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The ethnobotany and descriptive ecology of bitterroot, lewisia rediviva pursh (portulacaceae), in the… Bandringa, Robert W. 1999

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The Ethnobotany and Descriptive Ecology of Bitterroot, Lewisia rediviva Pursh (Portulacaceae), in the Lower Thompson River Valley, British Columbia: A Salient Root Food of the Nlaka'pamux First Nation  by  Robert W  Bandringa  A Thesis Submitted in Partial Fulfilment of the Requirements for the Degree of Master of Science in The Faculty of Graduate Studies (Department of Resource Management and Environmental Studies)  We accept the thesis as conforming to the required standard  The University of British Columbia October 1999 © Robert W  Bandringa, 1999  In  presenting  degree freely  at  this  the  thesis  in  partial  fulfilment  of  University  of  British  Columbia,  I agree  available for reference  copying  of  department publication  this or  thesis by  of this  for  his  or  thesis  and  her  DE-6 (2/88)  QcUer  Columbia  / fT,  requirements that the  agree  may  be  It  is  representatives.  for financial  Department  Date  I further  scholarly purposes  permission.  The University of British Vancouver, Canada  study.  the  gain shall  not  that  an  advanced  Library shall  permission for  granted  by  understood be  for  allowed  the  head  that without  make it extensive of  my  copying  or  my written  Abstract Bitterroot, Lewisia rediviva Pursh, is a geophytic, leaf-succulent perennial endemic to the arid, intermontaine grasslands o f western North America. Its fleshy tap root has been and remains an important food stuff for many indigenous groups, including the Nlaka'pamux First Nation in the Lower Thompson River Valley o f British Columbia. A m o n g the Nlaka'pamux, bitterroot's high salience as a root food vegetable is evidenced by its practical use as a powerful foodstuff delicacy and medicinal morsel. This is further heightened by traditional beliefs and mythologies linking it to human ancestry. Ethnobotanical texts o f the Nlaka'pamux encode an array o f sophisticated management strategies and harvesting techniques that have enhanced this plant resource. The surrounding anthropogenic influences were identified and openly weighed in direct connection with the autecology o f the species throughout the Lower Thompson River Valley. Descriptive ecological sampling was undertaken at the floristic level alongside a number o f environmental variables in order to evaluate the local status and community characteristics o f bitterroot. The gathered data exhibited high levels o f variability within and between populations, signifying adaptation to a disturbance regime likened to longterm, human-induced manipulation. These ethnobotanical and ecological findings serve to promote an integrated mediation o f the cultural and vegetational aspects o f the species.  Table of Contents  Abstract  ii  Table o f Contents  iii  List o f Tables  vi  List o f Figures  vii  Acknowledgements 1.0  Introduction  1  1.1  Cultural and Physical Landscape  3  1.1.1  Ethnographic Background  4  1.1.2  Geographic and Climatic Environment  7  1.2  2.0  ix  Botanical Description o f Bitterroot  8  1.2.1  Taxonomy and Nomenclature  8  1.2.2  Distribution and Habitat  11  1.2.3  Morphology  12  1.2.4  Phenological and Biological Development  13  Nlaka'pamux Ethnobotany o f Bitterroot  17  2.1  Data Collection  18  2.2  The Ethnobotanical Text  19  2.2.1  20  2.3  2.4  Traditional and Contemporary Use  Harvest Design; Strategies and Techniques  27  2.3.1  Ownership  27  2.3.2  Timing and Scheduling  28  2.3.3  Harvesting Persons  30  2.3.4  Collection, Preparation and Storage  32  Collection  32  Preparation  35  Storage  37  2.3.5  Digging Implements  38  2.3.6  Transplanting  43  Social Significance o f Harvest Season  45  iii  3.0  2.5  Nomenclature and Folk Classification  48  2.6  Mythology, Rituals and Traditional Beliefs  50  2.7  Trade  56  2.8  Similar Ethnobotanical Species  57  2.9  Traditional Ecological Knowledge  58  Autecology of Lewisia rediviva in the Lower Thompson River Valley 3.1  Methodology  65  3.1.1  Study Sites  65  3.1.2  Vegetation Description  70  Species Identification  70  3.1.3  Environmental Parameters  71  3.1.4  Lewisia rediviva Population Characteristics  73  3.2  Data Analysis  74  3.3  Results  76  3.4 4.0  64  Vegetation Analysis  76  Environmental Analysis  80  Analysis o f Lewisia rediviva  83  Discussion  85  Overall Discussion and Conclusions Ethnobotanical Aspects  88  Ecological Considerations  91  Developmental Pressures  95  Literature Cited Appendix I  106  Raw scores o f the species matrix; percent cover values o f the 38 species in the seven plots used for the ordination  Appendix III  100  Nli'kesentem, as recorded by Teit (1912, p.297); "obtained from Nkamtci 'nemux"  Appendix II  88  108  Raw scores o f the environmental matrix; not all values were used for the ordination  Appendix I V List o f all taxa discussed in the text or present in one o f the seven survey sites o f Lewisia rediviva; left column gives scientific  115  binomial (alphabetically arranged) and author, right column gives common English name as well as previously referenced Nlaka'pamux names in italics  116  v  L i s t of Tables  Table 2.1  Ethnobotanical use of Lewisia rediviva by the Nlaka'pamux  Table 2.2  Nutritional constituents o f Lewisia rediviva roots [per lOOg] (Kuhnlein and Turner 1991, p.356-7)  Table 2.3  24  Anthropomorphistic characteristics o f bitterroot as recognised by the Nlaka'pamux  Table 3.1  21  53  Survey site descriptions o f traditional bitterroot harvesting grounds in the Lower Thompson River Valley  67  Table 3.2  Environmental variables used in habitat analysis  72  Table 3.3  Variables used in enumeration of Lewisia rediviva  73  Table 3.4  D C A species output from graph; Pearson (parametric coefficients o f r and r-sq) and Kendall (nonparametric tau) correlations with ordination axes (N= 63). Large values o f r and tau, indicating species with significant effects on the ordination axes, have been boldfaced  Table 3.5  79  N M D S Environmental Output from Graph; Pearson (parametric coefficients o f r and r-sq) and Kendall (nonparametric tau) Correlations with Ordination Axes (N= 7); significant rankings have been boldfaced  83  vi  L i s t of Figures  Figure 1-1  M a p of Nlaka'pamux Territory (as modified from Tepper 1994, p.#x)  Figure 1-2  Lewisia rediviva i n flower  Figure 1-3  Developmental / seasonal stages of Lewisia rediviva (clockwise  6 13  from upper left): 1) rosette form (most obvious i n midwinter - April); 2) budding (May - June); 3) flowering (May - July); 4) a mature fruit disseminule (species remains dormant throughout summer months, July - September)  14  Figure 2-1  Freshly collected and peeled bitterroot prior to steaming  35  Figure 2-2  Traditional buckhorn digging stick; digging bitterroot did not require the long shafted sticks used for deeply buried geophytes. Shorter digging sticks like the one displayed sufficed  Figure 2-3  39  Intricately carved designs on handle o f digging stick made o f antler (Teit 1900, p. 137)  40  Figure 2-4  Nlaka'pamux rock writing (York et al. 1993)  41  Figure 2-5  Typical traditional camping spot in Venables Valley under a Ponderosa Pine  Figure 2-6  A n example of bitterroot "lovers" sometimes used i n amulet-like symbolism  Figure 3-1  46  54  Survey site locations of traditional bitterroot harvesting grounds i n the Lower Thompson River Valley; see Table 3.1 for corresponding descriptions  Figure 3-2  G r i d format of plots used in survey sampling. The nine squares represent quadrat placements; drawn to scale (0.9cm = 1.0m)  Figure 3-3  66  69  Quadrat (Site) ordination from D C A o f cover data. Site names: 1 (Venables Valley), 2 (Ashcroft Manor), 3 (Red H i l l ) , 4 (Basque  Figure 3-4  Ranch), 5 (Cornwall Creek), 6 (Spatsum), 7 (Klootchville)  77  Species ordination from D C A o f cover data  77  vii  Figure 3-5  Plot Ordination from N M D S o f environmental parameters. Plot numbers designate study sites: p i (Venables Valley), p2 (Ashcroft Manor), p3 (Red H i l l ) , p4 (Basque Ranch), p5 (Cornwall Creek), p6 (Spatsum), p7 (Klootchville)  Figure 3-6  80  Characteristics o f Lewisia rediviva measured at the seven plots. Y axis is a logarithmic scaling with weight categories in grams  84  viii  Acknowledgements Sincere thank you to my Supervisory Committee at the University o f British Columbia; Dr. Gary Bradfield (Associate Professor, Department o f Botany), Dr. Brian Compton (Honorary Research Associate, Department o f Botany), and Dr. Les Lavkulich (Director, Institute for Resources and Environment), as well as to Dr. Jack M a z e (Professor Emeritus, Department o f Botany) for serving as External Examiner. M u c h appreciation also to O l i v i a Lee ( U B C Herbarium), Dr. Terry Mcintosh (Biospherics Environmental Inc.) and Dr. Nancy Turner (School o f Environmental Studies) at the University o f Victoria. W i t h heartfelt gratitude I thank the Nlaka'pamux Nation Tribal Council for affording me the opportunity to participate in this study and to all those individuals who shared their knowledge, home, wisdom and experiences with me. Special thanks to Debbie Abbott, A n n Beckett, Evelyn Beckett, Lorraine Campbell, Leslie Edmonds (Chief, Ashcroft Band), Rita Haugen, Saraphine Kirkpatrick, Madeline Lanaro, Wilfred L u l u , Jack M i l l e r , Verna Miller, Robert Pasko (Chief, Oregon Jack Creek Band and Chief, Nlaka'pamux Nation Tribal Council), Nathan Spinks, Ruth Peters, Percy Minnabarriet, Marie Minnabarriet and M a r y Sampson. Recognition and thanks also to James Friesen for consulting support with maps and figures.  1.0  Introduction Bitterroot, Lewisia rediviva Pursh, is a geophyte native to the cool steppe,  intermontaine grasslands o f west central North America. Continental evaluation o f the species is considered to be 'not endangered', that is, in correspondence to definitions given by the 'Flora o f North America Project' (Taylor and M a c B r y d e 1977). Within British Columbia, however, this conventional ranking is challenged i n light o f the species rather limited and oft marginalized habitat abreast its traditional and provisional importance as a root food of Interior First Nations. M a n y view bitterroot's present and future status to be provincially threatened (Couplan 1998, Kuhnlein and Turner 1991). The Nlaka'pamux First Nation o f British Columbia have raised earnest and emphatic comment as to the species' localised diminishment caused in part by the cumulative effects o f development. A s contained within their territory, the area o f the Lower Thompson River is an historically rich locality for bitterroot. While being part o f the 'dry belt' biome in British Columbia, it remains a largely neglected region o f study for the species, in both botanical and cultural terms. Past research on bitterroot has been broad but shallow, especially in address o f anthropogenic influences. Studies have looked at its ecological life-history (Daubenmire 1975), ecophysiological characteristics (Marvel 1986) and systematic implications o f the wood anatomy o f Portulacaceae (Carlquist 1998). Perhaps the most fascinating and historically pertinent papers however are by Davidson, who in 1914 and 1915 recorded some preliminary information specific to the species in the Lower Thompson River Valley. O f interest also is a paper by Wilson et al. (1988) who included cultural means as a possible dispersal mechanism o f the species into southern Alberta. A s to the content  1  and nutritional value o f bitterroot, chemical analyses have also been made; Daubenmire (1975) cites a brief investigation made a century ago by Paillieux and Bois (1899) while more recently, Kuhnlein and Turner (1991) made a thorough documentation o f its nutritional constituents. Ethnographic research related to the species has been o f moderate consequence. A m o n g the many indigenous Nations o f arid North America, bitterroot is frequently mentioned and referenced as an important root food and medicinal plant as well as a valuable cash crop (Moerman 1998). However, these citations are within the context o f multiple plant inventories and little i f any attention has been given to it on an individual basis. Pertinent to the Nlaka'pamux, ethnographic study by Teit (1898, 1900) as well as inventorial ethnobotany by Steedman (1930) and Turner et al. (1990) have given introductory attention to the species. W i t h many intriguing ethnobotanical plants and subjects worthy o f exploration, it is significant to note that the genesis o f this study emerged through a felt need o f the Nlaka'pamux. Chiefs, Elders and administrators took initiative to cooperatively delve into the status and traditional knowledge o f bitterroot, the plant they so intimately know as IhQuoopen. The species remains to be a precious and delighted upon resource for their people, holding rich traditional and contemporary value. The need for attention to this species was born not only in protection o f the highly venerable plant but also in affirmation and sustentation o f their culture. It is in this complementary nexus o f biocultural diversity that ethnobotanical and ecological investigation shines. They are interrelated and coactive aspects o f the same history; human activity and influence on flora can affect the latter's ecology, while the  2  genetic and phenological makeup o f a species may govern its degree o f cultural significance. The objectives o f this study are twofold: 1) to add to the greater ethnobotanical text o f the Nlaka'pamux by summarising the cultural, spiritual, social and physical saliency o f the species' use and management, and 2) to give analytical attention to how the roles o f human activity and their consequences have influenced the structure and evolution o f local vegetation, thereby elucidating that the species ecology cannot be separated from its ethnobotany and vice versa. Subsequent to the remainder o f this chapter outlining the people and place o f the Nlaka'pamux as well as a botanical overview o f bitterroot, the following chapters explore the ethnobotany and ecology o f the species. Chapter 2 focuses on the traditional knowledge and use o f bitterroot by the Nlaka'pamux, while Chapter 3 describes its autecological status in the Lower Thompson River Valley o f British Columbia.  1.1  C u l t u r a l and P h y s i c a l Landscape  The unique geology, climate and biological environment o f the Lower Thompson River Valley has given rise to a delicate but unyielding land coloured with the desert hues o f sagebrush, cacti and bunchgrass. Its dry, sandy soil and undulating hills have provided a becoming backdrop for a kinship, enchanted and enacted between bitterroot and the Nlaka'pamux People. A s a semi-arid habitat, the Lower Thompson is unmatched in situation across the whole o f Canada. It has a profound and rich natural history that parallels a startling chronicle o f Nlaka'pamux connection to the land. Archaeological evidence suggests First Nations have occupied the region for over 9000 years (Bordon 1968) while oral  3  tradition affirms indwelling since time immemorial. The unique climate and terrain coupled with historical interaction o f the Nlaka'pamux has led to its emergence as a kind of 'biocultural epicentre'. Truly, it is a place o f invaluable biological and cultural wealth. 1.1.1 E t h n o g r a p h i c B a c k g r o u n d The Nlaka'pamux are an Interior Salish First Nation in the province o f British Columbia. Their language is one o f twenty-three Salishan languages and a member o f the Northern Interior subgroup o f the Interior Branch o f the family (Thompson and Thompson 1996). The traditional territory o f the Nlaka'pamux covers a large region o f south-western British Columbia and a portion o f northern Washington that encompasses a part or whole o f the Fraser, Thompson and N i c o l a River valleys (see Figure 1-1). Their culture is classed in the Plateau cultural area although the influences o f coastal (Northwest Coast) and northern (Athapaskan) traditions are also prevalent. These influences are due in part to historical intermediate trade and travel between the adjacent groups. Earlier this century, the ethnographer James Teit (1900) reported that the Nlaka'pamux lived in 66 village communities, arranging themselves into five distinct bands. Extensive contact with other First Nations combined with adaptation to dissimilar resource environments brought about notable cultural differences among the bands. Based on these geographical and lifestyle contrasts, Teit (op. cit.) gave reason to categorise the Nlaka'pamux into 'Upper' and ' L o w e r ' divisions. Roughly, the ' L o w e r ' division encompassed the Nlaka'pamux residing south o f Lytton whose sedentary lifestyle had a strong dependence on the salmon (Oncorhynchus  spp.) resources o f the  4  Fraser River. Members o f the 'Upper' division inhabited regions west o f Lytton whose semi-nomadic subsistence was based over a greater number o f natural environments. The semi-nomadic movements o f the Upper Nlaka'pamux (whose territories equate roughly with that o f the concerned bitterroot populations) did not cover great geographic distances but was based on more local, elevational transitions. In general, they would dwell in the valley bottom o f the Thompson River during the winter months, living on subsistent gatherings o f the previous seasons. From there, as temperatures warmed into summer, the Nlaka'pamux would follow game up into alpine regions, collecting plant materials and berrying along the way. Evidence o f sh.EEshtkin, or cache pits in which they temporarily stored gathered goods, spaced out at various elevations throughout the Valley also points to this local migration. The name Nlaka'pamux is thought to be formed from the lexical root nkukuma, meaning 'above' or 'to the north', combined with the suffix mux, meaning 'people' (Teit 1900). Depending on the orthography chosen,' Nlaka'pamux has been variously spelled Ntak a pamux, Nlha7kapmx, Ntlakapamuq, Nl'Akapmx and Ntlakyapamuk. Originally, this was an internal name in reference to the 'Nlaka'pamux' living towards the northern boundary o f the territory or those o f the 'Upper' division. However, it is now used commonly to denote the entire Nation. Past, non-indigenous names for the Nlaka'pamux have included the 'Couteau' or ' K n i f e ' people, as by early French explorers, and less recently the 'Thompson Indians', as they were called by settlers because o f their proximity to the Thompson River.  ' Unless otherwise noted, all orthographic transcriptions throughout this paper are as provided by Chief Robert Pasco on behalf of the Nlaka'pamux Nation Tribal Council.  5  Figure 1 - 1  M a p o f Nlaka'pamux Territory (as modified from Tepper 1994, p.#x)  6  Currently, as is the case with the majority o f First Nations in British Columbia, the Nlaka'pamux now organise themselves by way o f bands and tribal councils. O f late, the Nlaka'pamux Nation is made up o f 16 bands, with a population o f roughly 7000 within the commission o f three councils; namely the Fraser Canyon, the N i c o l a Valley and the Nlaka'pamux Nation Tribal Council. Despite traditional and contemporary cultural variations between the various bands and councils, the Nlaka'pamux remain to share a common identity, speak a common language, use a common name and cite a common origin (Wyatt 1998), a relationship strengthened by the sharing o f common resources as well. 1.1.2  Geographic and C l i m a t i c E n v i r o n m e n t  The Lower Thompson River Valley is located in the central interior o f southern British Columbia. It is a fringe land, nestled in the rainshadow outskirts o f the Coast Mountain Range while left hanging on the northern most fingers o f an arid belt reaching from the heart o f Mexico; consequently, mean annual precipitation is relatively low (206 mm). The climate is comprised of moderately dry and cold winters (mean daily minimum temperature in January is -10.1°C) but with especially dry and hot early summers (mean daily maximum temperature in July is 29.61°C) (Atmospheric Environment Service 1982). The regional area o f the Lower Thompson contains a handful o f biogeoclimatic zones; however, the boundaries o f this study are contained within a single zone, the Ponderosa pine - bunchgrass zone (Krajina et al. 1978). Although the plant communities of interior regions are less productive in terms o f biomass as compared to coastal forests,  7  they house a far greater diversity o f species. This makes the interior an extremely important and unique biome within British Columbia and all o f Canada. The jagged and rock-strewn channel coursed by the Lower Thompson River arose from the plate subduction o f a tectonic fault line. From this rugged volcanic beginning the valley opens up onto the fertile steppe plains that made early settlers in the nearby town o f Ashcroft famous for their vegetables. Gradually these plateaux round into windswept grassland hills where upper edges eventually give way to forest and alpine meadows. K n o w n as part o f British Columbia's dry belt, this picturesque intermontaine valley supports a vast array o f life. A l o n g with human inhabitants (Homo sapiens), mule deer (Odocoileus hemionus [Rafmesque]), black bear (Ursus americanus Pallus), cougar (Felis concolor Linnaeus), western rattlesnake (Crotalus viridis Rafmesque), osprey (Pandion haliatus [Linnaeus]), hummingbird (various species) and many other species commonly share the valley as home.  1.2  Botanical Classification and Description of Bitterroot  Bitterroot's rosette of fleshy, cylindrical leaves appear immediately after the snow melts and pump food into the thick, starchy root. By early May the leaves have completely disappeared and the flowers sprout off the ground without any sign of green, as if the plant was some leafless saprophyte (Cannings and Cannings 1996).  1.2.1  Taxonomy and Nomenclature  Lewisia rediviva is a member o f the Portulacaceae (Purslane Family). This dicot family, which is classed in Order Caryophyllales, contains 19 genera and roughly 500 species that are widespread in warm temperate climates around the world (Zomlefer 1994). The Family is especially abundant in southern Africa, southern America and western North America; succulence is recognised to be extensive (Hitchcock et al.  8  1964). The genus Lewisia, which contains 15 species, is endemic to western North America, residing almost entirely within the United States (Hitchcock and Cronquist 1973). Although Lewisia rediviva has been a well recognised and heavily used plant by many Indigenous Peoples o f western North America for millennia, it is a relatively recent addition to the floral inventories o f western science. Lewisia rediviva was first collected by Captain Meriwether Lewis (1774-1809) o f the famed Lewis and Clark expedition, purportedly on July 1 or 2 in the year 1806. The type specimen was collected by Lewis, after whom the Genus is named, near a gravelly stream at or near what is now known as Traveller's Rest, along L o l o Creek near its confluence with the Bitterroot River in Missoula County, Montana, which has since made bitterroot its state flower (McCourt 1999). The lectotype is presently housed at the Academy o f Natural Sciences in Philadelphia, P A . Frederic Pursh was the first to describe L e w i s ' specimen, establishing himself as the authority o f both the genus Lewisia and species L. rediviva in Flora Americce, published in September, 1814 (Jackson 1895); Lewisia rediviva remains the type species of the genus. Events surrounding the specimens' description are astonishing and curious (Daubenmire 1975). A gentleman by the name o f M r . M ' M a h o n , with hint that the plant still contained life though already being stored for some time, took the specimen out o f the herbarium and replanted it. Amazingly, it took root and lived for over one year! With this account in hand, as the Latin epithet suggests, Pursh gave testimony to its reclamation o f life; redivivus meaning to 'revive from a dry state', 'to restore', or 'to live again' (Featherly 1965). The plants reviviscence was also insinuated through a voucher  9  collected by John Davidson on the 15th o f May, 1915 and deposited at the University o f British Columbia's Herbarium (collection number not stated; Accession #063207). Anecdotal information as to the vouchers preparation reads that the "...specimens had to be dipped in boiling water to k i l l them in order to prevent them from growing after they were mounted on the paper." More recently, the author o f this paper faced the challenge of curating Lewisia rediviva by making use of a quick stint in a microwave oven! Succeeding nomenclatural history of Lewisia rediviva has remained relatively straight-forward. Although variations in perianth colour and flower size have been distinguished, with consequent names L. alba (for white flowers) K e l l . and L. minor (for small plant size) Rydb. respectively, their classification was not conferred by modern taxonomists, namely M u n z , 1968 (Hitchcock et al. 1964, Daubenmire 1975). The differences were seen as mere biotypical variations with only varietal status being given to the latter, L. rediviva var. minor (Rydb.) M u n z (Daubenmire 1975). N o other varieties or subspecies have been successfully described or brought forward. Lewisia rediviva is known in vernacular English as "bitterroot". A s reported by Coues in 1899, it appears the name arose as a literal translation o f racine amere, as given it by French explorers (Daubenmire 1975). Additional, more idiomatic names abound but are rarely applied today. These include "sandhill rose", "desert rose", "rock rose", "reviving lewisia" and "resurrection flower" among others. Names for the plant also have been plentiful among indigenous peoples, usually varying regionally from Nation to Nation. Spait'lum, spitlum, Ikupen, chita and kon-ah are readily used today; IhQuoopen as used by the Nlaka'pamux First Nation. O n the whole, however, "bitterroot" is widely accepted and well representative o f the species for those obligatory to common names. It  10  should be noted that in the Pacific Northwest, the hyphenated spelling varient "bitterroot" has also be used as one o f the common names for Apocynum androsaemifolium  L.  (Apocynaceae), as well as for other species in the genus Lewisia. 1.2.2  D i s t r i b u t i o n and H a b i t a t  Endemic to western North America, the overall distribution o f bitterroot reaches southward to southern California, eastward to Wyoming and northward into southern British Columbia. However, principal populations are found west o f the continental divide, being most widely throughout the northern cordillera o f the R o c k y Mountains. Within intermontaine steppe grasslands, bitterroot is limited to arid, mostly exposed locations where the majority o f precipitation falls during the winter. The edaphic ecology o f this species is characterised by thin, rocky to gravelly, heavy or serpentine soil that is dry and often desiccated in early summer. Terrain varies from scabland to rimrock areas throughout bunchgrass plains and lower elevation mountain slopes. The overall distribution o f bitterroot reveals a preference for areas with dry and hot summer patterns but with winter temperatures ranging from mild (as in California) to severe (as in Montana). The apparent broad discontinuities o f range in some o f the more southern and eastern states have been interpreted by Daubenmire (1975) as being o f a climatic nature. It is suggested that retractions moving in the north-west direction are a result o f "post-xerothermic weakening o f the westerlies" that have also been accompanied by northward range extensions into the warm valleys o f British Columbia (p. 11). Past xeric climatic changes with dispersal during the Altithermal have also been argued in explanation o f a newly discovered disjunct occurrence o f the species in southern Alberta (Wilson et al. 1988).  11  Within British Columbia, local distribution is on the east side o f the Cascades, being limited to the driest regions o f the southern interior, namely the Okanagan, southern Kootenay and lower Thompson River valleys. A brief scan o f provincial collections deposited at the University of British Columbia's herbarium reveals a strong southern representation o f the species in and around Penticton and Osoyoos with peripheral collections being few. A s a crude parallel to range limits, the easternmost locality is recorded near Kimberly with the northernmost collection being made near Clinton, a town roughly 35 kilometres north-northwest o f Ashcroft. 1.2.3  Morphology  Bitterroot is a succulent 2 - 6 cm tall geophytic herb (see Figure 1-2). Its root system is composed o f a thick, fusiform and often forked taproot with one to several lateral roots originating just below the hypocotyl. The roots are very tenacious and when stripped o f their thin brown peridermal layer reveal a bright white to slightly pink mucilaginous flesh. The foliage o f this ground-level, acaulescent plant is in the form o f a rosette, arising from a simple or branched stout woody base. The basal cluster o f lance-like leaves can be up to 10 - 12 cm in diameter. The leaves are succulent and numerous (up to 30), subterete and obtuse, dark green and glabrous, from 3 - 7 cm in length. They usually shrivel and turn red immediately prior to anthesis. The flowers arise from 2 - 6 cm high scapes, which are jointed just above middle of scarious bracts; although a rosette usually bears no more than 10 flowers, some plants were recorded with over 20 flowers collectively. The flowers are solitary, 3 - 5 cm broad. Sepals are 5 - 9 , oval and imbricate, 1 0 - 2 5 m m long with the inner ones  12  Figure 1-2  Lewisia rediviva in flower  appearing petal-like. The petals are 10 - 1 6 , oblong, entire to erose, 18 - 35 cm long. Petal colour ranges from white to rose to deep pink, at times displaying prominent pink veins. The fruits are capsules containing discoid seeds 2 - 2.2 m m in width. The seeds are black to dark brown, smooth and shiny. 1.2.4  Phenology and Biological Development  Bitterroot is a hardy perennial that flowers in M a y to June, habitually disappearing as quickly as its flowers first appeared in the spring. A s a winter ephemeral, this disappearance is due to a summer dormant period; after abscission o f the flowers, the leaves as well as scapes are completely withered, making it almost impossible to locate specimens between the months o f July to September. H i g h soil  13  Figure 1-3  Developmental / seasonal stages of Lewisia rediviva (clockwise from upper left): 1) rosette form (most obvious in midwinter - April); 2) budding (May - June); 3) flowering ( M a y - July); 4) a mature fruit disseminule (species remains dormant throughout summer months, July - September)  temperatures maintain the species' dormant condition while thermoperiod rather than photoperiod influences are thought to break its dormancy in the fall (Daubenmire 1975). A t least in the northern regions o f distribution, the entire growing season is contained in roughly a seven month window; early October to m i d M a y (Daubenmire 1975). Aestivation is broken in mature specimens with the first rains o f the wet season (usually in early October), when the short, erect, rosette foliage is at its smallest diameter. This autumn growth phase is also when germination o f seeds usually starts, with small taproots beginning to appear soon after. Foliage is maintained through the winter with leaf elongation continuing into the early spring months. M a x i m u m rosette size is reached just before the appearance o f floral buds. Anthesis usually begins mid M a y , roughly one month after buds become visible arising from the centre o f the rosette. Flowering occurs for up to three weeks with dissemination taking place shortly thereafter. Open most fully from midmorning to midafternoon (with full sun not always essential), individual flowers attract pollinators for one to two days. Pollination is thought to be accomplished by a wide variety o f w i l d bees (Daubenmire 1975); however, it should be mentioned that the author also commonly saw scores o f ants crawling among open flowers, signalling them as practicable pollinators as well. Seed dispersal occurs two to four weeks after initial pollination when the closed, dried flowers, serving as disseminules, drop from their respective peduncle. Seeds are arranged with free-central placentation and are loosely attached; Daubenmire (1975) found an average o f 17 seeds per flower in one specimen. Disseminules, which measure about three cm in diameter, are papery and light and weigh no more than 0.1 g  15  (Daubenmire 1975). This makes wind the most conspicuous proponent for natural, unaided dispersal.  2.0  N l a k a ' p a m u x Ethnobotany of Bitterroot Modern ethnobotany is defined by and concerned with the "totality o f the place o f  plants in a culture" (Ford 1978). It is the study o f contexualised plant use, or "planthuman interrelationships embedded in dynamic ecosystems made up o f natural and social components" (Alcorn 1995). A s a constituent within the greater discipline o f ethnoscience, ethnobotany examines the reciprocal relationships which occur between traditional societies and the natural world. Specifically, ethnobotany includes any such studies related to plants, including how they are classified and named, how they are used and managed, and how their exploitation has influenced their evolution (Cotton 1996). Ethnobotanical texts o f British Columbian First Nations are on the whole well documented. However, some texts remain fragmented, incomplete or even non-existent, at least in western academic formats. While the living knowledge o f First Nation ethnobotany w i l l continue to be a dynamic and growing process, recent attention has been given to view existing inventories in a more comprehensive manner. Ensuing special topics in First Nation ethnobotany has delved into distinct sub-topics such as archaeobotany, medicinal plants, plant foods, ethnoclassification systems and species investigations (Turner 1995). In regard to species investigations, various papers have already been written (Loewen 1998, Turner 1982, Turner 1988), incurring and bolstering the need for other salient species to be studied as to their use and management in autecological and specific terms.  17  2.1  D a t a Collection  Through the auspices o f the Nlaka'pamux Nation Tribal Council ( N N T C ) , representing the Lytton, Ashcroft, Oregon Jack Creek, Boothroyd and Boston Bar Bands, Nlaka'pamux Chiefs, Elders and other knowledgeable members were invited personally by the council to participate in the traditional use study on bitterroot. A n enthusiastic and generous cooperation was given from the Nlaka'pamux Nation as a whole with opportunity to share key interviews with twelve individuals. Listed alphabetically below, the participating Nlaka'pamux consultants represent a range o f demographics from a number o f different bands:  Evelyn Beckett (Ashcroft Band) Lorainne Campbell (Lytton Band) Chief Leslie Edmonds (Ashcroft Band) Rita Haugen (Lytton Band) Saraphine Kirkpatrick (Ashcroft Band) Madeline Lanaro (Lytton Band) M a r i a Miruiabarriet (Bonaparte Band; Secwepmc) Percy Minnabarriet (Cooks Ferry Band) Chief Robert Paska (Oregon Jack Creek Band) Ruth Peters (Lytton Band) M a r y Sampson (Ashcroft Band) Nathan Spinks (Lytton Band)  Informal qualitative methodologies were used to gather and document traditional botanical knowledge related to bitterroot . Open-ended (semi-structured) interviews with 2  the Nlaka'pamux consultants were recorded on audio tapes as well as in field notebooks. These interviews took place in participants' homes, places o f work and appropriate community settings with additional interviewing taking place on field trips to various  Research methodology for the interview process and study in general was approved by the NNTC and the Behavioural Research Ethics Board at the University of British Columbia. 2  18  local harvesting sites. Copies o f all interview records have been deposited at N N T C facilities for storage in their archives. It is recognised that the interviewing format was a limited and relatively brief process (from A p r i l to June 1999) insomuch as representing the vast and diverse knowledge and use o f bitterroot by the Nlaka'pamux in its entirety. A s given by Campbell et al. (1986) i f a species-area curve were to be graphed, with the number o f interviews and applications taking their respective x-y axis', a highly salient species such as bitterroot would reach asymptote a great deal slower than a species o f limited value or occasional use (cf. Balick 1994). Thus said, the research was not conclusive and should rather be viewed as a snapshot in time. However, the Chiefs, Elders and other knowledgeable Nlaka'pamux do represent a comprehensive core and a wealth o f knowledge that has been amassed over hundreds, i f not thousands o f years. The ethnobotanical data contains new information (that is at least previously unrecorded) that cannot help but strengthen the empirical text as to the place and plant o f bitterroot in the Lower Thompson, as instituted by the Nlaka'pamux.  2.2  T h e Ethnobotanical Text  Plants have always been integral and meaningful in Nlaka'pamux culture. A s confirmed by a plenitude o f names and uses for the many plants found throughout their territories, their ethnobotanical text is one of, and possibly the largest in Canada. In the 3  category o f edible plants for example, the Nlaka'pamux have used some 120 species as foods, flavourings or beverages (Kuhnlein and Turner 1991, p.20). A s a morphological  3  A s used b y A l c o r n (1995), an  ethnobotanical text,  i s " . . . d e r i v e d p a r t i a l l y f r o m the n a t u r a l , s o c i a l , a n d  cultural contexts ...around a h u m a n c o m m u n i t y ' s use and management o f vegetation (p.24)".  19  annex within this host o f plants, roots and their harvesting regimes are also prominent. Roots are often animate within Nlaka'pamux mythology and traditional calendars were even based on their consummation for digging (Steedman 1930); "...at Spences Bridge, the seventh moon was designated as 'the people dig roots' moon (p.478)". Roots have been used as sources o f food, medicine, dye, basket material and cordage (Steedman 1930), but in both abundance and significance, most distinguished as food. A m o n g edible root vegetables used by the Nlaka'pamux, bitterroot has been preeminent, lending itself to heavy use as the roots are thick, high i n starch and contain virtually no lignified xylem (Daubenmire 1975, Steedman 1930). It attained prized 4  stature as well, in part because not only was its availability limited on a temporal and spatial basis, even locally throughout their territory, but it was a comparatively high timeconsuming plant to harvest and prepare. Extensive systems o f cultural (e.g. ownership, timing, mythologies) and cultivational (e.g. use o f digging stick, transplanting) management strategies and techniques have surrounded its use. The resulting beliefs and practices o f the Nlaka'pamux have placed the species i n an almost ethereal light within their culture as well as creating an anthropogenic environment specific to the population and community scales which bitterroot grows. 2.2.1  T r a d i t i o n a l and C o n t e m p o r a r y Use  Although bitterroot has been a highly sought-after and cherished species o f the Nlaka'pamux, its role i n daily sustenance was not as extensive as other commodious-type root food species (i.e. Claytonia lanceolata, 'spring-beauty' and Erythronium grandiflorum, 'yellow glacier l i l y ' ) . Bitterroot is considered a delicacy or speciality food  The nutritional worth of bitterroot also proved to be particularly valuable as a survival food in times of winter and / or early spring scarcity (Turner and Davis 1993).  4  20  with prominence arising out o f its mythological, social, environmental and nutritional worth. Personal comments heeded by the Nlaka'pamux described bitterroot as a "strong plant", an "all-body healer", a "real concentrated food", the "best meal there i s " and a "powerful plant and a powerful food". Given its multiple and diverse uses listed below (see Table 2.1), the species should be regarded as a unique and highly salient root food rather than an everyday staple root food. Table 2.1  Ethnobotanical Use of Lewisia rediviva by the Nlaka'pamux  Categorical Use Food main dish  Specific Use and Preparation Notes dumpling-like stew; known as 'IhQuoopen soup' with salmon eggs [AQuen], saskatoon berries (Amelanchier alnifolia [shchAquem]), sugar or salt added (flour was also added for extra thickening into a gravy) fresh vegetable (alone); very lightly steamed, sometimes with salt and butter added or sugar lightly sprinkled on top fresh vegetable (mixed); steamed together with Yellow Bell bulbs  (Frittilaria pudica) boiled vegetable; soak the dried IhQuoopen in water and then boil delicacy / dessert  fresh vegetable; eaten raw while harvesting or peeling extra ingredient in bannock, a traditional flat bread; crush up a few dried  IhQuoopen and mix well soup-like pudding; mixture known by the name of its main ingredient IhQuoopen as well as flour, sugar and a little bit of beef fat all mashed together (the more sugar added prior to cooking, the less needs to be added after) Medicine general therapeutic  general all-body-healer medicine; "good for colds and everything", steep roots in boiling water and drink as a hot tea, or for a fuller effect eat entire preparation like a hot soup blood purifier and cleaner; cooked roots (preparation not specified) digestive tract & body cleanser; an after winter 'clean out food', eaten like a fresh vegetable as a 'first food' in the spring to clean digestive tract out after all the dried meat and dried fish consumed during winter months tonic; as a medicinal to keep one from ageing too quickly, keeps hair from going grey and skin is slow to wrinkle; used year round as a weekly supplement added to diet; (preparation not specified) eyesight enhancer (general); eyes will become clear when large volume of roots eaten quickly all at once (preparation not specified) lozenge and vocal chord enhancer; raw roots chewed and juices swallowed to prevent voice from growing hoarse while singing or chanting over long periods of time immune system enhancer; eaten (preparation not specified)  21  acute treatment  Other amulet spiritual offering ornamental  poultice; dry, ground up root made into a powdery ash-like poultice and applied directly on cuts and abrasions; noted that preparation does not sting eaten to soothe and heal stomach ulcers (preparation not specified) laxative; eaten or prepared as a tea eaten or prepared as a tea for treatment of diarrhoea, something to 'plug you up' upset stomach soother; eaten (preparation not specified) bronchitis [pleurisy]; eaten (preparation not specified) tuberculosis [consumption]; eaten (preparation not specified)  as used between newlyweds, two human shaped roots buried or stored together as a symbol of good marriage dried roots presented as an aim and offering by Nlaka'pamux members at inter-tribal Powwow gatherings occasionally transplanted to personal home gardens for practical and ornamental value  A s an edible plant, preparation o f bitterroot was not unlike other root foods used by the Nlaka'pamux. However, bitterroot was an extremely versatile plant in the sense that the roots could be eaten raw or cooked, alone or in a mixed dish; they were even steeped as a tea. If the roots were cured for storage, either before or after cooking, it was only a matter o f soaking them for a few minutes in warm water to reconstitute and tenderise them before consumption. Fresh roots were consumed raw or lightly steamed while the dried roots were usually boiled to be eaten alone or added to a variety o f souplike stews o f which salmon eggs were a common ingredient. A s in traditional times, along with other root food vegetables, a favourite but occasional method o f cooking bitterroot is to steam in subterraneous pit ovens (Frye 1993). Bitterroot was also prepared in bannock and dumplings which had an almost dessert-like appeal. Their basic recipe called for water, flour, salt and or sugar with any combination o f bitterroot, saskatoon berries (Amelanchier alnifolia) or other available berry ingredients. Even today, some Nlaka'pamux prepare this kind o f bannock and store it in a crock to be given to children as a treat like a fruit roll. O f late, however,  22  bitterroot is most often treated as a delicacy, being prepared for special occasions like a potlatch. A t gatherings, dried bitterroot is frequently presented to Elders as a respected take-home gift or served in a stew-type dessert soup o f which everyone present is welcome to partake from the communal pot. The bitter taste o f the root (which is often an indicator o f medicinal value in plants by signalling the presence o f alkaloids or other phytochemical compounds), is thought to vary on a seasonal, environmental and preparatory basis. Teit reported that the roots were only palatable after cooking because they were too bitter in their raw state (Steedman 1930). However, the experiences o f the Nlaka'pamux and the author found this to be quite the contrary. Never-the-less, the relative bitterness o f the root body is acknowledged by most Nlaka'pamux as being slight, although some o f the younger generations still prefer to sprinkle sugar or salt on the root as a countermeasure. O n the whole, the Nlaka'pamux recognise that the astringency seems to dissipate when one becomes accustomed to it. A s Chief Lesley Edmonds asserted, " i f you acquire a taste for it you crave it, ...every year you think about it and crave for it", the "...bitterness, you can't notice it". A l s o related to the culinary preparations o f bitterroot, Kuhnlein and Turner (1991) found differences in nutritional value based upon how the root was prepared (see Table 2.2). The consumption o f bitterroot via the drying process is the most widely used traditional and prevailing contemporary manner o f preparation. Although it appears that the greatest nutritional values are found in roots that were dried versus those that were assayed in fresh or frozen states, it can be accounted for as a result o f the dehydration process (i.e. lOOg's dry weight is a quantity o f greater concentration). The only notable  23  drawbacks to roots that had been dried were slightly lower or sometimes non-existent values for crude fibre, ash, some vitamins and other minerals. It should also be noted that although the outer skin or periderm o f the root could potentially contain some vitamins as well, the Nlaka'pamux have customarily peeled the skin and have not been known to have ever consumed them. Table 2.2  Nutritional constituents of Lewisia rediviva roots [per lOOg] (Kuhnlein and Turner 1991, p.356-7)  F o o d energy (kcal) Water (g) Protein (g) Fat (g) Carbohydrate (g) Crude Fibre (g) A s h (g) Thiamine (mg) R i b o f l a v i n (mg) N i a c i n (mg) V i t a m i n C (mg) Vitamin A (RE) C a l c i u m (mg) Phosphorus (mg) Sodium (mg) Potassium (mg) M a g n e s i u m (mg) Copper (mg) Z i n c (mg) Iron (mg) Manganese (mg) M o l y b d e n u m (mg) Chloride (mg)  dry roots  frozen roots  fresh roots  343 12 4.0 0.6 81.0  94 76 0.9 0.2 22.1 1.3 1.2 0.10 0.03  94 76 1.6 0.4 21.6 1.5 0.9 0.10 0.02  -  -  -  -  -  17.0  27.0  -  -  -  168  22  39  -  -  -  -  20 85 3.1 0.1 0.7 1.6  16 75 10.9  19.8  1.3 5.3  -  -  -  1.0 4.9  -  In defining the categorical use o f bitterroot, although it is commonly referenced as a root food, some Nlaka'pamux thought it more agreeable in earmarking it as a medicinal plant. This supposive duality as to the plants' application lies in the fact that the Nlaka'pamux, as with many Indigenous Peoples around the world, often do not delineate between 'sustenance' and 'medicine' (Kuhnlein and Turner 1991). In compilation o f a North American ethnobotany, Moerman (1998) balanced this dichotomy  24  in recognising that "...medicinal plants were not completely distinct from food plants indeed, there was often substantial overlap in species that were used for both food and medicine (p.8)". Regarding the medicinal, therapeutic and nourishment value o f bitterroot, Chief Bob Pasco put it succinctly; "... there is always the food value but we know just through the food value itself, there is always medicinal value to it... IhQuoopen is a medicinal plus food". In this way, as its varied medicinal uses suggest, the Nlaka'pamux also beheld bitterroot as a kind o f all-body healer, much in the same way ginseng (Panax sp.) is prized in modern herbal medicine. In fact, many elders gave reference to the recent prolificacy o f ginseng fields in the Ashcroft area as confusing and unnecessary. To them, the redundancy o f introducing a plant so similar to their native IhQuoopen was folly. One elder remarked that upon seeing an alike root anatomy and morphology as well as hearing o f comparable uses, found reason to believe that bitterroot and ginseng were onein-the-same species; "...it is the same thing". The vigour and effectiveness o f bitterroot as a medicine was repeatedly referenced to by the Nlaka'pamux. One example, first shared by Percy Minnabarriet, but also mentioned by other Nlaka'pamux elders, gives factual account o f its potency over tuberculosis. Percy's Grandmother, Nancy Minnabarriet, who had an unofficial role as traditional doctor, was often called upon and visited by local Nlaka'pamux for assistance with various illness and other physical duress. Roughly 50 years ago, a 14 year old Nlaka'pamux girl was diagnosed with tuberculosis and instead o f being conscripted to a sanatorium, sought Percy's Grandmother for healing. The young girl was cured o f  25  tuberculosis in just under one year after being directed to eat a few pieces o f steamed bitterroot every evening after dinner. However, the Nlaka'pamux use o f bitterroot as a medicine also has some discontinuities that may seem puzzling within western paradigms. What is presented as seemingly opposite applications in regard to its medicinal use as a treatment for both diarrhoea and as a laxative is a paradox o f traditional plant use inherent and well documented among some other Indigenous Peoples o f North America (Moerman 1998). In a self interpretation o f this antilogy, the Nlaka'pamux Elder Saraphine Kirkpatrick stated quite light-heartily, " I f you get too much o f the bathroom you eat it and it w i l l stop,  ...and i f you don't go to the bathroom you eat it and it w i l l start; I don't know  which is which [laughing]". This statement in a sense nulls reasoning that the discrepancy arose as an error in understanding on part of the investigator, the Nlaka'pamux consultant, or both. It could be explained as being a matter o f medicinal worldview where western beliefs counter disease allopathically while traditional logic leans towards more homeopathic treatments. Or, it could be a matter o f dosage or delicate differences in preparation. Whatever the case, Moerman (1998) is not quick to dismiss these apparent contradictions as nonsense; "...there is much in medicine, any form o f medicine, that resists logic, rationality and explanation (p. 15)". The more contemporary uses o f bitterroot are growing but are not always familiar to some o f the Nlaka'pamux elders. One use that has become especially popular at powwows, is as a vocal chord enhancer.  