Metallothionein and cellular energy allocation in the estuarine mysid shrimp Neomysis integer exposed to cadmium at different salinities

In the present study the induction of metallothioneins (MTs) and effects on the cellular energy allocation (CEA) in euryhaline crustacean Neomysis integer exposed to Cd at different salinities were studied. N. integer was exposed to the same sub-lethal concentration of free cadmium ion (1/5 of the cadmium activity of the reported 96 h LC₅₀ value) in hypo-osmotic (7.2 μg Cd/L at 5 psu), isosmotic (23.0 μg Cd/L at 16 psu) and hyper-osmotic media (38.1 μg Cd/L at 25 psu) for 7 days. By using the free Cd concentration as the basis for conducting the exposures, the effect of salinity on cadmium speciation was eliminated and therefore the true effect of salinity as an abiotic factor on the MT induction and CEA could be studied.MT content was quantified by differential pulse voltammetry (DPV); this is the first time that this method is applied to assays with N. integer. No significant differences in MT levels between the control and Cd-exposed groups were observed. The measured MT levels (ranging from 32.3 to 75.7 μg/mg_{(cytosolic protein)}) probably represent the constitutive MT levels responsible for binding essential metals. The differences in MT levels observed at the different salinities indicate a possible relationship between some physiological process (possibly osmoregulation) other than detoxification and MT induction. A decrease in salinity caused an increase in MT level in N. integer, and this was significantly correlated to the CEA values (Spearman correlation coefficient r = − 0.56, p = 0.016). Our results indicate that salinity can change the energy status and MT content of N. integer. These findings should be taken into account when using these biomarkers - and especially MTs - in field studies and environmental monitoring.     

Seasonal and spatial patterns in cellular energy allocation in the estuarine mysid Neomysis integer (Crustacea: Mysidacea) of the Scheldt estuary (The Netherlands)

The seasonal and spatial patterns in cellular energy allocation of the estuarine mysid Neomysis integer (Leach, 1814) were investigated in the Scheldt estuary over a 2-year period. Using the recently developed cellular energy allocation (CEA) assay, energy reserves (protein, lipid and sugar) and energy consumption (as derived from the cellular respiration rate) were integrated into a general indicator of physiological stress. Total energy reserves were relatively unaffected by sampling season or location, whereas the individual energy reserve fractions of N. integer were differentially influenced by sampling location and season. Seasonal effects were apparent for mysid weight and were related to the population biology, whereas spatial effects on the weight of N. integer may depend on pollution-induced effects on cellular energy allocation in the two most upstream sites (Bath and Doel). These upstream sites coincide with the most polluted part of the sampled area and were characterized by a significant increase in energy consumption, resulting in a significantly lower CEA. Due to the recent amelioration in the oxygen concentration at these sites, it can be expected that N. integer will migrate further upstream, similar to what is observed in other European estuaries. It will, therefore, be important to assess the physiological consequences and potential population effects on mysids from these polluted areas in the Scheldt estuary. This study provides evidence that the CEA assay has potential under field conditions as an in situ biomarker of pollutant effects.     

Trophodynamics of two interacting species of estuarine mysids, Praunus flexuosus and Neomysis integer, and their predation on the calanoid copepod Eurytemora affinis

Community structure is shaped by external factors (i.e., habitat, temperature, and food) frequently modified by interactions among its members. This study focusses on trophic interactions between two sympatric mysids Praunus flexuosus and Neomysis integer of the Elbe Estuary, northern Germany. Based on an experimental approach, intraguild predation was evaluated. Predation rate of P. flexuosus on N. integer was positively related to predator size and temperature. Predation rate was significantly correlated with prey size, juvenile N. integer released just from the mysid marsupium being most vulnerable. However, adult P. flexuosus were able to gain more energy in terms of body carbon by catching larger N. integer, whereas immature P. flexuosus assimilated more energy by capturing large numbers of the small-sized N. integer. In contrast to N. integer, P. flexuosus showed an efficient escape behaviour that prevented all stages of N. integer from preying on any size class of P. flexuosus. When Eurytemora affinis was offered as prey, both N. integer and P. flexuosus increased predation rates with predator size and temperature. In mixed prey (N. integer and E. affinis) experiments at 10 °C, predation rates of adult P. flexuosus on N. integer released just from the marsupium declined from 17±8 to 6±4 N. integer mysid⁻¹ day⁻¹. We conclude that intraguild predation exists between the two species but is one sided with small N. integer being strongly suppressed. This heavy predation pressure is modified by the addition of alternative food resources, in this case, E. affinis.     

