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Linked collectors and determiners for: Bathyphysa conifera (Studer, 1878) worldwide distribution review.
Natural history specimen data linked to collectors and determiners held within, "Bathyphysa conifera (Studer, 1878) worldwide distribution review". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/f9367d11-65f0-4206-82b4-5ff986afaa68">https://bionomia.net/dataset/f9367d11-65f0-4206-82b4-5ff986afaa68</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/f9367d11-65f0-4206-82b4-5ff986afaa68">https://gbif.org/dataset/f9367d11-65f0-4206-82b4-5ff986afaa68</a>. Formatted as a Frictionless Data package.
Fig. 4 in Revised classification of Acanthaceae and worldwide dichotomous keys
Fig. 4. Schematic molecular phylogeny of the Acanthaceae, which serves as the foundation for the present reclassification. Phylogeny represents current understanding of evolutionary relationships among major lineages of Acanthaceae based on numerous phylogenetic works, as cited throughout this study. Depicted are the 4 subfamilies (capital letters), 10 tribes (bold), and 19 subtribes (not in bold, not in caps) recognized in the present study. Key diagnostic morphological characters for the subfamilies and tribes are provided in Table 1 and Fig. 5. Asterisks and dashed lines indicate uncertain phylogenetic placement of Physacantheae, either within or sister to Ruellieae or Acantheae (see text).
Fig. 1 in Revised classification of Acanthaceae and worldwide dichotomous keys
Fig. 1. Floral diversity among worldwide Acanthaceae. Collector, collection number, location of photograph, and photographer provided where available. A, Dicliptera trifurca, Kiel & al. 122 (photo: C. Kiel), Costa Rica; B, Hypoestes phyllostachya, Kiel & Tripp 65 (photo: C. Kiel), Mexico (native to Old World, widespread); C, Justicia refractifolia, Kiel & al. 137 (photo: C. Kiel), Costa Rica; D, Justicia costaricana, Kiel & al. 81 (photo: C. Kiel), Costa Rica; E, Neuracanthus niveus, Not vouchered (photo: W. McCleland), Mali; F, Pachystachys spicata, Kiel & Velez 258 (photo: C. Kiel), Colombia; G, Tetramerium nervosum, Kiel & Tripp 75 (photo: C. Kiel), Mexico; H, Ruelliopsis setosa, Tripp & Dexter 799 (photo: E. Tripp), Namibia; I, Petalidium giessii, Tripp & Dexter 825 (photo: E. Tripp), Namibia; J, Blepharis pruinosa, Tripp & al. 884 (photo: E. Tripp), Namibia; K, Acanthopsis hoffmanseggiana, Tripp & al. 2073 (photo: E. Tripp), Namibia; L, Aphelandra aurantiaca, Tripp & al. 5739, Mexico; M, Acanthopale pubescens, Ballings & Wursten 1074 (photo: B. Wursten), Mozambique; N, Barleria oenotheroides, Tripp & al. 5755 (photo: E. Tripp), Mexico; O, Bravaisia integerrima, Tripp & Luján 519 (photo: E. Tripp), Venezuela; P, Brunoniella australis, Hosking 2952 (photo: J. Hosking), Australia; Q, Mendoncia aspera, Clarke & Tripp s.n. (photo: D. Clarke), Guyana; R, Dyschoriste repens, Tripp & Luján 516 (photo: E. Tripp), Venezuela; S, Barleria lancifolia, Tripp & Dexter 781 (photo: E. Tripp), Namibia; T, Louteridium donnellsmithii, Tripp & Medina 9680 (photo: E. Tripp), Mexico; U, Calacanthus grandiflorus, Not vouchered (photo S. Yadav), India; V, Dinteracanthus asper, Tripp & al. 2079 (photo: E. Tripp), Namibia; W, Anisosepalum alboviolaceum, Bytebier & al. 3279 (photo: Q. Luke), Dem. Repub. Congo; X, Ruellia megasphaera, Tripp & al. 5756 (photo: E. Tripp), Mexico; Y, Odontonema glabrum, Tripp & al. 5763 (photo E. Tripp), Mexico; Z, Anisotes formosissimus, Wursten 2020 (photo: B. Wursten), Mozambique; AA, Lepidagathis fischeri, Not vouchered (photo: I. Darbyshire), Tanzania; BB, Asystasia malawiana, Mphamba 122 (photo: T. Harris), Mozambique.