5  Traditional drummers from a number o f  different First Nations w i l l often masticate the root and swallow the juices to strengthen  Bitterroot is noted by Scully (1970) to be chewed by North American Indians in alleviation of sore throats (cf. Daubenmire 1975).  5  26  and keep their voices strong while they sing and chant, which can last for hours at a time. Another recent application at Powwows is as an offering for the Sundance. The Nlaka'pamux give bitterroot in representation o f the uniqueness o f their people and territories, just as a coastal nation may present seaweed (various species) or salmon as an offering.  2.3  Harvest Design; Strategies and Techniques 2.3.1  Ownership  Traditional concepts o f natural resource site ownership existed and were practised among many First Nations in British Columbia. Ownership o f vegetable and berry resource sites, along with hunting, trapping, fishing, and the clam bed areas o f coastal groups were usually the property o f upper-class families where ownership was through inheritance (Suttles 1951). However, for the Nlaka'pamux , bitterroot and its harvesting sites remained in the control o f the greater corporate Nation. The ground where the roots were dug was considered common property (Steedman 1930 p.478). The main bitterroot harvesting sites for the Nlaka'pamux were and remain to be in and around the Ashcroft area corridor. M a n y members o f the Upper Nlaka'pamux, from the Lytton and Merritt Bands for example, came yearly to this region for the bitterroot harvest. But not only were these harvesting grounds shared intra-tribally, they were also used heavily by the Secwepmc (Shuswap) First Nation, specifically the neighbouring Bonaparte Band. A s understood by M a r i a Minnaberriet, "nobody owned the harvesting grounds; the Nlaka'pamux and the Secwepmc would both share it".  27  This communal outlook on harvesting sites, however, did not lack a sense o f local jurisdiction and responsibility. The welfare o f bitterroot populations remained in the hands o f the Nlaka'pamux who dwelled in the area as it was they who most benefited from its trade and long-term sustainability. Chief Bob Pasco says that "...there was a lot of people who came in here. I don't think that it was sort o f owned, ...but the people who lived here, they harvested a lot o f it and traded it to other people within the nation and outside; so I guess there was a bit o f ownership to it in that sense. ...the Okanagan have their own area..., but it would be the northern people who would come down [to Ashcroft] cause it doesn't grow any farther north". 2.3.2  Timing and Scheduling  "LhQuoopen is one of thefirstthings to come around...; it is like a bird in the spring" (Chief Robert Pasco) Subsistence activities o f the Nlaka'pamux followed and were patterned after the cyclical seasons in nature. Migration patterns o f game and fish as well as the climatic particularities o f the seasons were adhered to; however, their variability also forced the Nlaka'pamux to prioritise their needs. In regards to the spring harvest o f bitterroot (varying from late A p r i l to late June), no other subsistence activity took obvious precedence as it was one o f the first important plants to be gathered in the vernal season. The inaugural and primary importance o f bitterroot is also evident in some o f the traditional "First Roots" ceremonies conducted by the Nlaka'pamux that were centred upon its fruition o f harvest (see Section 2.6). A s winter lapsed into spring, bitterroot was one o f the most available and recognised roots in the lower valleys. It was symbolic o f spring in and o f itself as there were no extrusive biological or environmental indicators observed by the Nlaka'pamux  28  to signal its arrival and eventual maturation. O n a tertiary basis as indicators o f the resource species, some Nlaka'pamux did bring reference to the flowering o f 'saskatoon' shrubs, the greening o f notable choke cherry bushes (Prunus virginiana) and the pocketed flowering o f the concurrently harvested 'balsamroot' (Balsamorhiza  sagittata).  Also noted was the scented flowering o f lilac bushes (Syringa vulgaris) as a more recent horticultural indicator species common to the home gardens o f many Nlaka'pamux. A l o n g with the seasonal cycles preferenced in Nlaka'pamux culture, the physiology o f bitterroot also had a role in the timing o f its harvest. The tap roots were dug in the early spring when the rosettes were largest and most easy to locate before the flowers bloomed. This timing also allowed for the largest specimens to be located as the rosettes (whose diameter seems to have a bearing on root size - wider diameter suggests larger roots) had not yet completely shrivelled. Moreover, once flowered, no matter the size o f root, all flowers were equally proportioned which made selection for the largest individuals troublesome. A s a further indicator o f this growth stage, the Nlaka'pamux also chose to harvest bitterroot after it had budded but before it reached anthesis. This made for a short but intense harvesting season as the species above-ground parts disintegrate and essentially disappear after flowering in order to conserve all energy in the roots during the hot summer months. Some o f the rationale behind this particular timing includes that thereafter the root becomes too bitter to eat or loses the majority o f its nutritious substance (Couplan 1998). Although nutritional values o f the root have not been quantified seasonally,  6  The drought resistant capabilities of bitterroot are well documented and relay the fact that the species relies almost entirely on total nonstructural carbohydrate (TNC) reserves built up during the spring to support its autumn growth and winter maintenance (Marvel 1986). With high photosynthetic capacities 6  29  Nlaka'pamux reasoning is predominantly pragmatic in that it becomes too hard to peel after it flowers; the root is too elastic and the outer periderm is difficult if not impossible to separate from the muscilous root body without a lot of rubbing. As stated by Saraphine Kirkpatrick, bitterroot will "...stretch when they are getting too old, ...they won't even get clean; and they are ugly, bitter. I wouldn't touch it when it gets old. You have to get it before it flowers or just getting flowers." In addition, others mentioned that if harvested too late or too early, the stripped and dried roots would not remain a bright white colour but would eventually turn a light orange-red that was also equated to a bitter taste. The specific timing in harvest was not only important to, but in some ways also required, by the Nlaka'pamux. As upheld by Ruth Peters, "you have to pick them quick at a certain time. After that you leave it alone cause it is quite bitter and is not safe to eat (emphasis the authors)". Although phytochemical and ethnobotanical databases give no mention to poisons in Lewisia rediviva, reference to other First Nation plant foods containing toxins (Compton 1993a) justifies the possibility of seasonal toxicity and the need for further investigation.  7  2.3.3  Harvesting Persons  Among the Nlaka'pamux, as with most foraging and pastoral societies around the world, women have been the principle gatherers of vegetable and berry resources. In terms of the caloric contribution of subsistence plants gathered, Hunn (1981) points out that for groups of the Columbia-Fraser Plateau, of which the Nlaka'pamux are a part, roughly 70% of food energy needs came from plant foods harvested by women. This  during the spring in which to recover the storage reserves used during the autumn and winter, Nlaka'pamux timing of harvest coincides with the highest T N C levels. Within Portulacaceae, there is citation of the presence of alkaloids (a fairly low measure of 300 ppm) in the leaves of Portulaca oleracea <http://www.ars-grin.gov/duke/highchem.html>. 7  30  finding is quite contrary to most historical ethnographic accounts which have emphasised hunting contributions by men as being most primary. Teit's (1900) description o f girls puberty rites among the Nlaka'pamux also highlights women's integral and assumed role in plant gathering. Girls, at reaching puberty, were separated from other people at which time they would practice various artful and industrial skills that would demonstrate their readiness to contribute to society and provide for a family. The girls undertook some physical feats as well such as gathering wood, running and digging trenches, the last o f which might show proficiency at root-digging (p. 313). This division o f labour exhibited in Nlaka'pamux culture can be traced back further to mythological beliefs. A s noted in Section 2.6 (Digging Implements), the Creator gave specific instruction to the Nlaka'pamux that the digging stick was to be the woman's tool while the bow and arrow was given as the man's. Even the process o f pit-cooking vegetables was accomplished by groups o f women. Traditionally, no men were even allowed near the pit oven while roots were being cooked (Frye 1993). The spiritual nature and seriousness with which women approached the procuration o f root foods is also mentioned by Teit (Steedman 1930) in reference to face and body painting traditionally practised by the Nlaka'pamux. Painting a portion o f ones body or face was common and practised by almost everyone, young and old, o f both sexes. Various colours and designs were applied for a multitude o f reasons, be it as an offering, to show deference, to obtain success, or for protection. In particular, painting ones entire face red was usually used to ward off danger in correlation to bad dreams or to protect one from harm. It was this painting regime that nearly all women used while  31  d i g g i n g r o o t s , as " . . . i t w a s t h o u g h t t o g i v e t h e m s u c c e s s a n d p r o t e c t i o n , h e l p t h e m t o f i n d roots, a n d to d i g t h e m m o r e e a s i l y ; a l s o to p r e s e r v e t h e m f r o m h a r m w h i l e e n g a g e d i n their avocations" (p.438). S p e c i f i c to bitterroot, the c e n t r a l r o l e w o m e n p l a y e d i n g a t h e r i n g is a l s o h i g h l i g h t e d i n the n a m e o f a t r a d i t i o n a l d i g g i n g area.  " K l o o t c h v i l l e " (as n o t e d i n S e c t i o n  3 . 1 ) , is a s t y l i s e d s l a n g f o r m o f " w o m a n ' s p l a c e " b y the N l a k a ' p a m u x ;  "klootch"  m e a n i n g w o m a n . A s S a r a p h i n e K i r k p a t r i c k e x p l a i n e d , "...they c a l l it K l o o t c h v i l l e  'cause  the I n d i a n s are d i g g i n g roots there too m u c h . A l l the I n d i a n s , e v e n f r o m L y t t o n are d i g g i n g there, y o u see n o t h i n g b u t b u m s [ i n r e f e r e n c e to the s t o o p e d h a r v e s t i n g p o s i t i o n ] d i g g i n g Indian roots there." minimised.  H o w e v e r , the effeminate nature o f r o o t d i g g i n g has b e e n  In recent times, both m e n and w o m a n c o m m o n l y d i g a n d c l e a n bitterroot  together, a l b e i t the b u l k o f d i g g i n g is d o n e b y the m e n w h i l e the enterprise o f p e e l i n g r e m a i n s to be d o n e m o s t l y b y w o m e n .  2.3.4  Collection, Preparation and Storage  Collection  "...the Indians never cleaned it all out, just leave some here and there. You know they should leave some so they transplant themselves. They leave some, some small, they leave it; they don't take it all. They just leave it just to retransplant themselves. But if you take it all, it is all gone." (Saraphine Kirkpatrick) A s m e n t i o n e d p r e v i o u s l y , a p o r t i o n o f the v a l u e a f f o r d e d bitterroot is d e r i v e d f r o m the l a r g e a m o u n t o f t i m e a n d effort r e q u i r e d f o r its c o l l e c t i o n a n d p r e p a r a t i o n . S o m e N l a k a ' p a m u x b r o u g h t contrast to this fact b y m e n t i o n i n g the ease o f d i g g i n g u p d o m e s t i c potatoes that c o u l d q u i c k l y f i l l a r o o t c e l l a r , o r the g a t h e r i n g o f h u c k l e b e r r i e s o r s a s k a t o o n berries that w o u l d a p t l y f i l l a b a s k e t i n the m o r n i n g a n d b e d r y o n m a t s i n the afternoon sun. T h e harvesting o f bitterroot, h o w e v e r , required concerted a n d p l a n n e d  32  effort, having to know exactly where and when to look as well. Nathan Spinks recalled that even after picking all day, "...they picked six or seven sacks and when they peeled them were lucky to get a small little bag out of it when its dry". The Nlaka'pamux also repeatedly mentioned the alertness one needs while digging bitterroot, for it is during the time of year rattlesnakes are out. To them the digging stick can also serve as a probe and for extra safety, some Nlaka'pamux like to bring a dog along while digging. In selecting which individual bitterroot plants to harvest, besides the physiology already mentioned, the Nlaka'pamux did not have any steadfast rules for digging. Generally, however, the largest to medium-sized individuals were harvested while all the small and seedling-staged specimens were passed over; in a cluster, only the largest individuals would be harvested with the rest being allowed to mature. Although the selection for larger specimens also made for easier and efficient handling and peeling, other Nlaka'pamux gave more attention to the number of individuals harvested. To them, the differences between rosette diameters were perceived as comparatively minuscule and they were not overly specific about specimen size, "...as long as you left some". During the harvest, although focusing on bitterroot, the Nlaka'pamux would also dig other root foods they came across. In particular, the small but tasty bulbs of yellow bells (Frittilaria  pudica), whose harvesting stage often overlapped, were gathered as they  would occasionally be prepared together in a dish with bitterroot. In digging bitterroot, although there were no obvious and systematic routines found in association to a gathering format, it was selective. Within a locality, Nlaka'pamux would roam randomly throughout and dig where bitterroot seemed to grow thickest, moving on to new areas if evidence of prior digging was visible. The Elder  33  Maria Minnabarriet also spoke of how at times bitterroot seemed to blend in with the ground and camouflage itself. She recalled how her Grandmother explained that this meant the bitterroot "was hiding from you" and that it did not want to be dug up and picked. It is interesting to note that in areas where bitterroot is marginalised, it often grows scattered or only protected underneath sagebrush. This exhibits an indirect form of conservation and may be an incidental way of giving reason to leave bitterroot alone where it is sparse and to only dig where it is thick and immediately obvious for the gatherer to harvest. Traditionally, baskets were used in gathering plant resources, the birch-bark variety for berrying, and woven baskets for the collection of roots (Teit 1909). At later times, flour or sugar sacks were used and today plastic buckets and even shopping bags are employed as containers. As a rough indicator of the amount of bitterroot traditionally harvested, the size of the 100 pound white flour sacks are thought to point towards large volumes. With dozens of camps throughout the valley and perhaps hundreds of people digging, the number of these sacks that were filled was significant. Recollections of Mary Sampson also suggest this; "...as kids with our grandmother, picking it by the sackfulls..., you could go out there for days, out on the wagon, sackfulls of IhQuoopen. My hands got tired of IhQuoopen, fingernails wore out." Although a qualitative estimate, hundreds of thousands of plants were harvested annually in the early spring by local and touring Nlaka'pamux. These numbers have dwindled in recent years, both in number of people harvesting and volumes harvested, as a parallel to the more incidental use and need of bitterroot.  34  Preparation Once bitterroot was dug out o f the ground, the thin, brown and somewhat flaky, exfoliated bark o f the root was stripped off (see Figure 2-1). Traditionally, after a day gathering the roots, this 'stripping' was done by groups o f women in the evening at the camps set up by the harvesting sites. In modern times, after a number o f roots have been gathered, most Nlaka'pamux prefer to. take them home to be stripped later that day or left to soak in water for a couple days to keep them easy to peel until they were ready to process them. Some elders are even known to bury the roots in sand to keep them fresh until they are ready to peel them, but most Nlaka'pamux peel bitterroot on the day o f harvesting.  Figure 2-1  Freshly collected and peeled bitterroot prior to steaming.  35  If harvested at the right time, the peeling o f bitterroot was a relatively quick and easy process, the point when it is just starting to bud being most desirable. A t this stage, the periderm peels off with little effort by merely rubbing and rolling the root between the palms o f ones hands. If this optimum time is missed slightly, the periderm w i l l still rub off but with more effort required. In this case the Nlaka'pamux w i l l often employ the hard, flat surface o f a rock on which to rub and build up considerable friction with their hands or feet. When roots are stripped, the Nlaka'pamux w i l l also remove what they call the plant's 'heart' - a small, orange-red structure in the hypocotyl region that is a bud-like core o f the following years growth - as it is said to be too bitter to eat. The 'hearts' o f the bitterroot are considered by the Nlaka'pamux to represent the male sex o f the plant and it is treated as the male's 'seed'.  8  When the hearts are removed from the roots they are  disposed o f inconsequentially, although the Nlaka'pamux say that i f planted, the seed w i l l grow into a new plant. The next processing step o f bitterroot, after they had been stripped and 'dehearted', was to clean them with a light rinse in water. Once clean, the roots were ready to be dried. Although an antiquated practice today, the Nlaka'pamux would traditionally sort the collected roots by size before dehydrating them in the sun. The smaller roots and broken segments were dried collectively and loose on a mat while the larger roots were singled out to be threaded on a string to cure. The mats were positioned on rooftops or out-of-the-way places where the roots would take one to two days to thoroughly dry. In recent times, all the roots are spread out on mats to be dried in the sun.  Botanically, the seemingly random occurrence of this 'heart' or bud-like core in some specimens (usually of larger size) may be attributed to a developmental stage of growth found in older individuals. 8  36  Although today some Nlaka'pamux currently air dry bitterroot indoors, M a r y Sampson gave reason as to why bitterroot should be dried in the sun; "when you dry IhQuoopen it should be outside, you can't dry them in the house. I tried that once..., but it didn't work up in the rafters, it turned really red; you have to have it outside in the sun." While the manner o f drying may seem trivial, recent studies point to the release o f otherwise inaccessible nutrients through the process o f sun dehydration (Kuhnlein and Turner 1991). This gives further value not only to the consumer, but to traditional food processing knowledge and techniques o f the Nlaka'pamux. Storage Traditionally, the Nlaka'pamux would store bitterroot, either fresh but most commonly dried, in underground caches. These were pits constructed in dry sandy areas, generally found in the arid plain regions o f lower valley elevations but also at times higher in the mountains. The Nlaka'pamux called these caches sh.EEshtkin, and they filled them with a variety o f food goods for indefinite safekeeping. In locating a site for the construction o f a sh.EEshtkin, the main features were to find a dry sandy area free o f dirt and excessive moisture. Once dug, the pits were lined heavily with dry needles o f Ponderosa Pine (Pinus ponderosd) upon which the food materials would be stratified and further layered with leaves o f other unidentified plants. Occasionally, bitterroot that had been processed into bannock cakes was also stored in the caches. More recently, the Nlaka'pamux also constructed large, partially subterranean root cellars for storage purposes. Dried roots and berries o f all kinds were stowed, with bitterroot being kept in large jars or hanging in flour sacks just below the rafters. These  37  sacks would be in rows, the main requirement being that they had to be off the ground. The dried roots were reported to never spoil. W i t h the introduction o f modern amenities, Nlaka'pamux storage o f bitterroot also makes use o f freezers and airtight containers. After the root is washed, it is patted dry and frozen fresh in sealed plastic bags to prevent them from growing too 'mushy'. Or, as is still largely the custom, bitterroot remains to be dried and stored with the only difference being the use o f plastic containers. Many Nlaka'pamux continue to keep small portions o f dried bitterroot in their cupboards year-round to be accessed and cooked at w i l l .  2.3.5  Digging Implements  To aid in collecting vegetal roots, the Nlaka'pamux made root diggers, known singularly in their language as a KalAhh.  The root diggers usually took the form o f a T-  shaped tool that could be fashioned from a number o f materials. A s a root harvesting technology, this was an implement common to the majority o f Indigenous Peoples throughout North America. Teit noted it as the only known implement for digging roots as used by the Nlaka'pamux (Steedman 1930). The simplest o f diggers were nothing more than a section o f branch from a birch tree (Betula sp.), 60 - 75 cm in length, with its point treated to a slight calcination to ensure toughness (Morice 1893, Teit 1900). Other diggers employed the hard wood o f a service-berry (Amelanchier sp.) for a shaft and had a birch-wood handle, while some shorter varieties were fashioned from a single piece o f caribou, deer, or elk antler (Teit 1909; see Figure 2-2). More recently, some Nlaka'pamux have made use o f broken rake prongs from old horse-drawn haying outfits by straightening out the prongs and putting a  38  T-handle on them. O f late, customised diggers are made out of aluminium pipe or solid iron, o f which the latter's strength and weight o f shaft made for easy digging even in the toughest o f grounds. These are important qualities when considering that bitterroot grows in a variety o f ground conditions, a number o f which are often rocky.  