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Figure 4 from: Hua B, Jiang L, Yue C (2014) Larval morphology of Panorpodes kuandianensis (Insecta, Mecoptera, Panorpodidae) and its evolutionary implications. ZooKeys 398: 69-82. https://doi.org/10.3897/zookeys.398.6675
Figure 4 - Thoracic leg, abdominal processes, spiracles and telson of the larva of Panorpodes kuandianensis. A Thoracic leg, inset shows magnification of the tarsus of thoracic leg B Proleg-like abdominal process C Prothoracic spiracle D Abdominal spiracle E Ventral view of abdominal segments II and III F Telson (ventral view). Abbreviations: AO = atrial orifice, Ap = aperture, Cx = coxa, Fm = femur, PP = proleg-like process, Tb = tibia, Ts = tarsus. Scale bars: (A) = 20 μm, (B) = 5 μm, (C) and (D) = 3 μm, (E) = 40 μm, (F) = 50 μm.
Figure 2 from: Hua B, Jiang L, Yue C (2014) Larval morphology of Panorpodes kuandianensis (Insecta, Mecoptera, Panorpodidae) and its evolutionary implications. ZooKeys 398: 69-82. https://doi.org/10.3897/zookeys.398.6675
Figure 2 - Larval head of Panorpodes kuandianensis. A Ventral view B Dorsal view C Lateral view D Antenna (ventral view) E Sensilla on flagellum (dorsal view). Abbreviations: An = antenna, AT = anterior tentorial pit, Cl = clypeus, EB = egg burster, EC = ecdysial cleavage, Fl = flagellum, Lb = labium, Lm = labrum, Md = mandible, Mx = maxilla, Oc = occiput, Pe = pedicel, SB = sensillum basiconicum, Sc = scape, SP = sensillum placodeum. Scale bars: (A)−(C) = 50 μm, (D) = 20 μm, (E) = 5 μm.
Figure 3 from: Hua B, Jiang L, Yue C (2014) Larval morphology of Panorpodes kuandianensis (Insecta, Mecoptera, Panorpodidae) and its evolutionary implications. ZooKeys 398: 69-82. https://doi.org/10.3897/zookeys.398.6675
Figure 3 - Larval mouthparts of Panorpodes kuandianensis. A Epipharyx, arrows show the inconspicuous sensilla basiconica B Maxilla (ventral view) C Maxilla (frontal view) D Labium. Abbreviations: Cas = cardo-stipes, Ep = epipharynx, Ga = galea, La = lacinia, Lb = labium, LP = labial palpus, Md = mandible, MP = maxillary palpus, Pf = palpifer, Pm = postmentum, Prm = prementum, SB = sensillum basiconicum, SC = sensillum campaniformium. Scale bars: (A), (C) and (D) = 10 μm, (B) = 20 μm.
Figure 13 from: Carter CG, Westbury H, Crear B, Simon C, Thomas C (2014) Agonistic behaviour in juvenile southern rock lobster, Jasus edwardsii (Decapoda, Palinuridae): implications for developing aquaculture. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 323-337. https://doi.org/10.3897/zookeys.457.6760
Figure 13 - Occurrence of Jasus edwardsii behavioural groups as a) mean (± SE) individual occurrence (occ. h-1) and b) mean (± SE) group occurrence per individual per hour (occ. ind-1 h-1). Individual occurrence (a): significant difference amongst behavioural groups (N = 20, P < 0.001, Kruskal-Wallis Test). Group occurrence (b): significant difference amongst behavioural groups (n = 4, P < 0.001, Kruskal-Wallis Test). No significant different amongst means with same letter.
Figures 5-8 from: Carter CG, Westbury H, Crear B, Simon C, Thomas C (2014) Agonistic behaviour in juvenile southern rock lobster, Jasus edwardsii (Decapoda, Palinuridae): implications for developing aquaculture. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 323-337. https://doi.org/10.3897/zookeys.457.6760
Figures 5-8 - Selected avoidance behaviours of Jasus edwardsii: 5 back away 6 walk away 7 side step away 8 flee.
Figure 2 from: Carvalho-Batista A, Negri M, Pileggi LG, Castilho AL, Costa RC, Mantelatto FL (2014) Inferring population connectivity across the range of distribution of the stiletto shrimp Artemesia longinaris Spence Bate, 1888 (Decapoda, Penaeidae) from DNA barcoding: implications for fishery management. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 271-288. https://doi.org/10.3897/zookeys.457.6569
Figure 2 - Dendrogram based on Neighbor-Joining distance method of COI gene sequences of individuals of Artemesia longinaris. Localities represent the analyzed specimens. Numbers are bootstrap support values (1000 replicates); values below 50% are not shown.
