Plant-biochar interactions drive the negative priming of soil organic carbon in an annual ryegrass field system

There is a knowledge gap on biochar carbon (C) longevity and its priming effects on soil organic carbon (SOC) and recent root-derived C under field conditions. This knowledge would allow the potential of biochar in long-term soil C sequestration to be established. However, most studies on biochar C longevity and its priming effect have been undertaken in plant-free laboratory incubations.A 388 d field study was carried out in the presence of an annual ryegrass (C₃) growing on a rhodic ferralsol with established C₃/C₄ plant-derived SOC (δ¹³C: −20.2‰) in a subtropical climate. A ¹³C-depleted hardwood biochar (δ¹³C: −35.7‰, produced at 450 °C) was applied at 0 and 30 dry t ha⁻¹ and mixed into the top 100-mm soil profile (equivalent to 3% w/w). We report on the differentiation and quantification of root respiration and mineralisation of soil-C and biochar-C in the field. Periodic ¹³CO₂ pulse labelling was applied to enrich δ¹³C of root respiration during two separate winter campaigns (δ¹³C: 151.5–184.6‰) and one summer campaign (δ¹³C: 19.8–31.5‰). Combined soil plus root respiration was separated from leaf respiration using a novel in-field respiration collar. A two-pool isotope mixing model was applied to partition three C sources (i.e. root, biochar and soil). Three scenarios were used to assess the sensitivity associated with the C source partitioning in the planted systems: 1) extreme positive priming of recent SOC derived from the current ryegrass (C₃) pasture; 2) equivalent magnitude of priming of SOC and labile root C; and 3) extreme positive priming of the native C4-dominant SOC.We showed that biochar induced a significant negative priming of SOC in the presence of growing plants but no net priming was observed in the unplanted soil. We also demonstrated the importance of experimental timeframe in capturing the transient nature of biochar-induced priming, from positive (day 0–62) to negative (day 62–388). The presence/absence of plants had no impact on biochar-C mineralisation in this ferralsol during the measurement period. Based on a two-pool exponential model, the mean residence time (MRT) of biochar varied from 351 to 449 years in the intensive pasture system to 415–484 years in the unplanted soils.     

Short‐term sequestration of slurry‐derived carbon and nitrogen in temperate grassland soil as assessed by 13C and 15N natural abundance measurements

Land application of animal wastes from intensive grassland farming has caused growing environmental problems during the last decade. This study aimed to elucidate the short‐term sequestration of slurry‐derived C and N in a temperate grassland soil (Southwest England) using natural abundance ¹³C and ¹⁵N stable isotope techniques. Slurry was collected from cows fed either on perennial ryegrass (C3) or maize (C4) silages. 50 m³ ha^—1 of each of the obtained C3 or C4 slurries (δ¹³C = —30.7 and —21.3‰, δ¹⁵N = +12.2 and + 13.8 ‰, respectively) were applied to a C₃ soil with δ¹³C and δ¹⁵N values of —30.0 ± 0.2‰ and + 4.9 ± 0.3‰, respectively. Triplicate soil samples were taken from 0—2, 2—7.5, and 7.5—15 cm soil depth 90 and 10 days before, at 2 and 12 h, as well as at 1, 2, 4, 7, and 14 days after slurry application and analyzed for total C, N, δ¹³C, and δ¹⁵N. No significant differences in soil C and N content were observed following slurry application using conventional C and N analysis techniques. However, natural abundance ¹³C and ¹⁵N isotope analysis allowed for a sensitive temporal quantification of the slurry‐derived C and N sequestration in the grassland soil. Our results showed that within 12 hours more than one‐third of the applied slurry C was found in the uppermost soil layer (0—2 cm), decreasing to 18% after 2 days, but subsequently increasing to 36% after 2 weeks. The tentative estimate of slurry‐derived N in the soil suggested a decrease from 50% 2 hours after slurry application to only 26% after 2 weeks, assuming that the increase in δ¹⁵N of the slurry plots compared to the control is proportional to the amount of slurry‐incorporated N. We conclude that the natural abundance tracer technique can provide a rapid new clue to the fate of slurry in agricultural C and N budgets, which is important for environmental impacts, farm waste management, and climate change studies.     

