<p> <b><span style="font-size:10.0pt;">The <i>Tityus serrulatus </i>scorpion is considered the most dangerous scorpion in Brazil and is responsible for several cases of human envenomation annually. In this study, we performed transcriptome profiling of the <i>T. serrulatus</i> venom gland. In addition to transcripts with housekeeping functions, such as those related to protein synthesis, energy supply and structural processes, transcripts from thirty-five families of venom peptides or proteins were identified. These transcripts included three new complete sequences of toxins and more than a dozen putative venom gland proteins/peptides. The venom gland transcriptome profile was verified by comparison with the previously determined proteomic profile. In conclusion, this transcriptome data provides novel insights into the putative mechanisms underlying the venomous character of <i>T. serrulatus</i>. The collected data of scorpion transcripts and proteins/peptides described herein may be an important resource for identifying candidate targets of molecular therapies and preventative measures.</span></b><b><span style="font-size:10.0pt;"></span></b> </p>

Biofloc technology (BFT) provides an additional feed source for aquatic organisms through the conversion of waste in microbial flocs. Because of this, the suitable protein level in a diet for animals in this system could be different from those in conventional systems. Our objective was to determine the suitable protein level in the diet of Nile tilapia juveniles reared with BFT. Two experiments were carried out with tilapia weighing~10 g (first experiment) and about 50 g (second experiment) during 61 and 98 days respectively. Five crude protein (CP) levels (within 17% and 33%) were tested. The increment of CP resulted in a reduction in dissolved oxygen, pH, alkalinity and an increase in dissolved phosphorus, total suspended solids and total ammonium nitrogen. The crude protein level had a significant effect (p < 0.05) on animal performance. The linear response plateau model was the best fit for the final weight and weight gain data in the two growth phases. In conclusion, tilapia juveniles of 10-60 g and 60-230 g in biofloc can be fed on diets with 28% of CP (26% of digestible protein) and 22% CP (20% of digestible protein) respectively. K E Y W O R D Sbiofloc technology, growth performance, Nile tilapia, nutrition

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Reproductive biology and feeding of Curimatella lepidura (Eigenmann & Eigenmann, 1889) were studied in Juramento reservoir, São Francisco River basin, Southeastern Brazil. Histological analyses and gonadosomatic indexes revealed females and males in reproductive activity from October to March and total spawning occurring from January to March coupled with the peak of spermiating males. In the dry season, the fishes accumulated energetic reserves for reproduction during a short rainy season. The species presented sexual dimorphism, being females larger than males and sexual maturation occurring close to 7.7 cm standard length for females and 7.1 cm for males. C. lepidura presented iliophagous feeding habit, ingesting mainly sediment/detritus and a small amount of acari, algae, Tricoptera insects and Ostracoda crustaceans, suggesting a probable role in nutrient recycling of the Juramento reservoir.

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The Nile tilapia (Oreochromis niloticus) is economically one of the most important freshwater fish and is an excellent model for studies under laboratory conditions. Temperature is considered a very important modulator of reproductive activity in fish, although few studies have specifically addressed the effects of this key factor on morphological and functional aspects of teleost testes. Therefore, our main objectives in the present study were to analyze the effects of different temperatures (20, 25, 30, and 35 degrees C) on testicular somatic and germ cells in sexually mature Nile tilapias. Compared with fish kept at other temperatures, tilapias maintained at 20 degrees C demonstrated increased (P < 0.05) Sertoli cell and Leydig cell proliferation, volume density and frequency of most type B spermatogonia, and germ cell apoptosis. Conversely, tubular fluid secretion was decreased (P < 0.05) in the same animals. Although not significant, type A spermatogonia proliferation followed the pattern established for Sertoli cell and Leydig cell mitotic activity, suggesting that they preferentially would proliferate at lower temperatures. Based on most results found in our study and considering that tilapias are nonseasonal breeders, we suggest a model for temperature action on tilapia testes in which lower temperature (20 degrees C) would favor type A spermatogonial renewal, Sertoli cell and Leydig cell proliferation, and germ cell apoptosis, whereas higher temperatures (30-35 degrees C) would trigger rapid germ cell differentiation. Thus, tilapias could potentially be utilized in studies involving hormones and factors related to Sertoli cell and Leydig cell proliferation and spermatogonial self-renewal or differentiation.

Fish germ cell transplantation presents several important potential applications for aquaculture, including the preservation of germplasm from endangered fish species with high genetic and commercial values. Using this technique in studies developed in our laboratory with adult male Nile tilapias (Oreochromis niloticus), all the necessary procedures were successfully established, allowing the production of functional sperm and healthy progeny approximately 2months after allogeneic transplantation. In the present study, we evaluated the viability of the adult Nile tilapia testis to generate sperm after xenogeneic transplant of germ cells from sexually mature Jundia catfish (Rhamdia quelen) that belong to a different taxonomic order. Therefore, in order to investigate at different time-periods post-transplantation, the presence and development of donor PKH26 labeled catfish germ cells were followed in the tilapia seminiferous tubules. From 7 to 20days post-transplantation, only PKH26 labeled spermatogonia were observed, whereas spermatocytes at different stages of development were found at 70days. Germ cell transplantation success and progression of spermatogenesis were indicated by the presence of labeled PKH26 spermatids and sperm on days 90 and 120 post-transplantation, respectively. Confirming the presence of the catfish genetic material in the tilapia testis, all recipient tilapias evaluated (n=8) showed the genetic markers evaluated. Therefore, we demonstrated for the first time that the adult Nile tilapia testis offers the functional conditions for development of spermatogenesis with sperm production from a fish species belonging to a different order, which provides an important new venue for aquaculture advancement.