Biochemical responses of the mussel Perna perna after exposure to environmental concentrations of the UV filter Benzophenone-3.

Personal care products, such as UV filters, are frequently present in aquatic ecosystems, but studies on their impact on marine organisms are still scarce. Here we addressed the effects of benzophenone-3 (BP-3) on the antioxidant status of Perna perna mussels exposed to concentrations of 0.1 and 3 µg.L-1 for 72 h and 7 days. Glutathione peroxidase (GPx), glutathione reductase (GR), glutathione S-transferase (GST), glucose-6-phosphate dehydrogenase (G6PDH) activity and lipoperoxidation (MDA) were evaluated in the gills. A significant reduction (p < 0.05) in the activity of G6PDH and GPx was observed after exposure for 7 days to 0.1 µg.L-1. However, no significant differences were observed in GST activity and MDA levels, independently of the exposure time. Principal component analysis (PCA) showed an association of BP-3 highest concentration with GR and MDA at 72 h and only with GR at 7 days of exposure. Similarly, the integrated biomarker response (IBR) demonstrated GR and MDA alterations. In conclusion, environmentally relevant concentrations of BP-3 altered antioxidant and auxiliary enzymes, which could cause long-term damage to P.perna mussels. The need to implement more efficient techniques in wastewater treatment systems is pointed out, especially in summer, when UV filters are used more frequently and abundantly.

Biochemical metal accumulation effects and metalloprotein metal detoxification in environmentally exposed tropical Perna perna mussels.

Marine bivalves have been widely applied as environmental contamination bioindicators, although studies concerning tropical species are less available compared to temperate climate species. Assessments regarding Perna perna mytilid mussels, in particular, are scarce, even though this is an extremely important species in economic terms in tropical countries, such as Brazil. To this end, Perna perna mytilids were sampled from two tropical bays in Southeastern Brazil, one anthropogenically impacted and one previously considered a reference site for metal contamination. Gill metallothionein (MT), reduced glutathione (GSH), carboxylesterase (CarbE) and lipid peroxidation (LPO) were determined by UV-vis spectrophotometry, and metal and metalloid contents were determined by inductively coupled plasma mass spectrometry (ICP-MS). Metalloprotein metal detoxification routes in heat-stable cellular gill fractions were assessed by size exclusion high performance chromatography (SEC-HPLC) coupled to an ICP-MS. Several associations between metals and oxidative stress endpoints were observed at all four sampling sites through a Principal Component Analysis. As, Cd, Ni and Se contents, in particular, seem to directly affect CarbE activity. MT is implicated in playing a dual role in both metal detoxification and radical oxygen species scavenging. Differential SEC-HPLC-ICP-MS metal-binding profiles, and, thus, detoxification mechanisms, were observed, with probable As-, Cu- and Ni-GSH complexation and binding to low molecular weight proteins. Perna perna mussels were proven adequate tropical bioindicators, and further monitoring efforts are recommended, due to lack of data regarding biochemical metal effects in tropical species. Integrated assessments, as performed herein demonstrate, are invaluable in evaluating contaminated aquatic environments, resulting in more accurate ecological risk assessments.

Effects of DCOIT (4,5-dichloro-2-octyl-4-isothiazolin-3-one) to the haemocytes of mussels Perna perna.

Bivalve molluscs rely only on an innate immune system to execute cellular and humoral processes. Haemocytes, the haemolymph circulating cells, play a major role in this type of immunity, principally regarding cellular defences. Considering that environmental pollutants can affect the immune system of invertebrates, this work evaluated the effects of the antifouling biocide 4,5-dicloro-2-n-octil-4-isotiazolin-3-ona (DCOIT) on the haemocytes of mussels Perna perna. Individuals were exposed to 0 (control), 0.1 µg L-1 and 10 µg L-1 of DCOIT for up to 96 h. The analysed parameters included: total (THC) and differential (DHC) haemocyte count, cellular viability, adhesion capacity, phagocytic activity, levels of reactive oxygen species and DNA damage. Moreover, the stress on stress (SOS) response of mussels was analysed as a general stress index. The results show that DCOIT increased the haemocyte adhesion capacity and caused a decrease in THC and in the haemocyte viability after 24 h of exposure. After 96 h of exposure, DCOIT only affected the haemocyte adhesion capacity, which was decreased by biocide exposure. Moreover, exposure to DCOIT for 96 h did not affect the capacity for air survival of mussels. These results indicate that DCOIT interferes in important parameters associated with the innate immunity of P. perna, mainly after 24 h of exposure. It is suggested that the animals were able to develop some compensatory response strategy, making them more resistant to the biocide.