Short-term effects of dairy slurry amendment on carbon sequestration and enzyme activities in a temperate grassland

Land application of animal wastes from intensive grassland farming has resulted in growing environmental problems relating to greenhouse gas emissions, ammonia volatilisation, and nitrate and phosphorus leaching into surface and groundwater. We examined the short-term effects of dairy slurry amendment on carbon sequestration and enzyme activities in a temperate grassland (Southwest England). Slurry was collected from cows fed either on perennial ryegrass (C₃) or maize (C₄) silages. Fifty m³ ha⁻¹ of each of the obtained C₃ or C₄ slurries (δ¹³C=−30.7 and −21.3‰, respectively) were applied to a C₃ pasture soil with δ¹³C of −30.0±0.2‰. We found that water soluble organic carbon (WSOC) content was two to three times higher in the slurry amended plots compared with the unamended control. No significant change in the soil microbial biomass (SMB) carbon content was observed in the four weeks (772 h) following slurry application. Natural abundance ¹³C isotope analysis suggested a rapid initial incorporation (>25% within 2 h of application) of slurry-derived C in the SMB-C and WSOC pools of the 0-2 cm layer. Linear relationships were found between slurry-derived C in the whole soil, SMB, and WSOC for the 0-2 cm depth in the soil. Applied slurry-derived C was sequestered in the SMB pool in two phases. The first phase (0-48 h) was dominated by the incorporation of labile slurry C from the liquid phase, whereas beyond 48 h slurry-derived C was mainly from less mobile particulate C. No significant differences between treatments were found for invertase and xylanase. Urease activity was always higher in slurry treatments. Cellobiohydrolase, β-N-acetyl-glucosamidase, β-glucosidase and acid phosphatase activities became significantly higher in slurry treatments after 336 h. However, the observed temporal changes in enzyme activities were not correlated with the amounts of slurry-C incorporated in the SMB and WSOC pool.     

Soil organic matter in soil depth profiles: Distinct carbon preferences of microbial groups during carbon transformation

This study investigates how carbon sources of soil microbial communities vary with soil depth. Microbial phospholipid fatty acids (PLFA) were extracted from 0–20, 20–40 and 40–60 cm depth intervals from agricultural soils and analysed for their stable carbon isotopes (δ¹³C values). The soils had been subjected to a vegetation change from C3 (δ¹³C≈?29.3‰) to C4 plants (δ¹³C≈?12.5‰) 40 years previously, which allowed us to trace the carbon flow from plant-derived input (litter, roots, and root exudates) into microbial PLFA. While bulk soil organic matter (SOM) reflected ≈12% of the C4-derived carbon in top soil (0–20 cm) and 3% in deeper soil (40–60 cm), the PLFA had a much higher contribution of C4 carbon of about 64% in 0–20 cm and 34% in 40–60 cm. This implies a much faster turnover time of carbon in the microbial biomass compared to bulk SOM. The isotopic signature of bulk SOM and PLFA from C4 cultivated soil decreases with increasing soil depth (?23.7‰ to ?25.0‰ for bulk SOM and ?18.3‰ to ?23.3‰ for PLFA), which demonstrates decreasing influence of the isotopic signature of the new C4 vegetation with soil depth. In terms of soil microbial carbon sources this clearly shows a high percentage of C4 labelled and thus young plant carbon as microbial carbon source in topsoils. With increasing soil depth this percentage decreases and SOM is increasingly used as microbial carbon source. Among all PLFA that were associated to different microbial groups it could be observed that (a) depended on availability, Gram-negative and Gram-positive bacteria prefer plant-derived carbon as carbon source, however, (b) Gram-positive bacteria use more SOM-derived carbon sources while Gram-negative bacteria use more plant biomass. This tendency was observed in all three-depth intervals. However, our results also show that microorganisms maintain their preferred carbon sources independent on soil depth with an isotopic shift of 3–4‰ from 0–20 to 40–60 cm soil depth.     

Formation and use of microbial residues after adding sugarcane sucrose to a heated soil devoid of soil organic matter

