Can biomass burning produce a globally significant carbon-isotope excursion in the sedimentary record?

Negative carbon-isotope excursions have been comprehensively studied in the stratigraphic record but the discussion of causal mechanisms has largely overlooked the potential role of biomass burning. The carbon-isotopic ratios (δ¹³C) of vegetation, soil organic matter and peat are significantly lower than atmospheric carbon dioxide (CO₂), and thereby provide a source of low ¹³C CO₂ when combusted. In this study, the potential role of biomass burning to generate negative carbon isotope excursions associated with greenhouse climates is modeled. Results indicate that major peat combustion sustained for 1000 yr increases atmospheric CO₂ from 2.5× present atmospheric levels (PAL) to 4.6× PAL, and yields a pronounced negative δ¹³C excursion in the atmosphere ( 2.4‰), vegetation ( 2.4‰) and the surface ocean ( 1.2‰), but not for the deep ocean ( 0.9‰). Release of CO₂ initiates a short-term warming of the atmosphere (up to 14.4 °C, with a duration of 1628 yr), which is consistent with the magnitude and length of an observed Toarcian excursion event. These results indicate that peat combustion is a plausible mechanism for driving negative δ¹³C excursions in the rock record, even during times of elevated pCO₂.     

Origin and age of thermal waters in Cieplice Spa, Sudeten, Poland, inferred from isotope, chemical and noble gas data

Isotope and hydrochemical data of the thermal water system in Cieplice laskie Zdrój (Spa) indicate the existence of two subsystems that greatly differ in volume and which meet at the fault zones of a granitic horst, where they discharge at an altitude of about 340m. One of the subsystems is very small (about 4 × 10³ m³) as indicated by the tritium age of the order of 10 years and a low outflow rate. Its recharge area found from the δ¹⁸O and δD values, is about 200m above the springs, most probably on the slopes of the foothills of the Karkonosze Mountains south-southwest of the spa. The large subsystem contains water which is free of tritium and whose ¹⁴C content is from 1 to 8 pmc with δ¹³C = −8.0 to −9.2‰. The isotopic composition of this water reflects either the climatic effect (low-altitude recharge during a cooler pre-Holocene climate) or the altitude effect (recharge in the early Holocene period at about 1000m at the heights of the Karkonosze assuming that the ¹⁴C concentration is strongly reduced by exchange with calcite in veins). For the former hypothesis, the recharge area of this water is probably either at the foot of the southeastern slopes of the Kaczawa Mountains or/and at the foot of the Rudawy Janowickie Mountains, to the east of Cieplice. The noble gas temperatures are more consistent with the pre-Holocene recharge. Similarly, the ⁴He excess and ⁴⁰Ar/³⁶Ar ratio support the hypothesis of a pre-Holecene age. The constant ³He/⁴He ratio of 26 × 10⁻⁸ for highly different helium contents indicates crustal origin of helium. For the pre-Holocene age of water its volume is calculated at >- 10⁹m³ (stagnant water in micropores and mobile water in fractures) and the hydraulic conductivity of the host granite massif is estimated at about 7 × 10⁻⁸ ms⁻¹. Two outflows from this subsystem have different and variable fractions of a modern water component (bomb age), most probably originating from the bank infiltration of a nearby stream.     

Late Pleistocene to Holocene composite speleothem O and C chronologies from South Island, New Zealand—did a global Younger Dryas really exist?

Oxygen and carbon data from eight stalagmites from northwest South Island are combined to produce composite records of δ¹⁸O and δ¹³C from 23.4 ka to the present. The chronology is anchored by 43 thermal ionization mass spectrometry (TIMS) uranium series ages. Delta ¹⁸O values are interpreted as having a first order positive relationship to temperature, but also to be influenced by precipitation in a complex manner. Delta ¹³C is interpreted as responding negatively to increases in atmospheric CO₂ concentration, biological activity and precipitation amount.

