clam tissue
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Toxins ◽  
2020 ◽  
Vol 12 (3) ◽  
pp. 178 ◽  
Author(s):  
Melissa Bolotaolo ◽  
Tomofumi Kurobe ◽  
Birgit Puschner ◽  
Bruce G Hammock ◽  
Matt J. Hengel ◽  
...  

Harmful cyanobacterial blooms compromise human and environmental health, mainly due to the cyanotoxins they often produce. Microcystins (MCs) are the most commonly measured group of cyanotoxins and are hepatotoxic, neurotoxic, and cytotoxic. Due to MCs ability to covalently bind to proteins, quantification in complex matrices is difficult. To analyze bound and unbound MCs, analytical methods were optimized for analysis in sediment and clam tissues. A clean up step was incorporated to remove lipids, improving percent yield. This method was then applied to sediment and clam samples collected from the Sacramento–San Joaquin River Delta (Delta) in the spring and fall of 2017. Water samples were also tested for intracellular and extracellular MCs. These analyses were used to quantify the partitioning of MCs among sediment, clams, and water, and to examine whether MCs persist during non-summer months. Toxin analysis revealed that multiple sediment samples collected in the Delta were positive for MCs, with a majority of the positive samples from sites in the San Joaquin River, even while water samples from the same location were below detection limit. These data highlight the importance of analyzing MCs in complex matrices to accurately evaluate environmental risk.


2019 ◽  
Vol 70 (4) ◽  
pp. 324 ◽  
Author(s):  
S. Bejaoui ◽  
I. Rabeh ◽  
F. Ghribi ◽  
F. Aouini ◽  
I. Chetoui ◽  
...  

This study aimed to provide information about the changes in fatty acid composition and quality in Ruditapes decussatus tissue after four culinary treatments (steamed, baked, grilled and fried). All treated samples showed a significant decrease in moisture and protein. In contrast, a significant increase in fat content resulted from the grilled and fried treatments. Saturated fatty acid was significantly higher in fresh clams than all cooking processes, except in fried ones. Monounsaturated fatty acid and polyunsaturated fatty acid varied significantly between fresh and cooked clams with high values recorded for fried clams. The n-3/n-6 ratio, peroxide index, EPA+DHA and atherogenicity index decreased significantly after the cooking processes particularly in fried clams. The mineral levels (Mg, Ca and Mn) of cooked clams decreased considerably with grilled and fried treatments. The impacts of cooking on the fatty acid composition and protein content in clam tissue was evaluated by lipid peroxidation (TBARS, PV, FFA, TOR) and protein oxidation (AOPP and PCO), which varied statistically in fried, steamed, grilled and baked samples; indicating alterations in cooked clam tissues structure. Based on our results, steaming is recommended for the preparation of clams because it preserves the most nutritional tissue quality.


2015 ◽  
Vol 75 (1) ◽  
pp. 8-12 ◽  
Author(s):  
YBM. Carvalho ◽  
LA. Romano ◽  
LHS. Poersch

The aim of this study was to determine the lethal salinity (LC50) for the yellow clam Mesodesma mactroides (Bivalvia: Mesodesmatidae) and identify histopathological alterations that could be used to diagnose structural changes in clam tissue. Clams in two size classes (adults and juveniles) were placed in 10 L chambers and exposed to salinities of 35, 30, 25, 20, 15, 10, and 5 g/L. There were triplicate chambers with seven clams each for each salinity. The LC50 values for a 48 h exposure were 6.5 g/L and 5.7 g/L for adults and juveniles, respectively. For a 96 h exposure, the LC50 values were 10.5 g/L for adults and 8.8 g/L for juveniles. The histological examination of yellow clams exposed to 10 g/L for 96 h showed intercellular oedema and necrotic foci in the epithelium of the digestive gland and occlusion of the lumen of the digestive gland. In conclusion, M. mactroides can be characterised as a moderately euryhaline species, tolerating salinities from 35 to 15 g/L.


2004 ◽  
Vol 6 (4) ◽  
pp. 378-385 ◽  
Author(s):  
Masaharu Ishikura ◽  
Kiyoshi Hagiwara ◽  
Kiyotaka Takishita ◽  
Miyuki Haga ◽  
Kenji Iwai ◽  
...  

1999 ◽  
Vol 85 (1) ◽  
pp. 30-34 ◽  
Author(s):  
Thaddeus K. Graczyk ◽  
Ronald Fayer ◽  
David Bruce Conn ◽  
Earl J. Lewis

1990 ◽  
Vol 47 (5) ◽  
pp. 904-914 ◽  
Author(s):  
Scott E. Belanger ◽  
Jerry L. Farris ◽  
Donald S. Cherry ◽  
John Cairns Jr.

Studies designed to evaluate impacts of copper (Cu) on Asiatic clams, Corbicula fluminea, in artificial stream and field environments were conducted. Adult and juvenile responses (survival and growth) to Cu, relevance to Cu bioaccumulation, site-specific comparisons, and the relation to observed densities of resident clams at an impacted site were assessed. Juveniles were more sensitive than adults; however, clam tissue and shell growth were significantly impaired (p < 0.001) for both juveniles and adults at 8.4–26.7 μg Cu/L in artificial streams. Tissue levels of Cu were 2.5–6 times greater at 8.4–26.7 μg/L exposure concentrations compared with background body burdens in unexposed clams. In studies conducted at the Clinch River, Virginia power plant, clam growth was reduced at 22.5–104.8 μg/L at a water hardness (180 mg/L) that was more than two times the hardness in artificial streams. Clam population densities in the river were well correlated with outcomes of field growth studies. Corbicula fluminea growth patterns are a clear and interpretable indicator of Cu contamination in natural and artificial streams and represent a viable alternative to contemporary chronic testing protocols.


1988 ◽  
Vol 71 (5) ◽  
pp. 994-999 ◽  
Author(s):  
Jean E Matusik ◽  
George P Hoskin ◽  
James A Sphon

Abstract Coprostanol is a major fecal sterol in humans and may, therefore, be a good indicator of sewage-polluted waters. Some types of edible seafood, such as clams, that live in these waters may be contaminated with coprostanol. Coprostanol from clam tissue extracts had been previously quantitated by gas chromatography (GC). In the present work, capillary column GC was used to separate coprostanol, and electron ionization mass spectrometry was used to confirm its identity. Confirmation of identity of coprostanol at the 75 ng level was obtained by comparing the spectrum of the authentic standard with spectra of the clam tissue extract obtained under the same instrumental conditions. Various other compounds can be eliminated as potential interferences by virtue of either their different GC retention times or their spectra.


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