The use of biomarkers in Daphnia magna toxicity testing. IV. Cellular Energy Allocation: a new methodology to assess the energy budget of toxicant-stressed Daphnia populations

The Cellular Energy Allocation (CEA) methodology wasdeveloped as biomarker technique to assess the effectof toxic stress on the energy budget of testorganisms. This short-term assay is based on thebiochemical assessment of changes in the energyreserves (total carbohydrate, protein and lipidcontent) and the energy consumption (electrontransport activity). The CEA methodology was evaluatedusing Daphnia magna juveniles exposed for 96hto sublethal lindane and mercury chlorideconcentrations. The ecological relevance of the CEAassay was assessed by comparing the sub-organismalresponse with population level parameters (obtainedfrom 21 day life table experiments) such as theintrinsic rate of natural increase (r_m) and themean total offspring per female. Two differentmethodologies were used to assess the effect levels:the no (lowest) observed effect level (NOAECs-LOAECs)approach and the regression-based approach. Bothtoxicants caused a significant decrease in the netenergy budget of D. magna, with a LowestObserved (Adverse) Effect Concentration (LOAEC) of0.18 mg/l and 5.6 µg/l for lindane andHgCl₂,respectively. Changes in the lipid content of theorganisms were detected at toxicant concentrationslower than those affecting the total carbohydrate andprotein content. Toxicant specific effects wereobserved on the electron transport activity.Comparison of the CEA results with those of thepopulation level tests revealed that for mercury theCEA based LOAEC was a three times lower than thatbased on r_m and the total brood size(18 µg/l). For lindane the CEA based LOAEC was twotimes lower than the LOAEC based on r_m(0.32 mg/l) but was higher than that based on thetotal number of offspring produced (0.1 mg/l).Using the regression-based approach, EC₁₀ valueswere calculated using three parameter sigmoid orlogistic models. Comparison between the CEA andr_m based EC₁₀ values demonstrates that forboth chemicals similar effect concentrations areobtained: the CEA-based EC₁₀ (0.20 mg/l) forlindane is 1.5 times higher than the r_m-basedEC₁₀ threshold (0.13 mg/l), while for mercury thebiomarker-based EC₁₀ value (9 µg/l) was 1.4times lower than the population-based EC₁₀ value(12.5 µg/l).From these results, we suggest that the short-term CEAassay may be useful for predicting long-term effectsat the population level. The consequences of theobserved effects on the energy budget of the testorganism are discussed in the context of the effectsemerging at the population and community level.     

Testosterone metabolism in Neomysis integer following exposure to benzo(a)pyrene

Cytochromes P450 (CYPs) are important enzymes involved in the regulation of hormone synthesis and in the detoxification and/or activation of xenobiotics. CYPs are found in virtually all organisms, from archae, and eubacteria to eukaryota. A number of endocrine disruptors are suspected of exerting their effects through disruption of normal CYP function. Consequently, alterations in steroid hormone metabolism through changes in CYP could provide an important tool to evaluate potential effects of endocrine disruptors. The aim of this study was to investigate the potential effects of the known CYP modulator, benzo(a)pyrene (B(a)P), on the testosterone metabolism in the invertebrate Neomysis integer (Crustacea; Mysidacea). N. integer were exposed for 96 h to 0.43, 2.39, 28.83, 339.00 and 1682.86 μg B(a)P L^− 1 and a solvent control, and subsequently their ability to metabolize testosterone was assessed. Identification and quantification of the produced phase I and phase II testosterone metabolites was performed using liquid chromatography coupled with multiple mass spectrometry (LC–MS²). Significant changes were observed in the overall ability of N. integer to metabolize testosterone when exposed to 2.39, 28.83, 339.00 and 1682.86 μg B(a)P L^− 1 as compared to the control animals.     

