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Figure 5 from: Garcia-Robledo C, Staines CL, Kress WJ (2015) A new species of bromeliad-feeding Cephaloleia Chevrolat (Coleoptera, Chrysomelidae, Cassidinae) from Costa Rica: evidence from DNA barcodes, larval and adult morphology and insect diets. ZooKeys 477: 143-155. https://doi.org/10.3897/zookeys.477.8220
Figure 5 - Differences in microstructures between larvae of Cephaloleia kuprewiczae (left column) and Cephaloleia histrionica (right column). A–B Head C–D Details of dorsal papillae and spiracles E–F Detail of spiracle and surrounding setae G–H Front leg. cl: clypeus, hy: hypopharynx, lb: labrum, lbi: labium, lp: labial palp, ma: malum, mn: mandibula, mp: maxillary palp, p: palpifer, se: seta, sp: spiracle, st: stipe.
Figure 6 from: Garcia-Robledo C, Staines CL, Kress WJ (2015) A new species of bromeliad-feeding Cephaloleia Chevrolat (Coleoptera, Chrysomelidae, Cassidinae) from Costa Rica: evidence from DNA barcodes, larval and adult morphology and insect diets. ZooKeys 477: 143-155. https://doi.org/10.3897/zookeys.477.8220
Figure 6 - A Frequency distributions of inter and intraspecific similarities for beetle COI sequences (paired comparisons, percentage of bases/residuals that are identical for each comparison for cytochrome oxidase I (COI) sequences included in Figure 6B). B Identification of Cephaloleia kuprewiczae sp. n. and Cephaloleia histrionica using cytochrome oxidase I (COI) sequences. Neighbor-joining tree includes bootstrap values (%) supporting species identifications. Filled circles represent DNA sequences obtained from adults. Empty circles represent DNA sequences obtained from larvae.
Figure 4 from: Garcia-Robledo C, Staines CL, Kress WJ (2015) A new species of bromeliad-feeding Cephaloleia Chevrolat (Coleoptera, Chrysomelidae, Cassidinae) from Costa Rica: evidence from DNA barcodes, larval and adult morphology and insect diets. ZooKeys 477: 143-155. https://doi.org/10.3897/zookeys.477.8220
Figure 4 - Larvae of Cephaloleia kuprewiczae (A) and Cephaloleia histrionica (B) feeding on their host plants. Scale bars = 3 mm.
Figure 3 from: Garcia-Robledo C, Staines CL, Kress WJ (2015) A new species of bromeliad-feeding Cephaloleia Chevrolat (Coleoptera, Chrysomelidae, Cassidinae) from Costa Rica: evidence from DNA barcodes, larval and adult morphology and insect diets. ZooKeys 477: 143-155. https://doi.org/10.3897/zookeys.477.8220
Figure 3 - A Egg B–C First instar larva (dorsal and ventral views) D–E Second instar larva (dorsal and ventral views). F Adult Cephaloleia histrionica. Scale bars in all panels = 1 mm. From García-Robledo et al. 2013a.
Figure 2 from: Garcia-Robledo C, Staines CL, Kress WJ (2015) A new species of bromeliad-feeding Cephaloleia Chevrolat (Coleoptera, Chrysomelidae, Cassidinae) from Costa Rica: evidence from DNA barcodes, larval and adult morphology and insect diets. ZooKeys 477: 143-155. https://doi.org/10.3897/zookeys.477.8220
Figure 2 - A–B Cephaloleia kuprewiczae A dorsal view B ventral view C–D Cephaloleia histrionica C Dorsal view D Ventral view. Scale bars = 3 mm.
Figure 1 from: Garcia-Robledo C, Staines CL, Kress WJ (2015) A new species of bromeliad-feeding Cephaloleia Chevrolat (Coleoptera, Chrysomelidae, Cassidinae) from Costa Rica: evidence from DNA barcodes, larval and adult morphology and insect diets. ZooKeys 477: 143-155. https://doi.org/10.3897/zookeys.477.8220
Figure 1 - Pitcairnia arcuata and Pitcairnia brittoniana (Bromeliaceae), host plants of Cephaloleia kuprewiczae. A Pitcairnia arcuata, habit B Detail of a rolled leaf used as a larval and adult food source and adult oviposition site C Pitcairnia arcuata Inflorescence D Pitcairnia brittoniana inflorescence E Leaf damage produced by a feeding adult Cephaloleia histrionica. Scale bars: A–C = 10 cm; D, E = 1 cm. Modified from García-Robledo et al. 2013a.
Figure 4 from: Stur E, Borkent A (2014) When DNA barcoding and morphology mesh: Ceratopogonidae diversity in Finnmark, Norway. ZooKeys 463: 95-131. https://doi.org/10.3897/zookeys.463.7964
Figure 4 - A, B Forcipomyia sp. 5 female A terminalia, in ventral view B head, in anterior view C, D Forcipomyia sp. 4 female C terminalia, in ventral view D head, in anterior view.
