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1,118 results for “CAPES”
Heroes: Do All of Them Wear Capes? | Islam and Muslim Civilizations | iBrary
<p>This video introduces the module “Heroes: Do All of Them Wear Capes?” from the course Islam and Muslim Civilizations, taught by Prof. Shafique N. Virani. You can download the complete online course, including this module, for free from <a href="https://www.youtube.com/redirect?event=video_description&redir_token=QUFFLUhqa29hdmEydkxSVkdmMk9BUmV5S29lS1c0dGFvd3xBQ3Jtc0tsNXc4M2lGTlhIUkhITnZJbEp2WHhDMzZXamJFMG9fVkhld1RSTlNBcEtUbUFUNkhzaU04UmtJTnpVZ2EzdGJCWWRqcXdWRFNWaEM4endIYTFuYjk1Z3ZtU1hINHloU3k3cFhmRDUxMDQ2NnZnUVd0OA&q=https%3A%2F%2Fwww.ecampusontario.ca%2F&v=9ch92zHt3To">https://www.ecampusontario.ca/</a>.</p>
Fig. 6 in Ground beetles (Coleoptera: Carabidae) from the region of Cape Emine (central Bulgarian Black sea coast). Part III. Spatial distribution and gradient analysis
Fig. 6. PCA distribution of the sampling sites and the subclasses of life forms (according to Sharova 1981): Z_Phytob – Zoophagous phytobionts; Z_Strat – Zoophagous stratobionts; M_Strat – Mixophytophagous stratobionts; M_Short – Mixophytophagous stratohortobionts; M_Geoh – Mixophytophagous geobionts.
Fig. 7 in Ground beetles (Coleoptera: Carabidae) from the region of Cape Emine (central Bulgarian Black sea coast). Part III. Spatial distribution and gradient analysis
Fig. 7. PCA distribution of the sampling sites and categories of life forms (according to SHAROVA 1981): Life form class 1. Zoophagous. Life form subclass: 1.1 – Phytobios; 1.2 – Epigeobios; 1.3 – Stratobios; 1.4 – Geobios. Life form groups: 1.1.2 – stemdwelling hortobionts; 1.1.3 – leaf-dwelling dendrohortobionts; 1.2.2 – large walking epigeobionts; 1.2.2(1) – large walking dendroepigeobionts; 1.2.3 – running epigeobionts; 1.2.4 – flying epigeobionts; 1.3(1) – series crevice-dwelling stratobionts; 1.3(1).1 – surface & litter-dwelling; 1.3(1).2 – litter-dwelling; 1.3(1).3 – litter & crevice-dwelling; 1.3(1).4 – endogeobionts; 1.3(1).5 – litter & bark-dwelling; 1.3(1).6 – bothrobionts; 1.3(2).1 – litter & soil-dwelling; 1.4.2(1) – large digging geobionts. Life form class 2. Mixophytophagous. Life form subclass: 2.1 – Stratobios; 2.2 – Stratohortobios; 2.3 – Geohortobios. Life form groups: 2.1.1 – crevice-dwelling stratobionts; 2.2.1 – stratohortobionts; 2.3.1 – harpaloid geohortobionts; 2.3.1(1) – crevice-dwelling harpaloid geohortobionts; 2.3.2 – zabroid geohortobionts; 2.3.3 – dytomeoid geohortobionts.
Fig. 4 in Ground beetles (Coleoptera: Carabidae) from the region of Cape Emine (central Bulgarian Black sea coast). Part III. Spatial distribution and gradient analysis
Fig. 4. Ordination of the sampling sites in relation to the humidity and vegetation. The calculations were performed by the use of the results from all of the sampling sites and all of the catches, standardized through the recalculation of the data as number of specimens per 100 trapdays.
