Elevated CO2 Improves Growth and Phosphorus Utilization Efficiency in Cereal Species Under Sub-Optimal Phosphorus Supply

Cultivars of Triticum aestivum, T. durum, and Secale cereale were grown at low (2 μM) and sufficient (500 μM) phosphorus (P) under ambient carbon dioxide (380 μmol mol^?1; aCO₂) and elevated CO₂ (700 μmol mol^?1, eCO₂) to study responses of cereal species in terms of growth and P utilization efficiency (PUE) under P x CO₂ interaction. Dry matter accumulation increased under eCO₂ with sufficient P. Nevertheless, dry matter accumulated at eCO₂ with low-P was similar to that obtained at aCO₂ with sufficient P. Leaf area was 43% higher under eCO₂ with sufficient P. Significant increase in lateral root density, length and surface area were noted at low-P under eCO₂. Phosphorus use efficience (PUE) increased by 59% in response to eCO_2­ in low-P plants. Thus, eCO₂ can partly compensate effect of low-P supply because of improved utilization efficiency. Among cereals, durum wheat was more suitable in terms of PUE under high CO₂ and limiting P supply.     

Elevated CO2 alters the structure of the bacterial community assimilating plant‐derived carbon in the rhizosphere of soya bean

Elevated CO₂ (eCO₂) increases rhizodeposits, which in turn alters the soil microbial community. However, it is not really known how the microbial community metabolizes plant‐derived carbon (C) in the rhizosphere under eCO₂, especially in agricultural soils. This study used a ¹³CO₂ labelling technique combined with DNA‐stable isotope probing (SIP) to fractionate the ¹³C‐DNA and ¹²C‐DNA from the rhizosphere of soya bean plants (Glycine max (L.) Merr. cv. Suinong 14) grown for 54 days under ambient CO₂ (aCO₂) (390 ppm) or eCO₂ (550 ppm). The DNA fractions were then subjected to Illumina Miseq sequencing. The results showed that eCO₂ decreased the richness and diversity of the ¹³C‐assimilating bacterial community compared to aCO₂ (p < 0.05). Elevated CO₂ decreased the abundances of genera, including Pseudarthrobacter, Gaiellales_uncultured, Microlunatus, Gemmatimonas, Gemmatimonadaceae_uncultured, Ramlibacter, Massilia, Luteimonas, Acidobacteriaceae_uncultured, Bryobacter and Candidatus_Solibacter. These genera were probably fast‐growing bacteria and sensitive to labile C. In contrast, eCO₂ stimulated the growth of genera Novosphingobium, Acidimicrobiales_uncultured, Bacillus, Flavisolibacter and Schlesneria, which were able to assimilate complex C compounds. Moreover, the increased population of Novosphingobium under eCO₂ might have accelerated electron flow from the oxidation of organic C. Correspondingly, eCO₂ did not affect the concentration of the dissolved organic C but increased the plant‐derived ¹³C in the rhizosphere. These results indicated that an eCO₂‐induced increase in non‐labile C in rhizodeposits contributed to the increase in population size of a number of the plant‐C‐metabolizing genera that might become the mechanism for the turnover of fresh C in the rhizosphere, modifying the soil C cycle under eCO₂ environments.     

Soil respiration of karst grasslands subjected to woody‐plant encroachment

The transition of grasslands to forests influences many ecosystem processes, including water and temperature regimes and the cycling of nutrients. Different components of the carbon biogeochemical cycle respond strongly to woody plant encroachment; as a consequence, the carbon balance of the invaded grasslands can change markedly. In our research, we studied the response of soil respiration (R_S) to natural succession of calcareous grassland. We established two research sites, called grassland and invaded site, at each of which eddy flux measurement were also performed. Within these sites, triplicate plots were fenced for soil flux measurements. At the invaded site, measurements were performed for forest patches and grassy spaces separately. Soil respiration was strongly dependent on temperature and reached 8–12 µmol CO₂ m^?2 s^?1 in mid‐summer; it was greater at the grassland than at the invaded site. R_S dependence on temperature and soil water content was similar between the different vegetation covers (grassland, gaps and forest patches). At a reference temperature of 10°C, the average R_S was 2.71 µmol CO₂ m^?2 s^?1. The annual sums of R_S were also similar between years and sites: 1345 ± 47 (2009) and 1150 ± 37 g C m^?2 year^?1 (2010) for grassland and 1324 ± 26 (2009) and 1268 ± 26 g C m^?2 year^?1 (2010) for the invaded site, which is at the upper range of the values reported in the literature. Cumulative R_S peaked in July, with about 200 g C m^?2. Large mid‐summer R_S rates rely on strong biological activity supported by high, but non‐extreme soil temperatures and by regular summer precipitation. A coupling of photosynthesis and R_S was revealed by a 24‐hour measurement, which showed asymmetrical clockwise hysteresis patterns.     