Six climatic phases are recognized. After adjustment of 1.2‰ for the ice volume effect, the δ¹⁸O record between 23 and 18 ka varies around −3.72‰ compared to the Holocene average of −3.17‰. Late-glacial warming commenced between 18.2 and 17.8 ka and accelerated after 16.7 ka, culminating in a positive excursion between 14.70 and 13.53 ka. This was followed by a significant negative excursion between 13.53 and 11.14 ka of up to 0.55‰ depth that overlapped the Antarctic Cold Reversal (ACR) and spanned the Younger Dryas (YD). Positive δ¹⁸O excursions at 11.14 ka and 6.91–6.47 ka represent the warmest parts of the Holocene. The mid-Holocene from 6 to 2 ka was marked by negative excursions that coincide with increased glacial activity in the South Island. A short positive excursion from 0.71 to 0.57 ka was slightly later than the Medieval Warm Period of Europe.

Delta ¹³C values were high until 17.79 ka after which there was an abrupt decrease to 17.19 ka followed by a steady decline to a minimum at 10.97 ka. Then followed a general increase, suggesting a drying trend, to 3.23 ka followed by a further general decline. The abrupt decrease in δ-values after 17.79 ka probably corresponds to an increase in atmospheric CO₂ concentration, biological activity and wetness at the end of the Last Glaciation, but the reversal identified in the δ¹⁸O record from 13.53 to 11.14 ka was not reflected in δ¹³C changes. The lowest δ¹³C values coincided with the early Holocene climatic suboptimum when conditions were relatively wet as well as mild.

Major trends in the δ¹⁸O_c record are similar to the Northern Hemisphere, but second order detail is often distinctly different. Consequently, at the millennial scale, a more convincing case can be made for asymmetric climatic response between the two hemispheres rather than synchronicity.     

Al depth profile in Apollo 15 drill core

Cosmic-ray-produced²⁶Al (t_1/2 = 7.05 × 10⁵ years) has been measured in the Apollo 15 long core (surface to 390 g/cm²—218 cm) for study of galactic cosmic ray production profiles, using accelerator mass spectrometry. The results are in general accord with non-destructive counting data obtained earlier, but systematically lower, and significantly higher precision. From this experiment the half-attenuation length for²⁶Al production can be calculated to be 122 g/cm² (150–400 g/cm² region) after normalizing the data to average chemical composition. The⁵³Mn (t_1/2 = 3.7 × 10⁶ years) production profile in deep cores was also compiled to date. The half-attenuation length for⁵³Mn production was calculated to be 123 g/cm² (150–400 g/cm² region).     

Bomb C time history recorded in two modern stalagmites — importance for soil organic matter dynamics and bomb C distribution over continents

Carbon 14 activity measurements made by Accelerator Mass Spectrometry on two modern stalagmites from the Han-sur-Lesse cave (Belgium) and from the Postojna Cave (Slovenia) permit the construction of ¹⁴C activity (a¹⁴C) time series over the last 50 years. A high precision chronology is given by annual laminae in the first stalagmite and by a specific mark (explosion in the Postojna Cave in 1944) in the second one. In both stalagmites, ¹⁴C activity increase due to nuclear tests in the atmosphere is remarkable. However, instead of a sharp peak like the one observed in the atmosphere around 1963–1964, the ¹⁴C activities of the stalagmite CaCO₃ show an abrupt increase, with an offset of 1–10 years, followed by a high activity plateau for the Han-sur-Lesse sample and a slight decrease for the Postojna sample. For both stalagmites, the variation of the a¹⁴C amplitude between pre- and post-bomb period is much lower than the atmospheric record, which demonstrates the damping effect of the soil carbon reservoir. We have modeled the CaCO₃ activities using fractionation processes between atmosphere CO₂, soil CO₂ and organic matter (OM), dissolved inorganic carbon and stalagmite CaCO₃. In both cases studied, the model and former soil studies suggest that CO₂ from soil organic matter (SOM) decomposition, which has a slow turnover (i.e. >1 y), is of major importance in winter, when the development of speleothem is the most important. Combined with the fact that 80–90% of the stalagmite carbon comes from soil CO₂, this produces a damping effect on the speleothem a¹⁴C. Consequently, the ‘geochemical time resolution', at least for speleothem carbon, is much lower than the structural resolution given by annual laminae alternations and is mainly controlled by soil carbon dynamics: a¹⁴C and δ¹³C are smoothed over several years. Differences between the ¹⁴C time series of the Han-sur-Lesse and Postojna stalagmites are likely to be due to the double amount of precipitation in Postojna, which produces a faster soil OM turnover and thus a ‘system' which is more sensitive to atmospheric changes.     

