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57 results for “depth distribution”
Data from: Subtle shift in groundfish depth distribution within the impact range of seismic surveying along a continental slope
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Dataset S2: Global Synechococcus pigment type distribution from metagenomes with co-located mixed layer depths and sea surface properties
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Data from: Predictive modelling of habitat selection by marine predators with respect to the abundance and depth distribution of pelagic prey
1. Understanding the ecological processes that underpin species distribution patterns is a fundamental goal in spatial ecology. However, developing predictive models of habitat use is challenging for species that forage in marine environments, as both predators and prey are often highly mobile and difficult to monitor. Consequently, few studies have developed resource selection functions for marine predators based directly on the abundance and distribution of their prey. 2. We analysed contemporaneous data on the diving locations of two seabird species, the shallow-diving Peruvian Booby (Sula variegata) and deeper diving Guanay Cormorant (Phalacrocorax bougainvilliorum), and the abundance and depth distribution of their main prey, Peruvian anchoveta (Engraulis ringens). Based on this unique data set, we developed resource selection functions to test the hypothesis that the probability of seabird diving behaviour at a given location is a function of the relative abundance of prey in the upper water column. 3. For both species, we show that the probability of diving behaviour is mostly explained by the distribution of prey at shallow depths. While the probability of diving behaviour increases sharply with prey abundance at relatively low levels of abundance, support for including abundance in addition to the depth distribution of prey is weak, suggesting that prey abundance was not a major factor determining the location of diving behaviour during the study period. 4. The study thus highlights the importance of the depth distribution of prey for two species of seabird with different diving capabilities. The results complement previous research that points towards the importance of oceanographic processes that enhance the accessibility of prey to seabirds. The implications are that locations where prey is predictably found at accessible depths may be more important for surface foragers, such as seabirds, than locations where prey is predictably abundant. 5. Analysis of the relative importance of abundance and accessibility is essential for the design and evaluation of effective management responses to reduced prey availability for seabirds and other top predators in marine systems.
Figure 4. Regression lines between average length and sampling depth for the 19 in Bathymetric trends in distribution and size of demersal fish species in the north Aegean Sea
Figure 4. Regression lines between average length and sampling depth for the 19 species with significant size-depth relationships.
Data from: Molecular assessment of Pocillopora verrucosa (Scleractinia; Pocilloporidae) distribution along a depth gradient in Ludao, Taiwan
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Data from: Predictive modelling of habitat selection by marine predators with respect to the abundance and depth distribution of pelagic prey
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Supplementary material 1 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Table S1
Figure 1 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Figure 1 Location of the study sites. 1 Doline next to Silická ľadnica Ice Cave 2 Vysoká Hill (both sites in Slovak Karst National Park) 3 Drienok Valley (Revúcka Highlands) 4 Belinské skaly (Cerová vrchovina Highlands) 5 Okopanec Hill (Malé Karpaty Mts.) 6–8 Three localities near the Zbrašov Aragonite Caves and Hůrka u Hranic (Moravian-Silesian Foothills) 9–11 Three localities in Chrudim region (Iron Mts.).
Supplementary material 2 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Table S2
Figure 4 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Figure 4 Graphical presentation of myriapod community characteristics in different fixative solutions (N = number of individuals). A Formaldehyde to ethylene glycol ratio of sampled centipede species from all study sites, where both fixating solutions were used B formaldehyde to ethylene glycol ratio of sampled millipede species from all study sites, where both fixating solutions were used.
Figure 2 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Figure 2 A Overall depth distribution of centipede individuals and species B values of Shannon's diversity index and Pielou's evenness index, calculated for centipedes, at each of the study sites C mean values of Shannon's diversity index (±SD) calculated for centipedes, at each depth of the gradient (summarised data from all localities) D overall depth distribution of millipede individuals and species E values of Shannon's diversity index and Pielou's evenness index, calculated for millipedes, at each of the study sites F mean values of Shannon's diversity index (±SD) calculated for millipedes, at each depth of the gradient.
Figure 5 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Figure 5 Vertical distribution of myriapods along the depth gradient in different fixative solutions (data recalculated for the same number of traps). Trend line: dashed = formaldehyde, dotted = ethylene glycol. A Vertical distribution of Chilopoda specimens along the depth gradient (5–95 cm) at five scree slopes in different fixative solutions B vertical distribution of centipede species along the depth gradient at five scree slopes in different fixative solutions C vertical distribution of Diplopoda specimens along the depth gradient (5–95 cm) at five scree slopes in different fixative solutions D vertical distribution of millipede species along the depth gradient at five scree slopes in different fixative solutions.
