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52 results for “independent origins”

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zenodo44/100

A molecular taxonomy of tumors independent of tissue-of-origin

<p>This tarball contains the pre-processed data in .Rda files required to compile our manuscript entitled &quot;A molecular taxonomy of tumors independent of tissue-of-origin&quot;</p>

opencc-by-4.0Aug 2020View details →
zenodo40/100

Convergent loss of chemoreceptors across independent origins of slave-making in ants

<p>Manual annotations and sequence files of olfactory and gustatory receptors in eight species of ants (slave-making ants, hosts and non-host species) spanning 3 independent origins of slave-making. These manual annotations were investigated for patterns of convergent gain or loss in slave-making ants compared to their hosts and vice versa. We highlighted extensive losses of chemoreceptors in slave-making ants compared to hosts, indicating a loss in perception accompanying the transition to social parasitism, with some degree of convergent molecular evolution at the level of individual genes.</p> <p>For the full study, see doi:10.1093/molbev/msab305</p>

opencc-by-4.0Oct 2021View details →
zenodo40/100

Fig. 1 in Comparison Of Biting Midges Of The Early Eocene Cambay Amber (India) And Late Eocene European Ambers Supports The Independent Origin Of European Ambers

Fig. 1. Eohelea sp. with unique structure of wing organ from Rovno amber: 1 — dorsal view, 2 — ventral view.

opencc-by-4.0Aug 2017View details →
zenodo40/100

Phylogenomics illuminates the phylogeny of flower weevils (Curculioninae) and reveals ten independent origins of brood-site pollination mutualism in true weevils

