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445 results for “karyotype”

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dryad32/100

Data from: Chromosomal rearrangements do not seem to affect the gene flow in hybrid zones between karyotypic races of the common shrew (Sorex araneus)

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publicSep 2011View details →
dryad32/100

Data from: Karyotype analysis of four jewel-beetle species (Coleoptera, Buprestidae) detected by standard staining, C-banding, AgNOR-banding and CMA3/DAPI staining

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publicApr 2012View details →
dryad32/100

Tempo and mode in karyotype evolution revealed by a probabilistic model incorporating both chromosome number and morphology

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publicApr 2021View details →
zenodo28/100

Fig. 2. Karyotypes arranged from C-banded chromosomes. a in Cytogenetic markers as tools in delimiting species of the highly diverse Neotropical fish Bryconamericus (Characiformes: Characidae)

Fig. 2. Karyotypes arranged from C-banded chromosomes. a. Bryconamericus aff. iheringii (Ijuí River, pattern II); b. B. aff. iheringii (Iguaçu River); c. B. coeruleus (pattern II); d. B. cf. ecai; e. B. cf. eigenmanni. Scales bar = 10 μm.

opencc-by-4.0Sep 2019View details →
zenodo28/100

Fig. 3. Karyotypes after FISH with 5S in Cytogenetic markers as tools in delimiting species of the highly diverse Neotropical fish Bryconamericus (Characiformes: Characidae)

Fig. 3. Karyotypes after FISH with 5S rDNA probes (red) and 18S rDNA probe (green). In the boxes, the intra-population variations that represent distinct patterns of localization of ribosomal genes. a. Bryconamericus aff. iheringii (Ijuí River, pattern II) - box I: pattern I; b. B. aff. iheringii (Iguaçu River); c. B. coeruleus (pattern II) - box I: pattern I; box III: pattern III; d. B. cf. ecai; e. B. cf. eigenmanni. Scales bar = 10 μm.

opencc-by-4.0Sep 2019View details →
zenodo28/100

Fig. 1. Karyotypes arranged from Giemsa-stained chromosomes. a in Contributions to the systematic of Pimelodidae (Osteichthyes, Siluriformes): basic and molecular cytogenetics on seven species of Pimelodus from three Brazilian hydrographic systems

Fig. 1. Karyotypes arranged from Giemsa-stained chromosomes. a. Pimelodus absconditus; b. Pimelodus britskii; c. Pimelodus maculatus; d. Pimelodus microstoma; e. Pimelodus mysteriosus; f. Pimelodus ortmanni; g. Pimelodus paranaensis. Pairs of the AgNORs and B chromosomes are in the boxes. Scales bar = 10 μm.

opencc-by-4.0Jun 2018View details →
zenodo28/100

Supplementary material 2 from: Li Y, Li Y, Li H, Wang J, Rong X, Li Y (2020) Niviventer confucianus sacer (Rodentia, Muridae) is a distinct species based on molecular, karyotyping, and morphological evidence. ZooKeys 959: 137-159. https://doi.org/10.3897/zookeys.959.53426

Figure S1–S7, Tables S2–S6. Partial morphological and molecular results

opencc-zeroAug 2020View details →
zenodo28/100

Figure 6 from: Li Y, Li Y, Li H, Wang J, Rong X, Li Y (2020) Niviventer confucianus sacer (Rodentia, Muridae) is a distinct species based on molecular, karyotyping, and morphological evidence. ZooKeys 959: 137-159. https://doi.org/10.3897/zookeys.959.53426

Figure 6 Principal component analysis of dorsal view (a), ventral view (b), lateral view (c) of skull, and lateral view of the mandible (d) of the three clades.

opencc-by-4.0Aug 2020View details →
zenodo28/100

Figure 1 from: Li Y, Li Y, Li H, Wang J, Rong X, Li Y (2020) Niviventer confucianus sacer (Rodentia, Muridae) is a distinct species based on molecular, karyotyping, and morphological evidence. ZooKeys 959: 137-159. https://doi.org/10.3897/zookeys.959.53426

Figure 1 Distribution of phylogenetic clades of N. confucianus species complex obtained from Cytb. The numbers correspond to the locality code in Suppl. material 1, Table S1.

opencc-by-4.0Aug 2020View details →
zenodo28/100

Figure 7 from: Li Y, Li Y, Li H, Wang J, Rong X, Li Y (2020) Niviventer confucianus sacer (Rodentia, Muridae) is a distinct species based on molecular, karyotyping, and morphological evidence. ZooKeys 959: 137-159. https://doi.org/10.3897/zookeys.959.53426

Figure 7 Thin plate splines of dorsal view (a), ventral view (b), lateral view (c) of skull, and lateral view of the mandible (d) of N. sacer, N. confucianus, and N. lotipes.

opencc-by-4.0Aug 2020View details →
zenodo28/100

Figure 5 from: Li Y, Li Y, Li H, Wang J, Rong X, Li Y (2020) Niviventer confucianus sacer (Rodentia, Muridae) is a distinct species based on molecular, karyotyping, and morphological evidence. ZooKeys 959: 137-159. https://doi.org/10.3897/zookeys.959.53426

Figure 5 Principal component analysis and discriminant analysis of external and skull morphological indices. Principal component plots of external and skull indices are shown in a and b. Discriminant function plots of external and skull indices are shown in c and d, respectively.

