Monograph |
Corresponding author: Jeffery M. Saarela ( jsaarela@mus-nature.ca ) Academic editor: Doug Soltis
© 2020 Jeffery M. Saarela, Paul C. Sokoloff, Lynn J. Gillespie, Roger D. Bull, Bruce A. Bennett, Serguei Ponomarenko.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Saarela JM, Sokoloff PC, Gillespie LJ, Bull RD, Bennett BA, Ponomarenko S (2020) Vascular plants of Victoria Island (Northwest Territories and Nunavut, Canada): a specimen-based study of an Arctic flora. PhytoKeys 141: 1-330. https://doi.org/10.3897/phytokeys.141.48810
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Victoria Island in Canada’s western Arctic is the eighth largest island in the world and the second largest in Canada. Here, we report the results of a floristic study of vascular plant diversity of Victoria Island. The study is based on a specimen-based dataset comprising 7031 unique collections from the island, including some 2870 new collections gathered between 2008 and 2019 by the authors and nearly 1000 specimens variously gathered by N. Polunin (in 1947), M. Oldenburg (1940s–1950s) and S. Edlund (1980s) that, until recently, were part of the unprocessed backlog of the National Herbarium of Canada and unavailable to researchers. Results are presented in an annotated checklist, including keys and distribution maps for all taxa, citation of specimens, comments on taxonomy, distribution and the history of documentation of taxa across the island, and photographs for a subset of taxa. The vascular plant flora of Victoria Island comprises 38 families, 108 genera, 272 species, and 17 additional taxa. Of the 289 taxa known on the island, 237 are recorded from the Northwest Territories portion of the island and 277 from the Nunavut part. Thirty-nine taxa are known on the island from a single collection, seven from two collections and three from three collections. Twenty-one taxa in eight families are newly recorded for the flora of Victoria Island: Artemisia tilesii, Senecio lugens, Taraxacum scopulorum (Asteraceae); Crucihimalaya bursifolia, Draba fladnizensis, D. juvenilis, D. pilosa, D. simmonsii (Brassicaceae); Carex bigelowii subsp. bigelowii, Eriophorum russeolum subsp. albidum (Cyperaceae); Anthoxanthum monticola subsp. monticola, Bromus pumpellianus, Deschampsia cespitosa subsp. cespitosa, D. sukatschewii, Festuca rubra subsp. rubra, Lolium perenne, Poa pratensis subsp. pratensis (Poaceae); Stuckenia filiformis (Potamogetonaceae); Potentilla × prostrata (Rosaceae); Galium aparine (Rubiaceae); and Salix ovalifolia var. ovalifolia (Salicaceae). Eight of these are new to the flora of the Canadian Arctic Archipelago: Senecio lugens, Draba juvenilis, D. pilosa, Anthoxanthum monticola subsp. monticola, Bromus pumpellianus, Deschampsia cespitosa subsp. cespitosa, Poa pratensis subsp. pratensis and Salix ovalifolia var. ovalifolia. One of these, Galium aparine, is newly recorded for the flora of Nunavut. Four first records for Victoria Island are introduced plants discovered in Cambridge Bay in 2017: three grasses (Festuca rubra subsp. rubra, Lolium perenne, and Poa pratensis subsp. pratensis) and Galium aparine. One taxon, Juncus arcticus subsp. arcticus, is newly recorded from the Northwest Territories. Of the general areas on Victoria Island that have been botanically explored the most, the greatest diversity of vascular plants is recorded in Ulukhaktok (194 taxa) and the next most diverse area is Cambridge Bay (183 taxa). The floristic data presented here represent a new baseline on which continued exploration of the vascular flora of Victoria Island – particularly the numerous areas of the island that remain unexplored or poorly explored botanically – will build.
biodiversity, Canadian Arctic Archipelago, checklist, floristics, herbarium, natural history collections, range extension, taxonomy
The Canadian Arctic Archipelago is a large group of islands occupying the northern third of Canada and comprising 94 islands greater than 130 km2 and 36,469 smaller islands (
The flora of an area (whether local, regional, national, continental or global) refers to all plant species and taxa at other ranks occurring in the area; it is a principal measure of biodiversity. Exploration and documentation of the vascular plant flora of the Canadian Arctic Archipelago has been ongoing since the earliest expeditions in search of the Northwest Passage, nearly 200 years ago, during which crew members obtained new scientific information on the natural history of the lands being explored, including collections of plants. Vascular plant specimens have accumulated from across the Archipelago through the decades, variously collected opportunistically or as part of botanical studies by both botanists and non-botanists alike. Many floristic studies of areas of the Canadian Arctic Archipelago have been published, ranging from simple lists of plants to more detailed accounts of plant biodiversity, including information about taxonomy, nomenclature, distribution and ecology (
In contrast to the flora of an area, which is based on presence or absence of species regardless of abundance, vegetation refers to assemblage(s) of plant species, often focused on or characterized by the subset of species that are dominant in ecological communities. Arctic vegetation is responding rapidly to the changing Arctic climate, which is warming at twice the rate of the rest of the planet (
Many regions of the Canadian Arctic Archipelago remain underexplored or unexplored botanically, given the massive size of the region, the short window of opportunity for making field collections during Arctic summer, the small number of taxonomically trained and oriented Arctic botanists conducting field research, and the great logistical challenges and costs associated with accessing remote Arctic areas (
Here, we report the results of a collections-based floristic study of Victoria Island in the western Canadian Arctic Archipelago. Our study synthesizes existing published and unpublished information on the flora of the island, including new results from five field seasons (2008, 2010, 2013, 2014 and 2016) of botanical collecting at sites across the island. A small subset of collections from our 2008 and 2010 trips, representing first records of the following species for Victoria Island (or first records with confirmed vouchers), were reported in
Victoria Island (217, 291 km2), about 3.8% larger than Great Britain, is the eighth largest island in the world and the second largest (after Baffin Island, 507,451 km2) in Canada. It is located in the western Canadian Arctic Archipelago (Fig.
Victoria Island was part of British Arctic territory from the 16th century to 1880, the year the British Arctic Territories were claimed by Canada and became part of the Northwest Territories. It remained wholly part of that territory until creation of the territory of Nunavut in 1999. Victoria Island now spans the two territories. The territorial border corresponds to the boundary of the Inuvialuit Settlement Region, which includes much of the western third of the island. The Northwest Territories portion of the island comprises the northern half of the western tip of Wollaston Peninsula, land north of the 70th parallel north except for a southern protrusion around most of Quunnqug Lake, and land east of the 110th meridian west. The Northwest Territories portion of the island is part of the Inuvik Region, and the Nunavut portion is part of the Kitikmeot Region. Victoria Island has been inhabited since approximately 4500 BP (
Victoria Island is fully within the Canadian Arctic ecozone, and of the three major Arctic regions recognized in Canada, it is part of the Northern Arctic, as is most of the Canadian Arctic Archipelago (
The Circumpolar Arctic Vegetation Map–an international effort to develop a unified terminology for describing global Arctic vegetation–divides the circumpolar Arctic into five bioclimate zones (
Ecological zones recognized on Victoria Island. A Locations of bioclimate subzones C and D according to the Circumpolar Arctic Vegetation Map (
The two communities on Victoria Island are located within bioclimate subzone D. Cambridge Bay has a mean annual air temperature of -13.9 °C for the climate normal period of 1981–2010 and the mean annual temperature in July is 8.9 °C and in February is -32.5 °C for the same period (
The Northwest Territories
With the establishment of the Canadian High Arctic Research Station (CHARS; Polar Knowledge Canada) in Cambridge Bay in 2015, new ecological research has been initiated on Victoria Island and the adjacent mainland, including long-term, experiment-based monitoring of the terrestrial ecosystem (
Detailed accounts of the glaciation, geomorphology and surficial geology of Victoria Island are given by
Victoria Island was overlain by the Laurentide ice sheet during the Wisconsin glaciation, and the post-glacial landscape of the lowlands is characterized by numerous glacial landforms, including drumlins, drumlinoid ridges, till plain, moraines, esker complexes, kame hills, abandoned river valleys and meltwater channels, and glacio-lacustrine deposits (clay and silts). Marine strand lines marking former post-glacial marine limits are conspicuous on the island; nearly half the island was, at one point, submerged. Other marine features in inland areas include marine shells, raised deltas, raised beach ridges, abandoned strand lines and marine sediments. Coastal parts of western Victoria Island are characterized by having large morainal belts that often reach heights of 30 m or higher. Morainal topography is particularly varied on Wollaston Peninsula, attaining maximum height at the summit of Mt. Bumpus. Morainal belts of eastern Victoria Island are much smaller. The island is further characterized by its abundant lakes and rivers, floodplain deposits, alluvial fans and deltas. Pingos are present on southeastern Victoria Island, particularly on Wollaston Peninsula.
Ovayok Territorial Park, the only protected area on Victoria Island and one of three territorial parks in the Kitikmeot Region of Nunavut, is located 15 km east of the community of Cambridge Bay (Fig.
The earliest botanical collections on Victoria Island were gathered during a four-year (1850–1854), two-ship (Enterprise and Investigator), British expedition in search of Sir John Franklin’s missing ships Erebus and Terror, and by John Rae in 1851. These collections are housed at the Royal Botanic Gardens Kew (K; herbarium acronyms follow
John Rae made collections along the “south shore” of Victoria Island in 1851 while exploring and mapping the area (
A substantial amount of information on the flora of Victoria Island accumulated in the 20th century. The herbaria in which the collections described below are housed are listed in the Annotated Checklist, unless otherwise indicated. Diamond Jenness, anthropologist, made collections on “Wollaston Land” (Wollaston Peninsula) in 1915, during the Canadian Arctic Expedition, 1913–1918. These were reported in
Considerable plant exploration of Victoria Island occurred in the 1940s, when many plant collections were made at fur trading posts on the eastern shore of Walker Bay (Fort Collinson), at Holman and Cambridge Bay, and on Read Island just off the south coast of the Wollaston Peninsula. Father Arthème Dutilly, associated with the Catholic University of America, collected in 1940 at Holman, at a site referred to on his collection labels as “Willows Patch” [Boot Inlet; see comments under Salix alaxensis about the location of this site], at Kookyoak River [=Kuujjua R.] and at Cambridge Bay (
Botanist A. Erling Porsild, with the National Museum of Canada, collected on Victoria Island in 1949 at several sites, spending no more than two days at each: Read Island (27 July), the interior of the Wollaston Peninsula (27 July), the head of Prince Albert Sound (4 August), Holman Island (Ulukhaktok; 8 August), “Jackpot Lake” (an unnamed lake east of the head of Minto Inlet; 16 August), Walker Bay (at Fort Collinson; 25 August), the head of Minto Inlet (2–3 August), Cambridge Bay (5 August), an unnamed lake ca. 60 miles north of Cambridge Bay (6 August), Tahoe Lake and Washburn Lake (4 August), and a few other places inland. Those collections reportedly doubled the number of species known from the island, bringing the then-known flora to 201 species (
Margaret Oldenburg, an amateur botanist from Grand Marais, Minnesota, travelled and botanized extensively across Victoria Island in the 1940s and 1950s. She travelled primarily by chartered aircraft, typically collecting during brief stops. In 1943, she made collections at Holman Island (=Ulukhaktok; 1 August) and Read Island (23–24, 31 August, 2–3 September). In 1944, she collected at Cambridge Bay (14–15 August) and again at Read Island (20 August). In 1945, she collected at Ulukhaktok (12 August), Walker Bay (12 August) and “Oldenburg Lake” (11 August), an unnamed lake on northwestern Victoria Island west of Peel Point. We determined the location of “Oldenburg Lake” (73.11750, -114.58) based on information in
Botanical documentation of the Victoria Island flora continued through the 1950s. Entomologists E. Smith and D.K. Sweatman, Department of Agriculture, Ottawa, collected in 1950 at Holman Island (Ulukhaktok). In 1952, entomologists D.P. Gray and B. Gibbard, also with the Dept. of Agriculture, made collections at Holman Island (Ulukhaktok). In 1959 and 1960, W.D. Stretton, Army Survey Establishment, made collections at Cambridge Bay and at numerous sites in interior Victoria Island, during defence mapping operations. Areas where Stretton collected include the north side and head of Prince Albert Sound, Berkeley Point, Burns Lake, Freshwater Bay, Gordon Point, Kuujjua River, Murray Point, Richard Collinson Inlet, Storkerson Peninsula, Ulukhaktok and the west end of the Diamond Jenness Peninsula. Botanists J.A. Calder, D.B.O. Savile and I. Kukkonen collected at Cambridge Bay on 12 August 1959.