<p><strong>Phylogenomics illuminates the phylogeny of flower weevils (Curculioninae) and reveals ten independent origins of brood-site pollination mutualism in true weevils (142 /150 characters)</strong></p> <p>Haran J.<sup>1*</sup>, Li X.<sup>2,3,4*</sup>, Allio R.<sup>5*</sup>, Shin S.<sup>3,4,6</sup>, Benoit L.<sup>1</sup>, Oberprieler R.G.<sup>7</sup>, Farrell B.D.<sup>8</sup>, Brown S.D.J.<sup>9</sup>, Leschen R.A.B.<sup>10</sup>, Kergoat G.J.<sup>5</sup> &amp; McKenna D.D.<sup>3,4</sup></p> <p>* Equal contribution</p> <p>&nbsp;</p> <p><strong>Affiliations</strong></p> <p><sup>1</sup> CBGP, CIRAD, INRAE, IRD, Institut Agro, Univ. Montpellier, Montpellier, France. ORCID: 0000-0001-9458-3785 (JH); 0000-0003-3740-5346 (LB)</p> <p><sup>2</sup> Department of Entomology, College of Plant Protection, China Agricultural University, Beijing 100193, China. ORCID: 0000-0002-0622-2064 (XL)</p> <p><sup>3</sup> Department of Biological Sciences, University of Memphis, Memphis, TN 38152 ORCID: 0000-0002-7823-8727 (DDM)</p> <p><sup>4</sup> Center for Biodiversity Research, University of Memphis, Memphis, TN 38152</p> <p><sup>5</sup> CBGP, INRAE, IRD, CIRAD, Institut Agro, Univ. Montpellier, Montpellier, France. ORCID: 000-0003-3885-5410 (RA); 0000-0002-8284-6215 (GJK)</p> <p><sup>6</sup> School of Biological Sciences, Seoul National University, Seoul 08826, Republic of Korea.</p> <p>ORCID: 0000-0002-4258-8661 (SS)</p> <p><sup>7</sup> CSIRO, Australian National Insect Collection, GPO Box 1700, Canberra, ACT 2601, Australia. ORCID: 0000-0002-1837-580X (RGO)</p> <p><sup>8</sup> Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, USA. ORCID: 0000-0002-6843-0539 (BDF)</p> <p><sup>9</sup> Bio-Protection Research Centre, P.O. Box 85084, Lincoln University, Lincoln 7647, New Zealand. Current address: The New Zealand Institute for Plant and Food Research, Mount Albert Research Centre, Private Bag 92169, Auckland 1142, New Zealand. ORCID: 0000-0001-7112-421X (SDJB)</p> <p><sup>10</sup> Manaaki Whenua - Landcare Research, PB 92170, Auckland, New Zealand. ORCID: 0000-0001-8549-8933 (RABL)</p> <p>&nbsp;</p> <p><strong>Abstract</strong></p> <p>Weevils are an unusually species-rich group of phytophagous insects, for which there is increasing evidence of frequent involvement in brood-site pollination. This study examines phylogenetic patterns in the emergence of brood-site pollination mutualism among one of the most speciose beetle groups, the flower weevils (subfamily Curculioninae). We analyzed a novel phylogenomic dataset consisting of 214 nuclear loci for 202 weevil species, with a sampling that mainly includes flower weevils as well as representatives of all major lineages of true weevils (Curculionidae). Our phylogenomic analyses establish a uniquely comprehensive phylogenetic framework for Curculioninae and provide new insights into the relationships among lineages of true weevils. Based on this phylogeny, statistical reconstruction of ancestral character states revealed at least ten independent origins of brood-site pollination in higher weevils through transitions from ancestral associations with reproductive structures in the larval stage. Broadly, our results illuminate the unexpected frequency with which true weevils &mdash; typically specialized phytophages and hence antagonists of plants &mdash; have evolved mutualistic interactions of ecological significance that are key to both weevil and plant evolutionary fitness and thus a component of their deeply intertwined macroevolutionary success.</p> <p>&nbsp;</p> <p><strong><em>Figures&nbsp;</em></strong></p> <p><strong>Figure 1&nbsp;(part I).</strong> Maximum-likelihood tree resulting from analyses of 214 nuclear protein-coding genes (focus on the CEGH clade and outgroups). Support at node refers to SH-aLRT values &ge; 80% and uBV &ge; 95% (**). Single * refer to SH-aLRT values &ge; 80% only. Clades with black branches and highlighted in blue are classified in Curculioninae sensu Caldara et al. (2014). Taxa displayed on the left: 1 - Hypsomus sp. (Styphlini); 2 - Myllorhinus sp. (Storeini s. lat.); 3 - Encosmia sp. (Storeini s. lat.).</p> <p><strong>Figure 1&nbsp;(part II).</strong> Maximum-likelihood tree resulting from analyses of 214 nuclear protein-coding genes (focus on the CCCMS clade). Node support values refer to SH-aLRT values &ge; 80% and uBV &ge; 95% (**). Single * refer to SH-aLRT values &ge; 80% only. Clades with black branches and highlighted in blue are classified in Curculioninae sensu Caldara et al., (2014). Clades highlighted in darker blue contain genera engaged in brood-site pollination mutualism and the corresponding genera are highlighted in orange (higher taxonomic rank when specific genera are not included in the tree). Other lineages of the CCCMS clade are in bold font. Taxa displayed on the right: 1 - Tychius sp. (Tychiini); 2 - Anthonomus sp. (Athonomini); 3 - Tachyerges sp. (Rhamphini); 4 - Derelomus sp. (Derelomini); 5 - Cionus sp. (Cionini); 6 - Daeneus sp. (Ochyromerini); 7 - Meriphus sp. (Eugnomini); 8 - Archarius sp. (Curculionini); 9 - Dorytomus sp. (Ellescini); 10 - Cleopomiarus sp. (Mecinini).</p> <p><strong>Figure 2.</strong>&nbsp;Results of the ASE analysis of larval tissue specialization carried out on the CCCMS clade, with an ER model and using a continuous-time reversible Markov model with 1000 simulations. In addition, red arrows are used to underline the independent origins of brood-site mutualism inferred in another ASE analysis (see Fig. S4). Two clades including brood-site pollinator genera that were not sampled in our study are also highlighted using red rectangles.</p> <p>&nbsp;</p> <p><strong><em>Additional files</em></strong></p> <p><strong>Figure&nbsp;S1</strong>. Full ML tree with support values.</p> <p><strong>Figure&nbsp;S2</strong>.&nbsp;Support for ML analyses.</p> <p><strong>Figure S3</strong>.&nbsp;Results of the ASE analysis of the evolution of the tissue specialization by weevil larvae in the CCCMS clade, with an ER model and using a continuous time-reversible Markov model with 1000 simulations.&nbsp;</p> <p><strong>Figure S4</strong>.&nbsp;Results of the ASE analysis on the evolution of brood-site pollination in the CCCMS clade, with an ER model and using a continuous time-reversible Markov model with 1000 simulations.</p> <p>&nbsp;</p> <p><strong><em>Zenodo supplementary files</em></strong></p> <p><strong>AHE_pipeline.txt </strong>shows&nbsp;the detailed step-by-step script used to generate the phylogeny obtained in this study&nbsp;from raw sequencing data.</p> <p><strong>ASE Analyses.zip</strong> contains the script and the associated raw results of the ASE analyses.</p> <p><strong>Cole_tcas_probes.fasta</strong>&nbsp;contains the Coleopteran probes used.</p> <p><strong>IBA results.zip</strong> contains IBA results.</p> <p><strong>IQ-TREE files.zip</strong> contains input and output files of the IQ-TREE analysis.</p> <p><strong>Scripts.zip</strong> contains the scripts associated with the file AHE_pipeline.txt.</p> <p>&nbsp;</p>

