Seasonal levels of water‐extractable cations and anions in soil under blight‐affected and healthy citrus trees

Abstract

Soil samples were collected under blight‐affected and healthy citrus trees at 30‐day intervals for 24 months, at 20‐to 50‐cm depth. Analyses of water extracts (1:1 soil: water) for K, Ca, Mg, Na, SO₄, and Cl showed few differences in cations, but lower anion levels under blighted trees. The cation/anion ratio was significantly higher under blight‐affected trees. Samples collected once at different locations in the same time period showed the same differences. In one location, K was lower and Na higher under healthy trees than under blight‐affected trees, in others K was higher too.     

四环素类抗生素在土壤和堆肥中的吸附和降解

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.     

食用菌富集微量元素的研究与展望

本文综述了食用菌富集微量元素的特点，研究所用的食用菌菌种及所富集微量元素的种类，富集微量元素的食用菌生理功能、应用前景与存在问题。     

Analysis of Some Divalent Metal Contents in Tobacco Expressing the Exogenous Soybean Ferritin Gene

Abstract

T2 tobacco lines overexpressing soybean ferritin in the plastids (+TPs) or apoplasm (AFs) under the regulation of CaMV 35S promoter were grown on MS nutrient solution. After 1 month growth, statuses of six major divalent‐metals (Ca, Cu, Fe, Mg, Mn, and Zn) were measured in leaves and roots. Both +TPs and AFs showed enhanced growth (max. 1.7×) in leaves than the control line. The Fe contents in leaves of +TPs and AFs were significantly larger (1.9–2.8×) than that of the control line. The other metal contents in leaves of +TPs and AFs were almost the same as or less than those of the control line. In contrast to the result of leaves, the growth enhancement in roots was not clear in +TPs, but in AFs. Also, some of the non‐ferrous metal contents in roots of +TPs and AFs were dramatically increased compared with those of the control line (Mn, 1.9–10.4×; Zn, 1.6–2.3×), whereas the differences in content of Fe, Cu, Ca, and Mg were insignificant. These results demonstrated that the ferritin overexpression in apoplasm was as effective for inducing Fe accumulation as that in plastid. Under the normal metal‐balanced condition, even if the activation of Fe uptake related enzymes leads to the accumulation of non‐specific accumulation of divalent metal ions in roots, an Fe loading/unloading system and/or an internal translocator in xylem and phloem might specifically deliver Fe to the upper part of plants.     

Effects of enhanced supplies of nitrogen and sulphur on rhizosphere and soil chemistry in a Norway spruce stand in SW Sweden

Rhizophere and bulk soil chemistry were investigated in a Norway spruce stand in SW Sweden. The rhizosphere and bulk soil chemistry in water extracts in control plots (C) and plots repeatedly treated with ammonium sulphate (NS) were compared. Treatment regime was started in 1988. Cylindrical core samples of the LFH-layer and mineral soil layers were collected in 1992 and used for water extract analyses. Samples of soil from LFH-layer and mineral soil layers were taken in 1991 and 1993 for determination of CEC and base saturation. Soil pH and NH₄-N, NO₃-N and SO₄-S, Al, Ca, K and Mg concentrations in water extracts were measured for rhizosphere and bulk soils. The pH-values of bulk and rhizosphere soils in NS plots decreased compared with those in control plots, whereas concentrations of NH₄-N, NO₃-N, SO₄-S, base cations and Al in water extract increased. In both bulk and rhizosphere soils the concentration of NH₄-N was much higher than that of NO₃-N. A significant difference in the pH and Mg concentration of bulk and rhizosphere soil between the treated and control plots was found only in the 0–10 cm layer. For all layers, there was a significant difference in NH₄-N concentrations in the bulk and rhizosphere soil between the NS treatment and control plots. Concentrations of exchangeable base cations and the base saturation level in the LFH-layer decreased in the NS plots. The concentration of extractable SO₄-S increased in the NS plots. The NS treatment enhanced the amount of litter in L-layer, owing to increases in needle biomass and litterfall but led to losses of base cations, mainly K and Mg, from LFH-layer. It was concluded that the NS treatment displaced cations from exchangeable sites in the LFH-layer leading to higher concentrations of these elements in both rhizosphere and bulk soil.     