Collections in the 1960s were focused on southeastern Victoria Island and in the 1970s in the Ulukhaktok area. Homer A. “Steve” Stephens (and his associate George M. Sutton) made extensive collections in 1962 in the vicinities of Cambridge Bay and Mount Pelly, in association with research on the White-rumped Sandpiper at Cambridge Bay. Stephens also made collections on Jenny Lind Island immediately southeast of Victoria Island in Queen Maud Gulf (
In the 1980s, Sylvia A. Edlund, Geological Survey of Canada, made substantial contributions to knowledge of the flora of Victoria Island, associated with research characterizing the relationships between surficial geology and plant communities. She made more than 1800 collections at numerous sites across the island, including many from sites where no other collections have been made. Sites visited and collected by Edlund in 1982 include Armstrong Point, Boot Inlet, Cape Baring, Cape Wollaston, Kugaluk River, Kuujjua River, the head of Minto Inlet, Mt. Bumpus, Murray Point, Natkusiak Peninsula, Peel Point, the north side and head of Prince Albert Sound, Richard Collinson Inlet, Sangraun Hills, Shaler Mountains near Richard Collinson Inlet, Tahiryuaq (a large lake north of the head of Prince Albert Sound), Ulukhaktok and southwestern Wollaston Peninsula (
Botanical exploration of Victoria Island continued in the 1990s. William T. Dushenko made collections at Byron Bay in 1992, in association with research on environmental contaminants (
Over three decades, ecologist Dietbert Thannheiser, University of Hamburg, Germany, conducted phytosociological research at sites on Victoria Island, including Cambridge Bay (1983, 1984, 1986, 1987, 1998), Holman (Ulukhaktok; 1986, 1973), the head of Minto Inlet (1986), Mt. Pelly (1984), Wellington Bay (1983), Hadley Bay (1986), Surrey Lake, Richardson Islands and Johansen Bay (
Despite over a century of exploration and documentation of the vascular flora of Victoria Island, only a small subset of the collection data has been published in detail. Material gathered on the island during the Canadian Arctic Expedition was published by
2008, 2010 and 2017
In July 2008, our team, comprising L.J. Gillespie, J.M. Saarela, L.L. Consaul and R.D. Bull (Canadian Museum of Nature), explored and collected plants along southern Victoria Island, Nunavut. Research was carried out under Nunavut Research Institute Scientific Research Licence 0401308N-A, Nunavut Wildlife Research Permit No. WL 2008-1039, Nunavut Water Board Permit No. 3BC-AFP0813 and Polar Continental Shelf Program (PCSP) Project Number 515-08. We established three base camps: (1) at a site ca. 13 km north of Oterkvik Point and 10 km north of the coast at Coronation Gulf (68°36'50"N, 112°34'21"W; 3–11 July); (2) 8 km east-northeast of Johansen Bay airstrip along the Nakoyoktok River at its outflow from a large unnamed lake (68°39'25"N, 110°42'30"W; 12–21 July); and (3) Sinclair Creek North Warning System site (abandoned DEW-line site) (68°45'5"N, 109°06'20"W; 22–24 July). In each area, we explored as many habitats as possible, by foot, at each camp, and made collections as we encountered taxa. Our aim was to document all of the vascular plant species in the vicinity of each of our three camps with at least one voucher specimen. We also explored several remote sites accessed by helicopter. Staging from Oterkvik Point, we visited five sites via helicopter on 7 July: two sites along a bay on Coronation Gulf east of Oterkvik Point (68°30'46"N, 112°33'60"W; 68°29'17"N, 112°40'13"W); an esker ca. 21 km north of the coast at Coronation Gulf and 24 km north-northeast of Oterkvik Point (68°41'59"N, 112°26'23"W); a low rocky ridge between two lakes near the previous locality (68°42'48"N, 112°30'08"W); low rocky hills at the coast in the vicinity of Oterkvik Point (68°31'32"N, 111°59'58"W; longitude coordinates recorded on specimen labels for this site as 112°59'58"W are erroneous). Collections made while exploring the Oterkvik Point area on foot and during the five helicopter stops noted above are recorded in the annotated checklist as being from Oterkvik Pt. Staging from Oterkvik Point, we also visited two more distant sites via helicopter on 8 July: the eastern-most slopes of the Colville Mountains (69°32'45"N, 112°41'27"W) and the vicinity of a river flowing into Clouston Bay, 3–4 km from the river mouth (69°02'39"N, 113°25'15"W). These are treated as separate sites in the annotated checklist. Staging from Johansen Bay we visited five sites via helicopter on 20 July: a flat-topped steep-sided hill, 11 km northeast of the Johansen Bay airstrip (68°39'12"N, 110°54'47"W); a pingo 23 km west of the Johansen Bay airstrip (68°26'23"N, 111°40'22"W); the Johansen Bay airstrip (68°35'50"N, 111°6'59"W); the west end of Johansen Bay at the mouth of Mackenzie Creek (68°36'4"N, 111°21'7"W); and Mackenzie Creek, about 1 km from its mouth at the west end of Johansen Bay, along a river canyon above a waterfall and rapids (68°36'28"N, 111°22'10"W). Collections made while exploring the Johansen Bay area on foot and during the five helicopter stops noted above are recorded in the annotated checklist as being from Johansen Bay. Staging from Sinclair Cr., we visited one site via helicopter on 21 July: Murray Point on the west side of Wilbank Bay (68°35'33.5"N, 110°18'24"W). Murray Point is treated as a separate site in the annotated checklist. In total we made 1091 collections (numbers) of vascular plants, one of lichens and 27 of bryophytes.
In July 2010, we conducted fieldwork on northwestern Victoria Island, Northwest Territories, again aiming to document all species present at each site visited. Our team comprised L.J. Gillespie, J.M. Saarela, Jennifer Doubt, R.D. Bull and P.C. Sokoloff (Canadian Museum of Nature). Research was carried out under Aurora Research Institute Licence No. 14733, Inuvialuit Land Administration Licence No. ILA10HN004, and PCSP Project Number 509-10. We established three base camps: (1) at a site ca. 8 km inland from the head of Minto Inlet adjacent to a Geo-Mapping for Energy and Minerals (GEM) program, Natural Resources Canada, camp (71°37'10"N, 115°26'22"W; 7–8, 19–26 July); (2) at a site on the northeast side of a small round unnamed lake (ca. 1 km diameter) ca. 4 km north of Boot Inlet on the north side of Minto Inlet (71°30'35"N, 117°20'35"W; 9–12 July); and (3) at a site on the southeast side of “Fish Lake” on the lower Kuujjua River between two small lakes, on the south side of Minto Inlet (71°12'28"N, 116°22'46"W; 12–18 July). Collections were also made in Ulukhaktok by J.M. Saarela and R.D. Bull (5–6 July; Saarela nos. 1410–1508). Staging from the Kuujjua River camp we visited three sites by helicopter on 17 July: the base of north-facing cliffs 68 km east-northeast of Ulukhaktok (71°2'60"N, 116°9'48"W); the sandy banks of the Kuujjua River south of “Fish Lake”, ca. 17 km southeast of the head of Minto Inlet (71°6'43"N, 116°6'21"W); the shore of the Kuujjua River delta at Minto Inlet (71°15'23"N, 116°49'35"W). Staging from the Minto Inlet camp we visited three sites via helicopter on 25 July: a deep canyon on an escarpment south of the head of Minto Inlet in the vicinity of large waterfall (71°25'30"N, 115°12'2"W), a coastal saline flat along the end of the eastern most inlet (north arm) at the head of Minto Inlet (71°31'7"N, 115°6'30"W), and an esker on a plain 3 km south of the head of Minto Inlet (71°27'10"N, 115°17'3"W). We made 1048 collections (numbers) of vascular plants, one of lichens, five of bryophytes and 14 of fungi. Jennifer Doubt made extensive collections of bryophytes during this expedition, which are not considered here.
In 2017, 20 collections were made in Cambridge Bay by J.M. Saarela (nos. 5296–5301) during the Canada C3 expedition (https://canadac3.ca/en/homepage/).
All 2008, 2010 and 2017 collections were dried in the field in standard plant presses. For each collection we preserved a small sample of leaf tissue in silica gel for future molecular analyses. In most cases, we tagged the plant from which we obtained the sample. These tissue samples are preserved in the National Biodiversity Cryobank of Canada at the Canadian Museum of Nature. These collections were variously determined by L.J. Gillespie, J.M. Saarela and P.C. Sokoloff unless otherwise indicated (Suppl. material
2013, 2014
Fieldwork was conducted by B.A. Bennett in the vicinity of Cambridge Bay in 2013 and the Cambridge Bay and broader vicinity in 2014. The aim of this work was to document all species of vascular plants in the area to contribute to understanding of the ecology of the greater Canadian High Arctic Research Station (CHARS) (Polar Knowledge Canada) research area. In 2013, collections were made at numerous sites within the community, along the road to Mt. Pelly, within Ovayok Territorial Park, at the east end of Greiner Lake, and along the road west of the community, as far west as the hills above Long Point. In 2014, collections were made within the hamlet, across the bay from the hamlet, north of the DEW line site, at Long Point and at three sites more distant from the hamlet: “30-Mile Creek”, near the Ekalluk River and the west end of Ferguson Lake, and “Trunsky Lake”. Vouchers of material collected in 2014 has been distributed to
2016, 2018 and 2019
Botanical fieldwork was conducted by CHARS ecologist S. Ponomarenko during three field seasons. From 3–18 August 2016 a vegetation survey was carried out for the CHARS Intensive Monitoring Area (IMA), an area restricted to two small watersheds within the Greiner Lake watershed that drains to the northern shore of Greiner Lake approximately 20–30 km to the northeast of Cambridge Bay, an area measuring about 50 km2. This work was conducted as part of the high resolution vegetation mapping of the CHARS IMA project (
In the 2018 and 2019 field seasons, floristic collections were obtained during helicopters surveys of a broader area. In 2018, five days of helicopter surveys were undertaken within the Greiner Lake watershed, an area measuring approximately 1,500 km2. In 2019, eight days of helicopter surveys were undertaken north and east of Greiner Lake watershed along the border of bioclimatic subzones C and D. This survey covered an area of about 2,000 km2 north and east from the Greiner Lake watershed. This work constituted a part of the vegetation inventory and mapping project aiming to assemble baseline data for the CHARS ERA.
Vouchers collected during these three years of fieldwork are housed at CAN and CHARS. In total more than 700 specimens were collected, of which 394 collections were reviewed for this work. The remaining 300 collections, mainly collected in 2019, are not yet processed.
Herbarium research and data curation
In addition to accounting for our new collections, we attempted to locate and confirm or revise determinations of all unique collections of vascular plants from Victoria Island. To find specimens collected previously from the study area, we manually searched the collections at CAN,
As part of the current study, three batches of unprocessed material gathered on Victoria Island in the 1940s, 1940s–50s and 1980s that was stored in the backlog collection of the National Herbarium of Canada were organized, identified, mounted and inserted into the permanent collection. One batch comprised 134 sheets collected by Nicholas Polunin at Cambridge Bay in 1947. The second batch comprised 498 sheets collected by Margaret Oldenburg at various sites across the island (see Introduction). The third batch comprised 359 collections gathered by Sylvia Edlund at various sites across the island in 1982, 1986 and 1987 (see Introduction). In the course of processing this material, we discovered that 38 of these Edlund backlog collections from Victoria Island had previously been assigned CAN accession numbers and were recorded in the museum database (and thus mobilized online), but the material remained unmounted, until now. These 991 collections–of which some were gathered 70+ years ago – are now available to the scientific community and are published here. The backlog material from Victoria Island dealt with here is a subset of larger backlog batches of Arctic specimens at CAN gathered by Edlund, Oldenburg and Polunin.
During the course of this study, imaging of all vascular plant material housed at CAN from Yukon, Northwest Territories and Nunavut was completed and all images were linked to the institutional database and mobilized via GBIF. GBIF tools were used to identify and fix putative data errors in Victoria Island records. The images also facilitated completion of data entry for CAN specimens from Victoria Island for which only “skeletal” records existed (i.e., taxon name and higher-level geographic provenance – country and province/territory) or for which data entry was otherwise incomplete.
We amalgamated all collection data obtained from different resources into a spreadsheet. Substantial manual cleaning of the complete dataset was undertaken to make the dataset useable, including standardizing names of collectors, date format and locality descriptions among specimens gathered by the same collector at the same site. We combined records of duplicate specimens housed in different collections into single records, maintaining information on the disposition(s) of the duplicate specimens.
We spent considerable time improving the georeferencing of records in our dataset. Most collections from Victoria Island were made long before the existence of the Global Positioning System and many before the existence of detailed topographical maps, or of maps, period. As such, many collections either lacked coordinates or included the following: (1) inaccurate or erroneous primary coordinates, (2) accurate or inaccurate secondary coordinates but no attribution or source information for the georeferenced coordinates, or (3) accurate but imprecise coordinates determined to the nearest minute, being within ca. one nautical mile of the site, assuming the coordinates are correct. Prior to the advent of digital mapping, this level of precision was generally sufficient for dot-based distribution maps presented at a fixed scale. For example, each dot in the maps in
Therefore, to improve accuracy of geographical coordinates, we secondarily georeferenced many sites following standard point-radius protocols, including determining estimates of coordinate uncertainty in metres, in cases where we were confident that existing location data could be improved upon. Georeferencing was done by J.M. Saarela and Paul Wise, Canadian Museum of Nature. Georeferencing data is included in Suppl. material
Distribution maps were generated in ArcMap 10.5.1. Additionally, using ArcMap 10.5.1, we generated maps showing the locations of all collecting sites on the island, maps showing the locations of collections made by S. Edlund, including for specimens previously accessioned into the CAN herbarium and for specimens that had been housed in backlog and were newly accessioned as part of this study, and collections made by A.E. Porsild, Gillespie et al., B. Bennett, S. Ponomarenko, and M. Oldenburg. A heat map showing the density of collections at sites on the island was generated using QGIS 3.4.
Annotated checklist
The vascular flora of Victoria Island is summarised in an annotated checklist. Classification of lycophytes and ferns follows
All species reported for the study area are documented by one or more voucher specimens, and only vouchered records are included and mapped. Observations of species noted by
To simplify publication of voucher information, we assigned each collection to a general area of the island. Where possible, we used general areas as described on specimen labels. In cases where no or vague site information is given on labels, however, we assigned specimens to a nearby named place. For example, collections by Edlund reported from south of Burns Lake were gathered in 1982 and 1987 at sites ca. 40–45 km south or south-southwest of the lake, but on the specimen labels the location is described only as “Geological Survey of Canada peat study location” along with the coordinates. In most cases, the toponyms we use are recognized by the Geographical Names Board of Canada. A few sites names, however, are not officially recognized. Examples include “Oldenburg Lake”, “Trunsky Lake” and “30-Mile Creek”, also known locally as “30 Mile River” and “Halovik River”. Locations of all general areas are shown in Fig.
Some toponyms on Victoria Island have changed in recent years. Ferguson Lake, a large lake north of Cambridge Bay that flows into Wellington Bay via the Ekalluk River, is officially known as Tahiryuaq, the Inuinnaqtun name. We use the English name for the lake to avoid confusion with two other lakes on Victoria Island also officially named Tahiryuaq. Both of these are in Northwest Territories, one north of Prince Albert Sound (70°56'2"N, 112°15'7"W) where collections were made by Edlund and the other southeast of the head of Minto Inlet (71°27'2"N, 114°45'8"W). The esker formerly known as Ovayuk/Mount Pelly, where many collections have been made, was renamed Uvayuq, effective 21 September 2012. The esker northwest of Mount Pelly and north of Cambridge Bay formerly known as Mount Lady Pelly (69°15'28"N, 104°48'37"W), where collections were made in 1962, was renamed Amaaqtuq, effective 21 September 2012.
For each taxon recorded from Victoria Island we summarize previous reports of the species occurrence on the island by site and indicate sites for which a taxon is newly recorded here. “Previously recorded” at a site means a species occurrence was stated or mapped for a site in one or more earlier published works, which are cited in the text here, regardless of whether or not voucher information was published, and the earlier report is supported by one or more vouchers cited in the text here, unless otherwise indicated. In most cases, the vouchers cited here are the collections on which the earlier records were based. In many cases, new material has been gathered from sites at which a species was previously reported, particularly those areas that are best collected, like Cambridge Bay and Ulukhaktok. Although we do not, in most cases, comment on the accumulation of material of a species at a particular site, we do cite all the relevant material known to us from each site.
“Newly recorded” at a site means the current study is the first to publish an occurrence of a species at a particular site. Such new records reported here include collections made during our fieldwork from 2008 on, earlier collections that previous workers did not consider in their floristic treatments, earlier collections that were not processed and available for study until recently, and new identifications of material known to previous authors, either because previous determinations were incorrect or in light of revised taxon circumscriptions. In all cases we include explicit citation of one or more voucher specimens supporting new records.