Inter- and intra-specific differences in euryhalinity determine the spatial distribution of mysids in a temperate European estuary

Mysids are an important component of estuarine hyperbenthos and a major prey item in the food web of many estuaries. Understanding the abiotic and biotic mechanisms determining mysid distributions is therefore important to comprehend the general processes structuring estuarine communities. We carried out field surveys and exposure-survival experiments for three species of mysids, Neomysis integer Leach Mesopodopsis slabberi van Beneden and Rhopalophthalmus tartessicus Vilas-Fernandez, Drake and Sorbe, to link salinity tolerances of different sex and life stages (adults and juveniles) to their spatial distributions within the Guadalquivir estuary, SW Spain. Despite being euryhaline, the three species of mysids were unevenly distributed along the saline gradient, with salinity being the environmental variable which best explained structure changes in the estuarine mysid assemblage. R. tartessicus remained confined to the outer and more marine part of the estuary and showed a higher temporal variation in its salinity-related distribution (position within the salinity gradient). M. slabberi and N. integer displayed wider estuarine distributions but remained associated with intermediate and low salinities, respectively. We found considerable inter- and intra-specific differences in tolerance to sudden salinity changes: N. integer, and juveniles of M. slabberi and R. tartessicus, showed a high tolerance to sudden salinity changes, whereas adults of M. slabberi and R. tartessicus were only tolerant to salinities close to their isosmotic points. For the less euryhaline species M. slabberi and R. tartessicus acclimation to unfavourable salinities decreased survival after exposure to sudden salinity changes. Both location and strength of the salinity gradient were important factors in determining spatial distribution, either directly to avoid osmotic stress and mortality risk (R. tartessicus and M. slabberi) or indirectly to reduce inter-specific mysid competition (N. integer). We suggest inter- and intra-specific euryhalinity differences determine the spatial distribution of mysids and the specific strategies they use to maintain this spatial structure in a highly variable environment.     

Altered expression of Autism-associated genes in the brain of Fragile X mouse model

Autism is a severe neurodevelopmental disorder, which typically emerges in early childhood. Most cases of autism have not been linked to mutations in a specific gene, and the etioloty of the disorder remains to be established [S.S. Moy, J.J. Nadler, T.R. Magnuson, J.N. Crawley, Mouse models of autism spectrum disorders: the challenge for behavioral genetics, Am. J. Med. Genet. 142 (2006) 40-51]. Fragile X syndrome is caused by mutation in the FMR1 gene and is characterized by mental retardation, physical abnormalities, and, in most case, autistic-like behavior [R.J. Hagerman, A.W. Jackson, A. Levitas, B. Rimland, M. Braden, An analysis of autism in fifty males with the Fragile X syndrome, Am. J. Med. Genet. 23 (1986) 359-374, C.E. Bakker, C. Verheij, R. Willemsen, R. van der Helm, F. Oerlemans, M. Vermeij, A. Bygrave, A.T. Hoogeveen, B.A. Oostra, E. Reyniers, K. De Boulle, R. D’Hooge, P. Cras, D. van Velzen, G. Nagels, J.J. Marti, P. De Deyn, J.K. Darby, P.J. Willems, Fmr1 knockout mice: a model to study Fragile X mental retardation, Cell 78 (1994) 23-33]. The FMR1 knockout (KO) mouse is one of the best characterized animal models for human disorders associated with autism [S.S. Moy, J.J. Nadler, T.R. Magnuson, J.N. Crawley, Mouse models of autism spectrum disorders: the challenge for behavioral genetics, Am. J. Med. Genet. 142 (2006) 40-51]. We have used real-time PCR to investigate changes in expression levels of three genes: WNT2, MECP2, and FMR1 in different brain regions of Fagile X mice and litter mate controls. We found major changes in the expression pattern for the three genes examined. FMR1, MECP2, and WNT2 expression were drastically down regulated in the Fragile X mouse brain.     

Potential predation pressure of littoral mysids on herring (Clupea harengus membras L.) eggs and yolk-sac larvae

The predation potential of littoral mysid shrimps (Mysidacea) on Baltic herring (Clupea harengus membras L.) eggs and yolk-sac larvae was studied experimentally. The results showed that littoral mysids feed actively on both eggs and yolk-sac larvae. It was shown that Neomysis integer preys on eggs, which are not attached to the substrate. Alternative food (yolk-sac larvae or zooplankton) did not decrease feeding rate on eggs. Only gravel as a bottom material lowered the ingestion rate to nearly zero. The largest of the mysid species Praunus flexuosus ate yolk-sac larvae more than other mysids and most efficiently. Mysids switched to feed on eggs when larvae and eggs were offered simultaneously, thus predation focused on eggs. It is possible that hydrodynamic signals of moving larvae induced mysids to prey and eggs were easier prey to catch as well as more numerous. In addition egg size is optimal and the nutritive value (measured as C:N ratio) is better compared with larvae. The results indicate that mysids may have local effects on populations of Baltic herring by eating the early life stages, mostly eggs. Especially when large swarms of N. integer shoal in the spawning areas. However, the effect on recruitment of herring is still hard to evaluate.     