Solar modulation of cosmogenic nuclide production over the last millennium: comparison between C and Be records

For about the last 30 years it has been recognized that the high frequency component of the tree rings ¹⁴C/¹²C record is dominated by the modulation of the cosmic ray flux by the solar wind. In particular, it has been demonstrated that the three most recent periods of low sunspot occurrence were characterized by high values of atmospheric ¹⁴C/¹²C. During the last millennium other periods of high ¹⁴C/¹²C values were observed but their solar origin is still debatable. In the present work we compare these fluctuations with an independent record of cosmogenic ¹⁰Be measured in ice from the South Pole to check the solar origin of the observed ¹⁴C/¹²C variations. In order to compare quantitatively the results obtained on ¹⁰Be and ¹⁴C, it is necessary to take into account the different behaviour of these two cosmogenic isotopes, and especially the damping effect of the carbon cycle in the case of ¹⁴C. As an input to a 12-box numerical model we used the relative fluctuations of the ¹⁰Be concentrations record measured in South Pole ice and converted it into a synthetic ¹⁴C record. We took into account the fact that ¹⁰Be modulation is enhanced in polar regions due to the orientation of the geomagnetic field. As expected, the fluctuations of the modelled ¹⁴C record are much smaller (a factor of 20) than those observed for the raw ¹⁰Be record. In addition, the variations are smoother and shifted in time by a few decades. The ¹⁰Be-based ¹⁴C variations closely resemble the ¹⁴C measurements obtained on tree rings (R = 0.81). In particular, it is easy to identify periods of maximal ¹⁴C/¹²C which correspond to solar activity minima centred at about 1060, 1320 (Wolf), 1500 (Spörer), 1690 (Maunder) and 1820 (Dalton) yr A.D. Cross-correlation calculations suggest that there is no significant lag between the ¹⁰Be-based ¹⁴C and the tree-ring ¹⁴C records. Our study strongly suggests the dominance of the solar modulation on the cosmonuclide production variations during the last millennium.     

Groundwater recharge and palaeoclimate in the Sirte and Kufra basins, Libya

Stable and radio-isotope results (C, H, O) for groundwaters from the Sirte and northern Kufra basins are used to determine the recharge history during the Holocene and late Pleistocene. Radiocarbon ages have been corrected on the basis of their stable carbon isotope ratios and on environmental samples from the areas, and two groups may be recognised: (1) low ¹⁴C activity groundwaters (13000–34000 yr. BP) with δ ¹³C-5.6 to −11.7‰; and (2) higher ¹⁴C activity groundwaters (5000–7800 yr. BP) enriched in ¹³C up to δ ¹³C = −3.2‰. There is a general correlation of age with depth.

A well defined freshwater (< 50 mg/l Cl⁻) channel can be traced within the aquifer for some 130 km through the region, which is considered to represent recharge from a former wadi. This water with an age of ± 7800 yr. BP is chemically and isotopically distinct from the regional groundwaters and provides direct evidence of a significant recharge event during the Holocene.

The stable isotope (O and H) composition of groundwater from the Kufra and Sirte basins are all related by an evaporative line with slope δ D = 4.5δ ¹³O − 35 with an intercept on the meteoric line of -11‰. This suggests a recharge source continuing into the Holocene from air masses, analogous to current heavy monsoon rain derived from south of the Sahara. The spatial and temporal distribution of groundwaters in relation to the evaporative line suggests a progressive change in character of the recharge which is controlled by a shift towards strongly convective rainfall during the Holocene.

