The Selection of Temperature for High Temperature Combustion of Carbon

The rate of oxidation of different organic matters varied greatly at combustion temperatures lower than 800 °C. While some materials were oxidized rapidly, others produced peaks with extremely long tails which were difficult to integrate accurately. At 550 °C, where calcium carbonate still remained intact, the determination of carbon consumed much more time and yielded a poorer accuracy when compared with combustion at 950°C. Above 550 °C calcium carbonate decomposes and produces peaks which overlap with those of organic carbon. An accurate correction for carbonate in the results of organic carbon analysis cannot thus be established, in practice, and separate determinations of total and inorganic carbon should be carried out, organic carbon being obtained by subtraction. To achieve the most accurate results the use of 950… 1000°C is recommended for the determination of both total, and carbonate, carbon.     

Geochemische und 13C/12C-isotopenchemische Untersuchung zur Herkunft der Kohlensäure in mineralhaltigen Wässern Nordhessens (Deutschland)

Geochemical and ¹³C/¹²C-isotopical Investigation of Mineral Waters in Northern Hessia (Germany) and the Origin of their CO₂ Content The dissolved carbonate originates from three sources: 1. biogenetic soil-CO₂, 2. volcanic CO₂ related to the evaporites of the Zechstein formation, and 3. carbonate derived from the dissolution of limestones and dolomites. Miocenic basaltic melts penetrated the evaporites of the Zechstein, and the related CO₂ was trapped in the intra- and intergranulars of the salt minerals. Circulating meteoric waters dissolve the salt minerals releasing CO₂ gas. Thus, the occurrence of basalt is related to the CO₂ contents of the evaporites, and the dissolution of only small amounts of salts rich in CO₂ may result in a high concentration of carbonic acid. In waters rich in carbonate, where volcanic CO₂ dominates over the other two sources of carbon, a δ¹³C-value of “salt-CO₂” of about –1‰ (PDB) is obtained. Water with less dissolved carbonate species have smaller quantities of salt-CO₂ down to about 20%.     

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).     

Fluxes of inorganic carbon from two forested catchments in the Appalachian mountains

This study uses long‐term records of stream chemistry, discharge and air temperature from two neighbouring forested catchments in the southern Appalachians in order to calculate production of dissolved CO₂ and dissolved inorganic carbon (DIC). One of the pair of catchments was clear‐felled during the period of the study. The study shows that: (1) areal production rates of both dissolved CO₂ and DIC are similar between the two catchments even during and immediately after the period of clear‐felling; (2) flux of total inorganic carbon (dissolved CO₂+ DIC) rises dramatically in response to a catchment‐wide acidification event; (3) DIC and dissolved CO₂ are dominantly released on the old water portion of the discharge and concentrations peak in the early autumn when flows in the study catchments are at their lowest; (4) total fluvial carbon flux from the clear‐felled catchment is 11·6 t km⁻² year⁻¹ and for the control catchment is 11·4 t km⁻² year⁻¹. The total inorganic carbon flux represents 69% of the total fluvial carbon flux. The method presented in the study provides a useful way of estimating inorganic carbon flux from a catchment without detailed gas monitoring. The time series of dissolved CO₂ at emergence to the stream can also be a proxy for the soil flux of CO₂. Copyright © 2005 John Wiley & Sons, Ltd.     

Long‐term carbon storage and hydrological control of CO2 exchange in tundra ponds in the Hudson Bay Lowland

Carbon dioxide fluxes and water balance were examined in 43 tundra ponds in the northern portion of the Hudson Bay Lowland near Churchill, Manitoba. Most of the ponds were hydrologically disconnected from their catchments during dry periods throughout the post‐melt season. However, episodic reconnection occurred following large precipitation events where depression storage was exceeded. Significant shifts in pond chemistry were observed following precipitation events, with the degree of CO₂ saturation increasing during these periods. Pond CO₂ concentrations rapidly fell to pre‐event levels following events, suggesting that hydrological connectivity can affect the magnitude and direction of CO₂ gas fluxes in tundra ponds. Atmospheric CO₂ invaded ponds with highly organic sediments for most of the summer, suggesting that terrestrially derived inorganic carbon was insufficient to meet the demands of algal net production. In contrast, ponds with highly mineral sediments continued to evade CO₂ during the summer. In a subset of 11 ponds, long‐term rates of carbon accumulation in sediment ranged from 0·6 to 2·2 mol C m^?2 year^?1. Very strong correlations existed between average sediment accumulation rates and pond perimeters and basin areas suggesting that peat may be a major source of sediment carbon. Aeolian transport is also a potentially large source of sediment carbon. Copyright © 2004 John Wiley & Sons, Ltd.     

