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Supplementary material 1 from: Praz C, Genoud D, Vaucher K, Bénon D, Monks J, Wood TJ (2022) Unexpected levels of cryptic diversity in European bees of the genus Andrena subgenus Taeniandrena (Hymenoptera, Andrenidae): implications for conservation. Journal of Hymenoptera Research 91: 375-428. https://doi.org/10.3897/jhr.91.82761
Table S1. Specimens used in genetic analyses. The unique identifiers are identical to the Sample-ID on BOLD
Scientific dataset for the manuscript "Implication of contrasting surface conditions on monsoonal heavy rainfall events over India"
<p>The observational and model simulated data for the Manuscript "Implication of contrasting surface conditions on monsoonal heavy rainfall events over India", submitted to the Journal of Applied Meteorology and Climatology are shared here. The details of the dataset provided are as follows: </p> <p>i) IMD daily gridded rainfall (mm) for each heavy rainfall case. <br> ii) WRF simulated daily average values from Noah and SLAB experiments. <br> iii) 3-hourly time series of air temperature (K) and specific humidity (kg/kg) at 2m from AWS stations and from model simulations at respective observation locations. These datasets are provided for Case 1 and Case 2 only. <br> iv) Volumetric soil moisture (m3/m3) daily climatology (2001-2013) averaged over central India from ESA CCI, GLDAS, and LDAS. <br> v) The 3-hourly time series of Volumetric soil moisture (m3/m3) average and standard deviations over central India for the period May 15-18, 2013, June 22-25, 2013, and August 15-18, 2013. The average values from GLDAS soil moisture are provided. </p>
Comparison of behavioural tendencies between 'dangerous dogs' and other domestic dog breeds – evolutionary context and practical implications
<p>Aggressive behaviour by dogs is a considerable social problem, but the ability to predict which individuals may have increased aggressive tendencies is very limited, restricting the development of efficient preventive measures. There is a common perception that certain breeds are more likely to exhibit aggressive behaviour, which has contributed to the introduction of breed-specific legislation. The rationale for such legislation explicitly assumes high heritability of this trait while also implying relatively little variation within breeds; these assumptions are largely untested. We compared behavioural tendencies between 8 breeds that are subject to legislation in at least one country and 17 breeds that are not subject to legislation using two validated psychometric tools: the Dog Impulsivity Assessment Scale (DIAS), which scores elements of impulsivity, including a tendency for aggressive behaviour, and Positive and Negative Activation Scale (PANAS), which scores sensitivity to positive and negative stimuli (which may trigger aggressive responses). We found that the two groups of breeds do not differ significantly in the specific DIAS factor relating to aggressive behaviour, "Aggression Threshold and Response to Novelty", or any other DIAS and PANAS factors. We found large variation in all behavioural tendencies measured by both psychometric scales within both groups and within each breed studied. Taken together, our findings indicate that breed alone is not a reliable predictor of individual behavioural tendencies, including those related to aggression, and therefore breed-specific legislation is unlikely to be an effective instrument for reducing risk.</p>
Figure 6 in Ecological niche overlap of two allopatric karst-adapted tiger geckos (Goniurosaurus) from northern Vietnam: microhabitat use and implications for conservation
Figure 6. (a) Scatterplots of all variable groups on coordinates of (1) Dim1–Dim2, (2) Dim3–Dim4 axes in the multiple factor analysis (MFA); (b) the first four important variables contributing to (1) Dim1, (2) Dim2, (3) Dim3, (4) Dim4; (c) scatter diagrams illustrating ecological spaces of Goniurosaurus huuliensis and Goniurosaurus luii on coordinates of (1) Dim1–Dim2, (2) Dim3–Dim4 axes.
Figure 4 in Ecological niche overlap of two allopatric karst-adapted tiger geckos (Goniurosaurus) from northern Vietnam: microhabitat use and implications for conservation
Figure 4. Microhabitat parameters and activity of Goniurosaurus huuliensis (1) and Goniurosaurus luii (2): (a) substrate type; (b) position to cave/ crevice; (c) activity status; (d) substrate moisture.