Ecotoxicological effects of losartan on the brown mussel Perna perna and its occurrence in seawater from Santos Bay (Brazil).

The antihypertensive losartan (LOS) has been detected in wastewater and environmental matrices, however further studies focused on assessing the ecotoxicological effects on aquatic ecosystems are necessary. Considering the intensive use of this pharmaceutical and its discharges into coastal zones, our study aimed to determine the environmental concentrations of LOS in seawater, as well as to assess the biological effects of LOS on the marine bivalve Perna perna. For this purpose, fertilization rate and embryolarval development were evaluated through standardized assays. Phase I (ethoxyresorufin O­deethylase EROD and dibenzylfluorescein dealkylase DBF) and II (glutathione S-transferase GST) enzymes, glutathione peroxidase (GPx), Cholinesterase (ChE), lipoperoxidation (LPO) and DNA damage were used to analyze sublethal responses in gills and digestive gland of adult individuals. Lysosomal membrane stability was also assessed in hemocytes. Our results showed the occurrence of LOS in 100% of the analyzed water samples located in Santos Bay, Sao Paulo, Brazil, in a range of 0.2 ng/L-8.7 ng/L. Effects on reproductive endpoints were observed after short-term exposure to concentrations up to 75 mg/L. Biomarker responses demonstrated the induction of CYP450 like activity and GST in mussel gills exposed to 300 and 3000 ng/L of LOS, respectively. GPx activity was also increased in concentration of exposure to 3000 ng/L of LOS. Cyto-genotoxic effects were found in gills and hemocytes exposed in concentrations up to 300 ng/L. These results highlighted the concern of introducing this class of contaminants into marine environments, and pointed out the need to include antihypertensive compounds in environmental monitoring programs.

Interannual variability in Dinophysis spp. abundance and toxin accumulation in farmed mussels (Perna perna) in a subtropical estuary.

This study evaluated an 8-year dataset (2007 to 2015, except 2008) in the attempt to identify the most susceptible periods for the occurrence of diarrheic shellfish poisoning (DSP) episodes associated with the presence of toxigenic dinoflagellates, Dinophysis spp., in the mussel farming area of Babitonga Bay (southern Brazil). Dinophysis acuminata complex was the most frequent (present in 66% of the samples) and abundant (max. 4100 cells L-1) taxon, followed by D. caudata (14%; max. 640 cells L-1) and D. tripos (0.9%; max. 50 cells L-1). There was a marked onset of the annual rise in Dinophysis spp. abundance during weeks 21-25 (early winter) of each year, followed by a second peak on week 35 (spring). Mussel (Perna perna) samples usually started testing positive in DSP mouse bioassays (MBA) in late winter. Positive results were more frequent in 2007 and 2011 when the mean D. acuminata complex abundance was ~ 500 cells L-1. Although positive DSP-MBA results were observed in only 11% of the samples during the studied period, the toxin okadaic acid (OA) was present in 90% of the analyzed mussels (max. 264 µg kg-1). MBA results were positive when D. acuminata complex cell densities exceed 1200 ± 300 cells L-1, while trace toxin amounts could be detected at cell densities as low as 150 ± 50 cells L-1 (free OA) to 200 ± 100 cells L-1 (conjugated OA). Low salinity and the meteorological conditions triggered by La Niña events were the main factors associated with both Dinophysis abundance and OA accumulation in mussels.

Continuous Exposure to Microplastics Does Not Cause Physiological Effects in the Cultivated Mussel Perna perna.