A 67-day incubation experiment was carried out with a soil initially devoid of any organic matter due to heating, which was amended with sugarcane sucrose (C₄-sucrose with a δ¹³C value of ?10.5‰), inorganic N and an inoculum for recolonisation and subsequently at day 33 with C₃-cellulose (δ¹³C value of ?23.4‰). In this soil, all organic matter is in the microbial biomass or in freshly formed residues, which makes it possible to analyse more clearly the role of microbial residues for decomposition of N-poor substrates. The average δ¹³C value over the whole incubation period was ?10.7‰ in soil total C in the treatments without C₃-cellulose addition. In the CO₂ evolved, the δ¹³C values decreased from ?13.4‰ to ?15.4‰ during incubation. In the microbial biomass, the δ¹³C values increased from ?11.5‰ to ?10.1‰ at days 33 and 38. At day 67, 36% of the C₄-sucrose was left in the treatment without a second amendment. The addition of C₃-cellulose resulted in a further 7% decrease, but 4% of the C₃-cellulose was lost during the second incubation period. Total microbial biomass C declined from 200 μg g^?1 soil at day 5 to 70 μg g^?1 soil at day 67. Fungal ergosterol increased to 1.5 μg g^?1 soil at day 12 and declined more or less linearly to 0.4 μg g^?1 soil at day 67. Bacterial muramic acid declined from a maximum of 35 μg g^?1 soil at day 5 to a constant level of around 16 μg g^?1 soil. Glucosamine showed a peak value at day 12. Galactosamine remained constant throughout the incubation. The fungal C/bacterial C ratio increased more or less linearly from 0.38 at day 5 to 1.1 at day 67 indicating a shift in the microbial community from bacteria to fungi during the incubation. The addition of C₃-cellulose led to a small increase in C₃-derived microbial biomass C, but to a strong increase in C₄-derived microbial biomass C. At days 45 and 67, the addition of N-free C₃-cellulose significantly decreased the C/N ratio of the microbial residues, suggesting that this fraction did not serve as an N-source, but as an energy source.     

Seasonal variations in natural 13C abundances in C3 and C4 plants collected in Thailand and the Philippines

Abstract

The natural ¹³C abundance (δ ¹³C) of plant leaves collected from fields in Thailand and the Philippines (Asian Monsoon tropics) was analyzed, and changes in the δ ¹³C values of C₃ and C₄ plants in wet and dry seasons were characterized. In Thailand, the δ ¹³C values of C₃ plants were ?29.2?±?1.04 (mean?±?standard deviation) ‰ in July and August (wet season) and ?28.6?±?1.05‰ in February and March (dry season): these values are not significantly different, whereas the values of C₄ plants were ?12.7?±?0.56‰ in the wet season and ?14.5?±?0.68‰ in the dry season (P?<?0.01, t-test). In the Philippines, where plants were collected only in October (late wet season), the δ ¹³C values of C₃ plants were ?29.5?±?1.28‰, whereas those of C₄ plants were ?12.6?±?1.11‰. These results suggest that under an Asian Monsoon climate, C₄ plants exhibit more negative δ ¹³C values in the dry season than in the wet season, whereas C₃ plants as a whole show no clear seasonal changes in δ ¹³C values.     

Long‐Term Changes in Soil Carbon Stocks in the Brazilian Cerrado Under Commercial Soybean

The net effect of agriculture on soil carbon is not yet fully understood. While a number of studies on shallow profiles have been published, evidence suggests that carbon stock changes occur in deeper layers. In this study we analyzed the effect of agriculture in the Cerrado soil C looking at changes in seven different profile depths from 0 to 100 cm in a commercial grain farm. We also used isotopic techniques to distinguish between the original Cerrado C₃ carbon and the C₄ carbon derived from the grasses used in agriculture. At 0–5 cm depth C stocks significantly decreased with cultivation time. The C stock did not change significantly when it was calculated using the 0–10, 0–20, 0–30, 0–50 or 0–75 cm profile (p > 0·05) but increased with cultivation time when the profile considered was 0–100 cm (p < 0·05). A two‐source isotope model revealed that there was a significant increase in carbon derived from C₄ grasses for all depths with cultivation time. Annual carbon sequestration rates for the upper 100 cm of soil were 1·1 Mg C ha⁻¹ year⁻¹ for total carbon and 0·8 Mg C₄ C ha⁻¹ year⁻¹ for C₄ carbon. The oldest area, with 23 years of cultivation, had a soil C stock increase compared to the native Cerrado soil of 17·6%. These findings suggest that commercial grain farms practices may increase soil C stock compared to native Cerrado soil, if a more complete soil profile down to 100 cm is used to assess C stocks. Copyright © 2015 John Wiley & Sons, Ltd.     

