Effect of climate warming on the annual terrestrial net ecosystem CO2 exchange globally in the boreal and temperate regions

Abstract

The net ecosystem CO2 exchange is the result of the imbalance between the assimilation process (gross primary production, GPP) and ecosystem respiration (RE). The aim of this study was to investigate temperature sensitivities of these processes and the effect of climate warming on the annual terrestrial net ecosystem CO2 exchange globally in the boreal and temperate regions. A database of 403 site-years of ecosystem flux data at 101 sites in the world was collected and analyzed. Temperature sensitivities of rates of RE and GPP were quantified with Q 10, defined as the increase of RE (or GPP) rates with a temperature rise of 10 °C. Results showed that on the annual time scale, the intrinsic temperature sensitivity of GPP (Q 10sG ) was higher than or equivalent to the intrinsic temperature sensitivity of RE (Q 10sR ). Q 10sG was negatively correlated to the mean annual temperature (MAT), whereas Q 10sR was independent of MAT. The analysis of the current temperature sensitivities and net ecosystem production suggested that temperature rise might enhance the CO2 sink of terrestrial ecosystems both in the boreal and temperate regions. In addition, ecosystems in these regions with different plant functional types should sequester more CO2 with climate warming.

Introduction

The ecosystem CO2 exchange is controlled by fluxes associated with assimilation and respiration processes, corresponding to the rates of gross primary production (GPP) and ecosystem respiration (RE), respectively1. The net CO2 exchange (NEE) of terrestrial ecosystems, resulting from a delicate balance between GPP and RE, influences carbon dynamics and budget and is vulnerable to climate disturbance2, 3. However, there is still no consensus over the magnitude and directions of the response to climate change of the physiological processes underpinning the ecosystem CO2 exchange4. This uncertainty often limits the ability to predict the carbon balance of terrestrial ecosystems5.

Both GPP and RE are sensitive to temperature changes6, 7. Future variations in temperature may therefore modify the carbon sequestration capacity of ecosystems by altering the balance between plant growth and soil carbon decomposition8. As a consequence, global warming may have important impacts on the CO2 balance at all levels of ecological organization, from individual organisms to entire ecosystems9. For this reason, it is of great importance to investigate and link biotic responses to climate drivers and carbon cycle processes10.

The effect of temperature on the ecological respiration processes has been commonly quantified using the temperature sensitivity index Q 10, which is defined as the increase of CO2 respiration rate with a temperature rise of 10 °C11. Q 10 values fitted to measured field data with statistical models are normally used to characterize the temperature sensitivity of ecological respiration process. This observed temperature sensitivity is the outcome of many interacting processes and is referred to apparent sensitivity to differentiate it from the intrinsic temperature sensitivity, which reflects the direct effect of temperature on the kinetics of chemical reactions12. The temperature sensitivities of respiration are different across biomes and temporal scales13. It has been reported that apparent Q 10 values of RE change with geographic locations, ecosystem types, and other factors14. Zhou et al.15 showed that apparent Q 10 values of RE ranged from 1.43 to 2.03 in different biomes. Jones et al.16 found that intrinsic Q 10 values of RE are in the range of 1.9 ± 0.4 to 2.1 ± 0.7 in the region from 5°N to 5°S. Using the FLUXNET database collected in the mid-latitude region of the northern hemisphere, Mahecha et al.17 obtained intrinsic Q 10 of RE close to a constant of 1.4 ± 0.1. Wang et al.18 showed that intrinsic Q 10 of RE ranged between 1.4 and 1.6 from more than 300 field measurements in the region from 19°N to 74°N.

The Q 10 approach is on the base of the relationship between reaction rates and temperature described by van’t Hoff19. As shown above, this exponential model has been widely used to study temperature sensitivity of RE at the subcellular and individual levels, as well as at the ecosystem level13, 17, 20, 21, including calculations of apparent and intrinsic temperature sensitivity indexes of RE. The relationship holds over the temperature range of normal activity, which can be up to 40 °C for most organisms22. Similar to respiration, assimilation is also a temperature related reaction process. Therefore, it is expected that the exponential model should be applicable to quantify the temperature sensitivity of CO2 assimilation rate. Applications of the same type of models to quantify the temperature effects on RE and GPP can make it easier to compare the difference of temperature sensitivities between RE and GPP. Nevertheless, applicability of the exponential model to temperature sensitivity of GPP needs to be further demonstrated.

With limited studies, some have shown that RE is more sensitive than GPP to climate warming23, 24. In contrast, others have reported that GPP was more sensitive than RE to climate warming25, 26. Lupascu et al.27 reported a permafrost ecosystem as a strong carbon sink, whereas Xue et al.28 showed a significant net carbon loss in permafrost-based tundra with climate warming. Some others have observed a simultaneous greening trend globally with climate warming29,30,31. The findings reported in the literature show that there is no consensus and that we still have no clear understanding of temperature sensitivities of the assimilatory and respiratory processes as well as their influence on the annual terrestrial NEE. We used extensive data to investigate the temperature dependency of the CO2 balance processes in terrestrial ecosystems at the global scale. Specifically, the objectives of this study were to examine intrinsic temperature sensitivities of the assimilatory and respiratory processes in terrestrial ecosystems of the boreal and temperate regions, in ecosystems featuring different plant functional types (PFTs), and to estimate the response of annual terrestrial NEE to climate warming.

