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FIGURE 5 in Two new species of the Suborder Senticaudata (Crustacea: Amphipoda) from the upper continental slope off Galicia (NW Iberian Peninsula)
FIGURE 5. Pareurystheus vitucoi sp. nov., Holotype, MHNUSC 10065. A, pereopod 6; B, pereopod 7. Scales: 0.1 mm.
FIGURE 8 in Two new species of the Suborder Senticaudata (Crustacea: Amphipoda) from the upper continental slope off Galicia (NW Iberian Peninsula)
FIGURE 8. Photis guerrai sp. nov., Holotype, MHNUSC 10068. A, mandible; B, mandible, composite setae on molar process; C, mandible, pappose seta on palp article 3; D, mandible, ornamentation of molar process; E, maxilla 1; F, maxilla 1, distal stout setae on outer plate; G, maxilla 2; H, maxilla 2, distal setae on outer plate; I, maxilliped; J, maxilliped, distal setae on inner plate; K, maxilliped, distal setae on outer plate. Scales: 0.1 mm.
FIGURE 7 in Two new species of the Suborder Senticaudata (Crustacea: Amphipoda) from the upper continental slope off Galicia (NW Iberian Peninsula)
FIGURE 7. Photis guerrai sp. nov., Holotype, MHNUSC 10068. A, habitus, lateral view; B, antenna 1; C, antenna 2. Scales: 0.5 mm.
FIGURE 4 in Two new species of the Suborder Senticaudata (Crustacea: Amphipoda) from the upper continental slope off Galicia (NW Iberian Peninsula)
FIGURE 4. Pareurystheus vitucoi sp. nov., Holotype, MHNUSC 10065. A, pereopod 5. Allotype, MHNUSC 10066. B, pereopod 5. Scales: 0.1 mm.
FIGURE 3 in Two new species of the Suborder Senticaudata (Crustacea: Amphipoda) from the upper continental slope off Galicia (NW Iberian Peninsula)
FIGURE 3. Pareurystheus vitucoi sp. nov., Holotype, MHNUSC 10065. A, gnathopod 1; B, gnathopod 1, setae along palmar margin; C, gnathopod 1, dactylus (detail); D, gnathopod 2; E, pereopod 3; F, pereopod 4. Scales: 0.1 mm.
FIGURE 11 in Two new species of the Suborder Senticaudata (Crustacea: Amphipoda) from the upper continental slope off Galicia (NW Iberian Peninsula)
FIGURE 11. Photis guerrai sp. nov., Holotype, MHNUSC 10068. A, pereopod 6; B, pereopod 6, accessory stout seta on dactylus; C, pereopod 7; D, uropod 1; E, uropod 2; F, uropod 3 and telson; G, telson (dorsal view). Scales: 0.1 mm.
FIGURE 6 in Figure 6 In A New Species Of Noblella (Amphibia: Strabomantidae) From The Western Slopes Of The Andes Of Ecuador
FIGURE 6. Taxonomically relevant characters in Glassfrogs. (A) Transparent pericardium, white hepatic and visceral peritonea (left; Hyalinobatrachium aureoguttatum); white pericardium, translucent hepatic and visceral peritonea (right; Centrolene buckleyi). (B) Absence of humeral spine (top; H. fleischmanni); presence of humeral spine (bottom; Espadarana callistomma).
FIGURE 2 in Figure 6 In A New Species Of Noblella (Amphibia: Strabomantidae) From The Western Slopes Of The Andes Of Ecuador
FIGURE 2. Egg deposition sites in Centrolenidae. Type A: On the anterior part of upper side of leaves (e.g., Centrolene bacatum, photo by JMG). Type B: On the tip of upper side of leaves (e.g., Nymphargus wileyi, photo by JMG). Type C: On the underside of leaves (e.g., Hyalinobatrachium crurifasciatum, photo by C. Barrio-Amorós). Type D: On the margin of under side of leaves (e.g., Teratohyla spinosa, photo by R. Puschendorf). Type E: On rocks (e.g., Sachatamia albomaculata, photo by R. Puschendorf).
