黑土长缓坡地形与横垄对土壤有机碳空间分异的交互作用

横坡垄作对坡耕地土壤有机碳（soil organic carbon,SOC）流失有一定的阻控作用,但黑土区特有长而缓的地形与横垄对坡耕地SOC空间分异会产生交互作用,而这种交互作用引发的SOC流失风险没引起足够的重视。该研究以典型黑土区黑龙江省黑河市北安分局红星农场为研究区域,2022年在横坡垄作与顺坡水线方向上共布设25个采样点,采用地理探测器模型、单因素方差分析（one-way ANOVA）和Pearson相关性分析,探讨土壤有机碳的空间分异及其交互作用。结果表明,横坡垄作方向上垄沟土壤有机碳含量从坡顶到水线呈现逐渐增大的变化趋势;在垄台从坡顶到水线呈现先增大后减小的变化趋势。顺坡水线方向,土壤有机碳含量在垄沟呈现从上坡到下坡增大的变化趋势;在垄台呈现先增大后减小的变化趋势。由于断垄产生水线,顺坡土壤有机碳含量上坡与下坡仍有显著差异（P＜0.05）。Pearson相关性分析表明, 有机碳与可蚀性K因子呈显著负相关（垄沟和垄台相关系数分别为–0.228和–0.238,P＜0.05）,与碳循环相关的β-葡萄糖苷酶和微生物生物量碳在垄沟呈极显著正相关（相关系数为0.398和0.676,P<0.01）。地理探测器分析表明,顺坡水线对土壤有机碳空间分异的影响最大,其对垄沟和垄台SOC的解释力分别达到61%和52%以上;顺坡水线与其他因子的交互作用共同增强了对土壤有机碳的解释力,尤其是顺坡水线与高程的交互作用最为明显。黑土区坡耕地土壤有机碳空间分异主要受顺坡水线与高程的交互作用,横坡垄作虽然能够拦截径流,但由于长缓坡地形影响产生的断垄会加剧土壤侵蚀诱发的有机碳流失。因此,黑土坡耕地治理需要同时考虑横垄与地形的共同影响,从而实现防蚀的优化效果。     

天津市产业碳排放的影响因素及贡献

[目的] 综合考虑“水—土—能—碳”相互关系,研究产业碳排放的影响因素及贡献,为天津市减排决策制定提供一定依据。[方法] 对天津市产业碳排放进行测算,将水土资源因素引入Kaya恒等式,运用LMDI模型计算产业碳排放各影响因素的贡献。[结果] 2004—2018年天津市各产业碳排放均呈现上升趋势;整体来看,水资源经济产出、人口数量促进天津市各产业碳排放,且前者为主要促进因素,水土资源因素抑制各产业碳排放,碳排放强度促进农业碳排放,而抑制其他产业碳排放,人均用地面积抑制农业碳排放,而促进其他产业碳排放;水土资源因素对各产业碳排放影响的变化与水土资源匹配度变化有较好的一致性,单位用地面积用水量越多,其对碳排放的促进作用越大。[结论] 为实现节能减排,应发展节水产业,优化城市水土资源开发利用,发挥水土资源因素对碳排放的抑制作用。     

国内外有机肥标准对比及风险评价

中国是人口最多的发展中国家,生产生活中产生的有机废弃物数量巨大,堆制有机肥是降低有机废物污染风险的重要方式,而有机肥标准则是防止有机肥成为新的土壤污染源,规范有机肥产业健康发展的重要保障。目前我国有机肥不合格现象时有发生,针对有机堆肥的标准仅有一个8年前的行业标准（NY 525—2012）的现状,本文对比了中国、日本、澳大利亚、欧盟、美国有机肥标准的重要指标,对存在的重金属残留、抗生素污染、病原体污染、营养富集及土壤盐渍化等有机肥质量安全风险问题进行分析,为我国有机肥行业未来绿色、健康、可持续发展提出建议。尽管我国现有有机肥质量标准,在具体指标要求方面优于美国,但和欧盟相比还有差距,比如我国重金属Cu、Zn、Ni限量缺失,对Cd等重金属限值要求不够严格,长期施用会导致土壤重金属含量超过风险筛选值,严重影响农作物安全;同时,由于部分畜禽养殖业不合理使用抗生素,加之有机肥生产企业技术的欠缺,农户施用时缺乏指导,监管部门执法不严等因素,我国有机肥施用过程存在较大风险隐患。因此,进一步完善有机肥标准体系,强化对原料中有毒有害物质的限制,要求选用原料批批检,加大准入和过程的落实力度,才能保障我国有机肥产业有序健康发展。     

