农田土壤施用系列新型氮肥后气态氮(NH3和N2O)减排效果比较:以夏玉米季为例

为了解不同品种新型氮肥相对常规施肥其氨(NH3)和氧化亚氮(N_2O)的减排效果,本文通过田间原位试验同步研究了夏玉米生长季氮肥施用后的农田NH_3挥发和N_2O排放及其主要驱动因子.以常规施肥(复合肥+尿素,CK)为对照,设置了5个肥料处理,分别为脲铵氮肥(UA)、稳定性复合肥料(UHD)、硫包衣氮肥(SCU)、脲甲醛复合肥(UF)和有机肥(OF),施氮量(以N计)均为300 kg·hm~(-2).相关分析结果表明,氨挥发和N_2O排放受环境因子影响,均与土壤WFPS呈显著负相关(P0.05),N_2O排放还与土壤硝态氮呈极显著正相关(P0.01).进一步回归分析表明,N_2O排放(F_(N_2O))主要取决于土壤硝态氮(x)含量的变化,而氨挥发(F_(NH_3))主要取决于土壤铵态氮(x)含量的变化.与CK相比,除了UA,其它肥料处理都降低了土壤的氨挥发,尤其是UF和OF处理减少了37%~43%.但对于N_2O排放,所有处理与CK皆无显著差异.进一步计算每种处理氨挥发和N_2O的气态氮损失总量,与CK相比,UHD、SCU、UF和OF分别减排了9%、5%、30%和23%,而UA增加了3%.     

Soil moisture determines the effectiveness of two urease inhibitors to decrease N<Subscript>2</Subscript>O emission

Among the mitigation strategies to prevent nitrogen (N) losses from ureic fertilizers, urease inhibitors (UIs) have been demonstrated to promote high N use efficiency by reducing ammonia (NH₃) volatilization. In the last few years, some field experiments have also shown its effectiveness in reducing nitrous oxide (N₂O) losses from fertilized soils under conditions of low soil moisture. An incubation experiment was carried out with the aim of assessing the main biotic mechanisms behind N₂O emissions once that the UIs N-(n-butyl) thiophosphoric triamid (NBPT) and phenil phosphorodiamidate (PPDA) were applied with Urea (U) under different soil moisture conditions (40, 60 and 80 % water-filled pore space, WFPS). In the same study we tried to analyze to what extent soil WFPS regulates the effect of these inhibitors on N₂O emissions. The use of PPDA in our study allowed us to compare the effect of NBPT with that of another commercially available urease inhibitor, aiming to see if the results were inhibitor-specific or not. Based on the results from this experiment, a WFPS (i.e. 60 %) was chosen for a second study (i.e. mesocosm experiment) aiming to assess the efficiency of the UIs to indirectly affect N₂O emissions through influencing the pool of soil mineral N. The N₂O emissions at 40 % WFPS were almost negligible, being significantly lower from all fertilized treatments than that produced at 60 and 80 % WFPS. When compared to U alone, NBPT+U reduced the N₂O emissions at 60 % WFPS but had no effect at 80 % WFPS. The application of PPDA significantly increased the emissions with respect to U at 80 % WFPS whereas no significant effect was found at 60 %. At 80 % WFPS, denitrification was the main source of N₂O emissions for all treatments. In the mesocosm study, the application of NBPT+U was an effective strategy to reduce N₂O emissions (75 % reduction compared to U alone), due to a lower soil ammonium (NH₄ ⁺) content induced by the inhibitor. These results suggest that adequate management of the UI NBPT could provide, under certain soil conditions, an opportunity for mitigation of N₂O emissions from fertilized soils.     

Urease inhibitor reduces N losses and improves plant-bioavailability of urea applied in fine particle and granular forms under field conditions

