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365 results for “Nereididae”
FIGURE 8. Nereis denhamensis Augener, 1913 in Nereididae (Annelida: Phyllodocida) from intertidal macroalgae in Western Australia
FIGURE 8. Nereis denhamensis Augener, 1913 (WAM V11644); A, head, dorsal view; B, proboscis, ventral dissection; C, parapodium, chaetiger 41, posterior view; D, notochaetae, homogomph falciger, chaetiger 41; E, neurochaetae, dorsal fascicle, homogomph spiniger, chaetiger 41; F, neurochaetae, ventral fascicle, heterogomph spiniger, chaetiger 41; G, neurochaetae, ventral fascicle, heterogomph falciger, chaetiger 41. Scale: A–B, 1 mm; C, 0.1 mm; D–G, 0.02 mm.
FIGURE 19 in Nereididae (Annelida: Phyllodocida) from intertidal macroalgae in Western Australia
FIGURE 19. Comparative material from Western Australia and the Northern Territory sourced from the Museum & Art Gallery of the Northern Territory. Neanthes cricognatha (Ehlers, 1904) (NTM W18357; 1.8 mm wide at chaetiger 1): A, anterior segments, dorsal view; B, anterior segments, ventral view. Neanthes unifasciata (Willey, 1905) (NTM W19021; 1.5 mm wide at chaetiger 1): C, anterior segments, dorsal view; D, proboscis, ventral dissection. Nereis cockburnensis Augener, 1913 (NTM W18361; 2.0 mm wide at chaetiger 1): E, anterior segments, dorsal view; F, proboscis, ventral dissection. Nereis denhamensis Augener, 1913 (NTM W19015; 1.5 mm wide at chaetiger 1): G, anterior segments, dorsal view; H, anterior segments, ventral view.
FIGURE 14. Platynereis antipoda Hartman, 1954 in Nereididae (Annelida: Phyllodocida) from intertidal macroalgae in Western Australia
FIGURE 14. Platynereis antipoda Hartman, 1954 (WAM V11676); A, head, dorsal view; B, head, ventral view; C, parapodium, chaetiger 52, anterior view; D, notochaetae, homogomph spiniger, chaetiger 52; E, notochaetae, homogomph falciger, chaetiger 52; F, neurochaetae, dorsal fascicle, heterogomph falciger, chaetiger 52; G, neurochaetae, ventral fascicle, heterogomph spiniger, chaetiger 52. Scale: A, 1 mm; B, 0.5 mm; C, 0.1 mm; D–G, 0.02 mm.
FIGURE 15. Platynereis polyscalma Chamberlin, 1919 in Nereididae (Annelida: Phyllodocida) from intertidal macroalgae in Western Australia
FIGURE 15. Platynereis polyscalma Chamberlin, 1919 (WAM V11684); A, head, dorsal view; B, head, ventral view; C, parapodium, chaetiger 35, posterior view; D, notochaetae, homogomph falciger, chaetiger 35; E, neurochaetae, dorsal fascicle, homogomph spiniger, chaetiger 35; F, neurochaetae, ventral fascicle, heterogomph spiniger, chaetiger 35; G, neurochaetae, ventral fascicle, heterogomph falciger, chaetiger 18; H, neurochaetae, ventral fascicle, heterogomph falciger, chaetiger 35. Scale: A–B, 1 mm; C, 0.05 mm; D–H, 0.02 mm.s
FIGURE 18 in Nereididae (Annelida: Phyllodocida) from intertidal macroalgae in Western Australia
FIGURE 18. Pseudonereis rottnestiana (Augener, 1913) (WAM V11696); A, head, dorsal view; B, head, ventral view; C, parapodium, chaetiger 35, anterior view; D, neurochaetae, dorsal fascicle, homogomph spiniger, chaetiger 35; E, neurochaetae, ventral fascicle, heterogomph falciger, chaetiger 35. Scale: A–B, 1 mm; C, 0.1 mm; D–E, 0.02 mm.