The environmental impact of microplastics is a challenging theme, especially under realistic experimental conditions. We investigated physiological responses to 0.1-1.0 µm PVC particles intake by the mussel Perna perna after a relative long-term exposure (90 days) at a less extreme concentration compared with previous studies (0.125 g/L). Microplastic intake was inferred by the presence of PVC in the feces of mussels, and physiological damages were assessed through ingestion rate, assimilation efficiency, growth rate, cellular and molecular biomarkers (lysosomal integrity, lipid peroxidation, and DNA damage), and condition index. All physiological responses showed nonsignificant effects of the microplastics on the exposed mussels. We suggest that, despite the experimental concentration of microplastics, mussels were able to acclimate to the exposure through their abilities for long-term recovery and tolerance to stresses. These data have positive implications for environmental health and in terms of human food resource because mussel farming is a worldwide practice that heavily relies on plastic materials, increasing the chances of microplastic exposure and mussels contamination.

Exposure to crack cocaine causes adverse effects on marine mussels Perna perna.

Our study aimed to evaluate crack cocaine effects in different life stages of the marine mussel Perna perna. For this purpose, fertilization rate, embryo-larval development, lysosomal membrane stability and DNA strand breaks were assessed. Effect concentrations in gametes and in larval development were found after 1h (IC50=23.53mg·L-1) and 48h (IC50=16.31mg·L-1), respectively. The highest tested concentration showing no acute toxicity (NOEC) was 10mg·L-1, while the lowest observed effect concentration (LOEC) was 20mg·L-1. NOEC concerning embryo-larval development was 0.625mg·L-1, while the LOEC was 1.25mg·L-1. Cyto-genotoxic effects were evidenced in mussels exposed to crack cocaine concentrations ranging from 5 to 500µg·L-1. Our results report the first data on effects of an illicit drug to marine organisms and should encourage further ecotoxicological studies of these contaminants of emerging concern in coastal ecosystems.

Hypoxia effects on oxidative stress and immunocompetence biomarkers in the mussel Perna perna (Mytilidae, Bivalvia).

This study investigated the effects of hypoxia on oxidative stress response and immune function in mussels Perna perna exposed to air for 6, 12, 24 and 48 h. In air-exposed mussels, the antioxidant enzymes superoxide dismutase (SOD), catalase, and glutathione reductase (GR) activities were lower in gill tissues (24-48 h) and digestive gland (12 h), while the glutathione peroxidase and GR activities were increased in the digestive gland (48 h). In both tissues, aerial exposure promoted a rapid (6 h) and persistent (up to 48 h) increase of glutathione levels. Decreased hemocyte count and viability, as well as increased phagocytic activity and cellular adhesion capacity were detected after prolonged aerial exposure (>12 h). In summary, induction of thiol pools, altered antioxidant enzyme activities, and activation of immune responses were detected in hypoxia exposed brown mussels, indicating hypoxia induced tissue-specific responses in both antioxidant and immune systems.

Detachment, displacement and reattachment activity in a freshwater byssate mussel (Limnoperna fortunei): the effects of light, temperature and substratum orientation.

The ability of the freshwater bivalve Limnoperna fortunei to voluntarily detach from the substratum, crawl and reattach as a function of illumination, temperature, substratum orientation, and mussel size was investigated. Thirty-two per cent of the 879 experimental animals detached and reattached elsewhere at least once during five- to eight-day experiments. The proportions of mobile mussels were significantly higher in permanent darkness than under permanent illumination. Displacement distances were also higher in darkness, but statistical differences with illuminated individuals were inconclusive. No evidence of circadian rhythms was detected. Mobile mussels were often significantly smaller than non-mobile individuals. It was not possible to detect the effect of water temperature (22°C and 31°C), or substratum orientation (topside and underside) on mussel mobility, but because the power of the statistical tests was low, future experiments are needed to confirm this result. The ability of mussels to voluntarily detach and reattach elsewhere has important implications for biofouling control.

Ecological relevance of Sentinels' biomarker responses: a multi-level approach.