A field lysimeter/mini plot experiment was established in a silt loam soil near Lincoln, New Zealand, to investigate the effectiveness of urea fertilizer in fine particle application (FPA), with or without the urease inhibitor N-(n-butyl) thiophosphoric triamide (NBPT - “Agrotain”), in decreasing nitrogen (N) losses and improving N uptake efficiency. The five treatments were: control (no N) and ¹⁵N-labelled urea, with or without NBPT, applied to lysimeters or mini plots (unlabelled urea), either in granular form to the soil surface or in FPA form (through a spray) at a rate equivalent to 100 kg N ha⁻¹. Gaseous emissions of ammonia (NH₃) and nitrous oxide (N₂O), nitrate (NO₃⁻) leaching, herbage dry-matter (DM) production, N-response efficiency, total N uptake and total recovery of applied ¹⁵N in the plant and soil varied with urea application method and with addition of NBPT. Urea with NBPT, applied in granular or FPA form, was more effective than in application without NBPT: N₂O emissions were reduced by 7-12%, NH₃ emissions by 65-69% and NO₃⁻ leaching losses by 36-55% compared with granular urea. Urea alone and with NBPT, applied in FPA form increased herbage DM production by 27% and 38%, respectively. The N response efficiency increased from 10 kg DM kg⁻¹ of applied N with granular urea to 19 kg DM kg⁻¹ with FPA urea and to 23 kg DM kg⁻¹ with FPA urea plus NBPT. Urea applied in FPA form resulted in significantly (P < 0.05) higher ¹⁵N recovery in the shoots compared with granular treatments and this was improved further when urea in FPA form was applied with NBPT. These results suggest that applying urea with NBPT in FPA form has potential as a management tool in mitigating N losses, improving N-response efficiency and increasing herbage DM production in intensive grassland systems.     

An inhibitor of urease activity effectively reduces ammonia emissions from soil treated with urea under Mediterranean conditions

Urea is an important source of ammonia (NH₃) emissions to the atmosphere from agricultural soils. Abatement strategies are necessary in order to achieve NH₃ emission targets by reducing those emissions. In this context, a field experiment was carried out on a sunflower crop in spring 2006 with the aim of evaluating the effect of the N-(n-butyl) thiophosphoric triamide (NBPT) in the mitigation of volatilized NH₃ from a urea-fertilised soil. Ammonia emission was quantified, using the integrated horizontal flux (IHF) method, following application of urea with and without the urease inhibitor NBPT. Urea and a mixture of urea and NBPT (0.14%, w/w) were surface-applied at a rate of 170 kg N ha⁻¹ to circular plots (diameter 40 m). The soil was irrigated with 10 mm of water just after the application of urea to dissolve and incorporate it into the upper layer of soil. Over the duration of the measurement period (36 days) three peaks of NH₃ were observed. The first peak was associated with hydrolysis of urea after irrigation and the others with the increase of ammonia in soil solution after changes in atmospheric variables such as wind speed and rainfall. The total NH₃ emission during the whole experiment was 17.3 ± 0.5 kg NH₃–N ha⁻¹ in the case of urea treated soils and 10.0 ± 2.2 kg NH₃–N ha⁻¹ where NBPT was included with the urea (10.1 and 5.9%, respectively, of the applied urea–N). The lower NH₃ emissions from plots fertilised with urea + NBPT, compared with urea alone, were associated with a reduction in urease activity during the first 9 days after inhibitor application. This reduction in enzymatic activity promoted a decrease in the exchangeable NH₄⁺ pool.     

负载NH4+-N生物炭对土壤N2O-N排放和NH3-N挥发的影响

利用生物炭吸附面源污染水体NH₄⁺-N并将其进行还田可实现此氮资源由水体到农田的安全有效迁移,而探索负载NH₄⁺-N生物炭对N₂O-N排放和NH₃-N挥发的影响则对于减施化肥和降低土壤氮素损失意义重大.本研究采用土柱试验,设置4个处理：对照（不施氮肥,CK）、单施化肥（NPK）、负载氮+化学磷钾肥（N-BC+PK）和生物炭+化肥（BC+NPK）.结果表明,相较NPK和BC+NPK处理,N-BC+PK处理N₂O-N累积排放量、NH₃-N累积挥发量、气态氮素累积损失量（以N计）分别显著降低了33.62%和24.64%、70.64%和79.29%、64.97%和73.75%（P<0.05）.特别需要说明的是,BC+NPK处理相比NPK处理显著增加了NH₃-N累积挥发量（P<0.05）.综上所述,负载NH₄⁺-N生物炭可显著减少N₂O-N排放和NH₃-N挥发,且其减排效果显著优于传统的生物炭化肥配施.本研究结果将为富营养化水体NH₄⁺-N农田回用和土壤气态氮素减排提供理论依据和数据支持.     

