Distribution of Radioactive and Stable Zinc in an Experimental Marine Ecosystem

1971 ◽  
Vol 28 (11) ◽  
pp. 1783-1788 ◽  
Author(s):  
Ford A. Cross ◽  
James N. Willis ◽  
John P. Baptist

The distribution of radioactive and stable Zn in an experimental marine ecosystem is described. We added 1 mCi of 65Zn to 2000 liters of sea water and a mixed community of planktonic and benthic algae in a fiberglass tank, after which the ecosystem was left undisturbed for 9 months. We then measured the 65Zn specific activities for (1) particulate Zn (0.45 μ filterable), (2) extractable Zn (from water passed through a 0.45-μ filter and then treated with dithizone), (3) total dissolved Zn (from samples passed through a 0.45-μ filter and treated with acid prior to extraction with dithizone), and (4) dialyzable Zn. Zinc-65 specific activities were not significantly different among the extractable, dialyzable, or acid-treated samples of the water. Further, absolute concentrations of 65Zn and total Zn were no higher in the acid-treated samples than in the extracted or dialyzed samples, which indicates that nearly all of the soluble Zn in the water was dithizone-extractable and dialyzable. Zinc-65 specific activities were significantly less, however, in the particulate material than in the water. This difference indicates that equilibrium of Zn between particulate material and water had not been reached after 9 months. Three months later (December 1969) 65Zn specific activities were determined again for particulate material and total dissolved Zn. The mean specific activity of 65Zn in the particulate samples showed a small but significant increase, but it was still less than in the water. Concentration factors in the particulate matter were 980 for 65Zn and 1400 for total Zn. Samples of benthic algae taken in March 1970 had a mean specific activity of 65Zn similar to the mean 65Zn specific activity of water samples taken 3 months earlier.

2017 ◽  
Vol 14 (3) ◽  
pp. 619-624
Author(s):  
Baghdad Science Journal

In this research the specific activity of natural radionuclides 226Ra, 232Th and 40K were determined by sodium iodide enhanced by thallium NaI(TI) detector and assessed the annual effective dose in Dielac 1 and 2 and Nactalia 1 and 2 for children of less than 1 year which are available in Baghdad markets. The specific activity of 40K has the greater value in all the types which is in the range of allowed levels globally that suggested by UNSCEAR. The mean value of annual effective doses were 2.92, 4.005 and 1.6325 mSv/y for 226Ra, 232Th and 40K respectively.


2010 ◽  
Vol 79 (9) ◽  
pp. S85-S91 ◽  
Author(s):  
Petr Dvořák ◽  
Petr Snášel ◽  
Katarína Beňová

The aim of the study was to find the sources of 137Cs in wild boar food in the natural ecosystem. The main emphasis is focused on the analyses of wild boar muscles and the content of wild boar stomach. Boars weighing 20 to 100 kg were killed at two locations. The highest specific activities of muscles were measured in boars originated from the Dvorce location; the average specific activity in boars killed on 14 April 2007 and 9 March 2008 achieved 132 Bq kg-1. Due to high fluctuation the differences between the mean values of 31 Bq kg-1 in males and 43 Bq kg-1 in females were not significant. Earthworms from grass fields with a specific activity of 16 Bq kg-1, rootlets from the Šabrava location with 200 Bq kg-1 and Elaphomyces granulatus fruiting bodies with 4,743 Bq kg-1 and 2,858 Bq kg-1 are the components of boar food with the 137Cs specific activities higher than that of the detection limit. Consequently, underground mushrooms probably represent the main source of radiocesium in the food chain of boars. A remarkable reduction of 137Cs specific activities in boar muscles is not expected at the post-Chernobyl radiocesium contaminated locations with the occurrence of Elaphomyces granulatus within next two decades.


2012 ◽  
Vol 79 (1) ◽  
pp. 177-184 ◽  
Author(s):  
Dana E. Hunt ◽  
Yajuan Lin ◽  
Matthew J. Church ◽  
David M. Karl ◽  
Susannah G. Tringe ◽  
...  

