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Text-fig. 1. Modern vegetation proxies as delivered by the Drudge 1 and 2 tools for Parschlug. Left column results from KovarEder et al. (2021) based on the floristic spectrum published by Kovar-Eder et al. (2004). The other three columns result from three variants using the enlarged floristic spectrum herein. Differences between variants 1–3 from this study are caused by differences in assignment of some taxa and morphotypes (see Appendix 1). European vegetation formations: Formation C – Subarctic, boreal and nemoral-montane open woodlands as well as subalpine and oro-Mediterranean vegetation; Formation D – Mesophytic and hygromesophytic coniferous and mixed broad-leaved-coniferous forests; Formation F – Mesophytic broadleaved deciduous and mixed broadleaved/conifer forests; Formation G – Thermophilous mixed deciduous broadleaved forests; Formation J – Mediterranean sclerophyllous forests and scrub; Formation K – Xerophytic coniferous forests, coniferous woodland and scrub. East Asian vegetation types: MCF China, Japan – Montane Coniferous Forests China, Honshu, Yakushima; BLDF N and NE Provinces, China – Broad-leaved Deciduous Forests of the Northern and Northeastern Provinces (China); BLDF Upper Yangtze, Honshu – Broad-leaved Deciduous Forest, Upper Yangtze Provinces, Mt. Emei, and Honshu; MMF China – Mixed Mesophytic Forest, Lower Yangtze Provinces; BLEF China, Japan – Broad-leaved Evergreen Forests, China, Japan; Meili Snow Mt. high altitude SCL and BLF, China – Meili Snow Mt., Sclerophyllous and broad-leaved forest zone (2,580-3,650 m alt.). (Designations of European vegetation formations follow Bohn et al. (2004) and Asian ones follow Kovar-Eder et al. (2021). in Floristic, Vegetation And Climate Assessment Of The Early/Middle Miocene Parschlug Flora Indicates A Distinctly Seasonal Climate
Text-fig. 1. Modern vegetation proxies as delivered by the Drudge 1 and 2 tools for Parschlug. Left column results from KovarEder et al. (2021) based on the floristic spectrum published by Kovar-Eder et al. (2004). The other three columns result from three variants using the enlarged floristic spectrum herein. Differences between variants 1–3 from this study are caused by differences in assignment of some taxa and morphotypes (see Appendix 1). European vegetation formations: Formation C – Subarctic, boreal and nemoral-montane open woodlands as well as subalpine and oro-Mediterranean vegetation; Formation D – Mesophytic and hygromesophytic coniferous and mixed broad-leaved-coniferous forests; Formation F – Mesophytic broadleaved deciduous and mixed broadleaved/conifer forests; Formation G – Thermophilous mixed deciduous broadleaved forests; Formation J – Mediterranean sclerophyllous forests and scrub; Formation K – Xerophytic coniferous forests, coniferous woodland and scrub. East Asian vegetation types: MCF China, Japan – Montane Coniferous Forests China, Honshu, Yakushima; BLDF N and NE Provinces, China – Broad-leaved Deciduous Forests of the Northern and Northeastern Provinces (China); BLDF Upper Yangtze, Honshu – Broad-leaved Deciduous Forest, Upper Yangtze Provinces, Mt. Emei, and Honshu; MMF China – Mixed Mesophytic Forest, Lower Yangtze Provinces; BLEF China, Japan – Broad-leaved Evergreen Forests, China, Japan; Meili Snow Mt. high altitude SCL and BLF, China – Meili Snow Mt., Sclerophyllous and broad-leaved forest zone (2,580-3,650 m alt.). (Designations of European vegetation formations follow Bohn et al. (2004) and Asian ones follow Kovar-Eder et al. (2021).
FIGURE 14 in A redescription of deep-channel ghost knifefish, Sternarchogiton preto (Gymnotiformes: Apteronotidae), with assignment to a new genus
FIGURE 14 | Sample of diversity of maxilla shape in Apteronotidae, emphasizing the Navajini. Maxillae are illustrated in lateral view and are not drawn to scale.
