Earth is currently experiencing the sixth mass extinction of complex multi-cellular life, the first at the hands of a single species. The documented extinctions of iconic (mostly vertebrate and plant) taxa dominate the discourse, while poorly known invertebrate species are disappearing ‘silently’, sometimes without having ever been described. Here, we highlight the decline of elements of the trapdoor spider (Mygalomorphae: Idiopidae) fauna of southern Australia – a taxonomically poorly documented yet diverse assemblage of long-lived fossorial predators. We show that a number of trapdoor spider species may be threatened after a century of intensive land clearing and stocking, and that remaining populations in some areas may be experiencing serious contemporary population declines. So, how do we conserve this fauna? We suggest that baseline systematic studies are crucial, and that follow-up surveys, including integrative citizen science solutions, should be used to assess where remnant populations still exist, and whether they can persist into the future. Detailed population genetic research on a handful of carefully chosen taxa could be broadly informative, and ongoing natural history studies remain invaluable. Although solutions may be limited in the face of ongoing habitat degradation and other threats, urgently quantifying declines has implications not just for spiders but for mitigating against the mass extinction of poorly known invertebrate taxa across the globe

The Australasian spiny trapdoor spiders of the family Idiopidae (subfamily Arbanitinae) are revised at the generic level, using a multi-locus molecular phylogenetic foundation and comprehensive sampling of all known lineages. We propose a new family- and genus-group classification for the monophyletic Australasian fauna, and recognise 10 genera in four tribes. The Arbanitini Simon includes Arbanitis L. Koch, 1874 (61 species), Blakistonia Hogg, 1902 (one species) and Cantuaria Hogg, 1902 (43 species). The Aganippini Simon includes Bungulla Rix, Main, Raven & Harvey, gen. nov. (two species), Eucanippe Rix, Main, Raven & Harvey, gen. nov. (one species), Eucyrtops Pocock, 1897 (two species), Gaius Rainbow, 1914 (one species) and Idiosoma Ausserer, 1871 (14 species). The Cataxiini Rainbow and Euoplini Rainbow include just Cataxia Rainbow, 1914 (11 species) and Euoplos Rainbow, 1914 (12 species), respectively. Two distinctive new genera of Aganippini are described from Western Australia, and several previously valid genera are recognised as junior synonyms of existing genus-group names, including Misgolas Karsch, 1878 (= Arbanitis; new synonymy), Aganippe O. P.-Cambridge, 1877 (= Idiosoma; new synonymy) and Anidiops Pocock, 1897 (= Idiosoma; new synonymy). Gaius stat. rev. is further removed from synonymy of Anidiops. Other previously hypothesised generic synonyms are supported by both morphology and molecular phylogenetic data from 12 genes, including the synonymy of Neohomogona Main, 1985 and Homogona Rainbow, 1914 with Cataxia, and the synonymy of Albaniana Rainbow & Pulleine, 1918, Armadalia Rainbow & Pulleine, 1918, Bancroftiana Rainbow & Pulleine, 1918 and Tambouriniana Rainbow & Pulleine, 1918 with Euoplos. At the species level, the identifications of Eucy. latior (O. P.-Cambridge, 1877) and I. manstridgei (Pocock, 1897) are clarified, and three new species are described: Bungulla bertmaini Rix, Main, Raven & Harvey, sp. nov., Eucanippe bifida Rix, Main, Raven & Harvey, sp. nov. and Idiosoma galeosomoides Rix, Main, Raven & Harvey, sp. nov., the latter remarkable for its phragmotic abdominal morphology. The Tasmanian species Mygale annulipes C. L. Koch, 1842 is here transferred to the genus Stanwellia Rainbow & Pulleine, 1918 (family Nemesiidae), comb. nov., Arbanitis mestoni Hickman, 1928 is transferred to Cantuaria, comb. nov. and Idiosoma hirsutum Main, 1952 is synonymised with I. sigillatum (O. P.-Cambridge, 1870), new synonymy. In addition to the morphological synopses and an illustrated key to genera, molecular diagnoses are presented for all nominal taxa, along with live habitus and burrow images to assist in field identification. The Australasian idiopid fauna is highly diverse, with numerous new species known from all genera. As a result, this study provides a taxonomic and nomenclatural foundation for future species-level analyses, and a single reference point for the monographic documentation of a remarkable fauna. http://zoobank.org/?lsid=urn:lsid:zoobank.org:pub:BACE065D-1EF9-40C6-9134-AADC9235FAD8

