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FIGURE 3 in The advertisement call of Chiasmocleis (Syncope) carvalhoi (Nelson, 1975) (Anura Microhylidae), with taxonomic remarks based on new morphological observations of specimens from Peruvian Amazonia
FIGURE 3. Audiospectrograms (upper graphs) and oscillograms (lower graphs) of the advertisement call of a male of Chiasmocleis (Syncope) carvalhoi (MCP 14420, 10.38 mm snout-vent length) recorded at Estación Biológica José Álvarez Alonso, Reserva Nacional Allpahuayo-Mishana, Peru. (A) A 9 s fragment of the recording with four calls and (B) a single call. Air temperature at time of recording = 22.6 °C.
FIGURE 2 in The advertisement call of Chiasmocleis (Syncope) carvalhoi (Nelson, 1975) (Anura Microhylidae), with taxonomic remarks based on new morphological observations of specimens from Peruvian Amazonia
FIGURE 2. One of the males of Chiasmocleis (Syncope) carvalhoi (MCP 14418, 9.74 mm snout-vent length, 23.5º C) recorded in this study. (A) Dorsolateral and (B) ventral views in life. (C) Ventral view of its right hand in preservative, white arrow indicates the palmar tubercle. (D) Lateral view of the head in preservative, white arrow indicates the tympanum. Scale bars = 0.5 mm.
FIGURE 1 in The advertisement call of Chiasmocleis (Syncope) carvalhoi (Nelson, 1975) (Anura Microhylidae), with taxonomic remarks based on new morphological observations of specimens from Peruvian Amazonia
FIGURE 1. Map of Loreto, Peru, with symbols showing the known localities of Chiasmocleis (Syncope) carvalhoi. Red diamond: Type locality: Estirón, río Ampiyacu. Black diamond: Estación Biológica José Álvarez Alonso, Reserva Nacional Allpahuayo-Mishana (EBJAA—RNAM). Black circles, specimens sequenced in other studies: 1. Puerto Almendra, Arboreto UNAP; 2. Umarital, río Ampiyacu; 3. Hacienda Zamora, Loreto, near to EBJAA—RNAM.
Summer circumpolar acoustic occurrence and call rates of Ross (Ommatophoca rossii) and leopard (Hydrurga leptonyx) seals in the Southern Ocean
<p>Two of the Antarctic pack ice seals, Ross, Ommatophoca rossii, and leopard, Hydrurga leptonyx, seals, are extremely dificult to study via traditional visual survey techniques, yet are ideal for an acoustic survey as they are highly vociferous and produce an array of underwater sounds during the austral summer. To determine their acoustic occurrence in the Antarctic pack ice, we use their calls, detected within 680 acoustic recordings made between 1999 and 2009 as part of two multinational programmes. Siren calls of Ross seals were detected mainly in January, and 9.88 calls per minute from low siren calls was the highest call rate for this species. High numbers of Ross seal calls were detected close to the ice edge in areas between 0° and 20° E and 60° and 130° E, suggesting these are important summer habitats. Leopard seal calls were detected mainly in December and January, and December had the highest percentage of calls. Call rate of 11.93 calls per minute from low double trills was the highest call rate for leopard seals. Leopard seal calls were detected throughout the Southern Ocean with more calls detected throughout the pack ice. There was little spatio-temporal overlap in call occurrence of Ross and leopard seals, but both species were more vocally active during the day. Longitude and latitude were the most important predictors of Ross seal occurrence, and month of the year highly predicted leopard seal occurrence. This is the irst study to examine the circumpolar acoustic occurrence of Ross and leopard seals in the Southern Ocean pack ice.</p>
FIGURE 1 in The advertisement call of Physalaemus caete Pombal & Madureira, 1997 (Anura Leptodactylidae: Leiuperinae), an endangered species endemic to Brazil's northern Atlantic Forest
FIGURE 1. (A–C) Spectrogram, oscillogram, and amplitude spectrum, respectively, of the advertisement call of Physalaemus caete from Igarassu (state of Pernambuco, northeastern Brazil). The dominant harmonic (H4) and adjacent harmonics (H3 and H5) are indicated. The fundamental and second harmonics are supposedly filtered out (see text). (D) Male voucher of P. caete (CHPUFRPE 5840; SVL = 23.0 mm).
