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Fig. 2 in Two new Cyrtodactylus (Squamata, Gekkonidae) from Northeast India
Fig. 2. Maximum Likelihood phylogeny of the Cyrtodactylus khasiensis group; numbers at nodes represent bootstrap support (preceding the species name is the NCBI accession number).
Fig. 1 in Two new Cyrtodactylus (Squamata, Gekkonidae) from Northeast India
Fig. 1. Elevation map showing the type localities for the two newly described species of Cyrtodactylus and the congeners compared in this paper: 1. Cyrtodactylus exercitus sp. nov. (red star). 2. C. siahaensis sp. nov. (blue star). 3. C. bengkhuaiai Purkayastha, Lalremsanga, Bohra, Biakzuala, Decemson, Muansanga, Vabeiryureilai, Chauhan & Rathee, 2021. 4. C. aaronbaueri Purkayastha, Lalremsanga, Bohra, Biakzuala, Decemson, Muansanga, Vabeiryureilai, Chauhan & Rathee, 2021. 5. C. karsticola Purkayastha, Lalremsanga, Bohra, Biakzuala, Decemson, Muansanga, Vabeiryureilai, Chauhan & Rathee, 2021. 6. C. agarwali Purkayastha, Lalremsanga, Bohra, Biakzuala, Decemson, Muansanga, Vabeiryureilai, Chauhan & Rathee, 2021. 7. C. montanus Agarwal, Mahony, Giri, Chaitanya & Bauer, 2018. 8. C. tripuraensis Agarwal, Mahony, Giri, Chaitanya & Bauer, 2018. 9. C. khasiensis (Jerdon, 1870). 10. C. jaintiaensis Agarwal, Mahony, Giri, Chaitanya & Bauer, 2018. 11. C. guwahatiensis Agarwal, Mahony, Giri, Chaitanya & Bauer, 2018. 12. C. urbanus Purkayastha, Das, Bohra, Bauer & Agarwal, 2020. 13. C. septentrionalis Agarwal, Mahony, Giri, Chaitanya & Bauer, 2018. 14. C. kazirangaensis Agarwal, Mahony, Giri, Chaitanya & Bauer, 2018. 15. C. nagalandensis Agarwal, Mahony, Giri, Chaitanya & Bauer, 2018. 16. C. arunachalensis Mirza, Bhosale, Ansari, Phansalkar, Swant, Gowande & Patel, 2021. 17. C. markuscombaii (Darevsky, Helfenberger, Orlov & Shah, 1998) and C. martinstolli Darevsky, Helfenberger, Orlov & Shah, 1998). 18. C. himalayicus (Annandale, 1906). 19. C. cayuensis Li, 2007. 20. C. tamaiensis (Smith, 1940). 21. C. ayeyarwadyensis Bauer, 2003. 22. C. mandalayensis Mahony, 2009.
Source parameter of hydraulic-fracturing-induced earthquakes in the Kiskatinaw area, northeast British Columbia
<p>Source parameter of 2475 hydraulic-fracturing-induced earthquakes (1927 events using P-wave estimates and 1882 events using S-wave estimates) in the Kiskatinaw area, northeast British Columbia between 1 July 2017 to 31 July 2020. The Study area covers parts of the Montney Formation, a major shale gas play within the Western Canada Sedimentary Basin. Source parameters include seismic moment, moment magnitude, spectral corner frequency, and static stress drop values using three different approaches (single spectrum fitting, a clustered event approach, and spectral-ratio method). Detailed information about the methods are stated in the corresponding publication:</p> <p>Roth, M. P., K. B. Kemna, R. M. Harrington, and Y. Liu (2022). Source properties of hydraulic-fracturing-induced earthquakes in the Kiskatinaw area, British Columbia, Canada. Journal of Geophysical Research: Solid Earth. <a href="https://doi.org/10.1029/2021JB022750">https://doi.org/10.1029/2021JB022750</a></p>
FIG. 3. — A in Contributions to the taxonomic status and molecular phylogeny of Asian Bronzeback Snakes (Colubridae, Ahaetuliinae, Dendrelaphis Boulenger, 1890), from Mizoram State, Northeast India
FIG. 3. — A, BI phylogenetic tree estimated by mitochondrial 16S rRNA and; B, partial COI sequences depicting the phylogenetic relationships of Dendrelaphis Boulenger, 1890 species with BPP/UFB support at the branch nodes. Sequences generated in this study are shown in bold.
FIG. 2. — A in Contributions to the taxonomic status and molecular phylogeny of Asian Bronzeback Snakes (Colubridae, Ahaetuliinae, Dendrelaphis Boulenger, 1890), from Mizoram State, Northeast India
FIG. 2. — A, Dendrelaphis biloreatus Wall, 1908 in life, showing anterior body and head from Kolasib, Mizoram, NE India. Inset: Dorso-lateral view of the head showing two loreal scales; B, juvenile Dendrelaphis biloreatus (MZMU1812) in life from MZU Campus, Mizoram, NE India, photographed by Tbc. Lalhruaitluangi. Inset: Antero-lateral view of the head showing single loreal scale, photographed by Romalsawma.