Fluvial carbon export and CO2 efflux in representative nested headwater catchments of the eastern La Plata River Basin

This study involved a baseline evaluation of fluvial carbon export and degas rates in three nested rural catchments (1 to 80 km²) in Taboão, a representative experimental catchment of the Upper Uruguay River Basin. Analyses of the carbon content in stream waters and the catchment carbon yield were based on 4‐year monthly in situ data and statistical modeling using the United States Geological Survey load estimator model. We also estimated p CO₂ and degas fluxes using carbonate equilibrium and gas‐exchange formulas. Our results indicated that the water was consistently p CO₂ saturated (~90% of the cases) and that the steep terrain favors high gas evasion rates. The mean calculated fluvial export was 5.4 tC·km^?2·year^?1 with inorganic carbon dominating (dissolved inorganic carbon:dissolved organic carbon ratio >4), and degas rates (~40 tC km^?2·year^?1) were nearly sevenfold higher than the downstream export. The homogeneous land use in this nested catchment system results in similar water‐quality characteristics, and therefore, export rates are expected to be closely related to the rainfall–runoff relationships at each scale. Although the sampling campaigns did not fully reproduce storm‐event conditions and related effects such as flushing or dilution of in‐stream carbon, our results indicated a potential link between dissolved inorganic carbon and slower hydrological pathways related to subsurface water storage and movement.     

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.     

Carbon and nutrients transfer from primary producers to lake sediments – A stoichiometric approach

We aimed to demonstrate different input of organic and inorganic carbon, nitrogen and phosphorus from three main groups of primary producers (phytoplankton, charophytes and vascular submerged macrophytes) to respective lake sediments. Studies were carried out in one eutrophic and two mesotrophic lakes. Samples of sediments were taken from profundal and from littoral zones, the latter divided into such overgrown by charophytes and others covered by vascular submerged macrophytes. We applied a stoichiometric approach to illustrate variable functional carbon to nutrients relationships. Among profundal sediments, the lowest organic to inorganic carbon ratio was found in sediments from the eutrophic lake due to precipitation of calcium carbonate during algal blooms. Extremely low inorganic carbon input to profundal sediment of one of the mesotrophic lakes may be explained by low phytoplankton production but also by dissolution of once deposited calcium carbonates. Charophyte-dominated littoral sediments contained significantly more inorganic carbon than other littoral and profundal sediments. Comparison of stoichiometric ratios between plant standing crop and underlying littoral sediments showed significant enrichment of sediments in nitrogen manifested by reduction of organic carbon to total nitrogen ratio during plant decomposition taking place both in charophyte and in vascular plant stands. We also attempted to divide phosphorus pool in sediments into organic P and calcium-bound P present in charophyte stands and in profundal sediments of eutrophic lake. In the former, calcium-bound P was estimated at 17–19 % of the total P pool while in profundal sediments it amounted 42 % of the total P. This difference suggests that calcium carbonate settling during algal blooms in a eutrophic lake may be more effective in P trapping than calcite encrustations covering charophyte plants in littoral sites. In conclusions, we underline the need of considering often neglected inorganic fractions of carbon and phosphorus to get better insight into carbon and nutrient burial in lake sediments.     

