163 research outputs found

    Influence of irrigated agriculture on soil carbon and microbial community structure

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    Increasing the amount of carbon (C) in soils is one method to reduce the concentration of carbon dioxide (CO2) in the atmosphere. We measured organic C stored in southern Idaho soils having long-term cropping histories that supported native sagebrush vegetation (NSB), irrigated moldboard plowed crops (IMP), irrigated conservation-chisel-tilled crops (ICT), and irrigated pasture systems (IP). The CO 2 emitted as a result of fertilizer production, farm operations, and CO2 lost via dissolved carbonate in irrigation water, over a 30-year period, was estimated and used to calculate net C fixation. Organic C in ecosystems decreased in the order IP>ICT>IMP> NSB. In February 2001, active fungal, bacterial, and microbial biomass was greater in IP soils than all other soils. Active fungal, bacterial, and microbial biomass was least in ICT soils at the 15-30-cm depth than all other soils. In August 2001, active bacterial biomass was greater in IMP soils than IP, ICT, and NSB soils. Active fungal biomass was greater in IP soils than all other soils. Whole-soil fatty acid profiles differed among management regimes and sampling dates and, to a lesser extent, with soil depth. FAME profiles from the NSB soils were distinct from the agricultural treatments and contained greater amounts of total fatty acids than the other treatments. The IMP and ICT soils yielded fatty acid profiles that were similar to each other, although those at the 15-30-cm depth were distinct from all other treatment-depth combinations. The IP FAME profiles suggest that arbuscular mycorrhizal fungi are more common in these soils than soils from the other treatments. Differences in carbon substrate utilization patterns (BIOLOG) among treatments were more variable and less pronounced that FAME results. In general, irrigated arid soils can both increase C storage while increasing microbial biomass and changing microbial diversity

    The influence of vegetation in riparian filterstrips on coliform bacteria: II. Survival in soils

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    Survival of total and fecal coliform bacteria was measured in the 0 to 5, 5 to 15, and 15 to 30 cm soil depths at 1, 3, 7, 14, and 90 to 120 d after swine (Sus scrofa) wastewater application to riparian filterstrips in southern Georgia during each season of the year. Vegetative treatments evaluated were: (i) 20 m grass-10 m forest, (ii) 10 m grass-20 m forest, and (iii) 10 m grass-20 m maidencane (Panicum hemitomon Schult.). During winter, spring, and summer vegetation type in riparian filterstrips did not affect survival of total and fecal coliform bacteria. Total and fecal coliform bacterial numbers were usually higher in the top 0 to 5 cm of soil than in the 5 to 15 and 15 to 30 cm soil depths in all treatments. Total and fecal coliform numbers in the 0 to 5, 5 to 15, and 15 to 30 cm depths declined approximately 10-fold every 7 to 14 d after waste application in all seasons of the year. At 90 to 120 d after waste application, total and fecal coliform numbers in the three soil depths did not differ from riparian filterstrips that did not have animal waste applied. Total coliform bacteria in the O to 5, 5 to 15, and 15 to 30 cm soil depths correlated with temperature and moisture in a curvilinear relationship (r2 = 0.80 , 0.77, and 0.64, respectively). Fecal coliform bacteria in 0 to 5, 6 to 15, and 16 to 30 cm of soil also correlated with temperature and moisture in a curvilinear relationship (r 2 = 0.56 , 0.53, and 0.53, respectively)

    The influence of vegetation in riparian filterstrips on coliform bacteria: I. Movement and survival in water

