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202 results for “reproductive behavior”
Fig. 7 in Population structure and reproductive behavior of Sinaloa cichlid Cichlasoma beani (Jordan, 1889) in a tropical reservoir
Fig. 7. Size at first maturity of the Sinaloa cichlid Cichlasoma beani in the Aguamilpa Reservoir in Nayarit, Mexico.
Fig. 5 in Population structure and reproductive behavior of Sinaloa cichlid Cichlasoma beani (Jordan, 1889) in a tropical reservoir
Fig. 5. Reproductive cycle of the Sinaloa cichlid Cichlasoma beani in the Aguamilpa Reservoir in Nayarit, Mexico.
Fig. 2 in Social and reproductive physiology and behavior of the Neotropical cichlid fish Cichlasoma dimerus under laboratory conditions
Fig. 2. Body color patterns associated with different social status; a) Schematic representation of the main features of Cichlasoma dimerus color pattern. A: red eye blotch; B: preopercular blotch, C: anterior longitudinal line; D: mid trunk blotch; E: posterior longitudinal line; F: peduncular blotch; G: dorsal transversal bars; H: ventral transversal bars. These features may "turn on" or "off" in different conditions; b) Gregarious individuals; c) Reproductive Territorial male (RT); d) Reproductive Territorial female. e) Non Reproductive Territorial male (nRnT); f) Non Reproductive non Territorial (nRnT) individual. Scale bar = 1 cm
Fig. 1 in Social and reproductive physiology and behavior of the Neotropical cichlid fish Cichlasoma dimerus under laboratory conditions
Fig. 1. Distribution of different social status fish on the experimental aquaria: a) Picture of the experimental aquaria; b) Schematic representation. Abbreviations of social statuses used: nRnT = non Reproductive non Territorial individuals; nRT = non Reproductive Territorial individual; RT = Reproductive Territorial individual. For a detailed description of these social statuses see Table 3.
Fig. 1. A in Reproductive behavior and parental roles of the cichlid fish Laetacara araguaiae
Fig. 1. A pair of Laetacara araguaiae with fry (arrows). The largest fish is the male. Photo: Elias F. Lopes de Freitas.
Fig. 5 in Reproductive behavior and parental roles of the cichlid fish Laetacara araguaiae
Fig. 5. Mean frequency (± SE) of threats (a) and attacks (b) given by male and female in the pre-spawning (n = 11), egg/ wriggler (n = 11) and free-swimming fry (n = 12) phases. * indicates significant difference between sexes (Wilcoxon signed-rank test). Different letters indicate significant differences between phases for each sex (Kuskal-Wallis followed by Dunn post hoc test).
Fig. 4 in Reproductive behavior and parental roles of the cichlid fish Laetacara araguaiae
Fig. 4. Mean frequency (± SE) of agonistic acts given by male and female in the pre-spawning (n = 11), egg/wriggler (n = 11) and free-swimming fry (n = 12) phases. NS is non significant values (Two-way ANOVA followed by Tukey post hoc test).
Fig. 2 in Reproductive behavior and parental roles of the cichlid fish Laetacara araguaiae
Fig. 2. Mean frequency (± SE) of nest digging in the prespawning phase by males and females of Laetacara araguaiae (Wilcoxon signed-rank test).
Fig. 5 in Reproductive behavior, development and eye regression in the cave armored catfish, Ancistrus cryptophthalmus Reis, 1987 (Siluriformes: Loricariidae), breed in laboratory
Fig. 5. Left eye size (diameter, in mm) versus total length (in mm) in the seven specimens (respectively a to g) of Ancistrus cryptophthalmus of the Passa Três 2004 offspring.
Fig. 2 in Reproductive behavior, development and eye regression in the cave armored catfish, Ancistrus cryptophthalmus Reis, 1987 (Siluriformes: Loricariidae), breed in laboratory
Fig. 2. Size (total length, in mm) versus age (in days) in four specimens of Ancistrus cryptophthalmus from Passa Três Cave born in laboratory in March 2003.
Fig. 4 in Reproductive behavior, development and eye regression in the cave armored catfish, Ancistrus cryptophthalmus Reis, 1987 (Siluriformes: Loricariidae), breed in laboratory
Fig. 4. Size (total length, in mm) versus age (in days) of two wild caught specimens of Ancistrus cryptophthalmus from Angélica Cave kept in laboratory.
