Influence of temperature on the accumulation and retention of 11 radionuclides by the marine alga Fucus vesiculosus (L.)

Accumulation of the radionuclides ²⁴¹Am, ^110mAg, ¹³³Ba, ¹⁰⁹Cd, ⁵⁷Co-cobalamine, ⁶⁰Co, ¹³⁴Cs, ¹⁵²Eu, ⁵⁴Mn, ¹⁰⁶Ru and ⁶⁵Zn in the brown macroalga Fucus vesiculosus (L.) Phaeophyceae, was compared at 2°C and 12°C in a series of laboratory radiotracer experiments. Concentration factors in the thallus were temperature-dependent and significantly decreased at 2°C for ^110mAg, ¹⁰⁹Cd, ⁶⁰Co, ⁵⁴Mn and ⁶⁵Zn (CF = 439, 51, 101, 92 and 162, respectively) but not for ²⁴¹Am, ¹³³Ba, ¹³⁴Cs, ¹⁵²Eu and organic ⁵⁷Co (CF = 329, 210, 3.3, 470 and 214, respectively); hence, for these last isotopes concentration factors in this species derived from temperate latitude (12°C) studies can probably be applied to radiological assessments made under Arctic conditions. Between 2 and 14 days of depuration, the radionuclides, except ¹³³Ba and ¹³⁴Cs, remained tightly bound to the alga. Our results suggest that: 1. temperature must be considered when modelling the radiological impact of radioactive waste dumping in the Arctic Seas; and 2. Fucus spp. would be excellent bioindicators of radionuclide contamination and dispersion in the Barents and Kara Seas.     

Summary of IAEA-MEL's investigation of Kara Sea radioactivity and radiological assessment

IAEA-MEL participated in five expeditions to the Kara Sea with the aim of assessing the radiological consequences of dumped radioactive wastes in the Novaya Zemlya Bays and Trough. The programme included sampling, in-situ underwater investigations, laboratory analyses of water, sediment and biota samples, the development of a marine radioactivity database, modelling and radiological assessment, the organization of intercomparison exercises and the evaluation of distribution coefficients. Radiometric investigations have shown that no radiologically significant environmental contamination has occurred. Leakages which have led to locally increased levels of radionuclides in sediment have only been observed in Stepovoy and Abrosimov Bays. Computer modelling results suggest that only radiological effects on local and regional scales may be of importance. The global radiological impact of the disposals in the Arctic Seas will be negligible.     

Pu, Cs and excess Pb in Russian Arctic sediments

The activity ratios of Pu and radiocesium isotopes have been used to delineate the major sources (such as global and close-in (debris) fallout, nuclear fuel reprocessing and fabrication plant effluents) in the environment. We have measured ²³⁸Pu, ^239,240Pu, ¹³⁷Cs, and excess ²¹⁰Pb concentrations in 107 surficial sediments as well as in 5 sediment cores collected in the summer months of 1993 and 1994 from the Ob and Yenisey Rivers (Russia) and the Kara sea. A comparison of the sediment core inventories of ^239,240Pu and ¹³⁷Cs, along with the ²³⁸Pu/^239,240Pu activity ratios, with those expected from global fallout allows us to estimate the relative amounts, if any, of reactor-derived ²³⁸Pu and ^239,240Pu from the dumped reactor sites in the study area.

