Abstract:The response of microbial respiration from soil organic carbon (SOC) decomposition to environmental changes plays a key role in predicting future trends of atmospheric CO2 concentration. However, it remains uncertain whether there is a universal trend in the response of microbial respiration to increased temperature and nutrient addition among different vegetation types. In this study, soils were sampled in spring, summer, autumn and winter from five dominant vegetation types, including pine, larch and birch f… Show more
“…Tian et al (2016) demonstrated that N addition does not influence soil microbial CO 2 emission from a topsoil in a laboratory incubation. Several field studies also reported lower soil microbial CO 2 emissions with N addition compared to controls due to changes in microbial composition (Bowden, Davidson, Savage, Arabia, & Steudler, 2004;Mo et al, 2008;Phillips & Fahey, 2007;Qian et al, 2016;, but here no changes were observed. The response of CO 2 emission to N addition might also be related to soil C substrate availability.…”
Section: Discussioncontrasting
confidence: 50%
“…Our result is supported by some previous studies. For example, Mori et al (2016) found that CO 2 emission rates in tropical forest soils were stimulated by P addition at high C concentrations (1 mg C/g soil was added as glucose) but not at low C conditions (0.1 mg g −1 soil), whereas Qian et al (2016) reported that there was no response of soil microbial CO 2 emission to P addition. Indeed, in this study, the EV-RT soil in Puerto Rico with the highest C content (7.21%) showed the strongest response to P addition among the four soils.…”
Section: Discussionmentioning
confidence: 99%
“…Nutrient availability may regulate microbial physiology and activity and eventually influence ecosystem C cycling (Jing et al, 2017;Mackenzie, Ver, & Lerman, 2002). However, although many fertilization experiments have been conducted in the field, there are limited studies on soil microbial CO 2 emissions in response to P addition (Cleveland, Townsend, & Schmidt, 2002;Qian, He, & Wang, 2016). Microbial biomass tends to be limited by P in tropical soils (Cleveland et al, 2002;Turner & Wright, 2014;Waring, Averill, & Hawkes, 2013;Warren et al, 2015).…”
Section: Introductionmentioning
confidence: 99%
“…One laboratory experiment also found that P accelerates leaf litter decay in a tropical dry forest, whereas added N retards it (Powers & Salute, ). However, Qian et al () incubated soils with five different vegetation types at different temperatures for 5–7 days and found that microbial respiration does not significantly respond to inorganic N or P addition. The effects of P and N additions are site specific in tropical forests and more studies are needed to reveal the underlying factors influencing soil microbial activities and soil CO 2 emissions.…”
Ecosystem functional responses such as soil CO 2 emissions are constrained by microclimate, available carbon (C) substrates and their effects upon microbial activity. In tropical forests, phosphorus (P) is often considered as a limiting factor for plant growth, but it is still not clear whether P constrains microbial CO 2 emissions from soils. In this study, we incubated seven tropical forest soils from Brazil and Puerto Rico with different nutrient addition treatments (no addition, Control; C, nitrogen (N) or P addition only; and combined C, N and P addition (CNP)). Cumulative soil CO 2 emissions were fit with a Gompertz model to estimate potential maximum cumulative soil CO 2 emission (C m ) and the rate of change of soil C decomposition (k). Quantitative polymerase chain reaction (qPCR) was conducted to quantify microbial biomass as bacteria and fungi. Results showed that P addition alone or in combination with C and N enhanced C m , whereas N addition usually reduced C m , and neither N nor P affected microbial biomass. Additions of CNP enhanced k, increased microbial abundances and altered fungal to bacterial ratios towards higher fungal abundance. Additions of CNP, however, tended to reduce C m for most soils when compared to C additions alone, suggesting that microbial growth associated with nutrient additions may have occurred at the expense of C decomposition. Overall, this study demonstrates that soil CO 2 emission is more limited by P than N in tropical forest soils and those effects were stronger in soils low in P.
Highlights• A laboratory incubation study was conducted with nitrogen, phosphorus or carbon addition to tropical forest soils. Soil CO 2 emission was fitted with a Gompertz model and soil microbial abundance was quantified using qPCR. Phosphorus addition increased model parameters C m and soil CO 2 emission, particularly in the Puerto Rico soils. Soil CO 2 emission was more limited by phosphorus than nitrogen in tropical forest soils.