Patterns of floristic diversity
To characterize patterns of floristic diversity on Victoria Island we scored, based on our dataset, the presence of species/taxa in the following regions: Nunavut and Northwest Territories, the six areas that we aimed to document comprehensively in 2008 and 2010, two additional well-collected areas (Cambridge Bay, Ulukhaktok), and Ovayok Territorial Park, the only protected area on the island (Table
We compiled a dataset of some 7031 unique collections of vascular plants from Victoria Island (Suppl. material
The vascular flora of Victoria Island comprises 38 families, 108 genera, 272 species, and 17 additional taxa (Table
Number of genera and species in each family of vascular plants recorded from Victoria Island. The higher level classification of angiosperms follows
Order | Family | Genera | Species/Taxa | |||
---|---|---|---|---|---|---|
Lycophytes | Lycopodiales | Lycopodiaceae | 1 | 1 | ||
Monilophytes | Equisetales | Equisetaceae | 1 | 3 | ||
Polypodiales | Cystopteridaceae | 1 | 1 | |||
Dryopteridaceae | 1 | 1 | ||||
Woodsiaceae | 1 | 1 | ||||
Monocots | Alismatales | Potamogetonaceae | 1 | 2 | ||
Tofieldiaceae | 1 | 2 | ||||
Asparagales | Orchidaceae | 1 | 1 | |||
Poales | Juncaceae | 2 | 7/8 | |||
Cyperaceae | 2 | 33/35 | ||||
Poaceae | 17 | 38/44 | ||||
Eudicots | Ranunculales | Ranunculaceae | 6 | 13 | ||
Papaveraceae | 1 | 4 | ||||
Superasterids | Caryophyllales | Plumbaginaceae | 1 | 1 | ||
Polygonaceae | 2 | 2 | ||||
Caryophyllaceae | 7 | 19/21 | ||||
Amaranthaceae | 1 | 1 | ||||
Montiaceae | 1 | 1 | ||||
Superasterids | Asterids | Ericales | Primulaceae | 2 | 3 | |
Ericaceae | 8 | 11 | ||||
Gentianales | Rubiaceae | 1 | 1 | |||
Gentianaceae | 2 | 2 | ||||
Boraginales | Boraginaceae | 1 | 2 | |||
Lamiales | Plantaginaceae | 2 | 2 | |||
Lentibulariaceae | 1 | 1 | ||||
Orobanchaceae | 2 | 8 | ||||
Asterales | Asteraceae | 13 | 25/26 | |||
Superrosids | Saxifragales | Saxifragaceae | 3 | 15 | ||
Haloragaceae | 1 | 1 | ||||
Rosids | Fabales | Fabaceae | 4 | 10 | ||
Rosales | Rosaceae | 3 | 13/15 | |||
Campanulaceae | 1 | 1 | ||||
Fagales | Betulaceae | 1 | 1 | |||
Celastrales | Celastraceae | 1 | 1 | |||
Malpighiales | Salicaceae | 1 | 10/11 | |||
Linaceae | 1 | 1 | ||||
Myrtales | Onagraceae | 2 | 2 | |||
Brassicales | Brassicaceae | 10 | 31/33 | |||
Total | 21 | 38 | 108 | 272/289 |
Three families are represented by more than ten genera: Asteraceae (13), Brassicaceae (10), and Poaceae (17). Of the remaining 35 families, 21 are represented by a single genus, eight by two genera, two by three, one by four, one by five, one by seven and one by eight (Table
The number of collections per taxon from Victoria Island ranges from 1 to 162 (mean 24 ± 23). Thirty-nine taxa are known on the island from a single collection: Eurybia sibirica, Senecio lugens (Asteraceae), Mertensia drummondii (Boraginaceae), Braya thorild-wulffii subsp. glabrata, Cardamine bellidifolia, Crucihimalaya bursifolia, Draba norvegica, D. pauciflora, Erysimum coarctatum, Parrya nudicaulis (Brassicaceae), Sabulina elegans, S. stricta, Sagina caespitosa (Caryophyllaceae), Eriophorum russeolum subsp. albidum (Cyperaceae), Andromeda polifolia (Ericaceae), Oxytropis deflexa var. foliolosa (Fabaceae), Luzula wahlenbergii (Juncaceae), Montia fontana (Montiaceae), Corallorhiza trifida (Orchidaceae), Castilleja pallida var. caudata, Pedicularis hirsuta (Orobanchaceae), Anthoxanthum nitens subsp. nitens, Bromus pumpellianus, Deschampsia cespitosa subsp. cespitosa, D. sukatschewii, Festuca rubra subsp. rubra, Lolium perenne, Poa pratensis subsp. pratensis (Poaceae), Stuckenia filiformis, S. vaginata (Potamogetonaceae), Pulsatilla nuttalliana (Ranunculaceae), Potentilla hyparctica subsp. hyparctica, P. × prostrata, P. vulcanicola, Rubus chamaemorus L. (Rosaceae), Galium aparine (Rubiaceae), Salix arctophila, S. ovalifolia var. ovalifolia, S. planifolia (Salicaceae). Seven taxa are known from two collections: Braya thorild-wulffii subsp. thorild-wulffii, Draba fladnizensis, D. oligosperma (Brassicaceae), Arenaria longipedunculata (Caryophyllaceae), Equisetum scirpoides (Equisetaceae), Anthoxanthum monticola subsp. monticola (Poaceae) and Ranunculus sulphureus (Ranunculaceae). Three taxa are known from three collections: Antennaria monocephala subsp. angustata, Artemisia tilesii (Asteraceae) and Carex bicolor (Cyperaceae). Of the remaining taxa, 26 are known from 4–5 collections, 31 from 6–10, 51 from 11–19, 41 from 21–30, 28 from 31–40, 27 from 41–50 and 16 from 51–59. Fifteen species are known from 61–91 collections: Parrya arctica (Brassicaceae), Sabulina rubella, Silene uralensis subsp. uralensis (Caryophyllaceae), Carex aquatilis subsp. stans, C. fuliginosa subsp. misandra, C. membranacea, C. scirpoidea subsp. scirpoidea (Cyperaceae), Pedicularis lanata (Orobanchaceae), Arctagrostis latifolia subsp. latifolia, Dupontia fisheri, Festuca baffinensis, Poa glauca subsp. glauca (Poaceae), Bistorta vivipara (Polygonaceae), Dryas integrifolia subsp. integrifolia (Rosaceae) and Salix richardsonii (Salicaceae). Three species are known from over 100 collections: Draba corymbosa (102), Salix arctica (162), Draba cinerea (114) and Stellaria longipes (113).
Twenty-one taxa in eight families are newly recorded for the flora of Victoria Island, namely Artemisia tilesii, Senecio lugens, Taraxacum scopulorum (Asteraceae), Crucihimalaya bursifolia, Draba fladnizensis, D. juvenilis, D. pilosa, D. simmonsii (Brassicaceae), Carex bigelowii subsp. bigelowii, Eriophorum russeolum subsp. albidum (Cyperaceae), Anthoxanthum monticola subsp. monticola, Bromus pumpellianus, Deschampsia cespitosa subsp. cespitosa, D. sukatschewii, Festuca rubra subsp. rubra, Lolium perenne, Poa pratensis subsp. pratensis (Poaceae), Stuckenia filiformis (Potamogetonaceae), Potentilla × prostrata (Rosaceae), Galium aparine (Rubiaceae) and Salix ovalifolia var. ovalifolia (Salicaceae). Eight of these are new to the flora of the Canadian Arctic Archipelago: Senecio lugens, Draba juvenilis, D. pilosa, Anthoxanthum monticola subsp. monticola, Bromus pumpellianus, Deschampsia cespitosa subsp. cespitosa, Poa pratensis subsp. pratensis, Salix ovalifolia var. ovalifolia. One of these, Galium aparine, is newly recorded for the flora of Nunavut. Four of these first records for Victoria Island are introduced plants discovered in Cambridge Bay in 2017: three grasses (Festuca rubra subsp. rubra, Lolium perenne, and Poa pratensis subsp. pratensis) and Galium aparine. One taxon, Juncus arcticus subsp. arcticus, is newly recorded from the Northwest Territories.
Considering diversity in the CAVM subzones present on the island, 157 taxa are recorded in subzone C, 283 in subzone D, and 149 taxa are recorded in both subzones (Suppl. material
Within the Northwest Territories, 125 taxa are recorded in the West Prince Albert Lowland Mid Arctic (MA) ecoregion, 37 in the West Prince Albert Upland MA ecoregion, six in the East Prince Albert Plain MA ecoregion, 51 in the Shaler Mountains MA ecoregion, 76 in the Tahiryuak Upland MA ecoregion, 29 in Wollaston Peninsula MA ecoregion and 231 in Prince Albert Coastlands Low Arctic-north ecoregion (Suppl. material
Of the eight general areas on Victoria Island that have been botanically explored the most, the greatest diversity of vascular plants is recorded in Ulukhaktok, where 194 taxa are known (Table
Species discovery curves for each of the six areas we aimed to document comprehensively in 2008 and 2010 each indicate a generally consistent increase in number of new species found with each additional day of exploration (Fig.
Vascular plants recorded from Victoria Island. The table records whether or not each taxon is recorded in Northwest Territories and Nunavut, eight sites on the island that have been explored comprehensively (NWT: Ulukhaktok, Boot Inlet, Kuujjua River, the head of Minto Inlet; NU: Oterkvik Point, Johansen Bay, Sinclair Creek, Cambridge Bay) as well as Ovayok Territorial Park, Nunavut, the only protected area on Victoria Island. Occurrences at other sites are recorded in the annotated checklist and on the distribution maps. Taxa are listed by major clade, and then alphabetically by family.
Family | Taxon | Ulukhaktok | Boot Inlet | Kuujjua River | Head of Minto Inlet | Northwest Territories | Oterkvik Point | Johansen Bay | Sinclair Creek | Cambridge Bay | Ovayok Territorial Park | Nunavut |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lycophytes | ||||||||||||
Lycopodiaceae | Huperzia arctica Sipliv. | • | ▲ | • | ▲ | |||||||
Monilophytes | ||||||||||||
Cystopteridaceae | Cystopteris fragilis (L.) Bernh. | • | • | • | • | ▲ | • | • | • | ▲ | ||
Dryopteridaceae | Dryopteris fragrans (L.) Schott | • | ▲ | • | ▲ | |||||||
Equisetaceae | Equisetum arvense subsp. alpestre (Wahlenb.) Schönsw. & Elven | • | • | • | • | ▲ | • | • | • | • | ▲ | |
Equisetum scirpoides Michx. | • | • | ▲ | |||||||||
Equisetum variegatum Schleich. ex F.Weber & D.Mohr subsp. variegatum | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Woodsiaceae | Woodsia glabella R.Br. | • | • | • | ▲ | • | • | • | • | ▲ | ||
Monocots | ||||||||||||
Cyperaceae | Carex aquatilis subsp. stans (Drejer) Hultén | • | • | • | • | ▲ | • | • | • | • | • | ▲ |
Carex atrofusca Schkuhr | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Carex bicolor All. | • | ▲ | • | • | ▲ | |||||||
Carex bigelowii subsp. lugens (Holm) T.V.Egorova | • | • | ▲ | • | • | • | • | ▲ | ||||
Carex bigelowii subsp. bigelowii | • | • | • | ▲ | ||||||||
Carex borealipolaris S.R.Zhang | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Carex capillaris subsp. fuscidula (V.I.Krecz. ex T.V.Egorova) Á.Löve & D.Löve | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Carex chordorrhiza L.f. | ▲ | • | ▲ | |||||||||
Carex fuliginosa subsp. misandra (R.Br.) Nyman | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Carex glacialis Mack. | • | ▲ | • | ▲ | ||||||||
Carex glareosa subsp. glareosa | • | ▲ | • | • | • | ▲ | ||||||
Carex krausei Boeckeler | • | • | • | ▲ | • | • | ▲ | |||||
Carex marina Dewey | • | • | • | • | ▲ | • | • | • | ▲ | |||
Carex maritima Gunnerus | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Cyperaceae | Carex membranacea Hook. | • | • | • | • | ▲ | • | • | • | • | • | ▲ |
Carex microglochin Wahlenb. | • | ▲ | • | ▲ | ||||||||
Carex myosuroides Vill. | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Carex nardina Fr. | • | • | • | • | ▲ | ▲ | ||||||
Carex petricosa subsp. petricosa | • | • | • | ▲ | ▲ | |||||||
Carex rariflora (Wahlenb.) Sm. | • | • | • | ▲ | • | • | • | ▲ | ||||
Carex rupestris All. | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Carex saxatilis L. | • | • | • | • | ▲ | • | • | • | ▲ | |||
Carex scirpoidea subsp. scirpoidea | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Carex simpliciuscula subsp. subholarctica (T.V.Egorova) Saarela | • | • | • | • | ▲ | • | • | • | ▲ | |||
Carex subspathacea Wormsk. | • | • | • | ▲ | • | • | • | ▲ | ||||
Carex ursina Dewey | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Carex vaginata Tausch | • | • | • | ▲ | • | • | • | ▲ | ||||
Eriophorum angustifolium Honck. | • | • | • | • | ▲ | • | • | ▲ | ||||
Eriophorum brachyantherum Trautv. & C.A.Mey. | • | • | • | ▲ | ▲ | |||||||
Eriophorum callitrix C.A.Mey. | • | • | • | ▲ | • | • | • | ▲ | ||||
Eriophorum russeolum subsp. albidum (F.Nyl.) Väre | ▲ | |||||||||||
Eriophorum scheuchzeri subsp. scheuchzeri | • | ▲ | • | ▲ | ||||||||
Eriophorum scheuchzeri subsp. arcticum M.S.Novos. | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Eriophorum triste (Th.Fr.) Hadač & Á.Löve | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Eriophorum vaginatum subsp. vaginatum | • | • | • | • | ▲ | • | • | ▲ | ||||
Juncaceae | Juncus arcticus subsp. alaskanus Hultén | • | • | ▲ | • | • | ▲ | |||||
Juncus arcticus subsp. arcticus | • | • | ▲ | • | • | ▲ | ||||||
Juncus biglumis L. | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Juncus leucochlamys V.J.Zinger ex V.I.Krecz. | • | • | • | ▲ | • | • | ▲ | |||||
Juncus triglumis subsp. albescens (Lange) Hultén | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Luzula confusa Lindeb. | • | • | ▲ | • | • | • | ▲ | |||||
Juncaceae | Luzula nivalis (Laest.) Spreng. | • | • | • | • | ▲ | • | • | • | • | ▲ | |
Luzula wahlenbergii Rupr. | • | ▲ | ||||||||||
Poaceae | Alopecurus borealis Trin. | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Anthoxanthum arcticum Veldkamp | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Anthoxanthum monticola subsp. monticola | ▲ | |||||||||||
Anthoxanthum monticola subsp. alpinum (Sw. ex Willd.) Soreng | • | • | ▲ | |||||||||
Anthoxanthum nitens subsp. nitens | • | ▲ | ||||||||||
