The role and relative importance of weather and cutting for the seasonal and inter-annual variability of the net ecosystem CO2 exchange (NEE) of a temperate mountain grassland was investigated. Eddy covariance CO2 flux data and associated measurements of the green plant area index and the major environmental driving forces acquired during 2001–2006 at the study site Neustift (Austria) were analyzed. Driven by three cutting events per year which kept the investigated grassland in a stage of vigorous growth, the seasonal variability of NEE was primarily modulated by gross primary productivity (GPP). The role of environmental parameters in modulating the seasonal variability of NEE was obscured by the strong response of GPP to changes in the amount of green plant area, as well as the cutting-mediated decoupling of phenological development and the seasonal course of environmental drivers. None of the environmental and management metrics examined was able to explain the inter-annual variability of annual NEE. This is thought to result from (1) a high covariance between GPP and ecosystem respiration (Reco) at the annual timescale which results in a comparatively small inter-annual variation of NEE, (2) compensating effects between carbon exchange during and outside the management period, and (3) changes in the biotic response to rather than the environmental variables per se. GPP was more important in modulating inter-annual variations in NEE in spring and before the first and second cut, while Reco explained a larger fraction of the inter-annual variability of NEE during the remaining periods, in particular the post-cut periods.
 Atmospheric carbon dioxide (CO2) is responsible for around 60% of anthropogenic global warming [Intergovernmental Panel on Climate Change, 2001]. Of the 7 Pg carbon (C) released on average each year to the atmosphere through fossil fuel burning, the terrestrial biosphere absorbs about one third (a similar share is absorbed by aquatic ecosystems; [Cannadell et al., 2007]). Quantifying the spatial patterns of the net exchange of CO2 (NEE) between land ecosystems and the atmosphere and projecting how NEE will be affected by likely future climate and land use is thus a critical issue in environmental science [Steffen et al., 1998; Running et al., 1999; Baldocchi et al., 2001] and requires understanding of the interactions and feedbacks within the carbon cycle and the way these are influenced by human interference [Pielke et al., 1998].
 The objective of the present paper is to quantify the seasonal and inter-annual variability of NEE of a temperate managed grassland and to analyze the role and relative importance of environmental drivers and cutting in determining this variability. To this end we use six years of eddy covariance CO2 flux measurements made above a mountain grassland in Austria, which is cut three times per year for hay production. We hypothesize that (1) cutting, through modifying the amount of photosynthetically active plant matter, will be the major control on the seasonal variability of NEE, and (2) that the inter-annual variability in NEE will be determined by inter-active effects of both weather and cutting.
2. Material and Methods
2.1. Site Description
 The study site is located at a meadow in the vicinity of the village Neustift (47°07′N, 11°19′E) in the Stubai Valley (Austria) at an elevation of 970 m a s l. in the middle of the flat valley bottom. The fetch is homogenous up to 300 m to the east and 900 m to the west of the instrument tower, the dominant day and nighttime wind directions, respectively. The average annual temperature is 6.5°C, average annual precipitation amounts to 852 mm. The vegetation has been classified as a Pastinaco-Arrhenatheretum and consists mainly of a few dominant graminoid (Dactylis glomerata, Festuca pratensis, Phleum pratensis, Trisetum flavescens) and forb (Ranunculus acris, Taraxacum officinale, Trifolium repens, Trifolium pratense, Carum carvi) species. The soil has been classified as a Fluvisol (FAO classification) and is approximately 1 m deep. Below a thin (0.001 m) organic layer, an A horizon, with an organic volume fraction of approximately 14%, extends down to 0.02 m, followed by the B horizon, which is best described as a (sandy) loam. Roots reach down to 0.5 m, but 80% of them are concentrated in the upper 0.13 m of the soil.