FIG. 6 in Contributions to the taxonomic status and molecular phylogeny of Asian Bronzeback Snakes (Colubridae, Ahaetuliinae, Dendrelaphis Boulenger, 1890), from Mizoram State, Northeast India
FIG. 6. — Two specimens of Dendrelaphis proarchos Wall, 1909 found sheltered inside a green bamboo: A, from Kepran,photographed by Tbc. Mapuia; B, from Tlangnuam, photographed by C. Mawitea.
FIG. 7. — A in Contributions to the taxonomic status and molecular phylogeny of Asian Bronzeback Snakes (Colubridae, Ahaetuliinae, Dendrelaphis Boulenger, 1890), from Mizoram State, Northeast India
FIG. 7. — A, Dendrelaphis cyanochloris (Wall, 1921) preying on adult Calotes emma Gray, 1845, photographed by R. Lalnunmawia; B, Dendrelaphis proarchos Wall, 1909 preying on adult Duttaphrynus melanostictus (Schneider,1799), photographed by Hawla Hmar Zote.
FIG. 5 in Contributions to the taxonomic status and molecular phylogeny of Asian Bronzeback Snakes (Colubridae, Ahaetuliinae, Dendrelaphis Boulenger, 1890), from Mizoram State, Northeast India
FIG. 5. — Elevation map showing the specimens location of Dendrelaphis proarchos Wall, 1909 (green shapes), Dendrelaphis biloreatus Wall, 1908 (yellow shapes), Dendrelaphis cyanochloris (Wall, 1921) (red shapes), Dendrelaphis cf. vogeli LSUHC 6768 (purple circle with dot), and Dendelaphis cf. ngansonensis CAS221428 (blue circle with dot) examined in this study. Confirmed populations of Dendrelaphis proarchos (green circles) and Dendrelaphis biloreatus (yellow triangles) are based on Vogel & van Rooijen (2011a, b).
FIG. 4 in Contributions to the taxonomic status and molecular phylogeny of Asian Bronzeback Snakes (Colubridae, Ahaetuliinae, Dendrelaphis Boulenger, 1890), from Mizoram State, Northeast India
FIG. 4. — BI phylogenetic tree estimated by mitochondrial Cytb sequences depicting phylogenetic relationships of Dendrelaphis Boulenger, 1890 species with BPP/UFB support at the branch nodes. Sequences generated in this study are shown in bold.
FIG. 1. — A in Contributions to the taxonomic status and molecular phylogeny of Asian Bronzeback Snakes (Colubridae, Ahaetuliinae, Dendrelaphis Boulenger, 1890), from Mizoram State, Northeast India
FIG. 1. — A, sub-adult Dendrelaphis proarchos Wall, 1909 from Mizoram, NE India; B, everted hemipenial sulcal side (right) and asulcal side (left) of Dendrelaphis proarchos from Mizoram, NE India; C, Adult Dendrelaphis cyanochloris (Wall, 1921) from Mizoram, NE India. Scale bar: B, 5 mm.
Fig. 3 in Ecology Of Avian Settlements In Lake Tonga (Northeast Algeria)
Fig. 3. Evolution of the specific richness of waterbirds at Lake Tonga. common coot is by far the most abundant. The purple swamphen Porphyrio porphyrio is also included in the IUCN Red List and therefore we can say that Lake Tonga is a very important site for waterbirds in our country (Boumezbeur, 1993; Benyacoub et al., 2011). It should be noted that Lake Tonga is the only nesting site of the Whiskered Tern Chlidonias hybrida in Algeria and North Africa (Bakaria et al., 2009).
Otolith annual growth increments for cod populations in the Northeast Atlantic
<p>Large-scale, climate-induced synchrony in the productivity of fish populations is becoming more pronounced in the world's oceans. As synchrony increases, a population's 'portfolio' of responses can be diminished, in turn reducing its resilience to strong perturbation. Here we argue that the costs and benefits of trait synchronization, such as the expression of growth rate are context dependent. Synchrony among individuals could actually be beneficial for populations if growth is optimized during favourable conditions and then declines under poor conditions when a broader portfolio of responses is needed. Importantly, growth synchrony among individuals within populations has seldom been measured, despite well-documented evidence of synchrony across populations. Here, we used century-scale time series of annual otolith growth to test for changes in growth synchronization among individuals within multiple populations of a marine keystone species (Atlantic cod, <em>Gadus morhua</em>). On the basis of 74,662 annual growth increments recorded in 13,749 otoliths, we detected a rising conformity in long-term growth rates within northeast Atlantic cod populations in response to both favorable growth conditions and a large-scale, multidecadal mode of climate variability similar to the East Atlantic Pattern. The within-population synchrony was distinct from the across-population synchrony commonly reported for large-scale environmental drivers. Climate-linked, among-individual growth synchrony was also identified in other Northeast Atlantic pelagic, deep-sea and bivalve species. We hypothesize that growth synchrony buffers marine populations to changing climate and growth conditions through its effect on the phenotypic expression of growth diversity, and thus provides an unexpected, but pervasive and stabilizing impact on marine population productivity.</p>
Fig. 2 in Cladoceras rovumense sp. nov. (Gentianales-Rubiaceae), a new species from southeast Tanzania and northeast Mozambique
Fig. 2. Species of Cladoceras Bremek. in the field. A–B. Cladoceras rovumense I.Darbysh., J.E.Burrows & Q.Luke sp. nov. (photos: A. Q. Luke; B. P.A. Luke, Mozambique). C–D. Cladoceras subcapitatum (K.Schum. & K.Krause) Bremek. (photos: W.R.Q. Luke, Base Titanium nursery, Kwale County, Kenya).
