31 research outputs found

    Soil morphology, depth and grapevine root frequency influence microbial communities in a Pinot noir vineyard

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    The composition of microbial communities responds to soil resource availability, and has been shown to vary with increasing depth in the soil profile. Soil microorganisms partly rely on root-derived carbon (C) for growth and activity. Roots in woody perennial systems like vineyards have a deeper vertical distribution than grasslands and annual agriculture. Thus, we hypothesized that vineyard soil microbial communities along a vertical soil profile would differ from those observed in grassland and annual agricultural systems. In a Pinot noir vineyard, soil pits were excavated to ca. 1.6–2.5m, and microbial community composition in ‘bulk’ (i.e., no roots) and ‘root’ (i.e., roots present) soil was described by phospholipid ester-linked fatty acids (PLFA). Utilization of soil taxonomy aided in understanding relationships between soil microbial communities, soil resources and other physical and chemical characteristics. Soil microbial communities in the Ap horizon were similar to each other, but greater variation in microbial communities was observed among the lower horizons. Soil resources (i.e., total PLFA, or labile C, soil C and nitrogen, and exchangeable potassium) were enriched in the surface horizons and significantly explained the distribution of soil microbial communities with depth. Soil chemical properties represented the secondary gradient explaining the differentiation between microbial communities in the B-horizons from the C-horizons. Relative abundance of Gram-positive bacteria and actinomycetes did not vary with depth, but were enriched in ‘root’ vs. ‘bulk’ soils. Fungal biomarkers increased with increasing depth in ‘root’ soils, differing from previous studies in grasslands and annual agricultural systems. This was dependent on the deep distribution of roots in the vineyard soil profile, suggesting that the distinct pattern in PLFA biomarkers may have been strongly affected by C derived from the grapevine roots. Gram-negative bacteria did not increase in concert with fungal abundance, suggesting that acidic pHs in lower soil horizons may have discouraged their growth. These results emphasize the importance of considering soil morphology and associated soil characteristics when investigating effects of depth and roots on soil microorganisms, and suggest that vineyard management practices and deep grapevine root distribution combine to cultivate a unique microbial community in these soil profiles

    Climate-smart agriculture global research agenda: Scientific basis for action

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    Background: Climate-smart agriculture (CSA) addresses the challenge of meeting the growing demand for food, fibre and fuel, despite the changing climate and fewer opportunities for agricultural expansion on additional lands. CSA focuses on contributing to economic development, poverty reduction and food security; maintaining and enhancing the productivity and resilience of natural and agricultural ecosystem functions, thus building natural capital; and reducing trade-offs involved in meeting these goals. Current gaps in knowledge, work within CSA, and agendas for interdisciplinary research and science-based actions identified at the 2013 Global Science Conference on Climate-Smart Agriculture (Davis, CA, USA) are described here within three themes: (1) farm and food systems, (2) landscape and regional issues and (3) institutional and policy aspects. The first two themes comprise crop physiology and genetics, mitigation and adaptation for livestock and agriculture, barriers to adoption of CSA practices, climate risk management and energy and biofuels (theme 1); and modelling adaptation and uncertainty, achieving multifunctionality, food and fishery systems, forest biodiversity and ecosystem services, rural migration from climate change and metrics (theme 2). Theme 3 comprises designing research that bridges disciplines, integrating stakeholder input to directly link science, action and governance. Outcomes: In addition to interdisciplinary research among these themes, imperatives include developing (1) models that include adaptation and transformation at either the farm or landscape level; (2) capacity approaches to examine multifunctional solutions for agronomic, ecological and socioeconomic challenges; (3) scenarios that are validated by direct evidence and metrics to support behaviours that foster resilience and natural capital; (4) reductions in the risk that can present formidable barriers for farmers during adoption of new technology and practices; and (5) an understanding of how climate affects the rural labour force, land tenure and cultural integrity, and thus the stability of food production. Effective work in CSA will involve stakeholders, address governance issues, examine uncertainties, incorporate social benefits with technological change, and establish climate finance within a green development framework. Here, the socioecological approach is intended to reduce development controversies associated with CSA and to identify technologies, policies and approaches leading to sustainable food production and consumption patterns in a changing climate

    Assessment of carbon in woody plants and soil across a vineyard-woodland landscape

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    <p>Abstract</p> <p>Background</p> <p>Quantification of ecosystem services, such as carbon (C) storage, can demonstrate the benefits of managing for both production and habitat conservation in agricultural landscapes. In this study, we evaluated C stocks and woody plant diversity across vineyard blocks and adjoining woodland ecosystems (wildlands) for an organic vineyard in northern California. Carbon was measured in soil from 44 one m deep pits, and in aboveground woody biomass from 93 vegetation plots. These data were combined with physical landscape variables to model C stocks using a geographic information system and multivariate linear regression.</p> <p>Results</p> <p>Field data showed wildlands to be heterogeneous in both C stocks and woody tree diversity, reflecting the mosaic of several different vegetation types, and storing on average 36.8 Mg C/ha in aboveground woody biomass and 89.3 Mg C/ha in soil. Not surprisingly, vineyard blocks showed less variation in above- and belowground C, with an average of 3.0 and 84.1 Mg C/ha, respectively.</p> <p>Conclusions</p> <p>This research demonstrates that vineyards managed with practices that conserve some fraction of adjoining wildlands yield benefits for increasing overall C stocks and species and habitat diversity in integrated agricultural landscapes. For such complex landscapes, high resolution spatial modeling is challenging and requires accurate characterization of the landscape by vegetation type, physical structure, sufficient sampling, and allometric equations that relate tree species to each landscape. Geographic information systems and remote sensing techniques are useful for integrating the above variables into an analysis platform to estimate C stocks in these working landscapes, thereby helping land managers qualify for greenhouse gas mitigation credits. Carbon policy in California, however, shows a lack of focus on C stocks compared to emissions, and on agriculture compared to other sectors. Correcting these policy shortcomings could create incentives for ecosystem service provision, including C storage, as well as encourage better farm stewardship and habitat conservation.</p

