Sediment respiration and lake trophic state are important predictors of large CO2 evasion from small boreal lakes

We show that sediment respiration is one of the key factors contributing to the high CO₂ supersaturation in and evasion from Finnish lakes, and evidently also over large areas in the boreal landscape, where the majority of the lakes are small and shallow. A subpopulation of 177 randomly selected lakes (<100 km²) and 32 lakes with the highest total phosphorus (P_tot) concentrations in the Nordic Lake Survey (NLS) data base were sampled during four seasons and at four depths. Patterns of CO₂ concentrations plotted against depth and time demonstrate strong CO₂ accumulation in hypolimnetic waters during the stratification periods. The relationship between O₂ departure from the saturation and CO₂ departure from the saturation was strong in the entire data set (r²=0.79, n=2 740, P<0.0001). CO₂ concentrations were positively associated with lake trophic state and the proportion of agricultural land in the catchment. In contrast, CO₂ concentrations negatively correlated with the peatland percentage indicating that either input of easily degraded organic matter and/or nutrient load from agricultural land enhance degradation. The average lake‐area‐weighted annual CO₂ evasion based on our 177 randomly selected lakes and all Finnish lakes >100 km² ( Rantakari & Kortelainen, 2005 ) was 42 g C m^?2 LA (lake area), approximately 20% of the average annual C accumulation in Finnish forest soils and tree biomass (covering 51% of the total area of Finland) in the 1990s. Extrapolating our estimate from Finland to all lakes of the boreal region suggests a total annual CO₂ evasion of about 50 TgC, a value upto 40% of current estimates for lakes of the entire globe, emphasizing the role of small boreal lakes as conduits for transferring terrestrially fixed C into the atmosphere.     

Seasonal Dynamics of CO2 Flux Across the Surface of Shallow Temperate Lakes

We used data collected from 1989 to 2009 from 151 shallow (mean depth < 3 m) temperate lakes in Denmark to explore the influence of lake trophic status, surface area and catchment size on the seasonal dynamics of the air–water flux of CO₂. Monthly CO₂ fluxes were derived from measurements of acid neutralizing capacity (ANC), pH, ionic strength, temperature, and wind speed. CO₂ fluxes exhibited large seasonal variability, in particular in oligo-mesotrophic lakes. Most of the lakes emitted CO₂ during winter (median rates ranging 300–1,900 mg C m⁻² day⁻¹), and less CO₂ during summer or, in the case of some of the highly eutrophic lakes, retained CO₂ during summer. We found that seasonal CO₂ fluxes were strongly negatively correlated with pH (r = −0.65, P < 0.01), which in turn was correlated with chlorophyll a concentrations (r = 0.48, P < 0.01). Our analysis suggests that lake trophic status (a proxy for pelagic production) interacts with the lake ANC to drive the seasonal dynamics of CO₂ fluxes, largely by changing pH and thereby the equilibrium of the free CO₂ and bicarbonate relation. Long-term observations from four lakes, which have all undergone a period of oligotrophication during the past two decades, provide further evidence that CO₂ efflux generally increases as trophic status decreases, as a consequence of decreased pH. Across these four lakes, the annual average CO₂ emission has increased by 32% during the past two decades, thus, demonstrating the strong link between lake trophic status and CO₂ flux.     

Ecosystem CO2 exchange and plant biomass in the littoral zone of a boreal eutrophic lake

• 1 In order to study the dynamics of primary production and decomposition in the lake littoral, an interface zone between the pelagial, the catchment and the atmosphere, we measured ecosystem/atmosphere carbon dioxide (CO₂) exchange in the littoral zone of an eutrophic boreal lake in Finland during two open water periods (1998–1999). We reconstructed the seasonal net CO₂ exchange and identified the key factors controlling CO₂ dynamics. The seasonal net ecosystem exchange (NEE) was related to the amount of carbon accumulated in plant biomass.
• 2 In the continuously inundated zones, spatial and temporal variation in the density of aerial shoots controlled CO₂ fluxes, but seasonal net exchange was in most cases close to zero. The lower flooded zone had a net CO₂ uptake of 1.8–6.2 mol m^?2 per open water period, but the upper flooded zone with the highest photosynthetic capacity and above‐ground plant biomass, had a net CO₂ loss of 1.1–7.1 mol m^?2 per open water period as a result of the high respiration rate. The excess of respiration can be explained by decomposition of organic matter produced on site in previous years or leached from the catchment.
• 3 Our results from the two study years suggest that changes in phenology and water level were the prime cause of the large interannual difference in NEE in the littoral zone. Thus, the littoral is a dynamic buffer and source for the load of allochthonous and autochthonous carbon to small lakes.

