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Figure 2 from: Villet MH, Edwards S (2021) The cicada genus Tugelana Distant, 1912 (Hemiptera, Cicadidae): phylogenetic position and conservation status. African Invertebrates 62(2): 399-410. https://doi.org/10.3897/afrinvertebr.62.66891
Figure 2 Geographical distribution of P. butleri and P. zuluensis within southern Africa, with insets of the two species (specimen scale lines = 10 mm). The distribution of P. butleri has a known standard Area of Occupancy (AOO) of 36 km2 (nine localities) and an Extent of Occurrence (EOO) of 6360 km2. Abbreviations: EC = Eastern Cape, eS = eSwatini, G = Gauteng, KZN = KwaZulu-Natal, L = Limpopo, Les = Lesotho, M = Mpumalanga, NC = Northern Cape, WC = Western Cape.
Supplementary material 2 from: Villet MH, Edwards S (2021) The cicada genus Tugelana Distant, 1912 (Hemiptera, Cicadidae): phylogenetic position and conservation status. African Invertebrates 62(2): 399-410. https://doi.org/10.3897/afrinvertebr.62.66891
Locality records
Figure 3 from: Villet MH, Edwards S (2021) The cicada genus Tugelana Distant, 1912 (Hemiptera, Cicadidae): phylogenetic position and conservation status. African Invertebrates 62(2): 399-410. https://doi.org/10.3897/afrinvertebr.62.66891
Figure 3 Bayesian Inference (BI) phylogenetic tree constructed using a codon nucleotide substitution model. Tugelana butleri is highlighted with a black box. Posterior probabilities (PP) from the two BI phylogenetic reconstructions are indicated above the nodes numerically (BIPPc = codon substitution model, BIPPn = nucleotide substitution model), and the bootstrap support values from the Maximum Likelihood analyses are shown in percentages below the nodes (MLBS). Nodes with BIPP > 0.95 and MLBS > 75 are considered well-supported.
Supplementary material 1 from: Villet MH, Edwards S (2021) The cicada genus Tugelana Distant, 1912 (Hemiptera, Cicadidae): phylogenetic position and conservation status. African Invertebrates 62(2): 399-410. https://doi.org/10.3897/afrinvertebr.62.66891
Table S1, Figures S1, S2
Figure 1 from: Villet MH, Edwards S (2021) The cicada genus Tugelana Distant, 1912 (Hemiptera, Cicadidae): phylogenetic position and conservation status. African Invertebrates 62(2): 399-410. https://doi.org/10.3897/afrinvertebr.62.66891
Figure 1 Urites of Tugelana butleri, Hamza ciliaris, Platypleura capensis and Platypleura zuluensis. AT = anal tube; LP = lateral process; MLP = medio-lateral process; MP = median process. Scale bar: 1 mm.
Figure 1 in New Parabathynellidae species in Africa: the first bathynellids from Chad and an assay of their phylogenetic position in the order Bathynellacea (Crustacea: Malacostraca) based on 18S sequences
Figure 1. Racovitzaibathynella dumonti sp. nov. Male habitus; 10× microscope photography (MNCN).
FIGURE 2 in The taxonomic position of Tonkinomys daovantieni (Rodentia: Muridae) based on karyological and molecular data
FIGURE 2. Karyotype of male Tonkinomys daovantieni, 2n=44. Sample voucher ZMMU S-190817
FIGURE 8 in A new hypogean species of Iberian Microtyphlus and review of the taxonomic position of Speleotyphlus and Aphaenotyphlus (Carabidae: Trechinae: Anillini)
FIGURE 8. Cave map of the "Surgencia de l'Orao."
FIGS 1, 2 in The water mite Rutripalpus limicola Sokolow, 1934: new data on morphology and biology, and considerations on the systematic position of the monotypic family Rutripalpidae (Acari, Hydrachnidia)
FIGS 1, 2. Rutripalpus limicola male, idiosoma. (1) Ventral view; (2) dorsal view. Bar 5 100 mm.
FIGS 34, 35 in The water mite Rutripalpus limicola Sokolow, 1934: new data on morphology and biology, and considerations on the systematic position of the monotypic family Rutripalpidae (Acari, Hydrachnidia)
FIGS 34, 35. Rutripalpus limicola larva. (34) Chelicera; (35) palp, lateral view. Bar 5 50 mm.