opencc-by-4.0Apr 2023View details →
dryad36/100

The origins of coca: museum genomics reveals multiple independent domestications from progenitor Erythroxylum gracilipes

<p>Coca is the natural source of cocaine as well as a sacred and medicinal plant farmed by South American Amerindians and mestizos. The coca crop comprises four closely related varieties classified into two species (Amazonian and Huánuco varieties<i> </i>within <i>Erythroxylum coca</i> Lam., and Colombian and Trujillo varieties within<i> E. novogranatense </i>(D.Morris) Hieron.) but our understanding of their wild progenitor(s) and origins remains rudimentary. In this study we use genomic data from natural history collections to estimate the geographic origins and genetic diversity of this economically and culturally important crop in the context of its wild relatives. Our phylogeographic analyses clearly demonstrate the four varieties of coca comprise two or three exclusive groups nested within the diverse lineages of the widespread, wild species <i>E. gracilipes</i>; establishing a new and robust hypothesis of domestication wherein coca originated two or three times from this wild progenitor. The Colombian and Trujillo coca varieties are descended from a single, ancient domestication event in northwestern South America. Huánuco coca was domesticated more recently, possibly in southeastern Peru. Amazonian coca either shares a common domesticated ancestor with Huánuco coca, or it was the product of a third and most recent independent domestication event in the western Amazon basin. This chronology of coca domestication reveals different Holocene peoples in South America were able to independently transform the same natural resource to serve their needs; in this case, a workaday stimulant.</p>

opencc-zeroSep 2020View details →
dryad36/100

Different molecular changes underlie the same phenotypic transition: Origins and consequences of independent shifts to homostyly within species

<p>The repeated transition from outcrossing to selfing is a key topic in evolutionary biology. However, the molecular basis of such shifts has been rarely examined due to lack of knowledge of the genes controlling these transitions. A classic example of mating system transition is the repeated shift from heterostyly to homostyly. Occurring in 28 angiosperm families, heterostyly is characterized by the reciprocal position of male and female sexual organs in two (or three) distinct, usually self-incompatible floral morphs. Conversely, homostyly is characterized by a single, self-compatible floral morph with reduced separation of male and female organs, facilitating selfing. Here, we investigate the origins of homostyly in <i>Primula vulgaris </i>and its microevolutionary consequences by integrating surveys of the frequency of homostyles in natural populations, DNA sequence analyses of the gene controlling the position of female sexual organs (<i>CYPᵀ</i>), and microsatellite genotyping of both progeny arrays and natural populations characterized by varying frequencies of homostyles. As expected, we found that homostyles displace short-styled individuals, but long-style morphs are maintained at low frequencies within populations. We also demonstrated that homostyles repeatedly evolved from short-styled individuals in association with different types of loss-of-function mutations in <i>CYPᵀ</i>. Additionally, homostyly triggers a shift to selfing, promoting increased inbreeding within and genetic differentiation among populations. Our results elucidate the causes and consequences of repeated transitions to homostyly within species, and the putative mechanisms precluding its fixation in <i>P. vulgaris</i>. This study represents a benchmark for future analyses of losses of heterostyly in other angiosperms.</p>

opencc-zeroDec 2021View details →
dryad36/100

The origins of coca: museum genomics reveals multiple independent domestications from progenitor Erythroxylum gracilipes

Open the record for dataset details and reuse information.