In response to the need for more sensitive and rapid indicators of environmental quality, sublethal effects on the lowest levels of biological organization have been investigated. The ecological relevance of these responses assumes a prevailing role to assure effectiveness as indicator of ecological status. This study aimed to investigate the linkages between biomarker responses of caged bivalves and descriptive parameters of macrobenthic community structure. For this purpose a multi-level environmental assessment of marine and estuarine zones was performed in São Paulo coast, Brazil. Multivariate analysis was applied to identify linkages between biological responses and ecological indices, as well as to characterizing the studied stations. Individuals of the marine mussel Perna perna caged along Santos Bay showed signs of oxidative stress, lysosomal membrane destabilization, histological alterations and reduced embryonic development. The estuarine oyster Crassostrea rhizophorae caged along Santos Port Channel showed alterations on biotransformation enzymes and antioxidant system, DNA damage and lysosomal membrane destabilization. The benthic community analysis showed reduced richness and diversity in the same areas of the Santos bay and estuary where biomarker responses were altered. Our results revealed that xenobiotics are inducing physiological stress, which may lead to changes of the benthic community structure and deterioration of the ecological status over time. Integrating biomarker responses and ecological indexes improved certainty that alterations found at community level could be related to xenobiotic as stressors, which was very useful to improve the discriminatory power of the environmental assessment.

[Metallothioneins in Perna viridis (Bivalvia: Mytilidae): seasonal variation and its relation to reproductive biology]. / Metalotioninas en Perna viridis (bivalvia: mytilidae): variación estacional y su relación con la biologia reproductiva.

Metallothionein is a cytosolic protein found in a variety of tissues and have been involved in the regulation of essential trace metals such as copper and zinc, and in the detoxification of essential and nonessential metals. With the aim to study their seasonal variation and their possible role in reproductive behavior, we evaluated metallothioneins (Mts) in Perna viridis, taken from Rio Caribe and Chacopata localities in the North coast of Sucre state, Venezuela. A total of 325 samples were obtained from February to December 2003. We determined the following biometric indices in bivalves: Condition Index (CI), meat yield (RC) and dry weight-length relationship (PSL). Besides, Mts in whole tissue were separated by molecular exclusion chromatography, Sephadex G-50 and quantified by saturation with cadmium. Our results showed that the biometric indices (RC and PSL) had seasonal variations between localities and maturity stages, with the exception of IC. No significant differences were found between sexes. Mts showed seasonal variations between localities, with the highest concentrations between February and March, and minimum ones between September and December, coinciding with the respectively high and low productivity periods in the area. The mussels from Rio Caribe had higher Mts concentration than those from Chacopata. Furthermore, immature mussels showed the highest Mts concentration while the lowest was found in spawned specimens. We found a significant negative relationship between Mts and CI. Our results demonstrated that MTs in Perna viridis are influenced by the condition index and reproductive status, as well as physico-chemical factors in the marine environment.

Metalotioninas en Perna viridis (Bivalvia: Mytilidae): variación estacional y su relación con la biología reproductiva / Metallothioneins in Perna viridis (Bivalvia: Mytilidae): seasonal variation and its relation to reproductive biology

Metallothionein is a cytosolic protein found in a variety of tissues and have been involved in the regulation of essential trace metals such as copper and zinc, and in the detoxification of essential and nonessential metals. With the aim to study their seasonal variation and their possible role in reproductive behavior, we evaluated metallothioneins (Mts) in Perna viridis, taken from Rio Caribe and Chacopata localities in the North coast of Sucre state, Venezuela. A total of 325 samples were obtained from February to December 2003. We determined the following biometric indices in bivalves: Condition Index (CI), meat yield (RC) and dry weight-length relationship (PSL). Besides, Mts in whole tissue were separated by molecular exclusion chromatography, Sephadex G-50 and quantified by saturation with cadmium. Our results showed that the biometric indices (RC and PSL) had seasonal variations between localities and maturity stages, with the exception of IC. No significant differences were found between sexes. Mts showed seasonal variations between localities, with the highest concentrations between February and March, and minimum ones between September and December, coinciding with the respectively high and low productivity periods in the area. The mussels from Rio Caribe had higher Mts concentration than those from Chacopata. Furthermore, immature mussels showed the highest Mts concentration while the lowest was found in spawned specimens. We found a significant negative relationship between Mts and CI. Our results demonstrated that MTs in Perna viridis are influenced by the condition index and reproductive status, as well as physicochemical factors in the marine environment.

