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FIG. 2 in Two new crustose Cladonia species with strepsilin and other new lichens from the Serra de Maracaju, Mato Grosso do Sul, Brazil
FIG. 2. — Cladonia zebrathallina Aptroot & Spielmann, sp. nov., holotype: A, habitus; B, pycnidium; C, conidia. Width of pictures: A, 10 mm, B, 250 µm, C, 120 µm.
Fig. 4. A, C, H, J, L in Four new species and two subspecies of the genus Pachyrhynchus Germar, 1824 (Coleoptera: Curculionidae: Pachyrhynchini) from Luzon Island, Philippines
Fig. 4. A, C, H, J, L – aedeagus in lateral view; B, D, I, K, M – aedeagus in ventral view; A, B – P.disargus sp. nov.; C, D – P.congestus ssp. aedamlayroni subsp. nov.; H, I – P.kirklayroni sp. nov.; J, K – P.sagittatus sp. nov.; L, M – P.tetramaculatus sp.nov.; E, F, G – female genitalia of P.phaleratus ssp. dannylayroni subsp. nov.; E – sternite VIII in ventral view; F – ovipositor in dorsal view; G – spermatheca. Scale bar 1.00 mm
Fig. 2. A in Four new species and two subspecies of the genus Pachyrhynchus Germar, 1824 (Coleoptera: Curculionidae: Pachyrhynchini) from Luzon Island, Philippines
Fig. 2. A - Dorsal habitus of P.disargus sp. nov. male; B – Lateral habitus of P.disargus sp. nov. male Female. Unknown.
Fig. 1 in Four new species and two subspecies of the genus Pachyrhynchus Germar, 1824 (Coleoptera: Curculionidae: Pachyrhynchini) from Luzon Island, Philippines
Fig. 1. Dorsal habitus of the following species: A – P. tetramaculatus sp. nov. male; B – P. tetramaculatus sp. nov. female; C – P.sagittatus sp. nov. male; D – P. kirklayroni sp. nov. male; P. congestus ssp. aedamlayroni subsp. nov. male; E - P.congestus ssp. aedamlayroni subsp. nov female
Fig. 2. A - P. schandenbergi Heller, 1912, B - P. multimaculatus Schultze, 1918, C - P. apicatus Schultze, 1922, D - P. multianulatus Heller, 1929 in Two new species of the genus Pseudapocyrtus Heller, 1912 (Coleoptera: Curculionidae: Pachyrhynchini) from Luzon Island, Philippines
Fig. 2. A - P. schandenbergi Heller, 1912, B - P. multimaculatus Schultze, 1918, C - P. apicatus Schultze, 1922, D - P. multianulatus Heller, 1929
Fig. 2c. Tillomorphites otiliae n in Two new fossil species of Tillomorphites Vitali (Coleoptera: Cerambycidae) and remarks on the morphological evolution, mimicry, biogeography and phylogeny of the tribe Tillomorphini
Fig. 2c. Tillomorphites otiliae n. sp., habitus, Fig. 2 e. Tillomorphites otiliae n. sp., reconstruction. Paratype, colour reconstruction.
Fig. 2 in Two New Aphaenogaster Species (Hymenoptera, Formicidae) From Baltic Amber
Fig. 2. Photos of Aphaenogaster ribbeckei Radchenko, sp. n., holotype, worker, body in lateral view. Scale bar 1 mm.
Fig. 3 in Two New Aphaenogaster Species (Hymenoptera, Formicidae) From Baltic Amber
Fig. 3. Photos of Aphaenogaster ribbeckei Radchenko, sp. n., holotype, worker, body in dorsal view. Scale bar 0.5 mm.
Fig. 1 in Two New Aphaenogaster Species (Hymenoptera, Formicidae) From Baltic Amber
Fig. 1. Photos of Aphaenogaster groehni Radchenko, sp. n., holotype, worker, body in dorso-lateral view. Scale bar 1 mm.
Figure 5 A,B – Dorsal setae c2 in Taxonomic comments on some species of the genusEustigmaeus Berlese (Trombidiformes: Stigmaeidae), with a revised checklist of Eustigmaeus and descriptions of two new species from Türkiye
Figure 5 A,B – Dorsal setae c2 andvi in females; C,D – Venter of gnathosoma in females – A,C – Eustigmaeus incisus n. sp., B,D – Eustigmaeus paraincisusn. sp. Scale bar: 40.
Figure 5 in Genetic difference between two Schistosoma japonicum isolates with contrasting cercarial shedding patterns revealed by whole genome sequencing
Figure 5. Gene ontology enrichment analysis of genes from genome regions with strong selective signals.
Figure 2 in Genetic difference between two Schistosoma japonicum isolates with contrasting cercarial shedding patterns revealed by whole genome sequencing
Figure 2. Box plots of diversity, Tajima's D of S. japonicum and their FST. (A) Nucleotide diversity estimated in 100-kb windows sliding in 10-kb steps throughout the genome. (B) Tajima's D estimated within a nonoverlapping 100-kb window throughout the genome. (C) pairwise FST computed in 100-kb windows sliding in 10-kb steps throughout the genome.