FIGURE 12 in Calling for a reassessment of rodent diversity in Colombia: description of a new species of Neacomys (Cricetidae: Oryzomyini) from the Magdalena Valley, with a new phylogenetic hypothesis for the genus and comments on its diversification
FIGURE 12. Illustration of Neacomys serranensis sp. nov. by wildlife artist and zoologist Velizar Simeonovski.
FIGURE 10 in Calling for a reassessment of rodent diversity in Colombia: description of a new species of Neacomys (Cricetidae: Oryzomyini) from the Magdalena Valley, with a new phylogenetic hypothesis for the genus and comments on its diversification
FIGURE 10. Comparison of the lateral profiles of the skulls of Trans-Andean species of Neacomys present in Colombia: A) Neacomys sp. nov. (UIS-MHN-M 1068, holotype). B) Neacomys tenuipes (UIS-MHN-M 1723). Note a more convex profile of the braincase, a thicker hamular process of the squamosal, a broader condylar process, a larger and laterally projected mental foramen, and the anterior margin of nasals without a hump in Neacomys sp. nov. con: condylar process; hp: hamular process of the squamosal; mf: mental foramen; nas: nasals.
FIGURE 8 in Calling for a reassessment of rodent diversity in Colombia: description of a new species of Neacomys (Cricetidae: Oryzomyini) from the Magdalena Valley, with a new phylogenetic hypothesis for the genus and comments on its diversification
FIGURE 8. Ventral perspectives of adult specimens illustrating the striking difference in ventral fur of the two Trans-Andean species of Neacomys present in Colombia: A) Holotype of Neacomys sp. nov (UIS-MHN-M 1068). B) Section of the holotype of Neacomys sp. nov. showing its characteristic gray-based ochraceous-buff ventral fur. C) Neacomys tenuipes (UIS-MHN-M 1723); note the contrasting entirely white ventral fur of this species.
FIGURE 7 in Calling for a reassessment of rodent diversity in Colombia: description of a new species of Neacomys (Cricetidae: Oryzomyini) from the Magdalena Valley, with a new phylogenetic hypothesis for the genus and comments on its diversification
FIGURE 7. Frontal perspectives of adult specimens belonging to the two Trans-Andean species of Neacomys present in Colombia: A) Holotype of Neacomys sp. nov (UIS-MHN-M 1068); note the distinctive broad ochraceous-orange patches in the sides of the muzzle of this species. B) Neacomys tenuipes (UIS-MHN-M 1723).
FIGURE 6 in Calling for a reassessment of rodent diversity in Colombia: description of a new species of Neacomys (Cricetidae: Oryzomyini) from the Magdalena Valley, with a new phylogenetic hypothesis for the genus and comments on its diversification
FIGURE 6. Dorsal perspectives of adult specimens belonging to the two Trans-Andean species of Neacomys present in Colombia: A) Holotype of Neacomys sp. nov (UIS-MHN-M 1068). B) Neacomys tenuipes (UIS-MHN-M 1723); note that a portion of the tail is missing in this specimen.
