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1.
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.  相似文献   

2.
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.  相似文献   

3.
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.  相似文献   

4.
Spatial and seasonal variations in CO2 and CH4 concentrations in streamwater and adjacent soils were studied at three sites on Brocky Burn, a headwater stream draining a peatland catchment in upland Britain. Concentrations of both gases in the soil atmosphere were significantly higher in peat and riparian soils than in mineral soils. Peat and riparian soil CO2 concentrations varied seasonally, showing a positive correlation with air and soil temperature. Streamwater CO2 concentrations at the upper sampling site, which mostly drained deep peats, varied from 2·8 to 9·8 mg l?1 (2·5 to 11·9 times atmospheric saturation) and decreased markedly downstream. Temperature‐related seasonal variations in peat and riparian soil CO2 were reflected in the stream at the upper site, where 77% of biweekly variation was explained by an autoregressive model based on: (i) a negative log‐linear relationship with stream flow; (ii) a positive linear relationship with soil CO2 concentrations in the shallow riparian wells; and (iii) a negative linear relationship with soil CO2 concentrations in the shallow peat wells, with a significant 2‐week lag term. These relationships changed markedly downstream, with an apparent decrease in the soil–stream linkage and a switch to a positive relationship between stream flow and stream CO2. Streamwater CH4 concentrations also declined sharply downstream, but were much lower (<0·01 to 0·12 mg l?1) than those of CO2 and showed no seasonal variation, nor any relationship with soil atmospheric CH4 concentrations. However, stream CH4 was significantly correlated with stream flow at the upper site, which explained 57% of biweekly variations in dissolved concentrations. We conclude that stream CO2 can be a useful integrative measure of whole catchment respiration, but only at sites where the soil–stream linkage is strong. Copyright © 2004 John Wiley & Sons, Ltd.  相似文献   

5.
Several sediment cores were collected from two proglacial lakes in the vicinity of Mittivakkat Glacier, south‐east Greenland, in order to determine sedimentation rates, estimate sediment yields and identify the dominant sources of the lacustrine sediment. The presence of varves in the ice‐dammed Icefall Lake enabled sedimentation rates to be estimated using a combination of X‐ray photography and down‐core variations in 137Cs activity. Sedimentation rates for individual cores ranged between 0·52 and 1·06 g cm−2 year−1, and the average sedimentation rate was estimated to be 0·79 g cm−2 year−1. Despite considerable down‐core variability in annual sedimentation rates, there is no significant trend over the period 1970 to 1994. After correcting for autochthonous organic matter content and trap efficiency, the mean fine‐grained minerogenic sediment yield from the 3·8 km2 basin contributing to the lake was estimated to be 327 t km−2 year−1. Cores were also collected from the topset beds of two small deltas in Icefall Lake. The deposition of coarse‐grained sediment on the delta surface was estimated to total in excess of 15 cm over the last c. 40 years. In the larger Lake Kuutuaq, which is located about 5 km from the glacier front and for which the glacier represents a smaller proportion of the contributing catchment, sedimentation rates determined for six cores collected from the centre of the lake, based on their 137Cs depth profiles, were estimated to range between 0·05 and 0·11 g cm−2 year−1, and the average was 0·08 g cm−2 year−1. The longer‐term (c. 100–150 years) average sedimentation rate for one of the cores, estimated from its unsupported 210Pb profile, was 0·10–0·13 g cm−2 year−1, suggesting that sedimentation rates in this lake have been essentially constant over the last c. 100–150 years. The average fine‐grained sediment yield from the 32·4 km2 catchment contributing to the lake was estimated to be 13 t km−2 year−1. The 137Cs depth profiles for cores collected from the topset beds of the delta of Lake Kuutuaq indicate that in excess of 27 cm of coarse‐grained sediment had accumulated on the delta surface over the last approximately 40 years. Caesium‐137 concentrations associated with the most recently deposited (uppermost) fine‐grained sediment in both Icefall Lake and Lake Kuutuaq were similar to those measured in fine‐grained sediment collected from steep slopes in the immediate proglacial zone, suggesting that this material, rather than contemporary glacial debris, is the most likely source of the sediment deposited in the lakes. This finding is confirmed by the 137Cs concentrations associated with suspended sediment collected from the Mittivakkat stream, which are very similar to those for proglacial material. Copyright © 2000 John Wiley & Sons, Ltd.  相似文献   

