Variability and transport of suspended sediment,particulate and dissolved organic carbon in the tidal freshwater Hudson River

Measurements of suspended matter, particulate organic carbon and dissolved organic carbon were made over a three year period at stations spanning 150 km of the tidal freshwater Hudson River. Suspended matter concentrations varied from year-to-year and were not related to freshwater discharge. The increase in suspended matter with depth in vertical profiles suggests that, during medium to low flow conditions, resuspension of bottom sediments was as important a source of sediment as loadings from tributaries. Particulate organic carbon showed significant variability among stations, and both autochthonous primary production and detrital organic matter are contributing to POC standing stocks. Dissolved organic carbon represented over half of the total organic carbon in the water column and showed little variation among stations.Examining downstream changes in transport showed that there was significant production of both suspended matter and POC within the study reach during the ice-free season. Tributary loadings within the study reach do not appear to be the cause of these increases in downstream transport. Dissolved organic carbon behaved conservatively in that there was no evidence for net production or net consumption within the river.The spatial/temporal patterns and analyses of transport suggest that suspended matter and POC, but not DOC, were controlled to a significant extent by processes occurring within the river and were not simply related to loadings from outside.     

Alternative explanations for rising dissolved organic carbon export from organic soils

Since 1988, there has been, on average, a 91% increase in dissolved organic carbon (DOC) concentrations of UK lakes and streams in the Acid Waters Monitoring Network (AWMN). Similar DOC increases have been observed in surface waters across much of Europe and North America. Much of the debate about the causes of rising DOC has, as in other studies relating to the carbon cycle, focused on factors related to climate change. Data from our peat‐core experiments support an influence of climate on DOC, notably an increase in production with temperature under aerobic, and to a lesser extent anaerobic, conditions. However, we argue that climatic factors may not be the dominant drivers of DOC change. DOC solubility is suppressed by high soil water acidity and ionic strength, both of which have decreased as a result of declining sulphur deposition since the 1980s, augmented during the 1990s in the United Kingdom by a cyclical decline in sea‐salt deposition. Our observational and experimental data demonstrate a clear, inverse and quantitatively important link between DOC and sulphate concentrations in soil solution. Statistical analysis of 11 AWMN lakes suggests that rising temperature, declining sulphur deposition and changing sea‐salt loading can account for the majority of the observed DOC trend. This combination of evidence points to the changing chemical composition of atmospheric deposition, particularly the substantial reduction in anthropogenic sulphur emissions during the last 20 years, as a key cause of rising DOC. The implications of rising DOC export for the carbon cycle will be very different if linked primarily to decreasing acid deposition, rather than to changes in climate, suggesting that these systems may be recovering rather than destabilising.     

海洋异养细菌利用溶解有机碳的定量评估

【目的】惰性溶解有机碳(refractory dissolved organic carbon,RDOC)是海洋总有机碳的主体组分,RDOC在深海中可保存数千年,构成了巨大的碳储库,在调节气候变化中有重要作用。但RDOC的定量评估尚未有统一的标准方法。通过测定环境中能被异养细菌利用的溶解有机碳(biodegradable DOC,BDOC)可以反过来评估RDOC的量。本文对BDOC测定中一些关键步骤进行验证,为制定海洋RDOC评估标准奠定基础。【方法】本文评估了3种过滤方式及5种滤膜对DOC测定的影响,并评估了瓶子效应和稀释效应对细菌生长和DOC利用的影响。【结果】研究发现,(1) GF/F滤膜、GF-75滤膜、聚四氟乙烯(PTFE)滤膜(孔径0.2μm)、聚碳酸酯(PC)滤膜(孔径0.2μm)和聚四氟乙烯材质针孔过滤器(HA)(孔径0.2μm) 5种滤膜不会引入DOC污染;抽滤过滤和重力过滤方式过滤效果稳定、无污染,而在线过滤效果不稳定,易污染;(2)不同大小培养体系(30–480 mL;表面积/体积比为:1.64–0.67 cm–1)之间的细菌生长速率和DOC利用量没有显著性差异;(3)培养体系稀释度越高,细菌生长速率越高,对数生长期细菌丰度及DOC利用量越低。【结论】综合考虑,建议BDOC和RDOC测定实验中采用抽滤过滤的方式及不进行稀释的培养体系;常用的滤膜和培养体积对BDOC评估无显著影响。结合研究结果,我们提出了评估海洋RDOC的方法。     

A long-term perspective of dissolved organic carbon transport in Sycamore Creek, Arizona, USA