双氰胺对冬闲稻田和油菜地N2O排放的影响

冬季的温室气体排放往往被忽视,而最新的研究结果表明,冬闲稻田和冬季油菜地N_2O排放仍较大,研究相应的减排措施及减排机制对于减少农田土壤N_2O排放有重要意义.在中国科学院桃源农业生态试验站选择冬闲稻田和油菜地两种不同土地利用方式,并设置添加和不添加双氰胺(DCD)处理,采用静态箱采集和气相色谱法结合监测N_2O排放动态,利用分子生物学手段分析氨氧化古菌(AOA)和氨氧化细菌(AOB)的群落结构和丰度变化.结果表明,添加DCD后明显抑制了冬闲稻田和油菜地N_2O排放,分别减少了36.7%和23.6%.DCD施入抑制了冬闲稻田AOA和AOB的丰度但只改变AOA的群落结构,DCD使AOA和AOB丰度分别减少了59.3%和73.7%.与此相反,添加DCD只改变油菜地AOB的群落结构同时只抑制了AOB的丰度.本研究表明,施加DCD能有效减少冬闲稻田和冬季油菜地N_2O排放,但减排机制不一致.     

氮肥与DCD配施对棚室黄瓜土壤NH3挥发损失及N2O排放的影响

以传统水氮管理为对照,进行了优化水氮管理条件下氮肥与DCD配施对大棚黄瓜土壤氨挥发损失及氧化亚氮排放的影响研究.试验结果表明,与传统水氮管理相比,优化水氮管理减少了氮肥用量及灌水量,但黄瓜产量并没有降低.各水氮处理的NH3挥发速率峰值出现在施肥灌水后的第3d,添加DCD的各优化水氮处理与传统水氮处理相比,土壤氨挥发累积量分别减少55.97%、43.68%、66.47%,4次追肥后W2N2+DCD、W2N3+DCD和W2N4+DCD的氨挥发速率峰值与累积量变化范围较小.不同水氮处理的N2O排放通量的峰值均出现在施肥灌水后的第4d,各追肥时期W2N2+DCD、W2N3+DCD和W2N4+DCD处理,土壤N2O排放通量峰值与N2O累计排放量均显著低于传统水氮处理W1N1,并且3个处理之间不存在显著差异,充分表明优化水氮管理中将氮肥与DCD配施对减少N2O排放起到了显著作用.     

优化施氮对河套灌区氧化亚氮排放和氨挥发的影响

以河套灌区盐化潮土为研究对象,采用静态暗箱-气相色谱法和通气法研究了4个施肥处理(不施肥(CK)、传统施肥(CON)、优化处理1(OPT1,减氮53.3%)、优化处理2(OPT2,减氮53.3%+硝化抑制剂))对河套灌区玉米农田氧化亚氮(N_2O-N)排放、氨挥发(NH_3-N)损失和玉米产量的影响.结果表明:氮肥减量显著降低了土壤N_2O-N排放和NH_3-N挥发;相比于CON处理,OPT1处理的N_2O-N排放量和NH_3-N挥发量分别降低了45.2%和68.8%(p0.05),但N_2O-N损失氮素比率增加了9.7%(p0.05).施用硝化抑制剂可显著降低土壤N_2O-N排放,与OPT1处理相比,OPT2处理可降低34.6%(p0.05)的N_2O-N排放和41.5%(p0.05)的N_2O-N损失氮素比率,但NH_3-N挥发增加了47.5%(p0.05).OPT1处理显著降低了玉米产量,降幅达22.1%(p0.05),而OPT2处理相对于OPT1处理增产32.9%(p0.05),与传统施肥处理无差异.因此,综合N_2O-N排放、NH_3-N挥发及玉米产量可知,OPT2是较为合理的施肥措施,值得在河套灌区推广.     

An overview of the revised 1996 IPCC guidelines for national greenhouse gas inventory methodology for nitrous oxide from agriculture

The IPCC Guidelines for National Greenhouse Gas Inventories provide default methodologies for estimating emissions of the most important greenhouse gases at a national scale. The methodology for estimating emissions of nitrous oxide (N₂O) from agriculture was revised in 1996 by an international working group. Here we summarize this new methodology and apply it to the global data. The new method aims at assessing the full nitrogen cycle and takes into account N₂O formation in agricultural fields (direct emissions), animal waste management systems (AWMSs) as well as indirect emissions taking place at remote places after nitrogen is lost from the agricultural fields. Using the IPCC method, we estimated that global agricultural N₂O emissions almost doubled between 1960 (3.5 Tg N₂O-N) and 1994 (6.2 Tg N₂O-N). Direct emissions, animal waste management systems and indirect emissions make about equal contribution to total current emissions.     

