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Figure 3 in Calling phenology of anurans in a tropical rainforest in South Mexico: testing predictive models
Figure 3. Rose-diagram of anuran assemblage relative calling intensity. The length and colour (light = low, dark = high) of the bars from the centre indicate the intensity of vocalisation for the temporal section. A Rayleigh z test for unimodal orientation was performed, resulting in significant evidence of non-uniform distribution of vocalisations across the year (P = 0.0303).
Figure 1 in Calling phenology of anurans in a tropical rainforest in South Mexico: testing predictive models
Figure 1. Study site location and land use, natural protected area of Nahá, Ocosingo, Chiapas, México.
Figure 2. a in Calling phenology of anurans in a tropical rainforest in South Mexico: testing predictive models
Figure 2. a) Calling anuran species recorded at temporary sections (7 months). The horizontal axis corresponds to temporary sections and the vertical to species. b) Average temperature T � (° C) (continuous line) and accumulated rainfall Ra (dashed line) by temporary section (32 in 7 months). Both graphs share the horizontal axis, where breaks indicate recording gaps, and the numbers are the days of the months covered.
FIGURE 3 in Mikrischyrum musicum, a new katydid species from montane rainforest in southern Ecuador with complex pure-tone calling song (Orthoptera: Tettigoniidae: Pseudophyllinae: Platyphyllini)
FIGURE 3. Calling song of Mikrischyrum musicum: A. oscillogram of complete pulse train (20°C, holotype, recording cbt-019s04r03), B. first group of four pulses of A in higher resolution (and photo of holotype staged at day), C. linear spectrogram, D. zero-crossing analysis of one pulse, E. field recording together with two other katydid species, the arrow points at first pulse of the M. musicum sequence (13°C, cbt019x01r01, 14 August 1998), F. spectrogram taken from this recording with the distinctive peak of the new species, G. spectrogram of an unknown katydid species, showing the M. musicum peak too, H. spectrogram of an undescribed species of Aemasia (also Platyphyllini, song known from collected males, Braun 2002: Figs. 6.2.4, 6.3.3), based on the second call right after the end of the M. musicum sequence.
FIGURE 2 in Mikrischyrum musicum, a new katydid species from montane rainforest in southern Ecuador with complex pure-tone calling song (Orthoptera: Tettigoniidae: Pseudophyllinae: Platyphyllini)
FIGURE 2. Mikrischyrum musicum: A. male habitus, B. male subgenital plate in ventral view, C. male left cercus in dorsal view, D. male pronotum in dorsal view, E. ovipositor of female (pencil drawings done in October 2003, after holotype and a paratype).
FIGURE 1 in Mikrischyrum musicum, a new katydid species from montane rainforest in southern Ecuador with complex pure-tone calling song (Orthoptera: Tettigoniidae: Pseudophyllinae: Platyphyllini)
FIGURE 1. Mikrischyrum musicum: A. male holotype in dorsal view, B. same in lateral view, C. female paratype to same scale as B (specimen cbt019s01).
Distribution. Most of Africa S of the Sahara Desert, except in lowland tropical rainforests. Spotted Hyenas have been extirpated from many areas of southern Africa. in Hyaenidae
Distribution. Most of Africa S of the Sahara Desert, except in lowland tropical rainforests. Spotted Hyenas have been extirpated from many areas of southern Africa.
Data from: Monadelpha (Euphorbiaceae, Plukenetieae), a new genus of Tragiinae from the Amazon rainforest of Venezuela and Brazil
<p class="MsoPlainText"><span><span><span><span><span><span><span><span><span><span><span><i>Monadelpha </i>L.J.Gillespie & Card.-McTeag., <b>gen. nov</b>.<i>,</i> is described as a new member of Euphorbiaceae tribe Plukenetieae subtribe Tragiinae, to accommodate <i>Tragia guayanensis</i>, a species known from western Amazonas, Venezuela and, newly reported here, from Amazonas, Brazil. The genus is unique in the subtribe for having 5-colpate pollen and staminate flowers with filaments entirely connate into an elongate, cylindrical staminal column terminated by a tight cluster of anthers. Phylogenetic analyses based on nuclear rDNA ITS and sampling 156 accessions across the diversity of Tragiinae (all 12 genera and 77 of ~195 species) also support <i>Monadelpha</i> as a distinct lineage that is separate from <i>Tragia</i>. A revised key to the genera of Tragiinae in South America and Central America is provided.</span></span></span></span></span></span></span></span></span></span></span></p>
Distribution. Sub-Saharan Africa from Mauritania and Senegal in the W to Sudan, Ethiopia and Djibouti in the E and S to South Africa. Absent from W & C African rainforests. in Mustelidae
Distribution. Sub-Saharan Africa from Mauritania and Senegal in the W to Sudan, Ethiopia and Djibouti in the E and S to South Africa. Absent from W & C African rainforests.
Distribution. Continuous distribution in W & C African rainforest blocks also including Dahomey Gap and Bioko I; reaches as easternand southernmost boundaries SW Kenya, extreme W Tanzania, NW Zambia, and N Angola. in Manidae
Distribution. Continuous distribution in W & C African rainforest blocks also including Dahomey Gap and Bioko I; reaches as easternand southernmost boundaries SW Kenya, extreme W Tanzania, NW Zambia, and N Angola.
