Seasonal reproductive biology of two species of freshwater catfish from the Venezuelan floodplains.

Oxydoras sifontesi and Pimelodus blochii are seasonal breeder fish. Spawn occurs once a year over a short interval of time, at the beginning of the rainy season. The gonadosomatic index (GSI), and plasma levels of steroid hormones of P. blochii and O. sifontesi were studied from fish samples, collected from the Portuguesa River (Portuguesa State, Venezuela) in 1998 and 2004-2005, respectively. Gonadal tissue samples were obtained and processed for histology. A macroscopic classification of the degree of gonadal maturation was performed using a six-stage maturity scale. Data was analyzed and compared as a function of the gonadal maturation stage. The GSI of both O. sifontesi and P. blochii increases from stages II to V (preparatory and prespawning periods) and decreases in the stage VI (postspawning). In males, the GSI was usually lower than in females. In both species, the higher plasmatic concentration of 17beta-estradiol (17beta-E) and testosterone (T) were obtained from specimens in stages IV or V. A significant decrease in both hormones was observed in stage VI, except for the males of P. blochii where T concentration did not change between gonadal stages IV-VI. The relevance of these results is discussed in relation to the seasonality and the particular hydrological conditions of the region.

Intracytoplasmic sperm injection using cryopreserved, fixed, and freeze-dried sperm in eggs of Nile tilapia.

Gamete preservation techniques are essential in animal husbandry as well as in assisted reproduction for humans. In this research we attempted to use 3 different sperm preservation techniques in combination with newly developed techniques for intracytoplasmic sperm injection (ICSI) to fertilize eggs of a teleost fish, the Nile tilapia (Oreochromis niloticus). Of 47 eggs injected with fresh sperm, 11 (23%) were fertilized, 5 developed abnormally, and 4 developed normally and hatched; from these, one grew to adulthood. Nuclear DNA content of 4 of the abnormal embryos indicated that they were diploid. Flow cytometric analysis of a blood sample from the surviving ICSI fish collected 2 months after fertilization indicated that the fish was diploid. Of 45 eggs injected with cryopreserved sperm, 9 (20%) developed to the blastula stage. Of 40 eggs injected with sperm preserved in 70% methanol, none were fertilized. No injections were possible with freeze-dried Nile tilapia sperm owing to technical difficulties during manipulation. Although the findings described here are limited, they provide the first steps toward using sperm preservation methods in addition to cryopreservation for fertilization in fishes.