     

CO2 evasion from boreal lakes: Revised estimate,drivers of spatial variability,and future projections

Lakes (including reservoirs) are an important component of the global carbon (C) cycle, as acknowledged by the fifth assessment report of the IPCC. In the context of lakes, the boreal region is disproportionately important contributing to 27% of the worldwide lake area, despite representing just 14% of global land surface area. In this study, we used a statistical approach to derive a prediction equation for the partial pressure of CO₂ (pCO₂) in lakes as a function of lake area, terrestrial net primary productivity (NPP), and precipitation (r² = .56), and to create the first high‐resolution, circumboreal map (0.5°) of lake pCO₂. The map of pCO₂ was combined with lake area from the recently published GLOWABO database and three different estimates of the gas transfer velocity k to produce a resulting map of CO₂ evasion (FCO₂). For the boreal region, we estimate an average, lake area weighted, pCO₂ of 966 (678–1,325) μatm and a total FCO₂ of 189 (74–347) Tg C year^?1, and evaluate the corresponding uncertainties based on Monte Carlo simulation. Our estimate of FCO₂ is approximately twofold greater than previous estimates, as a result of methodological and data source differences. We use our results along with published estimates of the other C fluxes through inland waters to derive a C budget for the boreal region, and find that FCO₂ from lakes is the most significant flux of the land‐ocean aquatic continuum, and of a similar magnitude as emissions from forest fires. Using the model and applying it to spatially resolved projections of terrestrial NPP and precipitation while keeping everything else constant, we predict a 107% increase in boreal lake FCO₂ under emission scenario RCP8.5 by 2100. Our projections are largely driven by increases in terrestrial NPP over the same period, showing the very close connection between the terrestrial and aquatic C cycle.     

Role of lakes for organic carbon cycling in the boreal zone

We calculated the carbon loss (mineralization plus sedimentation) and net CO₂ escape to the atmosphere for 79 536 lakes and total running water in 21 major Scandinavian catchments (size range 437–48 263 km²). Between 30% and 80% of the total organic carbon that entered the freshwater ecosystems was lost in lakes. Mineralization in lakes and subsequent CO₂ emission to the atmosphere was by far the most important carbon loss process. The withdrawal capacity of lakes on the catchment scale was closely correlated to the mean residence time of surface water in the catchment, and to some extent to the annual mean temperature represented by latitude. This result implies that variation of the hydrology can be a more important determinant of CO₂ emission from lakes than temperature fluctuations. Mineralization of terrestrially derived organic carbon in lakes is an important regulator of organic carbon export to the sea and may affect the net exchange of CO₂ between the atmosphere and the boreal landscape.     

A comparison of zooplankton communities in saline lakewater with variable anion composition

Although salinity and aquatic biodiversity are inversely related in lake water, the relationship between types of salts and zooplankton communities is poorly understood. In this study, zooplankton species were related to environmental variables from 12 lakes: three saline lakes with water where the dominant anions were SO₄ and CO₃, four saline lakes with Cl-dominated water, and five dilute, subsaline (0.5–3 gl^?1 total dissolved solids) lakes of variable anion composition. Although this study comprised only 12 lakes, distinct differences in zooplankton communities were observed among the two groups of chemically defined saline lakes. Canonical correspondence analysis identified total alkalinity, sulphate, chloride, calcium, sodium, potassium, and total phosphorus as all contributing to the first two ordination axes (λ₁ = 0.97 and λ₂ = 0.62, P<0.05). The rotifer Brachionus plicatilis and the harpactacoid copepod Cletocamptus sp. prevailed lakes with Cl-dominated water. In contrast, the calanoid copepods Leptodiaptomus sicilis and Diaptomus nevadensis were dominant in the SO₄/CO₃-dominated lake water with elevated potassium (79–128 mg l^?1) and total phosphorus concentrations (1322-2915 μg l^?1). The contrasting zooplankton species distribution among these two saline lake types is likely explained by variable selective pressure on zooplankton and their predators from differing physiological tolerances to salt stress and specific ions. While inland saline lakes with Cl as the dominant anion are relatively rare in Canada and SO₄/CO₃ are the common features, our study provided an opportunity to compare zooplankton communities across the two groups of lakes.     