Distribution. Discontinuously distributed, from Senegal to Ghana in W Africa, and in the C African rainforest block from Cameroon to Uganda, W Kenya, and W Tanzania, and south to extreme NW Angola, also present in Bioko I. Sightings from Dahomey Gap and S Nigeria remain unconfirmed. in Manidae
Distribution. Discontinuously distributed, from Senegal to Ghana in W Africa, and in the C African rainforest block from Cameroon to Uganda, W Kenya, and W Tanzania, and south to extreme NW Angola, also present in Bioko I. Sightings from Dahomey Gap and S Nigeria remain unconfirmed.
Distribution. Two disjunct areas across the lowland rainforest belt of W Africa (Guinea, Sierra Leone, Liberia, Ivory Coast, Ghana, Togo & Benin) and C Africa through the Congo Basin (Cameroon, Gabon, Republic of the Congo, DR Congo, Central African Republic & extreme SW Sudan), and five very small disjunct populations in mountainous areas in C Kenya. in Bovidae
Distribution. Two disjunct areas across the lowland rainforest belt of W Africa (Guinea, Sierra Leone, Liberia, Ivory Coast, Ghana, Togo & Benin) and C Africa through the Congo Basin (Cameroon, Gabon, Republic of the Congo, DR Congo, Central African Republic & extreme SW Sudan), and five very small disjunct populations in mountainous areas in C Kenya.
Distribution. Main tropical rainforest belt from Senegal and Guinea Bissau to NW Uganda and E DR Congo, reaching as S boundary N Angola (Cabinda); no recent records from Gambia or Chad and its presence is uncertain in S Sudan and SW Ethiopia. As a species that may range widely through gallery forests, it may also occur in adjacent countries. in Suidae
Distribution. Main tropical rainforest belt from Senegal and Guinea Bissau to NW Uganda and E DR Congo, reaching as S boundary N Angola (Cabinda); no recent records from Gambia or Chad and its presence is uncertain in S Sudan and SW Ethiopia. As a species that may range widely through gallery forests, it may also occur in adjacent countries.
FIGURE 3 in New species of Tintiyakus Cadena-Castañeda (Orthoptera: Anostostomatidae Lutosinae) from the Brazilian Mountain Amazon Rainforest
FIGURE 3. Tintiyakus lari sp. nov., paratype female. A: habitus, lateral view; B: habitus, dorsal view; C: head, frontal view; D–F: Terminalia in dorsal, ventral and lateral view respectively. Abbreviations: Cer: cerci; Pl: subgenital plate; Ovp: ovipositor.
FIGURE 2 in New species of Tintiyakus Cadena-Castañeda (Orthoptera: Anostostomatidae Lutosinae) from the Brazilian Mountain Amazon Rainforest
FIGURE 2. Tintiyakus lari sp. nov., holotype male. A: habitus, lateral view; B: habitus, dorsal view; C: head, frontal view; D–E: Terminalia in ventral and dorsal view respectively. Abbreviations: Cer: cerci; Sty: styli; Pl: subgenital plate.
Figure 2 in Flowers are essential to maintain high beetle diversity (Coleoptera) in a Neotropical rainforest canopy
Figure 2. Small white flowers of the generalist pollination syndrome in a lowland rainforest canopy, Venezuela. (a) Flowers of Hymenopus heteromorphus (Benth.) Sothers and Prance var. heteromorphus (Chrysobalanaceae), March 1999. (b) Macraspis festiva Burmeister (Scarabaeidae) mating on flowering Matayba guianensis Aubl. (Sapindaceae), September 1997.
Figure 3 in Flowers are essential to maintain high beetle diversity (Coleoptera) in a Neotropical rainforest canopy
Figure 3. Diversity of Chrysomelidae beetles visiting flowers of Hymenopus heteromorphus (Benth.) Sothers and Prance var. heteromorphus (Chrysobalanaceae), March 1999. (a) Colaspis Fabricius (Eumolpinae). (b) Coroicona danieli Bechyné (Alticini). (c) Griburius auricapillus (Suffrian) (Cryptocephalinae). (d) Hecataeus Jacoby (Galerucinae).
Figure 1 in Flowers are essential to maintain high beetle diversity (Coleoptera) in a Neotropical rainforest canopy
Figure 1. Specialised flower-visiting beetles often have mouth parts adapted to feed effectively on pollen and nectar. Adaptations can include prolonged mouthparts and dense brushes on the maxillae as in (a) Mecometopus Thomson sp. (Cerambycidae), or enlarged and securiform maxillary palpomeres as in (b) Mordellistena Costa sp. 3 (Mordellidae).
FIGURE 10 in A new species of planthopper from Costa Rica in the genus Oropuna from palms in lowland tropical rainforest
FIGURE 10. Holotype of Oropuna fusca; (A) head frontal view, (B) lateral view, (C) dorsal view and (D) ventral view of male terminalia (Harvard University, Cambridge MA; ©President and Fellows of Harvard College, used by permission).
FIGURE 8 in A new species of planthopper from Costa Rica in the genus Oropuna from palms in lowland tropical rainforest
FIGURE 8. Holotype of Phaciocephalus orba (now Oropuna orba); (A) frontal view of head, (B) dorsal view of body, (C) lateral view of body, (D) female pregenital plate, and (E) labels.
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.