La(NO3)3 对盐胁迫下黑麦草幼苗生长及抗逆生理特性的影响

为探讨稀土元素镧(La)对牧草盐胁迫伤害的缓解作用, 采用水培法研究了叶面喷施20 mg·L^-1La(NO₃)₃ 对NaCl 胁迫下黑麦草幼苗生长及其抗逆生理特性的影响。结果表明: 盐胁迫显著抑制黑麦草幼苗的生长, 提高叶片电解质渗漏率及丙二醛(MDA)、O₂^- 和H₂O₂ 含量, 其作用随盐浓度的增大而增强。超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、抗坏血酸过氧化物酶(APX)活性和抗坏血酸(AsA)、谷胱甘肽(GSH)、可溶性蛋白质、脯氨酸含量随盐浓度增大呈先升后降趋势, 可溶性糖和Na⁺/K⁺比逐渐增大, 质膜H⁺-ATP 酶活性逐渐降低, 过氧化物酶(POD)活性及POD 同功酶数量表达增强。喷施La(NO₃)₃ 处理可降低盐胁迫下黑麦草幼苗叶片的O₂^- 和H₂O₂ 含量, 提高SOD、CAT、POD、APX 和质膜H⁺-ATP 酶的活性及POD 同功酶的表达, 使AsA、GSH、可溶性蛋白质、可溶性糖和游离脯氨酸含量及幼苗生物量增加, Na⁺/K⁺比降低。表明La(NO₃)₃ 可通过提高抗氧化系统的活性和积累渗透溶质减轻盐胁迫伤害, 从而提高黑麦草的耐盐性。     

水培条件下CO2与NH+4/NO-3配比对番茄幼苗生育的影响

升高CO₂浓度能够促进作物的光合作用，提高作物的生物量和产量，但关于CO₂与NH⁺₄/NO^-₃比及其交互作用对作物影响的研究较少，为探索番茄幼苗生长发育对CO₂浓度升高的响应是否对NH⁺₄/NO^-₃配比有较强的依赖关系，本试验在营养液栽培条件下，以番茄(Lycopersicun esculentum Mill)为试材，研究正常大气CO₂浓度(360 μL/L)和倍增CO₂浓度(720 μL/L)与不同NH⁺₄/NO^-₃配比的交互作用对番茄幼苗生长的影响。结果表明：CO₂浓度升高提高了低NH⁺₄/NO^-₃比例处理中番茄叶片的光合速率和水分利用率，提高幅度随NH⁺₄/NO^-₃比例的降低而增强，光合速率增强最大达55%。在同一CO₂浓度处理下净光合速率与水分利用率均随NH⁺₄/NO^-₃比例的增加而显著降低。这说明CO₂浓度升高对番茄幼苗生长发育的促进作用随NH⁺₄/NO^-₃比例的降低而提高，但并没有减弱全NH⁺₄-N处理中番茄幼苗的受毒害作用。综上所述，CO₂浓度升高能提高植物生产的节水能力和水分生产力；水培条件下，NO^-₃-N是最适合番茄幼苗生长发育的氮源，其它NH⁺₄/NO^-₃比例对番茄幼苗的生长发育有一定的抑制作用，仅以NH⁺₄-N作氮源则番茄幼苗很难生长。     

肥液浓度对单膜孔入渗NO-3-N运移特性影响的室内试验研究

该文通过室内入渗试验，研究了不同浓度的单膜孔肥液入渗NO^-₃-N的分布特性。研究表明：不同浓度的膜孔肥液入渗土壤NO^-₃-N浓度的湿润锋运移距离与土壤水分运动的湿润锋一致；肥液浓度越大，相同入渗时间的NO^-₃-N浓度锋运移距离越大，土壤剖面NO^-₃-N浓度最大值越大，相同深度处土壤NO^-₃-N浓度也越大。肥液入渗土壤NO^-₃-N浓度分布特征与湿润体深度符合分段函数模型。供水入渗过程中，NO^-₃-N浓度锋运移距离和浓度最大值均随时间的延长而增大；再分布过程中，NO^-₃-N浓度锋运移距离继续增大，而NO^-₃-N浓度最大值逐渐减小。     