Riverine export of water,sediment and carbon during flood events in the arid to semi-arid Wuding River on the Chinese Loess Plateau

Floods have become increasingly important in fluvial export of water, sediment and carbon (C). Using high-frequency sampling, the export of water, sediment and C was examined in the Wuding River catchment on the Chinese Loess Plateau. With groundwater as an important contributor to runoff all year round, floods were relatively less important in the export of water. However, large floods were disproportionately important in exporting sediment and inorganic C (DIC) and organic C (DOC and POC). The three largest floods in each year transported 53.6–97.3 and 41.4–77% of the annual sediment and C fluxes, respectively. An extreme flood in 2017 alone contributed 94.6 and 73.1% of the annual sediment and C fluxes, respectively, in just 7 days, which included 20.3, 92.1 and 35.7% of the annual DOC, POC and DIC fluxes, respectively. A stable carbon isotope (δ¹³C) analysis of POC indicated that modern soils and C3 plants were its primary source. Furthermore, floods greatly accelerated CO₂ degassing due to elevated gas transfer velocity, although stream water CO₂ partial pressure (pCO₂) exhibited a decreasing trend with flow discharge. Although these results illustrated that increasing runoff diluted pCO₂, the timing and magnitude of floods were found to be critical in determining the response of pCO₂ to flow dynamics. Low-magnitude floods in the early wet season increased pCO₂ because of enhanced organic matter input, while subsequent large floods caused a lower pCO₂ due to greatly reduced organic matter supply. Finally, continuous monitoring of a complete flood event showed that the CO₂ efflux during the flood (2348 ± 664 mg C m^–2 day^–1) was three times that under low-flow conditions (808 ± 98 mg C m^–2 day^–1). Our study suggests that infrequent, heavy storm events, which are predicted to increase under climate change, will greatly alter the transport regimes of sediment and C. © 2020 John Wiley & Sons, Ltd.     

On the use of loss‐on‐ignition techniques to quantify fluvial particulate organic carbon

The fluvial flux of carbon (C) from terrestrial to marine environments represents an important component of the global C‐cycle, which can transfer C from the atmosphere to sedimentary storage. Fluvial fluxes of C are also an essential resource for freshwater ecosystems, critical for habitat heterogeneity and function. As such it is crucial that we are able to quantify this flux accurately. However, at present there are a number of different techniques used to quantify concentrations of fluvial C, and these techniques vary in their accuracy. In this article, we compare particulate organic carbon (POC) measurements derived from two commonly‐used techniques; a simple combustion and loss‐on‐ignition (LOI) technique, and an oxidative–combustion and carbon dioxide (CO₂) detection technique. The techniques were applied to water samples collected from 10 contrasting reference‐condition, temperate river ecosystems. The POC measurements derived from the LOI technique were up to 16 times higher (average four times higher), than those derived from the oxidative–combustion and CO₂ detection technique. This difference was highly variable both across the different river ecosystems and within each river ecosystem over time, suggesting that there is no simple way of converting the mass measured by LOI to estimates of fluvial POC. It is suggested that the difference in POC measured by these two techniques is a consequence of: (1) the loss of inorganic carbon at LOI combustion temperatures of > 425 °C, (2) the potential during the LOI combustion stage to lose hygroscopic and intercrystalline water, not completely driven off by the drying stage at temperatures of < 150 °C, and (3) the variable C content of fluvial organic matter, meaning that the simple application of a fixed correction factor to values obtained from the LOI technique may not be appropriate. These findings suggest that oxidative–combustion and CO₂ detection techniques are preferential for quantifying fluvial POC. Copyright © 2013 John Wiley & Sons, Ltd.     

Controls on fluvial carbon efflux from eroding peatland catchments

Global peatlands store an unparalleled proportion of total global organic carbon but it is vulnerable to erosion into fluvial systems. Fluvial networks are being recognized as areas of carbon transformation, with eroded particulate organic carbon processed to dissolved organic carbon and CO₂. Existing studies indicate biodegradation and photodegradation as key processes controlling the transformation of organic carbon in fluvial systems, with initial concentrations of dissolved organic carbon (DOC) identified as a control on the rate of carbon mineralization. This study manipulates temperature and incident light intensity to investigate carbon mineralization rates in laboratory simulations of peatland sediment transport into fluvial systems. By directly measuring gaseous CO₂ emissions from sampled stream water, the relationship of temperature and light intensity with carbon efflux is identified. In simulations where sediment (as particulate organic matter, POM) is absent, temperature is consistently the dominant factor influencing carbon efflux rates. This influence is independent of the initial DOC concentration of the water sample. In simulations where POM was added, representing a peatland river receiving eroded terrestrial sediment, initial DOC concentration predicts 79% of the variation in total gaseous carbon efflux whereas temperature and light intensity predict 12% and 3%, respectively. When sampled stream water's mineralization rates in the presence of added POM are analysed independently, removing DOC as a model variable, the dominant variable affecting CO₂ efflux is opposite for each sample. This study presents novel data suggesting peatland erosion introduces further complexity to dynamic stream systems where rates of carbon transformation processes and the influence of specific environmental variables are interdependent. Anthropogenic climate change is identified as a leading risk factor perpetuating peatland erosion; therefore, understanding the fate of terrestrial sediment in rivers and further quantifying the benefits of protecting peatland soils will be of increasing importance to carbon budgeting and ecosystem function studies.     