Figure 4 from: Carvalho-Batista A, Negri M, Pileggi LG, Castilho AL, Costa RC, Mantelatto FL (2014) Inferring population connectivity across the range of distribution of the stiletto shrimp Artemesia longinaris Spence Bate, 1888 (Decapoda, Penaeidae) from DNA barcoding: implications for fishery management. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 271-288. https://doi.org/10.3897/zookeys.457.6569
Figure 4 - Haplotype network of Artemesia longinarisaccording to Median-Joining analysis. Each circle represent one haplotype found in the localities (53 haplotypes in 60 specimens). The size of the circle of each haplotype is proportional to its frequency in the sample. Each small dash represents a mutational step.
Figure 1 from: Carvalho-Batista A, Negri M, Pileggi LG, Castilho AL, Costa RC, Mantelatto FL (2014) Inferring population connectivity across the range of distribution of the stiletto shrimp Artemesia longinaris Spence Bate, 1888 (Decapoda, Penaeidae) from DNA barcoding: implications for fishery management. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 271-288. https://doi.org/10.3897/zookeys.457.6569
Figure 1 - Southwest Atlantic collection sites. Map showing the localities of the specimens of Artemesia longinaris analyzed: 1 Macaé, Brazil 2 Ubatuba, Brazil 3 Santos, Brazil 4 Cananéia, Brazil 5 São Francisco do Sul, Brazil 6 Rio Grande, Brazil 7 Mar del Plata, Argentina. The gray band indicates the complete geographical distribution of Artemesia longinaris.
Figures 1-4 from: Carter CG, Westbury H, Crear B, Simon C, Thomas C (2014) Agonistic behaviour in juvenile southern rock lobster, Jasus edwardsii (Decapoda, Palinuridae): implications for developing aquaculture. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 323-337. https://doi.org/10.3897/zookeys.457.6760
Figures 1-4 - Selected aggressive behaviours of Jasus edwardsii: 1 attack 1 (low intensity) 2 clasp 3 rise 1 (low intensity) 4 rise 3 (high intensity).
Figures 9-12 from: Carter CG, Westbury H, Crear B, Simon C, Thomas C (2014) Agonistic behaviour in juvenile southern rock lobster, Jasus edwardsii (Decapoda, Palinuridae): implications for developing aquaculture. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 323-337. https://doi.org/10.3897/zookeys.457.6760
Figures 9-12 - Selected other behaviours of Jasus edwardsii: 9 cautious approach, 10 approach forward 11 anntennae touch 12 antennule touch.
Figure 3 from: Carvalho-Batista A, Negri M, Pileggi LG, Castilho AL, Costa RC, Mantelatto FL (2014) Inferring population connectivity across the range of distribution of the stiletto shrimp Artemesia longinaris Spence Bate, 1888 (Decapoda, Penaeidae) from DNA barcoding: implications for fishery management. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 271-288. https://doi.org/10.3897/zookeys.457.6569
Figure 3 - Phylogram for individuals of Artemesia longinaris inferred from Maximum Likelihood analysis of COI gene sequences. Localities represent analyzed specimens. Numbers are bootstrap support values (1000 replicates); values below 50% are not shown.
Figure 3 from: Zhao L, Gao T, Lu W (2015) Complete mitochondrial DNA sequence of the endangered fish (Bahaba taipingensis): Mitogenome characterization and phylogenetic implications. ZooKeys 546: 181-195. https://doi.org/10.3897/zookeys.546.5964
Figure 3 - Phylogenetic relationships among Sciaenidae species based on the combined 9988 bp nucleotide positions. The posterior probability value of BI analyses and bootstrap support values of ML analyses (in the order: BI, ML) are indicated near the branches.
Figure 2 from: Zhao L, Gao T, Lu W (2015) Complete mitochondrial DNA sequence of the endangered fish (Bahaba taipingensis): Mitogenome characterization and phylogenetic implications. ZooKeys 546: 181-195. https://doi.org/10.3897/zookeys.546.5964
Figure 2 - Potential secondary structure of the origin of L-strand replication (OL) of Bahaba taipingensis mtDNA.