In surficial sediment samples collected in 1993 and 1994, the ^239,240Pu concentrations varied between 4.2 and 856 mBq kg⁻¹, with a mean of 239 mBq kg⁻¹. In samples with a measurable ²³⁸Pu, the ²³⁸Pu/^239,240Pu activity ratios varied between 0.010 and 0.069, with an average value of 0.035 ± 0.014. This range can be compared to the average ²³⁸Pu/^239,240Pu activity ratio of 0.030 for the year 1993 from nuclear weapons testing and SNAP fallout obtained from soil studies, indicating very little (≤ 5%) additional sources of ²³⁸Pu to the sediments in the study area. The inventories of Pu in the 5 sediment cores from the study area varied between 2.67 ± 0.67 and 24.5 ± 2.2 Bq m⁻² with a mean value of 8.83 Bq m⁻². The ¹³⁷Cs concentrations in the upper 3 cm of the sediments varied between below detection limit to 71.4 Bq kg⁻¹, with a mean of 14.9 Bq kg⁻¹. The ¹³⁷Cs inventories in the 5 sediment cores varied between 156.7 ± 28.3 and 1600 ± 153.3 Bq m⁻², with a mean value of 583.3 Bq m⁻². The mean ratio of inventories of Pu to that of ¹³⁷Cs, 0.015, is comparable to the values in other places in the Arctic region. There is a significant correlation between total organic carbon and concentrations of ¹³⁷Cs, ^239,240Pu and ²¹⁰Pb, suggesting that organic matter-enriched fine particles are a likely carrier phase for these nuclides. The ratio of ¹³⁷Cs/^239,240Pu also suggests that most of these nuclides are derived from global fallout.     

Sulfate reduction using methane in sediments beneath a bathyal “cold seep” giant clam community off Hatsushima Island, Sagami Bay, Japan

Two sandy sediment cores (Cores D227-120 and D380) were collected from inside a deep-sea giant clam (Calyptogena soyoae) community off Hatsushima Island, western Sagami Bay, central Japan (35°59.9′N, 139°13.6′E; 1160 m deep) and a muddy sediment core (Core D227-202) was obtained from outside the community by the submersibleShinkai 2000. The chloride concentration of the pore waters is constant vertically and sulfate reduction using sedimentary organic matter occurs in Core D227-202 (21 cm long). The chloride concentrations are lower by 7% at the 7.5–9 cm depth in Core D227-120 (9 cm long) and by 3% at the 11–12 cm depth in Core D380 (16 cm long) than those of the overlying bottom waters in the cores from inside of the community. Sulfate concentration decreases remarkably and dissolved inorganic carbon, alkalinity, ammonium-N, and hydrogen sulfide concentrations increase significantly with increasing depth in Core D380.δ³⁴S values of sulfate ions increase from +20.5 to +35.3‰ andδ¹³C values of dissolved inorganic carbon decrease drastically from −7.0 to −45‰ with increasing depth from the top to the bottom of the core, although theδ¹³C values of the organic carbon of the sediments are−23.7 ± 0.9‰ in Core D380. These results indicate that sulfate reduction using methane is active within the sediments just beneath the living clams and that the hydrogen sulfide produced can be used by endosymbiotic sulfur oxidizing bacteria living in the gills ofC. soyoae in the community.     

Correlation of magnetic properties with Δ(Sr) of igneous rocks from the northeast Pacific and Gulf of California

The magnetic properties of basalts and diabases recovered under Legs 63 and 64 of the Deep Sea Drilling Project are summarized. They are first correlated with the measured grain sizes of the opaque minerals and the overall alteration states of the rocks, the latter measured by conventional chemical parameters such as water content, total volatiles content, and Fe₂O₃/FeO ratio. It is shown, however, that the decrease in ⁸⁷Sr/⁸⁶Sr upon leaching (Δ(^87/86Sr)) is perhaps the best quantifier of the overall alteration state of the whole rocks as well as of the degree of low-temperature oxidation suffered by the titanomagnetites. It is well correlated with Curie-point variations caused by changes in the Fe³⁺/Fe²⁺ ratio.     

Tin and organotin in water, sediments, and benthic organisms of Poole Harbour

Tributyltin (TBT) concentrations in waters of Poole Harbour ranged between 2–139 ng l⁻¹ (as Sn) and increased to 234–646 ng l⁻¹ within marinas. Seasonal trends in contamination coincided with boat usage patterns and peaked during summer months. A combination of poor tidal flushing and removal of TBT to particulates restricts high levels of contamination to areas closest to marinas and moorings; TBT concentrations in benthic sediments decreased from 0.52 μg g⁻¹ near such sites to 0.02 μg g⁻¹ at the harbour mouth. Organotin accumulations in several benthic invertebrates including polychaetes (Nereis diversicolor), snails (Littorina littorea) and clams (Scrobicularia plana, Mya arenaria) reflect the distribution of contamination in the environment, though concentration factors (relative to water) vary considerably between species and were highest in sediment dwelling clams, notably Mya (1.3×10⁵). Compared to organotins, biological availability of inorganic tin is low.