CO2 supersaturation along the aquatic conduit in Swedish watersheds as constrained by terrestrial respiration,aquatic respiration and weathering

We tested the hypothesis that CO₂ supersaturation along the aquatic conduit over Sweden can be explained by processes other than aquatic respiration. A first generalized‐additive model (GAM) analysis evaluating the relationships between single water chemistry variables and pCO₂ in lakes and streams revealed that water chemistry variables typical for groundwater input, e.g., dissolved silicate (DSi) and Mg²⁺ had explanatory power similar to total organic carbon (TOC). Further GAM analyses on various lake size classes and stream orders corroborated the slightly higher explanatory power for DSi in lakes and Mg²⁺ for streams compared with TOC. Both DSi and TOC explained 22–46% of the pCO₂ variability in various lake classes (0.01–>100 km²) and Mg²⁺ and TOC explained 11–41% of the pCO₂ variability in the various stream orders. This suggests that aquatic pCO₂ has a strong groundwater signature. Terrestrial respiration is a significant source of the observed supersaturation and we may assume that both terrestrial respiration and aquatic respiration contributed equally to pCO₂ efflux. pCO₂ and TOC concentrations decreased with lake size suggesting that the longer water residence time allow greater equilibration of CO₂ with the atmosphere and in‐lake mineralization of TOC. For streams, we observed a decreasing trend in pCO₂ with stream orders between 3 and 6. We calculated the total CO₂ efflux from all Swedish lakes and streams to be 2.58 Tg C yr^?1. Our analyses also demonstrated that 0.70 Tg C yr^?1 are exported to the ocean by Swedish watersheds as HCO₃^? and CO₃^2? of which about 0.56 Tg C yr^?1 is also a residual from terrestrial respiration and constitute a long‐term sink for atmospheric CO₂. Taking all dissolved inorganic carbon (DIC) fluxes along the aquatic conduit into account will lower the estimated net ecosystem C exchange (NEE) by 2.02 Tg C yr^?1, which corresponds to 10% of the NEE in Sweden.     

Effects of temperature and sediment properties on benthic CO2 production in an oligotrophic boreal lake

1. Temperature and many other physical and chemical factors affecting CO₂ production in lake sediments vary significantly both seasonally and spatially. The effects of temperature and sediment properties on benthic CO₂ production were studied in in situ and in vitro experiments in the boreal oligotrophic Lake Pääjärvi, southern Finland. 2. In in situ experiments, temperature of the water overlying the shallow littoral sediment varied seasonally between 0.5 and 15.7 °C, but in deep water (≥20 m) the range was only 1.1–6.6 °C. The same exponential model (r² = 0.70) described the temperature dependence at 1.2, 10 and 20 m depths. At 2.5 and 5 m depths, however, the slopes of the two regression models (r² = 0.94) were identical but the intercept values were different. Sediment properties (wet, dry, mineral and organic mass) varied seasonally and with depth, but they did not explain a significantly larger proportion of variation in the CO₂ output rate than temperature. 3. In in vitro experiments, there was a clear and uniform exponential dependence of CO₂ production on temperature, with a 2.7‐fold increase per 10 °C temperature rise. The temperature response (slope of regression) was always the same, but the basic value of CO₂ production (intercept) varied, indicating that other factors also contributed to the benthic CO₂ output rate. 4. The annual CO₂ production of the sediment in Lake Pääjärvi averaged 62 g CO₂ m^?2, the shallow littoral at 0–3 m depth releasing 114 g CO₂ m^?2 and deep profundal (>15 m) 30 g CO₂ m^?2. On the whole lake basis, the shallow littoral at 0–3 m depth accounted for 53% and the sediment area in contact with the summer epilimnion (down to a depth c. 10 m) 75% of the estimated total annual CO₂ output of the lake sediment, respectively. Of the annual production, 83% was released during the spring and summer. 5. Using the temperature‐CO₂ production equations and climate change scenarios we estimated that climatic warming might increase littoral benthic CO₂ production in summer by nearly 30% from the period 1961–90 to the period 2071–2100.     