The direct hydrogeological and geochemical evidence supports climatic models proposed by several workers in which discrete humid episodes during the Holocene are inferred.     

The water balance of a small lake using stable isotopes and tritium

A small maar lake, known as the Blue Lake, set in a karstic region of southeastern Australia, provides the municipal water supply for a population of 20,000. The lake has a volume of 3.6·10⁷m³, of which 10–15% is pumped from it each year. The lake is recharged almost entirely from groundwater and the main objective of this study was to estimate the total groundwater inflow and outflow rates. Estimation of groundwater throughflow in a lake is difficult to assess using classical hydrological techniques and an alternative method involving measurement of the concentrations of the environmental isotopes ³H, ¹⁸O, ²H and ¹⁴C in the lake water and in the recharging groundwater was used to establish the lake-water balance. The water-balance calculations indicated a total groundwater inflow to Blue Lake of between 5.0·10⁶ and 6.5·10⁶m³yr.⁻¹, corresponding to a residence time of water in the lake of 6 yr. It was not possible to derive the relative proportions of inflow to the lake from the two possible source aquifers, using these isotopes, because their concentrations did not show a sufficiently large contrast to distinguish the two water sources.     

Ice core record of Be over the past millennium from Dome Fuji, Antarctica: A new proxy record of past solar activity and a powerful tool for stratigraphic dating

The cosmogenic nuclide ¹⁰Be was analyzed by using accelerator mass spectrometry on an ice core drilled at the Dome Fuji station, inland Antarctica, for 700–1900 yr CE. The measured concentration of ¹⁰Be in the Dome Fuji ice core and the derived ¹⁰Be flux show similar fluctuations, with both increasing at known solar-activity minima over the last millennium in agreement with earlier observations of ¹⁰Be and ¹⁴C. Based on the similar nature of the ¹⁰Be flux to the reconstructed ¹⁴C production rate patterns, a ¹⁰Be–¹⁴C correlation age model for the Dome Fuji ice core was successfully constructed. This age model agrees well with the initial version of the tephrochronology of the core. The ¹⁰Be-flux record contains information on variability in the amount of cosmic radiation incident on the atmosphere, which is mainly attributable to high-frequency change in solar activity and low-frequency background intensity adjustment of the geomagnetic field. High-resolution ¹⁰Be analyses of the Dome Fuji ice cores promise to provide potentially important information on the history of cosmic radiation intensity over the past several hundred thousand years.     

A 53 year seasonally resolved oxygen and carbon isotope record from a modern Gibraltar speleothem: Reconstructed drip water and relationship to local precipitation

The response of a climate proxy against measured temperature, rainfall and atmospheric circulation patterns at sub-annual resolution is the ultimate test of proxy fidelity but very few data exist showing the level of correspondence between speleothem climate proxies and the instrumental climate record. Cave sites on the Gibraltar peninsula provide a unique opportunity to calibrate speleothem climate proxies with the longest known available precipitation isotopes and instrumental records. An actively growing speleothem sampled from New St. Michaels Cave in 2004 is composed of paired laminae consisting of light columnar calcite and a darker microsparitic calcite. Stable isotope analysis of samples micromilled in 100 μm steps at the equivalent of bi-monthly intervals reveals fabric-correlated annual cycles in carbon isotopes, oxygen isotopes and trace elements responding to seasonal changes in cave microclimate, hydrology and ventilation patterns. Calcite δ¹³C values reach a minimum in the light columnar fabric and evidence from trace element behaviour and cave monitoring indicates that this grows under cave ‘winter’ conditions of highest pCO₂, whereas the dark microsparitic calcite, characterised by elevated δ¹³C and δ¹⁸O values grows under low ‘summer’ pCO₂ conditions. Drip water δ¹³C_DIC reaches a minimum in March–April, at which time the attenuated δ¹⁸O signal becomes most representative of winter precipitation. An age model based on cycle counting and the position of the ¹⁴C bomb carbon spike yields a precisely dated winter oxygen isotope proxy of cave seepage water for comparison with the GNIP and instrumental climate record for Gibraltar. The δ¹⁸O characteristics of calcite deposited from drip water representing winter precipitation for each year can be derived from the seasonally resolved record and allows reconstruction of the δ¹⁸O drip water representing winter precipitation for each year from 1951–2004. These data show an encouraging level of correspondence (r² = 0.47) with the δ¹⁸O of rainfall falling each year between October and March and on a decadal scale the δ¹⁸O of reconstructed winter drip water mirrors secular change in mean winter temperatures.     

