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-Map of the Southern Hemisphere showing the locations of all samples used. Further details for each site are provided in table 1. Inset (modified from McLoughlin 2001): approximate alignment of the Gondwanan continental landmasses (NZ 5 New Zealand; AP 5 Antarctic Peninsula; SAm 5 South America) that have formed the basis for vicariant hypotheses. 

-Map of the Southern Hemisphere showing the locations of all samples used. Further details for each site are provided in table 1. Inset (modified from McLoughlin 2001): approximate alignment of the Gondwanan continental landmasses (NZ 5 New Zealand; AP 5 Antarctic Peninsula; SAm 5 South America) that have formed the basis for vicariant hypotheses. 

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Throughout the Southern Hemisphere many terrestrial taxa have circum-Antarctic distributions. This pattern is generally attributed to ongoing dispersal (by wind, water, or migrating birds) or relict Gondwanan distributions. Few of these terrestrial taxa have extant representatives in Antarctica, but such taxa would contribute to our understanding o...

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... climate cooling leading to the glaciation of Antarctica. This is likely to have occurred once the South Tasman Rise had cleared the Oates Land coast of East Antarctica (;32 MYA) and Drake's passage had opened to deep water circulation (;28 MYA) (McLoughlin 2001;Lawver and Gahagan 2003). Although the circum-Antarctic currents (and polar front, see fig. 1) were sufficient to iso- late Antarctica from other continental landmasses, glacia- tion of Antarctica did not reach its maximum extent until around 10 MYA (Miller and Mabin 1998;Roberts et al. 2003), and some species may have survived by shifting in a habitat following climate changes in a similar manner to glacier foreground ...
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... were made between 2001 and 2005 from four continental Antarctic sites (Trans-Antarctic Mountains, Ross Sea Region); in addition, taxonomically related spe- cies were targeted from three islands in close proximity to the Antarctic Peninsula, six subantarctic islands, Tasmania and mainland Australia, New Zealand, and Patagonia ( fig. 1 and table 1). Springtails were extracted from vegetation, soil, and the underside of rocks using a Tullgren funnel, floatation technique, or aspirator and preserved in 95% eth- anol and stored at ÿ20°C. All outgroup individuals were identified by Arne Fjellberg and ingroup individuals by Penelope Greenslade, with vouchers deposited at ...
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... tree (using a proportion of variable sites sensu Lockhart et al. 1994) was similar to the maximum-parsimony (MP) tree (with all sites and also removing third codon posi- tions), but these were not congruent with some groupings in the maximum likelihood (ML) tree (using general time Table 1 Species Examined (with codes), Location (see also fig. 1 reversible [GTR] 1 I 1 C; model chosen using Modeltest) or Bayesian analysis (using a separate model for each codon po- sition, first: F81 1 I; second and third: GTR 1 C)calculated in MrModeltest 2.1 (Nylander 2004) and implemented in MrBayes 3.1 (Ronquist and Huelsenbeck 2003) using four chains of five million generations, sampling ...
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... species; Cryptopygus sp. 2 from New Zealand (CA3), Cryptopygus sp. 3 from Patagonia (CA4), and Cryptopygus sp. 4 from Heard (CA5) and Macquarie Islands (CA2). Surprisingly, in group IV three Cryptopygus spp.-two from Marion Island (Cryptopygus dubius-CD and Cryp- topygus antarcticus travei-CAT) and a single subspecies from the nearby (see fig. 1) I ˆ les Crozet (Cryptopygus ant- arcticus reagens-CAR)-grouped with the Antarctic species Antarctophorus subpolaris (AS) and were sister to a group containing Cryptopygus sp. 5 from mainland Australia (CA6) and Cryptopygus sp. 6 from Tasmania (CA7) (fig. ...
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... our results, C. antarcticus sensu stricto (type locality: Gerlache Straits; Antarctic Peninsula) appears restricted to the Antarctic Peninsula and offshore islands (maritime Antarctica) (1.5%-6.3% divergence) ( fig. 1 and table 2). The level of sequence divergence (12.3%- 17.4%) between populations of C. a. maximus from I ˆ les Kerguelen (CAM1) and Macquarie Island (CAM2) in group I are consistent with levels reported elsewhere for recognized springtail (e.g., .14%; ...
