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2,331 results for “Polymorphic”
Fig. 1 in Population Genetics Of Philaenus Spumarius On The Istranca Mountains: Ii. Polymorphism And Phenotype Frequency
Fig. 1. Dorsal colour/pattern phenotypes of Philaenus spumarius found on the Istranca Mountains, Turkey (abbreviations are described in the text)
Fig. 3 in Population Genetics Of Philaenus Spumarius On The Istranca Mountains: Ii. Polymorphism And Phenotype Frequency
Fig. 3. Combined phenotype frequency distributions of Philaenus spumarius for three types of habitat on the Istranca Mountains, Turkey. Separate diagrams for females and males denote the habitats from top to the bottom: Mixed, Oak, and Beech forests respectively. From left to right, the bars of the diagrams indicate; 1: POP, 2: TYP, 3: TRI+VIT, 4: MAR+LAT, 5: FLA+LCE. The height of the bar
Fig. 1 in P H E N O T Y P I C P L A S T I C I T Y A N D N U C L E A R D N A Polymorphism Of Two Differing Pinus Sylvestris L. Open-Pollinated Families Originating From The Same Population
Fig. 1. Field trials with open-pollinated progeny of Lithuanian Pinus sylvestris L. populations, established in 1983. The tree samples for DNA analysis were taken from the labeled field trials.
Fig. 6 in P H E N O T Y P I C P L A S T I C I T Y A N D N U C L E A R D N A Polymorphism Of Two Differing Pinus Sylvestris L. Open-Pollinated Families Originating From The Same Population
Fig. 6. Distribution of genetic diversity values by Nei at 5 loci among the investigated Scots pine trials.
Fig. 4 in P H E N O T Y P I C P L A S T I C I T Y A N D N U C L E A R D N A Polymorphism Of Two Differing Pinus Sylvestris L. Open-Pollinated Families Originating From The Same Population
Fig. 4. Distribution of observed heterozygosity (HO) at 5 loci among the investigated Scots pine trials.
Fig. 8 in P H E N O T Y P I C P L A S T I C I T Y A N D N U C L E A R D N A Polymorphism Of Two Differing Pinus Sylvestris L. Open-Pollinated Families Originating From The Same Population
Fig. 8. Unweighted pair group method (UPGMA) dendrogram based on Nei's genetic distances among investigated half-sib open-pollinated families of one Lithuanian Pinus sylvestris L. population.
Fig. 5. The ill-defined acrocentric B in B chromosome and NORs polymorphism in Callichthys callichthys (Linnaeus, 1758) (Siluriformes: Callichthyidae) from upper Paraná River, Brazil
Fig. 5. The ill-defined acrocentric B chromosome: (a) Giemsa stained; (b) C-banded; stained by (c) CMA3 and by (d) DAPI. The bar represents 5µm.
Fig. 3 in B chromosome and NORs polymorphism in Callichthys callichthys (Linnaeus, 1758) (Siluriformes: Callichthyidae) from upper Paraná River, Brazil
Fig. 3. Callichthys callichthys metaphases spreads with the third NOR bearing chromosome. The arrowheads indicate the NORs, marked in the interstitial position stained by (a) CMA3 and confirmed by (b) DAPI; and in terminal position stained by (c) CMA3 and confirmed by (d) DAPI. The bar represents 5µm.
Fig. 2. C in B chromosome and NORs polymorphism in Callichthys callichthys (Linnaeus, 1758) (Siluriformes: Callichthyidae) from upper Paraná River, Brazil
Fig. 2. C-banded metaphases of Callichthys callichthys: the arrowhead indicates the third NORs bearing chromosome and the arrow indicates the (a) acrocentric B chromosome and the (b) ill-defined acrocentric B chromosome. The bar represents 5µm.
Fig. 1 in B chromosome and NORs polymorphism in Callichthys callichthys (Linnaeus, 1758) (Siluriformes: Callichthyidae) from upper Paraná River, Brazil
Fig. 1. Callichthys callichthys karyotypes stained by Giemsa: (a) with an acrocentric B chromosome and the third NORs bearing chromosome (interstitial) and (b) with the ill-defined acrocentric B chromosome and the third NORs bearing chromosome (terminal). The bar represents 5µm.
Figures 1−6 in Polymorphism and hybridization in species of Hottentotta Birula, 1908 (Scorpiones: Buthidae)
Figures 1−6: 1. F0 female of Hottentotta salei (pale morph). 2. F0 male of Hottentotta jayakari (dark morph). 3. Courtship and mating between F0 male (dark morph) and F0 female (pale morph). 4. F1 brood, on instar I. 5. F1 brood, on instar II. 6. F1 adult female (dark morph).
Fig. 15 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 15. Genitalia of Durgella pentata sp. nov. paratype CUMZ 14240. A: general view of the genital system and B: internal structure of the penis and epiphallus. White arrow indicates the end of the penis.
Fig. 14 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 14. Genitalia of Durgella libas CUMZ 14236. A: general view of the genital system and B: internal structure of the penis and epiphallus. White arrow indicates the end of the penis.
Fig. 11 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 11. Representative SEM images of the radula. A, B: D. birmanica CUMZ 14233. C, D: D. levicula CUMZ 14253. E, F: D. erratica CUMZ 14234. G, H: D. siamensis CUMZ 14232. Yellow arrow indicates the central tooth.
Fig. 10 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 10. Genitalia of Durgella species. A: D. erratica CUMZ 14234. B, C: D. siamensis CUMZ 14232; B: general view of the genital system; C: internal structure of the penis and epiphallus. White arrow indicates the end of the penis.
Fig. 8 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 8. Shells of Durgella species. A: D. rhaphiellus syntypes ZMB/MOLL 5033. B–D: D. siamensis; B: syntypes SMF 227168/1; C, D: CUMZ 14232.
Fig. 7 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 7. Shells of Durgella species. A–C: D. erratica; A: syntypes NHMUK 1895.1.1.4–6; B, C: specimen CUMZ 14234. D: D. concinna syntype NHMUK 1865.9.3.15.
Fig. 5 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 5. Shells of Durgella species. A: D. birmanica modified from Hanley and Theobald (1876). B, C: D. birmanica CUMZ 14233. D–F: D. levicula; D: NHMUK 1903.7.1.785; E: CUMZ 14251; F: CUMZ 14245.
Fig. 13 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 13. Microsculpture of Durgella shells: protoconch and early teleoconch (first column), and close-up view of protoconch (second column). A, B: D. libas CUMZ 14236. C, D: D. pentata sp. nov. paratype CUMZ 14240. E, F: D. nulla sp. nov. paratype CUMZ 14228.
Fig. 4 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 4. Eggs and mating behavior of Durgella species recorded in the field. A: eggs of D. libas from Wachirathan Waterfall, Chiang Mai Province. B: eggs of D. pentata sp. nov. from Tham Chiang Dao, Chiang Mai Province. C: eggs of D. nulla sp. nov. from Phu Pha Lom, Loei Province. D: mating pairs of D. nulla sp. nov. from Phu Pha Lom, Loei Province.
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