Arctagrostis latifolia subsp. latifolia | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Arctophila fulva (Trin.) Andersson | • | • | ▲ | • | ▲ | |||||||
Bromus pumpellianus Scribn. | ▲ | |||||||||||
Calamagrostis purpurascens R.Br. | • | • | • | • | ▲ | • | • | ▲ | ||||
Calamagrostis stricta subsp. groenlandica (Schrank) Á.Löve | • | ▲ | • | ▲ | ||||||||
Deschampsia brevifolia R.Br. | • | • | ▲ | • | • | ▲ | ||||||
Deschampsia cespitosa subsp. cespitosa | ▲ | |||||||||||
Deschampsia sukatschewii (Popl.) Roshev. | • | ▲ | ||||||||||
Dupontia fisheri R.Br. | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Elymus alaskanus subsp. alaskanus | • | • | • | • | ▲ | • | ▲ | |||||
Elymus alaskanus subsp. hyperarcticus (Polunin) Á.Löve & D.Löve | • | • | • | • | ▲ | • | • | • | ▲ | |||
Festuca baffinensis Polunin | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Festuca brachyphylla subsp. brachyphylla | • | • | • | ▲ | • | • | • | • | ▲ | |||
Festuca hyperborea Holmen ex Fred. | • | ▲ | ▲ | |||||||||
Festuca rubra subsp. arctica (Hack.) Govor. | • | • | • | • | ▲ | • | • | • | ▲ | |||
Festuca rubra subsp. rubra | • | ▲ | ||||||||||
Poaceae | Leymus mollis subsp. villosissimus (Scribn.) Á.Löve & D.Löve | • | • | • | ▲ | • | • | ▲ | ||||
Lolium perenne L. | • | ▲ | ||||||||||
Phippsia algida (Sol.) R.Br. | • | • | • | ▲ | • | • | ▲ | |||||
Pleuropogon sabinei R.Br. | • | ▲ | • | ▲ | ||||||||
Poa abbreviata subsp. abbreviata | • | • | ▲ | • | ▲ | |||||||
Poa arctica subsp. arctica | • | • | • | ▲ | • | • | • | • | ▲ | |||
Poa arctica subsp. caespitans Simmons ex Nannf. | • | • | ▲ | • | • | ▲ | ||||||
Poa glauca subsp. glauca | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Poa hartzii subsp. hartzii | • | • | ▲ | • | • | • | ▲ | |||||
Poa pratensis subsp. pratensis | • | ▲ | ||||||||||
Poa pratensis subsp. alpigena (Lindm.) Hiitonen | • | • | • | ▲ | • | • | • | • | • | ▲ | ||
Poa pratensis subsp. colpodea (Th.Fr.) Tzvelev | ▲ | |||||||||||
Puccinellia andersonii Swallen | • | • | • | ▲ | • | • | ▲ | |||||
Puccinellia angustata E.L.Rand & Redfield | • | • | • | • | ▲ | • | • | ▲ | ||||
Puccinellia arctica (Hook.) Fernald & Weath. | • | • | • | • | ▲ | • | • | • | ▲ | |||
Puccinellia banksiensis Consaul | • | • | • | ▲ | ||||||||
Puccinellia bruggemannii T.J.Sørensen | ▲ | |||||||||||
Puccinellia nuttalliana (Schult.) Hitchc. | • | ▲ | • | ▲ | ||||||||
Puccinellia phryganodes subsp. neoarctica (Á.Löve & D.Löve) Elven | • | • | • | • | ▲ | • | • | • | ▲ | |||
Puccinellia tenella subsp. langeana (Berlin) Tzvelev | • | • | • | • | ▲ | • | • | • | ▲ | |||
Puccinellia vaginata (Lange) Fernald & Weath. | • | • | ▲ | • | • | ▲ | ||||||
Puccinellia vahliana (Liebm.) Scribn. & Merr. | • | ▲ | • | ▲ | ||||||||
Trisetum spicatum (L.) K.Richt. | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Potamogetonaceae | Stuckenia vaginata (Turcz.) Holub | • | ▲ | |||||||||
Potamogetonaceae | Stuckenia filiformis (Pers.) Börner | ▲ | ||||||||||
Tofieldiaceae | Tofieldia coccinea Richardson | • | • | • | • | ▲ | • | ▲ | ||||
Tofieldia pusilla (Michx.) Pers. | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Eudicots | ||||||||||||
Amaranthaceae | Suaeda calceoliformis (Hook.) Moq. | • | • | ▲ | • | • | ▲ | |||||
Asteraceae | Antennaria friesiana subsp. friesiana | • | • | ▲ | • | • | ▲ | |||||
Antennaria media subsp. compacta (Malte) Chmiel. | • | • | • | • | ▲ | • | ▲ | |||||
Antennaria monocephala subsp. angustata (Greene) Hultén | • | ▲ | • | ▲ | ||||||||
Arnica angustifolia subsp. angustifolia | • | • | • | • | ▲ | • | • | ▲ | ||||
Artemisia borealis subsp. borealis | • | • | ▲ | • | ▲ | |||||||
Artemisia borealis subsp. richardsoniana (Besser) Korobkov | • | • | • | ▲ | • | • | ▲ | |||||
Artemisia hyperborea Rydb. | • | • | • | ▲ | ▲ | |||||||
Artemisia tilesii Ledeb. | • | • | ▲ | |||||||||
Askellia pygmaea (Ledeb.) Sennikov | • | • | ▲ | • | • | ▲ | ||||||
Erigeron compositus Pursh | • | • | • | ▲ | • | • | ▲ | |||||
Erigeron eriocephalus J.Vahl | • | ▲ | ▲ | |||||||||
Erigeron humilis Graham | ▲ | • | • | • | ▲ | |||||||
Erigeron porsildii G.L.Nesom & D.F.Murray | • | ▲ | ||||||||||
Eurybia sibirica (L.) G.L.Nesom | ▲ | |||||||||||
Hulteniella integrifolia (Richardson) Tzvelev | • | • | • | • | ▲ | • | • | ▲ | ||||
Petasites frigidus subsp. frigidus | • | • | • | • | ▲ | • | ▲ | |||||
Senecio lugens Richardson | ▲ | |||||||||||
Symphyotrichum pygmaeum (Lindl.) Brouillet & Selliah | • | • | • | ▲ | • | • | ▲ | |||||
Taraxacum ceratophorum (Ledeb.) DC. | • | • | • | • | ▲ | • | • | • | ▲ | |||
Taraxacum holmenianum Sahlin | • | • | ▲ | • | • | • | ▲ | |||||
Asteraceae | Taraxacum hyparcticum Dahlst. | • | • | • | • | ▲ | • | • | • | ▲ | ||
Taraxacum phymatocarpum J.Vahl | • | • | • | • | ▲ | • | • | • | ▲ | |||
Taraxacum scopulorum (A.Gray) Rydb. | • | ▲ | • | ▲ | ||||||||
Tephroseris frigida (Richardson) Holub | • | • | • | • | ▲ | • | ▲ | |||||
Tephroseris palustris subsp. congesta (R.Br.) Holub | • | • | • | ▲ | • | • | • | ▲ | ||||
Tripleurospermum maritimum subsp. phaeocephalum (Rupr.) Hämet-Ahti | • | • | ▲ | • | • | • | ▲ | |||||
Betulaceae | Betula glandulosa Michx. | • | • | • | ▲ | • | • | ▲ | ||||
Boraginaceae | Mertensia drummondii (Lehm.) G.Don | ▲ | ||||||||||
Mertensia maritima subsp. tenella (Th.Fr.) Elven & Skarpaas | • | • | • | • | ▲ | • | • | ▲ | ||||
Brassicaceae | Braya glabella subsp. glabella | • | • | • | • | ▲ | • | • | • | • | ▲ | |
Braya glabella subsp. purpurascens (R.Br.) Cody | • | • | ▲ | • | ▲ | |||||||
Braya humilis subsp. humilis | • | • | • | ▲ | • | • | • | • | ▲ | |||
Braya thorild-wulffii subsp. thorild-wulffii | • | ▲ | ▲ | |||||||||
Braya thorild-wulffii subsp. glabrata J.G. Harris | ▲ | |||||||||||
Cardamine bellidifolia L. | ▲ | |||||||||||
Cardamine digitata Richardson | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Cardamine polemonioides Rouy | • | • | • | ▲ | • | • | ▲ | |||||
Cochlearia groenlandica L. | • | • | • | ▲ | • | • | • | ▲ | ||||
Crucihimalaya bursifolia (DC.) D.A.German & A.L.Ebel | • | ▲ | ||||||||||
Descurainia sophioides (Fisch. ex Hook.) O.E.Schulz | • | • | • | ▲ | • | • | ▲ | |||||
Draba arctica J.Vahl | • | ▲ | • | ▲ | ||||||||
Draba cinerea Adams | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Draba corymbosa R.Br. ex DC. | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Draba fladnizensis Wulfen | • | ▲ | ▲ | |||||||||
Draba glabella Pursh | • | • | • | ▲ | • | • | • | • | ▲ | |||
Draba juvenilis Kom. | • | ▲ | • | • | • | ▲ | ||||||
Brassicaceae | Draba lactea Adams | • | • | • | ▲ | • | • | ▲ | ||||
Draba micropetala Hook. | • | ▲ | ||||||||||
Draba nivalis Lilj. | • | ▲ | • | • | • | ▲ | ||||||
Draba norvegica Gunn. | • | ▲ | ||||||||||
Draba oblongata R.Br. ex DC. | • | • | ▲ | • | ▲ | |||||||
Draba oligosperma Hook. | ▲ | |||||||||||
Draba pauciflora R.Br. | ▲ | |||||||||||
Draba pilosa Adams ex DC. | • | • | ▲ | • | • | • | ▲ | |||||
Draba simmonsii Elven & Al-Shehbaz | • | • | • | ▲ | • | • | ▲ | |||||
Draba subcapitata Simmons | • | • | ▲ | • | • | ▲ | ||||||
Erysimum coarctatum Fernald | ▲ | |||||||||||
Erysimum pallasii (Pursh) Fernald | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Eutrema edwardsii R.Br. | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Parrya arctica R.Br. | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Parrya nudicaulis (L.) Regel | ▲ | |||||||||||
Physaria arctica (Wormsk. ex Hornem.) O’Kane & Al-Shehbaz | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Campanulaceae | Campanula uniflora L. | • | • | • | ▲ | ▲ | ||||||
Caryophyllaceae | Arenaria humifusa Wahlenb. | • | ▲ | |||||||||
Arenaria longipedunculata Hultén | • | ▲ | ||||||||||
Cerastium arcticum Lange | • | • | • | • | ▲ | • | ▲ | |||||
Cerastium beeringianum Cham. & Schltdl. | • | • | • | ▲ | • | • | • | • | • | ▲ | ||
Cerastium regelii Ostenf. | • | • | ▲ | • | ▲ | |||||||
Honckenya peploides subsp. diffusa (Hornem.) Hultén | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Sabulina elegans (Cham. & Schltdl.) Dillenb. & Kadereit | • | • | • | ▲ | ▲ | |||||||
Sabulina rossii (R.Br. ex Richardson) Dillenb. & Kadereit | • | • | • | • | ▲ | • | • | ▲ | ||||
Sabulina rubella (Wahlenb.) Dillenb. & Kadereit | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Sabulina stricta (Sw.) Rchb. | • | ▲ | ||||||||||
Sagina caespitosa Lange | ▲ | |||||||||||
Sagina nivalis Fr. | • | ▲ | • | ▲ | ||||||||
Caryophyllaceae | Silene acaulis (L.) Jacq. | • | • | • | • | ▲ | • | • | • | • | ▲ | |
Silene involucrata subsp. involucrata | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Silene involucrata subsp. tenella (Tolm.) Bocquet | • | • | ▲ | • | ▲ | |||||||
Silene ostenfeldii (A.E.Porsild) J.K.Morton | • | • | ▲ | • | • | ▲ | ||||||
Silene uralensis subsp. uralensis | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Silene uralensis subsp. arctica (Th.Fr.) Bocquet | • | • | • | ▲ | • | • | • | • | ▲ | |||
Stellaria crassifolia Ehrh. | • | ▲ | • | • | ▲ | |||||||
Stellaria humifusa Rottb. | • | • | • | • | ▲ | • | • | ▲ | ||||
Stellaria longipes Goldie | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Celastraceae | Parnassia kotzebuei Cham. ex Spreng. | • | ▲ | • | ▲ | |||||||
Ericaceae | Andromeda polifolia L. | • | ▲ | |||||||||
Arctous alpina (L.) Nied. | • | • | ▲ | |||||||||
Arctous rubra (Rehder & E.H.Wilson) Nakai | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Cassiope tetragona subsp. tetragona | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Empetrum nigrum L. | • | ▲ | ||||||||||
Rhododendron lapponicum (L.) Wahlenb. | • | • | ▲ | • | • | ▲ | ||||||
Orthilia secunda subsp. obtusata (Turcz.) Böcher | • | • | ▲ | • | ▲ | |||||||
Pyrola grandiflora subsp. grandiflora | • | • | • | • | ▲ | • | • | ▲ | ||||
Vaccinium vitis-idaea subsp. minus (Lodd., G. Lodd. & W. Lodd.) Hultén | • | ▲ | ||||||||||
Fabaceae | Astragalus alpinus L. | • | • | • | • | ▲ | • | • | • | ▲ | ||
Astragalus richardsonii E.Sheld. | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Hedysarum americanum (Michx.) Britton | • | • | • | • | ▲ | • | • | • | ▲ | |||
Hedysarum boreale subsp. mackenziei (Richardson) S.L.Welsh | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Lupinus arcticus subsp. arcticus | ▲ | |||||||||||
Oxytropis arctica var. arctica | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Oxytropis arctobia Bunge | • | • | • | • | ▲ | • | • | ▲ | ||||
Oxytropis deflexa var. foliolosa (Hook.) Barneby | • | ▲ | ||||||||||
Fabaceae | Oxytropis maydelliana Trautv. | • | ▲ | • | • | • | • | ▲ | ||||
Oxytropis varians (Rydb.) K.Schum. | • | ▲ | ▲ | |||||||||
Gentianaceae | Gentianella propinqua subsp. propinqua | • | • | • | • | ▲ | ▲ | |||||
Lomatogonium rotatum subsp. rotatum | • | • | • | • | ▲ | • | ▲ | |||||
Haloragaceae | Myriophyllum sibiricum Kom. | • | • | ▲ | ||||||||
Lentibulariaceae | Pinguicula vulgaris L. | • | ▲ | • | ▲ | |||||||
Linaceae | Linum lewisii subsp. lewisii | • | • | • | ▲ | ▲ | ||||||
Montiaceae | Montia fontana L. | • | ▲ | ▲ | ||||||||
Onagraceae | Chamaenerion latifolium (L.) Sweet | • | • | • | • | ▲ | • | • | • | • | • | ▲ |
Epilobium arcticum Sam. | • | • | • | • | ▲ | • | • | • | ▲ | |||
Orchidaceae | Corallorhiza trifida Châtel. | • | ▲ | |||||||||
Orobanchaceae | Castilleja elegans Malte | • | • | • | • | ▲ | • | • | • | • | ▲ | |
Castilleja pallida var. caudata (Pennell) B.Boivin | • | ▲ | ||||||||||
Pedicularis albolabiata (Hultén) Kozhevn | • | • | • | • | ▲ | • | • | • | ▲ | |||
Pedicularis arctoeuropaea (Hultén) Molau & D.F.Murray | • | • | • | ▲ | • | • | • | ▲ | ||||
Pedicularis capitata Adams | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Pedicularis hirsuta L. | ▲ | |||||||||||
Pedicularis lanata Willd. ex Cham. & Schltdl. | • | • | • | • | ▲ | • | • | • | ▲ | |||
Pedicularis langsdorffii subsp. arctica (R.Br.) Pennell ex Hultén | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Papaveraceae | Papaver cornwallisense D.Löve | • | • | • | ▲ | • | • | ▲ | ||||
Papaver dahlianum Nordh. | • | • | • | ▲ | • | • | ▲ | |||||
Papaver hultenii Knaben | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Papaver lapponicum (Tolm.) Nordh. | • | • | • | ▲ | • | ▲ | ||||||
Plantaginaceae | Hippuris lanceolata Retz. | • | • | ▲ | • | • | • | ▲ | ||||
Plantago canescens Adams | • | • | • | • | ▲ | • | • | ▲ | ||||
Plumbaginaceae | Armeria scabra Pall. ex Roem. & Schult. | • | • | • | • | ▲ | • | • | • | • | ▲ | |
Polygonaceae | Bistorta vivipara (L.) Delarbre | • | • | • | • | ▲ | • | • | • | • | ▲ | |
Oxyria digyna (L.) Hill | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Primulaceae | Androsace chamaejasme subsp. andersonii (Hultén) Hultén | • | • | • | ▲ | • | • | • | ▲ | |||
Androsace septentrionalis L. | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Primula stricta Hornem. | • | ▲ | • | • | ▲ | |||||||