Isotopic discrimination during long-term decomposition in an arid land ecosystem

Discrimination in carbon and nitrogen isotopes of decomposing plant litter in the northern Chihuahuan Desert was determined for a 5-year period. Factors influencing isotopic change were assessed from inter-species comparisons of litter chemistry, mass loss patterns, and isotope values of associated soil. Average δ¹⁵N_litter values of buried roots increased 1.2 and 2.6‰ for Big Blue Stem (Schizachyrium gerardi, grass) and Varital (Drypetes glauca, hardwood) during the study, respectively. Small but inconsistent variations were observed for Slash Pine (Pinus elliotii, conifer) roots. Average δ¹⁵N values of wooden dowels from Ramin (Gonystlylus bancanus, hardwood) increased ca. 2.0‰ during years 1–4, and then decreased slightly during year 5. Changes in δ¹⁵N_litter were independent of N content, and may reflect microbial fractionation or preferential retention of ¹⁵N enriched substrates. Surprisingly, there was no clear relationship between litter N dynamics and C/N ratios. There were no discernable changes in δ¹³C_litter values for Gonystlylus bancanus and Pinus elliotii. Average δ¹³C_litter values for Schizachyrium gerardi decreased ∼2.0‰ during years 0–2 and then increased slightly. In contrast, average δ¹³C_litter values for Drypetes glauca increased ∼0.5‰ from years 0–1 then remained relatively constant until decreasing slightly in year 5. δ¹³C_litter discrimination may have been masked by interfering δ¹³C fractionations or feedbacks between decomposers and litter chemistry. Our data indicate that isotopic discrimination is characteristic of early litter decay stages. These results may highlight aspects of isotope discrimination and nutrient cycling unique to arid land environments. Additional studies will be needed to confirm this.     

Potential of mine land reclamation for soil organic carbon sequestration in Ohio

Soils are an effective sink for carbon storage and immobilization through biomass productivity and enhancement of soil organic carbon (SOC) pool. The SOC sink capacity depends on land use and management. Degraded lands lose large amounts of C through SOC decomposition, erosion, and leaching. Thus, restoration of disturbed and degraded mine lands can lead to increase in biomass productivity, improved soil quality and SOC enhancement and sequestration. Reclamation of mined lands is an aggrading process and offers significant potential to sequester C. A chronosequence study consisting of 0‐, 5‐, 10‐, 15‐, 20‐ and 25‐year‐old reclaimed mine soils in Ohio was initiated to assess the rate of C sequestration by pasture and forest establishment. Undisturbed pasture and forest were used as controls. The SOC pool of reclaimed pasture sites increased from 15·3 Mg ha⁻¹ to 44·4 Mg ha⁻¹ for 0–15 cm depth and from 10·8 Mg ha⁻¹ to 18·3 Mg ha⁻¹ for 15–30 cm depth over the period of 25 years. The SOC pool of reclaimed forest sites increased from 12·7 Mg ha⁻¹ to 45·3 Mg ha⁻¹ for 0–15 cm depth and from 9·1 Mg ha⁻¹ to 13·6 Mg ha⁻¹ for 15–30 cm depth over the same time period. The SOC pool of the pasture site stabilized earlier than that of the forest site which had not yet attained equilibrium. The SOC sequestered in 0–30 cm depth over 25 years was 36·7 Mg ha⁻¹ for pasture and 37·1 Mg ha⁻¹ for forest. Copyright © 2000 John Wiley & Sons, Ltd.     

The role of biological activity (roots,earthworms) in medium-term C dynamics in vertisol under a Digitaria decumbens (Gramineae) pasture

The natural abundance of ¹³C was used to estimate the turnover of the soil organic matter in a vertisol re-grassed with Digitaria decumbens (C4 plant) following intensive market gardening (C3 plants). In addition, the experimental design allowed us to determine the respective roles of roots and earthworms (Polypheretima elongata) in soil C stock restoration in D. decumbens pasture.The C stock increased from 31 to 37 Mg C ha⁻¹ in 5 years and the δ¹³C increased from −18.1‰ in market gardening soil to −15.5‰ in the 5-year-old pasture soil in the upper 20 cm. Below the 20 cm soil layer, the C stock and the δ¹³C did not change significantly in 5 years. The net gain of 6 Mg C ha⁻¹ was the balance of a loss of 5 Mg C ha⁻¹ derived from market gardening and a gain of 11 Mg C ha⁻¹ derived from D. decumbens. Effects of earthworms on the C dynamics were not discernible.     