Combined effects of phosphorus nutrition and elevated carbon dioxide concentration on chlorophyll fluorescence,photosynthesis, and nutrient efficiency of cotton

To examine the combined effects of phosphorus (P) nutrition and CO₂ on photosynthesis, chlorophyll fluorescence (CF), and nutrient utilization and uptake, two controlled‐environment experiments were conducted using 0.01, 0.05 and 0.20 mM external phosphate each at ambient and elevated CO₂ (aCO₂: 400 and eCO₂: 800 µmol mol^?1, respectively). The CF parameters were affected more by P nutrition than by CO₂ treatment. Photoinhibition of photosystem II (PSII) was due to increased minimal CF (Fo′) and decreased maximal CF (Fm′), and efficiency of energy harvesting (Fv′/Fm′). In addition, reduced electron transport rate (ETR), the quantum yield of PSII (Φ_PSII) and CO₂ assimilation ( ), and overall photochemical quenching in the P‐deficient leaves led to reduction in the efficiency of energy transfer to the PSII reaction center. Stimulation in the Φ_PSII/ and photorespiration (ETR/P_net) was found under P deficiency, whereas the opposite was the case under CO₂ enrichment. On average, photosynthetic rate (P_net) and stomatal conductance declined by 50–53% at 0.05 mM P and by 70–72% at 0.01 mM P as compared to the 0.20 mM P treatment. However, P deficiency, especially at eCO₂, tended to increase the intrinsic water‐use efficiency. In the P‐deficient plants, the decline in the P and N utilization efficiency (up to 91%) of biomass production was mainly associated with greater reduction in the biomass relative to the tissue P concentration as the P supply was reduced. However, it was significantly stimulated by eCO₂ especially at higher P supply. The CO₂ × P interaction was observed for some parameters such as Fo′, Fm′, P utilization efficiencies of photosynthesis and biomass production that might be attributed to the irresponsiveness of these parameters to eCO₂ under low P treatment. Thus, P deficiency limited the beneficial effect of eCO₂. A close relationship between total biomass and photosynthesis with the P and N utilization or uptake efficiencies was found. The P utilization efficiency of P_net appeared to be stable across a range of leaf P concentrations, whereas the N‐utilization efficiency markedly increased with leaf P and differed between CO₂ levels. An apparent effect of both the treatments (P and CO₂) on N‐uptake and utilization efficiency also indicated the alteration in N acquisition and assimilation in cotton plants.     

CO2, CH4 and N2O fluxes of upland black spruce (Picea mariana) forest soils after forest fires of different intensity in interior Alaska

Abstract

Forest fires can change the greenhouse gase (GHG) flux of borea forest soils. We measured carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) fluxes with different burn histories in black spruce (Picea mariana) stands in interior Alaska. The control forest (CF) burned in 1920; partially burned (PB) in 1999; and severely burned (SB1 and SB2) in 2004. The thickness of the organic layer was 22 ± 6 cm at CF, 28 ± 10 cm at PB, 12 ± 6 cm at SB1 and 4 ± 2 cm at SB2. The mean soil temperature during CO₂ flux measurement was 8.9 ± 3.1, 6.4 ± 2.1, 5.9 ± 3.4 and 5.0 ± 2.4°C at SB2, SB1, PB and CF, respectively, and differed significantly among the sites (P < 0.01). The mean CO₂ flux was highest at PB (128 ± 85 mg CO₂-C m^?2 h^?1) and lowest at SB1 (47 ± 19 mg CO₂-C m^?2 h^?1) (P < 0.01), and within each site it was positively correlated with soil temperature (P < 0.01). The CO₂ flux at SB2 was lower than that at CF when the soil temperature was high. We attributed the low CO₂ flux at SB1 and SB2 to low root respiration and organic matter decomposition rates due to the 2004 fire. The CH₄ uptake rate was highest at SB1 [–91 ± 21 μg CH₄-C m^?2 h^?1] (P < 0.01) and positively correlated with soil temperature (P < 0.01) but not soil moisture. The CH₄ uptake rate increased with increasing soil temperature because methanotroph activity increased. The N₂O flux was highest [3.6 ± 4.7 μg N₂O-N m^?2 h^?1] at PB (P < 0.01). Our findings suggest that the soil temperature and moisture are important factors of GHG dynamics in forest soils with different fire history.     

