Find research datasets worth reusing

opennotspecifiedDec 2009View details →

FIGURES 23–26. Figs. 23 and 24 in Revisiting the Brazilian fauna of masarine wasps: new records, an illustrated key to species and a description of the male of Trimeria rubra Hermes & Melo (Hymenoptera: Vespidae: Masarinae)

FIGURES 23–26. Figs. 23 and 24. Trimeria bequaerti, female: 23, head in lateral view; 24, mesosoma in lateral view. Figs. 25 and 26. T. howardi, female: 25, head in lateral view; 26, mesosoma in lateral view. Scale bars = 1 mm.

opennotspecifiedDec 2009View details →

FIGURES 37–42. Fig. 37 in Revisiting the Brazilian fauna of masarine wasps: new records, an illustrated key to species and a description of the male of Trimeria rubra Hermes & Melo (Hymenoptera: Vespidae: Masarinae)

FIGURES 37–42. Fig. 37. Trimeria howardi, female scutellum in dorsal view. Fig. 38. T. rubra, female scutellum in dorsal view. Figs. 39 and 41. T. americana: 39, female scutellum in dorsal view; 41, male scutellum in lateral view. Figs. 40 and 42. T. neotropica: 40, female scutellum in dorsal view; 42, male scutellum in lateral view. Scale bar for figs. 37–40 = 1 mm; figs. 41 and 42 = 0,5 mm.

opennotspecifiedDec 2013View details →

FIGURE 3. Fabia insularis Melo, 1971, A–C, E in Remarks on the sexual dimorphism and taxonomy of Fabia Dana, 1851 (Crustacea, Brachyura, Pinnotheridae)

FIGURE 3. Fabia insularis Melo, 1971, A–C, E, from Rio Grande do Sul (FURG-1235), D, from Rio de Janeiro, Brazil (MZUSP 3688), sub-adult female; A, dorsal view; B, ventral view; C, ventral view of thoracic sterna; D, P3, longer left and shorter right; E, left gonopod. Scale A–C = 2mm; D = 1.7 mm; E = 1 mm. (A–C, E from Martins & D'Incao, 1998; D, from Melo 1971).

Fig. 3 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)

Fig. 3. Maximum likelihood tkee based on COI sequences of analyzed specimens of Meloe %Eurymeloe). Only suppokted values of nodes %UFBootstkap, UFB ≥ 95 and SH-aLRT ≥ 80%) ake kepokted %SH-LRT/UFB).;ashes %–) indicate non-suppokted values. Coloked vektical baks on the kight shown species delimitation analysis kesults %ASAP, ad hoc, and mPTP) %https://inkscape.okg/it/).

Fig. 8 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)

Fig. 8. Thkee diffekent pattekns of biogeogkaphic discunction and theik kelative moleculak dating %with the 95%HP; in squake bkackets) obsekved in %A) M. orobates and M. digiuliorum; %B) M. apenninicus and M. rugosus ′ M. cfk. rugosus; and %C) M. b. baudii and M. b. glazunovi %https://inkscape.okg/it/).

Fig. 6 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)

Fig. 6. Male habitus, doksal view, of %A) M. b. baudii, %B) M. b. glazunovi, and %C) M. scabriusculus. Scale bak 1 mm %https://inkscape.okg/it/).

Fig. 2 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)

Fig. 2. Multilocus %16S, COI, CA;, and 28S) phylogenetic tkee of Meloe %Eurymeloe). Topology cokkesponds to the maximum likelihood %ML) tkee. Clades ake indicated with letteks %a–t). Only suppokted values of nodes %UFBootstkap, UFB ≥ 95 ands SH-aLRT ≥ 80%; postekiok pkobability, PP ≥ 0.95) ake kepokted %SH-LRT/ UFB/PP).;ashes %–) indicate non-suppokted values. Clades of species that weke not the main focus of the study ake collapsed. Fok a non-collapsed veksion of the tkee, see Supplementaky Fig. S4 %https://inkscape.okg/it/).

Fig. 7 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)

Fig. 7.;oksal and latekal views of male genitalia: %A–C) M. b. baudii, %;–F) M. b. glazunovi, and %G–I) M. scabriusculus. Scale bak 0.5 mm %https://inkscape.okg/it/).

Fig. 5 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)

Fig. 5.;oksal and latekal views of male genitalia: %A–C) M. orobates %fkom: Sánchez-Vialas et al. 2022), %;–F) M. digiuliorum sp. n., %G–I) M. apenninicus, %J–L) M. rugosus. Scale bak 0.5 mm %https://inkscape.okg/it/).

Fig. 1 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)

Fig. 1. Italian endemic taxa of Meloe (Eurymeloe) %uppek kow) and theik type localities %lowek kow): %A) M. digiuliorium sp. nov.; %B) M. apenninicus; %C) M. b. baudii; %;) Abkuzzo, L'Aquila pkov., Ovindoli, Fkeddo Mt. westekn slope; %E) Sicily, Messina pkov., Cesakò, nk. Poktella di femmina mokta; %F) Abkuzzo, L'Aquila pkov., Cekchio, basal westekn slope of the Sikente Mt. Photo's ckedits: A, L. Spagoni; B–E, A. Ricceki; F, M.A. Bologna %https://inkscape.okg/it/).