FIGURE 1 in Figure 6 In A New Species Of Noblella (Amphibia: Strabomantidae) From The Western Slopes Of The Andes Of Ecuador
FIGURE 1. Synapomorphies of Centrolenidae. (A) Partial (Nymphargus posadae, QCAZ 25090) and complete ventral transparency (Hyalinobatrachium aureoguttatum, QCAZ 32070). (B) Partial (N. wileyi, QCAZ 26029) and complete fusion between tibiale and fibulare (H. munozorum, KU 155497). (C) Medial process on Metacarpal III and intercalary element (Teratohyla spinosa, KU 32935). The presence of T or Y-shaped terminal phalanges is a synapomorphy of Allocentroleniae (Allophrynidae + Centrolenidae). Photos in (A) by M. Bustamante.
FIGURE 13 in Figure 6 In A New Species Of Noblella (Amphibia: Strabomantidae) From The Western Slopes Of The Andes Of Ecuador
FIGURE 13. Crista medialis, crista ventralis, and humeral spines in centrolenid adult males. Centrolene bacatum, KU 170116; C. geckoideum, ICN 5598; C. pipilatum, KU 143286; Cochranella euknemos, KU 77534; Cochranella litoralis, QCAZ 27693; Teratohyla spinosa, KU 32935; Nymphargus griffithsi, KU 288992 188148; N. cochranae, KU 123218; N. megacheirus, KU 143271; N. pluvialis, KU 173488; Sachatamia albomaculata, KU 65185; S. ilex, LACM 72910; Chimerella mariaelenae, QCAZ 21252; Vitreorana antisthenesi, KU 167775; V. eurygnatha, KU 93225; V. gorzulae, UTA 52240; Celsiella revocata, MHNLS 13352; Hyalinobatrachium bergeri, KU 162256; H. valerioi, KU 178091; Ikakogi tayrona, KU 169754. Note that the crista medialis of I. tayrona is almost as long as the humerus.
FIGURE 9 in Figure 6 In A New Species Of Noblella (Amphibia: Strabomantidae) From The Western Slopes Of The Andes Of Ecuador
FIGURE 9. Use of unranked taxa as a mean to increase name stability. (A) Accepted relationships and taxonomy until 2006. (B) Proposal by Frost et al. (2006); note the change in names and species contents. (C) Recognition of Allocentroleniae as an unranked name; note that clade names and clade contents are as those used before 2006, and the Centrolenidae + Allophrynidae clade is recognized.
FIGURE 5 in Figure 6 In A New Species Of Noblella (Amphibia: Strabomantidae) From The Western Slopes Of The Andes Of Ecuador
FIGURE 5. Previous taxonomic hypotheses for centrolenid frogs. (A) Taxonomy sensu Taylor (1949, 1951). (B) Taxonomy sensu Savage (1967). (C) Generic arrangement by Ruiz-Carranza and Lynch (1991a). (D) Hypothesis of relationships sensu Ruiz-Carranza and Lynch (1991a), as modified by Bolívar et al. (1999). (E) Hypothesis of relationships sensu Ruiz-Carranza and Lynch (1991a, 1995a, 1998). (F) Hypothesis of relationships sensu Ruiz-Carranza and Lynch (1991a), as modified by Savage (2002). (G) Hypothesis of relationships sensu Ruiz-Carranza and Lynch (1991a, 1995a, 1998), as modified by Duellman and Señaris (2003), Señaris and Ayarzagüena (2005), and Cisneros- Heredia and McDiarmid (2006a, b). (H) Hypothesis of relationships sensu Ruiz-Carranza and Lynch (1991a, 1995a, 1998), as modified by Cisneros-Heredia and McDiarmid (2007a); asterisks denote uncertain placement of eurygnathum, parvulum, and uranoscopum. Figure from Guayasamin et al. (2008a).
FIGURE 15 in Figure 6 In A New Species Of Noblella (Amphibia: Strabomantidae) From The Western Slopes Of The Andes Of Ecuador
FIGURE 15. Differences in hand webbing (Fingers III and IV) between Nymphargus and genera within Cochranellini. The following species are illustrated: Nymphargus posadae, QCAZ 25090; Espadarana prosoblepon, KU 132462; Chimerella mariaelenae, QCAZ 22363; Cochranella resplendens, KU 118053; Rulyrana flavopunctata, KU 121046; Sachatamia albomaculata, QCAZ 4325; Teratohyla spinosa, KU 164668; Vitreorana ametarsia, ICN 50847.
