Glacial atmospheric CO_2 decline in association with decrease of marine sedimentary phosphorus

Since the discovery from the ice-core record of South Pole revealed that atmospheric concentration of CO2 of the last glacial was 80―100 ppm less than that of Holocene[1], many researchers[2―6] have obtained a series of important findings to seek the dominant fac- tors controlling its change from marine physical, chemical and biological processes, among which the view has gained increasing attention that phosphorus, as a macronutrient, is a crucial limitation to marine primary production, a…     

Variations of near-surface atmospheric CO2 and H2O concentrations during summer on Muztagata

Expeditions during the summers of 2002 and 2003 implemented continuous monitoring of near-surface (2 m height) atmospheric CO₂ and H₂O concentrations at the 4500 m elevation on Muztagata. The resultant data sets reveal a slight decrease of CO₂ concentrations (of about 5 μmol·mol^-1) and changes in the diurnal variations from the end of June to the middle August. The daily maximum CO₂ concentrations occur between 02:30-05:30 AM (local time) and the minimum levels occur between 12:00-15:30 PM. The atmospheric CO₂ concentrations in the summer of 2002 were around 5 μmol·mol^-1 lower than those during the same period of 2003, whereas the diurnal amplitude was higher. In contrast, we found that the daily mean atmospheric H₂O content in 2003 was much lower than that in 2002 and there exists a striking negative correlation between CO₂ and H₂O concentrations. We therefore suggest that the near-surface atmospheric CO₂ concentration is affected not only by photosynthesis and respiration, but also by the air H₂O content in the glaciated region around Muztagata.     

Carbon isotopic compositions of organic matter across continental Cretaceous–Tertiary (K–T) boundary sections: Implications for paleoenvironment after the K–T impact event

To assess the environmental perturbation induced by the impact event that marks the Cretaceous–Tertiary (K–T) boundary, concentrations and isotopic compositions of bulk organic carbon were determined in sedimentary rocks that span the terrestrial K–T boundary at Dogie Creek, Montana, and Brownie Butte, Wyoming in the Western Interior of the United States. The boundary clays at both sites are not bounded by coals. Although coals consist mainly of organic matter derived from plant tissue, siliceous sedimentary rocks, such as shale and clay, may contain organic matter derived from microbiota as well as plants. Coals record δ¹³C values of plant-derived organic matter, reflecting the δ¹³C value of atmospheric CO₂, whereas siliceous sedimentary rocks record the δ¹³C values of organic matter derived from plants and microbiota. The microbiota δ¹³C value reflects not only the δ¹³C value of atmospheric CO₂, but also biological productivity. Therefore, the siliceous rocks from these sites yields information that differs from that obtained previously from coal beds.Across the freshwater K–T boundary at Brownie Butte, the δ¹³C values decrease by 2.6‰ (from − 26.15‰ below the boundary clay to − 28.78‰ above the boundary clay), similar to the trend in carbonate at marine K–T sites. This means that the organic δ¹³C values reflect the variation of δ¹³C of atmospheric CO₂, which is in equilibrium with carbon isotopes at the ocean surface. Although a decrease in δ¹³C values is observed across the K–T boundary at Dogie Creek (from − 25.32‰ below the boundary clay to − 26.11‰ above the boundary clay), the degree of δ¹³C-decrease at Dogie Creek is smaller than that at Brownie Butte and that for marine carbonate.About 2‰ decrease in δ¹³C of atmospheric CO₂ was expected from the δ¹³C variation of marine carbonate at the K–T boundary. This δ¹³C-decrease of atmospheric CO₂ should affect the δ¹³C values of organic matter derived from plant tissue. As such a decrease in δ¹³C value was not observed at Dogie Creek, a process that compensates the δ¹³C-decrease of atmospheric CO₂ should be involved. For example, the enhanced contribution of ¹³C-enriched organic matter derived from algae in a high-productivity environment could be responsible. The δ¹³C values of algal organic matter become higher than, and thus distinguishable from, those of plant organic matter in situations with high productivity, where dissolved HCO₃⁻ becomes an important carbon source, as well as dissolved CO₂. As the δ¹³C-decrease of atmospheric CO₂ reflected a reduction of marine productivity, the compensation of the δ¹³C decrease by the enhanced activity of the terrestrial microbiota means that the microbiota at freshwater environment recovered more rapidly than those in the marine environment.A distinct positive δ¹³C excursion of 2‰ in the K–T boundary clays is superimposed on the overall decreasing trend at Dogie Creek; this coincides with an increase in the content of organic carbon. We conclude that the K–T boundary clays include ¹³C-enriched organic matter derived from highly productive algae. Such a high biological productivity was induced by phenomena resulting from the K–T impact, such as nitrogen fertilization and/or eutrophication induced by enhanced sulfide formation. The high productivity recorded in the K–T boundary clays means that the freshwater environments (in contrast to marine environments) recovered rapidly enough to almost immediately (within 10 yr) respond to the impact-related environmental perturbations.     

