近红外光谱法快速鉴定干海参产地

该文采用近红外漫反射光谱法,对来自4个不同产地的96个干刺参样品,进行了产地鉴别分析。研究表明：在5 000～4 000 cm-1 波段,干海参样品具有丰富的光谱结构,且反映出了由于海参生长环境不同带来的差异性;对该波段的一次微分光谱数据进行主成分聚类（PCCA）计算,可成功实现对其产地的鉴定分析。该研究为动物性海洋食品的产地快速鉴别分析提供了新方法。     

Recovery and characterization of the metal polymeric organic fraction (polymerin) from olive oil mill wastewaters

A dark and complex metal polymeric organic mixture, named polymerin, was recovered from olive oil mill wastewaters (OMWW) and characterized by chemical analysis, diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), and atomic absorption spectrometry (AAS). Polymerin proved to be composed of carbohydrates (52.40 mg 100(-1), w/w), melanin (26.14 mg 100(-1)), and proteins (10.40 mg 100(-1)), and the respective composition of monosaccharides, phenols, and amino acids was determined. It also contained metals (11.06 mg 100(-1)), mainly K(+) and, to a lesser extent, Na(+), Ca(2+), Mg(2+), Zn(2+), Fe(3+), and Cu(2+), which were naturally bound and chelated through carboxylate anions and other characteristic nucleophilic functional groups naturally occurring in polymerin. The distribution of polymerin relative molecular size was assessed to be approximately between 500.0 and 2.0 kDa by calibrated molecular weight gel filtration chromatography, indicating also that a fraction consisted of protein, melanin, and polysaccharide, strongly aggregated to each other in a supramolecular status by a combination of covalent and hydrogen bonds and CH/Pi interactions, and another fraction of only free polysaccharide. Polymerin was transformed into a potassium salt deglycosylated derivative, named KSDpolymerin, which was also characterized by chemical analysis, DRIFTS, and AAS. KSDpolymerin consisted of carbohydrates (6.00 mg 100(-1)), melanin (52.49 mg 100(-1)), and proteins (35.40 mg 100(-1)), and the composition of monosaccharides, phenols, and amino acids was determined. It also contained metals (6.11 mg 100(-1)), mainly K(+) and to a lesser extent Na(+), Ca(2+), Mg(2+), Zn(2+) and Fe(3+), bound as in polymerin. All the organic components were strongly linked in a supramolecular aggregate status and the relative average molecular size proved to be 6.3 kDa. Finally, we briefly discuss the possible use of such polymerins in agriculture as bioamendments and macro- and microelement biointegrators and as a biofilter for toxic metal removal, in light of their similarity with humic acids.     

香石竹设施栽培土壤可溶性盐分主成分分析

为探索香石竹设施栽培土壤盐害的防治方法与技术途径,对香石竹设施栽培土壤可溶性盐分进行了主成分分析。结果表明:土壤中可溶性盐分可分为主成分1(SO42-、NO3-、Ca2+、Cl-、K+)和主成分2(CO32-、HCO3-)两个成分,主成分1中SO42-、NO3-、Ca2+与土壤EC值三次模型拟合度较高(R2>0.850**),并与土壤EC值呈不同强度的正相关性;土壤EC值与全盐量呈强正相关性(r=0.99**),并接近线性关系(线性模型R2=0.976**,三次模型R2=0.984**);土壤EC值可作为一个有效指标,反映土壤盐渍化及土壤可溶性盐分,特别是反映SO42-、NO3-、Ca2+的变动情况,盐害防治重点在于SO42-、NO3-、Ca2+。研究对指导香石竹设施栽培土壤管理与持续利用具有重要意义。     

The links between potassium availability and soil exchangeable calcium,magnesium, and aluminum are mediated by lime in acidic soil

Journal of Soils and Sediments - The aims of this study were to investigate the links between potassium (K) uptake by crops and soil K, exchangeable calcium (Ca2+), magnesium (Mg2+), and aluminum...     