Figure 3 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Figure 3 Generalised Additive Models of depth distribution pattern of A centipedes and B millipedes. Only species with significant pattern are illustrated. (F-values, * p < 0.05, ** p < 0.01): ALamyctes emarginatus (13.1**), Lithobius forficatus (17.2**), Lithobius lucifugus (5.0*), Lithobius nodulipes (9.7**) BArchiboreoiulus pallidus (22.7**), Cylindroiulus nitidus (5.4*), Glomeris connexa (5.4*), Hylebainosoma tatranum (5.4*), Leptoiulus proximus (7.3*), Mastigona bosniensis (10.5**), Megaphyllum projectum (5.4*), Melogona transsylvanica (15.2**), Polydesmus complanatus (13.1**), Trachysphaera acutula (5.4*), Unciger foetidus (4.9*).
Figure 3 from: Jakšová P, Ľuptáčik P, Miklisová D (2019) Distribution of Oribatida (Acari) along a depth gradient in forested scree slopes. Subterranean Biology 31: 29-48. https://doi.org/10.3897/subtbiol.31.36241
Figure 3 Monthly temperature fluctuations along the depth gradient of the investigated screes. Abbreviations: AJ – Ardovská jaskyňa Cave, BS – Belinské skaly Rocks, DK – Drienčanský kras Karst, MR – Malý Ružínok Valley, SL – Silická ľadnica Cave.
Figure 4 from: Jakšová P, Ľuptáčik P, Miklisová D (2019) Distribution of Oribatida (Acari) along a depth gradient in forested scree slopes. Subterranean Biology 31: 29-48. https://doi.org/10.3897/subtbiol.31.36241
Figure 4 Distribution of Oribatida along the vertical profile of the screes expressed as a total number of trapped individuals and species richness. Abbreviations: AJ – Ardovská jaskyňa Cave, BS – Belinské skaly Rocks, DK – Drienčanský kras Karst, MR – Malý Ružínok Valley, SL – Silická ľadnica Cave, *Number of individuals = 661.
Figure 1 from: Jakšová P, Ľuptáčik P, Miklisová D (2019) Distribution of Oribatida (Acari) along a depth gradient in forested scree slopes. Subterranean Biology 31: 29-48. https://doi.org/10.3897/subtbiol.31.36241
Figure 1 Localities of samplings. 1 – Ardovská jaskyňa Cave, 2 – Belinské skaly Rocks, 3 – Drienčanský kras Karst, 4 – Malý Ružínok Valley, 5 – Silická ľadnica Cave.
Figure 4 in Depth-related gradient of soft-bottom crustacean distribution along the Cilician shelf*
Figure 4. nMDS (A; see Figure 1 for depth code) and biplot of CCA (axes 1–2) performed on log-transformed (log 10 × [N + 1]) density values (N) of the crustacean taxa and environmental variables (arrows) at each replicate (B; see Figure 1 for depth and transect codes around the symbols) and at 7 depths of a combination of 3 transects each, including 7 stations (C) in each season. Arrows refer to the direction and relative importance of environmental variables in the ordination. Symbol size is proportional to depth of sampling sites variable, i.e. the largest symbol corresponds to the maximum depth. See Table 3 for the abbreviations of the environmental variables.
Figure 1 in Depth-related gradient of soft-bottom crustacean distribution along the Cilician shelf*
Figure 1. Study area (framed in rectangle) and sampling stations located on soft bottoms (1: 10 m, 2: 25 m, 3: 50 m, 4: 75 m, 5: 100 m, 6: 150 m, and 7: 200 m) across 3 transects, Erdemli (E), Limonlu (L), and Kumkuyu (K), in the Cilician shelf in 2000.
Figure 8 from: Robertson R (2014) A new Liopropoma sea bass (Serranidae, Epinephelinae, Liopropomini) from deep reefs off Curaçao, southern Caribbean, with comments on depth distributions of western Atlantic liopropomins. ZooKeys 409: 71-92. https://doi.org/10.3897/zookeys.409.7249
Figure 8 - The strict consensus of a maximum parsimony analysis of the COI region among western Atlantic Liopropoma and related taxa. The tree was rooted on Scorpaena plumieri, (CUR11401), and the non-liopropomin serranids Rypticus carpenteri (TOB9102) and Grammistes sexlineatus (MBIO1671) were included as additional outgroups. Photographs of Liopropoma rubre and Liopropoma mowbrayi by James Van Tassell and Ross Robertson; photos of Liopropoma pallidum and Liopropoma lunulatum by Jeffrey Williams (from Encyclopedia of Life); photo of Liopropoma tonstrinum by Richard Winterbottom (from Encyclopedia of Life).
Figure 4 from: Robertson R (2014) A new Liopropoma sea bass (Serranidae, Epinephelinae, Liopropomini) from deep reefs off Curaçao, southern Caribbean, with comments on depth distributions of western Atlantic liopropomins. ZooKeys 409: 71-92. https://doi.org/10.3897/zookeys.409.7249
Figure 4 - In-situ photograph of Liopropoma santi sp. n., taken from the Curasub submersible at 204 m on a reef slope off Jan Theil Bay, Curaçao, 5 Nov 2013. Photo courtesy of Substation Curaçao.
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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.