Elevated atmospheric CO2 reduces CH4 and N2O emissions under two contrasting rice cultivars from a subtropical paddy field in China

Elevated CO₂(eCO₂) and rice cultivars can strongly alter CH₄ and N₂ O emissions from paddy fields.However,detailed information on how their interaction affects greenhouse gas fluxes in the field is still lacking.In this study,we investigated CH4 and N₂ O emissions and rice growth under two contrasting rice cultivars(the strongly and weakly responsive cultivars) in response to eCO₂,200 μmol mol^-1 higher than the ambient ...     

Elevated carbon dioxide level along with phosphorus application and cyanobacterial inoculation enhances nitrogen fixation and uptake in cowpea crop

Climate change, as a result of increase in the concentration of greenhouse gases, influences growth and productivity of leguminous crops. A study was carried out to analyse the impacts of elevated carbon dioxide (CO₂) and cyanobacterial inoculation on growth, N₂ fixation and N availability and uptake in cowpea crop, under different doses of phosphorus. Cowpea crop was grown under ambient (400 µmol mol^?1) and elevated (550 ± 20 µmol mol^?1) CO₂ levels using Free-Air Carbon dioxide Enrichment facility. Elevated CO₂ level increased chlorophyll content in leaves, improved nodulation and nitrogen fixation by the crop. Increase in P dose up to 16 mg kg^?1 soil enhanced nodule development and N₂ fixation under high CO₂ condition. Cyanobacterial inoculation increased nodule weight, leghaemoglobin content in nodules and total nitrogenase activity. Although nitrogen concentration in cowpea seeds decreased in high CO₂ treatment, higher N uptake was recorded. Under elevated CO₂ condition, cyanobacterial inoculation and higher P doses led to enhanced root growth and N₂ fixation and availability of soil nitrogen. The study illustrated the synergistic effect of high CO₂ and cyanobacterial inoculation in enhancing crop growth and availability of soil N, mediated by biological N₂ fixation in cowpea under different levels of P.     

Influence of elevated CO2 and GM barley on a soil mesofauna community in a mesocosm test system

We hypothesized that the combined effect of rising levels of atmospheric carbon dioxide (CO₂) and increasing use of genetically modified (GM) crops in agriculture may affect soil food-webs. So we designed a study for the assessment of the effects of elevated CO₂ (eCO₂) concentrations and GM barley on a soil-mesofauna community employing a 2nd tier mesocosm test system. The GM barley, Hordeum vulgare cv. Golden Promise, had a modified content of amino acids and it was compared with three non-GM barley cultivated varieties including the isogenic line. Our mesocosm experiment was conducted in a greenhouse at ambient (aCO₂) and eCO₂ (+80 ppm) levels and included a multispecies assemblage of Collembola, Acari and Enchytraeidae with either a GM or conventional spring barley varieties. To detect food-web changes we added dried maize leaves naturally enriched in δ¹³C and δ¹⁵N relative to the soil substrate. Soil, plants and animals were collected after five and eleven weeks. We found that the eCO₂ concentration did not affect the plant biomass, but the predatory mite and two collembolan species showed significantly lower abundances at eCO₂. The densities of three collembolan species (Folsomia fimetaria, Proisotoma minuta and juveniles of Mesaphorura macrochaeta) was significantly lower in the GM treatment compared to some of the non-GM varieties. F. fimetaria was less abundant in presence of GM barley compared to the cultivated barley variety “Netto” at both CO₂ levels, while the density of P. minuta was significantly reduced with the GM barley compared to variety “Netto” at aCO₂ and the isogenic variety at eCO₂. Maize litter acted as a food source for the community, as it was revealed by δ¹³C values in microarthropods. Microarthropod δ¹³C decreased over time, which indicates a diet change of the species towards carbon derived from barley, due to maize litter decomposition. The industrially produced CO₂ gas also had a role as an isotopic marker, as the different δ¹³C values were reflected in the barley and in the collembolan species. GM barley did not affect δ¹³C and δ¹⁵N values of soil animals indicating that the overall trophic structure of the mesofauna community was not changed compared to the non-GM cultivated varieties. The mesocosm methodology integrating stable isotope analysis demonstrates the potential of the multi-species mesocosm as a tool to detect and track changes in the soil trophic interactions in response to environmental pressures, climate and novel agricultural crops.     