Las metalotioninas (Mts) son proteínas de baja masa molecular que juegan un rol importante en la detoxificación de metales, en vista de su papel ecotoxicológico se evaluaron las metalotioneínas (MTs) en 350 ejemplares del bivalvo Perna viridis en dos localidades de la costa norte del estado Sucre, desde febrero hasta diciembre 2003. Se determinaron los índices biométricos: índice de condición (IC), rendimiento de carne (RC) y relación peso seco-talla (PSL). Las Mts fueron separadas por cromatografía de exclusión molecular, Sephadex G-50 y se cuantificaron por saturación con cadmio. Los índices biométricos (RC y PSL) mostraron variaciones estacionales, entre localidades y estados de madurez, con la excepción del CI. No se encontraron diferencias significativas entre sexos. Las Mts mostraron variaciones estacionales, con concentraciones más elevadas entre febrero y marzo y mínimos entre septiembre y diciembre, que coincidieron con los períodos de alta y baja productividad en el área, respectivamente. Los mejillones de Río Caribe presentaron una mayor concentración de Mts que los de Chacopata. Los mejillones inmaduros mostraron la mayor concentración de Mts y la más baja en los desovados. Se encontró una relación negativa y significativa entre Mts y CI. Los resultados demuestran que las Mts de Perna viridis están influidas por el índice de condición y la condición reproductiva, asi como también pot los factores físico-químicos del ambiente marino.

Physiological energetics of the brown mussel Perna perna (L.) transplanted in the Itajaí-Açu river mouth, Southern Brazil.

Groups of the mussel Perna perna were transplanted to two points and at three different depths in the coastal region close to the Itajaí-Açu River mouth, an impacted river in the south of Brazil. With the objective of evaluating the physiology changes in the organisms in relation to the control area (origin of the organisms), the clearance, respiration and excretion rates, absorption efficiency and growth were estimated. The levels of metals in the organism tissue were determined in an attempt to explain the physiological changes occurring in the study area. Organisms from Point 2 placed near the bottom showed physiological changes in comparison to the control and the transplanted organisms from Point 1. Point 2 showed greater sediment resuspension and availability of trace metals to the organisms closer to the bed. The increase in Cr concentration in the tissues of the organisms (up to 0.21 mg kg(-1) ww) was not sufficient to explain the decrease in the inhibition of clearance (28.8%) and in the absorption efficiency (15.7%), or the increased excretion rate (282.5%), which led to the organisms having a reduced scope for growth (48.6%). This indicates the possible presence of other contaminants, which were not measured, and which probably had synergistic action with the trace metals investigated.

Food availability and reproduction affects lipid and fatty acid composition of the brown mussel, Perna perna, raised in suspension culture.

We examined the influence of the reproductive cycle and environmental factors on variations of the condition index (CI), tissue dry mass, shell size, total lipid content, and relative percent of fatty acids in the mussel, Perna perna. Spat or juveniles were reared to commercial size (70 mm) in suspension culture in the Golfo de Cariaco, Venezuela between May and October 2004. The dry mass of soft tissues and shell, a visual assessment of gonadal status and the organism lipid profile were established every fortnight. In parallel, we measured the environmental conditions, following chlorophyll a, salinity, temperature and seston levels. After an initial decrease, the CI rose and remained high until August after which it decreased continuously until October. Total lipid values also decreased initially, after which they showed two periods of rapid recuperation and depletion, the first between May and August and the second between August and October. Similar tendencies were noted in the fatty acids, C18:3n-3, C18:4n-3 and C22:6n-3. Correlation analysis found no significant relationships between environmental parameters and the variations in total lipids. However, significant correlations were noted between fatty acids and specific environmental parameters. In particular, temperature was inversely correlated with C14:0, C16:1n-7, C18:0, C18:1n-9 and 20:5n-3. Chlorophyll a was positively correlated with C14:0, C16:1n-7, C18:1n-7, C18:4n-3 and 20:4n-6. On the other hand, gametogenesis had an effect on C14:0, C16:1n-7, C18:1n-9 and C18:1n-7, while spawned and gonadal regression states had an effect on fatty acid 20:4n-6. Temperature and chlorophyll a levels strongly influenced the proportion of mussels spawning, suggesting that their influence upon lipid composition may be secondary to their impact upon reproduction. Despite the thermal stability of this tropical system, the lipid composition of mussels changed markedly during the study, reflecting the central role of diet and reproductive investment upon lipid composition.

