72 research outputs found

    Mountain Peatland Restoration: Assessment, Goals, and Approaches

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    The purpose of this document is to provide an up-to-date guide to restoring mountain peatlands. This guide will be updated regularly, so check back for updates. We are also interested in hearing from you. Please let us know if you find an error, have new techniques, restoration projects, or information you would like to see included in the next update.https://digitalcommons.mtu.edu/oabooks/1008/thumbnail.jp

    Arbuscular mycorrhizal inoculation has similar benefits to fertilization for Thuja occidentalis L. seedling nutrition and growth on peat soil over a range of pH: implications for restoration

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    Arbuscular mycorrhizal (AM) fungi are hypothesized to assist growth of northern white-cedar in acid peatlands, yet there is little direct evidence that they can provide sufficient resources, especially nitrogen (N), from unfertilized peat soils. Our objective was to determine mycorrhizal efficacy to support cedar growth and nutrient supply as part of a low-impact approach for ecological restoration of cedar in peatlands. We tested the effectiveness of AM inoculation in a greenhouse experiment in factorial combination with fertilization and liming. We also determined AM colonization rate in the different treatment combinations. We found that AM inoculation in the absence of fertilization significantly increased all growth parameters, phosphorus (P) concentrations, and N, P, and copper (Cu) content of the seedlings, and decreased N:P ratios. Fertilizer alone had a similar impact on plant growth and nutrient acquisition when compared to un-fertilized AM inoculation treatments. Liming alone was ineffective at increasing cedar growth and nutrient uptake. There were many interactions of AM inoculation with liming and fertilization. Specifically, the positive effect of AM inoculation on many growth and nutrition metrics was strongly reduced in the presence of fertilization, whereas the P benefit of mycorrhizas appeared to increase under liming. We conclude that addition of AM inoculation alone improved cedar growth and P acquisition, reducing the need for fertilizer and lime in peatlands. However, seedling N limitation might be a problem in strongly N-deficient peat soils

    Root biomass and production by two cushion plant species of tropical high-elevation peatlands in the andean páramo

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    High-elevation peatlands in the Andes are receiving increasing attention for their biodiversity and their high rates of carbon accumulation. However, the ecology of these peatlands and the environmental factors that control their carbon dynamics remain under-studied. Here we report on the patterns of root biomass productivity and turnover rates for two cushion plant species (Distichia muscoides, Plantago rigida) that commonly dominate high-elevation peatlands (\u3e 4200 m a.s.l.) in the Andean páramo landscape of Northern Ecuador. Root biomass for P. rigida ranged from 680 to 864 g m-2 and was approximately 40 % higher than for D. muscoides (507–620 g m-2). In contrast, root production was almost twice as high for D. muscoides (2000–2800 g m-2 yr-1) than for P. rigida (1030–1080 g m-2 yr-1). These patterns resulted in high root turnover rates, especially for D. muscoides (0.98–1.90 yr-1). Below-ground productivity (as C) at our sites conservatively ranged from 0.55 to 1.5 kg m–2 yr–1, representing approximately 30 % of the estimated total productivity for these species, which only accounts for root production down to 50 cm depth. These high productivity rates are in accordance with the extremely high rates of carbon accumulation that have been reported for high-elevation peatlands of the Andes

    Wetland and Hydric Soils

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    Soil and the inherent biogeochemical processes in wetlands contrast starkly with those in upland forests and rangelands. The differences stem from extended periods of anoxia, or the lack of oxygen in the soil, that characterize wetland soils; in contrast, upland soils are nearly always oxic. As a result, wetland soil biogeochemistry is characterized by anaerobic processes, and wetland vegetation exhibits specific adaptations to grow under these conditions. However, many wetlands may also have periods during the year where the soils are unsaturated and aerated. This fluctuation between aerated and nonaerated soil conditions, along with the specialized vegetation, gives rise to a wide variety of highly valued ecosystem services

    Challenges and opportunities for restoration of high-elevation Andean peatlands in Ecuador