Results

To demonstrate the applicability of the exponential model to temperature sensitivity, GPP data collected at the 403 site-years (see Supplementary Table 1) were fitted with the exponential model (Eq. 2, see the section of Methods) and a linear model. The measured RE data were also fitted with the exponential model. The fitting results of GPP and RE were compared using values of the coefficients of determination (R 2) and of the root mean square error (RMSE). The results of the comparison demonstrates that temperature sensitivities of both RE and GPP can be well characterized by the exponential model. As examples, fitting results of GPP and RE for some site-years, which represent ecosystems featuring with climate regions and PFT groups of temperate & forest, temperate & non-forest, boreal & forest, and boreal & non-forest, respectively, are shown in Fig. 1. Then the approximate intrinsic temperature sensitivity indexes of GPP (Q 10sG ) and RE (Q 10sR ) were determined on all site-years using the procedure of Mahecha et al.17 described in the section of Methods.

Figure 1
figure1

Fitting results using different models to gross primary production rates (GPP) and respiration rate (RE) vs. temperature. The exponential model (i.e., the Q 10 approach, Exp.) and the linear function model (Lin.) were used to gross primary production rates (GPP) vs. temperature at site-years of (a) FR-Fon.2005, (c) NL-Ca1.2003, (e) CA-Qfo.2005, and (g) FI-Kaa.2006, and the exponential model was used to fit respiration rates (RE) vs. temperature at site-years of (b) FR-Fon.2005, (d) NL-Ca1.2003, (f) CA-Qfo.2005, and (h) FI-Kaa.2006. Sites of FR-Fon, NL-Ca1, CA-Qfo, and FI-Kaa represent ecosystems featuring with climate regions (i.e., temperate and boreal) and plant functional types (PFTs) (i.e., forest and non-forest) of temperate & forest, temperate & non-forest, boreal & forest, and boreal & non-forest, respectively. Comparison of the fitting results was based on the coefficients of determination (R 2) and root mean square error (RMSE).

Temperature sensitivity indexes in the whole region

Considering the boreal and temperate areas as a whole region, the mean of Q 10sR was 1.43 ± 0.03 with the 95% confidence interval (95% CI) spanning from 1.37 to 1.50. The mean of Q 10sG was 1.69 ± 0.04 with the 95% CI from 1.62 to 1.76. The Wilcoxon rank-sum test showed that differences between Q 10sR and Q 10sG Q 10s  = Q 10sG  − Q 10sR ) among different sites were significant (two-tailed test, Z = 7.39, P < 0.0001), and generally GPP was more sensitive to temperature than RE. Values of Q 10sG were negatively correlated to the mean annual temperature (MAT) (Pearson’s r = −0.31, linear regression: F = −41.8, P < 0.0001), whereas Q 10sR values was not correlated to the MAT (r = −0.034, F = 2.65, P = 0.49) (Fig. 2).

Figure 2
figure2

Relationships between intrinsic temperature sensitivity indexes of (a) gross primary production rate (GPP, Q 10sG ) and (b) respiration rate (RE, Q 10sR ) vs. mean annual temperature (MAT) (GPP: Pearson’s r = −0.31, n = 403, F = 41.80, P < 0.0001; RE: r = −0.034, n = 403, F = 2.65, P = 0.49). The solid line in (a) represents the linear regression line.

Temperature sensitivity indexes between different climate regions and plant functional types

In the boreal region, the mean values of Q 10sR and Q 10sG were 1.41 and 1.81, respectively. In the temperate region, the mean values of Q 10sR and Q 10sG were 1.43 and 1.66, respectively (Table 1). Values of Q 10sG were significantly different to those of Q 10sR within the climate regions (boreal: Z = 5.44, P < 0.0001; temperate: Z = 5.56, P < 0.0001) (Fig. 3a,b). However, the temperature sensitivities were not significantly different between the climate regions for both GPP (Z = 1.78, P = 0.075) and RE (Z = −0.19, P = 0.85), also indicated by the similar values of the centers of confidence ellipses at the level of one standard deviation of probability distribution in Fig. 3c,d, respectively.

Table 1 Basic information, temperature sensitivity indexes of assimilation rate (GPP, Q 10sG ) and respiration rate (RE, Q 10sR ), and net ecosystem productivity (NEP, μmol · m−2 · yr−1) of different climate groups.
Figure 3
figure3

The intrinsic temperature sensitivity of gross primary production rate (Q 10sG ) vs. that of respiration rate (Q 10sR ) in (a) the boreal region and (b) the temperate region, and changes of (c) Q 10sG and (d) Q 10sR with the mean annual temperature (MAT) in the two regions. The confidence ellipses in (c,d) were derived at the level of one standard deviation of probability distribution and the symbol “+” indicates the center of ellipse.

In the forest sites, including deciduous broadleaf forest, evergreen needleleaf forest, and mixed forest, the mean values of Q 10sR and Q 10sG were 1.43 and 1.71, respectively. In the not-forest sites, including croplands, closed shrublands, grasslands, open shrublands, and permanent wetland, the mean values of Q 10sR and Q 10sG were 1.42 and 1.65, respectively (Table 2). Within a PFT group, the difference between Q 10sG and Q 10sR was significant (forest: Z = 6.56, P < 0.0001; non-forest: Z = 3.67, P = 0.0002) (Fig. 4a,b). However, the PFT groups did not significantly affect the temperature sensitivities of GPP (Z = −0.91, P = 0.36) and RE (Z = −0.13, P = 0.90), also shown by the similar values of the centers of confidence ellipses at the level of one standard deviation of probability distribution in Fig. 4c,d, respectively.