Trace metals in mussel shells and corresponding soft tissue samples: a validation experiment for the use of Perna perna shells in pollution monitoring.

The uptake of Cr, Mn, Ni, Cu, Zn, Cd and Pb in soft tissue of Perna perna mussels and their shells has been studied in aquarium experiments in which mussels were exposed for 30 or 60 days to seawater spiked with different concentrations of these contaminants (125 and 500 microg L(-1)). Tissue samples were analyzed after acid digestion by conventional solution nebulization ICP-MS. Laser ablation ICP-MS was used for the quantitative determination of trace elements in different areas of the corresponding shells. With the exception of Mn and Zn, all other elements studied showed a significant concentration enhancements in soft tissue, with the magnitude of this enhancement following the order: Cr > Ni > Cd > Cu > Pb. A corresponding increase in most contaminants, although less pronounced, was also observed in the newly formed growth rings of mussel shells, contributing to the validation of Perna perna mussel shell as a bioindicator of toxic elements.

Temporal genetic differentiation in cultured and natural beds of the brown mussel Perna perna (Mytilidae).

Perna perna is the most important cultivated mussel of Santa Catarina, Brazil, sustaining an important economic input for many local families. Natural stocks of P. perna are depleted by the extraction of adults and seeds for consumption and culture. The aim of the present study was to use the microsatellite locus pms-2 to study the variation of the genetic composition and diversity between natural and cultured stocks in samples of 2001 and 2005 from Penha, Santa Catarina. DNA was extracted from adductor muscle by Chelex/proteinase-K and phenol/chloroform protocols. Amplification by polymerase chain reaction was performed using specific primers for analyzing the pms-2 locus. Polymerase chain reaction products were submitted to vertical denatured 6% polyacrylamide gel electrophoresis and horizontal 2% agarose gel electrophoresis, and visualized by silver staining and ethidium bromide, respectively. Allele diversity and heterozygote deficiency were higher for samples of 2005 than for those of 2001. No significant genetic differentiation was found between natural and cultured stocks of 2001 by the chi(2) test, but G(2) (likelihood ratio) detected slight differences (I = 0.949; chi(2), P = 0.147; G(2), P = 0.046), while cultured and natural stocks of 2005 were very different (I = 0.798, P = 0.006). Between the years of 2001 and 2005, a large change in genetic composition was observed (I = 0.582; P < 0.001). Although nothing is known about natural changes in the genetic composition of this species with time, the results suggest a strong impact of human activities on natural stocks of P. perna, which is expected to be related to heavy extraction and farming.

Oxidative stress in Perna perna and other bivalves as indicators of environmental stress in the Brazilian marine environment: antioxidants, lipid peroxidation and DNA damage.

Oxidative stress can take place in marine bivalves under a series of environmental adverse conditions. The study of different systems related to oxidative stress in these organisms can give important information about their physiological status and also about environmental health. Bivalves have been proposed as good sentinel organisms in pollution monitoring studies through the analysis of biochemical biomarkers, and most of the biomarkers analyzed are those related to oxidative stress. However, it is very important to know how other environmental factors not associated to the presence of pollutants might affect these parameters. We have studied a series of mechanisms related to oxidative stress in mussels which inhabit the Brazilian coast, especially in Perna perna species, subjected to different stress conditions, such as the exposure to different contaminants in the laboratory and in the field, the exposure of mussels to air and re-submersion, simulating the tidal oscillations, and in mussels collected at different seasons. Both oxidative damage levels and antioxidant defense systems were strongly affected by the different environmental stress. This review summarizes the data obtained in some studies carried out in bivalves from the Brazilian coast.

