Isotopic Studies (isotopic + studies)

Distribution by Scientific Domains


Selected Abstracts


Digestion and Assimilation of the Free-living Nematode Panagrellus redivivus Fed to First Feeding Coregonid Larvae: Evidence from Histological and Isotopic Studies

JOURNAL OF THE WORLD AQUACULTURE SOCIETY, Issue 1 2005
Christian Schlechtriem
The free-living nematode Panagrellus redivivus is a potential source of live food for first feeding fish. The digestion and assimilation of nematodes by larval fish were investigated with the aid of a histological and stable isotope approach. Larvae of whitefish Coregonus lavaretus were reared for 8 d with nematodes and compared with an unfed control. Nematodes were readily ingested by 3-d-old larvae. Different stages of nematode digestion could be observed in transverse sections of fish larvae sampled on Day 6 at regular intervals after feeding. Nematodes were produced on corn medium. In this way nematodes with a stable carbon isotope signature clearly different from the isotopic pattern of the fish larvae could be obtained. Stable carbon isotope signatures for lipids and lipid-free matter of fish larvae sampled on Days 2 and 8 after first feeding were clearly influenced by the stable isotopic pattern of the nematodes. The high acceptance of the nematodes by Coregonus lavaretus larvae and the early onset of digestion and nutrient retention positively confirm the potential of PanagreUus redivivus as a live food for first feeding fish larvae. [source]


The role of mass spectrometry to study the Oklo,Bangombé natural reactors,

MASS SPECTROMETRY REVIEWS, Issue 5 2007
J.R. De Laeter
Abstract The discovery of the existence of chain reactions at the Oklo natural reactors in Gabon, Central Africa in 1972 was a triumph for the accuracy of mass spectrometric measurements, in that a 0.5% anomaly in the 235U/238U ratio of certain U ore samples indicated a depletion in 235U. Mass spectrometric techniques thereafter played a dominant role in determining the nuclear parameters of the reactor zones themselves, and in deciphering the geochemical characteristics of various elements in the U-rich ore and in the surrounding rock strata. The variations in the isotopic composition of a large number of elements, caused by a combination of nuclear fission, neutron capture and radioactive decay, provide a powerful tool for investigating this unique geological environment. Mass spectrometry can be used to measure the present-day elemental and isotopic abundances of numerous elements, so as to decipher the past history of the reactors and examine the retentivity/mobility of these elements. Many of the fission products have a radioactive decay history that have been used to date the age and duration of the reactor zones, and to provide insight into their nuclear and geochemical behavior as a function of time. The Oklo fission reactors and their near neighbor at Bangombé, some 30 km to the south-east of Oklo, are unique in that not only did they become critical some 2,×,109 years ago, but also the deposits have been preserved over this period of geological time. The long-term geochemical behavior of actinides and fission products have been extensively studied by a variety of mass spectrometric techniques over the past 30 years to provide us with significant information on the mobility/retentivity of this material in a natural geological repository. The Oklo,Bangombé natural reactors are therefore geological analogs that can be evaluated in terms of possible radioactive waste containment sites. As more reactor zones were discovered, it was realized that they could be classified into two groups according to their burial depth in the Oklo mine-site. Reactor Zones 10, 13, and 16 were buried more deeply, and were therefore less weathered than the other zones. The less-weathered zones are of great importance in mobility/retentivity studies and therefore to the question of radioactive waste containment. Isotopic studies of these natural reactors are also of value in physics to examine possible variations in fundamental constants over the past 2 billion years. © 2007 Wiley Periodicals, Inc., Mass Spec Rev 26:683,712, 2007 [source]


Basin geochemistry and isotopic ratios of fishes and basal production sources in four neotropical rivers

ECOLOGY OF FRESHWATER FISH, Issue 3 2007
David B. Jepsen
Abstract,,, We analysed stable carbon and nitrogen isotopic ratios of dissolved inorganic carbon (DIC), plants, detritus and fishes to estimate the relative importance of dominant production sources supporting food webs of four Venezuelan rivers with divergent geochemical and watershed characteristics. Based on samples taken during the dry season at each site, fishes from two nutrient-poor, blackwater rivers had significantly lower ,13C values (mean = ,31.4, and ,32.9,) than fishes from more productive clearwater and whitewater rivers (mean = ,25.2, and ,25.6, respectively). Low carbon isotopic ratios of fishes from blackwaters were likely influenced by low ,13C of DIC assimilated by aquatic primary producers. Although floodplains of three savanna rivers supported high biomass of C4 grasses, relatively little carbon from this source appeared to be assimilated by fishes. Most fishes in each system assimilated carbon derived mostly from a combination of microalgae and C3 macrophytes, two sources with broadly overlapping carbon isotopic signatures. Even with this broad overlap, several benthivorous grazers from blackwater and whitewater rivers had isotopic values that aligned more closely with algae. We conclude that comparative stable isotopic studies of river biota need to account for watershed geochemistry that influences the isotopic composition of basal production sources. Moreover, isotopic differences between river basins can provide a basis for discriminating spatial and temporal variation in the trophic ecology of fishes that migrate between watersheds having distinct geochemical characteristics. [source]