6.
The knowledge of the contribution of sediment sources to river networks is a prerequisite to understand the impact of land use change on sediment yield. We calculated the relative contributions of sediment sources in two paired catchments, one with commercial eucalyptus plantations (0.83 km2) and the other with grassland used for livestock farming (1.10 km2), located in the Brazilian Pampa biome, using different combinations of conventional [geochemical (G), radionuclide (R) and stable isotopes and organic matter properties (S)] and alternative tracer properties [spectrocolorimetric visible-based-colour parameters (V)]. Potential sediment sources evaluated were stream channel, natural grassland and oat pasture fields in the grassland catchment, and stream channel, unpaved roads and eucalyptus plantation in the eucalyptus catchment. The results show that the best combination of tracers to discriminate the potential sources was using GSRV tracers in the grassland catchment, and using GSRV, GSV and GS tracers in the eucalyptus catchment. In all these cases, samples were 100% correctly classified in their respective groups. Considering the best tracers results (GSRV) in both catchments, the sediment source contributions estimated in the catchment with eucalyptus plantations was 63, 30 and 7% for stream channel, eucalyptus stands and unpaved roads, respectively. In the grassland catchment, the source contributions to sediment were 84, 14 and 2% for natural grassland, stream channel and oats pasture fields, respectively. The combination of these source apportionment results with the annual sediment loads monitored during a 3-year period demonstrates that commercial eucalyptus plantations supplied approximately 10 times less sediment (0.1 ton ha−1 year−1) than the traditional land uses in this region, that is, 1.0 ton ha−1 year−1 from grassland and 0.3 ton ha−1 year−1 from oats pasture fields. These results demonstrate the potential of combining conventional and alternative approaches to trace sediment sources originating from different land uses in this region. Furthermore, they show that well-managed forest plantations may be less sensitive to erosion than grassland used for intensive livestock farming, which should be taken into account to promote the sustainable use of land in this region of South America.  相似文献   

7.
Spatial and temporal variability of hydrological responses affecting surface water dissolved organic carbon (DOC) concentrations are important for determining upscaling patterns of DOC export within larger catchments. Annual and intra‐annual variations in DOC concentrations and fluxes were assessed over 2 years at 12 sites (3·40–1837 km2) within the River Dee basin in NE Scotland. Mean annual DOC fluxes, primarily correlated with catchment soil coverage, ranged from 3·41 to 9·48 g m?2 yr?1. Periods of seasonal (summer–autumn and winter–spring) DOC concentrations (production) were delineated and related to discharge. Although antecedent temperature mainly determined the timing of switchover between periods of high DOC in the summer‐autumn and low DOC in winter‐spring, inter‐annual variability of export within the same season was largely dependent on its associated water flux. DOC fluxes ranged from 1·39 to 4·80 g m?2 season?1 during summer–autumn and 1·43 to 4·15 g m?2 season?1 in winter–spring.Relationships between DOC areal fluxes and catchment scale indicated that mainstem fluxes reflect the averaging of highly heterogeneous inputs from contrasting headwater catchments, leading to convergent DOC fluxes at catchment sizes of ca 100 km2. However, during summer–autumn periods, in contrast to winter–spring, longitudinal mainstem DOC fluxes continue to decrease, most likely because of increasing biological processes. This highlights the importance of considering seasonal as well as annual changes in DOC fluxes with catchment scale. This study increases our understanding of the temporal variability of DOC upscaling patterns reflecting cumulative changes across different catchment scales and aids modelling of carbon budgets at different stages of riverine systems. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