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    Páramo peatlands are a regional reservoir of biodiversity and ecosystem services, accumulating large amounts of carbon and buffering water flows. Despite their importance, they have a long history of use and impacts including drainage for agriculture and grazing, and water withdrawal for human uses. Here we present a preliminary assessment of the conservation status of páramo peatlands in Ecuador and, using a case study, discuss peatland restoration as a tool for mitigation and adaptation to the impacts of current climate change. Through a simple index assessing the cumulative presence of signs of human activities on 163 peatland sites, we found that the level of impact was higher for peatlands located in the Western branch of the cordillera, whereas current human population density, precipitation, and elevation were not significant predictors of the levels of impact. Also, starting in 2017, we implemented a pilot restoration initiative on a 21-ha peatland which had been drained and converted into pasture for at least 150 years. The restoration consisted of two ditch blocking techniques implemented to stop fast-moving water and promote the rewetting of the peatland. During the next 3 years, water table increased from 27 ± 3 cm below the soil surface to 7 ± 1 cm by 2021, while wetland plant communities are colonizing and closing the pools in the blocked ditches. Re-wetting of the peatland has led to an increase in the abundance of native species. This case study suggests that restoration initiatives are an efficient and cost-effective approach to a better management of páramo peatlands, with high potential as a tool for mitigation and adaptation to climate change

    Mapping mountain peatlands and wet meadows using multi-date, multi-sensor remote sensing in the Cordillera Blanca, Peru

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    Wetlands (called bofedales in the Andes of Peru) are abundant and important components of many mountain ecosystems across the globe. They provide many benefits including water storage, high quality habitat, pasture, nutrient sinks and transformations, and carbon storage. The remote and rugged setting of mountain wetlands creates challenges for mapping, typically leading to misclassification and underestimates of wetland extent. We used multi-date, multi-sensor radar and optical imagery (Landsat TM/PALSAR/RADARSAT-1/SRTM DEM-TPI) combined with ground truthing for mapping wetlands in Huascarán National Park, Peru. We mapped bofedales into major wetland types: 1) cushion plant peatlands, 2) cushion plant wet meadows, and 3) graminoid wet meadows with an overall accuracy of 92%. A fourth wetland type was found (graminoid peatlands) but was too rare to map accurately, thus it was combined with cushion peatland to form a single peatland class. Total wetland area mapped in the National Park is 38,444 ha, which is 11% of the park area. Peatlands were the most abundant wetland type occupying 6.3% of the park, followed by graminoid wet meadows (3.5%) and cushion wet meadows (1.3%). These maps will serve as the foundation for improved management, including restoration, and estimates of landscape carbon stocks

    Flooding tolerance of four tropical peatland tree species in a nursery trial

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    In order to facilitate hydrological restoration, initiatives have been conducted to promote tree growth in degraded and rewetted peatlands in Indonesia. For these initiatives to be successful, tree seedlings need to be able to survive flooding episodes, with or without shade. We investigated the survival rates and the formation of adventitious roots in the case of four tree species exposed to combinations of different shading and water levels under controlled conditions in a nursery, with artificial rainwater and with peat soil as the medium. The research focused on the following questions (i) whether trees can grow on flooded peat soils; and (ii) which plant traits allow plants to cope with inundation, with or without shade. The four tree species compared (Shorea balangeran, Cratoxylum arborescens, Nephelium lappaceum and Durio zibethinus) include two natural pioneer and two farmer-preferred fruit trees. The experiment used a split-split plot design with 48 treatment combinations and at least 13 tree-level replicates. The study found that S. balangeran and C. arborescens had relatively high survival rates and tolerated saturated condition for 13 weeks, while N. lappaceum and D. zibethinus required non-saturated peat conditions. S. balangeran and C. arborescens developed adventitious roots to adapt to the inundated conditions. D. zibethinus, S. balangeran and N. lappaceum grew best under moderate (30%) shading levels, while C. arborescent grew best in full sunlight

