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FIGURE 17 in Polka-dotted treasures: Revising a clade of ascidian- and bivalve-associated shrimps (Caridea: Palaemonidae)
FIGURE 17 Dasella herdmaniae (Lebour, 1938) from Herdmania momus (Savigny, 1816). A) RMNH.CRUS.D.53924, stn SEM.52; B) RMNH.CRUS.D.53535, stn TER.10. PHOTOGRAPHS BY C.H.J.M. FRANSEN
FIGURE 13 Anchistus gravieri Kemp, 1922, RMNH.CRUS.D.58052 in Polka-dotted treasures: Revising a clade of ascidian- and bivalve-associated shrimps (Caridea: Palaemonidae)
FIGURE 13 Anchistus gravieri Kemp, 1922, RMNH.CRUS.D.58052, Vanuatu (stn FR15), female, pocl. 4.2 mm. A) left second maxilliped, dorsal view; B) left third maxilliped, dorsal view; C) left first pereiopod, lateral view; D) right second pereiopod, ventral view; E) idem, chela, medial view. Scale A, B = 0.5 mm; C = 1.25 mm; D = 2 mm; E = 1 mm. ARTWORK BY C.H.J.M. FRANSEN
FIGURE 21 in Polka-dotted treasures: Revising a clade of ascidian- and bivalve-associated shrimps (Caridea: Palaemonidae)
FIGURE 21 Ensiger custoides (Bruce, 1977), RMNH.CRUS.D.41440, ovigerous female pocl. 9.1 mm. A) habitus, lateral view; B) anterior appendages, lateral view; C) idem, dorsal view; D) telson, dorsal view. Scale A= 4 mm; B, C, = 2 mm; D = 1 mm. ARTWORK BY C.H.J.M. FRANSEN
FIGURE 20 A–C in Polka-dotted treasures: Revising a clade of ascidian- and bivalve-associated shrimps (Caridea: Palaemonidae)
FIGURE 20 A–C) Ensiger custoides (Bruce, 1977) in Atrina vexillum (Born, 1778). A) RMNH.CRUS.D.58065, stn RAJ.08; B) RMNH.CRUS.D.58066, stn SER.24; C) RMNH.CRUS.D.53610, stn TER.36; D) Ensiger custos (Forskål, 1775) from Pinna bicolor Gmelin, 1791, RMNH.CRUS.D.41446, stn RBE.01. PHOTOGRAPHS BY C.H.J.M. FRANSEN Downloaded from Brill.com 06/24/2024 12:38:05AM via Open Access. This is an open access article distributed under the terms of the CC-BY 4.0 license. https://creativecommons.org/licenses/by/4.0/
FIGURE 27 in Polka-dotted treasures: Revising a clade of ascidian- and bivalve-associated shrimps (Caridea: Palaemonidae)
FIGURE 27 Ensiger custos (Forskål, 1775). A–C) RMNH.CRUS.D.41445, male pocl. 4.0 mm. A) left first pereiopod, lateral view; B) right second pereiopod chela, medial view; C) left second pereiopod chela, medial view; D, RMNH.CRUS.D.41448, ovigerous female pocl. 6.4 mm, right third pereiopod dactylus, medial view, propodal setae omitted. Scale A = 1 mm; B, C = 1 mm; D = 0.1 mm. ARTWORK BY C.H.J.M. FRANSEN
Рис. 2. Виды иЗученных районов и характер плЯЖевых осадков: A, B – Чьюн Ша (о-в Лантау); C, D – СтЭнли (о-в Гонконг); E – ракуша на плЯЖе в районе м. д'Агулар (включаЯ обломки балЯнусов); F – плЯЖ в районе м. д'Агулар (о-в Гонконг). in On the fauna of bivalve mollusks of Hong Kong (South China Sea)
Рис. 2. Виды иЗученных районов и характер плЯЖевых осадков: A, B – Чьюн Ша (о-в Лантау); C, D – СтЭнли (о-в Гонконг); E – ракуша на плЯЖе в районе м. д'Агулар (включаЯ обломки балЯнусов); F – плЯЖ в районе м. д'Агулар (о-в Гонконг).
Рис. 3. Виды иЗученных районов и характер плЯЖевых осадков: A, B – Шек О (о-в Гонконг); C, D – Хун Шин Йе (о-в Ламма). in On the fauna of bivalve mollusks of Hong Kong (South China Sea)
Рис. 3. Виды иЗученных районов и характер плЯЖевых осадков: A, B – Шек О (о-в Гонконг); C, D – Хун Шин Йе (о-в Ламма).
Рис. 5. Синтипы Arca globosa Reeve, 1844 (A–D и E–H – наруЖный и внутренний виды двух раковин), МуЗей естественной истории, Лондон, коллекциЯ Х. Каминга, рег. номер 1969166. in On the fauna of bivalve mollusks of Hong Kong (South China Sea)
Рис. 5. Синтипы Arca globosa Reeve, 1844 (A–D и E–H – наруЖный и внутренний виды двух раковин), МуЗей естественной истории, Лондон, коллекциЯ Х. Каминга, рег. номер 1969166.