Are Indicators for Critical Load Exceedance Related to Forest Condition?

The aim of this study was to evaluate the suitability of the (Ca?+?Mg?+?K)/Al and the Ca/Al ratios in soil solution as chemical criteria for forest condition in critical load calculations for forest ecosystems. The tree species Norway spruce, Sitka spruce and beech were studied in an area with high deposition of sea salt and nitrogen in the south-western part of Jutland, Denmark. Throughfall and soil water were collected monthly and analysed for pH, NO₃-N, NH₄-N, K, Ca, Mg, DOC and Al_tot. Organic Al was estimated using DOC concentrations. Increment and defoliation were determined annually, and foliar element concentrations were determined every other year. The throughfall deposition was highest in the Sitka spruce stand (maximum of 40 kg N ha^?1yr^?1) and lowest in the beech stand (maximum of 11 kg N ha^?1yr^?1). The Sitka spruce stand leached on average 12 kg N ha^?1yr^?1 during the period 1988–1997 and leaching increased throughout the period. Only small amounts of N were leached from the Norway spruce stand whereas almost no N was leached from the beech stand. For all tree species, both (Ca?+?Mg?+?K)/Al and Ca/Al ratios decreased in soil solution at 90 cm depth between 1989 and 1999, which was mainly caused by a decrease in concentrations of base cations. The toxic inorganic Al species were by far the most abundant Al species at 90 cm depth. At the end of the measurement period, the (Ca?+?Mg?+?K)/Al ratio was approximately 1 for all species while the Ca/Al ratio was approximately 0.2. The lack of a trend in the increment rates, a decrease in defoliation as well as sufficient levels of Mg and Ca in foliage suggested an unchanged or even slightly improved health condition, despite the decreasing and very low (Ca?+?Mg?+?K)/Al and Ca/Al ratios. The suitability of these soil solution element ratios is questioned as the chemical criteria for soil acidification under field conditions in areas with elevated deposition rates of sea salts, in particular Mg.     

Chemical Composition of Urban Wet Deposition in Amman,Jordan

Precipitation events were collected during the period from October 1996 to April 1997 from two sites in the city of Amman, Jordan. The samples were analyzed for major cations (Na+, K+, Ca2+, Mg2+ and NH4+), major anions (F-, Cl-, NO3- and SO42-), in addition to heavy metals (Cu2+, Cd2+, Zn2+, and Pb2+). High levels of Ca2+ and SO42- were observed. The results were comparable with some regional values and they indicate that about 58% of Na+ and Cl- are of marine origin, while Ca2+, K+ and a large fraction of SO42- are of soil dust origin. Heavy metals were detectable in most of the samples, zinc showed the highest concentrations. Significant correlation was obtained between zinc and lead, which may indicate automobile emission source.     

Pyruvate kinase activity as an indicator of the level of K(+), Mg(2+), and Ca(2+) in leaves and fruits of the cucumber: the role of potassium fertilization.

Little is known about the effects of K(+) fertilization on pyruvate kinase (PK) activities in cucumber (Cucumis sativus L. cv. Brunex) grown in the greenhouse on calcareous soils. Here, the effect of K rates on the concentrations of K(+), Mg(2+), and Ca(2+) and on the PK activity as a possible indicator of the levels of these cations in the leaves and fruits of cucumber plants has been studied. The treatments consisted of applications of three rates of K in the form of K(2)SO(4) (K1 = 0.075 mg mL(-)(1), K2 = 0.15 mg mL(-)(1), and K3 = 0.30 mg mL(-)(1)). In general, K(+) application in calcareous soils proved beneficial. The highest application of K(+) (K3) to the culture medium reduced, in both the leaves and fruits, the foliar concentrations of Mg(2+) and Ca(2+). These results are reflected by the lowest basal PK activities and the highest differences between the basal PK activity and activities stimulated by these two cations. The opposite effect resulted with K2, with maximal basal PK activity and minimal differences between this activity and activities stimulated by the cations, indicating a better balance in this treatment between the different cations under the experimental conditions. Finally, this trend might partly account for the highest commercial yield in plants treated with K2.     