Kinetics of oxygen exchange,photosynthesis, and respiration in rivers determined from time-delayed correlations between sunlight and dissolved oxygen

The application of both a simple rate equation and a novel cross-correlation computational technique to dissolved oxygen records has enabled a determination of the oxygen exchange constant, photosynthesis rate, and rate of respiration for several Swiss rivers. An extension of this method to determine total carbonate dynamics from continuous pH records is also described. Results for the Aare at Bern (March, 1974) are: 0.38 h^?1 for oxygen exchange constant, 0.6–0.8 mg/(1 h) for respiration rate, and 0.28 mg/(1 h) for mean photosynthesis rate. Moreover the exchange rate for dissolved (but not hydrated or ionized) CO₂ was 0.91 times that for oxygen, and the ratio of O₂ molecules released to CO₂ molecules consumed during photosynthesis was 1.2.     

Dissolved inorganic carbon isotopes of a typical alpine river on the Tibetan Plateau revealing carbon sources,wetland effect and river recharge

The Nyangqu River, the largest right bank tributary of the Yarlung Zangbo River in the Qinghai–Tibet Plateau, was representative of an alpine riverine carbon cycle experiencing climate change. In this study, dissolved inorganic carbon (DIC) spatial and seasonal variations, as well as their carbon isotopic compositions (δ¹³C_DIC) in river water and groundwater were systematically investigated to provide constraints on DIC sources, recharge and cycling. Significant changes in the δ¹³C_DIC values (from −2.9‰ to −23.4‰) of the water samples were considered to be the result of different contributions of two dominant DIC origins: soil CO₂ dissolution and carbonate weathering. Three types of rock weathering (dissolution of carbonate minerals by H₂CO₃ and H₂SO₄, and silicate dissolution by H₂CO₃) were found to control the DIC input into the riverine system. In DIC cycling, groundwater played a significant role in delivering DIC to the surface water, and DIC supply from tributaries to the main stream increased from the dry season to the wet season. Notably, the depleted δ¹³C_DIC ‘peak’ around the 88.9° longitude, especially in the September groundwater samples, indicated the presence of ‘special’ DIC, which was attributed to the oxidation of methane from the Jiangsa wetland located nearby. This wetland could provide large amounts of soil organic matter available for bacterial degradation, producing ¹³C-depleted methane. Our study provided insights regarding the role of wetlands in riverine carbon cycles and highlighted the contribution of groundwater to alpine riverine DIC cycles.     

Spatial variation of salt-marsh organic and inorganic deposition and organic carbon accumulation: Inferences from the Venice lagoon,Italy