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The Migidae are a family of austral trapdoor spiders known to show a highly restricted and disjunct distribution pattern. Here, we aim to investigate the phylogeny and historical biogeography of the group, which was previously thought to be vicariant in origin, and examine the biogeographic origins of the genus Moggridgea using a dated multi-gene phylogeny. Moggridgea specimens were sampled from southern Australia and Africa, and Bertmainus was sampled from Western Australia. Sanger sequencing methods were used to generate a robust six marker molecular dataset consisting of the nuclear genes 18S rRNA, 28S rRNA, ITS rRNA, XPNPEP3 and H3 and the mitochondrial gene COI. Bayesian and Maximum Likelihood methods were used to analyse the dataset, and the key dispersal nodes were dated using BEAST. Based on our data, we demonstrate that Moggridgea rainbowi from Kangaroo Island, Australia is a valid member of the otherwise African genus Moggridgea. Molecular clock dating analyses show that the inter-specific divergence of M. rainbowi from African congeners is between 2.27–16.02 million years ago (Mya). This divergence date significantly post-dates the separation of Africa from Gondwana (95 Mya) and therefore does not support a vicariant origin for Australian Moggridgea. It also pre-dates human colonisation of Kangaroo Island, a result which is further supported by the intra-specific divergence date of 1.10–6.39 Mya between separate populations on Kangaroo Island. These analyses provide strong support for the hypothesis that Moggridgea colonised Australia via long-distance trans-Indian Ocean dispersal, representing the first such documented case in a mygalomorph spider.

To determine the relationship between vitamin D status and upper respiratory tract infection (URTI) of physically active men and women across seasons (study 1). Then, to investigate the effects on URTI and mucosal immunity of achieving vitamin D sufficiency (25(OH)D ≥50 nmol•L-1) by a unique comparison of safe, simulated-sunlight or oral D3 supplementation in winter (study 2). Methods: In study 1, 1,644 military recruits were observed across basic military training. In study 2, a randomized controlled trial, 250 men undertaking military training received either placebo, simulated-sunlight (1.3x standard erythemal dose, three-times-per-week for 4-weeks and then once-per-week for 8-weeks) or oral vitamin D3 (1,000 IU•day-1 for 4-weeks and then 400 IU•day-1 for 8-weeks). URTI was diagnosed by physician (study 1) and Jackson common cold questionnaire (study 2). Serum 25(OH)D, salivary secretory immunoglobulin A (SIgA) and cathelicidin were assessed by LC-MS/MS and ELISA. Results: In study 1, only 21% of recruits were vitamin D sufficient during winter. Vitamin D sufficient recruits were 40% less likely to suffer URTI than recruits with 25(OH)D <50 nmol•L-1 (OR (95% CI) = 0.6 (0.4-0.9)); an association that remained after accounting for sex and smoking. Each URTI caused on average 3 missed training days. In study 2, vitamin D supplementation strategies were similarly effective to achieve vitamin D sufficiency in almost all (≥95%). Compared to placebo, vitamin D supplementation reduced the severity of peak URTI symptoms by 15% and days with URTI by 36% (P < 0.05). These reductions were similar with both vitamin D strategies (P > 0.05). Supplementation did not affect salivary SIgA or cathelicidin. Conclusion: Vitamin D sufficiency reduced the URTI burden during military training.