Fig. 1. Cladoceras rovumense I.Darbysh., J.E.Burrows & Q in Cladoceras rovumense sp. nov. (Gentianales-Rubiaceae), a new species from southeast Tanzania and northeast Mozambique
Fig. 1. Cladoceras rovumense I.Darbysh., J.E.Burrows & Q.Luke sp. nov. A. Habit, fruiting shoot. B. Habit, flowering shoot. C. Stipule, external face. D. Hairs revealed beneath fallen stipule. E. Portion of flowering stem showing indumentum. F. Leaf, adaxial indumentum. G. Leaf, abaxial indumentum. H. Dissected corolla with androecium. I. Style and stigma. J. Longitudinal section of ovary. K. Mature fruit. L. Fruit, partially dissected to reveal seeds. M. Seed in two views. A, E–G, K–M from S. Bidgood et al. 1357; B, H–I from Q. Luke 13883; C–D, J from Q. Luke et al. 10116. Drawn by Andrew Brown.
Fig. 9 in Taxonomic revaluation of the Ahaetulla prasina (H. Boie in F. Boie, 1827) complex from Northeast India: resurrection and redescription of Ahaetulla flavescens (Wall, 1910) (Reptilia: Serpentes: Colubridae)
Fig. 9. Map of Northeast India, showing the distribution records of Ahaetulla flavescens (Wall, 1910) comb. nov.; red star represents the type locality.
Fig. 8 in Taxonomic revaluation of the Ahaetulla prasina (H. Boie in F. Boie, 1827) complex from Northeast India: resurrection and redescription of Ahaetulla flavescens (Wall, 1910) (Reptilia: Serpentes: Colubridae)
Fig. 8. Ahaetulla flavescens (Wall, 1910) comb. nov. Live uncollected specimen from Mizoram, showing the usual green colouration which is dominant in this species. Photo: Ajay Karthik.
Fig. 7 in Taxonomic revaluation of the Ahaetulla prasina (H. Boie in F. Boie, 1827) complex from Northeast India: resurrection and redescription of Ahaetulla flavescens (Wall, 1910) (Reptilia: Serpentes: Colubridae)
Fig. 7. Ahaetulla flavescens (Wall, 1910) comb. nov. Live uncollected specimens from Arunachal Pradesh, showing the unusual buff or yellowish-brown colouration. Photo: Bharat Bhushan Bhatt.
Fig. 6. Dryophis prasinusvar. flavescens Wall, 1910 in Taxonomic revaluation of the Ahaetulla prasina (H. Boie in F. Boie, 1827) complex from Northeast India: resurrection and redescription of Ahaetulla flavescens (Wall, 1910) (Reptilia: Serpentes: Colubridae)
Fig. 6. Dryophis prasinusvar. flavescens Wall, 1910, lectotype (NHMUK 1908.6.23.58) and paralectotype (NHMUK 1908.6.23.59). Jar label. Photo: ©The Trustees of the Natural History Museum, London.
Fig. 5. Dryophis prasinus var. flavescens Wall, 1910 in Taxonomic revaluation of the Ahaetulla prasina (H. Boie in F. Boie, 1827) complex from Northeast India: resurrection and redescription of Ahaetulla flavescens (Wall, 1910) (Reptilia: Serpentes: Colubridae)
Fig. 5. Dryophis prasinus var. flavescens Wall, 1910, lectotype (NHMUK 1908.6.23.58). Head close-up showing the divided 4th supralabial on right side, a unique identifying character in ascertaining its type status. Photo: ©The Trustees of the Natural History Museum, London.
Fig. 2 in Taxonomic revaluation of the Ahaetulla prasina (H. Boie in F. Boie, 1827) complex from Northeast India: resurrection and redescription of Ahaetulla flavescens (Wall, 1910) (Reptilia: Serpentes: Colubridae)
Fig. 2. The bPTP output trees generated from three mitochondrial loci ML trees. Blue coloured branches and black bars indicate monophyly of that lineage, where validity of lineages is further ascertained with genetic divergence (genetic p-distance) and geographic isolation. The grey bars indicate the genetic distance (G1) and geographic isolation (G2) among lineages. The values on clades indicate the posterior probability. The A. prasina complex (Lineage 1 and Lineage 2) from northeast India shows a very low genetic divergence with continuous geographic distribution.
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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.