FIGURE 12 in A redescription of deep-channel ghost knifefish, Sternarchogiton preto (Gymnotiformes: Apteronotidae), with assignment to a new genus
FIGURE 12 | Collection localities of Tenebrosternarchus preto, star indicating type locality. Some points indicate multiple collections or lots from proximate locations.
FIGURE 4 in A redescription of deep-channel ghost knifefish, Sternarchogiton preto (Gymnotiformes: Apteronotidae), with assignment to a new genus
FIGURE 4 | Suspensorium, opercular series, and lower jaw of Tenebrosternarchus preto, MUSM 54617 (198 mm TL) in A. lateral and B. medial view (image reflected). Thin, unstained hard tissue associated with opercular bones shown in light gray. Abbreviations: ang, anguloarticular; ap, autopalatine cartilage; cm, coronomeckelian; d, dentary; enp, endopterygoid; h, hyomandibula; iop, interopercle; m, Meckel's cartilage; mpt, metapterygoid; op, opercle; pop, preopercle; q, quadrate; rar, retroarticular; sym, symplectic.
FIGURE 3 in A redescription of deep-channel ghost knifefish, Sternarchogiton preto (Gymnotiformes: Apteronotidae), with assignment to a new genus
FIGURE 3 | Illustrations of the neurocranium of Tenebrosternarchus preto MUSM 54617 (198 mm TL) in dorsal A., ventral B., and lateral C. views. Cartilage shown in black. Abbreviations: bao, basioccipital; epo, epioccipital; fro, frontal; let, lateral ethmoid; met, mesethmoid; obs, orbitosphenoid; par, parietal; pas, parasphenoid; pro, prootic; pto, pterotic; pts, pterosphenoid; soc, supraoccipital; spo, sphenotic; vet, ventral ethmoid; vom, vomer.
FIGURE 1 in A redescription of deep-channel ghost knifefish, Sternarchogiton preto (Gymnotiformes: Apteronotidae), with assignment to a new genus
FIGURE 1 | Lateral view of live Tenebrosternarchus preto. A. MUSM 54656 (243 mm TL) from the río Amazonas at Iquitos, Peru; B. ANSP 207797 (232 mm TL) from the rio Negro downstream from Barcelos, Brazil; and C. Detail of the head of ANSP 207797 (232 mm TL).
◂Fig. 6 A molecular phylogeny of 56 systematically representative Peridiniaceae, including 42 accessions assignable to P. cinctum from various geographic regions. Maximum likelihood tree (– ln = 21,884.93), as inferred from a rRNA nucleotide alignment (1137 parsimony-informative sites) and with strain number information. Numbers on branches are ML bootstrap (above) and Bayesian support values (below) for the clusters (asterisks indicate maximal support values, values under 50 and 0.90, respectively, are not shown). Clades are indicated (CZE Czech Republic, E East, GER Germany, HET Heterocapsaceae, N North, PPE Protoperidiniaceae, POL Poland, rbn ribotype n, S South, SWE Sweden, UKR Ukraine, W West) in Bumps on the back: An unusual morphology in phylogenetically distinct Peridinium aff. cinctum (= Peridinium tuberosum; Peridiniales, Dinophyceae)
◂Fig. 6 A molecular phylogeny of 56 systematically representative Peridiniaceae, including 42 accessions assignable to P. cinctum from various geographic regions. Maximum likelihood tree (– ln = 21,884.93), as inferred from a rRNA nucleotide alignment (1137 parsimony-informative sites) and with strain number information. Numbers on branches are ML bootstrap (above) and Bayesian support values (below) for the clusters (asterisks indicate maximal support values, values under 50 and 0.90, respectively, are not shown). Clades are indicated (CZE Czech Republic, E East, GER Germany, HET Heterocapsaceae, N North, PPE Protoperidiniaceae, POL Poland, rbn ribotype n, S South, SWE Sweden, UKR Ukraine, W West)
