土壤磷形态组分分级及31P-NMR 技术应用研究进展

农田生态系统中土壤磷形态转化,影响土壤磷对作物的有效供应。土壤磷分为无机磷和有机磷两大部分。化学连续提取法 (chemical sequential fractionation,CSF) 研究土壤磷形态分级,采用不同的化学提取剂,分级提取土壤中组成或分解能力接近的有机无机含磷化合物,是目前表征土壤磷素形态的重要方法。但该方法虽历经改进,仍难以确切反映土壤磷的实际组成,提取的不同磷形态间存在重叠,有机磷和无机磷组分分级存在一定的误差;不同分级磷组分对作物的有效性,需谨慎评估。核磁共振波谱技术 (nuclear magnetic resonance,NMR) 根据核磁共振波谱图上共振峰的位置、强度和精细结构来研究土壤中含磷化合物的分子结构。液相31P-NMR 可以同吋检测出土壤中多种磷组分,如正磷酸盐、磷酸单酯、磷酸二酯、膦酸脂、焦磷酸盐和多聚磷酸盐,识别土壤提取物磷形态,可将有机磷与无机磷分开。本文综述了应用31P-NMR 技术研究土壤磷形态组分的一些进展,总结了样品制备过程、NMR 测试参数及在土壤磷形态转化研究中的应用。二维31P-NMR 技术发展为鉴定分析土壤中更多种类的含磷化合物提供了契机。     

土壤中210Pbex背景值含量动态平衡模型

在利用土壤侵蚀模型估算侵蚀速率的过程中,背景值点选取的好坏直接关系到结论是否可靠,如果能通过科学计算得出研究区域背景值,将大大提高背景值的准确性,对研究土壤侵蚀具有重大意义。土壤未受到侵蚀和沉积的背景区,首先假设全球大气沉降量为定值,研究把²¹⁰Pb_ex沉降过程以一年为时间尺度划分为n年,经过n年以后（n=0,1,2,…,∞）,土壤中²¹⁰Pb_ex沉降量和经过衰变减少量达到平衡,土壤中²¹⁰Pb_ex含量趋于稳定。假设各地年平均降水量为定值,通过研究发现²¹⁰Pb_ex的大气沉降通量与年降水量之间存在极显著相关（P < 0.01）,区域年降水量是影响土壤中²¹⁰Pb_ex量的主要因素,由于年平均降水量不同,全球各地土壤中²¹⁰Pb_ex含量都会达到不同的稳定值,从而建立土壤中²¹⁰Pb_ex含量与年降水量关系模型。研究²¹⁰Pb_ex来源、沉降的连续性和稳定性,提出利用区域年平均降水量来计算该地区的²¹⁰Pb_ex背景值,建立土壤中²¹⁰Pb_ex背景值含量动态平衡模型,为准确确定²¹⁰Pb_ex背景值提供了方法,对研究土壤侵蚀具有重要的意义。     

黄土高原石灰性土壤不同形态磷组分分布特征

以黄土高原自北向南采集的12个0～20 cm耕层土壤为供试土样,采用Tiessen和Moir修正的Hedley土壤有机无机磷分级方法研究了黄土高原石灰性土壤中不同形态磷组分的分布特征。结果表明:供试土壤各形态P总体分布特征为:HCl-P>Residual-P>NaHCO3-Po>NaHCO3-Pi>NaOH-Po>NaOH-Pi>H2O-P,以HCl-P和Residual-P为主,分别占土壤全磷的54.00%～88.96%和0～39.11%。黄土高原土壤磷含量总体分布表现为南高北低。在各土壤类型间,NaOH-Po、Residual-P和全磷平均含量表现为干润砂质新成土<黄土正常新成土<简育干润均腐土<土垫旱耕人为土,自北向南依次增加;H2O-P和HCl-P表现为简育干润均腐土<黄土正常新成土<干润砂质新成土<土垫旱耕人为土,自北向南先降后升,且上升幅度较大。黄土高原土壤全氮与全磷及各形态磷含量相关性均达显著水平,其中与NaOH-Pi、NaOH-Po、HCl-P及全磷含量达到极显著水平。C/N、pH及砂粒与全磷及各形态磷含量呈负相关关系,其中pH与NaHCO3-Po呈显著负相关,与H2O-P、NaHCO3-Pi、NaOH-Pi及HCl-P呈极显著负相关;砂粒与NaHCO3-Pi、Residual-P及全磷呈显著负相关。除NaHCO3-Po、NaOH-Po及Residual-P,CaCO3与其他各形态磷含量具有一定程度负相关。除NaOH-Pi和NaOH-Po外黏粒与其他各形态磷及全磷也具有一定程度负相关。土壤各形态磷组分和有效磷的多元回归分析发现,各形态磷中对有效磷贡献最大的是H2O-P,其次为NaOH-Pi和NaHCO3-Po;土壤各形态磷组分和有效磷逐步回归分析结果,进一步说明H2O-P的有效性最高。     

