一种新的厌氧污泥比活性试验测定法

本文介绍了一种以医用血清瓶作发酵瓶、用医用注射器来量测所产沼气的厌氧污泥比活性试验测定法。实践表明此法简单实用、快速准确。     

世界大麦生产、贸易特征及对我国的影响与启示

摘要：中国啤酒大麦进口量连续多年占到了国内需求量的50%以上,国际大麦市场的诸多变动都将给中国大麦及啤酒产业带来重大影响。本文总结分析了世界大麦生产贸易格局变动以及啤酒大麦主要出口国的发展特征,在此基础上探讨了对中国的影响与启示。主要结论为：世界大麦生产、出口非常集中,进口相对分散,容易产生市场波动和价格垄断;啤酒大麦的出口市场主要由澳大利亚、加拿大和欧盟主导,其生产和贸易波动较大;“大国效应”能够起到“调节阀”的作用,我国可以利用进口大国地位获取价格话语权;我国大麦生产应该以“质”取胜,而不是以“量”取胜,国产大麦和进口大麦共存的局面将长期维持。关键词：大麦 啤酒 生产 贸易     

Pedogenic carbonate recrystallization assessed by isotopic labeling: a comparison of 13C and 14C tracers

The C isotopic composition (δ¹³C) of pedogenic carbonates reflects the photosynthetic pathway of the predominant local vegetation because pedogenic (secondary) CaCO₃ is formed in isotopic equilibrium with soil CO₂ released by root and rhizomicrobial respiration. Numerous studies show the importance of pedogenic carbonates as a tool for reconstructing paleoecological conditions in arid and semiarid regions. The methodological resolution of these studies strongly depends on the time scale of pedogenic carbonate formation, which remains unknown. The initial formation rate can be assessed by ¹⁴C labeling of plants grown on loess and subsequent incorporation of ¹⁴C from rhizosphere CO₂ into newly formed carbonate by recrystallization of loess CaCO₃. We tested the feasibility of ¹⁴C and ¹³C tracers for estimating CaCO₃ recrystallization rates by simultaneous ¹⁴C and ¹³C labeling and comparison with literature data. ¹⁴C labeling was more efficient and precise in assessing recrystallization rates than ¹³C labeling. This is connected with higher sensitivity of ¹⁴C liquid scintillation counting when compared with δ¹³C measurement by IRMS. Further, assessment of very low amounts of incorporated tracer is more precise with low background signal (natural abundance), which is true for ¹⁴C, but is rather high for ¹³C. Together, we obtained better reproducibility, higher methodological precision, and better plausibility of recrystallization rates calculated based on ¹⁴C labeling. Periods for complete CaCO₃ recrystallization, extrapolated from rates based on ¹⁴C labeling, ranged from 130 (125–140) to 240 (225–255) y, while it was ≈ 600 (365–1600) y based on the ¹³C approach. In terms of magnitude, data from late‐Holocene soil profiles of known age provide better fit with modeled recrystallization periods based on the ¹⁴C approach.     

秸秆添加对石灰性土壤有机与无机碳释放的影响

在富含碳酸盐的石灰性土壤上,土壤本身CO2释放不仅来自土壤有机碳（SOC）的分解,也源于无机碳（SIC）的溶解。在秸秆还田下,石灰性土壤CO2释放来源达到三个（秸秆碳、SOC和SIC）,由于区分技术的限制,当前区分CO2释放三源的研究,尚少见报道。以华北石灰性农田土壤为研究对象,采用13C标记玉米秸秆添加土壤进行室内培养32周,设置4个处理,分别为无添加对照（CK）、低量秸秆添加（S1,相当于田间秸秆还田量9.6 t?hm-2）、中量秸秆添加（S2,秸秆还田量28.8 t?hm-2）和高量秸秆添加（S3,秸秆还田量48.0 t?hm-2）,利用秸秆碳、SOC与SIC之间的δ13C差异,借助稳定同位素溯源模型IsoSource,区分土壤CO2的释放来源,明确秸秆添加对石灰性土壤有机与无机碳释放的影响。结果表明,随着培养时间的进行,土壤释放CO2中源于秸秆的贡献呈下降趋势;秸秆分解对土壤CO2释放的贡献随着秸秆添加量增加而增加,对于S1、S2和S3处理,土壤释放CO2中源于秸秆、SOC和SIC的贡献比值约分别为3:3:4、5:2:3和6:2:2;与CK相比,S1处理降低SOC分解的激发效应（程度为9%）,S2和S3处理反而增加了SOC分解的激发效应（程度分别为22%和57%）;秸秆和SOC矿化增加SIC溶解的释放,随秸秆添加量增加而增加,S1、S2和S3处理提高SIC源CO2的释放程度分别为368%、561%和652%。因此,秸秆添加不仅影响SOC源CO2的释放,也增加了SIC源CO2的释放,若忽略SIC溶解对土壤CO2释放的贡献,可能导致SOC矿化量的高估,进而影响SOC激发效应评估的准确度。     

