Phosphorus Use Efficiency of Wheat Genotypes Grown in Calcareous Soils

ABSTRACT

Phosphorus (P) deficiency and low P-use efficiency are induced by soil properties, especially in calcareous soils, which are dominant in semi-arid regions of the world such as the Mediterranean region. Alternative approaches to P fertilization involve exploiting plant genetics in order to achieve more efficient use of P by the growing crop. Accordingly, in a greenhouse pot experiment, we evaluated P-efficiency in wheat genotypes grown in typical calcareous soils in southern Turkey. Ten common local genotypes were grown in six soil series for eight weeks using five P application rates (0, 25, 50, 100, and 200 mg P kg^?1). Dry matter (DM) yield and P content were significantly increased by increasing P rates, with significant differences between soils. Some genotypes performed better under P stress because of better P utilization efficiency. Shoot DM was the most sensitive indicator of genetic variability under P-deficient conditions. Genotypes classified as efficient-responsive (Adana-99, 1014, Golia, Balatilla) had above average DM yield when P was not added, and responded well to P applications; efficient-non-responsive genotypes (Firat-93, Seri-82, Genc-99, Panda) had below average DM yield, but responded to P applications; inefficient-non-responsive genotypes (Fuat Bey and Ceyhan-99) had below average DM yield; and no genotypes were in the inefficient responsive category. Such P response categorization is needed for better breeding programs for nutrient-use efficiency. The study may aid in selecting P-efficient genotypes in low-P soils, especially where little P is used. The use of P-efficient genotypes should be seen as complement to, rather than a substitute for, chemical P fertilization depending on local conditions.     

Root Morphology,Proton Release,and Carboxylate Exudation in Lupin in Response to Phosphorus Deficiency

Narrow-leafed lupin (Lupinus angustifolius L.) is widely planted in infertile acidic soils where phosphorus (P) deficiency is one of the major limiting factors for plant growth. A hydroponic experiment was conducted to examine the morphological and physiological responses of roots of narrow-leafed lupin in response to altered P supply at 0, 1, 10, 25 or 75 μ M P as monopotassium phosphate (KH₂PO₄). Low P (P₀ and P₁) significantly decreased the plant biomass, but the supply of 10 μ M P was sufficient to produce similar plant biomass as the maximal P supply (P₇₅), indicating an efficient P acquisition by narrow-leafed lupin. Phosphorus deficiency did not enhance rates of carboxylate exudation and proton release by plant roots, indicating that carboxylate exudation and proton release are not the mechanisms for efficient P acquisition. In contrast, low P supply evidently modified the root morphology by increasing the primary root elongation, and developing a large number of cluster-like first-order lateral roots with dense root hairs, thus allowing efficient P acquisition by narrow-leafed lupin under low P supply.     

Assessing phosphorus efficiency and tolerance in maize genotypes with contrasting root systems at the early growth stage using the semi-hydroponic phenotyping system

Background

Development of an evaluation tool to determine genotypic variation in phosphorus (P) utilization efficiency is essential to ensure crop productivity and farmers’ income under low P environments.

Aims

This study aimed to develop an evaluation tool to determine genotypic variation in low-P tolerance and P use efficiency under low P environments.

Methods

Root response and P efficiency traits in 20 maize genotypes with contrasting root systems were assessed 32 days after transplanting into the semi-hydroponic root phenotyping system under low P (10 µM) or optimal P (200 µM) supply.

Results

Compared to optimal P, low P supply increased root-to-shoot biomass ratio by 48.7% (shoot dry weight decreased by 20.0% and root dry weight increased by 20.6%). Low P supply increased total root length by 17.8% but decreased primary root depth, with no significant change in lateral root number across all genotypes. Low P stress enhanced P utilization efficiency. Based on genotypic variation and correlations among the 17 measured plant traits in response to low P stress, nine traits were converted to low-P tolerance coefficients (LPTC), compressed by principal component analysis. The three principal component scores were extracted for hierarchical cluster analysis and classified the 20 genotypes into three groups with different P efficiency, including two P-efficient genotypes and nine P-inefficient genotypes.

Conclusions

The study demonstrated genotypic variation in response to low P stress. The P-efficient genotypes with higher LPTC values better adapted to low P environments by adjusting root architecture and re-distributing P and biomass in plant organs. The systematic cluster analysis using selected traits and their LPTC values can be used as an evaluation tool in assessing P efficiency among the genotypes.     

