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379 results for “species number”
Recurrent speciation rates on islands decline with species number
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Data from: The relationship between native species richness and exotic species richness or occurrence will always be negative when the total number of species is accounted for in statistical models: A response to Beaury et al.
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Data from: Genetic divergence and the number of hybridizing species affect the path to homoploid hybrid speciation
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Data from: Effective number of breeders, effective population size and their relationship with census size in an iteroparous species, Salvelinus fontinalis
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Numbers of sperm associated with the perivitelline layer of seabird (and other bird species) eggs
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Palm-primate interactions: Number of palm species and palm species identity in primate diets according to region (Africa, Asia, Madagascar, Neotropics); Parts of palm species consumed by primates according to region; palm species of high importance in primate diets according to region; palm seed dispersal by primates according to region
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Large numbers of putative miRNAs originate from DNA transposons and are coincident with a large species radiation in bats.
GEO Series GSE47593. Eptesicus fuscus; Canis lupus familiaris; Equus caballus. 4 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Copy number variation of genes (exons) in invasive Cottus compared to the parental species, Cottus rhenanus and Cottus perifretum.
GEO Series GSE93064. Cottus perifretum; Cottus rhenanus; Cottus. 24 samples. Type: Genome variation profiling by array.
Across-species comprehensive copy number analyses identifies subtype-specific drivers of breast cancer development
GEO Series GSE52173. Mus musculus; Homo sapiens. 201 samples. Type: Genome variation profiling by SNP array.
Number of seeds recorded from the feces of different species of mammals during the study
<p><span>Senna spectabilis, a native tree of tropical America is rapidly colonizing the forests of Western Ghats. We identified the Asian elephant (Elephas maximus) as the major disperser of Senna, with the dung facilitating germination of the species. The study provides critical information for the management of Senna in tropical Asia, elephants</span>, Western Ghats, <span>Senna spectabilis, and </span>seed dispersal.</p>
Fig. 10 in Extant diversity and estimated number of Gracillariidae (Lepidoptera) species yet to be discovered in the Neotropical region
Fig. 10. Annual variation in number of gracillariid species described for the Neotropical region.
Figure 2 from: Del Latte L, Bortolin F, Rota-Stabelli O, Fusco G, Bonato L (2015) Molecular-based estimate of species number, phylogenetic relationships and divergence times for the genus Stenotaenia (Chilopoda, Geophilomorpha) in the Italian region. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 31-47. https://doi.org/10.3897/zookeys.510.8808
Figure 2 - Frequency distribution of COI pairwise distances. A K2P distances. B p-distances.
Data from: Intraspecific variations in life history traits of two pecky rice bug species from Japan: mapping emergence dates and number of annual generations
<p>The mirid bugs Stenotus rubrovittatus and Trigonotylus caelestialium, which cause pecky rice, have become a threat to rice cultivation in Asia. Damage caused by these pests has rapidly become frequent since around 2000 in Japan. Their expansion pattern is not simple, and predicting their future spread remains challenging. Some insects with wide ranges have locally adapted variations in life-history traits. We performed laboratory rearing experiments to assess the geographical scale of intraspecific variations in life-history traits of S. rubrovittatus and T. caelestialium. The experiments were aimed at increasing the accuracy of occurrence estimates and the number of generations per year. These results were compared with previous research, and differences in development rates were observed between populations of different latitudes, but not of the same latitude. Finally, plotting the timing of adult emergence and the potential number of generations per year on maps with a 5-km grid revealed that they differed greatly locally at the same latitude. These maps can be used for developing more efficient methods of managing mirid bugs in integrated pest management.</p>
Copy Number Variation across 12 tribes of African cichlid species
GEO Series GSE117914. Cyathopharynx furcifer; Oreochromis alcalicus; Pseudocrenilabrus multicolor victoriae; Cyprichromis leptosoma; Labeotropheus fuelleborni; Oreochromis ndalalani; Astatotilapia flaviijosephi; Xenotilapia spiloptera; Julidochromis ornatus; Rhamphochromis longiceps; Coptodon fusiforme; Coptodon kottae; Sarotherodon lamprechti; Lobochilotes labiata; Sarotherodon galilaeus; Tropheus moorii; Haplochromis burtoni; Ophthalmotilapia ventralis; Boulengerochromis microlepis; Neolamprologus brichardi; Eretmodus cyanostictus; Hemichromis fasciatus; Stomatepia mariae; Copadichromis virginalis; Diplotaxodon greenwoodi; Pallidochromis tokolosh; Konia eisentrauti; Benthodesmus elongatus; Coptodon zillii; Cyphotilapia frontosa; Lepidiolamprologus elongatus; Sarotherodon melanotheron; Oreochromis grahami; Pungu maclareni; Nyassachromis microcephalus; Tropheops sp. 'red cheek'; Haplochromis thereuterion; Coptodon deckerti; Oreochromis niloticus; Astatotilapia calliptera; Callochromis
Data from: Intraspecific variations in life history traits of two pecky rice bug species from Japan: mapping emergence dates and number of annual generations
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Number of seeds recorded from the feces of different species of mammals during the study
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microRNA-196 regulates vertebral number and identity across species
GEO Series GSE53018. Mus musculus. 44 samples. Type: Expression profiling by high throughput sequencing.