Table 2 Basic information, temperature sensitivity indexes of assimilation rate (GPP, Q 10sG ) and respiration rate (RE, Q 10sR ), and net ecosystem productivity (NEP, μmol · m−2 · yr−1) of different plant functional types (PFTs).
Figure 4
figure4

The intrinsic temperature sensitivity of gross primary production rate (Q 10sG ) vs. that of respiration rate (Q 10sR ) in ecosystems with plant function types in (a) the forest site group and (b) the non-forest site group, and changes of (c) Q 10sG and (d) Q 10sR with the mean annual temperature (MAT) in the two plant groups. The forest site group includes deciduous broadleaf forest, evergreen needleleaf forest, and mixed forest. The non-forest site group includes croplands, closed shrublands, grasslands, open shrublands, and permanent wetland. The confidence ellipses in (c,d) were derived at the level of one standard deviation of probability distribution and the symbol “+” indicates the center of ellipse.

The annual net ecosystem CO2 exchange

Using values of Q 10sG and Q 10sR as well as current net ecosystem production (NEP 0), we determined the sign of the annual NEP (i.e., >0 for CO2 sink and <0 for CO2 source) in terrestrial ecosystems under a scenario of climate warming (ΔT > 0). According to Eq. (9) (see the section of Methods), if GPP 0RE 0 (i.e., NEP 0 0) and Q 10sG Q 10sR (i.e., ΔQ 10s  0), it derives that ΔNEP 0, indicating that the ecosystem should be a CO2 sink (or carbon neutral as ΔNEP = 0). If NEP 0 < 0 and ΔQ 10s  < 0, it derives ΔNEP < 0, indicating that the ecosystem should be a CO2 source to the atmosphere. If NEP 0 < 0 and ΔQ 10s  > 0 (or NEP 0 > 0 and ΔQ 10s  < 0), the NEE is dependent on the values of NEP 0, ΔQ 10s , and ΔT.

In the boreal region, the null hypothesis test showed that the current NEP (i.e., NEP 0 in Eq. (9)) ≈0 (Signed rank test: S = 397.5, P = 0.13) (Table 1). Using Eq. (9) with NEP 0 = 0 and ΔQ 10s  > 0 (S = 1352, P < 0.0001) (Table 1), it derived that ΔNEP > 0, indicating that ecosystems in the region will response to a mean temperature increase by moving from the current state of near carbon neutral to a carbon sink. Moreover, in the temperate region, NEP 0 > 0 (S = 19716, P < 0.0001) and ΔQ 10s  > 0 (S = 9168, P < 0.0001), thus ΔNEP > 0 (Table 1). Ecosystems in the temperate region should therefore remain to act as carbon sinks, in response to a mean temperature increase.

In ecosystems with PFTs in the forest group, the CO2 budget was determined by GPP > RE (NEP 0  > 0: S = 12513, P < 0.0001) and Q 10sG  > Q 10sR (S = 7601, P < 0.0001), thus we obtained ΔNEP > 0, indicating that the ecosystems will be carbon sinks with climate warming. In the same way, for ecosystems with PFTs in the non-forest group, NEP (NEP 0) > 0 (S = 3507, P < 0.0001) and ΔQ 10s  > 0 (S = 2046, P < 0.0001), temperature rise should also lead to carbon sinks (Table 2).

More generally, the response of NEP (or NEE) to a change in mean air temperature can also be determined using Eq. (7) (see the section of Methods). If GPP ≥ RE, we have

$$\frac{dNEP}{dT}\ge \frac{GPP}{10}\,\mathrm{ln}\,\frac{{Q}_{10sG}}{{Q}_{10sR}}$$
(1)

If Q 10sG  > Q 10sR , the system will be a carbon sink. If GPP = RE and Q 10sG  = Q 10sR , the system will be carbon neutral. If GPP < RE and Q 10sG  < Q 10sR , the system will be a carbon source. This equation is useful to predict the future direction of change of the NEE in the various regions.

Discussion

In this study, we used the SCAPE method17 to derive the intrinsic temperature sensitivity (Q 10s ), which relied on the high frequency fluctuations of measured time series and represent the short-term response of ecological processes to temperature change. The method reduces or excludes the influences of confounding factors (e.g., seasonal variability and water limitation)1, 17, 32, which should result in robust estimates of Q 10sG and Q 10sR .

GPP principally occurs through the photosynthesis, an endothermal reaction process, which requires distinctive activation energies for different ambient temperatures. More activation energy is required to complete the same reaction at a lower temperature33,34,35. Gillooly et al.20 have shown that Q 10 is positively correlated to activation energy. Therefore, the relationship between the temperature sensitivity of GPP and MAT (Table 1 and Fig. 2a) is attributable to the activation energy required in the different temperature zones.

On the contrary, respiration is a heat-releasing process that mainly depends on the availability of substrate (i.e., carbon sources). Because of the heterogeneity of carbon sources, it is expected that diverse activation energies and turnover times are required for decomposition of the different carbon pools in the ecosystem12, 36. The turnover time ranges from less than 1 yr for labile carbon pool to greater than 106 yr for recalcitrant carbon pool37, 38. As mentioned above, the Q 10sR reflected the temperature response of short-term decomposition of labile carbon pool. The required activation energy for decomposition of the labile carbon pool is considered to be a constant12, 20, 36. As a consequence, the temperature sensitivity of RE (Table 1 and Fig. 2b) was not significantly correlated to temperature, consistent with the result of Mahecha et al.17.

At the ecosystem level, the changes of GPP and RE with temperatures are different2, 39. Within the range of low temperatures in the boreal and temperate regions, GPP increases with temperature faster than RE, which results in an increase of CO2 uptake under climate warming scenarios40.