Computer simulation of the interactions of glyphosate with metal ions in phloem

Essential nutrients such as trace metal ions, amino acids, and sugars are transported in the phloem from leaves to other parts of the plant. The major chelating agents in phloem include nicotianamine, histidine, cysteine, glutamic acid, and citrate. A computer model for the speciation of metal ions in phloem has been used to assess the degree to which the widely used herbicide glyphosate binds to Fe(3+), Fe(2+), Cu(2+), Zn(2+), Mn(2+), Ca(2+), and Mg(2+) in this fluid over the pH range of 8 to 6.5. The calculations show that glyphosate is largely unable to compete effectively with the biological chelating agents in phloem. At a typical phloem pH of 8, 1.5 mM glyphosate binds 8.4% of the total Fe(3+), 3.4% of the total Mn(2+), and 2.3% of the total Mg(2+) but has almost no effect on the speciation of Ca(2+), Cu(2+), Zn(2+), and Fe(2+). As the pH decreases to 6.5, there are some major shifts of the metal ions among the biological chelators, but only modest increases in glyphosate binding to 6% for Fe(2+) and 2% for Zn(2+). The calculations also indicate that over 90% of the glyphosate in phloem is not bound to any metal ion and that none of the metal-glyphosate complexes exceed their solubility limits.     

土壤水溶性盐基离子的高光谱反演模型及验证

土壤水溶性盐基离子是诊断土壤盐渍化类型与盐渍化程度的重要依据,利用光谱技术快速获取土壤水溶性盐基离子含量数据,可为土壤盐渍化类型与盐渍化程度的诊断提供新的技术和手段。该研究通过采集新疆5个不同地区399个土样的反射率与水溶性盐基离子数据并进行31种光谱预处理方法,分析了不同水溶性盐基离子(HCO3-、Cl-、SO42-、K+、Na+、Ca2+、Mg2+)与高光谱反射率之间的相关性;采用K-S(Kennard-Stone)方法挑选出299个样品,针对每种离子使用偏最小二乘回归(partial least squares regression,PLSR)分别建立32个高光谱定量反演模型,优选最佳反演模型,并单独使用100个样品对估测模型进行检验。结果表明:不同离子的最佳反演模型所使用的预处理方法存在差异,其中仅有Cl-和Ca2+、SO42-和Mg2+所使用的预处理方法相同,其他离子则不同;不同离子的反演精度也不同,HCO3-和Ca2+构建的模型相对分析误差(relative percent deviation,RPD)分别为2.67、2.57,模型具有很好的预测能力。Cl-、SO42-和Mg2+所构建的模型RPD分别为2.05、2.10和2.14,表明这三者建立的模型具有较好的预测能力。K+建立的模型RPD仅为1.11,不能对样品进行预测。Na+构建的模型RPD为1.83,表明该离子所建模型只能对样品进行粗略估测。研究结果为探究水溶性盐基离子的高光谱反演增添了新的内容,为土壤盐渍化监测的深入和推进提供了新的思路和方法。     

