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294 results for “temporal pattern”
Fig. 1 in Local ecological knowledge of fishers about the life cycle and temporal patterns in the migration of mullet (Mugil liza) in Southern Brazil
Fig. 1. Santa Catarina State coast, data collection sites (triangles) and the number of interviewed fishermen (in parenthesis; total N=45).
Figure 5 in Temporal variation in the reproductive pattern of blood cockle Anadara antiquata from Pakistan (northern Arabian Sea)
Figure 5. Temporal variation in gonad index (GI) of male and female A. antiquata from Phitti Creek and Sonmiani.
Figure 3 in Temporal variation in the reproductive pattern of blood cockle Anadara antiquata from Pakistan (northern Arabian Sea)
Figure 3. Photomicrographs of A. antiquata: A–D: stages of spermatogenesis; E–H: stages of oogenesis. A, E: Developing; B, F: Ripe; C, G: Spawned out; D, H: Resorbing. Abbreviations: F - Follicle, Sc - Spermatocytes; St - Spermatids; Sz - Spermatozoa; Ef - Empty follicle; Ct - Connective tissue; Og - Oogonia; Pvo - Previtellogenic oocyte; Vo - Vitellogenic oocyte; N - Nucleus; n - nucleolus; Mo - Mature oocyte; Ao - Atretic oocyte.
Figure. General head scalation pattern for Elaphe sauromates (cs – anterior chin shields; cs' – posterior chin shields; f – frontal; g – gulars; in – internasal; l – loreal; la – upper labials; la' – lower labials; m – mental; p – parietals; pf – prefrontal; prn – prenasal; ptn – postnasal; pto – postocular; pro – preocular; r – rostral; so – supraocular; sbo – subocular; t – temporals; v – ventral shields). in Morphological characteristics of the elusive blotched snake (Elaphe sauromates) at its northwestern range limit (Romania)
Figure. General head scalation pattern for Elaphe sauromates (cs – anterior chin shields; cs' – posterior chin shields; f – frontal; g – gulars; in – internasal; l – loreal; la – upper labials; la' – lower labials; m – mental; p – parietals; pf – prefrontal; prn – prenasal; ptn – postnasal; pto – postocular; pro – preocular; r – rostral; so – supraocular; sbo – subocular; t – temporals; v – ventral shields).
Figure 4 in The partitioning of temporal movement patterns of breeding red-crowned crane (Grus japonensis) induced by temperature
Figure 4. Multiple comparisons of the moving distance among the four RCC breeding subseasons (M: mating, B: brooding, W: wading, G: growing).
Figure 3 in The partitioning of temporal movement patterns of breeding red-crowned crane (Grus japonensis) induced by temperature
Figure 3. Principal component analysis for the climatic variables and the moving distance. The first axis (PC1) explains 31.44% of total variation, and the second axis (PC2) accounts for 22.44% of total variation.
Figure 2 in Spatial and temporal nesting pattern of Sea Turtles in Alas Purwo National Park, and its implications for conservation management practices
Figure 2. Trend of sea turtle nesting in the past 40 years at APNP: (A) L.olivacea, (B) C. mydas, (C) E. imbricata, and (D) D. coriacea.
Figure 1 in Spatial and temporal nesting pattern of Sea Turtles in Alas Purwo National Park, and its implications for conservation management practices
Figure 1. Study location in Alas Purwo National Park's Pancur-Cungur Coast with six hypothetical stations (dot: sector benchmark point).
Figure 4 in Spatial and temporal nesting pattern of Sea Turtles in Alas Purwo National Park, and its implications for conservation management practices
Figure 4. Number of four sea turtles nesting in each month during survey period: (A) L.olivacea, (B) C. mydas, (C) E. imbricata, and (D) D. coriacea.
Fig. 10 in Patterns of spatio-temporal distribution as criteria for the separation of planktic foraminiferal species across the Danian-Selandian transition in Spain
Fig. 10. Lower/higher (L/H) latitude taxa ratio and quantitative stratigraphic distribution of planktic foraminiferal genera across the Danian–Selandian transition at Caravaca. Asterisks indicate climate warming events identified here.
