Agricultural Research Service - Southeast Area

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    1816 research outputs found

    Phosphate sorption by Pacific Northwest calcareous soils

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    Understanding phosphorus (P) sorption of calcareous soils is important for the development of successful fertilizer and manure management practices. This study was conducted to identify soil chemical properties controlling P sorption in semiarid calcareous soils of the Pacific Northwest. Sorption isotherms of 18 primarily calcareous soils ranging widely in soil physical and chemical properties were constructed by equilibrating 4 g of soil with 40 mL of 0.01M CaC12 containing between 0 and 700 mg P 1.- 1 for 24 h. The P sorption isotherms at low to medium P concentrations fit the Freundlich isotherm (r2 � 0.93). The slope of the isotherm generally increased abruptly at high P concentrations, suggesting Ca-P precipitation. The maximum P sorption prior to Ca-P precipitation was closely related to organically complexed Fe and Mn (R2 > 0.98), suggesting that such complexes may regulate P sorption in these soils. The equilibrium P concentration at the point where Ca-P precipitation begins to dominate was closely related to pH and organic carbon. A better understanding of the role of organically complexed metals in controlling P sorption in calcareous soils is needed to determine how P solubility is affected by organic matter additions and how this will ultimately impact the plant availability and potential off-site transport of P from these soils

    Separation of soil organic phosphorus compounds using reverse-phase ion-pair chromatography

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    Methods were developed for the extraction and separation of soil organic phosphorus compounds using reverse-phase ion-pair chromatography (RP-ICP). Nucleotides (ATP, ADP, and AMP) were separated using a mobile phase of 15 mM TBAHS, 15 mM KH2PO4, and 7% acetonitrile. Inositol hexakisphosphate was separated using a mobile phase composition of 0.05 M formic acid:methanol (49:51 v/v) and 1.5 mL/100 mL of TBAOH. Extraction procedures were developed for the nucleotides which would be compatible with the RP-ICP system developed for their separation

    Organic phosphorus composition and potential bioavailability in semi-arid arable soils of the Western United States

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    The organic P composition of semi-arid arable soils is largely unknown, but such information is fundamental to understanding P dynamics in irrigated agriculture. We used solution "P nuclear magnetic resonance (NMR) spectroscopy and phosphatase hydrolysis to characterize organic P in semi-arid arable soils from the western USA (organic C 2.0-30.7 g C kg' soil, clay 2-48%, pH 5.2-8.2, CaCO 3 <1-480 g kg -' soil). Total P concentrations ranged from 220 to 1210 mg P kg-1 soil, of which between 12 and 45% was extracted with NaOH-EDTA. Inorganic orthophosphate was the dominant P compound, but concentrations determined by solution 31P NMR spectroscopy were consistently greater than those determined by molybdate colorimetry. Concentrations of organic P were relatively small, and were dominated by orthophosphate monoesters (11-130 mg P kg-1 soil), with smaller concentrations of orthophosphate diesters (0-7 mg P kg-1 soil). Pyrophosphate was present in almost all soils at concentrations up to 14 mg P kg-1 soil. Bicarbonate-extractable organic P ranged from 1.7 to 22.8 mg P kg-1 soil, of which between 37 and 87% was hydrolyzed by phosphatase enzymes, suggesting its bioavailability. Soil organic P concentrations were positively correlated with mean annual precipitation, organic C, clay, and oxalate-extractable metals (Al, Fe, Mn), and negatively correlated with mean annual temperature and soil pH. However, CaCO3 concentrations were not significantly correlated with any soil property. These results indicate that equilibrium levels of organic P in semi-arid arable soils are controlled by a balance between the physical protection offered by the soil matrix and the suitability of the environment for biological productivit

    Deficiencies in the soil quality concept and its application

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    Soil quality is a concept that has deeply divided the soil science community. It has been institutionalized and advocated without full consideration of concept weaknesses and contradictions. Our paper highlights its disfunctional definition, flawed approach to quantification, and failure to integrate simultaneous functions, which often require contradictory soil properties and/or management. While the concept arose from a call to protect the environment and sustain the soil resource, soil quality indexing as implemented may actually impair some soil functions, environmental quality, or other societal priorities. We offer the alternative view that emphasis on known principles of soil management is a better expenditure of limited resources for soil stewardship than developing and deploying subjective indices which fail to integrate across the necessary spectrum of management outcomes. If the soil quality concept is retained, we suggest precisely specifying soil use, not function or capacity, as the criteria for attribute evaluation. Emphasis should be directed toward using available technical information to motivate and educate farmers on management practices that optimize the combined goals of high crop production, low environmental degradation, and a sustained resource