Carbon isotopes in submarine basalts

High-sensitivity stepped extraction reveals two isotopically distinct forms of carbon in submarine basalt glasses: an isotopically light carbon component released by combustion from 200 to 600°C and an isotopically heavy CO₂ liberated from vesicles (magmatic carbon) from 600 to 1200°C. The δ¹³C_PDB of the low release temperature carbon varies from −24 to −30‰ and is believed to be surficial organic contamination. A survey of various types of oceanic glasses demonstrates that the δ¹³C of magmatic CO₂ varies from −4.2 to −7.5‰ in mid-ocean ridge basalt (MORB), from −2.8 to −6.7‰ in glasses from Hawaii and Explorer Seamount and from −7.7 to −16.3‰ in glasses from the Scotia Sea and Mariana Trough. Magmatic CO₂ in back-arc basin basalts (BABB) is on average 5‰ lighter than equivalent CO₂ in MORB and can be explained by the mixing in the source regions for BABB magmas of juvenile (MORB-like) CO₂ with an organic carbon component from subducted pelagic sediments. It is inferred that significant amounts of pelagic carbonate carbon (δ¹³C 0‰) must be recycled into the mantle.     

新保安—沙城断裂带土壤气地球化学特征分析

测量断裂带土壤气浓度变化, 是监测断裂活动性和地震危险性的重要途径之一。 2014年5月, 我们在怀来地区新保安-沙城断裂测量了断层土壤气H₂、 He、 CO₂、 Rn、 Hg浓度以及CO₂、 Rn、 Hg的通量。 测量结果显示: H₂、 He、 CO₂、 Rn、 Hg浓度变化范围分别为, H₂: (0.4～34.2)×10^-6、 He: (2.8～7)×10^-6、 CO₂: (0.051～1.19)%、 Rn: (0.31～18.22) kBq/m³、 Hg: (2～54) ng/m³。 土壤气H₂和Rn是揭示断层位置的有效参数之一, 在断层附近以及有陡坎的地区有明显高值异常。 通过对怀来地区新保安-沙城断裂土壤气浓度及通量地球化学研究初步确定断裂带有较高的脱气强度, 与此区域地震活动性有一定的关系。     

Variation in water use efficiency and δC levels in Eucalyptus grandis clones

This study aimed to determine whether the δ¹³C levels in the foliage and twigs of four Eucalyptus grandis clones were related to their water use efficiency (WUE). This relationship has previously been demonstrated in a number of herbaceous species but not in mature trees. The study involved accurate measurements of tree trunk growth and water use over a period of 4 months, with subsequent isotopic analysis of mature foliage from the north and south side of the canopy, and young leaves from the top of the canopy.

The water use efficiencies were found to vary from 5.97 × 10⁻³ to 12.3 × 10⁻³ m³ m⁻³. Significant differences were observed between clonal-mean water use efficiencies averaged over six sampling periods. The average δ¹³C of the mature and young foliage was found to be significantly correlated with WUE. However, the correlation was weak, suggesting that the relationship between δ¹³C and WUE is more complex in trees than suggested in the literature on crop plants. It is suggested that differences between sample trees in carbon allocation and leaf-to-air vapour pressure deficits may account for the poor correlation between δ¹³C and WUE in the four E. grandis clones studied.     