The integrated response of an ecosystem may demonstrate the thermal optimality under temperature change and be interpreted as photosynthesis and respiration acclimation to temperature41, 42. The temperature acclimation process, also described as temperature adaption, indicates that with increasing global temperature, plants and microorganisms may generate reversible changes in a way that can optimize their functions under the warmer environment43, 44. Such adaptation mechanism should result in compensative responses of the ecological processes of GPP and RE for a change in temperature45,46,47. The changes of NEP response to temperature can be modulated by the disproportional extent of temperature acclimation of either GPP or RE48. It has been well documented that at the plant level, electron transport capacity and/or heat stability of Rubisco are enhanced with increasing temperature, which result in higher photosynthetic assimilation rates42. Furthermore, the increased CO2 uptake in warmer temperatures may also be contributed by extended growing seasons, increased nitrogen mineralization and root growth29, 49. Respiration generally increases with temperature, however, water stress and respiratory acclimation can offset or reverse the direct temperature effect50, 51.

Our results showed that ecosystems in the boreal and temperate regions with different PFTs would become carbon sink with climate warming. Evidences have shown that the Earth is becoming greener since 1980s, indicating an increase in GPP52. This increase in GPP is mainly attributable to the rising atmospheric CO2 level and temperature30, 31, 53. The potential greenhouse effect may further accelerate CO2 uptake of plants54. In fact, the climate regions and PFTs interactively affect the temperature sensitivities of CO2 balance processes55, 56. For instance, the needleleaf biome generally distributes in cold climates of the world57. Consequently, the temperature sensitivity results derived from the PFTs are generally consistent with those from the climate groups.

Besides the exponential function model (the Q 10 approach) used in this study, other models, such as linear function6 and convex curve models40, have been applied to characterize GPP changes vs. temperature. It is well documented that GPP is positively correlated to temperature, but very high temperatures should decrease CO2 assimilation rates58, 59. Therefore, any model to characterize the GPP vs. temperature relationship should be applicable only within the temperature range for normal plant growth. Within the temperature range of this study (MAT: −4.67~16.0 °C), conceptually the exponential function model and the convex curve model should cross at a certain high temperature and the linear function model should be between the exponential function and the convex curve models. These models should cross at least at one point at the reference temperature (GPP 0) (Fig. 5). Among the exponential function, linear function, and convex curve models, the exponential function model predicts the lowest GPP value for a given temperature. Thus, the NEP values calculated in this study are more conservative than those calculated using other models. In other words, the conclusion of NEE with “sink” for most of the cases in this study should hold when other models of GPP vs. temperature are applied.

Figure 5
figure5

Conceptual models of the gross primary production (GPP) rates vs. temperature.

It should be noted that the estimation of CO2 balance trends in this study was according to the GPP and RE results under a relatively short time scale. The GPP results were on an annual basis and the RE results were mainly related to the labile carbon pool with short turnover time in the ecosystem. The patterns of temperature sensitivities of GPP and RE, as well as the NEP changing with the climate regions and PFTs, provide valuable information to predict the CO2 balance processes in response to climate change at the global scale60, 61. However, in longer time scales, the effects of environmental constraints should become more profound, which may reduce sensitivities of the CO2 balance processes of terrestrial ecosystems to future climate warming12, 60. On the other hand, the wide range of kinetic properties demonstrate a diverse organic matter compounds of substrates and the recalcitrant organic carbon pool with longer turnover time is more sensitive to temperature than the labile organic carbon pool36. The long-term change of temperature sensitivities of GPP and RE should influence the responses and feedback of terrestrial ecosystem carbon dynamic to global temperature change. Therefore, further research is needed to explore the patterns of CO2 balance processes under long time scales.

Methods

Database

Time series of GPP and RE were assembled from the FLUXNET Database (http://www.fluxdata.org/, Open Data set), European Flux Database (European Fluxes Database Cluster http://gaia.agraria.unitus.it/), AmeriFlux (http://ameriflux.lbl.gov/), Distributed Active Archive Center for Biogeochemical Dynamics (ORNL DAAC http://daac.ornl.gov/). In total, 403 site-years at 101 sites throughout the world were collected. The datasets covered various ecosystems spanning between 40°N to 71°N. Except twelve site-years from Russia, other site-years were primarily from Europe and North America during the time period from 1991 to 2006 (see Supplementary Table S1).

Semi-continuous observations of NEE were obtained with the eddy covariance technique on a large number of experimental sites and ecosystem types47. All flux data were 30 min measured averages. Flux data sets were compiled according to site, year, ecosystem and vegetation type, environmental and physical variables, such as air temperature, latitude and longitude, precipitation, solar radiation, and NEE. The data were quality controlled following the procedures of Papale et al.62. The data were further interpolated (gap-filled) with the common procedures of the marginal distribution sampling method63 and the artificial neural network simulator64. The interpolation procedure of iterative singular spectrum analysis (SSA) was further used to reduce uncertainty65.

Daily ecosystem respiration rates were estimated from the mean NEE values measured during night17. At least five data points for each day and at least 255 measurements in each site were required for the estimations17. Mean air temperatures over the same periods for CO2 flux measurements were used as the corresponding temperatures for Q 10 calculations. For forest sites, GPP values were estimated with the methods of using exclusive daytime fluxes66. For other sites, GPP values were derived from nighttime fluxes63. Since the absolute values of NEE and NEP are the same, daily NEP values were determined directly from the daily NEE measurements.

Our database included two climate regions, that is, the boreal region (between 49 and 71°N) (93 site-years) and the temperate region (between 40 and 64°N) (310 site-years). The collected data were also classified in the different PFTs according to the International Geosphere-Biosphere Programme (IGBP, 2012, http://www.igbp.net)67. In this study, we divided the database into two groups based on the PFTs, i.e., the forest site group (310 site-years) and the non-forest site group (143 site-years). The forest site group included deciduous broadleaf forest, evergreen needleleaf forest, and mixed forest. The not-forest site group included croplands, closed shrublands, grasslands, open shrublands, and permanent wetland.

