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1.
茶树根际土壤铝形态演变规律及其影响因素 总被引：5，自引：1，他引：4
茶树是典型的喜酸聚铝植物,为了弄清茶树根际土壤铝的形态特征及其演变规律,本文采集了湖南省不同茶厂、不同母质和不同种植年限的茶树根际土壤,研究了茶树根际土壤铝的形态演变规律及其影响因素。结果表明,不同茶厂由于地域、母质、种植年限等的差异,茶树根际土壤铝形态含量有明显的差异,含量变化为腐殖酸铝铝的水合氧化物和氢氧化物≈交换态铝无机吸附态铝;除腐殖酸铝外,其他3种形态铝含量均以第四纪红色黏土发育的茶树根际土壤的含量最高,且不同形态铝含量有随着茶树种植年限延长而增高的趋势。土壤交换性酸与水解性酸对茶树根际土壤铝形态有显著的影响,而与p H的关系不大;土壤有机质含量影响茶树根际土壤铝形态特征,与无机吸附态铝呈显著正相关关系,与腐殖酸铝有极显著正相关关系。 相似文献
2.
单宁酸对不同pH茶园土壤中活性铝形态分布的影响 总被引：4，自引：0，他引：4
采集云南省普洱市和江西省南昌县两地典型的茶园土壤,通过添加HCl和Ca(OH)2调节土壤pH,研究不同pH(3.0、3.5、4.0、4.5)茶园土壤添加0.4 mmol·kg 1、2.0 mmol·kg 1、4.0 mmol·kg 1、8.0 mmol·kg 1、12.0 mmol·kg 1单宁酸后,活性铝形态交换态铝(Al3+)、单聚体羟基铝[Al(OH)2+、Al(OH)+2]、酸溶无机铝[Al(OH)03]和腐殖酸铝[Al-HA]的分布特征。结果表明:单宁酸添加量为0~0.4 mmol·kg 1和0~2.0 mmol·kg 1时,江西南昌和云南普洱茶园土壤中交换态铝随土壤pH的增加呈明显下降趋势,而羟基态铝、酸溶无机铝和腐殖酸铝呈逐渐上升趋势;当单宁酸浓度增至2.0 mmol·kg 1以上时,随土壤pH的增加,单宁酸对活性铝释放的抑制作用增强,各形态活性铝含量都较低,且不同pH处理土壤间的差异不显著。0~20 cm土层土壤与20~40 cm土层土壤变化规律大致相似,总体上看,下层土壤活性铝总量高于上层。云南普洱茶园土壤活性铝总量明显高于江西南昌的茶园土壤。相关分析表明,0~20 cm土层土壤中,pH与羟基态铝、腐殖酸铝、土壤酸碱缓冲容量(pHBC)呈正相关(r=0.796,P0.01;r=0.960,P0.01;r=0.852,P0.01);pHBC与交换态铝、羟基态铝呈负相关(r=0.904,P0.01;r=0.645,P0.05),而与腐殖酸铝呈正相关(r=0.795,P0.01)。同时,单宁酸加入浓度为0~0.4 mmol·kg 1时,土壤pH明显上升,之后随着单宁酸加入浓度的增加土壤pH持续下降,土壤pH(YpH)与单宁浓度(CDN)在此阶段基本符合方程:YpH=0.04CDN+3.82(R2=0.95,P0.01)的线性变化趋势,在单宁酸浓度达到8.0~12.0 mmol·kg 1时,土壤pH基本不再变化。 相似文献
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4.
土地利用方式与坡位土壤活性铝形态特征分析 总被引：7，自引：0，他引：7
以红壤坡地为材料,研究了地带性恢复林地、农作区、人工林地茶园和桔园等4种土地利用方式下土壤pH、有机质和铝形态的分异特征。结果表明,土壤pH、有机质和3种活性铝形态含量差异显著。和恢复区相比,农作区由于大量秸秆和根茬还土,土壤交换性铝的含量显著降低,而土壤吸附态羟基铝和有机络合态铝的含量则不同程度地提高;人工林地茶园和桔园则呈现出土壤交换性铝提高的特征,吸附态羟基铝和有机络合态铝含量下降。下坡位土壤表现为堆积,土壤pH值和有机质含量增加,土壤交换性铝含量比上坡位减少,吸附态羟基铝和有机络合态铝含量增加,降低了铝的毒性。相关分析表明,土壤pH值与土壤交换性铝呈显著负相关,y=-97.6x＋6009.2（R^2=0.7315）,与土壤吸附态羟基铝呈显著正相关,y=2810.8x-9293（R^2=0.9003）;而土壤有机质含量与土壤交换性铝呈显著负相关,y=-2963x＋17616（R^2=0.8977）,与土壤有机络合态铝呈显著正相关,y=553.4x-4779.1（R^2=0.4364）。说明土壤铝形态在坡面上的分异特征是坡面利用类型与地形部位共同作用的结果。 相似文献
5.
