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FIGURES FG1–FG5. Female genitalia, ventral aspect. Scale bar = 500µm. Genitalia slide numbers in parentheses. FG1a, Scardia amurensis (JFL1702, inset = 8th abdominal tergum); FG1b, Scardia anatomella (MIC6097, inset = 8th abdominal tergum); FG2, Triaxomera parasitella (MIC6619); FG3, Nemapogon cloacella (MIC6618); FG4, Elatobia montelliella (MIC6792); FG5, Tinea svenssoni (USNM130227). in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES FG1–FG5. Female genitalia, ventral aspect. Scale bar = 500µm. Genitalia slide numbers in parentheses. FG1a, Scardia amurensis (JFL1702, inset = 8th abdominal tergum); FG1b, Scardia anatomella (MIC6097, inset = 8th abdominal tergum); FG2, Triaxomera parasitella (MIC6619); FG3, Nemapogon cloacella (MIC6618); FG4, Elatobia montelliella (MIC6792); FG5, Tinea svenssoni (USNM130227).
FIGURES MG24–MG27. Male genitalia. Genitalia slide numbers in parentheses. MG24, Scythris sinensis (MIC6783); MG25, Altenia perspersella (MIC5351); MG26, Gnorimoschema jalavai (MIC5930); MG27, Scrobipalpa acuminatella (MIC5204). in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES MG24–MG27. Male genitalia. Genitalia slide numbers in parentheses. MG24, Scythris sinensis (MIC6783); MG25, Altenia perspersella (MIC5351); MG26, Gnorimoschema jalavai (MIC5930); MG27, Scrobipalpa acuminatella (MIC5204).
FIGURES MG20–MG23. Male genitalia. Scale bar = 200µm. Genitalia slide numbers in parentheses. MG20, Coleophora glitzella (MIC6610); MG21, Coleophora granulatella (MIC5225); MG22, Coleophora texanella (MIC3582); MG23, Coleophora vitisella (MIC6155). in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES MG20–MG23. Male genitalia. Scale bar = 200µm. Genitalia slide numbers in parentheses. MG20, Coleophora glitzella (MIC6610); MG21, Coleophora granulatella (MIC5225); MG22, Coleophora texanella (MIC3582); MG23, Coleophora vitisella (MIC6155).
FIGURES MG11–MG15. Male genitalia. Scale bar = 200µm. Genitalia slide numbers in parentheses. MG11, Plutella hyperboreella (MIC6191); MG12, Lyonetia pulverulentella (MIC6630); MG13a, Oegoconia deauratella (MIC6771); MG13b, Oegoconia novimundi (MIC5423); MG14, Blastobasis glandulella (MIC6603); MG15, Blastobasis maroccanella (DAdamski6067). in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES MG11–MG15. Male genitalia. Scale bar = 200µm. Genitalia slide numbers in parentheses. MG11, Plutella hyperboreella (MIC6191); MG12, Lyonetia pulverulentella (MIC6630); MG13a, Oegoconia deauratella (MIC6771); MG13b, Oegoconia novimundi (MIC5423); MG14, Blastobasis glandulella (MIC6603); MG15, Blastobasis maroccanella (DAdamski6067).
FIGURES MG6–MG10. Male genitalia. Scale bar = 200µm. Genitalia slide numbers in parentheses. MG6, Caloptilia suberinella (Jackh5988); MG7, Parornix betulae (MIC6205); MG8, Phyllonorycter maestingella (G. Deschka GenPrep1328); MG9, Paraswammerdamia albicapitella (MIC6790); MG10, Paraswammerdamia conspersella (MIC4141, genitalia; MIC6187, abdomen). in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES MG6–MG10. Male genitalia. Scale bar = 200µm. Genitalia slide numbers in parentheses. MG6, Caloptilia suberinella (Jackh5988); MG7, Parornix betulae (MIC6205); MG8, Phyllonorycter maestingella (G. Deschka GenPrep1328); MG9, Paraswammerdamia albicapitella (MIC6790); MG10, Paraswammerdamia conspersella (MIC4141, genitalia; MIC6187, abdomen).
FIGURES MG16–MG19. Male genitalia. Scale bar = 200µm. Genitalia slide numbers in parentheses. MG16, Blastobasis tarda (MIC5831); MG17, Agonopterix conterminella (MIC5361); MG18, Depressaria depressana (MIC6212); MG19, Coleophora atriplicis (MIC6208). in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES MG16–MG19. Male genitalia. Scale bar = 200µm. Genitalia slide numbers in parentheses. MG16, Blastobasis tarda (MIC5831); MG17, Agonopterix conterminella (MIC5361); MG18, Depressaria depressana (MIC6212); MG19, Coleophora atriplicis (MIC6208).