Effects of infection with Nosema pyrausta on survival and development of offspring of laboratory selected Bt-resistant and Bt-susceptible European corn borers

Infection with Nosema pyrausta Paillot lengthens developmental period of Bt-susceptible Ostrinia nubilalis (Hübner) to a similar extent as feeding on Cry1Ab-incorporated diet in Cry1Ab-resistant O. nubilalis, and these two factors combined lengthen developmental period further than either alone. Resistant O. nubilalis mating with infected susceptible, or infected resistant partners would produce partially- and fully-resistant offspring, respectively, infected with N. pyrausta. To investigate the impacts on the progeny of such matings, test crosses were set up to produce partially- and fully Cry1Ab-resistant O. nubilalis offspring transovarially infected and not infected with N. pyrausta, which were exposed to Cry1Ab toxin at doses of 0, 3, or 30 ng/cm² for 7 days. Transovarial infection with N. pyrausta significantly decreased 7 day survival of partially and fully-resistant O. nubilalis feeding on 30 ng/cm² Cry1Ab. In addition, N. pyrausta infection delayed larval development (as measured by weight) of partially- and fully-resistant O. nubilalis feeding on 3 and 30 ng/cm² Cry1Ab. Impacts of natural enemies on target pests may have the potential to impact evolution of resistance. N pyrausta-infected O. nubilalis are more strongly affected by feeding on Bt, and would be less likely to survive to adulthood to pass on resistance to the next generation. This indigenous microsporidium may work to delay evolution of resistance in O. nubilalis by lowering their ability to survive on Bt.     

Efficient catalytic turnover of cytochrome P450(cam) is supported by a T252N mutation

A Thr (or Ser) residue on the I-helix is a highly conserved structural feature of cytochrome P450 enzymes. It is believed to be indispensable as a proton delivery shuttle in the oxygen activation process. Previous work showed that P450_cin (CYP176A1), which contains an Asn instead of the conserved Thr, is fully functional in the catalytic oxidation of cineole [D.B. Hawkes, G.W. Adams, A.L. Burlingame, P.R. Ortiz de Montellano, J.J. De Voss, J. Biol. Chem. 277 (2002) 27725-27732]. To determine whether the substitution of Asn for Thr is specific or general, the conserved Thr252 in P450_cam (CYP101) was mutated to generate the T252N, T252N/V253T, and T252A mutants. Steady-state kinetic analysis of the oxidation of camphor by these mutants indicated that the T252N and T252N/V253T mutants have comparable turnover numbers but higher K_m values relative to the wild-type enzyme. Spectroscopic binding assays indicate that the higher K_m values reflect a decrease in the camphor binding affinity. Non-productive H₂O₂ generation was negligible with the T252N and T252N/V253T mutants, but, as previously observed, was dominant in the T252A mutant. Our results, and a structure model based on the crystal structures of the ferrous dioxygen complexes of P450_cam and its T252A mutant, suggest that Asn252 can stabilize the ferric hydroperoxy intermediate, preventing premature release of H₂O₂ and enabling addition of the second proton to the distal oxygen to generate the catalytic ferryl species.     

