The enigmatic rodlet cell has been observed in tissues of marine and freshwater teleosts. The origin and function of this cell remain unclear. We describe the association of the rodlet cell with the head-kidney tissue of the southern platyfish, Xiphophorus maculatus. We have observed rodlet cells in various tissues of X. maculatus, e.g., the hemopoietic compartments of the head kidney, gill epithelia, and ovarian tissue, and in melanotic tumors. Recently, we found rodlet cells within the mesothelium and musculature. Intrigued by these observations, we began our current study of the rodlet cell – head kidney association in X. maculatus. We discerned a series of developmental stages of the rodlet cell within the hemopoietic tissue of the head kidney, including early precursor cells through degraded terminal stages. Tight junctions and desmosomes were observed between mature rodlet cells and endothelial cells. Desmosomal junctions were occasionally seen between maturing rodlet cells and neighboring cells within intertubular areas. We never observed junctional complexes between adjacent rodlet cells at any stage. Rodlet sacs were released intact and were seen to interact with other cellular components. We relate our findings to those of others who have described the development and distribution of rodlet cells in teleosts.

Although the testis in teleosts has been investigated for many years, little attention has been paid to the structure of the outer layers that enclose the testis and to their possible contributions to its organization. The present study in a protogynous male labrid, Thalassoma bifasciatum (bluehead wrasse), describes the arrangement and cytology of these tissues (for convenience, referred to collectively as the outer wall, OW) which include: the outer peritoneal layer and subjacent collagen fibers, myoid cells and diverse other cells and tissues, e.g., fibrocytes, presumptive mesenchyme, macrophages, granulocytes, nerves, and blood vessels. Beneath the OW are two compartments; one is the gamete-laden spermatocysts, the other the interstitium, which is composed of cells and tissues that lie between the spermatocysts. Both OW and interstitium contain similar kinds of tissues and cells. Moreover, the layers of the OW immediately subjacent to the peritoneum are continuous with that in the interstitium. It is suggested that the continuity between these two areas provides opportunities for the exchange of cells that could aid in the maintenance and reorganization of the testis and with the myoid and neural tissue to establish an extensive, coordinated motile system that aids movement of sperm from spermatocysts to the ducts. A recent report on the reexamination of the germinal epithelium concept and its identification in the common snook, Centropomus undecimalis, stimulated us to examine the feasibility of applying this concept to gonad organization and gamete development in T. bifasciatum. In addition, the ultrastructure of the Sertoli cell and formation of spermatocysts are described. Spermatocysts increase in size during the development of gametes. Observations and discussion are presented suggesting how Sertoli cells may accommodate this growth and how new populations of these cells may arise in the mature adult. Finally, ultrastructural characteristics for each stage of spermatogenesis are presented and, using (3H)thymidine and autoradiography, data on the chronology of spermatogonia-sperm cycle are included.

Female to male successive hermaphroditism (protogyny) is common in several groups of marine fish. Thalassoma bifasciatum, the bluehead wrasse (Labridae), found in the reefs of the Caribbean normally undergoes sex reversal after receiving behavioral cues. This report deals with the successful use of human chorionic gonadotropin (hCG) in inducing gonad reversal in this species. Eighty percent (n = 40) of the treated fish showed signs of reversal in 1-6 weeks; only 11% (n = 54) of the control (nontreated) group showed signs of reversal during the same period. The number of fish undergoing reversal increased with the length of the treatment period, 55% after 1 week, 100% after 6 weeks. A bluehead color pattern, typical of the terminal male phase, also appeared more frequently in the longer treated groups. To determine the efficacy of hCG in inducing gonad reversal, morphological criteria for reversal had to be established. For the majority of treated fish, the presence of both spermatogenic cysts and degenerating oocytes was sufficient to label these gonads unambiguously as undergoing reversal. However, at the extremes of this process, i.e., onset (early) and endpoint (late) stages, ambiguity could arise in identifying a gonad as undergoing reversal, and, therefore, key criteria were established for these stages. In our hands, the most consistent and reliable criterion for the early stage reversal was appearance of male germ line cells, clusters of "spermatogonial-like" cells. For the late stage, recognizable remnants of late-state oocytes had to be present. Some details of the histological changes that occur during early, middle, and late stages of reversal are also described. It is suggested that these results with hCG shed new light on the endocrine control of gonad reversal in T. bifasciatum.

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The effects ofexogenous testosterone pellet implantsat 21 and 40days on the ovary of Thalassoma hifasciaturn, a protogynous marine fish, are described. The characteristic markings of the terminal blue phase appeared by 4 to 5 days and were complete by 18 days. There was no shift in sex ratio in the treated fish when compared to an untreated control group. None of the ovaries showed signs of precocious transformation, i.e., spermatogenic tissue was lacking, and there was no evidence of duct formation. Instead, however, the ovaries of the treated fish showed marked degenerative changes characterized by oocyte breakdown, fat infiltration, vacuolization, the accumulation of fibrous PAS+ material and the appearance of small eosinophilic cells.These findings conflict with earlier studies on the same organism that employed different procedures. However, they resemble more closely the results obtained from work on another protogynoid, the ricefield eel, Monoprerus afbus. They add new light on the role of sex hormones in the reversal process of T. bifasciaturn and hermaphroditic fishes in general.