8.
From 2011 to 2019, mercury (Hg) stores and fluxes were studied in the small forested catchment Lesní potok (LES) in the central Czech Republic using the watershed mass balance approach together with internal measurements. Mean input fluxes of Hg via open bulk deposition, beech throughfall and spruce throughfall during the periodwere 2.9, 3.9 and 7.6 μg m−2 year−1, respectively. These values were considerably lower than corresponding deposition Hg fluxes reported in the early years of the 21st century from catchments in Germany. Current bulk precipitation inputs at unimpacted Czech mountainous sites were lower than those in Germany. The largest Hg inputs to the catchment were via litterfall, averaging 22.6 and 17.8 μg m−2 year−1 for beech and spruce stands. The average Hg input, based on the sum of mean litterfall and throughfall deposition, was 23.0 μg m−2 year−1, compared to the estimated Hg output in runoff of 0.5 μg m−2 year−1, which is low compared to other reported values. Thus, only ~2% of Hg input is exported in stream runoff. Stream water Hg was only weakly related to dissolved organic carbon (DOC) but both concentrations were positively correlated with water temperature. The estimated total soil Hg pool averaged 47.5 mg m−2, only 4% of which was in the O-horizon. Thus Hg in the O-horizon pool represents 72 years of deposition at the current input flux and 3800 years of export at the current runoff flux. Age-dating by 14C suggested that organic soil contains Hg from recent deposition, while mineral soil at 40–80 cm depth contained 4400-year old carbon, suggesting the soil had accumulated atmospheric Hg inputs through millennia to reach the highest soil Hg pool of the soil profile. These findings suggest that industrial era intensification of the Hg cycle is superimposed on a slower-paced Hg cycle during most of the Holocene.  相似文献   

9.
We measured spatial and temporal variations in carbon concentrations, isotopic compositions and exports during a complete hydrological cycle in nine watercourses draining a lowland forested podzolized catchment, flowing into the Arcachon lagoon (France). In addition, integrated fluxes of CO2 across the water-atmosphere interface were estimated to assess the relative importance of CO2 evasion versus lateral carbon transport at the catchment scale. Watercourse similarities and specificities linked to the local catchment characteristics are discussed and compared with other riverine systems. Low concentrations of suspended particulate matter and particulate organic carbon (POC) were generally measured in all the watercourses (8.4 ± 3.4 and 1.6 ± 0.6 mg L?1, respectively), reflecting limited mechanical soil erosion. The generally high POC content in the suspended matter (20 %), low Chl a concentrations (1.3 ± 1.4 μg L?1) and the relatively constant δ13C-POC value (near ?28 ‰) throughout the year reveal this POC originates from terrestrial C3 plant and soil detritus. The presence of podzols leads to high levels of dissolved organic carbon (DOC; 6.6 ± 2.2 mg L?1). Similarly, high dissolved inorganic carbon (DIC) concentrations were measured in the Arcachon lagoon catchment (5.9 ± 2.2 mg L?1). The δ13C-DIC value around ?20 ‰ throughout the year in many small watercourses reveals the predominance of terrestrial carbon mineralisation and silicate rock weathering in soils as the major DIC source. With pCO2 between 1,000 and 10,000 ppmv, all watercourses were a source of CO2 to the atmosphere, particularly during the low river stage. Organic carbon parameters remained relatively stable throughout the year, whereas DIC parameters showed strong seasonal contrasts closely linked to the hydrological regime and hyporheic flows. In total, the carbon export from the Arcachon watershed was estimated at 15,870 t C year?1 or 6 t C km?2 year?1, mostly exported to the lagoon as DOC (35 %), DIC (24 %) and lost as CO2 degassing to the atmosphere (34 %).  相似文献   

10.