Figure 5 in Ecological niche overlap of two allopatric karst-adapted tiger geckos (Goniurosaurus) from northern Vietnam: microhabitat use and implications for conservation
Figure 5. The number of observed individuals of Goniurosaurus huuliensis and Goniurosaurus luii at different time intervals.
Figure 3 in Ecological niche overlap of two allopatric karst-adapted tiger geckos (Goniurosaurus) from northern Vietnam: microhabitat use and implications for conservation
Figure 3. Microhabitat characters of Goniurosaurus huuliensis and Goniurosaurus luii. (a) Air temperature; (b) substrate surface temperature; (c) animal temperature; (d) relative air humidity; (e) substrate angle; (f) occupied height; (g) canopy coverage; (h) elevation.
Figure 2 in Ecological niche overlap of two allopatric karst-adapted tiger geckos (Goniurosaurus) from northern Vietnam: microhabitat use and implications for conservation
Figure 2. (a) Karst mountain inhabited by Goniurosaurus huuliensis; (b) Microhabitat of Goniurosaurus luii; (c) G. huuliensis; and (d) G. luii on rock substrate. (Photographed by Hai N. Ngo.)
Figure 1 in Ecological niche overlap of two allopatric karst-adapted tiger geckos (Goniurosaurus) from northern Vietnam: microhabitat use and implications for conservation
Figure 1. Geographic distribution of Goniurosaurus huuliensis (violet circles enclosed by a violet line) and Goniurosaurus luii (pink triangles – northern Vietnam; pink squares – southern China – enclosed by a pink line). The orange square represents the distribution of another tiger gecko species, namely Goniurosaurus araneus, in China.
Figure 7 in Ecological niche overlap of two allopatric karst-adapted tiger geckos (Goniurosaurus) from northern Vietnam: microhabitat use and implications for conservation
Figure 7. Anthropogenic impacts in natural habitats of Goniurosaurus huuliensis and Goniurosaurus luii: (a) quarrying for cement production; (b) timber logging. (Photographed by Hai N. Ngo.)
Fig. 1 in Implications of a Dating Analysis of Hippoboscoidea (Diptera) for the Origins of Phoresis in Feather Lice (Psocodea: Phthiraptera: Philopteridae)
Fig. 1. Result of the MCMCTree dating analysis of the published Hippoboscoidea NCBI popset of four genes (CO1, CAD, 16s, 28s; Petersen et al. 2007). Bootstrap support is depicted to the left of nodes.The scale bar depicts divergence estimates in millions of years (Mya) and 95% highest probability distribution (HPD) are to the right of nodes. Red branches represent avian-feeding Hippoboscidae lineages. Feather louse images above scientific names indicate the genus or species below has records of louse phoresis (Ornithoctona has records of louse phoresis for three species, but the specimen analyzed was not identified to species level; a single record of louse phoresis exists for Crataerina, but is believed to be inaccurate because members of the genus are stenopterous; Corbet 1956, Keirans 1975). Illustrations of animals to the right of scientific names show host associations of Hippoboscoidea species with true ectoparasitism (Maa 1969).
Figure 38 in Diversity of schizomids (Arachnida: Schizomida) revealed by new fossil genera and species from mid-Cretaceous Burmese amber with implications for a Gondwanan origin of the Burma Terrane
Figure 38. Undescribed schizomids in Burmese amber (all from the Müller collection). A, BUB3556. B, BUB10. C, BUB007. D, BUB09. E, BUB3545. F, BUB3547. G, BUB3544. H, BUB3557. I, BUB1531. J, BUB559. K, BUB3554. L, BUB3551. Scale bars: 1 mm.
Figure 37 in Diversity of schizomids (Arachnida: Schizomida) revealed by new fossil genera and species from mid-Cretaceous Burmese amber with implications for a Gondwanan origin of the Burma Terrane
Figure 37. Undescribed schizomids in Burmese amber. A, Gröhn collection no. 11216. B, Gröhn collection no. 11215. C, Müller collection no. BUB08. D, Müller collection no. BUB561. E, Müller collection no. BUB1530. F, Müller collection no. BUB3546. G, Müller collection no. BUB08. Scale bars: 1 mm.
