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Fig. 5 in New herpetofaunal observations from Laos based on photo records
Fig. 5. (A) Chirixalus doriae in Xay District, Oudomxai Province; (B) C. nongkhorensis in Khounkham District, Khammouan Province; (C) Gracixalus quangi in Longcheng District, Xaisomboun Province; (D) G. quyeti in Khounkham District, Khammouan Province; (E) Rhacophorus kio in Bortaen District, Xaignabouli Province; (F) R. rhodopus in Mork District, Xiangkhouang Province. Photos by P. Brakels.
Fig. 4 in New herpetofaunal observations from Laos based on photo records
Fig. 4. (A) Ophryophryne pachyproctus in Longcheng District, Xaisomboun Province; (B) Xenophrys palpebralespinosa in Mork District, Xiangkhouang Province; (C) Glyphoglossus guttulatus in Pathoumphone District, Champasak Province; (D) G. molossus in Savannakhet Province; (E) Rana johnsi in Xaignabouli Province; (F) Sylvirana cubitalis in Thongmyxay District, Xaignabouli Province. Photos by P. Pawangkhanant (A), P. Brakels (B–C), K. Inkhavilay (D), N. Maury (E), and P. Phiapalath (F).
Fig. 9 in New herpetofaunal observations from Laos based on photo records
Fig. 9. (A) Bungarus candidus in Khongxedone District, Salavan Province; (B) Subsessor bocourti in Champhone District, Savannakhet Province; (C) Pareas carinatus in Keo Oudom District, Vientiane Province; (D) P. hamptoni in Longcheng District, Xaisomboun Province. Photos by P. Brakels (A–C) and P. Pawangkhanant (D).
Fig. 3 in New herpetofaunal observations from Laos based on photo records
Fig. 3. (A) Nanorana aenea in Mork District, Xiangkhouang Province; (B) dorsal view and (C) ventral view of Quasipaa verrucospinosa in Longcheng District, Xaisomboun Province; (D) dorsal view and (E) ventral view of Leptobrachella eos in Bortaen District, Xaignabouli Province; (F) Leptobrachium smithi in Xay District, Oudomxai Province. Photos: P. Brakels (A–B, D, F) and N. Maury (C, E).
Fig. 11 in New herpetofaunal observations from Laos based on photo records
Fig. 11. Ventral views of two Trimeresurus species from Laos, showing scalation and tail base; numbers correspond to subcaudal scale count. (A) Adult male of T. gumprechti from Bortaen District, Xaignabouli Province; (B) adult male of T. popeiorum in Xay District, Oudomxai Province. Photos by N. Maury.
Fig. 2 in New herpetofaunal observations from Laos based on photo records
Fig. 2. Various habitat types surveyed in Laos: (A) forest in Mt. Phou Samsoum, Mork District, Xiangkhouang Province; (B) forest in Phou Khao Khouay NPA, Vientiane Province; (C) forest in Bortaen District, Xaignabouli Province; (D) forest in Longcheng District, Xaisomboun Province; (E) karst forest in Phou Hin Poun NPA, Khammouan Province; (F) lowland habitat in the Pathoumphone District, Champasak Province. Photos by P. Brakels.
Fig. 7 in New herpetofaunal observations from Laos based on photo records
Fig. 7. (A) Boiga cyanea in Phiang District, Xaignabouli Province; (B) B. multomaculata in Nakay District, Khammouan Province; (C) lateral view and (D) ventral view of Dendrelaphis cf. cyanochloris in Xay District, Oudomxai Province; (E) Gonyosoma prasinum in Xay District, Oudomxai Province. Photos by P. Brakels.
Fig. 1 in New herpetofaunal observations from Laos based on photo records
Fig. 1. Map showing localities cited in the text. Sites surveyed: 1: Xay; 2: Phoukhoun; 3: Xayabury; 4: Phiang 1; 5: Phiang 2; 6: Thongmyxay; 7: Bortaen 1; 8: Bortaen 2; 9: Xanakharm; 10: Kasy; 11: Vangvieng; 12: Phonghong; 13: Keo Oudom 2; 14: Longcheng 1; 15: Longcheng 2; 16: Thapabath; 17: Hom; 18: Thathom; 19: Mork 1; 20: Xaychamphone; 21: Khounkham 1; 22: Khounkham 2; 23: Nakai; 24: Ngommalath; 25: Champhone 2; 26: Champhone 1; 27: Xonnabouly; 28: Phin; 29: Khongxedone; 30: Paksong 2; 31: Paksong 1; 32: Pathoumphone.
Figure 5 in First record of five fish species from Réunion Island observed during the inventory of the Marine Natural Zones of Interest for Ecology, Flora and Fauna (ZNIEFF)
Figure 5. – Specimen of Trichonotus marleyi photographed on 6 April 2017 at 20°55'30.54"S and 55°17'55.32"E.
Figure 3 in First record of five fish species from Réunion Island observed during the inventory of the Marine Natural Zones of Interest for Ecology, Flora and Fauna (ZNIEFF)
Figure 3. – Specimen of Fusigobius neophytus photographed on 22 November 2017 at 21°1'16.32"S and 55°13'31.84"E.
