28 research outputs found

    Age And Growth Of The Smooth Dogfish (Mustelus canis) In The Northwest Atlantic Ocean

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    The northwest Atlantic population of smooth dogfish (Mustelus canis) ranges from Cape Cod, Massachusetts, to South Carolina. Although M. canis is seasonally abundant in this region, very little is known about important aspects of its biology, such as growth and reproductive rates. In the early 1990s, commercial fishery landings of smooth dogfish dramatically increased on the east coast of the United States. This study investigated growth rates of the east coast M. canis population through analysis of growth patterns in vertebral centra. Marginal increment analysis, estimates of precision, and patterns in seasonal growth supported the use of vertebrae to age these sharks. Growth bands in vertebral samples were used to estimate ages for 894 smooth dogfish. Age-length data were used to determine von BertalanfFy growth parameters for this population: K = 0.292/yr, L-infinity = 123.57 cm, and t(0) = -1.94 years for females, and K = 0.440/yr, L-infinity = 105.17 cm, and t(0) = -1.52 years for males. Males matured at two or three years of age and females matured between four and seven years of age. The oldest age estimate for male and female samples was ten and sixteen years, respectively

    Environmental Emission of Pharmaceuticals from Wastewater Treatment Plants in the USA

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    The residual drugs, drug bioconjugates, and their metabolites, mostly from human and veterinary usage, are routinely flushed down the drain, and enter wastewater treatment plants (WWTP). Increasing population, excessive use of allopathic medicine, continual introduction of novel drugs, and existing inefficient wastewater treatment processes result in the discharge of large volumes of pharmaceuticals and their metabolites from the WWTPs into the environment. The effluent from the WWTPs globally contaminate ~25% of rivers and the lakes. Pharmaceuticals in the environment, as contaminants of emerging concerns, behave as pseudo-persistent despite their relatively short environmental half-lives in the environment. Therefore, residual levels of pharmaceuticals in the environment not only pose a threat to the wildlife but also affect human health through contaminated food and drinking water. This chapter highlights WWTPs as point-sources of their environmental emissions and various effects on the aquatic and terrestrial ecosystem

    Mechanisms for the Evolution of a Derived Function in the Ancestral Glucocorticoid Receptor

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    Understanding the genetic, structural, and biophysical mechanisms that caused protein functions to evolve is a central goal of molecular evolutionary studies. Ancestral sequence reconstruction (ASR) offers an experimental approach to these questions. Here we use ASR to shed light on the earliest functions and evolution of the glucocorticoid receptor (GR), a steroid-activated transcription factor that plays a key role in the regulation of vertebrate physiology. Prior work showed that GR and its paralog, the mineralocorticoid receptor (MR), duplicated from a common ancestor roughly 450 million years ago; the ancestral functions were largely conserved in the MR lineage, but the functions of GRs—reduced sensitivity to all hormones and increased selectivity for glucocorticoids—are derived. Although the mechanisms for the evolution of glucocorticoid specificity have been identified, how reduced sensitivity evolved has not yet been studied. Here we report on the reconstruction of the deepest ancestor in the GR lineage (AncGR1) and demonstrate that GR's reduced sensitivity evolved before the acquisition of restricted hormone specificity, shortly after the GR–MR split. Using site-directed mutagenesis, X-ray crystallography, and computational analyses of protein stability to recapitulate and determine the effects of historical mutations, we show that AncGR1's reduced ligand sensitivity evolved primarily due to three key substitutions. Two large-effect mutations weakened hydrogen bonds and van der Waals interactions within the ancestral protein, reducing its stability. The degenerative effect of these two mutations is extremely strong, but a third permissive substitution, which has no apparent effect on function in the ancestral background and is likely to have occurred first, buffered the effects of the destabilizing mutations. Taken together, our results highlight the potentially creative role of substitutions that partially degrade protein structure and function and reinforce the importance of permissive mutations in protein evolution

    p21WAF1/CIP1expression in stage I cutaneous malignant melanoma: its relationship with p53, cell proliferation and survival

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    The expression of p21, p53 and proliferating cell nuclear antigen (PCNA) was analysed by immunohistochemistry in a consecutive series of 369 clinical stage I cutaneous malignant melanoma patients. Correlation of the detected expression levels with each other, with clinicopathological data and with melanoma survival were statistically evaluated. p21 expression was significantly associated with p53 and PCNA expression levels. In addition, high levels of p53 and PCNA were significantly interrelated. Tumour thickness, recurrent disease, high TNM category and older (≥ 55 years) age at diagnosis were inversely associated with p21 expression. Gender, bleeding, tumour thickness, Clark's level of invasion, TNM category and p53 index were all important predictors of both recurrence-free and overall survival of melanoma. In Cox's multivariate analysis including 164 patients with a complete set of data, only high tumour thickness and bleeding predicted poor recurrence-free survival (P= 0.0042 and 0.0087 respectively) or overall survival (P= 0.0147 and 0.0033 respectively). Even though elevated p21 expression may be associated with more favourable prognosis in clinical stage I cutaneous melanoma, our results suggest that cell cycle regulatory effects of p21 can be overcome by some other and stronger, partly yet unknown, mechanisms. 1999 Cancer Research Campaig

    Mercury Accumulation and Effects in the Brain of the Atlantic Sharpnose Shark (Rhizoprionodon terraenovae)

