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FIGURE 26 in Revision of the soft scale genus Paralecanium (Hemiptera: Coccomorpha: Coccidae) with the introduction of three new genera and twenty new species
FIGURE 26. Discochiton trifasciatum (Green), adult female. Type series, Batticoloa, Ceylon, on?Hemicyclia sp.
FIGURE 17. Discochiton papillatum Hodgson, spec. n in Revision of the soft scale genus Paralecanium (Hemiptera: Coccomorpha: Coccidae) with the introduction of three new genera and twenty new species
FIGURE 17. Discochiton papillatum Hodgson, spec. n., adult female. Type series from Malaysia. Where dp = dermal papilla.
FIGURE 23. Discochiton sarawakense Hodgson, spec. n., adult female. Where A in Revision of the soft scale genus Paralecanium (Hemiptera: Coccomorpha: Coccidae) with the introduction of three new genera and twenty new species
FIGURE 23. Discochiton sarawakense Hodgson, spec. n., adult female. Where A = type series, Kerangas Forest, Sarawak, and B = from Kuala Boram, Sarawak.
FIGURE 19. Discochiton paucipedis Hodgson, spec. n., adult female. Where A in Revision of the soft scale genus Paralecanium (Hemiptera: Coccomorpha: Coccidae) with the introduction of three new genera and twenty new species
FIGURE 19. Discochiton paucipedis Hodgson, spec. n., adult female. Where A = leg structure of specimens from type series, Puri, Orissa, India, and B = leg structure of specimen from Ponnuthu, South India.
FIGURE 9 in Revision of the soft scale genus Paralecanium (Hemiptera: Coccomorpha: Coccidae) with the introduction of three new genera and twenty new species
FIGURE 9. Discochiton expansum (Green), adult female. Bundaberg, Queensland, Australia on Ficus sp. Identified as Lecanium expansum var. japonicum Green.
FIGURE 5 in Revision of the soft scale genus Paralecanium (Hemiptera: Coccomorpha: Coccidae) with the introduction of three new genera and twenty new species
FIGURE 5. Discochiton cocophyllae (Banks), adult female. As P. angkorense Takahshi, Angkor, Indo-China, on unknown host.
FIGURE 25 in Revision of the soft scale genus Paralecanium (Hemiptera: Coccomorpha: Coccidae) with the introduction of three new genera and twenty new species
FIGURE 25. Discochiton seychellarum Williams & Hodgson, spec. n., adult female. Jardin Marron, Silhouette, Seychelles.
FIGURE 49. Paralecanium morobeense Hodgson, spec. n in Revision of the soft scale genus Paralecanium (Hemiptera: Coccomorpha: Coccidae) with the introduction of three new genera and twenty new species
FIGURE 49. Paralecanium morobeense Hodgson, spec. n., adult female. Where * refers to pore-like structure, which may not be dorsal.
FIGURE 31. Paralecanium acinaces Hodgson, spec. n in Revision of the soft scale genus Paralecanium (Hemiptera: Coccomorpha: Coccidae) with the introduction of three new genera and twenty new species
FIGURE 31. Paralecanium acinaces Hodgson, spec. n., adult female. Where ar = areolations, ldp = large dorsal pore; mb = ventral marginal band; mo = marginal ornamentation; mrl = marginal radial lines, and ii, iii, iv, v, vi and vii = abdominal segmentation on venter.
FIGURE 3. Discochiton browni Hodgson, spec. n in Revision of the soft scale genus Paralecanium (Hemiptera: Coccomorpha: Coccidae) with the introduction of three new genera and twenty new species
FIGURE 3. Discochiton browni Hodgson, spec. n., adult female. Where ar = areolations; ca = clear area; g = gap without spiracular disc-pores; ls = leg stub; mb = ventral marginal band; mo = marginal ornamentation; mrl = marginal radial line; mt = membranous dermal tube with dorsal seta on apex; pp = preopercular pore; sr = stigmatic ray, and v, vi and vii = abdominal segmentation on venter.
FIGURE 1 in Revision of the soft scale genus Paralecanium (Hemiptera: Coccomorpha: Coccidae) with the introduction of three new genera and twenty new species
FIGURE 1. Insularicoccus carolinensis (Beardsley), adult female. Where ar = areolations; ca = clear area; cp = compound pore; mb = ventral marginal band; mo = marginal ornamentation; mrl = marginal radial line, and v, vi and vii = abdominal segmentation on venter.
Supplementary material 5 from: Cabezas MP, Ros M, Santos AM, Martínez-Laiz G, Xavier R, Montelli L, Hoffman R, Fersi A, Dauvin JC, Guerra-García JM (2019) Unravelling the origin and introduction pattern of the tropical species Paracaprella pusilla Mayer, 1890 (Crustacea, Amphipoda, Caprellidae) in temperate European waters: first molecular insights from a spatial and temporal perspective. NeoBiota 47: 43-80. https://doi.org/10.3897/neobiota.47.32408
: Explanation note: A Phylogenetic tree of nuclear 28S rRNA. Unfortunately, this gene could not be amplified in P.tenuis species. In P.pusilla, only two haplotypes were detected, differing only by the presence of an indel. B Phylogenetic tree of nuclear ribosomal internal transcribed spacer (ITS). No variation was observed among P.pusilla sequences. Trees were rooted with Caprelladanilevskii and Caprellaliparotensis. Values at the nodes correspond to ML bootstrap support and Bayesian posterior probabilities, respectively.