2.2. Eddy Covariance
 Eddy covariance (EC) measurements at this site began in 2001 and measurements continue as of this writing - within this paper data from the period 2001–2006 are presented. The net ecosystem CO2 exchange was measured using the eddy covariance method [Baldocchi et al., 1988] using the same instrumentation as and following the procedures of the EUROFLUX project [Aubinet et al., 2000]. The three wind components and the speed of sound were measured by a three-dimensional sonic anemometer (R3IA, Gill Instruments, Lymington, UK), CO2 mole fractions by a closed-path infra-red gas analyzer (Li-6262, Li-Cor, Lincoln, NE, USA). Air was sucked from the inlet, a distance of 0.1 m from the center of the sensor volume of the sonic anemometer mounted at 3 m above ground, through a 4 m Teflon tube of 0.004 m inner diameter through a filter (Acro 50, Gelman, Ann Arbor, MI, USA) to the infrared gas analyzer (IRGA) at a flow rate of 9 l min−1 (N035ANE, KNF Neuberger, Freiburg, Germany). The infrared gas analyzer was operated in the absolute mode, flushing the reference cell with dry N2 from a gas cylinder at 0.1 l min−1. Raw voltage signals of the CO2 mixing ratio were output at 10 Hz to the analogue input of the sonic, where they were synchronized with the sonic signals, which were measured at 20 Hz. All raw data were saved to a hard disc of a personal computer for post-processing using the EdiSol software (University of Edinburgh).
 Half-hourly mean eddy fluxes were calculated as the covariance between the turbulent departures from the mean of the vertical wind speed and the CO2 mixing ratio using the post-processing software EdiRe (University of Edinburgh). Means and turbulent departures there from were calculated by Reynolds (block) averaging. The tube induced time delay of the CO2 signal was determined by optimizing the correlation coefficient with the vertical wind velocity [McMillen, 1988] within a given time window. A three-axis co-ordinate rotation was performed aligning the co-ordinate system's vector basis with the mean wind streamlines [Kaimal and Finnigan, 1994]. Finally, frequency response corrections were applied to raw eddy fluxes accounting for low-pass (sensor separation, dynamic frequency response, scalar and vector path averaging, frequency response mismatch and the attenuation of concentration fluctuations down the sampling tube) and high-pass filtering following Moore  and Aubinet et al. . Experimentally derived frequency response correction factors, according to Aubinet et al. [2000, 2001], were used to calibrate and assess the validity of the theoretical low-pass filtering correction method, as described in detail by Wohlfahrt et al. .
 The net flux of CO2 was calculated as the sum of the corrected vertical eddy term and the storage fluxes, the latter being estimated from the time-rate-of-change of the CO2 mixing ratio at the reference height between the current and previous averaging interval, which in a previous comparison with a profiling system was found to be sufficiently accurate. Negative fluxes represent transport from the atmosphere toward the surface, positive ones the reverse.
2.3. Ancillary Data
 Supporting meteorological measurements of relevance to this study included incident photosynthetically active radiation (PAR) (BF3H, Delta-T, Cambridge, UK), air temperature (Tair) and humidity at 3 m height and soil temperature (Tsoil) at 0.05 m depth, measured by the means of a combined temperature/humidity sensor (RFT-2, UMS, Munich, Germany) and a thermocouple (TCAV, Campbell Scientific, Logan, UT, USA), respectively, soil heat flux measured by the means of heat flux plates (3 replicates at 0.05 m depth, corrected for the change in heat storage above that depth; HFP01, Hukseflux, Delft, Netherlands), volumetric soil water content (ML2x, Delta-T Devices, Cambridge, UK) and precipitation (52202, R. M. Young, Traverse City, MI, USA). Volumetric soil water content was converted to relative extractable soil water (REW) by normalizing between the water content at field capacity (100% REW) and the wilting point (0% REW), which were determined from water retention curve analysis [Hillel, 1980].
 The green plant area index (GAI, the area of green plant matter per ground area) was assessed (1) in a destructive fashion by clipping of square plots of 0.09 m2 (3–5 replicates) and subsequent plant area determination (Li-3100, Li-Cor, Lincoln, NE, USA) and (2) from measurements of maximum canopy height which was related to destructively measured GAI using the following relationship:
where L is the GAI (m2 m−2) and h is the canopy height (m). Continuous time series of the GAI were derived by fitting sigmoid and quadratic functions to measured data separately for each growing phase before and after the third cut, respectively.