Levels of TBT in parts of Poole Harbour exceed Environmental Quality Targets designed to protect marine life and may be responsible for poor recruitment, particularly in bivalves, at heavily contaminated sites.     

Anomalous strontium and lead isotope signatures in the off-rift Öræfajökull central volcano in south-east Iceland: Evidence for enriched endmember(s) of the Iceland mantle plume?

The currently active off-rift central volcano Öræfajökull in south-east Iceland sits unconformably on much older (10–12 Ma) and eroded crust. The composition of recent volcanics ranges from basalt to rhyolite, but the series is more sodic alkaline than the common rift zone tholeiitic suites. In this study we present Sr, Nd, Pb and O isotopic data for a suite of Öræfajökull samples. The complete suite shows typical mantle values for oxygen isotopes. The ⁸⁷Sr/⁸⁶Sr ratios (average of 15 SAMPLES=0.703702) of the modern Öræfajökull rocks (basalts as well as rhyolites) are much higher than observed so far for any other Icelandic rocks. The ¹⁴³Nd/¹⁴⁴Nd ratios (average=0.512947; n=15) are lower than for rift rocks, but similar to rocks of the off-rift Snæfellsnes volcanic zone. Furthermore, the Öræfajökull rocks are enriched in the ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb isotope ratios compared to Icelandic rift basalts. The enriched nature of the suite indicates that Öræfajökull samples a source component that has characteristics common with EM2 type mantle. Furthermore, it is concluded that the silicic rocks of Öræfajökull formed by fractional crystallization from mafic melts rather than by partial melting of older crust.     

Oxygen isotope evidence for the origin of enriched mantle beneath the mid-Atlantic ridge

Geochemical variations in mid-ocean ridge basalts have been attributed to differing proportions of compositionally distinct mantle components in their sources, some of which may be recycled crust. Oxygen isotopes are strongly fractionated by near-surface interactions of rocks with the hydrosphere, and thus provide a tracer of near-surface materials that have been recycled into the mantle. We present here oxygen isotope analyses of basaltic glasses from the mid-Atlantic ridge south of and across the Azores platform. Variations in δ¹⁸O in these samples are subtle (range of 0.47‰) and may partly reflect shallow fractional crystallization; we present a method to correct for these effects. Relatively high fractionation-corrected δ¹⁸O in these samples is associated with geochemical indices of enrichment, including high La/Sm, Ce/Pb, and ⁸⁷Sr/⁸⁶Sr and low ¹⁴³Nd/¹⁴⁴Nd. Our results suggest two first-order conclusions about these enriched materials: (1) they are derived (directly or indirectly) from recycled upper oceanic crustal rocks and/or sediments; and (2) these materials are present in the north Atlantic MORB sources in abundances of less than 10% (average 2–5%). Modeling of variations of δ¹⁸O with other geochemical variables further indicates that the enriched component is not derived from incorporation of sediment or bulk altered oceanic crust, from metasomatism of the mantle by hydrous or carbonate-rich fluids, or from partial melting of subducted sediment. Instead, the data appear to require a model in which the enriched component is depleted mantle that has been metasomatized by small-degree partial melts of subducted, dehydrated, altered oceanic crust. The age of this partial melting is broadly constrained to 250 Ma. Reconstructed plate motions suggest that the enriched component in the north Atlantic mantle may have originated by subduction along the western margin of Pangea.     

Mantle and crustal contribution in the genesis of Recent basalts from off-rift zones in Iceland: Constraints from Th, Sr and O isotopes

Along the two volcanic off-rift zones in Iceland, the Snfellsnes volcanic zone (SNVZ) and the South Iceland volcanic zone (SIVZ), geochemical parameters vary regularly along the strike towards the centre of the island. Recent basalts from the SNVZ change from alkali basalts to tholeiites where the volcanic zone reaches the active rift axis, and their⁸⁷Sr/⁸⁶Sr andTh/U ratios decrease in the same direction. These variations are interpreted as the result of mixing between mantle melts from two distinct reservoirs below Snfellsnes. The mantle melt would be more depleted in incompatible elements, but with^a higher³He/⁴He ratio (R/Ra≈ 20) beneath the centre of Iceland than at the tip of the Snfellsnes volcanic zone (R/Ra≈ 7.5).

