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Figures 26-30 from: Albertoni F, Krell F, Steiner J, Zillikens A (2014) Life history and description of larva and pupa of Platyphileurus felscheanus Ohaus, 1910, a scarabaeid feeding on bromeliad tissues in Brazil, to be excluded from Phileurini (Coleoptera, Scarabaeidae, Dynastinae). ZooKeys 389: 49-76. https://doi.org/10.3897/zookeys.389.6888
Figures 26-30 - Imago of Platyphileurus felscheanus Ohaus, 1910. 26, 27 and 28 male habitus, dorsal, ventral and lateral, respectively 29 mentum DMNS ZE.20187 30 hind leg ventral and dorsal view respectively DMNS ZE.20188. Photos: FF Albertoni (26–28), C Grinter (29–30).
Figures 11-13 from: Albertoni F, Krell F, Steiner J, Zillikens A (2014) Life history and description of larva and pupa of Platyphileurus felscheanus Ohaus, 1910, a scarabaeid feeding on bromeliad tissues in Brazil, to be excluded from Phileurini (Coleoptera, Scarabaeidae, Dynastinae). ZooKeys 389: 49-76. https://doi.org/10.3897/zookeys.389.6888
Figures 11-13 - Platyphileurus felscheanus Ohaus, 1910, third instar. 11 lateral view MZSP 010.245, AT I-IX – abdominal tergites I to IX, DO X – dorsum X, MS – mesothorax, MT – metathorax, PLL – pleural lobes, PR - prothorax 12 thorax and legs lateral view DMNS ZE.15758, CX – coxa, FE – femur, PROS – prothoracic spiracle, PRSC II – prescutum II, PRSC III – prescutum III,, TR – trochanter, TT – tibiotarsus 13 larval raster DMNS ZE.15760, ASL – anal slit, C – campus, LAL – lower anal lip, T – teges. Photos: FF Albertoni (11), C Grinter (12–13).
Figure 36-37 from: Albertoni F, Krell F, Steiner J, Zillikens A (2014) Life history and description of larva and pupa of Platyphileurus felscheanus Ohaus, 1910, a scarabaeid feeding on bromeliad tissues in Brazil, to be excluded from Phileurini (Coleoptera, Scarabaeidae, Dynastinae). ZooKeys 389: 49-76. https://doi.org/10.3897/zookeys.389.6888
Figure 36-37 - Imago of Mystacella sp., parasite of Platyphileurus felscheanus. 36 dorsal view 37 lateral view. Photos: FF Albertoni.
Figures 9-10 from: Albertoni F, Krell F, Steiner J, Zillikens A (2014) Life history and description of larva and pupa of Platyphileurus felscheanus Ohaus, 1910, a scarabaeid feeding on bromeliad tissues in Brazil, to be excluded from Phileurini (Coleoptera, Scarabaeidae, Dynastinae). ZooKeys 389: 49-76. https://doi.org/10.3897/zookeys.389.6888
Figures 9-10 - Platyphileurus felscheanus Ohaus, 1910, third instar mouth parts DMNS ZE.15758: 9 maxilla and labium ventral view, LP – labial palpus, MA – mala, MP – maxillary palpus, PLF – palpifer, PMP – post-mentum, PRM1, 2 – Prementum 1 and 2 10 maxilla and labium dorsal view, GA – galea, GL – glossa, LAC – lacinia, HSC – hypopharyngeal sclerome, SD – stridulatory teeth, UN – uncus. Photos: C Grinter.
Figures 14-18 from: Albertoni F, Krell F, Steiner J, Zillikens A (2014) Life history and description of larva and pupa of Platyphileurus felscheanus Ohaus, 1910, a scarabaeid feeding on bromeliad tissues in Brazil, to be excluded from Phileurini (Coleoptera, Scarabaeidae, Dynastinae). ZooKeys 389: 49-76. https://doi.org/10.3897/zookeys.389.6888
Figures 14-18 - Platyphileurus felscheanus Ohaus, 1910, pupa: 14 female pupa dorsal view, t8, t9 – tergite 8 and 9, respectively 15 female pupa ventral view 16 female pupa lateral view 17 male pupa, ventral view of apex with genital ampulla 18 female pupa, ventral view of apex with genital ampulla. Legends: s8, s9 – sternite 8 and 9, respectively; gamp – genital ampulla; gp – genital pore, vt9 – ventralized tergite 9. Drawings: FF Albertoni.
Figure 5 from: Spodek M, Ben-Dov Y, Ghanim M, Mendel Z (2012) Morphological and molecular taxonomy of Nidularia balachowskii Bodenheimer (Hemiptera, Coccoidea, Kermesidae) with notes on its life history in Israel. ZooKeys 254: 23-45. https://doi.org/10.3897/zookeys.254.3959
Figure 5 - Maximum likelihood trees of 28S (a) and COI (b) nucleotide sequences of Nidularia balachowskii and other Coccoidea species. Acyrthosiphon pisum (Aphididae) sequences are used as outgroup species for both trees. Trees were constructed using K2P distance model and numerical values are bootstrap support, based on 1000 replicates (n= number of replicates, * = sequences derived from GenBank).
Figure 6 from: Briones-Fourzán P (2014) Differences in life-history and ecological traits between co-occurring Panulirus spiny lobsters (Decapoda, Palinuridae). 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: 289-311. https://doi.org/10.3897/zookeys.457.6669
Figure 6 - Diet of Panulirus argus and Panulirus guttatus from Puerto Morelos, Mexico. For each food item the index of relative importance (IRI) is estimated as IRI = (% frequency × % weight)/100. (Data from Colinas-Sánchez and Briones-Fourzán 1990).