FIGURES NJ7–NJ12. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ7, Parornix betulae; NJ8, Phyllonorycter maestingella; NJ9, Paraswammerdamia albicapitella; NJ10, Paraswammerdamia conspersella; NJ11, Plutella hyperboreella; NJ12, Lyonetia pulverulentella. in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES NJ7–NJ12. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ7, Parornix betulae; NJ8, Phyllonorycter maestingella; NJ9, Paraswammerdamia albicapitella; NJ10, Paraswammerdamia conspersella; NJ11, Plutella hyperboreella; NJ12, Lyonetia pulverulentella.
FIGURES NJ1–NJ6. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ1, Scardia amurensis; NJ2, Triaxomera parasitella; NJ3, Nemapogon cloacella; NJ4, Elabotia montelliella; NJ5, Tinea svenssoni; NJ6, Caloptilia suberinella. in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES NJ1–NJ6. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ1, Scardia amurensis; NJ2, Triaxomera parasitella; NJ3, Nemapogon cloacella; NJ4, Elabotia montelliella; NJ5, Tinea svenssoni; NJ6, Caloptilia suberinella.
FIGURE 1 in Timoides agassizii Bigelow, 1904, little-known hydromedusa (Cnidaria), appears briefly in large numbers off Oman, March 2011, with additional notes about species of the genus Timoides
FIGURE 1. The eight monthly sampling stations along the coast of Oman and the location of the occurrence of Timoides agassizii at Sohar (24.38°N latitude, 56.74°E longitude).
FIGURES 5–8. Kiwigaster variabilis. Figure 5 in Kiwigaster gen. nov. (Hymenoptera: Braconidae) from New Zealand: the first Microgastrinae with sexual dimorphism in number of antennal segments
FIGURES 5–8. Kiwigaster variabilis. Figure 5: Partial mesosoma and base of hind wing, dorso-lateral, Arrow shows vannal lobe. Figure 6: Fore wing, dorsal. Figure 7: Partial metatibia and two first segments of metatarsus, dorso-lateral. Arrow shows metatibial inner spur. Figure 8: Meso and metasoma, dorsal. Arrows show metacoxa and metatibial spur.
Sperm competition risk affects ejaculate strategy in terms of sperm number but not sperm size in squid
<p><span><span><span><span><span><span><span><span><span><span><span>In polygamous species, the mode of sperm storage in females influences evolution of sperm quantitative and qualitative traits because it provides the arena for sperm competition, cryptic female choice and fertilization processes. In this study, we compared ejaculate traits of two squid species, <i>Heterololigo bleekeri </i>and <i>Loligo reynaudii</i>. Both species show dimorphic sperm traits associated with alternative reproductive tactics where consort and sneaker males transfer sperm to different storage sites within a female (on the oviduct and near the mouth, respectively). Due to differences in reproductive behaviours and sperm placement, sperm competition risk is expected to be higher in sneakers than in consorts of both species, and higher overall in <i>L. reynaudii</i>. Our results demonstrate that the instantaneous number of released sperm is adjusted to the expected sperm competition risk via an elaborate sperm package. Consort sperm are similar in size, however, sneaker sperm have a significantly longer flagellum in <i>H. bleekeri </i>than in <i>L. reynaudii</i>, most likely due to intra-tactic conflicts associated with sperm storage conditions. From consideration of the different mating tactics, we suggest that while levels of sperm competition determine quantitative traits, sperm quality traits are determined more by the mode of sperm storage and fertilization.</span></span></span></span></span></span></span></span></span></span></span></p>
Figure 1 in Evaluating evolutionary pressures and phylogenetic signal in earthworms: a case study - the number of typhlosole lamellae in Hormogastridae (Annelida, Oligochaeta)
Figure 1. An example of the variability in body size and number of lamellae in Hormogastridae: (A) Hormogaster castillana Qiu & Bouche, 1998 (21 lamellae); (B) Hormogaster pretiosa Michaelsen, 1889 from Segariu (13 lamellae); (C) Hormogaster joseantonioi Marchan et al., 2014 (nine lamellae); (D) Hormogaster redii Rosa, 1887 (seven lamellae); (E) Hormogaster elisae Alvarez, 1977 (five lamellae); (F) Ailoscolex lacteospumosus Bouche, 1969 (three lamellae). To the right the diagrams show how the typhlosole is located in the digestive tract, with different degrees of convolution shown.