ABSTRACTMarine microbial communities are complex and dynamic, and their ecology impacts biogeochemical cycles in pelagic ecosystems. Yet, little is known about the relative activities of different microbial populations within genetically diverse communities. We used rRNA as a proxy for activity to quantify the relative specific activities (rRNA/ribosomal DNA [rDNA or rRNA genes]) of the eubacterial populations and to identify locations or clades for which there are uncouplings between specific activity and abundance. After analyzing 1.6 million sequences from 16S rDNA and rRNA (cDNA) libraries from two euphotic depths from a representative site in the Pacific Ocean, we show that although there is an overall positive relationship between the abundances (rDNAs) and activities (rRNAs) among populations of the bacterial community, for some populations these measures are uncoupled. Different ecological strategies are exemplified by the two numerically dominant clades at this site: the cyanobacteriumProchlorococcusis abundant but disproportionately more active, while the heterotrophic SAR11 is abundant but less active. Other rare populations, such asAlteromonas, have high specific activities in spite of their low abundances, suggesting intense population regulation. More detailed analyses using a complementary quantitative PCR (qPCR)-based approach of measuring relative specific activity forProchlorococcuspopulations in the Pacific and Atlantic Oceans also show that specific activity, but not abundance, reflects the key drivers of light and nutrients in this system; our results also suggest substantial top-down regulation (e.g., grazing, viruses, or organismal interactions) or transport (e.g., mixing, immigration, or emigration) of these populations. Thus, we show here that abundance and specific activity can be uncoupled in open ocean systems and that describing both is critical to characterizing microbial communities and predicting marine ecosystem functioning and responses to change.


1989 ◽  
Vol 259 (2) ◽  
pp. 333-339 ◽  
Author(s):  
O Colard ◽  
M Breton ◽  
D Pepin ◽  
F Chevy ◽  
G Bereziat ◽  
...  

The origin of the arachidonate released from platelets on stimulation with thrombin was investigated by comparing the specific activities of released arachidonate and of arachidonoyl-containing phospholipids using rat platelets prelabelled with arachidonate. Quantification of the released arachidonate was determined in the presence of BW 755 C, a dual cyclo-oxygenase/lipoxygenase inhibitor, which was found not to modify the arachidonate mobilization between the platelet phospholipids. The phospholipid molecular species were analysed by h.p.l.c. of diradylglycerol benzoate derivatives of diacyl, alkylacyl and alkenylacyl classes. The labelled/unlabelled arachidonate ratio varied greatly in the phospholipids depending on whether an ether or acyl bond was present in sn-1 position of the glycerol, on the length and degree of unsaturation of this fatty chain and on the polar head group. Between 15 s and 5 min of stimulation by thrombin, the released arachidonate kept a constant specific activity which was considerably lower than the specific activity of diacyl-GPC. The specific activity of the released arachidonate was intermediate between the specific activities of the 16:0-20:4 and 18:0-20:4 species of diacyl-GPI and diacyl-GPE, and corresponded to the mean specific activity of alkylacyl-GPC. The data indicate that the released arachidonate cannot come directly from diacyl-GPC, and that two phospholipids in particular can act as direct precursors of the released arachidonate. These are (1) the alkylacyl-GPC and (2) the diacyl-GPE whose hydrolysis would induce an arachidonate transfer from diacyl-GPC.