珠江三角洲平原土壤磷剖面分布及形态特征研究

以珠江三角洲平原由三角洲沉积物、河流沉积物和滨海沉积物发育形成的水耕人为土(水稻土)为对象,研究了水田、果园、菜地3种利用方式下不同发生层土壤全磷(TP)、有机磷(Po)、有效磷(AP)、无机磷(Pi)组分的含量和剖面分布特征,并利用液相31P核磁共振(NMR)技术测定了耕层土壤中磷形态分布。结果表明,珠江三角洲平原农田土壤全磷、有机磷、有效磷和各形态无机磷含量随土层深度增加呈减小的趋势,耕层土壤中全磷、有效磷、Al-P和Fe-P明显富集;菜地和果园耕层土壤中全磷、有效磷、Al-P、Fe-P、Ca-P和O-P含量均高于水田。土壤磷素以无机磷形态为主,无机磷、有机磷占全磷比例平均值分别为71.3%和28.7%。土壤无机磷组分以O-P和Fe-P为主,Al-P最低。Al-P、Fe-P、Ca-P、O-P与全磷呈极显著或显著正相关,有效磷与Al-P、Fe-P、O-P、全磷呈极显著正相关;Fe-P和Al-P是土壤有效磷的主要贡献者。31P-NMR结果表明,耕层土壤磷形态均以正磷酸盐为主;土地利用方式影响土壤磷组分,菜地耕层土壤中磷形态包括正磷酸盐、磷酸单酯和焦磷酸盐,水田和果园包括正磷酸盐、磷酸单酯、磷酸二酯和焦磷酸盐;水田土壤中正磷酸盐所占比例最低,磷酸单酯和磷酸二酯所占比例最高;成土母质对水田耕层土壤各形态磷所占比例影响很小。     

