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FIGURE 10. A-D in Diversity and renewal of tropical elasmobranchs around the Middle Eocene Climatic Optimum (MECO) in North Africa: New data from the lagoonal deposits of Djebel el Kébar, Central Tunisia
FIGURE 10. A-D: Propristis cf. schweinfurti. A. Rostral denticle KEB 1-172, A1. Profile, A2. dorsal view; B. Rostral denticle KEB 1-173, Profile; C. Rostral denticle KEB 1-174, C1. Profile, C2. Dorsal view, C3. basal view; D. Rostral denticle KEB 1-175, D1. profile. D2. dorsal view; E: Pristis sp. Rostral denticle, KEB 1-165, dorsal view; F-G. Rhynchobatus cf. vincenti. F. anterior tooth KEB 1-176, F1. Occlusal view, F2. Basal view; G. anterior tooth KEB 1-177, occlusal view; H-I.?Torpedo sp. H. lateral tooth KEB 1-178, occlusal view, I. lateral tooth KEB 1-179, occlusal view.
FIGURE 9. A-F in Diversity and renewal of tropical elasmobranchs around the Middle Eocene Climatic Optimum (MECO) in North Africa: New data from the lagoonal deposits of Djebel el Kébar, Central Tunisia
FIGURE 9. A-F: Propristis cf. schweinfurti, A. Anterior oral tooth KEB 1-166, A1. Lingual view, A2. Occlusal view, A3. profile; B. Antero-lateral oral tooth KEB 1-167, B1. Occlusal view, B2. Lingual view, B3. Labial view; C. Anterior oral tooth KEB 1-168, C1. Lingual view, C2. Basal view, C3. Profile; D. lateral tooth KEB 1-169, D1. Lingual view, D2. Occlusal view, D3. Basal view, D4. Magnificence of crown-root boundary of D3; E.?male lateral tooth KEB 1-170, E1. Occlusal tooth, E2. Basal view; F.?male anterior tooth KEB 1-171, F1. Lingual view, F2. Occlusal view; G-L: Pristis sp. G. porterior tooth KEB 1-158, G1. Occlusal view, G2. Basal view; H. anterior tooth KEB 1-159, occlusal view; I. lateral tooth KEB 1-160, I1 occlusal view, I2., lingual view. J lateral tooth KEB 1-161, occlusal view; K. anterior tooth KEB 1-162, occlusal view; L. lateral tooth of?juvenile KEB 1-163, L1. Occlusal view, L2. Basal view; M. lateral tooth of juvenile KEB 1-164, M1. Occlusal view, M2. Profile.
FIGURE 1 in Diversity and renewal of tropical elasmobranchs around the Middle Eocene Climatic Optimum (MECO) in North Africa: New data from the lagoonal deposits of Djebel el Kébar, Central Tunisia
FIGURE 1. Paleotemperatures (ice-free deep-ocean T°/ tropical sea surface T°) and Thermic events during the "doubthouse" conditions of Eocene period (from Cramwinckel et al., 2018 modified with events dating from Hollis et al., 2019). Stratigraphically and geographical locations of the main deposits with Elasmobranch associations along the southwestern Tethys. Abbreviations: DAK: Dakhla (Adnet et al., 2010), GEN: Genam (Zouhri et al., 2017, in press); AZ: Aznag (Tabuce et al., 2005) PM: Phosphate ores (see Noubhani and Cappetta, 1997), Morocco; GAF: Gafsa basin (see Arambourg, 1952); KEBAR: Kébar (this work and Adnet et al., 2019); MBK: Mabrouk (see Sweydan et al., 2019), Tunisia; EG: ElGedida (see Strougo et al., 2007); KM: KM11 (see Adnet et al., 2011) MT: Minqar Tabaghbagh (see Zalmout et al., 2012); BQ: Birquet Qarun QS: Quar et Sa; GE: Genahamm Fm.; MI: Midawara FM. from Wadi al Hitan, see Underwood et al., 2011), Egypt; QD: Qa Faydat al Dahikya, Jordania, see Mustafat and Zalmout, 2002).