Effects of part and whole straw returning on soil carbon sequestration in C3–C4 rotation cropland

Long‐term no‐tillage management and crop residue amendments to soil were identified as an effective measure to increase soil organic carbon (SOC). The SOC content, SOC stock (SOCs), soil carbon sequestration rate (CSR), and carbon pool management index (CPMI) were measured. A stable isotopic approach was used to evaluate the contributions of wheat and maize residues to SOC at a long‐term experimental site. We hypothesized that under no‐tillage conditions, straw retention quantity would affect soil carbon sequestration differently in surface and deep soil, and the contribution of C3 and C4 crops to soil carbon sequestration would be different. This study involved four maize straw returning treatments, which included no maize straw returning (NT‐0), 0.5 m (from the soil surface) maize straw returning (NT‐0.5), 1 m maize straw returning (NT‐1), and whole maize straw returning (NT‐W). The results showed that in the 0–20 cm soil layer, the SOC content, SOCs, CSR and CPMI of the NT‐W were highest after 14 years of no‐tillage management, and there were obvious differences among the four treatments. However, the SOC, SOCs, and CSR of the NT‐0.5 and NT‐W were the highest and lowest in 20–100 cm, respectively. The value of δ¹³C showed an obviously vertical variability that ranged from –22.01‰ (NT‐1) in the 0–20 cm layer to –18.27‰ (NT‐0.5) in the 60–80 cm layer, with enriched δ¹³C in the 60–80 cm (NT‐0.5 and NT‐1) and 80–100 cm (NT‐0 and NT‐W) layers. The contributions of the wheat and maize‐derived SOC of the NT‐0.5, NT‐1 and NT‐W increased by 11.4, 29.5 and 56.3% and by 10.7, 15.1 and 40.1%, relative to those in the NT‐0 treatment in the 0–20 cm soil layer, respectively. In conclusion, there was no apparent difference in total SOC sequestration between the NT‐0.5, NT‐1, and NT‐W treatments in the 0–100 cm soil layer. The contribution of wheat‐derived SOC was higher than that of maize‐derived SOC.     

Influence of land use (savanna,pasture, Eucalyptus plantations) on soil carbon and nitrogen stocks in Brazil

In Brazil, most Eucalyptus stands have been planted on Cerrado (shrubby savanna) or on Cerrado converted into pasture. Case studies are needed to assess the effect of such land use changes on soil fertility and C sequestration. In this study, the influence of Cerrado land development (pasture and Eucalyptus plantations) on soil organic carbon (SOC) and nitrogen (SON) stocks were quantified in southern Brazil. Two contrasted silvicultural practices were also compared: 60 years of short‐rotation silviculture (EUC_SR) versus 60 years of continuous growth (EUC_HF). C and N soil concentrations and bulk densities were measured and modelled for each vegetation type, and SOC and SON stocks were calculated down to a depth of 1 m by a continuous function. Changes in SOC and SON stocks mainly occurred in the forest floor (no litter in pasture and up to 0.87 kg C m^?2 and 0.01 kg N m^?2 in EUC_SR) and upper soil horizons. C and N stocks and their confidence intervals were greatly influenced by the methodology used to compute these layers. C/N ratio and ¹³C analysis showed that down to a depth of 30 cm, the Cerrado organic matter was replaced by organic matter from newly introduced vegetation by as much as 75–100% for pasture and about 50% for EUC_HF, poorer in N for Eucalyptus stands (C/N larger than 18 for Eucalyptus stands). Under pasture, 0–30 cm SON stocks (0.25 kg N m^?2) were between 10 and 20% greater than those of the Cerrado (0.21 kg N m^?2), partly due to soil compaction (limit bulk density at soil surface from 1.23 for the Cerrado to 1.34 for pasture). Land development on the Cerrado increased SOC stocks in the 0–30 cm layer by between 15 and 25% (from 2.99 (Cerrado) to 3.86 (EUC_SR) kg C m^?2). When including litter layers, total 0–30 cm carbon stocks increased by 35% for EUC_HF (4.50 kg C m^?2) and 53% for EUC_SR (5.08 kg C m^?2), compared with the Cerrado (3.28 kg C m^?2), independently of soil compaction.     

Impact of litter quality on mineralization processes in managed and abandoned pasture soils in Southern Ecuador

