四棱豆新品种及栽培技术要点

四棱豆又称翼豆、龙豆、四角豆、杨桃豆等,为豆科一年生或多年生缠绕草本植物。叶、花、果均具观赏价值,尤其是果实。食用器官一般为嫩豆荚,口感脆嫩     

Phosphorus release from vivianite and hydroxyapatite by organic and inorganic compounds

Based on recent mining rates and the exhaustion of global phosphorus(P)reserves,there is a need to mobilize P already stored in soils,and its recovery from secondary resources such as Ca-and Fe-phosphates is important.The Ca-phosphate hydroxyapatite forms a good fertilizer source,while vivianite is formed in waterlogged soils and sediments.During sludge treatment,the formation of vivianite has been identified,being mainly Fe-phosphate.Long-term P release from both hydroxyapatite and vivianite was studied using different inorganic(CaCl2 and CaSO4)and organic(citric and humic acid)reagents during batch experiments.Reagents CaCl2 and CaSO4 represent the soil solution,while citric and humic acids as organic constituents affect P availability in the rhizosphere and during the process of humification.Additionally,the flow-through reactor(FTR)technique with an infinite sink was used to study the long-term P release kinetics.The cumulative P release was higher by organic acids than by inorganic compounds.The cumulative P release rates were higher in the FTR with CaCl2 as compared to the batch technique.The infinite sink application caused a continuously high concentration gradient between the solid and liquid phases,leading to higher desorption rates as compared to the batch technique.The predominant amount of the total P released over time was available for a short term.While inorganic anion exchange occurred at easily available binding sites,organic acids affected the more heavily available binding sites,which could be embedded within the mineral structure.The results showed that organic compounds,especially citric acid,play a superior role as compared to the inorganic constituents of the soil solution during the recovery of already stored P from the tertiary phosphates vivianite and hydroxyapatite.     

Nitrification inhibitor nitrapyrin does not affect yield-scaled nitrous oxide emissions in a tropical grassland

Urea is the most common nitrogen(N)fertilizer used in the tropics but it has the risk of high gaseous nitrogen(N)losses.Use of nitrification inhibitor has been suggested as a potential mitigation measure for gaseous N losses in N fertilizer-applied fields.In a field trial on a tropical Andosol pastureland in Costa Rica,gaseous emissions of ammonia(NH₃)and nitrous oxide(N₂O)and grass yield were quantified from plots treated with urea(U;41.7 kg N ha^-1application^-1)and urea plus the nitrification inhibitor nitrapyrin(U+NI;41.7 kg N ha^-1application^-1and 350 g of nitrapyrin for each 100 kg of N applied)and control plots(without U and NI)over a six-month period(rainy season).Volatilization of NH₃(August to November)in U(7.4%±1.3%of N applied)and U+NI(8.1%±0.9%of N applied)were not significantly different(P>0.05).Emissions of N₂O in U and U+NI from June to November were significantly different(P<0.05)only in October,when N₂O emission in U+NI was higher than that in U.Yield and crude protein production of grass were significantly higher(P<0.05)in U and U+NI than in the control plots,but they were not significantly different between U and U+NI.There was no significant difference in yield-scaled N₂O emission between U(0.31±0.10 g N kg^-1dry matter)and U+NI(0.47±0.10 g N kg^-1dry matter).The results suggest that nitrapyrin is not a viable mitigation option for gaseous N losses under typical N fertilizer application practices of pasturelands at the study site.     

Effects of the nitrification inhibitor nitrapyrin and the plant growth regulator gibberellic acid on yield-scale nitrous oxide emission in maize fields under hot climatic conditions

Nitrification inhibitors are widely used in agriculture to mitigate nitrous oxide(N₂O)emission and increase crop yield.However,no concrete information on their mitigation of N₂O emission is available under soil and environmental conditions as in Pakistan.A field experiment was established using a silt clay loam soil from Peshawar,Pakistan,to study the effect of urea applied in combination with a nitrification inhibitor,nitrapyrin(2-chloro-6-tri-chloromethyl pyridine),and/or a plant growth regulator,gibberellic acid(GA_3),on N₂O emission and the nitrogen(N)uptake efficiency of maize.The experimental design was a randomized complete block with five treatments in four replicates:control with no N(CK),urea(200 kg N ha^-1)alone,urea in combination with nitrapyrin(700 g ha^-1),urea in combination with GA_3(60 g ha^-1),and urea in combination with nitrapyrin and GA_3.The N₂O emission,yield,N response efficiency,and total N uptake were measured during the experimental period.The treatment with urea and nitrapyrin reduced total N₂O emission by 39%–43%and decreased yield-scaled N₂O emission by 47%–52%,relative to the treatment with urea alone.The maize plant biomass,grain yield,and total N uptake increased significantly by 23%,17%,and 15%,respectively,in the treatment with urea and nitrapyrin,relative to the treatment with urea alone,which was possibly due to N saving,lower N loss,and increased N uptake in the form of ammonium;they were further enhanced in the treatment with urea,nitrapyrin,and GA_3 by 27%,36%,and 25%,respectively,probably because of the stimulating effect of GA_3 on plant growth and development and the reduction in biotic and abiotic stresses.These results suggest that applying urea in combination with nitrapyrin and GA_3 has the potential to mitigate N₂O emission,improve N response efficiency,and increase maize yield.     