Glomalin-related soil protein responses to elevated CO2 and nitrogen addition in a subtropical forest: Potential consequences for soil carbon accumulation

According to the economy theory, plants should preferentially allocate photosynthate to acquire below-ground resources under elevated atmospheric carbon dioxide (eCO₂) but decrease below-ground C allocation when nitrogen (N) is sufficient for plant growth. Arbuscular mycorrhizae (AM) represent a critical mechanism of below-ground nutrient acquisition for plants. The dynamics of arbuscular mycorrhizal fungi (AMF) could therefore reflect the response of plant C allocation under eCO₂ and N addition. We examined the responses of glomalin-related soil protein (GRSP) to eCO₂ (approximately 700 μmol mol⁻¹ CO₂) and/or N addition (100 kg N ha⁻¹ yr⁻¹ as NH₄NO₃) in a modeled subtropical forest to better understand its potential influence on soil C storage. We hypothesized that GRSP would increase under eCO₂ and decrease under N addition. Furthermore, the positive effects of eCO₂ on GRSP would be offset by extra N addition, and GRSP would remain unchanged under combined eCO₂ and N addition. Our results showed that the mean concentrations of easily extractable GRSP (EE-GRSP) and total GRSP (T-GRSP) were 0.35 ± 0.05 and 0.72 ± 0.13 mg C cm⁻³, respectively, which accounted for 2.76 ± 0.53% and 5.67 ± 0.92% of soil organic carbon (SOC) in the 0–10 cm soil layer. Elevated CO₂ significantly increased T-GRSP by 35.02% but decreased EE-GRSP by 5.09% in the top 10 cm soil layer. The opposite responses of T-GRSP and EE-GRSP to eCO₂ might result from an unchanged photosynthate investment to AMF with possible changes in their decomposition rates. The effect of N on GRSP was contrary to our hypothesis, i.e., there was a 1.72%–48.49% increase in T-GRSP and a slightly increase in EE-GRSP. Both EE-GRSP and T-GRSP concentrations increased under the combination of eCO₂ and N addition, which was inconsistent with our hypothesis. The significant increase of EE-GRSP under the combination of eCO₂ and N addition was partly caused by more rapid plant growth and reduced microbial diversity, and the marginal increase of T-GRSP indicated that the interaction between eCO₂ and N addition offset their independent effects. In addition, the relatively higher accumulation ratios of GRSP (22.6 ± 13.6%) compared with SOC (15.9 ± 9.4%) indicated that more rapid GRSP deposition in the soil might accelerate SOC accumulation under eCO₂ and N addition. Our results will improve the understanding of the functioning of GRSP in soil C sequestration under global environmental change scenarios.     

SOIL CO2 FLUX IN GRASSLAND,AFFORESTED LAND AND RECLAIMED COALMINE OVERBURDEN DUMPS: A CASE STUDY

The aim of this study was to measure the in situ soil CO₂ flux from grassland, afforested land and reclaimed coalmine overburden dumps by using the automated soil CO₂ flux system (LICOR‐8100® infrared gas analyzer, LICOR Inc., Lincoln, NE). The highest soil CO₂ flux was observed in natural grassland (11·16 µmol CO₂ m⁻²s⁻¹), whereas the flux was reduced by 38 and 59 per cent in mowed site and at 15‐cm depth, respectively. The flux from afforested area was found 5·70 µmol CO₂ m⁻²s⁻¹, which is 50 per cent lower than natural grassland. In the reclaimed coalmine overburden dumps, the average flux under tree plantation was found to be lowest in winter and summer (0·89–1·12 µmol CO₂ m⁻²s⁻¹) and highest during late monsoon (3–3·5 µmol CO₂ m⁻²s⁻¹). During late monsoon, the moisture content was found to be higher (6–7·5 per cent), which leads to higher microbial activity and decomposition. In the same area under grass cover, soil CO₂ flux was found to be higher (8·94 µmol CO₂ m⁻²s⁻¹) compared with tree plantation areas because of higher root respiration and microbial activity. The rate of CO₂ flux was found to be determined predominantly by soil moisture and soil temperature. Our study indicates that the forest ecosystem plays a crucial role in combating global warming than grassland; however, to reduce CO₂ flux from grassland, mowing is necessary. Copyright © 2012 John Wiley & Sons, Ltd.     

