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Рис. 2. МежгоΔовое соотношение чисΛенного обиΛия семейств герпетобионтных жесткокрыΛых в пойме (2008–2011 гг.) Fig. 2. Inter-annual ratio of numerical abundance of herpetobiont beetle families in the floodplain (2008–2011) in Population Dynamics For Herpetobiont Beetles (Coleoptera) In The Floodplain Of A Small Tributary In The Lower Reaches Of The Irtysh
Рис. 2. МежгоΔовое соотношение чисΛенного обиΛия семейств герпетобионтных жесткокрыΛых в пойме (2008–2011 гг.) Fig. 2. Inter-annual ratio of numerical abundance of herpetobiont beetle families in the floodplain (2008–2011)
Figure 7 in Sex ratio, oocyte development and spawning season of Mediterranean moray eel (Muraena helena) from the northern coast of Tunisia
Figure 7. – Section of gonad, illustrating the spawning capable reproductive phase of ovary (CA = cortical alveolar oocyte; Vtg3 = tertiary vitellogenic oocyte).
Figure 5 in Sex ratio, oocyte development and spawning season of Mediterranean moray eel (Muraena helena) from the northern coast of Tunisia
Figure 5. – Section of gonad, illustrating the immature phase of ovary (PG = primary growth oocyte; OW = ovarian wall).
Figure 2 in Sex ratio, oocyte development and spawning season of Mediterranean moray eel (Muraena helena) from the northern coast of Tunisia
Figure 2. Seasonal variation of the gonadosomatic index (GSI), hepatosomatic index (HSI) and relative condition factor (CF) of Muraena helena from the northern coast of Tunisia. Bars are mean values (± 2 standard errors).
Fig. 4 in Use of otolith strontium:calcium and zinc:calcium ratios as an indicator of the habitat of Percophis brasiliensis Quoy & Gaimard, 1825 in the southwestern Atlantic Ocean
Fig. 4. Discriminant analysis of the otolith Sr:Ca and Zn:Ca ratios for Percophis brasiliensis. Plot of the first two discriminant functions for each age group (a-d). An association was observed between data for ER and SMG, which were separated from data for AUCFZ. Triangles: ArgentineUruguayan Common Fishing Zone (AUCFZ), stars: San Matías Gulf (SMG) and black circles: El Rincón (ER).
Fig. 2 in Use of otolith strontium:calcium and zinc:calcium ratios as an indicator of the habitat of Percophis brasiliensis Quoy & Gaimard, 1825 in the southwestern Atlantic Ocean
Fig. 2. Variation of Sr:Ca (a) and Zn:Ca (b) ratios of Percophis brasiliensis separated by age for the three sampling sites. Different letters indicate statistical significant differences among age groups (years) for each sampling site (p<0.05).
Fig. 3 in Use of otolith strontium:calcium and zinc:calcium ratios as an indicator of the habitat of Percophis brasiliensis Quoy & Gaimard, 1825 in the southwestern Atlantic Ocean
Fig. 3. Relationship between otolith Sr:Ca and Zn:Ca ratios (mmol mol-1) for Percophis brasiliensis from three areas. Data for ER and SMG tended to cluster, while data for AUCFZ tended to disperse. Separation of data of AUCFZ and ER-SMG is observed. Triangles: Argentine-Uruguayan Common Fishing Zone (AUCFZ), stars: San Matías Gulf (SMG) and black circles: El Rincón (ER).
Figure 5 in Microbial control of live/dead zooplankton ratio in Sevastopol Bay
Figure 5. Bacterioplankton average annual (2010 - 2011) abundance (N), cell volume (V), biomass (B), intracellular nucleic acids (FL1) and integral metabolic activity (FL1 × N) (± 95% CI) at St. 1 (grey) and St. 2 (black). Significant differences are marked (* p <0.05, ** p <0.01).
Figure 7 in Microbial control of live/dead zooplankton ratio in Sevastopol Bay
Figure 7. Fraction of live organisms (FLO) as a function of the decomposition-to-mortality ratio (d/m) in the model under steady-state conditions (mortality and specific growth rates are balanced, µ = m) and projections of natural zooplankton communities (St. 1 and 2) onto the model curve.
