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FIGURE 5 in Reproductive biology of seven fish species of commercial interest at the Ramsar site in the Baixada Maranhense, Legal Amazon, Brazil
FIGURE 5 | Relative frequency of gonadal maturation stages during the rainy and dry seasons. (A) Cichla monoculus; (B) Hassar affinis; (C) Hoplias malabaricus; (D) Plagioscion squamosissimus; (E) Prochilodus lacustris; (F) Pygocentrus nattereri; and G. Schizodon dissimilis, caught in Baixada Maranhense Protection Area, between January 2012 and December 2016. Immature (IP); Developing phase (DP); Spawning capable (SP); Regression (RP); Regeneration (RGP), F (Female) and M (Males).
FIGURE 2 in Reproductive biology of seven fish species of commercial interest at the Ramsar site in the Baixada Maranhense, Legal Amazon, Brazil
FIGURE 2 | Distribution of the relative frequency by length classes, gonadal maturation stages, and sexes: (A) Cichla monoculus; (B) Hassar affinis; (C) Hoplias malabaricus; (D) Plagioscion squamosissimus; (E) Prochilodus lacustris; (F) Pygocentrus nattereri; and (G) Schizodon dissimilis, caught in Baixada Maranhense Protection Area, between January 2012 and December 2016. Immature (IP); Developing phase (DP); Spawning capable (SP); Regression (RP); Regeneration (RGP), F (Female) and M (Males).
FIGURE 4 in Reproductive biology of seven fish species of commercial interest at the Ramsar site in the Baixada Maranhense, Legal Amazon, Brazil
FIGURE 4 | Gonadosomatic index indicating the spawning season for (A) Cichla monoculus; (B) Hassar affinis; (C) Hoplias malabaricus; (D) Plagioscion squamosissimus; (E) Prochilodus lacustris; (F) Pygocentrus nattereri; and (G) Schizodon dissimilis, caught in Baixada Maranhense Protection Area, between January 2012 and December 2016.
Figure 3 in Reproductive biology of Lophius budegassa (Lophiidae) in the North Aegean Sea
Figure 3. - Monthly percentage of each maturity stage for males (A) and females (B) black-bellied anglerfish. Maturity stages: I, Immature; II, Maturing; III, Mature; IV, Spawning; V, Post-Spawning.
Figure 2 in Reproductive biology of Lophius budegassa (Lophiidae) in the North Aegean Sea
Figure 2. - Length-number distribution of Lophius budegassa sampled in the Saros Bay by commercial vessel between September 2006 and September 2008.
Figure 4 in Reproductive biology of Lophius budegassa (Lophiidae) in the North Aegean Sea
Figure 4. - Monthly variation of gonadosomatic index for males (A) Figure 5. - Percentage of sexually mature males (A) and females and females (B) Lophius budegassa between September 2006 and (B) Lophius budegassa according to total length. September 2008. Vertical bars represent standard error with sample size values indicated between brackets. and GSI values in females and males. Therefore, the results suggest a main spawning period from December to March decreases with increasing depth that may reflect a seasonal for blackbellied anglerfish. In females, spawning and postsegregation (García-Rodríguez et al., 2005). Laurenson et spawning stages have been seen from December to March al. (2008) found that the proportion of L. piscatorius varies and in males from January to March (Fig. 3A, B). At the same with both depth and season in Scottish waters. Several state- time, GSI values in males were high except in August and ments can explain this difference. Differentiation in growth November, while female GSI values were the highest in Janrate between sexes can cause an unbalanced proportion, uary (Fig. 4A, B). The spawning males can be seen almost all since the sex presenting faster growth rate will go through year around (Duarte et al., 2001; Landa et al., 2014), and this the most vulnerable smaller size phase quickly and, there- could increase the chances for a mature female to encounter fore decrease the predation proportion. Conversely, the sex with slower growth rate will be more likely to pass predation, with its abundance decreased disproportion- Table I. - Length at 50% maturity (L50) of Lophius budegassa obtained by other authors. ately in next development phases (Vicentini and Araújo,
Fig. 2 in Reproductive potential and biological characteristics of the parasitoid Cotesia flavipes (Hymenoptera: Braconidae) in Diatraea saccharalis (Lepidoptera: Crambidae) depending on parasitoid-host ratio
Fig. 2. Progeny (A) and sex rato (B) of Cotesia flavipes density in Diatraea saccharalis: 1:1, 3:1, 6:1, 9:1, 12:1 (parasitoids to host) at 25 ± 2 °C, 70 ± 10% RH, and a 12:12 h (L:D) photoperiod.