Temporal genetic differentiation in cultured and natural beds of the brown mussel Perna perna (Mytilidae)

Perna perna is the most important cultivated mussel of Santa Catarina, Brazil, sustaining an important economic input for many local families. Natural stocks of P. perna are depleted by the extraction of adults and seeds for consumption and culture. The aim of the present study was to use the microsatellite locus pms-2 to study the variation of the genetic composition and diversity between natural and cultured stocks in samples of 2001 and 2005 from Penha, Santa Catarina. DNA was extracted from adductor muscle by Chelex/proteinase-K and phenol/chloroform protocols. Amplification by polymerase chain reaction was performed using specific primers for analyzing the pms-2 locus. Polymerase chain reaction products were submitted to vertical denatured 6% polyacrylamide gel electrophoresis and horizontal 2% agarose gel electrophoresis, and visualized by silver staining and ethidium bromide, respectively. Allele diversity and heterozygote deficiency were higher for samples of 2005 than for those of 2001. No significant genetic differentiation was found between natural and cultured stocks of 2001 by the c2 test, but G2 (likelihood ratio) detected slight differences (I = 0.949; c2, P = 0.147; G2, P = 0.046), while cultured and natural stocks of 2005 were very different (I = 0.798, P = 0.006). Between the years of 2001 and 2005, a large change in genetic composition was observed (I = 0.582; P < 0.001). Although nothing is known about natural changes in the genetic composition of this species with time, the results suggest a strong impact of human activities on natural stocks of P. perna, which is expected to be related to heavy extraction and farming

Physiological rates in different classes of sizes of Perna perna (Linnaeus, 1758) submitted to experimental laboratory conditions.

Physiological studies of the mussel Perna perna in Brazil are almost 30 years behind those of other, more exhaustively investigated species, such as Mytilus edulis. Little is known about the variations in physiological rates due to size and the consequences of maintaining P. perna in laboratory conditions. This work investigated the variations in respiration, clearance, excretion and absorption efficiency rates of P. perna, classified by size and acclimatized in a laboratory, monitoring the mussels respiration rates and biometry over a period of 30 days, in laboratory conditions. The respiration, clearance and excretion rates presented an allometric relation with the dry weight of the organisms, with b values of 0.66, 0.48 and 0.91 respectively. On the other hand, these same rates, when considered by weight (specific rates) showed a relationship that was inverse to the size of the organisms. Only the absorption efficiency was independent of the weight of the mussel. In terms of acclimatization, it was observed that it takes 10 days for the respiration rate of the mussel P. perna to stabilize in laboratory conditions, after which it follows a routine metabolism.

Confiabilidade do teste de salto vertical com 4 séries de 15 segundos / Reliability of the four series 15-second vertical jumping test

OBJETIVO: O objetivo deste estudo foi verificar a confiabilidade do teste e reteste do teste salto vertical com quatro séries de 15 segundos (TSVI). MÉTODO: Dezoito atletas do sexo masculino, divididos em 11 handebolistas (25,74 ± 4,71 anos; 85,84 ± 7,63kg; 182,14 ± 3,46cm) e sete basquetebolistas (18,60 ± 0,77 anos; 83,32 ± 10,02kg; 188,14 ± 5,76cm) foram os voluntários desse estudo. As variáveis estudadas para o teste e reteste foram o pico de potência (PP), potência média (PM), índice de fadiga (IF). Os desempenhos dessas variáveis foram mensurados através do teste de salto vertical com quatro séries de 15 segundos com 10 segundos de recuperação entre as séries. O tratamento estatístico foi realizado através da técnica descritiva e do coeficiente de correlação intraclasse (CCI). RESULTADOS: Os resultados demonstraram um alto CCI nas medidas repetidas em dias diferentes para todas as variáveis: PP (R = 0,992; p = 0,0360); PM (R = 0,993; p = 0,0107) e IF (R = 0,981; p = 0,0556); além disso, indicaram altos coeficientes de correlações entre teste e reteste para os indicadores de qualidade nas medidas da técnica de salto vertical com contramovimento sem auxílio dos membros superiores (CMJ) (R = 0,991; p = 0,0800), nos números de saltos em um trabalho de 15 e 60 segundos (NSV15s, R = 0,936; p = 0,0062 e NSV60s, R = 0,978; p = 0,0139) e na altura saltada, em um trabalho de 15 e 60 segundos (SV15s, R = 0,993; p = 0,0467; e SV60s, R = 0,988; p = 0,0014). CONCLUSÃO: A análise dos dados aponta para a existência de uma medida confiável do TSVI na estimativa da resistência de força explosiva através das variáveis PM e IF.