Identification of genomic regions associated with low phosphorus tolerance in japonica rice (Oryza sativa L.) by QTL-Seq

ABSTRACT

Phosphorus (P) is a major nutrient supporting rice productivity. Improving low-P tolerance of rice is expected to reduce dependence on P fertilizer, thereby reducing rice production costs and environmental impacts. This report describes the mapping of quantitative trait loci (QTL) associated with P deficiency tolerance in japonica rice. An F5 population derived from a cross of the low-P tolerant cultivar Akamai (Yamagata) and the sensitive cultivar Koshihikari was evaluated for shoot growth under low-P conditions. Then single nucleotide polymorphism (SNP) profiles of the low-P tolerant and sensitive bulks were compared on a genome-wide scale by QTL-Seq, a rapid QTL mapping method using next-generation sequencing technology. Results show a major QTL associated with low-P tolerance located on the long arm of chromosome 12. It has been named QTL for low-P tolerance 1 or qLPT1. SNPs were detected in 45 genes of qLPT1 region and the 5 genes were harboring synonymous SNPs, although none of them had been reported as involved in low-P tolerance. This result implies that the novel gene responsible for low-P tolerance exists in qLPT1. This study will contribute to the elucidation of mechanisms underlying low-P tolerance of Akamai and will facilitate the breeding of rice with low-P tolerance.     

Proton release by nodulated roots varies among common bean genotypes (Phaseolus vulgaris) under phosphorus deficiency

Responses of proton release to phosphorus (P) availability by nodulated roots of common bean (Phaseolus vulgaris L.) were investigated for lines BAT 477 and CocoT, inoculated with Rhizobium tropici CIAT 899 in hydroaeroponic culture under glasshouse conditions. Phosphorus was supplied as KH₂PO₄ at 15 and 60 μmol plant^–1 week^–1 (15P and 60P). Proton release was higher for BAT 477 than for CocoT under both P supplies. However, it was higher for 60P than 15P, whatever the line. The ratio of proton release per unit biomass of nodulated root was higher for BAT 477 than for CocoT, independent of P deficiency. Proton release was correlated with the nodulated‐root respiration for both genotypes and with the nodule respiration linked with nitrogen fixation for CocoT. Thus, the nodulation was more limited by 15P than root and shoot growth and more in CocoT than in BAT 477. It is concluded that independent of symbiotic N₂ fixation, proton release was higher in BAT 477 than in CocoT and that the nodulated legume releases a substantial amount of protons into its rhizosphere that is correlated with its nitrogen fixation that eventually depends upon the nodule permeability to O₂ diffusion.     

Characterization and selection for phosphorus deficiency tolerance in 99 spring wheat genotypes in Montana

Phosphorus (P) deficiency in soil is a common spring wheat production-limiting factor in Montana. In a pot experiment, three groups of spring wheat genotypes based on source (association mapping, 2016 off-station, and nested association mapping) were grown in 5 (P5) and 30 (P30) mg P kg^?1 potting mix conditions and screened for P deficiency tolerance. Plant height, tiller and head number, grain yields per pot measured were significantly different between P5 and P30 conditions (p?<?.05). Spring wheat genotypes: Unity, Peace, Vida, Reeder, CLTR 15134, ONeal and Fortuna yielded more grains, and equally took up more P in P5 conditions, revealing some degree of P deficiency tolerance. The genetic variability identified in this study for grain yields and P uptake could be used in wheat improvement programs for selecting genotypes with low P tolerance in P deficient soils as well as in organic spring wheat production.     

Winter soil CO2 efflux and its contribution to annual soil respiration in different ecosystems of a forest-steppe ecotone, north China

