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135 results for “natural world”
TYPES: Male holotype from Panama: Panama: Parque Nacional Altos de Campana, 1 hectare PANCODING Inventory, 895 m, 8.68333°, -79.92972°, June 14–19, 2007, M. Arnedo, D. Dimitrov, G. Hormiga, F. Labarque, M. Ramírez, deposited in MIUP, PBI_OON 42313; same data, 1 male paratype deposited in MACN-Ar 29895, PBI_OON 42312. ETYMOLOGY: A noun in apposition; in Greek religion and mythology, Pan is the god of the wild natural world, of shepherds, flocks, and mountains, and of hunting and rustic music. He has hindquarters, legs, and horns of a goat, and the name is here employed to note the large mac- rosetae at the eye region of males that resemble the horns in some illustrations of this god. DIAGNOSIS: This is one of the most autapomor- phic species from the Americas; males have the labium fused with the sternum (fig. 34B), small chelicerae, shorter than the endite length, with anterior blunt projections, and directed backward in lateral view (fig. 34D, E); clypeus directed back- ward (fig. 34D); two light areas on the sternum just below the endites (fig. 34B), carapace almost flat in lateral view and two strong macrosetae at the eye region, pointing forward (fig. 34C–E). Other characters of the male palp, such as the presence of two apophyses, also distinguish this species from others (fig. 38D–F). MALE (PBI_OON 42312): Total length 1.00. Habitus as in figure 34A–C. CEPHALOTHO- RAX: Carapace orange, with brown stripe along in Taxonomic Revision Of The Jumping Goblin Spiders Of The Genus Orchestina Simon, 1882, In The Americas (Araneae: Oonopidae)
TYPES: Male holotype from Panama: Panama: Parque Nacional Altos de Campana, 1 hectare PANCODING Inventory, 895 m, 8.68333°, -79.92972°, June 14–19, 2007, M. Arnedo, D. Dimitrov, G. Hormiga, F. Labarque, M. Ramírez, deposited in MIUP, PBI_OON 42313; same data, 1 male paratype deposited in MACN-Ar 29895, PBI_OON 42312. ETYMOLOGY: A noun in apposition; in Greek religion and mythology, Pan is the god of the wild natural world, of shepherds, flocks, and mountains, and of hunting and rustic music. He has hindquarters, legs, and horns of a goat, and the name is here employed to note the large mac- rosetae at the eye region of males that resemble the horns in some illustrations of this god. DIAGNOSIS: This is one of the most autapomor- phic species from the Americas; males have the labium fused with the sternum (fig. 34B), small chelicerae, shorter than the endite length, with anterior blunt projections, and directed backward in lateral view (fig. 34D, E); clypeus directed back- ward (fig. 34D); two light areas on the sternum just below the endites (fig. 34B), carapace almost flat in lateral view and two strong macrosetae at the eye region, pointing forward (fig. 34C–E). Other characters of the male palp, such as the presence of two apophyses, also distinguish this species from others (fig. 38D–F). MALE (PBI_OON 42312): Total length 1.00. Habitus as in figure 34A–C. CEPHALOTHO- RAX: Carapace orange, with brown stripe along
Figs 36-39 in Classification, Natural History, and Evolution of the Enopliinae GISTEL (Coleoptera Cleridae). Part IV. The New World genus Pyticara SPINOLA
Figs 36-39: Photographs of Pyticara and Chrysomelidae species. (36) P. lineatohumeralis. (37) P. simoata. (38) P. duponti. (39) Chrysomelidae: Monocesta depressa.
Figs 21-26 in Classification, Natural History, and Evolution of the Enopliinae GISTEL (Coleoptera Cleridae). Part IV. The New World genus Pyticara SPINOLA
Figs 21-26: Morphological organs of Pyticara championi GORHAM. 21-22 Heads. (21) Frontal view. (22) Ventral view. 23-25 Antennae. (23) Funicle. (24) Ninth antennomere. (25) Entire antenna. (26) Front leg.
Figs 27-30 in Classification, Natural History, and Evolution of the Enopliinae GISTEL (Coleoptera Cleridae). Part IV. The New World genus Pyticara SPINOLA
Figs 27-30: Morphological organs of Pyticara species. (27) Pyticara championi front leg ungues. (28) Pyticara championi, metatibial subapical secretory pit. (29) Pyticara duponti, posterior angle of prothorax. (30) Pyticara championi, elytral disc.