Fine Root Dynamics in Thinned and Limed Pitch Pine and Japanese Larch Plantations

ABSTRACT

To investigate fine root dynamics after thinning (50% of standing tree) and liming calcium magnesium carbonate[CaMg(CO₃)₂] 2 Mg ha^{? 1}, a 2-year study was performed in 40-year-old pitch pine (Pinus rigida Mill.) and 44-year-old Japanese larch (Larix leptolepis Gord.) plantations in central Korea. Mean total fine root mass (kg ha^{? 1}± SE) in the control, thinned, and limed plots were 1234 ± 32, 1346 ± 67, and 1134 ± 40 for the pitch pine plantation and 1655 ± 48, 1953 ± 58, and 1868 ± 70 for the Japanese larch plantation, respectively. Live fine root mass of pitch pine at 0-10 cm soil depth decreased after thinning and liming. In addition, liming significantly increased dead fine root mass of Japanese larch. Fine root production (kg ha^{? 1} yr^{? 1}± SE) in the control, thinned and limed plots was 1108 ± 148, 2077 ± 262, and 1686 ± 103 for the pitch pine plantation and 1762 ± 103, 1886 ± 277, and 2176 ± 271 for the Japanese larch plantation, respectively. Fine root turnover rates increased after liming for both plantations. Fine root nitrogen (N) and phosphorus (P) concentrations of Japanese larch (1.012% of N and 0.073% of P) were higher than those of pitch pine (0.809% of N and 0.046% of P) in the control. Also N and P inputs into soil through fine root turnover increased after treatments. Results indicated that comparing fine root dynamics among forest types and after forest management practices might influence differences in soil fertility and underground nutrient cycling.     

Carbon Dioxide Emission from Black Soil as Influenced by Land‐Use Change and Long‐Term Fertilization

Land‐use change and soil management play a vital role in influencing losses of soil carbon (C) by respiration. The aim of this experiment was to examine the impact of natural vegetation restoration and long‐term fertilization on the seasonal pattern of soil respiration and cumulative carbon dioxide (CO₂) emission from a black soil of northeast China. Soil respiration rate fluctuated greatly during the growing season in grassland (GL), ranging from 278 to 1030 mg CO₂ m^?2 h^?1 with an average of 606 mg CO₂ m^?2 h^?1. By contrast, soil CO₂ emission did not change in bareland (BL) as much as in GL. For cropland (CL), including three treatments [CK (no fertilizer application), nitrogen, phosphorus and potassium application (NPK), and NPK together with organic manure (OM)], soil CO₂ emission gradually increased with the growth of maize after seedling with an increasing order of CK < NPM < OM, reaching a maximum on 17 August and declining thereafter. A highly significant exponential correlation was observed between soil temperature and soil CO₂ emission for GL during the late growing season (from 3 August to 28 September) with Q₁₀ = 2.46, which accounted for approximately 75% of emission variability. However, no correlation was found between the two parameters for BL and CL. Seasonal CO₂ emission from rhizosphere soil changed in line with the overall soil respiration, which averaged 184, 407, and 584 mg CO₂ m^?2 h^?1, with peaks at 614, 1260, and 1770 mg CO₂ m^?2 h^?1 for CK, NPK, and OM, respectively. SOM‐derived CO₂ emission of root free‐soil, including basal soil respiration and plant residue–derived microbial decomposition, averaged 132, 132, and 136 mg CO₂ m^?2 h^?1, respectively, showing no difference for the three CL treatments. Cumulative soil CO₂ emissions decreased in the order OM > GL > NPK > CK > BL. The cumulative rhizosphere‐derived CO₂ emissions during the growing season of maize in cropland accounted for about 67, 74, and 80% of the overall CO₂ emissions for CK, NPK, and OM, respectively. Cumulative CO₂ emissions were found to significantly correlate with SOC stocks (r = 0.92, n = 5, P < 0.05) as well as with SOC concentration (r = 0.97, n = 5, P < 0.01). We concluded that natural vegetation restoration and long‐term application of organic manure substantially increased C sequestration into soil rather than C losses for the black soil. These results are of great significance to properly manage black soil as a large C pool in northeast China.     

Phosphorus fertilization of a grass-legume mixture: Effect on plant growth,nutrients acquisition and symbiotic associations with soil microorganisms

Adding P on Lotus tenuis and Festuca arundinacea, pure or mixed, on growth, nitrogen (N) and phosphorus (P) acquisition and associations with soil microorganisms was studied to investigate the establishment of Lotus for competing with Festuca. Triple-superphosphate was applied on a Typic Natraquoll where Lotus grows spontaneously. Biomass, N-P uptake, arbuscular mycorrhizal colonization and rhizobia nodulation were measured. Lotus achieved the highest biomass, N-P uptake in fertilized stands and Festuca the lowest in fertilized and non-fertilized stands. Mycorrhizal colonization decreased with P-fertilization in both plants. Rhizobia nodules in Lotus showed little changes with P-fertilization. In mixed fertilized-stands, Lotus promoted the growth, N-P uptake of Festuca. P-fertilization increases the ability of Festuca to compete with Lotus for available-P in soil. Lotus improves nutrient cycling, maintains high level of rhizobia nodules and arbuscular mycorrhizal colonization in roots. Adding P to limited N-P environments depress grasses growth to compete with legumes for resources.     