Most soil respiration measurements are conducted during the growing season. In tundra and boreal forest ecosystems, cumulative winter soil CO₂ fluxes are reported to be a significant component of their annual carbon budgets. However, little information on winter soil CO₂ efflux is known from mid-latitude ecosystems. Therefore, comparing measurements of soil respiration taken annually versus during the growing season will improve the accuracy of ecosystem carbon budgets and the response of soil CO₂ efflux to climate changes. In this study we measured winter soil CO₂ efflux and its contribution to annual soil respiration for seven ecosystems (three forests: Pinus sylvestris var. mongolica plantation, Larix principis-rupprechtii plantation and Betula platyphylla forest; two shrubs: Rosa bella and Malus baccata; and two meadow grasslands) in a forest-steppe ecotone, north China. Overall mean winter and growing season soil CO₂ effluxes were 0.15-0.26 μmol m⁻² s⁻¹ and 2.65-4.61 μmol m⁻² s⁻¹, respectively, with significant differences in the growing season among the different ecosystems. Annual Q₁₀ (increased soil respiration rate per 10 °C increase in temperature) was generally higher than the growing season Q₁₀. Soil water content accounted for 84% of the variations in growing season Q₁₀ and soil temperature range explained 88% of the variation in annual Q₁₀. Soil organic carbon density to 30 cm depth was a good surrogate for SR₁₀ (basal soil respiration at a reference temperature of 10 °C). Annual soil CO₂ efflux ranged from 394.76 g C m⁻² to 973.18 g C m⁻² using observed ecosystem-specific response equations between soil respiration and soil temperature. Estimates ranged from 424.90 g C m⁻² to 784.73 g C m⁻² by interpolating measured soil respiration between sampling dates for every day of the year and then computing the sum to obtain the annual value. The contributions of winter soil CO₂ efflux to annual soil respiration were 3.48-7.30% and 4.92-7.83% using interpolated and modeled methods, respectively. Our results indicate that in mid-latitude ecosystems, soil CO₂ efflux continues throughout the winter and winter soil respiration is an important component of annual CO₂ efflux.     

Phosphate additions have no effect on microbial biomass and activity in a northern hardwood forest

High rates of atmospheric nitrogen (N) deposition have raised questions about shifting patterns of nutrient limitation in northern hardwood forests. Of particular interest is the idea that increased supply of N may induce phosphorus (P) limitation of plant and microbial processes, especially in acid soils where P sorption by Al is high. In this study, we established field plots and plant-free laboratory mesocosms with P and Ca additions to test the hypotheses that 1) microbial biomass and activity are limited by P in the northern hardwood forest soils at the Hubbard Brook Experimental Forest in NH USA; 2) elevated Ca increases inherent P availability and therefore reduces any effects of added P and 3) P effects are more marked in the more carbon (C) rich Oie compared to the Oa horizon. Treatments included P addition (50 kg P ha⁻¹), Ca addition (850 kg Ca ha⁻¹) and Ca + P addition (850 kg Ca ha⁻¹ and 50 kg P ha⁻¹). The P treatments increased resin-available P levels and reduced phosphatase activity, but had no effect on microbial biomass C, microbial respiration, C metabolizing enzymes, potential net N mineralization and nitrification in the Oie or Oa horizon of either field plots or plant free mesocosms, in either the presence or absence of Ca. Total, prokaryote, and eukaryote PLFA were reduced by P addition, possibly due to reductions in mycorrhizal fungal biomass. These results suggest that increased N deposition and acidification have not created P limitation of microbial biomass and activity in these soils.     

Unfrozen water content moderates temperature dependence of sub-zero microbial respiration

Abrupt increases in the temperature sensitivity of soil respiration below 0 °C have been interpreted as a change in the dominance of other co-dependent environmental controls, such as the availability of liquid-state water. Yet the relationship between unfrozen water content and soil respiration at sub-zero temperatures has received little attention because of difficulties in measuring unfrozen water contents. Using a recently-developed semi-solid ²H NMR technique the unfrozen water content present in seasonally frozen boreal forest soils was quantified and related to biotic CO₂ efflux in laboratory microcosms maintained at temperatures between −0.5 and −8 °C. In both soils the unfrozen water content had an exponential relationship with temperature and was increased by addition of KCl solutions of defined osmotic potential. Approximately 13% unfrozen water was required to release the dependence of soil respiration on unfrozen water content. Depending on the osmotic potential of soil solution, this threshold unfrozen water content was associated with temperatures down to −6 °C; yet if temperature were the predictor of CO₂ efflux, then the abrupt increase in the temperature sensitivity of CO₂ efflux was associated with −2 °C, except in soils amended with −1500 kPa KCl which did not show any abrupt changes in temperature sensitivity. The KCl-amendments also had the effect of decreasing Q₁₀ values and activation energies (Ea) by factors of 100 and three, respectively, to values comparable with those for soil respiration in unfrozen soil. The disparity between the threshold temperatures and the reductions in Q₁₀ values and activation energies after KCl amendment indicates the significance of unfrozen water availability as an environmental control of equal importance to temperature acting on sub-zero soil respiration. However, this significance was diminished when soils were supplied with abundant labile C (sucrose) and the influences of other environmental controls, allied to the solubility and diffusion of respiratory substrates and gases, are considered to increase.     