Dissolved organic carbon (DOC) dynamics were examined over five years (1989–1993) in Sycamore Creek, a Sonoran Desert stream, specifically focusing on DOC concentration in surface and hyporheic waters, and rates of export. In 1989 and 1990, the years of lowest stream discharge (0.08 and 0.04 m³ s^–1 annual mean of daily discharge, respectively), DOC was high, averaging 7.37 and 6.22 mgC l^–1 (weighted annual means). In contrast, from 1991 through 1993, a period of increased flow (1.1, 1.2 and 4.3 m³ s^–1), concentration was significantly lower (P<0.001) with annual mean concentrations of 3.54, 3.49 and 3.39 mgC l^–1. Concentration exhibited little spatial variation between two sampling stations located 6 km apart along the mainstem or between surface and hyporheic waters. Annual export of DOC from Sycamore Creek varied 100-fold over the five-year period from a mean rate of only 24 kgC d^–1 in 1990 to 2100 kgC d^–1 in 1993. Ninety percent of DOC was exported by flows greater than 2.8 m³ s^–1, and 50% during flows greater than 27 m³ s^–1; flows of 2.8 and 24 m³ s^–1 occurred only 9 and 1% of the time. The export of organic matter in Sycamore Creek appears to be coupled to El Niño-Southern Oscillation phenomena. The years of highest export, 1991–1993, had El Niño conditions while 1989 and 1990 had medial conditions.     

亚热带河口陆基养虾塘水体溶解性碳浓度及沉积物-水界面碳通量时空动态特征

以福建闽江和九龙江河口陆基养虾塘为研究对象,通过野外原位观测和室内模拟培养实验,开展了河口陆基养虾塘养殖期间水体溶解性有机碳(DOC)和溶解性无机碳(DIC)及养虾塘沉积物-水界面碳交换通量变化特征的研究。结果表明:时间变化上,养虾塘水体溶解性碳浓度及沉积物-水界面碳通量在闽江河口呈现8月中旬10月中旬6月中旬的特征,在九龙江河口表现为随养殖阶段推移而增加的趋势;空间变化上,闽江河口养虾塘水体溶解性碳浓度及沉积物-水界面碳通量显著高于九龙江河口;沉积物释放溶解性碳速率与水体溶解性碳浓度呈现显著正相关关系,沉积物碳释放过程是引起养虾塘水体溶解性碳浓度时空变化的重要因素。表明河口区水产养虾塘碳循环研究时需考虑不同形态碳生物地球化学循环的时空差异性。     

氮素添加和CO2浓度升高对白羊草根际和非根际土壤水溶性有机碳、氮的影响

采用盆栽控制试验对黄土丘陵区白羊草在不同CO₂浓度(400和800 μmol·mol^-1)和施氮水平(0、2.5、5.0 g N·m^-2·a^-1)条件下根际和非根际土壤水溶性有机碳(DOC)和水溶性有机氮(DON)的变化特征进行研究.结果表明: CO₂浓度升高对白羊草根际和非根际土壤DOC、水溶性总氮(DTN)、DON、水溶性铵态氮(NH₄⁺-N)、水溶性硝态氮(NO₃^--N)含量均无显著影响.施氮显著提高了根际和非根际土壤DTN、NO₃^--N含量和根际土壤DON含量,显著降低了根际土壤DOC/DON.在各处理条件下,根际土壤DTN、NO₃^--N和DON含量均显著低于非根际土壤,根际土壤DOC/DON显著高于非根际土壤.短期CO₂浓度升高对黄土丘陵区土壤水溶性有机碳、氮含量无显著影响,而氮沉降的增加在一定程度上改善了土壤中水溶性氮素缺乏的状况,但并不足以满足植被对水溶性氮素的需求.     

