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Figure 1 from: Martynov A, Mehrotra R, Chavanich S, Nakano R, Kashio S, Lundin K, Picton B, Korshunova T (2019) The extraordinary genus Myja is not a tergipedid, but related to the Facelinidae s. str. with the addition of two new species from Japan (Mollusca, Nudibranchia). ZooKeys 818: 89-116. https://doi.org/10.3897/zookeys.818.30477
Figure 1 Comparison of Myjalongicornis Bergh, 1896 with other aeolidacean taxa that have been proposed to have relationships with it (Calma, Tergipes) and which are covered by present analysis [type species of the genus Facelina, F.auriculata (Müller, 1776)]. A–HMyjacf.longicornis from Thailand, living animal ca. 10 mm in length A dorsal view of hydroids in situ B lateral view of hydroids in situ (left), egg mass on the hydroid (right) C details of cerata D smooth masticatory processes of jaws (indicated by arrows), SEM E pharynx, dissected dorsally to show very narrow radula (indicated by an arrow), LM F whole radula, SEM G anteriormost part of radula to show sacoglossan-like small knife-shaped teeth, SEM H teeth from the middle part of radula, SEM; I, JMyjalongicornis Bergh, 1896 external view and radula (anterior part), reproduced from the first description by Bergh (1896); K–OFacelinaauriculata jaws and radula of a specimen from UK, collected together with neotype K masticatory process (well-defined denticles indicated by arrow), SEM L radula (arrow) on odontophore, to show that anteriormost teeth are not reduced, LM M anterior part of radula to show that teeth are not reduced N anteriormost tooth of radula O two anterior teeth of radula P radula (middle part) of Calmaglaucoides (Alder & Hancock, 1854) from Norway Q radula (middle part) Tergipestergipes (Forsskål in Niebuhr, 1775). Scale bars: 20 μm (D, N, O, Q); 50 μm (F, K); 10 μm (G, P); 5 μm (H); 100 μm (M). Photographs of living specimens by Chanon Ngernthongdee and Siwat Worachananant, SEM images by AV Martynov. Figures I and J are reproduced from Bergh (1896), the publication not currently under copyright.
Figure 4 from: Martynov A, Mehrotra R, Chavanich S, Nakano R, Kashio S, Lundin K, Picton B, Korshunova T (2019) The extraordinary genus Myja is not a tergipedid, but related to the Facelinidae s. str. with the addition of two new species from Japan (Mollusca, Nudibranchia). ZooKeys 818: 89-116. https://doi.org/10.3897/zookeys.818.30477
Figure 4 Reproductive systems of new species of the genus Myja. AMyjacf.longicornisBMyjakarin sp. n. CMyjahyotan sp. n. Abbreviations: am – ampulla; fgm – female gland mass; fo – female opening; p – penis; psh – penial sheath; rsp – proximal receptaculum seminis; vd – vas deferens.
Figure 2 from: Perissinotto R (2019) Description of Callophylla macrocephala sp. n. from southern Tanzania. ZooKeys 818: 129-136. https://doi.org/10.3897/zookeys.818.32269
Figure 2 Type localities of Callophyllamacrocephala sp. n. (blue circle) and Callophyllatakanoi Legrand, 2015 (red circle) in Central – East Africa.
Figure 4 from: Egizi AM, Robbins RG, Beati L, Nava S, Evans CR, Occi JL, Fonseca DM (2019) A pictorial key to differentiate the recently detected exotic Haemaphysalis longicornis Neumann, 1901 (Acari, Ixodidae) from native congeners in North America. ZooKeys 818: 117-128. https://doi.org/10.3897/zookeys.818.30448
Figure 4 SEM photos of larval H.longicornis from a colony started with specimens from Queensland, Australia (Accession # RML58949). a dorsal full body b dorsal capitulum c ventral full body d ventral capitulum.
Figure 3 from: Egizi AM, Robbins RG, Beati L, Nava S, Evans CR, Occi JL, Fonseca DM (2019) A pictorial key to differentiate the recently detected exotic Haemaphysalis longicornis Neumann, 1901 (Acari, Ixodidae) from native congeners in North America. ZooKeys 818: 117-128. https://doi.org/10.3897/zookeys.818.30448
Figure 3 SEM photos of nymphal H.longicornis from a colony started with specimens from Jeju-teukbyeoljachido, Republic of Korea (Accession # RML48803). a dorsal full body b dorsal capitulum c ventral full body d ventral capitulum.
Figure 3 from: Martynov A, Mehrotra R, Chavanich S, Nakano R, Kashio S, Lundin K, Picton B, Korshunova T (2019) The extraordinary genus Myja is not a tergipedid, but related to the Facelinidae s. str. with the addition of two new species from Japan (Mollusca, Nudibranchia). ZooKeys 818: 89-116. https://doi.org/10.3897/zookeys.818.30477
Figure 3 Myjahyotan sp. n., holotype. A dorsal view B ventral view C lateral view D details of cerata E dorsal view on hydroids in situ F jaw G smooth masticatory processes of jaws (indicated by arrows), SEM H radula on odontophore, to show reduced anteriormost teeth (arrow), LM I anterior teeth with strongly reduced anteriormost teeth, SEM J teeth from the middle part of radula K posterior part of radula to show smooth teeth. Scale bars: 100 μm (F); 50 μm (G, I); 10 μm (J, K). Photographs of living specimens by TA Korshunova and AV Martynov, SEM images by AV Martynov.