典型农业流域不同类型池塘水体CO2排放特征

内陆水体是大气CO₂收支估算的重要组成部分。农业流域分布着大量池塘景观水体,且具备蓄洪抗旱、消纳污染、水产养殖等多种功能。但是,农业流域不同功能的小型池塘CO₂排放特征尚不清楚。本研究以极具农业流域代表性的烔炀河流域为研究对象,选取流域中用于水产养殖(养殖塘)、生活污水承纳(村塘)、农业灌溉(农塘)、蓄水(水塘)的4个功能不同的景观池塘,基于为期1年的野外实地观测,以明确农业流域小型池塘CO₂排放特征。结果表明,不同功能池塘水体CO₂排放差异显著,受养殖活动、生活污水输入和农田灌溉等人类活动影响,养殖塘((80.37±100.39) mmol/(m²·d))、村塘((48.69±65.89) mmol/(m²·d))和农塘((13.50±15.81) mmol/(m²·d))是大气CO₂的热点排放源,其CO₂排放通量分别是自然蓄水塘((4.52±23.26) mmol/(m²·d))的18、11和3倍。统计分析也表明,该流域池塘CO₂排放变化总体上受溶解氧、营养盐等因素驱动。4个不同景观池塘CO₂排放通量全年均值为(37.31±67.47) mmol/(m²·d),是不容忽视的CO₂排放源,其中养殖塘和村塘具有较高的CO₂排放潜力,在未来研究中需要重点关注。     

Correlations between13C and ΣCO2 in surface waters and atmospheric CO2

¹³C and ΣCO₂ data from the North and South Atlantic, the Antarctic, and the North and South Pacific are given. The δ¹³C of the ΣCO₂ in the deep water (～3000m) decreases from 1.7‰ in the North Atlantic to ?0.10‰ in the North Pacific. This change is attributed to the addition of about 158 μmoles of CO₂ per kg of seawater. The in-situ oxidation of organic matter accounts for 83% of this increase in ΣCO₂, while the remainder is attributed to dissolution of calcium carbonate.The δ¹³C of the dissolved CO₂ in mid-latitude surface water samples is controlled by a quasi-steady-state equilibrium with atmospheric CO₂ at a mean temperature of 16°C. The δ¹³C and ΣCO₂ values of Antarctic surface water samples suggest that these waters are derived from a mixture of North Atlantic deep water and equilibrated surface water.     

13C/12C- und 18O16O-Signaturen von Calcit-Abscheidungen in Drainagesystemen

¹³C/¹²C- and ¹⁸O/16O-signatures of Calcite Precipitations in Drainage Systems Measurements of drainage waters show two distinct processes of calcite precipitation: 1. reprecipitation of calcium carbonate previously dissolved in groundwaters and 2. absorption of atmospheric CO₂ by alkaline solutions. Both processes may be distinguished by the stable isotopes of oxygen and carbon. Calcite precipitated from carbonate groundwater yields δ¹³C ≈ ?13%₀ (PDB) and δ¹⁸O ≈ 24%₀ (SMOW), whereas calcite produced by CO₂-absorption shows δ¹³C ≈ ?25%₀ (PDB) and δ¹⁸O ≈ 10%₀ (SMOW).     