黄棕壤植茶以后,土壤pH下降,土壤酸度随植茶年限的增长而增大,且上层土壤pH的减幅大于下层土壤。茶园土壤的酸化是与茶树对铝和氟的生物积聚、土壤交换性铝与铝络合物的增加以及土壤盐基的淋溶有关。茶树落叶中铝和氟的含量分别高达5836—6136 ppm和469—520ppm;茶树透冠水和土壤渗漏液中均有相当多的Al和F,茶园土壤系统中铝和氟的循环,不仅导致土壤Al3+及F-的增多,还使表土的有机络合态铝以及土壤交换性复合体和土壤溶液中的氟铝络合物积聚。因此,土壤中铝和氟的积累、转化及其生物地球化学循环是茶园土壤酸化的主要原因。 相似文献
6.
粤东凤凰山茶区土壤镉赋存形态特征及茶叶有效性 总被引：1，自引：0，他引：1
通过对粤东凤凰山茶区12个大型茶园土壤和茶叶进行采样,采用连续提取法将茶园土壤Cd分为可交换态、碳酸盐结合态、铁锰氧化物结合态、有机束缚态和残渣态,探讨了茶园土壤Cd的5种化学形态组成特征及其与土壤理化性质和茶叶Cd积累的关系。结果表明:(1)茶区土壤中镉的化学形态分布受到土壤pH值和有机质含量的影响,土壤中Cd的5种化学形态分布的规律为:残渣态>碳酸盐结合态>可交换态>铁锰氧化物结合态>有机束缚态;茶区土壤可交换态Cd和残渣态Cd与土壤中的pH值呈极显著负相关性关系,而有机结合态Cd与土壤pH值呈显著正相关关系;有机质含量与氧化物结合态Cd和有机束缚态Cd呈显著正相关关系,而与可交换态Cd和残渣态Cd呈显著负相关关系。(2)茶叶中Cd含量在0.30~0.98mg/kg,平均含量为0.65mg/kg;茶叶中的Cd含量与土壤中可交换态Cd有显著正相关关系,而与土壤pH值呈显著负相关关系。因此,可以通过调节茶园土壤pH值,影响土壤中Cd的化学形态分布,最终达到降低茶叶中Cd含量,提高茶叶品质的目的。 相似文献
7.
通过实验室模拟,研究不同含量外源有机质存在下（5%、10%和15%）,钙铝交互作用（钙/铝摩尔浓度比为1∶2、1∶1和2∶1）对茶园土壤铝的吸附能力和活性的影响。结果表明,钙铝交互作用显著增加了茶园土壤对铝的吸附量,外源有机质对钙铝交互作用下茶园土壤铝的吸附作用影响不明显;钙铝交互作用使茶园土壤水溶态铝含量增加,交换态铝含量下降,且随钙/铝比的增大交换态铝含量下降越显著;但外源有机质使钙铝交互作用下茶园土壤的水溶态铝含量下降,同时交换态铝含量显著增加。总的看,外源有机质使钙铝交互作用下茶园土壤活性铝含量增加,且随外源有机质含量的增加,活性铝含量增加的越显著。 相似文献
8.
对7个广西环江县果园土壤剖面的28个土样的铝形态空间变异特性进行分析;包括交换性铝、吸附态羟基铝、有机络合态铝三种形态;结果表明:该区土壤中铝形态具有显著空间结构性特点,明显受pH、成土母质、地形地势等自然因素的影响,同时受耕作管理措施等人为因素影响;建议在红壤果园上增施有机肥,控制化学肥料的施用,进行深耕土改,并且施用石灰石以升高pH。 相似文献
9.