硫素营养胁迫对水稻根系和叶片超微结构的影响

通过水培试验,用电镜技术研究了不同浓度硫(S)索营养对水稻根系和叶片超微结构的影响.结果表明,受S素营养胁迫的水稻,其根系及叶片的超微结构均发生了显著的变化:低S胁迫会造成水稻叶片叶肉细胞内的叶绿体结构肿胀,基粒片层松驰、散乱,细胞器减少,线粒体结构被破坏,根系细胞内几乎没有内含物;S 浓度高则会使叶片叶绿体基粒片层致密、浓缩,无规则化,根系细胞发生质壁分离.这就从微观上进一步解释了水稻S索营养胁迫严重影响其生长发育的原因与机理,也为水稻S索营养的早期诊断提供了解剖学与形态学的依据.     

辽宁省不同土地利用背景下土壤侵蚀空间分布规律

辽宁省地域辽阔,不同地区不同土地类别土壤侵蚀差异很大.定量研究辽宁省不同区域、不同地类土壤侵蚀空间分布规律,研究如何进行水土保持,防止土壤侵蚀,为辽宁省的可持续发展提供决策支持,具有深远意义.以前人研究手段为基础,以辽宁省第4次土壤侵蚀遥感成果为依据,对辽宁省不同土地利用背景下土壤侵蚀空间分布规律进行定量研究.研究表明,辽宁省各地类土壤侵蚀以水蚀为主,林地最为严重,耕地次之;风蚀以草地最为严重,同时风蚀对耕地的影响不容忽视.     

抱子芥高产优质栽培技术

抱子芥又称儿菜、娃娃菜,特点是茎和茎上功能叶的腋芽变态肥大呈肉质作为主要的食用部份,其质地柔嫩,鲜食清香略带甜味,是度春淡的最佳蔬菜作物之一。最早在四川、重庆栽培较广,现已扩大到浙江、湖北、湖南、上海等全国12个省市。许多地方引种栽培儿菜时,由于不了解儿菜的生物学特性和栽培技术,常出现先期抽薹、产量低等问题,本文介绍儿菜的生物学特性和栽培技术,供生产参考。     

秋洋芋实用栽培技术

秋洋芋是晚秋生产的重点作物,是在水稻、玉米收获后,充分利用小麦、油菜播栽前的空闲时段,开发种植的一季秋洋芋。秋洋芋种植不仅可提高复种指数,增加粮食产量,保障粮食安全;而且可有效解决城乡居民蔬菜秋淡问题,提高经济效益,增加农民收入。     

杜陵生态环境演变及恢复重建研究

概述了杜陵的区位、地形及自然环境条件.参照关中地区生态环境演变的具体过程,指出杜陵生态环境演变的影响因素为自然因素和人为因素并重,人为因素是导致杜陵环境演变的主要因素.在实地调查的基础上指出了杜陵生态环境现存的问题为生态景观严重不协调,商开发不合理,水资源不足,水土流失严重等.以因地制宜原则,可持续发展原则为指导,提出了杜陵生态环境恢复重建的具体措施为人口措施、产业结构调整、工程技术措施及植被恢复.     

Zinc sorption–desorption by sand,silt and clay fractions in calcareous soils of Iran

Zinc sorption–desorption by sand, silt and clay fractions of six representative calcareous soils of Iran were measured. Sand, silt and clay particles were fractionated after dispersion of soils with an ultrasonic probe. Zinc sorption analysis was performed by adding eight rates of Zn from 6 to 120 μmol g^?1. For the desorption experiment, samples retained after the measurement of Zn sorption were resuspended sequentially in 0.01 M NaNO₃ solution and shaken for 24 h. Results indicated that Zn sorption by soil fractions increased in the order clay > silt > sand, and correlated negatively with CaCO₃ content and positively with cation exchange capacity (CEC) and smectite content. Results indicated that for all fractions, the Langmuir equation described the sorption rates fairly well. In contrast to sorption, Zn desorption from soil fractions increased in the order sand > silt > clay, and correlated positively with CaCO₃ content, CEC and smectite content. Results showed that parabolic diffusion and two constant equations adequately described the reaction rates of Zn desorption. In general, for all soils studied, the coarser the particle size, the less Zn sorption and more Zn desorption, and this reflects much higher risk of Zn leaching into groundwater or plant uptake in contaminated soils.     