Methane,nitrous oxide and ammonia emissions during storage and after application of dairy cattle slurry and influence of slurry treatment

Slurries are a significant source of CH₄, NH₃ and N₂O emissions to the atmosphere. The research project aimed at quantifying CH₄, NH₃ and N₂O emissions from liquid manure stores and after manure application under field conditions. The influence of the manure treatment options “no treatment”, “slurry separation”, “anaerobic digestion”, “slurry aeration” and “straw cover” on the emission level was investigated. Approximately 10 m³ of differently treated slurry were stored in pilot scale slurry tanks. Emissions were followed for c. 80 days. After the storage period, slurries were applied to permanent grassland. Greenhouse gas emissions from slurry were mainly caused by methane emissions during storage and by nitrous oxide emissions after field application of manures. Mitigation of GHG emissions can be achieved by a reduction in slurry dry matter and easily degradable organic matter content. Ammonia emissions mainly occurred after field application. Untreated slurry emitted 226.8 g NH₃ m⁻³ and 92.4 kg CO₂ eq. m⁻³ (storage and field application). Slurry separation (liquid fraction and composting of the solid fraction) resulted in NH₃ losses of 402.9 g m⁻³ and GHG losses of 58.5 kg CO₂ eq. m⁻³. Anaerobic digestion was a very effective means to reduce GHG emissions. 37.9 kg CO₂ eq. m⁻³ were lost. NH₃ emissions were similar to those from untreated slurry. Covering the slurry store with a layer of chopped straw instead of a wooden cover increased NH₃ emissions to 320.4 g m⁻³ and GHG emissions to 119.7 kg CO₂ eq. m⁻³. Slurry aeration nearly doubled NH₃ emissions compared to untreated slurry. GHG emissions were reduced to 53.3 kg CO₂ eq. m⁻³.     

Effects of aeration method and aeration rate on greenhouse gas emissions during composting of pig feces in pilot scale

The aim of this study was to uncover ways to mitigate greenhouse gas(GHG) emissions and reduce energy consumption during the composting process. We assessed the effects of different aeration rates(0, 0.18, 0.36, and 0.54 L/(kg dry matter(dm)·min)) and methods(continuous and intermittent) on GHG emissions. Pig feces and corn stalks were mixed at a ratio of 7:1. The composting process lasted for 10 weeks, and the compost was turned approximately every 2 weeks. Results showed that both aeration rate and method significantly affected GHG emissions. Higher aeration rates increased NH3 and N2O losses,but reduced CH4 emissions. The exception is that the CH4 emission of the passive aeration treatment was lower than that of the low aeration rate treatment. Without forced aeration,the CH4 diffusion rates in the center of the piles were very low and part of the CH4 was oxidized in the surface layer. Intermittent aeration reduced NH3 and CH4 losses, but significantly increased N2 O production during the maturing periods. Intermittent aeration increased the nitrification/denitrification alternation and thus enhanced the N2 O production. Forced aeration treatments had higher GHG emission rates than the passive aeration treatment. Forced aeration accelerated the maturing process, but could not improve the quality of the end product. Compared with continuous aeration, intermittent aeration could increase the O2 supply efficiency and reduced the total GHG emission by 17.8%, and this reduction increased to 47.4% when composting was ended after 36 days.     

Effect of phosphogypsum and dicyandiamide as additives on NH3, N2O and CH4 emissions during composting

A laboratory scale experiment of composting in a forced aeration system using pig manure with cornstalks was carried out to investigate the effects of both phosphogypsum and dicyandiamide (DCD, C2H4N4) as additives on gaseous emissions and compost quality. Besides a control, there were three amended treatments with different amounts of additives. The results indicated that the phosphogypsum addition at the rate of 10% of mixture dry weight decreased NH₃ and CH₄ emissions significantly during composting. The addition of DCD at the rate of 0.2% of mixture dry weight together with 10% of phosphogypsum further reduced the N₂O emission by affecting the nitrification process. Reducing the phosphogypsum addition to 5% in the presence of 0.2% DCD moderately increased the NH₃ emissions but not N₂O emission. The additives increased the ammonium content and electrical conductivity significantly in the final compost. No adverse effect on organic matter degradation or the germination index of the compost was found in the amended treatments. It was recommended that phosphogypsum and DCD could be used in composting for the purpose of reducing NH₃, CH₄ and N₂O emissions. Optimal conditions and dose of DCD additive during composting should be determined with different materials and composting systems in further study.     