Effect of organic and inorganic sources of nutrients on soil microbial activity and soil organic carbon build-up under rice in west coast of India

The effect of medium-term (5 years) application of organic and inorganic sources of nutrients (as mineral or inorganic fertilizers) on soil organic carbon (SOC), SOC stock, carbon (C) build-up rate, microbial and enzyme activities in flooded rice soils was tested in west coast of India. Compared to the application of vermicompost, glyricidia (Glyricidia maculate) (fresh) and eupatorium (Chromolaena adenophorum) (fresh) and dhaincha (Sesbania rostrata) (fresh), the application of farmyard manure (FYM) and combined application of paddy straw (dry) and water hyacinth (PsWh) (fresh) improved the SOC content significantly (p < 0.05). The lowest (p < 0.05) SOC content (0.81%) was observed in untreated control. The highest (p < 0.05) SOC stock (23.7 Mg C ha^?1) was observed in FYM-treated plots followed by recommended dose of mineral fertilizer (RDF) (23.2 Mg C ha^?1) and it was lowest (16.5 Mg C ha^?1) in untreated control. Soil microbial biomass carbon (C_mb) (246 µg g^?1 soil) and C_mb/SOC (1.92%) were highest (p < 0.05) in FYM-treated plot. The highest (p < 0.05) value of metabolic quotient (qCO₂) was recorded under RDF (19.7 µg CO₂-C g^?1 C_mb h^?1) and untreated control (19.6 µg CO₂-C g^?1 C_mb h^?1). Application of organic and inorganic sources of nutrients impacted soil enzyme activities significantly (p < 0.05) with FYM causing highest dehydrogenase (20.5 µg TPF g^?1 day^?1), phosphatase (659 µg PNP g^?1 h^?1) and urease (0.29 µg urea g^?1 h^?1) activities. Application of organic source of nutrients especially FYM improved the microbial and enzyme activities in flooded and transplanted rice soils. Although the grain yield was higher with the application of RDF, but the use of FYM as an organic agricultural practice is more useful when efforts are intended to conserve more SOC and improved microbial activity.     

Methane uptake and nitrous oxide emission in Japanese forest soils and their relationship to soil and vegetation types

Abstract

To determine the means and variations in CH₄ uptake and N₂O emission in the dominant soil and vegetation types to enable estimation of annual gases fluxes in the forest land of Japan, we measured monthly fluxes of both gases using a closed-chamber technique at 26 sites throughout Japan over 2 years. No clear seasonal changes in CH₄ uptake rates were observed at most sites. N₂O emission was mostly low throughout the year, but was higher in summer at most sites. The annual mean rates of CH₄ uptake and N₂O emission (all sites combined) were 66 (2.9–175) µg CH₄-C m^?2 h^?1 and 1.88 (0.17–12.5) µg N₂O-N m^?2 h^?1, respectively. Annual changes in these fluxes over the 2 years were small. Significant differences in CH₄ uptake were found among soil types (P < 0.05). The mean CH₄ uptake rates (µg CH₄-C m^?2 h^?1) were as follows: Black soil (95 ± 39, mean ± standard deviation [SD]) > Brown forest soil (60 ± 27) ≥ other soils (20 ± 24). N₂O emission rates differed significantly among vegetation types (P < 0.05). The mean N₂O emission rates (µg N₂O-N m^?2 h^?1) were as follows: Japanese cedar (4.0 ± 2.3) ≥ Japanese cypress (2.6 ± 3.4) > hardwoods (0.8 ± 2.2) = other conifers (0.7 ± 1.4). The CH₄ uptake rates in Japanese temperate forests were relatively higher than those in Europe and the USA (11–43 µg CH₄-C m^?2 h^?1), and the N₂O emission rates in Japan were lower than those reported for temperate forests (0.23–252 µg N₂O-N m^?2 h^?1). Using land area data of vegetation cover and soil distribution, the amount of annual CH₄ uptake and N₂O emission in the Japanese forest land was estimated to be 124 Gg CH₄-C year^?1 with 39% uncertainty and 3.3 Gg N₂O-N year^?1 with 76% uncertainty, respectively.     