Ranunculaceae | Anemone parviflora Michx. | • | • | • | • | ▲ | • | • | • | • | • | ▲ |
Caltha palustris subsp. radicans (T.F.Forst.) Hook. | • | ▲ | ||||||||||
Halerpestes cymbalaria (Pursh) Greene | • | ▲ | • | • | ▲ | |||||||
Pulsatilla nuttalliana (DC.) Spreng. | ▲ | |||||||||||
Ranunculus arcticus Richardson | • | • | • | ▲ | • | • | • | • | ▲ | |||
Ranunculus codyanus B.Boivin | • | ▲ | • | ▲ | ||||||||
Ranunculus gmelinii subsp. gmelinii | • | • | ▲ | • | • | • | ▲ | |||||
Ranunculus hyperboreus subsp. hyperboreus | • | • | ▲ | • | ▲ | |||||||
Ranunculus nivalis L. | • | • | • | • | ▲ | • | ▲ | |||||
Ranunculus pygmaeus Wahlenb. | • | • | ▲ | • | • | ▲ | ||||||
Ranunculus sabinei R.Br. | ▲ | ▲ | ||||||||||
Ranunculus sulphureus Sol. | ▲ | |||||||||||
Rosaceae | Dryas integrifolia subsp. integrifolia | • | • | • | • | ▲ | • | • | • | • | ▲ | |
Potentilla anserina subsp. groenlandica Tratt. | • | ▲ | • | ▲ | ||||||||
Potentilla arenosa subsp. arenosa | • | • | • | ▲ | • | • | • | ▲ | ||||
Potentilla arenosa subsp. chamissonis (Hultén) Elven & D.F.Murray | • | • | ▲ | • | • | ▲ | ||||||
Potentilla hyparctica subsp. hyparctica | ▲ | |||||||||||
Potentilla nivea L. | • | • | ▲ | • | • | ▲ | ||||||
Potentilla pedersenii (Rydb.) Rydb. | • | • | • | ▲ | • | • | ▲ | |||||
Potentilla × prostrata Rottb. | • | ▲ | ||||||||||
Potentilla pulchella R.Br. | • | • | ▲ | • | • | • | ▲ | |||||
Potentilla subgorodkovii Jurtzev | • | • | • | ▲ | ▲ | |||||||
Potentilla subvahliana Jurtzev | • | • | • | ▲ | ▲ | |||||||
Potentilla tikhomirovii Jurtzev | ▲ | • | • | ▲ | ||||||||
Potentilla uschakovii Jurtzev | • | • | • | • | ▲ | • | • | • | ▲ | |||
Rosaceae | Potentilla vulcanicola Juz. | • | ▲ | |||||||||
Rubus chamaemorus L. | ▲ | |||||||||||
Rubiaceae | Galium aparine L. | • | ▲ | |||||||||
Salicaceae | Salix alaxensis var. alaxensis | • | • | • | ▲ | • | ▲ | |||||
Salix arctica × Salix polaris | • | • | • | ▲ | • | • | • | ▲ | ||||
Salix arctica Pall. | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Salix arctophila Cockerell ex A.Heller | • | ▲ | ||||||||||
Salix glauca var. stipulata Flod. | • | • | • | ▲ | ||||||||
Salix niphoclada Rydb. | • | • | • | • | ▲ | • | • | ▲ | ||||
Salix ovalifolia var. ovalifolia | ▲ | |||||||||||
Salix planifolia Pursh | ▲ | |||||||||||
Salix polaris Wahlenb. | • | • | ▲ | • | ▲ | |||||||
Salix reticulata L. | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Salix richardsonii Hook. | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Saxifragaceae | Chrysosplenium rosendahlii Packer | • | • | ▲ | • | ▲ | ||||||
Chrysosplenium tetrandrum Th.Fr. | • | • | ▲ | • | ▲ | |||||||
Micranthes foliolosa (R.Br.) Gornall | • | ▲ | ▲ | |||||||||
Micranthes hieraciifolia (Waldst. & Kit. ex Willd.) Haw. | • | ▲ | ||||||||||
Micranthes nivalis (L.) Small | • | • | • | ▲ | • | • | • | ▲ | ||||
Micranthes tenuis (Wahlenb.) Small | • | • | • | ▲ | ||||||||
Saxifraga rivularis subsp. arctolitoralis (Jurtzev & V.V.Petrovsky) M.H.Jørg. & Elven | • | ▲ | • | • | ▲ | |||||||
Saxifraga aizoides L. | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Saxifraga cernua L. | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Saxifraga cespitosa L. | • | • | • | • | ▲ | • | • | • | • | ▲ | ||
Saxifraga flagellaris subsp. platysepala (Trautv.) A.E.Porsild | ▲ | ▲ | ||||||||||
Saxifraga hirculus L. | • | • | • | • | ▲ | • | • | • | • | • | ▲ | |
Saxifraga hyperborea R.Br. | • | • | • | ▲ | • | • | ▲ | |||||
Saxifraga oppositifolia L. | • | • | • | • | ▲ | • | • | • | ▲ | |||
Saxifraga rivularis L. | • | ▲ | • | • | ||||||||
Saxifraga tricuspidata Rottb. | • | • | • | • | ▲ | • | • | • | • | • | ||
Total | 194 | 139 | 176 | 173 | 237 | 127 | 181 | 85 | 183 | 57 | 277 |
We recorded 272 species and 289 taxa on Victoria Island, including 21 taxa newly reported for the island. This represents an increase of 4.3% from the 277 taxa previously recorded from Victoria Island (
The greatest regional vascular plant diversity on Victoria Island is recorded from Ulukhaktok (188 species, seven infraspecific taxa, one hybrid) and the next-greatest diversity is recorded from Cambridge Bay (176 species, 11 infraspecific taxa, one hybrid), with about 3.5% fewer taxa recorded than Ulukhaktok. This was an unexpected result, as we had predicted the Cambridge Bay area to be richer because (1) there has been more exploration and collecting there (1422 unique collections in our dataset) compared to Ulukhaktok (915 unique collections), and (2) the Cambridge Bay area, as we have defined it, including the area east of the community along the road to Ovayok Territorial Park and west of the community to the Augustus Hills area, is considerably larger (200 km2) than the Ulukhaktok area (16.5 km2) where collections have been made. In addition to different levels of species richness, the floras of the two areas are dissimilar. Although a total of 150 taxa are documented in both areas, 43 are recorded from Uluhaktok that are not known from Cambridge Bay and 33 from Cambridge Bay that are not known from Ulukhaktok; 61 taxa recorded on the island are not recorded from either area (Table
The distribution maps presented here serve as updates to those produced over the decades (
There are few introduced vascular plant species in the Canadian Arctic Archipelago, and none that are considered to be invasive (
The numerous first records of taxa for Victoria Island reported by
In addition to first records for Victoria Island, the current study documents many new sites for species previously recorded from one or more sites on the island. The majority of these are collections that close major or minor gaps in species’ known distributions. For example, our 2008 fieldwork across southern Victoria Island–in areas where no or few collections had previously been made–resulted, as expected, in collections that close numerous gaps in distribution for taxa otherwise documented elsewhere on the island, across the Canadian Arctic Archipelago and on the adjacent mainland. Our fieldwork on southeastern Victoria Island resulted in collections from many sites that had not previously been explored or documented (e.g., the Greiner Lake watershed, “Trunsky Lake”, “30-Mile Creek”). Some new site records reported here variously represent extensions to the known ranges of species, to the north (Gentianella propinqua, Tofieldia pusilla), south (Festuca hyperborea) and west (Juncus arcticus subsp. arcticus). In a few cases, we report additional collections for species newly reported for the island in
Thirty-nine taxa are known on the island from a single collection, seven from two collections and three from three collections. All 47 of these taxa may be considered rare on the island, and efforts should be made to discover additional populations. Many of the taxa known from a single collection have not been seen in decades, being known only from collections made in 1915 (Eurybia sibirica, Mertensia drummondii), 1945 (Pedicularis hirsuta), 1946 (Potentilla hyparctica subsp. hyparctica), 1949 (Anthoxanthum nitens subsp. nitens, Montia fontana), 1952 (Potentilla vulcanicola), 1959 (Braya thorild-wulffii subsp. glabrata, Draba norvegica), 1962 (Salix ovalifolia var. ovalifolia), 1964 (Bromus pumpellianus, Erysimum coarctatum, Pulsatilla nuttalliana, Rubus chamaemorus, Salix planifolia, Senecio lugens), 1986 (Cardamine bellidifolia) and 1987 (Draba pauciflora, Sagina caespitosa). The exact original collecting sites for all the collections made prior to the 1980s would likely be impossible to re-locate, since locality information on specimen labels is brief and imprecise. For example, the 1964 collections are part of a larger set of 48 specimens gathered by J.D.H. Lambert from “Long Lake” (Kellogok), a linear lake some 10 km in length with its northwestern end included in (or surrounded by) the southeastern portion of Ovayok Territorial Park. Additional information provided on the labels is brief, including plot numbers 21–27, the coordinates 69°07'N, 104°34'W, and the habitat “sedge meadow” on a subset of collections. The coordinates mark a spot about 750 m west of the mid-point of the lake. We do not know how accurate these coordinates are, nor if they were determined by the collector or secondarily by another worker based on the named locality. The recorded plot numbers suggest the collections were made as part of an ecological study, but we have not been able to align them with published or unpublished research. Other species recorded by Lambert from “Long Lake” include the rare species Lupinus arcticus subsp. arcticus (three collections) and the heaths Empetrum nigrum, Rhododendron tomentosum subsp. decumbens, Vaccinium uliginosum and V. vitis-idaea subsp. minus, most of which are uncommon on the island. The presence of the heaths indicates acidic substrate in the “Long Lake” area, which on southeastern Victoria Island is otherwise known only from the Wellington Bay area. Efforts should be undertaken to explore the “Long Lake” area to try and re-locate the occurrence(s) of these rare taxa, most of which should be relatively conspicuous, particularly if/when in flower, and which have not been seen in the area in over 50 years.
The species discovery curves for the six sites on Victoria Island at which we aimed to document all vascular plant diversity present indicate, not surprisingly, that species discovery is directly correlated with search intensity: as more days were spent at a site, more species were found. Search intensity is also a function of the number of searchers active in an area and their field botany skills, taxonomic expertise and knowledge of and experience with the flora under study. Some Arctic species are difficult to identify, especially in the field (high-powered magnification is often needed to observe diagnostic characters), such as those in the genera Draba and Potentilla and in groups that field botanists – in the Arctic and elsewhere – tend to be less familiar with, like the grasses (Poaceae) and sedges (Cyperaceae). Specialist knowledge is usually needed to locate and recognize diversity in such challenging groups in the field. Our own experience on Victoria Island serves as an example of this: the Canadian Arctic flora was brand new to one of us (J.M. Saarela) on our 2008 expedition. Reflecting on experience gained with the Canadian Arctic vascular plant flora in both the field and herbarium over the subsequent ten-year period, it is likely that some species present at sites studied in the plant families focused on by that individual (grasses, sedges, rushes) during that expedition were overlooked (J.M. Saarela, pers. obs.). Reciprocally, Puccinellia expert Laurie Consaul, who was also part of the 2008 expedition, focused on documenting diversity in that challenging genus on Victoria Island. Results, based on targeted search efforts, included her locating new populations of P. banksiensis, a species described as new to science that same year that was not then known from the island (
Vascular plant species diversity in the Canadian Arctic is correlated with habitat diversity. A large subset of species in the Arctic tend to be dominant and widespread, present wherever suitable habitat occurs; these species are easy to find. On the other hand, many vascular plant species in the Arctic tend to be uncommon on the landscape and occur in microhabitats that do not reflect the dominant vegetation in an area. Examples of microhabitats we encountered on Victoria Island with interesting vascular plant diversity included bird perches (rocks, cliffs), shallow freshwater ponds and south-facing slopes. Locating and searching as many microhabitats as possible results in discovery of the greatest number of species, as we found on Victoria Island. Accordingly, the general locations of our camp sites were chosen by targeting areas that appeared, on topographical maps, to be topographically diverse, ideally including local variation in elevation, aspect, moisture and geology. Ability to survey as many habitats as possible in an area is related to the amount of time available for searching and the diversity of the landscape. The number of days we spent in each area were determined based on our estimate of how long it would take to thoroughly explore the local habitat diversity, though other factors also affected this, such as availability of helicopter support and weather, which greatly affects logistical planning in the Arctic. Exactly where we were able to establish base camps was dependant on suitable areas to land a Twin Otter plane on the tundra in order to establish a camp, the availability of helicopter support for establishing a camp, logistical and financial support for plane and helicopter time, and weather.