长期施肥褐土不同磷组分对磷素盈余的响应

  【目的】  研究褐土区玉米田长期不同磷源投入对土壤磷素形态和磷素累积的影响，通过对不同磷组分与磷素盈余之间进行相关性分析，研究不同施肥措施对土壤磷素形态转化的影响，为探索合理的磷肥调控措施，促进土壤中磷素向作物易于吸收的水溶态和碳酸氢钠溶解态转化，提高磷素利用效率提供依据。  【方法】  试验依托始于1992年位于山西省寿阳县北坪旱塬上的长期定位试验。9个施肥处理包括:无肥对照 (CK)、N₁P₁、N₂P₂、N₃P₃、N₄P₄、N₂P₁M₁、N₃P₂M₃、N₄P₂M₂、N₀P₀M₆，其中N₁、N₂、N₃、N₄分别为尿素N 60、120、180、240 kg/hm2，P₁、P₂、P₃、P₄分别为过磷酸钙P 16、33、49、66 kg/hm2，M为腐熟厩肥，M₁、M₂、M₃、M₆分别折合为施P量14、28、42和83 kg/hm2。1992—2016年，收获后取0—20 cm耕层土壤样品，分析土壤磷素形态及盈余量，并计算不同形态磷素与磷盈余量之间的相关性。  【结果】  连续施肥25年后，土壤磷组分发生了不同的变化，不施肥处理除H₂O-Pi、Residual-P外，各形态磷较试验初均有降低。施用无机肥各处理主要增加了土壤中HCl-P含量，以N₄P₄处理提高幅度最大，比试验初提高了127.7%。有机肥投入可以显著提高土壤中的活性磷含量，高量施用有机肥后，H₂O-P总含量较试验初提高了8倍之多，NaHCO₃-Pi年增加速率为11.50 mg/(kg·a)。不同施肥各处理土壤磷素盈余量为N₀P₀M₆ > N₃P₂M₃ > N₄P₄ > N₄P₂M₂ > N₃P₃ > N₂P₂ > N₂P₁M₁ > N₁P₁ > CK。磷素盈余是土壤磷组分变化的重要影响因素，各形态磷组分对磷素累积量响应大小为NaHCO₃-Pi > NaOH-Pi > HCl-P > NaHCO₃-Po > Residual-P > H₂O-Po > NaOH-Po > H₂O-Pi。  【结论】  长期施肥使土壤各组分磷素含量发生了显著变化，有机无机肥配施有利于土壤中活性磷的转化，过量施磷导致磷素在土壤中大量盈余，高量施用有机肥磷素盈余量最大。当以无机肥投入时，施用过磷酸钙P 33 kg/(hm2·a)基本可以满足作物生长发育的要求。当有机无机肥配施时，施用过磷酸钙P 16 kg/(hm2·a)，配施厩肥P 14 kg/(hm2·a) 时，土壤磷素盈余量最小。     

淹水对石灰性土壤无机磷形态转化的影响

  【目的】  磷肥施入土壤后大部分转化为与铁氧化物关系密切的Fe-P和O-P,而淹水后土壤中铁的氧化还原过程可能影响与铁氧化物结合的磷的形态及有效性的变化。研究不同施磷处理下淹水土壤Fe (II) 、无机磷组分等的变化,以期明确淹水后土壤无机磷形态及磷有效性变化及其与铁氧化还原过程的关系。  【方法】  用不施磷土壤 (P0) 和连续6年施用P 180 kg/hm2的土壤 (P180) 进行室内模拟培养试验。将土壤装于西林瓶内,加水模拟淹水条件,西林瓶密封后,分别在避光或者光照条件下,于 (30 ± 1)℃恒温培养40天。测定供试土壤以及淹水培养土壤中的速效磷、无机磷以及不同形态无机磷组分含量,测定培养过程Fe (II) 的动态变化,以探讨磷形态转化与铁氧化还原过程的关系。  【结果】  施用磷肥显著增加土壤中的速效磷含量和无机磷总量,P0处理土壤速效磷含量为 (7.65 ± 1.65) mg/kg,P180处理土壤速效磷含量高达 (33.5 ± 2.01) mg/kg。施入土壤中的磷只有很小部分以Ca₂-P存在,主要以Ca₁₀-P、Ca₈-P、Al-P和Fe-P形态存在。避光淹水培养后,土壤速效磷含量增加,P0和P180处理土壤速效磷含量的增量分别为8.44、2.95 mg/kg。淹水培养降低了土壤Ca₈-P含量,提升了Fe-P、O-P、Al-P含量。光照和避光条件下P180处理土壤中Ca₈-P含量分别降低106.8、156.2 mg/kg,Fe-P含量分别增加23.4、47.0 mg/kg,O-P含量分别增加64.1、92.9 mg/kg,Al-P含量分别增加38.8、34.7 mg/kg,避光时Ca₈-P降幅以及Fe-P和O-P的增量均大于光照条件下。避光条件下,铁还原量和还原最大速率与Ca₈-P变化量之间存在显著负相关关系,与Fe-P、O-P增量之间存在显著正相关关系。  【结论】  淹水条件下,石灰性土壤中的Fe (Ⅲ) 还原形成Fe (Ⅱ) 和Fe (Ⅲ) 混合物,增加了铁氧化物的比表面积和磷吸附点,可促进Ca₈-P向O-P、Fe-P和Al-P转化。光照降低了Fe (Ⅲ) 的还原量,可能是Ca₈-P向O-P、Fe-P和Al-P转化率低的原因之一。     