FIGURE 1 in Introduction of a novel freshwater species Setoseptoria guangxiensis sp. nov., with Setoseptoria baiyunensis nom. nov., in Lentitheciaceae, Pleosporales
FIGURE 1. The RAxML tree is generated from combined LSU, SSU, ITS and tef1-α sequence data analysis. Bootstrap support values for ML equal to or greater than 60% and Bayesian posterior probabilities (PP) equal to or greater than 0.95 are given above the nodes shown as "ML/PP". The tree is rooted to Massarina cisti (CBS 266.62) and Massarina eburnea (CBS 473.64). Type strains are indicated in bold, new species is marked in red, and new name is indicated in blue.
FIGURE 3 in Introduction of a novel freshwater species Setoseptoria guangxiensis sp. nov., with Setoseptoria baiyunensis nom. nov., in Lentitheciaceae, Pleosporales
FIGURE 3. Setoseptoria guangxiensis (ZHKUCC 23-1034). a A two-month-old colony on PDA (from above). b Ascoma produced in PDA after two months. c Colony on PDA (from below). d, e Asci. f–i Ascospores (i ascospore in Indian Ink). Scale bars: d–i = 20 µm.
FIGURE 2 in Introduction of a novel freshwater species Setoseptoria guangxiensis sp. nov., with Setoseptoria baiyunensis nom. nov., in Lentitheciaceae, Pleosporales
FIGURE 2. Setoseptoria guangxiensis (MHZU 23-0281, holotype). a, b Appearance of ascomata on the host. c, d Section of ascomata. e Structure of peridium. f Pseudoparaphyses. g, h Asci. i–n Ascospores (n ascospore in Indian Ink). o Germinated ascospore. p, q Colony on PDA (p from above, q from below). Scale bars: c, d = 50 µm, e–o = 20 µm.
Figure 4 in The introduction of three cryptic tree frog species in the Dutch coastal dunes challenges conservation paradigms
Figure 4. Majority rule consensus phylogenetic tree resulting from Bayesian inference for Hyla orientalis haplotypes. Grey branches indicate the backbone phylogeny with representatives for each Western Palearctic Hyla species; the relatively distinct H. meridionalis and H. carthaginiensis were used as outgroup and are not shown. The pink haplotype is newly identified in the Netherlands; black haplotypes have not been reported in the Netherlands. Haplotype labels correspond to supplementary table S1.
Figure 2 in The introduction of three cryptic tree frog species in the Dutch coastal dunes challenges conservation paradigms
Figure 2. Majority rule consensus tree resulting from Bayesian inference to allocate new Hyla haplotypes to species. Grey branches indicate the backbone phylogeny with representatives for each Western Palearctic Hyla species; the relatively distinct H. meridionalis and H. carthaginiensis were used as outgroup and are not shown. New haplotypes are coloured blue (H. arborea) or pink (H. orientalis). Haplotype labels correspond to supplementary table S1.
Figure 1 in The introduction of three cryptic tree frog species in the Dutch coastal dunes challenges conservation paradigms
Figure 1. Map of the Netherlands showing sampled localities for Hyla tree frogs. A rough outline of the natural tree frog distribution range is shaded grey. Pies are sampled localities. Pie slices are coloured according to haplotype and pie sizes reflect sample sizes. Previously identified haplotypes are labelled 'old' and those newly identified in this study 'new'. The five populations introduced in the coastal dunes are labelled with the (approximate) date of appearance. Sampling details are in supplementary table S1.
Figure 3 in The introduction of three cryptic tree frog species in the Dutch coastal dunes challenges conservation paradigms
Figure 3. Majority rule consensus phylogenetic tree resulting from Bayesian inference for Hyla arborea haplotypes. Grey branches indicate the backbone phylogeny with representatives for each Western Palearctic Hyla species; the relatively distinct H. meridionalis and H. carthaginiensis were used as outgroup and are not shown. Blue haplotypes are newly identified and orange haplotypes were previously reported haplotypes in the Netherlands; black haplotypes have not been reported in the Netherlands. Haplotype labels correspond to supplementary table S1.
Data from: Little evidence for morphological change in a resilient endemic species following the introduction of a novel predator
Human activities, such as species introductions, are dramatically and rapidly altering natural ecological processes, and often result in novel selection regimes. To date, we still have a limited understanding of the extent to which such anthropogenic selection may be driving contemporary phenotypic change in natural populations. Here we test whether the introduction of the piscivorous Nile perch, Lates niloticus, into East Africa's Lake Victoria and nearby lakes coincided with morphological change in one resilient native prey species, the cyprinid fish Rastrineobola argentea. Drawing on prior eco-morphological research, we predicted that this novel predator would select for increased allocation to the caudal region in R. argentea to enhance burst-swimming performance, and hence escape ability. To test this prediction, we compared body morphology of R. argentea across space (nine Ugandan lakes differing in Nile perch invasion history) and through time (before and after establishment of Nile perch in Lake Victoria). Spatial comparisons of contemporary populations only partially supported our predictions, with R. argentea from some invaded lakes having larger caudal regions and smaller heads compared to R. argentea from uninvaded lakes. There was no clear evidence of predator-associated change in body shape over time in Lake Victoria. We conclude that R. argentea have not responded to the presence of Nile perch with consistent morphological changes, and that other factors are driving observed patterns of body shape variation in R. argentea.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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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.