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    Swine (Sus scrofa) wastewater was applied to three separate 4 m wide x 30 m long riparian filterstrips consisting of 20 m grass and 10 m forest, 10 m grass and 20 m forest, and 10 m grass and 20 m maidencane (Panicum hemitomon Schult.) in Southern Georgia during each season. Total and fecal coliform numbers in the applied wastewater pulse did not decline as water moved downslope regardless of vegetation type or season. The pulse of applied wastewater did not move beyond 15 m in any treatment in autumn or summer (dry seasons) and only moved beyond 7.5 m in the 20 m grass-10 m forest treatment in the summer. Total and fecal coliform numbers in soil water and shallow ground water declined by approximately 10-fold every 7 d for the first 14 d regardless of vegetative treatment or season. Soil temperature and soil moisture correlated with total coliform bacteria in both 13 m wells (r2 = 0.89) and 2.0 m wells (r2 = 0.89), and with fecal coliform bacteria in 1.5 (r2 = 0.82) and 2.0 m (r2 = 0.76) wells. Animal production operations may need to locate in warm–dry climates so animal waste can be applied to lands to help ensure enteric bacteria input to surface and ground water will not occur

    Influence of C02 enrichment and nitrogen fertilization on tissue chemistry and carbon allocation in longleaf pine seedlings

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    One-year old, nursery-grown longleaf pine (Pinus palustris Mill.) seedlings were grown in 45-L pots containing a coarse sandy medium and were exposed to two concentrations of atmospheric CO2 (365 or 720 µmol?1) and two levels of nitrogen (N) fertility (40 or 400 kg N ha?1 yr?1) within open top chambers for 20 months. At harvest, needles, stems, coarse roots, and fine roots were separated and weighed. Subsamples of each tissue were frozen in liquid N, lyophilized at ?50 ?C, and ground to pass a 0.2 mm sieve. Tissue samples were analyzed for carbon (C), N, nonpolar extractives (fats, waxes, and oils = FWO), nonstructural carbohydrates (total sugars and starch), and structural carbohydrates (cellulose, lignin, and tannins). Increased dry weights of each tissue were observed under elevated CO2 and with high N; however, main effects of CO2 were significant only on belowground tissues. The high N fertility tended to result in increased partitioning of biomass aboveground, resulting in significantly lower root to shoot ratios. Elevated CO2 did not affect biomass allocation among tissues. Both atmospheric CO2 and N fertility tended to affect concentration of C compounds in belowground, more than aboveground, tissues. Elevated CO2 resulted in lower concentrations of starch, cellulose, and lignin, but increased concentrations of FWO in root tissues. High N fertility increased the concentration of starch, cellulose, and tannins, but resulted in lower concentrations of lignin and FWO in roots. Differences between CO2 concentrations tended to occur only with high N fertility. Atmospheric CO2 did not affect allocation patterns for any compound; however the high N treatment tended to result in a lower percentage of sugars, cellulose, and lignin belowgroun

    Understanding Behavioral Antitrust

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    Litterfall, litter decomposition and associated nutrient fluxes in Pinus halepensis: influence of tree removal intensity in a Mediterranean forest