FIGURE 12 in Figure 6 In A New Species Of Noblella (Amphibia: Strabomantidae) From The Western Slopes Of The Andes Of Ecuador
FIGURE 12. Derived fighting behavior between males of Espadarana andina. The illustrated character state is considered to be a synapomorphy of Centroleninae. Wrestling on leaves and amplexus-like fighting behavior (not shown) are hypothesized to be present in all species of Hyalinobatrachinae.
FIGURE 11 in Figure 6 In A New Species Of Noblella (Amphibia: Strabomantidae) From The Western Slopes Of The Andes Of Ecuador
FIGURE 11. Size of prepollex relative to Metacarpal I (dorsal view). Note that in Hyalinobatrachium the prepollex has a length ≤ 50% of the length of Metacarpal I. Also, note relative length of Fingers I and II. Species illustrated: Centrolene hesperium, FMNH 232502; Teratohyla spinosa, KU 32935; Hyalinobatrachium munozorum, KU 155497; Ikakogi tayrona, KU 169754.
FIGURE 8 in Figure 6 In A New Species Of Noblella (Amphibia: Strabomantidae) From The Western Slopes Of The Andes Of Ecuador
FIGURE 8. Maximum likelihood phylogeny of Glassfrogs inferred from mitochondrial genes (12S, 16S, ND1, 2842 aligned base-pairs; ln L = –74810.404) and nuclear genes (c-myc exon 2, RAG1, POMC, 1520 aligned base-pairs; ln L = –17244.283) using RAxML (Stamatakis 2006). Circles indicate significant support values for clades recovered by Bayesian (BA, posterior probability ≥ 0.95), maximum likelihood (ML, bootstrap ≥ 70%), and maximum parsimony (MP, bootstrap ≥ 70%) analyses. Monotypic genera (Chimerella and Ikakogy) are shown in bold. Figure modified from Guayasamin et al. (2008a).
FIGURE 7 in Figure 6 In A New Species Of Noblella (Amphibia: Strabomantidae) From The Western Slopes Of The Andes Of Ecuador
FIGURE 7. Common nuptial pad morphologies in Centrolenidae (sensu Cisneros-Heredia & McDiarmid 2007). Arrow indicates glandular cluster typical in species of Hyalinobatrachium, as defined herein. Note that Morphology IV has only been reported in Cochranella litoralis, and differs from the description provided by Cisneros-Heredia & McDiarmid (2007). Species illustrated: Type I, Cochranella posadae, QCAZ 26023; Type II, Centrolene lynchi, MCZ 97846 (figure modified from Flores 1985); Type III, Nymphargus armatus, UVC 9400 (figure modified from Lynch & Ruiz-Carranza 1996); Type IV, Cochranella litoralis, ICN 13821; Type V, Hyalinobatrachium aureoguttatum, QCAZ 27429. Morphology VI (glands distributed on the body) is not illustrated.
Fig. 2 in Microhabitat Preference of Great Plains Giant Tiger Beetle Larvae,Amblycheila cylindriformisSay (Coleoptera: Carabidae: Cicindelinae), is Influenced by Soil Slope Profile
Fig. 2. Three third-stage larval burrows of the Great Plains giant tiger beetle, Wallace Co., Kansas.
Fig. 4 in Microhabitat Preference of Great Plains Giant Tiger Beetle Larvae,Amblycheila cylindriformisSay (Coleoptera: Carabidae: Cicindelinae), is Influenced by Soil Slope Profile
Fig. 4. Frequency distribution of Great Plains giant tiger beetle larval burrows (n = 132) among a range of degrees of slope across a soil profile inclination, Wallace Co., Kansas, 1987.
Fig. 3 in Microhabitat Preference of Great Plains Giant Tiger Beetle Larvae,Amblycheila cylindriformisSay (Coleoptera: Carabidae: Cicindelinae), is Influenced by Soil Slope Profile
Fig. 3. Habitat of the Great Plains giant tiger beetle in the western short grasslands, Wallace Co., Kansas, 2009. Height of the exposed soil profile in the foreground is approximately 3 m.
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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.