Figure 2 from: Stur E, Borkent A (2014) When DNA barcoding and morphology mesh: Ceratopogonidae diversity in Finnmark, Norway. ZooKeys 463: 95-131. https://doi.org/10.3897/zookeys.463.7964
Figure 2 - Taxon-ID tree of the studied Ceratopogonidae specimens based on the neighbor joining algorithm from aligned COI sequences using partial deletion for areas with gaps and 1000 bootstrap replicates in MEGA 5.2. All included sequences were longer than 500 bp. Bootstrap values shown on branches supported by more than 90% of the bootstrap replicates.
Figure 3 from: Stur E, Borkent A (2014) When DNA barcoding and morphology mesh: Ceratopogonidae diversity in Finnmark, Norway. ZooKeys 463: 95-131. https://doi.org/10.3897/zookeys.463.7964
Figure 3 - A, B Forcipomyia hygrophila female A terminalia, in ventral view B head, in anterior view C, D Forcipomyia sp. 1 female C terminalia, in ventral view D head, in anterior view.
Figure 1 from: Stur E, Borkent A (2014) When DNA barcoding and morphology mesh: Ceratopogonidae diversity in Finnmark, Norway. ZooKeys 463: 95-131. https://doi.org/10.3897/zookeys.463.7964
Figure 1 - Sample sites for Ceratopogonidae in Finnmark, Norway, in 2010. Modified after Fig. 2 in Ekrem et al. (2012). Map by Marc Daverdin, NTNU University Museum.
Figure 4 from: Amora G, Hamada N, Fusari LM, Andrade-Souza V (2015) An Asiatic Chironomid in Brazil: morphology, DNA barcode and bionomics. ZooKeys 514: 129-144. https://doi.org/10.3897/zookeys.514.9925
Figure 4 - Frequency of occurrence of the ventral length of the cephalic capsule of a Brazilian Chironomus population (Diptera: Chironomidae) showing the four larval instars.
Figure 2 from: Amora G, Hamada N, Fusari LM, Andrade-Souza V (2015) An Asiatic Chironomid in Brazil: morphology, DNA barcode and bionomics. ZooKeys 514: 129-144. https://doi.org/10.3897/zookeys.514.9925
Figure 2 - NJ tree based on the COI sequences of the mtDNA of Chironomus (Diptera: Chironomidae) species. The sequence of Lipiniella fujiprimus was used as the outgroup. Bootstrap values > 50% are shown on branches. Accession numbers and countries are provided beside the species names. Species flagged with an asterisk (*) are neotropical species. Brazilian Chironomus population: Chironomus sp1BRA; Chironomus sp2BRA; Chironomus sp3BRA
Figure 1 from: Amora G, Hamada N, Fusari LM, Andrade-Souza V (2015) An Asiatic Chironomid in Brazil: morphology, DNA barcode and bionomics. ZooKeys 514: 129-144. https://doi.org/10.3897/zookeys.514.9925
Figure 1 - Adult male and pupae. Chironomus striatipennis, Indian population. A Wing D Hypopygium, dorsal view G Anal spur, dorsal view. Chironomus kiiensis, Japanese population B Wing E Hypopygium, dorsal view H Anal spur, dorsal view. Chironomus striatipennis, Brazilian population C Wing F Hypopygium, dorsal view I Anal spur, dorsal view. Scale bar: 500 µm (A, B, C, G, H, I); 200 µm (D, E, F).
Figure 3 from: Rozo-Lopez P, Mengual X (2015) Mosquito species (Diptera, Culicidae) in three ecosystems from the Colombian Andes: identification through DNA barcoding and adult morphology. ZooKeys 513: 39-64. https://doi.org/10.3897/zookeys.513.9561
Figure 3 - Maximum likelihood tree of the barcoding sequences of mosquito species listed for the Neotropics. Terminal branches have been collapsed in order to save space (see original tree in Suppl. material 7 and 8). Branches in colors indicate non-monophyletic genera. Red clusters represent groups with problems to discriminate species. Names with green asterisk indicate non-monophyletic species. Bootstrap values above 60 (1,000 replicates) are given at the nodes.
Figure 1 from: Rozo-Lopez P, Mengual X (2015) Mosquito species (Diptera, Culicidae) in three ecosystems from the Colombian Andes: identification through DNA barcoding and adult morphology. ZooKeys 513: 39-64. https://doi.org/10.3897/zookeys.513.9561
Figure 1 - Map of Colombia indicating the sampling sites of mosquitoes collected in this study: Belmira, Antioquia, paramo, 3,200 masl (red circle); Rio Sucio, Caldas, cloud forest, 1,960 masl (green circle); La Pintada, Antioquia, tropical dry forest, 660 masl (blue circle); Supia, Caldas, rural area, 1,150 masl (pink circle). Modified from Instituo Geográfico Agustín Codazzi (www.igac.gov.co) and Wikimedia Commons (by Addicted04).