恒电荷土壤及可变电荷土壤与离子间相互作用的研究 I.共存离子对NO_3~-吸附的影响

研究了我国典型３种可变电荷土壤和４种恒电荷土壤在陪伴阳离子分别为Ｋ十、Ｎａ十、Ｃａ２＋时和１ｍｍｏｌＬ－１ＫＣ１、Ｋ２ＳＯ４支持电解质中ＮＯ３－的吸附。结果表明，ＮＯ３－吸附量随ｐＨ的增加而减小。在添加相同浓度ＮＯ３－时，３种可变电荷土壤对ＮＯ３－的吸附量顺序为Ｃａ（ＮＯ３）２＞ ＫＮＯ３＞ＮａＮＯ３＞ＫＮＯ３十ＫＣＩ＞ＫＮＯ３＋Ｋ２ＳＯ４；在初始ＮＯ３－浓度０．５－５ｍｍｏｌＬ－１的范围内，吸附量随浓度变化的关系符合Ｌａｎｇｍｕｉｒ等温吸附式．由此求出与ＮＯ３－吸附结合能有关的常数（Ｋ）在不同共存离子存在下数值较小且差异不大，因此认为不同陪伴阳离子和不同伴随阴离子对ＮＯ３－吸附的电性机理影响不大，只是改变了土壤表面的正电荷数量从而使吸附量发生变化。４种恒电荷土壤对ＮＯ３－的吸附量通常很小，其中在Ｃａ（ＮＯ３）２介质中较在其他介质中稍大，最大吸附量仅为１．５～ｍｍｏｌ ｋｇ－１左右，约为可变电荷土壤的１／１０，且在浓度较低时常观察到负吸附。     

亚热带花岗岩地区土壤矿物风化过程中盐基离子的释放特征

矿物风化过程中盐基离子释放遵从一定的化学计量关系,这种化学计量关系一般只能通过模拟实验来获取。本研究采用pH 7.0的EDTA-乙酸铵溶液将土壤中的交换性盐基离子完全洗脱出来,然后用Batch方法模拟不同pH溶液淋溶洗脱盐基和未洗脱盐基土壤,旨在消除土壤中交换性盐基离子的影响后更为准确地判断土壤矿物风化的盐基离子释放特征。结果表明:未洗脱盐基土壤的淋出液pH由3.73±0.14逐渐上升到4.23±0.06,主要原因是淋溶液中有高浓度的NH_4~+;洗脱盐基土壤矿物风化后淋出液pH从7.39±0.02逐渐下降到5.39±0.17,主要是由于土壤中可风化矿物减少。土壤交换性盐基离子会改变盐基离子释放特征、释放总量:未洗脱盐基土壤经酸雨淋溶后,各盐基离子释放均呈现急速下降后逐渐平缓的趋势,洗脱盐基土壤矿物风化后,K~+及盐基离子释放总量呈波动上升趋势,且盐基离子释放总量比未洗脱盐基土壤低。土壤交换性盐基离子的存在还会改变淋出液中的盐基离子化学计量关系:未洗脱盐基土壤的K~+︰Ca~(2+)︰Mg~(2+)︰Na+化学计量关系为11︰13︰4︰1(当量比),而洗脱盐基土壤为7︰2︰2︰1。K~+是盐基离子中风化释放量最多的,大部分K~+来自于土壤中云母的风化。因此,只有利用洗脱盐基土壤的盐基离子释放量才能准确计算矿物风化速率并获得准确的化学计量关系。土壤矿物风化作用随着淋溶液酸度增大而增强,但模拟一年降雨量的情况下,p H 3.5、4.5和5.5三种不同p H溶液对矿物风化后盐基离子的释放在实验期间没有显著性影响,较长时间后的差异性有待观察。本研究表明,可以通过预洗脱盐基土壤然后模拟酸雨淋溶的方法,观察矿物风化特征,特别是盐基离子释放的化学计量特征。     