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... is dominated by 90% endemicity, indicating that they are not recent immigrants (Wise 1967). Second, the Antarctic species are geographically partitioned into four distinct biogeographic regions within the Trans-Antarctic Mountains, suggesting long-term glacial barriers have sep- arated these species assemblages that may have evolved in situ ( fig. 1; see also Wise 1967;). This is supported by high levels of sequence divergence (.25%) (table 2) between the Antarctic species and their respective closest phylogenetic neighbor (fig. 2); for exam- ple, A. subpolaris (AS) with C. dubius (CD) coincides to isolation around 21-14 MYA (20-15 MYA to each other); the Antarctic G. terranova ...

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... For Antarctic biota, there is a growing body of molecular evidence revealing long-term isolation and persistence of short-range endemic species on the Antarctic continent [7,[58][59][60][61][62][63][64]. For springtails that are a dominant driver for biodiversity patterns across the Antarctic realm [25] (figure 1), data show that these endemic species were likely present in ice-free refuges for at least 15-12 Ma [17,46,58]. ...
... For Antarctic biota, there is a growing body of molecular evidence revealing long-term isolation and persistence of short-range endemic species on the Antarctic continent [7,[58][59][60][61][62][63][64]. For springtails that are a dominant driver for biodiversity patterns across the Antarctic realm [25] (figure 1), data show that these endemic species were likely present in ice-free refuges for at least 15-12 Ma [17,46,58]. Endemism is present in most sectors of the continent [6,7], and this is supported by geological dating indicating long-term icefree conditions at sites (figure 2a; see also electronic 2 royalsocietypublishing.org/journal/rsbl Biol. ...
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... Another cluster (blue) seems not to have a predominant topic, but the words that stand out the most are 'strategy' and 'summer' suggesting some attention to life histories around phenological processes under macroclimatic conditions. This cluster could be considered the closest aggregation to our review topic because we also find related terms like 'cold tolerance', 'cold hardiness', ' Cryptopygus antarcticus ' (an Antarctic Collembola superspecies, ( Stevens et al., 2006 )), and 'lethal temperature', among others. On the other hand, a red cluster, highlights the topics 'abundance' and 'richness' as dominant, in turn suggesting the relevance of thermal tolerance limits to account for community level patterns and the geographic distribution of species. ...
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... In order to understand the dispersal, over short and long distances, of microarthropods in Victoria Land, molecular studies have been conducted on different springtail species [22,[27][28][29][30][31]. These have identified that the presence of glacial barriers strongly influences species distributions, and that these have likely limited gene flow between restricted and isolated refugia during various glacial maxima [22,28,32]. Analogous biogeographical patterns have been reported for the prostigmatid mite Stereotydeus mollis by Womersley and Strandtmann, 1963, in Victoria Land [33][34][35][36], although with higher genetic divergence, possibly due to higher activity levels and shorter generation time [33,37] and/or to a longer evolutionary history than for the springtails. ...
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... Stevens et al., 2006Stevens et al., , 2007Tilbrook, 1967; but had not been examined further until molecular data from populations previously identified as 'F. grisea' on the Antarctic continent (northern Victoria Land), South Shetland Islands, and further south on the Antarctic Peninsula showed wide divergence in mitochondrial DNA indicating that more than one species was likely .Friesea grisea, with the type locality on South Georgia, has recently been redescribed and, based on morphology, shown to have a distribution restricted to that sub-Antarctic island alone (Greenslade, 2018a). ...
... We targeted the commonly used mtDNA (COI) gene which has successfully delineated between Collembola species (e.g. Carapelli et al., 2020;Stevens & D'Haese, 2014Stevens et al., 2006). PCR products were amplified using the primers LCO1490 (forward) and HCO2198 (reverse) (Folmer et al., 1994) or primers specific to Collembola (Schneider et al., 2011;Schneider & D'Haese, 2013 and references therein) on the thermocycler (Eppendorf Mastercycler® EP gradient) under the following conditions: 94°C for 1 min for initial denaturation, 5 cycles of 94°C for 1 min, annealing at 47°C for 90 s and extension at 72°C for 1 min, followed by 35 cycles at 94°C for 60 s, 90 s at 51°C and 60 s at 72°C, with a final extension of 72°C for 5 min. ...