Figure 2-2  Traditional buckhorn digging stick; digging bitterroot did not require the long shafted sticks used for deeply buried geophytes. Shorter digging sticks like the one displayed sufficed.  39  To the Nlaka'pamux, a digging stick is a highly personalised tool that customarily holds spiritual and sentimental value for the owner, many o f which were often ornately decorated with carved designs symbolic o f the use o f the implement (Teit 1900, p. 137; see Figure 2-3). Digging sticks are used from year to year and are even passed down from generation to generation within a family. They are also commonly given as prized and respected gifts. The personal attachment to ones' digging stick was strong and people could even be identified by their KalAhh.  This individualised quality and affinity  was mentioned by Chief Leslie Edmonds; "...digging sticks are quite personal and when someone else is using someone else's, other people notice it. Everyone has their own."  Figure 2-3  Intricately carved designs on handle o f digging stick made o f antler; reverse side o f tip also shown (Teit 1900, p. 137)  40  A s w i l l be expanded upon in section 2.6, root digging was seen as a spiritual enterprise. Nlaka'pamux rock writings (especially in the Stein River Valley) illustrate the reverence and seriousness that Nlaka'pamux bestowed upon root resources and their digging sites. Traditionally, when a Nlaka'pamux received a dream about something, they would often consider and record them in the form o f a painting sketch on rock surfaces. One such writing (Figure 2-4) was recently located in the Lytton area, and as explained by the late Nlaka'pamux elder Annie York, gives particular reason and respect as to why and what kind o f digging stick is used (York et al. 1993): "These are women's things here. That's a digging stick on the left. That Sun M a n told them that a woman's instrument is not going to be the bow and arrow. It's just a stick like a hoe. That was his design but it wasn't comfortable to dig with. The next picture is the one designed by Xwekt 'xwektl, with the hilt on it... The two little dots below, they're the stuff that she wants to dig up. The next one to the right is another digging tool. It's shaped like a letter " P . " Above that is the sign for prayer, like two curlicues, back to back. That Xwekt 'xwektl told the old lady that she must pray and talk to that tool before she uses it. He says, " Y o u kneel down and talk to it before you start." O l d people do that. I seen them. I saw my grandmother do that..."  Figure 2-4  Nlaka'pamux rock writing [site E b R k 3] (York et al. 1993)  41  The use o f a digging stick is also integral to helping achieve a sustainable harvest. Firstly, as a harvesting implement, the precision with which a digging stick can unearth a desired root body, even the deepest o f tubers, is uncanny. More importantly, the skill and prudence employed by the Nlaka'pamux in digging also exhibits an effort to conserve and care for bitterroot as a resource. Together, these aspects avail themselves to a purposeful and conscious design o f stewardship by the Nlaka'pamux. A s made clear by Chief Leslie Edmonds: "...it (digging stick) also helps IhQuoopen because shovels tend to dig up too much dirt, where as with the KalAhh... its small little point... you just take the one that you want and leave all the little ones around it alone. I f you leave the little ones alone you w i l l have some for the years after. Y o u just take the biggest mature looking ones... those are the ones to use, the little ones you leave alone. The way the elders taught me was to not disturb the little ones, you leave them alone, you just take the big ones. So with the shovel, i f you had a big one with a bunch o f little ones around it, you would disturb all o f them just to get the big one." Despite the Nlaka'pamux's primary use o f a KalAhh, some Nlaka'pamux presently prefer the ease which a shovel affords the digger as it covers a larger area with more leverage available. However, the use o f a shovel is not very common and tends to be used only by Nlaka'pamux who have difficulty getting to remote digging locations (and therefore can wield a shovel because they can drive to the site accessible by road), or those who don't own a digging stick. However, the use o f a shovel also carries some social stigmas as disrespecting the earth because it tends to leave hole-like divots in the ground. A s put by Evelyn Beckett, there are no written rules o f conduct but one must decide for oneself and "...use whatever you think is fair". Overall, the practicality o f a root digger, it's easy carrying and precise extraction capabilities, and its traditional esteem make it an appreciated and the most used harvesting implement.  42  2.3.6  Transplantation  Cultural dispersal o f useful plants through transplanting has been recorded and is thought to have been o f occasional occurrence within traditional First Nation living (Compton 1993b, Loewen 1998, Turner et al. 1983). Specific to bitterroot, transplanting is viewed as a highly credible reason behind localised populations o f the species within some Native American territories as well as disjunct occurrences in southern Alberta (Wilson et al. 1988). Transplanting useful plants, which included the apt and hardy bitterroot, was also practised by the Nlaka'pamux. Although most Nlaka'pamux concurred that it was very difficult to know exactly how bitterroot first arrived in their territories, they did imply that it had grown there for a very long time. The elder Saraphine Kirkpatrick on the other hand, while agreeing that there had always been some bitterroot growing in the area, said that the main reason bitterroot proliferated was through transplanting done prior to the turn o f the century. In particular, Saraphine's mother-in-law Suzanne Magee, is reported to have transplanted large volumes o f bitterroot from Walhachin and other nearby regions in British Columbia's dry belt (possibly Savona) into the Ashcroft area. Other Nlaka'pamux also transplanted bitterroot along with other edible plants like spring beauty (Claytonia lanceolata), although the latter species are not known to have survived to the present. The recorded transplanting seemed to be done out o f a sense o f urgency in ensuring a future supply. Saraphine mentioned Nlaka'pamux men on horseback having to 'steal' the bitterroot from across the river in Walhachin in order to transplant it in the Ashcroft area; " . . i f you don't do that, there won't be any around here... but i f you transplant it, it flowers and multiply [sic]". It was also an intensive process where  43  Nlaka'pamux would travel considerable distance (e.g. over 30 k m east to Walhachin) on horseback to return with baskets and sacks filled with bitterroot. Saraphine described Suzanne Magee working "...for days and days and days..., transplanting them from way over there across the bridge (Walhachin), ...that is a long ways; she got them in a sack and a basket, a big basket that hangs on the saddle horse." The transplanting process began by digging up the living plants during the normal spring harvest with the roots being temporarily stored in a pit covered with dry dirt through the summer which coincided with its normal dormancy period. The bitterroot would then be transplanted to the new location in the late fall just after it began to rain or snow; many o f the plants were reported to have been transplanted to large areas known as 'Klootchville' (see Figure 3.1). Survival rate is not known, but Saraphine said "...some grow out and some didn't [sic]". The reasons behind transplanting bitterroot also succeeded immediate concerns for food. A s made clear by Saraphine's rendering o f Suzanne Magee's words, "...I am only doing this for my grandchildren to have something to eat when they grow up; ...when I die Sara[phine], and your children grow up and they w i l l know where to get their Indian roots." Bitterroot is also transplanted by the Nlaka'pamux in the present-day, but on a much more narrowed scale o f personal home gardens. M a n y Nlaka'pamux referred to the transplanting o f bitterroot as a tricky endeavour with whimsical results paralleled to their oft tried but relatively unsuccessful transplanting o f edible mushrooms. Nathan Spinks inferred that it seemed just too difficult to grow; "...a lot o f people try to transplant that [bitterroot], moving it from here to there, like mushrooms, but it doesn't work". However, other Nlaka'pamux do find success, transplanting bitterroot to their  44  homes for ornamental as well as practical reasons. Madeline Lanaro noted an Nlaka'pamux elder who transplanted a handful o f bitterroot to her personal gardens flower bed. They are said to have grown year after year, and along with w i l d harvesting, "...she likes to get out and dig some when they are just ready at her house too."  2.4  Social Significance of Harvest Season "From an examination of several Indian camping-places it was seen that the women evidently collect a supply of roots and return to camp to strip them. One can picture half a dozen Indian women, squatted before the camp-fire at the close of a day's digging, busy peeling the roots preparatory to packing them. The small heaps of skins left at most of the camps indicated that each party returned with many hundreds -perhaps thousands- of roots. " -John Davidson (1916) The harvesting o f bitterroot from the sagebrush plains near Ashcroft was a  notable and culturally meaningful time for the greater Nlaka'pamux nation. Families and groups o f families would camp for weeks at a time throughout the harvesting areas in an atmosphere o f festivity amongst the also earnest business o f subsistence gathering. A s communities o f bitterroot are limited, or at least pocketed and site specific within Nlaka'pamux territory, accessibility was not always an easy endeavour. Other than the Nlaka'pamux whose dwellings juxtaposed the harvest sites, the majority o f people had to travel considerable distances in order to dig the root. Nlaka'pamux arrived from all over their territories, representational o f present day place names like Merritt, Kamloops, Chase and Lytton. Nathan Spinks recalls that the Nlaka'pamux from the Lytton area "...would go over the mountain pass behind Botanie (Valley) by horse and wagon and come down in front o f Basque (Ranch). It was a big trip to get there, two days there and two days back." For the populous who travelled, caravan style entourages were the custom as large groups provided safety and a dynamic o f social enjoyment.  45  Although there were always camps surrounding the major harvesting sites, namely on the flats at 100's (known to the Nlaka'pamux as "Schuchem-elch", which means "Root-digging house" [Davidson 1916]), a sprinkling o f camps would also be present throughout the greater Lower Thompson River Valley (see Figure 2-5). Nlaka'pamux would generally remain for two or more days and up to a week in one harvesting location, for as some elders shared, there used to be so much bitterroot that moving from place to place too often was unnecessary.  Figure 2-5  Typical traditional camping spot in Venables Valley under a Ponderosa Pine  46  The spring harvest o f bitterroot would bring individuals and families together on an annual basis. The Nlaka'pamux would look forward to the harvest as it allowed for otherwise dispersed family units to be brought together communally i n a time when social visiting tended to be a luxury. The harvest period also provided opportunity for the transfer o f practical and cultural knowledge in an in-situ environment. Young children imitated and helped their parents and grandparents in the bitterroot harvest while many elders also remember countless fabled reminiscings o f the Nlaka'pamux arising from camp life during the harvest. In an overall description o f the bitterroot harvest, Chief Leslie Edmonds shared: "There used to be camps set up all over the flats in certain areas. People would be all over gathering it and just having a relaxing time while they did it; ...there used to be camps all over when I was little, all in the hills I used to ride around on saddle horse, ...just anywhere someone might be sitting there cleaning their IhQuoopen i n the shade of the sagebrush, ...it could spook your horse 'cause you can't see them. People from all over used to come, they would camp for about a week or two weeks and just visit around for a while like a social time. When they gathered enough, away they would go."  Nowadays, harvesting bitterroot is within the context o f day trips with small groups and families digging for extended hours instead o f days. Nlaka'pamux o f all ages still look forward to the chance to dig; bus trips to harvesting sites organised for seniors are especially popular on the M a y long weekend. Nlaka'pamux have also begun to travel a lot more widely throughout their territories and beyond to harvest bitterroot. Nlaka'pamux members have reported digging not only in the Ashcroft area, but also in Penticton, Keremeos and even across the border near places like Loomis and Omak in the state o f Washington.  47  2.5  Nomenclature and F o l k Classification  The Nlaka'pamux named plants through a variety o f stimuli, some o f which were according to use, size, shape, colour, pubescence, habitat o f growth, taste and relationship or resemblance to other plants (Steedman 1930). Evidently, the Nlaka'pamux did not choose to base the name of Lewisia rediviva according to the taste o f its root, as was the manner imparted in common English. This may appear somewhat quandarical as a number o f other plants were named via their bitter taste, as represented by the prefix tahht. Examples given by Teit (Steedman 1930) are taxqai.n, meaning 'bitter head" (Leptotaenia dissecta [modern equivalent is Lomatium dissectum]); taxtaxei'uk, meaning 'bitter w o o d ' (Cascara sagrada [modern equivalent is Rhamnus purshiana]); taxtexo 'xsa, meaning 'little bitter berry" (Amelanchier alnifolia).  Bitterroot also has  many traditional and recent references by the Nlaka'pamux as a plant growing in association with other species as well. For example, companion-type relations with Montia perfoliata (Turner et al. 1990 p.241), Fritillaria pudica and. Artemisia tridentata could have also served as the basis for naming. Similar to the way other First Nations gave a number o f names for a variety o f different reasons to the species, the Nlaka'pamux naming o f bitterroot also varied geographically within their territories. A s reported by Turner et al. (1990, p.242), bitterroot was known in the southern regions as sk-ep-n in reference to the manner by which it was traditionally prepared; meaning "come to be pierced, impaled, by stick, fork, hook or other sharp instrument". To the north, i n and around Ashcroft, bitterroot was known as s/pi-m; meaning to "rub bitterroot on rough rock to remove skin (/pi-my or "skin bitterroot with hands (/pe-m)". This varied naming could conceivably be  48  explained by the fact that the Nlaka'pamux in the southern or 'lower' territories often only received bitterroot in its prepared state through trade while the 'upper' Nlaka'pamux were the ones who actually harvested and stripped the root. Nlaka'pamux ethnoclassification systems position bitterroot in descending order under the broadly inclusive taxon "ground growth", subclassed within "food ground growth" then further subclassed as a "root food" (Turner 1989). Although the latter class of edible roots (and underground parts) are a major nomenclatural plant category and readily recognised as distinct in utilitarian terms, it is an unnamed class. Whether or not this taxon name has been lost or absorbed into a class o f 'weeds' through acculturative perceptions o f European culture remains to be seen (Turner 1989). L i k e l y , it was not because the class lacked cultural significance as the Nlaka'pamux did not differentiate between bulbs, rhizomes, corms and tubers, but all underground fleshy structures are traditionally seen as 'roots', the majority o f which were utilised as food (Steedman 1930). One possibility speculated by Turner (1987) is that i f the Nlaka'pamux language had continued to develop without outside influences, a taxon name for the incipient root category might have evolved through a process o f expansion, with perhaps bitterroot or yellow glacier lily (Erythronium grandiflorum) serving as the type specimen because o f their high cultural salience (p.75). Within the unnamed taxa o f edible roots, bitterroot has been referenced as the dominant member o f a restricted mid-range grouping of "bitterroot type" plants (Turner 1989). The criteria for recognition o f this mid-range plant grouping was based on a combination o f common habitat and morphological similarities that included Columbia bitterroot (Lewisia columbiana), Siberian montia (Montia sibirica) and possibly  49  twayblade (Listera sp.) (Turner 1989). In further support o f bitterroot as the 'type specimen' o f this intermediate folk category, Teit also listed a name o f bitterroot as tlkupeno 'e, literally meaning "basic bitterroot" (Steedman 1930, p.479). What is interesting to note, however, is that this classification may only be representative on a geographic basis and is not homogenous or universal for all Nlaka'pamux speakers. For members living solely within the dry-belt corridor in and around Ashcroft, bitterroot is independently classed as its own type specimen because the other bitterroot-like plants mentioned above are not ordinarily found in the area. When queried o f bitterroots relations to and ordering beside other plants, Saraphine Kirkpatrick said that "..Indian root (bitterroot) hasn't got no friends, they're themselves." Although there are many associations between plants and animals in Nlaka'pamux culture (Turner 1990), no direct relationships, either observed or perceived, are found specific to bitterroot. However, in more o f an indirect manner, some Nlaka'pamux brought forward with consistent repetition a 'folk' connection with rattlesnakes.  M a n y references were made to rattlesnakes and the danger thereof while  harvesting bitterroot although this could be seen as more o f an environmental hazard o f seasonal digging rather than a relationship.  2.6  M y t h o l o g y , R i t u a l s and T r a d i t i o n a l Beliefs  Alongside the utilitarian aspects o f bitterroot, socio-cultural and symbolic analyses as to how it is perceived are also important towards understanding its place in Nlaka'pamux culture. Bitterroot, like other significant vegetal resources, carries with it an array o f historical, mythological and ceremonial citations that can only be recognised and appreciated within appropriate cultural frameworks. This being said, the  50  Nlaka'pamux have many creation-type mythologies particular to place and organism within their territories. Notable, but not directly related to bitterroot, a number dealt with the origin and procuration o f plants. A s recorded by Teit (1912), a portion o f one such myth is as follows: A t last Old-One came to the woman, ...He told her to shut her eyes, and, when she opened them again, a large plant had grown up before her. He asked her to go to the birch-tree, and, after saying to it, " O friend! I require you," to strip off its bark. This she did, brought the bark to him, and he rolled the plant in it. N o w he told her to travel along that hillside, and throw away pieces o f the plant. She did as directed, and, each time she put her hand in the role, she pulled out a different kind o f bulb or seed. Thus she sowed all the different kinds of plants used by the Indians for food or medicine; and from these sprang up many, and they spread over the whole country. They grew as soon as they touched the ground. Old-One told her their names, and said, "These only are edible." Thus the Indians learned the edible varieties o f roots and the proper kinds o f herbs to use. When the plants had all been distributed, Old-One made the role o f birch into a basket. He also made a root-digger, and showed the woman how to dig roots (p.326).  A s to the abundance and specific distribution o f plants throughout Nlaka'pamux territory and beyond, Teit (1912) recorded another variant o f the creation myth particular to vegetable root foods (see Appendix I). Aligned with this, Nathan Spinks shared a similar but much abbreviated rendition o f this myth in recollection o f what was taught to him as a youth by his elders. Interestingly, Nathan's rendering also gives specific reason as to the place o f bitterroot and why it grows where it does in the Lower Thompson River Valley: " T w o old people talked to me a long time ago... old, and I was just young; when I lived up at Spences Bridge and one time when I lived down at Siska. They were telling me that story, a long time ago. I listened to that story about when they were making the earth, and he was telling me, he says, 'when the Creator came, He came right through the Stein. He started here, but He didn't dump anything here  51  from H i s basket, He went all over, all over North America, dumping a little bit; that's why you see bitterroot only in certain spots, and some trees, and all kinds when they were making it'; this old man was telling me that. A n d then another old man said the same story, at different times". Throughout British Columbia, along with stories o f the O l d One, the Creator, many mythologies also speak o f the magical roles Transformer Beings played in the evolution o f human, plant and animal life (Teit 1900). Besides helping to separate the first beings into humans and animals, these Transformers also gave instruction to the early people as to how to live and work with one another and the earth (York et al. 1993). This ancient era is what scholars have touted 'The Mythological A g e ' and the proximity with which the Nlaka'pamux continue to respect and honour these pedagogical understandings remains close and real. For the Nlaka'pamux, D a l y (York et al. 1993) points out, "even today it is said that all the flora and fauna retain an elusive, human-like form o f consciousness that harks back to the mythological era (p.#xi)". Besides pointing towards geneses in culture, mythological ancestries can also be indicators o f biological organism saliency. A s stated by Martin (1995), "by exploring... the symbolic interaction between culture and nature in myth... plants and animals which are considered anomalous -abnormal in their behaviour or morphology- often serve as symbolic mediators in their special ability to cure, nourish or protect people (p.l 15)." Relating this observation to the knowledge and use o f plants by the Nlaka'pamux, bitterroot exemplifies a number o f unique attributes, holding mythological and practical values. M a n y o f these beliefs stem from bitterroot's human-like 'transformer' root morphology and the notion that at one time, bitterroot were human themselves.  52  Although no accounts o f bitterroot's anthropomorphistic past are recorded in ethnographic archives, many Nlaka'pamux elders signified that at one time such a myth did exist but had since been lost. Throughout the interview process, many descriptive references o f the root were loaded with anthropomorphism's; 'the IhQuoopen are sitting', 'they are holding hands', 'they talk to one another', 'they are hiding from y o u ' (see Table 2.3). In fact, aligning bitterroot within a human ancestry remains very real to some Nlaka'pamux. A s shared by Saraphine Kirkpatrick, there is even a hesitancy in the present day at digging too many IhQuoopen, for her experiences growing up have confirmed for her bitterroot's humanness: "I got down on the ground and I was leaning there and I was talking to it (bitterroot). I said to it that 'my granny said that you could talk and everybody wonders what you are saying'; ...when I heard that talk (gives speaking sounds made) they were talking and looking at each other. The Indian root (bitterroot) seems to come alive, so I don't like to get them too much, ...the IhQuoopen is always alive, I used to talk to them and rub them around my face and talk to them and look at them. M y Mother used to tell me you are crazy, I told her they are people, ...I used to talk to them in Indian"  Table 2.3  Anthropomorphistic Characteristics o f Bitterroot as recognised by the Nlaka'pamux  Noted Attributes physical similarities  social allusions  spiritual connotations  • • • • • • • •  the red 'heart' in what would be the thoracic cavity the pale skin colour under the outer peridermal layer the neck-like hypocotyl the trunk, arm and leg-like appendages common in mature lateral root morphologies often growing in defined, community-type populations the existence of bitterroot 'lover' couplets as representative of the marriage union described as "...a white medicine that looks like a ghost" regarded and esteemed by some individuals as a guiding spirit  53  The traditional affinity of the Nlaka'pamux towards bitterroot has also been described in contemporary times as that o f a guiding spirit. Particular to married couples, the gendered qualities bestowed upon bitterroot, that being the folk categories o f female and male plants (as described in Section 2.9), has been used by the Nlaka'pamux in an amulet-like symbolism. Madeline Lanaro depicts how the more human-like forms o f bitterroot are sometimes used (see Figure 2-6): " . . . i f a couple is going to get married and they don't ever want to break up, get a male and a female IhQuoopen and bury them or put them under their pillow, sort o f like a wedding ceremony; ...they w i l l never break up cause they are together, those bitterroot is sort o f their guiding spirit. If you talk to them and tell for them not to argue, ...that's the way their life w i l l be. If they don't grow together or i f they can put them together, they can bury them after they prayed to it or talked to it."  