Tropical regions are currently undergoing remarkable rates of land use change accompanied by altered litter inputs to soil. In vast areas of Southern Ecuador forests are clear cut and converted for use as cattle pastures. Frequently these pasture sites are invaded by bracken fern, when bracken becomes dominant pasture productivity decreases and the sites are abandoned. In the present study implications of invasive bracken on soil biogeochemical properties were investigated. Soil samples (0-5 cm) were taken from an active pasture with Setaria sphacelata as predominant grass and from an abandoned pasture overgrown by bracken. Grass (C₄ plant) and bracken (C₃ plant) litter, differing in C:N ratio (33 and 77, respectively) and lignin content (Klason-lignin: 18% and 45%, respectively), were incubated in soils of their corresponding sites and vice versa for 28 days at 22 °C. Unamended microcosms containing only the respective soil or litter were taken as controls. During incubation the amount of CO₂ and its δ¹³C-signature were determined at different time intervals. Additionally, the soil microbial community structure (PLFA-analysis) as well as the concentrations of KCl-extractable C and N were monitored. The comparison between the control soils of active and abandoned pasture sites showed that the massive displacement of Setaria-grass by bracken after pasture abandonment was characterized by decreased pH values accompanied by decreased amounts of readily available organic carbon and nitrogen, a lower microbial biomass and decreased activity as well as a higher relative abundance of actinomycetes. The δ¹³C-signature of CO₂ indicated a preferential mineralization of grass-derived organic carbon in pasture control soils. In soils amended with grass litter the mineralization of soil organic matter was retarded (negative priming effect) and also a preferential utilization of easily available organic substances derived from the grass litter was evident. Compared to the other treatments, the pasture soil amended with grass litter showed an opposite shift in the microbial community structure towards a lower relative abundance of fungi. After addition of bracken litter to the abandoned pasture soil a positive priming effect seemed to be supported by an N limitation at the end of incubation. This was accompanied by an increase in the ratio of Gram-positive to Gram-negative bacterial PLFA marker. The differences in litter quality between grass and bracken are important triggers of changes in soil biogeochemical and soil microbial properties after land use conversion.     

Soil carbon turnover and sequestration in native subtropical tree plantations

Approximately 30% of global soil organic carbon (SOC) is stored in subtropical and tropical ecosystems but it is being rapidly lost due to continuous deforestation. Tree plantations are advocated as a C sink, however, little is known about rates of C turnover and sequestration into soil organic matter under subtropical and tropical tree plantations. We studied changes in SOC in a chronosequence of hoop pine (Araucaria cunninghamii) plantations established on former rainforest sites in seasonally dry subtropical Australia. SOC, δ¹³C, and light fraction organic C (LF C<1.6 g cm⁻³) were determined in plantations, secondary rainforest and pasture. We calculated loss of rainforest SOC after clearing for pasture using an isotope mixing model, and used the decay rate of rainforest-derived C to predict input of hoop pine-derived C into the soil. Total SOC stocks to 100 cm depth were significantly (P<0.01) higher under rainforest (241 t ha⁻¹) and pasture (254 t ha⁻¹) compared to hoop pine (176-211 t ha⁻¹). We calculated that SOC derived from hoop pine inputs ranged from 32% (25 year plantation) to 61% (63 year plantation) of total SOC in the 0-30 cm soil layer, but below 30 cm all C originated from rainforest. These results were compared to simulations made by the Century soil organic matter model. The Century model simulations showed that lower C stocks under hoop pine plantations were due to reduced C inputs to the slow turnover C pool, such that this pool only recovers to within 45% of the original rainforest C pool after 63 years. This may indicate differences in soil C stabilization mechanisms under hoop pine plantations compared with rainforest and pasture. These results demonstrate that subtropical hoop pine plantations do not rapidly sequester SOC into long-term storage pools, and that alternative plantation systems may need to be investigated to achieve greater soil C sequestration.     

Short-term C4 plant Spartina alterniflora invasions change the soil carbon in C3 plant-dominated tidal wetlands on a growing estuarine Island

Spartina alterniflora is an invasive C₄ perennial grass, native to North America, and has spread rapidly along the east coast of China since its introduction in 1979. Since its intentional introduction to the Jiuduansha Island in the Yangtze River estuary, Spartina alterniflora community has become one of the dominant vegetation types. We investigated the soil carbon in the Spartina alterniflora community and compared it with that of the native C₃Scirpus mariqueter community by measuring total soil carbon (TC), soil organic carbon (SOC), total soil nitrogen (TN), and the stable carbon isotope composition (δ¹³C) of various fractions. TC and SOC were significantly higher in Spartina alterniflora in the top 60 cm of soil. However, there was no significant difference in soil inorganic carbon (IC) between the two communities. Stable carbon isotopic analysis suggests that the fraction of SOC pool contributed by Spartina alterniflora varied from 0.90% to 10.64% at a soil depth of 0-100 cm with a greater percentage between 20 and 40 cm deep soils. The δ¹³C decreased with increasing soil depth in both communities, but the difference in δ¹³C among layers of the top 60 cm soil was significant (p<0.05), while that for the deeper soil layers (>60 cm) was not detected statistically. The changes in δ¹³C with depth appeared to be associated with the small contribution of residues from Spartina alterniflora at greater soil depth that was directly related to the vertical root distribution of the species.     