Fig. 3 in Reproductive potential and biological characteristics of the parasitoid Cotesia flavipes (Hymenoptera: Braconidae) in Diatraea saccharalis (Lepidoptera: Crambidae) depending on parasitoid-host ratio
Fig. 3. Rato of female produced by female (A) and body length (mm) (B) of Cotesia flavipes density in Diatraea saccharalis: 1:1, 3:1, 6:1, 9:1, 12:1 (parasitoids to host) at 25 ± 2 °C, 70 ± 10% RH, and a 12:12 h (L:D) photoperiod.
Fig. 1 in Reproductive potential and biological characteristics of the parasitoid Cotesia flavipes (Hymenoptera: Braconidae) in Diatraea saccharalis (Lepidoptera: Crambidae) depending on parasitoid-host ratio
Fig. 1. Parasitsm percentage of Diatraea saccharalis depending on Cotesia flavipes density: 1:1, 3:1, 6:1, 9:1, 12:1 (parasitoids to host) at 25 ± 2 °C, 70 ± 10% RH, and a 12:12 h (L:D) photoperiod. P = 0.05 (significance level).
Fig. 2 in Biological and reproductive parameters of Tribolium castaneum in Brazil nut
Fig. 2. Regression analysis of daily mean survival of adult Tribolium castaneum that fed on Brazil nuts.
Fig. 1 in Biological and reproductive parameters of Tribolium castaneum in Brazil nut
Fig. 1. Regression analysis of daily mean number of Tribolium castaneum eggs produced by individuals that fed on Brazil nuts.
Figure 4 in Population structure and reproductive biology of the fiddler crab Uca urvillei (Brachyura: Ocypodidae) in Maputo Bay (south Mozambique)
Figure 4. Monthly percentages of ovigerous females in each month in Uca urvillei (H. Milne Edwards, 1852). The same letters above bars indicate no statistical differences among months through Scheffe's test for multiple comparisons.
Figure 3 in Population structure and reproductive biology of the fiddler crab Uca urvillei (Brachyura: Ocypodidae) in Maputo Bay (south Mozambique)
Figure 3. Uca urvillei (H. Milne Edwards, 1852). Monthly variation of gonadosomatic index (GSI) of adult females (A) and males (B) throughout the study period. Error bars represent standard deviation.
Figure 5 in Population structure and reproductive biology of the fiddler crab Uca urvillei (Brachyura: Ocypodidae) in Maputo Bay (south Mozambique)
Figure 5. Uca urvillei (H. Milne Edwards, 1852): ln egg number plotted against ln carapace width (mm).
Figure 2 in Reproductive biology of Scinax fuscomarginatus (Anura, Hylidae) in south-eastern Brazil
Figure 2. Summary of the agonistic interactions between adult males of Scinax fuscomarginatus at Estação Ecológica de Itirapina, State of São Paulo, south-eastern Brazil.
Figure 1 in Reproductive biology of Scinax fuscomarginatus (Anura, Hylidae) in south-eastern Brazil
Figure 1. Distance between Scinax fuscomarginatus nearest males at Estação Ecológica de Itirapina during the calling activity. White bars represent distances where satellite males or agonistic interactions were observed; grey bars represent the distances when solitary males were observed calling without occurrence of agonistic interactions (Ntotal556).
Figure 1 in Reproductive biology and strategies of nine meloid beetles from Central Europe (Coleoptera: Meloidae)
Figure 1. Correlation between mean egg number per oviposition and female and the beetle's size (expressed as pronotum length), determined separately for each species (*not applicable for Meloe rufiventris, since four out of seven females had the same pronotum length).
Figure 2 in Reproductive biology and strategies of nine meloid beetles from Central Europe (Coleoptera: Meloidae)
Figure 2. Correlation between mean egg weight per oviposition and female and the beetle's size (expressed as pronotum length), determined separately for each species (*not applicable for Meloe rufiventris, since three out of four females had the same pronotum length).
Figure 2 in Ecology and reproductive biology of two species of Aplastodiscus (Anura: Hylidae) in the Atlantic forest, Brazil
Figure 2. Number of courtship displays observed for Aplastodiscus leucopygius (grey columns) and A. arildae (black columns) in the Serra do Japi, municipalty of Jundiai, State of São Paulo, Brazil.
Figure 1 in Ecology and reproductive biology of two species of Aplastodiscus (Anura: Hylidae) in the Atlantic forest, Brazil
Figure 1. (A) Maximum number of males of Aplastodiscus arildae in calling activity in the studied stream; (B) maximum number of males of A. leucopygius in calling activity in three habitats (stream, swamp, and lake) in the Serra do Japi, municipality of Jundiaı´, State of São Paulo, Brazil.
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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.