Understanding the asymmetry between advancing and receding microscopic contact angles.

By means of molecular dynamics simulation, the advancing and receding microscopic contact angles were analyzed for a shear flow of two mono-atomic fluids confined between parallel non-polar solid walls. We defined the microscopic dynamic contact angle based on the coarse-grained microscopic density distribution of the fluids (the instantaneous interface method [Willard and Chandler, J. Phys. Chem. B, 2010, 114, 1954-1958]) near the moving contact line. We have found that the asymmetric change of fluid density near the wall with respect to the moving contact line results in a different dependence between the advancing and receding contact angles on the contact line velocity in a system where the two fluids across the interface have unequal wettability to the solid wall. This difference between the advancing and receding contact angles leads to different flow resistance caused by the advancing and receding contact lines, which should have impact on the industrial applications of the fine fluid transportation with contact lines.

Genetic and developmental analysis of some new color mutants in the goldfish, Carassius auratus.

The genotypes of three color mutants in goldfish: a depigmentation character of larval melanophores, albinism and a recessive-transparent character, were analyzed by crossing experiments. The depigmentation character in the common goldfish is controlled by two dominant multiple genes, Dp1 and Dp2, and only fish with double recessive alleles dp1dp1 dp2dp2 can retain larval melanophores throughout life. Albinism is also controlled by double autosomal genes, p and c. The genotype of an albino fish is represented by PP CC; the non-albino fish is PP CC. Fish with either a pp CC or pp Cc genotype are albino when scored at the time of melanosome differentiation in the pigment retina, but after the time of skin melanophore diffrentiation, they change to the nonalbino type under the control of the C gene. The recessive-transparent character is controlled by a single autosomal gene, g. The mechanisms of gene expression of these characters were proposed as a result of observation and/or experimental data on the differentiation processes of their phenotypes, and the genotypes of these color mutant goldfish were considered in relation to the "gene duplication hypothesis in the Cyprinidae."

In vitro analysis of gene depression in goldfish choroidal melanophores.

The common goldfish depigments its larval choroidal melanophores as well as the skin melanophores for about two to three months following hatching. Thereafter it begins to show a characteristic xanthic coloration. This depigmentation is under the control of depigmentation genes Dp1 and Dp2. The larval choroidal melanophores of the common goldfish were cultured in vitro for more than four months without showing any sign of depigmentation. During the same period the skin and choroidal melanophores in the ACTH to the culture medium had no effect on depigmentation. The mechanisms of depigmentation in the goldfish are discussed.

Ultrastructural analysis of gene interaction and melanosome differentiation in the retinal pigment cells of the albino goldfish.

The genotype of albino goldfish is represented by pp,cc, and the non-albino fish is PP,CC. The P gene begins to control the melanosome formation of retinal pigment cells at St-21; and the C, which is epistatic to P and p, governs melanosome formation in the dermal melanophores and in retinal pigment cells after St-22. Then in the pp,CC fish, between St-21 and St-22, melanosomes of the pigmented retina are albino in type, but after St-22 they become non-albino in type. From ultrastructural observations on the melanosomes of these late-melanizing fish, it is apparent that the imcompletely melanized albino pigment granules can differentiate into normal melanosomes under the control of the C gene. The processes of melanosome maturation in the late-melanizing goldfish are evident from these observations.

Pigment granules in choroidal melanophores of the albino goldfish.

Pigment granules in choroidal melanophores of the albino goldfish contained fine particulate materials which were in various degrees aggregated in clumps. Tyrosinase was considered to be present in an inhibited state in these pigment granules.

Inhibition of melanosome transformation in embryonic chick pigment retina cultured in vitro.

When the retinal pigment epithelial cells of the chick embryo are transferred to monolayer cultures, they lose their phenotypic trait-- melanin granules-- after a few days. Within the first 24 hours almost all of the melanosomes and premelanosomes are transformed into the degradative structures of the dense bodies or the melanosome complexes. Then, within a few days, these structures disappear completely from the cytoplasm. Actinomycin D, added to the culture medium during the first four hours, almost completely prevents the transformation of melanosomes and premelanosomes. The inhibition of cell proliferation, caused by the addition of colcemid, does not prevent the transformation, though the time of initiation of transformation is delayed considerably. The mechanisms of the transformation of pigment granules are discussed.