Effects of phosphorus addition on soil microbial biomass and community composition in three forest types in tropical China

Elevated nitrogen (N) deposition in humid tropical regions may aggravate phosphorus (P) deficiency in forest on old weathered soil found in these regions. From January 2007 to August 2009, we studied the responses of soil microbial biomass and community composition to P addition (in two monthly portions at level of 15 g P m^?2 yr^?1) in three tropical forests in southern China. The forests were an old-growth forest and two disturbed forests (mixed species and pine dominated). The objective was to test the hypothesis that P addition would increase microbial biomass and change the composition of the microbial community, and that the old-growth forests would be more sensitive to P addition due to its higher soil N availability. Microbial biomass C (MBC) was estimated twice a year and the microbial community structure was quantified by phospholipid fatty acid (PLFA) analysis at the end of the experiment. Addition of P significantly increased the microbial biomass and altered the microbial community composition in the old-growth forest, suggesting that P availability is one of the limiting factors for microbial growth. This was also reflected by significant increases in soil respiration after P addition. In contrast, P addition had no effect on the microbial biomass and the microbial community composition in the pine forests. Also in the mixed forest, the microbial biomass did not significantly respond to P addition, but soil respiration and the ratio of fungal-to-bacteria was significantly increased.     

Temperature dependence of soil CO2 efflux is strongly modulated by seasonal patterns of moisture availability in a Mediterranean ecosystem

Extensive research has focused on the temperature sensitivity of soil respiration. However, in Mediterranean ecosystems, soil respiration may have a pulsed response to precipitation events, especially during prolonged dry periods. Here, we investigate temporal variations in soil respiration (R_s), soil temperature (T) and soil water content (SWC) under three different land uses (a forest area, an abandoned agricultural field and a rainfed olive grove) in a dry Mediterranean area of southeast Spain, and evaluate the relative importance of soil temperature and water content as predictors of R_s. We hypothesize that soil moisture content, rather than soil temperature, becomes the major factor controlling CO₂ efflux rates in this Mediterranean ecosystem during the summer dry season. Soil CO₂ efflux was measured monthly between January 2006 and December 2007 using a portable soil respiration instrument fitted with a soil respiration chamber (LI-6400-09). Mean annual soil respiration rates were 2.06 ± 0.07, 1.71 ± 0.09, and 1.12 ± 0.12 μmol m⁻² s⁻¹ in the forest, abandoned field and olive grove, respectively. R_s was largely controlled by soil temperature above a soil water content threshold value of 10% at 0-15 cm depth for forest and olive grove, and 15% for abandoned field. However, below those thresholds R_s was controlled by soil moisture. Exponential and linear models adequately described R_s responses to environmental variables during the growing and dry seasons. Models combining abiotic (soil temperature and soil rewetting index) and biotic factors (above-ground biomass index and/or distance from the nearest tree) explained between 39 and 73% of the temporal variability of R_s in the forest and olive grove. However, in the abandoned field, a single variable - either soil temperature (growing season) or rewetting index (dry season) - was sufficient to explain between 51 and 63% of the soil CO₂ efflux. The fact that the rewetting index, rather than soil water content, became the major factor controlling soil CO₂ efflux rates during the prolonged summer drought emphasizes the need to quantify the effects of rain pulses in estimates of net annual carbon fluxes from soil in Mediterranean ecosystems.     

Effect of cattle slurry in grassland on microbial biomass and on activities of various enzymes

We examined the long-term effects of cattle slurry, applied at high rates, on microbial biomass, respiration, the microbial quotient (qCO₂) and various soil enzyme activities. In March, June, July, and October 1991, slurry-amended grassland soils (0–10 cm) contained significantly higher levels of microbial biomass, N mineralization and enzyme activities involved in N, P, and C cycling. With microbial biomass as the relative value, the results revealed that the slurry treatment influenced enzyme production by the microbial biomass. High levels of urease activity were the result not only of a larger microbial biomass, but also of higher levels of enzmye production by this microbial biomass. The ratio of alkaline phosphatase and xylanase to microbial biomass was nearly constant in the different treatments. The metabolic quotient (qCO₂) declined with increased levels of slurry application. Therefore it appears that microorganisms in slurry-amended soils require less C and energy if there is no competition for nutrients. The results of this study suggest that urease activity, nitrification, and respiration (metabolic quotient) can be used as indicators of environmental stress, produced by heavy applications of cattle slurry.     

