Clifton-Brown, J. C., Breuer, J., Jones, M. B. (2007). Carbon mitigation by the energy crop, Miscanthus. Global Change Biology. 13 (11), 2296-2307 Sponsorship: EU JOUB-0069 / AIR-CT92-0294 RAE2008Biomass crops mitigate carbon emissions by both fossil fuel substitution and sequestration of carbon in the soil. We grew Miscanthus x giganteus for 16 years at a site in southern Ireland to (i) compare methods of propagation, (ii) compare response to fertilizer application and quantify nutrient offtakes, (iii) measure long-term annual biomass yields, (iv) estimate carbon sequestration to the soil and (v) quantify the carbon mitigation by the crop. There was no significant difference in the yield between plants established from rhizome cuttings or by micro-propagation. Annual off-takes of N and P were easily met by soil reserves, but soil K reserves were low in unfertilized plots. Potassium deficiency was associated with lower harvestable yield. Yields increased for 5 years following establishment but after 10 years showed some decline which could not be accounted for by the climate driven growth model MISCANMOD. Measured yields were normalized to estimate both autumn (at first frost) and spring harvests (15 March of the subsequent year). Average autumn and spring yields over the 15 harvest years were 13.4?1.1 and 9.0?0.7 t DW ha?1 yr?1 respectively. Below ground biomass in February 2002 was 20.6?4.6 t DW ha?1. Miscanthus derived soil organic carbon sequestration detected by a change in 13C signal was 8.9?2.4 t C ha?1 over 15 years. We estimate total carbon mitigation by this crop over 15 years ranged from 5.2 to 7.2 t C ha?1 yr?1 depending on the harvest time.Peer reviewe
Bioenergy from crops is expected to make a considerable contribution to climate change mitigation. However, bioenergy is not necessarily carbon neutral because emissions of CO 2 , N 2 O and CH 4 during crop production may reduce or completely counterbalance CO 2 savings of the substituted fossil fuels. These greenhouse gases (GHGs) need to be included into the carbon footprint calculation of different bioenergy crops under a range of soil conditions and management practices. This review compiles existing knowledge on agronomic and environmental constraints and GHG balances of the major European bioenergy crops, although it focuses on dedicated perennial crops such as Miscanthus and short rotation coppice species. Such second-generation crops account for only 3% of the current European bioenergy production, but field data suggest they emit 40% to >99% less N 2 O than conventional annual crops. This is a result of lower fertilizer requirements as well as a higher N-use efficiency, due to effective N-recycling. Perennial energy crops have the potential to sequester additional carbon in soil biomass if established on former cropland (0.44 Mg soil C ha À1 yr À1 for poplar and willow and 0.66 Mg soil C ha À1 yr À1 for Miscanthus). However, there was no positive or even negative effects on the C balance if energy crops are established on former grassland. Increased bioenergy production may also result in direct and indirect land-use changes with potential high C losses when native vegetation is converted to annual crops. Although dedicated perennial energy crops have a high potential to improve the GHG balance of bioenergy production, several agronomic and economic constraints still have to be overcome.Keywords: biofuel, carbon debt, carbon footprint, land management, methane, Miscanthus, nitrous oxide, short rotation coppice, soil organic carbon Greenhouse gas saving with bioenergy -a European perspectiveThe European Union has committed to increase the proportion of renewable energy from 9% in 2010 to 20% of Correspondence: Axel Don,
The substantial stocks of carbon sequestered in temperate grassland ecosystems are located largely below ground in roots and soil. Organic C in the soil is located in discrete pools, but the characteristics of these pools are still uncertain. Carbon sequestration can be determined directly by measuring changes in C pools, indirectly by using 13 C as a tracer, or by simulation modelling. All these methods have their limitations, but long-term estimates rely almost exclusively on modelling. Measured and modelled rates of C sequestration range from 0 to > 8 Mg C ha − 1 yr − 1 . Management practices, climate and elevated CO 2 strongly influence C sequestration rates and their influence on future C stocks in grassland soils is considered. Currently there is significant potential to increase C sequestration in temperate grassland systems by changes in management, but climate change and increasing CO 2 concentrations in future will also have significant impacts. Global warming may negate any storage stimulated by changed management and elevated CO 2 , although there is increasing evidence that the reverse could be the case.