    Quality soil management or soil quality management: Performance versus semantics

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    In the past 200 years, soil science has used reductionist research to develop agricultural technologies that have unlocked the hidden potential of earth's natural systems to feed, clothe, and provide raw materials to the human population of over six billion. The soil quality paradigm seeks to change that scientific approach, the nomenclature of soil science, and institutional priorities for soil management and research. The definition of soil quality is elusive and value-laden. Concerns exist for the paradigm's policy overtones, regional and taxonomic biases, failure to reconcile conceptual contradictions, as well as its ambiguous definitions that are confounded by countless circumstance-specific, function-dependent scenarios. The paradigm does not recognize or offer practical means to manage conflicting, and often contradictory soil management requirements for the multiple functions of soil that occur simultaneously. Implementation of the concept has delivered low index ratings for many of the most economically productive and least subsidized US soils and agricultural sectors, and high ratings for soils and regions with some of the lowest economic return and greatest subsidization. The paradigm's focus on arbitrarily selected function assessment has diverted research and management resources from efforts aimed directly at developing improved management capable of solving existing identified and prioritized problems. We attempt to articulate the dangers of shifting soil science away from the value-neutral tradition of edaphology and specific problem solving to a paradigm based on variable, and often subjective, societal perceptions of environmental holism. We submit that over-arching, philosophically driven indexing of soil status, as opposed to focused, specific soil status and property characterization, carries risks to the scientific assessment process, and to the scientist's role as a data interpreter and science mediator. Value intrusion in umbrella-style indices erodes the individual manager's access to objective data to make decisions. We suggest emphasizing quality soil management rather than soil quality management as a professional and scientific goal

    Seasonal phosphatase activities of mosses from Upper Teesdale, northern England

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    Changes in tissue nutrient concentrations and surface phosphatase activities of eight moss species were measured over one year in terrestrial and semi-aquatic environments on Widdybank Fell, Upper Teesdale National Nature Reserve, northern England. Rates of phosphatase activity in apical regions of moss shoots differed markedly between species, but were generally greatest in the winter and least in the summer in most species. Mean values for phosphomonoesterase activity (umol para-nitrophenol g-1 d.wt h-1) ranged from 18.2 for Polytrichum commune to 85.8 for Palustriella commutata var. falcata. Mean phosphodiesterase activity ranged from 3.1 for Polytrichum commune to 86.2 for Hylocomium splendens. In contrast, tissue nitrogen and phosphorus concentrations remained relatively constant throughout the year. Phosphatase activities were negatively correlated with tissue phosphorus concentration for several species, although few relationships were detected between ambient nutrient concentrations and phosphatase activity, tissue nitrogen, or tissue phosphorus concentration. These results demonstrate that phosphatase activities can provide a sensitive indicator of nutrient stress in terrestrial and semi-aquatic mosses, notably in the ectohydric Hylocomium splendens. However, further studies at sites with a wide range of nutrient levels are required to determine whether the technique can be used to indicate ambient nutrient status

    Irrigation increases carbon in agricultural soils

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    Irrigated agriculture sequesters significant amounts of organic C. Irrigation may also sequester significant amounts of inorganic C. Inorganic C reactions are important chemical reactions in irrigated soils and may contribute to the total amount of C sequestered. Calcium content of arid and semi-arid soils tends to be higher than rainfed temperate soils due to calcium rich parent material and low rainfall. Carbonate formation is usually controlled by carbonate equilibrium reactions in the solid and g as phase CO2 . Respiration in plant roots and soil microorganisms continually produce CO, increasing its concentration in the soil atmosphere, modifying carbonate solubility. Since irrigation water flows through a series of canals, where smaller amounts of water are directly exposed to incoming radiation, irrigation water usually has higher temperatures than stream or ground water. Carbon dioxide dissolves in water to form both CO2 as a gas and H2CO3 in solution. Warmer water increases reaction time and, in favourable conditions, precipitates CaCO3 .We measured organic and inorganic C stored in southern Idaho soils having long term land use histories that supported native sagebrush vegetation (NSB), irrigated mouldboard ploughed crops (IMP), irrigated conservation - chisel- tilled crops (ICT) and irrigated pasture systems (IP). Inorganic C and total C (inorganic + organic C) in soil decreased in the order IMP>ICT>IP>NSB. We use our findings to estimate the amount of possible organic, inorganic and total C sequestration if irrigated agriculture were expanded by 10%. If irrigated agricultural land were expanded by 10% worldwide and NSB were converted to IMP, a possible 1.90 x 10' Mg total (organic +inorganic) C (2.72 % of the total C emitted in the next 30 yr) could be sequestered in soil. If irrigated agricultural lands were expanded by 10% worldwide and NSB were converted to ICT, a possible 1.30 x 10' Mg total C (2.24 % of the total C emitted in the next 30 yr) could be sequestered in soil. If irrigated agricultural land were expanded worldwide and NSB were converted to IP a possible gain of 1.7 x 10 8 Mg total C (1.174 % of the total C emitted in the next 30 yr) could be sequestered in soils. Altering land use to produce crops on high output irrigated agriculture, while selected less-productive rainfed agricultural land were returned to temperate forest or native grassland. there could be meaningful reductions in atmospheric CO 2