外源铜和镍在土壤中的化学形态及其老化研究 总被引：2，自引：0，他引：2
采用连续提取法测定了外源铜和镍进入田间土壤后的化学形态分布,比较研究了这2种重金属在3种不同类型土壤(红壤,水稻土和潮土)中随老化时间的形态转化和分布.结果表明,外源铜以残留态(40%～60%)和EDTA可提取态(40%)为主;随老化时间,EDTA可提取态、易还原锰结合态及铁铝氧化态向残留态转化;外源镍在酸性红壤中以可交换态(40%)和残留态(30%～50%)为主,在中性水稻土中以EDTA可提取态(30%)和残留态(30%～50%)为主,在碱性潮土中以铁铝氧化态(20%)和残留态(40%)为主.随老化时间,水溶态、可交换态、EDTA可提取态等向残留态转化.土壤pH较低时水溶态和可交换态含量较高,但是同时随老化时间的降低量也明显;pH较高时有利于易还原锰结合态和有机质结合态的转化. 相似文献
10.
硅是水稻等禾本科作物生长发育不可或缺的营养元素,pH影响着土壤中硅的有效性和形态转化,而土壤磷与硅之间存在明显的竞争吸附效应。以常年水稻-瓜/菜轮作农田土壤为研究对象,进行等摩尔硅磷竞争吸附试验、土壤培养试验和硅分组试验,模拟探究土壤酸化和磷富集对土壤硅的有效性及移动性的影响,以期为农田硅、磷养分管理提供一定的理论依据。结果表明,在pH 3.5～6.4范围内,同时加入等摩尔浓度的硅和磷时,磷的存在会抑制土壤吸附硅,使土壤对硅的吸附量降低78%～350%。土壤对硅的吸附小于对磷的吸附,磷的添加导致了土壤中硅的解吸。土壤酸化和磷添加均降低了土壤对硅的吸附,且在pH较高时添加磷对降低土壤吸硅的效果更为显著。土壤酸化降低了可移动态硅、吸附态硅、有机结合态硅和铁铝锰（氢）氧化物结合态硅的含量,但增加无定形态硅含量。与pH 6.4相比,酸化使可移动态硅和吸附态硅含量分别降低了22.47%～54.32%、10.72%～33.40%;磷添加使可移动态硅含量增加了4.07%～9.40%,吸附态硅含量降低了1.19%～3.53%。pH可调控土壤硅的溶解与吸附-解吸过程,从而影响土壤硅的移动性;磷富集促进土... 相似文献
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《Communications in Soil Science and Plant Analysis》2012,43(22):3235-3245
Phyllostachys praecox f. preveynalis (Lei bamboo) cultivation with intensive management has high economic profits. However, soil acidification is a severe problem with bamboo plantations that may influence its sustainability in practice. In this study, soils of two sites with different bamboo cultivation times were collected from Lin-an City of Zhejiang Province, China, to understand bamboo soil acidification through analysis of various soil acidification indicators. Results showed that soil nutrients accumulated significantly within the bamboo plantation, but soil pH dropped dramatically. Soil exchangeable acid increased with increasing bamboo planting times, so did the ratio of exchangeable aluminum (Al) to total soil Al. However, the exchangeable base cation [potassium (K) + sodium (Na) + calcium (Ca) + magnesium (Mg)] content and its saturation decreased greatly. With a simple simulation of first-order decay equation, soil acidification rates differed from soil sites but the final pH was similar, which suggested that intensive management exerted an important effect on soil properties. 相似文献
12.
南方茶园土壤酸化特征及交换性酸在水稳性团聚体中的分布 总被引：8，自引：2，他引：6
通过采集浙江省杭州西湖龙井茶园土壤,研究茶园土壤剖面的酸度特征、养分变化以及交换性酸在水稳性团聚体中的分布特征,以了解南方茶园土壤的酸化过程。结果表明:茶园表层土壤(0-20cm)酸化严重,最低的pHH2O值达到4.0,并且有明显的深层化趋势;表土的有机质和速效磷含量较高,速效磷含量最高可达138.2mg/kg;表土团聚体分级表明茶园土壤有良好的团聚体结构,具有良好的水稳性;除了交换性H+在0.5～0.25mm和0.25～0.106mm水稳性团聚体之间没有明显差别外,交换性酸总量、交换性H+和交换性Al 3+含量均随着水稳性团聚体粒径的减小而降低;水稳性大团聚体中交换性Al 3+相对交换性H+占有明显的优势,而在0.106～0.05mm水稳性微团聚体中交换性H+占有明显的优势。交换性酸总量、交换性H+和交换性铝主要分布于>2mm和2～0.5mm水稳性团聚体中,同时在不同粒级团聚体中的分布随粒径的减小而降低。 相似文献
13.