Phosphorus‐31–nuclear magnetic–resonance spectroscopy to trace organic dung phosphorus in a temperate grassland soil

Cattle dung contributes to hot‐spot inputs of nutrients to grassland systems, but not much is known about its organic P (P_o) composition and fate in the grassland soils. We used ³¹Phosphorus (P)–Nuclear Magnetic–Resonance (NMR) spectroscopy of alkaline soil extracts to examine potentials for tracing of different functional P_o forms into a temperate grassland soil amended with dung. The proportion of monoester, DNA‐diester, and phospholipid+teichoic acid P were comparable in dung extracts, but the soil was dominated by monoester P. The temporal trends in the DNA‐diester P–to–monoester P (D_DNAM) and diester P–to–monoester P (DM) ratio of dung, native soil, and soil amended with dung were monitored in the 70 d field experiment. The D_DNAM and DM ratio in the dung‐amended soil (0–1 and 1–5 cm depth) were always intermediate between the dung and (unamended) control soil. Clearly, extracted soil P was a mixture of incorporated dung‐derived P and native soil P. The dung‐P contribution in the 0–1 cm samples peaked at 47% of the total extracted P at day 70 and at 15% after 42 d in the 1–5 cm soil depth (based on the DM ratio). The proportions of dung‐derived P and C in the soil were positively correlated with: 1) topsoil, using the D_DNAM ratio (r² = 0.975), and 2) top‐ and subsoil, using the DM ratio (r² = 0.656). We concluded that our D_DNAM and DM‐P ratios approach (obtained from solution‐³¹P NMR) did trace successfully the short‐term dynamics and fate of dung P_o in soil. It indicated that dung‐derived P_o varied as rapidly in soil as the dung‐derived C.     

Effect of tillage on soil organic carbon mineralization estimated from 13C abundance in maize fields

Three methods of cultivation, conventional tillage (CT), superficial tillage (ST) and no-tillage (NT), were applied for 17 years to continuous maize. Their effect on soil organic carbon content was investigated through measurements of carbon and ¹³C/¹²C ratios, using the natural difference in ¹³C content between C₃ plants and maize, which is a C₄ plant. Because the soil had carried C₃ plants before the experiment started, the organic carbon remaining from that time (C₃,-carbon), was distinguished from the carbon derived from maize. Comparison between continuous wheat and maize plots showed that organic matter from both maize and wheat decomposed without significant ¹³C enrichment, whereas older C₃-carbon was enriched by 1.5% compared to that of fresh wheat material. From the initial 3.6 kg C m^?2 in the topsoil (0–30 cm), 0.95 were mineralized in the CT treatment, but only 0.45 in NT. The mineralization was the same in the tilled layer of ST as in CT. The CT treatment accumulated 1.1 kg C m^?2 of maize-derived carbon and the NT treatment 0.8. The mineralization of initial C₃-carbon was the same at all depths between 0 and 30 cm in the NT treatment; 75% of the carbon derived from maize was found in the 0–5 cm layer.     

Organic matter turnover in soil physical fractions following woody plant invasion of grassland: Evidence from natural C and N

Soil physical structure causes differential accessibility of soil organic carbon (SOC) to decomposer organisms and is an important determinant of SOC storage and turnover. Techniques for physical fractionation of soil organic matter in conjunction with isotopic analyses (δ¹³C, δ¹⁵N) of those soil fractions have been used previously to (a) determine where organic C is stored relative to aggregate structure, (b) identify sources of SOC, (c) quantify turnover rates of SOC in specific soil fractions, and (d) evaluate organic matter quality. We used these two complementary approaches to characterize soil C storage and dynamics in the Rio Grande Plains of southern Texas where C₃ trees/shrubs (δ¹³C=−27‰) have largely replaced C₄ grasslands (δ¹³C=−14‰) over the past 100-200 years. Using a chronosequence approach, soils were collected from remnant grasslands (Time 0) and from woody plant stands ranging in age from 10 to 130 years. We separated soil organic matter into specific size/density fractions and determined their C and N concentrations and natural δ¹³C and δ¹⁵N values. Mean residence times (MRTs) of soil fractions were calculated based on changes in their δ¹³C with time after woody encroachment. The shortest MRTs (average=30 years) were associated with all particulate organic matter (POM) fractions not protected within aggregates. Fine POM (53-250 μm) within macro- and microaggregates was relatively more protected from decay, with an average MRT of 60 years. All silt+clay fractions had the longest MRTs (average=360 years) regardless of whether they were found inside or outside of aggregate structure. δ¹⁵N values of soil physical fractions were positively correlated with MRTs of the same fractions, suggesting that higher δ¹⁵N values reflect an increased degree of humification. Increased soil C and N pools in wooded areas were due to both the retention of older C₄-derived organic matter by protection within microaggregates and association with silt+clay, and the accumulation of new C₃-derived organic matter in macroaggregates and POM fractions.     