Fig. 5 in Revised classification of Acanthaceae and worldwide dichotomous keys
Fig. 5. Corolla aestivation types in Acanthaceae. Note that the "open" aestivation observed in some Acantheae is not illustrated here. A, Left-contort (Avicennioideae in part, Thunbergioideae in part, Physacantheae, Whitfieldieae, Ruellieae); B, Quincuncial (Barlerieae); C, Ascending-cochlear (Thunbergioideae in part, Acantheae, Andrographideae, Justicieae); D, Descending-cochlear (Nelsonioideae); E, Valvate (Avicennioideae in part); F, Induplicate (Neuracantheae).
Fig. 3 in Revised classification of Acanthaceae and worldwide dichotomous keys
Fig. 3. Examples of habitat diversity among worldwide Acanthaceae. Collector, collection number, location of photograph, and photographer provided where available. A, Petalidium crispum, Tripp & Dexter 4087 (photo: E. Tripp), Namibia; plants showing affinity for crevices of near-barren schist rocks and associated slopes, near Van Zyl's Pass; B, Avicennia marina, Not Vouchered (photo: I. Darbyshire), Tanzania; locally dominant in intertidal mangrove communities near Lindi; note the presence of pneumatophores; C, Barleria aristata, Not Vouchered [but same location as Bidgood & al. 5027] (photo: I. Darbyshire), Tanzania; locally common in dry Somalia-Masai woodland near the Lukosi River; D, Justicia fittonioides, Suleiman & al. 5536 (photo: I. Darbyshire), Tanzania; abundant on the floor of seasonally dry coastal forest at Ruawa Forest Reserve near Lindi; E, Ruelliopsis setosa, Tripp & Dexter 799 (photo: E. Tripp), Namibia; plants a dominant component of rocky savanna floor, acting as a "grass mimic"; F, Blepharis ferox, Tripp & Dexter 4094 (photo: K. Dexter), Namibia; plants comprising one of the most abundant shrubs on barren sand of Namib Desert, near Oropembe; G, Isoglossa dispersa, Not Vouchered (photo: P.K. Haba), Guinea; a mass-flowering plietesial species of moist lowland and mid-elevation forest, here at Simandou; H, Justicia fittonioides, Suleiman & al. 5536 (photo: I. Darbyshire), Tanzania; showing the rosulate habit of the plants in D; I, Pogonospermum salsola, Klaassen & al. 2537 (photo: E. Tripp), Namibia; plants represent the dominant shrubs on the floor of the Namib Desert, which is typical of numerous species of this genus and of Petalidium, Blepharis, and Barleria in Namibia; J, Petalidium welwitschii, Tripp & Dexter 4091 (photo: E. Tripp), Namibia; total dominance of Namib Desert near Hartmann's Valley in the northwestern Kaokoveld; K, Justicia americana, Daniel & Lott 10530 (photo: T. Daniel), U.S.A.; aquatic perennial herb at edge of Town Lake, Austin, Texas; L, Lankesteria glandulosa Benoist, Daniel & al. 10453 (photo: T. Daniel), Madagascar; dying perennial herb along trail in seasonally moist forest, Ankarana Special Reserve.
Fig. 2 in Revised classification of Acanthaceae and worldwide dichotomous keys
Fig. 2. Floral diversity among worldwide Acanthaceae. Collector, collection number, location of photograph, and photographer provided where available. A, Andrographis echioides, Luke & Chidzinga 16414B (photo: Q. Luke), Kenya (naturalised, native to Asia); B, Cephalophis lukei, Hyde 15.119.06 (photo: M. Hyde), Mozambique; C, Crabbea velutina, Ballings & Wursten 2391 (photo: B. Wursten), Zimbabwe; D, Crossandra puberula, Wursten & al. 1946 (photo: B. Wursten), Mozambique; E, Duosperma crenatum, Not vouchered (photo: B. Wursten), Mozambique; F, Champluviera populifolia, Cheek 7654 (photo: M. Cheek), Cameroon; G, Dyschoriste hildebrandtii, Wursten 951 (photo: B. Wursten), Mozambique; H, Ecbolium tanzaniense, Suleiman & al. TTSA 235 (photo: I. Darbyshire), Tanzania; I, Elytraria acaulis, Not vouchered (photo: B. Wursten), Mozambique; J, Isoglossa vulcanicola, Darbyshire & al. 1048 (photo: I. Darbyshire), Uganda; K, Justicia salviiflora, Tripp & al. 5773 (photo: E. Tripp), Mexico; L, Lankesteria elegans, Collector/photographer unknown, Cameroon; M, Lankesteria hispida, van der Burgt 1406 (photo: X. van der Burgt), Sierra Leone; N, Mackaya bella, Not vouchered (photo: I. Darbyshire), South Africa (cult.); O, Megalochlamys hamata, Not vouchered (photo: B. Wursten), Zimbabwe; P, Mimulopsis excellens, Darbyshire & al. 1056 (photo: I. Darbyshire), Uganda; Q, Physacanthus batanganus, Cheek in Kami 4132 (photo: M. Cheek), Dem. Repub. Congo; R, Schaueriopsis variabilis, Luke 12527 (photo: Q. Luke), Dem. Repub. Congo; S, Ruspolia seticalyx, Wursten 1859 (photo: B. Wursten), Mozambique; T, Thunbergia gregorii, Not vouchered (photo: I. Darbyshire), Kenya; U, Whitfieldia orientalis, Suleiman & al. 5534 (photo: I. Darbyshire), Tanzania; V, Stenostephanus sessilifolius, Hammel & al. 26074 (photo: C. Kiel), Costa Rica; W, Pseuderanthemum subviscosum, Not vouchered (photo: B. Wursten), Mozambique; X, Ruellia neesiana, Tripp & Medina 5957 (photo: E. Tripp), Brazil; Y, Leandriella valvata, Thulin & Razafindraibe 11880 (photo: M. Thulin), Madagascar; Z, Avicennia germinans, Daniel 11120 (photo: W. Eckerman), São Tomé; AA, Heteradelphia paulowilhelmia, Not vouchered (photo: T. Daniel), São Tomé; BB, Lepidagathis grandidieri, Daniel & al. 11066 (photo: T. Daniel), Madagascar; CC, Chlamydacanthus euphorbioides, Daniel & Ranarivelo 10584 (photo: T. Daniel), Madagascar.
Invasive ant and trade flows from continents to countries worldwide
<p>A major goal of invasion biology is to understand global species flows between donor and recipient regions. Our current view of such flows assumes that species are moved directly from their native to their introduced range. However, if introduced populations serve as bridgehead population that generate additional introductions, tracing intercontinental flows between donor and recipient regions misrepresents the introduction history. Our aim was to assess to what extent bridgehead effects distort our view of global species flows. We separately mapped "flows" of 252 alien ant species established on one to six continents, representing a gradient of relatively certain to completely unreliable flows. In 83% of countries, more than 50% of alien ants were established on six continents, indicating that flows to these countries are unreliable. Flows of species established on a single continent were linked to global trade flows, while flows including cosmopolitan species were not linked to global trade. It is crucial to account for bridgehead effects when assessing the biogeography and intercontinental flows of alien species. This is urgent for improving our understanding of how species are moved around the planet.</p>
Fig. 4. Neanthes helenae Kinberg, 1865. A–C, I–P in Redescriptions of Neanthes Kinberg, 1865 (Annelida: Errantia: Nereididae) species from worldwide regions
Fig. 4. Neanthes helenae Kinberg, 1865. A–C, I–P. Holotype of Nereis (Neanthes) nanciae Day, 1949 (NHMUK 1950.1.5.72-95) from Jamestown, St Helena Island, atokous. A. Entire body in dorsal view. B. Anterior end in dorsal view.C. Anterior region in ventral view, arrow indicates ventrolateral projection. I. Left parapodium from chaetiger 1 in posterior view. J. Left parapodium from chaetiger 7 in posterior view. K. Right parapodium from chaetiger 21 in anterior view. L. Left parapodium from chaetiger 30 in posterior view with ventral cirri contracted and hidden behind the neuroacicular ligule. M. Right parapodium from chaetiger 60 in anterior view. N. Heterogomph fused falciger from supracicular neurochaetae (chaetiger 30). O. Heterogomph falciger from subacicular neurochaetae (chaetiger 7). P. Heterogomph falciger from subacicular neurochaetae (chaetiger 30). — D–H, Q. Paratype of Nereis (Neanthes) nanciae Day, 1949 (NHMUK 1950.1.5.72-95) from Jamestown, St Helena Island, atokous. D. Anterior region in lateral view, arrow indicates ventrolateral projection. E. Left jaw in dorsal and ventral views, respectively. F. Inner canals of jaws in ventral view. G. Non-everted pharynx in ventral view. H. Area VI of oral ring of non-everted pharynx in ventral view, arrows indicate p-bars. Q. Posterior end in dorsal view. Roman numerals refer to the areas and Arabic numbers to chaetigers. Scale bars: A–C, Q = 1 mm; D–E, G = 0.5 mm; F, J–L = 0.2 mm; H–I, M = 0.1 mm; N–P = 20 µm.
