Thermoluminescence studies on the function of Photosystem II in the desiccation tolerant lichen Cladonia convoluta

The effect of desiccation and rehydration on the function of Photosystem II has been studied in the desiccation tolerant lichen Cladonia convoluta by thermoluminescence. We have shown that in functional fully hydrated thalli thermoluminescence signals can be observed from the recombination of the S₂₍₃₎Q_B ^– (B band), S₂Q_A ^– (Q band), Tyr-D⁺Q_A ^– (C band) and Tyr-Z⁺(His⁺)Q_A ^– (A band) charge stabilization states. These thermoluminescence signals are completely absent in desiccated thalli, but rapidly reappear on rehydration. Flash-induced oscillation in the amplitude of the thermoluminescence band from the S₂₍₃₎Q_B ^– recombination shows the usual pattern with maxima after 2 and 6 flashes when rehydration takes place in light. However, after rehydration in complete darkness, there is no thermoluminescence emission after the 1 st flash, and the maxima of the subsequent oscillation are shifted to the 3rd and 7th flashes. It is concluded that desiccation of Cladonia convoluta converts PS II into a nonfunctional state. This state is characterized by the lack of stable charge separation and recombination, as well as by a one-electron reduction of the water-oxidizing complex. Restoration of PS II function during rehydration can proceed both in the light and in darkness. After rehydration in the dark, the first charge separation act is utilized in restoring the usual oxidation state of the water-oxidizing comples.Abbreviations Chl chlorophyll - DCMU 3-(3,4-dichlorophenyl)-1,1-dimethylurea - DT desiccation tolerant - PS II Photosystem II - TL thermoluminescence - P₆₈₀ reaction center Chl of PS II - Q_A and Q_B puinone electron acceptors of PS II - S₀,...,S₄ the redox states of the water-oxidizing complex - Tyr-Z and Tyr-D redox-active tyrosine electron donors of PS II     

Desiccation of Panagrolaimus rigidus (Nematoda): survival,reproduction and the influence on the internal clock

Following the life-table experimental schedule, cohorts of aparthenogenetic strain of the free-living nematode Panagrolaimus rigidus were desiccated for six days at theages of4, 8, 12, and 19 d (age effect) and cohorts aged 8 d weredried for15, 20, 40, and 60 days (time effect) to determine theirability torecover and to reproduce.Nematode age had poor effect on recovery after 6 days ofdesiccation until the mean longevity of the nematode (19 daysinhydrated medium) is approached, while increasing times ofdesiccation (from 6 to 60 d) remarkably decreased capacity forrecovery (from 80 to 8%). Anhydrobiosis experienced atdifferentages or for different durations modified the timing of thenematodelife cycle events, but not the pattern of age-specificfecunditynor survival curves. The age-specific fecundity is largelyretainedfollowing anhydrobiosis, but when matched to that of thenematodeskept hydrated (controls), it declines for increasing durationsofdesiccation. Anhydrobiosis appears to cause a reset of theanimalsinternal clock, that is dependent on the duration ofdesiccation.     

The wheat wcs120 gene family. A useful model to understand the molecular genetics of freezing tolerance in cereals

Winter, as compared with spring cereals, possess better acclimation mechanisms that allow them to overwinter and survive freezing temperatures. This difference is genetically programmed and involves a complex genetic system. To understand the nature of this system and its regulation by low temperature, genes associated with freezing tolerance in wheat ( Triticum aestivum L.) were identified and characterized. Among these, the wcs120 gene family encodes a group of proteins ranging in size from 12 to 200 kDa. As shown by biochemical, immunohistochemical, molecular and genetic analyses, this gene family is specific to the Poaceae, highly abundant and coordinately regulated by low temperature. Furthermore, accumulation of WCS protein is directly correlated with the development of freezing tolerance. These analyses also revealed a regulatory control of the vernalization process over low temperature gene expression in winter cereals. Recent studies suggest that the molecular mechanisms controlling the expression of these genes involve negative regulatory factors that are modulated by phosphorylation.     