FIGURE 2 in A new species of Perinereis Kinberg, 1865 (Annelida: Nereididae) and invalidation of two congeners from Western India
FIGURE 2. Sites and type of habitats present in the Gujarat coast, west India. A. Hard mud flats in low tide of Kamboi. B. Mounds of soft and hard calcrete mudflat at Kamboi. C. Excavated block of hard calcrete substratum, arrow indicates burrowing and boring pattern of worms, scale bar: 7 cm.
FIGURE 3 in A new species of Perinereis Kinberg, 1865 (Annelida: Nereididae) and invalidation of two congeners from Western India
FIGURE 3. Perinereis khambhatiensis sp. nov. from Kamboi, Gujarat, India. A, H–N, atoke holotype (MSUB-ZL-AN-PCh- 01); B–G, atoke paratype (ZSI-WRC ANN/25). A. Whole body in dorsolateral view. B. Anterior region and everted proboscis in dorsal view. C. Everted proboscis in ventral view. D. Paragnaths of areas III and IV, arrows pointing at lateral isolated paragnaths on area III. E. Left jaw in ventral view and right jaw in dorsal view, respectively. F. Close-up of jaw in ventral view, arrow pointing inner canals. G. Paired oesophageal caeca (arrows) in ventral view. H–L. Parapodia in anterior view, numbers refer to the chaetiger. M. Homogomph spiniger from notopodia (chaetiger 45). N. Heterogomph falciger from neuropodial subacicular fascicle (chaetiger 48). Scale bars: A, 7 mm; B, 0.8 mm; C, E, 0.4 mm; D, 0.5 mm; F, 0.2 mm; G, 1 mm; H–L, 200 μm; M, 40 μm; N, 25 μm.
A Taxonomic Information System for Nereididae (Annelida): morphological datasets supporting description, interactive identification and phylogenetic analysis of the family
<p>Nereididae (Polychaeta)–A DELTA database of genera, and Australian species</p><p>Robin S. Wilson1,2 , Christopher J. Glasby3,4 , Torkild Bakken5</p><p> </p><p>1 Sciences Department, Museums Victoria Research Institute, Museums Victoria, GPO Box 666 Melbourne, Victoria 3001, Australia</p><p>2 The University of Melbourne, Melbourne, Victoria 3010, Australia</p><p>3 Museum and Art Gallery Northern Territory, PO Box 4646, Darwin NT 0801, Australia</p><p>4 Australian Museum Research Institute, Australian Museum, 1 William Street, Sydney, NSW 2010, Australia</p><p>5 Norwegian University of Science and Technology, NTNU University Museum, NO-7491 Trondheim, Norway</p><p> </p><p>Corresponding author: Robin S. Wilson (<a href="mailto:rwilson@museum.vic.gov.au">rwilson@museum.vic.gov.au</a>)</p><p>Scope</p><p>This Nereididae (Annelida) Delta database is the work of Robin Wilson, Torkild Bakken & Chris Glasby and was used to generate sections of Wilson et al. (2023a). Status of genera and nominal subfamily placements follow WoRMS <a href="https://www.marinespecies.org/polychaeta/">https://www.marinespecies.org/polychaeta/</a>.</p><p>The version distributed here includes only Nereididae genera and is part of the Wilson et al. (2023b) Zenodo repository which also includes other outputs: Nexus files as .nex and natural language output of taxon descriptions and character lists as .rtf files. </p><p>Updates including fixes to any errors found, and including new taxa and new taxonomic revisions, will be uploaded to Zenodo as new versions (the doi above will resolve to the most recent version). We intend that future versions will include all Nereididae species known from Australia; and all Nereididae species known from bathyal-abyssal depths (~2,000 m and deeper).</p><p>This repository contains an interactive key using the Delta Intkey software version by the Atlas of Living Australia (2014) <strong>but not yet that of Dallwitz (2020)</strong>.</p><p>References</p><p>Atlas of Living Australia (2014) Open-delta. A Java port of the Delta - DEscription Language for TAxonomy suite of applications into Java. Available from: https://github.com/AtlasOfLivingAustralia/open-delta (July 12, 2023).</p><p>Dallwitz MJ (2020) Installing and running the programs of the DELTA System. Reports, Division of Entomology CSIRO Australia. Available from: https://www.delta-intkey.com/www/programs.htm (January 31, 2023).