Fig. 1 in Towards a ground pattern reconstruction of bivalve nervous systems: neurogenesis in the zebra mussel Dreissena polymorpha
Fig. 1 Development of Dreissena polymorpha from gastrula to early veliger stage. a, g, h, and i Scanning electron micrographs. b, c Confocal microscope Zprojection images. d, e, and f Single optical sections of c. Acetylated α-tubulin-lir (green), HCS CellMask (pink), and cell nuclei counter staining (blue). Apical is always up. Lateral views. Scale bars are 15 μm. a Ciliated gastrula stage (16 h post fertilization, hpf) with blastopore (bp) on the vegetal pole. b Elongated early trochophore (22 hpf) with prominent apical tuft (at) and prototroch (pt). c Early-trochophore (23 hpf) with apical tuft (at), prototroch (pt), and telotroch (tt). d Early trochophore (23 hpf). e, f Early trochophore (23 hpf) in different optical planes with foregut (fg) and shell field (sf) invagination. g Early veliger (39 hpf) with embryonic shell (s) and expanded velum (ve). h 46 hpf old veliger. i Late veliger larva (188 hpf)
Карта-схема района исследований. 1А, 1Б, 1В – станции раЗреЗа 1; 2А, 2Б, 2В – станции раЗреЗа 2; 3А, 3Б, 3В – станции раЗреЗа 3. A schematic map of the research area. 1A, 1Б, 1В – stations of line 1; 2A, 2Б, 2В – stations of line 2; 3A, 3Б, 3В – stations of line 3. in Pelagic larvae of bivalve mollusks in meroplankton in the coastal waters of Aniva Bay (southern Sakhalin, Sea of Okhotsk)
Карта-схема района исследований. 1А, 1Б, 1В – станции раЗреЗа 1; 2А, 2Б, 2В – станции раЗреЗа 2; 3А, 3Б, 3В – станции раЗреЗа 3. A schematic map of the research area. 1A, 1Б, 1В – stations of line 1; 2A, 2Б, 2В – stations of line 2; 3A, 3Б, 3В – stations of line 3.
Рис. 2. Схема станΔартных промеров раковины Δвустворчатых моΛΛюсков по А. А. Зютину: L — ΔΛина раковины; H — тоΛщина раковины; D — ширина / выпукΛость Fig. 2. Scheme of bivalve mollusk shell standard measurements: L — shell length; H — shell thickness; D — width / convexity (according to A. A. Zyutin) in Morphometric characteristics of Black Sea mussels Mytilus galloprovincialis Lam. as biomarkers of the anthropogenic impact on the Black Sea coastal biocenoses in tourist destinations
Рис. 2. Схема станΔартных промеров раковины Δвустворчатых моΛΛюсков по А. А. Зютину: L — ΔΛина раковины; H — тоΛщина раковины; D — ширина / выпукΛость Fig. 2. Scheme of bivalve mollusk shell standard measurements: L — shell length; H — shell thickness; D — width / convexity (according to A. A. Zyutin)
Fig. 10 in A mosaic of conserved and novel modes of gene expression and morphogenesis in mesoderm and muscle formation of a larval bivalve
Fig. 10 Muscle systems in bivalve lineages. a Bivalve phylogeny (after Combosch et al. (2017)) with larval muscle systems in various clades.?: unknown, numbers: number of paired retractors/adductors,>: set of paired mantle retractors, a.m.: after metamorphosis. Colour code indicates individual muscle systems. Comparative analysis implies that five major muscle systems were present in the last common ancestor (LCA) of autobranch bivalve larvae: The velum musculature including three or four pairs of velum retractors and a velum muscle ring, the larval retractors (one or two pairs), the adductor system containing the anterior as well as the posterior adductor,
Fig. 5 in A mosaic of conserved and novel modes of gene expression and morphogenesis in mesoderm and muscle formation of a larval bivalve
Fig. 5 Expression of myosin II heavy chain (Dro-mhc_c1) and myogenesis in Dreissena rostriformis veliger larvae. Lateral view in all images, anterior faces upwards and dorsal to the left except in c which is a dorso-anterior view, e and f which are anterior views (dorsal is up), and i which is a posterior view (dorsal is up). Arrowheads indicate the stomodaeum. Scale bar equals 20 µm. Brightfield images of the gene expression (a and e) and confocal images (b–d and f–i) with F-actin (yellow–red), cilia (green), and cell nuclei staining (cyan). a Expression of Dro-mhc_c1 is in the central and dorsal mesoderm. Velum (ve). b First distinct muscle bundles are the dorsal velum retractor (dv), the ventral velum retractor (vv), and the larval retractor (lr). First appearance of the velum muscle ring (vr), the (pal-
Fig. 3 in A mosaic of conserved and novel modes of gene expression and morphogenesis in mesoderm and muscle formation of a larval bivalve
Fig. 3 Expression of myosin II heavy chain (Dro-mhc_c1) and immunofluorescence staining in Dreissena rostriformis trochophore larvae. Anterior is up. Arrowheads indicate the stomodaeum, sf marks the shell field, dotted line outlines the region of the prototroch (pt). Scale bar equals 20 µm. Brightfield images (a, b) of the gene expression and confocal images (c, d) with F-actin (red), cilia (green; pt: prototroch; tt: telotroch), and cell nuclei staining (cyan). a Dro-mhc_c1 expression is first present in the anterior mesoderm. b Anterior mesodermal expression in dorsal view. c First F-actinpositive domain in the mesoderm below the shell field in the dorso-median region. d Slightly further developed trochophore larva showing two developing myofilaments in the median region. A, anterior; D, dorsal; P, posterior; V, ventral
Figure 3 in The ecology of freshwater bivalves in the Lake Sapanca basin, Turkey
Figure 3. Length–frequency distribution of (a) Unio crassus, (b) Unio pictorum, (c) Anodonta anatina, (d) Anodonta cygnea in the Lake Sapanca basin.