Determination of paclitaxel and metabolites in mouse plasma,tissues, urine and faeces by semi-automated reversed-phase high-performance liquid chromatography

We have developed and validated a sensitive and selective assay for the quantification of paclitaxel and its metabolites 6α,3′-p-dihydroxypaclitaxel, 3′-p-hydroxypaclitaxel and 6α-hydroxypaclitaxel in plasma, tissue, urine and faeces specimens of mice. Tissue and faeces were homogenized (approximately 0.1–0.2 g/ml) in bovine serum albumin (40 g/I) in water, and urine was diluted (1:5, v/v) in blank human plasma. Sample pretreatment involved liquid-liquid extraction of 200–1000 μl of sample with diethyl ether followed by automated solid-phase extraction using cyano Bond Elut column. 2′-Methylpaclitaxel was used as internal standard. The overall recovery of the sample pretreatment procedure ranged from 76 ot 85%. In plasma, the lower limit of detection (LOD) and the lower limit of quantitation (LLQ) are 15 and 25 ng/ml, respectively, using 200 μl of sample. In tissues, faeces and urine the LLQs are 25–100 ng/g, 125 ng/g and 25 ng/ml, respectively, using 1000 μl (faeces: 200 μl) of homogenized or diluted sample. The concentrations in the various biological matrices, for validation procedures spiked with known amounts of the test compounds, are read from calibration curves constructed in blank human plasma in the range 25–100 000 ng/ml for paclitaxel and 25–500 ng/ml for the metabolites. The accuracy and precision of the assay fall within the generally accepted criteria for bio-analytical assays.     

Influence of tris(2,3-dibromopropyl) isocyanurate on the expression of photosynthesis genes of Nannochloropsis sp.

The proteins encoded by psaA and psaB form a heterodimer, an essential compound of photosystem; while the protein encoded by psbC binds with chlorophyll a in photosystem II, serving as antennae in photosystem. Here we report that a heterocyclic brominated flame retardant, tris(2,3-dibromopropyl) isocyanurate (TBC), inhibited the expression of psaA and psbC, then leads to the decrease of Nannochloropsis sp.'s growth biomass. TBC exposure inhibited the expression of psaA and psbC at 10, 100 ng/mL slightly and 1000 ng/mL significantly. In addition, TBC was found to slow down the growth of Nannochloropsis sp. at concentrations ranging from 10 to 1000 ng/mL. These results indicated that TBC influenced both photosynthesis and growth performance of Nannochloropsis sp.     

Temperature and salinity effects on post-marsupial growth of Neomysis integer (Crustacea: Mysidacea)

There has been an increasing interest in using the brackish water mysid Neomysis integer as a toxicological test species for Western European estuarine systems. In this respect, more data on growth, moulting and development in this species is needed. The influence of prevailing environmental variables (e.g. temperature, salinity) and age on these processes as well as their optimal range have to be known in order to develop optimal laboratory cultures and to differentiate between chemically induced variability and natural variability in toxicity testing. Individual post-marsupial growth (size, intermoult period, growth factor) was studied from first day neonates until adulthood at eight environmentally relevant temperature-salinity conditions. Three salinities (5, 15 and 30 psu) were tested at 15 and 20 °C, and two more extreme temperatures (8 and 25 °C) were tested at a salinity of 5 psu.Survival and growth of N. integer were detected within the whole range tested, but sexual maturation was only possible in the narrower range of 15-25 °C and 5-15 psu. The size at maturity of N. integer increased with decreasing temperature and increasing salinity. Salinity seems to have a stronger effect than temperature on the duration of maturation. The sigmoid von Bertalanffy growth model was fitted to the individual and pooled data, except for the 8 °C experiment where growth was linear. Estimates from pooled data were comparable with individually based estimates, but generally underestimated the asymptotic length. Temperature was negatively correlated with the asymptotic length and positively correlated with the growth constant K. Higher temperatures caused smaller intermoult periods but had no effect on the growth increment, while salinity effects were less straightforward and dependent on the water temperature. A tool is provided to estimate the age, moult number, intermoult period, growth factor and growth rate from the body standard length of N. integer. Experimentally derived von Bertalanffy parameter estimates resulted in a higher growth performance index compared with field-based estimates for the Schelde estuary and Galgenweel populations of N. integer.     