High carbon emissions from thermokarst lakes and their determinants in the Tibet Plateau

Thermokarst lakes are potentially important sources of methane (CH₄) and carbon dioxide (CO₂). However, considerable uncertainty exists regarding carbon emissions from thermokarst lakes owing to a limited understanding of their patterns and motivators. In this study, we measured CH₄ and CO₂ diffusive fluxes in 163 thermokarst lakes in the Qinghai–Tibet Plateau (QTP) over 3 years from May to October. The median carbon emissions from the QTP thermokarst lakes were 1440 mg CO₂ m⁻² day⁻¹ and 60 mg CH₄ m⁻² day⁻¹, respectively. The diffusive rates of CO₂ and CH₄ are related to the catchment land cover type. Sediment microbial abundance and hydrochemistry explain 51.9% and 38.3% of the total variance in CH₄ diffusive emissions, respectively, while CO₂ emissions show no significant relationship with environmental factors. When upscaling carbon emissions from the QTP thermokarst lakes, the annual average CH₄ release per lake area is equal to that of the pan-Arctic region. Our findings highlight the importance of incorporating in situ observation data with different emission pathways for different land cover types in predicting carbon emissions from thermokarst lakes in the future.     

Links between Terrestrial Primary Production and Bacterial Production and Respiration in Lakes in a Climate Gradient in Subarctic Sweden

We compared terrestrial net primary production (NPP) and terrestrial export of dissolved organic carbon (DOC) with lake water heterotrophic bacterial activity in 12 headwater lake catchments along an altitude gradient in subarctic Sweden. Modelled NPP declined strongly with altitude and annual air temperature decreases along the altitude gradient (6°C between the warmest and the coldest catchment). Estimated terrestrial DOC export to the lakes was closely correlated to NPP. Heterotrophic bacterial production (BP) and respiration (BR) were mainly based on terrestrial organic carbon and strongly correlated with the terrestrial DOC export. Excess respiration over PP of the pelagic system was similar to net emission of CO₂ in the lakes. BR and CO₂ emission made up considerably higher shares of the terrestrial DOC input in warm lakes than in cold lakes, implying that respiration and the degree of net heterotrophy in the lakes were dependant not only on terrestrial export of DOC, but also on characteristics in the lakes which changed along the gradient and affected the bacterial metabolization of allochthonous DOC. The study showed close links between terrestrial primary production, terrestrial DOC export and bacterial activity in lakes and how these relationships were dependant on air temperature. Increases in air temperature in high latitude unproductive systems might have considerable consequences for lake water productivity and release of CO₂ to the atmosphere, which are ultimately determined by terrestrial primary production.     

Controls of organic and inorganic carbon in randomly selected Boreal lakes in varied catchments

Organic and inorganic carbon concentrations in lakes and the links to catchment and water quality were studied in variable landscapes using the Finnish Lake Survey data base including 874 randomly selected lakes sampled during autumn overturn. The median total organic carbon (TOC) in these boreal lakes was 7.8 mg l^?1, the median total inorganic carbon (TIC) 1.6 mg l^?1 and the median partial pressure of CO₂ (pCO₂) 900 μatm. When the data was divided into subgroups according to land use in the catchment, the proportion of TIC of the total carbon (TC) in lakes was highest (31%) in agricultural areas and lowest (10%) in peatland areas. Elevated TIC concentrations were associated with agricultural land in the catchment, whereas elevated TOC concentrations were observed in lakes with high peatland proportion in the catchment. Two contrasting important sources of CO₂ in lakes were identified on the basis of statistical analysis of the data; weathering processes in the catchments and decomposition of organic matter. CO₂ was also strongly associated with total nutrients TN and TP, implying the importance of quality of organic matter and availability of nutrients for the decomposition processes.     