publicOct 2020View details →
dryad36/100

Different molecular changes underlie the same phenotypic transition: Origins and consequences of independent shifts to homostyly within species

Open the record for dataset details and reuse information.

publicDec 2021View details →
dryad32/100

Data from: Genetic analysis of the peatmoss Sphagnum cribrosum (Sphagnaceae) indicates independent origins of an extreme infra-specific morphology shift

Within Sphagnum cribrosum, a dioicous aquatic peatmoss, a unique morphological variant (the "waveform"), found at only two lakes in North Carolina, has a branching architecture that is extremely differentiated from anything otherwise known in Sphagnum, though the plants are microscopically indistinguishable from S. cribrosum. At one site where the two morphologies co-occur, sixty years of field observations demonstrate the persistence of each morphology, even where the two forms grow intermixed. We conducted a reciprocal transplant experiment in which waveform and normal plants maintained their divergent morphologies for eight months. We sampled populations throughout the range and conducted genetic and phylogenetic analyses with microsatellite markers and DNA sequences to investigate the genetic context of the waveform morphology within S. cribrosum. Haplotype networks from DNA sequences showed the two waveform populations are separated by 11 substitutions across three loci. Microsatellite analyses using non-parametric clustering and admixture models also indicated genetic dissimilarity between genotypes with waveform morphology at the two lakes. Both molecular datasets suggest that the waveform morphology had at least two independent origins despite proximity of the two lakes where it uniquely occurs. Given the clonal nature of the waveform, it is unlikely to form a cohesive evolutionary lineage deserving of taxonomic status. The analysis also revealed a genetically diverse population in Georgia as the potential source of variation found in all other populations of S. cribrosum.

opencc-zeroDec 2011View details →
dryad32/100

Data from: Genetic structure reveals a history of multiple independent origins followed by admixture in the allopolyploid weed Salsola ryanii

It has recently become clear that many invasive species have evolved in situ via hybridization or polyploidy from progenitors which themselves are introduced species. For species formed by hybridization or polyploidy, genetic diversity within the newly formed species is influenced by the number of independent evolutionary origins of the species. For recently formed species, an analysis of genetic structure can provide insight into the number of independent origin events involved in the formation of the species. For a putative invasive allopolyploid species, the number of origins involved in the species formation, the genetic diversity present within these origins, and the level of gene flow between independent origins determines the genetic composition of the neospecies. Here we analyze the genetic structure of the newly formed allopolyploid species, Salsola ryanii, a tumbleweed which evolved within the last 20–100 years in California. We utilize the genetic structure analysis to determine that this new species is the result of at least three independent allopolyplodization events followed by gene flow between the descendants of independent origins.

opencc-zeroDec 2015View details →
dryad32/100

Data from: Unraveling independent origins of two tetraploid Achillea species by amplicon sequencing

<p>Allopolyploidy is a significant mechanism of plant speciation, and many allopolyploid species have arisen recurrently. However, the probability that allopolyploidization between the same two parental species may lead to the origin of different taxa has received little attention. Here we used a new progenitor-specific amplicon sequencing method to demonstrate the independent origins of two yarrow species, <i>Achillea alpina</i> and <i>A. wilsoniana</i>, via allotetraploidy from the same diploid progenitor species pair, <i>A. acuminata</i> and <i>A. asiatica</i>. Based on the sequences of 17 nuclear genes from 21 wild populations of the four <i>Achillea </i>species investigated, a clear view of  genetic structure and demographic history was obtained with each species. Significant genetic differentiation was evident between the two tetraploid species. Two genetically distinguishable groups were detected within one of the progenitor, <i>A. acuminata</i>, and ancestors belonging to those two groups contributed to the two tetraploid species, respectively. Excluding fixed heterozygosity, we detected extremely low genetic diversity in many populations of both tetraploid species. Approximate Bayesian computation indicated that both tetraploid species originated before the Last Glacial Maximum, and nearly all diploid lineages went through population declines after the allopolyploidization events. Our study demonstrates that independent allopolyploidization events between the same <i>Achillea</i> parental species have generated two genetically and ecologically distinct taxa.</p>

opencc-zeroOct 2019View details →
dryad32/100

Data from: Tempo and mode of performance evolution across multiple independent origins of adhesive toe pads in lizards