Isotope geochemistry of Pantelleria volcanic fluids, Sicily Channel rift: a mantle volatile end-member for volcanism in southern Europe

Chemical and isotopic ratio (He, C, H and O) analysis of hydrothermal manifestations on Pantelleria island, the southernmost active volcano in Italy, provides us with the first data upon mantle degassing through the Sicily Channel rift zone, south of the African–European collision plate boundary. We find that Pantelleria fluids contain a CO₂–He-rich gas component of mantle magmatic derivation which, at shallow depth, variably interacts with a main thermal (100°C) aquifer of mixed marine–meteoric water. The measured ³He/⁴He ratios and δ¹³C of both the free gases (4.5–7.3 R_a and −5.8 to −4.2‰, respectively) and dissolved helium and carbon in waters (1.0–6.3 R_a and −7.1 to −0.9‰), together with their covariation with the He/CO₂ ratio, constrain a ³He/⁴He ratio of 7.3±0.1 R_a and a δ¹³C of ca. −4‰ for the magmatic end-member. These latter are best preserved in fluids emanating inside the active caldera of Pantelleria, in agreement with a higher heat flow across this structure and other indications of an underlying crustal magma reservoir. Outside the caldera, the magmatic component is more affected by air dilution and, at a few sites, by mixing with either organic carbon and/or radiogenic ⁴He leached from the U–Th-rich trachytic host rocks of the aquifer. Pantelleria magmatic end-member is richer in ³He and has a lower (closer to MORB) δ¹³C than all fluids yet analyzed in volcanic regions of Italy and southern Europe, including Mt. Etna in Sicily (6.9±0.2 R_a, δ¹³C=−3±1‰). This observation is consistent with a south to north increasing imprint of subducted crustal material in the products of Italian volcanoes, whose He and C (but also O and Sr) isotopic ratios gradually evolve towards crustal values northward of the African–Eurasian plate collision boundary. Our results for Pantelleria extend this regional isotopic pattern further south and suggest the presence of a slightly most pristine or ‘less contaminated’, ³He-richer mantle source beneath the Sicily Channel rift zone. The lower than MORB ³He/⁴He ratio but higher than MORB CO₂/³He ratio of Pantelleria volatile end-member are compatible with petro-geochemical evidence that this mantle source includes an upwelling HIMU–EM1-type asthenospheric plume component whose origin, according to recent seismic data, may be in the lower mantle.     

Implanted radiogenic and other noble gases in crustal diamonds from Northern Kazakhstan

Noble gases were extracted in steps from grain size fractions of microdiamonds ( < 100 μm) from the Kokchetav Massif, Northern Kazakhstan, by pyrolysis and combustion. The concentration of ⁴He in the diamonds proper (liberated by combustion) shows a 1/r dependence on grain size. For grain diameters > 15 μm the concentration also decreases with the combustion step. Both results are clear evidence that ⁴He has been implanted into the diamonds from -decaying elements in the surrounding matrix. The saturation concentration of ⁴He(5.6 × 10⁻⁴ cm³ STP/g) is among the very highest observed in any terrestrial diamonds. Fission xenon from the spontaneous fission of ²³⁸U accompanies the radiogenic ⁴He; the ¹³⁶Xe_f/⁴He ratio of (2.5 ± 0.3) × 10⁻⁹ agrees well with the production ratio of 2.3 × 10⁻⁹ expected in a reservoir where Th/U 3.3. Radiogenic ⁴⁰Ar is predominantly ( > 90%) set free upon combustion; it also resides in the diamonds and appears to have been incorporated into the diamonds upon their formation.