Figure 2-6  A n example of bitterroot "lovers" sometimes used in amulet-like symbolism  54  The high esteem, identification and relational connection felt by the Nlaka'pamux towards bitterroot also spread beyond mere mythological sentiments. The Nlaka'pamux engaged themselves in a plenitude or rituals surrounding the root and its harvest. A number o f these adherences took the form o f ceremonially observing the first bitterroot harvested each spring. Teit (Steedman 1930) reported that these First Fruit ceremonies, lesser known as First Root ceremonies, were common to a number o f gathered food resources; they "...were observed by the Thompson (Nlaka'pamux) before and after the gathering of roots or fruits... the former were conducted to ensure and increase productivity, the latter as a thanksgiving (p.453)". For many o f the Nlaka'pamux o f late, the specifics o f these prayerful ceremonies have been generally forgotten and their carrying out largely ceased, but their meanings and purposes remain. A s Madeline Lanaro explains, "I recall prayers happening when the first IhQuoopen o f the year was picked when I was a little kid, but I don't remember i f anybody does it anymore; ...when we go out now we just do our prayers quietly". Traditionally, along with ceremonies and a stringent air o f reverence during the harvest, personal conduct also played a high role. The Nlaka'pamux took great care in digging and respect in honour o f the root itself and where it came from. In modern times, although many o f these self readying practices are overlooked i f not lost from memory, some elders continue to remind the younger generations o f these attitudes. One commentary, in echo o f these traditions, says to comb out ones hair thoroughly before taking to dig bitterroot; the connection being that i f one had messy hair, they would dig up roots that were matted, bushy and stringy instead o f long straight and thick roots that were the preferred norm. Moreover, and not entirely viewed in a disciplinary light, when  55  children are helping to dig bitterroot, good behaviour is expected and required in edification o f the serious and spiritual nature of the enterprise. Madeline Lanaro remembers being taught as a child that i f one misbehaved while digging, "you are going to make IhQuoopen upset".  2.7  Trade  Bitterroot served as a traditionally important cash crop trade item for the Nlaka'pamux. Roots were traded both intra-tribally to the Lower Nlaka'pamux and to other surrounding Nations for a variety o f items, the most common o f which was dried salmon (Perry 1952, Turner et al. 1990). Even today, trade remains prevalent though on a far more limited basis than in the past. Nlaka'pamux who attend inter-tribal powwows are frequently approached by members o f other nations to exchange or barter for bitterroot. Bitterroot was traded in a processed condition (i.e. stripped, peeled and dried), either collectively in a sack or bundle, or in the manner upon which its name is derived, that being threaded on a string. Besides making for ease in curing and light handling, the threaded and dried segments o f roots were used in order that trade value and market worth could be determined and accounted for in a uniform manner. Teit (1900) gives reference to bitterroot as a commonly traded item though he did not list it as a 'principle commodity o f trade' like the status given dried salmon, dressed skins and woven baskets.  A s enumerated, 10 bundles o f bitterroot were considered to  be o f equitable exchange for one large dressed buckskin (p.261). Elsewhere, it was even reported by an early explorer that a sack o f its roots could buy a good horse (Lyons 1952). Although the amounts o f ' b u n d l e ' and 'sack' are unquantified, it can be granted  56  that these were dry amounts representing considerable energy and effort to collect and prepare. The Nlaka'pamux consider bitterroot and the trade thereof a sacred overture to its stewardship. The Elder Nathan Spinks shared in a vein o f reverence and concern that natural resources o f the Nlaka'pamux are a gift o f the Creator and should be regarded as such: The Creator gave IhQuoopen to the Nlaka'pamux for a reason and that's why it only grows in certain spots, to trade and share; ...trade it with people who don't have it for other things like salmon. O r what is good is to give it away to someone who is travelling. If you don't treat things with respect they w i l l disappear like when the people who started to sell salmon...; now the salmon doesn't come back the way they used to because they took too much and didn't treat salmon with respect. A n d that is like IhQuoopen...; you must treat it with respect and not sell it for money. White people would call IhQuoopen a commodity because it is important and it only grows in some spots and only some people can get it. In Indian we don't have a word like that cause we all share and trade, but that is like what it is.  2.8  S i m i l a r Ethnobotanical Species  Within Portulacaceae, only one other species matches the prolific use and importance attained by bitterroot. Claytonia lanceolata, commonly known as 'Western Spring Beauty' or 'Indian Potato' is also a highly salient root food o f many interior First Nations; a mountain range, the 'Potato Mountains', is even named after this plant in the territories o f the nearby Tsilhqot'in First Nation. Other notable but not as heavily used species include Montiaperfoliata, or 'Miner's-Lettuce', used by the Nlaka'pamux as a medicine for sore eyes (Turner et al. 1990) and as the common name implies, also used as a salad green by early prospectors. Other species used by the Nlaka'pamux includes Lewisia columbiana and Lewisia pygmaea, both o f which were used as sources o f food,  57  the latter o f which was sometimes thought to cause insanity (Steedman 1930, Turner et al. 1990). In identifying Lewisia pygmaea, which can be quite similar to Lewisia rediviva,  any misgivings can be resolved in recognising that it only has two sepals, much  fewer petals, its narrow leaves are usually a great deal longer than the stalks and it has a higher elevation habitat (Parish, Coupe and L l o y d 1996). Modern ornamental use o f Portulacaceae also includes species o f more than usual horticultural interest and application (Hitchcock and Cronquist 1973, Mathew 1989, Zomlefer 1994). For obvious reasons, the genera Talinum, Claytonia and Lewisia are sought for their stunning, delicate and often opulent nature o f flower. In regards to bitterroot, though a desirable species for the rock gardens o f desert plants enthusiasts, when transplanted to the more temperate climates found west o f the Cascades, it does not do well without careful care and attention in as it is overly prone to root rot.  2.9  T r a d i t i o n a l Ecological K n o w l e d g e  For thousands ofyears, aboriginal peoples around the world have used knowledge of their local environment to sustain themselves and to maintain their cultural identity. Only in the past decade, however, has this knowledge been recognised by the scientific community as a valuable source of ecological information (Johnson 1992).  Nlaka'pamux traditional knowledge o f bitterroot and other natural resources is in effect an overflow to the deep-seated, locally inherent understandings they hold as an indigenous people. This has resulted in appropriate, working knowledge systems o f 9  flora, fauna and overall ecology in the area. Aspects o f this indigenous knowledge are  As such, indigenous is in dynamic reference to "...early peoples of an area whose traditional cultures are rooted in particular landscapes with which they are essentially and specifically identified." (Elder and Wong 1994, p.7).  58  often lumped under the phrase Traditional Ecological Knowledge (abbreviated T E K ) and as stressed in The Brundtland Commission's report, Our Common Future (1987), there associated with the concept o f 'sustainability'. The sustainable use and awareness o f how, where and when to harvest bitterroot grew from familiarity with habitat requirements as well as physiological understandings o f the species. While Nlaka'pamux T E K o f bitterroot is not entirely obvious as to habitational reasons why it grows where it does (locally around Ashcroft), there was consensus as to what ideal growing situations are. Climatic conditions stated to bring about large, favourable roots are dependant upon the winter months. If there was little or no snow or rain, bitterroot was said to have abnormally small roots in the spring. However, i f the winter did provide enough moisture in the ground and it was not too cold, "...they w i l l grow big". Edaphic requirements are seen as equally important. M a n y Nlaka'pamux conveyed that bitterroot grows better in sandy soils, where it is generally hot and dry, but where the soil is still able to retain some moisture. Furthermore, where the soil is soft it tends to grow bigger and they are easier to dig. A s Saraphine Kirkpatrick states, "when it rains it (bitterroot) grows, but when its no rain it dries up just like a stick. When it is too rocky and dry they don't come out right [sic]." In regards to physiological differences between bitterroot populations, it has been reported that some First Nation groups recognise varying degrees o f astringency, believing that only certain populations produce palatable roots (Hitchcock et al. 1964); the Nlaka'pamux do not fully concur. While they recognise that environmental factors may bring about certain nutritional or physiological differences, the variations are noted as being on a year to year basis, not changing greatly over time. The Nlaka'pamux  59  interpret physiological variations as arising from environmental or climatic factors. A s Ruth Peters shared, "...in different parts o f the country they come in different sizes", however, "...they are the same kind". T E K o f the Nlaka'pamux also accounts for the reproductive dynamics o f bitterroot, influencing and contributing greatly to the species' propagation as well. In general, traditional terms, Teit reported that although it may have not been entirely accurate scientifically , the Nlaka'pamux did have concepts o f sex in plants; this being explainable through greater plant size usually attributed to that o f the male (Steedman 1930, p.453-4). In regards to bitterroot, morphological size remains to have sway over plant engenderment, that is, along with the presence or absence o f 'hearts' as previously mentioned. However, Ruth Peters shares that one can locate female individuals without digging to compare root size or the presence o f a heart; "...just like everything, there is female and male. Vegetables, everything, even the lilac bush (Syringa vulgaris) out in front [of her home] is a female because it has saplings underneath it. The females are the ones who have all the little ones around, ...it is the same with the flowers". Relating these understandings to the propagation o f bitterroot, the Nlaka'pamux recognise the male 'heart' o f the root as also being the male 'seed'. Further, mentionings from various Elders correspond to the fact that "...you can go and plant the male seed and it w i l l grow", or "...the one with the heart is the male and that seed is to grow more [plants]". While all Nlaka'pamux interviewed confirmed that the 'hearts' were removed from the edible portion o f the root due to its bitter taste, no one gave reference to replanting it as a fertile propagule once it was removed. From what was shared, any replanting o f the root or its propagule was incidental as the male 'seeds' were cast away  60  indiscriminately without any formal thought to where it landed. However, because o f many references to the 'seeds' self reproductive abilities, it is foreseeable that at one time, a replanting process may have been on a much more intentional, outright basis.  10  Nlaka'pamux management strategies surrounding bitterroot and other plant food resources are many. It should be mentioned, however, that one o f the most prominent examples in illustration o f the comprehensive nature o f their T E K is the use o f fire. Periodic controlled burning o f resource sites was a prominent factor in maintaining and enhancing floral resources by keeping competitive species at bay and releasing nutrients into the soil. In fact, the persistence with which Interior First Nations have used burning (Lewis 1973, 1982, Turner 1995, 1997) has allowed fire to be the dominant force in selecting for fire-resistant species. A s a grassland geophyte, it can be ascertained that bitterroot is a species potentially enhanced through burning although few referrals were given by the Nlaka'patmux attributing or connecting this process specifically to the bitterroot harvest. Traditional burning is a well recognised management tool throughout Nlaka'pamux territory though it has evolved into a rare safety practice in prevention o f large, unintentional fires since governmental repression earlier this century. To many Nlaka'pamux, fire was known to have been used moderately throughout the Ashcroft area; modern ecological interpretations o f the landscape in many ways attributes change to the present lack o f burning. Landscape and habitat degradation in the area is also addressed and interpreted through T E K and other recollections made by Nlaka'pamux Elders. M a n y times,  Further quantitative study as to the ability of bitterroots 'heart' to act as a propagule is needed for verification. 10  61  remarks as to the fact bitterroot roots were getting smaller were charged to the introduction o f cattle. Madeline Lanaro recognised this; "...they grew nice and big but the cows have all trampled them... they are little now, ...it is not as good as it used to [be]". So noticeable has the introduction o f cattle been that in digging areas where grazing is heavy, the Nlaka'pamux have identified a loose relationship between bitterroot and sagebrush (Artemisia tridentata). It seems that through trampling and grazing and the effects o f soil compaction and erosion", bitterroot is conscripted to grow most favourably under the shelter and protection o f sagebrush. Consequently, although not mentioned as a traditional exercise, probing and digging underneath sagebrush is now a common spot to harvest bitterroot. A l o n g with traditional observation o f bitterroot's interactions with indigenous mammals, that is, the leaf herbivory o f small rodents (various species) and mule deer, domestic livestock have also entered the scene although on a much more detrimental level. Saraphine Kirkpatrick distinguishes that cattle not only trample bitterroot, they consume flowers before the plant can set seed: "...the cows eat all the flowers and that's what kills them. They are eating the seeds, you know the flowers, and they are eating the seeds and that's why it won't transplant. That is not nice. It isn't nice to have cows in there cause they are eating the seeds too. I wonder i f it grows now, cause a long time ago they [bitterroot] were just riding each other, you know on top o f each other; you dig anywhere and you see lots o f roots coming up." Through the above information presented on the ethnobotany and T E K o f the Nlaka'pamux, humans are, o f course, prominent users o f bitterroot as well. It is strongly evident that they were not merely passive gatherers of such natural resources. M u c h o f  This is thought to be due in part to the loss of microbiotic crust (that is the vegetative layer made up predominately of byrophytes) and the protective role it plays in relation to substrate conditions; e.g. 1 1  62  the knowledge surrounding bitterroot and its procuration stemmed from a deep appreciation for and understanding o f intricate ecological systems. In all, the Nlaka'pamux were acutely aware and active in the sustainable management o f bitterroot.  helping to retain soil moisture or i n prevention o f w i n d erosion (Cannings and Cannings 1996).  63  3.0  Autecology of Lewisia rediviva i n the L o w e r T h o m p s o n R i v e r V a l l e y A s outlined in the previous chapter, Nlaka'pamux ethnobotany of Lewisia  rediviva is a complex and integrated text that manifests a clear and purposeful sense o f stewardship. While the cultural salience o f the species is implicit and obvious as to reasons why and factors o f how it has been maintained, ecological characteristics and inquiry as to the reciprocal effects management activities have wrought are much more abstruse and locally unknown. The historical and contemporary place o f the plant among the Nlaka'pamux incurs the need to view Lewisia rediviva''s status on an autecological basis in order to understand or even approach a balanced consensus o f the structure and dynamics o f its populations. The ecological component o f this research employed an inductive approach to describe vegetation rather than using experimental, hypothesis testing methodologies. With the objective to document habitat requirements and to develop a preliminary baseline survey o f the species' local distribution and abundance for future reference and comparison, data sets related to ecosystem properties were collected through a variety o f environmental (essentially abiotic) and species (biotic) site parameters. Vegetation description was at the floristic level with Lewisia rediviva and associated plant species valued through cover estimations respective to seven anthropogenic communities spread throughout the Lower Thompson River Valley.  64  3.1  Methodology 3.1.1  Study Sites  The most recognised and still existent bitterroot harvesting sites o f the Nlaka'pamux were selected in which to conduct ecological surveying. Seven locations were chosen to give an even and complete cross-section o f traditional sites based upon historical records and contemporary mentionings delineating them as such. A l l surveying took place during one field season (in the spring o f 1999) at a time when bitterroot is customarily harvested, that is just prior to flowering, between late A p r i l to early June. None o f the study areas exhibited the prolific bitterroot populations as documented earlier this century (Davidson 1916), but they did represent the most productive, present-day populations found in the Lower Thompson River Valley. Figure 3-1 displays the seven site locations, with Table 3.1 containing general descriptions o f the sites. O f the seven sites selected, all were located within the Thompson 'Bunchgrass' biogeoclimatic zone. Within this zone, sites were divided between Very D r y Hot (BGxh2) and Very D r y Warm ( B G x w ) subzone variants, representing the hottest, driest biogeoclimatic zones in British Columbia. Overall, observed vegetation was dominated by big sagebrush (Artemisia tridentata) and bluebunch wheatgrass (Agropyron spicatum), with pasture sage (Artemisia frigida), rabbit-brush (Chrysothamnus nauseosus), and Kentucky bluegrass (Poa pratensis) as co-dominants.  65  F i g u r e 3-1  Survey site locations o f traditional bitterroot harvesting grounds in the Lower Thompson River Valley; see Table 3.1 for corresponding descriptions.  66  Table 3.1  Survey site descriptions of traditional bitterroot harvesting grounds i n the Lower Thompson River Valley.  No.  Name (common name)  Site Locality and Description (Date surveyed; latitude - longitude; elevation; slope angle; slope aspect as from true north; biogeoclimatic subzone variant [explanation]; land title and use [disturbance]; location and directions; population area Lewisia rediviva in hectares [phenological state]; principal associated co-occurring species [alphabetical]; comments)  l  Venables Valley  08 May 1999; 50° 34'N - 121° 19W; 511m; 4°; 327°; BG xh2 (very dry hot bunchgrass); crown land being leased by the Oregon Jack Creek Band and used for cattle grazing (heavy); 1 km south up Venables Valley Rd. (gravel), plot is 50 m east of road near barbwire fence (transecting north to south); 2-3 ha (only rosettes, no buds); Agropyron cristatum, Androsace occidentalis, Antennaria dimorpha, Arabis holboellii, Artemisia tridentata, Poa pratensis; old flat-topped Pinus ponderosa found nearby is where Percy Minnabarriet's Grandma used to camp for weeks at a time while harvesting Lewisia rediviva.  2  Ashcroft Manor  12 May 1999; 50° 43'N - 121° 19'W; 481m; 1°; 352°; BG xh2 (very dry hot bunchgrass); Ashcroft Reserve (IR 4) land laying vacant with no grazing; directly east off Highway 1, 20m in on the left side of entrance road (gravel) to Nl'Akapmx Eagle Motorplex; 0.5 -1 ha (small buds showing); Antennaria dimorpha, Artemisia tridentata, Frittilaria pudica, Lomatium macrocarpum, Poa pratensis; Lewisia rediviva grew in intensive clump-like pockets, this is a well known and easily accessible harvesting area.  3  Red Hill  13 May 1999; 50° 38'N - 121 ° 21'W; 465m; 6°; 72°; BG xw (very dry warm Bunchgrass); private land (Ashcroft Ranch) being used for cattle grazing (heavy); 50m west off Highway 1 directly across from Red Hill Reststop area; 0.5 ha (buds well developed); Agropyron spicatum, Androsace occidentalis, Antennaria dimorpha, Arabis holboellii, Artemesia frigida, Opuntia fragilis, Phacelia linearis; traditional camp sites were very common here while harvesting Lewisia rediviva, evidence of'discing' near plot site.  4  Basque Ranch  14 May 1999; 50° 38'N - 121° 19'W; 373m; 18°; 108°; BG xh2 (very dry hot bunchgrass); Basque Ranch Reserve land (IR 18), Cooks Ferry Band, used for cattle grazing (light); on the northwestern perimeter of middlefieldadjacent to dry creekbed and barbwire fence (east to west); 0.5 - 1.0 ha (majority in full flower); Agropyron spicatum, Artemisia tridentata, Delphinium nuttallianum, Opuntia fragilis, Poa pratensis, Sporobolus crypytandrus; last grazed in 1996.  67  5  Cornwall Creek  16 May 1999; 50° 4 4 ' N - 121° 19'W; 610 m; 24°; 328°; B G xw (very dry warm bunchgrass); 105 Mile Post Reserve (IR 2), Ashcroft Band, used for cattle grazing (heavy); on the south side, 400m west up unmarked road (dirt) west off Highway 1 across from Nl'Akapmx Eagle Motorplex; 1 ha (few rosettes, small buds showing); Antennaria dimorpha, Arabis holboellii, Artemisia tridentata, Lomatium macrocarpum, Poa pratensis, Tragopogon dubius; Lewisia rediviva was not found on slopes > 30°, evidence of herbivory on some rosettes. Area traditionally known as nKa.chEEn, meaning 'dry place'.  6  Spatsum  17 May 1999; 50° 32'N - 121° 17'W; 320m; 9°; 218°; B G xh2 (very dry hot bunchgrass); Shpapzchinh Reserve (IR 20), Cooks Ferry Band, used for occasional grazing (light); 100m east off road (dirt) 2 km north of Spatsum near large scree slope; 10 ha (majority in flower, some in bud); Agropyron spicatum, Androsace occidentalis, Arabis holboellii, Opuntia fragilis, Phacelia linearis, Poa pratensis; 2-3km's of sparse Lewisia rediviva with punctuated pockets throughout.  7  Klootchville  18 May 1999; 50° 4 2 ' N - 121° 22'W; 709m; 8°; 97°; B G xw (very dry warm bunchgrass); private land (Ashcroft Ranch) used for cattle grazing (heavy); upper meadows of Ashcroft Ranch, 400m down slope (east) of thinly forested area, 600m northwest of the older southem-most corral, 20 east off unmarked road (dirt); 1 - 2 ha (rosettes still present, majority in beginning to bud); Agropyron spicatum, Artemisia frigida, Fritillaria pudica, Lappula redowskii, Poa pratensis, Tragopogon dubius; traditionally important harvesting site with access now extremely limited.  