施用畜禽粪便堆肥品的蔬菜地CH4、N2O和NH3排放特征

农田是重要的温室气体排放来源之一,其中蔬菜地的温室气体排放日益受到人们关注.以北京市郊某温室种植的油麦菜地为研究对象,通过大棚试验,考察和比较了油麦菜地施用不同类型畜禽粪便堆肥产品的CH4、N2O和NH3排放特征及其影响因素.结果表明,油麦菜地NRM、RM、CF处理的CH4排放系数分别为0.2%、0.027%、0.004%;N2O排放系数分别为0.18%、0.63%、0.74%;NH3排放系数分别为2.00%、3.98%、2.53%.CH4排放通量与土壤温度和地表湿度相关,N2O排放通量与土壤温度、地表温度和湿度相关,CH4、N2O和NH3排放通量均受土壤含水率影响,而温室中的气温不是影响CH4、N2O和NH3排放的主要因素.     

秸秆还田方式对东北农田土壤NH3挥发和N2O排放的影响

秸秆还田是有效利用资源、增加土壤有机质含量和培肥地力的有效措施,但也会影响土壤NH₃挥发和N₂O的排放.探索不同秸秆还田方式对NH₃挥发和N₂O排放的影响对于减少土壤氮素损失和保护生态环境具有重要意义.采用田间小区试验,利用Los Gatos Research（LGR）超便携NH₃分析仪和密闭式静态箱-气相色谱法探究不同秸秆还田方式下土壤NH₃挥发和N₂O排放的特征,试验设4个处理（覆盖还田,即表面覆盖玉米秸秆,0~20和20~40 cm土壤分层扰动后填回,记为JG0-0;常规还田,即秸秆与0~20 cm土壤混合,20~40 cm土壤扰动后填回,记为JG0-20;深还田,秸秆与20~40 cm土壤混合,0~20 cm土壤挖出后填回,记为JG20-40;对照处理,即无玉米秸秆还田,0~20和20~40 cm土壤分层扰动后填回,记为CK）.结果表明:①相比于CK,不同秸秆还田方式均显著降低了土壤NH₃挥发量,增加了土壤N₂O排放量.与CK相比,JG0-0、JG0-20和JG20-40处理下土壤NH₃累积排放量分别减少了12.38%、9.87%和5.73%;土壤N₂O累积排放量分别增加了30.19%、82.82%和36.53%,其中JG0-0和JG20-40处理之间无显著性差异.②JG20-40处理下玉米产量显著高于其他处理,比CK增加了23.15%,JG0-0处理下玉米产量高于CK和JG0-20处理,但并未达到显著水平.③对于NH₃和N₂O这两种气体的总累积排放量,各处理间均达到显著性差异.与CK相比,JG0-0、JG0-20和JG20-40处理下NH₃和N₂O总累积排放量分别增加了16.67%、52.08%和22.92%.④不同秸秆还田方式下的氮素气态损失率均高于CK,JG0-0、JG0-20和JG20-40处理下氮素气态损失率分别比CK增加了17.50%、52.50%和22.50%.因此,综合考虑土壤NH₃挥发量、N₂O排放量和玉米产量等因素,JG0-0处理优于JG20-40、JG0-20处理.      

Managing the nitrogen cycle to reduce greenhouse gas emissions from crop production and biofuel expansion