◂Fig. 4 A molecular tree of 51 systematically representative Peridiniaceae, including all 28 accessions assignable to P. volzii. Maximum Likelihood tree (–ln = 22,017.62), as inferred from a rRNA nucleotide alignment (1,129 parsimony-informative sites) and with strain number information. Numbers on branches are ML bootstrap (above) and Bayesian support values (below) for the clusters (asterisks indicate maximal support values, values under 50 and 0.90, respectively, are not shown). Clades are indicated (abbreviations: HET, Heterocapsaceae; PPE, Protoperidiniaceae) in Morphological and molecular variability of Peridinium volzii Lemmerm. (Peridiniaceae, Dinophyceae) and its relevance for infraspecific taxonomy
◂Fig. 4 A molecular tree of 51 systematically representative Peridiniaceae, including all 28 accessions assignable to P. volzii. Maximum Likelihood tree (–ln = 22,017.62), as inferred from a rRNA nucleotide alignment (1,129 parsimony-informative sites) and with strain number information. Numbers on branches are ML bootstrap (above) and Bayesian support values (below) for the clusters (asterisks indicate maximal support values, values under 50 and 0.90, respectively, are not shown). Clades are indicated (abbreviations: HET, Heterocapsaceae; PPE, Protoperidiniaceae)
BRAIN Journal-Computational Intelligence in a Human Brain Model-Figure 3. Assigning ` the "SAH" Human Brain Model the role of the Chess Pieces
<p>The components are not topically subordinated to each other but in a strong interoperability and used for outputs reflected as result of thinking, actions to receiving information from the sensor of the interfaces, movement or speaking. </p>
Experiment Result Plots of Data Stewardship (FAIR - Assignment 1)
<p>These plots show the results of the experiment by creating a scatterplot of the variables and a line plot.</p>
Anomaly-free, flavour-dependent U(1) charge assignments for Standard Model/Standard Model plus three right-handed neutrino fermionic content
<p>We present lists of anomaly-free charge combinations up to a maximum magnitude charge Qmax given by the number at the end of the filename. Filenames beginning "SMcharges" are for the Standard Model fermion content, whereas "SMnuRcharges" are for Standard Model plus three right-handed neutrino fermion content. Use the bunzip2 program to unpack the larger files with a bz2 suffix.</p> <p>The files searchU1.cpp and searchU1.h contain C++ files (in the 2014 standard) to produce the solutions. runme.sh is a bash script that compiles the programs and then runs it several times, once to produce each file.</p> <p>filterNeut.cpp contains an example program that reads in one of the solution lists, applies a filter to it, and only prints out solutions that satisfy the filter.</p> <p>These data and programs are based on this paper: https://arxiv.org/abs/1812.04602</p> <p> </p>
Figure 4 in Microhabitat partitioning of closely related Sarawak (Malaysian Borneo) frog species previously assigned to the genus Hylarana (Amphibia: Anura)
Figure 4. NMDS configuration showing ecological groupings from microhabitat characteristics of Sarawak frogs. Each point represents a species: Hba = Pulchrana baramica (N = 62 individuals), Hg = Pulcharana glandulosa (N = 10 individuals), Hsig = Pulcharana signata (N = 26 individuals), Hp = Pulcharana picturata (N = 27 individuals, Hra = Chalcorana raniceps (N = 112 individuals), He = Hylarana erythraea (N = 46 individuals), and Oh = Odorrana hosii (N = 21 individuals).
Figure 2 in Microhabitat partitioning of closely related Sarawak (Malaysian Borneo) frog species previously assigned to the genus Hylarana (Amphibia: Anura)
Figure 2. Dendrogram of Morisita's similarity resulting from average linkage clustering using the unweighted pair-group (UPGMA) method on data based on counts of individuals of frogs' species associated with habitats and microhabitats.