SO42-和Cl-对稻田土壤养分及其吸附解吸特性的影响

利用长期定位试验 ,比较了长期施用含SO₄^2-和Cl^- 化肥 22年后稻田土壤的 pH值、养分状况及其吸附解吸特性。结果表明 ,长期施用含SO₄^2-化肥 ,土壤有机质、速效氮和速效钾的含量较高 ,但全量氮磷钾的含量较低 ;长期施用含Cl^- 化肥 ,土壤全量氮磷钾和速效磷的含量较高 ,但pH值相对较低。长期施用含上述二种阴离子的化肥后 ,土壤对H₂PO₄^-的最大吸附量均较大 ,且在Cl^- 处理下土壤对H₂PO₄^-吸附的结合能较大 ,而SO₄^2-处理下土壤在同等吸附量时对H₂PO₄^-的解吸量相应较多。长期施用含SO₄^2-的化肥亦使土壤对钾素的供应强度较大 (ΔK0的绝对值较大 )、缓冲能力增强 (AR0值较高 ) ,而长期施用含Cl^- 的化肥时则与SO₄^2-相反     

宁夏引黄灌区稻田氮素浓度变化与迁移特征

过量施氮与不合理灌水是农田面源污染加剧的主要原因。为了寻求较优的水氮管理模式以促进农业生产和减少农田退水对黄河水体的污染, 在宁夏引黄灌区典型稻田中开展了不同水氮条件下稻田氮素迁移转化规律研究。结果表明: 不同水氮条件下稻田田面水NH₄⁺-N 与NO₃^--N 浓度伴随施肥出现明显峰值, NO₃^--N 峰值出现时间较NH₄⁺-N 晚, 且变化较平缓。3 次追肥时期和整个生育期田面水NH₄⁺-N 平均浓度与施氮量和灌水量都呈显著相关, 田面水NO₃^--N 平均浓度与施氮量呈显著正相关, 与灌水量相关性不显著。稻田30 cm与60 cm 深度的直渗水NH₄⁺-N 浓度受施肥影响较大, 与田面水NH₄⁺-N 浓度变化规律相似, 90 cm 处直渗水NH₄⁺-N 浓度峰值出现较为滞后, 且浓度较上层土体低, 120 cm 处直渗水NH₄⁺-N 浓度大体呈现持续上升趋势,整个生育期直渗水NH₄⁺-N 平均浓度与施氮量呈显著相关, 仅30 cm 处NH₄⁺-N 平均浓度与灌水量呈负相关, 其他土层深度不显著。30 cm 与60 cm 直渗水NO₃^--N 浓度在首次灌水后急剧下降, 在施肥后有较小幅度上升, 90 cm 与120 cm 直渗水NO₃^--N 浓度下降缓慢, 仅30 cm 处NO₃^--N 平均浓度与施肥量显著正相关。总的结果表明减少施肥或灌水均可达到减少农田氮素淋失的目的。     

NO-3胁迫下K+、Ca2+对黄瓜幼苗膜质过氧化及活性氧清除酶系统的影响

通过水培试验探讨了NO-3胁迫下K+、Ca2+对黄瓜幼苗膜质过氧化及活性氧清除酶系统的影响.结果表明,在相同NO-3浓度胁迫7d后, Ca2+浓度越大,膜脂过氧化产物丙二醛(MDA)含量越高,而K+浓度越大,电解质相对渗透率越高,由此说明K+、Ca2+对细胞膜造成伤害的机理不同.黄瓜幼苗活性氧清除酶系统对K+、Ca2+的响应亦不同,在一定程度上,K+和Ca2+ 可提高SOD、POD和CAT活性,保护植物免受自由基伤害,继而可增强植物对逆境的适应能力.     

NO-3胁迫下K+、Ca2+对黄瓜幼苗膜质过氧化及活性氧清除酶系统的影响

通过水培试验探讨了NO3-胁迫下K 、C a2 对黄瓜幼苗膜质过氧化及活性氧清除酶系统的影响。结果表明,在相同NO3-浓度胁迫7d后,C a2 浓度越大,膜脂过氧化产物丙二醛(M DA)含量越高,而K 浓度越大,电解质相对渗透率越高,由此说明K 、C a2 对细胞膜造成伤害的机理不同。黄瓜幼苗活性氧清除酶系统对K 、C a2 的响应亦不同,在一定程度上,K 和C a2 可提高SOD、POD和CAT活性,保护植物免受自由基伤害,继而可增强植物对逆境的适应能力。     

