不同超富集、富集植物-玉米间作模式对玉米中镉吸收、转运的影响研究

为了研究Cd污染条件下,玉米分别与苋菜、黑麦草、龙葵间作对重金属Cd吸收和转运的特点,从而选择适宜与玉米间作的富集植物,同时达到修复重金属Cd污染土壤的目的。该文以镉(Cd)污染的河南棕壤黏土为供试土壤,通过盆栽试验,基于玉米各器官中Cd含量、富集系数、转运系数、土壤有效态Cd含量的变化,研究了间作苋菜、黑麦草、龙葵对玉米各器官Cd的积累特性的影响及其迁移转运机制。结果表明：(1)龙葵、苋菜、黑麦草间作使得玉米地上部Cd含量显著性降低(P<0.05),其中以籽粒中Cd含量的下降最为显著。间作苋菜、黑麦草、龙葵,玉米籽粒中Cd含量分别下降了67.6%、75.7%和79.9%。(2)间作苋菜、黑麦草、龙葵使得玉米的富集系数较单作处理下玉米的富集系数分别下降了49.3%、39.7%和68.5%,且差异达到显著水平。(3)与苋菜、黑麦草间作相比,间作龙葵的玉米转运系数分别下降了27.5%、24.2%,且差异均达到显著水平。通过对人体每天摄入Cd量的安全值计算得出间作后土壤中Cd全量应低于2.26 mg·kg-1,土壤有效态Cd含量低于0.88 mg·kg-1。该污染农田在间作模式下,食用玉米Cd暴露对居民健康不存在风险。间作苋菜、黑麦草、龙葵能够抑制玉米对Cd的吸收,同时阻控玉米地上部Cd向地上部的转移,尤其是向籽粒转移。通过间作苋菜、黑麦草、龙葵,不仅降低了主栽作物玉米的Cd累积量,实现玉米安全、优质种植,同时也达到了修复污染土壤的目的。     

高效优化非分裂PML边界二阶标量波方程数值模拟方法

卷积完全匹配层（convolution perfectly matched layer,CPML）吸收边界是一种高效处理波动方程数值模拟中人工边界反射波的方法。本文基于传统的一阶系统CPML吸收边界条件推广并推导了新的二阶系统CPML边界条件（NCPML）。与常规二阶系统CPML边界条件不同,新边界条件推导的核心思想是在复数-频率域中忽略部分衰减因子空间变化特性,避免其在时间域产生复杂卷积算子,然后反变换至时间域得到基于CPML吸收条件的二阶标量波方程,并应用于二阶标量波方程数值模拟。均匀介质模型测试验证了NCPML吸收条件在内存使用上相对于常规二阶系统CPML与SPML（split PML）吸收条件更少。在对人工边界反射的吸收效果上,NCPML稍逊色于常规二阶系统CPML,但二者均相对于SPML优势明显。最后通过层状模型和Marmousi模型测试验证了NCPML的稳定性及其在效率上的优势。     

Do CRISTA Experiment/Campaign Data Represent a Typical Situation or Not?

Data from four A3 radio wave circuits in central Europe are used to analyse the representativeness of the ionization and gravity wave activity pattern in the lower ionosphere (85 – 100 km) in the CRISTA experiment interval (3 – 12 November 1994) for the given conditions. It has been found that the CRISTA experiment interval was run under conditions, which are highly representative both of October – November 1994 and autumn, low-moderate solar activity, the descending phase of solar cycle conditions, i.e. CRISTA measurements may be considered to provide values identical with, or close to climatological values (at least for central Europe, h = 85 – 100 km).     

Dehydration experiments on natural omphacites: qualitative and quantitative characterization by various spectroscopic methods

A series of natural omphacites from a wide range of P, T occurrences were investigated by electron microprobe (EMP), infrared (IR)-, Mössbauer (MS)- and optical spectroscopy in the UV/VIS spectral range (UV/VIS), secondary ion mass spectrometry (SIMS) and single crystal structure refinement by X-ray diffraction (XRD) to study the influence of hydrogen loss on valence state and site occupancies of iron. In accordance with literature data we found Fe²⁺ at M1 as well as at M2, and in a first approach assigned Fe³⁺ to M1, as indicated by MS and XRD results. Hydrogen content of three of our omphacite samples were measured by SIMS. In combination with IR spectroscopy we determined an absorption coefficient: ε _i,tot = 65,000 ± 3,000 lmol_H2O ^?1 cm^?2. Using this new ε _i,tot value, we obtained water concentrations ranging from 60 to 700 ppm H₂O (by weight). Hydrogen loss was simulated by stepwise heating the most water rich samples in air up to 800°C. After heat treatment the samples were analyzed again by IR, MS, UV/VIS, and XRD. Depending on the type of the OH defect, the grade of dehydration with increasing temperature is significantly different. In samples relatively poor in Fe³⁺ (<0.1 Fe³⁺ pfu), hydrogen associated with vacancies at M2 (OH bands around 3,450 cm^?1) starts to leave the structure at about 550°C and is completely gone at 780°C. Hydrogen associated with Al³⁺ at the tetrahedral site (OH bands around 3,525 cm^?1, Koch-Müller et al., Am Mineral, 89:921–931, 2004) remains completely unaffected by heat treatment up to 700°C. But all hydrogen vanished at about 775°C. However, this is different for a more Fe³⁺-rich sample (0.2 Fe³⁺ pfu). Its IR spectrum is characterized by a very intense OH band at 3,515 cm^?1 plus shoulder at 3,450 cm^?1. We assign this intense high-energy band to vibrations of an OH dipole associated with Fe³⁺ at M1 and a vacancy either at M1 or M2. OH release during heating is positively correlated with decrease in Fe²⁺ and combined with increase in Fe³⁺. That dehydration is correlated with oxidation of Fe²⁺ is indirectly confirmed by annealing of one sample in a gas mixing furnace at 700°C under reducing conditions keeping almost constant OH^? content and giving no indication of Fe²⁺-oxidation. Obtained data indicate that in samples with a relatively high concentration of Fe²⁺ at M2 and low-water concentrations, i.e., at a ratio of Fe^{2+ M2}/H > 10 dehydration occurs by iron oxidation of Fe²⁺ exclusively at the M2 site following the reaction: \( {\left[ {{\text{Fe}}^{{{\text{2 + [ M2]}}}}{\text{OH}}^{ - } } \right]} = {\left[ {{\text{Fe}}^{{{\text{3 + [ M2]}}}} {\text{O}}^{{{\text{2}} - }} } \right]} + {\text{1/2}}\;{\text{H}}_{{\text{2}}} \uparrow . \) In samples having relatively low concentration of Fe²⁺ at M2 but high-water concentrations, i.e., ratio of Fe^{2+ M2}/H < 5.0 dehydration occurs through oxidation of Fe²⁺ at M1.     