Effects of Different Rates of Ca2+ Addition on Respiration and Sorption of Water-Extractable Organic C to a Vertisol Subsoil

It is well known that calcium (Ca²⁺) plays an important role in binding organic matter to clay. However, most previous studies were conducted with either topsoil or pure aluminosilicates. Less is known about the effect of Ca²⁺ on binding of organic matter to clay-rich subsoils, which have lower organic-matter contents than topsoils, and their clays are more strongly weathered than pure aluminosilicates. Two experiments were conducted with a Vertisol subsoil (69% clay): a laboratory incubation and a batch sorption. The mineral substrate in the incubation experiment was pure sand alone or sand amended with 300 g clay kg^?1. Powdered calcium sulfate (CaSO₄) at rates of 0, 5, 10, and 15 g Ca kg^?1 and mature wheat residue at a rate of 20 g kg^?1 were added to this mineral substrate and the water content was adjusted to 70% of water-holding capacity. Carbon dioxide release was measured for 28 days. Cumulative respiration per g soil organic carbon (C) (SOC from clay and residues) was increased by clay addition. Increasing Ca²⁺ addition rate decreased cumulative respiration in the sand with clay but had no effect on respiration in the pure sand. Clay and Ca²⁺ addition had no significant effect on microbial biomass carbon (MBC) per g SOC but clay addition reduced the concentration of potassium sulfate (K₂SO₄)–extractable C per g SOC. For the batch sorption experiment, the subsoil was mixed with 0 to 15 g Ca kg^?1 and water-extractable organic C (WEOC) derived from mature wheat straw was added at 0, 1485, 3267, and 5099 mg WEOC kg^?1. Increasing Ca²⁺ addition rate increased sorption of WEOC, particularly at the greatest concentration of WEOC added, and decreased desorption. This study confirmed the importance of Ca²⁺ in binding organic matter to clay and suggests that Ca²⁺ addition to clay-rich subsoils could be used to increase their organic C sequestration.     

沙粒中添加Ca2+、粘土以及富粘土对水溶性有机碳呼吸作用及其吸附的影响研究

Clay addition to light-textured soils is used to ameliorate water repellency and to increase nutrient retention. However, clay addition may also increase the potential to bind organic matter and thus C sequestration. Divalent calcium ions （Ca2＋） play an important role in binding of organic matter to clay because they provide the bridge between the clay particles and organic matter which are both negatively charged. In the first experiment, quartz sand was mixed with clay isolated from a Vertosol at rates of 0, 50 and 300 g kg-1, finely ground mature wheat residues （20 g kg-1） and powdered CaSO4 at 0, 5 and 10 g kg-1. Soil respiration was measured over 28 d. Compared to the sand alone, addition of isolated clay at 300 g kg-1 increased cumulative respiration with a stronger increase than that at 50 g kg-1. Addition of CaSO4 increased electrical conductivity, decreased sodium adsorption ratio and reduced cumulative respiration. The latter can be explained by enhanced sorption of organic matter to clay via Ca2＋ bridges. In a second experiment, isolated clay or subsoil of the Vertosol without or with powdered CaSO4 at 10 g kg-1 were used for a batch sorption with water-extractable organic C （WEOC） from wheat straw followed by desorption with water. Addition of 10 g kg-1 CaSO4 increased sorption and decreased desorption of WEOC in both subsoil and isolated clay. In the third experiment, subsoil of the Vertosol was used for a batch sorption in which WEOC was added repeatedly. Repeated addition of WEOC increased the concentration of sorbed C but decreased the sorbed proportion of the added WEOC. This indicates that sorption of WEOC may be underestimated if it is added only once in batch sorption experaments.     