不同形态氮素添加下三江源区高寒草甸草场氮素分配与利用

【目的】研究三江源区高寒草甸牧草对不同形态氮素的吸收利用和残留氮素在土壤中的去向及分配,以期为制定三江源区高寒草甸草场养分科学添加方案提供理论依据。【方法】于2020年6月至2021年9月,在青海省称多县高寒草甸试验站开展¹⁵N田间微区示踪试验,试验设置3个不同氮素形态处理,分别为(¹⁵NH₄)₂SO₄、Ca(¹⁵NO₃)₂、CO(¹⁵NH₂)₂,各处理的氮素施用量均为N 300 kg/hm²。分析了施肥当年和次年不同形态氮素在高寒草甸牧草地上部、地下部中的含量,及在0—15、15—30 cm土层土壤中的去向及分配。【结果】1)在施肥当年,与Ca(¹⁵NO₃)₂、(¹⁵NH₄)₂SO_4<...     

磷肥减施对玉米根系生长及根际土壤磷组分的影响

【目的】 我国农业过量和不合理施用磷肥现象普遍存在,导致磷资源的浪费,对环境也造成潜在威胁。研究减少磷肥用量对玉米产量、根系形态及根际中磷转化特征的影响,为集约化农业生产体系中磷肥合理施用提供技术基础。 【方法】 在河北省衡水小麦玉米轮作体系下连续三年进行了田间试验,在冬小麦季设置4个P₂O₅用量处理:0、112.5、150.0、187.5 kg/hm2,收获后在原处理小区免耕播种夏玉米。利用WinRHIZO根系分析系统分析获取根长、直径等数据,测定玉米籽粒产量、生物量和地上部磷含量及根际土壤中磷形态等指标。 【结果】 与农民习惯磷肥用量(P₂O₅187.5 kg/hm2)相比,3年磷肥用量减施20%~40%处理(P₂O₅150和112.5 kg/hm2),玉米籽粒产量、根系长度与直径和土壤有效磷含量尚未发生明显变化。但3年不施磷处理,根际土壤有效形态磷含量和玉米籽粒产量开始出现下降趋势。2009年和2010年玉米收获期,不施磷肥处理根际土壤有机磷含量低于非根际土壤。2008年玉米苗期和收获期土壤有机磷分组中,中等活性有机磷含量最高;磷肥减施20%~40%处理苗期根际中中等活性有机磷含量显著低于非根际土壤。土壤无机磷形态分组研究发现:从玉米苗期到收获期,各磷肥处理根际和非根际土壤中Ca₂-P下降明显;而不同磷肥处理间土壤中Ca₁₀-P、Ca₈-P、O-P (闭蓄态磷)、Al-P和Fe-P含量差异不显著。减施磷肥处理2008年玉米苗期根际土壤微生物量P含量较非根际土壤高;与习惯施肥量相比,磷肥减施未明显降低根际土壤微生物量磷。 【结论】 在华北小麦玉米轮作种植体系下,在土壤肥力水平较高地区,连续3年将小麦季磷肥的习惯用量减少20%~40%,对夏玉米产量、根系形态以及根际土壤无机磷、有机磷、微生物量磷含量影响尚不明显,因此,该地区磷肥施用量可从习惯用量的P₂O₅180 kg/hm2减至112.5 kg/hm2。     