³He, on the other hand is mainly released during pyrolysis and hence is apparently carried by ‘contaminants’. The concentration in the diamonds proper is of the order of 4 × 10⁻¹² cm³ STP/g, with a ³He/⁴He ratio of 1 × 10⁻⁸. Excess ²¹Ne, similarly, appears to be present in contaminants as well as in diamonds proper. These two nuclides in the contaminants must have a nucleogenic origin, but it is difficult to explain their high concentrations.     

Accretion, core formation, H and C evolution of the Earth and Mars

Recent understandings of planetary accretion have suggested that accumulation of a small number of large planetesimals dominates intermediate to final growth stages of the terrestrial planets, with impact velocity high enough to induce extensive melting of the planetesimal and target materials, resulting in formation of a large molten region in which gravitational segregation of silicate and metal, that is, core formation proceeds. In case of homogeneous accretion, volatiles contained in each planetesimal are likely subjected to partitioning among gas, silicate melt, and molten metallic iron at significantly high temperatures and pressures in such a massive molten region. Each phase would subsequently form the proto-atmosphere, -mantle, or-core, respectively. Such chemical reprocessing of H and C associated with core formation, which is followed by both degassing from mantle and atmospheric escape, may result in a diverse range of H₂O/CO₂ in planetary surface environments, which mainly depends on the H and C content relative to metallic iron in planetary building stones. This may explain inferred difference in volatile distribution between the Earth's (relatively H₂O-rich, CO₂-poor) and the martian (H₂O-poor, CO₂-rich) surface environments. Such volatile redistribution may be systematically described by using the retentivity of H₂O, ξ, defined as follows: ξ = 1 − ([CO]⁰ + 2[CH₄]⁰ + 2[C(gr)]⁰)/[H₂O]⁰, where [i]⁰ represents mol number of species i partitioned into non-metallic phases, that is, gas and silicate melt in impact-induced molten region. When ξ > 0.5, relatively H₂O-rich and CO₂-poor surface environment may eventually evolve, although a small portion of H₂O partitioned into the NON=metallic phases are possibly consumed by subsequent chemical reactions with reduced C-species with producing CO₂ and H₂. When ξ< 0.5, on the contrary, H₂O consumption by the above reactions and selective loss of H₂ to space may result in relative H₂O-depleted and CO₂-rich surface environment. Given the building stone composition by the two-component model by Ringwood (1977) and Wänke (1981), ξ is found to decrease with increasing the mixing fraction of the volatile-rich component: ξ > 0.5 for the mixing fraction smaller than about 15–20% and ξ < 0 for the mixing fraction larger than about 20–30%. This is not significantly dependent on temperature and pressure in molten region and H/C ratio in the building stone. The estimated mixing fraction of the volatile-rich component, about 10% for the Earth and 35% for Mars, is consistent with the observed difference in volatile distribution between the surfaces of both planets.     

Organic carbon isotope geochemistry of clayey deposits and their associated porewaters, southern Alberta

The organic carbon cycle of slowly permeable, clayey glacial till deposits in the Western Interior Great Plains, southern Alberta, was investigated by examining the relationship between solid organic matter (SOM) in the till sediments and dissolved organic carbon (DOC) in the till porewaters. Geochemically, the tills can be divided into two distinct zones: an upper oxidized (low SOM) till zone, and a lower unoxidized (high SOM) till zone. Till porewaters in both zones are characterized by high DOC contents. Radiocarbon dating and comparison of SOM and DOC fractions suggest DOC in the deep unoxidized zone originated during deglaciation, and is probably representative of groundwater ages in this till zone. In the oxidized zone, DOC originates from variable mixtures of soluble organic matter emplaced during deglaciation, and Cretaceous age coal fragments in this till zone. SOM in the upper till zone was mainly oxidized to CO₂ gas during lowered water table conditions of the Altithermal climatic period. The subsurface production of fossil CO₂ gas has serious implications for using the conventional dissolved inorganic carbon (DIC) ¹⁴C groundwater dating method in these clayey till porewaters.     

