川西南柳杉早材、晩材年表与温度和降雨的关系

年轮宽度和气候要素的相关或响应分析已大量应用在气候 树木生长的相互作用研究中。以川西南区瓦屋山自然保护区速生树种柳杉（Cryptomeria fortunei）的71个样芯,探讨了温度和降雨与柳杉早材、晩材年表的关系,结果表明早材径向生长对温度变化比较敏感,早材年轮指数序列与当年4月的平均温度、4月平均最高温度、上年9、10月平均最高温度间呈显著正相关关系,与当年7月平均温度以及上年11月最低温度间均存在显著负相关关系;晚材年轮序列与当年10月的平均最高温度呈显著正相关关系。柳杉早材年轮的生长过程中气温“滞后效应”表现明显,特别是在上个生长季的9～10月,最高温度的变化对柳杉当年生长季节形成较宽的年轮有重要的作用。不同的季节温度、降水量变化影响早材、晚材年轮的形成与生长     

济南市环境空气中PM_(2.5)的碳组成与特征分析

对济南市环境空气中PM2.5中碳组分污染特征的研究结果表明,济南市环境空气细颗粒物中碳主要以有机碳(OC)和元素碳(EC)的形式存在,二者浓度以冬季最高,且变化趋势相同;OC占总碳比例较高;冬季二次有机气溶胶(SOC)浓度最高,与污染源排放及气象条件有关。     

Photolytic degradation of decabromodiphenyl ethane (DBDPE)

The photolytic degradation of decabromodiphenyl ethane (DBDPE), an alternative flame retardant to decabromodiphenyl ether, was investigated in a variety of matrixes (n-hexane, tetrahydrofuran, methanol/water, humic acid/water, and silica gel) by irradiation under ultraviolet light and in n-hexane under natural light. Photolytic degradation of DBDPE occurs in all the matrixes investigated within the irradiation period (<320 min). The degradation experiments showed varied reaction rates, dependent on the matrixes, with increasing half-lives (t_1/2) in the order of tetrahydrofuran (t_1/2 = 6.0 min) > n-hexane (t_1/2 = 16.6 min) > humic acid/water (30 < t_1/2 < 60) > silica gel (t_1/2 = 75.9 min) > methanol/water (t_1/2 > 240 min). The reaction in tetrahydrofuran, n-hexane, and silica gel matrixes can be described by the pseudo first order kinetics. Nevertheless, the matrixes have little effect on the degradation product distributions of DBDPE. A numbers of debrominated intermediates were identified. The degradation involves the initial formation of nona-BDPEs and the subsequent decomposition of these congeners to lower brominated congeners (octa- and hepta-BDPEs) within the irradiation time. To our knowledge, the present work is the first attempt to investigate the photolytic degradation kinetics and the identification of intermediates, as well as the degradation mechanism, during the degradation of DBDPE. Further research is needed to understand the photolytic degradation pattern of DBDPE in the natural environment.     

Efficient bio-deodorization of aniline vapor in a biotrickling filter: metabolic mineralization and bacterial community analysis

A biotrickling filter inoculated with commercial mixed microorganisms B350 was employed to treat N-containing odorous vapor - aniline. Results indicated no aniline could be detected when empty bed residence time (EBRT) was larger than 110s at inlet concentration of 0.30 g m(-3). The variation of inlet concentration did not change removal efficiencies when concentration is less than 0.21 g m(-3) at fixed EBRT 110s. Biodegradation mechanism of aniline was tentatively proposed based on identified intermediates and predicted biodegradation pathway as well as final mineralized products. Aniline was firstly biodegraded to catechol, and then to levulinic acid and subsequently to succinic acid. Finally, about 62% aniline carbon was completely mineralized to CO(2), while about 91% aniline nitrogen was converted into ammonia and nitrate. Bacterial community in biotrickling filter was found that at least seven bands microbes were identified for high efficiencies of bioreactor at stable state. In all, biotrickling filter seeded with B350 would be a better choice for the purification odorous gas containing high concentration aniline.     