Changes of Soil Phosphorus Fractionation According to pH in Red Soils of China: An Incubation Experiment

Phosphorus (P) deficiency is one of the main problems limiting crop growth in red soils of southern China. The primary objective of this study was to examine P availability as a function of soil acidity. Soils were sampled from a long-term fertilization experiment and are referred as low-P (No P fertilization) and high-P (120 kg P₂O₅ ha^–1). Both low-P and high-P treatments were incubated adjusting soil pH to seven levels from 3.0 to 6.5 for 10, 20, 30 and 45 days. The pH, DIP, and Olsen-P were determined after each incubation period, and inorganic P fractions were measured at the end of incubation. For both low-P and high-P treatments, DIP decreased with rising pH value and increased with decreasing soil pH. Olsen-P, Ca-P (Ca₂-P, Ca₈-P, and Ca₁₀-P) and Al-P increased significantly with soil pH in low-P treatment. In high-P, Olsen-P increased with pH between 3.4 and 5.0 and was stable at higher pH. Moreover, Ca-P and Al-P increased significantly but Fe-P decreased with soil pH increase. The redundancy analysis showed that Ca-P, Al-P, and pH had positive effects on Olsen-P, but Occluded-P showed a negative correlation with Olsen-P in both soils. Our results confirmed that soil P availability was influenced by pH and that the changes in DIP and Olsen-P were linked to changes of inorganic fractions from occluded to Ca- and Al-bound forms. Managing soil acidity is a key issue regarding the availability of P in red soils of China and our results suggest that at least a pH of 5.0 should be targeted.     

Grazing intensity in subarctic tundra affects the temperature adaptation of soil microbial communities

Grazing by large ungulates, such as reindeer (Rangifer tarandus L.), in subarctic tundra exerts a considerable effect on the soil microclimate. Because of higher insulation by the aboveground vegetation in light versus heavily grazed areas, soil temperatures during the growing season are considerably higher under heavy grazing. Here, we hypothesized that these grazer-induced changes in soil microclimate affect the temperature sensitivity of soil microbial activity. To test this hypothesis, we conducted soil incubations at different temperatures (4 °C, 9 °C and 14 °C) for six weeks using soils from sites with contrasting long-term grazing intensities. Microbial respiration at low temperature (4 °C) was significantly higher in soils under light grazing than in soils under heavy grazing; however, grazing intensity did not affect respiration rates at 9 °C and 14 °C. In soils under light grazing, post-incubation β-glucosidase (BG) activity at 4 °C was higher in soils that had been incubated at 4 °C than in soils incubated at 14 °C, suggesting functional adaptation of the soil microbial community to low temperature. Similar adaptation was not detected in soils under heavy grazing. Ion Torrent sequencing of bacterial 16S rRNA genes showed major differences in the bacterial community composition in soils incubated at different temperatures. Overall, our results indicate that tundra soil microorganisms may be more cold-adapted under low than high grazing intensity. Due to this difference in temperature adaptation, the consequences of climate warming on soil microbial processes may be dependent on the grazing intensity.     

Carbon pulses but not phosphorus pulses are related to decreases in microbial biomass during repeated drying and rewetting of soils