Physicochemical properties of the soils associated with shifting cultivation in Northern Thailand with special reference to factors determining soil fertility

Abstract

Recently agricultural activity in the mountainous area of northern Thailand has increased and problems relating to soil fertility have arisen. In order to gain basic information about the soil properties associated with shifting cultivation, physicochemical properties of the surface soils (0–10 cm) and subsoils (30–40 cm) were investigated in selected villages in the area. The physicochemical properties of the soils studied are summarized as follows: 1) The soils were rich in organic matter, content of which ranged from 11.4 to 63.3 g C kg^?1 in the surface soil. 2) The pH(H₂O) of the soils mostly ranged from 5 to 7 and soil acidity was more pronounced in the deeper horizons. In the surface soils, exchangeable Ca and Mg were generally dominant, whereas exchangeable Al was often predominant in the subsoils. 3) Most of the soils showed a medium to fine texture with more than 30% clay. The clay mineral composition was characterized by various degrees of mixture of kaolin minerals and clay mica with, in some cases, a certain amount of 2:1-2:1:1 intergrades. 4) According to the ion adsorption curves, most of the B horizon soils were characterized by the predominance of permanent negative charges. On the other hand, organic matter contributed to the increase of variable negative charges in the surface soils. The content of organic matter and the percentage of the clay fraction were essential for determining the CEC of the soils of the surface 10 and 30–40 cm depths, respectively. Under the field conditions, the composition of exchangeable cations largely reflected the soil acidity. In addition, the content of organic matter also showed a significant correlation with that of available N in the surface soils. Thus, soil acidity both in the surface soils and subsoils, organic matter content in the surface soils, and clay content in the subsoils were considered to be the main factors that affected soil chemical fertility in the area.     

The forms and availability to plants of soil potassium as related to mineralogy for upland Oxisols and Ultisols from Thailand

Potassium (K) deficiency is widespread in crops on highly weathered upland soils under a tropical monsoonal climate. Critical assessment of the forms of K in soils and of the ability of soils to release K for plant uptake is important for the proper management of K in crop production. The relationships between different pools of K were investigated as a function of silt and clay mineralogy for 14 upland Oxisols and 26 upland Ultisols soils from Thailand. Most soils contained no K-minerals in the silt fraction. XRD showed that kaolinite is the dominant clay mineral with variously minor or moderate amounts of illite, hydroxy-Al interlayered vermiculite and smectite present in some soils. For some soils, both conventional and synchrotron XRD were unable to detect illite. Analytical TEM including EFTEM of individual clay crystals showed that clay in the apparently illite-free samples contained very small amounts of illite. Many kaolinite particles appear to contain K which may be present in illite interleaved with kaolinite crystals. A glasshouse K-depletion experiment was conducted to assess the K supply capacity and changes in chemical forms of K and K-minerals using exhaustive K depletion by Guinea grass (Panicum maximum). Potassium deficiency symptoms and mortality of plants occurred on light textured soils, whereas plants survived for six harvests for Oxisols with clay texture, relatively high CEC and higher NH₄OAc-K (exchangeable K plus water-soluble K). There is a strong linear relationship of unit slope between NH₄OAc-K and cumulative K uptake by plants indicating that NH₄OAc-K is a major form of K available to plants. Thus K-bearing minerals contributed little K to plants over the time scale of the experiment and XRD patterns of whole soil samples, silt and clay from soils after cropping mostly showed no change from those for the initial soil. An exception was for a single surface soil clay where a minor amount of smectite was formed from illite by K release to plants.     

胡敏酸对铵钾在粘土矿物上交互作用的影响

Interaction of ammonium (NH+4) and potassium (K+) is typical in field soils. However, the effects of organic matter on interaction of NH+4 and K+have not been thoroughly investigated. In this study, we examined the changes in major physicochemical properties of three clay minerals (kaolinite, illite, and montmorillonite) after humic acid (HA) coating and evaluated the influences of these changes on the interaction of NH+4 and K+on clay minerals using batch experiments. After HA coating, the cation exchange capacity (CEC) and specific surface area (SSA) of montmorillonite decreased significantly, while little decrease in CEC and SSA occurred in illite and only a slight increase in CEC was found in kaolinite. Humic acid coating significantly increased cation adsorption and preference for NH+4, and this effect was more obvious on clay minerals with a lower CEC. Results of Fourier transform infrared spectrometry analysis showed that HA coating promoted the formation of H-bonds between the adsorbed NH+4 and the organo-mineral complexes. HA coating increased cation fixation capacity on montmorillonite and kaolinite, but the opposite occurred on illite. In addition, HA coating increased the competitiveness of NH+4 on fixation sites. These results showed that HA coating affected both the nature of clay mineral surfaces and the reactions of NH+4 and K+with clay minerals, which might influence the availability of nutrient cations to plants in field soils amended with organic matter.     