    Andes, Bofedales, and the Communities of Huascarán National Park, Peru

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    Universidad Nacional Agraria La Molina. Escuela de Posgrado. Maestría en Producción AnimalMountain wetlands are abundant in the high elevations of the tropical Andes. Wetlands occupy ~11% of the total park area and are mostly found in the large mountain valleys. Wetlands occur up to 5000 m asl, but most occur between 4,000–4,700 m asl. The highest elevation wetlands are typically dominated by cushion plants, while lower elevation wetlands are more commonly occupied by graminoids. About 60% of all wetlands are peatlands and the remainder are mineral soil wet meadows. The peatlands are up to 11 m deep and 12,000 years old, storing an average of 2,101 Mg C ha-1, which is comparable to lowland tropical peatlands. Our work in Huascarán National Park in Peru is also showing the importance of wetlands in a coupled natural-human system. These wetlands and alpine landscapes are shaped in part by legacies of past human land use, including ancient pastoralism and farming, and are also affected by millions of downstream users dependent upon wetlands and glacier-fed streams for water and energy production. Biodiversity and endemism is high among taxonomic groups such as plants, birds, fish, amphibians and insects. Currently the tropical Andes are in ecological flux due to rapid land cover changes caused by both biophysical and socioeconomic drivers. In addition, the high Andes are experiencing warming and rapid glacial retreat that is resulting in hydroecological changes and socioeconomic changes to the traditional Andean societies that feed back to changes in wetland sustainability

    Variation in carbon and nitrogen concentrations among peatland categories at the global scale

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    Publisher Copyright: © 2022 This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.Peatlands account for 15 to 30% of the world's soil carbon (C) stock and are important controls over global nitrogen (N) cycles. However, C and N concentrations are known to vary among peatlands contributing to the uncertainty of global C inventories, but there are few global studies that relate peatland classification to peat chemistry. We analyzed 436 peat cores sampled in 24 countries across six continents and measured C, N, and organic matter (OM) content at three depths down to 70 cm. Sites were distinguished between northern (387) and tropical (49) peatlands and assigned to one of six distinct broadly recognized peatland categories that vary primarily along a pH gradient. Peat C and N concentrations, OM content, and C:N ratios differed significantly among peatland categories, but few differences in chemistry with depth were found within each category. Across all peatlands C and N concentrations in the 10-20 cm layer, were 440 ± 85.1 g kg-1 and 13.9 ± 7.4 g kg-1, with an average C:N ratio of 30.1 ± 20.8. Among peatland categories, median C concentrations were highest in bogs, poor fens and tropical swamps (446-532 g kg-1) and lowest in intermediate and extremely rich fens (375-414 g kg-1). The C:OM ratio in peat was similar across most peatland categories, except in deeper samples from ombrotrophic tropical peat swamps that were higher than other peatlands categories. Peat N concentrations and C:N ratios varied approximately two-fold among peatland categories and N concentrations tended to be higher (and C:N lower) in intermediate fens compared with other peatland types. This study reports on a unique data set and demonstrates that differences in peat C and OM concentrations among broadly classified peatland categories are predictable, which can aid future studies that use land cover assessments to refine global peatland C and N stocks.Peer reviewe

    Are riparian bur oak phreatophytic? A stable water isotope study in Homestead National Monument, Nebraska

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    Recently, it has been found that several species of oaks (e.g. Q. douglasii) are phreatophytes, or predominately use groundwater. The objectives of our study were to determine if riparian bur oak (Quercus macrocarpa) also used groundwater. This study took place in Homestead National Monument (Homestead, NM), Nebraska, where bur oak grow within the historical floodplain of Cub Creek with groundwater six to seven meters below the surface. Plant and soil samples for isotopic analysis were collected from three sites during 2008 and 2009. Water table depth was measured continuously, and river stage and precipitation were monitored daily by Homestead NM staff. We analyzed river water, groundwater, twig xylem water, and soil water for natural abundance of oxygen isotopes (which can be used as a natural tracer to identify different sources of water). A three-pool mixing model indicated that bur oak were using from 70% to 88% groundwater, 10% to 12% deep soil water, and a maximum of only 8% from shallow soil water. This, in conjunction with diel groundwater fluctuations, indicates that these riparian bur oak are likely phreatophytic and are using groundwater as their predominant source of water
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