The study has unequivocally demonstrated that siliceous sponges Spirastrella cuspidifera and Prostylyssa foetida from the same microecological niche exhibit a high degree of species specificity, while accumulating a host of heavy metal ions (Ni, Cr, Cd, Sn, Ti, Mo, Zr). S. cuspidifera accumulated, in addition, 60 Co and 63 Ni, showing discrimination against other radionuclides, 137 Cs and 131 I, present in the ambient waters receiving controlled low level waste discharges from a B. W. R. nuclear power station. P. foetida , on the other hand, accumulated only 131 I and showed discrimination against other radionuclides including 60 Co, although the stable iodine concentrations in both the sponges were the same. The specific activity of 60 Co (in becquerels per gram of 59 Co) in S. cuspidifera and 131 I (in becquerels per gram of 127 I) in P. foetida were at least two orders of magnitude greater than in the ambient sea water. That of 63 Ni (in becquerels per gram of 62 Ni) in S. cuspidifera , on the other hand, was lower by two orders of magnitude than in either abiotic matrices from the same environment. Thus, not only did both the species show bioaccumulation of a specific element, but also preferential uptake of isotopes of the same element, though they were equally available for intake. Such differential uptake of isotopes can possibly be explained in terms of two quite different mechanisms operating, each applicable in a particular case. One is that the xenobiotic isotope enters the environment in a physicochemical form or as a complex different from that of its natural counterpart. If equilibration with the latter is slow, so that the organism acquires the xenobiotic in an unfamiliar chemical context, it may treat it as a chemically distinct entity so that its concentration factor differs from that of stable isotope, thus changing the specific activity. Alternatively, if the xenobiotic is present in the same chemical form as the stable isotope, the only way in which specific activities can be modified is by fractionation on the basis of mass of isotope. In view of the remarkable concentration factors observed for stable and radioactive isotopes of the same element and the specific activities reached, it is desirable that species of sponges, especially from the coastal and estuarine environments, be monitored to detect levels of pollution due to anthropogenic substances.


2020 ◽  
Vol 2020 ◽  
pp. 1-11
Author(s):  
Lucia Nyiva Munyao ◽  
Daniel Kipngetich Ketui ◽  
Calford Otieno ◽  
Margaret Wairimu Chege

Construction sand is naturally polluted with radionuclides of terrestrial origin. In this study, specific activities of 238U, 232Th, and 40K in 30 sand samples collected along the Ekalakala River, Machakos County, Kenya, were measured using a high-purity germanium γ-ray spectrometer. The specific activities ranged between 9.7 Bqkg−1 and 24.0 Bqkg−1, 11.5 Bqkg−1 and 26.2 Bqkg−1, and 820 Bqkg−1 and 1850 Bqkg−1 for 238U, 232Th, and 40K, respectively. While the mean specific activities for 238U and 232Th were less than half of the world average values of 33 Bqkg−1 and 45 Bqkg−1, respectively, the average specific activity of 40K was significant since it was three times the global mean value of 420 Bqkg−1. A calculated absorbed radiation dose rate for the sand varied between 46.8 nGyh−1 and 94.2 nGyh−1 with a mean of 68.5 ± 13.3 nGyh−1. This is not significantly different from the world average dose rate of 60 nGyh−1 for geological samples. The AEDR and Hex had maximum values of 0.29 mSvy−1 and 0.52, respectively, both within the recommended limits of radiation exposure for members of the general public. Based on these results, the sand from Ekalakala River does not pose significant health implication to the sand harvesters as well as the inhabitants of the houses constructed using this sand.


1993 ◽  
Vol 69 (05) ◽  
pp. 430-435 ◽  
Author(s):  
Colin Longstaff ◽  
Man-Yu Wong ◽  
Patrick J Gaffney

SummaryAn international collaborative study has been carried out to investigate the reproducibility of hirudin assays in 13 laboratories using four recombinant hirudins and one natural, sulphated product. A simple assay procedure was proposed involving the titration of α-thrombin with inhibitor and measurement of residual activity using a chromogenic substrate. A standard α-thrombin preparation was supplied to ensure that this reagent was of uniform quality throughout the study. The method appeared to present no difficulties and laboratories reported similar potencies for the 5 hirudin samples, in line with expected values. This gave 200–222 Thrombin Inhibitory Units/ampoule (TIU/ampoule) of lyophilised hirudin, with geometric coefficient of variation (gcv) values ranging from 10.15–15.97%. This corresponds to specific activities of approximately 14,300–15,900 TIU/mg protein. This is close to the upper limit of previously reported values of specific activity. We conclude that the precision of this determination compared with the wider range of values in the literature (8,000–16,000 thrombin inhibitory units [TIU]/mg) results from the use of good quality standard α-thrombin by all laboratories. This study has important implications for hirudin standardisation.