Drying and rewetting cycles are known to be important for the turnover of carbon (C) in soil, but less is known about the turnover of phosphorus (P) and its relation to C cycling. In this study the effects of repeated drying-rewetting (DRW) cycles on phosphorus (P) and carbon (C) pulses and microbial biomass were investigated. Soil (Chromic Luvisol) was amended with different C substrates (glucose, cellulose, starch; 2.5 g C kg⁻¹) to manipulate the size and community composition of the microbial biomass, thereby altering P mineralisation and immobilisation and the forms and availability of P. Subsequently, soils were either subjected to three DRW cycles (1 week dry/1 week moist) or incubated at constant water content (70% water filled pore space). Rewetting dry soil always produced an immediate pulse in respiration, between 2 and 10 times the basal rates of the moist incubated controls, but respiration pulses decreased with consecutive DRW cycles. DRW increased total CO₂ production in glucose and starch amended and non-amended soils, but decreased it in cellulose amended soil. Large differences between the soils persisted when respiration was expressed per unit of microbial biomass. In all soils, a large reduction in microbial biomass (C and P) occurred after the first DRW event, and microbial C and P remained lower than in the moist control. Pulses in extractable organic C (EOC) after rewetting were related to changes in microbial C only during the first DRW cycle; EOC concentrations were similar in all soils despite large differences in microbial C and respiration rates. Up to 7 mg kg⁻¹ of resin extractable P (P_resin) was released after rewetting, representing a 35-40% increase in P availability. However, the pulse in P_resin had disappeared after 7 d of moist incubation. Unlike respiration and reductions in microbial P due to DRW, pulses in P_resin increased during subsequent DRW cycles, indicating that the source of the P pulse was probably not the microbial biomass. Microbial community composition as indicated by fatty acid methyl ester (FAME) analysis showed that in amended soils, DRW resulted in a reduction in fungi and an increase in Gram-positive bacteria. In contrast, the microbial community in the non-amended soil was not altered by DRW. The non-selective reduction in the microbial community in the non-amended soil suggests that indigenous microbial communities may be more resilient to DRW. In conclusion, DRW cycles result in C and P pulses and alter the microbial community composition. Carbon pulses but not phosphorus pulses are related to changes in microbial biomass. The transient pulses in available P could be important for P availability in soils under Mediterranean climates.     

Stoichiometric responses of soil microflora to nutrient additions for two temperate forest soils

The ratios of soil carbon (C) to nitrogen (N) and C to phosphorus (P) are much higher in Chinese temperate forest soils than in other forest soils, implying that N and P might limit microbial growth and activities. The objective of this study was to assess stoichiometric responses of microbial biomass, enzyme activities, and respiration to N and P additions. We conducted a nutrient (N, P, and N + P) addition experiment in two temperate soils under Korean pine (Pinus koraiensis) plantation and natural broadleaf forest in Northeast China and measured the microbial biomass C, N, P; the activities of β-glucosidase (BG), N-acetyl-β-glucosaminidase (NAG), and acid and alkaline phosphomonoesterase (AP); and the microbial respiration in the two soils. Nitrogen addition increased microbial biomass N and decreased microbial biomass C-to-N ratio and microbial respiration in the two soils. Nitrogen addition decreased NAG activity to microbial biomass N ratio, P addition decreased AP activity to microbial biomass P ratio, and N, P, and N + P additions all increased BG activity to microbial biomass C ratio. These results suggest that microbial stoichiometry is not strictly homeostatic in response to nutrient additions, especially for N addition. The responses of enzyme activities to nutrient additions support the resource allocation theory. The N addition induced a decline in microbial respiration, implying that atmospheric N deposition may reduce microbial respiration, and consequently increase soil C sequestration in the temperate region.     

Influence of mouldboard plough and rotary harrow tillage on microbial biomass and nutrient stocks in two long-term experiments on loess derived Luvisols

The nutrient-specific effects of tillage on microbial activity (basal respiration), microbial biomass (C, N, P, S) indices and the fungal cell-membrane component ergosterol were examined in two long-term experiments on loess derived Luvisols. A mouldboard plough (30 cm tillage depth) treatment was compared with a rotary harrow (8 cm tillage depth) treatment over a period of approximately 40 years. The rotary harrow treatment led to a significant 8% increase in the mean stocks of soil organic C, 6% of total N and 4% of total P at 0–30 cm depth compared with the plough treatment, but had no main effect on the stocks of total S. The tillage effects were identical at both sites, but the differences between the sites of the two experiments were usually stronger than those between the two tillage treatments. The rotary harrow treatment led to a significant increase in the mean stocks of microbial biomass C (+18%), N (+25%), and P (+32%) and to a significant decrease in the stocks of ergosterol (−26%) at 0–30 cm depth, but had no main effect on the stocks of microbial biomass S or on the mean basal respiration rate. The mean microbial biomass C/N (6.4) and C/P (25) ratios were not affected by the tillage treatments. In contrast, the microbial biomass C/S ratio was significantly increased from 34 to 43 and the ergosterol-to-microbial biomass C ratio significantly decreased from 0.20% to 0.13% in the rotary harrow in comparison with the plough treatment. The microbial biomass C-to-soil organic C ratio varied around 2.1% in the plough treatment and declined from 2.6% at 0–10 cm depth to 2.0 at 20–30 cm depth in the rotary harrow treatment. The metabolic quotient qCO₂ revealed exactly the inverse relationships with depth and treatment to the microbial biomass C-to-soil organic C ratio. Rotary harrow management caused a reduction in the microbial turnover in combination with an improved microbial substrate use efficiency and a lower contribution of saprotrophic fungi to the soil microbial community. This contrasts the view reported elsewhere and points to the need for more information on tillage-induced shifts within the fungal community in arable soils.     