FIGURE 5. A in Calling for a reassessment of rodent diversity in Colombia: description of a new species of Neacomys (Cricetidae: Oryzomyini) from the Magdalena Valley, with a new phylogenetic hypothesis for the genus and comments on its diversification
FIGURE 5. A) Montane forest habitat along the left Bank of the La San Guillerma stream, adjacent to the type locality of Neacomys sp. nov. (municipality of El Carmen de Chucurí) (Photograph by Juliette Gualdrón) B) View of the forest remnant where the second specimen of Neacomys sp nov. was collected (municipality of Hato) (Photograph by Juliette Gualdrón). C) Topography of the western slope of the Serranía de los Yariguíes from the campsite "Finca Buenos Aires"; near the type locality of Neacomys sp. nov. D) Educational activity with members of the community in the municipality of El Carmen del Chucurí, Vereda la Bodega, Sector Manchurrias, illustrating the importance of government funded projects (like Santander BIO expeditions), not only to inventory the biodiversity of remote areas, but also to teach local people to preserve it.
FIGURE 4 in Calling for a reassessment of rodent diversity in Colombia: description of a new species of Neacomys (Cricetidae: Oryzomyini) from the Magdalena Valley, with a new phylogenetic hypothesis for the genus and comments on its diversification
FIGURE 4. Scatterplots of the Principal Components Analyses: PC1 and PC2 are represented in the graphics. A. PCA of the external and craniodental variables of all the small-bodied species of Neacomys; B. PCA of the craniodental variables of N. tenuipes and Neacomys sp. nov. Miniatures in the right side correspond to the Bayesian Cytb phylogeny recovered here (FIGURE 3): species in the scatterplots and the phylogenies are same colored.
FIGURE 3 in Calling for a reassessment of rodent diversity in Colombia: description of a new species of Neacomys (Cricetidae: Oryzomyini) from the Magdalena Valley, with a new phylogenetic hypothesis for the genus and comments on its diversification
FIGURE 3. Bayesian Inference topology based on Cytb sequence data used to assess the position of Neacomys sp. nov. in relation to other species in the genus (BI and ML analyses resulted in congruent topologies). Support values are indicated for each node (Bayesian posterior probabilities to the left, and percentages of 1,000 bootstrap replicates to the right). Each terminal is identified by country of origin, the next largest political unit, and GenBank accession number (in red). For specimens of N. tenuipes and Neacomys sp. nov. sequenced here, collection numbers are provided, as well as a number referring to localities mapped in FIGURE 2 and listed in Appendix I. Shaded colored boxes enclose the species groups proposed by Hurtado & Pacheco (2017) and Semedo et al. (2020). Abbreviations: BO (Bolivia), BR (Brazil), CO (Colombia), EC (Ecuador), FG (French Guyana), GU (Guyana), PE (Peru), and SU (Suriname).
FIGURE 11 in Calling for a reassessment of rodent diversity in Colombia: description of a new species of Neacomys (Cricetidae: Oryzomyini) from the Magdalena Valley, with a new phylogenetic hypothesis for the genus and comments on its diversification
FIGURE 11. Selected qualitative morphological traits differentiating Trans-Andean species of Neacomys present in Colombia: A), C), E) Neacomys sp. nov. B), D), F) N. tenuipes. Note the tegmen tympani exposed above the dorsal surface of the ectotympanic, the opened ectotympanic ring, the larger orbicular apophysis of the malleus, the bifurcated paraoccipital process, the deeper folds of the upper molars, and the divided mesoflexus of M1 in the new species. ab: auditory bullae; adeect: anterodorsal edge of the ectotympanic; hyp: hypoflexus; hp: hamular process of the squamosal; M1 prc: procingulum of first upper molar; mes: mesoflexus; met: metaflexus; mt: mastoid tubercle; oa: orbicular apophysis; par: paraflexus; pgf: postglenoid foramen; pp: paraoccipital process; pro: protoflexus; ssf: subsquamosal fenestra; tt: tegmen tympani.