Figure 2 from: Martynov A, Mehrotra R, Chavanich S, Nakano R, Kashio S, Lundin K, Picton B, Korshunova T (2019) The extraordinary genus Myja is not a tergipedid, but related to the Facelinidae s. str. with the addition of two new species from Japan (Mollusca, Nudibranchia). ZooKeys 818: 89-116. https://doi.org/10.3897/zookeys.818.30477
Figure 2 Myjakarin sp. n. A–D holotype A dorsal view B ventral view C lateral view D animal with egg mass E details of cerata F lateral view on hydroids in situ G, H veligers; I–N paratype I jaws J smooth masticatory processes of jaws (inidicated by arrows), SEM K radula on odontophore, to show narrow teeth and reduced anteriormost teeth (arrow), LM L whole radula, SEM M teeth from the middle part of radula N anterior teeth. Scale bars: 100 μm (I); 50 μm (J, L); 10 μm (M); 5 μm (N). Photographs of living specimens by TA Korshunova and AV Martynov, SEM images by AV Martynov.
Figure 1 from: Perissinotto R (2019) Description of Callophylla macrocephala sp. n. from southern Tanzania. ZooKeys 818: 129-136. https://doi.org/10.3897/zookeys.818.32269
Figure 1 Dorsal (A) and ventral (B) habitus of Callophyllamacrocephala sp. n., with details of clypeus (C), pygidium (D) and aedeagus in dorsal (E) and lateral (F) view (photographs Lynette Clennell).
Figure 1 from: Egizi AM, Robbins RG, Beati L, Nava S, Evans CR, Occi JL, Fonseca DM (2019) A pictorial key to differentiate the recently detected exotic Haemaphysalis longicornis Neumann, 1901 (Acari, Ixodidae) from native congeners in North America. ZooKeys 818: 117-128. https://doi.org/10.3897/zookeys.818.30448
Figure 1 SEM photos of female H.longicornis from a colony started with specimens from Jeju-teukbyeoljachido, Republic of Korea (Accession # RML48803) a dorsal full body b dorsal capitulum c ventral full body d ventral capitulum.
Figure 5 from: Martynov A, Mehrotra R, Chavanich S, Nakano R, Kashio S, Lundin K, Picton B, Korshunova T (2019) The extraordinary genus Myja is not a tergipedid, but related to the Facelinidae s. str. with the addition of two new species from Japan (Mollusca, Nudibranchia). ZooKeys 818: 89-116. https://doi.org/10.3897/zookeys.818.30477
Figure 5 Phylogenetic tree of aeolidacean nudibranchs based on concatenated molecular data (COI + 16S + H3) represented by Bayesian Inference (BI). Numbers above branches represent posterior probabilities from Bayesian Inference. Numbers below branches indicate bootstrap values for Maximum Likelihood. The key clades and illustrated taxa are highlighted in colour. Two taxa with highly convergent external morphology but very distantly related according to the molecular analysis, the Tergipedidae and the genus Myja, are connected by a dotted red line. Neotype ZMMU Op-669 of Facelinaauriculata (Müller, 1776) is illustrated on the tree (photograph BE Picton).
Figure 1 from: Kondratieff BC, DeWalt RE, Verdone CJ (2019) Plecoptera of Canada. In: Langor DW, Sheffield CS (Eds) The Biota of Canada – A Biodiversity Assessment. Part 1: The Terrestrial Arthropods. ZooKeys 819: 243-254. https://doi.org/10.3897/zookeys.819.23535
Figure 1 The percent of the Canadian Plecoptera fauna represented by each family. The numbers represent rounded percentages and do not total 100.
Figure 1 from: Langor DW (2019) The diversity of terrestrial arthropods in Canada. In: Langor DW, Sheffield CS (Eds) The Biota of Canada – A Biodiversity Assessment. Part 1: The Terrestrial Arthropods. ZooKeys 819: 9-40. https://doi.org/10.3897/zookeys.819.31947
Figure 1 Terrestrial ecozones of Canada as included in the Canadian Biodiversity Ecosystem Status and Trends 2010 report (Federal, Provincial, and Territorial Governments of Canada 2010). [Reprinted with permission from Environment and Climate Change Canada]
Figure 2 from: Langor DW (2019) The diversity of terrestrial arthropods in Canada. In: Langor DW, Sheffield CS (Eds) The Biota of Canada – A Biodiversity Assessment. Part 1: The Terrestrial Arthropods. ZooKeys 819: 9-40. https://doi.org/10.3897/zookeys.819.31947
Figure 2 Collection points for the 375 species of Cerambycidae (Coleoptera) in Canada based on 81,555 records extracted from 106 Canadian and USA collections (Bousquet et al. 2017).