Acidity controls on dissolved organic carbon mobility in organic soils

Dissolved organic carbon (DOC) concentrations in surface waters have increased across much of Europe and North America, with implications for the terrestrial carbon balance, aquatic ecosystem functioning, water treatment costs and human health. Over the past decade, many hypotheses have been put forward to explain this phenomenon, from changing climate and land management to eutrophication and acid deposition. Resolution of this debate has been hindered by a reliance on correlative analyses of time series data, and a lack of robust experimental testing of proposed mechanisms. In a 4 year, four‐site replicated field experiment involving both acidifying and deacidifying treatments, we tested the hypothesis that DOC leaching was previously suppressed by high levels of soil acidity in peat and organo‐mineral soils, and therefore that observed DOC increases a consequence of decreasing soil acidity. We observed a consistent, positive relationship between DOC and acidity change at all sites. Responses were described by similar hyperbolic relationships between standardized changes in DOC and hydrogen ion concentrations at all sites, suggesting potentially general applicability. These relationships explained a substantial proportion of observed changes in peak DOC concentrations in nearby monitoring streams, and application to a UK‐wide upland soil pH dataset suggests that recovery from acidification alone could have led to soil solution DOC increases in the range 46–126% by habitat type since 1978. Our findings raise the possibility that changing soil acidity may have wider impacts on ecosystem carbon balances. Decreasing sulphur deposition may be accelerating terrestrial carbon loss, and returning surface waters to a natural, high‐DOC condition.     

A comparative study of dissolved organic carbon transport and stabilization in California forest and grassland soils

For soil carbon to be effectively sequestered beyond a timescale of a few decades, this carbon must become incorporated into passive reservoirs or greater depths, yet the actual mechanisms by which this occurs is at best poorly known. In this study, we quantified the magnitude of dissolved organic carbon (DOC) leaching and subsequent retention in soils of a coniferous forest and a coastal prairie ecosystem. Despite small annual losses of DOC relative to respiratory losses, DOC leaching plays a significant role in transporting C from surface horizons and stabilizing it within the mineral soil. We found that DOC movement into the mineral soil constitutes 22% of the annual C inputs below 40 cm in a coniferous forest, whereas only 2% of the C inputs below 20 cm in a prairie soil could be accounted for by this process. In line with these C input estimates, we calculated advective transport velocities of 1.05 and 0.45 mm year⁻¹ for the forested and prairie sites, respectively. Radiocarbon measurements of field-collected DOC interpreted with a basic transport-turnover model indicated that DOC which was transported and subsequently absorbed had a mean residence time of 90–150 years. Given these residence times, the process of DOC movement and retention is responsible for 20% of the total mineral soil C stock to 1 m in the forest soil and 9% in the prairie soil. These results provide quantitative data confirming differences in C cycles in forests and grasslands, and suggest the need for incorporating a better mechanistic understanding of soil C transport, storage and turnover processes into both local and regional C cycle models.     

可溶性有机碳在米槠天然林不同土层中的迁移特征

选取我国中亚热带典型的常绿阔叶林米槠天然林(Castanopsis carlesii)为研究对象,采集林内米槠凋落物并通过挖剖面法分6个土层采集土样至1m。通过浸提米槠凋落物得到可溶性有机碳(dissolved organic carbon,DOC)溶液并在室内模拟其在不同土层的淋溶过程,不仅分析了土壤性质对DOC淋溶的影响,还研究了淋溶前后DOC化学结构的变化,以阐明DOC在不同土层中的迁移特征及影响因素,探寻米槠天然林土壤的固碳潜力和DOC在土壤有机碳循环中的作用。结果表明:(1)下层土壤比上层土壤吸附DOC的能力更强,亲水性DOC与疏水性DOC间会争夺土壤颗粒表面的吸附位点,而且芳香化合物和大分子物质等疏水性DOC组分会被优先吸附;(2)红外光谱表明,芳香类和醚类等疏水性物质会优先被吸附,烷烃类物质却不易被吸附,土壤中原有的酚、醇类亲水性物质会被初始DOC中的疏水性物质置换出来;(3)土壤DOC的截留能力与粘粒、游离氧化铁含量呈极显著正相关,而与土壤有机碳和砂粒含量呈极显著负相关,其中土壤有机碳的含量是影响米槠天然林不同土层DOC截留量的关键因素。     

富营养化湖泊溶解性有机碳生物可利用性研究进展

富营养化湖泊溶解性有机碳(DOC)包括内源和外源性碳源,不同来源碳源在物质化学结构组成和分子量级等方面具有显著差异,进而影响到对细菌的生物可利用性和碳素在食物网中的传递效率。根据国内外文献,综述了内外源DOC在碳稳定同位素值域上的显著差异,建议通过对DOC碳稳定同位素的分析来识别富营养化湖泊中DOC的主要来源;通过对比内外源DOC在碳水化合物、结合态中性糖和腐殖质含量上的差异,并结合细菌生长参数如细菌二级生产力、细菌呼吸作用及细菌生长效率来分析内外源DOC对细菌的生物可利用性。从富营养化湖泊DOC来源的角度探讨其生物可利用性和碳素传递效率,有助于了解富营养化湖泊食物网中碳素循环特征,加强对湖泊生态学的认识,为湖泊环境治理与保护提供科学依据。     