opencc-by-4.0Aug 2020View details →
zenodo28/100

Supplementary material 1 from: Li Y, Li Y, Li H, Wang J, Rong X, Li Y (2020) Niviventer confucianus sacer (Rodentia, Muridae) is a distinct species based on molecular, karyotyping, and morphological evidence. ZooKeys 959: 137-159. https://doi.org/10.3897/zookeys.959.53426

Tables S1. Sampling and Genbank sequences information

opencc-zeroAug 2020View details →
zenodo28/100

Karyotypes of the water scavenger beetles (Coleoptera: Hydrophilidae): new data and review of published records

<p>The dataset includes original photos of mitotic and meiotic nuclei and all working karyograms used for the paper, including those not published on the plates in the paper.</p>

opencc-by-4.0Jul 2020View details →
zenodo28/100

Figure 3 from: Wang L-J, Gao M-D, Sheng M-Y, Yin J (2020) Cluster analysis of karyotype similarity coefficients in Epimedium (Berberidaceae): insights in the systematics and evolution. PhytoKeys 161: 11-26. https://doi.org/10.3897/phytokeys.161.51046

Figure 3 Diagram of cluster analysis of karyotype similarity coefficients in 51 Epimedium taxa and two Vancouveria species.

opencc-by-4.0Sep 2020View details →
zenodo28/100

Figure 2 from: Wang L-J, Gao M-D, Sheng M-Y, Yin J (2020) Cluster analysis of karyotype similarity coefficients in Epimedium (Berberidaceae): insights in the systematics and evolution. PhytoKeys 161: 11-26. https://doi.org/10.3897/phytokeys.161.51046

Figure 2 Mitotic metaphase chromosomes in 27 Epimedium taxa and two Vancouveria species. 25E. sagittatum26E. sagittatum var. glabratum27E. dolichostemon28E. truncatum29E. brevicornu30E. myrianthum31E. stellulatum32E. fargesii33E. elachyphyllum34E. koreanum35E. grandiflorum var. grandiflorum36E. grandiflorum var. thunbergianum37E. grandiflorum var. higoense38E. grandiflorum var. coelestre39E. sempervirens40E. sempervirens var. hypoglaucum41E. sempervirens var. multifoliolatum42E. trifoliatobinatum43E. diphyllum44E. cremeum45E. kitamuranum46E. setosum47E. alpinum48E. pubigerum49E. pinnatum subsp. colchicum50E. pinnatum cv. "Elegans" 51E. perralderianum52V. hexandra53V. chrysantha. Scale bars: 5 μm.

opencc-by-4.0Sep 2020View details →
zenodo28/100

Figure 1 from: Wang L-J, Gao M-D, Sheng M-Y, Yin J (2020) Cluster analysis of karyotype similarity coefficients in Epimedium (Berberidaceae): insights in the systematics and evolution. PhytoKeys 161: 11-26. https://doi.org/10.3897/phytokeys.161.51046

Figure 1 Mitotic metaphase chromosomes in 24 Epimedium species. 1E. ecalcaratum2E. shuichengense3E. platypetalum4E. davidii5E. pauciflorum6E. flavum7E. ilicifolium8E. mikinorii9E. membranaceum10E. lishihchenii11E. acuminatum12E. wushanense13E. leptorrhizum14E. baojingense15E. chlorandrum16E. luodianense17E. pudingense18E. glandulosopilosum19E. pseudowushanense20E. franchetii21E. enshiense22E. sutchuenense23E. zhushanense24E. pubescens. Scale bars: 5 μm.

opencc-by-4.0Sep 2020View details →
zenodo28/100

Supplementary material 1 from: Wang L-J, Gao M-D, Sheng M-Y, Yin J (2020) Cluster analysis of karyotype similarity coefficients in Epimedium (Berberidaceae): insights in the systematics and evolution. PhytoKeys 161: 11-26. https://doi.org/10.3897/phytokeys.161.51046

Table S1. Karyotype resemblance-near coefficients in 51 Epimedium taxa and two Vancouveria species

opencc-zeroSep 2020View details →
zenodo28/100

FIGURE 191. Karyotype S in Generic relationships of New World Jerusalem crickets (Orthoptera: Stenopelmatoidea:Stenopelmatinae), including all known species of Stenopelmatus

FIGURE 191. Karyotype S. zimapan.

opennotspecifiedJan 2021View details →
zenodo28/100

FIGURE 109. Karyotype S in Generic relationships of New World Jerusalem crickets (Orthoptera: Stenopelmatoidea:Stenopelmatinae), including all known species of Stenopelmatus

FIGURE 109. Karyotype S. perote.

opennotspecifiedJan 2021View details →
dryad28/100

Data from: Karyotype and genome size variation in genus Ajuga L. (Ajugoideae–Lamiaceae)

Chromosome number changes and karyotype evolution play an important role in plant genome diversification and eventually in speciation. The genus Ajuga L. (Lamiaceae) has approximately 50 species distributed in temperate to subtropical regions. Four of these species are currently recognized in Korea (A. decumbens Thunb., A. multiflora Bunge, A. nipponensis Makino and A. spectabilis Nakai). Understanding the karyotype evolution in Ajuga has been hampered by the small size of their chromosomes and symmetrical karyotypes. Here we used classic Feulgen staining to establish chromosome numbers and construct karyotypes of the four species of Ajuga recognized in Korea and flow cytometry was used to study their variation in genome. The chromosome number of all investigated plants was 2n = 32. Still, the 2C DNA content ranged from 2.18 pg (A. decumbens) to 4.53 pg (A. multiflora). While the chromosome numbers were the same for all investigated species, the genome size variation could potentially be used as a taxonomic marker.

opencc-zeroDec 2018View details →

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