Preceding crop affects grain cadmium and zinc of wheat grown in saline soils of central Iran

Enhanced Cd concentrations in wheat (Triticum aestivum L.) grain produced on saline soils of central Iran have been recently reported. Because wheat bread is a major dietary component for the Iranian people, practical approaches to decrease Cd concentration in wheat grain were investigated. This study investigated the influence of sunflower-wheat vs. cotton-wheat rotations on extractable Cd and on Cd uptake by wheat in these salt-affected soils. Two fields with different levels of Cd contamination (1.5 and 3.2 mg total Cd kg(-1) dry soil) were cropped with different rotations (cotton-wheat and sunflower-wheat) in Qom province, central Iran. Seeds of cotton (Gossypium L.) or sunflower (Helianthus annuus L. cv. Record) were planted in plots. After harvesting of the plants and removal of crop residues, wheat (cv. Rushan) was seeded in all plots. For both studied soils, the concentrations of Cd extracted by 0.04 M EDTA and 1 M CaCl(2) were significantly (P < or = 0.05) greater after cotton than after sunflower. Accordingly, the total amount of Cd in sunflower shoot was significantly (P < or = 0.05) greater than in the cotton shoot. Shoot Cd content in wheat plants grown after cotton and sunflower were significantly different; wheat shoots after cotton accumulated more Cd (two to four times) than after sunflower. Wheat grain Cd concentration after sunflower was much lower (more than seven times) than after cotton. The results of this study showed that sunflower in rotation with wheat in salt-affected soils of central Iran significantly reduced the risk of Cd transfer to wheat grain.     

Removal of linear alkylbenzene sulfonates and their degradation intermediates at low temperatures during activated sludge treatment

The degradation of linear alkylbenzene sulfonates and their degradation intermediates (sulfophenylcarboxylic acids) has been characterized at 9 degrees C in an activated sludge pilot plant. After an adequate adaptation period (20 days), LAS primary degradation exceeds 99% and takes place preferentially for long alkyl chain homologues and external isomers. LAS homologues in the reactor are preferentially sorbed onto particulate matter, while sulfophenylcarboxylic acids (SPCs) are present predominantly in solution, due to their lower hydrophobicity. During the adaptation period the most abundant LAS biodegradation intermediates were long chain sulfophenylcarboxylic acids (SPCs) (C(9)-C(13)SPC). However once this system is fully adapted, the microorganisms are capable of degrading SPCs efficiently. SPCs with 7-9 carbon atoms in the carboxylic chain predominate due to their degradation being slower than for the rest of the SPCs. The presence of C(13)SPC confirms that LAS degradation in wastewater starts with a omega-oxidation on the alkylic chain. A preferential degradation of SPC isomers of the types 2phiC(n)SPC to 6phiC(n)SPC was also detected, as shown by the relatively higher SPC concentrations of the remaining ones.     

Presence of surfactants and their degradation intermediates in sediment cores and grabs from the Cadiz Bay area

The occurrence and distribution of the major surfactants--LAS, AES, APEOs and AEOs--and their degradation intermediates--SPCs, AP and APECs--in a marine-estuarine environment at Spain are presented. Results show that their concentration in surface sediments is clearly correlated with their usage and the existence of wastewater discharges. The degradation processes appear to lead to the formation of SPCs in the case of LAS, and to the shortening of the average ethoxylated chain length in the case of NPEOs, AEOs and AES. Vertical profiles for AEOs and AES are reported for the first time and present the highest values nearest the surface, followed by a sharp decrease with depth for all surfactants, as well as the appearance of degradation intermediates in deeper sedimentary layers. Shorter LAS homologues and SPCs tend to be present in pore water while strongly non-polar intermediates like NP are firmly attached to the sediments.     

Environmental impact assessment of non-wood based pulp production by soda-anthraquinone pulping process

