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Figure 7 from: Wang Z-T, Li C-D (2021) Three new species, and new distributional data, of Haltichella (Hymenoptera, Chalcididae) from China. ZooKeys 1060: 1-16. https://doi.org/10.3897/zookeys.1060.70427
Figure 7 Haltichella nipponensis, (female) A habitus, lateral view B head, front view C forewing D head, dorsal view E antenna F propodeum G hind leg H metasoma I mesosoma, dorsal view.
Figure 4 from: Wang Z-T, Li C-D (2021) Three new species, and new distributional data, of Haltichella (Hymenoptera, Chalcididae) from China. ZooKeys 1060: 1-16. https://doi.org/10.3897/zookeys.1060.70427
Figure 4 Haltichella clavicornis, (female) A habitus, lateral view B head, front view C antenna D forewing E mesosoma, dorsal view.
Figure 1 from: Wang Z-T, Li C-D (2021) Three new species, and new distributional data, of Haltichella (Hymenoptera, Chalcididae) from China. ZooKeys 1060: 1-16. https://doi.org/10.3897/zookeys.1060.70427
Figure 1 Haltichella bimaculata sp. nov. (holotype female) A habitus, lateral view B head, front view C antenna D head and part of mesosoma, dorsal view E forewing F propodeum G metasoma H head and mesosoma, dorsal view I hind leg.
Figure 5 from: Wang Z-T, Li C-D (2021) Three new species, and new distributional data, of Haltichella (Hymenoptera, Chalcididae) from China. ZooKeys 1060: 1-16. https://doi.org/10.3897/zookeys.1060.70427
Figure 5 Haltichella clavicornis, (female) A hind leg B metasoma C propodeum D head and mesosoma, dorsal view.
Figure 2 from: Wang Z-T, Li C-D (2021) Three new species, and new distributional data, of Haltichella (Hymenoptera, Chalcididae) from China. ZooKeys 1060: 1-16. https://doi.org/10.3897/zookeys.1060.70427
Figure 2 Haltichella bomiana sp. nov. (holotype male) A habitus, lateral view B head, front view C antenna D head and part of mesosoma, dorsal view E forewing F propodeum G hind leg H metasoma I mesosoma, dorsal view.
Figure 3 from: Wang Z-T, Li C-D (2021) Three new species, and new distributional data, of Haltichella (Hymenoptera, Chalcididae) from China. ZooKeys 1060: 1-16. https://doi.org/10.3897/zookeys.1060.70427
Figure 3 Haltichella strigata sp. nov. (holotype male) A habitus, lateral view B head, front view C antenna D head, dorsal view E forewing F propodeum G hind leg H metasoma I mesosoma, dorsal view.
Figure 1 in A review of the biology of Neochalcis Kirby (Hymenoptera, Chalcididae) with a new host and biological data for N. breviceps (Masi)
Figure 1. (a–e) Drynaria quercifolia (L.) J. Sm.
Figure 1 in New data on the crabronid fauna of Saudi Arabia (Hymenoptera: Apoidea (Spheciformes): Crabronidae) from Jazan Province, with the description of three new species and the hitherto unknown male of Miscophus chrysis Kohl, 1894
Figure 1. Map of the Saudi Arabia, showing the locality of Jazan.