 Snow cover duration was determined from weekly site visits and measured time courses of albedo and soil heat flux, which changed markedly with the presence/absence of snow cover.
 Half-hourly flux data were screened for validity by removal of time periods with (1) the CO2 signal outside a specific range, (2) the coefficient of variation for CO2 mixing ratio and pressure within the IRGA outside a specific range, (3) the third rotation angle exceeding ±10° [McMillen, 1988], (4) the stationarity test for the CO2 flux exceeding 60% [Foken and Wichura, 1996], (5) the deviation of the integral similarity characteristics larger than 60% [Foken and Wichura, 1996], and (6) the maximum of the footprint function [Hsieh et al., 2000] outside the boundaries of the meadow [cf. Novick et al., 2004]. In order to avoid the potential underestimation of nighttime ecosystem respiration during calm and stable conditions [Gu et al., 2005], nighttime NEE data were excluded when friction velocity (u*) was below 0.2 m s−1 [Wohlfahrt et al., 2005]. Together with gaps due to failure of the PC logging system, these quality control measures led to the exclusion of 59 (47) % of all possible (vegetation period only) data (Table 1).
Table 1. Annual Net Ecosystem CO2 Exchange (NEE), Gross Primary Production (GPP), Ecosystem Respiration (Reco) and Data Coveragea
NEE, gC m−2 a−1
GPP, gC m−2 a−1
Reco, gC m−2 a−1
Data Coverage, %
Numbers in parenthesis refer to random and systematic uncertainty of annual net ecosystem CO2 exchange, respectively. Average ± one standard deviation over the six study years are given in lowermost line.
−42 (±6 ± 35)
69 (±7 ± 11)
49 (±7 ± 13)
−23 (±7 ± 28)
67 (±7 ± 21)
−11 (±7 ± 21)
18 ± 49
1568 ± 87
1586 ± 92
39 ± 5
 In order to derive continuous time series of NEE, required for calculating the annual balance of NEE, the following gap filling procedure was employed at Neustift: Gaps less than two hours were filled by linear interpolation. Larger gaps were filled by means of functional relationships between NEE and Tsoil (using Arrhenius-type relationships) and PAR (using Michaelis-Menten-type relationships) during nighttime and daytime, respectively. In the presence of snow cover, CO2 fluxes were noisy and the variability of soil temperature was too small for deriving defensible relationships with NEE and thus an average NEE value was used for gap-filling during winter. An uncertainty analysis, accounting for both random and systematic errors [Moncrieff et al., 1996], was conducted in order to obtain confidence intervals for the annual CO2 balances. Details on the uncertainty analysis are provided in the Appendix.
 Ecosystem respiration (Reco) was estimated from nighttime NEE measurements and for daytime conditions by extrapolating these using the functional relationships with soil temperature also used for gap-filling (see above). Gross primary production (GPP) was calculated as GPP = −NEE + Reco. The inter-annual variance of NEE was decomposed into the variance of GPP, Reco and the covariance between GPP and Reco according to
where FNEE, FGPP and FReco refer to NEE, GPP and Reco.
3.1. Environmental Conditions and Canopy Development
 The six-year study period was characterized by a wide range of environmental conditions (Figure 1): The warmest years were 2002 and 2003 with annual averages of 7.7 and 7.1°C, respectively, the coldest year was 2005 with an annual average of 5.6°C. With average annual temperatures of 6.3–6.8°C, the remaining years were close to the long-term (1980–2000) average of 6.5°C. Precipitation ranged from 582 mm a−1 in 2006 to 948 and 984 mm a−1 in 2001 and 2002, and was somewhat below the long-term (1980–2000) average of 852 mm a−1 during 2003–2005 (745–786 mm a−1). Monthly averages of relative extractable soil water ranged from above 100% in spring and late autumn, when parts of the soil were frozen, down to values below 30% in May, August and September 2003, June 2005 and July 2006 (Figure 1). Following Granier et al.  in assuming water stress to occur when REW drops below 40%, 109 days with water stress were counted during the vegetation period April-September of 2003, for 2004–2006 this value ranged from 17–35 days, while not a single day with REW < 40% occurred in 2001 and 2002. The year with the highest mean VPD of 0.43 kPa was 2003 (2001–2006 average: 0.35 kPa; data not shown). Snow cover duration (Figure 2) ranged from 93 days (2002) to 128 days (2001). Snow melting dates varied from 7 March (2003) to 30 March (2005) and increased linearly by 0.2 days for each mm of winter precipitation (r2 = 0.90, p = 0.01). The permanent winter snow cover established between 18 November (2005) and 20 December (2004). The amount of GAI ranged from close to nil after snowmelt up to 7.6 m−2 m−2 shortly before cutting (Figure 2). The meadow was cut three times a year, the three cuts taking place between 2 and 16 June, 24 July and 12 August, and 21 September and 28 October. Cutting resulted in an immediate reduction of GAI down to 0.5–2.0 m−2 m−2 (Figure 2).