氨基酸对三种石灰性土壤磷素有效性的影响及其作用差异机制

磷是农作物生长发育的必需元素,为了保证我国粮食安全,提高农作物的产量,提高磷肥有效性十分重要。本试验选取三种石灰性土壤（郑州潮土、周口褐土和昌图风沙土）为研究对象,通过90天的室内埋土试验,在三种土壤中研究氨基酸与磷酸一铵配施对提高土壤中磷肥有效性的影响。研究结果表明:（1）氨基酸在三种石灰性土壤中均能够提高磷酸一铵的有效性,郑州潮土、周口褐土和昌图风沙土的磷肥有效性与单施磷酸一铵相比分别提高了21.16%、10.87%和4.06%;（2）氨基酸的加入降低了土壤中Ca₂-P向Ca₈-P或其他难溶形态磷的转化,通过对三种土壤进行相关性和通径分析的得出在郑州潮土、周口褐土和昌图风沙土中主要决策因子是Ca₂-P,决策系数分别到达了0.836、0.946和0.712（P < 0.05）,郑州潮土、周口褐土主要限制因子是Ca₈-P,决策系数分别为?0.066、?0.401（P < 0.05）,昌图风沙土主要限制因子是Ca₈-P和Fe-P,决策系数分别为?0.080和?0.105（P < 0.05）;（3）氨基酸的加入能够降低三种石灰性土壤的pH和CaCO₃含量,有利于提高磷肥有效性;（4）通过对三种土壤的有效磷含量与土壤理化性质进行冗余分析,得出有机质（SOM）和碳酸钙 （CaCO₃）是影响磷肥在三种土壤中固定速率差异的主要原因,SOM和CaCO₃分别解释了有效磷含量全部变异的36.5%和25.6% （P < 0.05）。氨基酸在三种石灰性土壤中均能够提高磷肥有效性,主要途径是降低土壤的pH和CaCO₃含量,抑制Ca₂-P的快速转化。在三种石灰性土壤中,氨基酸作用有差异的主要原因是三种土壤中SOM和CaCO₃含量的差异,提高SOM,降低土壤中CaCO₃能够降低土壤对磷的固定,提高磷肥有效性。     

氮锌配施对冬小麦根土界面锌有效性及形态分级的影响

【目的】 氮能够促进冬小麦根系对锌的吸收及在籽粒中的积累。研究氮锌配施对冬小麦根土界面锌有效性及形态分级的影响,有助于探究氮锌配施促进冬小麦吸收锌的可能机制,为合理施用氮肥来提高冬小麦籽粒锌含量提供一定的理论依据。 【方法】 以冬小麦为试材进行了根箱培养试验。分别设置三个氮水平 (0、0.2和0.4 g/kg) 和两个锌水平 (0和10 mg/kg),分析了冬小麦地上部锌含量、根际土和非根际土有效锌含量、pH以及六种锌形态含量。 【结果】 氮锌配施 (N_0.2Zn₁₀和N_0.4Zn₁₀) 处理显著提高了冬小麦地上部干物质重和锌含量。在不施锌 (Zn₀) 条件下,N_0.4处理显著提高根际土壤的有效锌含量;在Zn₁₀条件下,N_0.4和N_0.2处理均显著降低根际土有效锌含量,却提高了非根际土有效锌含量。无论施锌与否,N_0.4和N_0.2处理均显著降低根际土壤的pH,但对非根际土壤的pH影响不大。在Zn₀条件下,N_0.4和N_0.2处理显著降低了根际土壤交换态锌、碳酸盐结合态锌及非根际土氧化物结合态锌含量,提高了非根际土交换态锌、根际与非根际土壤残渣态锌含量。在Zn₁₀条件下,N_0.4和N_0.2处理显著提高了根际和非根际土交换态锌、非根际土松结有机态和紧结有机态锌及根际土残渣态锌含量,降低了根际土松结有机态、碳酸盐结合态锌及根际与非根际土壤残渣态锌含量。 【结论】 氮锌配施提高冬小麦锌含量,促进冬小麦锌的吸收,可能是由于氮锌配施与冬小麦根系共同作用降低了根际土壤pH,促进土壤中锌从松结有机态和碳酸盐结合态向交换态转化,从而提高了土壤锌的有效性。      

A study of soil and fertilizer phosphorus intake by Barley plants,using Radioactive tracer technique

Introduction

Phosphorus applied on a phosphate deficient soil, by increasing the root development of the plant, or by stimulating the soil microflora especially in the rhizosphere, may increase the amount of phosphorus which the plant takes up from the soil. This present paper is a report on a pot culture investigation of such an effect of added phosphorus.     