From southwest to northeast along the SIVZ, the basalts change from alkali basalts to FeTi basalts and quartz-normative tholeiites. TheTh/U ratio of the Recent basalts increases and both (²³⁰Th/²³²Th) andδ¹⁸O values decrease in the same direction. This reflects an important crustal contamination of the FeTi-rich basalts and the quartz tholeiites. The two types of basalts could be produced through assimilation and fractional crystallization in which primary alkali basaltic and olivine tholeiitic melts ‘erode’ and assimilate the base of the crust. The increasingly tholeiitic character of the basalts towards the centre of Iceland, which reflects a higher degree of partial melting, is qualitatively consistent with increasing geothermal gradient and negative gravity anomaly.

The highest Sr isotope ratio in Recent basalts from Iceland is observed inÖrfajökull volcano, which has a³He/⁴He ratio (R/Ra≈ 7.8) close to the MORB value, and this might represent a mantle source similar to that of Mauna Loa in Hawaii.     

Derived concentration factors for caesium-137 in edible species of North Sea fish

Concentration factor (CF=Bq kg⁻¹ fillet/Bq kg⁻¹ filtered sea water) values for ¹³⁷Cs in fillets of cod (Gadus morhua), haddock (Merlanogrammus aeglefinus), plaice (Pleuronectes platessa) and whiting (Merlangius merlangius), were derived from fish and filtered seawater concentrations. Samples were collected in twelve sampling boxes in the North Sea over an eight-year period—1978–1985. The range of results with species, between species, and between surveys are discussed. Mean CF values of 92, 58, 39, and 150 were found in cod, haddock, plaice, and whiting respectively. These support the IAEA recommended CF value of 100 for fish in generalised dose assessments.     

Biokinetics of Radiocobalt in the Asteroid Asterias rubens (Echinodermata): Sea Water and Food Exposures

Uptake and loss of cobalt-57 were investigated in the starfish Asterias rubens, in order to assess its value as a sentinel organism for nearshore radionuclide contamination. Whole-body uptake from sea water was linear over a 32-day exposure period and reached wet weight concentration factor (CF) of 23 ± 5. Bioaccumulation of ⁵⁷Co was dependent upon body compartment, the aboral part of the body wall concentrating cobalt to the greatest degree (wet weight CF: 77 ± 16). After restoration of uncontaminated conditions, radiocobalt was released following an exponential loss kinetics characterized by a biological half-life (T_b1/2) of 27 ± 6 day. Dietary radiocobalt (taken up during a short-term feeding for 24 h on radiolabelled mussels) showed a much more rapid turnover time (T_b1/2: 14 ± 4 d), suggesting that A. rubens accumulates this radionuclide predominantly from sea water. A. rubens, and more particularly the aboral part of its body wall, would readily reveal the presence of an environmental contamination by radiocobalt and could preserve this information over a period of few months.     

Bioconcentration factors for petroleum hydrocarbons, PAHs, LABs and biogenic hydrocarbons in the blue mussel

Bioconcentration factors (K_bc) for petroleum hydrocarbons, PAHs, LABs and biogenic hydrocarbons in Mytilus edulis were measured in field experiments using time-integrating water samplers. Seven deployments at five sites gave lipid weight K_bcs for total hydrocarbons ranging from 0.99 × 10⁶ to 3.1 × 10⁶ (mean 1.6 × 10⁶)—a narrower range than has been obtained previously. Bioconcentration factors for the PAHs were similar to those for total hydrocarbons where the major hydrocarbon source was oil. However, at other sites the factors for PAHs were an order of magnitude lower than those for petroleum and for hydrocarbons originating from algae. Compositional profiles for the linear alkyl benzenes (LABs) suggested that these compounds were assimilated primarily from the dissolved phase, despite their greater abundance on particles.     

