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Figure 7 in Replacement name for the homonym of subgenus Trimorus (Neotrimorus) (Hymenoptera: Platygastroidea: Scelionidae) with description of two new species from India
Figure 7. Trimorus (Lochana) scutellospinosus (Rajmohana and Narendran 1997), male. (a) Habitus; (b) head and pleuron; (c) antennae; (d) frons; (e) metasoma.
FIGURE 1 in Referral of Thyone neofusus Deichmann, 1941, Thyone adinopoda (Pawson & Miller, 1981 and Havelockia obunca (Lampert, 1885) to the genus Sclerothyone Thandar, 1990, and a replacement name for the preoccupied genus Neothyone Deichmann, 1941 (Echinodermata: Holothuroidea: Dendrochirotida)
FIGURE 1. Sclerothyone neofusus comb. nov. (Deichmann, 1941), paratype (MCZ, AHF no. 30). A. calcareous ring of paratype (mid-dorsal view); B. tables of body wall; C. corroded rods of tube feet; D. rods of tentacles; E. rosettes of tentacles. (A—scale 1; B–E scale 2). Sclerothyone obunca comb. nov. (Lampert, 1885), F. calcareous ring, mid-dorsal view; G. tables of body wall; H. tables of tentacles; I. tables of introvert [(all copied from Östergren (1938), perhaps from holotype)]. (r = radial plate; ir = interradial plate); A. Scale 1; B–E Scale 2; F. Scale 3; G. Scale 6; H. Scale 4; I. Scale 5).
Supplementary Videos - Mild paravalvular leak may pose an increased thrombogenic risk in transcatheter aortic valve replacement (TAVR) patients - Insights from patient specific in vitro and in silico studies
<p>Supplementary Videos for manuscript in Bioengineering Special Issue "“Mathematical Modeling of Aortic Diseases " </p> <p>Mild paravalvular leak may pose an increased thrombogenic risk in transcatheter aortic valve replacement (TAVR) patients - Insights from patient specific in vitro and in silico studies</p> <p>Brandon J. Kovarovic PhD<sup>1</sup>, Oren M. Rotman PhD<sup>1</sup>, Puja B. Parikh MD, MPH<sup>2</sup>, Marvin J. Slepian MD<sup>3,4</sup>, and Danny Bluestein PhD<sup>1,</sup> *</p> <p><sup>1</sup> Biofluids Research Group, Department of Biomedical Engineering, Stony Brook University, Stony Brook, NY, USA.</p> <p><sup>2</sup> Division of Cardiovascular Medicine, Department of Medicine, Stony Brook University, Stony Brook, NY, USA.</p> <p><sup>3</sup> Department of Medicine, Sarver Heart Center, University of Arizona, Tucson, AZ, USA</p> <p><sup>4</sup> Department of Biomedical Engineering, College of Engineering, University of Arizona, Tucson, AZ USA</p> <p><strong>*</strong> Correspondence: danny.bluestein@stonybrook.edu</p> <p><strong>*</strong> Correspondence: danny.bluestein@stonybrook.edu</p>
FIGURE 1 in Hansarsia nom. nov., a replacement name for Nematoscelis G.O. Sars, 1883 (Crustacea: Euphausiidae), a junior homonym of Nematoscelis Wollaston, 1867 (Coleoptera: Staphylinidae: Aleocharinae)
FIGURE 1. Syntype of Nematoscelis filipes Wollaston, 1867 (Coleoptera: Staphylinidae: Aleocharinae) and associated labels.
FIGURE 1 in Rhagadiolus edulis (Cichorieae, Compositae), a replacement name for Lapsana rhagadiolus L. or a name of a new taxon?
FIGURE 1. Lectotype of Rhagadiolus edulis Gaertner at TUB, with QR code TUB011867. Image by courtesy of the Herbarium TUB, reproduced with permission.
Figure 2 in A two-species distribution model for parapatric newts, with inferences on their history of spatial replacement
Figure 2. Two-species distribution model derived from Triturus cristatus and Triturus marmoratus records over France along with a suite of environmental variable (for details, see main text), extrapolated over neighbouring areas. The colours show the probability for any eligible locality to be occupied by T. cristatus (P c), from deep red for T. cristatus to deep blue for T. marmoratus. Intermediate colours, such as orange and green, represent intermediate probabilities (see the colour scale, which ranges from P c at zero to P c at unity). Areas in black have an elevation of> 1500 m a.s.l. A, model with forestation as documented. B, C, the mutual species distribution under the assumption that western Europe would be completely forested (full forest; B) and devoid of forestation (zero forest; C). The white line approximates the mutual species border as modelled in A. Note that large areas in the south-east of France are devoid of Triturus newts (cf. Fig. 1) and that Italy has another crested newt species (Triturus carnifex), but that a parapatric contact zone is being modelled nevertheless.