Fig. 5 in Redescriptions of Neanthes Kinberg, 1865 (Annelida: Errantia: Nereididae) species from worldwide regions
Fig. 5. Neanthes mossambica (Day, 1957). Holotype (NHMUK 1961.16.22) from Morrumbene, Mozambique, atokous female. A. Entire body in dorsal view. B. Anterior end in dorsal view. C. Noneverted pharynx in ventral view (arrow indicates p-bar). D. Area VI of non-everted pharynx in ventral view (arrow pointing anteriorly). E. Left parapodium from chaetiger 1 in posterior view. F. Right parapodium from chaetiger 9 in anterior view. G. Left parapodium from chaetiger 21 in posterior view. H. Right parapodium from chaetiger 40 in anterior view. I. Right parapodium from chaetiger 63 in anterior view with ventral cirri contracted and hidden behind the neuroacicular ligule. J. Homogomph spiniger from notochaetae (chaetiger 9). K. Heterogomph spiniger from subacicular neurochaetae (chaetiger 9). L. Heterogomph falciger from supracicular neurochaetae (chaetiger 9). M. Heterogomph falciger from subacicular neurochaetae (chaetiger 9). Roman numerals refer to the areas and Arabic numbers to chaetigers. Scale bars: A = 2 mm; B = 1 mm; C = 0.5 mm; D = 0.1 mm; E–I = 0.2 mm; J–M = 20 µm.
Fig. 1 in Redescriptions of Neanthes Kinberg, 1865 (Annelida: Errantia: Nereididae) species from worldwide regions
Fig. 1. Neanthes chilkaensis (Southern, 1921). Lectotype (NHMUK 1938.5.7.27) from Chilika Lake, Orissa, India, atokous. A. Entire body in dorsal view (inset: approach of pygidium). B. Anterior end in dorsal view. C. Non-everted pharynx in ventral view. D. Dorsum of oral ring of non-everted pharynx in ventral view. E. Left parapodium from chaetiger 2 in posterior view. F. Left parapodium from chaetiger 13 in posterior view. G. Right parapodium from chaetiger 26 in anterior view. H. Right parapodium from chaetiger 38 in anterior view with ventral cirri contracted and hidden behind the neuroacicular ligule. I. Parapodium from chaetiger 52 in anterior view. J. Homogomph spiniger from notochaetae (chaetiger 13). K. Homogomph spiniger from supracicular neurochaetae (chaetiger 13). L. Heterogomph spiniger from subacicular neurochaetae (chaetiger 2). M. Heterogomph falciger from subacicular neurochaetae (chaetiger 13). Roman numerals refer to the areas and Arabic numbers to chaetigers. Scale bars: A = 3 mm; B = 1 mm; C = 0.5 mm; D–I = 0.2 mm; J–M = 20 µm.
Fig. 3. Neanthes helenae Kinberg, 1865. A–B, E–Q in Redescriptions of Neanthes Kinberg, 1865 (Annelida: Errantia: Nereididae) species from worldwide regions
Fig. 3. Neanthes helenae Kinberg, 1865. A–B, E–Q. Complete syntype (SMNH Type-457) from Jamestown, St Helena Island, atokous. C–D. Incomplete syntype (SMNH Type-457) from Jamestown, St Helena Island, atokous. A. Entire body in dorsal view. B. Anterior end in dorsal view. C. Everted pharynx in dorsal view. D. Everted pharynx in ventral view. E. Right parapodium from chaetiger 1 in anterior view with ventral cirri missing. F. Right parapodium from chaetiger 8 in anterior view. G. Right parapodium from chaetiger 27 in anterior view. H. Right parapodium from chaetiger 42 in anterior view with ventral cirri missing. I. Right parapodium from chaetiger 60 in anterior view. J. Homogomph spiniger from notochaetae (chaetiger 27). K. Heterogomph spiniger from subacicular neurochaetae (chaetiger 1). L. Heterogomph falciger from subacicular neurochaetae (chaetiger 1). M. Heterogomph, fused falciger from supracicular neurochaetae (chaetiger 42). N. Heterogomph falciger from supracicular neurochaetae (chaetiger 60). O. Heterogomph falciger from subacicular neurochaetae (chaetiger 13). P. Heterogomph falciger from subacicular neurochaetae (chaetiger 60). Q. Posterior end in dorsal view. A–D, Q: stained with Shirlastain A. Roman numerals refer to the areas and Arabic numbers to chaetigers. Scale bars: A–B = 1 mm; C–D, Q = 0.5 mm; E–I = 0.1 mm; J–P = 20 µm.