Air-sea CO2 fluxes in the southern Yellow Sea: An examination of the continental shelf pump hypothesis

The southern Yellow Sea (SYS), located to the north of the East China Sea (ECS), was considered part of the ECS when Tsunogai et al. (1999) proposed the “continental shelf pump” (CSP) hypothesis. However, the original CSP carbon dioxide (CO₂) uptake flux (2.9 mol C m⁻² yr⁻¹) appears to have been overestimated, primarily due to the differences between the SYS and the ECS in terms of their CO₂ system. In this paper, we estimated air-sea CO₂ fluxes in the SYS using the surface water partial pressure of CO₂ (pCO₂) measured in winter, spring, and summer, as well as that estimated in fall via the relationship of pCO₂ with salinity, temperature, and chlorophyll a. The results indicate that overall, the entire investigated area was a net source of atmospheric CO₂ during summer, winter, and fall, whereas it was a net sink during spring. Spatially, the nearshore area was almost a permanent CO₂ source, while the central SYS shifted from being a CO₂ sink in spring to a source in the other seasons of the year. Overall, the SYS is a net source of atmospheric CO₂ on an annual scale, releasing ∼7.38 Tg C (1 Tg=10¹² g) to the atmosphere annually. Thus, the updated CO₂ uptake flux in the combined SYS and ECS is reduced to ∼0.86 mol C m⁻² yr⁻¹. If this value is extrapolated globally following Tsunogai et al. (1999), the global continental shelf would be a sink of ∼0.29 Pg C yr⁻¹, instead of 1 Pg C yr⁻¹ (1 Pg=10¹⁵ g).The SYS as a net annual source of atmospheric CO₂ is in sharp contrast to most mid- and high-latitude continental shelves, which are CO₂ sinks. We argue that unlike the ECS and the North Sea where carbon on the shelf could be exported to the open ocean, the SYS lacks the physical conditions required by the CSP to transport carbon off the shelf effectively. The global validity of the CSP theory is thus questionable.     

New insights into the spatial variability of the surface water carbon dioxide in varying sea ice conditions in the Arctic Ocean

In the summer of 2005, continuous surface water measurements of fugacity of CO₂ (fCO₂^sw), salinity and temperature were performed onboard the IB Oden along the Northwest Passage from Cape Farwell (South Greenland) to the Chukchi Sea. The aim was to investigate the importance of sea ice and river runoff on the spatial variability of fCO₂ and the sea–air CO₂ fluxes in the Arctic Ocean. Additional data was obtained from measurements of total alkalinity (A_T) by discrete surface water and water column sampling in the Canadian Arctic Archipelago (CAA), on the Mackenzie shelf, and in the Bering Strait. The linear relationship between A_T and salinity was used to evaluate and calculate the relative fractions of sea ice melt water and river runoff along the cruise track. High-frequency fCO₂^sw data showed rapid changes, due to variable sea ice conditions, freshwater addition, physical upwelling and biological processes. The fCO₂^sw varied between 102 and 678 μatm. Under the sea ice in the CAA and the northern Chukchi Sea, fCO₂^sw were largely CO₂ undersaturated of approximately 100 μatm lower than the atmospheric level. This suggested CO₂ uptake by biological production and limited sea–air CO₂ gas exchange due to the ice cover. In open areas, such as the relatively fresh water of the Mackenzie shelf and the Bering Strait, the fCO₂^sw values were close to the atmospheric CO₂ level. Upwelling of saline and relatively warm water at the Cape Bathurst caused a dramatic fCO₂^sw increase of about 100 μatm relative to the values in the CAA. At the southern part of the Chukchi Peninsula we found the highest fCO₂^sw values and the water was CO₂ supersaturated, likely due to upwelling. In the study area, the calculated sea–air CO₂ flux varied between an oceanic CO₂ sink of 140 mmol m⁻² d⁻¹ and an oceanic source of 18 mmol m⁻² d⁻¹. However, in the CAA and the northern Chukchi Sea, the sea ice cover prevented gas exchange, and the CO₂ fluxes were probably negligible at this time of the year. Assuming that the water was exposed to the atmosphere by total melting and gas exchange would be the only process, the CO₂ undersaturated water in the ice-covered areas will not have the time to reach the atmospheric CO₂ value, before the formation of new sea ice. This study highlights the value of using high-frequency measurements to gain increased insight into the variable and complex conditions, encountered on the shelves in the Arctic Ocean.     