Eddy covariance technique was used to measure carbon flux during two growing seasons in 2003 and 2004 over typical steppe in the Inner Mongolia Plateau, China. The results showed that there were two different CO2 flux diurnal patterns at the grassland ecosystem. One had a dual peak in diurnal course of CO2 fluxes with a depression of CO2 flux after noon, and the other had a single peak. In 2003, the maximum diurnal uptake and emitting value of CO2 were −7.4 and 5.4 g·m−2·d−1 respectively and both occurred in July. While in 2004, the maximum diurnal uptake and release of CO2 were −12.8 and 5.8 g·m−2·d−1 and occurred both in August. The grassland fixed 294.66 and 467.46 g CO2·m−2 in 2003 and 2004, and released 333.14 and 437.17 g CO2·m−2 in 2003 and 2004, respectively from May to September. Water availability and photosynthetic active radiation (PAR) are two important factors of controlling CO2 flux. Consecutive precipitation can cause reduction in the ability of ecosystem carbon exchange. Under favorable soil water conditions, daytime CO2 flux is dependent on PAR. CO2 flux, under soil water stress conditions, is obviously less than those under favorable soil water conditions, and there is a light saturation phenomena at PAR=1200 μmol·m−2·s−1. Soil respiration was temperature dependent when there was no soil water stress; otherwise, this response became accumulatively decoupled from soil temperature.

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11.
Estimates of greenhouse gas evasion from rivers have been refined over the past decades to constrain their role in global carbon cycle processes. However, despite 55% of the human population living in urban areas, urban rivers have had limited attention. We monitored carbon dynamics in an urbanized river (River Kelvin, 331 km2, UK) to explore the drivers of dissolved carbon lateral and vertical export. Over a 2-year sampling period, riverine methane (CH4) and carbon dioxide (CO2) concentrations were consistently oversaturated with respect to atmospheric equilibria, leading to continual degassing to the atmosphere. Carbon stable isotopic compositions (δ13C) indicated that terrestrially derived carbon comprised most of the riverine CH4 and dissolved CO2 (CO2*) load while dissolved inorganic carbon (DIC) from groundwater was the main form of riverine DIC. The dynamics of CH4, CO2*, and DIC in the river were primarily hydrology-controlled, that is, [CH4] and [CO2*] both increased with elevated discharge, total [DIC] decreased with elevated discharge while the proportion of biologically derived DIC increased with increasing discharge. The concentration of dissolved organic carbon (DOC) showed a weak relationship with river hydrology in summer and autumn and was likely influenced by the combined sewer overflows. Carbon emission to the atmosphere is estimated to be 3.10 ± 0.61 kg C·m−2·yr−1 normalized to water surface area, with more than 99% emitted as CO2. Annual carbon loss to the coastal estuary is approximately 4.69 ± 0.70 Gg C yr−1, with annual DIC export approximately double that of DOC. Per unit area, the River Kelvin was a smaller carbon source to the atmosphere than natural rivers/streams but shows elevated fluxes of DIC and DOC under comparable conditions. This research illustrates the role urban systems may have on riverine carbon dynamics and demonstrates the potential tight link between urbanization and riverine carbon export.  相似文献   

12.
The stable isotopic composition of dissolved inorganic carbon (δ13C‐DIC) was investigated as a potential tracer of streamflow generation processes at the Sleepers River Research Watershed, Vermont, USA. Downstream sampling showed δ13C‐DIC increased between 3–5‰ from the stream source to the outlet weir approximately 0·5 km downstream, concomitant with increasing pH and decreasing PCO2. An increase in δ13C‐DIC of 2·4 ± 0·1‰ per log unit decrease of excess PCO2 (stream PCO2 normalized to atmospheric PCO2) was observed from downstream transect data collected during snowmelt. Isotopic fractionation of DIC due to CO2 outgassing rather than exchange with atmospheric CO2 may be the primary cause of increased δ13C‐DIC values downstream when PCO2 of surface freshwater exceeds twice the atmospheric CO2 concentration. Although CO2 outgassing caused a general increase in stream δ13C‐DIC values, points of localized groundwater seepage into the stream were identified by decreases in δ13C‐DIC and increases in DIC concentration of the stream water superimposed upon the general downstream trend. In addition, comparison between snowmelt, early spring and summer seasons showed that DIC is flushed from shallow groundwater flowpaths during snowmelt and is replaced by a greater proportion of DIC derived from soil CO2 during the early spring growing season. Thus, in spite of effects from CO2 outgassing, δ13C of DIC can be a useful indicator of groundwater additions to headwater streams and a tracer of carbon dynamics in catchments. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