Savanna-derived organic matter remaining in arable soils of the South African Highveld long-term mixed cropping: Evidence from C and N natural abundance

Sustainable agriculture requires the formation of new humus from the crops. We utilized ¹³C and ¹⁵N signatures of soil organic matter to assess how rapidly wheat/maize cropping contributed to the humus formation in coarse-textured savanna soils of the South African Highveld. Composite samples were taken from the top 20 cm of soils (Plinthustalfs) cropped for lengths of time varying from 0 to 98 years, after conversion from native grassland savanna (C4). We performed natural ¹³C and ¹⁵N abundance measurements on bulk and particle-size fractions. The bulk soil δ¹³C values steadily decreased from −14.6 in (C4 dominated) grassland to −16.5‰ after 90 years of arable cropping. This δ¹³C shift was attributable to increasing replacement of savanna-derived C by wheat crop (C3) C which dominated over maize (C4) inputs. After calculating the annual C input from the crop yields and the output from literature data, by using a stepwise C replacement model, we were able to correct the soil δ¹³C data for the irregular maize inputs for a period of about one century. Within 90 years of cropping 41-89% of the remaining soil organic matter was crop-derived in the three studied agroecosystems. The surface soil C stocks after 90 years of the wheat/maize crop rotation could accurately be described with the Rothamsted Carbon Model, but modelled C inputs to the soil were very low. The coarse sand fraction reflected temporal fluctuations in ¹³C of the last C₃ or C₄ cropping and the silt fraction evidenced selective erosion loss of old savanna-derived C. Bulk soil ¹⁵N did not change with increasing cropping length. Decreasing δ¹⁵N values caused by fertilizer N inputs with prolonged arable cropping were only detected for the coarse sand fraction. This indicated that the present N fertilization was not retained in stable soil C pool. Clearly, conventional cropping practices on the South African highlands neither contribute to the preservation of old savanna C and N, nor the effective humus reformation by the crops.     

Field-applying an inexpensive, 13C-depleted,labile carbon source to study in situ fate and short-term effects on soils

Background

Labile carbon (C_labile) limits soil microbial growth and is critical for soil functions like nitrogen (N) immobilization. Most experiments evaluating C_labile additions use laboratory incubations. We need to field-apply C_labile to fully understand its fate and effects on soils, especially at depth, but high cost and logistical difficulties hinder this approach.

Aims

Here, we evaluated the impact of adding an in situ pulse of an inexpensive and ¹³C-depleted source of C_labile—crude glycerol carbon (C_glyc), a by-product from biodiesel production—to agricultural soils under typical crop rotations in Iowa, USA.

Methods

We broadcast-applied C_glyc at three rates (0, 216, and 866 kg C ha⁻¹) in autumn after soybean harvest, tracked its fate, and measured its impact on soil C and N dynamics to four depths (0–5, 5–15, 15–30, and 30–45 cm). Nineteen days later, we measured C_glyc in microbial biomass carbon (MBC), salt-extractable organic C, and potentially mineralizable C pools. We paired these measurements with nitrate N (NO₃⁻–N) and potential net N mineralization to examine short-term effects on N cycling.

Results

C_glyc was found to at least 45-cm depth with the majority in MBC (18%–23% of total C_glyc added). The δ¹³C values of the other measured C pools were too variable to accurately track the C_labile fate. NO₃⁻–N was decreased by 13%–57% with the 216 and 866 kg C ha⁻¹ rates, respectively, and was strongly related to greater microbial uptake of C_glyc (i.e., immobilization via microbial biomass). Crude glycerol application had minor effects on soil pH—the greatest rate decreased pH 0.18 units compared to the control.

Conclusions

Overall, glycerol is an inexpensive and effective way to measure in situ, C_labile dynamics with soil depth—analogous to how mobile, dissolved organic C might behave in soils—and can be applied to rapidly immobilize NO₃⁻–N.