    Potential contribution of lysed bacterial cells to phosphorus solubilisation in two rewetted Australian pasture soils

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    Soil drying renders considerable amounts of phosphorus soluble upon rewetting, which may be partly derived from lysed microbial cells. Using direct bacterial cell counting in water and tetra-sodium pyrophosphate extracts of two Australian pasture soils, we found that almost all extractable cells were lysed following the rewetting of dry soils. The amounts of phosphorus in the lysed cells corresponded closely to the increases in water-extractable phosphorus following soil drying, suggesting that bacterial cell lysis is a major source of the released phosphorus

    Quantification of myo-inositol hexakisphosphate in alkaline soil extracts by solution 31P NMR spectroscopy and spectral deconvolution

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    Inositol phosphates are the dominant class of organic phosphorus (P) compounds in most soils, but they are poorly understood because they are not easily identified in soil extracts. This study reports a relatively simple technique using solution 31P NMR spectroscopy and spectral deconvolution for the quantification of myo-inositol hexakisphosphate (phytic acid), the most abundant soil inositol phosphate, in alkaline soil extracts. An authentic myo-inositol hexakisphosphate standard added to a re-dissolved soil extract gave signals at 5.85, 4.92, 4.55, and 4.43 ppm in the ratio 1:2:2:1. Spectral deconvolution quantified these signals accurately (102 ± 4%) in solutions containing a mixture of model P compounds by resolving the envelope of signals in the orthophosphate monoester region. In NaOH-EDTA extracts from a range of lowland permanent pasture soils in England and Wales, concentrations of myo-inositol hexakisphosphate determined by spectral deconvolution ranged between 26 and 189 mg P kg- 1 soil, equivalent to between 11 and 35% of the extracted organic P. Concentrations were positively correlated with oxalate-extractable aluminum and iron but were not correlated with total carbon, total nitrogen, clay, or the microbial biomass. This suggests that myo-inositol hexakisphosphate accumulates in soils by mechanisms at least partially independent of those controlling organic matter stabilization and dynamics. Furthermore, myo-inositol hexakisphosphate concentrations were positively correlated with plant-available inorganic P and negatively correlated with the carbon-to-organic P ratio, suggesting that biological P availability may, in part, regulate myo-inositol hexakisphosphate concentrations in soils, perhaps because organisms capable of degrading this compound are favored in more P-limited environments. Solution 31P NMR spectroscopy and spectral deconvolution offers a relatively simple method of quantifying myo-inositol hexakisphosphate in soil extracts

    A new tall fescue with a beneficial endophyte

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    Researchers from the University of Arkansas, University of Missouri, and the USDA Agricultural Research Service cooperated in an effort to produce a new cultivar of tall fescue (Festuca arundinacea Schreb.) containing an endophyte (Neotyphodium coenophialum) which does not produce ergot alkaloids. Our objective was to select and introduce an endophyte which was not toxic to livestock be that retained the beneficial characteristic of enhancing plant drought tolerance. Studies were conducted in Arkansas and Missouri to test the safety and persistence of the cultivar HiMag with a nontoxic endophyte, referred to here as ArkPlus. ArkPlus was shown to produce steer weight gains as high as HiMag fescue without endophyte, and significantly higher than Kentucky-31 fescue with its natural, toxic endophyte. Stand persistence of ArkPlus was as good as toxic Kentucky-31 and better than endophyte-free HiMag in southwest Arkansas. ArkPlus Brand tall fescue is currently being marketed by FFR Cooperative and through its associated cooperatives throughout most states in the southeast

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