氯酚类化合物对紫背浮萍生长及叶绿素含量的影响

以我国本土水生植物紫背浮萍为受试物种,利用其生长抑制和叶绿素含量的变化评价了3种氯酚类化合物的毒性效应.结果显示:2,4-二氯酚(2,4-DCP), 2,4,6-三氯酚(2,4,6-TCP)和五氯酚(PCP)对紫背浮萍的96h IC50值分别为12.73,8.49,1.12mg/L.根据化学物质对水生生物毒性分级标准,3种物质均为高毒.2,4-DCP,2,4,6-TCP和PCP对紫背浮萍基于叶绿素含量变化的最大可接受浓度(MATC)分别为2.24,1.58, 0.35mg/L,对应的急慢性毒性比(ACR)分别为5.68,5.37和3.20.     

湿地挺水植物根系土壤中的磷形态变化与分析

以野鸭湖湿地中扁秆藨草、芦苇和茭白3种优势挺水植物为研究对象,利用化学连续提取法对根际和非根际土壤中不同形态无机磷和有机磷进行分级提取,分析了不同形态磷的含量特点和分布规律,探讨了植物对磷素的潜在吸收机制.结果表明,根际Ca-P含量均显著低于非根际,Ex-P、Fe-P和Oc-P相反.4种形态有机磷含量均为根际高于非根际,表现出累积的趋势.根际Ca-P/TP值显著小于非根际,说明植物将有效性低的Ca-P形态大量转化为其他形态无机磷以供自身利用;根际HR-OP/TP值小于非根际,而MR-OP/TP大于非根际,表明稳定有机磷形态有向活性高的有机磷转化的趋势;TIP/TP均为根际小于非根际,而TOP/TP根际大于非根际,推测根系在吸收利用磷素的过程中主要吸收无机磷,同时积聚大量有机磷供转化后利用.     

Assessing the P fractionation in a tropical river-estuarine system of South India

Seasonal variations in dissolved and particulate P forms were assessed in the estuarine system of Chalakudy River, Kerala, South India – a tropical river having substantial relics of riparian vegetation. The contribution of the reactive P form extended to 84–96% compared with the residual fraction. Geographical and human activities have had effects on the phosphorus-loading capacity at various locations, which reveal pronounced variability in P distribution. Not all forms of phosphate in suspended particulate matter are likely to be released, and thus the nature of the P forms within the stock is a sensitive factor that can be utilised. Ca-bound P in suspensates increases to a highly significant level in the estuarine area, whereas Fe/Al-bound P predominates at the riverine and catchment areas during both the monsoon and non-monsoon seasons. Thus, calcium compounds determine the availability of P in the alkaline estuarine environment, whereas in the riverine environment, Al and Fe control P solubility. The comparatively low P load in upstream waters indicates that, under ambient situations, vegetative riparian zones can be very important P filters.     

Isolation and Chemical Characterization of Dissolved and Colloidal Organic Matter

An overview of the methods used for the isolation and characterization of organic matter in natural waters is presented. Commonly used techniques for the concentration and isolation of organic matter from water, such as preparative chromatography, ultrafiltration and reverse osmosis, and the methods used to analyze the organic matter obtained by these methods are reviewed. the development of methods to obtain organic matter that is associated with fractions of the dissolved organic carbon other than humic substances, such as organic bases, hydrophilic organic acids and colloidal organic matter are discussed. Methods specifically used to study dissolved organic nitrogen and dissolved organic phosphorous are also discussed.     

Influence of Dissolved Organic Matter On the Bio-Availability and Toxicity of Metals in Soils and Aquatic Systems

Cations in soil are essential for the growth of plants and micro-organisms. Their availability is dependent on soil organic matter. Soil organic matter (SOM) is heterogeneous comprising amino, aliphatic and phenolic acids, but particularly humic substances. All these substances can complex cations selectively. Mechanisms of complexation with dissolved organic matter are discussed. Such complexation can lead to the apparently contradictory observations that dissolved organic matter (DOM) can either increase the concentration of some less soluble nutrients, making them more available for plant uptake, or make them less available and hence less toxic. the importance of DOM is discussed in relation to soil solution, particularly the rhizosphere, and also in relation to aquatic systems. the latter systems contain mainly dissolved humic substances whereas in the soil, non-humic substances assume a greater importance.