Data from: Re-examination of species limits in Aspergillus section Flavipedes using advanced species delimitation methods and description of four new species
<p><span>Since the last revision in 2015, the taxonomy of section <i>Flavipedes</i> evolved rapidly along with the availability of new species delimitation techniques. This study aims to re-evaluate the species boundaries of section <i>Flavipedes </i>members using modern delimitation methods applied to an extended set of strains (n=90) collected from various environments. The analysis used DNA sequences of three house-keeping genes (<i>benA</i>, <i>CaM</i>, <i>RPB2</i>) and consisted of two steps: application of several single-locus (GMYC, bGMYC, PTP, bPTP) and multi-locus (STACEY) species delimitation methods to sort the isolates into putative species, which were subsequently validated using DELINEATE software that was applied for the first time in fungal taxonomy. As a result, four new species are introduced, i.e. <i>A. alboluteus</i>, <i>A. alboviridis</i>, <i>A. inusitatus</i> and <i>A. lanuginosus</i>, and <i>A. capensis</i> is synonymized with <i>A. iizukae</i>. Phenotypic analyses were performed for the new species and their relatives and the results showed that the growth parameters at different temperatures and colonies characteristics were useful for differentiation of these taxa. The revised section harbors 18 species, most of them are known from soil. However, common species from the section are ecologically diverse, occurring in indoor environment (6 species), clinical samples (5 species), food and feed (4 species), droppings (4 species) and other less common substrates/environments. Due to the occurrence of section <i>Flavipedes</i> species in the clinical material/hospital environment, we also evaluated the susceptibility of 66 strains to six antifungals (Amphotericin B, Itraconazole, Posaconazole, Voriconazole, Isavuconazole, Terbinafine) using the reference EUCAST method. These results showed some potentially clinically relevant differences in susceptibility between species. For example, MICs higher than those observed for wild-type <i>A. fumigatus</i> were found for both triazoles and amphotericin B for <i>A. ardalensis, A. iizukae, </i>and<i> A. spelaeus</i> whereas <i>A. lanuginosus, A. luppiae, A. movilensis, A. neoflavipes, </i>and<i> A. olivimuriae</i> were comparable to or more susceptible as <i>A. fumigatus</i>. Finally, terbinafine was <i>in vitro</i> active against all species except <i>A. alboviridis</i>.</span></p>
Figure 6 from: Hofman S, Grego J, Fehér Z, Erőss ZP, Rysiewska A, Osikowski A, Falniowski A (2021) New data on the valvatiform-shelled Hydrobiidae (Caenogastropoda, Truncatelloidea) from southern Greece. ZooKeys 1062: 31-47. https://doi.org/10.3897/zookeys.1062.64746
Figure 6 A shell of lectotype of Valvata hellenica presented by Reischütz and Sattmann (1993)B shell measurements: a – shell height, b – body whorl breadth, c – aperture height, d – spire height, e – aperture breadth, α – apex angle.
Figure 3 from: Hofman S, Grego J, Fehér Z, Erőss ZP, Rysiewska A, Osikowski A, Falniowski A (2021) New data on the valvatiform-shelled Hydrobiidae (Caenogastropoda, Truncatelloidea) from southern Greece. ZooKeys 1062: 31-47. https://doi.org/10.3897/zookeys.1062.64746
Figure 3 Shells of gastropods: D. longipeniaA–D locality 2 (holotype, 2A32, 2B26, 2B27) E locality 1 (2A29); Daphniola hadeiF locality 3 (2A27) G locality 4 (2B19) H locality 5 (2B20) ID. louisi, locality 6 (2A33) J–KGraecoarganiella parnassiana, locality 7 (2A28, 2B23) L–OIsimeropeL locality 8 (2A30) M locality 9 (2A31) N locality 10 (2B21) O locality 11 (2A22) P cf. Islamia sp., locality 12 (2A34). Scale bar: 1 mm.
Figure 2 from: Hofman S, Grego J, Fehér Z, Erőss ZP, Rysiewska A, Osikowski A, Falniowski A (2021) New data on the valvatiform-shelled Hydrobiidae (Caenogastropoda, Truncatelloidea) from southern Greece. ZooKeys 1062: 31-47. https://doi.org/10.3897/zookeys.1062.64746
Figure 2 Type locality of Daphniola longipenia sp. nov. Panagitsa, Arcadia, Peloponnese A spring reservoir B spring head.
Figure 4 from: Hofman S, Grego J, Fehér Z, Erőss ZP, Rysiewska A, Osikowski A, Falniowski A (2021) New data on the valvatiform-shelled Hydrobiidae (Caenogastropoda, Truncatelloidea) from southern Greece. ZooKeys 1062: 31-47. https://doi.org/10.3897/zookeys.1062.64746
Figure 4 Pallial and renal section of female reproductive organs of Daphniola longipenia [bc – bursa copulatrix, cbc – duct of bursa, ga – albuminoid gland, gn – nidamental gland, gp – gonoporus, ov – oviduct, ovl – loop of (renal) oviduct, rs – seminal receptacles (in black) rs1 and rs2 (as defined by Radoman 1973, 1983): rs1 – distal, rs2 – proximal]. Scale bar: 250 μm.
Figure 8 from: Hofman S, Grego J, Fehér Z, Erőss ZP, Rysiewska A, Osikowski A, Falniowski A (2021) New data on the valvatiform-shelled Hydrobiidae (Caenogastropoda, Truncatelloidea) from southern Greece. ZooKeys 1062: 31-47. https://doi.org/10.3897/zookeys.1062.64746
Figure 8 Phylogenetic tree inferred from connected COI and H3 sequences. Bootstrap supports (>60%) and Bayesian probabilities are given.