Public policies are promoting biofuels as an alternative to fossil fuel consumption in order to mitigate greenhouse gas (GHG) emissions. However, the mitigation benefit can be at least partially compromised by emissions occurring during feedstock production. One of the key sources of GHG emissions from biofuel feedstock production, as well as conventional crops, is soil nitrous oxide (N₂O), which is largely driven by nitrogen (N) management. Our objective was to determine how much GHG emissions could be reduced by encouraging alternative N management practices through application of nitrification inhibitors and a cap on N fertilization. We used the US Renewable Fuel Standards (RFS2) as the basis for a case study to evaluate technical and economic drivers influencing the N management mitigation strategies. We estimated soil N₂O emissions using the DayCent ecosystem model and applied the US Forest and Agricultural Sector Optimization Model with Greenhouse Gases (FASOMGHG) to project GHG emissions for the agricultural sector, as influenced by biofuel scenarios and N management options. Relative to the current RSF2 policy with no N management interventions, results show decreases in N₂O emissions ranging from 3 to 4 % for the agricultural sector (5.5–6.5 million metric tonnes CO₂?eq.?year^?1; 1 million metric tonnes is equivalent to a Teragram) in response to a cap that reduces N fertilizer application and even larger reductions with application of nitrification inhibitors, ranging from 9 to 10 % (15.5–16.6 million tonnes CO₂?eq.?year^?1). The results demonstrate that climate and energy policies promoting biofuel production could consider options to manage the N cycle with alternative fertilization practices for the agricultural sector and likely enhance the mitigation of GHG emissions associated with biofuels.     

Methane and nitrous oxide emissions from a subtropical coastal embayment (Moreton Bay, Australia)

Surface water methane (CH₄) and nitrous oxide (N₂O) concentrations and fluxes were investigated in two subtropical coastal embayments (Bramble Bay and Deception Bay, which are part of the greater Moreton Bay, Australia). Measurements were done at 23 stations in seven campaigns covering different seasons during 2010-2012. Water-air fluxes were estimated using the Thin Boundary Layer approach with a combination of wind and currents-based models for the estimation of the gas transfer velocities. The two bays were strong sources of both CH₄ and N₂O with no significant differences in the degree of saturation of both gases between them during all measurement campaigns. Both CH₄ and N₂O concentrations had strong temporal but minimal spatial variability in both bays. During the seven seasons, CH₄ varied between 500% and 4000% saturation while N₂O varied between 128 and 255% in the two bays. Average seasonal CH₄ fluxes for the two bays varied between 0.5 ± 0.2 and 6.0 ± 1.5 mg CH₄/(m²·day) while N₂O varied between 0.4 ± 0.1 and 1.6 ± 0.6 mg N₂O/(m²·day). Weighted emissions (t CO₂-e) were 63%-90% N₂O dominated implying that a reduction in N₂O inputs and/or nitrogen availability in the bays may significantly reduce the bays' greenhouse gas (GHG) budget. Emissions data for tropical and subtropical systems is still scarce. This work found subtropical bays to be significant aquatic sources of both CH₄ and N₂O and puts the estimated fluxes into the global context with measurements done from other climatic regions.     

Effect of C/N ratio, aeration rate and moisture content on ammonia and greenhouse gas emission during the composting

Gaseous emission (N₂O, CH₄ and NH₃) from composting can be an important source of anthropogenic greenhouse gas and air pollution. A laboratory scale orthogonal experiment was conducted to estimate the effects of C/N ratio, aeration rate and initial moisture content on gaseous emission during the composting of pig faeces from Chinese Ganqinfen system. The results showed that about 23.9% to 45.6% of total organic carbon (TOC) was lost in the form of CO₂ and 0.8% to 7.5% of TOC emitted as CH₄. Most of the nitrogen was lost in the form of NH₃, which account for 9.6% to 32.4% of initial nitrogen. N₂O was also an important way of nitrogen losses and 1.5% to 7.3% of initial total nitrogen was lost as it. Statistic analysis showed that the aeration rate is the most important factor which could affect the NH₃ (p = 0.0189), CH₄ (p = 0.0113) and N₂O (p = 0.0493) emissions significantly. Higher aeration rates reduce the CH₄ emission but increase the NH₃ and N₂O losses. C/N ratio could affect the NH₃ (p = 0.0442) and CH₄ (p = 0.0246) emissions significantly, but not the N₂O. Lower C/N ratio caused higher NH₃ and CH₄ emissions. The initial moisture content can not influence the gaseous emission significantly. Most treatments were matured after 37 days, except a trial with high moisture content and a low C/N ratio.     

