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      Effects of Hardwood Biochar on Methane Production, Fermentation Characteristics, and the Rumen Microbiota Using Rumen Simulation

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          Abstract

          Biochar is a novel carbonized feed additive sourced from pyrolyzed biomass. This compound is known to adsorb gasses and carbon, participate in biological redox reactions and provide habitat biofilms for desirable microbiota proliferation. Therefore, biochar holds potential to modify rumen fermentation characteristics and reduce enteric CH 4 emissions. The objective of this study was to investigate the effect of hardwood biochar supplementation on fermentation parameters, methane (CH 4) production and the ruminal archaeal, bacterial, and fungal microbiota using the in vitro RUSITEC (rumen simulation technique) system. Treatments consisted of a control diet (oaten pasture: maize silage: concentrate, 35:35:30 w/w) and hardwood biochar included at 400 or 800 mg per day (3.6 and 7.2% of substrate DM, respectively), over a 15-day period. Biochar supplementation had no effect ( P ≥ 0.37) on pH, effluent (mL/d), total gas (mL/d), dry matter (DM) digestibility or CH 4 production (mg/d). The addition of 800 mg biochar per day had the tendency ( P = 0.10) to lower the % of CH 4 released in fermentation compared to 400 mg/d biochar treatment. However, no effect ( P ≥ 0.44) was seen on total VFA, acetate, propionate, butyric, branched-chain VFA, valerate and caproate production and the ratio of acetate to propionate. No effect ( P > 0.05) was observed on bacterial, archaeal or fungal community structure. However, biochar supplementation at 800 mg/d decreased the abundance of one Methanomethylophilaceae OTU (19.8-fold, P = 0.046) and one Lactobacillus spp. OTU (31.7-fold, P < 0.01), in comparison to control treatments. Two fungal OTUs classified as Vishniacozyma victoriae (5.4 × 10 7 increase) and Sporobolomyces ruberrimus (5.4 × 10 7-fold increase) were more abundant in the 800 mg/d biochar samples. In conclusion, hardwood biochar had no effects on ruminal fermentation characteristics and may potentially lower the concentration of enteric CH 4 when included at higher dosages by manipulating ruminal microbiota abundances.

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          454 Pyrosequencing analyses of forest soils reveal an unexpectedly high fungal diversity.

          * Soil fungi play a major role in ecological and biogeochemical processes in forests. Little is known, however, about the structure and richness of different fungal communities and the distribution of functional ecological groups (pathogens, saprobes and symbionts). * Here, we assessed the fungal diversity in six different forest soils using tag-encoded 454 pyrosequencing of the nuclear ribosomal internal transcribed spacer-1 (ITS-1). No less than 166 350 ITS reads were obtained from all samples. In each forest soil sample (4 g), approximately 30 000 reads were recovered, corresponding to around 1000 molecular operational taxonomic units. * Most operational taxonomic units (81%) belonged to the Dikarya subkingdom (Ascomycota and Basidiomycota). Richness, abundance and taxonomic analyses identified the Agaricomycetes as the dominant fungal class. The ITS-1 sequences (73%) analysed corresponded to only 26 taxa. The most abundant operational taxonomic units showed the highest sequence similarity to Ceratobasidium sp., Cryptococcus podzolicus, Lactarius sp. and Scleroderma sp. * This study validates the effectiveness of high-throughput 454 sequencing technology for the survey of soil fungal diversity. The large proportion of unidentified sequences, however, calls for curated sequence databases. The use of pyrosequencing on soil samples will accelerate the study of the spatiotemporal dynamics of fungal communities in forest ecosystems.
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            Redox properties of plant biomass-derived black carbon (biochar).

            Soils and sediments worldwide contain appreciable amounts of thermally altered organic matter (chars). Chars contain electroactive quinoid functional groups and polycondensed aromatic sheets that were recently shown to be of biogeochemical and envirotechnical relevance. However, so far no systematic investigation of the redox properties of chars formed under different pyrolysis conditions has been performed. Here, using mediated electrochemical analysis, we show that chars made from different feedstock and over a range of pyrolysis conditions are redox-active and reversibly accept and donate up to 2 mmol electrons per gram of char. The analysis of two thermosequences revealed that chars produced at intermediate to high heat treatment temperatures (HTTs) (400-700 °C) show the highest capacities to accept and donate electrons. Combined electrochemical, elemental, and spectroscopic analyses of the thermosequence chars provide evidence that the pool of redox-active moieties is dominated by electron-donating, phenolic moieties in the low-HTT chars, by newly formed electron accepting quinone moieties in intermediate-HTT chars, and by electron accepting quinones and possibly condensed aromatics in the high-HTT chars. We propose to consider chars in environmental engineering applications that require controlled electron transfer reactions. Electroactive char components may also contribute to the redox properties of traditionally defined "humic substances".
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              Nutritional management for enteric methane abatement: a review

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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                10 July 2019
                2019
                : 10
                : 1534
                Affiliations
                [1] 1Sydney School of Veterinary Science, Faculty of Science, The University of Sydney , Camperdown, NSW, Australia
                [2] 2School of Life and Environmental Sciences, Faculty of Science, The University of Sydney , Camperdown, NSW, Australia
                [3] 3Department of Agricultural, Forestry and Food Science, University of Turin , Turin, Italy
                [4] 4Lacombe Research and Development Centre, Agriculture and Agri-Food Canada , Lacombe, AB, Canada
                [5] 5School of Materials Science and Engineering, University of New South Wales , Sydney, NSW, Australia
                [6] 6School of Agriculture and Food Sciences, Faculty of Science, The University of Queensland , Gatton, QLD, Australia
                Author notes

                Edited by: Antonio Faciola, University of Florida, United States

                Reviewed by: Anusorn Cherdthong, Khon Kaen University, Thailand; Biswarup Sen, Tianjin University, China

                *Correspondence: Alex V. Chaves, alex.chaves@ 123456sydney.edu.au

                This article was submitted to Systems Microbiology, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2019.01534
                6635593
                dbb28203-6fd1-408d-9bd5-4420d78f369e
                Copyright © 2019 Teoh, Caro, Holman, Joseph, Meale and Chaves.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 01 April 2019
                : 19 June 2019
                Page count
                Figures: 4, Tables: 5, Equations: 0, References: 88, Pages: 13, Words: 0
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                16s rrna gene abundance,fungal its1 region,pyrolyzed biomass,ruminant feeds,rusitec system

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