EGCG溶液浓度与酸碱度对黄壤Al、Fe和Mn形态的影响 总被引：2，自引：0，他引：2
植物多酚可通过络合作用改变元素的存在形态。采用双因素完全随机试验设计,通过浸提试验研究表没食子儿茶素没食子酸脂(EGCG)溶液浓度、酸碱度、浓度与酸碱度互作对黄壤可溶态、游离态、无定形态和络合态铝(Al)、铁(Fe)和锰(Mn)的影响。结果表明:EGCG溶液浓度对黄壤可溶态和络合态Al、Fe、Mn及无定形态Al、Fe均产生极显著影响,EGCG溶液酸碱度对黄壤可溶态及无定形态Al、Fe、Mn均产生显著或极显著影响,EGCG溶液浓度与酸碱度对黄壤可溶态Al、Fe、Mn,无定形态和络合态Al也有极显著或显著的互作效应。相关分析结果显示,土壤中3种元素的无定形态氧化物含量与对应的可溶态氧化物含量呈显著或极显著负相关,表明EGCG溶液主要通过改变氧化物形态,特别是无定形态氧化物含量,影响元素活化,进而改变其可溶态含量;Al和Mn的活化会使土壤滤液pH降低,在pH降低幅度较大时,可能导致土壤酸化。本试验一方面为研究酸性茶园土壤酸化的来源提供了方向,另一方面也可为植物Al/Mn毒害的防治提供参考,但在利用植物多酚类物质防治土壤Al/Mn毒害的同时要处理好土壤酸化与治理毒害的关系。 相似文献
14.
土壤组分对广东省酸性水稻土磷吸附参数的影响 总被引：9，自引：2，他引：7
Soil components affecting phosphate sorption parameters were studied using acid paddy soils derived from basalt, granite, sand-shale and the Pearl River Delta sediments, respectively, in Guangdong Province.For each soil, seven 2.50 g subsamples were equilibrated with 50 mL 0.02 mol L-1 (pH=7.0) of KCl containing 0, 5, 10, 15, 25, 50 and 100 ng P kg-1, respectively, in order to derive P sorption parameters (P sorption maximum, P sorption intensity factor and maximum buffer capacity) by Langmuir isotherm equation. It was shown that the main soil components influencing phosphate sorption maximum (Xm) included soil clay, pH,amorphous iron oxide (Feo) and amorphous aluminum oxide (Alo), with their effects in the order of Alo ＞Feo ＞ pH ＞ clay. Among these components, pH had a negative effect, and the others had a positive effect.Organic matter (OM) was the only soil component influencing P sorption intensity factor (K). The main components influencing maximum phosphate buffer capacity (MBC) consisted of soil clay, OM, pH, Feo and Alo, with their effects in the order of Alo ＞ OM ＞ pH ＞ Feo ＞ clay. Path analysis indicated that among the components with positive effects on maximum phosphate buffer capacity (MBC), the effect was in the order of Alo ＞ Feo ＞ Clay, while among the components with negative effects, OM ＞ pH. OM played an important role in mobilizing phosphate in acid paddy soils mainly through decreasing the sorption intensity of phosphate by soil particles. 相似文献
15.
工业副产品改良土壤酸度和铝毒的潜力 总被引：12，自引：0，他引：12
It is imperative to choose some low cost, available and effective ameliorants to correct soil acidity in southern China for sustainable agriculture. The present investigation dealt with the possible role of industrial byproducts, i. e., coal fly ash (CFA), alkaline slag (AS), red mud (RM) and phosphogypsum (PG) in correcting acidity and aluminum (Al) toxicity of soils under tea plantation using an indoor incubation experiment. Results indicated that CFA, AS and RM increased soil pH, while PG decreased the pHs of an Ultisol and an Alfisol. The increment of soil pH followed the order of RM > AS > CFA. All the industrial byproducts invariably decreased exchangeable Al and hence increased exchangeable Ca, Mg, K and Na and effective cation exchange capacity. RM, AS and lime decreased total soluble Al, exchangeable Al and organically bound Al. Formation and retention of hydroxyl-Al polymers were the principal mechanism through which Al phytotoxicity was alleviated by application of these amendments. In addition, the heavy metal contents in the four industrial byproducts constituted a limited environmental hazard in a short time at the rates normally used in agriculture. Therefore, the short-term use of the byproducts, especially AS and RM, as amendments for soil acidity and Al toxicity in acid soils may be a potential alternative to the traditional use of mined gypsum and lime. 相似文献
16.