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    The online version of this article (doi:10.1007/s10342-015-0893-z) contains supplementary material, which is available to authorized users[EN] Our knowledge about the influence of silvicultural treatments on nutrient cycling processes in Mediterranean forests is still limited. Four levels of tree removal were compared in an Aleppo pine forest in eastern Spain to determine the effects on litterfall, litter decomposition and the associated nutrient fluxes after 12 years. Removal treatments included clearfelling, two shelterwood intensities (60 and 75 % of basal area removed) and untreated controls. Twelve years later, the basal area removed still explained 60 % of litterfall mass variance and 60 % of C, 52 % of N, 45 % of P, 17 % of K, 47 % of Ca and 60 % of Mg return variances. Litter decomposed somewhat more slowly in clearfellings compared to controls (p = 0.049), accumulated more Ca and released less K compared to the other three treatments. This was explained by contamination with mineral particles due to the poorly developed O horizon in clearfellings. We conclude that the management practices reduced the nutrient return via litterfall, but the nutrient release through decomposition seems poorly sensitive to canopy disturbance. In order to accurately quantify the harvesting impacts on nutrient cycling in this Mediterranean forest system, it is necessary to measure the litterfall of the understory layer.This work has been supported by a fellowship from the Generalitat Valenciana, Conselleria de Educacion, Formacion y Empleo awarded to L. Lado-Monserrat (BFPI/2008/041). Silvicultural treatments were carried out by the Mediterranean Centre for Environmental Studies (CEAM) through programme "I + D en relacion con la restauracion de la cubierta vegetal y otros aspectos de investigacion forestal". Dataloggers and probes were provided by the Generalitat Valenciana through Project "Efecto de diferentes sistemas de aclareo de masa forestal sobre la disponibilidad de agua, nutrientes y la regeneracion de la masa arborea y arbustiva en parcelas de pinar" (GV06/126). We acknowledge Joana Oliver, Ruth M. Tavera and Daniel Fortanet for their help in the laboratory and in the field. The authors wish to thank Francisco Galiana for his assistance, including help in fieldwork and providing information about the experimental design of the silvicultural treatments. Thanks also go to Rafael Herrera from the Centro de Ecologia, Instituto Venezolano de Investigaciones Cientificas, Caracas, Venezuela and two anonymous reviewers for critically reviewing the manuscript.Lado Monserrat, L.; Lidón, A.; Bautista, I. (2015). Litterfall, litter decomposition and associated nutrient fluxes in Pinus halepensis: influence of tree removal intensity in a Mediterranean forest. European Journal of Forest Research. 134(5):833-844. https://doi.org/10.1007/s10342-015-0893-zS8338441345Almagro M, Martínez-Mena M (2012) Exploring short-term leaf-litter decomposition dynamics in a Mediterranean ecosystem: dependence on litter type and site conditions. Plant Soil 358:323–335Alvarez A, Gracia M, Vayreda J, Retana J (2012) Patterns of fuel types and crown fire potential in Pinus halepensis forests in the Western Mediterranean Basin. For Ecol Manage 270:282–290Austin AT, Vivanco L (2006) Plant litter decomposition in a semi-arid ecosystem controlled by photodegradation. Nature 442:555–558Bates JD, Svejcar TS, Miller RF (2007) Litter decomposition in cut and uncut western juniper woodlands. J Arid Environ 70:222–236Binkley D (2008) Three key points in the design of forest experiments. For Ecol Manage 255:2022–2023Blair JM, Crossley DA Jr (1988) Litter decomposition, nitrogen dynamics and litter microarthropods in a southern Appalachian hardwood forest 8 years following clearcutting. J Appl Ecol 25:683–698Blanco JA, Zavala MA, Imbert JB, Castillo FJ (2005) Sustainability of forest management practices: evaluation through a simulation model of nutrient cycling. For Ecol Manage 213:209–228Blanco JA, Imbert JB, Castillo FJ (2006) Influence of site characteristics and thinning intensity on litterfall production in two Pinus sylvestris L. forests in the western Pyrenees. For Ecol Manage 237:342–352Blanco JA, Imbert JB, Castillo FJ (2008) Nutrient return via litterfall in two contrasting Pinus sylvestris forests in the Pyrenees under different thinning intensities. For Ecol Manage 256:1840–1852Blanco JA, Imbert JB, Castillo FJ (2011) Thinning affects Pinus sylvestris needle decomposition rates and chemistry differently depending on site conditions. Biogeochemistry 106:397–414Caldentey J, Ibarra M, Hernández J (2001) Litter fluxes and decomposition in Nothofagus pumilio stands in the region of Magallanes, Chile. For Ecol Manage 148:145–157Christensen JH, Krishna Kumar K, et al. (2013) Climate phenomena and their relevance for future regional climate change. In: Stocker TF, Qin D, Plattner G-K et al (Eds.) Climate change 2013: the physical science basis. Contribution of Working Group I to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change. Cambridge University Press, Cambridge, United Kingdom and New York, NY, USACortina J, Vallejo VR (1994) Effects of clearfelling on forest floor accumulation and litter decomposition in a radiata pine plantation. For Ecol Manage 70:299–310Entry JA, Rose CL, Cromack K Jr (1991) Litter decomposition and nutrient release in ectomycorrhizal mat soils of a Douglas fir ecosystem. Soil Biol Biochem 23:285–290Fabbio G, Merlo M, Tosi V (2003) Silvicultural management in maintaining biodiversity and resistance of forests in Europe—the Mediterranean region. J Environ Manage 67:67–76Galiana F, Pérez-Badía R, Camarero E, Estruch V, Currás R (2001) Estimación de la Radiación solar incidente en pinares de Pinus halepensis sometidos a tratamientos selvícolas de cortas finales. In: Junta de Andalucía. Consejería de Medio Ambiente (Ed.) Actas del III Congreso Forestal Español. Junta de Andalucía. Granada (Original in Spanish)García-Plé C, Vanrell P, Morey M (1995) Litter fall and decomposition in a Pinus halepensis forest on Mallorca. J Veg Sci 6:17–22González Utrillas N, González Pérez E, Galiana F (2005) Variación del crecimiento diametral de la masa de pinar de carrasco en cortas finales experimentales, en los montes de Tuejar y Chelva (Valencia). IV Congreso Forestal Español. Zaragoza. Soc. Esp. Cien. For. (Original in Spanish)Guo LB, Sims REH (1999) Litter decomposition and nutrient release via litter decomposition in New Zealand eucalypt short rotation forests. Agric Ecosyst Environ 75:133–140GVA (1995) Mapa de Suelos de la Comunidad Valenciana. Chelva (666). Proyecto LUCDEME (Icona), Centro de Investigaciones sobre Desertificación y Conselleria d’Agricultura i Mig Ambient. Generalitat Valenciana. Valencia, Spain. (Original in Spanish)Hennessey TC, Dougherty PM, Cregg BM, Wittwer RF (1992) Annual variation in needle fall of a loblolly pine stand in relation to climate and stand density. For Ecol Manage 51:329–338Inagaki Y, Kuramoto S, Torii A, Shinomiya Y, Fukata H (2008) Effects of thinning on leaf-fall and leaf-litter nitrogen concentration in hinoki cypress (Chamaecyparis obtusa Endlicher) plantation stands in Japan. For Ecol Manage 255:1859–1867Jonard M, Misson L, Ponette Q (2006) Long-term thinning effects on the forest floor and the foliar nutrient status of Norway spruce stands in the Belgian Ardennes. Can J For Res 36:2684–2695Kim C, Sharik TL, Jurgensen MF (1996a) Canopy cover effects on mass loss, and nitrogen and phosphorus dynamics from decomposing litter in oak and pine stands in northern Lower Michigan. For Ecol Manage 80:13–20Kim C, Sharik TL, Jurgensen MF (1996b) Litterfall, nitrogen and phosphorus inputs at various levels of canopy removal in oak and pine stands in northern lower Michigan. Am Midl Nat 135:195–204Kim C, Son Y, Lee WK, Jeong J, Noh NJ, Kim SR, Yang AR, Ju NG (2012) Influence of forest tending (Soopkakkugi) works on litterfall and nutrient inputs in a Pinus densiflora stand. For Sci Technol 8:83–88Kimmins JP (2004) Forest ecology, a foundation for sustainable management and environmental ethics in forestry. 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For Ecol Manage 269:206–213Navarro FB, Romero-Freire A, Del Castillo T, Foronda A, Jiménez MN, Ripoll MA, Sánchez-Miranda A, Hutsinger L, Fernández-Ondoño E (2013) Effects of thinning on litterfall were found after years in a Pinus halepensis afforestation area at tree and stand levels. For Ecol Manage 289:354–362Olson JS (1963) Energy storage and the balance of producers and decomposers in ecological systems. Ecology 44:322–331Pérez Cueva AJ (1994) Atlas Climático de la Comunidad Valenciana. Colección Territori nº 4. Generalitat Valenciana. Conselleria d’Obres Publiques, Urbanisme i Transport, ValenciaPetritsch R, Hasenauer H, Pietsch SA (2007) Incorporating forest growth response to thinning within biome-BGC. For Ecol Manage 242:324–336Prescott CE (1997) Effects of clearcutting and alternative silvicultural systems on rates of decomposition and nitrogen mineralization in a coastal montane coniferous forest. 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    Effect of Biocontrol Agent Pseudomonas fluorescens 2P24 on Soil Fungal Community in Cucumber Rhizosphere Using T-RFLP and DGGE

