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993 results for “T Dwarfs”

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Figure 5 in Comparison of non-native dwarf eelgrass (Zostera japonica) and native eelgrass (Zostera marina) distributions in a northeast Pacific estuary: 1997-2014

Figure 5: Area of Zostera marina and Zostera japonica as a function of distance from the mouth of Yaquina Estuary, from August normalised classifications of the digital orthophotographs obtained in 1997 and 2007.

opennotspecifiedJun 2015View details →
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Figure 8 in Comparison of non-native dwarf eelgrass (Zostera japonica) and native eelgrass (Zostera marina) distributions in a northeast Pacific estuary: 1997-2014

Figure 8: Perimeters of Zostera japonica patches in Idaho Flat embayment, mapped via DGPS on foot (June 23, 2000 and August 13, 2014).

opennotspecifiedJun 2015View details →
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Figure 3 in Comparison of non-native dwarf eelgrass (Zostera japonica) and native eelgrass (Zostera marina) distributions in a northeast Pacific estuary: 1997-2014

Figure 3: Seasonal variation in area of selected Zostera japonica meadows within Sallys Bend embayment, mapped via DGPS from a hovercraft (April 2011–November 2012).

opennotspecifiedJun 2015View details →
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Figure 6 in Comparison of non-native dwarf eelgrass (Zostera japonica) and native eelgrass (Zostera marina) distributions in a northeast Pacific estuary: 1997-2014

Figure 6: Total (August normalised) area of intertidal Zostera marina (A) and Zostera japonica (B) in lower Yaquina Estuary from orthophotograph image classifications (Year 1 is 1997, Year 11 is 2007) and best-fit equations with 95% CI.

opennotspecifiedJun 2015View details →
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Spectral ANalog of Dwarfs (SAND) model atmospheres and Evolutionary Extension to SAND (SANDee) evolutionary models for low-mass stars and brown dwarfs

<p>Spectral ANalog of Dwarfs (SAND) is a new grid of model atmospheres for low-mass stars and brown dwarfs at a variety of chemical compositions, characteristic of various components of the Milky Way, including the galactic halo and globular clusters. The models were calculated using <strong>PHOENIX 15</strong></p> <p>A detailed description of SAND is available in RNAAS 2024 by Alvarado, Gerasimov, Burgasser, Brooks, Aganze and Theissen <a href="https://ui.adsabs.harvard.edu/abs/2024RNAAS...8..134A/abstract">[ADS]</a></p> <p>Evolutionary Extension to SAND (SANDee) is a new grid of evolutionary models that uses the SAND models for synthetic photometry and as atmosphere boundary conditions. SANDee is the first set of models that can reproduce the observed star/brown dwarf transition in globular clusters. SANDee models were calculated using&nbsp;<strong>MESA 23.05.1</strong></p> <p>A detailed description of SANDee is available in ApJ 2024 by Gerasimov, Bedin, Burgasser, Apai, Nardiello, Alvarado and Anderson <a href="https://ui.adsabs.harvard.edu/abs/2024arXiv240501634G/abstract">[ADS]</a></p> <p>&nbsp;</p> <p><strong>Directory structure:</strong></p> <pre><code>SAND.zip : SAND model atmospheres recommended : Subset of SAND atmospheres whose synthetic photometry maintains continuity as a function of temperature rest : The rest of SAND models (see notes on convergence below) SANDee.zip : SANDee evolutionary models BC : MESA atmosphere boundary condition tables for tau=100 at each chemistry MESA : MESA evolutionary models, organized first by chemistry, then by initial mass isogen.zip : Python script to generate model isochrones from SANDee and SAND models isogen.py : The script itself demo.ipynb : Jupyter notebook that demonstrates how the script can be used &nbsp; &nbsp; vega_bohlin_2004.dat &nbsp;: &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; Standard spectrum of Vega for VEGAMAG photometry<br>&nbsp; &nbsp; Other *.dat &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; : &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; Transmission profiles for JWST filters used by the demo notebook custom.patch : Patch with author's changes to the MESA codebase HBL.mrt : Estimated true hydrogen-burning limits for each SAND/SANDee chemistry</code></pre>

opencc-by-4.0Apr 2024View details →
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FIGURE 13 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex

FIGURE 13. Habitat of species of the Lygodactylus tolampyae complex. A. Dry deciduous forest at Ampijoroa (Ankarafantsika) where L. morii sp. nov. occurs in high densities. B. View of remains of dry deciduous Ampondrabe forest (habitat of L. morii sp. nov. and L. herilalai sp. nov.) with large areas of forest destroyed by fire in the foreground. C, D. Transitional forest on Sahamalaza Peninsula, habitat of L. schwitzeri sp. nov. E. Forest in the Tsingy de Bemaraha, habitat of L. tolampyae. All photos by the authors except A by P. Galán.

opennotspecifiedJun 2024View details →
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FIGURE 11 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex

FIGURE 11. Ventral views of the heads of the holotypes of the three new species of Lygodactylus described herein, and one representative specimen of L. tolampyae. The images on the right show the mental region magnified and strongly sharpened to improve visibility of sutures between scales. For the holotype of L. morii sp. nov., the typical arrangement of scales in the mental region in this species complex is labelled: M, mental scales (semi-divided by incomplete sutures), PM, post-mentals (typically three), IL1, first infralabial (which maintains a broad contact with the mental). Scale bars (referring to the images on the left) represent 1 mm.

