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根据国内外大量实际资料,从碘的分布情况及其所处的地质条件,结合石油和天然气形成过程、油气藏类型及其分布特点,探讨高碘卤水分布的规律及其形成条件,在此基础上指出了我国的找碘方向。 相似文献
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Iodine contents of soils developed over the major rock formations of the northern zone of the Eastern Pontide Tectonic Belt
(Northeastern Turkey) have been investigated with respect to soil-parent rock relationship, effect of topography, elevation,
and climate to construe its effect on the health of the local population. Samples were collected from the A and B horizons
of the soils developed over the major stratigraphic units constituting the eastern Pontides, including the Lower Basic Complex
of Jurassic-Lower Cretaceous age, the Berdiga limestone (Jurassic-lower Cretaceous), the Dagbasi granitoid (Upper Cretaceous),
volcano-sedimentary sequence of Upper Cretaceous age, ore-bearing and barren dacites of Upper Cretaceous age, and Neogene
alkaline basalts. Chemical analyses of soil samples indicate significantly lower iodine abundances for all the soils studied
(5–28 ppm) in comparison to the average abundance of iodine in analogous soils of other parts of the world (22–93 ppm). The
concentration of iodine in soils developed over the same geologic formation decrease with increasing elevation. In certain
cases, this decrease may reach up to 70%. Goiter is highly common throughout this region in Turkey. The results of this study
suggest that the iodine deficiency of region’s soils may be a principal underlying cause for this area of Turkey being an
endemic goiter region. 相似文献
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Lisa K. Whalley Kate L. Furneaux Tom Gravestock Helen M. Atkinson Catherine S. E. Bale Trevor Ingham William J. Bloss Dwayne E. Heard 《Journal of Atmospheric Chemistry》2007,58(1):19-39
A Laser Induced Fluorescence (LIF) instrument has been developed to detect iodine monoxide (IO) radicals in the atmosphere.
An all solid-state Nd:YAG pumped Ti:Sapphire laser operating at approximately 445 nm was used to excite the (2,0) band of
the IO A2Π3/2 ← X2Π3/2 electronic transition, with off-resonance fluorescence in the (2,5) band detected at 521 nm. The sensitivity of the instrument
was determined by calibration. IO (between 10 and 150 pptV) was generated following the 184.9 nm photolysis of N2O/CF3I/N2 mixtures with O3 actinometry used to determine the photolysis flux. The detection limit was determined to be 0.3 pptV for a 300 s integration
period, with an uncertainty of 23% (1σ). The instrument was deployed in August/September 2006 during the RHaMBLe (Reactive Halogens in the Marine Boundary Layer)
campaign in Roscoff, France. Located on a small jetty, a few metres from the water’s edge at high tide, the instrument measured
significant levels of IO on 11 days, with a maximum of 27.6 ± 3.2 pptV observed on one day (averaged over 10 s) representing
the highest IO mixing ratio recorded in the marine boundary layer to date. IO displayed a clear diurnal profile with a maximum
at low tide during the daytime. These results represent the first point measurements of IO in the atmosphere by LIF. 相似文献
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根据国内外大量实际资料,从碘的分布情况及其所处的地质条件,结合石油和天然气形成过程、油气藏类型及其分布特点,探讨高碘卤水分布的规律及其形成条件,在此基础上指出了我国的找碘方向。 相似文献
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Iodine enrichment in the Atacama Desert of northern Chile is widespread and varies significantly between reservoirs, including nitrate-rich “caliche” soils, supergene Cu deposits and marine sedimentary rocks. Recent studies have suggested that groundwater has played a key role in the remobilization, transport and deposition of iodine in Atacama over scales of millions-of-years. However, and considering that natural waters are also anomalously enriched in iodine in the region, the relative source contributions of iodine in the waters and its extent of mixing remain unconstrained. In this study we provide new halogen data and isotopic ratios of iodine (129I/I) in shallow seawater, rivers, salt lakes, cold and thermal spring water, rainwater and groundwater that help to constrain the relative influence of meteoric, marine and crustal sources in the Atacama waters. Iodine concentrations in surface and ground waters range between 0.35 μM and 26 μM in the Tarapacá region and between 0.25 μM and 48 μM in the Antofagasta region, and show strong enrichment when compared with seawater concentrations (I = ∼0.4 μM). In contrast, no bromine enrichment is detected (1.3–45.7 μM for Tarapacá and 1.7–87.4 μM for Antofagasta) relative to seawater (Br = ∼600 μM). These data, coupled to the high I/Cl and low Br/Cl ratios are indicative of an organic-rich sedimentary source (related with an “initial” fluid) that interacted with meteoric water to produce a mixed fluid, and preclude an exclusively seawater origin for iodine in Atacama natural waters. Iodine isotopic ratios (129I/I) are consistent with halogen chemistry and confirm that most of the iodine present in natural waters derives from a deep initial fluid source (i.e., groundwater which has interacted with Jurassic marine basement), with variable influence of at least one atmospheric or meteoric source. Samples with the lowest isotopic ratios (129I/I from ∼215 to ∼1000 × 10−15) strongly suggest mixing between the groundwater and iodine storage in organic-rich rocks (with variable influence