基于GIS与分区Kriging的采煤沉陷区土壤有机碳含量空间预测

中国煤炭产量占世界煤炭总产量的46.9%,年塌陷的耕地面积约为200 km~2,对农田土壤有机碳库扰动十分剧烈。由于农田的土壤有机碳库是减少陆地生态系统碳排放的最大潜在因素,中国以及世界上的其他煤炭开采大国必须更好地对煤炭开采区的土壤有机碳库进行科学管理,这也是煤炭低碳开采的重要途径。而预测精度好的煤炭开采沉陷区土壤有机碳含量空间预测方法是科学管理煤炭开采沉陷区土壤有机碳库的前提。该文以徐州九里煤炭开采沉陷区作为研究区,通过普通Kriging插值法和以结合沉陷积水情况为辅助变量的分区Kriging插值法这2种方法来对研究区的土壤有机碳含量进行了空间预测,并通过比较验证样点的预测值与实测值来对比2种方法的预测精度,确定每种方法的可行性。研究发现,结合区域内部积水情况来进行的分区Kriging插值法求得到的预测值与实测值的相关系数为0.7564,远高于直接进行Kriging插值得到的预测值与实测值的相关系数0.5086,并且两者的均方根误差分别为0.35和0.55,说明前者的预测精度更高。因此结合沉陷积水情况的分区Kriging插值模式是更适宜煤炭开采沉陷区土壤有机碳含量的空间预测模型。     

有机酸对红壤磷素吸附特性的影响

以不同供磷水平的旱地红壤为材料,探讨了柠檬酸、酒石酸和草酸对红壤磷素吸附特性的影响。试验结果表明,经有机酸培育后的红壤磷的吸附曲线与Langmuir方程吻合性很好,相关系数可达0.949~0.999。有机酸可使磷的吸附曲线类型发生转变,柠檬酸可使土壤磷的吸附等温线由第Ⅱ类型转化为第Ⅲ类型,酒石酸可改变CK与NPK处理的吸附类型,而草酸没有影响。柠檬酸可使土壤的Xm降低30%~75.3%,以PM处理中的降低程度最大。酒石酸和草酸却在不同程度上使土壤的Xm增大,二者可使Xm分别增加0.8~2.3倍和0.1~0.3倍。三种有机酸均可减小平衡常数K值,提高土壤磷素的吸附饱和度,对磷素吸附特征值的影响程度大小顺序为:柠檬酸>酒石酸>草酸。在磷素利用率低的红壤中,增施有机肥或配施有机肥是提高土壤磷素生物有效性的最佳途径。     

滇中本地和外来植物群落对紫色土理化性质的影响

在同一"气候-母质"条件下,本文研究了滇中飒马场流域4种处于不同演替阶段的本地植被群落和1种外来植被群落对酸性紫色土理化性质的影响。结果表明:随着灌草丛、云南松、针阔混交林到次生常绿阔叶林的本地植物群落演替过程,土壤的容重、pH、水溶性盐阳离子含量明显降低,而土壤粘粒、水解性酸、活性铝、有机碳、全氮含量显著增加,同时表层土壤有机碳和全氮占其剖面总含量的比例有降低的趋势。次生常绿阔叶林土壤0~150 cm土层的有机碳、全氮贮存量比灌草丛土壤的分别高出35 Mg hm-2和1.2 Mg hm-2,而其pH则比灌草丛土壤的低0.33。这反映出酸性紫色土的富铝化过程、生物富集过程和粘化过程随着植被演进而加强。桉树林土壤有机碳、全氮贮量和pH分别为93.04 mg hm-2、2.45 mg hm-2和4.49,与针阔混交林土壤的有机碳、全氮贮量和pH没有显著差异,但是其水解性酸度和活性铝含量均显著高于针阔混交林土壤的,表明长期种植桉树有加速土壤酸化的可能。     