Soil microbial activity and community composition: Impact of changes in matric and osmotic potential

As saline soils dry, the salt in the remaining solution phase is concentrated and the microbes are subjected to both water and osmotic stress. However, little is known about the interactive effect of matric potential (MP) and osmotic potential (OP) on microbial activity and community structure. We conducted an experiment in which two non-saline soils, a sand and a sandy loam, were pre-incubated at optimal water content (for microbial activity) but different osmotic potentials achieved by adding NaCl. The EC of the saturated paste (ECe) ranged between 1.6 and 11.6 dS m⁻¹ in the sand and between 0.6 and 17.7 dS m⁻¹ in the sandy loam. After the 14-day pre-incubation, the soils were dried to different water contents: 25-35 g kg⁻¹ in the sand and 95-200 g kg⁻¹ in the sandy loam. Water potential (WP, the sum of osmotic + matric potential) ranged from −0.7 to −6.8 MPa in the sand and from −0.1 to −4.4 MPa in the sandy loam. After addition of ground pea straw to increase the concentration of readily available substrate, respiration was measured over 14 days and microbial community composition was assessed by phospholipid fatty acid analysis (PLFA) at the end of the experiment. In both soils, cumulative respiration at a given soil water content (WC) decreased with decreasing osmotic potential, but the effect of decreasing water content differed between the two soils. In the sand, cumulative respiration at the two lowest water contents (WC25 and WC28) was always significantly lower than that at the highest water content (WC35). In the sandy loam, cumulative respiration was significantly lower at the lowest water content (WC95) compared to the highest water content (WC200) only in treatments with added salt. The reduction of cumulative respiration at a given WP was similar in the two soils with a 50% reduction compared to the control (optimal water content, no salt added) at WP −3 MPa. In the sand at WP <−2 MPa, the reduction in fungal fatty acids was greater than that of bacterial fatty acids whereas in the sandy loam, the response of bacteria and fungi to decreasing WP was similar. In both soils, microbial biomass decreased by 35-50% as WP decreased to about −2 MPa but then remained stable with further decreases of WP. Microbial community composition changed with WP in both soils. Our results suggest that there are two strategies by which microbes respond to water potential. A decrease in WP up to −2 MPa kills a proportion of the microbial community, but the remaining microbes adapt and maintain their activity per unit biomass. At lower WP however, the adaptation mechanisms are not sufficient and although the microbes survive, their activity per unit biomass is reduced.     

Fumigation-extraction and substrate-induced respiration derived microbial biomass C,and respiration rate in limed soil of Scots pine sapling stands

The effect of liming on microbial biomass C and respiration activity was studied in four liming experiments on young pine plantations. One of the experimental sites had been limed and planted 12 years before, two 5 years before, and one a year before soil sampling. The youngest experimental site was also treated with ash fertilizer. Liming raised the pH_KCl of the humus layer by 1.5 units or less. Microbial biomass was measured using the fumigation-extraction and substrate-induced respiration methods. Liming did not significantly affect microbial biomass C, except in the experiment which had been limed 11 years ago, where there was a slight biomass increase. Basal respiration, which was measured by the evolution of CO₂, increased in the limed soils, except for the youngest experiment, where there was no effect. Ash fertilization raised the soil pH_KCl by about 0.5 unit, but did not influence microbial biomass C or basal respiration. Fumigation-extraction and substrate-induced respiration derived microbial biomass C values were correlated positively with each other (r=0.65), but substrate-induced respiration gave approximately 1.3 times higher results. In addition, the effect of storing the soil samples at +6 and -18°C was evaluated. The effects were variable but, generally, the substrate-induced respiration derived microbial biomass C decreased, and the fumigation-extraction derived microbial biomass C and basal respiration decreased or were not affected by storage.