of volcanic fluids) and pre-anthropogenic meteoric water, while samples with higher values (∼2000–93,700 × 10−15) indicate the input of anthropogenic meteoric fluid. Taking into account the geological, hydrologic and climatic features of the Atacama region, we propose that the mean contribution of anthropogenic 129I is associated with 129I releases during nuclear weapon tests carried out in the central Pacific Ocean until the mid 1990's (129I/I = ∼12,000 × 10−15). This source reflects rapid redistribution of this radioisotope on a global scale. Our results support the notion of a long-lived continental iodine cycle in the hyperarid margin of western South America, which is driven by local hydrological and climate conditions, and confirm that groundwater was a key agent for iodine remobilization and formation of the extensive iodine-rich soils of Atacama. 相似文献
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Previous studies have shown that brines in an Ordovician paleokarst reservoir of the Lunnan oilfield in the Tarim Basin, China, are the product of mixing of paleo-evaporated seawater in the east with paleometeoric waters in the west. In order to put time constraints on the brine and related hydrocarbons in this field, 10 brine samples were collected, for which the iodine concentrations and 129I/I ratios were measured and discussed. The iodine concentration (3.70–31.2 mg/L) and the 129I/I ratio (189–897 × 10−15) show that the iodine in the paleoseawater and meteoric water (MW) had different origins and 129I characteristics. The paleoseawater has a high iodine content (∼31 mg/L), indicating that iodine was introduced into the reservoir along with thermally generated hydrocarbons, possibly in the Cretaceous, from the Caohu Sag in the eastern area. Based on consideration of all possible origins of iodine and 129I in the brines, it is suggested that the meteoric water maintained its initial iodine content (0.01 mg/L) and 129I/I ratio (1500 × 10−15), whereas the iodine-enriched paloseawater (IPSW) exhibited a secular 129I equilibrium (Nsq = 39 atom/μL) as a result of fissiogenic 129I input in the reservoir over a long period of time. The model of brine evolution developed on that basis confirmed that meteoric water entered the reservoir in the Miocene at about 10 Ma, and partially mixed with the iodine-enriched paleoseawater. The movement of meteoric water was facilitated by faults created during the Himalayan orogeny, then became more dense after dissolving Paleogene halite and infiltrated into the reservoir at high pressure. The iodine and 129I concentration in the brine contains information about the path and history of the fluid in the reservoir. This may be useful in oil exploration, since the movement of water was, to some extent, related to hydrocarbon migration. 相似文献
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Short-lived halocarbons were measured in Arctic sea–ice brine, seawater and air above the Greenland and Norwegian seas (~81°N, 2–5°E) in mid-summer, from a melting ice floe at the edge of the ice pack. In the ice floe, concentrations of C2H5I, 2-C3H7I and CH2Br2 showed significant enhancement in the sea ice brine, of average factors of 1.7, 1.4 and 2.5 times respectively, compared to the water underneath and after normalising to brine volume. Concentrations of mono-iodocarbons in air are the highest ever reported, and our calculations suggest increased fluxes of halocarbons to the atmosphere may result from their sea–ice enhancement. Some halocarbons were also measured in ice of the sub-Arctic in Hudson Bay (~55°N, 77°W) in early spring, ice that was thicker, colder and less porous than the Arctic ice in summer, and in which the halocarbons were concentrated to values over 10 times larger than in the Arctic ice when normalised to brine volume. Concentrations in the Arctic ice were similar to those in Antarctic sea ice that was similarly warm and porous. As climate warms and Arctic sea ice becomes more like that of the Antarctic, our results lead us to expect the production of iodocarbons and so of reactive iodine gases to increase. 相似文献
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The concentrations of 129I in seawater samples from two sites (off Sekine and the Toyama Bay) in the Japan Sea were determined by accelerator mass spectrometry. The observed concentrations exceed amounts expected from natural origin and globally distributed fallout due to nuclear weapons testing. Because the fraction of natural origin and global fallout is 2% and 8.9–13.8%, respectively, the residual more than 80% of the concentration must come primarily from nuclear fuel reprocessing plants. This result indicates a rapid distribution of 129I through atmospheric transport on a global scale. The depth distribution of 129I at the Toyama Bay in the Japan Sea shows that the 129I maximum is in the mixed layer and that concentrations decrease with depth. The inventory of 129I in water column is four times higher than that measured in the Gulf of Mexico which has almost the same depth at the Toyama Bay. This higher inventory probably reflects: (1) the rapid water sinking in the Japan Sea, (2) the difference of distance in sampling locations with respect to major 129I releasing plants and (3) the strong increase in emissions from nuclear fuel reprocessing plants after the profile of the Gulf of Mexico was taken. 相似文献