13.
In order to investigate the relation between water chemistry and functional landscape elements, spatial data sets of characteristics for 68 small (0·2–1·5 km2) boreal forest catchments in western central Sweden were analysed in a geographical information system (GIS). The geographic data used were extracted from official topographic maps. Water sampled four times at different flow situations was analysed chemically. This paper focuses on one phenomenon that has an important influence on headwater quality in boreal, coniferous forest streams: generation and export of dissolved organic carbon (DOC). It is known that wetland cover (bogs and fens) in the catchment is a major source of DOC. In this study, a comparison was made between a large number of headwater catchments with varying spatial locations and areas of wetlands. How this variation, together with a number of other spatial variables, influences the DOC flux in the streamwater was analysed by statistical methods. There were significant, but not strong, correlations between the total percentages of wetland area and DOC flux measured at a medium flow situation, but not at high flow. Neither were there any significant correlations between the percentage of wetland area connected to streams, nor the percentage of wetland area within a zone 50 m from the stream and the DOC flux. There were, however, correlations between catchment mean slope and the DOC flux in all but one flow situations. This study showed that, considering geographical data retrieved from official sources, the topography of a catchment better explains the variation in DOC flux than the percentage and locations of distinct wetland areas. This emphasizes the need for high‐resolution elevation models accurate enough to reveal the sources of DOC found in headwater streams. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

14.
Utilising newly available instrumentation, the carbon balance in two small tropical catchments was measured during two discharge events at high temporal resolution. Catchments share similar climatic conditions, but differ in land use with one draining a pristine rainforest catchment, the other a fully cleared and cultivated catchment. The necessity of high resolution sampling in small catchments was illustrated in each catchment, where significant chemical changes occurred in the space of a few hours or less. Dissolved and particulate carbon transport dominated carbon export from the rainforest catchment during high flow, but was surpassed by degassing of CO2 less than 4 h after the discharge peak. In contrast, particulate organic carbon dominated export from the cleared catchment, in all flow conditions with CO2 evasion accounting for 5–23% of total carbon flux. Stable isotopes of dissolved inorganic carbon (DIC) in the ephemeral rainforest catchment decreased quickly from ~1.5 ‰ to ~ ?16 ‰ in 5 h from the flood beginning. A two‐point mixing model revealed that in the initial pulse, over 90% of the DIC was of rainwater origin, decreasing to below 30% in low flow. In the cultivated catchment, δ13CDIC values varied significantly less (?11.0 to ?12.2 ‰) but revealed a complex interaction between surface runoff and groundwater sources, with groundwater DIC becoming proportionally more important in high flow, due to activation of macropores downstream. This work adds to an increasing body of work that recognises the importance of rapid, short‐lived hydrological events in low‐order catchments to global carbon dynamics. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

15.
Li  Yingnian  Sun  Xiaomin  Zhao  Xinquan  Zhao  Liang  Xu  Shixiao  Gu  Song  ZhangG  Fawei  Yu  Guirui 《中国科学:地球科学(英文版)》2006,49(2):174-185