适宜无机盐及浓度抑制麦胚脂肪酶存在时油水界面张力

为了探明无机盐稳定化脂肪酶的潜在机理,该文以小麦胚芽脂肪酶为研究对象,基于界面酶学的分析方法,研究添加浓度介于1.0×10-9~1.0×10-2 mol/L的Na~+、K+、Ca~(2+)、Mg~(2+)的氯化物对小麦胚芽脂肪酶存在的油-水界面特性的影响。结果表明,当小麦胚芽脂肪酶体系浓度为1.7×10-6 mol/L时,一价金属中Na~+更有利于抑制油-水界面的表面张力(P0.05),对麦胚脂肪酶存在时的油水界面特性影响也较大;二价金属离子Ca~(2+)对界面张力的影响趋势与一价离子不同,在高浓度时反而增加界面张力;当油水界面上存在脂肪酶的催化底物(三油酸甘油酯)和产物(油酸)时,添加浓度分别为10-6、10-6、10-4和10-9mol/L的Na~+、K~+、Ca~(2+)、Mg~(2+)均可一定程度上降低油水界面张力,从而降低麦胚脂肪酶的作用效果,三油酸甘油酯存在时Mg~(2+)的作用效果最明显(P0.05),油酸存在时Na+的作用效果最明显(P0.05)。综上,无机盐金属离子主要通过影响麦胚脂肪酶在油水界面的聚集行为及底物结构状态起到钝化麦胚脂肪酶的作用,该结果可为麦胚脂肪酶存在时界面的活性调控及麦胚的稳定化处理提供参考。     

地理加权回归模型结合高光谱反演盐生植物叶片盐离子含量

快速、无损地估算盐生植物叶片盐离子含量在植物生长监测、耐盐植物筛选和土壤盐渍化监测等方面有实用价值。该研究以新疆艾比湖保护区内盐生植物为研究对象,通过分析植物叶片盐离子(K~+、Na~+、Ca~(2+)、Mg~(2+))含量与冠层高光谱数据的光谱变换和二维植被指数(比值型植被指数(ratiovegetationindex,RVI)、差值型植被指数(difference vegetation index,DVI)、归一化型植被指数(normalized difference vegetation index,NDVI))的相关性选取特征波段,构建基于地理加权回归模型(geographically weighted regression,GWR)的叶片盐离子含量估算模型,并与BP神经网络模型(back propagation neural network)进行对比,研究基于GWR模型估算干旱区盐生植物叶片盐离子的可行性。结果表明,选取特征波段集中表现在红及短波红外波段:K~+含量在反射率倒数的对数选取的红光区域内波段使用GWR估算效果最佳;Na~+的特征波段在光谱变换下集中于短波红外区域,二维植被指数集中在近红外、短波近红外及黄、橙、红区域,各种波段选取下GWR对Na~+的含量估算均有较好效果,但反射率对数的一阶估算效果最好;Ca~(2+)含量在反射率平方根的一阶微分下选取的短波红外波段通过GWR模型估算效果最好;Mg~(2+)含量在DVI选取的位于红光区域特征波段估算效果最佳,但使用GWR模型对Mg~(2+)的估算精度不及BP模型。分析基于GWR盐离子模型估算模型发现,含量较高的离子估算效果更好,K~+、Na~+的模型精度优于Ca~(2+)、Mg~(2+)。在使用GWR模型估算植物叶片盐离子含量时,特征波段均指向红及短波红外波段,符合植被光谱机理的响应。     