Figure 3 from: Briones-Fourzán P (2014) Differences in life-history and ecological traits between co-occurring Panulirus spiny lobsters (Decapoda, Palinuridae). 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: 289-311. https://doi.org/10.3897/zookeys.457.6669
Figure 3 - Diet of Panulirus gracilis and Panulirus inflatus from Zihuatanejo, Mexico. For each food item the index of relative importance (IRI) is estimated as IRI = (% frequency × % weight)/100. (Data from Lozano-Álvarez and Aramoni-Serrano 1996).
Figure 2 from: Briones-Fourzán P (2014) Differences in life-history and ecological traits between co-occurring Panulirus spiny lobsters (Decapoda, Palinuridae). 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: 289-311. https://doi.org/10.3897/zookeys.457.6669
Figure 2 - Differences in some life-history traits between Panulirus gracilis and Panulirus inflatus from Zihuatanejo, Mexico. A carapace length (CL) distribution (n Panulirus gracilis: 2162, n Panulirus inflatus: 1873) B mean size C growth rate of males (mm CL week–1, n Panulirus gracilis: 148, n Panulirus inflatus: 34) D brood size (number of eggs per clutch) versus CL relationship. Error bars denote 95% confidence intervals. (Data from A, B Briones-Fourzán and Lozano-Álvarez 1992, C Briones-Fourzán and Lozano-Álvarez 2003, D Gracia 1985, Fernández-Lomelín 1992).
Figure 5 from: Briones-Fourzán P (2014) Differences in life-history and ecological traits between co-occurring Panulirus spiny lobsters (Decapoda, Palinuridae). 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: 289-311. https://doi.org/10.3897/zookeys.457.6669
Figure 5 - Differences in some life-history traits between Panulirus argus and Panulirus guttatus from Puerto Morelos, Mexico. A carapace length (CL) distribution (n Panulirus argus: 717, n Panulirus guttatus: 450) B mean size C growth rate of males (mm CL week–1, n Panulirus argus: 148, n Panulirus guttatus: 57) D brood size (number of eggs per clutch) versus CL relationship. Error bars denote 95% confidence intervals. (Data from A, B Lozano-Álvarez et al. 2007, Briones-Fourzán and Lozano-Álvarez 2013, C Negrete-Soto et al. 2002, D Fonseca-Larios and Briones-Fourzán 1998, Briones-Fourzán and Contreras-Ortiz 1999).
Figure 1 from: Briones-Fourzán P (2014) Differences in life-history and ecological traits between co-occurring Panulirus spiny lobsters (Decapoda, Palinuridae). 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: 289-311. https://doi.org/10.3897/zookeys.457.6669
Figure 1 - Geographic distribution of the two pairs of sympatric Panulirus species addressed in the text.
Figure 4 from: Briones-Fourzán P (2014) Differences in life-history and ecological traits between co-occurring Panulirus spiny lobsters (Decapoda, Palinuridae). 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: 289-311. https://doi.org/10.3897/zookeys.457.6669
Figure 4 - Potential ecological interactions between Panulirus gracilis and Panulirus inflatus in a rocky site ("Site A") in Zihuatanejo, Mexico. A lobster density (number of individuals ha–1) B relative abundance of molluscs (percentage of molluscs in benthic samples) C condition factor of lobsters. Error bars denote 95% CI. (Data from A Lozano et al. 1982, B Aramoni-Serrano 1982, C Lozano-Álvarez and Aramoni-Serrano 1996).
Figure 7 from: Por F (2014) Sulfide Shrimp? Observations on the concealed life history of the Thermosbaenacea (Crustacea). Subterranean Biology 14: 63-77. https://doi.org/10.3897/subtbiol.14.7927
Figure 7 - Thermosbaena mirabilis Monod. Female, translocating a membrane-protected batch of developing eggs to the brooding pouch (drawing by Zilch 1972).
Figure 5 from: Por F (2014) Sulfide Shrimp? Observations on the concealed life history of the Thermosbaenacea (Crustacea). Subterranean Biology 14: 63-77. https://doi.org/10.3897/subtbiol.14.7927
Figure 5 - Juvenile Tethysbaena ophelicola Wagner (intestine filled with bacteria (?)) (photo N. Ben Eliahu).
Figure 4 from: Por F (2014) Sulfide Shrimp? Observations on the concealed life history of the Thermosbaenacea (Crustacea). Subterranean Biology 14: 63-77. https://doi.org/10.3897/subtbiol.14.7927
Figure 4 - Tethysbaena argentarii Stella. Backdown swimming recovery after disturbance (filmed sequence by Olesen et al. 2006).
Figure 1 from: Por F (2014) Sulfide Shrimp? Observations on the concealed life history of the Thermosbaenacea (Crustacea). Subterranean Biology 14: 63-77. https://doi.org/10.3897/subtbiol.14.7927
Figure 1 - The extremophilic Thermosbaena mirabilis Monod from, El Hamma, Tunisia, a little known illustration (Barker 1962).
Figure 9 from: Por F (2014) Sulfide Shrimp? Observations on the concealed life history of the Thermosbaenacea (Crustacea). Subterranean Biology 14: 63-77. https://doi.org/10.3897/subtbiol.14.7927
Figure 9 - Schematic presentation of the suggested life strategy of a thermosbaenacean (for explanations see text).
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.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
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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.