不同水文情景下洪泽湖二氧化碳排放通量特征及影响因素

内陆水域二氧化碳(CO₂)排放是全球碳平衡的重要组成部分,全球CO₂排放通量估算通常有很大不确定性,一方面源于CO₂排放数据观测的时空离散性,另一方面也是缺少水文情景与CO₂排放通量关联性的研究.本文观测了2018年洪泽湖不同水文情景表层水体CO₂排放通量特征,并探讨其影响因素.结果表明,洪泽湖CO₂排放通量为丰水期((106.9±73.4) mmol/(m²·d))>枯水期((18.7±13.6) mmol/(m²·d))>平水期((5.2±15.5) mmol/(m²·d)),且碳通量由丰(310.2~32.0 mmol/(m²·d))、枯(50.8~2.2 mmol/(m²·d))、平(-17.3~39.8 mmol/(m²·d))3种水文情景的交替表现出湖泊碳源到弱碳汇的转变,空间上CO₂排放通量总体呈现北部成子湖区低、南部过水湖区高的分布趋势.洪泽湖CO₂排放对水文情景响应敏感,特别是上游淮河流域来水量的改变,是主导该湖CO₂排放时空分异的重要因子.丰水期湖泊接纳了淮河更多有机和无机碳的输入,外源碳基质的降解和矿化显著促进了水体CO₂的生产与排放,同时氮、磷等营养物质的大量输入,加剧了水体营养化程度,进一步提高CO₂排放量,间接反映出人类活动对洪泽湖CO₂变化的深刻影响.平、枯水期随着上游淮河来水量的减少,驱动水体CO₂排放的因素逐渐由外源输入转变为水体有机质的呼吸降解.此外,上游河口区DOM中陆源类腐殖质的累积与矿化能够促进CO₂的排放,而内源有机质组分似乎并没有直接参与CO₂的排放过程.研究结果揭示了水文情景交替对湖库CO₂排放的重要影响,同时有必要进行高频观测以进一步明晰湖泊的碳通量变化及其控制因素.     

Net primary productivity and its control of the Middle Jurassic peatlands: An example from the southern Junggar coalfield

The Jurassic is an important period of global coal formation, including the development of several large coalfields in central Asia and northern China. Individual seams within these peatlands represent sustained periods of terrestrial carbon accumulation and a key environmental indicator attributed to this record is the rate of carbon accumulation. Determining the rate of carbon accumulation requires a measure of time contained within the coal and this study aimed at determining the rate via the identification of Milankovitch orbital cycles using spectral analysis. Spectral analyses of geophysical data from two thick coal seams, No. 43(35.9 m) and No. 3(13.2 m), of the Middle Jurassic of the southern Junggar coalfield were conducted to identify significant signals of variations in ash content. The results showed that the variations in ash content of the coal showed spatial cycles at 0.2, 0.7 and 1.1 m~(-1), which were interpreted to represent 123 ka(eccentricity), 37.1 ka(obliquity), and 21.2 ka(precession) orbital periodicities, respectively. Using this timeframe, the depositional time of the No. 43 and No. 3 coal seams were calculated to be 876–970 and 322–357 ka, respectively. In combination with an understanding of carbon loss during coalification, the carbon accumulation rates of these Middle Jurassic peatlands were calculated to be 58.6–64.9 and60.3–66.8 g C m~(-2) a~(-1) for the No. 43 and No. 3 coal seams, respectively. Given that the net primary productivity(NPP) was 4.3 times the value of the carbon accumulation in a mid-latitude region of 40°–45°N, an NPP of 251.8–279.1 and259.1–287.1 g C m~(-2) a~(-1) was calculated for the No. 43 and No. 3 coal seams, respectively. In the context of the same paleolatitude(40°–45°N) and peat type, the NPP values of the Middle Jurassic strata in the study area were higher than those of the peatlands of the Holocene and Permian, and were similar to the NPP values of Early Cretaceous peatlands. Considering the NPP of a peatland is predominantly controlled by atmospheric CO_2 and O_2 levels and temperature, the lower content of CO_2 and an excessive O_2 level in the temporal atmosphere would lead to a decrease in peatland NPP. Therefore, it is inferred that the CO_2 level during the Middle Jurassic was higher than that of the icehouse Permian and Holocene periods, and it was similar to the CO_2 level of the greenhouse Cretaceous period. The results are consistent with the global CO_2 variation curve of Berner. In conclusion, Milankovitch orbital cycles calculated from geophysical logs can be used to infer the NPP of temporal peatlands during different geological periods, based on which the deep-time paleoclimates can be analyzed.     