Influence of artificial groundwater lakes on the abundance and activity of bacteria in adjacent subsurface systems

Bacterial abundances and activity, estimated by 4′,6-diamidino-2-phenylindole staining (DAPI) and the reduction of 2-(p-iodophenyl)-3-(p-nitrophenyl)-5-phenyl tetrazolium chloride (INT), were investigated in two oligotrophic artificial groundwater lakes and the surrounding aquifers. To evaluate the effect of lake water on groundwater downstream, samples were taken from wells at different distances from the lakes, and the total number of bacteria and the number of active bacteria in these samples were compared with samples collected upstream. In addition, sterilized sandy sediments were exposed in groundwater wells to measure the number and activity of bacteria attached to particles. At one of the study sites, where the lake sediments were disturbed by dredging, total bacterial abundance and the number of respiring bacteria in the groundwater aquifer was clearly influenced by the lake water. The average bacterial abundances decreased from 2.6 ± 1.9 × 10⁵ cells ml⁻¹ in the well closest to the lake (S2) to 2.9 ± 3.8 × 10⁴ cells ml⁻¹ in the most distant one (S4), which was equivalent to cell numbers in the upstream well. The number of respiring bacteria showed a similar tendency with 1.3 ± 2.7 × 10⁴ active cells ml⁻¹ in S2 and 1.9 ± 1.5 × 10³ active cells ml⁻¹ in S4. At the second study site, which was not influenced by dredging, bacteria in the downstream wells seemed not to be affected by the lake water. The number and activity of bacteria, which colonized exposed sediments, were not significantly different in the upstream and downstream wells, indicating a minor influence of lake water on this habitat. Our results suggest that gravel-pit lakes may influence the free living bacterial assemblages in nearshore groundwater systems, but do not visibly affect numbers and activity of bacteria attached to the surface of aquifer sediments.     

Noble gases in submarine pillow basalt glasses from the Lau Basin: Detection of a solar component in backarc basin basalts

Noble gas elemental and isotopic abundances have been analysed in eight samples of youthful basaltic glass dredged from three different locations within the Lau Backarc Basin: (1) the King's Triple Junction, (2) the Central Lau Spreading Centre at 18°S and (3) the Eastern Lau Spreading Centre at 19°S. Samples from the Lau central and eastern spreading centres have MORB-like helium isotopic ratios of approximately 1.2 × 10⁻⁵ (8.5 R/R_A). In contrast, the samples from the King's Triple Junction yield helium isotopic ratios averaging 9.4 (±0.8) × 10⁻⁶ (6.7 ± 0.6 R/R_A), systematically lower than the MORB-like value, which may be reflecting the addition of radiogenic ⁴He released from the descending slab. Neon isotopic ratios are enriched in ²⁰Ne and ²¹Ne with respect to atmospheric ratios by as much as 23% and 62% respectively. These observations further confirm that non-atmospheric neon is a common characteristic of samples derived from the mantle. The helium and neon isotopic signatures in the samples can be explained by mixing of a primordial solar component, radiogenic and nucleogenic components produced by radioactive processes inside the Earth, and an atmospheric component. This reconnaissance survey of noble gases in a backarc basin indicates that current volcanism is dominated by magmas from the mantle wedge, a source similar to that from which MORBs are derived. The heavier noble gases (argon, krypton and xenon), however, show more atmosphere-like compositions, either indicating strong interaction of the magmas with the atmosphere or the presence of a recycled component derived from the underlying subducting slab.     

中国三个大地震的震源参数及讨论

大地震的震源机制及地震矩、应力降等参数,不(又对认识地震的破裂过程,而且对预报强地面运动都是非常重要的。一些文章对板内地震应力降的特点、地震矩与高频源谱的关系及区域特征的讨论,使我们可直接由长周期体波或面波得出的地震矩M₀估计出不同地区中大地震的高频源谱,以供强地面运动预报参考。 由于对发生在中国板内的1976年11月6日盐源地震（M_s=6.5）和1976年11月15日宁河地震（M_s=6.3）的震源参数还没有详尽的报道;另外,对1973年7月14日