Fig. 3 in Ground beetles (Coleoptera: Carabidae) from the region of Cape Emine (central Bulgarian Black sea coast). Part III. Spatial distribution and gradient analysis
Fig. 3. Distribution of the permanent species in relation to the humidity and vegetation. The analysis included only the permanent species – those with a frequency above 50% (see TEOFILOVA 2015): A aenea – Amara aenea; A anth – Amara anthobia; A famil – Amara familiaris; Ac megac – Acinopus megacephalus; Agon sp – Agonum (Europhilus) sp.; Br crep – Brachinus crepitans; Br expl – Brachinus explodens; C ambig – Calathus ambiguus; C cinct – Calathus cinctus; C fuscip – Calathus fuscipes; Car conv – Carabus convexus; Car cor – Carabus coriaceus; Car ullr – Carabus ullrichi; Chl nit – Chlaenius nitidulus; H dimid – Harpalus dimidiatus; H dist – Harpalus distinguendus; H flavic – Harpalus flavicornis; H rubrip – Harpalus rubripes; H tardus – Harpalus tardus; Laem ter – Laemostenus terricola; Lei ruf – Leistus rufomarginatus; M maurus – Microlestes maurus; M minut – Microlestes minutulus; Myas ch – Myas chalybaeus; N brevic – Nebria brevicollis; O azur – Ophonus azureus; Par mend – Parophonus mendax; Ps rufip – Pseudoophonus rufipes; Pt melas – Pterostichus melas; Tr q – Trechus quadristriatus.
A high-resolution regional data-assimilative ocean modeling output near Cape Hatteras in 2017
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Environmental heterogeneity explains contrasting plant species richness between the South African Cape and southwestern Australia
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A high-resolution regional data-assimilative ocean modeling output near Cape Hatteras in 2018
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Data and code for: Previous assessments of faecal glucocorticoid metabolites in Cape Mountain zebra (Equus zebra zebra) were flawed
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Cape Marsh Rock Magnetics & U-Pb Zircon Data
<p>Raw rock magnetic and U-Pb zircon data for manuscript "­­New evidence of a Campanian age for the Cretaceous fossil-bearing strata of Cape Marsh, Robertson Island, Antarctica­­"</p>
High-CAPE summer convection in large-domain large-eddy simulations with ICON - model and observational data sets
<p>Data sets including all observational and ICON model data for publication in Atmosperic Chemistry and Physics Journal (ACP) - "High-CAPE summer convection in large-domain large-eddy simulations with ICON"</p>
Fig. 4 in New scale insects (Homoptera: Coccinea) from the Cape Floristic Region
Fig. 4. Cryptinglisia millari Gavrilov-Zimin sp. nov., adult female, holotype.
Fig. 5 in New scale insects (Homoptera: Coccinea) from the Cape Floristic Region
Fig. 5. Cryptinglisia millari Gavrilov-Zimin sp. nov., adult females in life.
Fig. 2 in New scale insects (Homoptera: Coccinea) from the Cape Floristic Region
Fig. 2. Coccidohystrix daedalea Gavrilov-Zimin sp. nov., adult female, holotype.
Fig. 3 in New scale insects (Homoptera: Coccinea) from the Cape Floristic Region
Fig. 3. Mirococcopsis ptilura Gavrilov-Zimin sp. nov., adult female (holotype) and primolarva (L1).