Effects of wood char and activated carbon on the hydrolysis of cellobiose by β-glucosidase from Aspergillus niger

Biochar amendments to soils have been suggested as a strategy to sequester carbon and therefore mitigate global climate change. The enrichment of soils with charred materials also increases their fertility. This fertilising effect of biochar may be caused by various mechanisms; an acceleration of nutrient cycling has been suggested as one such mechanism. The rate-limiting step in nutrient cycling is thought to be the extracellular enzymatic attack on biological macromolecules. In this study, therefore, the effects of chestnut wood char (specific surface area 2.0 m² g⁻¹) and of activated carbon (specific surface area approximately 900 m² g⁻¹) on an extracellular enzymatic reaction involved in the degradation of cellulose (i.e., hydrolysis of cellobiose by β-glucosidase from Aspergillus niger) were investigated. Cellobiose was not adsorbed by chestnut wood char, whereas activated carbon absorbed more than 97% of it. Both charred materials adsorbed more than 99% of β-glucosidase. For chestnut wood char, adsorption of the enzyme caused a decrease of approximately 30% in the reaction rate, whereas for activated carbon, the nearly complete absorption of both substrate and enzyme entirely inhibited the reaction. These results show that β-glucosidase from A. niger retains most of its activity when adsorbed to chestnut wood char and that the reaction it catalyses in nature is only slightly affected by this charred material. On the other hand, a material characterised by a high specific surface area and high porosity, such as activated carbon, can make even a highly soluble substrate unavailable for soil enzymes and therefore completely inhibit the reaction. Thus, charred materials may affect nutrient cycling mainly by regulating the availability of substrates: the degradation of highly soluble substrates may be accelerated by materials with low specific surface area, which maintain an active and protected enzyme pool, whereas materials with high specific surface and high porosity may slow down the degradation by making substrates unavailable.     

Short term soil priming effects and the mineralisation of biochar following its incorporation to soils of different pH

The aim of this work was to determine the magnitude of the priming effect, i.e. short-term changes in the rate (negative or positive) of mineralisation of native soil organic carbon (C), following addition of biochars. The biochars were made from Miscanthus giganteus, a C4 plant, naturally enriched with ¹³C. The biochars were produced at 350 °C (biochar350) and 700 °C (biochar700) and applied with and without ryegrass as a substrate to a clay-loam soil at pH 3.7 and 7.6. A secondary aim was to determine the effect of ryegrass addition on the mineralisation of the two biochars.After 87 days, biochar350 addition caused priming effects equivalent to 250 and 319 μg CO₂-C g⁻¹ soil, in the low and high pH soil, respectively. The largest priming effects occurred at the start of the incubations. The size of the priming effect was decreased at higher biochar pyrolysis temperatures, which may be a way of controlling priming effects following biochar incorporation to soil, if desired. The priming effect was probably induced by the water soluble components of the biochar. At 87 days of incubation, 0.14% and 0.18% of biochar700 and 0.61% and 0.84% of biochar350 were mineralized in the low and high pH soil, respectively. Ryegrass addition gave an increased biochar350 mineralisation of 33% and 40%, and increased biochar700 at 137% and 70%, in the low and high pH soils, respectively. Certainly, on the basis of our results, if biochar is used to sequester carbon a priming effect may occur, increasing CO₂-C evolved from soil and decreasing soil organic C. However, this will be more than compensated for by the increased soil C caused by biochar incorporation. A similar conclusion holds for accelerated mineralisation of biochar due to incorporation of fresh labile substrates. We consider that our results are the first to unequivocally demonstrate the initiation, progress and termination of a true positive priming effect by biochar on native soil organic C.     