FIGURE 2 in Calling for a reassessment of rodent diversity in Colombia: description of a new species of Neacomys (Cricetidae: Oryzomyini) from the Magdalena Valley, with a new phylogenetic hypothesis for the genus and comments on its diversification
FIGURE 2. Map showing collection localities of the named and unamed small-bodied species of Neacomys (except N. pictus) along with salient topographic features of northern South America. Localities of N. tenuipes and Neacomys sp. nov are numbered according to Appendix I. Localities of the remaining species are detailed in Voss et al. (2001), Sánchez-Vendizú et al. (2018), and Semedo et al. (2020). Miniature in the right side of the map corresponds to the Bayesian Cytb phylogeny recovered here (FIGURE 3): species in the map and phylogeny are same colored; the numbers in some nodes correspond to the median divergence times estimated by Upham et al. (2019) within Neacomys.
FIGURE 1 in Calling for a reassessment of rodent diversity in Colombia: description of a new species of Neacomys (Cricetidae: Oryzomyini) from the Magdalena Valley, with a new phylogenetic hypothesis for the genus and comments on its diversification
FIGURE 1. Map of collecting localities of the specimens of Neacomys sp. nov. (stars) 1. Colombia, Department of Santander, Municipality of El Carmen de Chucurí, vereda La Bodega, sector Manchurrias, western slope of the Serranía de los Yariguíes, Finca Buenos Aires, in the basin of the La San Guillerma stream (Type locality); 2. Colombia, Department of Santander, Municipality of Hato, vereda Hoya Negra. Numbers also correspond to the localities listed in Appendix I. Dashed lines represent boundaries of the municipalities encompassing the two localities. Green polygon represents the area comprised by the Serranía de los Yariguíes National Natural Park.
FIGURE 9 in Calling for a reassessment of rodent diversity in Colombia: description of a new species of Neacomys (Cricetidae: Oryzomyini) from the Magdalena Valley, with a new phylogenetic hypothesis for the genus and comments on its diversification
FIGURE 9. Comparison of the dorsal and ventral views of the skulls of Trans-Andean species of Neacomys present in Colombia: A), C) Neacomys sp. nov. (UIS-MHN-M 1068, holotype). B), D) Neacomys tenuipes (UIS-MHN-M 1723). Note the nasals more expanded anteriorly, the shallower zygomatic notches, the less developed supraorbital ridges, the procingulum of M1 flattened laterally, and the incisive foramina extending almost to anterior alveolus of M1 in Neacomys sp. nov. if: incisive foramen; M1 prc: procingulum of first upper molar; nas: nasal bone; sob: supraorbital beads; zn: zygomatic notch.
Data from: Acoustic identification of Mexican bats based on taxonomic and ecological constraints on call design
Monitoring global biodiversity is critical for understanding responses to anthropogenic change, but biodiversity monitoring is often biased away from tropical, megadiverse areas that are experiencing more rapid environmental change. Acoustic surveys are increasingly used to monitor biodiversity change, especially for bats as they are important indicator species and most use sound to detect, localise and classify objects. However, using bat acoustic surveys for monitoring poses several challenges, particularly in megadiverse regions. Many species lack reference recordings, some species have high call similarity or differ in call detectability, and quantitative classification tools, such as machine learning algorithms, have rarely been applied to data from these areas. Here, we collate a reference call library for bat species that occur in a megadiverse country, Mexico. We use 4685 search-phase calls from 1378 individual sequences of 59 bat species to create automatic species identification tools generated by machine learning algorithms (Random Forest). We evaluate the improvement in species-level classification rates gained by using hierarchical classifications, reflecting either taxonomic or ecological constraints (guilds) on call design, and examine how classification rate accuracy changes at different hierarchical levels (family, genus and guild). Species-level classification of calls had a mean accuracy of 66%, and the use of hierarchies improved mean species-level classification accuracy by up to 6% (species within families 72%, species within genera 71·2% and species within guilds 69·1%). Classification accuracy to family, genus and guild-level was 91·7%, 77·8% and 82·5%, respectively. The bioacoustic identification tools we have developed are accurate for rapid biodiversity assessments in a megadiverse region and can also be used effectively to classify species at broader taxonomic or ecological levels. This flexibility increases their usefulness when there are incomplete species reference recordings and also offers the opportunity to characterise and track changes in bat community structure. Our results show that bat bioacoustic surveys in megadiverse countries have more potential than previously thought to monitor biodiversity changes and can be used to direct further developments of bioacoustic monitoring programs in Mexico.