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    Fungi and fungal community play important roles in the soil ecosystem, and the diversity of fungal community could act as natural antagonists of various plant pathogens. Biological control is a promising method to protect plants as chemical pesticides may cause environment pollution. Pseudomonas fluorescens 2P24 had strong inhibitory on Rastonia solanacearum, Fusarium oxysporum and Rhizoctonia solani, etc., and was isolated from the wheat rhizosphere take-all decline soils in Shandong province, China. However, its potential effect on soil fungal community was still unknown. In this study, the gfp-labeled P. fluorescens 2P24 was inoculated into cucumber rhizosphere, and the survival of 2P24 was monitored weekly. The amount decreased from 108 to 105 CFU/g dry soils. The effect of 2P24 on soil fungal community in cucumber rhizosphere was investigated using T-RFLP and DGGE. In T-RFLP analysis, principle component analysis showed that the soil fungal community was greatly influenced at first, digested with restriction enzyme Hinf I and Taq I. However, there was little difference as digested by different enzymes. DGGE results demonstrated that the soil fungal community was greatly shocked at the beginning, but it recovered slowly with the decline of P. fluorescens 2P24. Four weeks later, there was little difference between the treatment and control. Generally speaking, the effect of P. fluorescens 2P24 on soil fungal community in cucumber rhizosphere was just transient

