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687 results for “Central Mexico”
Figure 10 in A third species of Haroldiellus Gordon and Skelley, 2007 from Mexico and Central America (Coleoptera: Scarabaeidae: Aphodiinae: Aphodiini)
Figure 10. Distribution map of Haroldiellus lansbergei (blue) as currently known from specimen labels and literature records. Chiapas, Mexico is striped because it is a literature record that may represent the new species H. woodruffi described herein. Map made with SimpleMappr (Shorthouse 2010).
FIGURE 1 in Trophic strategies of the invasive Twospot livebearer (Pseudoxiphophorus bimaculatus, Teleostei: Poeciliidae) in a gradient of environmental quality in central Mexico
FIGURE 1 | Geographic location of study area and sampling sites located in the Lerma-Chapala River basin and Pánuco River basin in central Mexico. XOT = El Xote; CHI = El Charco del Ingenio; GAL = Los Galvanes; PRC = Presa del Carmen; PVA = Paso de Vaqueros; OAS = Oasis; EXT = Extoraz; BUC = Bucareli.
FIGURE 2 in Trophic strategies of the invasive Twospot livebearer (Pseudoxiphophorus bimaculatus, Teleostei: Poeciliidae) in a gradient of environmental quality in central Mexico
FIGURE 2 | Physicochemical parameters of water in each study site in central Mexico: temperature (°C), TDS= Total dissolved solids (g/L) and DO= Dissolved oxygen (mg/L). XOT = El Xote; CHI = El Charco del Ingenio; GAL = Los Galvanes; PRC = Presa del Carmen; PVA = Paso de Vaqueros; OAS = Oasis; EXT = Extoraz; BUC = Bucareli.
Fig. 9 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 9. Population fluctuation of Thrips tabaci in the onion crops at Axochiapan, Morelos, Mexico, 2010–2011. Sufficient thermal units (180 degree days) occurred to support 1 life cycle of T. tabaci from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.
Fig. 6 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 6. Population fluctuation of Frankliniella occidentalis related with tomato crops at Tlayacapan and Atlatlahucan, Morelos, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.
Fig. 2 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 2. Population fluctuation of Frankliniella occidentalis in the cucumber crops at Tlayacapan, Morelos, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.
Fig. 7 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 7. Population fluctuation of Frankliniella occidentalis in the tomatillo crops at Tlayacapan, Morelos, and Tepeojuma, Puebla, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.
Fig. 4 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 4. Population fluctuation of Frankliniella occidentalis in the zucchini crops at Tlayacapan, Tepalcingo and Atlatlahucan, Morelos, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st red vertical arrow and between consecutive red arrows.
Fig. 5 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 5. Population fluctuation of Frankliniella occidentalis in the pepper crops at Izucar de Matamoros and Tepeojuma, Puebla, and Tlayacapan, Morelos, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.
Fig. 1 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 1. Population fluctuation of Frankliniella occidentalis in the cucumber crops at Atlatlahucan and Tepalcingo, Morelos, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.
Fig. 10 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 10. Population fluctuation of Thrips tabaci in the onion crops at Tilapa and Tepeojuma, Puebla, Mexico, 2010–2011. Sufficient thermal units (180 degree days) occurred to support 1 life cycle of T. tabaci from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.
Figures 3–6 in Andrena nahua, a new bee species from central Mexico (Hymenoptera: Andrenidae: Andreninae)
Figures 3–6. Andrena nahua, new species, male terminalia. 3. Sternum 7. 4. Sternum 8. 5. Genital capsule, lateral view. 6. Genital capsule, dorsal view.
Figures 1–2. Andrena nahua, new species. 1 in Andrena nahua, a new bee species from central Mexico (Hymenoptera: Andrenidae: Andreninae)
Figures 1–2. Andrena nahua, new species. 1. Lateral view, holotype, scale bar = 1.0 mm. 2. Facial frontal view, holotype, scale bar = 0.5 mm.
Fig. 29 in A review of the cleptoparasitic bee genus Epeolus Latreille, 1802 (Hymenoptera: Apidae) in the Caribbean, Central America and Mexico
Fig. 29. Antenna (basal portion) of female. A. E. minimus (Robertson, 1902), in which F2 is noticeably longer than wide. B. E. asperatus Cockerell, 1910, in which F2 is not noticeably longer than wide. Scale bars = 0.5 mm.
Fig. 27 in A review of the cleptoparasitic bee genus Epeolus Latreille, 1802 (Hymenoptera: Apidae) in the Caribbean, Central America and Mexico
Fig. 27. Head of female, lateral view. A. E. luteipennis Friese, 1916, in which the frontal keel lacks a tooth-like process. B. E. odyneroides sp. nov., holotype (KUNHM SM0253729), in which the frontal keel has a small tooth-like process (blue arrow). C. E. australis Mitchell, 1962, in which the frontal keel (blue arrow) is strongly raised. D. E. brumleyi Onuferko, 2018, paratype, in which the frontal keel (blue arrow) is weakly protuberant by comparison. Scale bars = 1 mm.
Fig. 26 in A review of the cleptoparasitic bee genus Epeolus Latreille, 1802 (Hymenoptera: Apidae) in the Caribbean, Central America and Mexico
Fig. 26. Epeolus spp., habitus of female, ventral view. A. E. basili Onuferko, 2018, paratype showing antennae, legs, and metasomal sterna with similar reddish-orange coloration. B. E. pusillus Cresson, 1864 showing color contrast between reddish-orange legs and dark brown antennae and metasomal sterna. Scale bars = 3 mm.
Fig. 25 in A review of the cleptoparasitic bee genus Epeolus Latreille, 1802 (Hymenoptera: Apidae) in the Caribbean, Central America and Mexico
Fig. 25. Metasoma of female, dorsal view. A. E. novomexicanus Cockerell, 1912. B. E. basili Onuferko, 2018, paratype. Scale bars = 2 mm.
Fig. 28 in A review of the cleptoparasitic bee genus Epeolus Latreille, 1802 (Hymenoptera: Apidae) in the Caribbean, Central America and Mexico
Fig. 28. Pygidial plate of male, dorsal view. A. E. australis Mitchell, 1962 (longer than wide and apically narrowed). B. E. brumleyi Onuferko, 2018, allotype (about as long as wide and broadly rounded apically). Scale bars = 1 mm.
Fig. 24 in A review of the cleptoparasitic bee genus Epeolus Latreille, 1802 (Hymenoptera: Apidae) in the Caribbean, Central America and Mexico
Fig. 24. Mandibles of female A. E. ainsliei Crawford, 1932, each of which lacks a preapical tooth. B. E. rufulus Cockerell, 1941, each of which has a blunt, obtuse preapical (almost submedial) tooth (blue arrow). Scale bars = 0.5 mm.
Fig. 23 in A review of the cleptoparasitic bee genus Epeolus Latreille, 1802 (Hymenoptera: Apidae) in the Caribbean, Central America and Mexico
Fig. 23. Head of male, posterior view. A. E. ainsliei Crawford, 1932, in which the preoccipital ridge joins the hypostomal carina (blue arrow). B. E. rufulus Cockerell, 1941, in which the preoccipital ridge does not join the hypostomal carina (blue arrow). Scale bars = 1 mm.
ScienceDex guides
Understand access before you commit
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.