Calculation of Q 10 values of GPP and RE

The relationship between reaction rates and temperature can be described by19:

$$R={R}_{r}{{Q}_{10}}^{\frac{T-{T}_{r}}{10}}$$
(2)

here T is the temperature (°C), T r is the reference temperature, R and R r are the measured reaction rates corresponding to T and T r , respectively (g C m−2 d−1), and Q 10 is the temperature sensitivity index of the reaction. Equation (2) can be linearized as follows:

$$\mathrm{ln}\,R=\,\mathrm{ln}\,{R}_{r}+\frac{T-{T}_{r}}{10}\,\mathrm{ln}\,{Q}_{10}$$
(3)

By fitting Eq. (3) with measured R values at different temperatures, the apparent Q 10 can be estimated by linear regression.

To study the annual ecosystem processes response to temperature changes, we are specifically interested in the sensitivity of these processes to fast temperature fluctuations. The SSA procedure was applied to extract the fast temperature fluctuations of the ecosystem processes directly from measured data68, 69. According to the procedure, a time series of measured data can be decomposed into sums of sub-signals of characteristic frequency ranges and overall mean values as follows17:

$$R(i)=\sum _{m=1}^{M}R{(i)}_{fm}+\langle R\rangle \quad i=1,2,\ldots ,N$$
(4)
$$T(i)=\sum _{m=1}^{M}T{(i)}_{fm}+\langle T\rangle \quad i=1,2,\ldots ,N$$
(5)

here R(i) is the series of reaction rates, T(i) is the corresponding temperature time series, the subscript fm represent the mth frequency band, M is the total number of predefined frequency bands, which should cover the whole frequency range, N is the time series length, and 〈 〉 denotes the overall time series mean. According to the scale parameter estimation (SCAPE) principle, different sub-signals are associated with parameters corresponding to different time scales. Reaction rates at high frequency bands reflect the fast temperature fluctuations, i.e., the direct responses to temperature, which is defined as the intrinsic temperature sensitivity17. The use of reaction rates and corresponding temperatures at high frequency bands should disentangle the effect of temperature on GPP and RE from all the other environmental factors. Therefore, the intrinsic temperature sensitivity can be related to the high frequency portions of R(i) and T(i) by ref. 17

$$\mathrm{ln}\,R{(i)}_{fh}=\frac{T{(i)}_{fh}-{T}_{r}}{10}\,\mathrm{ln}\,{Q}_{10s}$$
(6)

where the subscript fh represents the high frequency series and Q 10s is the intrinsic temperature sensitivity index. With measurement series of GPP and RE rates at different temperatures, the approximate intrinsic temperature sensitivity indexes of GPP (Q 10sG ) and RE (Q 10sR ) can be determined using the procedure of Mahecha et al.17 on the basis of Eqs (4) to (6).

The annual net CO2 exchange (i.e., the CO2 source or sink) of terrestrial ecosystems at increasing temperature can be defined as the sensitivity of NEP to temperature, which is related to the intrinsic temperature sensitivity indexes of GPP and RE as follows:

$$\frac{dNEP}{dT}=\frac{d(GPP-RE)}{dT}=\frac{GPP}{10}\,\mathrm{ln}\,{Q}_{10sG}-\frac{RE}{10}\,\mathrm{ln}\,{Q}_{10sR}$$
(7)

More specifically, at an initial condition (T = T 0) and temperature rise to T 1, the NEP values are calculated, respectively, with the following forms:

$$NE{P}_{0}=GP{P}_{0}-R{E}_{0}=GP{P}_{r}{Q}_{10sG}^{\frac{{T}_{0}-{T}_{r}}{10}}-R{E}_{r}{Q}_{10sR}^{\frac{{T}_{0}-{T}_{r}}{10}}$$
(8a)
$$NE{P}_{1}=GP{P}_{1}-R{E}_{1}=GP{P}_{r}{Q}_{10sG}^{\frac{{T}_{1}-{T}_{r}}{10}}-R{E}_{r}{Q}_{10sR}^{\frac{{T}_{1}-{T}_{r}}{10}}$$
(8b)

where GPP r and RE r are the GPP and RE values at the reference temperature, respectively. Therefore, with a temperature increase ΔT = T 1 − T 0, the change of NEP is:

$$\begin{array}{rcl}{\rm{\Delta }}NEP & = & NE{P}_{1}-NE{P}_{0}=GP{P}_{r}({Q}_{10sG}^{\frac{{T}_{1}-{T}_{r}}{10}}-{Q}_{10sG}^{\frac{{T}_{0}-{T}_{r}}{10}})-R{E}_{r}({Q}_{10sR}^{\frac{{T}_{1}-{T}_{r}}{10}}-{Q}_{10sR}^{\frac{{T}_{0}-{T}_{r}}{10}})\\ & = & GP{P}_{0}({Q}_{10sG}^{\frac{{\rm{\Delta }}T}{10}}-1)-R{E}_{0}({Q}_{10sR}^{\frac{{\rm{\Delta }}T}{10}}-1)\\ & = & GP{P}_{0}[{({Q}_{10sR}+{\rm{\Delta }}{Q}_{10s})}^{\frac{{\rm{\Delta }}T}{10}}-1)-R{E}_{0}({Q}_{10sR}^{\frac{{\rm{\Delta }}T}{10}}-1)\end{array}$$
(9)

where ΔQ 10s  = Q 10sG  − Q 10sR .

Data analysis

The uncertainty of mean Q 10 values and confidence intervals were evaluated with the nonparametric bootstrap method70. This method is more advantageous than the normal distribution method to deal with uncertain population distributions with comparably small sample sizes. The bootstrap sample size was set as 10000, which is an appropriate value to ensure the reliability of results.