The study by the eddy covariance technique in the alpine shrub meadow of the Qinghai-Tibet Plateau in 2003 and 2004 showed that the net ecosystem carbon dioxide exchange (NEE) exhibited noticeable diurnal and annual variations, with more distinct daily changes during the warmer seasons. The CO2 emission of the shrub ecosystem culminated in April and September while the CO2 absorption capacity reached a maximum in July and August. The absorbed carbon dioxide during the two consecutive years was 231.4 and 274.8 g CO2·m−2 respectively, yielding an average of 253.1 gCO2·m−2 per year: that accounts for a large proportion of absorbed CO2 in the region. Obviously, the diurnal carbon flux was negatively related to temperature, radiation and other atmospheric factors. Still, minute discrepancies in kurtosis and duration of carbon emission/absorption were detected between 2003 and 2004. It was found that the CO2 flux in the daytime was similarly affected by photosynthetic photon flux density in both years. Temperature appears to be the most important determinant of CO2 flux: specifically, the high temperature during the plant growing season inhibits the carbon absorption capacity. One potential explanation is that soil respiration is enhanced under such condition. Analysis of biomass revealed that the annual net carbon fixed capacity of aboveground and belowground biomass was 544.0 in 2003 and 559.4 g C·m−2 in 2004, which coincided with the NEE absorption capacity (63.1 g C·m−2 in 2003 and 74.9 g C·m−2 in 2004) in the corresponding plant growing season.

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16.
Agricultural, forestry-impacted and natural catchments are all vectors of nutrient loading in the Nordic countries. Here, we present concentrations and fluxes of total nitrogen (totN) and phosphorus (totP) from 69 Nordic headwater catchments (Denmark: 12, Finland:18, Norway:17, Sweden:22) between 2000 and 2018. Catchments span the range of Nordic climatic and environmental conditions and include natural sites and sites impacted by agricultural and forest management. Concentrations and fluxes of totN and totP were highest in agricultural catchments, intermediate in forestry-impacted and lowest in natural catchments, and were positively related %agricultural land cover and summer temperature. Summer temperature may be a proxy for terrestrial productivity, while %agricultural land cover might be a proxy for catchment nutrient inputs. A regional trend analysis showed significant declines in N concentrations and export across agricultural (−15 μg totN L−1 year−1) and natural (−0.4 μg NO3-N L−1 year−1) catchments, but individual sites displayed few long-term trends in concentrations (totN: 22%, totP: 25%) or export (totN: 6%, totP: 9%). Forestry-impacted sites had a significant decline in totP (−0.1 μg P L−1 year−1). A small but significant increase in totP fluxes (+0.4 kg P km−2 year−1) from agricultural catchments was found, and countries showed contrasting patterns. Trends in annual concentrations and fluxes of totP and totN could not be explained in a straightforward way by changes in runoff or climate. Explanations for the totN decline include national mitigation measures in agriculture international policy to reduced air pollution and, possibly, large-scale increases in forest growth. Mitigation to reduce phosphorus appears to be more challenging than for nitrogen. If the green shift entails intensification of agricultural and forest production, new challenges for protection of water quality will emerge possible exacerbated by climate change. Further analysis of headwater totN and totP export should include seasonal trends, aquatic nutrient species and a focus on catchment nutrient inputs.  相似文献   

17.
Wang  Chunlin  Yu  Guirui  Zhou  Guoyi  Yan  Junhua  Zhang  Leiming  Wang  Xu  Tang  Xuli  Sun  Xiaomin 《中国科学:地球科学(英文版)》2006,49(2):127-138