Complementary (secondary) metabolites in an octocoral competing with a scleractinian coral: effects of varying nutrient regimes

Competitive interactions between two sessile, epibenthic species were investigated on the Great Barrier Reef (GBR) in the presence and absence of added nutrients, as part of the Enrichment of Nutrients on Coral Reefs Experiment (ENCORE). Sarcophyton ehrenbergi Marenzeller (Octocorallia: Alcyonacea), an alcyonacean soft coral, and Pocillopora damicornis (Linnaeus), a scleractinian coral, were relocated and placed in contact with each other on large plastic grids on each of 12 micro-atolls within the One Tree Island (OTI) lagoon (23°30′S, 152°96′E, GBR). These micro-atolls were allocated in equal-sized groups to three enrichment treatments (addition of nitrogen, N; addition of phosphorus, P; addition of both nitrogen and phosphorus, N+P) and one control. Non-relocated (NR) and relocated colonies were also monitored as controls. After relocation and 1 year of nutrient enrichment, concentrations of a terpenoid complementary metabolite—sarcophytoxide—and wax esters were analyzed in colonies of S. ehrenbergi that had been exposed to elevated concentrations of N, P, N+P and compared with colonies on the non-nutrient-enriched control. Non-relocated control colonies from the natural environment were monitored over a period of 1 year and compared to colonies relocated to the control micro-atolls to assess handling effects. Analyses were performed on non-interacting S. ehrenbergi colonies, S. ehrenbergi colonies in experimental contact with P. damicornis colonies, and on non-interacting S. ehrenbergi colonies from the site of initial collection. Significant differences were found between sarcophytoxide levels in colonies of S. ehrenbergi in contact with P. damicornis vs. control/non-contact colonies; contact colonies had higher levels of this metabolite. Non-relocated control colonies of S. ehrenbergi exhibited significantly higher levels of sarcophytoxide than relocated control colonies. Augmentation of nutrient levels in micro-atolls significantly increased sarcophytoxide levels in S. ehrenbergi colonies relative to colonies on the control micro-atolls, although this response was not strong. Concentrations of fatty esters increased significantly through time in S. ehrenbergi colonies in their natural setting (non-relocated controls). This variability was not observed in relocated colonies in the treatment and control micro-atolls, irrespective of contact with P. damicornis. Concentrations of fatty esters in colonies of S. ehrenbergi in contact with P. damicornis were significantly lower than control/non-contact colonies, indicating that there is a cost in terms of stored energy reserves for the production of additional complementary metabolites when involved in competition for space. Augmentation of P levels in micro-atolls induced significant increases in fatty ester levels within S. ehrenbergi colonies vs. colonies in control micro-atolls, or in micro-atolls treated with added N or N+P together. These findings indicate that interspecific competition for space between a scleractinian coral and an alcyonacean soft coral and/or changes in the environmental nutrient regime can influence concentrations of complementary/secondary metabolites in the alcyonacean coral and the organism's stored energy reserves.     

Aerobic biodegradation characteristics and metabolic products of quinoline by a Pseudomonas strain

A bacterial strain, BW003, which utilized quinoline as its sole C, N and energy source, was isolated and identified as Pseudomonas sp. BW003 degraded 192–911 mg/l quinoline within 3–8 h with removal rates ranging from 96% to 98%. The optimum conditions for the degradation were 30 °C and pH 8. In the process of biodegradation, at least 43% of quinoline was transformed into 2-hydroxyquinoline, then 0.69% of 2-hydroxyquinoline was transformed into 2,8-dihydroxyquinoline, and then, presumably, into 8-hydroxycoumarin. Meanwhile, at least 48% of the nitrogen in quinoline was directly transformed into ammonia-N. An extra carbon source enhanced the nitrogen transformation from ammonia-N. Further experiments showed that, besides cell synthesis, BW003 transformed less than 6% of ammonia-N into nitrate through heterotrophic nitrification. In addition, BW003 contained a large plasmid, which may be involved in quinoline metabolism. The study indicates that quinoline and its metabolic products can be eliminated from wastewater by controlling the C/N ratio using BW003 as the bioaugmentation inoculum.     

Efficacy of Ethoprop on Meloidogyne hapla and M. chitwoodi and Enhanced Biodegradation in Soil

Responses of egg masses, free eggs, and second-stage juveniles (J2) ofMeloidogyne hapla and M. chitwoodi to ethoprop were evaluated. The results indicated that J2 were the most sensitive, followed by free eggs and egg masses. In general, M. chitwoodi was more susceptible to ethoprop than M. hapla. Ethoprop at 7.2 μg a.i./g soil protected tomato roots from upward migrating M. chitwoodi for 5 weeks. The zone of protection was extended to 10 and 20 cm below the root zone when 3.6 and 7.2 cm water were applied over 8 days. Ethoprop at 1.8, 3.6, and 7.2 μg a.i./g soil degraded faster and killed fewer M. chitwoodi J2 in potato field soil previously exposed to ethoprop than in unexposed soil or sterilized exposed soil. The enhanced biodegradation property of the exposed soil lasted 17 months after the last application of ethoprop. The limited downward movement of ethoprop in the soil, migration of M. chitwoodi J2 into the treated zone, presence of resistant life stage(s) at the time of application, and loss of efficacy due to enhanced biodegradation may have a significant effect on the performance of ethoprop.     