</p><p>Wilson RS, Glasby CJ, Bakken T (2023a) The Nereididae (Annelida) – diagnoses, descriptions, and a key to the genera. ZooKeys 1182: 35–134. <a href="https://doi.org/10.3897/zookeys.1182.104258">https://doi.org/10.3897/zookeys.1182.104258</a></p><p>Wilson RS, Bakken T, Glasby CJ (2023b) A Taxonomic Information System for Nereididae (Annelida): morphological datasets supporting description, interactive identification and phylogenetic analysis of the family. <a href="https://doi.org/10.5281/zenodo.7776745">https://doi.org/10.5281/zenodo.7776745</a></p>
Fig. 2 in Two New Species of Composetia (Annelida: Nereididae) from Small Estuaries in the Ryukyu Islands, Southern Japan, with a List of All Species Currently Belonging to Composetia
Fig. 2. Composetia kumensis sp. nov. A, dorsal view of prostomium and peristomium of a paratype (NSMT-Pol P-772). B–H, holotype (NSMT-Pol H-766): B, dorsal view of the everted proboscis; C, ventral view of the everted proboscis; D, anterior view of left parapodium 1; E, posterior view of right parapodium 5; F, anterior view of right parapodium 5; G, posterior view of right parapodium 20; H, posterior view of right parapodium 41. Abbreviations: g, glandular patch; i, neuropodial inferior lobe; ne, neuroacicula; no, notoacicula; p, neuropodial postchaetal lobe. Scale bars: 1 mm (A–C); 0.1 mm (D–H).
Figure 4 from: Núñez J, Glasby CJ, Naranjo M (2020) Groundwater annelids from Gran Canaria and Fuerteventura (Canary Islands), with the description of two new species of Namanereis (Namanereidinae, Nereididae, Polychaeta). Subterranean Biology 36: 35-49. https://doi.org/10.3897/subtbiol.36.55090
Figure 4 Namanereis canariarum sp. nov. a jaw pieces of the pharynx, ventral view b parapodium, detail of the acicular lobes c pseudospiniger blade tip d subneuroacicular heterogomph falciger, chaetiger 60. Namanereis llanetensis sp. nov. e Holotype, detail of the basal spinulation, hererogomph spiniger, chaetiger 10 f Holotype, detail of spinulation, subneuroacicular heterogomph falciger, chaetiger 10.
Figure 3 from: Núñez J, Glasby CJ, Naranjo M (2020) Groundwater annelids from Gran Canaria and Fuerteventura (Canary Islands), with the description of two new species of Namanereis (Namanereidinae, Nereididae, Polychaeta). Subterranean Biology 36: 35-49. https://doi.org/10.3897/subtbiol.36.55090
Figure 3 Namanereis llanetensis sp. nov. a anterior end, dorsal view b everted pharynx with jaws, dorsal view c jaws ventral view d posterior end, dorsal view e parapodium from chaetiger 3 f parapodium from chaetiger 60 g supraneuroacicular falciger, chaetiger 60 h subneuroacicular falciger, chaetiger 3 i supraneuroacicular falciger, chaetiger 3 j subneuroacicular falciger, chaetiger 3 k supraneuroacicular spiniger, blade not fully shown, chaetiger 3 l subneuropodial spiniger, blade not fully shown, chaetiger 10 m subneuroacicular spiniger, blade fully shown, chaetiger 60 n supraneuroacicular spiniger, blade fully shown, chaetiger 60.
Figure 2 from: Núñez J, Glasby CJ, Naranjo M (2020) Groundwater annelids from Gran Canaria and Fuerteventura (Canary Islands), with the description of two new species of Namanereis (Namanereidinae, Nereididae, Polychaeta). Subterranean Biology 36: 35-49. https://doi.org/10.3897/subtbiol.36.55090
Figure 2 Namanereis canariarum sp. nov. a anterior end, everted pharynx, dorsal view b jaw pieces of the pharynx, frontal view c parapodium from chaetiger 10 d parapodium from chaetiger 60 e supraneuroacicular falciger, chaetiger 30 f subneuroacicular falciger, chaetiger 10 g subneuroacicular pseudospiniger, chaetiger 30 h supraneuroacicular spiniger, blade not fully shown, chaetiger 10 i supraneuroacicular spiniger, blade fully shown, chaetiger 10 j subneuroacicular pseudospiniger, chaetiger 10 k supraneuroacicular falciger, chaetiger 30 l subneuroacicular falciger, chaetiger 30.
