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Fig. 3 in Seasonal response of benthic foraminifera to anthropogenic pressure in two stations of the Gulf of Trieste (northern Adriatic Sea, Italy): the marine protected area of Miramare versus the Servola water sewage outfall
Fig. 3: Potentially toxic elements (PTE) concentration in the Ser (a) and Res (b) stations calculated for the 0-1 cm level. PTEs are expressed in micrograms per gram (µg/g).
Fig. 1 in Seasonal response of benthic foraminifera to anthropogenic pressure in two stations of the Gulf of Trieste (northern Adriatic Sea, Italy): the marine protected area of Miramare versus the Servola water sewage outfall
Fig. 1: Study area and location of the Ser (Servola) and Res (Riserva Naturale Marina di Miramare) stations. The Servola pipeline is evidenced in the enlarged square.
Fig. 2 in Seasonal response of benthic foraminifera to anthropogenic pressure in two stations of the Gulf of Trieste (northern Adriatic Sea, Italy): the marine protected area of Miramare versus the Servola water sewage outfall
Fig. 2: Vertical profiles of temperature, salinity, pH, oxygen saturation and chlorophyll a at Ser and Res stations during the seasonal sampling.
Fig. 15 in Seasonal dynamics of small-scale fisheries in the Adriatic Sea
Fig. 15: Size-frequency distributions of trammel net landings. TL = total length; CL = carapace length; ML = mantle length. Vertical lines: minimum landing size.
Fig. 7 in Seasonal dynamics of small-scale fisheries in the Adriatic Sea
Fig. 7: Composition of traps landings. ITA_17_A = Italy GSA17 traps for S. officinalis; ITA_17_B = Italy GSA17 traps for T. mutabilis; SLOV = Slovenia; CRO = Croatia.
Fig. 6 in Seasonal dynamics of small-scale fisheries in the Adriatic Sea
Fig. 6: Composition of trammel net landings. CRO_rocky = Croatia rocky bottoms; CRO_soft = Croatia soft bottoms; ITA_18 = Italy GSA18; MONT = Montenegro; SLOV = Slovenia.
Fig. 5 in Seasonal dynamics of small-scale fisheries in the Adriatic Sea
Fig. 5: Composition of gillnet landings. CROA = Croatia; ITA_17 = Italy GSA17; ITA_18 = Italy GSA18; MONT = Montenegro; SLOV = Slovenia.
Fig. 6 in Occurrence Of Dactylogyrus Infection Linked To Seasonal Changes And Host Fish Size On Four Cyprinid Fishes In Lake Manyas, Turkey
Fig. 6. Prevalence (broken line) (❍: D. cornu, ∆: D. difformis) and mean intensity (solid line) of the parasite species (●: D. cornu, ▲: D. difformis) on Vimba vimba and Scardinius erythrophthalmus in
Fig. 3 in Occurrence Of Dactylogyrus Infection Linked To Seasonal Changes And Host Fish Size On Four Cyprinid Fishes In Lake Manyas, Turkey
Fig. 3. Prevalence (broken line) and mean intensity (solid line) of D. crucifer on R. rutilus in Lake Manyas over two years
Fig. 2 in Occurrence Of Dactylogyrus Infection Linked To Seasonal Changes And Host Fish Size On Four Cyprinid Fishes In Lake Manyas, Turkey
Fig. 2. Prevalence (broken line) and mean intensity (solid line) of D. sphyrna on B. bjoerkna in Lake Manyas over two years, and the water temperature (*) of the Lake during the study period (surface)
Fig. 5 in Occurrence Of Dactylogyrus Infection Linked To Seasonal Changes And Host Fish Size On Four Cyprinid Fishes In Lake Manyas, Turkey
Fig. 5. Prevalence (broken line) (❍: D. sphyrna, ∆: D. crucifer) and mean intensity (solid line) of the parasite species (●: D. sphyrna, ▲: D. crucifer) on Blicca bjoerkna and Rutilus rutilus in relation to
Fig. 4 in Occurrence Of Dactylogyrus Infection Linked To Seasonal Changes And Host Fish Size On Four Cyprinid Fishes In Lake Manyas, Turkey
Fig. 4. Prevalence (broken line) (❍: D. cornu, ∆: D. difformis) and mean intensity (solid line) of the parasite species (●: D. cornu, ▲: D. difformis) on Vimba vimba and Scardinius erythropthalmus in Lake Manyas over two years
Figs 3–4. 3 in Seasonal Changes In The Sex Ratio Of Nyctalus Species In North-East Hungary
Figs 3–4. 3 = The numbers of males and females of N. lasiopterus grouped into 15 day periods. 4 = Sex ratios of N. leisleri in different parts of Europe [source: 1 (HELVERSEN & WEID); 2 (GAISLER 1975); 3 (HEISE 1982); 4 (LICHACEV 1980); 5 (ABELENCEV et al. 1956) in BOGDANOWICZ & RUPRECHT 2004]
Moss species and precipitation mediate experimental warming stimulation of growing season N2 fixation in subarctic tundra