Figure 3 in Microhabitat partitioning of closely related Sarawak (Malaysian Borneo) frog species previously assigned to the genus Hylarana (Amphibia: Anura)
Figure 3. Final coordinate dimension (FDC) 1(A) and 2(B) of NMDS (PROXSCAL) of microhabitat characteristics of Sarawak frogs.
Fig. 4. Geothelphusa marginata fulva. a in A New Species Of The Freshwater Crab, Previously Assigned To Geothelphusa Miyazakii (Miyake & Chiu, 1965) (Crustacea: Decapoda: Potamidae), From Yaeyama Group, Southern Ryukyus, Japan
Fig. 4. Geothelphusa marginata fulva. a, carapace, dorsal view; b, carapace, frontal view; c, gonopod 1, ventral view; d, gonopod 1, dorsal view; e, gonopod 2. All figures indicate holotype (RUMF-ZC-62). Scales: a, b, 10 mm; c–e, 1 mm.
Fig. 3. Geothelphusa marginata marginata. a in A New Species Of The Freshwater Crab, Previously Assigned To Geothelphusa Miyazakii (Miyake & Chiu, 1965) (Crustacea: Decapoda: Potamidae), From Yaeyama Group, Southern Ryukyus, Japan
Fig. 3. Geothelphusa marginata marginata. a, carapace, dorsal view; b, carapace, frontal view; c, left mandible; d, maxilla; e, gonopod 1, ventral view; f, gonopod 1, dorsal view; g, gonopod 2. a, b, e-g, RUMF-ZC-59 (holotype); c, d, RUMF-ZC-87. Scales: a, b, 10 mm; c–g, 1 mm.
Fig. 1 in 1H, 13C, 15N Chemical Shift Assignments for Mesd12-155
Fig. 1. Pangerpeton sinensis gen. et sp. nov. A. Holotype specimen (IVPP V14244) from Wubaiding Village, Lingyuan City, Liaoning Province, China, probably contemporaneous with the salamander−bearing horizon at Daohugou, Inner Mongolia, Late Jurassic/Early Cretaceous, showing ventral impression of a nearly complete skeleton. B. High−fidelity cast of holotype showing skull, forelimbs and pectoral girdle. C. Line drawing of skull and atlas, taken from cast.
Fig. 2 in 1H, 13C, 15N Chemical Shift Assignments for Mesd12-155
Fig. 2. Fifty percent Majority Rule Consensus of 28 most parsimonious trees resulting from a phylogenetic analysis using PAUP* (see character description in http://spaces.msn.com/members/ywangivpp, and matrix of taxon and character states in Table 2).
Dataset related to the publication "Measurement and assignment of J = 5 to 9 rotational energy levels in the 9070-9370 cm-1 range of methane using optical frequency comb double-resonance spectroscopy"
<p>The files contain the normalized interleaved double-resonance spectra recorded with four different pump transitions, indicated in the file name. The first column is the wavenumber, the second column is the transmission intensity.</p>
Linked collectors and determiners for: Dyticodopoea And Pygmaeodopoea, New Genera For The Central American Cicada Species Previously Assigned To Odopoea Stål, 1861 (Hemiptera: Cicadoidea: Cicadidae: Cicadinae: Zammarini).
Natural history specimen data linked to collectors and determiners held within, "Dyticodopoea And Pygmaeodopoea, New Genera For The Central American Cicada Species Previously Assigned To Odopoea Stål, 1861 (Hemiptera: Cicadoidea: Cicadidae: Cicadinae: Zammarini)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/fe944f68-7821-4adb-a603-9397b2cb8b68">https://bionomia.net/dataset/fe944f68-7821-4adb-a603-9397b2cb8b68</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/fe944f68-7821-4adb-a603-9397b2cb8b68">https://gbif.org/dataset/fe944f68-7821-4adb-a603-9397b2cb8b68</a>. Formatted as a Frictionless Data package.
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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.