The sites varied in size from < 1 hectare (Red H i l l ) to nearly 10 hectares (Spatsum). In all, the region o f study constituted an area o f roughly 250 square kilometres along the western and eastern flanks o f the lower Thompson River, from north beyond Spences Bridge to the southern perimeter o f Cache Creek (Spences Bridge to Cache Creek=42krn). A s mentioned, survey sites were selected for their historical and contemporary significance as a bitterroot digging area. Specific sampling locations within sites were subjectively chosen based upon culturally guided factors rather than chance or pure randomness. After a brief scouting o f each locale, one plot o f 100m2 was demarcated at each site in an area that represented general physiognomic uniformity as w e l l as fair portrayal o f an anthropogenic bitterroot population. In order to conduct floristic  68  description at each site, plot layout was that o f a 10 X 10m transect grid with set sampling placements throughout (see Figure 3-2). Hence, sampling within each plot objective and fixed, being carried out in a structured, predetermined manner.  10m  1m -1m-  F i g u r e 3-2  10m  G r i d format o f plots used in survey sampling. The nine squares represent quadrat placements; drawn to scale (0.9cm = 1.0m)  3.1.2  Vegetation Description  The 10 X 10m transect grid system, made up o f nine 1 X l m quadrats was set up in order to record species abundance by way o f estimating percent cover values. These quadrats were evenly spaced and sampled at the corners, meridians and central points o f each plot using a portable 1 X l m quadrat frame. The data collected was subjective in nature as cover estimates were made by eye using a modified Braun-Blanquet scale methodology (Kent and Coker 1992). Cover value percentages used were augmented from 0.25, 0.5, 1.0, 1.5, 2.0, 2.5 and continuing on in whole percentages from 3.0 and greater. A l l herbaceous plants and shrubs in the quadrats at the time o f surveying were recorded and their percent cover estimated.  12  Larger woody bushes and trees were  uncommon at the sites and did not occur in any o f the grid plots. Bryophytes were amalgamated under the heading 'microbiotic crust', and were treated as a single species, being given appropriate percent cover values per quadrat. Except for the most common and dominant plant species in the area, collections were made o f species within the quadrats to aid in identification and to serve as herbarium vouchers for the study. Species Identification Nomenclature for the vascular plants identified in plot surveys followed the four volume series by Douglas, Straley and Meidinger (1989, 1990, 1991, 1994). For instances where species identification proved difficult in the field, collections were made for closer examination and comparison at the University o f British Columbia's Herbarium. These specimens were collected in duplicates on a random basis among the plot sites and have been deposited in the herbarium at the University o f British Columbia  It is recognised that some species in the plots were overlooked because they were not yet visible above ground. 12  70  and the repositorial facilities o f the Nlaka'pamux Nation Tribal Council. Occasionally, triplicate specimens were also collected to be sent to the Royal Provincial Museum Herbarium in Victoria or other appropriate herbaria. 3.1.3  E n v i r o n m e n t a l Parameters  Overall site descriptions, both quantitative and qualitative, were carried out at each o f the seven plot areas under the following domains: landforms (aspect, slope, latitude & longitude), climate (elevation, exposure), vegetation (physiognomical and floristic features,  13  biogeoclimatic zone and variants), soils (compaction, rockiness, p H ,  texture, colour) and disturbance (grazing). Table 3.2 outlines the environmental variables derived from these domains and how their respective values were calculated to be adopted into analyses. Soil compaction and rockiness were amalgamated into a single category. Measurements were taken with a makeshift aluminium soil probe and gauged through taking the average depth (cm) of ten random probes within each grid area. Other substrate variables were evaluated off site. Three samples from the uppermost soil horizon were collected randomly from each o f the seven plots in order to determine 14  average p H , colour and texture qualities (these samples were composed primarily o f organic rather than mineral matter). Soil p H was measured by diluting approximately 4 grams o f roughly sifted soil in 20 m l o f distilled water. The mixture was stirred for 30 minutes and left to settle for another 60 minutes before being assayed with an electrometric meter (Orion p H meter - model 420A) at an ambient temperature o f 25.0° C ; the meter was first calibrated with p H 4.0 and 7.0 buffering solutions. Soil colour  13  14  Considered here as an environmental parameter in characterising habitat type. Ranging from a depth of 3 - 10 cm, in representation of the region of bitterroot growth.  71  qualities were gauged using the Munsell Soil Colour Chart while soil texture was valued by applying a standardised hand Texture B y Feel Guide test.  Table 3.2  15  Environmental variables used in habitat analysis  Variable aspect  Definition Slope aspect, transformed as cos(Amax - A ) + 1, where Amax = 202.5 (S-SW), and A is azimuth from true north; S-SW=2, N-NE=0  slope  Slope angle in degrees  elevation  Elevation in metres above sea level (ASL)  lat  Latitude (converted to a decimal number)  long  Longitude (converted to a decimal number)  exposure  Categorical variable, 3 levels: full direct sun(3); sloped, direct sun(2); partial shade(l)  comp-rock  Compaction and rockiness index, values from 0 to 30 cm (high numbers = more compaction and greater rockiness)  pH  Upper substrate pH (to one decimetre equating with root depth)  texture  Substrate texture index calculated on a 1-10 scale, where l=clay, 5=silt and 10=sand  colour  Substrate colour calculated using Hurst Colour Index ([Hue X Chroma] / Value)  microcrust  Microbiotic crust percent cover values (means for 9 quadrats per site)  barerock  Percent cover values for bare soil and rock (means for 9 quadrats per site)  shrub  Categorical variable, 3 levels: large sagebrush(3); low sagebrush(2); bunchgrass(l)  herbcover  Sum of average percent cover values (means for 9 quadrats per site) for all associated vascular species  alphadiv  Representative of the mean number of vascular species present within the 9 quadrats per site; used as an index of species richness and biodiversity  betadiv  Calculated here as the total number of species recorded at a site divided by the average number of species per quadrat; used as a measure of the degree of floristic change within a site (higher numbers = greater variance)  intro-spp  Number of introduced vascular species present at each site  native-spp  Number of native vascular species present at each site  grazing  Categorical variable, 3 levels: no grazing(l); light grazing(2); heavy grazing(3)  15  as found at <http://ltpwww.gsfc.nasa.gov/globe/tbf/tbfguide.htm>  72  3.1.4  Lewisia rediviva Population Characteristics  Data specific to Lewisia rediviva were collected to further understand the nature of environmental controls on plant growth. In addition to an estimation o f the population area of the species at each site (as mentioned in the original site descriptions; see Table 3.1), quantification o f harvestable root bodies was also made. For this purpose, a 1 X l m quadrat was subjectively positioned within the plot in an area that contained the most prominent, aboveground growth o f bitterroot (regardless o f whether or not it fell along grid transects). The aim was to characterise the maximum harvestable growth output for the various bitterroot populations in terms o f numbers and biomass that could also be applied in estimation o f species health and vigour. Species variables enumerated for each plot area are outlined in Table 3.3. The net dry weight o f harvested root material was determined after preparing the roots in the traditional fashion o f stripping off the outer periderm, rinsing in water and setting to cure in the sun (in this case, bitterroot 'hearts' were not removed). The processed root bodies were then dried further in an oven (Fisher Scientific Isotemp Oven model-655F) at 60° C for 72 hours before being weighed on a microscale ( A N D HF-400).  Table 3.3 Variable  Variables used in enumeration o f Lewisia rediviva Definition  lewisiamax  Maximum number of harvestable Lewisia rediviva in a 1X1 meter quadrat at each site (excludes seedlings)  total-weight  Total dry weight of roots (in grams) taken from lewisiamax; used as a measurement of biomass  indiv-weight  Average individual dry weight of roots (in grams) taken from lewisiamax; used as a measurement of biomass  73  3.2  D a t a Analysis  Vegetation data used in analyses consisted o f cover values for a total o f 38 species in 63 quadrats 16  17  from the seven plots. Environmental data and the growth  characteristics of Lewisia rediviva corresponded to the seven plots, thus avoiding grid redundancy in treating each quadrat on an individual basis. Analyses used to examine the above data involved indirect ordination methods to assess vegetation and environmental properties. The growth data on Lewisia rediviva were incorporated in a subsequent step to examine possible relationships between population characteristics and vegetation / site features. Examination o f the species data (n=63 quadrats) collected was carried out independently o f the environmental data (n=7 plots) because the low number o f plots surveyed (limited by few local traditional harvesting sites) was unsuited for the complexities o f reciprocal averaging techniques found in direct or canonical analyses (i.e. meanings could potentially be lost in the stabilising process because o f the differences in sample size between the species and environmental data). Therefore, the species data were analysed using Detrended Correspondence Analysis ( D C A ) , a widely used and well accepted methodology since the early 1980's, and cited as the overall preferred indirect ordination technique for practical and descriptive ecology very much similar to the concerned survey (pers. comm. Bradfield 1999, Kent and Coker 1992). N o downweighting o f rare species (those being scarce to the quadrats) was instituted as the breadth o f the data set proved relatively trim; regardless, instalment o f the  For inclusion and simplicity in analysis, the species represented were reduced to an eight character code, that being a combination of the number of its alphabetical position along with the first three letters of the genus and the first three letters of the specific epithet (e.g. Lewisia rediviva Pursh became 281ewred) 16  74  downweighting option produced differences perceived as insignificant between ordinations . Axes were rescaled according to the default settings (number o f segments = 26; threshold = .00) in the programme used ( P C - O R D for Windows, Version 3.17). N o additional data transformations were performed on the species cover values. In a separate analysis of the environmental data, a total o f 19 variables were selected and used (on the basis o f the parameter having a numerical value) i n forming a plot matrix prepatory to ordination. Using methodologies available on P C - O R D , ordination was carried out through Non-metric Multidimensional Scaling ( N M D S ) . This methodology was chosen due to the limited sample size and non-parametric nature o f some o f the environmental variables. A s sampling sites fell within the confines o f a single watershed and were not spread out on a wide biogeoclimatic basis, N M D S was used because o f its overall strengths in treating small test groups that are similar on a local scale (pers. comm. Bradfield 1999). For useful comparison, Principal Component Analysis ( P C A ) was also run on the environmental data, however, the results were perceived as differing little and offered no additional insights than those gathered from N M D S . The N M D S options used included the use o f Euclidean distance as a measure o f interplot similarity, with starting coordinates selected on a random basis particular to two axes. The harvestable growth outputs recorded for Lewisia rediviva were in regards to the maximum number o f individuals and their biomass weights specific to the seven plots. This data was analysed separately from the above ordinations using a logarithmic graphing option in Microsoft Excel (Version 5.0).  Quadrats were numbered 1 through 63 as they were distributed evenly in groups of nine among seven plots (e.g. numbers 10 through 18 equated to the nine quadrats from plot number two) 17  75  3.3  Results Vegetation Analysis The D C A ordination o f the sixty-three quadrats at the seven sites based on species  cover data is shown in Figure 3-3 (see Appendix II for the raw scores o f species cover; plant stratification was minimal and did not result in cover values o f over 100%). N o distinct groups are apparent among the quadrats corporately other than an ill-defined clumping o f quadrats near the middle o f A x i s 2. However, sites 2, 3, 5, 6 and 7 do show obvious clustering among quadrats indicating greater vegetation homogeneity than at sites 1 and 4. The positions o f outlying quadrats in the ordination are attributable to abnormally high percent cover values o f certain species within the plots. For example, the bottom right outlier in plot 2 was pulled askew by an 8% cover of Agropyron spicatum in quadrat number 15, while the upper right outlier in plot number 6 was pulled askew by a 20% cover o f Chyrsothamnus nauseosus in quadrat number 48. This interpretation was based on inspection o f the raw cover data (Appendix II) in combination with the species ordination shown in Figure 3-4. Figure 3-4 was generated simultaneously with the quadrat ordination but displays the relative similarities among the species based on their patterns o f distribution and abundance at the seven sites. Again, no highly distinctive groups are apparent other than the nestling o f species towards the centre o f both axes. V i e w e d beside Figure 3-3, the pull o f some quadrats towards the lower and upper right corners o f the graph is clearly seen by way o f directional groups o f species gravitating towards the same two corners in Figure 3-4. The slight intersection o f quadrats and species that occurs in both these  76  sites A A  V  T O  CM CO  O  O  A  £  •  V A  o  O  X  <  /  •  A  o  o T  •  O  oo o o T  1  1  1  2 3 4 5 6 7  w  ^ V  V  v  v  r  Axis 1 F i g u r e 3-3  Quadrat (Site) ordination from D C A o f cover data. Site names: (Venables Valley), 2 (Ashcroft Manor), 3 (Red H i l l ) , 4 (Basque Ranch), 5 (Cornwall Creek), 6 (Spatsum), 7 (Klootchville).  16Chrnau 35Poasec  8Artdra 26Guetri  CO  x  <  3 3 p h a |  .  ? 1 0 n l l f r a  M  CN  18Dessop  27Lapred , 17Delnut 15Choten 14Cenbie 28Lewred 34Poapra 36Spocry 22Erilin SAntdim 7Arahol •'lUputra 2Agrc  10Arttri  12Brotec  ri  13Cendif  »™pud  °?Ach i, 11Astpur 21Erifla 23Erisp. 38Zigven 30Lommac 37Tradub 29Litrud 9Artfri 4 A n d  19Encom  20Ericor  m  3Agrspi  6Antumb  320pupol 24Eryinc  Axis 1 Figure 3-4  Species ordination from D C A of cover data  n  figures can be interpreted as representing an average plot area with its corresponding plant associations common to all the survey sites. Although the majority o f species present in the quadrats can be equated as loose associates of Lewisia rediviva throughout the study area, the centrally positioned grouping o f species in Figure 3-4 represents the most common associates. Species commonly associated with grazing disturbances, such as Opuntia fragilis, Antennaria dimorpha, Poa pratensis, Achillea millifolium, Lappula redowskii, Centaurea diffusa, Tragopogon dubius and Erigeron compositus are highly evident in this central group, suggesting that Lewisia rediviva could be suffering from grazing effects throughout the valley. A s seeded for fodder, the proximity of Agropyron cristatum adds further complication to the effects o f grazing despite its presence in only i n one o f the seven plots (Venables Valley). A l s o notable in the central grouping o f species is the traditionally recognised association between Lewisia rediviva and Fritillaria pudica, evidence that this historical linkage between populations is still intact. Table 3.4 lists the species correlations with the first two D C A axes. B y viewing this table in combination with the previous two figures, additional explanations for the overall form o f the ordination can be explored. Most o f the correlations are weak (i.e. between -0.3 and +0.3) indicating that the majority o f species are randomly distributed. O f particular interest are the strong correlations shown by Agropyron spicatum, Artemisia tridentata, Phacelia linearis, and Poa pratensis, suggesting that these species are responding to the dominant environmental gradients within the Lewisia rediviva vegetation. Correlation values with opposite signs indicate an opposite response by the corresponding species to the gradient in question. It is no surprise that this "gradient-  78  indicating", species association is also representative o f the greater biogeoclimatic zone in the area, the 'bunchgrass - sagebrush' community type. Table 3.4  Species  lAchmil 2Agrcri 3Agrspi 4Andocc 5Antdim 6Antumb 7Arahol 8Artdra 9Artfri lOArttri 1 lAstpur 12Brotec 13Cendif 14Cenbie 15Choten 16Chrnau 17Delnut 18Dessop 19Ericom 20Ericor 21Erifla 22Erilin 23Erisp. 24Eryinc 25Fripud 26Guetri 27Lapred 28Lewred 29Litrud 30Lommac 310pufra 320pupol 33Phalin 34Poapra 35Poasec 36Spocry 37Tradub 38Zigven  D C A species output from graph; Pearson (parametric coefficients o f r and r-sq) and Kendall (nonparametric tau) correlations with ordination axes (N= 63). Large values o f r and tau, indicating species with significant effects on the ordination axes, have been boldfaced. Axis 1 r .175 -.220 .670 .216 -.171 .177 .070 -.153 .264 -.670 .271 .287 -.199 -.231 .044 .259 .284 .175 -.061 -.072 .064 -.212 -.106 .105 -.171 -.210 .217 .103 -.048 -.063 .256 .105 .463 -.467 -.036 -.067 -.103 .029  Axis 2 r-sq .031 .048 .449 .046 .029 .031 .005 .023 .070 .448 .073 .083 .040 .053 .002 .067 .080 .031 .004 .005 .004 .045 .011 .011 .029 .044 .047 .011 .002 .004 .066 .011 .215 .218 .001 .004 .011 .001  tau .216 -.147 .613 .177 -.225 .156 .122 -.132 .199 -.676 .248 .361 -.148 -.215 .023 .158 .205 .138 -.039 -.040 .012 -.189 -.124 .080 -.127 -.198 .209 .106 -.098 -.190 .334 .080 .475 -.310 .015 -.121 -.098 .010  r .036 .118 -.681 -.011 .225 -.340 .155 .096 -.387 .110 -.078 .228 -.021 .234 .028 .388 .025 .237 .092 -.032 -.087 .262 -.007 -.331 .065 .089 .042 .190 -.104 -.259 -.017 -.331 .045 .385 .268 .069 -.103 -.087  r-sq .001 .014 .464 .000 .051 .115 .024 .009 .150 .012 .006 .052 .000 .055 .001 .151 .001 .056 .008 .001 .008 .069 .000 .110 .004 .008 .002 .036 .011 .067 .000 .110 .002 .148 .072 .005 .011 .008  tau -.034 .140 -.495 -.009 .174 -.256 .134 .115 -.380 .144 -.108 .078 -.045 .256 .011 -.017 .012 .197 .104 -.063 -.029 .315 -.004 -.178 -.009 .157 -.139 .167 .033 -.131 -.115 -.178 -.175 .349 .222 .044 -.035 -.070  79  Environmental Analysis The N M D S ordination o f plots based on the environmental parameters is shown in Figure 3-5 (see Appendix III for the raw scores o f these environmental values). Overall, no strong groupings o f plots are noticeable along either axis other than some similarities among plots 1,2 and 3; plots 6 and 7 are plausible outliers. Interpretation o f the environmental gradients represented by the two ordination axes was facilitated by using the overlay option available in P C - O R D (i.e. by varying the symbol sizes in the plot points), and by examining the correlations o f environmental variables with the ordination axes as listed in Table 3.5.  NMS ENVIRON 4  P  P  •  6  • P  3  •  p1  •  CM1  21  p5 •  p7 •  T  1  1  1  1  1  1  1  Axis 1 Figure 3-5  Plot Ordination from N M D S o f environmental parameters. Plot numbers designate study sites: p i (Venables Valley), p2 (Ashcroft Manor), p3 (Red H i l l ) , p4 (Basque Ranch), p5 (Cornwall Creek), p6 (Spatsum), p7 (Klootchville).  80  The majority o f the variables were factors (however superfluously) to the gradients o f both axes. H i g h positive values were given to comp-rock and barerock on A x i s 1 with comparably high values given to elevation, latitude, longitude, exposure, herbcover and introduced spp. on A x i s 2 (refer to bolded values in Table 3.5). Nevertheless, even though these gradients are strong, definition o f the gradient's makeup gives reason for their high values. In illustration o f the association between elevation, latitude and longitude on both axes, plot 6 has the lowest elevation (320 m), and is one o f the most southern study areas (32'N), while plot 7 has the highest elevation (709 m), and is one o f the most northern study areas (44' N ) ; all other plots were somewhere inbetween these two poles. A s the study area was located along a short stretch o f river running north to south and represented an overall limited landbase (see Figure 3-1), this association o f variables is conceivably unavailing i f not effectively neutralised. The positive correlation on both axes between bare-rock (representative o f unvegetated soil) and compaction-rock (an index o f soil compaction and rockiness) is also o f interest. W i t h greater amounts o f bare soil, sites tend to have greater soil compaction. This relationship hints at the negative effects cattle ranching has on the area with grazing and trampling compounding each others' disturbance. However, there is a negative correlation on both axes as well; sites with lower herb cover tend to be found at lower elevations along with having reduced microbiotic crusts. This also points to conceivably heavier grazing in the more accessible regions o f the lower plains. In regards to the centrality o f plots 1, 2 and 3, the grouping is moderately diffused with plot 2 being the most central o f the points. A s the distance between points represents an approximate measure o f the degree o f similarity or difference to each other  81  (closer points = greater environmental homogeneity), plot 2 serves as an average plot or provisional centroid for the 7 plots in the study; with perhaps plots 4 and 5 being transitional between this central grouping and the previously described, dis-similarities o f plots 6 and 7. What is overwhelmingly the most noteworthy manner in which to separate this plot from the others is via the microbiotic crust, bare rock and grazing variables. Although plot 2 cannot be classified as totally undisturbed, being that it is adjacent to a high traffic area (see Table 3.1), it was the only site surveyed that was not currently used for or had a detectable history o f grazing. Plot 2 also had by far the highest percent cover of intact microbiotic crust (an average o f 70%) as well as the lowest percent cover o f bare rock / soil (an average o f 9%), which again gives indirect implication as to the possible effects o f grazing. The centrality o f plot 2 along with the moderate to high correlation values registered by grazing could be explained in that the grazing variable was categorically and subjectively valued but more likely because grazing was widespread throughout the entire valley, albeit with varying intensity. This leads to the fact that although the other variables mentioned are congruent with the gradient given, the most functional premise to draw out and separate the plots on an environmental basis seems to be in reference to the surrounding effects o f grazing.  82  Table 3 . 5  Domains  N M D S Environmental Output from Graph; Pearson (parametric coefficients o f r and r-sq) and Kendall (nonparametric tau) Correlations with Ordination Axes (N= 7); significant rankings have been boldfaced.  Axis 1  Axis 2 r  r-sq  tau  r  r-sq  tau  .267  .071  .238  -.533  .284  -.238  slope elevation  -.287 -.354  .082  -.143  .045  .002  -.048  .125  -.238  lat  -.787  .620  -.586  .035  .001  .056  .998 .654 .762  .997 .427 .581  exposure comp-rock  -.429 .595  .184 .354  -.436 .429  .579 -.265  .336 .070  1.000 .488 .507 .546  PH texture colour  -.431  .186  -.048  -.359  .129  -.333  .160 .013  .025 .000  .206 -.056  -.066 -.253  .004 .064  -.206 .282  microcrust  -.705 .831  .496 .690  -.048  .059  .003  .048  .810  -.593  .352  -.429  -.229  .052  -.109  .087  .008  .218  -.792  .628  -.714  .058  -.134  .018  .098 -.195  .151 .085  .333  .241  .389 .292 -.182  .033  -.098  intro-spp native-spp  .243  .059  .233  .662  .438  .467  .230  .053  .098  .187  .035  .293  grazing  .461  .213  .350  .544  .296  .467  aspect  long  barerock shrub herbcover alphadiv betadiv  -.238  .293  Analysis o f Lewisia rediviva The third step in analysis involved quantifying characteristics of Lewisia rediviva for each o f the seven plots. Figure 3-6 displays the values obtained from the quadrats with maximum Lewisia rediviva growth at each plot. A s the intention o f this analysis was geared towards measuring the harvestable numbers and biomass o f the species, seedlings and immature individuals were not included. However, on a purely subjective level, seedlings appeared to be present in equal numbers throughout all the plots. Conversely, among the quadrats within each plot, seedling numbers were more variable because o f their tendency to grow in tight clumps.  