The species discovery curves (Fig.
Vascular plant biodiversity in the Arctic is correlated with summer warmth, with diversity declining substantially from south to north. A total of 75–150 species is expected in local floras across bioclimate subzone C and 125–250 in subzone D, based on research by
Comparisons of documented levels of vascular plant diversity among the various bioclimate and ecological zones defined on Victoria Island and with diversity recorded within the subzones elsewhere in the Canadian Arctic provides insight into how complete current documentation of the vascular flora is across the island. Several taxa on the island recorded from both bioclimate subzones C and D are known from single occurrences in subzone C. Although uncommon (or poorly documented) in subzone C on the island, all but one are common and/or known from multiple collections elsewhere in the subzone either in the eastern and northern Arctic (Cystopteris fragilis) or more or less throughout the subzone (western, eastern and northern) (Equisetum arvense subsp. alpestre, Huperzia arctica, Woodsia glabella). Their rareness in subzone C on the island may therefore be a result of collection bias, which seems likely for E. arvense, or lack of appropriate habitat, which seems likely for the fern taxa, which grow on acidic substrates that are uncommon on Victoria Island. The presence of Carex vaginata in subzone C is a borderline occurrence, as the species is known elsewhere in that subzone only from one area of Banks Island. Of the seven species recorded in subzone C but not in subzone D on Victoria Island, four occur elsewhere in subzone D in Canada: Cardamine bellidifolia, which is widespread in several parts of subzone D, and Puccinellia bruggemannii, Ranunculus sabinei and R. sulphureus, which are recorded mostly along the northern edge of subzone D (
There is also considerable variation in levels of vascular plant diversity recorded within subzone C on Victoria Island. For example, within the Nunavut portion of subzone C, lower diversity (101 taxa) is recorded from the northern part of the subzone, here arbitrarily defined as comprising Storkerson Peninsula, the head of and west side of Hadley Bay, and Natkusiak Peninsula, than is recorded from the rest of the subzone in Nunavut. Of the species recorded from the more northerly Nunavut portion of subzone C, 18 are not recorded from the more southerly Nunavut portion of the subzone (Caltha palustris subsp. radicans, Cardamine bellidifolia, Carex nardina, Cerastium arcticum, Chamaenerion latifolium, Eriophorum angustifolium, Micranthes foliolosa, Papaver dahlianum, Pleuropogon sabinei, Potentilla uschakovii, Puccinellia angustata, P. vaginata, P. vahliana, Ranunculus hyperboreus subsp. hyperboreus, R. nivalis, R. sulphureus, Sagina nivalis, Saxifraga flagellaris subsp. platysepala). All but four of these (Cardamine bellidifolia, Micranthes foliolosa, Ranunculus sulphureus and Saxifraga flagellaris subsp. platysepala) are recorded in the Nunavut portion of subzone D on the island. It is therefore likely that the remaining 13 species occur within the southern Nunavut portion of subzone C, but are as yet unrecorded. Reciprocally, there are 43 species recorded in the southern Nunavut portion of subzone C on Victoria Island that are not recorded in the northern Nunavut portion of the subzone (Armeria scabra, Arnica angustifolia subsp. angustifolia, Astragalus richardsonii, Braya thorild-wulffii subsp. glabrata, Carex atrofusca, C. bigelowii subsp. lugens, C. borealipolaris, C. chordorrhiza, C. fuliginosa subsp. misandra, C. maritima, C. saxatilis, C. simpliciuscula subsp. subholarctica, Cassiope tetragona subsp. tetragona, Deschampsia cespitosa subsp. cespitosa, Draba arctica, D. glabella, D. nivalis, D. pauciflora, D. simmonsii, Elymus alaskanus subsp. alaskanus, Equisetum arvense subsp. alpestre, Erigeron eriocephalus, Eriophorum brachyantherum, E. callitrix, Festuca rubra subsp. arctica, Juncus triglumis subsp. albescens, Oxytropis maydelliana, Papaver lapponicum, Potentilla subgorodkovii, Puccinellia arctica, Ranunculus codyanus, R. gmelinii subsp. gmelinii, R. pygmaeus, Salix alaxensis var. alaxensis, S. arctica × S. polaris, S. niphoclada, S. polaris, Saxifraga aizoides, Silene uralensis subsp. arctica, Symphyotrichum pygmaeum, Taraxacum ceratophorum, T. hyparcticum, Tofieldia pusilla, Woodsia glabella). A subset of these are expected to be present within the northern Nunavut portion of the subzone, given their documented occurrences on nearby islands to the north and east (
Species are not distributed evenly throughout subzone D across southern Victoria Island. The composition of the vascular flora of the southeastern part of the island differs somewhat from the southwestern part. As a way to quantitatively assess this, we arbitrarily divided the subzone at Wellington Bay. We found that 178 species are known from both east and west of Wellington Bay, 216 are recorded from east of the bay and 224 from west of the bay. These differences are likely due to a combination of the historical biogeography of the region, in that a subset of species present on the southwestern part of the island, such as those with western or Beringian distributions that are at the edges of their ranges on western and southwestern Victoria Island, are likely absent on the southeastern part, and collection bias, in that some species that are present have not yet been documented in areas east or west of the bay. Species recorded from subzone D on southwestern but not southeastern Victoria Island that are not known from nor expected to occur on the southeastern part of the island, given knowledge of their broader distributions (
Our data indicate very low documented species diversity for most of the Northwest Territories ecological regions. With the exception of the Prince Albert Coastlands Low Arctic North ecoregion, which includes Ulukhaktok and the areas around Minto Inlet we intensively surveyed in 2010 (Kuujjua River, head of Minto Inlet and Boot Inlet) and that several other collectors have visited, low recorded diversity is due to collection bias rather than reflecting true levels of vascular plant diversity. Aside from our 2010 efforts, there has been no attempt to comprehensively document local floras at sites/areas within the ecological regions, and most have only been cursorily explored. For example, in the East Prince Albert Plain Mid-Arctic Ecoregion, spanning 9,866 km2, only six species are known, all recorded from one site, by S. Edlund, on the east side of Richard Collinson Inlet. Within the West Prince Albert Upland Mid-Arctic Ecoregion collections representing 37 taxa were been made by M. Oldenburg at a single site, “Oldenburg Lake”, all of which are newly reported here. In the Shaler Mountains Mid-Arctic Ecoregion 51 taxa are recorded, in the Wollaston Peninsula Mid-Arctic Ecoregion just 29 taxa are recorded, and collections representing 76 taxa have been made in the Tahiryuak Upland Mid-Arctic Ecoregion. Considerable field work will be needed to accurately document levels of vascular plant diversity in most of these regions, which may be considered underexplored botanically.
This study has substantially increased our understanding of the diversity and distribution of the vascular plant flora of Victoria Island. The results represent a new baseline of knowledge on which continued exploration of the flora of the island can build. We have provided documentation of several taxa new to the island and increased knowledge of the spatial distribution of taxa across the island. Study of existing herbarium material, which was greatly facilitated by recent mass-digitization efforts at several institutions, revealed a large number of occurrence records that have been overlooked in previous efforts to document the vascular flora of Vascular Island. Nearly 50 taxa on the island are rare, known by three or fewer collections. Although more than 7000 unique collections of vascular plants have been made on Victoria Island, many areas remain unexplored or poorly explored botanically. Numerous species that are expected to occur within bioclimate subzones C on the island have not yet been recorded there, while many species reach their northern limits in bioclimate subzone D on the island. We expect (and hope) that many new collections of vascular plants will be gathered over the coming years, particularly related to CHARS research activity in the Cambridge Bay area, on southeastern Victoria Island and across the entire island, and that the information on the distribution and diversity of vascular plant diversity on the island presented here will help guide future documentation efforts. The complete, specimen-based dataset published here will allow future workers to generate updated distribution maps including new occurrence records. We strongly encourage all researchers conducting botanical or plant-related ecological research on Victoria Island and throughout the Canadian Arctic to document species occurrences with specimens, and to deposit the material in one or more publically accessible herbaria, so that the collections may contribute to the centuries long mission to document Arctic biodiversity.
1 | Plants not producing flowers or seeds, reproducing by spores | 2 |
– | Plants producing flowers and seeds | 4 |
2 | Stems conspicuously jointed, bearing at each node a whorl of small, scale-like leaves united at the base | Equisetaceae |
– | Stems not conspicuously jointed, bearing green leaves or leaf-like structures, leaves not whorled, usually not scale-like | 3 |
3 | Leaves lanceolate to triangular, not divided; sporangia axillary | Lycopodiaceae |
– | Leaves (fronds) pinnately divided; sporangia borne on lower surface of leaves | Polypodiales |
4 | Leaves usually parallel-veined; parts of the perianth usually in threes or sixes; seeds with a single cotyledon | Monocots |
– | Leaves usually net-veined; parts of the perianth usually in fours or fives; seeds with two cotyledons | Eudicots |
1 | Fronds once pinnate, lower pinnae sometimes notched or toothed; sori with a divided, hair-like indusium | Woodsiaceae |
– | Fronds 2–3 pinnate or pinnatifid; sori with a hooded lateral indusium, or without indusia | 2 |
2 | Sori with a distinct lateral indusium; fronds thin, somewhat translucent; stipe thin, fragile, more or less translucent, easily disarticulated from a lateral rhizome | Cystopteridaceae |
– | Sori without an indusium; fronds stout; stipe stout, not fragile, firmly attached to a stout rootstock | Dryopteridaceae |
1 | Perianth absent or inconspicuous and of bracts, scales or bristles | 2 |
– | Perianth present, in two distinct whorls | 4 |
2 | Flowers not enclosed in or subtended by bracts, scales or bristles; plants aquatic; leaves submersed or floating; stipules present, adnate to the blade for 2/3 to nearly the entire length of the stipule; inflorescences submersed | Potamogetonaceae |
– | Flowers enclosed in or subtended by bracts, scales or bristles; plants usually terrestrial, rarely aquatic; leaves erect, rarely floating (Arctophila, Pleuropogon); stipules absent; inflorescences never submersed if plants aquatic | 3 |
3 | Stems round, hollow between nodes; leaves 2-ranked; leaf sheaths usually open, sometimes closed; anthers attached at the middle; fruit a caryopsis | Poaceae |
– | Stems triangular or round, solid; leaves 3-ranked; leaf sheaths closed; anthers attached at the base; fruit an achene | Cyperaceae |
4 | Plants rootless and leafless, mycotrophic; flowers zygomorphic | Orchidaceae |
– | Plants with roots and leaves, autotrophic; flowers actinomorphic | 5 |
5 | Perianth conspicuous, deciduous; tepals white, yellowish-green, greenish, pinkish cream or deep crimson; leaves equitant (having the base folded and partly enclosing the leaf above), laterally flattened | Tofieldiaceae |
– | Perianth relatively inconspicuous, persistent; tepals green to brown or purplish black; leaves not equitant, dorsi-ventrally flattened or round | Juncaceae |
1 | Plants aquatic | 2 |
– | Plants terrestrial | 4 |
2 | Leaf blades entire | Plantaginaceae (Hippuris) |
– | Leaf blades finely divided | 3 |
3 | Leaves in whorls; flowers unisexual, 4-merous, petals lacking or inconspicuous and pinkish | Haloragaceae |
– | Leaves alternate; flowers bisexual, 5-merous, petals conspicuous, yellow or white | Ranunculaceae (Ranunculus) |
4 | Plants with woody or partly lignified creeping or erect stems (shrubs or sub-shrubs) | 5 |
– | Plants herbaceous | 9 |
5 | Leaves finely divided or lobed | Asteraceae (Artemisia) |
– | Leaves not divided or lobed, the margins at most crenulate or serrate | 6 |
6 | Petals absent; flowers arranged in catkins | 7 |
– | Petals present; flowers variously arranged, not in catkins | 8 |
7 | Plants monoecious; fruits 2-winged samaras, 1-seeded, seeds lacking hairs | Betulaceae |
– | Plants dioecious; fruits capsules, many seeded, seeds bearing a tuft of hairs | Salicaceae |
8 | Stamens 10 or fewer | Ericaceae (Andromeda , Arctous , Cassiope , Empetrum , Rhododendron , Vaccinium) |
– | Stamens 50+ | Rosaceae (Dryas) |
9 | Flowers arranged in dense heads on a common receptacle (the inflorescence having the appearance of a single flower) | Asteraceae |
– | Flowers arranged variously, but not on a common receptacle | 10 |
10 | Flowers with a single perianth | 11 |
– | Flowers with a double perianth | 15 |
11 | Leaves whorled | Rubiaceae |
– | Leaves not whorled | 12 |
12 | Leaves divided or deeply lobed | Ranunculaceae (Anemone , Anemonastrum , Pulsatilla) |
– | Leaves not deeply lobed or divided | 13 |
13 | Stipules present, fused and sheathing (ocrea) | Polygonaceae |
– | Stipules absent | 14 |
14 | Annuals; fruit a utricle | Amaranthaceae |
– | Perennials; fruit a capsule | Saxifragaceae (Chrysosplenium) |
15 | Petals fused | 16 |
– | Petals distinct, not fused | 23 |
16 | Stems scapose | 17 |
– | Stems leafy | 20 |
17 | Scape 1-flowered; plants carnivorous (leaves sticky and glandular, trapping and digesting insects) | Lentibulariaceae |
– | Scape several-flowered; plants not carnivorous | 18 |
18 | Inflorescences simple, spicate | Plantaginaceae (Plantago) |
– | Inflorescences compound | 19 |
19 | Inflorescences umbels; fruits capsular | Primulaceae |
– | Inflorescences dense hemispheric heads of scorpioid cymes; fruits dry, enclosed by persistent calyces | Plumbaginaceae |
20 | Leaves alternate | 21 |
– | Leaves opposite | 22 |
21 | Inflorescence a single flower; corolla campanulate; ovary inferior; fruit a capsule | Campanulaceae |
– | Inflorescences corymbose; corolla tubular or funnel-form; ovary superior; fruit an aggregate of nutlets | Boraginaceae |
22 | Flowers actinomorphic | Gentianaceae |
– | Flowers zygomorphic | Orobanchaceae |
23 | Cauline leaves opposite | 24 |
– | Cauline leaves alternate, or plants with a basal rosette | 26 |
24 | Plants annual | Montiaceae |
– | Plants perennial | 25 |
25 | Ovary inferior | Onagraceae (Epilobium) |
– | Ovary superior | Caryophyllaceae |
26 | Flowers strongly zygomorphic | Fabaceae |
– | Flowers actinomorphic or slightly zygomorphic | 27 |
27 | Pistils 2-several | 28 |
– | Pistil 1 | 31 |
28 | Perianth and androecium attached to the receptacle below the ovary (hypogynous) | 29 |
– | Perianth and androecium fused at the base to form a hypanthium (perigynous) | 30 |
29 | Staminodes present | Celastraceae |
– | Staminodes absent | Ranunculaceae |
30 | Stipules present | Rosaceae (Potentilla, Rubus) |
– | Stipules absent | Saxifragaceae (Micranthes) |
31 | Petals 4 | 32 |
– | Petals 5 | 34 |
32 | Ovary inferior | Onagraceae (Chamaenerion) |
– | Ovary superior | 33 |
33 | Sepals 4; stamens 6, in two distinct whorls, outer ones short, inner ones long; ovary 2-locular | Brassicaceae |
– | Sepals 2; stamens many, not in two distinct whorls; ovary 1-locular | Papaveraceae |
34 | Ovary 1-locular | Saxifragaceae (Saxifraga) |
– | Ovary 2-several-locular | 35 |
35 | Leaves basal (or appearing so), blades ovate, broadly ovate, elliptic, orbiculate, round or subreniform; petals green, greenish white, yellowish white, white, pinkish, or reddish | Ericaceae (Orthilia, Pyrola) |
– | Leaves cauline, blades linear, linear-lanceolate or linear-oblanceolate; petals usually blue, sometimes whitish | Linaceae |
Lycopodiales
Lycopodiaceae [1/1]
Huperzia Bernh. [1]
Huperzia arctica
(Grossh. ex Tolm.) Sipliv. (H. selago subsp. arctica (Grossh. ex Tolm.) Á.Löve & D.Löve, Lycopodium selago subsp. arcticum Grossh. ex Tolm.), Fig.
