162 research outputs found
Collembola of Canada
The state of knowledge of diversity of Collembola in Canada was assessed by examination of literature and DNA barcode data. There are 474 described extant Collembola species known from Canada, a significant change compared to the 520 species estimated to occur in Canada in 1979 (Richards 1979) and the 341 reported in the most recent national checklist (Skidmore 1993). Given the number of indeterminate or cryptic species records, the dearth of sampling in many regions, and the growing use of genetic biodiversity assessment methods such as Barcode Index Numbers, we estimate the total diversity of Collembola in Canada to be approximately 675 species. Advances in Collembola systematics and Canadian research are discussed
Globally invariant metabolism but density-diversity mismatch in springtails.
Soil life supports the functioning and biodiversity of terrestrial ecosystems. Springtails (Collembola) are among the most abundant soil arthropods regulating soil fertility and flow of energy through above- and belowground food webs. However, the global distribution of springtail diversity and density, and how these relate to energy fluxes remains unknown. Here, using a global dataset representing 2470 sites, we estimate the total soil springtail biomass at 27.5 megatons carbon, which is threefold higher than wild terrestrial vertebrates, and record peak densities up to 2 million individuals per square meter in the tundra. Despite a 20-fold biomass difference between the tundra and the tropics, springtail energy use (community metabolism) remains similar across the latitudinal gradient, owing to the changes in temperature with latitude. Neither springtail density nor community metabolism is predicted by local species richness, which is high in the tropics, but comparably high in some temperate forests and even tundra. Changes in springtail activity may emerge from latitudinal gradients in temperature, predation and resource limitation in soil communities. Contrasting relationships of biomass, diversity and activity of springtail communities with temperature suggest that climate warming will alter fundamental soil biodiversity metrics in different directions, potentially restructuring terrestrial food webs and affecting soil functioning
Global fine-resolution data on springtail abundance and community structure
Springtails (Collembola) inhabit soils from the Arctic to the Antarctic and comprise an estimated ~32% of all terrestrial arthropods on Earth. Here, we present a global, spatially-explicit database on springtail communities that includes 249,912 occurrences from 44,999 samples and 2,990 sites. These data are mainly raw sample-level records at the species level collected predominantly from private archives of the authors that were quality-controlled and taxonomically-standardised. Despite covering all continents, most of the sample-level data come from the European continent (82.5% of all samples) and represent four habitats: woodlands (57.4%), grasslands (14.0%), agrosystems (13.7%) and scrublands (9.0%). We included sampling by soil layers, and across seasons and years, representing temporal and spatial within-site variation in springtail communities. We also provided data use and sharing guidelines and R code to facilitate the use of the database by other researchers. This data paper describes a static version of the database at the publication date, but the database will be further expanded to include underrepresented regions and linked with trait data.</p
Global fine-resolution data on springtail abundance and community structure
CODE AVAILABILITY : Programming R code is openly available together with the database from Figshare.SUPPLEMENTARY MATERIAL 1 : Template for data collectionSUPPLEMENTARY MATERIAL 2 : Data Descriptor WorksheetSpringtails (Collembola) inhabit soils from the Arctic to the Antarctic and comprise an estimated ~32% of all terrestrial arthropods on Earth. Here, we present a global, spatially-explicit database on springtail communities that includes 249,912 occurrences from 44,999 samples and 2,990 sites. These data are mainly raw sample-level records at the species level collected predominantly from private archives of the authors that were quality-controlled and taxonomically-standardised. Despite covering all continents, most of the sample-level data come from the European continent (82.5% of all samples) and represent four habitats: woodlands (57.4%), grasslands (14.0%), agrosystems (13.7%) and scrublands (9.0%). We included sampling by soil layers, and across seasons and years, representing temporal and spatial within-site variation in springtail communities. We also provided data use and sharing guidelines and R code to facilitate the use of the database by other researchers. This data paper describes a static version of the database at the publication date, but the database will be further expanded to include underrepresented regions and linked with trait data.Open Access funding enabled and organized by Projekt DEAL.http://www.nature.com/sdatahj2024Plant Production and Soil ScienceSDG-15:Life on lan
Ceratophysella brevisensillata Yosii 1961
C. brevisensillata Yosii, 1961 – Ceratophysella brevisensillata Yosii, 1961: 251 – Hypogastrura pseudarmata Yosii, 1960: 261, nec Folsom, 1916 AK Fjellberg 1985; Skidmore 1995; Babenko & Fjellberg 2006; Babenko & Skarżyński 2011 Remarks: This species was originally described from the northeastern part of the USA (Massachusetts) and is now recorded up to the Ural Mountains in mid Palaearctic. It is rather polymorphic within this wide range and several species may be involved (Babenko & Skarżyński 2011). General distribution: Nearctic and Eastern Palaearctic.Published as part of Babenko, Anatoly, Stebaeva, Sophya & Turnbull, Matthew S., 2019, An updated checklist of Canadian and Alaskan Collembola, pp. 1-125 in Zootaxa 4592 (1) on page 16, DOI: 10.11646/zootaxa.4592.1.1, http://zenodo.org/record/265692
Sminthurides pumilis
S. pumilis (Krausbauer, 1898) – Sminthurus pumilis Krausbauer, 1898: 495 AK Weber 1950; Christiansen & Bellinger 1981, 1998; Ryan 1981; Skidmore 1995; Babenko & Fjellberg 2006 YT Hammer 1953 NT Hammer 1953; Christiansen & Bellinger 1981, 1998; Rusek 1994; Skidmore 1995; Babenko & Fjellberg 2006 BC Marshall et al. 1990; Skidmore 1995; Addison et al. 2003; Cannings 2010 AB Lindo 2014 MB McClure 1943; Maynard 1951; Hammer 1953; Scott 1964; Christiansen & Bellinger 1981, 1998; Skidmore 1995 QC Rochefort 2006 Remarks: The record of this species in AB is an assumption based on species occurrence in analogous communities of the United States noted by Brand & Dunn (1998). General distribution: Holarctic.Published as part of Babenko, Anatoly, Stebaeva, Sophya & Turnbull, Matthew S., 2019, An updated checklist of Canadian and Alaskan Collembola, pp. 1-125 in Zootaxa 4592 (1) on page 95, DOI: 10.11646/zootaxa.4592.1.1, http://zenodo.org/record/265692
Isotomurus palustroides Folsom 1937
I. palustroides Folsom, 1937 – Isotomurus palustroides Folsom, 1937: 77 AK Weber 1950; Danks 1981; Skidmore 1995 MB Aitchison 1984, 1984c; Skidmore 1995 ON Folsom 1937; Christiansen & Bellinger 1980, 1998; Skidmore 1995 QC Therrien et al. 1999, 1999a; Chagnon et al. 2000 NS Christiansen & Bellinger 1980, 1998; Skidmore 1995 NF Arulnayagam 1995; Puvanendran et al. 1997 Remarks: The status of this species is not as complex as with I. palustris, although Christiansen & Bellinger (1980, p. 684) also noted that “it is not certain that our species is the same as Folsom’s”. General distribution: Nearctic.Published as part of Babenko, Anatoly, Stebaeva, Sophya & Turnbull, Matthew S., 2019, An updated checklist of Canadian and Alaskan Collembola, pp. 1-125 in Zootaxa 4592 (1) on page 73, DOI: 10.11646/zootaxa.4592.1.1, http://zenodo.org/record/265692
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