Figure 2 from: Dixie B, White H, Hassall M (2015) Effects of microclimate on behavioural and life history traits of terrestrial isopods: implications for responses to climate change. In: Taiti S, Hornung E, Štrus J, Bouchon D (Eds) Trends in Terrestrial Isopod Biology. ZooKeys 515: 145–157. https://doi.org/10.3897/zookeys.515.9399
Figure 2 - Responses of relative growth rates to temperature and relative humidity. Responses to differences in temperature by a) Oniscus asellus, (F1, 36 = 0.905, P = 0.348) and. b) by Porcellio dilatatus, (F1, 36 = 5.112, P = 0.030); to differences in relative humidity of c) Oniscus asellus, (F1, 36 = 17.125, P < 0.001) and d) Porcellio dilatatus, (F1, 36 = 84.326, P < 0.001). Asterisks denote differences signficance at P < 0.05.
Figure 3 from: Dixie B, White H, Hassall M (2015) Effects of microclimate on behavioural and life history traits of terrestrial isopods: implications for responses to climate change. In: Taiti S, Hornung E, Štrus J, Bouchon D (Eds) Trends in Terrestrial Isopod Biology. ZooKeys 515: 145–157. https://doi.org/10.3897/zookeys.515.9399
Figure 3 - Response of mortality to temperature and relative humidity. Responses to temperature by a) Oniscus asellus, (U = 3097.0, P = 0.640. and b) by Porcellio dilatatus, (U = 2254.5, P = 0.016) and to relative humidity by c) Oniscus asellus (U = 1851.5, P < 0.001) and d) by Porcellio dilatatus (U = 2277.5 P < 0.001). Asterisks denote differences signficance at P < 0.05.
Figure 1 from: Dixie B, White H, Hassall M (2015) Effects of microclimate on behavioural and life history traits of terrestrial isopods: implications for responses to climate change. In: Taiti S, Hornung E, Štrus J, Bouchon D (Eds) Trends in Terrestrial Isopod Biology. ZooKeys 515: 145–157. https://doi.org/10.3897/zookeys.515.9399
Figure 1 - Responses in aggregation index to differences in temperatures and relative humidity: Responses to different temperatures by a) Oniscus asellus, (F 4, 249 = 12.22; P < 0.001) and b) by Porcellio scaber (F4,249 = 3.76; P < 0.001). and to different relative humidies by c) Oniscus asellus, (F 4, 230 = 25.39; P < 0.001) and d) by Porcellio dilatatus (F4,171 = 16.85; P < 0.001). Means sharing the same letter are not significantly different from each other at P < 0.05.
Figure 1 from: Edgecombe GD, Vahtera V, Giribet G, Kaunisto P (2015) Species limits and phylogeography of Newportia (Scolopendromorpha) and implications for widespread morphospecies. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 65-77. https://doi.org/10.3897/zookeys.510.8573
Figure 1 - Map of Mesoamerica, the Caribbean and northern South America showing geographic distribution of Newportia specimens analyzed herein (see Table 1 for coordinates of samples).
Figure 2 from: Edgecombe GD, Vahtera V, Giribet G, Kaunisto P (2015) Species limits and phylogeography of Newportia (Scolopendromorpha) and implications for widespread morphospecies. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 65-77. https://doi.org/10.3897/zookeys.510.8573
Figure 2 - Strict consensus of two optimal cladograms for Newportia under parameter set 111 for parsimony (POY) analysis. Abbreviations: BRA, Brazil; COL, Colombia; CR, Costa Rica; DR, Dominican Republic; ECU, Ecuador; FRG, French Guiana; GUA, Guatemala; HON, Honduras; MEX, Mexico.
Figure 2 from: Mertens J, Jocqué M, Geeraert L, De Beenhouwer M (2016) Newly discovered populations of the Ethiopian endemic and endangered Afrixalus clarkei Largen, implications for conservation. ZooKeys 565: 141-146. https://doi.org/10.3897/zookeys.565.7114
Figure 2 - Distribution map of Afrixalus clarkei. Green polygons represent previously known distribution. Red triangles represent new records.
Figure 1 from: Mertens J, Jocqué M, Geeraert L, De Beenhouwer M (2016) Newly discovered populations of the Ethiopian endemic and endangered Afrixalus clarkei Largen, implications for conservation. ZooKeys 565: 141-146. https://doi.org/10.3897/zookeys.565.7114
Figure 1 - Afrixalus clarkei; calling male (A), frontal view of male (B), dorsal view of female (C). Pictures: J. Mertens.
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.