Figs. 5–8 in First elucidation of a blood fluke (Electrovermis zappum n. gen., n. sp.) life cycle including a chondrichthyan or bivalve
Figs. 5–8. Sporocyst and cercaria of Electrovermis zappum Warren and Bullard n. gen., n. sp. (Digenea: Aporocotylidae) infecting variable coquina clam, Donax variabilis Say, 1822 (Bivalvia: Cardiida: Donacidae). (5) Sporocyst showing four cercarial bodies among several germ bodies, ventral view. (6) Photo of live sporocyst showing three germ bodies (*). (7) Body of live cercaria, ventral view. (8) Body of mounted cercaria (USNM No. 1578578–1578583), ventral view. Mouth (mo), concentric spines (cs), dorsal fin fold (df), penetration gland (pg), lateral body spines (s), gonadal anlage (ga), excretory duct (ed), tail stem (ts), nuclei (n), and furca (f).
Fig. 16 in First elucidation of a blood fluke (Electrovermis zappum n. gen., n. sp.) life cycle including a chondrichthyan or bivalve
Fig. 16. Cercaria infecting green jackknife clam, Solen viridis Say, 1821 (Bivalvia: Adapedonta: Solenidae). (16) Body of mounted cercaria (USNM No. 1578587–1578589), ventral view. Mouth (mo), penetration gland (pg), excretory vesicle (ev), tail stem (ts), and furca (f).
Fig. 17–21 in First elucidation of a blood fluke (Electrovermis zappum n. gen., n. sp.) life cycle including a chondrichthyan or bivalve
Fig. 17–21. Cercaria infecting green jackknife clam, Solen viridis Say, 1821 (Bivalvia: Adapedonta: Solenidae). (17) Cercarial body showing mouth (m), anterior-most row of spines (arrow), and connection with tail (tl). (18) Anterior end showing concentric rows of minute spines about anterior body end, lateral view. (19) High magnification view of spine (arrow) and spine rows in anterior region of cercarial body near mouth, lateral view. (20 & 21) Granular material near tegumental pore.
Figs. 9–15 in First elucidation of a blood fluke (Electrovermis zappum n. gen., n. sp.) life cycle including a chondrichthyan or bivalve
Figs. 9–15. Scanning electron microscopy and histopathology of cercaria of Electrovermis zappum Warren and Bullard n. gen., n. sp. (Digenea: Aporocotylidae) infecting variable coquina clam, Donax variabilis Say, 1822 (Bivalvia: Cardiida: Donacidae). (9) Whole body, arrow = dorsal fin fold. (10) Body, white arrows = possible secretion masses from penetration glands; white bar = anterior-most end including concentric spines; white arrows = lateral body spine rows, lateral view (11) Higher magnification of lateral body margin, arrows = tegumental papillae. (12) Higher magnification of anterior body end, showing space between spines of anterior sucker and those of the lateral body margin. (13) Histological section of infected gonad adjacent to intestinal arms (ia) and digestive diverticulum (dd). (14) Histological section showing infiltration of hemocytes (*) surrounding intestinal arm (ia), spororcysts (sp), and ooctyes (arrow). (15) Higher magnification of sporocyst containing developed cercaria (arrow) adjacent to digestive diverticulum (dd).
Fig. 22 in First elucidation of a blood fluke (Electrovermis zappum n. gen., n. sp.) life cycle including a chondrichthyan or bivalve
Fig. 22. Life cycle of Electrovermis zappum Warren and Bullard n. gen., n. sp. (Digenea: Aporocotylidae) infecting the heart of the lesser electric ray, Narcine bancroftii (Griffith and Smith, 1834) Carvalho, 2001 (Torpediniformes: Narcinidae), and the variable coquina clam, Donax variabilis Say, 1822 (Bivalvia: Cardiida: Donacidae). (22) Letters indicate the life history: A) egg or miracidium emerges from definitive host, N. bancroftii; B) miracidium infects the intermediate host, D. variabilis; C) clonal asexual reproduction occurs in sporocyst and cercariae emerge; D) cercariae infect neonates, juveniles, or adults of N. bancroftii.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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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.
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