Figure 1. A in A two-species distribution model for parapatric newts, with inferences on their history of spatial replacement
Figure 1. A, the outer range borders of the crested newt, Triturus cristatus (c; southern border shown by continuous line) and the marbled newt, Triturus marmoratus (m; northern and eastern border shown by dashed line) in continental France, after Castanet & Guyetant (1989) and Lescure & De Massary (2012). Departments mentioned in the text are as follows: DS, Deux-Sevres; M, Mayenne; V, Vienne. The Lower Rhône T. cristatus population is indicated by LR. The base map was downloaded from MapsLand (https://www.mapsland.com), under a Creative Commons Attribution-ShareAlike 3.0 Licence. B, the area of T. cristatus–T. marmoratus range overlap in Mercator projection, with the generalized species border as inferred from a two-species distribution model (see Fig. 2). The open circles represent documented species occurrences that strongly contradict the model, for T. cristatus (probability of occurrence, Pc ≤ 0.2, in red) and T. marmoratus (Pc ≥ 0.8, in blue). Large symbols represent multiple observations at close range. The drawings of animals, with T. cristatus at the top and T. marmoratus at the bottom, are by Bas Blankevoort, Naturalis Biodiversity Center.
Figure 4 in A two-species distribution model for parapatric newts, with inferences on their history of spatial replacement
Figure 4. Model of the two-species distribution of Triturus cristatus and Triturus marmoratus for climatic conditions as foreseen for 50 years from now under the CMCC-ESM2_ SSP126 scenario. Results were simplified to a binary representation, with red for T. cristatus (probability of occurrence, Pc> 0.5) and blue for T. marmoratus (Pc <0.5). Grey areas predict the presence of one species or the other, depending on zero or full forestation (for details, see main text). The white line approximates the mutual species border as modelled for the present day (Fig. 2A). Note that the contact zone would have to move at a pace of> 10 km/ year to keep up with the projected change. Three other scenarios yielded even larger contact zone displacements (Supporting Information, Fig. S2).
Figure 3 in A two-species distribution model for parapatric newts, with inferences on their history of spatial replacement
Figure 3. Models of the two-species distribution of Triturus cristatus and Triturus marmoratus for climatic conditions as reconstructed for the Holocene, under the assumption that western Europe would be entirely forested (left panel) or entirely deforested (right panel). Colour key as in Figure 2. Results for nine different scenarios (for details, see main text) were averaged; for scenarios shown individually, see the Supporting Information (Fig. S1). The white line approximates the mutual species border as modelled for the present day in Figure 2.
FIGURE 1 in A replacement name for Salsolicola Oatley, 2004 (Aves: Muscicapidae), preoccupied by Salsolicola Kuznetsov, 1960 (Lepidoptera: Tortricidae)
FIGURE 1. The two generally accepted subspecies of Karoo Scrub-Robin: nominate coryphoeus (left) and cinerea (right). Artist: Andrew Tilsley.
FIGURES 1–3 in Replacement names for three preoccupied genus-group names of Cetoniinae (Coleoptera: Scarabaeidae)
FIGURES 1–3. Adult cetoniines, dorsal and ventral views and specimen label. 1, Ixorida (Emas) thoracica (Wallace, 1867). 2, Ruteraetia (Legrandetia) pahangensis Jákl, 2019 (holotype from Jákl 2019b). 3, Walsternoplus schaumii (White, 1856), new combination.
FIGURES 23–28 in Letrasilta, a new genus for the Striatella cernyi Volynkin species-group with description of a new species from Xizang, China, and a replacement name for the genus group name Striatella Volynkin & S.-Y. Huang, 2019 (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
FIGURES 23–28. Female genitalia of Letrasilta spp. and the type species of the genera Striatochrista nom. n., Aberrasine, Indiania, and Idopterum. Depositories of the slides: 23 in TAAHU, 24, 25 and 28 in MWM/ZSM, 26 and 27 in SCAU.
FIGURES 20–22 in Letrasilta, a new genus for the Striatella cernyi Volynkin species-group with description of a new species from Xizang, China, and a replacement name for the genus group name Striatella Volynkin & S.-Y. Huang, 2019 (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
FIGURES 20–22. Male genitalia of the type species of the genera Aberrasine, Indiania and Idopterum. Depositories of the slides: 20 in MWM/ZSM, 21 and 22 in SCAU.