土壤溶解性有机碳在陆地生态系统碳循环中的作用

土壤溶解性有机碳(DOC)是有机碳库的活跃组分,在陆地生态系统碳循环中发挥重要作用.本文从碳循环重要性着手,综述了土壤DOC在土壤碳固持与温室气体排放中的作用;结合我国的现实情况(如土壤酸化、气候变暖等),探讨了土壤DOC的相关影响因素如土壤性质、环境因素、人为活动对土壤DOC的影响及作用机制,对进一步理解土壤DOC在陆地生态系统碳循环与温室气体减排中的作用具有重要意义.     

The effect of land use on dissolved organic carbon and nitrogen uptake in streams

1. Agricultural and urban land use may increase dissolved inorganic nitrogen (DIN) concentrations in streams and saturate biotic nutrient demand, but less is known about their impacts on the cycling of organic nutrients. To assess these impacts we compared the uptake of DIN (as ammonium, NH₄⁺), dissolved organic carbon (DOC, as acetate), and dissolved organic nitrogen (DON, as glycine) in 18 low‐gradient headwater streams in southwest Michigan draining forested, agricultural, or urban land‐use types. Over 3 years, we quantified uptake in two streams in each of the three land‐use types during three seasons (spring, summer and autumn). 2. We found significantly higher NH₄⁺ demand (expressed as uptake velocity, V_f) in urban compared to forested streams and NH₄⁺V_f was greater in spring compared to summer and autumn. Acetate V_f was significantly higher than NH₄⁺ and glycine V_f, but neither acetate nor glycine V_f were influenced by land‐use type or season. 3. We examined the interaction between NH₄⁺ and acetate demand by comparing simultaneous short‐term releases of both solutes to releases of each solute individually. Acetate V_f did not change during the simultaneous release with NH₄⁺, but NH₄⁺V_f was significantly higher with increased acetate. Thus, labile DOC V_f was not limited by the availability of NH₄⁺, but NH₄⁺V_f was limited by the availability of labile DOC. In contrast, neither glycine nor NH₄⁺V_f changed when released simultaneously indicating either that overall N‐uptake was saturated or that glycine and NH₄⁺ uptake were controlled by different factors. 4. Our results suggest that labile DOC and DON uptake can be equivalent to, or even higher than NH₄⁺ uptake, a solute known to be highly bioreactive, but unlike NH₄⁺ uptake, may not differ among land‐use types and seasons. Moreover, downstream export of nitrogen may be exacerbated by limitation of NH₄⁺ uptake by the availability of labile DOC in headwater streams from the agricultural Midwestern United States. Further research is needed to identify the factors that influence cycling of DOC and DON in streams.     

Photochemical transformations and bacterial utilization of high-molecular-weight dissolved organic carbon in a southern Louisiana tidal stream (Bayou Trepagnier)

UVirradiation of dissolved organic carbon (DOC) in the laboratory can producesmall, labile organic compounds utilizable by microbes, but few studies haveattempted to document this process in situ. ¹³Cnuclear magnetic resonance (NMR) was used to examine the bulk chemicalcomposition of natural and laboratory-irradiated high-molecular-weight DOC(HMW-DOC) from shaded (150 mol m^–2s^–1 average light in surface water) and open (1500mol m^–2 s^–1) field sitesoverone and a half years. ¹³C NMR revealed only small differences incarbon functional groups between laboratory irradiated and non-irradiatedHMW-DOC. However, bacterial protein productivity per cell (BPP) was enhanced innaturally irradiated samples of HMW-DOC in a field mesocosm experiment (p <0.05), suggesting that bacterial growth was enhanced by photochemicalproductionof labile DOC substrates. Absorbance characteristics such as spectral slope,absorbance at 350 nm, and the absorbance ratio 250nm/365 nm revealed that HMW-DOC was photoreactive,yetno differences in these values were found between samples irradiated with andwithout UV-B. In experiments conducted with simulated solar radiation in thelaboratory and with natural light in the field mesocosm experiment, UV-A(320–400 nm) and photosynthetically active radiation (PAR;400–700 nm) were more effective than UV-B (280–320nm) in HMW-DOC photolysis.     