<p>Climate change in high latitude regions leads to both higher temperatures and more precipitation but their combined effects on terrestrial ecosystem processes are poorly understood. In nitrogen (N) limited and often moss-dominated tundra and boreal ecosystems, moss-associated N<sub>2</sub> fixation is an important process that provides new N. We tested if high mean annual precipitation enhanced experimental warming effects on growing season N<sub>2</sub> fixation in three common arctic-boreal moss species adapted to different moisture conditions and evaluated their N contribution to the landscape level. We measured <em>in situ</em> N<sub>2</sub> fixation rates in <em>Hylocomium splendens</em>, <em>Pleurozium schreberi</em> and <em>Sphagnum</em> spp. from June to September in subarctic tundra in Sweden. We exposed mosses occurring along a natural precipitation gradient (mean annual precipitation: 571-1155 mm) to eight years of experimental summer warming using open-top chambers before our measurements. We modelled species-specific seasonal N input to the ecosystem at the colony and landscape level. Higher mean annual precipitation increased N<sub>2</sub> fixation, especially during peak growing seasons and in feather mosses. For <em>Sphagnum-</em>associated N<sub>2</sub> fixation,<em> </em>high mean annual<em> </em>precipitation reversed a small negative warming response. By contrast, in the dry-adapted feather moss species higher mean annual precipitation led to negative warming effects<em>.</em> Modelled total growing season N inputs for <em>Sphagnum </em>spp. colonies were 2-3 times that of feather mosses on an area basis. However, at the landscape level where feather mosses were more abundant, they contributed 50% more N than <em>Sphagnum</em>. The discrepancy between modelled estimates of species-specific N input via N<sub>2</sub> fixation at the moss core versus ecosystem scale exemplifies how moss cover is essential for evaluating the impact of altered N<sub>2</sub> fixation. Importantly, combined effects of warming and higher mean annual precipitation may not lead to similar responses across moss species, which could affect moss fitness and their abilities to buffer environmental changes. </p>
Figure 4 in Population Dynamics of Amoeboid Protists in a Tropical Desert: Seasonal Changes and Effects of Vegetation and Soil Conditions
Figure 4. Relationship between amoeboid protist richness and soil parameters during the wet season in three microhabitats by CCA: PL: Pr. laevigata, PP: Pa. praecox, and BS: bare soil. The names and abbreviations of the amoeboid protist species can be found in table 3.
Figure 2 in Population Dynamics of Amoeboid Protists in a Tropical Desert: Seasonal Changes and Effects of Vegetation and Soil Conditions
Figure 2. Cumulative richness plots of amoeboid protists present under Pr. laevigata (PL), Pa. praecox (PP) and bare soil (BS) during dry and wet seasons at 0–30 cm. a) eruptive pseudopods, and b) acanthopodial pseudopods. ND: not determined.
Figure 1 in Population Dynamics of Amoeboid Protists in a Tropical Desert: Seasonal Changes and Effects of Vegetation and Soil Conditions
Figure 1. Study area, showing vegetation patches in the desert of Tehuacán, Puebla, Mexico. In addition, the analyzed microhabitats are shown: Pr. laevigata, Pa. praecox and bare soil.
Fig. 3 in Spatial, seasonal and ontogenetic changes in food resource use by a piscivore fish in two Pantanal lagoons, Brazil
Fig. 3. Diet composition of Plagioscion ternetzi by size class in Sinhá Mariana lagoon (a) and in Chacororé lagoon (b) (EIG: Eigenmannia spp.; PIM: Pimelodella spp.; ROE: Roeboides spp.; PCU: Psectrogaster curviventris; CDO: Curimatella dorsalis; BRA: Brachyhypopomus spp.; SMA: Synbranchus marmoratus; TAR: Tetragonopterus argenteus; HOR: Hemiodus orthonops; LOR: Loricariichthys spp.; SBR: Schizodon borellii; AST: Astyanax spp.; SMG: Serrasalmus marginatus; LEP: Leporinus spp.; OF: other fish; SH: shrimp; INS: insect; FR: fish remains).
Fig. 5 in Seasonal analysis of condition, biochemical and bioenergetic indices of females of Brazilian flathead, Percophis brasiliensis
Fig. 5. Seasonal variation of inorganic matter content (ash) in muscle, gonad and liver of Percophis brasiliensis.
Fig. 1 in Seasonal analysis of condition, biochemical and bioenergetic indices of females of Brazilian flathead, Percophis brasiliensis
Fig. 1. Seasonal variation of mean and standard deviation of hepatosomatic index (HSI), gonadosomatic index (GSI) and condition index (K) estimated for Percophis brasiliensis.
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.