第四纪红色粘土发育的红壤中营养元素的淋失

A red soil derived from Quaternary red clay was employed to study nutrient leaching with soil columns repacked in laboratory. The objective was to identify the effects of fertilization practices on leaching patterns and magnitudes of Ca²⁺, Mg²⁺, K⁺, NH₄⁺, and NO₃^-. The treatments were CK (as a control), CaCO₃, CaSO₄, MgCO₃, Ca(H₂PO₄)₂, urea, KCl, and multiple (a mixture of the above-mentioned fertilizers). The fertilizers were added to the bare surface of the soil columns, and then the columns were leached with 120 mL deionized water daily through peristaltic pumps over a period of 92 days. Leaching processes of NH₄⁺, and NO₃^- were only measured in CK, urea, and multiple treatments which were directly related to N leaching. Results showed that sole application of CaSO₄, and Ca(H₂PO₄)₂ scarcely had any effect on the leaching losses of Ca²⁺, Mg²⁺, and K⁺; the application of MgCO₃ stimulated the leaching of Mg²⁺; the application of CaCO₃ promoted the leaching of Ca²⁺, Mg²⁺ and K⁺; urea treatment also promoted the leaching of K⁺ and NH₄⁺, and NO₃^- leaching mainly occurred at late stage of leaching process in particular; under KCl treatment, leaching of Ca²⁺, Mg²⁺, and K⁺ was promoted to a large extent; under multiple treatment, leaching of Ca²⁺, Mg²⁺, K⁺, NH₄⁺, and NO₃^- was all increased and NO₃^- was mainly leached at the end of leaching process and still had a trend of increase.     

可变电荷土壤和矿物Pb2+ and Cu2+吸附动力学: Ⅶ. Pb2+吸附后H+释放的动力学

The kinetics of H⁺ releasing after Pb²⁺ adsorption was studied by the potentiometric method combined with the acid-base titration curve technique. Results showed that pH of latosol, red soil and kaolinite suspensions dropped sharply, and then decreased gradually. Most of the H⁺ exchanged, more than 60%, was displaced at the first minute after Pb²⁺ was added into the suspension. More H⁺ was released at a higher concentration of Pb²⁺ added for a given sample and the amount of H⁺ released decreased in the order of red soil > latosol > kaolinite at a given concentration. The time-dependent data of H⁺ releasing of latosol, red soil and kaolinite at two concentrations could be fitted best with the second-order equation among the six equations, including second-order equation, two-constant equation, Elovich equation, parabolic diffusion equation, first-order equation and exponential equation. The H⁺/Pb²⁺ exchange stoichiometry increased with time, and a stable ratio of H⁺/Pb²⁺, being 1.73, 1.92 and 2.01 for kaolinite, latosol and red soil, respectively, was reached 25 minutes later.     

3 种挺水植物吸收水体NH4+、NO3-、H2PO4- 的动力学特征比较

本文用动力学试验研究了具有景观价值的3 种挺水植物—— 水生美人蕉(Canna generalis)、细叶莎草(Cyperus papyrus)、紫芋(Colocasia tonoimo)对H₂PO₄^-、NH₄⁺、NO₃^- 的吸收特征及差异。试验结果表明: 3 种挺水植物吸收H₂PO₄^- 时, 美人蕉的吸收速率最快, 且在较低离子浓度条件下也可以吸收该离子, 说明其具有嗜磷特性, 能够适应广范围浓度H₂PO₄^- 环境; 吸收NO₃^- 时, 细叶莎草的速率最快, 但对低浓度NO₃^- 环境的适应能力较差, 美人蕉吸收NO₃^- 的特性与细叶莎草刚好相反; 吸收NH₄⁺ 时, 细叶莎草的吸收速率最快, 且在低浓度NH₄⁺ 环境下仍能吸收该离子, 而美人蕉的吸收速率最慢, 但能在低浓度NH₄⁺ 环境下吸收该离子。说明不同植物对养分的吸收特性存在较大差异, 各自的污染水体修复适用范围也不同。美人蕉可用于各种浓度H₂PO₄^- 污染的水体修复; 而NO₃^- 污染严重的水体最适宜用细叶莎草作先锋植物, 修复到一定程度后再种植美人蕉来维持水质; 细叶莎草在各种浓度NH₄⁺ 污染的水体中均适用, NH₄⁺ 污染较轻的水体也可用美人蕉修复。     