Figure 9 from: Sroka P, Godunko RJ, Rutschmann S, Angeli KB, Salles FF, Gattolliat J-L (2019) A new species of Bungona in Turkey (Ephemeroptera, Baetidae): an unexpected biogeographic pattern within a pantropical complex of mayflies. Zoosystematics and Evolution 95(1): 1-13. https://doi.org/10.3897/zse.95.29487
Figure 9 Molecular reconstruction including representative set of taxa of the Cloeodes-complex (comprising Bungona (Chopralla) pontica sp. n.) and additional taxa of other lineages. Bayesian inference was used to reconstruct the tree based on the mitochondrial DNA barcoding gene cytochrome c oxidase subunit 1. Bayesian posterior probabilities > 0.8 are indicated. Scale bar represents substitutions per site. Geographic origins of the specimens are indicated. Colours: green = Bungona (Bungona); blue = Bungona (Chopralla); purple = Bungona (Centroptella); yellow = Cloeodes; white = other genera.
Figure 8 from: Sroka P, Godunko RJ, Rutschmann S, Angeli KB, Salles FF, Gattolliat J-L (2019) A new species of Bungona in Turkey (Ephemeroptera, Baetidae): an unexpected biogeographic pattern within a pantropical complex of mayflies. Zoosystematics and Evolution 95(1): 1-13. https://doi.org/10.3897/zse.95.29487
Figure 8 Distribution of Bungona (Chopralla) spp. Marked occurrence in Turkey encompass the position of both known localities of Bungona (Chopralla) pontica sp. n.
Figure 7 from: Sroka P, Godunko RJ, Rutschmann S, Angeli KB, Salles FF, Gattolliat J-L (2019) A new species of Bungona in Turkey (Ephemeroptera, Baetidae): an unexpected biogeographic pattern within a pantropical complex of mayflies. Zoosystematics and Evolution 95(1): 1-13. https://doi.org/10.3897/zse.95.29487
Figure 7 A Type locality of Bungona (Chopralla) pontica sp. n. (Dipsiz Önü stream near Gemicıler village). B Valley of Dipsiz Önü stream approximately 400 m downstream from the type locality.
Figure 6 from: Sroka P, Godunko RJ, Rutschmann S, Angeli KB, Salles FF, Gattolliat J-L (2019) A new species of Bungona in Turkey (Ephemeroptera, Baetidae): an unexpected biogeographic pattern within a pantropical complex of mayflies. Zoosystematics and Evolution 95(1): 1-13. https://doi.org/10.3897/zse.95.29487
Figure 6 Difference in the arrangement of the posterior margin of pronotum between Bungona (Chopralla) pontica sp. n. (A) and Bungona (Chopralla) liebenauae (B).
Figure 5 from: Sroka P, Godunko RJ, Rutschmann S, Angeli KB, Salles FF, Gattolliat J-L (2019) A new species of Bungona in Turkey (Ephemeroptera, Baetidae): an unexpected biogeographic pattern within a pantropical complex of mayflies. Zoosystematics and Evolution 95(1): 1-13. https://doi.org/10.3897/zse.95.29487
Figure 5 Bungona (Chopralla) pontica sp. n., thorax and abdomen. A Setae on abdominal sterna IV, V and VI. B Part of metathorax with vestigial hind wing pad. C Surface and posterior margin of abdominal terga II, V and VIII. D Paraproct. E Abdominal tergum X. F Gills.
Figure 4 from: Sroka P, Godunko RJ, Rutschmann S, Angeli KB, Salles FF, Gattolliat J-L (2019) A new species of Bungona in Turkey (Ephemeroptera, Baetidae): an unexpected biogeographic pattern within a pantropical complex of mayflies. Zoosystematics and Evolution 95(1): 1-13. https://doi.org/10.3897/zse.95.29487
Figure 4 Bungona (Chopralla) pontica sp. n., legs. A Scales on surface of legs. B Foretibia (dorsal). C Middle tibia (dorsal). D Hind tibia (dorsal). E Claw. F Detail of claw apex. Abbreviations: s–scale, ss–scale socket, pts–patella-tibial suture.
Figure 3 from: Kondratieff BC, DeWalt RE, Verdone CJ (2019) Plecoptera of Canada. In: Langor DW, Sheffield CS (Eds) The Biota of Canada – A Biodiversity Assessment. Part 1: The Terrestrial Arthropods. ZooKeys 819: 243-254. https://doi.org/10.3897/zookeys.819.23535
Figure 3 Cluster analysis of Plecoptera assemblages for Canadian provinces. For meaning of province abbreviations, see Figure 2 legend. The assemblages of Newfoundland (NF) and Labrador (LB) were kept separate in this analysis.
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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.