Fig. 3 in A new species of Quadrivisio (Amphipoda, Maeridae) from coastal tropical lagoons (Benin, West Africa)
Fig. 3. Quadrivisio laleyei sp. nov. A., C. Holotype, ♂, 7.5 mm, MNHN IU-2017-209, gnathopod. B., D. Paratype, ♀, 7.0 mm, MNHN IU-2017-211, gnathopod.
Fig. 2 in A new species of Quadrivisio (Amphipoda, Maeridae) from coastal tropical lagoons (Benin, West Africa)
Fig. 2. Quadrivisio laleyei sp. nov., ♂, holotype, 7.5 mm, MNHN IU-2017-209. A. Habitus (scale 1). B. Lower lip (scale 3). C. First antenna (scale 2). D. Second antenna (scale 2). E. Left mandible (scale 4). F. Maxilliped palp (scale 3).
Fig. 5 in A new species of Quadrivisio (Amphipoda, Maeridae) from coastal tropical lagoons (Benin, West Africa)
Fig. 5. Quadrivisio laleyi sp. nov. A–D., F. Holotype, ♂, 7.5 mm, MNHN IU-2017-209. E. Paratype, ♀, 7.0 mm, MNHN IU-2017-211. A. Male uropod 1 (scale 1). B. Male uropod 2 (scale 1). C. Male urosome (scale 1). D. Male uropod 3 (scale 1). E. Female uropod 3 (scale 1). F. Male telson (scale 2).
Fig. 4 in A new species of Quadrivisio (Amphipoda, Maeridae) from coastal tropical lagoons (Benin, West Africa)
Fig. 4. Quadrivisio laleyi sp. nov. A–B., D–E. Holotype, ♂, 7.5 mm, MNHN IU-2017-209. C. Paratype, ♂, 7.6 mm, MNHN IU-2017-210. A. Pereopod 3. B. Pereopod 4. C. Pereopod 5. D. Pereopod 6. E. Pereopod 7.
Landscape and biodiversity indicators for Curonian Lagoon
<p>Landscape and biodiversity indicators have been identified as crucial for detecting changes in the Land Cover/Habitat map target classes and evaluating threats and intense impacts on certain areas of a site. This analysis is useful to prevent future ecosystem degradation, update the preservation strategies or take immediate mitigation actions.</p> <p>Regarding Curonian Lagoon, Landscape and biodiversity indicators were generated for 2013-2014. The Land Cover/Habitat map and Object-ID raster files were used as input to estimate the indicators. The outputs include a raster file of each indicator and a file “indValues.csv” containing the values of indicators per object.</p> <p>The calculated indicators are: (i) PLAND; (ii) PD; (iii) SHAPE_MN; (iv) CA; (v) MPS; (vi) MESH; (vii) AWMPFD. Indicator files are accompanied by INSPIRE metadata XML. Detailed information can be found in the “Readme.pdf” included in the zip containing the dataset.</p>
Figure 2 in Carbon primary sources and estuarine habitat use by two congeneric ariid catfishes in a subtropical coastal lagoon
Figure 2. Carbon isotope ratios (d13C) and total length (TL, mm) of individuals of Genidens genidens (closed circles) and Genidens barbus (open circles) collected in the interface between the estuarine and freshwater zones of Patos Lagoon in present study. DISCUSSION According to the model of the life cycle suggested by ARAúJO (1988), G. barbus move between freshwater to the estuary during their first year of life. After reaching sexual maturity, adults migrate to the ocean, returning to freshwater to spawn. Our work with stable isotopes corroborates the general movement pattern proposed in this model by providing evidence that the primary producers at the estuary are an important source of carbon for juveniles of G. barbus during the initial phase of their development. There is no current model describing the life cycle of G. genidens at the Patos Lagoon. ARAúJO (1988) mentioned that this species remains in the upper limit of the estuarine zone or in the limnetic portion of the lagoon and that its juveniles are occasionally found in the estuary. Based on fish sampling restricted to the mixohaline zone of the Patos Lagoon, some authors classified this species as estuarine resident (CHAO et al. 1985, ARAúJO 1988). However, VIEIRA et al. (2010) demonstrated that G. genidens occurs from the estuary to the uppermost northern portion of the lagoon, which is located ~180 km from the lagoon's connection with the sea, and can remain year round at freshwater. Our work provides new evidence that this catfish species derives energy from the estuarine and freshwater zones of
Figure 4 in New record of an oyster species from Chilika Lagoon, Odisha, north-western Bay of Bengal
Figure 4. Ligament area, hinge dentition and white layer showing layer of mother pearl in I. ephippium.