Fig. 1 in Reproductive behavior, development and eye regression in the cave armored catfish, Ancistrus cryptophthalmus Reis, 1987 (Siluriformes: Loricariidae), breed in laboratory
Fig. 1. (a) Reproductive adults of Ancistrus cryptophthalmus from Passa Três Cave kept in laboratory: two females (to the left) and male (to the right, dorso-posterior region of the head red-colored); arrow indicates the entrance of the shelter occupied by the male. Photograph taken on April 2004. (b) Cluster of eggs adhered to the ceiling of the shelter, average diameter = 4.0 mm. (c) Area around the shelter entrance (within the white circle) defended by the male (close to the center of the circle). (d) Clockwise from the top left: embrio (eyes visible), newly hatched larva (10.4 mm TL), more advanced larva (12.5 mm TL), with yolk-sac almost completely absorbed. (e) Top: 53 mm long juvenile from Passa Três Cave, with regressed eyes; arrow indicates the orbit reduced to a small depression covered with skin. Bottom: 53 mm long juvenile from Angélica Cave, probable the same age as the former, showing non-regressed eyes. (f) Detail of the head of the juvenile from Passa Três; arrows indicate the first primordia of tentacles.
Fig. 6 in Reproductive behavior, development and eye regression in the cave armored catfish, Ancistrus cryptophthalmus Reis, 1987 (Siluriformes: Loricariidae), breed in laboratory
Fig. 6. Eye size (diameter, in mm) versus age (in days) in three selected specimens (from left to right) of Ancistrus cryptophthalmus from Passa Três Cave; right eye on the top, left eye on the bottom.
Automatic extraction of opinions of users of social networks on reproductive behavior issues
<p>The database contains an upload of text comments in Russian from the social network Vkontakte in .tsv format (UTF-8 encoding). Comments are collected from communities, which discuss pregnancy, childhood, motherhood, paternity, etc. Comments are collected from communities, which discuss pregnancy, childhood, motherhood, paternity, etc. <br> The database contains train, test and valid sets for machine learning processing. For the analysis of opinions in the field of reproductive behavior, nine groups of the social network Vkontakte were selected, in the names or descriptions of which the words "childfree" and their variations were clearly present, and 341 groups, in the names or descriptions of which the keywords "mother", " mothers "," children ", etc. and the number of subscribers of which was more than 10,000 people. This distribution of groups depended on the different activity of groups - supporters of a childless lifestyle produced significantly more posts and comments on our topics. Using data from different groups of the social network Vkontakte avoids data homogeneity - one of the weak points of sentiment analysis. Thus, the presented database is suitable for the analysis of specific demographic groups, which we conditionally called “anti-natalists” and “pronatalists”. Note that in the group of pronatalists there are largely representatives of a small child model of reproductive behavior. The sample contains data about stance on 6 topics: "maternity capital / benefits", "abortion", "large families", "childlessness", "parental leave", "individualism".The topics are selected by a set of keywords such as abortion, childfree, rest, no child and so on.</p> <p>Sentences from the collected sample were randomly selected for annotator marking. Each sentence was marked with three annotators. Since each sentence could discuss several issues, the annotator marked each sentence on all seven topics. The proposals were marked up mainly by professional demographers and linguists.</p>
Reproductives signature revealed by protein profiling and behavioral bioassays in termite
<p>Proteins are known to be social interaction signals in many species in the animal kingdom. The aim of this project is to explore the potential role of cuticular polar compounds in reproductive recognition on termites. Cuticular polar fractions were extracted from reproductives and workers. These extracts were used for molecular profiling, top-down proteomics and tested in behavioral bioassays to measure behavioral response in termite.</p>
Alteration of reproductive behaviors by aromatase inhibition is population-dependent in an African cichlid fish
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Reproductive experience drives changes in behavior and physiology in male California mice (Peromyscus californicus)
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Food and social cues modulate reproductive development but not migratory behavior in a nomadic songbird, the Pine Siskin (Pinus spinus)
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Managing the tradeoff between reproduction and survival requires flexibility in behavior and gene regulation in three-spined stickleback
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Multiple stressors lead to complex responses in reproductive behaviors in an African cichlid
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Allen Brain Atlas
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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
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