不同铵钾比对高铵下拟南芥地上部和根系生长的影响

钾在缓解植物铵毒害的过程中起着重要的作用。本文研究了高铵(30 mmol/L)条件下,不同铵钾比(7.5︰1和150︰1)对拟南芥(Col-0)主根、侧根以及地上部生长的影响。结果表明:30 mmol/L NH4+条件下,高铵钾比(150)处理显著加重了拟南芥铵毒害现象,地上部和根系生长所受的抑制作用更为明显并导致更严重的氧化胁迫。相比低铵钾比水平,在高铵处理下,高铵钾比使得拟南芥主根伸长量降低57.4%,侧根数量减少33.3%,而地上部鲜重减轻69.9%。DAB(3,3￠-二氨基联苯胺,3,3￠-diaminobenzidine)叶片染色结果表明,不加铵处理下,外源不同钾水平(0.2和4.0 mmol/L)对拟南芥叶片的氧化胁迫作用没有显著差异;而高铵处理下,相比低铵钾比处理,高铵钾比显著增加了叶片中过氧化氢的含量,加重了其氧化胁迫。伊文思蓝(Evans blue,EB)染色结果表明,不加铵处理下,外源不同钾水平对拟南芥地上部和根部的膜透性没有显著差异,而高铵处理下,高铵钾比显著增强了拟南芥地上部和根部的膜透性,表明其对细胞的伤害程度加重。可见,高铵抑制拟南芥根系和地上部生长,高铵钾比则会加重这种抑制,其原因除了高浓度钾能减少植物对铵的吸收外,可能与高铵钾比条件加剧了植物的氧化胁迫有关。因此,适宜的铵钾比在植物应对铵毒害的过程中发挥重要作用。     

聚天门冬氨酸钙盐对水稻田面水中三氮动态变化的影响

利用桶栽试验探究不同浓度水平的聚天门冬氨酸钙盐(PASP-Ca)对水稻田面水中铵态氮(NH_4~+)、硝态氮(NO_3~-)和总氮(TN)浓度动态变化的影响。结果表明,施氮后,田面水中TN、NH_4~+和NO_3~-分别于第1,3,9天达到最大值,随后逐渐降低。NO_3~-/TN多在0.1以下,(NH_4~++NO_3~-)/TN多在0.5以上。因此,可以将NH_4~+和TN作为农田水污染防治的主要监测指标,NO_3~-作为辅助指标。添加一定浓度的PASP—Ca能对田面水中氮素浓度的变化起到缓释作用,其中0.3%浓度水平的PASP—Ca效果相对较好,田面水中NH_4~+和TN的下降速率分别为3.452,4.806mg/(L·d),与单施氮肥(CK)相比,分别降低了11.68%和16.25%;同时,NH_4~+的平均浓度为6.999mg/L,较CK低了3.88%;NO_3~-的平均浓度为0.396mg/L,较CK低了24.83%;TN的平均浓度为20.077mg/L,较CK提升了3.10%。施氮后田面水中TN浓度随时间呈对数递减,而NH_4~+浓度在施氮后3天内随时间呈对数增加,之后随时间呈对数递减趋势。施氮后的9天内是防止稻田田面水中氮素流失的关键时期。     

外源精胺对NO_3~-胁迫下黄瓜幼苗抗氧化酶活性及光合作用的影响

采用营养液培养方法,研究了添加不同浓度的精胺(Spm)对NO3-胁迫下黄瓜幼苗生长、叶片抗氧化酶活性及光合作用的影响。结果表明,140 mmol/L NO3-胁迫下,外加1 mmol/L Spm,10 d后,黄瓜幼苗叶片超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、过氧化物酶(POD)、抗坏血酸过氧化物酶(APX)活性显著增加,电解质渗漏率和丙二醛(MDA)含量显著降低;气孔导度(Gs)、胞间CO2浓度(Ci)和净光合速率(Pn)显著升高,气孔限制值(Ls)显著降低。说明1 mmol/L Spm处理能增强黄瓜幼苗对活性氧的清除能力,降低膜脂过氧化程度;降低气孔关闭,改善叶片的气体交换,幼苗生长势增加,对高浓度NO3-胁迫的抗性增强。当Spm浓度高达1.5~2 mmol/L时,与1mmol/L Spm相比,SOD、POD、APX、CAT活性均开始降低,电解质渗漏率和MDA含量增加,Gs、Ci和Pn显著降低,黄瓜幼苗生长受到抑制。可见,外加一定浓度的Spm可通过提高抗氧化酶活性、降低膜脂过氧化程度及改善光合作用来缓解NO3-胁迫对黄瓜幼苗的影响。     