PURPOSE: The purpose of this study was to check the reliability of the vertical jumping test and re-test in four series of the 15-seconds test (IVJT). METHOD: Eighteen male volunteer athletes participated in this study, and they were divided as follows: eleven handball players (25.74 ± 4.71 years; 85.84 ± 7.63 kg; 182.14 ± 3.46 cm), and seven basketball players (18.60 ± 0.77 years; 83.82 ± 10.02 kg; 188.14 ± 5.76 cm). The assessed variables for the test and re-test were: power peak (PP), mean power (MP), and fatigue index (FI). The performances attained by them in these variables were measured through the vertical jumping test in four series of the 15-seconds test with 10 seconds recovery between series. The statistical treatment was performed through the descriptive technique and the intraclass correlation coefficient (ICC). RESULTS: The results have shown a high ICC in the repeated measurements performed in different days for every variable: PP (r = 0.992; p = 0.0360); MP (r = 0.993; p = 0.0107); and FI (r = 0.981; p = 0.0556). Added to this, it was found high correlation coefficients between the test and re-test as to the quality indicators in the measurements of the vertical jumping technique with counter-movement without the help of the upper limbs (CMJ) (r = 0.991; p = 0.0800), for the amount of jumps together with a 15 and 60 seconds work (AVJ15s, r = 0.936; p = 0.0062, and AVJ60s, r = 0.978; p = 0.0139) and in the jumped height, in a 15 and 60 seconds work (VJ15s, r = 0.993; p = 0.0467, and VJ60s, r = 0.988; p = 0.0014). CONCLUSION: The data analysis pointed out the existence of a reliable measurement of the IVJT when assessing the explosive strength resistance through the MP and FI variables.

OBJETIVO: El objetivo de este estudio era verificar la fiabilidad de la prueba y retesteo de la prueba el salto vertical con cuatro series de 15 segundos (TSVI). MÉTODO: Dieciocho atletas varones, divididos en once handbolistas (25,74 ± 4,71 años; 85,84 ± 7,63 kg; 182,14 ± 3,46 centímetros) y siete basquetbolistas (18,60 ± 0,77 años; 83,32 ± 10,02 kg; 188,14 ± 5,76 centímetros) todos voluntarios de ese estudio. VARIABLES: Se estudiaron para la prueba y los retesteos de pico de potencia (PP), la potencia (PM), el índice de fatiga (SI). Las acciones de los primeros variaron de moderado a través de la prueba de salto vertical con cuatro series de 15 segundos con 10 segundos de recuperación entre cada serie. El tratamiento estadístico fue cumplido a través de la técnica descriptiva, y del coeficiente de intra-clase de la correlación (CCI). RESULTADOS: Los resultados demostraron una CCI alta en las medidas repetidas en días diferentes para todas las variables: PP (R = 0,992; el p = 0,0360); PM (R = 0,993; el p = 0,0107) y SI (R = 0,981; el p = 0,0556); además, ellos indicaron coeficientes altos de correlaciones entre la prueba y retesteo para los indicadores de calidad en las medidas de la técnica de salto vertical CMJ (R = 0,991; el p = 0,0800), en los números de saltos en un trabajo de 15 y 60 segundos (NSV15s, R = 0,936; el p = 0,0062 y NSV60s, R = 0,978; el p = 0,0139) y en la altura saltada, en un trabajo de 15 y 60 segundos (SV15s, R = 0,993; el p = 0,0467; y SV60s, R = 0,988; el p = 0,0014). CONCLUSIONES: El análisis de los datos aponta para la existencia de una medida fiable de TSVI en la estimación de la resistencia de fuerza explosiva a través de las variables PM y SI.