我国主要菜区耕层土壤盐分总量及离子组成

【目的】评价全国主要菜区温室、 大棚和露地菜田土壤盐分及离子组成状况,为土壤次生盐渍化防治、 蔬菜合理施肥和土壤可持续利用提供一定的理论依据。【方法】在我国北方3个区域(东北、 华北、 西北地区)和南方4个区域(华中、 西南、 华东、 华南地区)主要蔬菜种植区不同栽培方式典型菜田耕层土壤展开调查,共采集501个土壤样品,分析了盐分总量及其离子组成。【结果】 1)全国主要菜区设施(温室和大棚)菜田土壤盐分总量及其各离子含量(NO-3、 SO2-4、 Cl-、 Na+、 K+、 Ca2+、 Mg2+)均显著高于露地菜田土壤,盐分总量平均高69.3%,离子组成增加幅度在36.2%~170.0%之间。2)设施菜田土壤次生盐渍化的土样数比例显著高于露地菜田土壤,但设施菜田土壤盐化程度总体上较轻,居于轻度盐化水平的比例占38.2%,处于中度盐化以上水平的比例仅占4.7%。 3)设施菜田土壤盐分总量及主要盐分离子(NO-3、 SO2-4和Ca2+)含量积累总体上随种植年限的延长呈先增后降并趋于平缓的变化趋势,在连续种植5~6年时达到高峰期,之后因采取的各种管理措施而有所降低,但仍显著高于露地菜田土壤。 4)设施菜田土壤盐分离子组成以NO-3和SO2-4为主,其次是Ca2+,分别占盐分总量的27.9%、 26.9%和15.3%。露地菜田土壤主要盐分离子组成总体上是SO2- 4 NO- 3 Ca2+、 HCO-3,分别平均占盐分总量的29.0%、 21.1%、 16.1%和14.1%,但西北地区露地菜田土壤盐分离子组成以HCO-3为主,其次是SO2-4、 NO-3和Ca2+。【结论】设施菜田土壤次生盐渍化的土样数比例虽然显著高于露地菜田土壤,但土壤盐化程度总体上较轻,盐分离子主要是NO-3、 SO2- 4和Ca2+,NO-3、 SO2-4含量大于Ca2+含量; 露地菜田主要盐分离子是SO2-4、 NO- 3、 Ca2+和HCO-3,含量为SO2- 4 NO- 3 Ca2+、 HCO-3。     

Theoretical speciation of ethylenediamine-N-(o-hydroxyphenylacetic)-N'-(p-hydroxyphenylacetic) acid (o,p-EDDHA) in agronomic conditions

The presence of ethylenediamine-N-(o-hydroxyphenylacetic)-N'-(p-hydroxyphenylacetic) acid (o,p-EDDHA) as the second largest component in commercial EDDHA iron chelates has recently been demonstrated. Here is reported the speciation of o,p-EDDHA by the application of a novel methodology through the determination of the complexing capacity, protonation, and Ca(2+), Mg(2+), Cu(2+), and Fe(3+) stability constants. The pM values and species distribution in solution, hydroponic, and soil conditions were obtained. Due to the para position of one phenol group in o,p-EDDHA, the protonation constants and Ca and Mg stability constants have different values from those of o,o-EDDHA and p,p-EDDHA regioisomers. o,p-EDDHA/Fe(3+) stability constants are higher than those of EDTA/Fe(3+) but lower than those of o,o-EDDHA/Fe(3+). The sequence obtained for pFe is o,o-EDDHA/Fe(3+) >/= o,p-EDDHA/Fe(3+) > EDTA/Fe(3+). o,p-EDDHA/Fe(3+) can be used as an iron chelate in hydroponic conditions. Also, it can be used in soils with limited Cu availability.     

Influence of herbicide structure,clay acidity,and humic acid coating on acetanilide herbicide adsorption on homoionic clays

Adsorption of chloroacetanilide herbicides on homoionic montmorillonite was studied by coupling batch equilibration and FT-IR analysis. Adsorption decreased in the order metolachlor > acetochlor > alachlor > propachlor on Ca(2+)- or Mg(2+)-saturated clays and in the order metolachlor > alachlor > acetachlor > propachlor on Al(3+)- or Fe(3+)-saturated clays. FT-IR spectra showed that the carbonyl group of the herbicide molecule was involved in bonding. For the same herbicide, adsorption of alachlor, acetachlor, and metolachlor on clay followed the order Ca(2+) approximately Mg(2+) < Al(3+) < or = Fe(3+), which coincided with the increasing acidity of homoionic clays. Adsorption of propachlor, however, showed an opposite dependence, suggesting a different governing interaction. In clay and humic acid mixtures, herbicide adsorption was less than that expected from independent additive adsorption by the individual constituents, and the deviation was dependent on the clay-to-humic acid ratio, with the greatest deviation consistently occurring at a 60:40 clay-to-humic acid ratio.     

