Impact of trace metal contamination and in situ remediation on microbial diversity and respiratory activity of heavily polluted Kastanozems

Biology and Fertility of Soils - Agriculturally used soils (Kastanozems) of experimental fields in the Mashavera Valley in southeast Georgia show various degrees of trace metal contamination (Cd,...     

Isolation and characterization of <Emphasis Type="Italic">Serratia rubidaea</Emphasis> from dark brown spots of tomato fruits

Bacterial contamination of fresh tomato fruits is of great concern. From naturally infected tomato fruits showing dark brown irregularly shaped spots, 36 bacterial isolates were recovered and identified on phenotypic characteristics and sequences of the gene encoding the 16S rRNA. Five isolates showing spots on tomato fruits in the pathogenicity test with healthy tomato fruits belong to the genus Serratia on the basis of phenotypic characteristics. One representative isolate of these has been further identified as a Serratia rubidaea by sequencing of the 16S rRNA gene. This is the first evidence showing that a S. rubidaea strain can cause spots on tomato fruits. Virulence of the S. rubidaea was also confirmed by the production and secretion of a large variety of enzymes capable of degrading the complex polysaccharides of the plant cell wall and membrane constituents. Nineteen bacterial isolates of the 36 did not induce any spot symptoms in a pathogenicity test on artificially infected tomato fruits although these are known as phytopathogenic bacteria. Five of these 19 bacterial isolates were identified as Ralstonia species on the basis of biochemical tests. Sequencing of the 16S ribosomal gene of one representative isolate revealed that the isolate is closely related to Ralstonia solanacearum. Six isolates of the 19 were related to Xanthomonas vesicatoria on the basis of biochemical tests and eight were related to the Enterobacteriaceae. One representative isolate of the Enterobacteriaceae could be identified by the 16S rRNA gene as Enterobacter cloacae subsp. dissolvens. The 12 other strains were related to Proteus mirabilis based on the 16S RNA gene sequence of one representative isolate. The isolates related to P. mirabilis did not produce any symptoms on artificially infected tomato fruits. The nucleotide sequences of S. rubidaea strain E9, E. cloacae strain E23, P. mirabilis strain E11, and R. solanacearum strain E15 have been deposited in the GenBank nucleotide sequence database under accession numbers HM585373 to HM585376.     

Oily waste containing natural radionuclides: does it cause stimulation or inhibition of soil bacterial community?

Contamination with oily wastes containing natural radionuclides is a potential hazard for soil health and function. Our study aimed to reveal both structural and functional changes of the microbial community resistant to and able to decompose oily wastes in soil. To do this, we determined CO₂ efflux, microbial biomass (by the extraction‐fumigation method), and community structure (by PCR‐SSCP) for 120 d after application of radioactive oily wastes to the soil at the ratio 1:4. The addition of the waste resulted in an increase of the activity concentration of ²²⁶Ra by 130 times (up to 643 Bq kg^?1) and of ²³²Th by 29 times (up to 254 Bq kg^?1). The calculated weighted dose for the radionuclide ²²⁶Ra was found to be below the values that are known to affect microorganisms. However, the cumulative effect of a repeated deposition of radioactive oily waste may result in an increase of the weighted dose up to an effective level. During the incubation, the hydrocarbon (HC) content of the waste‐treated soil decreased from 156 to 54 g kg^?1 of soil indicating intensive decomposition of added organics by soil microorganisms. The waste application, however, led to an inhibition of soil microbial biomass compared with the control (by 26–47%). Microbial respiration was stimulated in the first month of incubation and then decreased until the end of the incubation period (by up to 74% compared to the control). The qCO₂ was estimated to be 3‐fold higher than the control on day 1 of incubation and equal to the control on day 120 of incubation. The bacterial diversity decreased in the contaminated soil compared with the control soil. The bacterial community structure was altered by domination of new oil degrader species belonging to the genera Dyella, Pseudoxanthomonas, Sinobacter, and Parvibaculum. Thus, disposal of radioactive petroleum waste strongly altered the structure of the microbial community resulting in the selection of resistant species able to decompose pollutants and also affected the community function (inhibition of microbial biomass and stimulation of respiration) which tended to stabilize after long‐term incubation.     

Stimulation of methane oxidation by CH<Subscript>4</Subscript>-emitting rose chafer larvae in well-aerated grassland soil

In this study, the impact of rose chafer (Cetonia aurata L.) larvae on net and gross methane (CH₄) fluxes in soil from an old permanent grassland site (Giessen, Germany) was investigated. Previous studies at this site suggested the existence of Scarabaeidae larvae-induced “CH₄-emitting hot spots” within the soil profile which may subsequently lead to increased CH₄ oxidation. The net (soil + larvae) and gross (soil and larvae separated) CH₄ fluxes were studied in a 3-month laboratory incubation. Addition of larvae changed the soil from a net sink (?330 ± 11 ng CH₄ kg^?1 h^?1) to a net source (637 ± 205 ng CH₄ kg^?1 h^?1). Supply of plant litter to the soil + larvae incubation jars tended to increase CH₄ emissions which was not significant due to large variability. After 11–13 weeks of incubation, the net soil CH₄ oxidation was significantly stimulated by 13–21% in the treatments containing larvae when these were taken out. Analysis of archaeal 16S rRNA genes revealed that the majority of the obtained clones were closely related to uncultured methanogens from guts of insects and other animals. Other sequences were relative to cultivated species of Methanobrevibacter, Methanoculleus, and Methanosarcina. Hence, Scarabaeidae larvae in soils (i) may represent an underestimated source of CH₄ emissions in aerobic upland soils, (ii) may stimulate gross CH₄ consumption in their direct soil environment, and, thus, (iii) contribute to the spatial heterogeneity often observed in the field with closed-chamber measurements. Long-term CH₄-flux balances may be wrongly assessed when “exceptional” net CH₄ flux rates (due to larvae hot spots) are excluded from data sets.