Studies on Cepaea I. The genetics of some morphs and varieties of Cepaea nemoralis (L.)

The following segregants of shell colour are described: pale brown, faint brown, faint pink, yellow-white. Faint pink is dominant to dark and pale yellow and recessive to pale pink. Murray’s finding that the hyalozonate gene when homozygous pales shell colour as well as removing the lip and banding pigment is confirmed; faint pink or yellow-white shells homozygous for hyalozonate may be genetically faint pink or pale pink. Deep pink hyalozonates exist and transmit their phenotype to their offspring; in these the paling effect is not noticeable. Shells with no bands but a strip of fascialbate opaque material in the position for bordering the middle band are genetically mid-banded. The condition is due to a multifactorial suppression of the pigmented band. Spread-banded is described in the five-banded form as well as the m id-banded; the strong linkage between it and shell colour previously suggested is confirmed, but crossovers are recorded. White lip (with normally pigmented bands) is recessive to normal lip, linked to the locus for shell-colour, and allelic to hyalozonate. The normal lip/white lip heterozygote appears to be palelipped, but the degree of pallor is modified by the presence of yellow or pink shell colour. White lip, when homozygous, may reduce the intensity of shell colour in some cases, as does hyalozonate. Hyalozonate is shown to be linked to the banding locus, which itself is strongly linked to that for shell colour. Orange-banded is complementary to hyalozonate, not allelic to it as is the very similar form lurida described by Murray in Cepaea hortensis . A form of the var. punctata producing only traces of bands and occasionally a definite punctate band is described, which is linked to the shell colour locus and dominant to normal bands. This and the form figured by Lang and by Taylor with well-developed punctate bands (the segregation of which from normal bands is confirmed) may well be alleles. A segregation of medium grey to very pale body is described, with medium grey dominant to pale. It appears to be unlinked to shell colour, banding and mid-banded.

2018 ◽  
Vol 28 (3) ◽  
pp. 113-118
Author(s):  
I. P. Shepeleva

A comparative analysis of the camera eyes of gastropod pulmonate molluscs Cepaea nemoralis and Cepaea hortensis was carried out on the basis of original and published data. It was demonstrated that the eyeballs and their main components in C. nemoralis and C. hortensis have more similarities in morphological and optical properties than in anatomical parameters.


2008 ◽  
Vol 133 (4) ◽  
pp. 569-578 ◽  
Author(s):  
Jessica G. Barb ◽  
Dennis J. Werner ◽  
Robert J. Griesbach

Stokes aster [Stokesia laevis (J. Hill) Greene] is a herbaceous perennial endemic to the coastal plains of the southeastern United States. Anthocyanin and copigment aglycones from flowers were characterized using high-performance liquid chromatography. Blue, lavender, violet, and albescent flowers each contained the anthocyanidin petunidin, although albescent flowers contained a substantially smaller amount. Pale pink flowers were found to contain only cyanidin. Anthocyanins and carotenoids were not present in pale yellow flowers of this species. All flowers contained the flavone luteolin. Genetic analysis of F1, F2, and BC1 populations suggested that flower color in stokes aster is controlled by at least three loci. F2 populations of blue × albescent and blue × pale yellow flowering plants segregated in a 3:1 ratio of blue to albescent or pale yellow flowered progeny, indicating that albescent and pale yellow flower colors were recessive and each controlled by a single locus with two alleles. BC1 populations supported these results. We propose the symbols A and Y: AA and YY plants synthesize a normal amount of anthocyanins, aa plants synthesize a reduced amount of anthocyanins, and yy plants do not synthesize anthocyanins. When the two mutant phenotypes (i.e., albescent [aa] and pale yellow [yy]) were crossed, the F1s were blue, and the F2 segregated in a 9 blue:3 albescent:4 yellow ratio, indicating that the recessive locus (y), when homozygous, was epistatic to other loci involved in anthocyanin production (e.g., A), and that the genotypes of the parents used in these crosses were aaYY (albescent) and AAyy (pale yellow). F1, F2, and BC1 populations of blue (petunidin) × pale pink (cyanidin) flowering plants revealed that cyanidin production was recessive and controlled by a single locus, P, with two alleles, whereby PP plants synthesize petunidin and pp plants synthesize cyanidin. It was difficult to distinguish albescent- and pale pink-flowered progeny in segregating generations, therefore three genetic models were proposed and tested to determine the genotype(s) (i.e., AApp, Aapp, or aapp) of the pale pink-flowered plants. Based on these analyses, we propose a theoretical biochemical pathway for flavonoid biosynthesis in stokes aster.


Sign in / Sign up

Export Citation Format

Share Document