Carbon sequestration in forest soils: effects of soil type, atmospheric CO2 enrichment, and N deposition

Soil contains the major part of carbon in terrestrial ecosystems, but the response of this carbon to enriching the atmosphere in CO₂ and to increased N deposition is not completely understood. We studied the effects of CO₂ concentrations at 370 and 570 μmol CO₂ mol^?1 air and increased N deposition (7 against 0.7 g N m^?2 year^?1) on the dynamics of soil organic C in two types of forest soil in model ecosystems with spruce and beech established in large open‐top chambers containing an acidic loam and a calcareous sand. The added CO₂ was depleted in ¹³C and thus the net input of new C into soil organic carbon and the mineralization of native C could be quantified. Soil type was the greatest determining factor in carbon dynamics. After 4 years, the net input of new C in the acidic loam (670 ± 30 g C m^?2) exceeded that in the calcareous sand (340 ± 40 g C m^?2) although the soil produced less biomass. The mineralization of native organic C accounted for 700 ± 90 g C m^?2 in the acidic loam and for 2800 ± 170 g C m^?2 in the calcareous sand. Unfavourable conditions for mineralization and a greater physico‐chemical protection of C by clay and oxides in the acidic loam are probably the main reasons for these differences. The organic C content of the acidic loam was 230 g C m^?2 more under the large than under the small N treatment. As suggested by a negligible impact of N inputs on the fraction of new C in the acidic loam, this increase resulted mainly from a suppressed mineralization of native C. In the calcareous sand, N deposition did not influence C concentrations. The impacts of CO₂ enrichment on C concentrations were small. In the uppermost 10 cm of the acidic loam, larger CO₂ concentrations increased C contents by 50–170 g C m^?2. Below 10 cm depth in the acidic loam and at all soil depths in the calcareous sand, CO₂ concentrations had no significant impact on soil C concentrations. Up to 40% of the ‘new’ carbon of the acidic loam was found in the coarse sand fraction, which accounted for only 7% of the total soil volume. This suggests that a large part of the CO₂‐derived ‘new’ C was incorporated into the labile and easily mineralizable pool in the soil.     

Root and rhizomicrobial respiration: A review of approaches to estimate respiration by autotrophic and heterotrophic organisms in soil

Partitioning the root‐derived CO₂ efflux from soil (frequently termed rhizosphere respiration) into actual root respiration (RR, respiration by autotrophs) and rhizomicrobial respiration (RMR, respiration by heterotrophs) is crucial in determining the carbon (C) and energy balance of plants and soils. It is also essential in quantifying C sources for rhizosphere microorganisms and in estimation of the C contributing to turnover of soil organic matter (SOM), as well as in linking net ecosystem production (NEP) and net ecosystem exchange (NEE). Artificial‐environment studies such as hydroponics or sterile soils yield unrealistic C‐partitioning values and are unsuitable for predicting C flows under natural conditions. To date, several methods have been suggested to separate RR and RMR in nonsterile soils: 1) component integration, 2) substrate‐induced respiration, 3) respiration by excised roots, 4) comparison of root‐derived ¹⁴CO₂ with rhizomicrobial ¹⁴CO₂ after continuous labeling, 5) isotope dilution, 6) model‐rhizodeposition technique, 7) modeling of ¹⁴CO₂ efflux dynamics, 8) exudate elution, and 9) δ¹³C of CO₂ and microbial biomass. This review describes the basic principles and assumptions of these methods and compares the results obtained in the original papers and in studies designed to compare the methods. The component‐integration method leads to strong disturbance and non‐proportional increase of CO₂ efflux from different sources. Four of the methods (5 to 8) are based on the pulse labeling of shoots in a ¹⁴CO₂ atmosphere and subsequent monitoring of ¹⁴CO₂ efflux from the soil. The model‐rhizodeposition technique and exudate‐elution procedure strongly overestimate RR and underestimate RMR. Despite alternative assumptions, isotope dilution and modeling of ¹⁴CO₂‐efflux dynamics yield similar results. In crops and grasses (wheat, ryegrass, barley, buckwheat, maize, meadow fescue, prairie grasses), RR amounts on average to 48±5% and RMR to 52±5% of root‐derived CO₂. The method based on the ¹³C isotopic signature of CO₂ and microbial biomass is the most promising approach, especially when the plants are continuously labeled in ¹³CO₂ or ¹⁴CO₂ atmosphere. The “difference” methods, i.e., trenching, tree girdling, root‐exclusion techniques, etc., are not suitable for separating the respiration by autotrophic and heterotrophic organisms because the difference methods neglect the importance of microbial respiration of rhizodeposits.     