Salt marshes are ubiquitous features of the tidal landscape governed by mutual feedbacks among processes of physical and biological nature. Improving our understanding of these feedbacks and of their effects on tidal geomorphological and ecological dynamics is a critical step to address issues related to salt-marsh conservation and response to changes in the environmental forcing. In particular, the spatial variation of organic and inorganic soil production processes at the marsh scale, a key piece of information to understand marsh responses to a changing climate, remains virtually unexplored. In order to characterize the relative importance of organic vs. inorganic deposition as a function of space, we collected 33 shallow soil sediment samples along three transects in the San Felice and Rigà salt marshes located in the Venice lagoon, Italy. The amount of organic matter in each sample was evaluated using Loss On Ignition (LOI), a hydrogen peroxide (H₂O₂) treatment, and a sodium hypochlorite (NaClO) treatment following the H₂O₂ treatment. The grain size distribution of the inorganic fraction was determined using laser diffraction techniques. Our study marshes exhibit a weakly concave-up profile, with maximum elevations and coarser inorganic grains along their edges. The amount of organic and inorganic matter content in the samples varies with the distance from the marsh edge and is very sensitive to the specific analysis method adopted. The use of a H₂O₂+NaClO treatment yields an organic matter density value which is more than double the value obtained from LOI. Overall, inorganic contributions to soil formation are greatest near the marsh edges, whereas organic soil production is the main contributor to soil accretion in the inner marsh. We interpret this pattern by considering that while plant biomass productivity is generally lower in the inner part of the marsh, organic soil decomposition rates are highest in the better aerated edge soils. Hence the higher inorganic soil content near the edge is due to the preferential deposition of inorganic sediment from the adjacent creek, and to the rapid decomposition of the relatively large biomass production. The higher organic matter content in the inner part of the marsh results from the small amounts of suspended sediment that makes it to the inner marsh, and to the low decomposition rate which more than compensates for the lower biomass productivity in the low-lying inner zones. Finally, the average soil organic carbon density from the LOI measurements is estimated to be 0.044 g C cm⁻³. The corresponding average carbon accumulation rate for the San Felice and Rigà salt marshes, 132 g C m⁻² yr⁻¹, highlights the considerable carbon stock and sequestration rate associated with coastal salt marshes.     

Total waterborne carbon export and DOC composition from ten nested subarctic peatland catchments—importance of peatland cover,groundwater influence,and inter‐annual variability of precipitation patterns

Waterborne carbon (C) export from terrestrial ecosystems is a potentially important flux for the net catchment C balance and links the biogeochemical C cycling of terrestrial ecosystems to their downstream aquatic ecosystems. We have monitored hydrology and stream chemistry over 3 years in ten nested catchments (0.6–15.1 km²) with variable peatland cover (0%–22%) and groundwater influence in subarctic Sweden. Total waterborne C export, including dissolved and particulate organic carbon (DOC and POC) and dissolved inorganic carbon (DIC), ranged between 2.8 and 7.3 g m^–2 year^–1, representing ~10%–30% of catchment net ecosystem exchange of CO₂. Several characteristics of catchment waterborne C export were affected by interacting effects of peatland cover and groundwater influence, including magnitude and timing, partitioning into DOC, POC, and DIC and chemical composition of the exported DOC. Waterborne C export was greater during the wetter years, equivalent to an average change in export of ~2 g m^–2 year^–1 per 100 mm of precipitation. Wetter years led to a greater relative increase in DIC export than DOC export due to an inferred relative shift in dominance from shallow organic flow pathways to groundwater sources. Indices of DOC composition (SUVA₂₅₄ and a₂₅₀/a₃₆₅) indicated that DOC aromaticity and average molecular weight increased with catchment peatland cover and decreased with increased groundwater influence. Our results provide examples on how waterborne C export and DOC composition might be affected by climate change. Copyright © 2012 John Wiley & Sons, Ltd.     

Dissolved inorganic carbon sourcing using δ13CDIC from a karst influenced river system

Rivers, representing the primary conduits of dissolved inorganic carbon (DIC) from the continents to the oceans, are important components to the global carbon cycle. To better understand the complex carbon cycling dynamics within two nested, mixed lithology watersheds, two sites were studied along the karst influenced upper Green River in south‐central Kentucky, USA. Weekly samples were collected from June 2013 through May 2014 and analyzed for δ¹³C_DIC. The mixing model IsoSource was employed to better understand source partitioning differences over seasonal time spans and across the two nested basins. In both the lithologically mixed upstream basin (53% carbonate rocks, 47% siliciclastic) and carbonate rock dominated downstream basin (96% carbonate rocks in the drainage area between Greensburg and Munfordville, 78% in the total area upstream from Munfordville), DIC was primarily derived from soil respiration. The proportion of DIC from dissolved carbonate minerals derived from the downstream carbonate rock dominated basin was similar to the upstream basin, due to carbonate mineral dissolution having such a consistent effect on the overall DIC content of the river. Seasonally, soil respiration provided the most DIC from fall to winter. Early spring precipitation, combined with limited seasonal photosynthesis, shifted groundwater to be the primary source of DIC, bringing in a flush of carbonate mineral‐rich water during higher flows. This study provides insight into carbon dynamics across multiple lithologies and the important influence of seasonality using carbon isotope sourcing to determine carbonate mineral dissolution variability and aid in understanding its contribution to global carbon flux quantification. Copyright © 2015 John Wiley & Sons, Ltd.     