A shotgun lipidomics approach in Sinorhizobium meliloti as a tool in functional genomics

A shotgun lipidomics approach that allowed the analysis of eight lipid classes directly from crude extracts of the soil bacterium Sinorhizobium meliloti is presented. New MS-MS transitions are reported for the analysis of monomethylphosphatidylethanolamines, dimethylphosphatidylethanolamines, and three bacterial non-phosphorus-containing lipid classes [sulfoquinovosyldiacylglycerols, ornithines, and diacylglyceryl-(N,N,N-trimethyl)-homoserines]. Unique MS-MS transitions allowed the analysis of isomeric species from various lipid classes without chromatography. Analyses required small sample amounts and minimal preparation; thus, this methodology has excellent potential to be used as a screening tool for the analysis of large numbers of samples in functional genomics studies. FA distributions within lipid classes of S. meliloti are described for the first time, and the relative positions of fatty acyl substituents (sn-1, sn-2) in phospholipids are presented. FA distributions in diacylglyceryl-(N,N,N-trimethyl)-homoserines were identical to those of phospholipids, indicating a common biosynthetic origin for these lipids. The method was applied to the analysis of mutants deficient in the PhoB regulator protein. Increased lipid cyclopropanation was observed in PhoB-deficient mutants under P_i starvation.     

Respiration,energy balance and development during growth and starvation of Carcinus maenas L. larvae (Decapoda:Portunidae)

In all larval stages of Carcinus maenas L. oxygen consumption was measured at three temperatures (12,18,25 °C). Values increased during development and were in the range of 0.037 ± 0.01 (zoea-1, 12°C, $\text{x}\text{?}\text{± 95\% CL}$) to 0.734 ± 0.047 μl O₂ · h^?1 · ind^?1 (megalopa, 25 °C). Growing larvae showed temperature dependent trends in weight specific respiration rates (referred to dry wt; DW), with values between ≈2.4 and 9.4 μl O₂· h^?1·mg DW^?1. Increase in oxygen consumption of megalops did not differ much at temperatures between 18 and 25 °C. This points to an exceptional physiological position of this stage. Fed zoea-1 of C. maenas (18 °C) revealed growth rates in terms of 40% DW, 20% carbon (C), 30% nitrogen (N) and 65% hydrogen (H). At the same time larvae gained individual energy by 13% (J · ind^?1), while weight specific energy dropped by ≈ 19% (J · mg DW^?1) during the first day and remained constant until the moult. Starved zoea-1 of C. maenas (18 ° C) gained ≈ 20 % in DW through the first day, probably caused by inorganic salts which enter the organism after the moult of the prezoea. DW dropped to ≈ 25 % of initial value, when starvation continued. Single components decreased by ≈50% (C), 54% (N), 57% (J · ind^?1). Weight specific energy (J · mg DW^?1) decreased by 40% during the first 4 days of starvation, remaining constant thereafter. Individual respiration rate (R) dropped by 61 %, weight specific respiration rate (QO₂) by 55 %. Individual energy loss in starved zoea-1 was 0.077 J over a period of 11 days. In this period ≈ 9.3 μl O₂·ind^?1 were consumed. Thus effective oxygen capacity was lower than in growing larvae. It dropped to 5.3 J·mlO₂^?1 after 4 days and remained constant if starvation continued, i.e. 65 % of possible energy loss occurred during the first 4 days. Decrease in requirement for oxygen and its effective capacity were both recognized as independent components of survival during starvation. Partitioning of energy through individual larval development of C. maenas was investigated for all five larval stages. The cumulative budget could be calculated: consumption (C) = 28.23 J, growth (G) = 0.92 J, exoskeleton (Ex) = 0.20 J, metabolism (M) = 5.30 J, egestion and excretion (E) = 21.82 J. Mean gross and net growth efficiency were, K₁ = 3.3% and K₂ = 14.8%, respectively.