The effect of life cycle stage and genotype on desiccation tolerance in the colonizing parthenogenetic cockroach Pycnoscelus surinamensis and its sexual ancestor P. indicus

We compared the desiccation tolerance of nymphs of diploid and triploid clones of the colonizing parthenogenetic cockroach, Pycnoscelus surinamensis, and strains of its sexual ancestor, P. indicus, as a test of the general-purpose genotype hypothesis and the polyploidy hypothesis for geographic parthenogenesis in this species complex. Desiccation tolerance is strongly associated with nymphal size. Clones of P. surinamensis are highly variable in nymphal desiccation tolerance, adjusted for body weight by analysis of covariance. This heterogeneity is mirrored by significant differences among recently isolated sublines of a lab population of P. indicus. As a group, the clones are not more tolerant than the sexual strains. Likewise, the four triploid clones were not more resistant to desiccation than the four diploid clones tested. A second experiment revealed a negative association between adult and last instar desiccation tolerance, due to developmental factors not associated with size. These patterns of variation in the sexual and parthenogenetic forms are consistent with the conclusion that extensive genetic variation in desiccation tolerance in the sexual ancestor has been preserved in the clonal lineages, but that desiccation tolerance has not been selected on strongly during the dispersal of clones of P. surinamensis.     

Significance of Thiol-Disulfide Exchange in Resting Stages of Plant Development

Abstract: Desiccation tolerance is a fundamental principle for resting stages of plant development which include the dormancy of seeds and the quiescent stages of resurrection plants. To prevent the deleterious effects of cellular desiccation, a complex interplay of several adaption mechanisms is required. The ability to cope with free radicals, the formation of which is well documented in desiccated tissues, is one of these basic requirements. Detoxification of free radicals by several antioxidants and scavenging enzymes include reactions of reduced glutathione (GSH) resulting in the formation of glutathione disulfide (GSSG). In free radical processing pathways GSSG is considered to be immediately reduced back to GSH by the action of glutathione reductase (EC 1.6.4.2.). However, in desiccated tissues GSSG accumulates. Protein-glutathione mixed disulfides (PSSG) are also reported to increase in plants under drought leading to the hypothesis that glutathione protects protein thiol groups from auto-oxidation. The irreversible formation of intramolecular disulfides resulting in denaturation of proteins would be one of the primary sites of desiccation injury. We suggest that PSSG is formed by the reaction of GSSG with high molecular weight thiols and introduce a thiol-disulfide cycle that involves reduction/oxidation processes of glutathione and protein thiol groups during the dehydration/rehydration processes in desiccation tolerant tissues.     

Desiccation as a mitigation tool to manage biofouling risks: trials on temperate taxa to elucidate factors influencing mortality rates

The desiccation tolerance of biofouling taxa (adults and early life-stages) was determined under both controlled and ‘realistic’ field conditions. Adults of the ascidian Ciona spp. died within 24 h. Mortality in the adult blue mussel Mytilus galloprovincialis occurred within 11 d under controlled conditions, compared with 7 d when held outside. The Pacific oyster Crassostrea gigas was the most desiccation-tolerant taxon tested (up to 34 d under controlled conditions). Biofouling orientated to direct sunlight showed faster mortality rates for all the taxa tested. Mortality in Mytilus juveniles took up to 24 h, compared with 8 h for Ciona, with greater survival at the higher temperature (18.5°C) and humidity (~95% RH) treatment combination. This study demonstrated that desiccation can be an effective mitigation method for a broad range of fouling taxa, especially their early life-stages. Further work is necessary to assess risks from other high-risk species such as algae and cyst forming species.     

