Oral and integumental uptake of free exogenous glycine by the Japanese spiny lobster Panulirus japonicus phyllosoma larvae.

The possibility of direct integumental absorption of the amino acid glycine from a solution in seawater was investigated in 250-260 day old (16.9-50.0 mg wet mass) phyllosoma larvae of the Japanese spiny lobster Panulirus japonicus Von Siebold 1824. The uptake of the amino acid was assessed by autoradiography and liquid scintillation counting (LSC) of larvae incubated with [2-(3)H]glycine and the net uptake was estimated by a time course high-performance liquid chromatography (HPLC) analysis of the concentration of glycine in the incubation medium. Autoradiography revealed the presence of labelled glycine in the cuticle, epidermis and internal tissues (digestive system, muscle, haemocytes) within 30 min of the onset of incubation. Absorption through the integument was confirmed by autoradiography and LSC as glycine uptake was observed even in larvae whose mouths were artificially sealed with cyanoacrylate bond prior to incubation. Scanning electron microscopic examination of the body surface revealed no bacterial population that could have mediated the uptake. HPLC revealed a consistent net uptake (0.29-0.39 micromol g(-1) body mass h(-1)) of glycine in larvae incubated in 6 micromol l(-1) glycine and high individual variation (e.g. absorption or release) in larvae incubated at higher concentrations (30 and 60 micromol l(-1)). Thus, the results of this study provide clear confirmation that, in addition to the known mode of oral feeding on macroscopic food masses, P. japonicus phyllosoma larvae are also able to absorb nutrients directly from the surrounding medium.

Dynamics and histological characteristics of gonadal sex differentiation in pejerrey (Odontesthes bonariensis) at feminizing and masculinizing temperatures.

This study evaluated the effects of different temperatures on the histological process of sex differentiation in the pejerrey Odontesthes bonariensis, a fish with marked temperature-dependent sex determination (TSD), at feminizing, neutral, and masculinizing temperatures. Fish reared at three temperatures (17 degrees C, 24 degrees C, and 29 degrees C) from hatching were sampled weekly until 11 weeks and their gonads were examined by histology. The percentages of females at 17 degrees C, 24 degrees C, and 29 degrees C were 100%, 73%, and 0%, respectively. Sex differentiation occurred earlier and at a smaller body size at higher temperatures in both sexes. The first signs of ovarian differentiation were observed at 4 and 7 weeks at 24 degrees C and 17 degrees C, respectively, and those of testicular differentiation at 4 and 7 weeks at 29 degrees C and 24 degrees C, respectively. Body or gonadal growth rates before sex differentiation were not proportional to temperature and showed no sexual dimorphism at 24 degrees C, where both sexes were present. Thus, differential growth rate is probably not a factor in TSD or histological sex differentiation in pejerrey. Blood vessels were formed before sex differentiation in both sexes and at all temperatures, and may be important for sex differentiation. No signs of intersexuality were found in any of the groups, and this characterizes pejerrey as the differentiated type of gonochorist even at feminizing and masculinizing temperatures. Ovaries were formed by the same histological processes at feminizing (17 degrees C) and neutral (24 degrees C) temperatures and without any pathological features such as germ cell degeneration. The process of testicular formation was generally similar at 24 degrees C and 29 degrees C, but some fish at 29 degrees C had widespread germ cell degeneration before sex differentiation. This suggests that pathological processes leading to germ cell death, such as heat-induced dysfunction of the supporting somatic cells, could be involved in masculinization of the genetic females at high temperatures.

Differential expression and cellular localization of activin and inhibin mRNA in the rainbow trout ovary and testis.

An inhibin cDNA from rainbow trout consisted of 1305 bp, which coded for 352 amino acid residues. The deduced amino acid sequence of mature inhibin was 50 to 60% identical to mammalian sequences. Distribution of inhibin alpha and activin beta A and beta B in different ovarian and testis compartments was studied in rainbow trout by in situ hybridization with complementary RNA probes. In testis tissue, inhibin alpha and activin beta A and beta B were expressed only in the testicular interstitia between the seminal lobules, where Sertoli cells and Leydig cells are distributed. The localizations and intensities of the reactions were constant throughout the maturation of the testis. Within ovarian tissue, the theca cell layers of follicles showed strong reactions of Dig-labeled antisense mRNA probes hybridizing against inhibin alpha and activin beta A and beta B in all samples over the same sampling period. In regressing oocytes, a positive reaction was observed in the granular cell layer of the follicles.

Biomechanical stress in bone surrounding an implant under simulated chewing.

The concept of reducing nonaxial loading of dental implants has been widely regarded as the standard procedure. The aim of this study was to reveal the biomechanical stress distribution in supporting bone around an implant and a natural tooth under chewing function. Three-dimensional finite element models of the mandibular first molar and the titanium implant both with the mandible in the molar region were constructed. The directions of displacement constraints were determined according to the angles of the closing pathways of chopping type and grinding type chewing patterns. The tooth model showed smooth stress distribution in the supporting bone with low stress concentration around the neck of the tooth. The implant model showed stress concentration in the supporting bone around the neck of the implant, especially in the buccal area. The grinding type model of the implant showed higher tensile stress concentration than the chopping type model at the lingual neck of the implant. The results of this study suggested the importance of considering occlusion under chewing function for understanding the biomechanics of oral implants.

Effect of salinity on the oxygen consumption of larvae of the silversides Odontesthes hatcheri and O. bonariensis (Osteichthyes, Atherinopsidae)

Starved larvae of the silversides O. hatcheri (2- and 5-days-old) and Odontesthes bonariensis (5-days-old) were used to compare the oxygen consumption rates at 0, 5, 10, 20 and 30 ppt salinity. Oxygen consumption of O. hatcheri and O. bonariensis was minimal at 0 and 10 ppt, respectively, salinities close to those encountered in areas inhabited by these fishes. In both species, oxygen consumption rates thereafter increased with increasing salinity, and then abruptly decreased at 30 ppt. Lower consumption at extreme salinities might be a result of reduced activity, which in itself was salinity-modulated. Differences in activity may explain the fact that oxygen consumption rates of 5-day-old larvae were higher than 2-day-old larvae, which still possess yolk-sac. In this case, starved larvae incurred in higher metabolic demand due to the continuous swimming in the search for food.

As larvas em inanição de peixe-rei O. hatcheri (2 e 5 dias de idade) e Odontesthes bonariensis (5 dias de idade) foram usadas para comparar as taxas de consumo de oxigênio em salinidades de 0, 5, 10, 20 e 30 ppt. As taxas de consumo de oxigênio de O. hatcheri e O. bonariensis foram mínimas a 0 e 10 ppt, respectivamente, salinidades próximas aquelas encontradas nas áreas onde estes peixes habitam. Em seguida, em ambas as espécies, as taxas de consumo de oxigênio aumentaram com o incremento da salinidade, e abruptamente caíram a 30 ppt. As taxas de consumo mais baixas em salinidades extremas podem ser resultado da atividade reduzida, sendo portanto modulada pela salinidade. Diferenças na atividade possivelmente explicam o fato das taxas de consumo de oxigênio de larvas de 5 dias de idade serem maiores em comparação a larvas de 2 dias, ainda com saco vitelínico. Neste caso, larvas em inanição impõem um maior gasto metabólico devido a natação contínua em busca de alimento.