不同铵硝配比对弱光下白菜氮素吸收及相关酶的影响

以黑色遮阳网覆盖模仿弱光环境, 使光照强度为自然光的20%左右, 以自然光照为对照, 采用精确控制水培溶液氮素营养, 研究NH₄⁺-N/NO₃^--N 比例分别为0/100、25/75、50/50、75/25、100/0 对弱光下白菜氮代谢及硝酸还原酶和谷氨酰胺合成酶活性的影响。结果表明, 弱光下, 白菜的鲜重及叶片总氮量以NH₄⁺-N/NO₃^--N 比为25/75 时最大, NH₄⁺-N/NO₃^--N 比为100/0 时最低。随弱光处理的进行, 白菜叶片中硝酸还原酶活性及谷氨酰胺合成酶活性均呈下降趋势, 但NH₄⁺-N/NO₃^--N 比为25/75 时, 可维持叶片内较高的硝酸还原酶活性及谷氨酰胺合成酶活性。试验表明, NH₄⁺-N/NO₃^--N 比25/75 是白菜在弱光下生长的较适宜氮素形态配比。     

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.     

铁铝氢氧化物对两种土壤和高岭石表面K+和NH4+解吸的影响

Potassium (K) and nitrogen (N) are essential nutrients for plants. Adsorption and desorption in soils affect K+ and NH + 4 availabilities to plants and can be affected by the interaction between the electrical double layers on oppositely charged particles because the interaction can decrease the surface charge density of the particles by neutralization of positive and negative charges. We studied the effect of iron (Fe)/aluminum (Al) hydroxides on desorption of K+ and NH + 4 from soils and kaolinite and proposed desorption mechanisms based on the overlapping of diffuse layers between negatively charged soils and mineral particles and the positively charged Fe/Al hydroxide particles. Our results indicated that the overlapping of diffuse layers of electrical double layers between positively charged Fe/Al hydroxides, as amorphous Al(OH) 3 or Fe(OH) 3 , and negatively charged surfaces from an Ultisol, an Alfisol, and a kaolinite standard caused the effective negative surface charge density on the soils and kaolinite to become less negative. Thus the adsorption affinity of these negatively charged surfaces for K+ and NH + 4 declined as a result of the incorporation of the Fe/Al hydroxides. Consequently, the release of exchangeable K+ and NH +4 from the surfaces of the soils and kaolinite increased with the amount of the Fe/Al hydroxides added. The greater the positive charge on the surfaces of Fe/Al hydroxides, the stronger was the interactive effect between the hydroxides and soils or kaolinite, and thus the more release of K+ and NH + 4 . A decrease in pH led to increased positive surface charge on the Fe/Al hydroxides and enhanced interactive effects between the hydroxides and soils/kaolinite. As a result, more K+ and NH + 4 were desorbed from the soils and kaolinite. This study suggests that the interaction between oppositely charged particles of variable charge soils can enhance the mobility of K+ and NH + 4 in the soils and thus increase their leaching loss.     

阴离子对可变电荷土壤吸附铜离子的影响机理

根据NO-3、Cl-和SO24-对可变电荷土壤和恒电荷土壤吸附Cu2+的影响的比较,探讨了阴离子对可变电荷土壤吸附Cu2+的影响机理。结果表明,当3种阴离子的浓度相同时,在SO24-体系中铁质砖红壤对Cu2+的吸附率较在NO3-和Cl-体系中大得多,而在浓度相同的3种阴离子体系中,黄棕壤对Cu2+的吸附率相差不大。在离子强度相近的NaCl体系中,砖红壤对Cu2+的吸附率相近。在3种阴离子体系中,随着pH升高,砖红壤对Cu2+的吸附率均增大;但在NO-3体系和Cl-体系中Cu2+的吸附率相近;而在SO24-体系中Cu2+的吸附率最大。随着Na2SO4浓度的增大,铁质砖红壤和砖红壤对Cu2+的吸附率减小。但在0.005 mol L-1和0.05 mol L-1Na2SO4体系中,Cu2+的吸附率大于在不含Na2SO4的体系中者。而在0.5 mol L-1Na2SO4体系中,Cu2+吸附率小于在不含Na2SO4体系中者。在3种浓度的Na2SO4体系中,黄棕壤对Cu2+的吸附率均小于在不含Na2SO4体系中者。总之,阴离子可通过离子强度、专性吸附和形成离子对影响土壤对Cu2+的吸附。在可变电荷土壤中,阴离子对Cu2+吸附的影响机理较在恒电荷土壤中复杂得多。