Figure 35 in Diversity of schizomids (Arachnida: Schizomida) revealed by new fossil genera and species from mid-Cretaceous Burmese amber with implications for a Gondwanan origin of the Burma Terrane
Figure 35. Distribution of species with a 1 + 2 setation on the anterior process in present times (A) and in same locations at 160 Mya (B), modified after Seton et al. (2021). Abbreviations: AF, Africa; ANT, Antarctica; AS, Asia; AU, Australia; BT, Burma Terrane; EUR, Europe; G, Greenland; I, India; NA, North America; SA, South America.
Figure 31. Specimen GPIH04892 in Diversity of schizomids (Arachnida: Schizomida) revealed by new fossil genera and species from mid-Cretaceous Burmese amber with implications for a Gondwanan origin of the Burma Terrane
Figure 31. Specimen GPIH04892, †Muellerizomus amandae sp. nov., female paratype, details. A, female flagellum in dorsal view, photograph. B, same, interpretative drawing. See Material and methods for explanation of abbreviations. Scale bar: 0.50 mm.
Figure 39 in Diversity of schizomids (Arachnida: Schizomida) revealed by new fossil genera and species from mid-Cretaceous Burmese amber with implications for a Gondwanan origin of the Burma Terrane
Figure 39. Undescribed schizomids in Burmese amber (all from the Müller collection except for D, Gröhn collection). A, BUB3550. B, BUB11. C, BUB3543. D, Gröhn collection no. 11207. E, BUB3555. F, BUB562. G, BUB560. H, BUB3558. I, BUB3552. J, BUB3564. K, BUB3548. L, BUB3549. Scale bars: 1 mm.
Figure 34. Specimen GPIH04894 in Diversity of schizomids (Arachnida: Schizomida) revealed by new fossil genera and species from mid-Cretaceous Burmese amber with implications for a Gondwanan origin of the Burma Terrane
Figure 34. Specimen GPIH04894, †Muellerizomus palicaudatus sp. nov., holotype, details. A, flagellum in dorsal view, photograph. B, same, interpretative drawing. C, flagellum in ventral view, photograph. D, same, interpretative drawing. See Material and methods for explanation of abbreviations. Scale bars: 0.25 mm.
Figure 29. Specimen GPIH04892 in Diversity of schizomids (Arachnida: Schizomida) revealed by new fossil genera and species from mid-Cretaceous Burmese amber with implications for a Gondwanan origin of the Burma Terrane
Figure 29. Specimen GPIH04892, †Muellerizomus amandae sp. nov., female paratype. A, specimen in dorsal view, photograph. B, same, interpretative drawing. C, specimen in ventral view, photograph. D, same, interpretative drawing. See Material and methods for explanation of abbreviations. Scale bars: 1 mm.
Figure 30. Specimen GPIH04892 in Diversity of schizomids (Arachnida: Schizomida) revealed by new fossil genera and species from mid-Cretaceous Burmese amber with implications for a Gondwanan origin of the Burma Terrane
Figure 30. Specimen GPIH04892, †Muellerizomus amandae sp. nov., female paratype, details. A, propeltidium in dorsal view, photograph. B, same, interpretative drawing. C, metapeltidium in dorsal view, photograph. D, same, interpretative drawing. See Material and methods for explanation of abbreviations. Scale bars: 0.5 mm (A, B); 0.25 mm (C, D).
Figure 32. Specimen GPIH04894 in Diversity of schizomids (Arachnida: Schizomida) revealed by new fossil genera and species from mid-Cretaceous Burmese amber with implications for a Gondwanan origin of the Burma Terrane
Figure 32. Specimen GPIH04894, †Muellerizomus palicaudatus sp. nov., holotype. A, specimen in dorsal view, photograph. B, same, interpretative drawing. C, specimen in ventral view, photograph. D, same, interpretative drawing. See Material and methods for explanation of abbreviations. Scale bars: 1 mm.
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.