Figure 2 from: Rozo-Lopez P, Mengual X (2015) Mosquito species (Diptera, Culicidae) in three ecosystems from the Colombian Andes: identification through DNA barcoding and adult morphology. ZooKeys 513: 39-64. https://doi.org/10.3897/zookeys.513.9561
Figure 2 - Neighbour-Joining tree of the barcoding sequences of mosquito species listed for Neotropics, based on Tamura-Nei genetic distances. Terminal branches have been collapsed in order to save space (see original tree in Suppl. material 5 and 6). Branches in colors indicate non-monophyletic genera. Red clusters represent groups with problems to discriminate species. Names with green asterisk indicate non- monophyletic species. Bootstrap values above 60 (1,000 replicates) are given at the nodes.
Figures 12-17 from: Huemer P, Mutanen M (2015) Alpha taxonomy of the genus Kessleria Nowicki, 1864, revisited in light of DNA-barcoding (Lepidoptera, Yponomeutidae). ZooKeys 503: 89-133. https://doi.org/10.3897/zookeys.503.9590
Figures 12-17 - Kessleria male genitalia. 12 Kessleria alternans, Switzerland, Graubünden, SE Sils-Maria, 1820–1870 m, 13.7.1989, leg. Huemer, Karsholt & Tarmann, gen. slide YPO 22 (TLMF) 13 idem, distal part of phallus enlarged 14 Kessleria cottiensis sp. n., paratype, Italy, Prov. Torino, Alpi Cozie, V. delle Finestre, 1700 m, 27.7.1990, leg. Huemer & Tarmann, gen. slide YPO 66 (TLMF) 15 idem, distal part of phallus enlarged 16 Kessleria dimorpha sp. n., paratype, France, Dep. Hautes-Alpes, Col Agnel, 2770 m, 4.8.2010, leg. Huemer gen. slide YPO 149 (TLMF) 17 idem, holotype, gen. slide YPO 158, distal part of phallus enlarged.
Figures 2-7 from: Huemer P, Mutanen M (2015) Alpha taxonomy of the genus Kessleria Nowicki, 1864, revisited in light of DNA-barcoding (Lepidoptera, Yponomeutidae). ZooKeys 503: 89-133. https://doi.org/10.3897/zookeys.503.9590
Figures 2-7 - Kessleria adults in dorsal view. 2 Kessleria alternans, ♂, Switzerland, Graubünden, SE Sils-Maria, 1820–1870 m, 13.7.1989, leg. Huemer, Karsholt & Tarmann (TLMF) 3 Kessleria alternans, ♀, same data (TLMF) 4 Kessleria cottiensis sp. n., ♂, paratype, Italy, Prov. Torino, Alpi Cozie, V. delle Finestre, 1700 m, 27.7.1990, leg. Huemer & Tarmann (TLMF) 5 Kessleria cottiensis sp. n., ♀, paratype, same data (TLMF) 6 Kessleria dimorpha sp. n., ♂, paratype, France, Dep. Hautes-Alpes, Col Agnel, 2770 m, 4.8.2010, leg. Huemer (TLMF) 7 Kessleria dimorpha sp. n., ♀, paratype, same data (TLMF).
Figures 63-66 from: Huemer P, Mutanen M (2015) Alpha taxonomy of the genus Kessleria Nowicki, 1864, revisited in light of DNA-barcoding (Lepidoptera, Yponomeutidae). ZooKeys 503: 89-133. https://doi.org/10.3897/zookeys.503.9590
Figures 63-66 - Kessleria female genitalia, details of VIII abdominal segment enlarged. 63 Kessleria klimeschi, paratype, Italy, Prov. Udine, Montasio, Malga Pecol, 1600 m, 24.6.1989 e.l., leg. Huemer & Tarmann, gen. slide YPO 76 (TLMF) 64 Kessleria inexpectata, paratype, France, Dep. Alpes Maritimes, Marguareis W-Hang, Navela, 2100–2200 m, 21.-23.7.1990, leg. Huemer & Tarmann, gen. slide YPO 74 (TLMF) 65 Kessleria orobiae sp. n., paratype, Zambla Alta – Plassa, 1160 m, 24.6.2013, leg. Huemer, gen. slide YPO 161 (TLMF) 66 Kessleria albescens, Italy, Monte Baldo, Bocca di Navene, 14.7.1987, leg. Huemer & Tarmann (TLMF).
Figures 24-26 from: Huemer P, Mutanen M (2015) Alpha taxonomy of the genus Kessleria Nowicki, 1864, revisited in light of DNA-barcoding (Lepidoptera, Yponomeutidae). ZooKeys 503: 89-133. https://doi.org/10.3897/zookeys.503.9590
Figures 24-26 - Kessleria female genitalia. 24 Kessleria dimorpha sp. n., paratype, France, Dep. Hautes-Alpes, Col Agnel, 2770 m, 4.8.2010, leg. Huemer, gen. slide YPO 159 (TLMF) 25 Kessleria wehrlii, paratype, France, Dep. Alpes Maritimes, Mont Gelas Massiv, Mont Colomb W, 2450 m, 24.7.1990, leg. Huemer & Tarmann, gen. slide YPO 69 (TLMF) 26 Kessleria alpmaritimae sp. n., paratype, France, Dep. Alpes Maritimes, Marguareis W-Hang, Navela, 2100–2200 m, 18.-19.7.1991, leg. Huemer & Tarmann (TLMF).
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)
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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.