小麦–玉米轮作体系长期施肥对塿土微生物量碳、氮及酶活性的影响

以20年塿土小麦玉米轮作体系长期肥料定位试验为平台,探讨不同施肥模式下土壤化学肥力要素、微生物量碳氮及酶活性的响应。试验包括不施肥（CK）、单施氮肥（N）、氮磷（NP）、磷钾（PK）、氮磷钾（NPK）、NPK+秸秆（SNPK）以及不同量有机肥+NPK（M1NPK、M2NPK）等8种施肥模式。结果表明,与CK相比,长期施用NP提高土壤有机碳含量达34.0%、全氮34.0%、全磷58.5%、速效磷608.9%、微生物量碳23.3%、微生物量氮54.0%、蔗糖酶53.9%、脲酶132.6%、碱性磷酸酶29.9%以及脱氢酶40.9%。长期施用NPK与NP效果相似,钾素效果甚微。作物秸秆还田配合氮磷钾化肥与氮磷钾相比没有明显影响土壤有机碳、氮和磷水平,但是显著提高微生物量碳的含量（29.5%）、碱性磷酸酶（23.0%）和脱氢酶（26.9%）的活性。有机肥配合氮磷钾与其它施肥处理相比,显著提升土壤化学肥力要素、微生物量碳氮和酶活性,特别是引起了磷素的大量富集（速效磷含量大于150 mg/kg）。因此,塿土不施有机物情况下,氮磷配合可以提高土壤化学和生物肥力,作物秸秆还田配合氮磷钾化肥的培肥效果优于氮磷钾化肥配合,而合理的有机无机肥配合是塿土提升化学肥力和保证生物健康的最佳施肥模式。     

Characterization of humus-protease complexes extracted from soil

Pyrophosphate (140 mM, pH 7.1) extracts of two arable soils and one pasture soil were ultrafiltrated separating the extracted material into three fractions: A_I with nominal molecular weight (nmw) > 100 kD, A_II with nmw between 10 kD and 100 kD and R with nmw < 10 kD. Protease activity was determined in the fractions by using three different substrates: N-benzoyl-l-argininamide (BAA), specific for trypsin; N-benzyloxy-carbonyl-l-phenylalanyl l-leucine (ZPL), specific for carboxypeptidases; and casein, essentially a non-specific substrate. The derivative fractions were also analysed for their amino acid N and humic (HA) and fulvic (FA) acid contents. The organic matter of extracts and derivative fractions obtained from the pasture soil was analysed by isoelectric focusing (IEF) and that of fractions analysed by pyrolysis gas chromatography (Py-GC). Activities of the extract were monitored for their thermal stability and those of the extract and derivative fractions for their optimal pH.Due to the mechanical disintegrating action of sodium pyrophosphate over the humic substances during the fractionation process the amount of total organic C and FA in the fractions was ranked as R > A_II > A_I. The lowest amino acid N/organic C was found in the R fraction, whereas A_II fraction was rich in humic acids, carbohydrates and amino acid N and A_I fraction showed the lowest carbohydrate content. At least 70% of the total BAA- and ZPL-hydrolysing activity was associated to particles with nmw higher than 10 kD and at least 30% of these activities were present in particles with nmw higher 100 kD. Casein-hydrolysing activity was quite evenly distributed among the three fractions (A_I, A_II and R). The extracted protease-organic complexes were resistant to thermal denaturation and some of them showed optimal activity at pH values higher than 10 as a result of the polyanionic characteristics of the humic material surrounding enzyme molecules and of the presence of alkaline protease. Comparison of data obtained in Py-GC analyses and in protease activity suggests that BAA-hydrolysing activity was associated to a highly condensed humic matter and ZPL-hydrolysing activity to less resistant humic substances, while at least some of the extracted casein-hydrolysing activity was present as glyco-proteins not associated to humus. BAA-hydrolysing activity was probably inhibited by fresh organic matter of carbohydrate origin whereas lignin derived organic matter probably inhibited ZPL- and casein-hydrolysing activity.