Complementary pathways of dissolved organic carbon removal pathways in clear-water Amazonian ecosystems: photochemical degradation and bacterial uptake

Dissolved organic carbon (DOC) photochemical reactions establish important links between DOC and planktonic bacteria. We hypothesize that seasonal changes in DOC quality, related to the flood pulse, drive the effects of light-DOC interactions on uptake by planktonic bacteria uptake in clear-water Amazonian ecosystems. Water samples from two ecosystems (one lake and one stream) were incubated in sunlight during different hydrological periods and were then exposed to bacterial degradation. Photochemical and bacterial degradation were driven by seasonal DOC inputs. Bacterial mineralization was the main degradation pathway of autochthonous DOC in the lake, while allochthonous DOC was more available for photochemical oxidation. We suggest that sunlight enhances the bacterial uptake of refractory DOC but does not alter uptake of labile forms. We also observed a positive relationship between sunlight and bacterial degradation of DOC, instead of competition. We conclude that photochemical reactions and bacteria complementarily degrade the different sources of DOC during the flood pulse in Amazonian clear-water aquatic ecosystems.     

森林转换对地表径流可溶性有机碳输出浓度和通量的影响

米槠次生林转换成米槠人工幼林和米槠人工促进天然更新幼林(以下简称"人促幼林")后,以这三种森林类型为研究对象,连续监测每次降雨后地表径流量及径流水中可溶性有机碳(DOC)的含量及通量,比较不同森林类型观测结果的差异,并分析降雨对实验结果的影响。结果表明:米槠人工幼林单次产流量是米槠次生林的1.5—19.0倍,观测期间总径流量为5.9倍;米槠人促幼林单次径流量和总径流量均与米槠次生林无显著差异(P0.05)。观测期间米槠次生林、人工幼林、人促幼林径流水DOC浓度值范围为5.9—18.4 mg/L,4.3—13.5 mg/L和3.2—9.9 mg/L,米槠次生林径流水浓度均值(12.6 mg/L)分别是米槠人促幼林(7.6 mg/L)和米槠人工幼林(5.3 mg/L)的1.6和2.4倍。回归分析表明,径流水中DOC浓度与降雨前土壤含水率呈显著相关;降雨前土壤含水率20.8%是一个临界值,含水率低于20.8%时,径流水DOC浓度与降雨前含水率呈显著正相关(P0.05);高于20.8%时,径流水DOC浓度与降雨前土壤含水率呈显著负相关(P0.05)。米槠人工幼林地表径流DOC输出通量是米槠次生林的0.7—5.4倍,观测期间总输出通量为2.1倍;米槠人促林DOC单次通量和观测期间总通量均与米槠次生林差异不显著(P0.05)。三种森林类型DOC输出通量均与降雨量呈显著相关(P0.05)。可见,米槠次生林转变成米槠人工幼林后DOC输出浓度降低,但径流量显著增加,导致DOC输出通量增加;而转变成米槠人促幼林后DOC输出浓度也降低,但径流量并未增加,因而并未增加DOC输出通量。     

Distribution of dissolved organic carbon and dissolved fulvic acid in mesotrophic Lake Biwa, Japan

The dissolved organic carbon (DOC) concentrations in mesotrophic Lake Biwa were determined by a total organic carbon (TOC) analyzer, and DOC molecular size distributions were determined by size exclusion chromatography (SEC) using a fluorescence detector at excitation/emission (Ex/Em) levels of 300/425 nm with the eluent at pH 9.7. The fluorescence wavelengths for detection were chosen from the result of excitation–emission matrix spectrometry (EEM) analysis for dissolved fulvic acid (DFA) extracted from Ado River (peak A, Ex/Em = 260–270/430–440 nm; peak B, Ex/Em = 300–310/420–430 nm). Ado River DFA was eluted with a retention time (RT) of 7.4–8.9 min and the apparent molecular weight was estimated at 22–87 kDa based on the elution curve for the spherical protein molecular weight standard. A DFA peak eluted at the same retention time as Ado River DFA also appeared in all the samples of Lake Biwa water. From the linear relationship between the peak areas with an RT of 7.4–8.9 min by SEC analysis and DOC values of DFA by TOC analysis of a series of DFA samples (r² = 0.9995), the concentrations of DFA in the lake water were roughly calculated. DFA was distributed within the range 0.25–0.43 mg C l⁻¹ and accounted for 15%–41% of DOC, with the highest ratios observed at a depth of 70 m in August and the lowest at 2.5 m in May.     