Helium isotope geochemistry of mid-ocean ridge basalts from the South Atlantic

We report new helium isotope results for 49 basalt glass samples from the Mid-Atlantic Ridge between 1°N and 47°S.³He/⁴He in South Atlantic mid-ocean ridge basalts (MORB) varies between 6.5 and 9.0 R_A (R_A is the atmospheric ratio of1.39 × 10⁻⁶), encompassing the range of previously reported values for MORB erupted away from high³He/⁴He hotspots such as Iceland. He, Sr and Pb isotopes show systematic relationships along the ridge axis. The ridge axis is segmented with respect to geochemical variations, and local spike-like anomalies in³He/⁴He, Pb and Sr isotopes, and trace element ratios such as(La/Sm)_N are prevalent at the latitudes of the islands of St. Helena, Tristan da Cunha and Gough to the east of the ridge. The isotope systematics are consistent with injection beneath the ridge of mantle “blobs” enriched in radiogenic He, Pb and Sr, derived from off-axis hotspot sources. The variability in³He/⁴He along the ridge can be used to refine the hotspot source-migrating-ridge sink model.

MORB from the 2–7°S segment are systematically the least radiogenic samples found along the mid-ocean ridge system to date. Here the depleted mantle source is characterized by⁸⁷Sr/⁸⁶Sr of 0.7022, Pb isotopes close to the geochron and with²⁰⁶Pb/²⁰⁴Pb of 17.7, and³He/⁴He of 8.6–8.9 R_A. The “background contamination” of the subridge mantle, by radiogenic helium derived from off-ridge hotspots, displays a maximum between 20 and 24°S. The HePb and HeSr isotope relations along the ridge indicate that the³He/⁴He ratios are lower for the hotspot sources of St. Helena, Tristan da Cunha and Gough than for the MORB source, consistent with direct measurements of³He/⁴He ratios in the island lavas. Details of the HeSrPb isotope systematics between 12 and 22°S are consistent with early, widespread dispersion of the St. Helena plume into the asthenosphere, probably during flattening of the plume head beneath the thick lithosphere prior to continental breakup. The geographical variation in theHe/Pbratio deduced from the isotope systematics suggests only minor degassing of the plume during this stage. Subsequently, it appears that the plume component reaching the mid-Atlantic ridge was partially outgassed of He during off-ridge hotspot volcanism and related melting activity.

Overall, the similar behavior of He and Pb isotopes along the ridge indicates that the respective mantle sources have evolved under conditions which produced related He and Pb isotope variations.     

Effect of Bioremediation on the Microbial Community in Oiled Mangrove Sediments

Bioremediation was conducted in the field on a mature Rhizophora stylosa mangrove stand on land to be reclaimed near Fisherman’s Landing Wharf, Gladstone Australia. Gippsland crude oil was added to six large plots (>40 m²) and three plots were left untreated as controls. Bioremediation was used to treat three oiled plots and the remaining three were maintained as oiled only plots. The bioremediation strategy consisted of actively aerating the sediment and adding a slow-release fertilizer in order to promote oil biodegradation by indigenous micro-organisms. Oil addition stimulated the numbers of alkane-degrading bacteria slightly to levels of 10⁴–10⁵/g sediment. Bioremediation of the oiled sediment had a marked effect on the alkane-degrading population, increasing the population size by three orders of magnitude from 10⁵ to 10⁸ cells/g of sediment. An effect of bioremediation on the growth of aromatic-degraders was detected with numbers of aromatic-degraders increasing from 10⁴ to 10⁶ cells/g of sediment. Active aeration and nutrient addition significantly stimulated the growth of hydrocarbon-degraders in oiled mangrove sediment in the field.     