Figure 1 in Microbial control of live/dead zooplankton ratio in Sevastopol Bay
Figure 1. Fluorescein diacetate- (FDA) and neutral red (NR) -based estimates of the average annual FLO in the open coastal waters (St. 1 in this study) and the polluted bay (St. 2 in this study) in 2010 – 2011. Calculated from the data presented in Litvinyuk et al. (2011).
Figure 6 in Microbial control of live/dead zooplankton ratio in Sevastopol Bay
Figure 6. Fraction of live organisms (FLO) in zooplankton versus bacterioplankton abundance (N). Data on FLO (2010-2011) are from Litvinyuk et al. (2011).
Figure 4 in Microbial control of live/dead zooplankton ratio in Sevastopol Bay
Figure 4. Initial bacterial abundances in the experiment (No, left plot) and frequency distribution of the copepod decomposition stages on the fourth day of exposition at St. 1 and 2 (right plot). Means and standard deviations are presented.
Figure 4 in Carbon-to-chlorophyll-a ratio in the phytoplankton of the Black Sea surface layer: variability and regulatory factors
Figure 4. Seasonal dynamic of monthly average values of C:Chl a ratio (mg С·mg Chl а-1) and their standard deviation (vertical lines) for all stations, located in the Black Sea coastal waters (during period 2000–2010).
Figure 3 in Carbon-to-chlorophyll-a ratio in the phytoplankton of the Black Sea surface layer: variability and regulatory factors
Figure 3. Seasonal variability of C:Chl a ratio (mg С·mg Chl а-1), phytoplankton biomass, water temperature, nitrate and ammonium concentrations in the surface water layer of Sevastopol Bay, as well as solar radiation intensity, which can reach the sea surface.
Figure 6 in Carbon-to-chlorophyll-a ratio in the phytoplankton of the Black Sea surface layer: variability and regulatory factors
Figure 6. Spatial distribution of chlorophyll a, phytoplankton biomass, relative share of diatoms in the total biomass of nano- and microphytoplankton and C:Chl a ratio in the surface water layer of the Black Sea in October 2010.
Figure 5 in Carbon-to-chlorophyll-a ratio in the phytoplankton of the Black Sea surface layer: variability and regulatory factors
Figure 5. Spatial distribution of chlorophyll a, phytoplankton biomass, relative share of diatoms in the total biomass of nano- and microphytoplankton and C:Chl a ratio in the surface water layer of the Black Sea in August 2011.
Рис. 2.Соотношение виΑов рыб на ΛитораΛи Тауйской губы: А — по их зоогеографической принаΑΛежности; Б — по принаΑΛежности к ихтиоцену. Обозначения см. в табΛице 1 Fig. 2. Ratio of fish species in the littoral zone of Tauysk Bay: А — according to their zoogeographic affiliation; Б — by belonging to the ichthyocene. Designations are similar to those in Table 1. in Species diversity and dominant species of the littoral area fishes of Tauysk bay, the Sea of Okhotsk
Рис. 2.Соотношение виΑов рыб на ΛитораΛи Тауйской губы: А — по их зоогеографической принаΑΛежности; Б — по принаΑΛежности к ихтиоцену. Обозначения см. в табΛице 1 Fig. 2. Ratio of fish species in the littoral zone of Tauysk Bay: А — according to their zoogeographic affiliation; Б — by belonging to the ichthyocene. Designations are similar to those in Table 1.
Fig. 6 in Habitat Use and Migratory Life History of Salangid Icefish (Salangidae) Revealed by Otolith Sr/Ca Ratios
Fig. 6. Icefish (Salanx ariakensis) collected from the Yangtze River estuary show diverse otolith Sr/Ca profiles that represent whole-life residence in the sea (a), the movement from the river to the sea at during juvenile stage (b) and the movement from the sea to the river at adult stage (c).
Fig. 5 in Habitat Use and Migratory Life History of Salangid Icefish (Salangidae) Revealed by Otolith Sr/Ca Ratios
Fig. 5. Icefish (Neosalanx anderssoni) collected from Qinhuangdao (Bohai Sea) display variably high otolith Sr/Ca ratios, indicating marine residence for the fish.
Fig. 4 in Habitat Use and Migratory Life History of Salangid Icefish (Salangidae) Revealed by Otolith Sr/Ca Ratios
Fig. 4. Icefish (Neosalanx tangkahkeii) collected from the Pearl River estuary display consistently high otolith Sr/Ca ratios, indicating brackish and marine residence for these 10 fish.
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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.