Species distribution maps. Lycopodiaceae: A Huperzia arctica. Equisetaceae: B Equisetum arvense subsp. alpestre C Equisetum scirpoides D Equisetum variegatum subsp. variegatum. Cystopteridaceae: E Cystopteris fragilis. Woodsiaceae: F Woodsia glabella. Dryopteridaceae: G Dryopteris fragrans. Tofieldiaceae: H Tofieldia coccinea I Tofieldia pusilla. Potamogetonaceae: J Stuckenia filiformis K Stuckenia vaginata. Orchidaceae: L Corallorhiza trifida.
Previously recorded from Ulukhaktok (
NORTHWEST TERRITORIES. Ulukhaktok: Edlund 476, 745 (CAN), Porsild 17234, 17235 (CAN). NUNAVUT. Ferguson L. [Tahiryuaq]: Bennett et al. 14-0432 (BABY). Johansen B.: Gillespie et al. 7958 (CAN, O). Mukta [?] L.: Hainault 2124 (
Equisetales
Equisetaceae [1/3]
Equisetum L. [3]
Key to Equisetum [adapted from Porsild and Cody (1980) and Hauke (1993)]:
1 | Stems annual (persisting one year or less), bearing whorls of branches; cones terminal on brown unbranched reproductive stems or green branched stems; cone apex rounded | E. arvense subsp. alpestre |
– | Stems evergreen (persisting more than one year), unbranched or forking; cones terminal on green stems; cone apex pointed | 2 |
2 | Teeth 3 per sheath; stem ridges 6; stems inclined and tortuous | E. scirpoides |
– | Teeth 3–12 per sheath; stem ridges same number as teeth; stems stiff and straight | E. variegatum subsp. variegatum |
Equisetum arvense
subsp. alpestre (Wahlenb.) Schönsw. & Elven, Figs
A Equisetum arvense subsp. alpestre strobilus (left) and habit (right), Gillespie et al. 10109 B Equisetum variegatum subsp. variegatum habit, Gillespie et al. 8499 C Cystopteris fragilis habit, Gillespie et al. 9990 D Dryopteris fragrans habit, Johansen Bay, 18 July 2008 E Woodsia glabella habit F Woodsia glabella habitat G Tofieldia coccinea inflorescences, Kuujjua River, NT, 18 July 2010 H Tofieldia coccinea habit, Gillespie et al. 9749. Photos A, C by L.J. Gillespie B, D, G by R.D. Bull H by J.M. Saarela and E, F by B.A. Bennett.
Previously recorded from Cambridge Bay, Ferguson L., the head of Minto Inl. (Porsild obs., conf.), Mt. Pelly, inland from the head of Prince Albert S., Ulukhaktok (Porsild obs., conf.) and Walker B. (Porsild obs.) (
NORTHWEST TERRITORIES. Boot Inl.: Edlund 576 (CAN), Gillespie et al. 9576 (
Equisetum scirpoides
Michx., Fig.
The only previous record (unconfirmed) for Victoria I. is from Johansen B. (
NORTHWEST TERRITORIES: Boot Inl.: Gillespie et al. 9616 (
Equisetum variegatum
Schleich. subsp. variegatum, Figs
Previously recorded from Anderson B., Cambridge Bay, C. Wollaston, Ferguson L., Hadley B., Kuujjua R., the head of Minto Inl., Mt. Pelly, Namaycush L., Natkusiak P., the head of Prince Albert S. (Porsild obs.), Richard Collinson Inl., Storkerson P., Tahoe L. (Porsild obs.) and Ulukhaktok (
NORTHWEST TERRITORIES. Boot Inl.: Gillespie et al. 9588 (CAN). C. Wollaston: Edlund 28 (CAN). Kuujjua R.: Edlund 643 (CAN), Gillespie et al. 9826 (
Cystopteridaceae [1/1]
Cystopteris Bernh. [1]
Cystopteris fragilis
(L.) Bernh., Figs
Previously recorded from Cambridge Bay, Ferguson L., the head of Minto Inl., Mt. Pelly, the head of Prince Albert S. (Porsild obs.), Richard Collinson Inl., Ulukhaktok, Walker B. and Washburn L. (Porsild obs.) (
NORTHWEST TERRITORIES. Boot Inl.: Gillespie et al. 9596 (
Woodsia R.Br. [1]
Woodsia glabella
R.Br., Figs
Previously recorded from Byron B., Cambridge Bay, Ferguson L., Hadley B., the head of Minto Inl., Mt. Pelly, the head of Prince Albert S. (Porsild obs.), Ulukhaktok and Walker B. (
NORTHWEST TERRITORIES. Kuujjua R.: Gillespie et al. 9867 (
Dryopteris Adans. [1]
Dryopteris fragrans
(L.) Schott, Figs
Previously recorded from Ulukhaktok and Ferguson L. (
NORTHWEST TERRITORIES. Ulukhaktok: Bandringa 342 (CAN,
Alismatales
Tofieldiaceae [1/2]
Tofieldia Hudson [2]
Key to Tofieldia [adapted from
1 | Bracts deeply 3-lobed; bracteoles absent; tepals white, cream, yellowish white or sometimes greenish white; capsules 2.5–3 mm; seeds 0.6–0.8 mm | T. pusilla |
– | Bracts ovate, margins ± entire (sometimes absent distally); bracteoles 3-lobed; tepals white or pale pink, often tinged pink to deep purplish; capsules 2–2.3 mm; seeds ca. 1 mm | T. coccinea |
Tofieldia coccinea
Richardson, Figs
Previously recorded from Ulukhaktok and Walker B. (
NORTHWEST TERRITORIES. Boot Inl.: Gillespie et al. 9671 (CAN). Kuujjua R.: Gillespie et al. 9749 (
Tofieldia pusilla
(Michx.) Pers., Fig.
Previously recorded from Ulukhaktok and Walker B. (
NORTHWEST TERRITORIES. Boot Inl.: Gillespie et al. 9590 (
Stuckenia Börner [2]
Key to Stuckenia [adapted from
1 | Leaf sheaths closed and tubular at base (connate) at least when young; stems freely branching proximally, sparsely branching distally; stipules with distinct ligules to 20 mm, especially on distal stipules; summit of midstem stipules tight to stem, about the ± same width as stem; fruit 2–3 mm | S. filiformis |
– | Leaf sheaths open at base, even when young, often with shortly overlapping edges (convolute); stems freely branching proximally to distally; stipules without ligules or ligules to 2 mm on distal stipules; summit of midstem stipules inflated at least 2 times width of stem; fruit 3–3.8 mm | S. vaginata |
Stuckenia filiformis
(Pers.) Börner (Potamogeton filiformis Pers., S. filiformis var. borealis (Raf.) H.St.John, S. filiformis subsp. alpina (Blytt) R.R.Haynes, Les & M.Král), Fig.
Newly recorded for Victoria I., where discovered growing in a small lake (shallow water with Hippuris lanceolata) near Greiner L. in 2016. The site marks the northern edge of the species’ range in the central Canadian Arctic. Elsewhere in the Canadian Arctic Archipelago known only from Sylvia Grinnell Territorial Park on Baffin I. and two sites on Southampton I. (
NUNAVUT. Greiner L.: Ponomarenko CB52 (CAN).
Stuckenia vaginata
(Turcz.) Holub (Potamogeton vaginatus Turcz., S. subretusa (Hagstr.) Holub), Fig.
Known from a single locality in the vicinity of Johansen B., discovered in 2008; see
NUNAVUT. Johansen B.: Gillespie et al. 8048 (
Orchidaceae [1/1]
Corallorhiza Gagnebin [1]
Corallorhiza trifida
Châtel., Fig.
Known from a single collection we made in 2008 at Johansen B.; see details in
NUNAVUT. Johansen B.: Gillespie et al. 8093 (CAN).
Juncaceae [2/7/8]
Key to Juncaceae
1 | Capsules many-seeded; leaves glabrous, sheaths open | Juncus |
– | Capsules 3-seeded; leaves hairy, sheaths closed | Luzula |
Key to Juncus [adapted from
1 | Inflorescences lateral cymes, sympodial; bracts erect, terete, appearing to be continuation of culms; bracteoles 2, at base of perianth; basal leaves bladeless, cauline leaves absent; flowers borne singly, not in heads (J. arcticus) | 2 |
– | Inflorescences terminal panicles or racemes of several heads or a single terminal head, sympodial or monopodial; bracteoles absent at base of perianth; basal leaves (at least some) usually with blade, cauline leaves present or absent; flowers in multiflowered heads | 3 |
2 | Flowers usually 2–5 per inflorescence; bract c. ¼–1/8 of culm | J. arcticus subsp. arcticus |
– | Flowers 3–10 per inflorescence; bract 1/7–1/10 of culm | J. arcticus subsp. alaskanus |
3 | Plants strongly rhizomatous, culms solitary; inflorescences of 1–3(–5) heads, each 2–10-flowered; tepals lanceolate, 4.5–6.6 mm | J. leucochlamys |
– | Plants cespitose, culms clustered; inflorescences single heads, each 1–2(–4)-flowered; tepals oblong or oblong-lanceolate, 2.5–5 mm | 4 |
4 | Primary bract much longer than inflorescence; capsule apex retuse; filaments 1–1.5 mm | J. biglumis |
– | Primary bract nearly equal to or shorter than inflorescence; capsule apex obtuse, mucronate; filaments 2.5–4 mm | J. triglumis subsp. albescens |
Juncus arcticus
Willd. subsp. arcticus, Fig.
Juncus arcticus s.l. was previously recorded from Cambridge Bay, the head of Minto Inl. and Ulukhaktok (
NORTHWEST TERRITORIES. Minto Inl. (head): Edlund 164 (CAN), Porsild 17375 (CAN). Ulukhaktok: Edlund 778 (CAN). NUNAVUT. Cambridge Bay: Saarela & Teeter 5289 (CAN). Oterkvik Pt.: Gillespie et al. 7690 (CAN, O).
Juncus arcticus
subsp. alaskanus Hultén (J. balticus var. alaskanus (Hultén) A.E.Porsild), Fig.
Recorded from Kuujjua R., the head of Minto Inl., “30-Mile Cr.”, Cambridge Bay, Clouston B. and Johansen B. This western subspecies is the common one on the island. Elsewhere in the Canadian Arctic Archipelago it is recorded from Banks I., and on the mainland it extends to Bathurst Inl. and southeastern mainland Nunavut (
NORTHWEST TERRITORIES. Kuujjua R.: Edlund 651 (CAN), Gillespie et al. 9911 (
Juncus biglumis
L., Figs
Previously recorded from Cambridge Bay, the head of Minto Inl., Natkusiak P., Richard Collinson Inl., Storkerson P., Washburn L. (Porsild obs., conf.) and Ulukhaktok (
NORTHWEST TERRITORIES. Boot Inl.: Gillespie et al. 9559 (
Juncus leucochlamys
V.J.Zinger ex V.I.Krecz. | (J. castaneus Sm. pro parte., J. castaneus subsp. leucochlamys (V.J.Zinger ex V.I.Krecz.) Hultén), Figs
Previously recorded from Cambridge Bay, C. Wollaston, the head of Minto Inl. and Ulukhaktok (
NORTHWEST TERRITORIES. C. Wollaston: Edlund 65 (CAN). Kuujjua R.: Gillespie et al. 9860 (CAN), 9901 (ari, CAN, O). Minto Inl. (head): Edlund 125 (CAN), Gillespie et al. 10227 (
Juncus triglumis
subsp. albescens (Lange) Hultén (J. albescens Lange, J. triglumis var. albescens Lange), Figs
Previously recorded from Cambridge Bay, C. Peel, C. Wollaston, Hadley B., the head of Minto Inl., Mt. Bumpus, Namaycush L., east of the head of Prince Albert S. and Ulukhaktok.
NORTHWEST TERRITORIES. Boot Inl.: Gillespie et al. 9555 (
Key to Luzula [adapted from
1 | Inflorescences open, paniculate cymes, flowers solitary at the end of the capillary branches; seeds 1.2–1.6 mm | L. wahlenbergii |
– | Inflorescences spike-like with flowers in heads; seeds 0.8–1.2 mm | 2 |
2 | Basal leaves ± flat, usually up to 5 cm, (2–)3–4 mm wide, tip obtuse, often slightly swollen, with a spinuliform mucro; cauline leaves (1–)2, 1–2(–3) cm; bracteole apices sparsely ciliate | L. nivalis |
– | Basal leaves ± subcanaliculate to ± flat, up to 6–9 cm, 1.5–2.5 mm wide, tip acuminate; cauline leaves 1–2, usually 2–4 cm; bracteole apices fimbriate-ciliate | L. confusa |
Luzula confusa
Lindeb., Fig.