Impacts of changing climate and atmospheric deposition on N and S drainage losses from a forested watershed of the Adirondack Mountains, New York State

Biogeochemical responses to changing climate and atmospheric deposition were investigated using nitrogen (N) and sulfur (S) mass balances, including dry deposition and organic solutes in the Arbutus Lake watershed in the Adirondack Mountains, New York State. Long‐term monitoring of wet‐only precipitation (NADP/NTN, 1983–2001) and dry deposition (AIRMoN, 1990–2001) at sites adjacent to the watershed showed that concentrations of SO₄^2? in precipitation, SO₄^2? in particles,and SO₂ vapor all declined substantially (P<0.005) in contrast to no marked temporal changes observed for most N constituents (NH₄⁺ in precipitation, HNO₃ vapor, and particulate NO₃^?), except for NO₃^? in precipitation, which showed a small decrease in the late 1990s. From 1983 to 2001, concentrations of SO₄^2? in the lake outlet significantly decreased (?2.1 μeq L^?1 yr^?1, P<0.0001), whereas NO₃^? and dissolved organic N (DON) concentrations showed no consistent temporal trends. With the inclusion of dry deposition and DON fluxes into the mass balance, the retained portion of atmospheric N inputs within the main subcatchment increased from 37% to 60%. Sulfur outputs greatly exceeded inputs even with the inclusion of dry S deposition, while organic S flux represented another source of S output, implying substantial internal S sources. A significant relationship between the annual mean concentrations of SO₄^2? in lake discharge and wet deposition over the last two decades (r=0.64, P<0.01) suggested a considerable influence of declining S deposition on surface water SO₄^2? concentrations, despite substantial internal S sources. By contrast, interannual variations in both NO₃^? concentrations and fluxes in lake discharge were significantly related to year‐to‐year changes in air temperature and runoff. Snowmelt responses to winter temperature fluctuations were crucial in explaining large portions of interannual variations in watershed NO₃^? export during the months preceding spring snowmelt (especially, January–March). Distinctive response patterns of monthly mean concentrations of NO₃^? and DON in the major lake inlet to seasonal changes in air temperature also suggested climatic regulation of seasonal patterns in watershed release of both N forms. The sensitive response of N drainage losses to climatic variability might explain the synchronous patterns of decadal variations in watershed NO₃^? export across the northeastern USA.     

Concentrations of CO2 and CH4 in water columns of two stratified boreal lakes during a year of atypical summer precipitation

We measured CO₂ and CH₄ concentrations throughout the water columns of two boreal lakes with contrasting trophic status and water color during a wet summer. Previous work suggested that rainfall was important for carbon gas evasion. During the stratified period, precipitation generated unexpected variabilities in CO₂, CH₄, and DOC concentrations below the euphotic zone, especially in the metalimnion. The DOC concentrations after the rains rose to 22 and 10 mg L^?1 from the initial 13 and 8 mg L^?1, in the humic and clear-water lakes respectively, simultaneously with an increase in carbon gas concentrations. In both lakes, the water column was stable, suggesting that the high gas concentrations were not due to transport from hypolimnia rich in carbon gases. The high concentrations of CH₄, which can only be produced in anoxic conditions, in the oxic metalimnion and epilimnion in comparison to the hypolimnetic concentrations indicated that a considerable proportion of the pelagic CH₄ originated from the catchment and/or the littoral zone. Thus, as a consequence of high levels of precipitation, carbon gas concentrations during summer stratification can increase, which can have overall importance in annual carbon budgets.     