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    Few published studies have examined whether the elevated concentrations of the nonessential toxic metal mercury (Hg) often observed in shark muscle also occur in the shark brain or whether Hg accumulation affects shark neurophysiology. Therefore, this study examined accumulation and distribution of Hg in the shark brain, as well as effects of Hg on oxidative stress in the shark central nervous system, with particular focus on the Atlantic sharpnose shark (Rhizoprionodon terraenovae). Sharks were collected along the southeastern U.S. coast throughout most of this species’ U.S. geographical range. Total Hg (THg) concentrations were measured in and compared between shark muscle and brain, whereas known biomarkers of Hg-induced neurological effects, including glutathione depletion, lipid peroxidation, and concentrations of a protein marker of glial cell damage (S100b), were measured in shark cerebrospinal fluid. Brain THg concentrations were correlated with muscle THg levels but were significantly lower and did not exceed most published thresholds for neurological effects, suggesting limited potential for detrimental responses. Biomarker concentrations supported this premise, because these data were not correlated with brain THg levels. Hg speciation also was examined. Unlike muscle, methylmercury (MeHg) did not comprise a high percentage of THg in the brain, suggesting that differential uptake or loss of organic and inorganic Hg and/or demethylation of MeHg may occur in this organ. Although Hg accumulation in the shark brain generally fell below toxicity thresholds, higher THg levels were measured in the shark forebrain compared with the midbrain and hindbrain. Therefore, there is potential for selective effects on certain aspects of shark neurophysiology if brain Hg accumulation is increased

    The Genetic Connectivity of a Euryhaline Elasmobranch, the Atlantic Stingray (Dasyatis sabina)

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    Identifying the genetic connectivity of elasmobranchs inhabiting coastal waters remains an important global priority, as these species are particularly susceptible to human mediated impacts and declines given their close proximity to highly populated areas. The Atlantic stingray (Dasyatis sabina), a small, coastal species whose range spans the western North Atlantic (Florida to Chesapeake Bay) and Gulf of Mexico, is one of the few elasmobranchs capable of occupying both estuarine and freshwater habitats. Within Florida waters, a putative ‘resident’ population inhabits the freshwater St. Johns River System (SJRS); however, the extent of this population’s connectivity to the remainder of its distribution remains unknown. To examine the genetic connectivity of the Atlantic stingray across its southern US distribution, including the SJRS, a total of 312 individuals from 11 sampling locations were genotyped at nine species-specific microsatellite loci. Population- and individual-level analyses identified high levels of genetic population structure among collections, with coastal populations within the Gulf of Mexico showing high genetic structure (FST = 0.011 – 0.034; P \u3c0.05) and a signal of isolation by distance (R2 = 0.957; P = 0.041). Interestingly, individual-based analyses showed that freshwater SJRS animals were differentiated from other locations, suggesting that these individuals may truly represent a ‘resident’ freshwater population. The presence of high genetic population structure, coupled with what may be locally adapted populations, suggests that care must be taken to conserve this species, as the extinction of even a single population may result in the irreversible loss of genetic diversity and adaptive potential

    Diet shift and site-fidelity of oceanic whitetip sharks Carcharhinus longimanus along the Great Bahama Bank

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    Identifying the driving forces behind oceanic pelagic shark movements is key to a better understanding of their life history. Some oceanic pelagic shark species have been shown to aggregate in specific regions to mate and/or exploit abundant food resources. The oceanic whitetip shark Carcharhinus longimanus, a subtropical, ectothermic, oceanic pelagic shark that has experienced severe population declines, aggregates seasonally around Cat Island (CI) in The Bahamas. Large pelagic teleosts (e.g. billfish, tunas, and dolphinfish) are abundant in this region and oceanic whitetips are anecdotally reported to feed heavily on recreationally caught teleosts. However, it was unknown whether feeding habits at CI substantially differ from longer-term feeding habits. We used tag-recapture to assess site-fidelity of adult oceanic whitetips to CI and stable isotope analysis (SIA) of 2 different tissues (blood plasma and white muscle) to compare short- and long-term feeding patterns. The relatively high recapture rate (20.3%) confirmed that individual whitetips exhibit site-fidelity to CI. The aggregation consisted of adult individuals; females were more common, more than half were gravid, and no physical or behavioral evidence of mating or parturition was observed at CI. SIA-based Bayesian mixing model estimates of short-term (near CI) diets showed more large pelagic teleosts (72%) than in long-term diets (47%), showing a spatiotemporal difference in oceanic whitetip feeding habits. This suggests that availability of large teleost prey is a possible mechanism underpinning site-fidelity and aggregation of whitetips at CI. These results provide insight into the function of one of the last known aggregations of this once-abundant top predator

    Associations between total mercury, trace minerals, and blood health markers in Northwest Atlantic white sharks (Carcharodon carcharias)

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    The ecology and life-histories of white sharks make this species susceptible to mercury bioaccumulation; however, the health consequences of mercury exposure are understudied. We measured muscle and plasma total mercury (THg), health markers, and trace minerals in Northwest Atlantic white sharks. THg in muscle tissue averaged 10.0 mg/kg dry weight, while THg in blood plasma averaged 533 μg/L. THg levels in plasma and muscle were positively correlated with shark precaudal length (153-419 cm), and THg was bioaccumulated proportionally in muscle and plasma. Nine sharks had selenium:mercury molar ratios in blood plasma \u3e1.0, indicating that for certain individuals the potential protective effects of the trace mineral were diminished, whereas excess selenium may have protected other individuals. No relationships between plasma THg and any trace minerals or health markers were identified. Thus, we found no evidence of negative effects of Hg bioaccumulation, even in sharks with very high THg
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