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1,245 results for “dating”
Figure 8 in Phytoseiidae from date palms in Israel with descriptions of two new taxa and a key to the species found on date palms worldwide (Acari: Mesostigmata)
Figure 8. Typhlodromus athiasae. (A) Dorsal view; (B) ventral view; (C) chelicera; (D) spermatheca; (E) leg IV; (F) male spermatodactyl.
Figure 6 in Phytoseiidae from date palms in Israel with descriptions of two new taxa and a key to the species found on date palms worldwide (Acari: Mesostigmata)
Figure 6. Neoseiulus bicaudus. (A) Dorsal view; (B) ventral view; (C) chelicera; (D) spermatheca; (E) leg IV; (F) male spermatodactyl.
Figure 2 in Phytoseiidae from date palms in Israel with descriptions of two new taxa and a key to the species found on date palms worldwide (Acari: Mesostigmata)
Figure 2. Neoseiulus cozae. (A) Dorsal view; (B) ventral view; (C) chelicera; (D) spermatheca; (E) leg IV.
Figure 1 in Phytoseiidae from date palms in Israel with descriptions of two new taxa and a key to the species found on date palms worldwide (Acari: Mesostigmata)
Figure 1. Proprioseiopsis beatus. (A) Dorsal view; (B) ventral view; (C) chelicera; (D) spermatheca; (E) leg IV.
Figure 3 in Phytoseiidae from date palms in Israel with descriptions of two new taxa and a key to the species found on date palms worldwide (Acari: Mesostigmata)
Figure 3. Neoseiulus marginatus. (A) Dorsal view; (B) ventral view; (C) chelicera; (D) spermatheca; (E) leg IV; (F) male ventrianal shield; (G) male spermatodactyl.
FIGURE 1 in The dates of publication of L.A.G. Bosc's Histoire naturelle des Crustacés
FIGURE 1. The title-pages of the first (left) and second (right) volumes of the Histoire naturelle des Crustacés (Bosc 1801a, b). Note the uncertainty in the date of the publication in the anonymous annotation on the title-page of the first volume. From a work no longer in copyright held by the Smithsonian Institution and digitised under the Biodiversity Heritage Library initiative (http://dx.doi.org/10.5962/bhl.title.39831).
FIGURE 1 in The leucosiid crabs described by Thomas Bell in 1855: original description and dates of publication (Crustacea: Decapoda: Brachyura)
FIGURE 1. Two of Bell's (1855) publications on the Leucosiidae Samouelle, 1819. A, title-page of Bell's (1855d) Catalogue of Crustacea in the Collection of the British Museum; B, plate 34 from Bell (1855c) published in the Transactions of the Linnean Society. From publications no longer in copyright (A, Google Books, www.books.google.com; B, the Biodiversity Heritage Library, www.biodiversitylibrary.org).
Figs. 1–3. Javeta pallida. 1 in First Report of the Indian Date Palm Leaf Miner, Javeta pallida Baly (Coleoptera: Chrysomelidae: Cassidinae: Coelaenomenoderini), on Pygmy Date Palm, Phoenix roebelenii O'Brien (Arecaceae)
Figs. 1–3. Javeta pallida. 1) Adult; 2) Infestation on Phoenix roebelenii in Kerala, India; 3) Infested leaflets.
Figure 3 in Molecular dating and diversification of the South American lizard genus Liolaemus (subgenus Eulaemus) based on nuclear and mitochondrial DNA sequences
Figure 3. Posterior probability distributions for mean rates of evolution estimated from the combined data under a partitioned analysis for the mitochondrial (A) and nuclear genes (B). The middle line of each box plot represents mean rates and the top and bottom lines indicate the 95% credibility intervals. CMOS; MXRA-5.
Figure 2 in Molecular dating and diversification of the South American lizard genus Liolaemus (subgenus Eulaemus) based on nuclear and mitochondrial DNA sequences
Figure 2. Age posterior probability distributions for each of the Eulaemus crown groups. Vertical black line represents the Miocene-Pliocene boundary (5.33 Mya).
Figure 1 in Molecular dating and diversification of the South American lizard genus Liolaemus (subgenus Eulaemus) based on nuclear and mitochondrial DNA sequences
Figure 1. Fifty per cent majority rule phylogram from the partitioned BEAST analyses of the combined data set (cytochrome b, 12S, CMOS, and MXRA5). Numbers above and below the nodes represent posterior probability values and mean estimates of divergence dates (in millions of years), respectively.
FIGURES 1–5 in A new species of Neoseiulus Hughes, with records of seven species of predatory mites associated with date palm in Saudi Arabia (Acari: Phytoseiidae)
FIGURES 1–5. Neoseiulus saudiensis Negm, Alatawi & Aldryhim n. sp. Female, 1. idiosoma dorsum, 2. idiosoma venter, 3. spermatheca, 4. chelicera, 5. genu, tibia and basitarsus IV.
Figure 8 in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 8. Divergence ages (median and 95% HPD) for all dating models, shown for the main groups of Folivora of the present classification. Time scale in million years ago.
Figure 5 in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 5. Estimated rate multipliers for anatomical partitions in each model. Partition colours as in Figure 1.
Figure 2 in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 2. Diversity through time for sloth genera sampled and its association with geological epochs. Time scale in million years ago.
Figure 1 in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 1. Anatomical partitions and partitioning schemes. Coloured anatomical regions in the skeleton of Paramylodon harlani (modified from Stock, 1925) correspond to the maximally partitioned data subsets, as used in model A7, whereas their combinations into composite partitions used in schemes A1 to A6 are indicated by other colours in the table. UN, unpartitioned model.
Figure 4 in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 4. Selected trees, with node supports (Poisson boostrap and posterior probabilities), depicting the overall variation in topologies obtained. A, parsimony IW100. B, parsimony IW5. C, Bayesian UN_p. D, Bayesian IW100_e. All topologies and branch lengths for Bayesian trees are available in the Supporting Information (File S9).
Figure 3. A in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 3. A, marginal likelihoods of Bayesian models. B, normalized Robinson–Foulds (nRF) distances among topologies (with IW100_e used as reference). C, distribution of node supports, with posterior probabilities for Bayesian inferences and bootstrap values for maximum parsimony.
Figure 7 in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 7. Stratigraphic fit of maximum parsimony and Bayesian topologies evaluated with two metrics, considering fossil age intervals as known ranges or as stratigraphic uncertainty. A, stratigraphic consistency index (SCI). B, gap excess ratio (GER).
Figure 10 in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 10. Relative rates (median and 95% HPD) of speciation, extinction and fossilization obtained with a skyline fossilized birth-death process for seven consecutive time bins.
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