John C. Clifton-Brown, Paul F. Stampfl, Michael B. Jones (2004). Miscanthus biomass production for energy in Europe and its potential contribution to decreasing fossil fuel carbon emissions. Global Change Biology, 10 (4)509-518 RAE2008Field trials throughout Europe over the past 15 years have confirmed the potential for high biomass production from Miscanthus, a giant perennial rhizomatous grass with C4 photosynthesis. However, policies to promote the utilization of biomass crops require yield estimates that can be scaled up to regional, national and continental areas. The only way in which this information can be reliably provided is through the use of productivity models. Here, we describe MISCANMOD, a productivity model, which was used in conjunction with a GIS to plot potential, non-water-limited yields across Europe. Modelled rainfed yields were also calculated using a water balance approach based on FAO estimates of plant available water in the soil. The observed yields were consistent with modelled yields at 20 trial sites across Europe. We estimate that if Miscanthus was grown on 10% of suitable land area in the European Union (EU15), 231 TWh yr?1 of electricity could be generated, which is 9% of the gross electricity production in 2000. Using the same scenario, the total carbon mitigation could be 76 Mt C yr?1, which is about 9% of the EU total C emissions for the 1990 Kyoto Protocol baseline levels.Peer reviewe
The urgency for mitigation actions in response to climate change has stimulated policy makers to encourage the rapid expansion of bioenergy, resulting in major land-use changes over short timescales. Despite the potential impacts on biodiversity and the environment, scientific concerns about large-scale bioenergy production have only recently been given adequate attention. Environmental standards or legislative provisions in the majority of countries are still lagging behind the rapid development of energy crops. Ranging from the field to the regional scale, this review (i) summarizes the current knowledge about the impact of biomass crops on biodiversity in temperate regions, (ii) identifies knowledge gaps and (iii) drafts guidelines for a sustainable biomass crop production with respect to biodiversity conservation. The majority of studies report positive effects on biodiversity at the field scale but impacts strongly depend on the management, age, size and heterogeneity of the biomass plantations. At the regional scale, significant uncertainties exist and there is a major concern that extensive commercial production could have negative effects on biodiversity, in particular in areas of high nature-conservation value. However, integration of biomass crops into agricultural landscapes could stimulate rural economy, thus counteracting negative impacts of farm abandonment or supporting restoration of degraded land, resulting in improved biodiversity values. Given the extent of landconversion necessary to reach the bioenergy targets, the spatial layout and distribution of biomass plantations will determine impacts. To ensure sustainable biomass crop production, biodiversity would therefore have to become an essential part of risk assessment measures in all those countries which have not yet committed to making it an obligatory part of strategic landscape planning. Integrated environmental and economic research is necessary to formulate standards that help support long-term economic and ecological sustainability of biomass production and avoid costly mistakes in our attempts to mitigate climate change.
HighlightsThe impact of grazing on SOC is climate-dependent.Grazing increases SOC for C4 but decreases it for C3 and C3-C4 mixed grasslands.Grazing increases TN and BD but has no effect on soil pH.