Chlorophyll-specific absorption coefficients and pigments of phytoplankton off Sanriku, northwestern North Pacific

The variety in shape and magnitude of thein vivo chlorophyll-specific absorption spectra of phytoplankton was investigated in relation to differences in pigment composition off Sanriku, northwestern North Pacific. Site-to-site variations of the absorption coefficients,a _ph ^* (λ), and pigment composition were clearly observed. At warm-streamer stations, higher values ofa _ph ^* (440) anda _ph ^* (650) were found with relatively high concentrations of chlorophyllb (a green algae marker). At stations located in the Oyashio water (cold streamer),a _ph ^* (440) values were lower and fucoxanthin (a diatom marker) concentrations were higher, compared to the other stations. The peak in the absorption spectra at the Oyashio stations was shifted toward shorter wavelengths, which was probably due to the presence of phaeopigments. In a Kuroshio warm-core ring, the magnitude ofa _ph ^* (440) was in between those at the warm-streamer and Oyashio stations, and the diagnostic pigment was peridinin (a dinoflagellate marker). These findings indicated that major differences in phytoplankton absorption spectra of each water mass were a result of differences in the phytoplankton pigment composition of each water mass, which was probably related to the phytoplankton community.     

太湖流域昆承湖春季颗粒物和有色可溶性有机物吸收特性

利用2010年4月23日在昆承湖采集的水体吸收系数数据,对总悬浮物颗粒物、浮游植物色素颗粒物、非色素颗粒物和有色可溶性有机物的吸收特征进行研究.结果表明,春季昆承湖水体除675 nm附近具有叶绿素吸收峰的红光波段外,非色素颗粒物吸收系数大于浮游植物色素颗粒物吸收系数,总颗粒物吸收系数光谱分布与非色素颗粒物的吸收光谱类似...     

高矿化度沙漠湖泊水体的光学特性

沙漠湖泊水体和东部大型湖泊如太湖等存在较大差异.为深入研究沙漠湖泊水体的光学特性,利用腾格里沙漠月亮湖实测水面ASD高光谱数据和同步采集的水样,对水体矿化度与叶绿素a、DOC、悬浮物的含量进行相关性分析,比较沙漠湖泊水体和其它水体的黄色物质、浮游植物、非藻类悬浮物吸收特征光谱,探讨不同波段中水深和矿化度对水体反射率的影...     

养马岛附近海域藻华期间有色溶解有机质的生物可利用性研究

本研究利用吸收光谱和荧光激发-发射矩阵光谱-平行因子分析(EEMs-PARAFAC),研究了养马岛附近海域海水中有色溶解有机质(CDOM)的浓度、组成、来源和生物可利用性,并估算了浮游植物生长繁殖对CDOM及具有生物可利用性CDOM的贡献。结果表明,表、底层海水中CDOM浓度(以吸收系数a₃₅₀计)平均值分别为1.62±0.42 m^-1和1.30±0.47 m^-1,光谱斜率(S_275-295)平均值分别为0.022±0.003 nm^-1和0.023±0.003 nm^-1。利用PARAFAC模型识别出4种荧光组分,分别为陆源类腐殖酸C1、类色氨酸C2、类酪氨酸C3和微生物源类腐殖酸C4。荧光指数(FIX)、腐殖化指数(HIX)和生物指数(BIX)显示,CDOM受陆源输入和海洋自生源的综合影响。降解实验结果显示,表、底层海水中生物可利用性CDOM百分比(%△a₃₅₀)平均值分别为(23.36%±17.94%)和(8.93%±20.30%)。C1、C2和C4组分的荧光强度在培养之后降低,而C3组分的荧光强度上升。各荧光组分生物可利用性依次递减的顺序为:%△C1(23.75%±8.96%)＞%△C4(20.83%±11.71%)＞%△C2(11.67%±38.87%)＞%△C3(-29.61%±39.90%),显示培养之后CDOM的平均分子量和腐殖化程度降低。表层海水中a₃₅₀、%△a350与Chl a之间存在显著线性相关关系,据此可以估算出浮游植物生长繁殖对CDOM的贡献为36.9%,对具有生物可利用性CDOM的贡献为85.0%。