四环素类抗生素在土壤和堆肥中的吸附和降解 总被引：6，自引：0，他引：6
Two agricultural soils were collected from Dahu and Pinchen counties and swine manure compost (SMC) from Ping-tung County in Taiwan, China to investigate the sorption and dissipation of three tetracyclines (TCs), i.e., oxytetracycline (OTC), tetracycline (TC) and chlortetracycline (CTC), in compost, soils and soil/compost mixtures with different organic carbon (OC) contents. There were seven treatments in total. TCs were most strongly adsorbed to SMC in all treatments due to the high OC content. When SMC was present in the soils, the sorption of TCs was significantly enhanced, which might be attributed to the increased OC content and CEC. The adsorption of TCs showed non-linear adsorption isotherms and fitted well to the Freundlich model. After 49 d of incubation at 25 ℃ in soils and soil/compost mixtures in the dark, TCs elapsed in all substrates, with the time required for 50% degradation (DT50) between 20 and 41 d, and the time for 90% degradation (DT90) between 68 and 137 d. Soil amended with compost enhanced the stability of TCs and reduced their mobility. The dissipation of TCs in a soil environment was slow, indicating that these compounds might be persistent in soil. 相似文献
17.
集约经营下南方竹园土壤酸化特征与缓冲容量研究 总被引：2，自引：0，他引：2
高强度集约经营下竹园土壤质量退化是制约竹笋持续丰产高效的主要障碍因素。通过研究集约经营雷竹林典型土壤剖面的酸度特征、养分变化以及土壤酸碱缓冲容量,以期探明集约经营下雷竹林衰退的可能因素。结果表明,雷竹种植后,表层土壤呈现明显的酸化现象,表土的最低pHH2O值达到了3.75;表土的有机质和速效磷含量明显提高,表土(0~20 cm)速效磷含量最高可达350 mg kg-1;竹林土壤铝的形态分析表明,有机配合态铝在表土中的含量较高,并随剖面深度的降低而降低;土壤交换态铝含量与pHH2O和pHKCl呈极显著负相关,有机配合态铝含量与有机质和速效磷含量呈极显著正相关;竹园土壤的酸碱缓冲容量在8.58~14.31 mmol kg-1之间,有机质含量是影响竹园土壤缓冲容量的主要因素。 相似文献
18.
《Communications in Soil Science and Plant Analysis》2012,43(11-12):1467-1478
Abstract The accumulation of heavy metals in tea leaves is of concern because of its impact on tea quality. This study characterized long‐term changes of soil properties and heavy‐metal fractions in tea gardens and their effect on the uptake of metals from soils by the plants. Soil and tea leaf samples were collected from five plantations with a history of 2–70 years in Jinghua, Zhejiang Province, southeast China. The six chemical fractions (water‐soluble, exchangeable, carbonate‐bound, organic‐matterbound, oxide‐bound, and residual forms) of cadmium (Cd), chromium (Cr), copper (Cu), iron (Fe), nickel (Ni), manganese (Mn), lead (Pb), and zinc (Zn) in the soils were characterized. Dissolved organic‐matter accumulation in the soils and effects of low‐molecular‐weight organic acids on solubility of soil heavy metals were also tested. Long‐term tea plantation use resulted in accumulation of dissolved organic matter, decrease of soil pH, and elevation of water‐soluble and exchangeable metal fractions, thereby increasing metal contents in leaves. The influence was more significant when soil pH was less than 4.4. The results indicated that both acidification and accumulation of dissolved organic matter induced by tea plantations were also important causes of increased accumulation of the metals in the tea leaves. This was particularly true for the soils polluted with low concentration of heavy metals, because availability of the metals in these soils was mainly controlled by pH and dissolved organic matter. 相似文献