APPENDIX Individuals included in the genetic and/or skull morphology analyses are presented with source and locality information (reference to sites in Fig. 1 are given in parentheses when available). Voucher numbers are provided for individuals that were collected: AMNH — American Museum of Natural History, New York, NY, USA, BMNH — Natural History Museum, London, UK, FMNH — Field Museum, Chicago, IL, USA, HZM — Harrison Zoological Museum, Kent, UK, MCZ — Museum of Comparative Zoology, Harvard, MA, USA, MZB — Muzeum Zoologicum Bogoriense, Bogor, Indonesia, RMNH — National Museum of Natural History Naturalis, Leiden, Netherlands, SEN — Senckenberg Museum, Frankfurt, Germany, TK — tissue collection and TTU — specimen numbers; Texas Tech. University, Lubbock, TX, USA, and USNM — Smithsonian Institute, Washington D.C., USA. All specimens from peninsular Malaysia with THK or MBCRU field numbers were collected by A. Zubaid, and the specimens or duplicate wing punches were deposited at UKM (Universiti Kebangsaan Malaysia, Bangi, Selangor, Malaysia). The original taxonomy of type specimens (type) are listed. Haplotypes (Hap) are given for individuals of H. bicolor (=H. bicolor-131) and H. kunzi (=H. bicolor-142). GenBank accession numbers are given for one representative of each unique haplotype in A new species in the Hipposideros bicolor group (Chiroptera: Hipposideridae) from Peninsular Malaysia
APPENDIX Individuals included in the genetic and/or skull morphology analyses are presented with source and locality information (reference to sites in Fig. 1 are given in parentheses when available). Voucher numbers are provided for individuals that were collected: AMNH — American Museum of Natural History, New York, NY, USA, BMNH — Natural History Museum, London, UK, FMNH — Field Museum, Chicago, IL, USA, HZM — Harrison Zoological Museum, Kent, UK, MCZ — Museum of Comparative Zoology, Harvard, MA, USA, MZB — Muzeum Zoologicum Bogoriense, Bogor, Indonesia, RMNH — National Museum of Natural History Naturalis, Leiden, Netherlands, SEN — Senckenberg Museum, Frankfurt, Germany, TK — tissue collection and TTU — specimen numbers; Texas Tech. University, Lubbock, TX, USA, and USNM — Smithsonian Institute, Washington D.C., USA. All specimens from peninsular Malaysia with THK or MBCRU field numbers were collected by A. Zubaid, and the specimens or duplicate wing punches were deposited at UKM (Universiti Kebangsaan Malaysia, Bangi, Selangor, Malaysia). The original taxonomy of type specimens (type) are listed. Haplotypes (Hap) are given for individuals of H. bicolor (=H. bicolor-131) and H. kunzi (=H. bicolor-142). GenBank accession numbers are given for one representative of each unique haplotype
List of specimens, species codes, localities (NI, Northern Iberia; CI, Central Iberia; SI, Southern Iberia; AU, Austria; BL, Bulgaria; CR, Croatia; CZ, Czech Republic; DK, Denmark; FR, France; GE, Germany; GR, Greece; HN, Hungary; SD, Sweden; SW, Switzerland; TK, Turkey), haplotypes codes for species and GenBank accession numbers of the samples used for an overall molecular screening of bat cryptic diversity in Iberia using a mtDNA cytb fragment in The Iberian contribution to cryptic diversity in European bats
List of specimens, species codes, localities (NI, Northern Iberia; CI, Central Iberia; SI, Southern Iberia; AU, Austria; BL, Bulgaria; CR, Croatia; CZ, Czech Republic; DK, Denmark; FR, France; GE, Germany; GR, Greece; HN, Hungary; SD, Sweden; SW, Switzerland; TK, Turkey), haplotypes codes for species and GenBank accession numbers of the samples used for an overall molecular screening of bat cryptic diversity in Iberia using a mtDNA cytb fragment
FIGURE. Phylogenetic tree derived from Bayesian analysis, based on nrITS1-5.8S-ITS2 region data. Posterior probability (PP> 0.95) values from the Bayesian analysis are added at the nodes. The scale bar represents the number of nucleotide changes per site. (T) indicates the type specimen for this species. The new species are in bold. in Four new species of Entoloma (Entolomataceae, Agaricomycetes) subgenera Cyanula and Claudopus from Vietnam and their phylogenetic position
FIGURE. Phylogenetic tree derived from Bayesian analysis, based on nrITS1-5.8S-ITS2 region data. Posterior probability (PP> 0.95) values from the Bayesian analysis are added at the nodes. The scale bar represents the number of nucleotide changes per site. (T) indicates the type specimen for this species. The new species are in bold.
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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.