Geographic classification of spanish and Australian tempranillo red wines by visible and near-infrared spectroscopy combined with multivariate analysis

Visible (vis) and near-infrared (NIR) spectroscopy combined with multivariate analysis was used to classify the geographical origin of commercial Tempranillo wines from Australia and Spain. Wines (n = 63) were scanned in the vis and NIR regions (400-2500 nm) in a monochromator instrument in transmission. Principal component analysis (PCA), discriminant partial least-squares discriminant analysis (PLS-DA) and linear discriminant analysis (LDA) based on PCA scores were used to classify Tempranillo wines according to their geographical origin. Full cross-validation (leave-one-out) was used as validation method when PCA and LDA classification models were developed. PLS-DA models correctly classified 100% and 84.7% of the Australian and Spanish Tempranillo wine samples, respectively. LDA calibration models correctly classified 72% of the Australian wines and 85% of the Spanish wines. These results demonstrate the potential use of vis and NIR spectroscopy, combined with chemometrics as a rapid method to classify Tempranillo wines accordingly to their geographical origin.     

A DSC study on the gel-sol transition of a starch and hsian-tsao leaf gum mixed system

Differential scanning calorimetric analysis was performed on the admixture of 4% hsian-tsao leaf gum and 8% wheat starch as a function of salt types and concentrations. The salt concentrations (C(s)) studied were 5-100 mM for sodium and potassium chloride, and 3.4-34 mM for calcium and magnesium chloride. It was found that hsian-tsao leaf gum or starch alone did not present a readily recognizable exothermic peak or endothermic peak during cooling or heating in DSC. However, mixing these two polymers promoted the intermolecular binding and subsequent gelation of the mixtures as evidenced by the DSC exothermic and endothermic peaks during cooling and heating, respectively. The setting and melting temperatures of such a mixed system shifted progressively to higher temperatures with increasing concentrations of added salts. It was considered that the aggregated mixed polymers formed thermally stable junction zones with higher binding energies. The thermal behavior change was more remarkable by the addition of K(+) than by Na(+), and by Ca(2+) than by Mg(2+). For monovalent cations, the DSC heating and cooling curves showed a single endothermic and exothermic peak. For divalent cations at low concentration, the DSC curves showed a single peak. However, with sufficient divalent cations, the DSC curves eventually developed a bimodal character. A mixed system with sufficient Ca(2+) could form firm gel that was difficult to remelt completely upon heating to 130 degrees C, indicating the possibility of the formation of ionic bonds through cross-links with the carboxyl groups in hsian-tsao leaf gum.     

河套灌区乌拉特灌域春季土壤盐碱化空间分布特征

盐碱化状况是干旱区灌区水盐合理调控及水土资源合理利用的基础。为掌握内蒙古河套灌区下游乌拉特灌域春季耕地土壤盐碱化状况的空间分布，通过野外调查采样和实验室检测，对0~20 cm和20~40 cm土层中的全盐量（Total Salt，TS）、pH值、CO32-、HCO3-、Cl-、SO42-、Ca2+、Mg2+、K++Na+含量、交换性Na+含量、阳离子交换量（Cation Exchange Capacity，CEC）、碱化度（Exchangeable Sodium Percentage，ESP）等反映土壤盐碱化特征的指标进行了测定和计算，采用经典统计学、地统计学和多指标综合评价方法对土壤盐碱化指标的空间分布特征进行分析。结果表明：1）0～20 cm土层中的TS含量更大一些，可溶性盐分离子主要以HCO3-、SO42-、Cl-、Na+为主。HCO3-、CEC、交换性Na+和ESP的变异系数在10%～100%之间，属于中等变异，其中交换性Na+和ESP的变异系数接近100%；TS、Cl-、SO42-和Na+的变异系数均大于100%，属于强变异。2）土壤pH、TS和ESP的空间分布规律基本一致，在东西方向上，各指标西部低，东部高；在南北方向上，中间低，南、北两侧高。土壤pH值基本在7.5～8.5之间，从TS空间分布来看，灌域内有32%的土壤存在盐渍化问题，且以轻度盐渍化土为主，约占26%；从ESP分布来看，有97%的土壤存在碱化问题，其中轻度碱化土约占40%，中度碱化土和碱土均约占23%。因此灌域内土壤碱化问题比盐化问题更为突出。3）通过因子分析得出TS、Cl-、Na+、交换性Na+、ESP和CEC是乌拉特灌域土壤盐碱化程度的主要影响因子，公因子综合得分值在-0.78~3.38之间，公因子综合得分能排除指标间个体差异，比较客观地评价土壤盐碱化整体水平。     