Influences of PAR, temperature and water vapor concentration on gas exchange by ferns

The effects of photosynthetically active radiation (PAR), leaf temperature and the leaf-to-air water vapor concentration drop on net CO₂ uptake and water vapor conductance were surveyed for 14 species of ferns. Most previous studies indicated that ferns have extremely low maximal rates of net CO₂ uptake, below 2 umol m^?2 s^?1, whereas the average maximal rate observed here at 25⁰ C was 7 umol m^?2 s^?1. Net CO₂ uptake reached 90% of saturation at an average PAR (400 to 700 nm) of only 240 umol m^?2 s^?1, consistent with the typically shaded habitats of most ferns. Maximal CO₂ uptake rates were positively correlated with the PAR for 90% saturation (r²=0.59), the chlorophyII per unit leaf area (r²=0.30), the water vapor conductance (r²=0.65), and the CO₂ residual conductance (r²=0.69). A higher water vapor conductance (gwv) was correlated with a greater fractional change in gwv as the leaf-to-air water vapor concentration drop (Δc_wv) was raised from 5to20 g m^?3 (r²=0.90). Specifically, for species with low g_wv of about I mm s^?1 the ratio of g_wv at Δc_wv= 5 g m^?3 to that at Δc_wv= 20 g m^?3 was near 1, but it was near 2 for species with g_wv of about 4 mm s^?1. Such a relationship, which can prevent excessive transpiration, has apparently not previously been pointed out in surveys of other plant groups.     

Carbon Dioxide in Boreal Surface Waters: A Comparison of Lakes and Streams

The quantity of carbon dioxide (CO₂) emissions from inland waters into the atmosphere varies, depending on spatial and temporal variations in the partial pressure of CO₂ (pCO₂) in waters. Using 22,664 water samples from 851 boreal lakes and 64 boreal streams, taken from different water depths and during different months we found large spatial and temporal variations in pCO₂, ranging from below atmospheric equilibrium to values greater than 20,000???atm with a median value of 1048???atm for lakes (n?=?11,538 samples) and 1176???atm for streams (n?=?11,126). During the spring water mixing period in April/May, distributions of pCO₂ were not significantly different between stream and lake ecosystems (P?>?0.05), suggesting that pCO₂ in spring is determined by processes that are common to lakes and streams. During other seasons of the year, however, pCO₂ differed significantly between lake and stream ecosystems (P?<?0.0001). The variable that best explained the differences in seasonal pCO₂ variations between lakes and streams was the temperature difference between bottom and surface waters. Even small temperature differences resulted in a decline of pCO₂ in lake surface waters. Minimum pCO₂ values in lake surface waters were reached in July. Towards autumn pCO₂ strongly increased again in lake surface waters reaching values close to the ones found in stream surface waters. Although pCO₂ strongly increased in the upper water column towards autumn, pCO₂ in lake bottom waters still exceeded the pCO₂ in surface waters of lakes and streams. We conclude that throughout the year CO₂ is concentrated in bottom waters of boreal lakes, although these lakes are typically shallow with short water retention times. Highly varying amounts of this CO₂ reaches surface waters and evades to the atmosphere. Our findings have important implications for up-scaling CO₂ fluxes from single lake and stream measurements to regional and global annual fluxes.     

Carbon exchange of grazed pasture on a drained peat soil

Land‐use changes have contributed to increased atmospheric CO₂ concentrations. Conversion from natural peatlands to agricultural land has led to widespread subsidence of the peat surface caused by soil compaction and mineralization. To study the net ecosystem exchange of carbon (C) and the contribution of respiration to peat subsidence, eddy covariance measurements were made over pasture on a well‐developed, drained peat soil from 22 May 2002 to 21 May 2003. The depth to the water table fluctuated between 0.02 m in winter 2002 to 0.75 m during late summer and early autumn 2003. Peat soil moisture content varied between 0.6 and 0.7 m³ m^?3 until the water table dropped below 0.5 m, when moisture content reached 0.38 m³ m^?3. Neither depth to water table nor soil moisture was found to have an effect on the rate of night‐time respiration (ranging from 0.4–8.0 μmol CO₂ m^?2 s^?1 in winter and summer, respectively). Most of the variance in night‐time respiration was explained by changes in the 0.1 m soil temperature (r²=0.93). The highest values for daytime net ecosystem exchange were measured in September 2002, with a maximum of ?17.2 μmol CO₂ m^?2 s^?1. Grazing events and soil moisture deficiencies during a short period in summer reduced net CO₂ exchange. To establish an annual C balance for this ecosystem, non‐linear regression was used to model missing data. Annually integrated (CO₂) C exchange for this peat–pasture ecosystem was 45±500 kg C ha^?1 yr^?1. After including other C exchanges (methane emissions from cows and production of milk), the net annual C loss was 1061±500 kg C ha^?1 yr^?1.     