Alkaline syenites in eastern Cathaysia (South China): link to Permian–Triassic transtension

Two alkaline syenite plutons, the Tieshan and Yangfang plutons, have recently been recognized within NE-trending fault zones in eastern Cathaysia, South China. The rocks are very enriched in K₂O (6.28–9.39 wt.%), rare earth elements (REE; particularly light REE) and large ion lithophile elements, but are relatively low in high field strength elements. Isotopically, they are characterized by high initial ⁸⁷Sr/⁸⁶Sr (0.7093 to 0.7123) and low _Nd(t) values (−5.64 to −10.63). The geochemical data suggest that the alkaline syenites most likely formed via fractional crystallization of enriched mantle-derived magmas. Sensitive High-Resolution Ion Microprobe zircon U–Pb dating indicates that these two intrusions have Late Permian (254±4 Ma) and Early Triassic (242±4 Ma) crystallization ages, respectively. Our data suggest that a tectonic regime dominated by transtension probably existed from at least the latest Permian into the Triassic and was responsible for the formation of the Tieshan and Yangfang alkaline syenites. When combined with previous paleomagnetic, structural, and sedimentology data, we suggest that the transtension along the NE-trending strike-slip fault zones was related to oblique subduction of the Pacific plate underneath South China.     

Organic pollutants in sediment cores of NE-Germany: comparison of the marine Arkona Basin with freshwater sediments

During a contamination survey in NE-Germany sediment cores were sampled at 5 locations with freeze-coring devices and conventional box-coring systems. In total more than 40 samples were analysed for several organic compounds (136 PCDD/F, 33 PCB, 39 PAH, 10 DDX, 4 HCH, 4 CB), sedimentological parameters (TOC, TC, TIC, LOI), some total trace metals (Pb, Cd, Cr, Cu, Zn) and dated by measurement of the ²¹⁰Pb and ¹³⁷Cs activity. The deepest segment of the cores from the Arkona Basin and the freshwater lakes were dated back to the end of the 19th century. A comparison of marine versus freshwater data is presented. The contamination levels of Arkona Basin were often lower than anthropogenically influenced freshwater sediments and more similar to a freshwater sediment core only influenced by deposition, with an additional Oder River inflow. Differences in patterns and contamination levels are discussed.     

Bioaccumulation of radiocaesium in Arctic seals

Seals are high trophic level feeders that bioaccumulate many contaminants to a greater degree than most lower trophic level organisms. Their trophic status in the marine food web and wide-spread distribution make seals useful sentinels of arctic environmental change. The purpose of this investigation is to document the levels and bioaccumulation potential of radiocaesium in high latitude seal species for which data have not previously been available. The study was carried out on harp, ringed, and bearded seals caught north of the island archipelago of Svalbard (82°N) in 1999. The results are then compared with previous studies in order to elucidate factors responsible for bioaccumulation in Arctic seals. Concentrations of ¹³⁷Cs were determined in muscle, liver and kidney samples from a total of 10 juvenile and one adult seal. The mean concentration in muscle samples for all animals was 0.23±0.045 Bq/kg f.w. ¹³⁷Cs concentrations in both liver and kidney samples were near detection limits (≈0.2 Bq/kg f.w.). The results are consistent with previous studies indicating low levels of radiocaesium in Arctic seals in response to a long term trend of decreasing levels of ¹³⁷Cs in the Barents Sea region. Bioconcentration factors (BCFs) estimated for seals from NE Svalbard are low, ranging from 34 to 130. Comparing these values with reported BCFs for Greenland seals from other sectors of the European Arctic, we suggest that the combination of physiological and ecological factors on radiocaesium bioaccumulation is comparable among different Arctic seal populations. The application of this work to Arctic monitoring and assessment programs is discussed.     