Figure 1 in First record of five fish species from Réunion Island observed during the inventory of the Marine Natural Zones of Interest for Ecology, Flora and Fauna (ZNIEFF)
Figure 1. – Location of the observation stations of the 5 fish species present- ed in this study on a geomorphological map of the Reunionese coastline.
Figure 4 in First record of five fish species from Réunion Island observed during the inventory of the Marine Natural Zones of Interest for Ecology, Flora and Fauna (ZNIEFF)
Figure 4. – Specimen of Samariscus triocellatus photographed on 4 May 2016 at 21°6'20.92"S and 55°46'16.72"E.
Figure 2 in First record of five fish species from Réunion Island observed during the inventory of the Marine Natural Zones of Interest for Ecology, Flora and Fauna (ZNIEFF)
Figure 2. – Specimen of Fusigobius inframaculatus photographed on 8 April 2016 at 21°21'18.54"S and 55°47'31.31"E.
Figure 6 in Observations of plume moths on North Andros Island, Bahamas, and notes on new records and species previously recorded from the Bahamas (Lepidoptera: Pterophoridae)
Figure 6. Larva and pupa of Adaina perplexus: a) larva (prepupa), dorsal view; b) larva (prepupa) lateral view; c) pupa, dorsal view; d) pupa, lateral view.
Figure 3–5 in Observations of plume moths on North Andros Island, Bahamas, and notes on new records and species previously recorded from the Bahamas (Lepidoptera: Pterophoridae)
Figure 3–5. Male genitalia of Hellinsia and Adaina: 3a) H. chlorias, slide DM 717; 3b) aedeagus, same individual; 4a) H. unicolor, slide DM 536; 4b) aedeagus, same individual; 5a) A. perplexus, slide DM 1625; 5b) aedeagus, same individual.
Figure 2 in Observations of plume moths on North Andros Island, Bahamas, and notes on new records and species previously recorded from the Bahamas (Lepidoptera: Pterophoridae)
Figure 2. Pterophoridae from North Andros Island: a) Lioptilodes albistriolatus; b) Stenoptilodes brevipennis; c) Sphenarches anisodactylus; d) Exelastis pumilio; e) Adaina perplexus; f) A. sp.
Figs. 1–2. Lisposoma josehermana Lamoral, 1979 in New Records and Observations on the Natural History of Lisposoma elegans and L. josehermana (Scorpiones: Bothriuridae)
Figs. 1–2. Lisposoma josehermana Lamoral, 1979, adult?, in life. 1. Natural light. 2. Ultraviolet light. Scale bar 5 10 mm.
Fig. 9 in New Records and Observations on the Natural History of Lisposoma elegans and L. josehermana (Scorpiones: Bothriuridae)
Fig. 9. Map showing the known distributions of Lisposoma elegans Lawrence, 1928 (n) and Lisposoma josehermana Lamoral, 1979 (m) in Namibia (contour interval 600 m; major sand systems stippled).
Fig. 6. Courtship movements recorded for a in Intertidal life: field observations on the clingfish Gobiesox barbatulus in southeastern Brazil
Fig. 6. Courtship movements recorded for a pair of Gobiesox barbatulus in the wild. Each cycle did not exceed 30 min of duration, and always started with one of the three "pre-mating" positions [i.e., (a, e, and h)]. After mating the pair did not stay in contact (b or f), and the larger individual performed parental behavior (b). They restarted the cycle after moving to a spot without eggs, following new approximation (c, d, and g). It is important to note that there are many sequences possible based in such events, since they can alternate.
Data for: Zebra finch song ecology: monitoring of breeding, observational transects, focal and year-round acoustic recordings, and a large-scale simultaneous playback experiment
<p class="MsoNormal">Male songbirds sing to establish territories and to attract mates. However, increasing reports of singing in non-reproductive contexts and by females show that song use is more diverse than previously considered. Therefore, alternative functions of song, such as social cohesion and synchronisation of breeding, by and large were overlooked even in such well-studied species as the zebra finch (<em>Taeniopygia guttata</em>). In these social songbirds only the males sing and pairs breed synchronously in loose colonies following aseasonal rain events in their arid habitat. As males are not territorial, and pairs form long-term monogamous bonds early in life, conventional theory predicts that zebra finches should not sing much at all; yet they do and their song is the focus of hundreds of lab-based studies. We hypothesise that zebra finch song functions to maintain social cohesion and to synchronise breeding. Here we test this idea using data from five years of field studies, including observational transects, focal and year-round audio recordings, and a large-scale playback experiment. We show that zebra finches frequently sing while in groups, that breeding status influences song output at the nest and at aggregations, that they sing year-round, and that they predominantly sing when with their partner, suggesting that song remains important after pair formation. Our playback reveals that song actively features in social aggregations as it attracts conspecifics. Together, these results demonstrate that birdsong has important functions beyond territoriality and mate choice, illustrating its importance in coordination and cohesion of social units within larger societies.</p>
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.