Contribution of Sediment Respiration to Summer CO2 Emission from Low Productive Boreal and Subarctic Lakes

We measured sediment production of carbon dioxide (CO₂) and methane (CH₄) and the net flux of CO₂ across the surfaces of 15 boreal and subarctic lakes of different humic contents. Sediment respiration measurements were made in situ under ambient light conditions. The flux of CO₂ between sediment and water varied between an uptake of 53 and an efflux of 182 mg C m⁻² day⁻¹ from the sediments. The mean respiration rate for sediments in contact with the upper mixed layer (SedR) was positively correlated to dissolved organic carbon (DOC) concentration in the water (r² = 0.61). The net flux of CO₂ across the lake surface [net ecosystem exchange (NEE)] was also closely correlated to DOC concentration in the upper mixed layer (r² = 0.73). The respiration in the water column was generally 10-fold higher per unit lake area compared to sediment respiration. Lakes with DOC concentrations <5.6 mg L⁻¹ had net consumption of CO₂ in the sediments, which we ascribe to benthic primary production. Only lakes with very low DOC concentrations were net autotrophic (<2.6 mg L⁻¹) due to the dominance of dissolved allochthonous organic carbon in the water as an energy source for aquatic organisms. In addition to previous findings of allochthonous organic matter as an important driver of heterotrophic metabolism in the water column of lakes, this study suggests that sediment metabolism is also highly dependent on allochthonous carbon sources.     

Total Organic Carbon (TOC) of Lake Water During the Holocene Inferred from Lake Sediments and Near-infrared Spectroscopy (NIRS) in Eight Lakes from Northern Sweden

The aim of this study is to infer past changes in total organic carbon (TOC) content of lake water during the Holocene in eight boreal forest, tree-limit and alpine lakes using a new technique – near-infrared spectroscopy (NIRS). A training set of 100 lakes from northern Sweden covering a TOC gradient from 0.7 to 14.9 mg l⁻¹ was used to establish a relationship between the NIRS signal from surface sediments (0–1 cm) and the TOC content of the water mass. The NIRS model for TOC has a root mean squared error (RMSECV) of calibration of 1.6 mg l⁻¹ (11% of the gradient) assessed by internal cross-validation (CV), which yields an R²_cv of 0.61. The results show that the most dramatic change among the studied lakes occurs in both tree-line lakes around 1000 yrs BP when the TOC content decreases from ca. 7 to 3 mg l⁻¹ at the present, which is probably due to a descending tree-limit. The TOC content in the alpine lakes shows a declining trend throughout most of the Holocene indicating that TOC may be more directly correlated to climate in alpine lakes than forest lakes. All boreal forest lakes show a declining trend in TOC during the past 3000 yrs with the largest amplitude of change occurring in the lake with a connected mire. The results indicate that a change to a warmer and more humid climate can increase the TOC levels in lakes, which in turn may increase the saturation of CO₂ in lake waters and the emission of CO₂ to the atmosphere.     