3.2. Seasonal Variability in NEE
 The grassland acted as a net source of CO2 as long as snow covered the ground (Figures 2–3) . After snowmelt, the meadow continued to emit CO2 on a daily basis until it eventually reached a reversal point (on average after 25 days), when GPP exceeded Reco (Figures 3–4) , and the meadow became a net sink and remained so until the first cut (Figure 3). The first cut turned the ecosystem into a net source of CO2 and it took GPP on average 16 days to exceed Reco, which varied comparably little with time, and thus the meadow to become (on a daily basis) a net sink for CO2 again (Figures 3–4). This pattern repeated itself after the second and third cut, although the meadow did not quite recover from the third cut (Figures 3–4), instead the grassland kept losing CO2 until the continuous winter snow cover established and then further until the end of the year (Figure 3). Daily average rates of net CO2 uptake and loss before and after cutting, respectively, decreased from the first to the third cut (Figure 3). On the basis of these seasonal patterns, which represent the combined effects of changes in phenology and anthropogenic interference, we divided the annual cycle of NEE into several periods:
 1. Wintertime: Delimited by the presence of snow cover;
 2. Spring: Starts after snowmelt and ends at the reversal point when the meadow turns, on a daily basis, into a net sink;
 3. Pre-cut periods: Comprise the periods of daily net carbon gain preceding the three cutting events and are referred to as pre-cut1-3;
 4. Post-cut periods: Are assigned the periods between the cuts and the recovery of the (daily) net sink capacity and are referred to as post-cut1-3; the post-cut3 period ends with the establishment of the continuous winter snow cover.
 During the later parts of the three pre-cut phases, NEE exhibited signs of saturation and even declined in some years (Figures 2–3). As shown in Figure 5, this was due to GPP saturating (and sometimes decreasing) with increasing GAI. GPP saturated at values of 10.7 and 9.7 gC m2 d−1 once GAI exceed 3 m2 m−2 before the first and second cut, respectively, and at a value of 7.0 gC m2 d−1 before the third cut once GAI exceed 2 m2 m−2 (Figure 5). The seasonal decrease in saturation GPP was related to day length, which decreased from around 18 to 13 h between the first and third cut, respectively. After the third cut, the GAI did not exceed 4 m2 m−2 (Figure 2) and no saturation was observed (Figure 5).
 The response of NEE, GPP and Reco to the main environmental drivers changed with time during and varied substantially between the various periods - patterns were more conclusive for GPP and Reco, as opposed to NEE, as well as for PAR as opposed to Tair, VPD and REW (Figure 6): The correlation between GPP and PAR was poor shortly after snowmelt and the cuts and then quickly increased with the developing GAI (Figure 6). The correlation between NEE and PAR largely mirrored the one of GPP (Figure 6). Reco was significantly positively correlated with Tair except for spring, when the correlation was initially negative; no clear patterns were found for Tair-GPP and Tair-NEE (Figure 6). VPD was strongly correlated with Tair (data not shown) and the response to VPD thus largely mirrored the one to Tair (Figure 6). REW was most of the time negatively related to GPP and Reco (Figure 6), which reflected the inverse correlation to PAR, Tair and VPD (data not shown).