    Soil biological and chemical properties in restored perennial grassland in California. Restoration Ecology

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    Abstract Restoration of California native perennial grassland is often initiated with cultivation to reduce the density and cover of non-native annual grasses before seeding with native perennials. Tillage is known to adversely impact agriculturally cultivated land; thus changes in soil biological functions, as indicated by carbon (C) turnover and C retention, may also be negatively affected by these restoration techniques. We investigated a restored perennial grassland in the fourth year after planting Nassella pulchra, Elymus glaucus, and Hordeum brachyantherum ssp. californicum for total soil C and nitrogen (N), microbial biomass C, microbial respiration, CO 2 concentrations in the soil atmosphere, surface efflux of CO 2 , and root distribution (0-to 15-, 15-to 30-, 30-to 60-, and 60-to 80-cm depths). A comparison was made between untreated annual grassland and plots without plant cover still maintained by tillage and herbicide. In the uppermost layer (0-to 15-cm depth), total C, microbial biomass C, and respiration were lower in the tilled, bare soil than in the grassland soils, as was CO 2 efflux from the soil surface. Root length near perennial bunchgrasses was lower at the surface and greater at lower depths than in the annual grass-dominated areas; a similar but less pronounced trend was observed for root biomass. Few differences in soil biological or chemical properties occurred below 15-cm depth, except that at lower depths, the CO 2 concentration in the soil atmosphere was lower in the plots without vegetation, possibly from reduced production of CO 2 due to the lack of root respiration. Similar microbiological properties in soil layers below 15-cm depth suggest that deeper microbiota rely on more recalcitrant C sources and are less affected by plant removal than in the surface layer, even after 6 years. Without primary production, restoration procedures with extended periods of tillage and herbicide applications led to net losses of C during the plant-free periods. However, at 4 years after planting native grasses, soil microbial biomass and activity were nearly the same as the former conditions represented by annual grassland, suggesting high resilience to the temporary disturbance caused by tillage

    Biodiversity and multiple ecosystem functions in an organic farmscape

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    To increase ecosystem services provided by their lands, farmers in the United States are managing non-production areas to create a more biodiverse set of habitats and greater landscape heterogeneity. Relatively little is known, however, of the actual environmental outcomes of this practice, termed 'farmscaping'. We inventoried communities of plant and soil organisms and monitored indicators of ecosystem functions in six distinct habitats of an organic farm in California's Central Valley to better understand the ecological costs and benefits of farmscaping. A riparian corridor, hedgerows, a system of drainage ditches, and tailwater ponds supported different plant life history/functional groups and greater native plant diversity than the two production fields. Differences were less pronounced for belowground organisms, i.e.;nematode functional groups, microbial communities (based on phospholipid fatty acid (PLFA) analysis) and earthworm taxa. Partial ordination analysis showed that environmental variables, rather than spatial location, explained much of the distribution of soil and plant taxa across the farmscape. Riparian and hedgerow habitats with woody vegetation stored 18% of the farmscape's total carbon (C), despite occupying only 6% of the total area. Infiltration rates in the riparian corridor were &gt;230% higher than those observed in the production fields, and concentrations of dissolved organic carbon (DOC) in soil solution were as much as 65% higher. The tailwater pond reduced total suspended solids in irrigation runoff by 97%. Drainage ditches had the highest N2O-N emissions (mean values of 16.7Όgm-2h-1) and nitrate (NO3--N) leaching (12.1gm-2year-1 at 75cm depth). Emissions of N2O-N and leaching of NO3--N were, however, quite low for all the habitats. Non-production habitats increased biodiversity (particularly plants) and specific ecosystem functions (e.g. water regulation and carbon storage). Extrapolating relative tradeoffs to the entire farmscape showed that greater habitat enhancement through farmscaping could increase both biodiversity and multiple ecosystem functions of agricultural lands with minor loss of production area. © 2010 Elsevier B.V

    Bacterial community dissimilarity in soils is driven by long‐term land‐use practices

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    Land‐use practices impact soil microbial functionality and biodiversity, with reports suggesting that anthropogenic activities potentially result in reduced microbial functions and loss of species. The objective of this study was to assess the effect of long‐term (\u3e50 yr) land use (natural forest and grassland, and agricultural land) on soil bacterial community structure. A high‐throughput sequencing‐by‐synthesis approach of the 16S rRNA gene was used to study bacterial community and predicted functional profiles of Alfisols, as affected by variables including land‐use (forest, grass, agricultural) and soil/crop management (rotation and tillage) in long‐term experimental plots in Hoytville, OH. The distribution of the abundant phyla was different across samples. No‐till soils showed higher diversity indices than the plow‐till (PT) soils. Ordinations across locations suggested that no‐till soils had distinctly different community structure compared with plow‐till soils, while crop rotation within the no‐till plot had highest number of taxa. Overall land use (forest, grass, agronomic treatment) and tillage (within agricultural soils) were found to be significant when evaluating bacterial community dissimilarity. Predictive functional profiles showed that the forest soil had greatest proportion of PICRUSt‐assignable gene functions followed by the no‐till and grassland soils whereas plow‐till soils had the lowest predicted gene abundances across all samples. The results provide a view of soil bacterial diversity and predictive functional capacity in long‐term land‐use and soil/crop management practices, with a potential to inform future experiments to increase our understanding of long‐term impacts of land use on microbial community structure and function
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