Fig. 4 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)

Fig. 4. Male habitus, doksal view, of %A) M. orobates %fkom: Sánchez-Vialas et al. 2022), %B) M. digiuliorum sp. n., %C) M. apenninicus, %;) M. rugosus. Scale bak 1 mm %https://inkscape.okg/it/).

opencc-by-4.0Jun 2016View details →

Supplementary material 1 from: Monteiro M, Reino L, Melo M, Beja P, Bastos-Silveira C, Ramos M, Rodrigues D, Neves IQ, Consciência S, Figueira R (2016) The collection of birds from São Tomé and Príncipe at the Instituto de Investigação Científica Tropical of the University of Lisbon (Portugal). ZooKeys 600: 155-167. https://doi.org/10.3897/zookeys.600.7899

Species lists referred in Tables 1 and 2 showing correspondence between scientific and common names between IOC and BirdLife Internaction/IUCN nomenclatures : Explanation note: Nomenclatural differences between International Ornithological Council and BirdLife International/IUCN lists (2016) for endemic species and endemic subspecies of São Tomé and Príncipe.

Figure 3 in Nesting biology and behavioural ecology of the solitary bee Monoeca haemorrhoidalis (Smith) and its cleptoparasite Protosiris gigas Melo (Hymenoptera: Apidae: Tapinotaspidini; Osirini)

Figure 3. Percentage of pollen grains found in samples collected from females and males of Monoeca haemorrhoidalis.

Figure 2 in Nesting biology and behavioural ecology of the solitary bee Monoeca haemorrhoidalis (Smith) and its cleptoparasite Protosiris gigas Melo (Hymenoptera: Apidae: Tapinotaspidini; Osirini)

Figure 2. (A) Female Monoeca haemorrhoidalis building a tumulus around the nest entrance; (B) female entering its nest with a mixture of pollen and oil on its scopae; (C) a "nesting female" inside its nest and an "invader female" in the surroundings; (D) an "invader female" entering the nest after the "nesting female" left; (E) a female with exuvial remains entering a nest when the "nesting female" was away; (F) males trying to copulate with a newly emerged female; (G) a cluster of males trying to copulate with a female; (H) M. haemorrhoidalis copulation; (I) a copulation attempt between a M. haemorrhoidalis male and a Protosiris gigas male; (J) a female M. haemorrhoidalis on flowers of Niedenzuella acutifolia; (K) a female with a pollinarium of Grandiphyllum divaricatum on its front; (L) a male M. haemorrhoidalis on flowers of Coccocypselum condalia.

Figure 4 in Nesting biology and behavioural ecology of the solitary bee Monoeca haemorrhoidalis (Smith) and its cleptoparasite Protosiris gigas Melo (Hymenoptera: Apidae: Tapinotaspidini; Osirini)

Figure 4. (A) Female Heterostylum maculipennis hovering over a nest of M. haemorrhoidalis; (B) an individual of Tetraolytta gerardi eating pollen on flowers of Niedenzuella acutifolia; (C) an individual of Pyrogaster moestus preying on a male Monoeca haemorrhoidalis; (D) a female Pseudomethoca melanocephala excavating a closed nest of M. haemorrhoidalis; (E) Protosiris gigas copulation; (F) a female P. gigas leaving a nest after parasitizing it; (G) a female P. gigas removing earth pellets from a nest entrance; (H) a specimen P. gigas visiting flowers of Coccocypselum condalia; (I) a female P. gigas perching on leaves of Coccocypselum condalia.

Figure 1 in Nesting biology and behavioural ecology of the solitary bee Monoeca haemorrhoidalis (Smith) and its cleptoparasite Protosiris gigas Melo (Hymenoptera: Apidae: Tapinotaspidini; Osirini)

Figure 1. Monthly variation in relative air humidity, annual rainfall and temperature, measured from March 2005 to February 2007 in the Meteorological Station of Pinhais, southern Brazil.

opencc-zeroOct 2022View details →

dryad32/100

Data for: Metagenomics show high spatiotemporal virus diversity and ecological compartmentalisation: virus infections of melon, Cucumis melo, crops and adjacent wild communities

Emergence of viral diseases results from novel transmission dynamics between wild and crop plant communities. The bias of studies towards pathogenic viruses of crops has distracted from knowledge of non-antagonistic symbioses in wild plants. Here we implemented a high throughput approach to compare the viromes of melon (Cucumis melo), and wild plants of crop (Crop) and adjacent boundaries (Edge). Each of the 41-plant species examined was infected by at least one virus. The interactions of 104 virus operational taxonomic units (OTUs) with these hosts occurred largely within ecological compartments of either Crop or Edge, Edge having traits of a reservoir community. The positive correlation of virus and plant richness at each site, the tendency for increased specialist host use through seasons, and specialist host use by OTUs observed only in Melon, characterised local-scale patterns of infection. In this study of systematically sampled viromes of crop and adjacent wild communities most hosts showed no disease symptoms, suggesting non-antagonistic symbioses are common. The coexistence of viruses within species-rich ecological compartments of agro-systems might promote the evolution of a diversity of virus strategies for survival and transmission. These communities, including those suspected as reservoirs, are subject to sporadic changes in assemblages, and so too are the conditions that favour the emergence of disease.

opencc-zeroMay 2023View details →

Supplementary material 2 from: Souza CS, Mattox GMT, Vita G, Ochoa LE, Melo BF, Oliveira C (2023) Molecular species delimitation and description of a new species of Phenacogaster (Teleostei, Characidae) from the southern Amazon basin. ZooKeys 1164: 1-21. https://doi.org/10.3897/zookeys.1164.102436

Best-score results of Assemble Species by Automatic Partitioning (ASAP) delimitation of species of Phenacogaster