1972 ◽  
Vol 71 (1) ◽  
pp. 24-36 ◽  
Author(s):  
Ariel Gordin ◽  
Pirkko Saarinen

ABSTRACT An account is given of a methodological study of the double-antibody radioimmunoassay of human TSH, using highly purified labelled human TSH as tracer. It was shown that conventional paper electrophoresis was not adequate for studying the purity of labelled human TSH. When polyvinylchloride (Pevikon®) electrophoresis was used, four subfractions could still be separated, even though, on paper electrophoresis, the material seemed to be homogeneous. Only two of the four Pevikon fractions were immunoreactive. Purification of labelled human TSH by Pevikon electrophoresis also improved the sensitivity of the assay. Specific activities of about 100 mCi/mg gave the highest initial binding capacity, produced least damage to the labelled hormone and showed the best stability of the tracer without influencing the sensitivity of the method. In different storage conditions, labelled human TSH was found to be most stable at −20°C and diluted 1/100. Only in pregnancy did the addition of HCG seem necessary. The mean TSH value in healthy subjects was 3.6 ± 1.4 μU/ml (mean±sd) with a range from 1.6 μU/ml to 8.8 μU/ml.


2021 ◽  
Vol 9 (3) ◽  
pp. 522
Author(s):  
Lyudmila V. Gromova ◽  
Elena I. Ermolenko ◽  
Anastasiya L. Sepp ◽  
Yulia V. Dmitrieva ◽  
Anna S. Alekseeva ◽  
...  

In recent years, great interest has arisen in the use of autoprobiotics (indigenous bacteria isolated from the organism and introduced into the same organism after growing). This study aimed to evaluate the effects of indigenous bifidobacteria on intestinal microbiota and digestive enzymes in a rat model of antibiotic-associated dysbiosis. Our results showed that indigenous bifidobacteria (the Bf group) accelerate the disappearance of dyspeptic symptoms in rats and prevent an increase in chyme mass in the upper intestine compared to the group without autoprobiotics (the C1 group), but significantly increase the mass of chyme in the colon compared to the C1 group and the control group (healthy animals). In the Bf group in the gut microbiota, the content of opportunistic bacteria (Proteus spp., enteropathogenic Escherichia coli) decreased, and the content of some beneficial bacteria (Bifidobacterium spp., Dorea spp., Blautia spp., the genus Ruminococcus, Prevotella, Oscillospira) changed compared to the control group. Unlike the C1 group, in the Bf group there was no decrease in the specific activities of maltase and alkaline phosphatase in the mucosa of the upper intestine, but the specific activity of maltase was decreased in the colon chyme compared to the control and C1 groups. In the Bf group, the specific activity of aminopeptidase N was reduced in the duodenum mucosa and the colon chyme compared to the control group. We concluded that indigenous bifidobacteria can protect the microbiota and intestinal digestive enzymes in the intestine from disorders caused by dysbiosis; however, there may be impaired motor function of the colon.


Genetics ◽  
1982 ◽  
Vol 100 (1) ◽  
pp. 79-87
Author(s):  
Daniel W Nebert ◽  
Nancy M Jensen ◽  
Hisashi Shinozuka ◽  
Heinz W Kunz ◽  
Thomas J Gill

ABSTRACT Forty-four inbred and four randombred rat strains and 20 inbred mouse strains were examined for their Ah phenotype by determining the induction of liver microsomal aryl hydrocarbon (benzo[a]pyrene) hydroxylase activity (EC 1.14.14.1) by intraperitoneal treatment with either β-naphthoflavone or 3-methylcholanthrene. All 48 rat strains were found to be Ah-responsive. The maximally induced hydroxylase specific activities of the ALB/Pit, MNR/Pit, MR/Pit, SHR/Pit, and Sprague-Dawley strains were of the same order of magnitude as the basal hydroxylase specific activities of the ACI/Pit, F344/Pit, OKA/Pit, and MNR/N strains. Six of the 20 mouse strains were Ah-nonresponsive (i.e. lacking the normal induction response and presumably lacking detectable amounts of the Ah receptor). The basal hydroxylase specific activities of the BDL/N, NFS/N, STAR/N, and ST/JN mouse strains were more than twice as high as the maximally induced hydroxylase specific activity of the CBA/HT strain.——To date, 24 Ah-nonresponsive mouse strains have been identified, out of a total of 68 known to have been characterized. The reasons for not finding a single Ah-nonresponsive inbred rat strain—as compared with about one Ah-nonresponsive inbred mouse strain found for every three examined—remain unknown.


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