Global warming contributions from wheat,sheep meat and wool production in Victoria,Australia – a life cycle assessment

This paper compares the life cycle global warming potential of three of Australia’s important agricultural production activities – the production of wheat, meat and wool in grazed subterranean clover (sub-clover) dominant pasture and mixed pasture (perennial ryegrass/phalaris/sub-clover/grass and cape weed) systems. Two major stages are presented in this life cycle assessment (LCA) analysis: pre-farm, and on-farm. The pre-farm stage includes greenhouse gas (GHG) emissions from agricultural machinery, fertilizer, and pesticide production and the emissions from the transportation of these inputs to paddock. The on-farm stage includes GHG emissions due to diesel use in on-farm transport and processing (e.g. seeding, spraying, harvesting, topdressing, sheep shearing), and non-CO₂ (nitrous oxide (N₂O), and methane (CH₄)) emissions from pastures and crop grazing of lambs.The functional unit of this life cycle analysis is the GHG emissions (carbon dioxide equivalents – CO₂ -e) from 1 kg of wheat, sheep meat and wool produced from sub-clover, wheat and mixed pasture plots. The GHG emissions (e.g. CO₂, N₂O and CH₄ emission) from the production, transportation and use of inputs (e.g. fertilizer, pesticide, farm machinery operation) during pre-farm and on-farm stages are also included. The life cycle GHG emissions of 1 kg of wool is significantly higher than that of wheat and sheep meat. The LCA analysis identified that the on-farm stage contributed the most significant portion of total GHG emissions from the production of wheat, sheep meat and wool. This LCA analysis also identified that CH₄ emissions from enteric methane production and from the decomposition of manure accounted for a significant portion of the total emissions from sub-clover and mixed pasture production, whilst N₂O emissions from the soil have been found to be the major source of GHG emissions from wheat production.     

厌氧条件下砂壤水稻土N2、N2O、NO、CO2和CH4排放特征

了解厌氧条件土壤反硝化气体(N2、N2O和NO)、CO2和CH4排放特征,是认识反硝化过程机制的基础,并有助于制定合理的温室气体减排措施.定量反硝化产物组成,可为氮转化过程模型研发制定正确的关键过程参数选取方法或参数化方案.本研究选取质地相同(砂壤土)的两个水稻土为研究对象,通过添加KNO3和葡萄糖的混合溶液,将培养土壤的初始NO-3和DOC含量分别调节到50 mg·kg-1和300 mg·kg-1,采用氦环境培养-气体及碳氮底物直接同步测定方法,研究完全厌氧条件下土壤N2、N2O、NO、CO2和CH4的排放特征,并获得反硝化气态产物中各组分的比率.结果表明,在整个培养过程中,两个供试土壤的N2、N2O和NO累积排放量分别为6~8、20和15~18 mg·kg-1,这些气体排放量测定结果可回收土壤NO-3变化量的95%~98%,反硝化气态产物以N2O和NO为主,其中3种组分的比率分别为15%~19%(N2)、47%~49%(N2O)和34%~36%(NO);但反硝化气体产物组成的逐日动态均显现为从以NO为主逐渐过渡到以N2O为主,最后才发展到以N2为主.以上结果说明,反硝化气体产物组成是随反硝化进程而变化的,在以气体产物组成比率作为关键参数计算各种反硝化气体产生率或排放率的模型中,很有必要重视这一点.     

Stepwise multiple regression method of greenhouse gas emission modeling in the energy sector in Poland

The energy sector in Poland is the source of 81% of greenhouse gas (GHG) emissions. Poland, among other European Union countries, occupies a leading position with regard to coal consumption. Polish energy sector actively participates in efforts to reduce GHG emissions to the atmosphere, through a gradual decrease of the share of coal in the fuel mix and development of renewable energy sources. All evidence which completes the knowledge about issues related to GHG emissions is a valuable source of information. The article presents the results of modeling of GHG emissions which are generated by the energy sector in Poland. For a better understanding of the quantitative relationship between total consumption of primary energy and greenhouse gas emission, multiple stepwise regression model was applied. The modeling results of CO₂ emissions demonstrate a high relationship (0.97) with the hard coal consumption variable. Adjustment coefficient of the model to actual data is high and equal to 95%. The backward step regression model, in the case of CH₄ emission, indicated the presence of hard coal (0.66), peat and fuel wood (0.34), solid waste fuels, as well as other sources (− 0.64) as the most important variables. The adjusted coefficient is suitable and equals R² = 0.90. For N₂O emission modeling the obtained coefficient of determination is low and equal to 43%. A significant variable influencing the amount of N₂O emission is the peat and wood fuel consumption.