FIGURES 12–15 in Letrasilta, a new genus for the Striatella cernyi Volynkin species-group with description of a new species from Xizang, China, and a replacement name for the genus group name Striatella Volynkin & S.-Y. Huang, 2019 (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
FIGURES 12–15. Adults of the type species of the genera Indiania and Idopterum. Depositories of the specimens: 12 and 13 in SCAU; 14 in CKC; 15 in MWM/ZSM.
FIGURES 16–19 in Letrasilta, a new genus for the Striatella cernyi Volynkin species-group with description of a new species from Xizang, China, and a replacement name for the genus group name Striatella Volynkin & S.-Y. Huang, 2019 (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
FIGURES 16–19. Male genitalia of Letrasilta spp. and the type species of the genus Striatochrista nom. n. Depositories of the slides: 16 in TAAHU, 17 and 19 in MWM/ZSM, 18 in OUMNH.
FIGURES 2–11 in Letrasilta, a new genus for the Striatella cernyi Volynkin species-group with description of a new species from Xizang, China, and a replacement name for the genus group name Striatella Volynkin & S.-Y. Huang, 2019 (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
FIGURES 2–11. Adults of Letrasilta spp. and the type species of the genera Striatochrista nom. n. and Aberrasine. Depositories of the specimens: 2 and 3 in TAAHU; 4, 5, 7 and 9 in MWM/ZSM; 6 in OUMNH; 8 in CKC; 10, 11 in SCAU.
FIGURE 1 in Letrasilta, a new genus for the Striatella cernyi Volynkin species-group with description of a new species from Xizang, China, and a replacement name for the genus group name Striatella Volynkin & S.-Y. Huang, 2019 (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
FIGURE 1. Molecular phylogenetic tree recovered from the Bayesian inference analysis of the combined dataset with the bestfit partitioning strategy. The clades unrelevant to the present study were all collapsed. The Letrasilta clade was marked out by yellow ground colour. The order of the values on the nodes is as follows: ultrafast bootstrap values (UFBS) in IQtree / posterior probabilities (PP) of the Bayesian analysis.
FIGURES 6–9 in Description of a new Brazilian species of Acanthoderini, new records in American Cerambycinae and Lamiinae, and a replacement name for a genus (Coleoptera, Cerambycidae)
FIGURES 6–9. Penaherreraus birai sp. nov., holotype female: 6) Dorsal habitus; 7) Ventral habitus; 8) Lateral habitus; 9) Head, frontal view.
FIGURES 1–5. 1 in Description of a new Brazilian species of Acanthoderini, new records in American Cerambycinae and Lamiinae, and a replacement name for a genus (Coleoptera, Cerambycidae)
FIGURES 1–5. 1) Susuacanga rotundipennis (Bates, 1884), female from Mexico (Jalisco), dorsal habitus. 2) Psyrassa xestioides (Bates, 1872), male from Mexico (Oaxaca), dorsal habitus. 3) Anisopodus dispar Bates, 1885, female from Nicaragua, dorsal habitus; 4) Lasiolepturges zikani Melzer, 1928, male from Brazil (Pará), dorsal habitus; 5) Urgleptes navarretei Santos-Silva, Nascimento, Botero & McClarin, 2021, male from Ecuador, dorsal habitus.
Replaced feathers, degree of bill corrugation, and bill coloration in 19 Central American hummingbird species
<p>We document molt extent; age-specific molt patterns, plumages, and percent of the bill with corrugations; the presence or absence of delayed plumage maturation and bill color changes in males of some species; and molt timing in the 19 resident hummingbird species of Belize. Molt strategies and rates of bill smoothing were similar to North American species, with all species showing limited to partial preformative molts, replacing only body feathers and some wing coverts and retaining all remiges and rectrices. Extent of bill corrugations reduced to ≤10% of bill length in all species by the time definitive cycle basic plumage is achieved. Males in sexually dichromatic species showed delayed maturation in plumage characteristics and/or bill coloration, and in two dichromatic species, some older females showed male-like plumage. Nine species representing multiple clades showed advanced timing to the second prebasic molt, indicating that this trait may be a proximal response to individuals not breeding during the first molt cycle. Species with advanced second prebasic molts replaced fewer wing coverts during the preformative molt than species with later molt timing.</p>
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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)
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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.