土壤中结合态苯氧羧酸类除草剂的测定

利用超临界ＣＯ２流体萃取的方法提取２甲４氯(ＭＣＰＡ),２,４－Ｄ和除草醚在三种土壤中的结合残留．结果表明,在培养２００ｄ的时间内,ＭＣＰＡ的结合残留量为１．０ｌ－５．１２ｍｇ·ｋｇ－１,占添加总量的２．０－１０．１%;２,４－Ｄ的结合残留量为０．２４－２．６５ｍｇ·ｋｇ－１,占添加总量的０．５－５．３%;除草醚的结合残留量为６．５３－１９．３０ｍｇ·ｋｇ－１,占添加总邑的１２．９—３８．２%．农药结合态与游离态含量的比值随时间的延长而增加．     

地震与环境生态

基于地震环境生态破坏的实际资料,我们讨论了以下的问题;（1）从Ⅸ度地震烈度开始就会引起环境生态的破坏;（2）初步划分Ⅸ－Ⅻ度情况下地地震对环境生态破坏程度;（3）得出了在发生6．7级－8．5级地震时环境生态破坏的面积;（4）提出了地震引起环境生态破坏的恢复和补救对策。     

CH4 and N2O emissions from Spartina alterniflora and Phragmites australis in experimental mesocosms

Spartina alterniflora, a perennial grass with C(4)-photosynthesis, shows great invading potential in the coastal ecosystems in the east of China. We compared trace gas emissions from S. alterniflora with those from a native C(3) plant, Phragmites australis, by establishing brackish marsh mesocosms to experimentally assess the effects of plant species (S. alterniflora vs. P. australis), flooding status (submerged vs. non-submerged), and clipping (plants clipped or not) on trace gas emissions. The results show that trace gas emission rates were higher in S. alterniflora than P. australis mesocosms due to the higher biomass and density of the former, which could fix more available substrates to the soil and potentially emit more trace gases. Meanwhile, trace gas emission rates were higher in non-submerged than submerged soils, suggesting that water might act as a diffusion barrier in the brackish marsh mesocosms. Interestingly, methane (CH(4)) emission rates were lower in clipped non-submerged mesocosms than in non-clipped submerged mesocosms, but nitrous oxide (N(2)O) emissions were enhanced. CH(4) emissions were significantly correlated with the plant biomass and stem density (R(2)>0.48, P<0.05) for both species, suggesting that both the two species might play important roles in CH(4) production and transport and also act as suppliers of easily available substrates for the methanogenic bacteria in wetland ecosystems. N(2)O emissions, however, were not significantly correlated with plant biomass and density (P>0.05).     

China's natural wetlands: past problems, current status, and future challenges

Natural wetlands, occupying 3.8% of China's land and providing 54.9% of ecosystem services, are unevenly distributed among eight wetland regions. Natural wetlands in China suffered great loss and degradation (e.g., 23.0% freshwater swamps, 51.2% costal wetlands) because of the wetland reclamation during China's long history of civilization, and the population pressure and the misguided policies over the last 50 years. Recently, with an improved understanding that healthy wetland ecosystems play a vital role in her sustainable economic development, China started major efforts in wetland conservation, as signified by the policy to return reclaimed croplands to wetlands, the funding of billions of dollars to restore degraded wetlands, and the national plan to place 90% of natural wetlands under protection by 2030. This paper describes the current status of the natural wetlands in China, reviews past problems, and discusses current efforts and future challenges in protecting China's natural wetlands.     

紫外光作用下氯酚的矿化程度比较

有关氯酚污染物光化学降解的研究,已有报道。ＨｕａｎｇＣＰ的工作较有系统性,他研究了四类深度化学氧化过程,检测指标是氯酚浓度。本文研究了在紫外光以及其它因素作用下,氯酚混合溶液的矿化程度,以溶液总有机磷浓度ＴＯＣ作为指标。所得结论,对于含有氯酚废水的治理,具有指导意义;对于难降解     

Unravelling the effects of complexation of transition metal ions on the hydroxylation of catechol over the whole pH region

Catechol pollutants (CATPs) serving as chelating agents could coordinate with many metal ions to form various CATPs-metal complexes. Little information is available on the effects of complexation of metal ions on CATPs degradation. This work presents a systematical study of •OH-mediated degradation of catechol and catechol-metal complexes over the whole pH range in advanced oxidation processes (AOPs). Results show that the pH-dependent complexation of metal ions (Zn²⁺, Cu²⁺, Ti⁴⁺ and Fe³⁺) promotes the deprotonation of catechol under neutral and even acidic conditions. The radical adduct formation (RAF) reactions are both thermodynamically and kinetically favorable for all dissociation and complexation species, and OH/O⁻ group-containing C positions are more vulnerable to •OH attack. The kinetic results show that the complexation of the four metal ions offers a wide pH range of effectiveness for catechol degradation. At pH 7, the apparent rate constant (k_app) values for different systems follow the order of catechol+Ti⁴⁺ ≈ catechol+Zn²⁺ > catechol+Cu²⁺ > catechol+Fe³⁺ > catechol. The mechanistic and kinetic results would greatly improve our understanding of the degradation of CATPs-metal and other organics-metal complexes in AOPs. The toxicity assessment indicates that the •OH-based AOPs have the ability for decreasing the toxicity and increasing the biodegradability during the processes of catechol degradation.