Gas hazard assessment in a densely inhabited area of Colli Albani Volcano (Cava dei Selci, Roma)

The northwestern flank of the Colli Albani, a Quaternary volcanic complex near Rome, is characterised by high pCO₂ values and Rn activities in the groundwater and by the presence of zones with strong emission of gas from the soil. The most significant of these zones is Cava dei Selci where many houses are located very near to the gas emission site. The emitted gas consists mainly of CO₂ (up to 98 vol%) with an appreciable content of H₂S (0.8–2%). The He and C isotopic composition indicates, as for all fluids associated with the Quaternary Roman and Tuscany volcanic provinces, the presence of an upper mantle component contaminated by crustal fluids associated with subducted sediments and carbonates. An advective CO₂ flux of 37 tons/day has been estimated from the gas bubbles rising to the surface in a small drainage ditch and through a stagnant water pool, present in the rainy season in a topographically low central part of the area. A CO₂ soil flux survey with an accumulation chamber, carried out in February–March 2000 over a 12 000 m² surface with 242 measurement points, gave a total (mostly conductive) flux of 61 tons/day. CO₂ soil flux values vary by four orders of magnitude over a 160-m distance and by one order of magnitude over several metres. A fixed network of 114 points over 6350 m² has been installed in order to investigate temporal flux variations. Six surveys carried out from May 2000 to June 2001 have shown large variations of the total CO₂ soil flux (8–25 tons/day). The strong emission of CO₂ and H₂S, which are gases denser than air, produces dangerous accumulations in low areas which have caused a series of lethal accidents to animals and one to a man. The gas hazard near the houses has been assessed by continuously monitoring the CO₂ and H₂S concentration in the air at 75 cm from the ground by means of two automatic stations. Certain environmental parameters (wind direction and speed; atm P, T, humidity and rainfall) were also continuously recorded. At both stations, H₂S and CO₂ exceeded by several times the recommended concentration thresholds. The highest CO₂ and H₂S values were recorded always with wind speeds less than 1.5 m/s, mostly in the night hours. Our results indicate that there is a severe gas hazard for people living near the gas emission site of Cava dei Selci, and appropriate precautionary and prevention measures have been recommended both to residents and local authorities.     

粤东五华河流域的化学风化与CO2吸收

基于对粤东五华河干流和支流水体的物理、化学组成测试数据,应用质量平衡法和相关分析法探讨湿热山地丘陵地区岩石化学风化过程对大气CO₂的吸收.结果表明:五华河水体的总溶解性固体含量(77.11 mg/L)接近于世界河流的平均值(65 mg/L);离子组成以Ca²⁺、Na⁺和HCO₃^-为主,可溶性Si次之.五华河流域化学径流组成主要源自硅酸盐矿物化学风化过程的贡献,碳酸盐矿物的贡献较少;大气和土壤CO₂是流域内岩石化学风化的主要侵蚀介质.与同一气候带其他河流相比较,五华河流域岩石化学风化过程对大气CO₂的吸收通量(2.14×105mol/(km²·a))较低,这主要是由于流域内缺乏碳酸盐岩所导致.     

Dissolved carbon dioxide in basaltic glasses: concentrations and speciation

Carbon dioxide dissolved in both synthetic Ca±Mg-bearing silicate glasses and natural basaltic glasses has been characterized using infrared spectroscopy. CO₂ is inferred to be dissolved in these glasses as distorted Ca or Mg carbonate ionic complexes that result in unique infrared absorption bands at 1515 cm⁻¹ and 1435 cm⁻¹. This speciation contrasts with the case of CO₂-bearing sodium aluminosilicate glasses, which contain both dissolved molecular CO₂ and dissolved Na-carbonate ionic-complexes. The difference in speciation in Ca±Mg-bearing melts may result in part from a higher activity of oxygens that react with CO₂ molecules to produce carbonate.Dissolved CO₂ contents of natural basaltic glasses can be determined from the intensities of the carbonate absorption bands at 1515 cm⁻¹ and 1435 cm⁻¹. The uncertainty of the method is estimated to be ± 15% of the amount present. The infrared technique is a powerful tool for the measurement of dissolved CO₂ contents in natural basaltic glasses since it is non-destructive, can be aimed at regions of glass a few tens of microns in size, and can discriminate between dissolved carbonate and carbon present as carbonate alteration, contained in fluid inclusions, or adsorbed on the glass.A set of submarine basaltic glasses dredged from a variety of locations contain 0–400 ppm dissolved CO₂, measured using the infrared technique. These concentrations are lower than most previous reports for similar basaltic glasses. No general relationship is observed between dissolved CO₂ content and depth of magmatic eruption, although some correlation might be present in restricted geographic locales.     

