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666 results for “type locality”
Figure 5 in First record of Oligosarcus itau (Characiformes: Characidae) outside the type locality, and second after the description
Figure 5. La Ciénaga dam 24°25'50.10''S, 65°16'41.0''W. El Carmen Department, Jujuy Province.
Figure 4 in First record of Oligosarcus itau (Characiformes: Characidae) outside the type locality, and second after the description
Figure 4. Las Pavas River at 24º26'37.7''S, 65º13'01.3"W, El Carmen Department, Jujuy Province.
Figs. 21-22 in Rediscovery of Zubovskya morii (Bey-Bienko, 1931) (Orthoptera: Acrididae), the nearly forgotten endemic grasshopper in North Korea with revised checklist from its type locality, Mount Baekdusan
Figs. 21-22. Mount Baekdusan with caldera lake 'Cheonji' on the top (7 July, 2005).
Fig. 1. Geographic distribution of bogidiellid amphipods. Large map: type localities of: 1, Bogidiella veneris n. sp.; 2, Bogidomma australis; 3, Xystriogidiella capricornea; and 4, Xystriogidiella juliani on the Australian continent (with kind permission of demis.nl). Insert map: global distribution of Bogidiellidae and several, possibly closely related taxa (modified after Koenemann and Holsinger, 1999).
Fig. 1. Geographic distribution of bogidiellid amphipods. Large map: type localities of: 1, Bogidiella veneris n. sp.; 2, Bogidomma australis; 3, Xystriogidiella capricornea; and 4, Xystriogidiella juliani on the Australian continent (with kind permission of demis.nl). Insert map: global distribution of Bogidiellidae and several, possibly closely related taxa (modified after Koenemann and Holsinger, 1999).
Figure 7. Type locality. Santiago 15 in Two new species of plume moths (Lepidoptera: Pterophoridae) from Atacama Desert (Chile)
Figure 7. Type locality. Santiago 15 km ENE Camino a Farellones, 02.ii.2017 (photo by A. Pototski).
Figure 15. Type locality for Trichonotuloides aphoderrans n in Trichonotuloides aphoderrans, n.sp. (Coleoptera: Scarabaeidae: Aphodiinae), a new genus and species for the United States
Figure 15. Type locality for Trichonotuloides aphoderrans n. sp.
Fig. 2. Acanthocobitis pavonacea, NRM 40422, 96.6 in Type locality and synonymy of Paracanthocobitis marmorata and notes on Acanthocobitis (Teleostei: Nemacheilidae)
Fig. 2. Acanthocobitis pavonacea, NRM 40422, 96.6 mm; India: aquarium. (Photograph by M. Kottelat).
Figs 10–12 in Notes on the preimaginal stages and the type locality of Cissatsuma berezowskii Krupitsky, 2018 (Lepidoptera: Lycaenidae)
Figs 10–12. Adult, label and type locality. 10 – male of Cissatsuma berezowskii Krupitsky,
Figs 1–6 in Notes on the preimaginal stages and the type locality of Cissatsuma berezowskii Krupitsky, 2018 (Lepidoptera: Lycaenidae)
Figs 1–6. Development of Cissatsuma berezowskii Krupitsky, 2018. 1, 2 – last-instar
Local habitat type influences bumble bee pathogen loads and bee species distribution
<p>Bumble bees (<em>Bombus </em>spp.) perform important ecological services in both managed and natural ecosystems. Anthropogenically-induced change, however, has altered the availability of floral resources, climatic suitability, and exposure to insecticides, factors that impact overall health and disease levels in these bees. Habitat management presents a solution for improving bee health and biodiversity, but this requires better understanding of how different pathogens and bee species respond to habitat conditions. Herein, we take advantage of the washboard of repeated ridges (forested) and valleys (mostly unforested and developed) in central Pennsylvania to examine whether local variation in habitat type and other landscape factors influence bumble bee community composition and the levels of four leading pathogens in the common eastern bumble bee, <em>Bombus impatiens</em>. Loads of viral pathogens (deformed wing virus and black queen cell virus) were found to be lowest in forest habitats, whereas loads of a gut parasite, <em>Crithidia bombi</em>, were highest in forests. Ridgetop forests hosted the most diverse bumble bee communities, including several habitat specialists. <em>B. impatiens</em> was most abundant in valleys, and showed higher incidence in areas of greater disturbance, including more developed, unforested, and lower floral resource sites, a pattern that mirrors its success in the face of anthropogenic change. Additionally, DNA barcoding revealed that <em>B. sandersoni</em> is much more common than is apparent from databases, likely due to misidentification as mimics <em>B. perplexus</em> and <em>B. vagans</em>. Our results provide evidence that habitat type can play a large role in pathogen load dynamics, but in ways that differ by pathogen type, and point to a need for consideration of habitat at both macro-ecological and local spatial scale</p>
QL1706 Plus Neoadjuvant Chemotherapy Followed by Type I Hysterectomy for Locally Advanced Cervical Cancer
ClinicalTrials.gov study NCT07205497. IPD Sharing: YES. Countries: 1. Publications: 8.
A Study of Nimotuzumab Combinated With Gemcitabine in K-RAS Wild-type Locally Advanced and Metastatic Pancreatic Cancer
ClinicalTrials.gov study NCT02395016. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Irinotecan and Cetuximab With or Without Bevacizumab in Treating Patients With RAS Wild-Type Locally Advanced or Metastatic Colorectal Cancer That Cannot Be Removed by Surgery
ClinicalTrials.gov study NCT02292758. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Local habitat type influences bumble bee pathogen loads and bee species distribution
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Fruit-, seed- and seedling-related fitness traits after self-pollination and two types of cross-pollination in regionally and locally common and rare plant species
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Glucocorticoids link forest type to local abundance in tropical birds
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Distribution. Endemic to S India (Kolar district, Karnataka), known only from type locality. Previously also on nearby Therahalli, where now absent. in Family Hipposideridae (Old World Leaf-nosed Bats)
Distribution. Endemic to S India (Kolar district, Karnataka), known only from type locality. Previously also on nearby Therahalli, where now absent.
Distribution. Endemic to Madagascar, where it is just known from type locality and Androimpano Cave, near Itampolo, Toliara Province. in Hipposideridae
Distribution. Endemic to Madagascar, where it is just known from type locality and Androimpano Cave, near Itampolo, Toliara Province.
Subspecies and Distribution. R.f. frantisi Soisook et al, 2015 - known only from a few localities in N, SW & S Borneo. R.f. thailandicus Soisook & Bates, 2015 — known only from type locality in SW Thailand. Genetic data suggest that the species may also occur in Vietnam, but this requires more research. in Rhinolophidae
Subspecies and Distribution. R.f. frantisi Soisook et al, 2015 - known only from a few localities in N, SW & S Borneo. R.f. thailandicus Soisook & Bates, 2015 — known only from type locality in SW Thailand. Genetic data suggest that the species may also occur in Vietnam, but this requires more research.
FIGURE4.Map of selected records of Siphamia species recorded in Queensland and Papua New Guinea waters in 2003–2005, including the type locality of Siphamia guttulata. Some symbols represent more than one specimen. in Redescription and distributional range extension of the Speckled Siphonfish, Siphamia guttulata (Pisces: Apogonidae)
FIGURE4.Map of selected records of Siphamia species recorded in Queensland and Papua New Guinea waters in 2003–2005, including the type locality of Siphamia guttulata. Some symbols represent more than one specimen.
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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)
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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.