Alkalinity generation and sediment CO2 uptake influence establishment of Sparganium angustifolium in softwater lakes

1. Softwater lakes are generally dominated by slow growing, small, isoetid plant species that are adapted to the carbon‐ and nutrient‐limited conditions in these lakes. We investigated the strategy of a fast growing species, Sparganium angustifolium, for occupying softwater lakes. A field survey was carried out in Norwegian carbon‐limited Isoëteto‐Lobelietum softwater lakes to compare abiotic conditions at locations with and without S. angustifolium. In addition, long term abiotic changes (1995–2008) related to the sudden establishment of the species on experimentally limed plots were studied. Based on the results, the carbon acquisition mechanism of S. angustifolium was tested in eco‐physiological laboratory experiments. 2. The redox potential was significantly lower at locations with S. angustifolium (220 ± 2.3) compared to locations without S. angustifolium (338.1 ± 13.9). The lower redox potential was accompanied by significantly higher concentrations of HCO₃^?, CO₂ and Fe²⁺ in the sediment pore water, indicating in‐lake alkalinity generation due to higher iron reduction rates in the generally iron‐rich sediments. In addition, the lower redox potential was accompanied by a higher nutrient availability (NH₄⁺ and PO₄^3?) in the sediment pore water. Since there were no differences in water quality between the lakes, the ability of S. angustifolium to grow in softwater lakes very likely depends upon the higher dissolved inorganic carbon (DIC) and nutrient concentrations present in the sediment pore water. 3. Results from the liming experiment revealed that appearance of S. angustifolium on limed plots was related to the dissolution of Ca and Mg carbonates and development of a lower redox potential in the sediment. These processes were accompanied by a sustained increase in the availability of DIC in the sediment pore water. 4. The eco‐physiological experiments indicated that S. angustifolium can increase in biomass and produce floating leaves at a relatively high DIC availability in the root medium. In addition, it appeared that S. angustifolium can take up CO₂ by the roots. As far as we know, the ability to use sediment CO₂ has only been described as an adaptation typical for isoetid plant species. Use of the relatively large sediment CO₂ pools present in these sediment types (>1000 μmol L^?1) to enable development of long floating leaves for additional uptake of atmospheric CO₂ is a very different strategy to colonise softwater lakes as compared to isoetid plant species.     

Nitrous oxide emissions from grass swards during the eighth year of elevated atmospheric pCO2 (Swiss FACE)

Emissions of N₂O were measured during the growth season over a year from grass swards under ambient (360 μL L^?1) and elevated (600 μL L^?1) CO₂ partial pressures at the Free Air Carbon dioxide Enrichment (FACE) experiment, Eschikon, Switzerland. Measurements were made following high (56 g N m^?2 yr^?1) and low (14 g N m^?2 yr^?1) rates of fertilizer application, split over 5 re‐growth periods, to Lolium perenne, Trifolium repens and mixed Lolium/Trifolium swards. Elevated pCO₂ increased annual emissions of N₂O from the high fertilized Lolium and mixed Lolium/Trifolium swards resulting in increases in GWP (N₂O emissions) of 179 and 111 g CO₂ equivalents m^?2, respectively, compared with the GWP of ambient pCO₂ swards, but had no significant effect on annual emissions from Trifolium monoculture swards. The greater emissions from the high fertilized elevated pCO₂Lolium swards were attributed to greater below‐ground C allocation under elevated pCO₂ providing the energy for denitrification in the presence of excess mineral N. An annual emission of 959 mg N₂O‐N m^?2 yr^?1 (1.7% of fertilizer N applied) was measured from the high fertilized Lolium sward under elevated pCO₂. The magnitude of emissions varied throughout the year with 84% of the total emission from the elevated pCO₂Lolium swards measured during the first two re‐growths (April–June 2001). This was associated with higher rainfall and soil water contents at this time of year. Trends in emissions varied between the first two re‐growths (April–June 2001) and the third, fourth and fifth re‐growths (late June–October 2000), with available soil NO₃^? and rainfall explaining 70%, and soil water content explaining 72% of the variability in N₂O in these periods, respectively. Caution is therefore required when extrapolating from short‐term measurements to predict long‐term responses to global climate change. Our findings are of global significance as increases in atmospheric concentrations of CO₂ may, depending on sward composition and fertilizer management, increase greenhouse gas emissions of N₂O, thereby exacerbating the forcing effect of elevated CO₂ on global climate. Our results suggest that when applying high rates of N fertilizer to grassland systems, Trifolium repens swards, or a greater component of Trifolium in mixed swards, may minimize the negative effect of continued increasing atmospheric CO₂ concentrations on global warming.