83  In general, as with the seedlings, mature Lewisia rediviva plants often occurred in clumps. This was especially true in sites that were heavily grazed, as individuals that reached maturity usually did so in clumps under the protection o f sagebrush {Artemisia tridentata). A t times, the more matted o f the clumps constituted strikingly large, intertwined growths o f two to four, thin individuals.  100  10 • lew isiamax B total w eight • individual w eight  0.1  Figure 3 - 6  Characteristics o f Lewisia rediviva measured at the seven plots; Y axis is on a logarithmic scaling with weight categories in grams.  Recorded biomass weights among the plots were, on the whole, consistent and evenly proportioned. However, some of the sites did exhibit irregularities, the most noteworthy o f which were in plots 6 and 7. These two plots, which were also on opposite poles from each other concerning environmental variables, differed the most in total numbers and individual weights o f roots. The differences in root size could be attributed to temperature and moisture conditions during the autumnal growth phase o f the plant in the same manner that rosette diameter is dependent (Marvel 1986).  18  Alternatively, root  size could be affected by higher light and moisture levels in the vernal season when maximum carbohydrate storage capacities are realised (Marvel 1986). Likewise, in  84  either case for plots 6 and 7, biomass variability could be induced through a variety o f environmental conditions along an elevation gradient; higher elevation being equated to larger root size through greater moisture levels. Apart from the foregoing speculations, there appeared to be little difference in Lewisia  rediviva characteristics  among the seven  plots. 3.4  Discussion  The complex structure and dynamics o f plant communities, combined with a highly variable 'environmental complex', places very real limitations on any conclusiveness in plant ecology. Despite these limitations, however, this study has identified what may be some o f the contributing factors as to the status o f bitterroot in the Lower Thompson River Valley. B y concentrating on conditions where bitterroot occurred, that is through culturally guided means, a comparative description o f population structure and associated habitat features was attained. It can be expected that with a narrow data set, any ordination method would be constrained drawing out gradients in a manner accurate and meaningful to all the sites, as was particularly true for this information gathered. However, the data gathered at the seven sites were in-depth, and in all probability, may be representative o f bitterroot throughout its range. While no strong ecophysiological trends were detected to suggest what optimal growth and reproduction requirements might be for the species at large, the fact that bitterroot grew in highly site specific areas throughout the Valley does point to both micro- and macro-scale limitations to its distribution and abundance. This is also seen in the narrow range o f environmental conditions represented, indicating at least an appearance o f the species being confined to a particular type o f habitat.  18  Overall, climatic differences between the plots are perceived as slight. 85  What brought complementary expression to the status o f bitterroot was species composition and associations throughout the seven sites. To further these findings and to serve as an intriguing diachronic comparison, Davidson (1916) made some poignant observations o f bitterroot populations in the Ashcroft area earlier this century. Although presumably made on a descriptive level, the principal plant species associated with bitterroot were listed as the following (modern binomial equivalents given in brackets were applicable): Phacelia menziesii (P. linearis), Triticum glaucum occidentale (Agropyron spicatum), Erigeron peucophyllus (E. linearis), Opuntia polycantha borealis (O.fragilis), Artemisia tridentata and Artemisia frigida (p. 135). While all the species listed occurred within quadrats o f the present survey (offering some continuity), their overall weight in ordination appeared minimal as compared to species commonly associated with overgrazing (that is, as previously mentioned: Antennaria dimorpha, Poa pratensis, Achillea millifolium, Lappula redowskii, Centaurea diffusa, Tragopogon dubius and Erigeron compositus, excluding Opuntia fragilis and the association o f Agropyron spicatum - Artemisia tridentata). This leads to an inference that the change in environmental conditions seemingly brought on from continued grazing (in addition to introduced seeding o f Agropyron cristatum) have altered plant population structure, resulting in a substantially changed vegetation from that described by Davidson nearly 100 years ago. In summary o f variation in the vegetation data, ordination revealed a strong representation o f species commonly associated with disturbance and overgrazing; the majority o f other species had weak correlations. Comparatively, ordination o f the environmental data identified gradients which separated the seven sites primarily by way  86  of substrate conditions, which may be associated with disturbance and overgrazing (e.g. soil compaction, low microbiotic crust cover). Through indirect means, these two ordinations were linked to the extent that they meshed through gradients thought to be attributed to disturbance. However, in analysis o f bitterroot numbers and biomass, the effects o f disturbance, and thus overgrazing, did not prove as critical as temperature and moisture requirements found to be related in some degree to local elevation. Overall, the results o f this analysis point to the indication that bitterroot populations in the Lower Thompson River Valley are contained in, and adapted to, a disturbance regime. Species composition, while having some variability within sites, was found to be highly variable between sites. The weak relationship o f vegetation and environmental variation found between sites is most likely a direct consequence o f historical anthropogenic influences; i.e. bitterroot and its associated vegetation was not able to establish a 'natural', stable order because o f sustained human manipulation and intervention. Thus, enduring and identifiable connections could not develop, offering explanation as to why no obvious plant community or environmental gradients could be seen. If associative relationships did occur at one time, they have been severely masked by various kinds and levels o f disturbance, be it root harvesting, grazing, or combinations of both.  87  4.0  Overall Discussion and Conclusions "God creates. People rearrange " -Joseph Casey The relationship between ethnobotany and ecology, or more befitting, the  Nlaka'pamux people and bitterroot, is a closely knit but blurred weave o f agency and adaptation. The Lower Thompson River Valley is host to an extensive and intensive history o f anthropogenic association, making it conceptually difficult i f not impossible to differentiate between what are natural and what are humanly engineered environments; locally, they are one and the same. Moreover, philosophical rhetoric may not even allow for a distinction to be made, after all, the centricism o f believing humankind is not a part of nature is obvious and myopic. A l l told, the Lower Thompson River Valley is seen by the Nlaka'pamux as possessing a unique vegetal richness. A s contributory to bitterroot, these anthropogenic populations should be seen and approached in the light o f coevolution; this being an evolution articulated in the reciprocal relationship between plants and the people who manage them. Ethnobotanical Aspects Anthropogenic plant communities arise near human populations, both in proximity and persuasion. In part, they are ecological niches that show evidence o f human involvement and manipulation, being created through these disturbances. In broad terms, tracing the perpetuity o f the form and function o f plants and their use, Ford (1978) maintains that the theoretical road to domestication is often abbreviated by not recognising the place o f anthropogenic plant communities: "Adherence by a culture to general principle for manipulating vegetation does not preclude the creation o f new plant forms or communities. In fact, following rules like 'take only the part you w i l l  88  use' is precisely the process which leads to selection for larger leaves or seeds characteristic o f domesticated plants (p.251)". Recent theories as to the origins o f proto-agricultural traditions stem from a continuum o f people and plant interactions; from simple collecting, to cultivation and modification o f plant growth, to full-scale domestication where plant survival is entirely dependant on human input (Cotton 1996). Although conventional agriculture was not traditionally practised by the Nlaka'pamux, modes o f plant-food production once perceived as limited to w i l d foraging are in fact much more complex. In regards to bitterroot, the Nlaka'pamux were not passive and indifferent to its procuration as a plant resource but employed many practices (essentially horticultural) to secure and be active in its maintenance and development. In this manner, the Nlaka'pamux were able to obtain substantial benefit and yield while keeping the intensity o f their repair (upkeep contributions) to a minimum. B y taking advantage o f the combination o f natural and artificial selection techniques, bitterroot communities were strengthened and enhanced. Sustainability was achieved by allowing for genetic diversity to be maintained while still acquiring desirable phenotypes. Although it may be controvertible whether or not aspects o f this management were incidental or highly controlled and deliberate, the main point is that it was directed and purposeful. The sustainability o f bitterroot and their harvesting sites throughout the Lower Thompson River Valley over hundreds, perhaps thousands o f years, denotes that a management system was in place. The bitterroot harvest carried design on both cultural and cultivational fronts. Mythological and ritualistic beliefs as well as traditional concepts o f ownership infused a conscience o f accountability and responsibility on a personal and corporate level. In many ways this intimacy was crafted and required by the  89  Nlaka'pamux to ensure not only the species' survival but its long-term prolificacy as well. Timing and scheduling of the harvest was also important and was arranged and established according to a specific stage of bitterroot growth. Harvesting sites at lower elevations along the river contained plants that reached anthesis sooner than those at higher and thus cooler elevations which allowed roughly a two-week window of optimum digging for each site. This harvest practice was low in impact and prevented site over-harvesting while in turn stretching the seasonal harvest over a period of up to eight weeks from population to population. The physical manner and criteria by which bitterroot was harvested also played a pivotal role in its sustainability. A s compared to the harvesting of renewable plant parts (e.g. bark, stems, leaves), roots require special attention because in strict utilitarian terms their harvesting usually requires that the individual plant be destroyed. This presents a danger that over-utilisation could lead to site depletion or even species extinction if conservation measures are not in place (Turner 1981). Although the 'digging' of bitterroot is destructive in nature, it proved to be restorative and even productive in practice. The Nlaka'pamux maintained and enhanced bitterroot populations through harvest techniques that included selective digging (leaving seedlings and immature specimens to continue to grow), tilling of the soil (the use of a digging stick aerated and loosened the soil) and periodic transplantation of root bodies (instituting or enhancing populations at desirable sites).  90  Ecological Considerations While the prevalence and richness o f ethnobotanical species such as Erythronium grandiflorum has in itself contributed to their favourable use among many northern First Nations (Loewen 1998), the local distribution and abundance o f bitterroot in the Lower 19  Thompson River Valley may be a direct response to it first being valued as a food. Wide ethnobotanical use o f bitterroot is well documented throughout arid regions o f western North America -being a much sought after and heavily traded species- and may have propelled the Nlaka'pamux to bolster already occurring populations and possibly adding expediency to the creation o f new ones through transplantation. Within the continental distribution o f bitterroot, there seems to be a trend o f recession from the southern areas o f California combined with a northward-spreading range into the valleys o f southern British Columbia. Nlaka'pamux Elders speak o f the Lower Thompson River Valley becoming drier all the time, as evidenced by now dry channels that are still named on maps as remnants o f creeks and streams. W h i l e there is no denying a natural shift o f the species into the southern valleys o f British Columbia that are slowly becoming warmer and drier, it is arguable as to whether this extension northward was also encouraged by cultural rather than solely environmental, climatic or other natural means. Phytogeographic change is troublesome to delineate, especially in regards to a heavily used species such as bitterroot. A s reported by Wilson et al. (1988), this is the case for many ethnobotanical species, citing Reeve (1980), as encountering "...similar difficulties in assessing cultural vs. natural dispersal in terms o f the modern flora o f the  See Loewen (1998); ecological research done on the comparably harvested root food, the 'Yellow glacier lily', in many ways confers to the same disturbance regimes as that of bitterroot. 19  91  Yellowstone National Park area of Wyoming" (p.521). Although there are no pronounced discontinuities in the local distribution of bitterroot that would suggest human intervention outright, the empirical record of First Nation skill in plant dispersal and transplantation (Compton 1993b) does furnish evidence that what is accepted as the common range of the species may more correctly be its extended range. Among the Nlaka'pamux, transplanting appears to have been a common practice with a number root foods although maybe not on as an extensive a level as bitterroot. With transplantation being known to have occurred over distances of at least 30 km's (from Walhachin west to Ashcroft), expertise needed for successful transplantation is explicit; i.e. familiarity with ideal growing conditions and localities as well as phenological development. This can be seen through a variety of comments like, "...it is too rocky and dry and they don't come out right", "...they grow best here, but over there it is dry", or "...now they are growing good because it is damp". Moreover, incidental means of distribution should also be considered. Saraphine Kirkpatrick shared how Suzanne Magee, while transporting large baskets of bitterroot for transplantation by horse and cart, "...said she was coming across the river (Thompson) and she needed help and it was deep and the horse needed help and it all spilled over, the cart and everything was into the river [laughing]." Overall, occurrence of bitterroot in the Lower Thompson River Valley is pocketed and site-specific which does coincide with human agency as a possible mode of introduction. Nonetheless, in light of the continental distribution of the species, these pocketed occurrences cannot be considered disjunct; they may be better seen as exemplifying a kind of range extension or 'pushed dispersal' at the hands of the  92  Nlaka'pamux.  A d d i n g to the p l a n t s c o n s p i q u i t y i n the r e g i o n , c u l t u r a l d i s p e r s a l m a y , i n  t h e e n d , p r o v e t o o f f e r m o r e a n s w e r s t h a n first a n t i c i p a t e d . I n l i g h t o f o n l y w i n d a i d e d d i s s e m i n a t i o n , D a u b e n m i r e ( 1 9 7 5 ) states:  " H o w effective d i s s e m i n a t i o n is a c c o m p l i s h e d across tracts o f i n i m i c a l habitats c a n o n l y b e j u d g e d b y the w i d e s p r e a d o c c u r r e n c e o f the species. A b r e e z e b a r e l y s t r o n g e n o u g h to p i c k u p a n a v e r a g e d r y leaf w o u l d carry a disseminule easily. H o w e v e r , o n l y a rather v i o l e n t w i n d c o u l d result i n dissemination across l a n d supporting an abundance o f plants even a decimetre i n height, for such vegetation lifts breezes s u f f i c i e n t l y a b o v e the g r o u n d to l e a v e the d i s s e m i n u l e trapped indefinitely (p.21)." O b v i o u s l y t h e r e i s n o e n d t o p o s s i b i l i t i e s a n d r e a s o n s as t o h o w b i t t e r r o o t r e a c h e d i t s p r e s e n t d i s t r i b u t i o n . A s e x p l a i n e d b y W i l s o n et a l . ( 1 9 8 8 ) , " c l e a r l y , t h e s e q u e s t i o n s a r e o f m o r e than l o c a l interest, a n d their u l t i m a t e r e s o l u t i o n w i l l be o f great s i g n i f i c a n c e i n terms o f the p h y t o g e o g r a p h y o f w e s t e r n N o r t h A m e r i c a " (p.521). A b u n d a n c e o f b i t t e r r o o t i n the L o w e r T h o m p s o n R i v e r V a l l e y is a l s o n o t a b l e i n r e l a t i o n to a n t h r o p o g e n i c i n f l u e n c e s o f the N l a k a ' p a m u x . W h i l e there are n o n o n - h u m a n e x a m p l e s o f d i r e c t d i s t u r b a n c e s o n b i t t e r r o o t ( s u c h as t h e c a s e w i t h o t h e r r o o t v e g e t a b l e s b e i n g d u g u p b y bears for e x a m p l e ) , there w a s repeated l a r g e - s c a l e d i s t u r b a n c e b y the N l a k a ' p a m u x through harvesting. A l t h o u g h this d i d not imitate any k n o w n natural disturbances, h a r v e s t i n g m a y h a v e inadvertently a c c u s t o m e d i f not e n h a n c e d the species.  It i s n o t h a r d t o s e e h o w u p t u r n e d s o i l f r o m d i g g i n g h a d a p o s i t i v e e f f e c t o n s e e d g e r m i n a t i o n e s p e c i a l l y c o n s i d e r i n g that s e l e c t i v e h a r v e s t i n g left s o m e s p e c i m e n s i n c l u m p e d areas j u x t a p o s e d to f r e s h l y d i s t u r b e d substrate; to anthesis.  a n d this w a s i m m e d i a t e l y p r i o r  M o r e o v e r , w i n d is seen to be the m a i n d i s s e m i n a t i o n a g e n t o n l o c a l scales  f o r b i t t e r r o o t , p a r t i c u l a r l y as d i s s e m i n u l e s c a n b e c a u g h t o n e v e n t h e s m a l l e s t o f r i d g e s  93  (Daubenmire 1975). U p o n examination o f one harvesting site well into the month o f August, disseminules were located on the ground with seeds and calyptra laying beside obvious and recent evidences o f digging. For the Nlaka'pamux, as shared by Madeline Lanaro, the exact process is not always known, but the persistence o f bitterroot is undeniable; "I don't know how IhQuoopen propagates, but I imagine like any other plant, by the seeds. The IhQuoopen... seed themselves and just keep growing." Enhancement o f vegetative means o f propagation is also highly probable through the harvesting process. Although no studies have been done to quantify the extent o f vegetative propagation in bitterroot, it is often the case that the root bodies o f fleshy, tuberous geophytes can spread by way o f propagules. Moreover, horticultural literature notes bitterroot as the easiest 'lewisia' to grow (provided certain conditions are met) and outlines the relative ease o f increasing bitterroot vegetatively through 'notching' and splitting the root-stock and caudex (Mathew 1989). In traditional harvesting methods, root breakage is common as a result o f manually using a digging stick; rarely is a bitterroot removed without a lateral or taproot appendage being left in the ground. The viability o f plant multiplication through root breakage is also backed by natural, undisturbed multiplication processes. One growth formation found by Daubenmire (1975) exhibited below ground root grafting, while many other specimens were located with lateral roots producing caudices through a manner o f sympodial branching:  "Although a plant may continue to have but one caudex as it ages, adventitious buds arising well below the soil surface on thick lateral roots may produce additional caudices that rise to the surface, each bearing a rosette o f leaves, with the plant eventually exhibiting several orders o f branching (p. 15)".  94  Although untested, another more coincidental means o f vegetative propagation may have arisen through the traditional processing o f bitterroot. Traditionally, after a days harvest, the 'male' roots were 'de-hearted' on site at the same time as all the roots were peeled. A s the 'hearts' o f bitterroot are bud-like cores o f the following years new growth and traditionally recognised as male 'seeds' capable o f propagation, it can be seen that even though these 'hearts' were reportedly disposed o f in haphazard fashion, the chance o f some o f these 'seeds' inadvertently taking root must also be considered. Assessment o f the environmental impacts o f long-term root extraction and surrounding maintenance activities are difficult to measure. Ultimately, human induced effects on bitterroot in the Lower Thompson can only be measured and determined by comparing the diachronic behaviour o f those populations which are harvested with those that are not. This is because any human influence on a natural environment (in this case root harvesting, their cultivation and propagation) is superimposed upon the natural population dynamics o f an area. A s Cotton (1996) points out, "...comparative sampling of natural populations and populations which are subject to varying degrees o f harvesting intensities must be undertaken in order to investigate the sustainability o f different harvesting regimes" (p.361/62). It is recognised that without more systematic research, all environmental change and impact reporting o f anthropogenic influences is limited i f not speculative. Developmental Pressures Since the introduction o f cattle ranching in Ashcroft and surrounding areas during the m i d 1800's (Wier 1964), substantial disturbances to the vegetation o f the Lower Thompson River Valley has taken place. Although the physiognomic appearance o f the  95  rangeland has been retained through grazing, the floristic make-up of the species has been greatly affected. As a traditional management technique, periodic landscape burning selected for and was a benefit to root foods by keeping weedy species at bay. However, with the introduction of cattle ranching, these competing species were now allowed the chance to survive and establish themselves. This botanical transpiration can in some ways be accounted for morphologically; harvestable 'root foods' were largely geophytic, that is having an energy storing body and shoot apices located below ground. Competing therophytic plants (i.e. grasses) also grow in meadowlands but have their apical meristem tissue above ground where fire can destroy them but where grazing disturbance encourages them. Thus, a lack of burning allowed less palatable grasses and other weedy species a chance to increase or invade at the expense of geophytes and preferred, native, grazing plants such as Bluebunch Wheatgrass. The physiognomy of the Lower Thompson River Valley has remained a grassland primarily because larger plant morphologies have not had an opportunity to establish themselves because of grazing. However, it is not merely the presence of cattle that concerns the Nlaka'pamux, for as Ruth Peters recalled, "there used to be thousands a head of cattle in Ashcroft, now they don't have as many anymore, not like during the war". Not only is herbivory an issue, but the main concern lies in the effects of localised trampling and overgrazing caused by some ranchers. As related to bitterroot the loss of microbiotic crusts and the compaction of soil is severely damaging. Chief Lesley Edmonds explained: "LhQuoopen is harmed by cattle if they hang out in one area. Years ago the old time ranchers used to move their cattle around everyday so that they don't overgraze. Now people in 4x4's do it but  96  from a much more casual way; the cattle stay in one area and they trample the ground until it is packed rock hard." Compounding the effects of grazing, seeding of the fodder Crested Wheatgrass through the process of discing destroys natural plant communities of which bitterroot can often be apart (and in so doing, appears to be the distinguishing factor that separates the seemingly positive effects of traditional digging disturbance from the seemingly destructive effects of discing, not to mention that discing is only instituted in areas of which the natural plant community is already severely eroded through grazing). The only retribution offered through discing is alleviating future pressure off certain bitterroot harvesting sites. As shared by Chief Robert Pasco, "...it has become a lot better now where the IhQuoopen is growing and now doing well; the animals aren't out there because they are in the seeded area." In measuring the detrimental effects of grazing on bitterroot, many Nlaka'pamux have given reference to 'the way things were'; the roots were bigger and more of them. In the words of Saraphine Kirkpatrick, "...it was not very much long ago and you walk all over and you got to watch where you step cause you might step on it (bitterroot)". In casual comparison of root body sizes, a voucher specimen collected by Davidson in 1915 from Schuchem-elch (U.B.C. Accn #063207), did not visually differ in any way from specimens collected for present vouchers; likely, small differences in size could be recorded from year to year or locality to locality. However, graphic accounts by the Nlaka'pamux as well as Davidson (1916) of past bitterroot abundance is irrefutable and dumbfounding: "The bitter-root region covers several square miles of open undulating country. The plants are present in the millions; at one point twenty-two plants were counted on one square foot of ground.  