Experimental stream acidification — the influence of sediment and streambed vegetation

An acidification experiment was conducted on a small stream in the Loch Ard area of central Scotland. The stream was chosen because of its large, flow related, variation in pH (5.9-4.0). Two acid additions were made to approximately pH 3.5–3.7. The results indicated a strong correlation between labile aluminium and hydrogen, and a noticeable hysteresis in the response of calcium and hydrogen. It is hypothesised that divalent cation response is a result of ion-exchange mechanisms involving the streambed vegetation, with aluminium release resulting primarily from exchange reactions with streambed sediment stores. Data from a program of stream spot sampling have been analysed in an attempt to elucidate the contribution of different sources of aluminium under different flow conditions. Streambed sources of aluminium contribute significantly under low flow conditions; however, at high flow, additional sources of aluminium must contribute to match observed streamwater chemistry.     

An oceanic calcium problem?

Recent published data on dissolved calcium in seawater reveal an apparent excess of calcium over that predicted from the changes in alkalinity. In the South Pacific this excess calcium is approximately 40 μmoles/kg. We suggest that this arises from an in-situ titration of some of the alkalinity by protons derived from the redox changes associated with oxidative decomposition of organic matter. This postulates an effective flux of nitric and phosphoric acids into the deep water. Other redox changes, such as in the oxidation of reduced sulfur, may also contribute protons, but these are more difficult to evaluate. This concept changes current thinking on the oceanic CO₂-carbonate system. It increases the amount of calcium carbonate believed to have dissolved in the ocean by ca. 25%; and alters the proportions of abyssal CO₂ believed to be derived from respiration versus carbonate dissolution by about 10%.     

喀斯特筑坝河流中生物碳泵效应的碳施肥及对水化学时空变化的影响——以贵州平寨水库及红枫湖为例

耦联水生光合作用的碳酸盐风化碳汇是全球碳循环的重要组成部分,而生物碳泵效应是稳定碳酸盐风化碳汇的关键机制.河流筑坝后,生物碳泵效应的变化、控制因素及对水化学影响的研究甚少.本研究对2个喀斯特筑坝河流平寨水库和红枫湖进行系统采样,以研究河流筑坝后生物碳泵效应的变化、控制因素及对水化学的影响.研究结果表明,入库河流的水化学变化不明显,而2个水库的水化学则表现出显著的季节变化特征,具体表现为水库的水温和pH均呈现出夏季高、冬季低的变化特征,而电导率（EC）、HCO₃^-浓度和pCO₂则表现出夏季低、冬季高的季节变化特征.以叶绿素a（Chl.a）浓度和溶解氧（DO）饱和度指代的生物碳泵效应则是在夏季最强、冬季最弱.生物碳泵效应利用溶解性无机碳（DIC）,形成有机质并释放出氧气,是造成夏季水库pH值和DO饱和度升高,电导率（EC）、HCO₃^-浓度和pCO₂降低的主要因素.空间上,水库的Chl.a浓度及DO饱和度均大于河水,EC、HCO₃^-浓度和pCO₂均小于河水,这表明河流筑坝后,由于水库的“湖泊化”导致水库的生物碳泵效应显著提高.通过对Chl.a与碳、氮和磷浓度及化学计量比的相关性分析发现,平寨水库和红枫湖的生物碳泵效应受到碳施肥的影响.平寨水库和红枫湖水库生物碳泵效应碳施肥机制的发现,表明在喀斯特地区,生物碳泵效应不仅受到氮磷元素的控制,也受到碳元素的控制,因此在富营养化湖泊治理时,也应考虑碳的影响.