Figure 6 in New record of an oyster species from Chilika Lagoon, Odisha, north-western Bay of Bengal
Figure 6. Sessile organisms on the shell of I. ephippium. A. Calcareous tube of marine polychaeta, B. Gastropod full egg capsule, C. Reminiscent of attached bivalve and barnacles, D. Empty gastropods egg capsule over oyster shell collected from "Arakhkuda" region.
Figure 3 in New record of an oyster species from Chilika Lagoon, Odisha, north-western Bay of Bengal
Figure 3. (A&B). Exterior of the Bivalve Isognomon ephippium, (C&D). Internal part of I. ephippium.
Figure 5. A in New record of an oyster species from Chilika Lagoon, Odisha, north-western Bay of Bengal
Figure 5. A. Mangrove vegetation at outer channel area of Chilika lagoon. B. Large bivalve colony exposed during low tide period at mangrove vegetation of "Bhabakundaleswar" region, C. Occurrence of multiple colonies of Isognomon ephippium in the sea grass bed at "Arakhkuda", D. Single colony of I.ephippium from mangrove vegetation.
Figure 1 in First record of Ophichthus johnmccoskeri (Ophichthidae: Ophichthinae) from Chilika lagoon, India
Figure 1. Ophichthus johnmccoskeri Mohapatra, Ray, Mohanty, Mishra, 2018 from Chilika lagoon, Odisha, India.
Figure 2 in Impacts of environmental factors on zooplankton taxonomic diversity in coastal lagoons in Turkey
Figure 2. Venn diagram showing identified zooplankton taxa distribution and number of taxa (in parentheses) in the lagoons.
Figure 3 in Tintinnina (Ciliophora) and Foraminifera in plankton of hypersaline Lagoon Bardawil (Egypt): spatial and temporal variability
Figure 3. Dependence of number of found tintinnid species on number of analyzed samples in Lagoon Bardawil (a) and the Mediterranean Sea (b).
Figure 2 in Tintinnina (Ciliophora) and Foraminifera in plankton of hypersaline Lagoon Bardawil (Egypt): spatial and temporal variability
Figure 2. Dependence of total tintinnid abundance on number of tintinnid species in Lagoon Bardawil during 2009 and 2010 (a- winter, b- all seasons).
Figure 1 in Assessment of the zooplankton community structure of the coastal Uzungöl Lagoon (Kızılırmak Delta, Turkey) based on community indices and physicochemical parameters
Figure 1. Geographical location of study area, coordinates of sampling points. Station 1: 41°32'33.85"N - 36°04'56.80"E; Station 2: 41°33'36.66"N - 36°05'22.24"E; Station 3: 41°34'11.10"N - 36°05'40.67"E; Station 4: 41°34'44.82"N - 36°06'0.14"E; Station 5: 41°35'7.57"N - 36° 06'20.14"E.
Figure 6 in Assessment of the zooplankton community structure of the coastal Uzungöl Lagoon (Kızılırmak Delta, Turkey) based on community indices and physicochemical parameters
Figure 6. Zooplankton community indices (Shannon Diversity, Pielou evenness and Species richness) during the study period.
Figure 3 in Assessment of the zooplankton community structure of the coastal Uzungöl Lagoon (Kızılırmak Delta, Turkey) based on community indices and physicochemical parameters
Figure 3. Seasonal density (ind. m -3) changes of nauplii larvae and copepodit individuals in Uzungöl Lagoon.
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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.