Chemical and isotopic signatures of Na/HCO3/CO2 -rich geofluids, North Portugal

GEOFLUIDS (ELECTRONIC), Issue 4 2006
J. M. MARQUES
Abstract Geochemical and isotopic studies have been undertaken to assess the origin of CO2 -rich waters issuing in the northern part of Portugal. These solutions are hot (76°C) to cold (17°C) Na,HCO3 mineral waters. The ,2H and ,18O signatures of the mineral waters reflect the influence of altitude on meteoric recharge. The lack of an 18O-shift indicates there has been no high temperature water,rock interaction at depth, corroborating the results of several chemical geothermometers (reservoir temperature of about 120°C). The low 14C activity (up to 9.9 pmC) measured in some of the cold CO2 -rich mineral waters (total dissolved inorganic carbon) is incompatible with the presence of 3H (from 1.7 to 4.1 TU) in those waters, which indicates relatively short subsurface circulation times. The ,13C values of CO2 gas and dissolved inorganic carbon range between ,6, and ,1, versus Vienna-Peedee Belemnite, indicating that the total carbon in the recharge waters is being diluted by larger quantities of CO2 (14C-free) introduced from deep-seated (upper mantle) sources, masking the 14C-dating values. The differences in the 87Sr/86Sr ratios of the studied thermal and mineral waters seem to be caused by water,rock interaction with different granitic rocks. Chlorine isotope signatures (,0.4, < ,37Cl < +0.4, versus standard mean ocean chloride) indicate that Cl in these waters could be derived from mixing of a small amount of igneous Cl from leaching of granitic rocks. [source]


Photosynthetic pathways, spatial distribution, isotopic ecology, and implications for pre-Hispanic human diets in central-western Argentina

INTERNATIONAL JOURNAL OF OSTEOARCHAEOLOGY, Issue 2 2009
C. Llano
Abstract In a number of areas around the world researchers have begun to use the isotopic values of subsistence resources as a means of determining diets of human populations. The objective of the present study is to classify the plant species present at distinct altitudes in southern Mendoza Province, Argentina, considering photosynthetic pathways in order to determine their ,13C isotopic signature. This will help to understand the relationships between diets and the isotopic values observed in archaeological human remains. Data compiled from various sources are used to establish the photosynthetic pathways and mean ,13C values. The results indicate that C3 species are dominant at high-altitude settings, and that the few identified C4 species were found primarily at lower altitudes. These results are intended to serve as a foundation for future isotopic studies designed to address relationships among species at different trophic levels. Copyright © 2009 John Wiley & Sons, Ltd. [source]


The petrous bone,A new sampling site for identifying early dietary patterns in stable isotopic studies

AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, Issue 2 2009
Marie Louise S. Jřrkov
Abstract Intraskeletal variation in the composition of carbon (,13C) and nitrogen (,15N) stable isotopes measured in collagen is tested from various human bones and dentine. Samples were taken from the femur, rib, and petrous part of the temporal bone from well-preserved skeletons of both adults (n = 34) and subadults (n = 24). Additional samples of dentine from the root of 1st molars were taken from 16 individuals. The skeletal material is from a medieval cemetery (AD 1200,1573) in Holbćk, Denmark. Our results indicate that the petrous bone has an isotopic signal that differs significantly from that of femur and rib within the single skeleton (P < 0.001 and P < 0.001, respectively), with only minor variation seen between femur and rib. On the other hand, there was no significant difference between the petrous bone and the 1st molar. The intraskeletal variation may reflect differences in turnover rate among skeletal elements. The inner periosteal layer of the petrous bone is formed in uterus and does not undergo any further remodelling after the age of 2 years, whereas the rib and femur have a continuous turnover rate of ,5 and 10,20 years, respectively. From the results of this study it is believed the petrous bone may be a new useful bone element and a supplement or a proxy for teeth in the analysis of early dietary patterns as it may reflect diet in fetal stages and early years of life. Am J Phys Anthropol 2009. © 2008 Wiley-Liss, Inc. [source]


REE, Mn, Fe, Mg and C, O Isotopic Geochemistry of Calcites from Furong Tin Deposit, South China: Evidence for the Genesis of the Hydrothermal Ore-forming Fluids

RESOURCE GEOLOGY, Issue 1 2010
Yan Shuang
Abstract The Furong tin deposit in the central Nanling region, South China, consists of three main types of mineralization ores, i.e. skarn-, altered granite- and greisen-type ores, hosted in Carboniferous and Permian strata and Mesozoic granitic intrusions. Calcite is the dominant gangue mineral intergrown with ore bodies in the orefield. We have carried out REE, Mn, Fe, and Mg geochemical and C, and O isotopic studies on calcites to constrain the source and evolution of the ore-forming fluids. The calcites from the Furong deposit exhibit middle negative Eu anomaly (Eu/Eu*= 0.311,0.921), except for one which has an Eu/Eu* of 1.10, with the total REE content of 5.49,133 ppm. The results show that the calcites are characterized by two types of REE distribution patterns: a LREE-enriched pattern and a flat REE pattern. The LREE-enriched pattern of calcites accompanying greisen-type ore and skarn-type ore are similar to those of Qitianling granite. The REE, Mn, Fe, and Mg abundances of calcites exhibit a decreasing tendency from granite rock mass to wall rock, i.e. these abundances of calcites associated with altered granite-type and greisen-type ores are higher than those associated with skarn-type ores. The calcites from primary ores in the Furong deposit show large variation in carbon and oxygen isotopic compositions. The ,13C and ,18O of calcites are ,0.4 to ,12.7, and 2.8 to 16.4,, respectively, and mainly fall within the range between mantle or magmatic carbon and marine carbonate. The calcites from greisen and altered granite ores in the Furong deposit display a negative correlation in the diagram of ,13C versus ,18O, probably owing to the CO2 -degassing of the ore-forming fluids. From the intrusion to wall-rock, the calcites display an increasing tendency with respect to ,13C values. This implies that the carbon isotopic compositions of the ore-bearing fluids have progressively changed from domination by magmatic carbon to sedimentary carbonate carbon. In combination with other geological and geochemical data, we suggest that the ore-forming fluids represent magmatic origin. We believe that the fluids exsolved from fractionation of the granitic magma, accompanying magmatism of the Qitianling granite complex, were involved in the mineralization of the Furong tin polymetallic deposit. [source]