SOM in the rhizosphere is derived from plant, microbial and animal remains but much, especially the water-soluble compounds, are acquired through root exudation. Exudation has important consequences for enhanced nutrient availability as a result of the production of non-humic substances such as amino, aliphatic and phenolic acids. in future, the role of root exudation in relation to DOM and nutrient availability should be investigated more fully, particularly as predicted elevated CO₂ levels are likely to have a major impact on root exudation, nutrient availability, and possibly ecosystem community structure and functioning. It is likely that more information will become available on aquatic systems as more highly sensitive techniques and equipment capable of dealing with low concentrations of DOM in these systems become available.     

Fish as an indicator of aquatic environment: Multielemental neutron activation analysis of nutrient and pollutant elements in fish from Indian coastal areas

Fish is the main food in coastal areas and its analysis for toxic metals has been used as an indicator of the pollution status of the aquatic environment. Several different fish species from the three Indian coasts, Visakhapatnam in the east, Mumbai in the west and Mangalore in the south west and also inland freshwater fish from Nagpur in the central region for comparison were analyzed for up to 20 elements (As, Au, Ba, Br, Cl, Co, Cr, Cu, Fe, Hg, K, Mn, Na, P, Rb, Sb, Sc, Se, Sr, Zn) by instrumental neutron activation analysis (INAA). Dried fish samples in powdered form were irradiated with thermal neutrons in a nuclear reactor followed by high resolution gamma ray spectrometry at different intervals. Several Reference Materials (RMs) of biological origin were analyzed for quality assurance and data validation. Elemental contents in different fish species vary in a wide range depending on the species, its size, location, and aquatic environment. Fish from Mangalore showed highest mean contents of Cr (14.8?±?29.9?µg?g^?1), Cu (1005?±?643?µg?g^?1) and Sb (849?±?888?ng?g^?1) whereas those from Mumbai exhibited highest Hg (2066?±?2146?ng?g^?1) and P (20.3?±?4.63?µg?g^?1) but lowest Cu (6.30?±?3.10?µg?g^?1) contents. Fish from all the regions showed significant amounts of nutrient elements such as Na, K, P, Mn, Fe, Se and Zn as well as some pollutant elements (Br, Cr, Sb, Hg). No regularity in variation of elemental contents with the size was observed. Prawn (Panaeus latisulcatus), a popular fish species from four different regions showed wide variation in elemental contents of Cr, Mn, Fe, Zn, Se, P including toxic pollutants, Sb and Hg. An attempt has been made to calculate daily dietary intake (DDI) for some nutrient elements from Indian fish. Elemental data for Cr, Cu, Fe, Hg, Se, and Zn have been compared with those from other fish exporting countries.     

Ecotoxicological effects of Trichloroethene upon plankton

A case study in an experimental pond was performed to evaluate the ecotoxic effects of Trichloroethene (TRI) upon the population density and productivity of phyto‐ and zooplankton. TRI was continuously released into two pond enclosures over 11 weeks (mean concentrations 1.5 and 7.5 mg/l). The chronic chemical treatment showed distinctive toxic influences upon the biota. Following the high TRI concentration, the phytoplankton density slightly increased; the productivity per single cells, however, was significantly reduced compared to the controls and the low TRI concentration. Cryptophyceae were the most sensitive algae taxa. The density and reproductivity of Daphniae and Phyllopodae decreased by the high TRI concentration. Most of the Rotatoriae were not negatively influenced. With increasing TRI concentrations two different bacteria forms showed a mass development. Small amounts of Trichloroacetic acid were detected in both enclosures as a conversion product of TRI (～3 μg/l after 80 days treatment).     

Bioaccumulation of heavy metals in flora and fauna of Hooghly estuary,east coast of India

Spectroscopic determinations of Fe, Zn, Mn, Cu, Co and Ni were carried out in 23 organisms including seaweeds, zooplankters, molluscs and fishes from Hooghly estuary at the confluence of Bay of Bengal. Seaweeds and gastropods were more efficient in accumulating levels while zooplankters bivalves and fishes showed intermediate levels. Analyses were performed on the sediment, water and on the individual dissected organs of a mussel, oyster and teleost fish. Bioaccumulation of Fe, Zn, Mn and Cu in the soft body parts (gills, mantle, liver etc.) of the three species showed a high degree of organ specificity in some cases. Major sources of the micropollutants include natural weathering, catchment runoff, urban and industrial discharges that may pose an ecological risk to the local estuarine ecosystem.     