“…Tian et al (2016) demonstrated that N addition does not influence soil microbial CO 2 emission from a topsoil in a laboratory incubation. Several field studies also reported lower soil microbial CO 2 emissions with N addition compared to controls due to changes in microbial composition (Bowden, Davidson, Savage, Arabia, & Steudler, 2004;Mo et al, 2008;Phillips & Fahey, 2007;Qian et al, 2016;, but here no changes were observed. The response of CO 2 emission to N addition might also be related to soil C substrate availability.…”
Section: Discussioncontrasting
confidence: 50%
“…Our result is supported by some previous studies. For example, Mori et al (2016) found that CO 2 emission rates in tropical forest soils were stimulated by P addition at high C concentrations (1 mg C/g soil was added as glucose) but not at low C conditions (0.1 mg g −1 soil), whereas Qian et al (2016) reported that there was no response of soil microbial CO 2 emission to P addition. Indeed, in this study, the EV-RT soil in Puerto Rico with the highest C content (7.21%) showed the strongest response to P addition among the four soils.…”
Section: Discussionmentioning
confidence: 99%
“…Nutrient availability may regulate microbial physiology and activity and eventually influence ecosystem C cycling (Jing et al, 2017;Mackenzie, Ver, & Lerman, 2002). However, although many fertilization experiments have been conducted in the field, there are limited studies on soil microbial CO 2 emissions in response to P addition (Cleveland, Townsend, & Schmidt, 2002;Qian, He, & Wang, 2016). Microbial biomass tends to be limited by P in tropical soils (Cleveland et al, 2002;Turner & Wright, 2014;Waring, Averill, & Hawkes, 2013;Warren et al, 2015).…”
Section: Introductionmentioning
confidence: 99%
“…One laboratory experiment also found that P accelerates leaf litter decay in a tropical dry forest, whereas added N retards it (Powers & Salute, ). However, Qian et al () incubated soils with five different vegetation types at different temperatures for 5–7 days and found that microbial respiration does not significantly respond to inorganic N or P addition. The effects of P and N additions are site specific in tropical forests and more studies are needed to reveal the underlying factors influencing soil microbial activities and soil CO 2 emissions.…”
Ecosystem functional responses such as soil CO 2 emissions are constrained by microclimate, available carbon (C) substrates and their effects upon microbial activity. In tropical forests, phosphorus (P) is often considered as a limiting factor for plant growth, but it is still not clear whether P constrains microbial CO 2 emissions from soils. In this study, we incubated seven tropical forest soils from Brazil and Puerto Rico with different nutrient addition treatments (no addition, Control; C, nitrogen (N) or P addition only; and combined C, N and P addition (CNP)). Cumulative soil CO 2 emissions were fit with a Gompertz model to estimate potential maximum cumulative soil CO 2 emission (C m ) and the rate of change of soil C decomposition (k). Quantitative polymerase chain reaction (qPCR) was conducted to quantify microbial biomass as bacteria and fungi. Results showed that P addition alone or in combination with C and N enhanced C m , whereas N addition usually reduced C m , and neither N nor P affected microbial biomass. Additions of CNP enhanced k, increased microbial abundances and altered fungal to bacterial ratios towards higher fungal abundance. Additions of CNP, however, tended to reduce C m for most soils when compared to C additions alone, suggesting that microbial growth associated with nutrient additions may have occurred at the expense of C decomposition. Overall, this study demonstrates that soil CO 2 emission is more limited by P than N in tropical forest soils and those effects were stronger in soils low in P.
Highlights• A laboratory incubation study was conducted with nitrogen, phosphorus or carbon addition to tropical forest soils. Soil CO 2 emission was fitted with a Gompertz model and soil microbial abundance was quantified using qPCR. Phosphorus addition increased model parameters C m and soil CO 2 emission, particularly in the Puerto Rico soils. Soil CO 2 emission was more limited by phosphorus than nitrogen in tropical forest soils.
“…Furthermore, the two to four month lag length of NDVI in response to temperature for distinct sub-watersheds reveals that the vegetation may not have a synchronous response to temperature changes. As vegetation mainly accumulates nutrients and organic matter in spring and grows in summer and autumn [29], the distinct dominant and diversity of the vegetation types would be the main cause of different legacy effect for NDVI in response of the temperature. The agricultural area (upstream) presented a faster responce to temperature than the forest conservation area in the midstream and forest-urban mixed area in the downstream, which may be due to the short growth cycle and rapid growth rate of the crops [30].…”
Hydrothermal and climatic conditions determine vegetation productivity and its dynamic changes. However, the legacy effect and the causal relationships between these climatic variables and vegetation growth are still unclear, especially in the dry regions. Based on multi-statistical methods, including bivariate correlation analysis and composite Granger causality tests, we investigated the correlation, causality, and lag length between temperature/precipitation and the vegetation growth (Normalized Difference Vegetation Index, NDVI) in three typical sub-watersheds in the Luanhe River Basin, China. The results show that: (1) Precipitation and temperature are the Granger causes of NDVI variation in the study catchment; (2) temperature and precipitation are not strictly positively correlated with NDVI during growing seasons along with the whole sequence, and excessive warmth and precipitation inhibits vegetative growth; (3) the lag length of vegetation growth in response to temperature/precipitation was shorter in agriculture areas (~2 months) than the forest-dominant area, which have indicated 3-4 months lag length; and (4) anthropogenic disturbance did not result in notable negative effects on vegetation growth at the Luanhe River Basin. Our study further suggests that use of these multi-statistical methods could be a valuable approach for comprehensively understanding the correlation between vegetation growth and climatic variations. We have also provided an avenue to bridge the gaps between stationary and non-stationary sequence, as well as to eliminate pseudo regression problems. These findings provide critical information for developing cost-efficient policies and land use management applications for forest conservation in arid and semi-arid area.
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