Atmospheric nitrate deposition and the microbial degradation of cellobiose and vanillin in a northern hardwood forest

Human activity has increased the amount of N entering terrestrial ecosystems from atmospheric NO₃⁻ deposition. High levels of inorganic N are known to suppress the expression of phenol oxidase, an important lignin-degrading enzyme produced by white-rot fungi. We hypothesized that chronic NO₃⁻ additions would decrease the flow of C through the heterotrophic soil food web by inhibiting phenol oxidase and the depolymerization of lignocellulose. This would likely reduce the availability of C from lignocellulose for metabolism by the microbial community. We tested this hypothesis in a mature northern hardwood forest in northern Michigan, which has received experimental atmospheric N deposition (30 kg NO₃⁻-N ha⁻¹ y⁻¹) for nine years. In a laboratory study, we amended soils with ¹³C-labeled vanillin, a monophenolic product of lignin depolymerization, and ¹³C-labeled cellobiose, a disaccharide product of cellulose degradation. We then traced the flow of ¹³C through the microbial community and into soil organic carbon (SOC), dissolved organic carbon (DOC), and microbial respiration. We simultaneously measured the activity of enzymes responsible for lignin (phenol oxidase and peroxidase) and cellobiose (β-glucosidase) degradation. Nitrogen deposition reduced phenol oxidase activity by 83% and peroxidase activity by 74% when compared to control soils. In addition, soil C increased by 76%, whereas microbial biomass decreased by 68% in NO₃⁻ amended soils. ¹³C cellobiose in bacterial or fungal PLFAs was unaffected by NO₃⁻ deposition; however, the incorporation of ¹³C vanillin in fungal PLFAs extracted from NO₃⁻ amended soil was 82% higher than in the control treatment. The recovery of ¹³C vanillin and ¹³C cellobiose in SOC, DOC, microbial biomass, and respiration was not different between control and NO₃⁻ amended treatments. Chronic NO₃⁻ deposition has stemmed the flow of C through the heterotrophic soil food web by inhibiting the activity of ligninolytic enzymes, but it increased the assimilation of vanillin into fungal PLFAs.     

The use of environmental radionuclides as tracers in soil erosion and sedimentation investigations: recent advances and future developments

Although much of the recent attention on the environmental problems has focused on climatic change, there is also increasing concern that accelerated soil erosion and associated land degradation represent a major problem for sustainable development and environmental protection. There is an urgent need to obtain reliable quantitative data on the extent and rates of soil erosion worldwide to provide a more comprehensive assessment of the magnitude of the problems and to underpin the selection of effective soil conservation measures. The use of environmental radionuclides, in particular ¹³⁷Cs, affords an effective and valuable means for studying erosion and deposition within the landscape. The key advantage of this approach is that it can provide retrospective information on medium-term (30–40 years) erosion/deposition rates and spatial patterns of soil redistribution, without the need for long-term monitoring programmes. Advantages and limitations of the technique are highlighted. The launching of two closely linked International Atomic Energy Agency (IAEA) research networked projects in 1996 involving some 25 research groups worldwide has made a major contribution to co-ordinating efforts to refine and to standardise the ¹³⁷Cs technique. The efficacy and value of the approach has been demonstrated by investigations in a number of environments. Significant developments that have been made to exploit its application in a wide range of studies are reported in this review paper. Other environmental radionuclides, such as unsupported ²¹⁰Pb and ⁷Be offer considerable potential for use in soil erosion investigations, both individually and complementary to ¹³⁷Cs. The IAEA through research networks and other mechanisms is promoting further development and applications of these radionuclides in soil erosion and sedimentation studies for a sustainable resource use and environmental protection.     