Both parametric and non-parametric tests were applied to examine the differences of Q 10 among factors. Other statistical methods used for data analyses, included the null hypothesis test, the Wilcoxon rank-sum test, and the Kruskal-Wallis test71, 72. The SAS 9.3 software was used for the above analyses.

References

  1. 1.

    Carrara, A., Janssens, I. A., Curiel Yuste, J. & Ceulemans, R. Seasonal changes in photosynthesis, respiration and NEE of a mixed temperate forest. Agr. Forest Meteorol. 126, 15–31 (2004).

  2. 2.

    Valentini, R. et al. Respiration as the main determinant of carbon balance in European forests. Nature 404, 861–865 (2000).

  3. 3.

    Luyssaert, S. et al. CO2 balance of boreal, temperate, and tropical forests derived from a global database. Glob. Chang. Biol 13, 2509–2537 (2007).

  4. 4.

    Perkins, D. M. et al. Environmental warming and biodiversity-ecosystem functioning in freshwater microcosms: partitioning the effects of species identity, richness and metabolism. Adv. Ecol. Res. 43, 177–209 (2010).

  5. 5.

    Reiss, J. et al. When microscopic organisms inform general ecological theory. Adv. Ecol. Res 43, 45–85 (2010).

  6. 6.

    Hirata, R. et al. Spatial distribution of carbon balance in forest ecosystems across East Asia. Agr. Forest Meteorol. 148, 761–775 (2008).

  7. 7.

    Mäkelä, A. et al. Developing an empirical model of stand GPP with the LUE approach: analysis of eddy covariance data at five contrasting conifer sites in Europe. Glob. Chang. Biol. 14, 92–108 (2008).

  8. 8.

    Allen, A. P., Gillooly, J. F. & Brown, J. H. Linking the global carbon cycle to individual metabolism. Funct. Ecol. 19, 202–213 (2005).

  9. 9.

    Walther, G.-R. et al. Ecological responses to recent climate change. Nature 416, 389–395 (2002).

  10. 10.

    Cox, P. M., Betts, R. A., Jones, C. D., Spall, S. A. & Totterdell, I. J. Acceleration of global warming due to carbon-cycle feedbacks in a coupled climate model. Nature 408, 184–187 (2000).

  11. 11.

    Davidson, E. A., Janssens, I. A. & Luo, Y. On the variability of respiration in terrestrial ecosystems: moving beyond Q 10. Glob. Chang. Biol 12, 154–164 (2006).

  12. 12.

    Davidson, E. A. & Janssens, I. A. Temperature sensitivity of soil carbon decomposition and feedbacks to climate change. Nature 440, 165–173 (2006).

  13. 13.

    Yvon-Durocher, G. et al. Reconciling the temperature dependence of respiration across timescales and ecosystem types. Nature 487, 472–476 (2012).

  14. 14.

    Peng, S., Piao, S., Wang, T., Sun, J. & Shen, Z. Temperature sensitivity of soil respiration in different ecosystems in China. Soil Biol. Biochem. 41, 1008–1014 (2009).

  15. 15.

    Zhou, T., Shi, P., Hui, D. & Luo, Y. Global pattern of temperature sensitivity of soil heterotrophic respiration (Q 10) and its implications for carbon-climate feedback. J. Geophys. Res-Biogeosci. 114, G02016 (2009).

  16. 16.

    Jones, C. D., Cox, P. & Huntingford, C. Uncertainty in climate–carbon-cycle projections associated with the sensitivity of soil respiration to temperature. Tellus B 55, 642–648 (2003).

  17. 17.

    Mahecha, M. D. et al. Global convergence in the temperature sensitivity of respiration at ecosystem level. Science 329, 838–840 (2010).

  18. 18.

    Wang, X. et al. Are ecological gradients in seasonal Q 10 of soil respiration explained by climate or by vegetation seasonality? Soil Biol. Biochem. 42, 1728–1734 (2010).

  19. 19.

    van’t Hoff, J. H. & Lehfeldt, R. A. Lectures on theoretical and physical chemistry (1899).

  20. 20.

    Gillooly, J. F., Brown, J. H., West, G. B., Savage, V. M. & Charnov, E. L. Effects of size and temperature on metabolic rate. Science 293, 2248–2251 (2001).

  21. 21.

    Enquist, B. J. et al. Scaling metabolism from organisms to ecosystems. Nature 423, 639–642 (2003).

  22. 22.

    Brown, J. H., Gillooly, J. F., Allen, A. P., Savage, V. M. & West, G. B. Toward a metabolic theory of ecology. Ecology 85, 1771–1789 (2004).

  23. 23.

    Woodwell, G. M. Biotic effects on the concentration of atmospheric carbon dioxide: a review and projection. In: Changing Climate 216–241 (Natl. Acad. Press, Washington D. C., USA, 1983).

  24. 24.

    Jenkinson, D. S., Adams, D. E. & Wild, A. Model estimates of CO2 emissions from soil in response to global warming. Nature 351, 304–306 (1991).

  25. 25.

    Myneni, R. B., Keeling, C. D., Tucker, C. J., Asrar, G. & Nemani, R. R. Increased plant growth in the northern high latitudes from 1981 to 1991. Nature 386, 698–702 (1997).

  26. 26.

    Welp, L. R., Randerson, J. T. & Liu, H. P. The sensitivity of carbon fluxes to spring warming and summer drought depends on plant functional type in boreal forest ecosystems. Agr. Forest Meteorol. 147, 172–185 (2007).

  27. 27.

    Lupascu, M. et al. High Arctic wetting reduces permafrost carbon feedbacks to climate warming. Nat. Clim. Change 4, 51–55 (2014).

