The eggshells of 56 chelonians were examined by electron microscopy and X-ray diffractometry. They were classified into six types in terms of the matrix structure of their calcareous layer; type I was composed of a thin calcareous layer with minerals in an amorphous structure; type II with shell units composed of mammillary cores calcified with aragonite crystals; type III with shell units composed of mammillary cores, plus a single palisade layer also calcified with aragonite crystals, and with each shell unit separated; type IV with shell units the same as type III, but tightly packed together; type V with shell units composed of mammillary cores plus two palisade layers; and type VI with a cuticle layer calcified with calcite crystals over the same structure as that of type V. X-ray diffraction analyses at the outer surface of eggshells showed a gradual change in crystal disposition from the random disposition of type II to the single direction-oriented disposition of type V. The shell height was approximately parallel to the development of the palisade-layer matrix. The limiting membrane of all eggshell types was perforated with canals and that of type I was partially missing. Type I had a parchment shell, types II and III had a pliable shell (some were rigid) and types IV to VI had rigid shells. The present study showed that the hardness of eggshells can be determined by the composition of the shell matrices, as shell matrices are the framework for mineralization.
The structure and mineral composition of eggshell cuticles were studied in species of birds. The approximate thickness of the cuticle layer at the top of shell columns was about m in the Red Junglefowl ( ), about m in the White Pelican ( ), about m in the Japanese quail ( ), about m in the Greater Flamingo ( ) and about m in the Humboldt Penguin ( ). The matrix of the cuticle layer decalcified with EDTA was composed of vesicles in a variety of sizes in all birds. Major elements in cuticle materials detected by X-ray microanalysis were O, C, Ca and P, and their percentage numbers of atoms decreased in this order. The concentration of P was significantly higher in the cuticles of the quail, flamingo, and penguin than in those of the junglefowl and pelican. Ca mapping on electron-microscopic images showed strong signals in the shell layer and weaker ones in the cuticle layer, whereas P mapping showed that signals were mostly confined in the cuticle layer. X-ray di raction analyses on the inside of the shell layer showed a profile of calcite crystals of calcium carbonates in all birds. In the cuticle materials, the profile was of calcite in the junglefowl, and a mixture of calcite and vaterite in the pelican. The profiles in cuticle materials of the quail, flamingo and penguin showed no specific signals, indicating that mineral compounds are amorphous in these forms. It was suggested that the diversity of mineral structures in the cuticle layer is caused by the presence of phosphorous, in addition to the structure of the cuticle matrix.
Clone loaches reproduce unisexually in a wild population of Hokkaido Island, Japan. These clone loaches produce genetically identical unreduced eggs which develop to diploid individuals without any genetic contribution of sperm donors. In the present study, sex reversal of clone loaches was attempted and the reproductive potential of resultant clone males was examined. Clone loaches administered 0.5 ppm of 17-alpha methyltestosterone (MT) for 30 days from 1 month after hatching differentiated into physiological males. These sex-reversed clone males produced fertile spermatozoa with a diploid DNA content. Diploid spermatozoa had significantly larger heads than normal haploid sperm, but had a normal shape showing a head, mid-piece, and tail. The motility of diploid spermatozoa was low after ambient water was added. Concentration of diploid spermatozoa per unit of sperm was lower than that of control haploid spermatozoa. Microsatellite genotyping revealed that triploid progeny from the cross between a normal diploid female and a sex-reversed clone male had two alleles specific to the diploid clone male and one allele of the mother loach. These results indicated that the sex-reversed clone males produced fertile diploid spermatozoa genetically identical to the clone lineage.
To examine the pluripotency of cryopreserved blastomeres, we transplanted them into blastula. Donor blastomeres were prepared from blastula of goldfish (Carassius auratus) and cryopreserved in liquid nitrogen for two months. Fifty-five percent and 44% of blastomeres survived after thawing. Cryopreserved blastomeres were transplanted to the blastula of triploid crucian carp (C. a. longsdorfii), which reproduces gynogenetically in nature. At four days after the operation, resultant chimeric embryos transplanted with cryopreserved blastomeres showed a survival rate (41.6%) lower than that of embryos transplanted with unfrozen blastomeres (57.1%). Transplanted blastomeres were histologically identified in various organs derived from all three germ layers. A primordial germ cell differentiated from a cryopreserved blastomere was detected in one of the 32 chimeric fish examined. These results suggest blastomeres that survive after cryopreservation retain their pluripotency and are able to differentiate into both somatic and germ cell lines.
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