青贮玉米-牛粪尿体系的15N标记及氮素转化研究

15N示踪技术已开始应用于畜禽粪便氮素循环与利用研究领域,而15N在畜禽粪便不同组分和不同形态氮素中的丰度与数量将直接影响到畜禽粪便15N示踪去向与氮素实际去向的一致性。为了解15N在畜禽粪便标记过程的转化特点和在标记粪尿的分布特征,本文首先采用改进的、含有15N标记硫酸铵(60 atom%15N)的Hoagland营养液砂培种植15N玉米,然后将15N玉米和普通玉米以55∶45的氮配比作为混合青贮饲料饲喂1头已空腹2 d的2龄黄牛,饲喂4 d后停喂2 d,收集全部牛粪尿并对其不同组分和形态氮素的15N丰度和数量进行分析。结果表明:标记玉米、混合青贮饲料、牛粪尿的15N丰度分别为48.024%、26.579%和8.044%;标记玉米对硫酸铵15N的回收率为26.3%,牛粪尿对标记玉米15N回收率为36.0%。在收集的牛粪尿氮中,牛粪全氮、牛尿全氮、牛粪铵态氮和牛尿铵态氮量分别占70.25%、29.75%、5.44%和0.03%,其15N丰度分别为9.223%、5.261%、6.505%和5.419%。在短期内通过饲喂黄牛15N青贮饲料制备的标记牛粪尿中,15N丰度在不同组分和形态氮素中的分布并不相同,牛尿氮的15N丰度低于牛粪氮,矿质态和易于矿化态氮的15N丰度低于不易矿化态氮。     

Effect of biochar amendment on soil carbon balance and soil microbial activity

We investigated the behavior of biochars in arable and forest soil in a greenhouse experiment in order to prove that these amendments can increase carbon storage in soils. Two qualities of biochar were produced by hydrothermal pyrolysis from ¹³C labeled glucose (0% N) and yeast (5% N), respectively. We quantified respiratory losses of soil and biochar carbon and calculated mean residence times of the biochars using the isotopic label. Extraction of phospholipid fatty acids from soil at the beginning and after 4 months of incubation was used to quantify changes in microbial biomass and to identify microbial groups utilizing the biochars. Mean residence times varied between 4 and 29 years, depending on soil type and quality of biochar. Yeast-derived biochar promoted fungi in the soil, while glucose-derived biochar was utilized by Gram-negative bacteria. Our results suggest that residence times of biochar in soils can be manipulated with the aim to “design” the best possible biochar for a given soil type.     

基于相关系数法与遗传算法的啤酒酒精度近红外光谱分析

以啤酒的酒精度的快速检测为研究对象,针对采用偏最小二乘(Partial Least Squares,PLS)法建立近红外光谱预测模型时波长筛选问题,提出将相关系数法与遗传算法(Genetic Algorithms,GA)相结合提取光谱有效信息,提高预测模型的精度的方法。结果表明：该方法应用于啤酒酒精度近红外光谱检测中,吸收光谱和一阶导数光谱的预测建模的波长个数分别减少了83%、82%,预测平均相对误差分别降低了0.42%、0.64%,不仅简化、优化了模型,而且增强了预测建模型的预测能力,是一种采用PLS法建立预测模型前行之有效的降低和优选波长的方法。     

Linking Microbial Community Dynamics Associated with Rhizosphere Carbon Flow in a Biofuel Crop (Jatropha curcas L.)