The reasons for these requirements can be summarized as follows. Biomass with moisture contents below Miscanthus spp. are high-yielding perennial C 4 grasses, native to 200 to 250 g kg Ϫ1 fresh matter can be stored safely Asia, that are being investigated in Europe as potential biofuels. Production of economically viable solid biofuel must combine high without the danger of self ignition (Clausen, 1994) and biomass yields with good combustion qualities. Good biomass com-burns more efficiently while ash lowers the heating value bustion quality depends on minimizing moisture, ash, K, chloride, N, of the biomass and causes slagging of the boiler heat and S. To this end, field trials at five sites in Europe from Sweden exchangers (Hartmann et al., 1999). High levels of K to Portugal were planted with 15 different genotypes including M. ϫ are undesirable because it decreases the ash melting giganteus, M. sacchariflorus, M. sinensis, and newly bred M. sinensis point, but critical levels will depend on combustion techhybrids. Yield and combustion quality at an autumn and a late winter/ nique. Chloride can lead to corrosion through reaction early spring harvest were determined in the third year after planting with water to form HCl or with K to form gaseous when the stands had reached maturity. As expected, delaying the KCl, both of which are corrosive and reduce boiler life harvest by three to four months improved the combustion quality of (Baumbach et al., 1997). Furthermore, high chloride all genotypes by reducing ash (from 40 to 25 g kg Ϫ1 dry matter), K (from 9 to 4 g kg Ϫ1 dry matter), chloride (from 4 to 1 g kg Ϫ1 dry concentrations can lead to emissions of dioxine and matter), N (from 5 to 4 g kg Ϫ1 dry matter), and moisture (from furane (Siegle and Spliethoff, 1999). Nitrogen concen-564 to 291 g kg Ϫ1 fresh matter). However, the delayed harvest also trations in biofuels need to be as low as possible to decreased mean biomass yields from 17 to 14 t ha Ϫ1 . There is a strong minimize fertilizer off-takes and to reduce emissions interaction among yield, quality, and site growing conditions. Results of NO x during combustion. To avoid SO 2 emissions, show that in northern regions of Europe, M. sinensis hybrids can be biomass S concentrations also need to be as low as recommended for high yields (yielding up to 25 t ha Ϫ1 ), but M. sinensis possible. (nonhybrid) genotypes have higher combustion qualities. In mid-and To date, most research on Miscanthus sp. as an energy south Europe, M. ϫ giganteus (yielding up to 38 t ha Ϫ1 ) or specific crop has concentrated on maximizing the yield of a high-yielding M. sinensis hybrids (yielding up to 41 t ha Ϫ1 ) are more genotypes selected, there were four acquisitions of M. ϫ gigan-
SummaryBackground and objectives This study was designed to investigate the causes of alternative pathway dysregulation in a cohort of patients with dense deposit disease (DDD).Design, setting, participants, & measurements Thirty-two patients with biopsy-proven DDD underwent screening for C3 nephritic factors (C3Nefs), factor H autoantibodies (FHAAs), factor B autoantibodies (FBAAs), and genetic variants in CFH. C3Nefs were detected by: ELISA, C3 convertase surface assay (C3CSA), C3CSA with properdin (C3CSAP), two-dimensional immunoelectrophoresis (2DIEP), and immunofixation electrophoresis (IFE). FHAAs and FBAAs were detected by ELISA, and CFH variants were identified by Sanger sequencing.Results Twenty-five patients (78%) were positive for C3Nefs. Three C3Nef-positive patients were also positive for FBAAs and one of these patients additionally carried two novel missense variants in CFH. Of the seven C3Nef-negative patients, one patient was positive for FHAAs and two patients carried CFH variants that may be causally related to their DDD phenotype. C3CASP was the most sensitive C3Nef-detection assay. C3CASP and IFE are complementary because C3CSAP measures the stabilizing properties of C3Nefs, whereas IFE measures their expected consequence-breakdown of C3b.Conclusions A test panel that includes C3CSAP, IFE, FHAAs, FBAAs, and genetic testing for CFH variants will identify a probable cause for alternative pathway dysregulation in approximately 90% of DDD patients. Dysregulation is most frequently due to C3Nefs, although some patients test positive for FHAAs, FBAAs, and CFH mutations. Defining the pathophysiology of DDD should facilitate the development of mechanism-directed therapies.
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