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FIGURE 3 in Description of Hypocambala zizhongi sp. nov. and the new combination, Glyphiulus polytrichus (Golovatch et al., 2011) comb. nov., based on morphological and molecular data (Spirostreptida: Cambalidea: Cambalopsidae)
FIGURE 3. Phylogenetic tree based on the concatenated dataset (COI + 16S + 18S + 28S). Numbers at nodes are Bayesian posterior probabilities (left) and maximum likelihood percent bootstrap values (right).
FIGURE 10 in New data on the subfamily Opiinae (Hymenoptera: Braconidae) from Iran
FIGURE 10. Phaedrotoma pseudonitidus (Fahringer, 1943): A. Habitus, lateral view; B. Head, dorsal view; C. Head, frontal view; D. Mesosoma, dorsal view; E. Mesosoma, lateral view; F. Fore wing; G. Propodeum, dorsal view; H. Metasoma, dorsal view; I. Hind leg, lateral view; J. Ovipositor sheath.
FIGURE 9 in New data on the subfamily Opiinae (Hymenoptera: Braconidae) from Iran
FIGURE 9. Opius (Opiothorax) phytobiae Fischer, 1959: A. Habitus, lateral view; B. Head, lateral view; C. Mesosoma, lateral view; F. Metasoma, lateral view; D. Fore wing.
FIGURE 6 in New data on the subfamily Opiinae (Hymenoptera: Braconidae) from Iran
FIGURE 6. Opius (Misophthora) mischa Fischer, 1968: A. Habitus, lateral view; B. Head, frontal view; C. Head, dorsal view; D. Mesosoma, dorsal view; E. Mesosoma, lateral view; F. Fore wing; G. Hind leg, lateral view; H. Propodeum, dorsal view; I. Metasoma, dorsal view.
FIGURE 5 in New data on the subfamily Opiinae (Hymenoptera: Braconidae) from Iran
FIGURE 5. Desmiostoma parvulum (Wesmael, 1835): A. Habitus, dorsal view; B. Head, lateral view; C. Head, dorsal view; D. Mesosoma, dorsal view; E. Mesosoma, lateral view; F. Fore wing; G. First metasomal tergite, dorsal view.
FIGURE 4 in New data on the subfamily Opiinae (Hymenoptera: Braconidae) from Iran
FIGURE 4. Bitomus (Bitomus) multipilis Fischer, 1990: A. Habitus, lateral view; B. Head, frontal view; C. Head, lateral view; D. Mesosoma, lateral view; E. Mesosoma, dorsal view; F. Fore wing; G. Hind leg, lateral view.
FIGURE 3 in New data on the subfamily Opiinae (Hymenoptera: Braconidae) from Iran
FIGURE 3. Biosteres (Chilotrichia) advectus Papp, 1979: A. Habitus, lateral view; B. Head, dorsal view; C. Head, frontal view; D. Head, lateral view; E. Mesosoma, dorsal view; F. Mesosoma, lateral view; G. Fore wing; H. Hind leg, lateral view.
FIGURE 8 in New data on the subfamily Opiinae (Hymenoptera: Braconidae) from Iran
FIGURE 8. Opius (Opiothorax) attributus Fischer, 1962: A. Habitus, ateral view, B. Head, frontal view; C. Mesosoma, dorsal view; D. Mesosoma, lateral view; E. Propodeum, dorsal view; F. Fore wing; G. Hind leg, lateral view; H. Metasoma, dorsal view.
FIGURE 1 in New data on the subfamily Opiinae (Hymenoptera: Braconidae) from Iran
FIGURE 1. Apodesmia posticatae (Fischer, 1957): A. Habitus, lateral view; B. Head, dorsal view; C. Head, frontal view; D. Mesosoma, dorsal view; E. Mesosoma, lateral view; F. Fore wing; G. Hind leg, H. Propodeum, dorsal view; I. First metasomal tergite, dorsal view; J. Metasoma, dorsal view.
FIGURE 2 in New data on the subfamily Opiinae (Hymenoptera: Braconidae) from Iran
FIGURE 2. Apodesmia striatula (Fischer, 1957): A. Habitus, lateral view, B. Head, frontal view; C. Mesosoma, dorsal view; D. Mesosoma, lateral view; E. Fore wing; F. Hind leg, lateral view; G. First metasomal tergite, dorsal view; H. Metasoma, dorsal view.
FIGURE 11 in New data on the subfamily Opiinae (Hymenoptera: Braconidae) from Iran
FIGURE 11. Utetes curtipectus (Fischer, 1958): A. Habitus, lateral view; B. Head, frontal view; C. Head, dorsal view; D. mesosoma, dorsal view; E. Mesosoma, lateral view; F. Fore wing; G. Propodeum, dorsal view; H. Ovipositor sheath.
FIGURE 7 in New data on the subfamily Opiinae (Hymenoptera: Braconidae) from Iran
FIGURE 7. Opius (Misophthora) rufimixtus Fischer, 1958: A. Habitus, lateral view; B. Head, lateral view; C. Mesosoma, dorsal view; D. Mesosoma, lateral view; E. Propodeum, dorsal view; F. Fore wing; G. Hind leg, lateral view; H. Metasoma, dorsal view.
FIGURE 3 in New taxonomic and phylogeographic data on three nominal species of the genus Septaria Férussac, 1807 (Gastropoda: Cycloneritida: Neritidae)
FIGURE 3: Cloud of points representing the L/W and L/H ratios of Septaria borbonica, S. porcellana and S. tahitiana.