Figure 7 from: Hofman S, Grego J, Fehér Z, Erőss ZP, Rysiewska A, Osikowski A, Falniowski A (2021) New data on the valvatiform-shelled Hydrobiidae (Caenogastropoda, Truncatelloidea) from southern Greece. ZooKeys 1062: 31-47. https://doi.org/10.3897/zookeys.1062.64746
Figure 7 Phylogenetic tree for COI showing relationships between the studied snails. Bootstrap supports (>60%) and Bayesian probabilities are given.
Supporting data from: The distribution of leaf form among indigenous woody angiosperms in New Zealand
<p>New Zealand's woody indigenous eudicot flora comprises a variety of leaf shapes and features and occupies environments extending from subtropical to cold temperate climates. We used a dataset of over 300,000 occurrences of 557 indigenous woody eudicot species to investigate patterns and trends in the occurrence of six leaf features (leaf pubescence, leaf margin teeth, leaf size, leaf apex and base shape, and leaf length to width ratio) along critical climate gradients. Major climate variables examined included temperature, precipitation, moisture deficit and solar radiation. Our results reveal strong latitudinal gradients in toothed leaves and leaf area with both declining at higher latitudes. Leaf base and leaf apex angle are also aligned latitudinally, both declining in northern areas. In contrast, the occurrence of pubescent leaves and leaf length to width ratio are independent of other leaf features and latitudinal gradients. Larger leaves are positively associated with warmer climates while serrated margins are more common in warmer and wetter zones. The occurrence of pubescent leaves is greatest in seasonally dry environments with low annual precipitation. Long thin leaves (high length to width ratio) were more common in areas with a high rainfall to potential evapotranspiration ratio. Leaf apex angle is negatively correlated with temperature while leaf base angle distribution in relation to climate was highly variable. Overall, results confirm global patterns for leaf size and climate, highlighting the importance of small leaves limiting heat loss in cool climates. The positive correlation between leaf teeth and warmer climates has not been found elsewhere. High occurrence of pubescent leaves in low rainfall and highly moisture deficient environments in New Zealand suggests that the trait is associated with water retention in dry climates.</p>
Figures 1-6 from: Gess F (2012) A new species of Masarina Richards 1962 from southern Africa, description of the female of M. ceres Gess 1997 and supplementary data on three other species of the genus (Hymenoptera, Vespidae, Masarinae). Journal of Hymenoptera Research 25: 83-92. https://doi.org/10.3897/jhr.25.2442
Figures 1-6 - Masarina gabymariae 1 ♀, lateral view (actual length 6.7 mm) 2 ♂, lateral view (actual length 6.0 mm) 3 ♀, dorsal view 4 ♂, dorsal view 5 ♀, head, front view (actual width 2.1 mm), tongue not extended 6 ♂, head, front view (actual width 1.9 mm), tongue extended.
Figure 6 from: Nelson W, Dalen J, Neill K (2013) Insights from natural history collections: analysing the New Zealand macroalgal flora using herbarium data. PhytoKeys 30: 1-21. https://doi.org/10.3897/phytokeys.30.5889
Figure 6 - Number of taxa unique to each region by division (BAAC = Bounty, Antipodes, Auckland, Campbell Islands).
Figure 4 from: Nelson W, Dalen J, Neill K (2013) Insights from natural history collections: analysing the New Zealand macroalgal flora using herbarium data. PhytoKeys 30: 1-21. https://doi.org/10.3897/phytokeys.30.5889
Figure 4 - Number of taxa in the collections by decade of collection and division (green, brown, and red algae).
Figure 1 from: Nelson W, Dalen J, Neill K (2013) Insights from natural history collections: analysing the New Zealand macroalgal flora using herbarium data. PhytoKeys 30: 1-21. https://doi.org/10.3897/phytokeys.30.5889
Figure 1 - Map of New Zealand indicating the boundaries of the regions investigated in this study (1 Kermadec Is 2 Three Kings Is 3 North I. (NI) North 4 NI Bay of Plenty (BOP) 5 NI East 6 NI West 7 Wairarapa-Cook 8 South I. (SI) Northwest (NW) 9 SI Kaikoura 10 Chatham Is 11 SI Southeast (SE) 12 SI Westland 13 SI Fiordland 14 SI Southern 15 Stewart I. 16 Snares Is 17 Bounty Is 18 Antipodes Is 19 Auckland Is 20 Campbell I).
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.