Data from: Effect of ecological momentary assessment, goal-setting and personalized phone-calls on adherence to interval walking training using the InterWalk application among patients with type 2 diabetes – a pilot randomized controlled trial
Objectives: The objective was to investigate the feasibility and usability of structured text-messages, goal-setting and phone-calls on adherence to a 12-week self-conducted interval walking training (IWT) program, delivered by the InterWalk smartphone among patients with type 2 diabetes (T2D). Methods: In a two-arm pilot randomized controlled trial (Denmark, March 2014 to February 2015), patients with T2D (18-80 years with a Body Mass Index of 18 and 40 kg/m2) were randomly allocated to 12 weeks of IWT with (intervention) or without additional support (control). The primary outcome was the difference between groups in accumulated time of interval walking training across 12 weeks. All patients were encouraged to use the InterWalk application to perform IWT for ≥90 minute/week. Patients in the intervention group made individual goals regarding lifestyle change, received automated text-messages once a week, inquiring about exercise adherence. In case of consistent non-adherence, the patients would receive a phone-call inquiring about the reason for non-adherence. The control group did not receive additional support. Information about training adherence was assessed objectively. Usability of structured text-messages was assessed based on response rates and self-reported satisfaction after 12-weeks. Results: Thirty-seven patients with T2D (66 years, 65% female, hemoglobin 1Ac 50.3 mmol/mol) where included (n=18 and n=19 in intervention and control group, respectively). The retention rate was 83%. The intervention group accumulated [95%CI] 345 -7, 698 minutes of IWT more than the control group. The response rate for the text-messages was 83% (68% for males and 90% for females). Forty-one percent of the intervention and 25% of the control group were very satisfied with their participation. Conclusion: The combination of structured text-messages, goal-setting with the possibility of follow-up phone calls are considered feasible interventions to attain training adherence when using the InterWalk app during a 12-week period in patients with T2D. Some uncertainty about the effect size of adherence remains.
Data from: Why does noise reduce response to alarm calls? Experimental assessment of masking, distraction and greater vigilance in wild birds
1. Environmental noise from anthropogenic and other sources affects many aspects of animal ecology and behaviour, including acoustic communication. Acoustic masking is often assumed in field studies to be the cause of compromised communication in noise, but other mechanisms could have similar effects. 2. We tested experimentally how background noise disrupted the response to conspecific alarm calls in wild superb fairy-wrens, Malurus cyaneus, assessing the effects of acoustic masking, distraction and changes in vigilance. We first examined the birds' response to alarm-call playbacks accompanied by different amplitudes of background noise that overlapped the calls in acoustic frequency. We then scored and videoed their response to alarm calls in two types of background noise, that did or did not overlap call frequency, but were broadcast at a constant amplitude. 3. Birds were less likely to flee to alarm calls in higher amplitudes of overlapping noise, demonstrating that noise itself compromised communication independently of environmental correlates. Background noise affected the response only if it overlapped in frequency with the alarm calls, implying that the effect was not due to distraction. Further, birds were equally vigilant during background noise of overlapping or non-overlapping frequency, indicating that the lack of response to alarm calls in overlapping noise was not due to enhanced vigilance and awareness that there was no predator. 4. We conclude that alarm-call reception was compromised by masking, a mechanism that is often assumed but rarely tested in an ecological context. Masking compromised reception of high-frequency 'aerial' alarm calls and so could reduce survival in background noise of similar frequency. While anthropogenic noise, which is often of lower frequency, is unlikely to affect communication with these calls, it could affect reception of acoustic cues of danger, or other conspecific or heterospecific alarm calls.
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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)
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.