3.3. Inter-Annual Variability in NEE
 Annual NEE varied from −42 gC m−2 a−1 to +69 gC m−2 a−1, with a six-year average NEE of +18 ± 49 gC m−2 a−1 (Table 1 and Figure 3). The random and systematic uncertainties of these numbers varied between 6–7 and 11–35 gC m−2 a−1, respectively (Table 1). The annual NEEs of 2001–2003 and 2005 may thus be regarded significantly different from zero. Annual ecosystem respiration varied between 1455–1696 gC m−2 a−1, gross primary production between 1449–1687 gC m−2 a−1 (Table 1).
 The inter-annual variance of daily average NEE was in all periods but spring and post-cut1 dominated by the covariance between GPP and Reco (Figure 3) which was positive and thus acted to reduce the variance in NEE (equation (2)). The variance of daily average GPP exceeded the one of Reco in spring and pre-cut1-2, while the reverse was true for all post-cut phases and pre-cut3 (Figure 3). The coefficient of variation of daily average NEE was smallest during winter (0.05), largest during pre-cut3 (0.52) and between 0.15–0.29 for all other phases (Figure 3). On the annual timescale, the covariance term was about twice as large as the variance of GPP and Reco, which were of almost equal magnitude (data not shown).
 The most influential periods for annual NEE were post-cut1 and pre-cut3, which explained 45% (p = 0.15) and 47% (p = 0.13) of the variability in annual NEE, respectively - larger carbon losses in post-cut1 and larger carbon gains during pre-cut3 were associated with larger annual losses and gains, respectively. No significant lagged effects, i.e., correlations with NEE in antecedent periods or previous years, could be determined. Snow cover duration and cardinal dates, such as the timing of snowmelt, the establishment of the continuous winter snow cover, the cuts, the duration of the inter-cut periods, and the duration between snowmelt and first cut and the third cut and the establishment of the continuous winter snow cover all explained less than 30% of the inter-annual variability of NEE (data not shown). As shown in Figure 7, snowmelting dates though explained significant fractions of the inter-annual variability in NEE before the first cut: While wintertime CO2 losses were smaller for early snowmelting dates, carbon losses were larger during spring and NEE was less negative during pre-cut1 in years with earlier snowmelts (Figure 7). Up to the first cut, the positive effect of early snowmelts on wintertime carbon losses was thus outweighed by smaller carbon gains thereafter, leading to an increase (i.e., smaller net carbon gain) in cumulative NEE by 1.5 gC m−2 for each day snowmelt occurred earlier.
 Environmental control on the inter-annual variability in NEE and its two component processes, GPP and Reco is explored in Table 2, which shows the results of a linear correlation analysis: On an annual timescale, the only significant correlation was found for Reco, which increased significantly with Tair, but as GPP increased with Tair as well, no significant effect on NEE was found (Table 2). No significant relationships could be found between annual NEE and environmental controls during the various periods (data not shown). Broken down to the timescale of the various periods, Tair was the variable which most frequently yielded significant correlations, followed by PAR and REW, and VPD. The only significant correlation for NEE was found during post-cut1, when it increased with Tair (Table 2). GPP was negatively correlated with Tair during spring and positively before and after the third cut. During pre-cut3 Tair was positively correlated with PAR (as well as VPD) and negatively with REW, resulting in a positive and negative correlation of these two environmental variables with GPP, respectively (Table 2). Reco was positively related to temperature during all post-cut periods as well as during pre-cut3 (Table 2), when the auto-correlation between Tair and the other environmental variables resulted in the same correlation pattern observed for GPP. The same reasoning holds for the correlation between Reco and REW and PAR during post-cut2 and post-cut3, respectively (Table 2).
Table 2. Results (Correlation Coefficients) of Linear Regression Analysis With Daily Average NEE, GPP and Reco as Independent and Daily Average PAR, Tair, VPD and REW as Independent Variables (*… p < 0.05, **… p < 0.01, ***… p < 0.001; n = 6)a
Significant correlation coefficients are shown in bold letters for clarity. Correlations with soil temperature are both quantitatively and qualitatively similar to Tair and are thus not shown.