The Dinghushan flux observation site, as one of the four forest sites of ChinaFLUX, aims to acquire long-term measurements of CO2 flux over a typical southern subtropical evergreen coniferous and broad-leaved mixed forest ecosystem using the open path eddy covariance method. Based on two years of data from 2003 to 2004, the characteristics of temporal variation in CO2 flux and its response to environmental factors in the forest ecosystem are analyzed. Provided two-dimensional coordinate rotation, WPL correction and quality control, poor energy-balance and underestimation of ecosystem respiration during nighttime implied that there could be a CO2 leak during the nighttime at the site. Using daytime (PAR > 1.0 μmol−1·m−2·s−1) flux data during windy conditions (u* > 0.2 m·s−1), monthly ecosystem respiration (Reco) was derived through the Michaelis-Menten equation modeling the relationship between net ecosystem C02 exchange (NEE) and photosynthetically active radiation (PAR). Exponential function was employed to describe the relationship between Reco and soil temperature at 5 cm depth (Ts05), then Reco of both daytime and nighttime was calculated respectively by the function. The major results are: (i) Derived from the Michaelis-Menten equation, the apparent quantum yield (α) was 0.0027±0.0011 mgCO2·μmol−1 photons, and the maximum photosynthetic assimilation rate (Amax) was 1.102±0.288 mgCO2·m−2·s−1. Indistinctive seasonal variation of α or Amax was consistent with weak seasonal dynamics of leaf area index (LAf) in such a lower subtropical evergreen mixed forest, (ii) Monthly accumulated Reco was estimated as 95.3±21.1 gC·m−2mon−1, accounting for about 68% of the gross primary product (GPP). Monthly accumulated WEE was estimated as −43.2±29.6 gC·m−2·mon−1. The forest ecosystem acted as carbon sink all year round without any seasonal carbon efflux period. Annual NEE of 2003 and 2004 was estimated as −563.0 and −441.2 gC·m−2·a−1 respectively, accounting for about 32% of GPP.

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18.
Solute concentrations and fluxes in rainfall, throughfall and stemflow in two forest types, and stream flow in a 90 ha catchment in southern Chile (39°44′S, 73°10′W) were measured. Bulk precipitation pH was 6·1 and conductivity was low. Cation concentrations in rainfall were low (0·58 mg Ca2+ l?1, 0·13 mg K+ l?1, 0·11 mg Mg2+ l?1 and <0·08 mg NH4–N l?1), except for sodium (1·10 mg l?1). Unexpected high levels of nitrate deposition in rainfall (mean concentration 0·38 mg NO3–N l?1, total flux 6·3 kg NO3–N ha?1) were measured. Concentrations of soluble phosphorous in bulk precipitation and stream flow were below detection limits (<0·09 mg l?1) for all events. Stream‐flow pH was 6·3 and conductivity was 28·3 μs. Stream‐water chemistry was also dominated by sodium (2·70 mg l?1) followed by Ca, Mg and K (1·31, 0·70 and 0·36 mg l?1). The solute budget indicated a net loss of 3·8 kg Na+ ha?1 year?1, 5·4 kg Mg2+ ha?1 year?1, 1·5 kg Ca2+ ha?1 year?1 and 0·9 kg K+ ha?1 year?1, while 4·9 kg NO3–N ha?1 year?1 was retained by the ecosystem. Stream water is not suitable for domestic use owing to high manganese and, especially, iron concentrations. Throughfall and stemflow chemistry at a pine stand (Pinus radiata D. Don) and a native forest site (Siempreverde type), both located within the catchment, were compared. Nitrate fluxes within both forest sites were similar (1·3 kg NO3–N ha?1 year?1 as throughfall). Cation fluxes in net rainfall (throughfall plus stemflow) at the pine stand generally were higher (34·8 kg Na+ ha?1 year?1, 21·5 kg K+ ha?1 year?1, 5·1 kg Mg2+ ha?1 year?1) compared with the secondary native forest site (24·7 kg Na+ ha?1 year?1, 18·9 kg K+ ha?1 year?1 and 4·4 kg Mg2+ ha?1 year?1). However, calcium deposition beneath the native forest stand was higher (15·9 kg Ca2+ ha?1 year?1) compared with the pine stand (12·6 kg Ca2+ ha?1 year?1). Copyright © 2002 John Wiley & Sons, Ltd.  相似文献   

19.
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.  相似文献   

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