opennotspecifiedJun 2024View details →
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FIGURE 12 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex

FIGURE 12. Lateral views of the heads of the holotypes of the three new species of Lygodactylus described herein, and one representative specimen of L. tolampyae. The scale bar represents 1 mm.

opennotspecifiedJun 2024View details →
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FIGURE 10 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex

FIGURE 10. Preserved holotypes of the three new species of the Lygodactylus tolampyae complex described herein, photographed in May 2023.

opennotspecifiedJun 2024View details →
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FIGURE 4 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex

FIGURE 4. Individuals of Lygodactylus tolampyae from Tsingy de Bemaraha National Park, all photographed in 2006. The upper three individuals are not unambiguously assignable to voucher specimens but correspond to samples included in the mitochondrial tree (Fig. 1) and grouped in lineage A+B; the lowermost picture shows the female ZSM 6/2006 (FGZC 676).

opennotspecifiedJun 2024View details →
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FIGURE 9 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex

FIGURE 9. Female holotype of Lygodactylus schwitzeri sp. nov., ZSM 419/2000 (FGMV 2000.155), from Berara Forest, Sahamalaza, in life, photographed in February 2000.

opennotspecifiedJun 2024View details →
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FIGURE 5 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex

FIGURE 5. Male holotype of Lygodactylus morii sp. nov., ZSM 501/2001 (FGMV 2001.300) from Ampijoroa, Ankarafantsika National Park, in life, photographed in February 2001.

opennotspecifiedJun 2024View details →
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FIGURE 2 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex

FIGURE 2. Map of Madagascar with genetically confirmed sampling localities of the Lygodactylus tolampyae complex. Colours correspond to those used for mitochondrial lineages. The black square marks the town Morondava from which no samples were analyzed; it is likely that the type locality of L. tolampyae is located in the wider Morondava area.

opennotspecifiedJun 2024View details →
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FIGURE 6 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex

FIGURE 6. Individuals of Lygodactylus morii sp. nov. from near Ampijoroa (Ankarafantsika National Park) in life, photographed in November 2022. A. specimen with sample number MVTIS 33402/33488 (not collected). B. paratype ZSM 159/2022 (ZCMV 15703).

opennotspecifiedJun 2024View details →
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FIGURE 8 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex

FIGURE 8. Female holotype of Lygodactylus herilalai sp. nov., ZSM 161/2022 (ZCMV 15707) from Ampondrabe, Ankarafantsika National Park, in life, photographed November 2022.

opennotspecifiedJun 2024View details →
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FIGURE 1 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex

FIGURE 1. Maximum Likelihood tree calculated from DNA sequences of the mitochondrial 16S rRNA gene (alignment length: 517 bp) for 70 samples of the L. tolampyae complex. A sample of L. bivittis was used as outgroup. Numbers are bootstrap support values in percent (500 replicates). Clades are defined on the basis of an analysis with ASAP.

opennotspecifiedJun 2024View details →
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FIGURE 7 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex

FIGURE 7. Four individuals of Lygodactylus morii sp. nov. photographed in November 2022 at different sites near Ampijoroa (Ankarafantsika National Park) in life, resting at night on terminal twigs of trees as is typical for the L. tolampyae complex. Individuals not individually assignable to sample or voucher specimen numbers, but corresponding to sequences included in Fig. 1.

opennotspecifiedJun 2024View details →
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Unveiling the nature of two dwarf novae: CRTS J080846.2+313106 and V416 Dra

<p>The observed spectra of two dwarf novae, CRTS J080846.2+313106 and V416 Dra, have been uploaded.&nbsp;</p>

opencc-by-4.0Jul 2024View details →
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FIGURE 5 in Molecular phylogenetics and taxonomy of dwarf hamsters Cricetulus Milne-Edwards, 1867 (Cricetidae, Rodentia): description of a new genus and reinstatement of another

FIGURE 5. Timescale of major divergence events among taxa of Cricetinae based on nuclear gene data. The chronogram was reconstructed under the autocorrelated clock model imрlemented in MCMCTree software. The divergence times corresрond to the mean рosterior estimate of their age in Myr. The bars reрresent the 95% HPD interval.

opennotspecifiedFeb 2018View details →
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FIGURE 2 in Molecular phylogenetics and taxonomy of dwarf hamsters Cricetulus Milne-Edwards, 1867 (Cricetidae, Rodentia): description of a new genus and reinstatement of another

FIGURE 2. The Bayesian рhylogeny of Cricetinae as inferred from the comрlete cytb gene sequence in MrBayes. Outgrouрs are not shown. Values above/below branches denote Bayesian рosterior рrobabilities (BPP) and bootstraр suррort in Maximum Likelihood (ML) and Maximum Parsimony (MP) analyses. The asterisks indicate the highly suррorted nodes in all analyses (BPP&gt;0.95, ML and MP bootstraр suррort&gt;90%). The ML analysis was рerformed in Treefinder based on either nucleotide (nuc) or рrotein (AA) sequence alignment. In the latter case a mixed рrotein model (mixture of mtREV, mtMam and mtArt) with emрirical state frequencies and a gamma distribution of rates across sites was used. Transitions at the 3rd codon рositions were removed from the ML analysis of the nucleotide alignment via usage of GTR2 model.

opennotspecifiedFeb 2018View details →

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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.

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OpenNeuro

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