Kinetics of 110mAg, 60Co, 137Cs and 54Mn Bioaccumulation from Water and Depuration by the Crustacean Daphnia Magna

As part of a research program on the transfer withinfreshwater ecosystems of the radionuclides present inthe weakly radioactive liquid effluents from nuclearpower stations, this article presents an assessment ofthe dynamics of zooplankton contamination from water.The experiments were carried out on young pre-adultdaphnids, placed at a density of 250 individualsL^-1, in 0.45 m filtered river water. Inorder to maintain the radionuclide contamination at ahigh level and to limit alterations in the chemicalcharacteristics of the medium, the water was reneweddaily. The dynamics of contamination were described bya one (¹³⁷Cs) or a two compartmental model(^110mAg, ⁶⁰Co and ⁵⁴Mn), taking intoaccount the fluctuations of the radionuclideconcentration in the water, as well as the growth rateof the daphnids. The contamination levels weredescribed by the steady state value of theconcentration factor, which was 2870 mL g^-1 wetweight, 320 mL g^-1 wet weight, 265 mL g^-1wet weight and 30 mL g^-1 wet weight, for^110mAg, ⁵⁴Mn, ⁶⁰Co and ¹³⁷Cs,respectively. During the depuration phase,radioactivity decrease in daphnids was a very fastphenomenon indicating that radionuclide adsorption tothe surface was the major process involved in thecontamination of daphnids. The two correspondinghalf-lives of the depuration kinetics were 10 min and7 d, 20 min and 1 d and 3 hr and 1.5 d for⁶⁰Co, ^110mAg and ⁵⁴Mn, respectively.The loss of ¹³⁷Cs was characterised by a singlehalf-life of 0.3 d.     

Nutrient Solution and Nutrient Soil Solution Parameter Evolution in Tomato with Dynamic Fertigation under Saline Conditions

This trial was carried out to study the evolution of the nutrient parameters of the nutrient solution applied to tomato plants (Lycopersicum sculentum Mill. Forteza) cultivated in Mediterranean greenhouse conditions under different fertigation management models. The dynamic model is based on soil water content, which was measured by tensiometers, and on soil solutions obtained with suction cups (porous ceramic cup water samplers). The local traditional method consists of following technical recommendations, and the classical model requires the estimation of Crop Factor (Kc) and knowing the nutrient extraction. Nutrient solution and water applied are functions of the fertigation management criteria. The water used for fertigation was classified as C₄-S₃ according to the Riverside classification system. The cultivation period lasted from 15 August to 20 April. The nutrient parameters studied in nutrient and soil solution were pH, electrical conductivity (EC), nitrate (NO₃ ^?), phosphate (H₂PO₄ ^?), potassium (K⁺), calcium (Ca²⁺), magnesium (Mg²⁺), sodium (Na⁺), and chloride (Cl^?). The pH shows similar trends under the different treatments. Electrical conductivity is in the range of 2.8–4.5 dS m^?1. Chloride, sodium, magnesium, and sulfate are exclusively modified by the salt concentration in the irrigation water, so it can be assumed that the three treatments vary equally. Nitrate, potassium, phosphate, and calcium are modified depending on each fertigation management method. Soil solution is modified by the nutrient solution applied. Dynamic management allows low nutrient concentration in the nutrient solution to be maintained and keeps soil nutrient concentration low, reducing fertilizer losses and therefore aquifer contamination.     