FIGURE 6 in New taxonomic and phylogeographic data on three nominal species of the genus Septaria Férussac, 1807 (Gastropoda: Cycloneritida: Neritidae)
FIGURE 6. Haplotype network of the nominal species Septaria borbonica and S. porcellana according to the median-joining method. The circles are proportional to the frequency of occurrence, the number of mutations is indicated on the branches by dashes.
FIGURE 5 in New taxonomic and phylogeographic data on three nominal species of the genus Septaria Férussac, 1807 (Gastropoda: Cycloneritida: Neritidae)
FIGURE 5. Bayesian analysis of the gene of the sub-unit 1 of the Cytochrome oxydase (COI). FP French Polynesia, JP Japan, KM Comoros, MU Mauritius, RI Reunion Island.
FIGURE 1. A in New taxonomic and phylogeographic data on three nominal species of the genus Septaria Férussac, 1807 (Gastropoda: Cycloneritida: Neritidae)
FIGURE 1. A Septaria porcellana (Linnaeus, 1758), MNHN-IM-2013-62871 (Okinawa, Japan) B Septaria borbonica (Bory de Saint-Vincent, 1804), MNHN-IM-2013-78206 (Mohéli, Comoros) C Septaria tahitiana Eichhorst, 2016, MNHN-IM-2013- 62864 (Moorea, French Polynesia). From left to right: Ventral view, dorsal view, dorsal view without periostracum, side view. Scale bars: 10 mm.
FIGURE 4. A, B in New taxonomic and phylogeographic data on three nominal species of the genus Septaria Férussac, 1807 (Gastropoda: Cycloneritida: Neritidae)
FIGURE 4. A, B. Samples supposed to belong to Septaria borbonica but for which the identification is doubtful. A MNHN- IM-2013-78211 (Mayotte, Comoros) B MNHN-IM-2013-78212 (Mayotte, Comoros), dorsal view without periostracum. Scale bar: 10 mm.
FIGURE 7. A, B in New taxonomic and phylogeographic data on three nominal species of the genus Septaria Férussac, 1807 (Gastropoda: Cycloneritida: Neritidae)
FIGURE 7. A, B. Two other different external patterns of the shell, found in Septaria porcellana. A. MNHN-IM-2013-62872 (Okinawa, Japan) B. MNHN-IM-2013-62867 (Okinawa, Japan). C–H. Samples of S. borbonica from different islands in the Indian Ocean have a common external pattern. C. MNHN-IM-2016-7863 (Reunion Island) D. MNHN-IM-2016-7857 (Mauritius) E. MNHN-IM-2016-7874 (Seychelles) F. MNHN-IM-2016-7880 (Mayotte, Comoros) G. MNHN-IM-2016-7887 (Anjouan, Comoros) H. MNHN-IM-2016-7892 (Grande-Comore, Comoros). Dorsal view without periostracum, below. Scale bars: 10 mm.
FIGURE 4. Combined haplotype networks from CytB data for Laminatubus paulbrooksi n in Laminatubus (Serpulidae, Annelida) from eastern Pacific hydrothermal vents and methane seeps, with description of two new species
FIGURE 4. Combined haplotype networks from CytB data for Laminatubus paulbrooksi n. sp. (top) from Pacific Costa Rica margin and Gulf of California (Mexico) localities and L. joycebrooksae n. sp. (bottom) from Costa Rica. There was little variability among the L. joycebrooksae n. sp. sequences and a distinct break to L. paulbrooksi n. sp. This corresponds to a minimum 6.4% uncorrected distance. Laminatubus paulbrooksi n. sp. showed marked intraspecific variability with distinct breaks among the three main sites; Costa Rica (9°N), Pescadero (23°N) and Guaymas Basin (27°N). * indicates the holotypes for L. paulbrooksi n. sp. and L. joycebrooksae n. sp. respectively.
Data from: Abundance data applied to a novel model invertebrate host sheds new light on parasite community assembly in nature
<ol> <li>Understanding how environmental drivers influence the assembly of parasite communities, in addition to how parasites may interact at an infracommunity level, are fundamental requirements for the study of parasite ecology. Knowledge of how parasite communities are assembled will help to predict the risk of parasitism for hosts, and model how parasite communities may change under variable conditions. However, studies frequently rely on presence-absence data and examine multiple host species or sites, metrics which may be too coarse to characterise nuanced within-host patterns.</li> <li>We utilised a novel host system, the freshwater mussel <i>Anodonta anatina</i>, to investigate the drivers of community structure and explore parasite interactions. In addition, we aimed to highlight consistencies and inconsistencies between presence-absence and abundance data.</li> <li>Our analysis incorporated 14 parasite taxa and 720 replicate infracommunities. Using redundancy analysis, a joint species distribution model and a Markov random fields approach, we modelled the impact of both host-level and environment-level characteristics on parasite structure, as well as parasite-parasite correlations after accounting for all other factors. This approach was repeated for both the presence and abundance of all parasites.</li> <li>We demonstrated that the regional species pool, individual host characteristics (mussel length and gravidity) and predicted parasite-parasite interactions are all important but to varying degrees across parasite species, suggesting that applying generalities to parasite community construction is too simplistic. Further, we showed that presence-absence data fails to capture important density-dependent effects of parasite load for parasites with high abundance, and in general performs poorly for high-intensity parasites.</li> <li>Host and parasite traits, as well as broader environmental factors, all contribute to parasite community structure, emphasising that an integrated approach is required to study community assembly. However, care must be taken with the data used to infer patterns, as presence-absence data may lead to incorrect ecological inference.</li> </ol>
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.