  28. 28.

    Xue, K. et al. Tundra soil carbon is vulnerable to rapid microbial decomposition under climate warming. Nat. Clim. Change 6, 595–600 (2016).

  29. 29.

    Churkina, G., Schimel, D., Braswell, B. H. & Xiao, X. Spatial analysis of growing season length control over net ecosystem exchange. Glob. Chang. Biol. 11, 1777–1787 (2005).

  30. 30.

    Piao, S., Friedlingstein, P., Ciais, P., Zhou, L. & Chen, A. Effect of climate and CO2 changes on the greening of the Northern Hemisphere over the past two decades. Geophys. Res. Lett. 33, L23402 (2006).

  31. 31.

    Pan, Y. et al. A large and persistent carbon sink in the world’s forests. Science 333, 988–993 (2011).

  32. 32.

    Falge, E. et al. Seasonality of ecosystem respiration and gross primary production as derived from FLUXNET measurements. Agr. Forest Meteorol. 113, 53–74 (2002).

  33. 33.

    Laidler, K. J. A glossary of terms used in chemical kinetics, including reaction dynamics. In: Pure and Applied Chemistry (IUPAC Recommendations, 1996).

  34. 34.

    Blankenship, R. E. Molecular mechanisms of photosynthesis. John Wiley & Sons (2013).

  35. 35.

    Cai, J., Wu, W. & Liu, R. An overview of distributed activation energy model and its application in the pyrolysis of lignocellulosic biomass. Renew. Sust. Energ. Rev. 36, 236–246 (2014).

  36. 36.

    Knorr, W., Prentice, I. C., House, J. I. & Holland, E. A. Long-term sensitivity of soil carbon turnover to warming. Nature 433, 298–301 (2005).

  37. 37.

    Davidson, E. A., Trumbore, S. E. & Amundson, R. Biogeochemistry: Soil warming and organic carbon content. Nature 408, 789–790 (2000).

  38. 38.

    Trumbore, S. Age of soil organic matter and soil respiration: Radiocarbon constraints on belowground C dynamics. Ecol. Appl. 10, 399–411 (2000).

  39. 39.

    Huxman, T. E., Turnipseed, A. A., Sparks, J. P., Harley, P. C. & Monson, R. K. Temperature as a control over ecosystem CO2 fluxes in a high-elevation, subalpine forest. Oecologia 134, 537–546 (2003).

  40. 40.

    Niu, S. et al. Thermal optimality of net ecosystem exchange of carbon dioxide and underlying mechanisms. New Phytol. 194, 775–783 (2012).

  41. 41.

    Loreau, M. Evolution of ecosystems and ecosystem properties. 225–259 (Princeton University Press, 2010).

  42. 42.

    Sage, R. F. & Kubien, D. S. The temperature response of C3 and C4 photosynthesis. Plant Cell Environ. 30, 1086–1106 (2007).

  43. 43.

    Luo, Y., Wan, S., Hui, D. & Wallace, L. L. Acclimatization of soil respiration to warming in a tall grass prairie. Nature 413, 622–625 (2001).

  44. 44.

    Saxe, H., Cannell, M. G. R., Johnsen, Ø., Ryan, M. G. & Vourlitis, G. Tree and forest functioning in response to global warming. New Phytol. 149, 369–399 (2001).

  45. 45.

    Lloyd, J. & Taylor, J. A. On the temperature dependence of soil respiration. Funct. Ecol. 8, 315–323 (1994).

  46. 46.

    Tjoelker, M. G., Oleksyn, J., Reich, P. B. & ŻYtkowiak, R. Coupling of respiration, nitrogen, and sugars underlies convergent temperature acclimation in Pinus banksiana across wide-ranging sites and populations. Glob. Chang. Biol. 14, 782–797 (2008).

  47. 47.

    Baldocchi, D. et al. FLUXNET: A new tool to study the temporal and spatial variability of ecosystem–scale carbon dioxide, water vapor, and energy flux densities. Bull. Amer. Meteorol. Soc. 82, 2415–2434 (2001).

  48. 48.

    Atkin, O. K., Scheurwater, I. & Pons, T. L. High thermal acclimation potential of both photosynthesis and respiration in two lowland Plantago species in contrast to an alpine congeneric. Glob. Chang. Biol. 12, 500–515 (2006).

  49. 49.

    Peñuelas, J. & Filella, I. Phenology-Responses to a warming world. Science 294, 793–795 (2001).

  50. 50.

    Irvine, J., Law, B. E., Martin, J. G. & Vickers, D. Interannual variation in soil CO2 efflux and the response of root respiration to climate and canopy gas exchange in mature ponderosa pine. Glob. Chang. Biol. 14, 2848–2859 (2008).

  51. 51.

    Scott, R. L., Jenerette, G. D., Potts, D. L. & Huxman, T. E. Effects of seasonal drought on net carbon dioxide exchange from a woody-plant-encroached semiarid grassland. J. Geophys. Res-Biogeosci. 114, G04004 (2009).

  52. 52.

    Zhu, Z. et al. Greening of the Earth and its drivers. Nat. Clim. Change 6, 791–795 (2016).

  53. 53.

    Lucht, W. et al. Climatic control of the high-latitude vegetation greening trend and Pinatubo effect. Science 296, 1687–1689 (2002).

  54. 54.

    Johnson, J. M. F., Franzluebbers, A. J., Weyers, S. L. & Reicosky, D. C. Agricultural opportunities to mitigate greenhouse gas emissions. Environ. Pollut. 150, 107–124 (2007).

  55. 55.

    Chapin, F. S., Sala, O. E. & Huber-Sannwald, E. Global biodiversity in a changing environment: scenarios for the 21st century. Vol. 152 (Springer Science & Business Media, 2001).