Utility of the QSAR modeling system for predicting the toxicity of substances on the European inventory of existing commercial chemicals∗

Many chemicals are in common commercial use for which no information on the environmental fate or toxicity exists. Recent legislation requires that many substances be assessed for their toxicity to aquatic organisms within a very short time and determine which of these chemicals need to be studied in greater detail. It would be impossible to measure the acute and chronic effects of all of these compounds on a single organism, let alone a battery of different types of organisms, communities or ecosystems. Initially, the chemicals on the European Inventory of Existing Commercial Chemical Substances (EINECS) need to be screened and relative hazard to the environment determined. In response to OECD directives, there has been a great deal of activity by government and industry scientists. At the International Workshop on Advances in Environmental Hazard and Risk Assessment it was concluded that quantitative structure activity relationships (QSAR) could and should be used in the hazard assessment process. Papers published in that volume outline the advantages, disadvantages, limitations, advances and research requirements.

The QSAR, structure‐activity based chemical modeling and information system, which was developed by the US‐Environmental Protection Agency was used to predict the acute toxicity of 113 substances from the “Old Substances”; list of the German government to the four commonly used aquatic toxicity test organisms: Daphnia magna (DM), fathead minnow (FHM), rainbow trout (RBT), and blue‐gill sunfish (BG).

Of these compounds the QSAR system predicted the acute toxicity of 87 substances towards fathead minnow. For the other three species examined the QSAR system could be used to predict toxicity for 78 compounds.

The predicted toxicities were compared to observed toxicities of compounds which have been evaluated and stored in the “Aquire”; data base. Observed toxicity values were available for at least one species for 38 compounds. The toxicities of some compounds are well predicted while those of other compounds were not well predicted. Overall, the QSAR system accurately classified the acute toxicity ranges of 50%, 64%, 56% and 56% of the compounds investigated for DM, FHM, RBT and BG, respectively. Of the compounds studied 10 were very poorly predicted, of these the QSAR system overpredicted the toxicity of three, while underpredicting the toxicity of seven. Of these seven compounds, five contained amino groups.     

Acute toxicity of benzophenone-type UV filters and paraben preservatives to freshwater planarian,Dugesia japonica

Fourteen benzophenone-type UV filters and four paraben preservatives were selected to examine their acute toxicities on Dugesia japonica. The 48-h LC₅₀ values for planarians exposed to benzophenone-type UV filters can be ranked as oxybenzone?>?mexenone?>?5-chloro-2-hydroxybenzophenone?> 2,4-dihydroxybenzophenone?>?2-hydroxybenzophenone?>?dioxybenzone?>?benzophenone?>?2,2′,4,4′-tetrahydroxybenzophenone?>?4-hydroxybenzophenone?> 3-hydroxybenzophenone?>?4,4′-dihydroxybenzophenone?>?2,2′-dihydroxy-4,4′-dimethoxybenzophenone?>?2,3,4-trihydroxybenzophenone?>?sulisobenzone with a range from 0.9 to 145?mg?L^?1 with a similar sequence for the 96?h LC₅₀ values, ranging from 0.5 to 77?mg?L^?1. The 48 and 96?LC₅₀ values for planarians exposed to paraben preservatives can be ranked as butylparaben?>?propylparaben?>?ethylparaben?>?methylparaben. Among all the tested chemicals, oxybenzone was the most toxic and sulisobenzone the least toxic chemical to planarian at each exposure period. Most benzophenone-type UV filters are toxic to aquatic animals with 48?h LC₅₀ values less than 10 mg?L^?1, except for 2,2′-dihydroxy-4,4′-dimethoxybenzophenone, 2,3,4-trihydroxybenzophenone, and sulisobenzone. Because of their common occurrence in aquatic environment, more studies on aquatic toxicities of benzophenone-type UV filters and paraben preservativs are needed to provide important information to adequately assess their ecological risk.