Previously recorded from Cambridge Bay, Ferguson L. [Tahiryuaq], “Long L.”, the head of Minto Inl. and Ulukhaktok (
NORTHWEST TERRITORIES. Minto Inlet (head): Porsild 17378 (CAN). Ulukhaktok: Edlund 811, 845 (CAN), Porsild 17264 (CAN). NUNAVUT. Cambridge Bay: Bennett et al. 13-0304 (
Luzula nivalis
(Laest.) Spreng. (L. arctica Blytt), Figs
Previously recorded from Anderson B., Collinson P., Greely Haven, Hadley B., the head of Minto Inl., Namaycush L., Natkusiak P., Shaler Mts., Storkerson P. and Ulukhaktok (
NORTHWEST TERRITORIES. Boot Inl.: Gillespie et al. 9667 (
Luzula wahlenbergii
Rupr., Fig.
Known from a single collection we made in 2008 at Johansen B.; see
NUNAVUT. Johansen B.: Gillespie et al. 8170 (CAN).
Key to Cyperaceae [adapted from
1 | Flowers and achenes partially to completely enclosed in scalelike structure (perigynium); perigynium in axil of scale; flowers unisexual; perianth absent | Carex |
– | Flowers and achenes not enclosed in scalelike perigynium; flowers in axil of scale; flowers usually bisexual, sometimes some, rarely all, flowers unisexual; perianth persistent, of 10–25 smooth, hairlike bristles | Eriophorum |
Key to Carex [adapted from
1 | Margins of perigynium open; terminal and distal spikelets usually 1-flowered, staminate; proximal spikelets 1-flowered and pistillate, or 2–4-flowered and bisexual with 1 pistillate flower proximally and 1–3 staminate flowers distally | 2 |
– | Margins of perigynium fused; all spikelets 1-flowered | 4 |
2 | Inflorescences compound; basal leaf sheaths dull, base of blade usually persistent | C. simpliciuscula subsp. subholarctica |
– | Inflorescences simple; basal leaf sheaths somewhat glossy, bladeless | 3 |
3 | Perigynia 2–3.5 mm, margins free to base; scales ovate, 2–3.5 mm; midvein distinct almost to tip; anthers 1–1.5 mm; achenes 2–2.8 mm | C. myosuroides |
– | Perigynia 3.5–5.5 mm, margins connate near base; scales obovate-circular, 3.5–5 mm; midvein distinct only near base; anthers 2–3 mm; achenes 2.6–4 mm | C. borealipolaris |
4 | Spikes solitary | 5 |
– | Spikes compound | 9 |
5 | Pistillate scales early deciduous; perigynia deflexed at maturity | C. microglochin |
– | Pistillate scales persistent; perigynia not deflexed at maturity | 6 |
6 | Stigmas 2; plants densely cespitose | 7 |
– | Stigmas 3; plants cespitose or loosely cespitose | 8 |
7 | Spike gynaecandrous (staminate flowers proximal, pistillate flowers distal); perigynia 1.5–2 mm; plants of seashores | C. ursina |
– | Spike androgynous (pistillate flowers proximal, staminate flowers distal); perigynia 3–5 mm; plants of dry, exposed tundra | C. nardina |
8 | Plants dioecious, rarely monoecious; rhizomes short, sometimes inconspicuous; perigynia hairy | C. scirpoidea subsp. scirpoidea |
– | Plants monoecious, spike androgynous; rhizomes long; perigynia glabrous | C. rupestris |
9 | Spikes all bisexual and sessile | 10 |
– | Spikes mostly unisexual, the terminal one staminate or bisexual | 13 |
10 | Some or all spikes androgynous | 11 |
– | Some or all spikes gynaecandrous | 12 |
11 | Plants rhizomatous, stolons lacking; perigynium beak 0.5–1 mm | C. maritima |
– | Plants rhizomatous and long-stoloniferous (vegetative stems ascending to erect when young, becoming prostrate stolons at maturity); perigynium beak 0.3–0.6 mm | C. chordorrhiza |
12 | Plants loosely cespitose; culms erect, 10–15(–30) cm; spikes 2–3(–4); lateral spikes gynecandrous, containing 3–8 perigynia, oblong-clavate; perigynia elliptic, green-white proximally, pale brown distally, often brown in age; beak indistinct | C. marina |
– | Plant densely cespitose; culms often arching, weak, 10–25 cm; spikes 2–4; lateral spikes pistillate, containing 5–10(–15) perigynia, oblong-linear; perigynia broadly elliptic-obovate to lanceolate, light to pale brown, often gray-brown at maturity; beak short | C. glareosa |
13 | Stigmas 2 | 14 |
– | Stigmas 3 | 19 |
14 | Terminal spike gynecandrous | C. bicolor |
– | Terminal spike staminate | 15 |
15 | Perigynia somewhat glossy, glabrous, more or less inflated, beak distinct; lateral spikes usually pendant | C. saxatilis |
– | Perigynia dull, usually papillose, sometimes glabrous, not inflated, beak indistinct; lateral spikes erect | 16 |
16 | Pistillate scales with a prominent, scabrous awn on at least the proximal scales; leaf blades involute, 1–2 mm wide | C. subspathacea |
– | Pistillate scales with apex acute, acuminate, or mucronate, lacking a prominent, scabrous awn; leaf blades not involute, the widest > 2 mm wide | 17 |
17 | Proximal bract longer than inflorescence (usually at least 1.5× as long) | C. aquatilis subsp. stans |
– | Proximal bract shorter than or equal to inflorescence (C. bigelowii) | 18 |
18 | Perigynia green, spotted purple-black on apical 1/2, minutely papillose; stipe 0.15–0.45 mm; proximal pistillate spike loosely flowered, base often attenuate, less often cuneate | C. bigelowii subsp. bigelowii |
– | Perigynia green, often white at maturity, uniformly purple-brown on apical 1/2, strongly or minutely papillose; stipe 0–0.15 mm; proximal pistillate spike densely flowered, base cuneate, less often attenuate | C. bigelowii subsp. lugens |
19 | Terminal spike gynaecandrous | 20 |
– | Terminal spike staminate | 21 |
20 | Perigynia lanceolate, 3.3–5.5 mm, margins ciliate; pistillate scales ovate, 2.8–4.2 mm; staminate scales oblong-obovate or obovate, 3–5 mm; achenes 1.5–2 × 0.9–1 mm | C. fuliginosa subsp. misandra |
– | Perigynia lanceolate to ovate-lanceolate, 1.5–3.3 mm, margins entire or serrulate; pistillate scales obovate or obovate-circular, 1.6–2.1 mm; staminate scales oblong-ovate 2–2.8 mm; achenes 1.1–1.4 × 0.6–0.9 mm | C. krausei |
21 | Inflorescence capitate, the lateral spikes short-peduncled | C. glacialis |
– | Inflorescence not capitate | 22 |
22 | Pistillate spikes sessile or nearly sessile | C. membranacea |
– | Pistillate spikes on peduncles as long or longer than the spikes | 23 |
23 | Plants tufted | 24 |
– | Plants rhizomatous | 25 |
24 | Pistillate scales black with pale midvein, ovate or oblong-ovate, 3–4.8 × 0.9–1.6 mm; lateral spikes 4–7 mm wide; terminal spike 6–15 × 2–5 mm, usually over-topping lateral spikes, sometimes overlapping some of them | C. atrofusca |
– | Pistillate scales medium to dark brown with pale midvein, ovate, obovate or obovate-circular, 2.3–3.5 × 0.8–1.2 mm; lateral spikes 3–4 mm wide; terminal spike 4–10 × 0.7–1.4 mm, level with or over-topped by some of the lateral spikes | C. capillaris subsp. fuscidula |
25 | Lateral spikes ± erect; proximal perigynia loosely arranged; perigynium beak distinct, (0.4–)0.6–1.8(–2.2) mm | C. vaginata |
– | Lateral spikes drooping, at least the lowermost ones; proximal perigynia densely arranged; perigynium beak absent or indistinct, to 0.5 mm | 26 |
26 | Perigynia pale green; proximal bracts of inflorescence 0.5–2 cm; spikes 2–4 | C. rariflora |
– | Perigynia pale yellow proximally, brown or black distally; proximal bracts of inflorescences 0.5–14 cm; spikes 3–8 | C. petricosa subsp. petricosa |
Carex aquatilis
subsp. stans (Drejer) Hultén (C. aquatilis var. minor Boott, C. stans Drejer), Figs
Species distribution maps. Cyperaceae: A Carex aquatilis subsp. stans B Carex atrofusca C Carex bicolor D Carex bigelowii subsp. bigelowii E Carex bigelowii subsp. lugens F Carex borealipolaris G Carex capillaris subsp. fuscidula H Carex chordorrhiza I Carex fuliginosa subsp. misandra J Carex glacialis K Carex glareosa subsp. glareosa L Carex krausei.
A Carex aquatilis subsp. stans habit, 18 July 2010 B Carex atrofusca habit, head of Minto Inlet, 25 July 2010 C Carex borealipolaris inflorescence, Gillespie et al. 9900 D Carex borealipolaris habit, Gillespie et al. 9900 E Carex fuliginosa subsp. misandra habit, Kuujjua River, NT, 18 July 2010. Photos by J.M. Saarela.
Previously recorded from Cambridge Bay, C. Wollaston, Hadley B., Kuujjua R., Mt. Bumpus, Namaycush L., Natkusiak P., north and southeast of the head of Prince Albert S., Richard Collinson Inl., Storkerson P., Tahiryuaq and Ulukhaktok (
NORTHWEST TERRITORIES. Boot Inl.: Dutilly 18706 (
Care
x atrofusca Schkuhr, Figs
Previously recorded from Cambridge Bay, Ferguson L., Jonnessee L., the head of Minto Inl., Mt. Pelly, Tahiryuaq and Ulukhaktok (
NORTHWEST TERRITORIES. Boot Inl.: Dutilly 18705a (
Carex bicolor
Bellardi ex All., Fig.
Newly reported from Victoria I. and the western Canadian Arctic Archipelago based on a collection we made in 2008 in the Johansen B. area; see
NORTHWEST TERRITORIES. Kuujjua R.: Edlund 646 (CAN). NUNAVUT. Cambridge Bay: Bennett et al. 13-0199 (BABY, CAN). Johansen B.: Gillespie et al. 8118 (CAN).
Carex bigelowii
Torr. ex Schwein. subsp. bigelowii, Fig.
Newly recorded for Victoria Island, known from Cambridge Bay, Ferguson L., Johansen B. and Oterkvik Pt. The Ferguson L. records were not previously determined to subspecies. This is a primarily eastern Arctic taxon recorded elsewhere in the Canadian Arctic from numerous mainland sites as well as Baffin, Devon, Ellesmere and Southampton islands (
NUNAVUT. Cambridge Bay: Polunin s.n. (CAN). Ferguson L. [Tahiryuaq]: Hainault 2077, 2134 (
Carex bigelowii
subsp. lugens (Holm) T.V.Egorova (C. consimilis Holm, C. lugens Holm), Fig.
Previously known from Ulukhaktok and the head of Prince Albert S. (
NORTHWEST TERRITORIES. Minto Inl. (head): Gillespie et al. 10269 (
Carex borealipolaris
S.R.Zhang (Kobresia sibirica (Turcz. ex Ledeb.) Boeckeler, K. hyperborea A.E.Porsild), Figs
Previously recorded from Cambridge Bay, Namaycush L., Ulukhaktok and Walker B. (
NORTHWEST TERRITORIES. Boot Inl.: Gillespie et al. 9557 (
Carex capillaris
subsp. fuscidula (V.I.Krecz. ex T.V.Egorova) Á.Löve & D.Löve, Fig.
Previously recorded from Cambridge Bay, Read I., Tahoe L. (Porsild obs.), Ulukhaktok (Porsild obs., conf.) and Walker B. (Porsild obs.) (
NORTHWEST TERRITORIES. Boot Inl.: Gillespie et al. 9675 (CAN). Kuujjua R.: Gillespie et al. 9774 (CAN, MT, O), 9946 (
Carex chordorrhiza
L.f., Fig.
Previously recorded from Tahoe L., where collected in 1949, and a lake edge 1.6 km northeast of Cambridge Bay (
NORTHWEST TERRITORIES. Wollaston P.: Oldenburg 54-504A (
Carex fuliginosa
subsp. misandra (R.Br.) Nyman (C. misandra R.Br.), Figs
Previously recorded from Anderson B., Byron B., Cambridge Bay, the head of Minto Inl., Natkusiak P., Namaycush L., N of a large lake in the Ekalluk River system about 90 km NNE of Cambridge Bay, Mt. Bumpus, Storkerson P., Tahiryuaq, Ulukhaktok and Walker B. (
NORTHWEST TERRITORIES. Boot Inl.: Gillespie et al. 9668 (ari, CAN, MT, O), 9669 (CAN), 9676 (CAN, O). Kuujjua R.: Gillespie et al. 9726 (CAN, O). Minto Inl. (head): Edlund 91 (CAN), Gillespie et al. 9488 (
Carex glacialis
Mack., Fig.
Previously known from near the head of Prince Albert S. (mapped erroneously in
NORTHWEST TERRITORIES. Kuujjua R.: Gillespie et al. 9909 (
Carex glareosa
Wahlenb. subsp. glareosa (C. glareosa var. amphigena Fernald), Fig.
Previously recorded from Ulukhaktok (
NORTHWEST TERRITORIES. Ulukhaktok: Porsild 17249 (
Carex krausei
Boeckeler (C. capillaris subsp. robustior (Lange) Böcher), Figs
Previously recorded from Ulukhaktok and the south side of Prince Albert S. (
NORTHWEST TERRITORIES. Boot Inl.: Gillespie et al. 9541 (
Carex marina
Dewey (C. amblyorhyncha V.I.Krecz.), Figs
A Carex krausei habit, Gillespie et al. 9977 B Carex krausei inflorescence, Gillespie et al. 8114 C Carex marina habit D Carex marina habitat E Carex maritima habit, Johansen Bay, NU, 18 July 2008 F Carex membranacea inflorescence. Photos A, F by J.M. Saarela C, D by B.A. Bennett and B, E by R.D. Bull.
Species distribution maps. Cyperaceae: A Carex marina B Carex maritima C Carex membranacea D Carex microglochin E Carex myosuroides F Carex nardina G Carex petricosa subsp. petricosa H Carex rariflora I Carex rupestris J Carex saxatilis K Carex scirpoidea subsp. scirpoidea L Carex simpliciuscula subsp. subholarctica.
Previously recorded from Cambridge Bay, the head of Minto Inl. and Ulukhaktok (Porsild obs., conf.) (
NORTHWEST TERRITORIES. Boot Inl.: Gillespie et al. 9640 (