Properties of sub soils in relation to various measures of surface area and water content

Neither the specific surface area values (from N₂ sorption) nor the ethylene glycol monoethyl ether (EGME) retention values of 21 soil samples from New Zealand and Fiji could all be accounted for by the sum of the contributions from their component minerals. Much EGME is probably retained by internal surfaces of inter layered and interstratified clay minerals. EGME retention correlated well with cation exchange capacity (CEC) and a number of measures of water content of these soils. The water contents of air-dried soils (measured as ‘moisture factors’ or the ratios of air-dry and oven-dry weights) showed almost as close a relationship to CEC as EGME retention for this set of 21 subsoils. Moisture factors and CEC were closely related, within groups defined by dominant clay mineralogies, for a much wider selection of 1318 New Zealand soil horizons with low carbon contents. The relationships between surface area and a number of other soil properties including dispersibility of soils were also examined.     

Sorption of dissolved organic nitrogen by acid subsoil horizons and individual mineral phases

Dissolved organic matter is important in translocation and export of nutrients from forest ecosystems. Its mobility in soil is restricted by sorption to mineral surfaces which depends on its chemical properties. Carboxyl and hydroxyl groups form strong bondings to mineral surfaces, whereas the role of N‐containing functional groups in the sorption process is less well understood. We examined in laboratory experiments the binding of dissolved organic matter from the forest floor to amorphous Al(OH)₃, goethite, kaolinite, and illite and to subsoils in order to compare the sorption and desorption of dissolved organic C with that of dissolved organic N. The mineral samples were equilibrated with acidic solutions of organic matter at pH 4. In the equilibrium solutions organic C and N and their contribution to two operationally defined fractions, namely the so‐called hydrophilic and hydrophobic fractions, were determined. We measured neutral and acidic amino sugars to discover the nature of the binding of organic N. Within the hydrophilic and hydrophobic fractions, the sorption and desorption of organic C and N did not differ, indicating that there was no preferential binding of N‐containing compounds. The hydrophilic fraction contained more N and sorbed less than the hydrophobic fraction, and so the overall retention of organic N by the mineral phases and subsoils was smaller than that of organic C. Among the amino sugar compounds, muramic acid was preferentially removed from the solution, whereas the neutral amino sugars were sorbed similar to organic C. The results suggest that the sorption of N‐containing compounds is favoured by acidic groups and not by amino groups.     

Azimsulfuron sorption--desorption on soil

The sorption and desorption of the herbicide azimsulfuron, N-[[(4-dimethoxypyrimidin-2-yl)amino]carbonyl]1-methyl-4-(2-methyl-2H-tetrazole-5-yl)1H-pyrazole-5-sulfonamide, were studied using five soils. Sorption isotherms conformed to the Freundlich equation. It was found that pH is the main factor influencing the sorption and that the sorption on soils was negatively correlated with pH. The highest level of sorption was measured on soils with low pH and high organic carbon content. Moreover, inorganic soil colloids, for example, smectite clay minerals and iron oxides, contributed to the sorption of azimsulfuron. Desorption was hysteretic on soils with high organic and inorganic colloid contents.     

Short‐time clay‐mineral evolution in a soil chronosequence in Oléron Island (France)

Major weathering sequences in soils are well established; however, knowledge on rates of mineral transformations remains unknown, because it is often difficult to date precisely soil processes. This work was carried out on soils developed on recent (< 188 y) sand dunes on the W coast of Oléron Island (France). The coast has been protected against marine and wind erosion by constructing five consecutives barriers close to the coastline since 1820 (1820, 1864, 1876, 1889, 1948) defining the maximum age of the soil parent material, as before the areas between the barriers were under water. Soils on the older dunes have low clay content (> 94% of sand) and exhibit a bleached E horizon that overlies a yellowish brown B horizon. The process responsible for their formation is podzolization promoted by the high permeability of the material and complexing organic matter produced by coniferous vegetation. Initial mineralogy of C horizons is homogenous and constituted of chlorite, illite, illite/smectite mixed‐layer minerals, and kaolinite, quartz, calcite (≈ 8% related to shell fragments), and feldspars. The initial clay‐mineral assemblage of the E horizons is dominated by illite (well‐crystallized WCI and poorly crystallized PCI) and chlorite. With progressive podzolization, poorly crystallized illite is first transformed to illite/smectite mixed‐layer minerals and in a further step into smectite. In addition, transformation of well‐crystallized illite leads to formation of ordered illite/smectite mixed‐layer minerals in the E horizons, which is not commonly described in soils. In the B horizons, illite/smectite mixed‐layer minerals are present with traces of smectite, as well as Al and Fe oxi‐hydroxides as revealed by DCB and oxalate chemical extractions. This chronosequence illustrates that over short distances and short time (< 188 y) intense mineral weathering and soil development occur. Major clay‐mineral changes occur between 132 and 188 y in agreement with development of the pine forest producing acidic litter.