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376 results for “morphological divergence”
Figure 20. Lectotype Pseudoanthidium eversmanni. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 20. Lectotype Pseudoanthidium eversmanni. A, dorsal view; B, ventral metasoma; C, labels; D, S5 showing sternal combs; E, S7.
Figure 9. Dorsal habitus, females. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 9. Dorsal habitus, females. A, vertex Pseudoanthidium nanum (Kalpetran, Switzerland); B, vertex P. scapulare (Rich, Morocco); C, mesonotum P. nanum (Kalpetran, Switzerland); D, mesonotum P. scapulare (Rich, Morocco); E, metasoma P. nanum (Kalpetran, Switzerland); F, metasoma P. scapulare (Rich, Morocco).
Figure 4. Lectotype, Pseudoanthidium reptans. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 4. Lectotype, Pseudoanthidium reptans. A, face; B, dorsal view; C, labels; D, ventral view; E, apex of metasoma, showing tips of gonostyli.
Figure 3 in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 3. Best-scoring maximum likelihood tree based on analyses of the (A) 75% UCE matrix and (B) 100% UCE matrix. Numbers shown at nodes are maximum likelihood bootstrap values based on 1000 bootstrap replicates in RAxML. Only bootstrap values greater than 50% are shown. Terminals are labelled with a DNA extraction code corresponding to the whole-body extraction performed for UCE sequencing, the DNA extraction code for the same specimen based on single leg extractions performed for barcode sequencing, the species name, collection locality and either as male (m) or female (f). Three specimens (1800, 1802 and 1805) were only sequenced following the UCE protocol and thus have only a UCE extraction code.
Figure 1. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 1. A, nest of Pseudoanthidium stigmaticorne, in a capsule of Tulipa biflora Pall. (Lisya Bay, Crimea). Insert in lower right shows close-up of the same nest. Three males eventually emerged (photo Alexander V. Fateryga); B, Pseudoanthidium stigmaticorne nesting in a stem of Crambe maritima L. (Arabatskaya Strelka sand spit, Crimea). A pin is inserted to mark the nest (photo Sergey P. Ivanov).
Figure 17. Dorsal habitus, females. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 17. Dorsal habitus, females. A, vertex Pseudoanthidium stigmaticorne (Arzens, France); B, vertex P. cribratum (Bukhara, Uzbekistan); C, mesonotum P. stigmaticorne (Arzens, France); D, mesonotum P. cribratum (Bukhara, Uzbekistan); E, metasoma P. stigmaticorne (Arzens, France); F, metasoma P. cribratum (Bukhara, Uzbekistan).
Fig. 2 in Genetic and morphological divergence among Gravel Bank Grasshoppers, Chorthippus pullus (Acrididae), from contrasting environments
Fig. 2 Morphometric distances measured on each individual of C. pullus sampled for the study. For descriptions of numbered traits, see Table 1
Fig. 1 in Genetic and morphological divergence among Gravel Bank Grasshoppers, Chorthippus pullus (Acrididae), from contrasting environments
Fig. 1 Geographic locations and genetic composition of the seven populations of the Gravel Bank Grasshopper included in the study. ISA, LOI and LIN (Bavaria, Germany) are gravel bank populations (solid circles); OPP, GRU (both Brandenburg, Germany), UHY (Saxony, Germany) and MIS (Ukraine) are heath populations (open circles). Population composition shown in pie-diagrams, with slice size proportional to frequency of corresponding allele (coded as in Table 2); the two most frequent alleles (A and C) represented in grey and black, respectively; all others in white. Shaded area is the species' range (Maas et al. 2002; I. Landeck unpublished data)
Fig. 3 Haplotype network derived from the Cpunl-1 in Genetic and morphological divergence among Gravel Bank Grasshoppers, Chorthippus pullus (Acrididae), from contrasting environments
Fig. 3 Haplotype network derived from the Cpunl-1 data set; alleles coded as in Table 2. Pie diameters proportional to number of individuals carrying that particular haplotype (see inlet at bottom right); numbers next to pies or pie slices indicate how many individuals carried that particular haplotype. Shading of pies and slices (see inlet at top right) reflects frac- tions of haplotypes contributed by the different populations; Bavarian and eastern German (Brandenburg + Saxony) populations presented as two pools based on pairwise FST values (no significant differentiation detected within either region). Solid dots represent missing haplotypes; dashed lines indicate that multiple connections among haplotypes are possible but not favored
Figs. 1–5 in A Morphologically Divergent New Genus and Species of Eurygeniinae from California, USA (Coleoptera: Anthicidae)
Figs. 1–5. Rastrogenius ambrosiaphilus, new genus and species, holotype male. 1) Dorsal; 2) Ventral; 3) Lateral;
FIGURE 18 in The glandulous Specklinia: morphological convergence versus phylogenetic divergence
FIGURE 18. Micrographs of the outer surface of the sepals of Specklinia species. A. Specklinia alajuelensis 1 (Pupulin 8470). B. Specklinia alajuelensis 2 (Karremans 6460). C. Specklinia chontalensis (Pupulin 6543). D. Specklinia gersonii (Karremans 6025). E. Specklinia glandulosa (Karremans 6306). F. Specklinia vittariifolia (Chinchilla 1111). Photographs by A.P. Karremans.
FIGURE 8 in The highly divergent New World Artemia species (Branchiopoda, Anostraca), A. franciscana and A. persimilis, show subtle differences in morphological traits involved in mating
FIGURE 8. Frontal knob variants in A. franciscana from El Convento (A, B) and Pichilemu (C–E), central Chile.
FIGURE 7 in The highly divergent New World Artemia species (Branchiopoda, Anostraca), A. franciscana and A. persimilis, show subtle differences in morphological traits involved in mating
FIGURE 7. Interpopulation variation in frontal knob morphology. A. franciscana from Chaxa (A), Los Vilos (B) and Rinconada (C); A. persimilis from Torres del Paine (D) and Cisnes lagoone (E).
Figure 9 in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 9. Bayesian chronogram for the best-fitting dating model (FBD_TK02_TIP). Shaded bars depict uncertainty in estimates of node and tip ages. Main sloth clades are named on the right.
A conserved transcriptional regulator governs fungal morphology in widely diverged species [expression data]
GEO Series GSE32550. Saccharomyces cerevisiae. 8 samples. Type: Expression profiling by array.
FIGURE 1 in The highly divergent New World Artemia species (Branchiopoda, Anostraca), A. franciscana and A. persimilis, show subtle differences in morphological traits involved in mating
FIGURE 1. Artemia sites in Chile.
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International Brain Laboratory public data
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