Activity Disequilibrium between 234U and 238U Isotopes in Southern Baltic

The aim of the work was to determine the concentration of ²³⁴U and ²³⁸U and calculate the values of the ²³⁴U/²³⁸U activity ratio in samples of living organisms, bottom water, surface and interstitial water and also sediments from the various regions of southern Baltic Sea. The knowledge of ²³⁴U/²³⁸U activity ratio in ecosystem allows getting know about the mechanisms and processes of uranium transport and origin.The activities of the analyzed uranium radionuclides in samples were measured using alpha spectrometry. The results of researches revealed diversified concentrations of uranium in the sediments of the southern Baltic Sea (sea and coastal waters) and increase of uranium with sediment depth, suggesting the diffusion of uranium from sediments to water through interstitial water and diagenesis processes in sediment material. The nuclides of uranium ²³⁴U and ²³⁸U were radioactive state equilibrium in most of the sediments. The values of the ²³⁴U/²³⁸U activity ratio oscillate around one. In bottom, surface, interstitial water and living organisms mean values of the ²³⁴U/²³⁸U activity ratio are between 1.12 and 1.15. Higher uranium concentration was observed in samples of sediments and seawater after flood in 1997 and torrential rainfalls in 2000–2001. River waters are characterized by higher ²³⁴U/²³⁸U activity ratio. The values of the ²³⁴U/²³⁸U activity ratio equal 1.27 in sediments and 1.34–1.38 in seawater indicate the influence of fresh waters.     

应用15N稀释法测定土壤氮素初级转化速率的一些关键技术

本文综合评述了应用~(15)N库稀释法测定土壤氮素初级转化速率的一些关键技术,即~(15)N标记土壤氮库的方法、~(15)N的加入量、丰度和标记物种类的选择,以及初始取样时间的确定。只有合理地运用这些关键技术,才能更准确地测定土壤氮素初级转化速率,进而更真实地表征土壤氮素的实际周转状况。     

Radioactive cesium distribution in bamboo [Phyllostachys reticulata (Rupr) K. Koch] shoots after the TEPCO Fukushima Daiichi Nuclear Power Plant disaster

Abstract

Radioactivity levels of cesium (Cs)-134 and ¹³⁷Cs in bamboo [Phyllostachys reticulata (Rupr) K. Koch] sprouts grown from April to June 2011 over a wide area (including Fukushima Prefecture) were elevated (max. 3100 Bq kg^?1 fresh weight) after the Tokyo Electric Power Company, Inc. (TEPCO) Fukushima Daiichi Nuclear Power Plant disaster in March 2011. Bamboo sprouts in 2012 also contained high radioactivity levels. Radioactivity imaging analysis of bamboo sprouts harvested in 2012 showed increasing concentration gradients of radioactivity from the lower parts to the top of the sprouts. The peels were individually separated from the sprouts, and the inner edible part (trunk) was cross-sectioned at the internodal sections from the top to the lower parts. Each segmented trunk and its corresponding peel were analyzed for radioactive cesium (¹³⁴Cs and ¹³⁷Cs) and stable cesium (¹³³Cs). The concentrations of ¹³⁴Cs and ¹³⁷Cs showed significant increases from the lower part to the top, whereas ¹³³Cs showed an almost constant value in the trunk and peel except in the peel of the top node. We speculated that ¹³⁴Cs and ¹³⁷Cs in newly emerging bamboo sprouts in 2012 were translocated mainly from various plant tissues (where the fallout was layered on the bamboo tissues) in older bamboo, while ¹³³Cs was translocated from the soil through the roots of the new bamboo sprouts and was present in the roots and stems.     

Plant uptake of dual-labeled organic N biased by inorganic C uptake: Results of a triple labeling study

Direct plant uptake of organic nitrogen (N) is often studied using the dual-labeling approach (¹⁵N + ¹³C or ¹⁵N + ¹⁴C). However, the method might be hampered by uptake of labeled inorganic carbon (C) produced by mineralization of labeled organic compounds. Here we report the results from a triple labeling experiment (¹⁵N + ¹³C + ¹⁴C) investigating whether root uptake of labeled inorganic C can bias the results obtained in studies of organic N uptake using dual-labeled amino acids (¹⁵N, ¹³C). In a rhizosphere tube experiment we investigated ¹³C and ¹⁴C uptake by maize either supplied with labeled glycine or , but found no differences in uptake rates between these C-sources. The uptake of inorganic C to the shoot tissue was higher for maize grown in full light compared to shading, which indicates a passive uptake of inorganic C with water. We conclude that uptake of inorganic C produced by mineralization of amino acids can significantly bias the interpretations of organic N uptake studies using dual-labeling.