Figure 4 in Genetic difference between two Schistosoma japonicum isolates with contrasting cercarial shedding patterns revealed by whole genome sequencing
Figure 4. Distribution of p ratios (pST/pHX) and FST values calculated in 100-kb windows sliding in 10-kb steps throughout the genome. Data points colored red and blue were identified as selected regions in ST (red dots) and in HX (blue dots), respectively. These points correspond to the 5% left and right tails of the empirical p ratio distribution, where the p ratios are 0.092 and 1.643, respectively (vertical dashed lines), and the 5% right tail of the empirical FST distribution, where FST is 0.965 (horizontal dashed line).
Figure 3 in Genetic difference between two Schistosoma japonicum isolates with contrasting cercarial shedding patterns revealed by whole genome sequencing
Figure 3. Box plots of diversity and relationship of two sample groups. (A) Nucleotide diversity estimated in 100-kb windows sliding in 10-kb steps throughout the genome. (B) Tajima's D estimated within a nonoverlapping 100-kb window throughout the genome. (C) FST between computed in 100-kb windows sliding in 10-kb steps throughout the genome.
Figures 9–14 in Two new species of Aristocleidus (Monogenea) from the gills of the Mexican mojarra Eugerres mexicanus (Perciformes, Gerreidae) from southwestern Mexico
Figures 9–14. Haptoral and copulatory complex sclerites of Aristocleidus lacantuni n. sp. from the gills of Eugerres mexicanus. 9: dorsal anchor; 10: ventral anchor; 11: ventral bar; 12: dorsal bar; 13: hook; 14: Copulatory complex. Figures are drawn to the following scales: 20 µm (Figs. 9–12 and 14) and 5 µm (Fig. 13).
Figures 1–8. Aristocleidus mexicanus n in Two new species of Aristocleidus (Monogenea) from the gills of the Mexican mojarra Eugerres mexicanus (Perciformes, Gerreidae) from southwestern Mexico
Figures 1–8. Aristocleidus mexicanus n. sp. from the gills of Eugerres mexicanus. 1: whole-mount (composite, ventral view); 2: ventral anchor (Sh, shaft; Au, angular union; Po, point); 3: copulatory complex (dorsal view); 4: dorsal anchor; 5: Ventral bar; 6: dorsal bar; 7: vagina; 8: hook. Figures are drawn to the following scales: 100 µm (Fig. 1), 25 µm (Figs. 2–7), and 10 µm (Fig. 8).
Fig. 4 in Population counts and potential impact of two successful invaders in a town of Northern Italy: the case of ring-necked parakeet and Alexandrine parakeet in Reggio Emilia
Fig. 4 - One of the four Savi's pipistrelles killed by RNPs in Reggio Emilia. / Uno dei quattro pipistrelli di Savi uccisi da parrocchetti dal collare a Reggio Emilia.
Fig. 3 in Population counts and potential impact of two successful invaders in a town of Northern Italy: the case of ring-necked parakeet and Alexandrine parakeet in Reggio Emilia
Fig. 3 - Mean consumption (and standard deviations) of persimmons by RNPs, APs and AP×RNP hybrids in 2019 and 2020. / Consumo medio percentuale (e deviazione standard) di cachi per pianta da parte di parrocchetti dal collare, parrocchetti di Alessandro e ibridi nel 2019 e nel 2020.
Fig. 1 in Population counts and potential impact of two successful invaders in a town of Northern Italy: the case of ring-necked parakeet and Alexandrine parakeet in Reggio Emilia
Fig. 1 - Male individuals of ring-necked parakeet (left) and Alexandrine parakeet (right) in Reggio Emilia. / Individui di sesso maschile di parrocchetto dal collare (sinistra) e parrocchetto di Alessandro (destra) a Reggio Emilia. (Photo: / Foto: S. Manfredini).
Fig. 2 in Population counts and potential impact of two successful invaders in a town of Northern Italy: the case of ring-necked parakeet and Alexandrine parakeet in Reggio Emilia
Fig. 2 - Population counts at night roosts showing the growing trends of both RNPs and APs in Reggio Emilia. Counts recorded during our 2019-2020 survey are shown in a blue rectangle. The 2008-2018 counts were obtained from the literature and citizen-science web platforms (Chessa, 2020). / Conteggi di parrocchetti ai dormitori notturni, con tendenze crescenti sia di parrocchetto dal collare sia di parrocchetto di Alessandro a Reggio Emilia. I conteggi del 2019-2020 sono riportate nel rettangolo blu. I conteggi 2008-2018 sono stati ottenuti da letteratura e da piattaforme web di citizen-science (Chessa, 2020).
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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.