Paper pulp manufacturing is the main non-food industrial utilization of plant biomass. Non-wood and agricultural residues are potential raw materials in the production of specialty papers. This chapter aims to quantify the environmental impacts associated with non-wood high quality paper pulp manufacture via soda-anthraquinone (AQ) cooking process by means of the application of LCA methodology in a cradle-to-gate analysis. Hemp (Cannabis sativa) and Flax (Linum usitatissimum) were evaluated as raw materials for the production of high quality non-porous pulp. A specialty paper pulp mill was analysed in detail and process chain was divided in six subsystems: agricultural activities, chemicals production, electricity production, transport, pulp production and waste treatment. Inventory data came from interviews and surveys (on-site measurements). When necessary, the data were completed with bibliographic resources.Abiotic resources depletion (AD), global warming (GW), ozone layer depletion (OLD), human toxicity (HT), ecotoxicity, photochemical oxidant formation (POF), acidification (A) and eutrophication (E) were the impact categories analysed in this study. According to the results, the environmental impact is mainly caused by the production of chemicals, electricity and fibres (agricultural activities) due to greenhouse gases emissions, phosphorous and nitrogen compounds emissions. The activities inside the pulp mill present minor contribution to almost all impact categories, excluding GW (15%) and E (6%) as well as OLD (25%). This study provides useful information for non-wood based industries related not only to pulp manufacture but also to panels or biorefineries with the aim of increasing their sustainability.     

Ostracoda and foraminifera as short-term tracers of environmental changes in very polluted areas: the Odiel Estuary (SW Spain)

The analysis of 17 cores collected in the Odiel Estuary (SW Spain) permits delimiting the recent evolution of this zone during the past decades and the influence of natural and anthropogenic factors on the distribution of Ostracoda and Foraminifera. In the upper estuary, the coincidence of acid waters, prolonged subaerial exposure, and coarse sediments may explain the absence or the disappearance of these microorganisms during the industrial period (1966-1985) in the major part of this area. In the lower estuary, sedimentary evolution and industrial wastes are the main factors influencing both the distribution and trends of the populations of these two groups. Finally, the main changes observed in the marine estuary are due to the sedimentary effects of the construction of two banks and the dredging of the main estuarine channel.     

Assessing a Quick Monitoring Method Using Rocky Intertidal Communities as a Bioindicator: A Multivariate Approach in Algeciras Bay

A multivariate approach was used to test the value of intertidal communities as a bioindicator of environmental conditions at Algeciras Bay, southern Spain. The study area is located in the Strait of Gibraltar and it is subjected to a variety of anthropic impacts. Eight localities (5 inside and 3 outside the bay) were selected, and four transects were undertaken in each locality to characterise the fauna and flora. The spatial distribution of the intertidal species reflected the physico-chemical conditions of Algeciras Bay. The stations located outside the bay, characterised by high hydrodynamism and dissolved oxygen and low sedimentation and turbidity, had a higher diversity and species richness than the inner stations. According to the BIO-ENV procedure and CCA, water turbidity was the factor which best correlated with the intertidal assemblages. SIMPER showed that the molluscs Chtamalus stellatus, Mytilus cf edulis, Littorina neritoides and Balanus perforatus, and the algae Gelidium pusillum, Corallina elongata, Asparagopsis armata, Colpomenia sinuosa and Fucus spiralis were the species that most contributed to the dissimilarity between internal and external sites. The present study, based on the spatial distribution of intertidal taxa, yielded similar results to those previously obtained in the area with costly physico-chemical analysis based on complex matrices of subtidal epifaunal communities. Consequently, the intertidal sampling method proposed in this study is presented here as a quick, effective alternative strategy, and can be useful in environmental monitoring programs, since these communities are easily accessible and amenable to sample, and the sessile nature of the majority of the species makes future, long-term monitoring relatively simple.     

Biomass from phytopathogens and culture conditions improve Penicillium chrysogenum antimicrobial activity and antifungal compounds production

The present study evaluated the effect of culture conditions and phytopathogenic strain co-culture on the production of antimicrobial metabolites and antifungal activity of Penicillium chrysogenum R1, which PCR identified. Antimicrobial activity was determined using the Hunter-Hunter experimental design with three factors (pH, incubation temperature, and inoculum, at two levels each). The antifungal metabolites, β 1-3 glucanase and chitinase, produced in the presence of live and inactivated Fusarium oxysporum Fsox C11 biomass, were evaluated using HPLC-MS and GC-MS. Results showed that P. chrysogenum inhibited the growth of five phytopathogenic fungal strains, and the most significant inhibition was observed for F. oxysporum Fsox C11. The best conditions to achieve the highest antifungal activity of the cell-free extract were pH 7, 28°C, 1 × 10⁶ spores/mL, and 144 h of fermentation, observing 86% inhibition of F. oxysporum Fsox C11 growth. Production of antifungal metabolites such as 1,4-benzoquinone imine, viridicatic acid, phenol-5-methyl-2-(1-methyl ethyl), and hydrolytic enzymes β 1-3 glucanase and chitinase was detected. The results define the perspective in designing new processes and products for biocontrol phytopathogens.