Seasonal patterns of viruses, bacteria and dissolved organic carbon in a riverine wetland

SUMMARY 1. Viral and bacterial abundances were studied in relation to environmental attributes over an annual period, for both planktonic and attached (sediment, aquatic macrophyte and submerged wood) habitats, in a riverine wetland.
2. Annual mean abundance of planktonic viruses ranged from 2.3 × 10⁵−3.8 × 10⁵ particles mL⁻¹ and varied according to sampling site. Significant seasonal patterns in viral abundance were evident and appeared to be linked to variations in bacterial abundance, dissolved organic carbon and inorganic nutrients.
3. Annual mean abundance of viruses associated with surfaces ranged from 1.3 × 10⁶ particles cm⁻² on aquatic macrophytes to 1.1 × 10⁷ particles cm⁻² on wood and also showed seasonal patterns. The difference in viral dynamics among the different sites emphasizes the importance of considering habitat diversity within wetlands when examining microbial communities.     

Nitrogen loading into an urban estuary: Lake Pontchartrain (Louisiana,U.S.A.)

We constructed a nitrogen loading budget for the Lake Pontchartrain watershed located north of New Orleans, Louisiana (U.S.A.). Water quality measurements, discharge estimates, and literature values were used to establish the annual and seasonal variations in loading rates for total nitrogen and nitrate. The relatively stable annual loadings (million kg N) are about 10× that of the pre-settlement nitrogen loading, and come from atmosphere (1.3), the watershed (7.8), pumped urban runoff from New Orleans (1.0), and leakage through the Bonnet Carré flood control structure (0.5–0.9). Relatively minor additional amounts come from nitrogen fixation in the Lake. Occasional openings of the Bonnet Carré Spillway (for flood protection) could triple the annual average loading within 1–2 months. Proposed smaller diversions (for wetland restoration) could raise present N loadings by 50%. The results of water quality management, flood protection and wetland restoration may thus have conflicting effects on the Lake's phytoplankton community, which is primarily nitrogen limited. Lowering the total nitrogen loading, however, seems quite possible, especially given that the present loadings are almost all reducible through existing technology, especially sewerage treatment. The analysis demonstrates that the consequences of ecosystem restoration efforts, continued population growth and flood protection to estuarine nitrogen budgets are intertwined with each other, have a seasonal component, and are changing as policies evolve.     

Environmental variability in the reactivity of freshwater dissolved organic carbon to UV-B

Reductions in the global stratospheric ozone layer arethought to be increasing the amount of ultraviolet B (UV-B) radiationreaching the planets surface and may be affecting the chemistry ofdissolved organic carbon (DOC) in surface waters. We studied theabundance of chromophores in DOC collected in four different aquaticenvironments in southwestern Nova Scotia using ¹³C nuclearmagnetic resonance (¹³C NMR) spectroscopy. We showed a clearseasonal pattern in the distribution of structural carbon related tolight-sensitive chromophores. There seemed to be little variation in theUV-B related chemical structure of DOC between lakes and streams, thoughwater from a bog pool showed large differences from the other samples. Thesepatterns of potential UV-B reactivity tend to be dampened however, byvariations in DOC concentrations which also occur seasonally.     

Microbial control of dissolved organic carbon in lakes: research for the future

The dissolved organic carbon (DOC) of lakes dominates any budget of organic carbon in these systems. Limnologists are still limited by techniques and particularly by the lack of measurements of rates of microbial transformation and use of this DOC. There are now four different approaches to the study of the microbial control of DOC in lakes. The first is through measurements of the total DOC. Recent advances in measurement with high temperature combustion will likely lead to higher and more consistent measurements in freshwaters than previously. It is possible that a biologically active fraction may be identified. The second approach is through measurements of microbial incorporation and respiration of ¹⁴C-labeled organic matter. The kinetics of this process are well known but advances in measurement of the size of the substrate pool are still being made. The third approach is to use bacterial growth in batch or continuous flow experiments in order to understand how much of the total DOC can be decomposed by microbes. The assay in this approach may be microbial growth (thymidine incorporation, biomass changes) or change in the DOC (total concentrations, specific compounds, or fractions of the DOC by molecular weight). These methods are promising but are not developed enough for routine use. For example, growth measurements in the laboratory are all subject to experimental artifacts caused by changes in the DOC and in the bacterial populations. Finally, the fourth approach is through the use of isotopes of the natural DOC. In the sea this approach has given the age of the bulk DOC (¹⁴C data). In freshwaters it has great potential for differentiating between bacterial use of terrestrial DOC vs. use of algal-derived DOC (13C data). Stable isotopes are also useful for experimentally labeling DOC produced by algae and following the use of this material by bacteria.