  56. 56.

    Lloret, F., Peñuelas, J. & Estiarte, M. Experimental evidence of reduced diversity of seedlings due to climate modification in a Mediterranean-type community. Glob. Chang. Biol. 10, 248–258 (2004).

  57. 57.

    Woodward, F. I., Lomas, M. R. & Kelly, C. K. Global climate and the distribution of plant biomes. Philos. T. R. Soc. B 359, 1465–1476 (2004).

  58. 58.

    Bernacchi, C. J., Singsaas, E. L., Pimentel, C., Portis, A. R. Jr & Long, S. P. Improved temperature response functions for models of Rubisco-limited photosynthesis. Plant Cell Environ. 24, 253–259 (2001).

  59. 59.

    Alonso, A., Pérez, P., Morcuende, R. & Martinez-Carrasco, R. Future CO2 concentrations, though not warmer temperatures, enhance wheat photosynthesis temperature responses. Physiol. Plantarum. 132, 102–112 (2008).

  60. 60.

    Frank, D. C. et al. Ensemble reconstruction constraints on the global carbon cycle sensitivity to climate. Nature 463, 527–530 (2010).

  61. 61.

    Randerson, J. T. et al. Systematic assessment of terrestrial biogeochemistry in coupled climate–carbon models. Glob. Chang. Biol. 15, 2462–2484 (2009).

  62. 62.

    Papale, D. et al. Towards a standardized processing of Net Ecosystem Exchange measured with eddy covariance technique: algorithms and uncertainty estimation. Biogeosciences 3, 571–583 (2006).

  63. 63.

    Reichstein, M. et al. On the separation of net ecosystem exchange into assimilation and ecosystem respiration: review and improved algorithm. Glob. Chang. Biol. 11, 1424–1439 (2005).

  64. 64.

    Papale, D. & Valentini, R. A new assessment of European forests carbon exchanges by eddy fluxes and artificial neural network spatialization. Glob. Chang. Biol. 9, 525–535 (2003).

  65. 65.

    Mahecha, M. D. et al. Comparing observations and process‐based simulations of biosphere‐atmosphere exchanges on multiple timescales. J. Geophys. Res-Biogeosci. (2005–2012) 115 (2010).

  66. 66.

    Lasslop, G. et al. Separation of net ecosystem exchange into assimilation and respiration using a light response curve approach: critical issues and global evaluation. Glob. Chang. Biol. 16, 187–208 (2010).

  67. 67.

    Díaz, S. et al. The global spectrum of plant form and function. Nature 529, 167–171 (2016).

  68. 68.

    Golyandina, N., Nekrutkin, V. & Zhigljavsky, A. A. Analysis of time series structure: SSA and related techniques (CRC press, 2001).

  69. 69.

    Ghil, M. et al. Advanced spectral methods for climatic time series. Rev. Geophys. 40, 1003 (2002).

  70. 70.

    Efron, B. & Tibshirani, R. J. An introduction to the bootstrap (CRC press, 1994).

  71. 71.

    Larson, M. G. Analysis of variance. Circulation 117, 115–121 (2008).

  72. 72.

    Hollander, M., Wolfe, D. A. & Chicken, E. Nonparametric statistical methods (John Wiley & Sons, 2013).

Download references

Acknowledgements

This study was supported by grants from the National Natural Science Foundation of China (No. 41471181). We thank Dr. Miguel Mahecha for sharing the source codes of SCAPE model and his valuable guidance, and thank Dr. Carmen Emmel and Dr. Asko Noormets for the suggestions during the manuscript preparation. We also acknowledge all the principal investigators and data providers for sharing their flux data (all sites are listed in supporting information). The following networks provided flux data: FLUXNET, AmeriFlux, ORNL DAAC, European Fluxes Database Cluster. This work used eddy covariance data mostly acquired by the FLUXNET community, which is in particular provided by the following networks: AmeriFlux [U.S. Department of Energy, Biological and Environmental Research, Terrestrial Carbon Program (DE‐FG02‐04ER63917 and DE‐FG02‐04ER63911)], CarboEuropeIP, CarboItaly, CarboMont, Fluxnet‐Canada (supported by CFCAS, NSERC, BIOCAP, Environment Canada, and NRCan), GreenGrass, KoFlux, LBA, NECC, OzFlux, TCOS‐Siberia, USCCC. We acknowledge the financial support to the eddy covariance data harmonization provided by CarboEuropeIP, FAO‐GTOS‐TCO, iLEAPS, Max Planck Institute for Biogeochemistry, National Science Foundation, University of Tuscia, Université Laval and Environment Canada and US Department of Energy and the database development and technical support from Berkeley Water Center, Lawrence Berkeley National Laboratory, Microsoft Research eScience, Oak Ridge National Laboratory, University of California-Berkeley, University of Virginia.

Author information

Z.Z. and R.Z. designed the research. J.Z. collected the data. Z.Z. and R.Z. performed the research and analyzed the data. Z.Z., R.Z., A.C. and G.W. drafted the manuscript. Z.Z., R.Z., A.C., G.W., N.B., G.C., F.M., J.P., T.H., K.T, and L.M. contributed in the discussion of the results and in writing the manuscript.

Correspondence to Renduo Zhang.

Ethics declarations

Competing Interests

The authors declare that they have no competing interests.

Additional information

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Zhang, Z., Zhang, R., Cescatti, A. et al. Effect of climate warming on the annual terrestrial net ecosystem CO2 exchange globally in the boreal and temperate regions. Sci Rep 7, 3108 (2017). https://doi.org/10.1038/s41598-017-03386-5

Download citation

Further reading

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.