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... Species closely related to C. antarcticus, i.e., belonging to Cryptopygus sensu Rusek, have also been found in this study in South Africa (see below) but their status remain unsolved because of the taxonomic and molecular complexity of this group (Deharveng, 1981;Stevens et al. 2006;McGaughran et al. 2010 Description. Body size 0.7-0.9 ...
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... The first, second, and third codon positions were partitioned and we applied a relaxed uncorrelated lognormal molecular clock with Yule speciation process and general time reversible plus a gamma site heterogeneity model (GTR+ ⌫). Based on Stevens et al. (2006) and McGaughran et al. (2010), we used an arthropod strict molecular clock conservative calibration of 1.5%-2.3% divergence per million years (0.0115 substitutions/site) as derived from comparisons between geological and molecular data (Brower 1994;Gaunt and Miles 2002;Quek et al. 2004;Papadopoulou et al. 2010;Ho and Lo 2013). ...
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The invertebrate terrestrial fauna of Antarctica is being investigated with increasing interest to discover how life interacts with the extreme polar environment and how millions of years of evolution have shaped their biodiversity. Classical taxonomic approaches, complemented by molecular tools, are improving our understanding of the systematic relationships of some species, changing the nomenclature of taxa and challenging the taxonomic status of others. The springtail Friesea grisea has previously been described as the only species with a “pan-Antarctic” distribution. However, recent genetic comparisons have pointed to another scenario. The latest morphological study has confined F. grisea to the sub-Antarctic island of South Georgia, from which it was originally described, and resurrected F. antarctica as a congeneric species occurring on the continental mainland. Molecular data demonstrate that populations of this taxon, ostensibly occurring across Maritime and Continental Antarctica, as well as on some offshore islands, are evolutionarily isolated and divergent and cannot be included within a single species. The present study, combining morphological with molecular data, attempts to validate this hypothesis and challenges the taxonomic status of F. antarctica, suggesting that two additional new species, described here as Friesea gretae sp. nov. and Friesea propria sp. nov., are present in Continental Antarctica.
... van Vuuren, Lee, Convey, & Chown, 2018), often indicating allopatric speciation processes (e.g. Allegrucci, Carchini, Convey, & Sbordoni, 2012;Stevens, Greenslade, Hogg, & Sunnucks, 2006). At a finer scale, intra-island population differentiation has been detected for several species, aligning with historical barriers to gene flow such as glaciers and topography (e.g. ...
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Human‐mediated transport of species outside their natural range is a rapidly growing threat to biodiversity, particularly for island ecosystems which have evolved in isolation. The genetic structure underpinning island populations will largely determine their response to increased transport and thus help to inform biosecurity management. However, this information is severely lacking for some groups, such as the soil fauna. We therefore analysed the phylogeographic structure of an indigenous and an invasive springtail species (Collembola: Poduromorpha), each distributed across multiple remote sub‐Antarctic islands, where human activity is currently intensifying. For both species, we generated a genome‐wide SNP dataset and additionally analysed all available COI barcodes. Genetic differentiation in the indigenous springtail Tullbergia bisetosa is substantial among (and, to a lesser degree, within) islands, reflecting low dispersal and historic population fragmentation, while COI patterns reveal ancestral signatures of post‐glacial recolonisation. This pronounced geographic structure demonstrates the key role of allopatric divergence in shaping the region's diversity and highlights the vulnerability of indigenous populations to genetic homogenisation via human transport. For the invasive species Hypogastrura viatica, nuclear genetic structure is much less apparent, particularly for islands linked by regular shipping, while diverged COI haplotypes indicate multiple independent introductions to each island. Thus, human transport has likely facilitated this species’ persistence since its initial colonisation, through the ongoing introduction and inter‐island spread of genetic variation. These findings highlight the different evolutionary consequences of human transport for indigenous and invasive soil species. Yet both demonstrate the need for improved intraregional biosecurity among remote island systems, where the policy focus to date has been on external introductions.