外辐射带区域新建地磁场经验模型的定量研究

准确的磁场模型对于辐射带粒子环境研究至关重要.本文利用美国Van Allen Probes（VAP）在2012至2018年期间测量的磁场数据和GOES15在2011至2017年期间测量的磁场数据,定量地评估了三个较新的外磁场经验模型（TS05、TA15和TA16）对外辐射带区域（3~6.6R_E）磁场的描述性能.本文选择预测效率（Prediction Efficiency,PE）作为评估指标,定量分析各模型在不同空间范围（Lm值）、不同地磁活动水平（Kp）以及不同磁地方时（MLT）下的性能表现,并且计算了观测磁场与模型磁场的夹角θ,以评估模型的磁场方向预测能力.结果表明：PE随Lm值增大,随地磁扰动增强而下降;θ随Lm值增大,随地磁扰动增强而增大.在Lm=5~6.5R_E范围内,PE呈现晨昏不对称性,MLT=12-21时的PE值小于MLT=0-9时的值,说明三个磁场模型可以较好地描述晨侧磁场的强度,但它们并不能很好地反映下午至昏侧磁场的大小;在地球同步轨道附近（Lm~6.6R_E）,PE呈现昼夜不对称性,MLT=9-15时的PE值大于其他时区的值,说明三个磁场模型可以很好地反映昼侧磁场大小,但在夜侧可能存在较大的误差.θ在MLT=6-12时的值小于其他时区的值,呈现昼夜不对称性,说明三个磁场模型可以较好地描述昼侧磁力线的分布位型,但在夜侧存在较大的方向描述误差.在外辐射带3~6.5R_E内,TA16模型与VAP磁场观测数据最为接近,PE均大于0.7,θ均小于3°;在地球同步轨道高度（6.6R_E）,TS05模型与GOES15卫星磁场观测数据最为接近,PE约为0.75,θ约为7°.相关的研究结果可以为我国星载高能粒子探测器探测数据的在轨交叉定标、辐射带高能粒子动态模型研究和相关的磁层环境理论/应用研究提供地磁场模型选择方面的参考.     

Iodine-129 concentrations in marginal seas of the north Pacific and Pacific-influenced waters of the Arctic Ocean

Water sampling during the 1993 IV Russian–US Joint Expedition to the Bering and Chukchi Seas (BERPAC) indicates that Pacific Ocean burdens of the long-lived radionuclide ¹²⁹I are relatively low in the Pacific-influenced Arctic, particularly compared to high latitude waters influenced by the North Atlantic. These low concentrations occur despite the presence of potential submerged anthropogenic sources in the East Sea (Sea of Japan), and in the northwest Pacific Ocean, east of the Kamchatka Peninsula. The concentration of ¹²⁹I entering the Arctic Ocean through Bering Strait, 0.7×10⁸ atoms kg⁻¹, is only slightly higher than observed in deep Pacific waters. Similar concentrations (0.44–0.76×10⁸ atoms kg⁻¹) measured in Long Strait indicate no significant transfer of ¹²⁹I eastward into the Chukchi Sea in the Siberian Coastal Current from the Siberian marginal seas to the west. However, the concentrations reported here are more than an order of magnitude higher than the Bering Strait input concentration estimated (1.0×10⁶ atoms kg⁻¹) from bomb fallout mass balances, which supports other existing evidence for a significant atmospheric deposition term for this radionuclide in surface ocean waters. Near-bottom water samples collected in productive waters of the Bering and Chukchi Seas also suggest that sediment regeneration may locally elevate ¹²⁹I concentrations, and impact its utility as a water mass tracer. As part of this study, two deep ¹²⁹I profiles were also measured in the East Sea in 1993–1994. The near-surface concentration of ¹²⁹I ranged from 0.12 to 0.31×10⁸ atoms kg⁻¹. The ¹²⁹I concentration showed a steady decrease with depth, although because of active deep water ventilation, the entire 3000 m water column exceeded natural concentrations of the radionuclide. Atom ratios of ¹²⁹I/¹³⁷Cs in the East Sea also suggest an excess of ¹²⁹I above bomb fallout estimates, also possibly resulting from atmospheric deposition ultimately originating from nuclear facilities.     

晋冀鲁豫交界地区震源参数特征

利用晋冀鲁豫交界地区邯郸地震台网记录的地震波形资料,选取2005—2016年M_L≥1.8地震事件,采用Brune震源模型,结合遗传算法得到该区中小地震震源参数,并分析各参数形态特征。研究表明：①晋冀鲁豫交界地区中小地震的地震矩取值范围1.34×10¹¹—2.63×10¹⁵ N·m,震源半径取值范围132—1 044 m,拐角频率f_c取值范围1.25—9.82 Hz,应力降取值范围0.036 4—11.063 1 MPa;②震源参数之间相互关系;③按照震中分区分析不同区域应力降分布特征,河北邯郸、邢台等地及附近地区应力降范围为0 MPa<Δσ≤5 MPa,河南濮阳以及范县和山西黎城等地及附近地区应力降范围为5 MPa <Δσ≤11.063 1 MPa,该区处于高应力背景场状态。