Understanding macroevolutionary dynamics of trait evolution is an important endeavor in evolutionary biology. Ecological opportunity can liberate a trait as it diversifies through trait space, while genetic and selective constraints can limit diversification. While many studies have examined the dynamics of morphological traits, diverse morphological traits may yield the same or similar performance and as performance is often more proximately the target of selection, examining only morphology may give an incomplete understanding of evolutionary dynamics. Here we ask whether convergent evolution of pad-bearing lizards have followed similar evolutionary dynamics, or whether independent origins are accompanied by unique constraints and selective pressures over macroevolutionary time. We hypothesized that geckos and anoles each have unique evolutionary tempos and modes. Using performance data from 59 species, we modified Brownian Motion (BM) and Ornstein-Uhlenbeck (OU) models to account for repeated origins estimated using Bayesian ancestral state reconstructions. We discovered that adhesive performance in geckos evolved in a fashion consistent with Brownian Motion with a trend, whereas anoles evolved in bounded performance space consistent with more constrained evolution (an Ornstein-Uhlenbeck model). Our results suggest that convergent phenotypes can have quite distinctive evolutionary patterns, likely as a result of idiosyncratic constraints or ecological opportunities.

opencc-zeroDec 2016View details →
zenodo32/100

Fig. 3 in Phylogenetic evidence for multiple independent origins of functional kleptoplasty in Sacoglossa (Heterobranchia, Gastropoda)

Fig. 3 Phylogeny of the Sacoglossa based on Bayesian analysis (50 % majority rule consensus tree). Numbers at nodes indicate Posterior Probability (PP), black circles indicate PP=100, and black asterisks indicate PP=95–99. The inner dark gray circle borders functional-retention information of taxa, the outer food sources (displayed are only three major food sources per species). The scale bar displays substitutions per site. Yellow highlighted is the "outgroup", pink the Oxynoacea, purple the Platyhedylidae, green the " Limapontioidea ", and blue the

opennotspecifiedDec 2014View details →
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Fig. 2 in Phylogenetic evidence for multiple independent origins of functional kleptoplasty in Sacoglossa (Heterobranchia, Gastropoda)

Fig. 2 Maximum quantum yield measurements (Fv/Fm) of Elysia clarki. Specimens of E. clarki were either starved under 40 μmol quanta m−2 s−1 (diamonds) or in complete darkness (rectangles) over a period of 49 days. Error bars indicate standard deviation between different specimens for each measuring point. Because specimens were fixed at certain intervals, finally only one individual was left at day 49

opennotspecifiedDec 2014View details →
dryad32/100

Phylotranscriptomics points to multiple independent origins of multicellularity and cellular differentiation in the volvocine algae

<p class="western">The volvocine algae, which include the single-celled species <i>Chlamydomonas reinhardtii</i> and the colonial species <i>Volvox carteri</i>, serve as a model in which to study the evolution of multicellularity and cellular differentiation. Studies reconstructing the history of this group have by and large relied on datasets of one to a few genes for phylogenetic inference and ancestral character state reconstruction. As a result, volvocine phylogenies lack concordance depending on the number and/or type of genes (i.e., chloroplast vs nuclear) chosen for phylogenetic inference. While multiple studies suggest that multicellularity evolved only once in the volvocine algae, that each of its three colonial families is monophyletic, and that there have been at least three independent origins of cellular differentiation in the group, other studies call into question one or more of these conclusions. An accurate assessment of the evolutionary history of the volvocine algae requires inference of a more robust phylogeny. We performed RNA sequencing (RNA-seq) on 55 strains representing 47 volvocine algal species and obtained similar data from curated databases on 13 additional strains. We then compiled a dataset consisting of transcripts for 40 single-copy, protein-coding, nuclear genes, and subjected the predicted amino acid sequences of these genes to maximum likelihood, Bayesian inference, and coalescent-based analyses. These analyses show that multicellularity independently evolved at least twice in the volvocine algae and that the colonial family Goniaceae is not monophyletic. Our data further indicate that cellular differentiation arose independently at least four, and possibly as many as six times, within the volvocine algae. Altogether, our results demonstrate that multicellularity and cellular differentiation are evolutionarily labile in the volvocine algae, affirming the importance of this group as a model system for the study of major transitions in the history of life.</p>

opencc-zeroDec 2020View details →
zenodo32/100

FIGURES 46–51. Notophlebia jobi. 46–49 in New Oriental tribe Iscini, new non-dilatognathan species of Notophlebia Peters & Edmunds 1970 and independent origin of Dilatognathus-type mouth apparatus in Atalophlebiinae (Ephemeroptera: Leptophlebiidae)