Figs 1-20 in Classification, Natural History, and Evolution of the Enopliinae GISTEL (Coleoptera Cleridae). Part IV. The New World genus Pyticara SPINOLA
Figs 1-20: Morphological organs of Pyticara species. 1-6 Antennae. (1) Pyticara batesiana; (2) P. duponti. (3) P. championi. (4) P. implana. (5) P. lineatohumeralis; (6) P. simoata. 7-12 Pronota. (7) P. batesiana. (8) P. championi. (9) P. duponti. (10) P. implana. (11) P. lineatohumeralis. (12) P. simoata. 13-20 Aedeagi. (13) P. batesiana phallus. (14) P. batesiana tegmen. (15) P. championi phallus. (16) P. championi tegmen. (17) P. duponti phallus. (18) P. duponti tegmen. (19) P. lineatohumeralis phallus. (20) P. lineatohumeralis phallus.
Fig. 32-35 in Classification, Natural History, and Evolution of the Enopliinae GISTEL (Coleoptera Cleridae). Part IV. The New World genus Pyticara SPINOLA
Fig. 32-35: Photographs of Pyticara species. (32) P. batesiana. (33) P. championi. (34) P. duponti. (35) P. implana.
Fig 70 in ClassiIication, Natural History, and Evolution oI the SubIamily Peloniinae OPITZ (Coleoptera, Cleroidea, Cleridae). Part XIII. The New World genera oI checkered beetles of the Labasiella complex
Fig 70: The known geographic distribution of species as noted.
Figs 59-60 in ClassiIication, Natural History, and Evolution oI the SubIamily Peloniinae OPITZ (Coleoptera, Cleroidea, Cleridae). Part XIII. The New World genera oI checkered beetles of the Labasiella complex
Figs 59-60: Head and antenna of Amphelissus meieri. (59) Head, ventral view. (60) Antenna.
Figs 57-58 in ClassiIication, Natural History, and Evolution oI the SubIamily Peloniinae OPITZ (Coleoptera, Cleroidea, Cleridae). Part XIII. The New World genera oI checkered beetles of the Labasiella complex
Figs 57-58: Head and mouthparts of Amphelissus meieri. (57) Head, frontal view. (58) Mouthparts.
Fig. 90-91 in Classification, Natural History, and Evolution of the Subfamily Peloniinae O (Coleoptera: Cleroidea: Cleridae). Part IX. Taxonomic revision of the New World genus Muisca S
Fig. 90-91: Metatarsus. (90) M. octonotata, ungues. (91) M. octonotata, 4th tarsomere.
Fig. 96 in Classification, Natural History, and Evolution of the Subfamily Peloniinae O (Coleoptera: Cleroidea: Cleridae). Part IX. Taxonomic revision of the New World genus Muisca S
Fig. 96: Geographic distribution of Muisca species as listed.
Data associated with: Recording animal-view videos of the natural world using a novel camera system and software package
<p>Data associated with Vasas V, Lowell MC*, Villa J*, Jamison QD*, Siegle AG*, Katta PVR*, Bhagavathula P*, Kevan PG, Fulton D, Losin N, Kepplinger D, Salehian S, Forkner RE, Hanley D (2023) Recording animal-view videos of the natural world using a novel camera system and software package. PLoS Biology. DOI: 10.1371/journal.pbio.3002444</p>
Final Diorama-Nature Reclaimed-"World On Fire"
This piece was made as a part of my Nature Reclaimed project. Please provide any constructive comments you think might help me. Thank you Source: Objaverse 1.0 / Sketchfab
Diaspore traits specialized to animal adhesion and sea current dispersal are positively associated with the naturalization of European plants across the World
<p>Understanding what drives non-native species naturalization (the establishment of a self-sustainable population outside its native range) is a central question in invasion science. Plants' capacity for long distance dispersal (LDD) is likely to influence the spread and naturalization of non-native species differently according to their introduction pathways. These pathways include intentional introductions (for economic use, e.g. for agriculture), unintentional introductions (e.g. seed contaminants), plant dispersal via human infrastructures (e.g. roads), and plant spread from an adjacent region where the species was previously introduced. Herein, we tested the relationship between sets of LDD traits (syndromes) of 10,308 European plant species and their global naturalization incidence (i.e. whether a species has become naturalized or not) and extent (i.e. the number of regions where a species has become naturalized) using the most comprehensive database of naturalized plants worldwide (GloNAF). Diaspore traits allowed the identification of four traditional LDD syndromes, namely those with specializations for dispersal by: wind (anemochorous), animal ingestion (endozoochorous), attached to animals (epizoochorous), and sea currents (thalassochorous). These evolutionary specializations have been historically interpreted by biologists even though actual dispersal is not always related to diaspore syndromes. We found that while epizoochorous and thalassochorous traits are positively associated with global plant naturalization incidence, anemochorous and endozoochorous traits show a negative relationship. Species´ residence time outside their native range, their economic use and presence of epizoochorous traits (such as hooks, hairs and adhesive substances) are positively associated with global naturalization extent. Furthermore, we found that plants' economic use reduces the influence of LDD syndromes on the naturalization incidence of intentionally introduced plants. While the success of non-native plants is influenced by a broad array of species- and context-specific factors, LDD syndromes play an important role in this context depending on the economic use of plants.</p>
Fig. 1 in Beyond the raccoon roundworm: The natural history of non-raccoon Baylisascaris species in the New World
Fig. 1. Generalized life cycle scheme for Baylisascaris spp.
Fig. 41 in Classification, Natural History, and Evolution of the Enopliinae GISTEL (Coleoptera Cleridae). Part IV. The New World genus Pyticara SPINOLA
Fig. 41: Geographic distribution of Pyticara championi.
Fig. 31 in Classification, Natural History, and Evolution of the Enopliinae GISTEL (Coleoptera Cleridae). Part IV. The New World genus Pyticara SPINOLA
Fig. 31: Phylogenetic hypothesis of Pyticara species.
Fig. 40 in Classification, Natural History, and Evolution of the Enopliinae GISTEL (Coleoptera Cleridae). Part IV. The New World genus Pyticara SPINOLA
Fig. 40: Geographic distribution of species as noted.
Wildlife documentaries present a diverse, but biased, portrayal of the natural world
<p>1. Wildlife-documentary production has expanded over recent decades, while studies report reduced direct contact with nature. The role of documentaries and other electronic content in educating people about biodiversity is therefore likely to be growing increasingly important. This study investigated whether the content of wildlife documentaries is an accurate reflection of the natural world and whether conservation messaging in documentaries has changed over time.</p> <p>2. We sampled an online film database (n = 105) to quantify the representation of taxa and habitats over time, and compared this with actual taxonomic diversity in the natural world. We assessed whether the precision with which an organism could be identified from the way it was mentioned varied between taxa or across time, and whether mentions of conservation and anthropogenic impacts on the natural world changed over time.</p> <p>3. Mentions of organisms (n = 374) were very biased towards vertebrates (81.1% of mentions) relative to invertebrates (17.9% of mentions), despite vertebrates representing only 3.4% of described species, compared to 74.9% for invertebrates. Mentions were highly variable across groups and between time periods, particularly for insects, fish and reptiles. Plants had a consistently low representation across time periods.</p> <p>4. A range of habitats was represented, the most common being tropical forest and the least common being deep ocean, but there was no change over time.</p> <p>5. Mentions identifiable to species were significantly different between taxa, with 41.8% of mentions of vertebrates identifiable to species compared with just 7.5% of invertebrate mentions and 10% of plant mentions. This did not change over time.</p> <p>6. Conservation was mentioned in 16.2% of documentaries overall but in almost 50% of documentaries in the current decade. Anthropogenic impacts were mentioned in 22.1% of documentaries and never before the 1970s.</p> <p>7. Our results show that documentaries provide a diverse picture of nature with an increasing focus on conservation, with likely benefits for public awareness. However, they overrepresent vertebrate species, potentially directing public attention towards these taxa. We suggest widening the range of taxa featured to redress this and call for a greater focus on threats to biodiversity to improve public awareness.</p>
Does Belimumab Modify the Natural History of SLE? A Propensity Score-matched, Real-world Study
ClinicalTrials.gov study NCT07056621. IPD Sharing: NO. Countries: 1. Publications: 6.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.