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444 results for “Mesoamerica”
FIGURE 4 in The largest blindsnake in Mesoamerica: a new species of Typhlops (Squamata: Typhlopidae) from an isolated karstic mountain in Honduras
FIGURE 4. Montaña de Santa Bárbara, Depto. Santa Bárbara, Honduras, seen from the community of El Cedral, 1580 m elevation, in the vicinity of the type locality of Typhlops tycherus. The highest part of the mountain is>2700 m elevation. Photographed 28 January 2008 by JHT.
FIGURE 2 in The largest blindsnake in Mesoamerica: a new species of Typhlops (Squamata: Typhlopidae) from an isolated karstic mountain in Honduras
FIGURE 2. Scalation of the head of the holotype of Typhlops tycherus. A = dorsal view, B = lateral view.
FIGURE 1 in The largest blindsnake in Mesoamerica: a new species of Typhlops (Squamata: Typhlopidae) from an isolated karstic mountain in Honduras
FIGURE 1. Distribution of Typhlops in eastern Nuclear Central America, shaded areas indicate>1000 m elevation. Triangle = T. tycherus n. sp., diamonds = T. costaricensis, squares = T. stadelmani.
FIGURE 1 in A new combination in Nasa (Loasaceae) from Mesoamerica
FIGURE 1. Comparison between Nasa rudis (A-C), Nasa dyeri subsp. australis (D), Nasa dyeri subsp. dyeri (E-F) and Nasa triphylla subsp. papaverifolia (G-I). (A) Stem, notice the dark green callus near the petiole base and the abundant stinging trichomes (San José, Costa Rica; photo by Rafael Acuña). (B) Mature flower, notice the two long, filiform, apical petal appendages (San José, Costa Rica; photo by Elena Farries). (C) Capsule and distal stem, notice the stem is sparsely verrucose (San José, Costa Rica; photo by Jacob Rehage). (D) Stem, notice the partially suberized callus neat the petiole base and the scarcity of stinging trichomes (cultivated material; photo by Maximilian Weigend). (E) Mature flower, notice the two long, filiform, apical petal appendages (Zamora-Chinchipe, Ecuador; photo by Ruth Ripley). (F) Capsule and distal stem, the latter densely verrucose (Zamora-Chinchipe, Ecuador; photo by Rafael Acuña). (G) Stem, notice the lack of a conspicuous raised or suberized callus (Tungurahua, Ecuador; photo by Rafael Acuña), (H) Mature flower, notice the difference in the nectar scale shape and color pattern, as well as the apical petal appendages, that are much shorter than in the other taxa (Antioquia, Colombia; photo by Daniel Mesa). (I) Capsule, the distal stem is mostly non-verrucose (Huila, Colombia; photo by Jorge Peña).
Data from: Ups and downs: genetic differentiation among populations of the Podocarpus (Podocarpaceae) species in Mesoamerica
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Data from: Tree species composition, breeding systems, pollination and dispersal syndromes in three forest successional stages in a tropical dry forest in Mesoamerica
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Data from: Historical reconstruction of climatic and elevation preferences and the evolution of cloud forest-adapted tree ferns in Mesoamerica
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Data from: Interglacial genetic diversification of Moussonia deppeana (Gesneriaceae), a hummingbird-pollinated, cloud forest shrub in northern Mesoamerica
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Data from: A jungle tale: molecular phylogeny and divergence time estimates of the Desmopsis - Stenanona clade (Annonaceae) in Mesoamerica
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Data from: A diversification relay race from Caribbean-Mesoamerica to the Andes: historical biogeography of Xylophanes hawkmoths
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Data from: Phylogeography of Liquidambar styraciflua (Altingiaceae) in Mesoamerica: survivors of a Neogene widespread temperate forest (or cloud forest) in North America?
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Data from: Influence of Pleistocene glacial/interglacial cycles on the genetic structure of the mistletoe cactus Rhipsalis baccifera (Cactaceae) in Mesoamerica
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FIG. 8 in The use of animals in Northern Mesoamerica, between the Classic and the Conquest (200-1521 AD). An attempt at regional synthesis on central Mexico
FIG. 8. — Right mandible of Geomyidae (cf. Cratogeomys sp.) from Mich.31 showing evidences of cooking: burnt marks are located on the most prominent part of the bone, lateral side. Scale bar = 1 cm
FIG. 2 in The use of animals in Northern Mesoamerica, between the Classic and the Conquest (200-1521 AD). An attempt at regional synthesis on central Mexico
FIG. 2. — Graphical representation of NSP, NISP and NTAXA in the different assemblages. Sites where sieving has been done are indicated by (Y).
FIG. 3 in The use of animals in Northern Mesoamerica, between the Classic and the Conquest (200-1521 AD). An attempt at regional synthesis on central Mexico
FIG. 3. — Matrix of the nestedness analysis on taxonomic list per site (black=present; white=absent) showing a high
FIGURE 10 in Haruchlora maesi, a new emerald moth genus and species from Mesoamerica (Lepidoptera, Geometridae, Geometrinae)
FIGURE 10. The collecting site in the Selva Negra estate, Matagalpa, Nicaragua.
FIGURE 9 in Haruchlora maesi, a new emerald moth genus and species from Mesoamerica (Lepidoptera, Geometridae, Geometrinae)
FIGURE 9. Haruchlora maesi, sp. nov., male specimen on screen before it has been trapped.
FIGURE 1 in Review of the Ambrysus stali La Rivers species complex (Heteroptera: Nepomorpha: Naucoridae) with the description of a new species from Mesoamerica
FIGURE 1. Distribution of species in the Ambrysus stali species complex.
FIGURE 5 in A new species of Oiovelia (Heteroptera: Gerromorpha: Veliidae) from Mesoamerica, with an identification key to the genus
FIGURE 5. Geographical records of all species of Oiovelia.
Figure 1 in Ecological niche differentiation among Aztec fruit-eating bat subspecies (Chiroptera: Phyllostomidae) in Mesoamerica
Figure 1. Ocurrence records for the three subspecies of Artibeus aztecus: Artibeus aztecus aztecus (yellow),Artibeus aztecus minor (blue) and Artibeus aztecus major (light red).
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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