Figure 2 in Evaluating evolutionary pressures and phylogenetic signal in earthworms: a case study - the number of typhlosole lamellae in Hormogastridae (Annelida, Oligochaeta)
Figure 2. Ultrametric tree used as the phylogenetic input for the phylogenetic generalized least squares (PGLS) analysis. Number of typhlosole lamellae and average weight are shown as red and green bars for taxa with available information. The colour code for the branches show the main Hormogastridae clades (for details, see Appendix S4).
FIGURE. Cumulative number of ferns and lycophytes, including varieties and hybrids, that were added to the Honduran flora since 1975 (A). Cumulative number of authors contributing to the addition of new records to the flora since 1975 (B). in Ferns and Lycophytes of Honduras: A new annotated checklist
FIGURE. Cumulative number of ferns and lycophytes, including varieties and hybrids, that were added to the Honduran flora since 1975 (A). Cumulative number of authors contributing to the addition of new records to the flora since 1975 (B).
FIGURE. Map of Mexico, indicating the number of families, genera, and species of Mexican Vascular Epiphytes by state. in Mexican Vascular Epiphytes: Richness and Distribution
FIGURE. Map of Mexico, indicating the number of families, genera, and species of Mexican Vascular Epiphytes by state.
Text-fig. 10. Upper cheek teeth of Sayimys giganteus from Keseköy and Yapıntı (= YAP numbers) shown as right specimens. Left side specimens are shown in mirror image, these have underlined specimen numbers. in An Exceptional Large Sample Of The Early Miocene Ctenodactyline Rodent Sayimys Giganteus, Specific Variation And Taxonomic Implications
Text-fig. 10. Upper cheek teeth of Sayimys giganteus from Keseköy and Yapıntı (= YAP numbers) shown as right specimens. Left side specimens are shown in mirror image, these have underlined specimen numbers.
Text-fig. 9. Lower molars and premolars of Sayimys giganteus from Keseköy and Yapıntı (= YAP numbers) shown as right specimens. Left side specimens are shown in mirror image, these have underlined specimen numbers. in An Exceptional Large Sample Of The Early Miocene Ctenodactyline Rodent Sayimys Giganteus, Specific Variation And Taxonomic Implications
Text-fig. 9. Lower molars and premolars of Sayimys giganteus from Keseköy and Yapıntı (= YAP numbers) shown as right specimens. Left side specimens are shown in mirror image, these have underlined specimen numbers.
Raw data for: Modes of grain number determination differentiate barely row-types
<p>Gaining knowledge on intrinsic interactions of various yield components is crucial to improve the yield potential in small grain cereals. It is well known in barley that increasing the grain number (GN) preponderantly improves their yield potential; however, the yield components determining GN and their association in barley row-types are less explored. In this study, we assessed different yield components like potential spikelet number (PSN), spikelet survival (SSL), spikelet number (SN), grain set (GS), and grain survival (GSL), as well as their interactions with GN by using a selected panel of two- and six-rowed barley types. Also, to analyze the stability of these interactions, we performed the study in two growth conditions, greenhouse and field. From this study, we found that in two-rowed, GN determination is strongly influenced by PSN rather than SSL and/or GS in both growth conditions. Conversely, in six-rowed, GN is associated with SSL instead of PSN and/or GS. Thus, our study exemplified that increasing GN might be possible by augmenting PSN in two-rowed genotypes, while for six-rowed genotypes, the ability of SSL needs to be improved. We speculate that this disparity of GN determination in barley row-types might be due to the fertility of lateral spikelets. Collectively, this study revealed that GN of two-rowed largely depends on the developmental trait, PSN, while in six-rowed, it mainly follows the ability of SSL.</p>
A framework for the quantification of soundscape diversity using Hill numbers
<p>This is the data underlying the case study and supplementary material described in Luypaert et al. (2021): A framework for the quantification of soundscape diversity using Hill numbers. </p>
FIGURE. Bayesian tree of New Zealand spider orchids (Corybas) based on DNA sequence data from ITS, trnL-trnF and psbJ-petA. Major clades are indicated by open bars and capital letters, members of the C. trilobus aggregate are shaded, and posterior probabilities/ bootstrap percentages (≥50) indicated by numbers near each node. NI: North Island, SI: South Island, MCQI: Macquarie Island, CHI: Chatham Island in Five new species of Corybas (Diurideae, Orchidaceae) endemic to New Zealand and phylogeny of the Nematoceras clade
FIGURE. Bayesian tree of New Zealand spider orchids (Corybas) based on DNA sequence data from ITS, trnL-trnF and psbJ-petA. Major clades are indicated by open bars and capital letters, members of the C. trilobus aggregate are shaded, and posterior probabilities/ bootstrap percentages (≥50) indicated by numbers near each node. NI: North Island, SI: South Island, MCQI: Macquarie Island, CHI: Chatham Island
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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)
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.