Figs. 37–41. Xenysmoderes consularis. 37 in Taxonomic Position of a Taiwanese Ceutorhynchine, Mecysmoderes consularis Pascoe (Coleoptera: Curculionidae), with Description of an Allied New Species from Lanhsu Island
Figs. 37–41. Xenysmoderes consularis. 37) A pair of adults mating on a bract of Alpinia sp.;
Figs. 29–33 in Taxonomic Position of a Taiwanese Ceutorhynchine, Mecysmoderes consularis Pascoe (Coleoptera: Curculionidae), with Description of an Allied New Species from Lanhsu Island
Figs. 29–33. Female genitalia of Xenysmoderes spp. 29–30, 32) Xenysmoderes consularis.
Figs. 21–24 in Taxonomic Position of a Taiwanese Ceutorhynchine, Mecysmoderes consularis Pascoe (Coleoptera: Curculionidae), with Description of an Allied New Species from Lanhsu Island
Figs. 21–24. Male genitalia of Xenysmoderes consularis. 21) Aedeagus, dorsal view; 22)
Figs. 25–28 in Taxonomic Position of a Taiwanese Ceutorhynchine, Mecysmoderes consularis Pascoe (Coleoptera: Curculionidae), with Description of an Allied New Species from Lanhsu Island
Figs. 25–28. Male genitalia of Xenysmoderes ruficollis. 25) Aedeagus, dorsal view; 26)
Figs. 5–8. Xenysmoderes consularis, male. 5 in Taxonomic Position of a Taiwanese Ceutorhynchine, Mecysmoderes consularis Pascoe (Coleoptera: Curculionidae), with Description of an Allied New Species from Lanhsu Island
Figs. 5–8. Xenysmoderes consularis, male. 5) Pronotum; 6) elytron; 7) pro-, meso- and
Figs. 13–14 in Taxonomic Position of a Taiwanese Ceutorhynchine, Mecysmoderes consularis Pascoe (Coleoptera: Curculionidae), with Description of an Allied New Species from Lanhsu Island
Figs. 13–14. Antennae of Xenysmoderes spp. 13) Xenysmoderes consularis; 14) Xenysmo-
Figs. 1–4 in Taxonomic Position of a Taiwanese Ceutorhynchine, Mecysmoderes consularis Pascoe (Coleoptera: Curculionidae), with Description of an Allied New Species from Lanhsu Island
Figs. 1–4. Habitus of Xenysmoderes spp. 1–2) Xenysmoderes consularis, male. 1) Dorsal
An expanded character set for evaluating the phylogenetic position of Homo floresiensis
<p>The hominin character matrix of Dembo et al. (2016) has been updated with additional character states for <i>Ar. ramidus</i>, <i>Au. anamensis</i>, <i>H. antecessor</i>, and <i>H. floresiensis</i>. These characters were published and described in Wood (2020).</p>
Positive genetic covariance and limited thermal tolerance constrain tropical insect responses to global warming
<p>Tropical ectotherms are particularly vulnerable to global warming because their physiologies are assumed to be adapted to narrow temperature ranges. This study explores three mechanisms potentially constraining thermal adaptation to global warming in tropical insects: 1. tradeoffs in genotypic performance at different temperatures (the jack-of-all-trades hypothesis) 2. positive genetic covariance in performance, with some genotypes performing better than others at viable temperatures (the 'winner and 'loser genotypes hypothesis) or 3. limited genetic variation as the potential result of relaxed selection and the loss of genes associated with responses to extreme temperatures (the gene decay hypothesis). We estimated changes in growth and survival rates at multiple temperatures for three tropical rain forest insect herbivores (<i>Cephaloleia</i> rolled-leaf beetles, Chrysomelidae). We reared 2746 individuals in a full-sibling experimental design, at temperatures known to be experienced by this genus of beetles in nature (<i>i.e.</i>, 10-35°C). Significant genetic covariance was positive for 16 traits, supporting the 'winner and 'loser genotypes hypothesis. Only two traits displayed negative cross-temperature performance correlations. We detected a substantial contribution of genetic variance in traits associated with size and mass (0-44%), but low heritability in plastic traits such as development time (0-6%) or survival (0-4%). Lowland insect populations will most likely decline if current temperatures increase beyond 2°C. It is concerning that local adaption is already lagging behind current temperatures. The consequences of maintaining the current global warming trajectory would be devastating for tropical insects. However, if humans can limit or slow warming, many tropical ectotherms might persist in their current locations, and potentially adapt to warmer temperatures.</p>
Fig. 73 in Postcranial Osteology Of Azendohsaurus Madagaskarensis (?Middle To Upper Triassic, Isalo Group, Madagascar) And Its Systematic Position Among Stem Archosaur Reptiles
Fig. 73. The relationships of the major clades of early archosauromorphs found in the analyses of this study.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.