Weight width carapace relationship in the crab hepatus-pudibundus (herbst, 1785) (crustacea, decapoda, calappidae) of the Ubatuba region, SP, Brazil

In populational studies, the weight/width carapace relationship analysis, can furnish indications about the individual physiological variations as a function of the environment, and it can indicate sexual dimorphism. The goal of this research is to find the mathematical expressions of weight/width carapace relationship in the crab Hepatus pudibundus. This study was accomplished by analysing the crabs that were sampled monthly with a shrimp fishing boat equipped with 2 otter-trawl nets, during the period from november/1988 to october/1989. A total of 624 specimens were obtained composed of 244 males and 380 females. In each group the sex, the weight (PE) and the carapace width (LC) were determined. The obtained values agree with the studied range, showing variations during male and female development, represented by the potential function of the equation Y = aX(b). Such variations are probably related to reproductive strategies.

Appraisal of the chelipeds size on Hepatus-pudibundus (Herbst, 1785) (Crustacea, Calappidae) in function of sex and maturation

This paper appraises the influence of chelipeds on sexual and maturation phasis of the crab Hepatus pudibundus (Herbst, 1785), collected in Ubatuba (SP) region. The allometric constants obtained from the regression (carapace width X cheliped weight) adjusted to a power function (Y=aX(b)) were analysed. It was verified that males show larger chelipeds than females. The mean percentage of the chelipeds weight differs in sex and maturation.

Ecologia e biologia populacional do caranguejo Heptus pudibundus (Herbst, 1785) (Crustacea, Decapoda, Aethroidea) na região de Ubatuba, São Paulo, Brasil

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Análise temporal da composição, abundância, diversidade dos Cladocera e crescimento alométrico da Daphnia spp. O. F. Müeller, 1785 na Lagoa do Camargo, lateral ao Rio Paranapanena em sua zona de desembocadura na Represa do Jurumirim

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Eterogeneità delle proprietà fisico – chimiche della proteina prionica patologica e variabilità fenotipica ceppo specifica nella malattia di Creutzfeldt – Jakob

Transmissible spongiform encephalopathies (TSEs), or prion diseases, are neurodegenerative disorders that affect humans and mammals. Creutzfeldt-Jakob disease (CJD), the most common TSE in humans, can be sporadic (sCJD), genetic (gCJD), or acquired by infection. All TSEs are characterised by the accumulation of PrPSc, a misfolded form of the cellular protein PrPC. PrPSc is insoluble in detergents, partially resistant to proteolysis and shows a highly enriched β-sheet secondary structure. Six clinico-pathological phenotypes of sCJD have been characterized which correlate at the molecular level with two types (1 or 2) of PrPSc with distinctive physicochemical properties and the genotype at the polymorphic (methionine or valine) codon 129 of the prion protein gene. According to the protein-only hypothesis, which postulates that prions are composed exclusively of PrPSc, the strains of prions that are largely responsible for the wide spectrum of TSE phenotypes are enciphered in PrPSc conformation. In support to this view, studies mainly conducted in experimental scrapie, have shown that several prion strains can be identified based on distinguishing PrPSc biochemical properties. To further contribute to the understanding of the molecular basis of strains and to develop more sensitive strain typing assays in humans we have analyzed PrPSc biochemical properties in two experimental setting. In the first we compared the size of the core after protease digestion and the glycoform pattern of PrPSc before and after transmission of human prions to non human primates or bank voles, whereas in the second we analyzed the conformational stability of PrPSc associated with sCJD, vCJD or fCJD using guanidine hydrochloride (GdnHCl) as denaturant. Combining the results of the two studies, we were able to distinguish five human strains for at least one biochemical property. The present data extend our knowledge about the extent of strain variation and its relationship with PrPSc properties in human TSEs.

Sleep-wake disturbances in sporadic Creutzfeldt-Jakob disease

BACKGROUND: The prevalence and characteristics of sleep-wake disturbances in sporadic Creutzfeldt-Jakob disease (sCJD) are poorly understood. METHODS: Seven consecutive patients with definite sCJD underwent a systematic assessment of sleep-wake disturbances, including clinical history, video-polysomnography, and actigraphy. Extent and distribution of neurodegeneration was estimated by brain autopsy in six patients. Western blot analyses enabling classification and quantification of the protease-resistant isoform of the prion protein, PrPSc, in thalamus and occipital cortex was available in four patients. RESULTS: Sleep-wake symptoms were observed in all patients, and were prominent in four of them. All patients had severe sleep EEG abnormalities with loss of sleep spindles, very low sleep efficiency, and virtual absence of REM sleep. The correlation between different methods to assess sleep-wake functions (history, polysomnography, actigraphy, videography) was generally poor. Brain autopsy revealed prominent changes in cortical areas, but only mild changes in the thalamus. No mutation of the PRNP gene was found. CONCLUSIONS: This study demonstrates in sporadic Creutzfeldt-Jakob disease, first, the existence of sleep-wake disturbances similar to those reported in fatal familial insomnia in the absence of prominent and isolated thalamic neuronal loss, and second, the need of a multimodal approach for the unambiguous assessment of sleep-wake functions in these patients.