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484 results for “reproductive biology”
Figure 6 in Growth and reproductive biology of the amphidromous shrimp Palaemon pandaliformis (Decapoda: Caridea) in a Neotropical river from northeastern Brazil
Figure 6. Monthly length frequency distribution of males and females of Palaemon pandaliformis collected from September 2009 and August 2010 in Rio Salsa, Canavieiras, Bahia, Brazil. Dotted line at 4.53 mm was drawn for illustrative purposes, indicating recruitment of small individuals into the population, according to PASCHOAL et al. (2013b).
Figure 5 in Growth and reproductive biology of the amphidromous shrimp Palaemon pandaliformis (Decapoda: Caridea) in a Neotropical river from northeastern Brazil
Figure 5. Minimum, maximum (whiskers), median (horizontal line) and mean (black square) carapace and total length values for males and females of Palaemon pandaliformis collected from September
Fig. 3 in Biology and reproductive capacity of Spodoptera eridania (Cramer) (Lepidoptera, Noctuidae) in different soybean cultivars
Fig. 3. Total number of eggs and larvae of Spodoptera eridania during the oviposition period in cultivars TMG Tabarana, BRS/MT Pintado, FMT Tucunaré and Monsoy 8757.
Figure 6 in Age, growth, and reproductive biology of Atlantic bonito (Sarda sarda Bloch, 1793) from the Turkish coasts of the Black Sea and the Sea of Marmara
Figure 6. Micrographs from gonad cross-sections of immature stage (a), nonspawning mature stage (b), spawning stage (c), and postovulatory stage (d).
Figure 1 in Age, growth, and reproductive biology of Atlantic bonito (Sarda sarda Bloch, 1793) from the Turkish coasts of the Black Sea and the Sea of Marmara
Figure 1. Length–frequency distribution for females, males, unidentified specimens, and all samples of S. sarda (n = 212).
Figure 5 in Reproductive biology of the greater lizardfish, Saurida tumbil (Bloch, 1795), in Bushehr coastal waters of Iran
Figure 5. Monthly variations in the GSI and HSI of greater lizardfish (Saurida tumbil, Synodontidae) (confidence intervals, 95%).
Figure 3 in Reproductive biology of the greater lizardfish, Saurida tumbil (Bloch, 1795), in Bushehr coastal waters of Iran
Figure 3. Monthly variations in the sexual stages of male greater lizardfish (Saurida tumbil, Synodontidae).
Figure 1 in Reproductive biology of the greater lizardfish, Saurida tumbil (Bloch, 1795), in Bushehr coastal waters of Iran
Figure 1. Length frequency for greater lizardfish (Saurida tumbil, Synodontidae) collected in this study.
Figure 3 in Reproductive biology of pink cuttlefish Sepia orbignyana in the Aegean Sea (eastern Mediterranean)
Figure 3. Monthly average length and standard deviation distribution of S. orbignyana in the Aegean Sea.
Figure 4 in An investigation on some biological and reproduction characteristics of Eriphia verrucosa (Forskål, 1775) in the South Black Sea (Turkey)
Figure 4. Nonlinear regressions between carapace width (CW) and carapace length (CL) and crab weight (W) for E. verrucosa from the study area.
Figure 3 in An investigation on some biological and reproduction characteristics of Eriphia verrucosa (Forskål, 1775) in the South Black Sea (Turkey)
Figure 3. Carapace width (CW) frequency distribution of male (black), nonovigerous females (gray), and ovigerous females (white) of E. verrucosa collected from the study area between February 2012 and January 2013.
Figure 7 in An investigation on some biological and reproduction characteristics of Eriphia verrucosa (Forskål, 1775) in the South Black Sea (Turkey)
Figure 7. Fecundity–carapace width and fecundity–crab weight relationship of E. verrucosa (CW = carapace width; W = crab weight).
Figure 2 in An investigation on some biological and reproduction characteristics of Eriphia verrucosa (Forskål, 1775) in the South Black Sea (Turkey)
Figure 2. Sex ratio of males (black; N = 958), females (gray; N = 317), and ovigerous females (white; N = 85) of E. verrucosa from the study area.
Figure 6 in An investigation on some biological and reproduction characteristics of Eriphia verrucosa (Forskål, 1775) in the South Black Sea (Turkey)
Figure 6. Monthly variations in number of female (gray) and ovigerous females (white) (A), and monthly changes of gonadosomatic index values (B) of E. verrucosa.
Fig. 2 in Effect of different diets on biology, reproductive variables and life and fertility tables of Harmonia axyridis (Pallas) (Coleoptera, Coccinellidae)
Fig. 2. Survival probability (lx), expressed in percentage, and specific fertility (mx) expressed as average number of eggs per day of Harmonia axyridis (Pallas, 1773) fed on Brevicoryne brassicae Linnaeus, 1758. Temperature 25 ± 1 ◦C, 70 ± 10% RU and humidity and 12:12 h L:D.
Fig. 1 in Effect of different diets on biology, reproductive variables and life and fertility tables of Harmonia axyridis (Pallas) (Coleoptera, Coccinellidae)
Fig. 1. Survival probability (lx), expressed in percentage, and specific fertility (mx) expressed as average number of eggs per day of Harmonia axyridis (Pallas, 1773) fed on Cinara atlantica (Wilson, 1919). Temperature 25 ± 1 ◦C, 70 ± 10% RU and humidity and 12:12 h L:D.
Fig. 3 in Effect of different diets on biology, reproductive variables and life and fertility tables of Harmonia axyridis (Pallas) (Coleoptera, Coccinellidae)
Fig. 3. Survival probability (lx), expressed in percentage, and specific fertility (mx) expressed as average number of eggs per day of Harmonia axyridis (Pallas, 1773) fed on Anagasta kuehniella (Zeller, 1879). Temperature 25 ± 1 ◦C, 70 ± 10% RU and humidity and 12:12 h L:D.
Figure 6 in Reproductive biology of Tylototriton yangi (Urodela: Salamandridae), with suggestions on its conservation
Figure 6. Habitat destruction of Tylototriton yangi in southern Yunnan Province, China. a) Coal mining site at Yangjie, Mengzi, Yunnan Province, China; b) illegal tin mining at the type locality of T. yangi in Gejiu, Yunnan, China; c) Deforestation and infrastructure constructions at the type locality of T. yangi in Gejiu, Yunnan, China. Photographs by Kai WANG.
Fig. 1 in Reproductive biology of Tylototriton yangi (Urodela: Salamandridae), with suggestions on its conservation
Fig. 1. Location of the study site (the type locality of Tylototriton yangi) at Gejiu, Honghe Prefecture, Yunnan Province, PR China. Numbered locations of potential breeding pools (abbreviated as PBP) are shown in yellow.
Fig. 5 in Reproductive biology of Tylototriton yangi (Urodela: Salamandridae), with suggestions on its conservation
Fig. 5. Developmental series from fertilized embryos to newly metamorphosed juvenile of Tylototriton yangi. Clockwise from the upper left: a) fertilized embryos of T. yangi; embryos sank to the bottom of water, and were not adhesive to plants, the bottom of the container, or to one another; b) newly hatched larvae with one pair of balancers 6-day post-hatch; c) larva 17-days post-hatch, in which the forelimbs became visible; d) larva 50-days post-hatch; e) larva 75-days post-hatch; f) pre-metamorphic larva 95-days post hatch; g) newly metamorphosed individual 115-day post hatch. Photographs by Kai WANG and Guangyu LI.
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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.