Fig. 2. Neanthes galetae Fauchald, 1977. A–B, E–M in Redescriptions of Neanthes Kinberg, 1865 (Annelida: Errantia: Nereididae) species from worldwide regions
Fig. 2. Neanthes galetae Fauchald, 1977. A–B, E–M. Holotype (USNM 53088) from Galeta Reef, Panama, atokous. C–D. Paratype (USNM 53089) from Galeta Reef, Panama, atokous. A. Entire body in dorsal view. B. Anterior end in dorsal view. C. Non-everted pharynx in ventral view, black arrow indicates merged paragnaths. D. Right jaw in dorsal view, white arrow indicates canals. E. Right parapodium from chaetiger 2 in anterior view. F. Right parapodium from chaetiger 8 in anterior view. G. Right parapodium from chaetiger 16 in anterior view. H. Right parapodium from chaetiger 33 in anterior view. I. Right parapodium from chaetiger 47 in anterior view. J. Supracicular (Sp) and subacicular (Sb) neurochaetae (chaetiger 1). K. Homogomph spiniger from supracicular neurochaetae (chaetiger 47). L. Heterogomph falciger from supracicular neurochaetae (chaetiger 47). M. Heterogomph falciger from subacicular neurochaetae (chaetiger 47). Roman numerals refer to the areas and Arabic numbers to chaetigers. Scale bars: A = 0.5 mm; B = 0.2 mm; C–I = 0.1 mm; J = 20 µm; K–M = 10 µm.
Fig. 113. Albunea gibbesii Stimpson, 1859 in A Worldwide Revision Of The Recent And Fossil Sand Crabs Of The Albuneidae Stimpson And Blepharipodidae, New Family (Crustacea: Decapoda: Anomura: Hippoidea)
Fig. 113. Albunea gibbesii Stimpson, 1859: A–J, Ƌ, 10.6 mm cl, AMNH 10247. A. Carapace, branchiostegite, and ocular peduncles, dorsal view. B. Ocular peduncles, dorsal view. C. Left antennule, lateral view. D. Left antenna, lateral view. E. Left mandible, mesial view. F. Left maxillule, lateral view. G. Left maxilla, lateral view. H. Left maxilliped I, lateral view. I. Left maxilliped II, lateral view. J. Left maxilliped III, lateral view. Scale = 1.6 mm (B, E, F), 2.2 mm (I), and 3.3 mm (A, C, D, G, H, J).
Fig. 111. Albunea steintizi Holthuis, 1958 in A Worldwide Revision Of The Recent And Fossil Sand Crabs Of The Albuneidae Stimpson And Blepharipodidae, New Family (Crustacea: Decapoda: Anomura: Hippoidea)
Fig. 111. Albunea steintizi Holthuis, 1958: A, Ƌ, 10.8 mm cl, ZMTAU E62/3614; B–J, Ƌ, 9.9 mm cl, USNM 304308. A. Carapace, branchiostegite, and ocular peduncles, dorsal view. B. Ocular peduncles, dorsal view. C. Left antennule, lateral view. D. Left antenna, lateral view. E. Left mandible, mesial view. F. Left maxillule, lateral view. G. Left maxilla, lateral view. H. Left maxilliped I, lateral view. I. Left maxilliped II, lateral view. J. Left maxilliped III, lateral view. Scale = 1.6 mm (B, F), 2.2 mm (E, I), 3.3 mm (C, D, G, H, J), and 4.5 mm (A).
Fig. 110 in A Worldwide Revision Of The Recent And Fossil Sand Crabs Of The Albuneidae Stimpson And Blepharipodidae, New Family (Crustacea: Decapoda: Anomura: Hippoidea)
Fig. 110. Graph of length of distal peduncular segments plotted against carapace length for Albunea paretii and Albunea catherinae, n. sp. Data points are for 68 specimens of A. paretii (5.0– 27.4 mm cl) and 50 specimens of A. catherinae, n. sp. (6.8–22.1 mm cl). O, Albunea catherinae, n. sp. -, Albunea paretii.
