Iron requirement and siderophore production in Rhizobium ciceri during growth on an iron-deficient medium

Under conditions of iron limitation many rhizospheric bacteria produce siderophores, ferric iron-specific ligands, which may enhance plant growth by increasing the availability of iron near the roots. Thirty-five strains of Rhizobium ciceri, specific to chickpea (Cicer arietinum L.), were screened for their ability to grow on iron-deficient medium and to produce siderophores. Maximal growth of all strains previously depleted in iron was obtained in medium containing 5 to 10 m of ferric iron. When iron limitation was achieved by the addition of 2,2-bipyridyl or EDDHA [ethylene diamine di(o-hydroxyphenyl) acetic acid] to the medium, only two strains were able to scavenge iron and grow. Siderophore production by these two strains was detected by the Chrome Azurol S assay (CAS), a universal test for siderophores. No hydroxamate-type siderophores were detected in the supernatants of Rhizobium ciceri cultures. However, some strains secreted salicylic acid and 2,3-dihydroxybenzoic acid as phenolate-type siderophores. Addition of ferric iron to the culture medium increased growth yield significantly but depressed the production of siderophores. Although these compounds are produced in response to iron deficiency, nutritive components of the culture medium significantly affected their production. It seems that CuII, MoVI and MnII ions bound competitively with iron to siderophores, resulting in a 34 to 100% increase in production.     

Energy and greenhouse gas balance of bioenergy production from poplar and willow: a review

Short‐rotation woody crops (SRWC) such as poplar and willow are an important source of renewable energy. They can be converted into electricity and/or heat using conventional or modern biomass technologies. In recent years many studies have examined the energy and greenhouse gas (GHG) balance of bioenergy production from poplar and willow using various approaches. The outcomes of these studies have, however, generated controversy among scientists, policy makers, and the society. This paper reviews 26 studies on energy and GHG balance of bioenergy production from poplar and willow published between 1990 and 2009. The data published in the reviewed literature gave energy ratios (ER) between 13 and 79 for the cradle‐to‐farm gate and between 3 and 16 for cradle‐to‐plant assessments, whereas the intensity of GHG emissions ranged from 0.6 to 10.6 g CO₂ Eq MJ_biomass^?1 and 39 to 132 g CO₂ Eq kWh^?1. These values vary substantially among the reviewed studies depending on the system boundaries and methodological assumptions. The lack of transparency hampers meaningful comparisons among studies. Although specific numerical results differ, our review revealed a general consensus on two points: SRWC yielded 14.1–85.9 times more energy than coal (ER_coal～0.9) per unit of fossil energy input, and GHG emissions were 9–161 times lower than those of coal (GHG_coal～96.8). To help to reduce the substantial variability in results, this review suggests a standardization of the assumptions about methodological issues. Likewise, the development of a widely accepted framework toward a reliable analysis of energy in bioenergy production systems is most needed.     

Karyomorphology of six taxa in Chrysanthemum sensu lato (Anthemideae) in Egypt and their genetic relationships by Giemsa C‐banding

Abstract Giemsa C‐banding was applied to the chromosome complements of six diploid species belonging to six genera in Chrysanthemum sensu lato (Anthemideae) distributed in Egypt. Four types of C‐banding distribution were observed in the taxa as follows: (i) negative C‐banding in Anacyclus monanthos (L.) Thell.; (ii) all bands in terminal regions in Achillea fragrantissima (Forssk.) Sch. Bip, which showed 32 bands on 18 chromosomes; (iii) all eight bands at centromeric regions on eight chromosomes in Matricaria recutita L.; and (iv) bands at terminal and centromeric regions in Brocchia cinerea Vis. (12 terminal and six centromeric bands on 12 chromosomes), Cotula barbata DC. (four terminal, six centromeric, and eight short arm bands on 16 chromosomes), and Glebionis coronaria (L.) Cass. ex Spach. (eight terminal on the short arms and four large bands in centromeric regions on 12 chromosomes).