Photosynthetically derived rhizodeposits are an important source of carbon (C) for microbes in root vicinity and can influence the microbial community dynamics. Pulse labeling of carbon dioxide (¹³CO₂) coupled with stable isotope probing techniques have potential to track recently fixed photosynthate into rhizosphere microbial taxa. Therefore, the present investigation assessed the microbial community change associated with the rhizosphere and bulk soil in Jatropha curcas L. (a biofuel crop) by combining phospholipid fatty acid (¹³C-PLFA) profiling using a stable isotope ¹³CO₂ labeling approach. The labeling (¹³C) took place after 45 days of germination, PLFAs were extracted from both soils (rhizosphere and bulk) after 1 and 20 days pulse labeling and analyzed by gas chromatography-isotope ratio mass spectrometry. There was no significant temporal effect on the PLFA profiles in the bulk soil, but significantly increased abundance of Gram positive (i15:0) and Gram negative (16:1ω7c and 16:1ω5c) biomarkers was observed in the rhizosphere soil from day 1 to day 20 after labeling. The Gram negative (16:1ω7c) decreased and fungal (18:2ω6,9c) increased significantly in rhizospheric soil compared to bulk soil after day 1 of labeling. Whereas, after 20 days of labeling, the Gram negative biomarker (16:1ω7c and 18:1ω7c) decreased and Gram positive (a15:0) increased significantly in rhizospheric soil compared to bulk soil. One day following labeling, i15:0, a15:0, i16:0, 16:1ω5c, 16:0, i17:0, a17:0, 18:2ω6,9c, 18:1ω9c, and 18:0 PLFAs were significantly more enriched in δ¹³C in the rhizosphere than in the bulk soil. Twenty days after labeling, 16:1ω5c (Gram negative) and 18:2ω6,9c (fungal) were significantly more enriched in δ¹³C in the rhizosphere than in the bulk soil. These results shows the effectives of PLFA coupled using the pulse chase labeling technique to examine the microbial community changes in response to recently fixed photosynthetic C flow in rhizodeposits.     

Variable use of plant- and soil-derived carbon by microorganisms in agricultural soils

In this study we used compound specific ¹³C and ¹⁴C isotopic signatures to determine the degree to which recent plant material and older soil organic matter (SOM) served as carbon substrates for microorganisms in soils. We determined the degree to which plant-derived carbon was used as a substrate by comparison of the ¹³C content of microbial phospholipid fatty acids (PLFA) from soils of two sites that had undergone a vegetation change from C3 to C4 plants in the past 20-30 years. The importance of much older SOM as a substrate was determined by comparison of the radiocarbon content of PLFA from soils of two sites that had different ¹⁴C concentrations of SOM.The ¹³C shift in PLFA from the two sites that had experienced different vegetation history indicated that 40-90% of the PLFA carbon had been fixed since the vegetation change took place. Thus PLFA were more enriched in ¹³C from the new C4 vegetation than it was observed for bulk SOM indicating recent plant material as preferentially used substrate for soil microorganisms. The largest ¹³C shift of PLFA was observed in the soil that had high ¹⁴C concentrations of bulk SOM. These results reinforce that organic carbon in this soil for the most part cycles rapidly. The degree to which SOM is incorporated into microbial PLFA was determined by the difference in ¹⁴C concentration of PLFA derived from two soils one with high ¹⁴C concentrations of bulk SOM and one with low. These results showed that 0-40% of SOM carbon is used as substrate for soil microorganisms. Furthermore a different substrate usage was identified for different microorganisms. Gram-negative bacteria were found to prefer recent plant material as microbial carbon source while Gram-positive bacteria use substantial amounts of SOM carbon. This was indicated by ¹³C as well as ¹⁴C signatures of their PLFA. Our results find evidence to support ‘priming’ in that PLFA indicative of Gram-negative bacteria associated with roots contain both plant- and SOM-derived C. Most interestingly, we find PLFA indicative of archeobacteria (methanothrophs) that may indicate the use of other carbon sources than plant material and SOM to a substantial amount suggesting that inert or slow carbon pools are not essential to explain carbon dynamics in soil.     

基于RFlD技术的动物标识及疫病可追溯体系

研究旨在通过基于RFID技术的动物标识及疫病可追溯体系的建立,提供可靠真实的相关信息,帮助国家对重大动物疫病防控和动物产品安全问题进行有效追踪、溯源并及时解决。在介绍RF1D技术原理及其主要特点的同时,提出了RFID技术在动物的饲养和屠宰中的应用设想,并对RFID在动物标识及疫病可追溯体系中的技术应用进行了展望。