亚热带湿润地区城市公园重建强度对其土壤酸化和土壤中重金属的影响

Soil quality is a major concern in the management of urban parks. In this study, the soils at 0–3, 3–13, and 13–23 cm depths were sampled from six urban parks, differing in reconstruction intensity(mainly changes made during conversion of natural forests into parklands), in the Pearl River Delta, China to determine how reconstruction intensity influenced the extent of acidification and heavy metal levels in the soils of urban parks in a humid subtropical environment. High reconstruction intensity(HRI) was practiced in three parks and low reconstruction intensity(LRI) in three other parks. The LRI soils were strongly to extremely acidic(with low exchangeable Ca, Mg, and K concentrations) while the HRI soils were much less acidic. Both total and extractable concentrations of soil heavy metals were related to the specific management practices and age of the park, but did not differ significantly between LRI and HRI parks or among soil depths. Soil p H was significantly related to soil exchangeable cation concentrations and base saturation but was weakly related or unrelated to soil heavy metal levels. Our results suggest that high intensity but not low intensity reconstruction significantly reduces the extent of soil acidification in the urban parks in a humid subtropical environment.     

Assessment of sugar maple tree growth in relation to the partitioning of elements in xylem along a soil acidity gradient

Partitioning of elements in tree xylem is being increasingly studied, as it suggests that elements are potentially mobile within the xylem long after their uptake. A recent study revealed that only the most mobile xylem fraction (water-soluble) of base cations (calcium [Ca], magnesium [Mg], and potassium [K]) increased at higher soil acidity, while the two mobile fractions (water- and acid-soluble) of acidic metals—potentially phytotoxic aluminium (Al), cadmium (Cd) and manganese (Mn)—were significantly enhanced on very acid soils. The current paper presents an investigation of soil-wood chemistry relationships with basal area tree growth. It was hypothesized that the growth of sugar maple would be reduced by low base cation and high acidic metal concentrations in the xylem mobile fractions. Sugar maple trees (n = 55) from six watersheds in southern Quebec, Canada were analysed by sequential chemical extractions for the water-soluble, acid-soluble and residual fractions of base cations (Ca, K, Mg) and acidic metals (Al, Cd, Mn) in xylem. Generally, tree growth was positively correlated to concentrations of base cations in wood (ρ = 0.27-0.50) and soil (ρ = 0.41-0.67), and negatively correlated to concentrations of acidic metals in wood (ρ = −0.33 to −0.52) and soil (ρ = −0.67). However, these relations differed depending on the element fraction considered. Water- and acid-soluble xylem concentrations of base cations and Al were among the best predictors of growth trends (R² = 0.46-0.51). The relationship between acidic metals and tree growth is further discussed.     

Evaluation of elemental depletion weathering rate estimation methods on acid-sensitive soils of north-eastern Alberta, Canada

Immobile element-based weathering estimation methods assume that Zr (or Ti) is an immobile element, and that weathering rates of other elements can be estimated according to the enrichment of Zr in weathered horizons relative to an unweathered parent material. This approach was used to estimate base cation weathering rates for 33 soil profiles on acid-sensitive terrain in north-eastern Alberta. Zirconium generally showed enrichment within the rooting zone, but the deepest (subsoil) samples were not always associated with the lowest Zr concentrations. Weathering rates estimated with the Zr depletion and Pedological Mass Balance (PMB) methods were generally low (ranges: 0-51 and 0-58 mmol_c m^− 2 yr^− 1, respectively); however, low base cation oxide concentrations and heterogeneity within soil profiles complicated weathering rate calculations and net base cation gains were calculated for several (six) sites. Evaluation of the Zr depletion and PMB weathering estimates against those calculated with the process-oriented PROFILE model at a subset (n = 9) of the sites indicated the estimates were poorly related, with PROFILE rates typically being higher. The effects-based emissions management strategy for acid precursors in this region requires spatial coverage of soil properties (including weathering rates) across a large area, but the apparent limitations associated with the immobile element based methods in this region: identifying representative parent soils and deriving weathering rate estimates comparable to more robust methods are arguments against their candidacy for future use.