Elevated CO<Subscript>2</Subscript> alters the abundance but not the structure of diazotrophic community in the rhizosphere of soybean grown in a Mollisol

The effect of elevated CO₂ (eCO₂) on rhizospheric diazotrophic community in cropland has little been studied, although eCO₂ facilitates nodulation and N₂ fixation in legumes. In this study, four soybean cultivars (Xiaohuangjin, Suinong 8, Suinong 14, and Heinong 45) were grown in Mollisols for 65 days under ambient CO₂ (aCO₂) (390 ppm) or eCO₂ (550 ppm). Quantitative PCR and Illumina MiSeq sequencing targeting the nifH gene that reflects the composition of diazotrophic community were determined. Elevated CO₂ significantly increased the abundance of nifH gene copies in the rhizospheres of the Suinong 8 and Heinong 45 cultivars, but not in the Suinong 14 and Xiaohuangjin cultivars. The nifH abundance correlated negatively with nodule density (p?≤?0.01) but positively with nodule size (p?≤?0.01). Elevated CO₂ did not significantly alter the composition of diazotrophic community, nor shift dominant bacterial operational taxonomic units (OTUs). These results indicated that eCO₂ stimulated the growth but did not alter the community composition of diazotrophs in the rhizosphere of soybean, which depended on cultivar and might contribute to nodulation responses to eCO₂.     

水稻叶际细菌群对二氧化碳升高的不同响应特征

A vast number of microorganisms colonize the leaf surface of terrestrial plants, known as the phyllosphere, and these microorganisms are thought to be of critical importance in plant growth and health. However, the taxonomic identities and ecological functions of the microorganisms inhabiting the rice phyllosphere remain poorly understood. Using a massive, parallel pyrosequencing technique, we identified the phyllosphere bacterial taxa of four different rice varieties and investigated the microbial response to elevated CO2 （eCO2） in a rice field of a free-air CO2 enrichment （FACE） facility located in Jiangsu Province, China. The results showed that the dominant phylotype, the Enterobacteriaceae family of Gammaproteobacteria~ accounted for 70.6%-93.8% of the total bacterial communities in the rice phyllosphere. The dominant phylotype was stimulated by eCO2, with its relative abundance increasing from 70.6%-75.2% at ambient CO2 （aCO2） to 86.5%-93.8% at eCO2 in the phyllosphere of rice varieties IIYou084 （TY-084）, YangLiangYou6 （YLY-6）, and ZhenXian96 （ZX-96）. The rare phylotypes, including the bacterial taxa of Sphingobacteriaceae, Xanthomonadaceae, Oxalobacteraceae, Clostridiaceae, and Pseudomonadaceae, were suppressed and their relative abundance decreased from 13.4%-23.0% at aCO2 to 1.47% 6.11% at eGO2. Furthermore, the bacterial diversity indices decreased at eCO2 in the phyllosphere of the rice varieties TY-084, YLY-6, and ZX-96. In contrast, an opposite response pattern was observed for the rice variety of YangDao8 （YD-8）. In the phyllosphere of this variety, the relative abundance of the dominant phylotype, Enterobacteriaceae, decreased from 94.1% at aCO2 to 81.4% at eCO2, while that of the rare phylotypes increased from 3.37% to 6.59%. In addition, eCO2 appeared to stimulate bacterial diversity in the rice variety YD-8. Our results suggest that the phyllosphere microbial response to eCO2 might be relative abundance-dependent in paddy fields.     

Methane and nitrous oxide fluxes, and carbon dioxide production in boreal forest soil fertilized with wood ash and nitrogen

Wood ash has been used to alleviate nutrient deficiencies and acidification in boreal forest soils. However, ash and nitrogen (N) fertilization may affect microbial processes producing or consuming greenhouse gases: methane (CH₄), nitrous oxide (N₂O) and carbon dioxide (CO₂). Ash and N fertilization can stimulate nitrification and denitrification and, therefore, increase N₂O emission and suppress CH₄ uptake rate. Ash may also stimulate microbial respiration thereby enhancing CO₂ emission. The fluxes of CH₄, N₂O and CO₂ were measured in a boreal spruce forest soil treated with wood ash and/or N (ammonium nitrate) during three growing seasons. In addition to in situ measurements, CH₄ oxidation potential, CO₂ production, net nitrification and N₂O production were studied in laboratory incubations. The mean in situ N₂O emissions and in situ CO₂ production from the untreated, N, ash and ash + N treatments were not significantly different, ranging from 11 to 17 μg N₂O m^?2 h^?1 and from 533 to 611 mg CO₂ m^?2 h^?1. However, ash increased the CH₄ oxidation in a forest soil profile which could be seen both in the laboratory experiments and in the CH₄ uptake rates in situ. The mean in situ CH₄ uptake rate in the untreated, N, ash and ash + N plots were 153 ± 5, 123 ± 8, 188 ± 10 and 178 ± 18 μg m^?2 h^?1, respectively.