 The seasonal and inter-annual variability of NEE reflects the variability of the governing environmental forcing variables at these timescales, as well as changes in the ecosystem's response to these [Stoy et al., 2005; Richardson et al., 2007]. Through modifying the amount of photosynthetically active plant matter, cutting and grazing fundamentally alter how grassland ecosystems respond to environmental forcings [Wohlfahrt, 2004; Nieveen et al., 2005; Rogiers et al., 2005] and thus have the potential to modulate the seasonal and inter-annual variability of NEE. The objective of the present paper is to examine the role and relative importance of weather and cutting for the seasonal and inter-annual variability of the NEE of a temperate mountain grassland in Austria. To this end we analyzed eddy covariance CO2 flux data and associated measurements of the GAI and the major environmental driving forces acquired during 2001–2006 at the study site Neustift.
4.1. Seasonal Variability in NEE
 The seasonal variability of the NEE of the investigated mountain grassland combined features typical for natural ecosystems (which we define here as ecosystems not managed on an annual or finer timescale), but was also characterized by human-induced, step-change temporal patterns typical for agricultural ecosystems [Falge et al., 2002a, 2002b].
 No management activities occurred at the site between the establishment of the continuous snow cover in late autumn and the first cut in early summer (i.e., the wintertime, spring and pre-cut1 periods), except for the application of manure in late autumn, which had no discernable influence on NEE though. During these periods, the seasonal course of NEE was modulated primarily by the physical environment, such as the presence/absence of snow (Figure 2) and the seasonal changes in environmental drivers (Figure 1), and compared well with the progression from dormancy and associated net CO2 losses to active sink activity observed for natural temperate ecosystems during that same period [Falge et al., 2002a]. The period of snow cover was characterized by net losses of CO2 to the atmosphere which were small in magnitude (Figures 2–3), but due to the length of the snow cover period (3–4 months), accounted for an appreciable fraction of the annual NEE as found for other high-elevation or -latitude ecosystems [Aurela et al., 2002; Monson et al., 2002; Lafleur et al., 2003].
 In between the first cut and the establishment of the continuous snow cover, the most obvious consequence of the three cuts the grassland is subject to each year, was the recurrent progression of NEE from CO2 source to sink which resulted in a characteristic seasonal time course of NEE (Figure 3) typical for repeatedly cut/grazed grasslands [Sousanna et al., 2007; Veenendaal et al., 2007]. Cutting thereby led to a decoupling of the phenological plant development, which is reinitiated by cutting [Wohlfahrt and Cernusca, 2002], and the seasonal progression of environmental conditions. As a consequence, the seasonal variability of NEE during the vegetation period was modulated primarily by changes in GPP rather than Reco, which was much less variable in time (Figure 4). This was reflected also by the relationships between environmental drivers and NEE, which largely mirrored the response of GPP to these drivers (Figure 6). As a further result of this decoupling, GPP and Reco were strongly out of phase between the first cut and the establishment of the continuous snow cover, which is again a typical feature of agricultural ecosystems [Falge et al., 2002a].
 The response of NEE and its two component process, GPP and Reco, to the main environmental drivers changed rapidly with time, reflecting the active growth of the canopy (and associated changes in GAI) and thus changes in what Richardson et al.  termed the ecosystem's “biotic response”. The response of NEE, GPP and Reco to the main environmental drivers also varied substantially between the various periods, reflecting the above mentioned decoupling of phenological development and the seasonal progression of environmental conditions. As in addition, the investigated environmental parameters were inter-correlated, it was very difficult to defensibly attribute seasonal changes in NEE, GPP and Reco to certain environmental parameters or combinations thereof.