Fig. 98 in A Worldwide Revision Of The Recent And Fossil Sand Crabs Of The Albuneidae Stimpson And Blepharipodidae, New Family (Crustacea: Decapoda: Anomura: Hippoidea)
Fig. 98. Albunea symmysta (Linnaeus, 1758): A, ♀, 14.8 mm cl, USNM 68613; B–J, ♀, 16.9 mm cl, ZMUC 2713. A. Carapace, branchiostegite, and ocular peduncles, dorsal view. B. Ocular peduncles, dorsal view. C. Left antennule, lateral view. D. Left antenna, lateral view. E. Left mandible, mesial view. F. Left maxillule, lateral view. G. Left maxilla, lateral view. H. Left maxilliped I, lateral view. I. Left maxilliped II, lateral view. J. Left maxilliped III, lateral view. Scale = 2.2 mm (F), 3.0 mm (B, E), 3.3 mm (I), 4.4 mm (D, H), 5.0 mm (A), 5.9 mm (C), and 6.7 mm (G, J).
Fig. 103. Albunea elegans A in A Worldwide Revision Of The Recent And Fossil Sand Crabs Of The Albuneidae Stimpson And Blepharipodidae, New Family (Crustacea: Decapoda: Anomura: Hippoidea)
Fig. 103. Albunea elegans A. Milne Edwards and Bouvier, 1898: A–F, Ƌ, 10.4 mm cl, AMNH 18079; G, ♀, 13.8 mm cl, AMNH 18079. A. Right pereopod I, lateral view. B. Left pereopod II, lateral view. C. Right pereopod III, lateral view. D. Left pereopod IV, lateral view. E. Abdominal somites I– VI, dorsal view. F. Telson of Ƌ, dorsal view. G. Telson of ♀, dorsal view. Scale = 2.2 mm (F, G), 3.3 mm (B, D, E), and 4.4 mm (A, C).
Fig. 116. Albunea thurstoni Henderson, 1893 in A Worldwide Revision Of The Recent And Fossil Sand Crabs Of The Albuneidae Stimpson And Blepharipodidae, New Family (Crustacea: Decapoda: Anomura: Hippoidea)
Fig. 116. Albunea thurstoni Henderson, 1893: A, B, D, F, ♀, 6.8 mm cl, BMNH 1894.11.3.4–5, syntype; C, E, ♀, 5.4 mm cl, BMNH 1901.4.20.11–12. A. Right pereopod I, lateral view. B. Left pereopod II, lateral view. C. Left pereopod III, lateral view. D. Right pereopod IV, lateral view. E. Abdominal somites I–VI, dorsal view. F. Telson of immature Ƌ, dorsal view. G. Telson of ♀, dorsal view. Scale = 0.8 mm (F), 1.8 mm (E), 2.2 mm (A, B, D), and 2.5 mm (C).
Fig. 97. Albunea groeningi, n in A Worldwide Revision Of The Recent And Fossil Sand Crabs Of The Albuneidae Stimpson And Blepharipodidae, New Family (Crustacea: Decapoda: Anomura: Hippoidea)
Fig. 97. Albunea groeningi, n. sp.: A–F, Ƌ, 9.2 mm cl, AM P5340, paratype; G, ♀, 13.9 mm cl, MOV J40194, paratype. A. Left pereopod I, lateral view. B. Left pereopod II, lateral view. C. Left pereopod III, lateral view. D. Left pereopod IV, lateral view. E. Abdominal somites I–VI, dorsal view. F. Telson of Ƌ, dorsal view. G. Telson of ♀, dorsal view. Scale = 1.7 mm (F), 2.2 mm (G), and 3.3 mm (A–E).
Fig. 96. Albunea groeningi, n in A Worldwide Revision Of The Recent And Fossil Sand Crabs Of The Albuneidae Stimpson And Blepharipodidae, New Family (Crustacea: Decapoda: Anomura: Hippoidea)
Fig. 96. Albunea groeningi, n. sp.: A–J, Ƌ, 9.2 mm cl, AM P5340, paratype. A. Carapace, branchiostegite, and ocular peduncles, dorsal view. B. Ocular peduncles, dorsal view. C. Left antennule, lateral view. D. Left antenna, lateral view. E. Left mandible, mesial view. F. Left maxillule, lateral view. G. Left maxilla, lateral view. H. Left maxilliped I, lateral view. I. Left maxilliped II, lateral view. J. Right maxilliped III, lateral view. Scale = 1.1 mm (B), 1.6 mm (E, F, I), 2.2 mm (C, D, H), and 3.3 mm (A, G, J).
ScienceDex guides
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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.