FIGURES 46–51. Notophlebia jobi. 46–49, third segment of maxillary palp (46 and 48, ventral side; 47 and 49, dorsal side); 50–51, base of third segment of labial palp, dorsal side).

opennotspecifiedFeb 2014View details →
zenodo32/100

FIGURES 31–45. 31–38 in New Oriental tribe Iscini, new non-dilatognathan species of Notophlebia Peters & Edmunds 1970 and independent origin of Dilatognathus-type mouth apparatus in Atalophlebiinae (Ephemeroptera: Leptophlebiidae)

FIGURES 31–45. 31–38, Notophlebia ganeshi sp. n.; 39–45, Notophlebia jobi. 31–34 and 40–43, tergalii of I, II, V and VI pairs (ventral lamella turned back); 35, claw; 36 and 44, pronotum and mesonotum of last instar larva; 37 and 45, posterior margin of abdominal sternum IX of mature male larva and protopenis, dorsal view (gonoducts lined by cuticle shown by interrupted lines); 38 and 39, posterior margin of larval abdominal tergum VI (37, 38, holotype).

opennotspecifiedFeb 2014View details →
zenodo32/100

FIGURES 52–54. Notophlebia jobi. 52 in New Oriental tribe Iscini, new non-dilatognathan species of Notophlebia Peters & Edmunds 1970 and independent origin of Dilatognathus-type mouth apparatus in Atalophlebiinae (Ephemeroptera: Leptophlebiidae)

FIGURES 52–54. Notophlebia jobi. 52, distal part of larval fore tibia, posterior side; 53, the same, anterior side; 54, distal part of larval middle tibia, anterior side. Abbreviations: a, row of stout setae on anterior side; h, hair-like setae on outer side; p, row of stout setae on posterior side.

opennotspecifiedFeb 2014View details →
zenodo32/100

FIGURES 11–20 in New Oriental tribe Iscini, new non-dilatognathan species of Notophlebia Peters & Edmunds 1970 and independent origin of Dilatognathus-type mouth apparatus in Atalophlebiinae (Ephemeroptera: Leptophlebiidae)

FIGURES 11–20. Notophlebia ganeshi sp. n. 11, male imaginal mesonotum; 12, male subimaginal exuviae of right half of mesonotum. 13–19, legs at the same magnification (arrows show ontogenesis): 13, fore leg of male imago; 14, fore leg of male larva (long hair-like setae not shown); 15–17, fore, middle and hind legs of male subimago; 18, hind leg of male imago; 19, fore leg of female imago. 20, tarsus of larval hind leg before molt to subimago (larval cuticle shown as optic section by black; subimaginal cuticle shown by integral lines; imaginal claw developing under subimaginal cuticle shown by interrupted lines). 21, posterior margin of abdominal sternum IX of mature female larva; 22, the same, of female imago (12–18, holotype). Abbreviations: LPs, lateroparapsidal suture; MNS, mesonotal suture; MPs, medioparapsidal suture.

opennotspecifiedFeb 2014View details →
zenodo32/100

FIGURES 4–10 in New Oriental tribe Iscini, new non-dilatognathan species of Notophlebia Peters & Edmunds 1970 and independent origin of Dilatognathus-type mouth apparatus in Atalophlebiinae (Ephemeroptera: Leptophlebiidae)

FIGURES 4–10. Notophlebia ganeshi sp. n. Larval mouthparts (at the same magnification, except 6). 4, hypopharynx and superlinguae; 5, labrum (setae of distal transverse row not shown, their bases shown as dots and levels of their apices shown by dotted line); 6, apex of maxilla, ventral view; 7, maxilla, ventral view (apical and median setae not shown, their apices shown by dotted lines); 8, labium (dorsal view at left, ventral view at right); 9, apex of labial palp, dorsal view; 10, left mandible (5, 10, holotype).

opennotspecifiedFeb 2014View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record