Inductively coupled plasma optical emission spectrometric determination of minerals in thyme honeys and their contribution to geographical discrimination

Twenty-four Spanish thyme honey samples were analyzed using inductively coupled plasma optical emission spectrometry (ICP-OES). Twenty-four minerals were quantified for each honey. The elements Al, As, Ba, Ca, Cr, Cu, Fe, K, Li, Mg, Mn, Na, P, Pb, S, Se, Si, Sr, and Zn were detected in all samples; seven elements are very abundant (Ca, K, Mg, Na, P, S, and Si), and six are not abundant (Al, Cu, Fe, Li, Mn, and Zn). Eleven of them are trace elements (As, Ba, Cd, Co, Cr, Ni, Mo, Pb, Se, Sr, and V) at <1 mg kg(-)(1). Classification of thyme honeys according to their origin (coast, mountains) was achieved by pattern recognition techniques on the mineral data. By means of principal component analysis, a good separation by geographical origin is obtained when scores for the two first principal components are plotted. Classification functions of 11 metals (Al, As, Cr, Cu, K, Li, Mg, Na, P, S, and V) were obtained using stepwise discriminant analysis and applied to classify correctly approximately 100% of the honey samples.     

秦皇岛市蔬菜大棚全盐及盐分组成离子变化的研究

通过对不同棚龄、不同土层、不同季节的蔬菜大棚土壤全盐及盐分组成离子变化的研究表明,大棚土壤全盐含量明显高于相邻棚外土壤,大棚土壤全盐含量随着棚龄的增加而增加,大部分大棚土壤已达到中度盐渍化的程度,同棚龄不同土层全盐含量由上而下呈下降的趋势,大棚土壤全盐含量季节变化2月份明显高于9月份。不同棚龄的大棚土壤盐分组成离子Na+、K+、Ca2+、Mg2+、Cl-、SO42-、HCO3-、NO3-含量,在0～20cm土层中均明显高于相邻棚外土壤,其含量随着棚龄的增加而增加,其中,K+、Ca2+、NO3-、SO42-最为明显,是造成大棚土壤表层盐渍化的主要离子。造成大棚土壤盐渍化的主要原因是大量使用化学肥料,另外,耕作、灌溉等管理方式不当也是造成棚内土壤盐渍化的原因。     

Analysis of protein structures and interactions in complex food by near-infrared spectroscopy. 2. Hydrated gluten

Hydrated gluten, treated with various salts, was analyzed by near-infrared (NIR) spectroscopy to assess the ability of this method to reveal protein structure and interaction changes in perturbed food systems. The spectra were pretreated with second-derivative transformation and extended multiplicative signal correction for improving the band resolution and removing physical and quantitative spectral variations. Principal component analysis of the preprocessed spectra showed spectral effects that depended on salt type and concentration. Although both gluten texture and the NIR spectra were little influenced by treatment with salt solutions of low concentrations (0.1-0.2 M), they were significantly and diversely affected by treatment with 1.0 M salt solutions. Compared to hydration in water, hydration in 1.0 M sulfate salts caused spectral effects similar to a drying-out effect, which could be explained by salting-out.