Figure 1 from: Núñez J, Glasby CJ, Naranjo M (2020) Groundwater annelids from Gran Canaria and Fuerteventura (Canary Islands), with the description of two new species of Namanereis (Namanereidinae, Nereididae, Polychaeta). Subterranean Biology 36: 35-49. https://doi.org/10.3897/subtbiol.36.55090
Figure 1 a Distribution in Canary Islands of Namanereis canariarum sp. nov. (yellow dot) and Namanereis llanetensis (red dot) bNamanereis canariarum sp. nov. live specimen, dorsal view cNamanereis llanetensis sp. nov. live specimen, dorsal view d Los Llanetes water mine (Valsequillo, Gran Canaria) type locality of N. llanetensis sp. nov.
Figure 9 from: Azmi SS, Ibrahim YS, Angsupanich S, Sumpuntarat P, Sato M (2021) Epitokous metamorphosis, reproductive swimming, and early development of the estuarine polychaete, Neanthes glandicincta Southern, 1921 (Annelida, Nereididae) on the east coast of the Malay Peninsula. ZooKeys 1011: 1-24. https://doi.org/10.3897/zookeys.1011.59780
Figure 9 Early development of Neanthes glandicincta (Southern, 1921) after fertilisation in the laboratory. The material from the Lower Songkhla Lagoon, Thailand A fertilised egg surrounded by a jelly layer (j), 10 min after fertilisation; many sperm were trapped in the jelly layer; lipid (oil) drops (o) surrounded the germinal vesicle B 4-cell stage, 1 h and 10 min after fertilisation C early trochophore stage, 7 h and 30 min after fertilisation; ciliary movement of the prototroch (p) began within the jelly layer D free-swimming trochophore larva just after hatching out of the jelly layer, 8 h after fertilisation; ciliary bands of the prototroch and telotroch (t) were present E free-swimming early-metatrochophore larva, 20 h after fertilisation; two pairs of chaetal tufts (c) were present F free-swimming 2-chaetiger late-metatrochophore larva, 21 h after fertilisation; two pairs of chaetal tufts well developed G free-swimming early 3-chaetiger nectochaeta larva, 22 h after fertilisation; three pairs of chaetal tufts were developed; the prototroch and lipid drops remained in the anterior body H demersal late 3-chaetiger nectochaeta larva, 48 h after fertilisation; a pair of eyes (e), antennae (a), and anal cirri (ac) appeared. Lipid drops disappeared. Scale bars: 0.2 mm.
Figure 5 from: Azmi SS, Ibrahim YS, Angsupanich S, Sumpuntarat P, Sato M (2021) Epitokous metamorphosis, reproductive swimming, and early development of the estuarine polychaete, Neanthes glandicincta Southern, 1921 (Annelida, Nereididae) on the east coast of the Malay Peninsula. ZooKeys 1011: 1-24. https://doi.org/10.3897/zookeys.1011.59780
Figure 5 Female epitoke of Neanthes glandicincta (Southern, 1921) collected from Kuala Ibai, Malaysia (UMTAnn 449) A dorsal view of the whole-body B enlargement of anterior end C enlargement of eyes D rupture of body wall at the ventral surface in the posterior body (arrow). Scale bars: 1 mm (A); 0.5 mm (B–D).
Figure 3 from: Azmi SS, Ibrahim YS, Angsupanich S, Sumpuntarat P, Sato M (2021) Epitokous metamorphosis, reproductive swimming, and early development of the estuarine polychaete, Neanthes glandicincta Southern, 1921 (Annelida, Nereididae) on the east coast of the Malay Peninsula. ZooKeys 1011: 1-24. https://doi.org/10.3897/zookeys.1011.59780
Figure 3 Epitokous males (A, C) and females (B, D) of Neanthes glandicincta (Southern, 1921) collected from the Lower Songkhla Lagoon, Thailand (PMBC 20732) in comparison with an atoke from the same locality (E) (PMBC 21209) A dorsal view of the whole body of a male B dorsal view of the anterior body of a female C–E enlargement of anterior dorsal end of a male epitoke (C), a female epitoke (D), and an atoke (E). Scale bars: 5 mm (A, B); 0.5 mm (C–E).