Fig. 9 in Patterns of spatio-temporal distribution as criteria for the separation of planktic foraminiferal species across the Danian-Selandian transition in Spain
Fig. 9. Cluster analyses based on Morisita's index for relative abundance data of species from Caravaca in the Acarinina uncinata Zone (4a) and in the Morozovella cf. albeari Zone (4b); l1 = Simpson's diversity index in sample j; l2 = Simpson's diversity index in sample k; xij = percentage of species i in sample j; xik = percentage of species i in sample k.
Fig. 2 in Patterns of spatio-temporal distribution as criteria for the separation of planktic foraminiferal species across the Danian-Selandian transition in Spain
Fig. 2. Comparison of some planktic foraminiferal zonations proposed for the D–S transition in low and middle latitudes. Correlation with the chronostratigraphic and magnetostratigraphic scales based on data from the Zumaia stratotype. (*) Probable biostratigraphic position of the base of the Igorina pusilla Zone by Toumarkine and Luterbacher (1985), and Canudo and Molina (1992), based on data from Zumaia. (**) Biostratigraphic position of the P3a/P3b boundary by Berggren and Pearson (2005), assuming that their species concept of I. albeari includes Morozovella crosswicksensis by Blow (1979) and Arenillas and Molina (1997) and/or M. cf. albeari by Arenillas et al. (2008). FOD, first occurrence data; L/H, lower/higher latitude, LOD, last occurence data.
Fig. 3 in Patterns of spatio-temporal distribution as criteria for the separation of planktic foraminiferal species across the Danian-Selandian transition in Spain
Fig. 3. Quantitative stratigraphic distribution of planktic foraminiferal species across the Danian–Selandian transition at Caravaca. The shown stratigraphic interval does not include the lower part of the A. uncinata Zone, where Globoconusa species were found (see Arenillas and Molina 1997).
FIGURE 1 in Larval fish assemblages in nearshore waters of southeast Gulf of California: vertical and temporal patterns
FIGURE 1 | A. Map of the study area, nearshore waters in front of the Huizache-Caimanero estuarine system, located in the southeast Gulf of California, Sinaloa, Mexico. Sampling sites are indicated by black circles. B. Detail of the study area and sampling sites located in front of the Presidio River inlet.
FIGURE 4 in Larval fish assemblages in nearshore waters of southeast Gulf of California: vertical and temporal patterns
FIGURE 4 | Boxplots for diversity and evenness for the sampled months from September 1994 to June 1995. A. Diversity, B. Evennes. Line: median; box: 25th to 75th percentiles; whiskers: minimum to maximum value range. Differences in GLM p-values are shown by lowercase letters, different letters mean significant differences for the indexes (p-value <0.05).
FIGURE 7 in Larval fish assemblages in nearshore waters of southeast Gulf of California: vertical and temporal patterns
FIGURE 7 | Vertical distribution of the abundance of the species found in the study. Bars indicate the mean value (individuals m-3) and error bars the Standard Error.
FIGURE 3 in Larval fish assemblages in nearshore waters of southeast Gulf of California: vertical and temporal patterns
FIGURE 3 | Water temperature and salinity profiles at each sampling site, for each sampled month from September 1994 to June 1995.
FIGURE 5 in Larval fish assemblages in nearshore waters of southeast Gulf of California: vertical and temporal patterns
FIGURE 5 | Correlation triplot of the db-RDA showing the relationship between explanatory (temperature and salinity) and response variables (species). Black labels indicate the position of species in the ordination; their size increase according to the abundance of the species to achieve a better visualization. Samples are coded by depths and months. The angles between species and explanatory variables reflect their correlations; a small angle implies a positive correlation, a large one suggests a negative correlation, and a 90° angle indicates no correlation between two variables.
FIGURE 2 in Larval fish assemblages in nearshore waters of southeast Gulf of California: vertical and temporal patterns
FIGURE 2 | A. Box plots showing temporal variations in temperature and salinity during the sampling period (1994–1995). Line: median; box: 25th to 75th percentiles; whiskers: minimum to maximum value range. Months with the same letters do not significantly differ using Dunn's test. B. Monthly variability of salinity from October 2011 to August 2014, dots indicate the mean value and error bars the Standard Deviation.
FIGURE 6 in Larval fish assemblages in nearshore waters of southeast Gulf of California: vertical and temporal patterns
FIGURE 6 | Temporal and vertical variations of the abundance of the most abundant species found in the study. Dots indicate the mean value and error bars the Standard Error. SEP: September, DEC: December, Apr: April, JUN: June.
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.