Leaf margins in a deciduous lineage from the Greater Cape Floristic Region track climate in unexpected directions
<p>Premise of the study: The functional significance of leaf margins has long been debated. In this study we explore influences of climate, leaf lobing, woodiness, and shared evolutionary history on two leaf margin traits within the genus Pelargonium.</p> <p>Methods: Leaves from 454 populations of Pelargonium (161 species) were collected in the Greater Cape Floristic Region and scored for tooth presence/absence and degree of lobing. Tooth density (number of teeth per interior perimeter distance) was measured for a subset of these. We compared five hypotheses to explain tooth presence and density using mixed effect models.</p> <p>Key results: Tooth presence/absence was best predicted by the interaction of leaf lobing and mean annual temperature (MAT), but often in patterns opposite to the previous literature: species were more likely to be toothed with warmer temperatures. This was particularly the case for unlobed and highly lobed leaves. In contrast, tooth density was best predicted by the interaction of MAT and the season of most rain; density declines with temperature as consistent with expectations, but only in winter- rain dominated areas. Woody and non-woody species within Pelargonium both have similar associations between tooth presence/absence and MAT, contrary to the expectation that patterns within non-woody species would be insignificant.</p> <p>Conclusions: We conclude Pelargonium leaf margins show predictable responses to climate, but these responses are complex and can contradict those found for global patterns across plant communities.</p>
West Point Cadet's Cape and Uniform
Authentic West Point United States Military Academy cadet's cape and uniform belonging to Charles Young, the third African-American graduate in the academy's history. Scanned using the Peel 3D hand-held scanner. Source: Objaverse 1.0 / Sketchfab
Figure 3. - ATruncatoflabellumzuluense, paratype, USNM 91751, MD ZK-20, South Africa B Truncatoflabellumpusillum, holotype, USNM 81978, Albatross 5178, Philippines C Truncatoflabellumangustum, USNM 98894, MUSORSTOM 8-1016, Vanuatu D Truncatoflabellumangiostomum, USNM 96643, Cape Jaubert, Western Australia. Scale bars: all 10 mm, except for basal scar views, which are 5 mm.
Figure 3. - ATruncatoflabellumzuluense, paratype, USNM 91751, MD ZK-20, South Africa B Truncatoflabellumpusillum, holotype, USNM 81978, Albatross 5178, Philippines C Truncatoflabellumangustum, USNM 98894, MUSORSTOM 8-1016, Vanuatu D Truncatoflabellumangiostomum, USNM 96643, Cape Jaubert, Western Australia. Scale bars: all 10 mm, except for basal scar views, which are 5 mm.
Figure 1. - Representative specimens of the nine Epicephala species in Japan. Wing pattern of Epicephalaparasitica is sexually dimorphic, so specimens of both sexes are shown for this species. A Epicephalaanthophilia (Amami Island, Kagoshima, ♀, holotype) B Epicephalabipollenella (Henoko, Okinawa, ♀) C Epicephalalanceolatella (Cape Hedo, Okinawa, ♀, holotype) D Epicephalaperplexa (Cape Hedo, Okinawa, ♀, holotype) E Epicephalaobovatella (Tomogashima, Wakayama, ♂, paratype) F Epicephalacorruptrix (Takae, Okinawa, ♀, holotype) G Epicephalavitisidaea (Yona, Okinawa, ♀) H Epicephalaparasitica (Yonaguni Island, Okinawa, ♀, holotype) I Epicephalaparasitica (Hateruma Island, Okinawa, ♂) J Epicephalanudilingua (Watarase-yusuichi, Tochigi, ♀, holotype). Scale bar: 5 mm.
Figure 1. - Representative specimens of the nine Epicephala species in Japan. Wing pattern of Epicephalaparasitica is sexually dimorphic, so specimens of both sexes are shown for this species. A Epicephalaanthophilia (Amami Island, Kagoshima, ♀, holotype) B Epicephalabipollenella (Henoko, Okinawa, ♀) C Epicephalalanceolatella (Cape Hedo, Okinawa, ♀, holotype) D Epicephalaperplexa (Cape Hedo, Okinawa, ♀, holotype) E Epicephalaobovatella (Tomogashima, Wakayama, ♂, paratype) F Epicephalacorruptrix (Takae, Okinawa, ♀, holotype) G Epicephalavitisidaea (Yona, Okinawa, ♀) H Epicephalaparasitica (Yonaguni Island, Okinawa, ♀, holotype) I Epicephalaparasitica (Hateruma Island, Okinawa, ♂) J Epicephalanudilingua (Watarase-yusuichi, Tochigi, ♀, holotype). Scale bar: 5 mm.
Circulation and Retention of River Plumes Around Capes
<p>Supporting data for the JGR-Oceans Manuscript: Circulation and Retention of River Plumes Around Capes by Pareja-Roman, Chant, Mazzini, and Cole.</p>
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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