The stable isotopic composition of modern soil carbonate and its relationship to climate

The oxygen isotopic composition of modern soil carbonate is well correlated with the isotopic composition of local meteoric water. The carbon isotopic cycle for CO₂ in soils can be described in terms of the proportion of biomass using the C₄ photosynthetic pathway and the CO₂ respiration rate of the soil; at low soil respiration rates significant atmospheric CO₂ mixing can occur. In general, the carbon isotopic composition of soil carbonate is related to the proportion of C₄ biomass present in soil, but soils that freeze to the depth of carbonate formation often have a significant atmospheric component. This suggests that freezing of the soil solution should be considered as another important mechanism for soil carbonate formation. Because of these relationships, the isotopic composition of soil carbonate may be a paleoclimatic and paleoecologic indicator in cases in which diagenetic alteration has not occurred.     

Formation of High-Alkali Groundwater in Upper Aquifers

Generalized observational data on groundwater chemistry and the results of modeling geochemical processes allowed us to establish that the formation of high-carbonate alkaline waters follows two ways, i.e., calcium and soda. It is shown that the formation of alkaline waters in semiarid and arid zones can be facilitated by acid atmospheric precipitation, which forms the concentration of Ca in groundwater sufficiently high to initiate ion exchange processes resulting in the formation of H₂CO₃–Na waters. Ion exchange is shown to be a boundary process, which facilitates the transition from calcium to soda way of groundwater metamorphization with subsequent increase in the carbonate content and alkalinity of groundwater.     

Relationship between13C and18O fractionation and changes in major element composition in a recent calcite-depositing spring — A model of chemical variations with inorganic CaCO3 precipitation

A theoretical model is derived in which isotopic fractionations can be calculated as a function of variations in dissolved carbonate species on CO₂ degassing and calcite precipitation. This model is tested by application to a calcite-depositing spring system near Westerhof, Germany. In agreement with the model,¹³C of the dissolved carbonate species changes systematically along the flow path. The difference in δ values between the upper and lower part of the stream is about 1‰. The¹³C content of the precipitated calcite is different from that expected from the theoretical partitioning. The isotopic composition of the solid CaCO₃ is similar to that of the dissolved carbonate, though in theory it should be isotopically heavier by about 2.4‰. The¹⁸O composition of dissolved carbonate and H₂O is constant along the stream. Calculated calcite-water temperatures differ by about +5°C from the observed temperatures demonstrating isotopic disequilibrium between the water and precipitated solid. This is attributed to kinetic effects during CaCO₃ deposition from a highly supersaturated solution, in which precipitation is faster than equilibration with respect to isotopes.Plant populations in the water have virtually no influence on CO₂ degassing, calcite saturation and isotopic fractionation. Measurements of P_CO2, S_C and¹³C within a diurnal cycle demonstrate that metabolic effects are below the detection limit in a system with a high supply-rate of dissolved carbonate species. The observed variations are due to differences in CO₂ degassing and calcite precipitation, caused by continuously changing hydrodynamic conditions and carbonate nucleation rates.     

Reduction of thermohaline circulation during deglaciation: the effect on atmospheric radiocarbon and CO2

A two-? ocean reservoir model is employed to examine the combined effects of vertical ocean circulation, organic matter extraction and cosmic ray production on the¹⁴C/¹²C in the atmosphere, ocean and sediment. In this model, dissolution of deep-sea calcium carbonate sediment is assumed to respond to the supply of particulate carbonate from the surface ocean and to the dissolved carbonate-ion concentration of the deep-sea.If the vertical ocean circulation decreased by 50% during the maximum rate of deglaciation, the atmospheric¹⁴C/¹²C would have increased concurrently by 10% relative to the pre-bomb present. Further, if cosmic ray production of¹⁴C was 50% greater than present at about 7800 years B.P. as suggested by archeomagnetic measurements, a double maximum of 10% occurs. The first is at about 10.5 ka and the second at 6.5 ka. This result is similar to the variation of¹⁴C/¹²C over the last 10,000 years calculated from the¹⁴C dates measured by Stuiver on the varved Lake of the Clouds. The result is not sensibly altered if 10¹⁷ moles of organic carbon is extracted from the ocean during sea-level rise.Reduction of the thermohaline ocean circulation by 50% over a one- to two-thousand-year interval would not be sensibly detected in the dating of deep-sea sediment. If Broecker's organic nutrient extraction occurs in conjunction with reduction of vertical circulation, a decrease in the atmospheric P_CO2 will precede the eventual rise.     