97  Over large areas one finds an average o f twelve plants per square foot...(p.l35)." These numbers are not even approached anywhere in the valley at present. The small, localised harvesting areas that remain are few and even they are becoming eroded to the point that many Nlaka'pamux view bitterroot as now locally threatened i f not endangered. This erosion has serious implications for continuance o f the species throughout the Lower Thompson River Valley. Not only is the environment being slowly degraded and altered, but the cultural fixations upon which it adapted to is also eroding. This could be said o f other traditional foods as well. It should also be mentioned that through traditional territories being pre-empted earlier this century, many harvesting sites, some o f the best included, have become the private property o f non-Nlaka'pamux people. In one case, the most prominent o f areas, commonly referred to as "100-Mile Flats" and known to the Nlaka'pamux as "Schuchemelch", which means "Root-digging house" (Davidson 1916), is now privately owned in its entirety by Ashcroft Ranch; the main digging area is now a winter holding pen for cattle that has utterly destroyed the bitterroot that used to be found there. In other cases, land holders do not allow Nlaka'pamux access to their traditional harvesting sites purportedly for fear that it w i l l provide more incentive and momentum for reclamation of the land. Given the situation, some Nlaka'pamux have resorted to harvesting bitterroot in relatively secret digging sites where they can actively and responsibly conserve the plant along with aspects o f culture and tradition surrounding its use. Ultimately, the threat to bitterroot and other vegetation o f the Lower Thompson River Valley is not found solely in ranching nor in its array o f cumulative maintenance hazards that include discing. The real threat is in 'habitat loss' through development  98  pressures brought on through urban sprawl such as the 'Wastech' garbage dump, a woodchip mill, irrigated hayfields or the expansion of tarpaulined ginseng monoculture. Bitterroot is not an alpine meadow plant that may enjoy temporary isolation from development pressures at least by distance; the localised micro-environments in which bitterroot is found lays close to human habitation and may have been the one of the reasons why humans gathered there in the first place. For the future, bitterroot must be purposefully insulated and accounted for in all natural resource management decisions. In beholding a population of these plants in flower, one is drawn to the tension found in the delicateness of light pink petals against the often rocky and arduous landscape. For the Nlaka'pamux, it is a picture of balance, a sense of place drawn out like a dance over time. They are the ones who have partaken of the valley's rich volcanic soils a plant whose root body incarnates past generations. How different would bitterroot and surrounding ecologies be valued if everyone affirmed this heritage rather than the pursuit of a narrowly defined sense of wealth? As Chief Leslie Edmonds shared, " i f the mighty big wheel of progress doesn't take these things into consideration, it will all be lost...". Bitterroot's long-term sustainability resonates in the fertile traditions of the Nlaka'pamux. Their stewardship will continue to be a rich and innovative source of vegetal and natural resource management for years to come. Living up to the more recent, western scientific name of 'rediviva', it is hoped that with some attentiveness and respect, populations of bitterroot that were once so profound can satisfy its spirited name and 'live again'.  99  Literature Cited Alcorn, J.B. 1995. The Scope and A i m s o f Ethnobotany i n a developing World. In Schultes, R . E . and S. von Reis. Ethnobotany: Evolution of a Discipline. Dioscorides Press, Portland, pp. 23-39. Atmospheric Environment Service. 1982. Temperature and Precipitation: 19511980, British Columbia. Environment Canada, Ottawa. Balick, M . J . 1994. Ethnobotany, Drug Development and Biodiversity Conservation: Exploring Linkages. In Prance, G.T., D . J . Chadwick and J. Marsh (eds.). Ethnobotany and the Search for New Drugs. Ciba Foundation Symposium, 185. John W i l e y and Sons, West Sussex, pp.228-239. 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University o f North  105  Appendix I  Nli'kesentem, as recorded by Teit (1912, p.297); "obtained from Nkamtci 'nemux"  When Nli 'kesentem was ready to be lowered down by the spider and his wife, the latter put four stones in the basket, saying, "Throw one o f these stones overboard when you reach each o f the four obstacles." She also gave him a present o f four articles o f clothing, a coat, shirt, leggings, and moccasins o f buckskin, and some food to eat on the way, consisting o f four bundles o f roots which grew plentifully in the upper world. Each bundle was o f a different variety (see below). When Nli 'kesentem reached the earth, he ran four times with the slack o f rope, twice to the east and twice to the west. He tugged the rope four times, -twice at each quarter; then the spider pulled the basket up. He cached his present o f clothes at Lytton, but carried the roots on his back to Beta 'ni (Botanie). Although he ate o f them, they did not decrease in number. He overtook four old women on the trail, -the Ant, Beetle, etc., and learned from them that his wife, Lqo 'qena (the teal duck), had been taken by his father. H e overtook his other wife, and where he told her to camp, he created a spring which runs at the present day. When out hunting one day, he was carrying his lunch o f roots, as usual, and he felt them heavy. He thought to himself, "These roots are heavy, and do not decrease when I eat them. What shall I do with them?" Then the spiders wife called from the sky, saying, "Throw them on the earth to the people." Nli 'kesentem took some roots from the bundle containing tatu 'en, and threw some to the east, saying, " Y o u shall hence forth live on the earth, and grow plentifully in that direction. People w i l l dig you and eat you in great numbers." Then he threw some to each o f the other quarters, addressing the roots  106  in the same fashion. Taking some roots from each o f the other bundles, he did the same thing with them. Thus these roots from the sky became plentiful all over the mountains of the earth. Still most o f the roots remained in the bundles, so Nli 'kesentem emptied them out in the Beta 'ni valley, saying, " Y o u w i l l become very plentiful here, and this place w i l l become a noted root-digging resort." Therefore the Beta 'ni valleys are celebrated for the great quantity and variety of roots to be found there. [note: one bundle contained tatu 'e«-roots ( W i l d Potato or Indian Potato, likely Claytonia lanceolata); another bundle consisted o f skametc-roots (Yellow Adder Tongue L i l y , likely Erythronium grandiflorum). The roots in the other two bundles are uncertain.]  107  Appendix II R a w scores of the species matrix; percent cover values o f the 38 species in the seven plots used for the ordination  Venables Valley Quadrats (% cover) Species 1) Achillea millefolium 2) Agropyron cristatum 3) Agropyron spicatum 4) Androsace occidentalis 5) Antennaria dimorpha 6) Antennaria umbrinnella 7) Arabis holboellii 8) Artemisia dracunculus 9) Artemisia frigida 10) Artemisia tridentata 11) Astragalus purshii 12) Bromus tectorum 13) Centaurea diffusa 14) Centaurea maculosa 15) Chorispora tenella 16) Chrysothamnus nauseosus 17) Delphinium nuttallianum 18) Descuriania sophia 19) Erigeron compositus 20) Erigeron corymbosus 21) Erigeron flagellaris 22) Erigeron linearis 23) Erigeron sp. 24) Erysimum inconspicuum 25) Fritillaria pudica 26) Guem triflorum 27) Lappula redowskii 28) Lewisia rediviva 29) Lithospurmum ruderale 30) Lomatium macrocarpum 31) Opuntia fragilis 32) Opuntia polyocantha 33) Phacelia linearis 34) Poa pratensis 35) Poa secunda 36) Sporobolus crypytandrus 37) Tragopogon dubius 38) Zigadenus venenosus Bare rock/earth Microbiotic crust Total herb cover Number of species Lewisia rediviva (individuals)  la  lb  lc  Id  8 2 0.5  4 0.5 2.5  0.5 4  le  lf  1.5  3 1.5  2  4.5  0.5 2  0.5 2.5  2  0.5 3  0.5  0.5  1  1 1 1  1  1  lh  lg  li  1.5  1 1  1 30  4.5  2  0.5 35  5  0.5 1.5  1  1.5  0.5  1 1  2 3  2 6 1  1.5  1  1 1  1.5 0.5  0.5  1 2  1.5  1.5  0.5  0.5  1.5  1  2 1  2  1.5  1  3  40 3 17.5 8 26  1.5  30 17 14.5 7 17  1.5  35 5 10.5 9 21  20 20 13.5 10  4  50 1 13 9 19  1 1  1 2.5  1  2.5 1  1.5  1  3 7 43.5 9 9  7 40 49 12 19  0.5 40 15 19.5 8 17  50 5 17 11 7  108  Ashcroft Manor  Quadrats (% cover) Species  Achillea millefolium Agropyron cristatum 3) Agropyron spicatum 4) Androsace occidentalis 5) Antennaria dimorpha 6) Antennaria umbrinnella 7) Arabis holboellii 8) Artemisia dracunculus 9) Artemisia frigida 10) Artemisia tridentata 11) Astragalus purshii 12) Bromus tectorum 13) Centaurea diffusa 14) Centaurea maculosa 15) Chorispora tenella 16) Chrysothamnus nauseosus 17) Delphinium nuttallianum 18) Descuriania sophia 19) Erigeron compositus 20) Erigeron corymbosus 2 1 ) Erigeron flagellaris 2 2 ) Erigeron linearis 2 3 ) Erigeron sp. 24) Erysimum inconspicuum 2 5 ) Fritillaria pudica 2 6 ) Guem triflorum 2 7 ) Lappula redowskii 2 8 ) Lewisia rediviva 2 9 ) Lithospurmum ruderale 3 0 ) Lomatium macrocarpum 31) Opuntia fragilis 3 2 ) Opuntia polyocantha 3 3 ) Phacelia linearis 34) Poa pratensis 35) Poa secunda 3 6 ) Sporobolus crypytandrus 3 7 ) Tragopogon dubius 38) Zigadenus venenosus  2a  2b  2c  2d  2f  2e  2h  2g  2i  1)  2)  1.5  1  1  1  2.5  2  0.5  0.5  8  1 2.5  1.5  1.5  35  20  35  0.5 1  1  1.5  0.5  3  6  5  4  4.5  14  0.5  2  1  0.5  1  0.5  1.5  2  0  0.25  1  0.5  0.5  0  0.25  2.5  3  0.5  1  1.5  0.5  0  0  0.5  4  3  2.5  4  1.5  1.5  1.5  12  3 2  6  2.5  2  2  0.5  0.5  7  8  15  15  5  2  20  3  7  M i c r o b i o t i c crust  75  60  65  70  45  90  60  85  80  T o t a l herb c o v e r  14  13.5  11.75  12  26.75  20.5  43.5  28.5  54.5  7  5  7  8  10  7  6  7  6  45  0  3  0  1  2  0  0  3  B a r e rock/earth  N u m b e r o f species  Lewisia rediviva ( i n d i v i d u a l s )  109  Red Hill  Quadrats (% cover) Species Achillea millefolium Agropyron cristatum Agropyron spicatum Androsace occidentalis Antennaria dimorpha Antennaria umbrinnella Arabis holboellii Artemisia dracunculus Artemisia frigida Artemisia tridentata 11) Astragalus purshii 12) Bromus tectorum 13) Centaurea diffusa 14) Centaurea maculosa 15) Chorispora tenella 16) Chrysothamnus nauseosus 17) Delphinium nuttallianum 18) Descuriania sophia 19) Erigeron compositus 20) Erigeron corymbosus 21) Erigeron flagellaris 22) Erigeron linearis 23) Erigeron sp. 24) Erysimum inconspicuum 25) Fritillaria pudica 26) Guem triflorum 27) Lappula redowskii 28) Lewisia rediviva 29) Lithospurmumruderale 30) Lomatium macrocarpum 1) 2) 3) 4) 5) 6) 7) 8) 9) 10)  3b  3a  3c 1  7 0.5 2  4 0.5 0.5  12  0.5  0.5  6  3.5  0.5  1.5  6  35 0.5  0.5  0.5  0.5  1.5  1  4  1 1  0.5  3h  3g  0.5  1.5  3i 2.5  27  10  3.5  1.5  0.5  0.5  0.5  1 1  4 2  4 1.5  35 0.5 1 2 0.5 2  1  0.5  0.5  1.5  1  1  1.5  1  0.5  1 1  0.5  1.5  31) Opuntia fragilis 32) Opuntia polyocantha 33) Phacelia linearis 34) Poa pratensis 35) Poa secunda 36) Sporobolus crypytandrus  0.5 0.5  0.5 0.5  0.5  37) Tragopogon dubius 38) Zigadenus venenosus  1.5  1  0.5  55  60 4.5 12.5  65 1.5 21.5 11 17  Microbiotic crust Total herb cover Number of species Lewisia rediviva (individuals)  3f  17 0.5 1  0.5  Bare rock/earth  3e  3d  5 20.5 11 7  10 8  0.5  1  1  0.5  1  1  0.5 1  3 0.5  0.5 0.5  0.5  1  1 65 1 23  80 16  40 4 41.5  20 4 40.5  55 10 25.5  15 8 44  9 14  9 6  9 10  10  10 10  9 4  4  8  110  Basque Ranch  Quadrats (% cover) Species  4a  Achillea millefolium Agropyron cristatum Agropyron spicatum Androsace occidentalis Antennaria dimorpha Antennaria umbrinnella Arabis holboellii Artemisia dracunculus 9) Artemisia frigida 10) Artemisia tridentata 11) Astragalus purshii 12) Bromus tectorum 13) Centaurea diffusa 14) Centaurea maculosa 15) Chorispora tenella 16) Chrysothamnus nauseosus 17) Delphinium nuttallianum 18) Descuriania sophia 19) Erigeron compositus 20) Erigeron corymbosus 21) Erigeron Jlagellaris 22) Erigeron linearis 23) Erigeron sp. 24) Erysimum inconspicuum 25) Fritillaria pudica 26) Guem triflorum 27) Lappula redowskii 28) Lewisia rediviva 29) Lithospurmum ruderale 30) Lomatium macrocarpum 31) Opuntia fragilis 32) Opuntia polyocantha 33) Phacelia linearis 34) Poa pratensis 35) Poa secunda 36) Sporobolus crypytandrus 37) Tragopogon dubius 38) Zigadenus venenosus  4b  1) 2) 3) 4) 5) 6) 7) 8)  Bare rock/earth Microbiotic crust Total herb cover Number o f species  Lewisia rediviva (individuals)  4c  3  4d  6.5  4f  4e  3  1.5  4h  4g  1.5  2  4i  3.5  2.5  2  1.5  4  8  70  5  1  0.5  0.5  3  1 0.5  3  40  3  0.5  1.5 0.5  6  1.5 0.5  0.5  1  0.5  11  1  1  2.5  1  1  1  0.5  1.5  0.5  3.5  0.5  1.5  3  2.5  4  1  1.5  1  40 2.5 18.5 8 7  65 5  4 1  15 6 7  80 6 26|  40 2 11.5 6 4  0.5  1  4.5 1.5  1.5  0.5  0.5  3.5 6  3  0.5 1.5  1.5  2.5 1 58 9 1  30 1  1  0.5 55 3.5 10 7 5  15 3 25.5 9 42  60 4 13.5 6 1  14 9 1  111  Species  5a  1) Achillea millefolium 2) Agropyron cristatum 3) Agropyron spicatum 4) Androsace occidentalis 4 5) Antennaria dimorpha 6) Antennaria umbrinnella 0.5 7) Arabis holboellii 0.5 8) Artemisia dracunculus 9) Artemisia frigida 20 10) Artemisia tridentata 11) Astragalus purshii 12) Bromus tectorum 13) Centaurea diffusa 14) Centaurea maculosa 15) Chorispora tenella 16) Chrysothamnus nauseosus 17) Delphinium nuttallianum 18) Descuriania sophia 19) Erigeron compositus 20) Erigeron corymbosus 21) Erigeron flagellaris 22) Erigeron linearis 0.5 23) Erigeron sp. 24) Erysimum inconspicuum 25) Fritillaria pudica 26) Guem triflorum 27) Lappula redowskii 2 28) Lewisia rediviva 29) Lithospurmum ruderale 0.5 30) Lomatium macrocarpum 31) Opuntia fragilis 32) Opuntia polyocantha 33) Phacelia linearis 25 34) Poa pratensis 35) Poa secunda 36) Sporobolus crypytandrus 1.5 37) Tragopogon dubius 38) Zigadenus venenosus 15 Bare rock/earth 35 Microbiotic crust 54.5 Total herb cover 9 Number of species Lewisia rediviva (individuals) 27  Cornwall Creek Quadrats (% cover) 5d 5e 5f 5g  5c  5b  5h  5i  1 2  15  0.5 0.5 2  6  10  1  0.5  1  0.5  3  10  2  0.5 0.5 1  0.5 1.5  1  1.5  0.5  0.5  1  1  2  35  40  20  0.5  1  0.5  0.5  1 0.5 0.5  1  1  1.5  0.5  2  2  1  1.5  0.5  12  1.5 1  1.5  1  1.5  2  2  1  2  2 0.5 0.5  20  30  25  20  25  20  20  15  0.5  1.5 1 6 70 73.5 10 18  1.5  1  1.5  2  1.5  5 35 85.5 11 24  15 40 45.5 7 12  70 20 47 7 26  30 20 33.5 12 34  10 30 45 9 37  1 0.5 25 20 34.5 11 33  1 0.5  15 45 29.5 12 23  112  Spatsum Quadrats (% cover) Species  6a  6b  1)Achillea millefolium 2)Agropyron cristatum 9 3)Agropyron spicatum 0.5 4)Androsace occidentalis 5)Antennaria dimorpha 6)Antennaria umbrinnella 0.5 7)Arabis holboellii 8)Artemisia dracunculus 9)Artemisia frigida 10)Artemisia tridentata 1 11)Astragalus purshii 12)Bromus tectorum 13) Centaurea diffusa 14) Centaurea maculosa 15) Chorispora tenella 16) Chrysothamnus nauseosus 17)Delphinium nuttallianum 18)Descuriania sophia 19)Erigeron compositus 20) Erigeron corymbosus 21)Erigeron flagellaris 22) Erigeron linearis 23)Erigeron sp. 24)Erysimum inconspicuum 25) Fritillaria pudica 26) Guem triflorum 27)Lappula redowskii 28)Lewisia rediviva 1 29)Lithospurmum ruderale 30)Lomatium macrocarpum 31) Opuntia fragilis 1.5 32) Opuntia polyocantha 33)Phacelia linearis 1 2.5 34)Poa pratensis 35) Poa secunda 36) Sporobolus crypytandrus 37) Tragopogon dubius 38)Zigadenus venenosus Bare rock/earth 70 Microbiotic crust 5 Total herb cover 17 Number of species 8 Lewisia rediviva (individuals) 10  6c  6d  6e  6f  6g  6h  6i  0.5 4 0.5 1  3 0.5 1  6  8  3  0.5  0.5  0.5  0.5  0.5  10 0.5  1  1 1.5  1  20 1  3 0.5  10  1 1  2  10 0.5  1.5  12 0.5 1.5  3.5 0.5  1  0.5  1 1.5  1 0.5  1.5  1  0.5 0  0.5 2  25 30 21 10 0  1  3.5 0.5  65 5 32 10 13  0.5 1.5  2  1  0.5 3  4 4  1 1  0.5 2.5 0.5  1.5  10  4  0.5  1.5  3.5 3  3 1.5  2 4  2 1.5  1.5 3.5  2.5 2  1  1  60 40 4 2 23 20.5 10 11 21 25  20 20 4 2 31 23.5 8 9 6 46  40 20 3 4 28.5 21.5 14 11 39 79  113  Species 1) Achillea millefolium 2) Agropyron cristatum 3) Agropyron spicatum 4) Androsace occidentalis 5) Antennaria dimorpha 6) Antennaria umbrinnella 7) Arabis holboellii . 8) Artemisia dracunculus 9) Artemisia frigida 10) Artemisia tridentata 11) Astragalus purshii 12) Bromus tectorum 13) Centaurea diffusa 14) Centaurea maculosa 15) Chorispora tenella 16) Chrysothamnus nauseosus 17) Delphinium nuttallianum 18) Descuriania sophia 19) Erigeron compositus 20) Erigeron corymbosus 21) Erigeron jlagellaris 22) Erigeron linearis 23) Erigeron sp. 24) Erysimum inconspicuum 25) Fritillaria pudica 26) Guem triflorum 27) Lappula redowskii 28) Lewisia rediviva 29) Lithospurmum ruderale 30) Lomatium macrocarpum 31) Opuntia fragilis 32) Opuntia polyocantha 33) Phacelia linearis 34) Poa pratensis 35) Poa secunda 36) Sporobolus crypytandrus 37) Tragopogon dubius 38) Zigadenus venenosus Bare rock/earth Microbiotic crust Total herb cover Number of species  Lewisia rediviva (individuals)  7a  7b  Klootchville Quadrats (% cover) 7e 7f 7d 7g  7c  7h  7i  1.5 7  3  4  4  6  1  2  9 1  5  0.5  1  3  10  7  8  3  1 0.5  0.5 0.5  4  4  3 0.5  1.5  2  2.5  0.5 1 0.5  0.5  0.5  1.5 1.5  1.5 0.5  0.5 1.5 7 1  0.5  1  1 3  1 2.5  1 1  5 1.5  8 1.5  0.5  4  3  4  6  2 1.5 5 1 31 10 5  1 0.5 10 0.5 34 14 33  1.5  1 6 1 27 12 34  0.5  0.5  1  0.5  0.5 1 2 5  1.5 0.5  1 2  1 2.5  1 0.5  4  7 1  8  10  4  6  5 1 34.5 11 26  2 1.5 10 1 30 9 29  4  2  15  3  2 0.5 20 3 19.5 10 6  1  45 1 31 11 12  1  10 2 32.5 10 5  6 2 19.5 11 9  114  1 landforms 1 aspect(degrees) 1 slope angle (degrees)  | Environmental Domains  Venables Valley |  00  c o J <*S  o  «  5t  X X  CN  %  o.  1 J j J 1  1 1 1 1 |  | | |  \Lewisia redivia 1 population area 1 max. number in IXlm. 1 total dry weight (roots) 1 net dry weight (roots)  1 human management 1 title 1 use/disturbance crown | heavy grazing |  reserve| vacant |  private | heavygrazing |  reserve| light grazing |  reserve| heavy grazing|  18.580g| 0.4425g|  Tf CN  24.747g| 0.4883g|  0.5-1 hai •3ci  15.431g| 0.5133 g|  0.5-1.0 ha|  0.5 ha| OO  2-3 hai  7.051  7.11|  7.021  6.981 7.031  6.1 cm| 7.16|  reserve | light grazing |  private | heavy grazing!  25.922g| 0.7307g|  1-2 ha|  10 ha 21.697g| 0.3041g|  chroma 21  IOYR|  chroma 21  YR  7.06) 7.06| sandy loam | sandy clay loam| grayish brown | dk. grayish brown| 10 value 4| value 5 1  3.95 cm  in  21.652g| 0.4547g|  |  CN  20.169g| 0.5824 g|  value 41 chroma 21  value 31 chroma 31  value 51 chroma 21  YR  6.971  7-44 sandy clay loam | dk. grayish brown | 10  YR  (  6.641| 6.8211  OO Cl  value 51 chroma 21  YR  1  7 . 1 6 1| 7.13 loamy sand grayish brown J lOYR]  18.5 cm|  7.71 | 7.75|| 7.37|1 7.61 clay loam | dark brown j 10  CS oo 43 CN  value 41 chroma 21  IOYRI  1  7.841 loamy sand grayish brown J 10  NO  1 texture 1 colour 1 hue 1 value 1 chroma  7.061 6.991 sandy loam | dk. grayish brown 1  11.2cm||  CQ  6.961  | 7.12 1  CQ  5.3 cm  partial shade|  O  |  <r>  CN 4= X  1 pH#3 1 pH average  00  O  8.1511 7.761  WN CN 42 X  1  "3-  bunchgrass | BG xw| very dry warm|  NO  low sagebrush | | very dry hot|  ci  large sagebrush | BG XW: very dry warm |  CN  bunchgrass | bunchgrass | BGxw | very dry warm | very dry hot |  CN Cl  full direct sun|  CN  partial shade|  ?  stp. slope; full sun|  r~  sloped; full sun1  o  1  | Klootchville  ON  1 soils 1 depth (10 probe average) 9.25 cm j  CN  8.8 cm 6.931  r~ low sagebrush | BG xh2 | very dry hot|  CN N O  | large sagebrush | BGxh2| | very dry hot |  oo o oo  1 vegetation types 1 height of vegetation 1 biogeoclimatic zone 1 subzone variant  o  ON  |  Spatsum  32'N-17'W  |  fN fN  | full direct sun  Cornwall Creek  OO TICN CS  44'N-19'W |  |  CN  o  38'N - 19'W |  Plot Sites | Basque Ranch  <N  38'N - 21'W |  Red Hill  OO  oo  1 full direct sun  43'N - 19'W |  CN Cl  CN in ci  34-N-19'W|j  Ashcroft Manor |  ON  1 climate 1 elevation (m) 1 exposure  |  | |  Appendix III R a w scores of the environmental matrix; not all values were used for the ordination  11  A p p e n d i x I V List o f all taxa discussed in the text or present in one o f the seven survey sites of Lewisia rediviva; left column gives scientific binomial (alphabetically arranged) and author, right column gives common English name as well as previously referenced Nlaka'pamux names in italics  Scientific name Achillea millefolium L . Agropyron cristatum (L.) Gaertn. Agropyron spicatum (Pursh) Scribn. & Smith Amelanchier alnifolia Nutt. Androsace occidentalis Pursh Antennaria dimorpha (Nutt.) T. & G . Antennaria umbrinella Rydb. Arabis holboellii Hornem. Artemisia dracunculus L . Artemisia frigida W i l l d . Artemisia tridentata Nutt. Astragalus purshii Dougl. Betula L . Bromus tectorum L . Balsamorhiza sagittata (Pursh) Nutt. Centaurea diffusa L a m . Centaurea maculosa L a m . Chorispora tenella (Pall.) D C . Claytonia lanceolata Pursh Chrysothamnus nauseosus (Pall.) Britt. Delphinium nuttallianum Pritz. Descuriania sophia (L.) Webb Erigeron compositus Pursh Erigeron corymbosus Nutt. Erigeron flagellaris Gray Erigeron linearis (Hook.) Piper Erysimum inconspicuum (Wats.) M a c M . Erythronium grandiflorum Pursh Frittilaria pudica (Pursh) Spreng. Geum triflorum Pursh Lappula redowskii (Hornem.) Greene Lewisia columbiana (Howell) Robins. Lewisia pygmaea (Gray) Robins. Lewisia rediviva Pursh Listera R. B r . Lithospurmum ruderale Dougl. Lomatium dissectum (Nutt.) Math. & Const. Lomatium macrocarpum (Nutt.) Coult. & Rose  C o m m o n name Yarrow Crested Wheat Grass Bluebunch Wheat Grass Saskatoon, Serviceberry Western Fairy-candelabra L o w Pussy-toes Umber Pussy-toes Holboell's Rockcress Tarragon Pasture Sage B i g Sagebrush Woollypod Milk-vetch Birch Cheat Grass Balsamroot; shchAquem Tumble Knapweed Spotted Knapweed Chorispora, Blue Mustard Western Spring Beauty C o m m o n Rabbitbrush Upland Larkspur Flixweed Cut-leaved Daisy Long-leaved Daisy Trailing Daisy Fine-leaved Daisy Small Wallflower Y e l l o w Glacier L i l y Y e l l o w Bells O l d M a n ' s Whiskers Western Stickseed Columbia Lewisia Alpine Lewisia Bitterroot; IhQuoopen Twayblade Lemonweed Fern-leaved Desert-parsley Large-fruited Desert-parsley  116  Montia perfoliata (Donn) Howell Montia sibrica (L.) Howell Opuntia fragilis (Nutt.) Haw. Opuntia polyocantha Haw. Panax L . Phacelia linearis (Pursh) Holz. Pinus ponderosa Dougl. Poa pratensis L . Poa secunda J.S. Presl in C B . Presl Prunus virginiana L . Rhamnus purshiana D C . Sporobolus cryptandrus (Torr.) Gray Syringa vulgaris L . Talinum Adans. Tragopogon dubius Scop. Zigadenus venenosus Wats.  M i n e r ' s-lettuce Siberian Miner's-lettuce Brittle Prickly-pear Cactus Plains Prickly-pear Cactus Ginseng Threadleaf Phacelia Ponderosa Pine Kentucky Bluegrass Sandberg Bluegrass Comon Chokecherry Cascara Sand Dropseed C o m m o n Lilac Fameflower Y e l l o w Salsify Death-camas  117  

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