    Clustering of cancer among families of cases with Hodgkin Lymphoma (HL), Multiple Myeloma (MM), Non-Hodgkin's Lymphoma (NHL), Soft Tissue Sarcoma (STS) and control subjects

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    <p>Abstract</p> <p>Background</p> <p>A positive family history of chronic diseases including cancer can be used as an index of genetic and shared environmental influences. The tumours studied have several putative risk factors in common including occupational exposure to certain pesticides and a positive family history of cancer.</p> <p>Methods</p> <p>We conducted population-based studies of Hodgkin lymphoma (HL), Multiple Myeloma (MM), non-Hodgkin's Lymphoma (NHL), and Soft Tissue Sarcoma (STS) among male incident case and control subjects in six Canadian provinces. The postal questionnaire was used to collect personal demographic data, a medical history, a lifetime occupational history, smoking pattern, and the information on family history of cancer. The family history of cancer was restricted to first degree relatives and included relationship to the index subjects and the types of tumours diagnosed among relatives. The information was collected on 1528 cases (HL (n = 316), MM (n = 342), NHL (n = 513), STS (n = 357)) and 1506 age ± 2 years and province of residence matched control subjects. Conditional logistic regression analyses adjusted for the matching variables were conducted.</p> <p>Results</p> <p>We found that most families were cancer free, and a minority included two or more affected relatives. HL [(OR<sub>adj </sub>(95% CI) <b>1.79 (1.33, 2.42)]</b>, MM <b>(1.38(1.07, 1.78))</b>, NHL <b>(1.43 (1.15, 1.77)</b>), and STS cases <b>(1.30(1.00, 1.68)) </b>had higher incidence of cancer if any first degree relative was affected with cancer compared to control families. Constructing mutually exclusive categories combining "family history of cancer" (yes, no) and "pesticide exposure ≥10 hours per year" (yes, no) indicated that a positive family history was important for HL <b>(2.25(1.61, 3.15))</b>, and for the combination of the two exposures increased risk for MM <b>(1.69(1.14,2.51))</b>. Also, a positive family history of cancer both with <b>(1.72 (1.21, 2.45)) </b>and without pesticide exposure <b>(1.43(1.12, 1.83)) </b>increased risk of NHL.</p> <p>Conclusion</p> <p>HL, MM, NHL, and STS cases had higher incidence of cancer if any first degree relative affected with cancer compared to control families. A positive family history of cancer and/or shared environmental exposure to agricultural chemicals play an important role in the development of cancer.</p
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