Figure 2 from: Azmi SS, Ibrahim YS, Angsupanich S, Sumpuntarat P, Sato M (2021) Epitokous metamorphosis, reproductive swimming, and early development of the estuarine polychaete, Neanthes glandicincta Southern, 1921 (Annelida, Nereididae) on the east coast of the Malay Peninsula. ZooKeys 1011: 1-24. https://doi.org/10.3897/zookeys.1011.59780
Figure 2 Atokes (A–F) and an epitoke (G) of Neanthes glandicincta (Southern, 1921) collected from the Lower Songkhla Lagoon, Thailand A prostomium of an atoke (ind. no. 10 with BW of 1.7 mm, PMBC 21209) B anterior view of an everted proboscis, showing a pair of small nipple-like round papillae on area VI in an atoke (ind. no. SL-2 with BW of 1.5 mm, PMBC 21212) C–F paragnaths in areas I (C), II (anterior and middle parts of left side, D), III (central part, E), and IV (right side, F) of an atoke (ind. no. 1 with BW of 2.3 mm, PMBC 21209) G dorsal (upper) and ventral (lower) views of the right jaw of a male epitoke (ind. no. 3M with BW of 1.2 mm, PMBC 20732).
Figure 4 from: Azmi SS, Ibrahim YS, Angsupanich S, Sumpuntarat P, Sato M (2021) Epitokous metamorphosis, reproductive swimming, and early development of the estuarine polychaete, Neanthes glandicincta Southern, 1921 (Annelida, Nereididae) on the east coast of the Malay Peninsula. ZooKeys 1011: 1-24. https://doi.org/10.3897/zookeys.1011.59780
Figure 4 Male epitoke of Neanthes glandicincta (Southern, 1921) collected from Kuala Ibai, Malaysia (UMTAnn 453) A dorsal view of the whole body (incomplete, with the pre-natatory and natatory regions) B dorsal view of the proboscis with pigmentation C ventral view of the proboscis with pigmentation. Scale bars: 1 mm (A); 0.5 mm (B, C).
Figure 7 from: Azmi SS, Ibrahim YS, Angsupanich S, Sumpuntarat P, Sato M (2021) Epitokous metamorphosis, reproductive swimming, and early development of the estuarine polychaete, Neanthes glandicincta Southern, 1921 (Annelida, Nereididae) on the east coast of the Malay Peninsula. ZooKeys 1011: 1-24. https://doi.org/10.3897/zookeys.1011.59780
Figure 7 Epitokous males (A, B, E) and a female (C, D) of Neanthes glandicincta (Southern, 1921) collected from the Lower Songkhla Lagoon, Thailand (PMBC 20732) A anterior view of left parapodium of chaetiger 5 in the pre-natatory region of a male epitoke B anterior view of right modified parapodium of chaetiger 34 in the natatory region of the same male as (A) C posterior view of right parapodium of chaetiger 3 of a female epitoke D posterior view of right parapodium of chaetiger 37 of the same female as (C) E enlargement of an epitokous paddle chaeta of another male epitoke. Abbreviations: dc, dorsal cirrus; vc, ventral cirrus. Scale bars: 0.1 mm (A, C); 0.5 mm (B, D); 0.05 mm (E).
Figure 1 from: Azmi SS, Ibrahim YS, Angsupanich S, Sumpuntarat P, Sato M (2021) Epitokous metamorphosis, reproductive swimming, and early development of the estuarine polychaete, Neanthes glandicincta Southern, 1921 (Annelida, Nereididae) on the east coast of the Malay Peninsula. ZooKeys 1011: 1-24. https://doi.org/10.3897/zookeys.1011.59780
Figure 1 Map showing the collection sites (closed circles) in two estuaries on the east coast of the Malay Peninsula A lower Songkhla Lagoon, Thailand B mangrove area in Kuala Ibai branched from Sungai Ibai in Terengganu, Malaysia.
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