4.2. Inter-Annual Variability in NEE
 None of the variables looked at in the present paper was able to explain, in a statistically significant fashion, the inter-annual variability of annual NEE. The investigated variables included metrics like the length of the vegetation period and the snowmelting date (which varied by up to a month) for which Baldocchi and Wilson , Baldocchi et al. [2001, 2005], Carrara et al. , Aurela et al. , among others, found clear correlations with NEE. Even environmental drivers such as PAR, temperature, soil moisture and vapor pressure deficit, for which the short-term response of NEE is well established [Stoy et al., 2005], did not yield significant relationships at the annual timescale. One reason for the failure of weather-based metrics in explaining the inter-annual variability of NEE may be that the variance in annual NEE is to be attributed to the biotic response to rather than the environmental drivers per se [Hui et al., 2003; Richardson et al., 2007]. In the present case, the response to environmental forcings may have been obscured by inter-annual variations in the timing of the cutting events and thus the seasonal courses of GAI. Cutting dates varied by 2–5 weeks, so that for a given time of the year the ecosystem's response to environmental drivers may have greatly differed because of cutting-mediated differences in GAI. In addition, we observed a high covariance between GPP and Reco at the annual timescale, resulting in a comparatively small inter-annual variation in NEE [Dunn et al., 2006; Jacobs et al., 2007; Richardson et al., 2007]. This covariance also held with regard to the controls by environmental drivers, causing annually averaged/integrated environmental parameters being better predictors of GPP and Reco than NEE (Table 1). Very weak correlations between annual NEE and weather-based indices, resulting from compensating influences of GPP and Reco, have been reported also by Reichstein et al.  in an analysis of 23 European flux tower sites. Generally, few studies have reported statistically significant relationships between annual NEE and single annually integrated/averaged environmental drivers, but rather multiple regression models had to be used for sufficient predictive power [Saigusa et al., 2005; Dunn et al., 2006; Barr et al., 2006]. Along this line, environmental conditions during certain cardinal periods, as opposed to annually integrated/averaged values, were generally more successful in predicting annual NEE [e.g., Hollinger et al., 2004; Zha et al., 2004], although this did not apply in the present case.
 Contrary to our expectations, the timing of the cutting events, the time duration between cutting events, between snowmelt and first cut, and third cut and the establishment of the continuous snow cover did not yield significant relationships with annual NEE. Even the amounts of carbon gained or lost during the various pre- and post-cut periods, which form part of the annual NEE, were not significantly correlated with annual NEE. The poor explanatory power of these management-related metrics may reflect that cutting, while significantly modulating the seasonal course of NEE, affects NEE only during approximately half of the year. During the rest of the year environmental conditions may lead to compensating or opposing effects as for example in year 2001, which due sustained carbon losses during the spring period caused by a late snow fall had the lowest cumulative NEE up to the first cut. Comparatively large carbon gains after the first and second cut (Figure 3), however, compensated for this, causing year 2001 to top out with the highest annual net carbon gain observed during the six year study. Because the biotic response to environmental drivers changes abruptly with cutting [Wohlfahrt, 2004; Rogiers et al., 2005; G. Wohlfahrt, manuscript submitted, 2007] and because cutting acts as to decouple weather and phenology, any legacies from antecedent periods are quickly blurred after cutting. This became obvious in case of the significant correlation between snowmelting dates and NEE cumulated up to the first cut (Figure 7), which was completely lost when the integration period was extended beyond the first cut. In natural ecosystems, the effects of early/late snowmelting often persist and sometimes even dominate annual NEE, as shown by Aurela et al.  for a subarctic fen (even if the effect was of opposite sign in this study).
 Several studies have ascribed inter-annual variability in NEE to variability in either GPP [Janssens et al., 2001; Griffis et al., 2003; Saigusa et al., 2005; Urbanski et al., 2007] or Reco [Goulden et al., 1998; Valentini et al., 2000; Morgenstern et al., 2004]. While the strong covariance between GPP and Reco prevented us from doing so at the annual timescale (see above), we found distinct differences in the control of inter-annual variability of NEE at sub-annual timescales (Figure 3). Although the covariance between GPP and Reco generally dominated also at these timescales, GPP was clearly more important in modulating inter-annual variance in NEE during spring and pre-cut1-2. Reco explained a larger fraction of the variance in NEE during pre-cut3 and all post-cut periods, which is remarkable if we recall that the seasonal dynamics of NEE during the post-cut periods were driven by rapid changes in GPP (Figure 4). Since Reco increased significantly with temperature during all post-cut periods, it follows that high temperatures after cutting contribute to higher annual CO2 losses, even if this is supported by statistics only during post-cut1 (Table 2). NEE during pre-cut3 not only stood out by being characterized by the highest coefficient of variation, in contrast to the other pre-cut periods, its NEE was also modulated more by Reco than GPP (Figure 3). Because GPP and Reco were driven in the same direction by the same environmental drivers during this period (Table 2), it is difficult to unambiguously assess what controlled the observed large variability in NEE. In any case, NEE during pre-cut3 explained 47% of the variability in annual NEE (p = 0.13), and thus constituted not only a climatologically very sensitive, but also the quantitatively most influential period for annual NEE.