Continuous chemical monitoring of volcanic gas in Izu-Oshima volcano, Japan

A new continuous monitoring system has been developed for the measurement of volcanic gas from the steam well located 3 km north from the summit of Izu-Oshima volcano, Japan. After removing the water vapor using three sequential dehydration methods, CO₂ and SO₂ contents are measured using IR sensors, and O₂ and H₂ using a zirconia sensor and a semiconductor sensor, respectively. This system has been in operation without any significant trouble for 3 years.The dehydrated volcanic gas from the well consists of a mixture of CO₂, O₂ and N₂. A decreasing trend of the CO₂ content was observed from 1995 to 1998 together with a decrease of volcanic activity. Seasonal changes have also been observed in CO₂ and O₂ contents, CO₂ being higher and O₂ lower in summer, which suggests larger contribution of magmatic components in summer. While changes in short-term variation in CO₂ and O₂ are influenced by atmospheric pressure changes; the CO₂ content correlates inversely with atmospheric pressure unlike O₂ with some hours delay. In contrast, the H₂ content increased intermittently up to 1200 ppm one to several hours after a sudden drop in the atmospheric pressure and without any apparent correlation with seasonal changes.This system allows us to study temporal variation in chemical composition of volcanic gas during quiescent periods of volcanic activity of Izu-Oshima volcano, and might help us detect anomalous changes before future eruptive events.     

Comparative study on CO2 sources in soil developed on carbonate rock and non-carbonate rock in Central Guizhou

In this paper, by using concentration and carbon stable isotope the CO₂ sources of soil profiles developed on limestone, dolostone and claystone basements in Central Guizhou, China are comparatively studied. The results show that CO₂ concentration of soil profiles developed on different basements is different, having the following sequence: limestone ; dolostone;claystone. Below the soil depth of 20 cm from the surface the δ₁₃ value of CO₂ in soil profile developed on limestone ranges from -12.811%. - -13.492%.(PDB), that in soil profile developed on dolostone varys from -13.212%. - -14.271%.(PDB) and that in soil profile developed on claystone is about-20.234%. - -21.485%.(PDB). Taking the carbon isotope of soil organic matter and carbonate rock as two isotopic endmembers, the proportion of soil CO₂ generated by dissolution of carbonate rock is calculated, about 21%–25% for soil profile developed on limestone basement, 19%–21% for soil profile developed on dolostone basement. There is almost no influx of CO₂ generated by the dissolution of carbonate rock in soil profile developed on claystone basement.     

Tidal pumping and biogeochemical processes: Dissolution within the tidal capillary fringe of eogenetic coastal carbonates

Growing evidence suggests microbial respiration of dissolved organic carbon (DOC) may be a principal driver of subsurface dissolution and cave formation in eogenetic carbonate rock. Analyses of samples of vadose zone gasses, and geochemical and hydrological data collected from shallow, uncased wells on San Salvador Island, Bahamas, suggest tidally varying water tables may help fuel microbial respiration and dissolution through oxygenation. Respiration of soil organic carbon transported to water tables generates dysaerobic to anaerobic groundwater, limiting aerobic microbial processes. Positive correlations of carbon dioxide (CO₂), radon-222 (²²²Rn) and water table elevation indicate, however, that tidal pumping of water tables pulls atmospheric air that is rich in oxygen, and low in CO₂ and ²²²Rn, into contact with the tidal capillary fringe during falling tides. Ratios of CO₂ and O₂ in vadose gas relative to the atmosphere indicate this atmospheric oxygen fuels respiration within newly-exposed, wetted bedrock. Deficits of expected CO₂ relative to O₂ concentrations indicate some respired CO₂ is likely removed by carbonate mineral dissolution. Tidal pumping also appears capable of transferring oxygen to the freshwater lens, where it could also contribute to respiration and dissolution; dissolved oxygen concentrations at the water table are at least 5% saturated and decline to anaerobic conditions 1–2 m below. Our results demonstrate how tidal pumping of air to vadose zones can drive mineral dissolution reactions that are focused near water tables and may contribute to the formation of laterally continuous vuggy horizons and potentially caves. © 2020 John Wiley & Sons, Ltd.