5. Summary and Conclusions
 The NEE of the investigated mountain grassland combined features typical for both natural and agricultural ecosystems resulting in characteristic temporal patterns and complex interactions between phenological development, cutting and weather conditions. Our results show that the investigated mountain grassland, under present climate and management, exhibits a stable near-neutral NEE. Driven by three cutting events per year which kept the investigated mountain grassland in a stage of vigorous growth throughout most of the vegetation period, the seasonal variability of NEE was primarily modulated by GPP. The role of environmental parameters in modulating the seasonal variability of NEE was obscured by the strong response of GPP to changes in GAI, as well as the cutting-mediated decoupling of phenological development and the seasonal course of environmental drivers. None of the weather and management metrics examined in the present paper was able to explain, in a statistically significant fashion, the inter-annual variability of annual NEE. This is thought to result from (1) a high covariance between GPP and Reco at the annual timescale which results in a comparatively small inter-annual variation of NEE, (2) compensating effects between carbon exchange during and outside the management period, and (3) changes in the biotic response to rather than the environmental variables per se. GPP was more important in modulating inter-annual variations in NEE in spring and before the first and second cut, while Reco explained a larger fraction of the inter-annual variability of NEE during the remaining periods, in particular the post-cut periods. Inter-annual variations in temperature accounted for significant fractions of the variability in Reco suggesting a potential sensitivity to predicted changes in climate.
Appendix A:: Uncertainty Analysis
 The random uncertainty of the half-hourly CO2 flux measurements was determined based on measurements under similar environmental conditions during adjacent days [Hollinger and Richardson, 2005]. The probability density distributions of the random CO2 flux uncertainty, which followed a Laplace rather than a normal distribution, are shown in Figure A1 separately for wintertime and the vegetation period. In accordance with Richardson et al.  a good linear correlation between the random uncertainty and the magnitude of NEE was found, which was used to estimate the random uncertainty of each valid half-hourly flux measurement (Figure A2). The random uncertainty of the parameters of the functional relationships between NEE and Tsoil and PAR was then estimated with a Simulated Annealing algorithm nested within a bootstrapping loop with 1000 iterations using the absolute deviation criterion as the objective function [Hollinger and Richardson, 2005]. During wintertime the mean CO2 flux uncertainty (Figure A1) was assigned to all measurements.
 The largest systematic uncertainty in annual NEE is due to the potential underestimation of ecosystem respiration during calm nighttime conditions and the choice of the u* threshold for excluding these. In order to assess the systematic uncertainty associated with rejecting nighttime ecosystem respiration measurements according to friction velocity, we calculated annual CO2 balances without filtering for u* and with the default value of 0.2 m s−1 [Wohlfahrt et al., 2005] and estimated the systematic uncertainty as the difference between these two [cf. Morgenstern et al., 2004]. Following recommendations by Moncrieff et al. , we report the annual NEE and its uncertainty as average ± random uncertainty ± systematic uncertainty.
 This study was financially supported by the EU FP 5 project CARBOMONT (EVK2-CT2001-00125), the Austrian National Science Fund (P17560), and the Tyrolean Science Fund (Uni-404/33). Family Hofer (Neustift, Austria) is thanked for granting us access to the study site. Long-term temperature and precipitation data have been generously provided by the Austrian Hydrographic Service.