Effect of moisture evaporation from diatomaceous earth pellets on storage stability of Steinernema glaseri

Induction of anhydrobiosis and storage stability of entomopathogenic nematodes are influenced by moisture availability. Decreasing moisture content in diatomaceous earth (DE) pellets containing the Steinernema glaseri NJ-43 strain and its effect on survival time and infectivity of the nematode were determined. Pelletisation was performed in a vortex mixer, using DE Celite® 209 as the desiccant material. Pellets were stored at room temperature (23?±?2°C) and high relative humidity (96–100%). Nematode survival and infectivity against last instar greater wax moth, Galleria mellonella, were tested daily. Initial average and average equilibrium moisture content in pellets were 66.7% and 13.6%, respectively, and the infective juveniles mean survival time was 8.8 days. A moisture transfer model based on diffusion and evaporation was evaluated to predict moisture fluctuations within the pellets. We concluded that 84% of variation in S. glaseri infectivity on G. mellonella larvae was explained by the survival of the nematode, whereas 52% of variation in S. glaseri survival was explained by the loss of moisture from the pellets. The moisture transfer model achieved 78% reliability in predicting moisture content and fluctuations. Therefore, the mechanisms of moisture diffusion and evaporation from the surface to the surrounding atmosphere contribute significantly to moisture loss from the pellets.     

Water‐level fluctuations affect sediment properties,carbon flux and growth of the isoetid Littorella uniflora in oligotrophic lakes

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Chlorophyll Fluorescence of Lichens Containing Green and Blue-Green Algae During Hydration by Water Vapor Uptake and by Addition of Liquid Water*

The fluorescence yield at room temperature of the lichens Ramalina maciformis and Peltigera rufescens, containing either green or blue-green algae (Cyanobacteria) as phycobionts, has been investigated during rehydration of the dry lichens by water vapor uptake or by wetting with liquid water. In the dry state the fluorescence yield with all reaction centers open, F_o, was low and no variable fluorescence could be induced with both species. Whereas R. maciformis, containing green algae, regained normal fluorescence behavior during water vapor uptake, the photosynthetic apparatus of the blue-green algae-containing P. rufescens stayed inhibited and could be reactivated only by addition of liquid water. During stepwise rehydration at increasing air humidities, a pattern was established for the recovery of the different fluorescence parameters in R. maciformis. At a dry-weight related water content between 30 and 40%, F_o rose sharply. Maximal variable fluorescence yield expressed as (F_v)_m/F_o, strongly increased in the same range of water content and remained constant above a water content of 50%. Non-photochemical fluorescence quenching, q_NP, determined at the end of a period of actinic illumination, decreased with increasing water vapor uptake. While spraying the lichen with liquid water did not induce a further decrease of q_NP, slow dehydration at lowered air humidity led to a minimal value of q_NP at a water content of 65 % indicating optimal photosynthetic rate under these conditions. These results extend the conclusions drawn from earlier gas exchange experiments that blue-green algae-containing lichens are unable to reactivate photosynthesis by water vapor uptake. During a re- and de-hydration cycle, no hysteresis in the hydration dependence of the fluorescence parameters was found. From this and the presence of a stable and low F_o value at prolonged incubation in nearly water vapor saturated air, we conclude that the reactivation of photosynthesis in blue-green algae-containing lichens is not prevented through high diffusion resistances for water.     

PHOTOSYNTHESIS,DARK RESPIRATION AND DESICCATION RESISTANCE OF THE INTERTIDAL SEAWEEDS HESPEROPHYCUS HARVEYANUS AND PELVETIA FASTIGIATA F. GRACILIS12

Rates of net photosynthesis and dark respiration were determined under submersed and emerged conditions for Hesperophycus harveyanus S. & G. and Pelvetia fastigiata f. gracilis (Decne.) S. & G. Both species exhibited submersed photosynthesis-light relationships and dark respiration rates similar to those established for other closely related intertidal, fucoids. Maximal net photosynthesis of H. harveyanus (0.21 mmol O₂ g dry wt.^-1· h^-1; 0.18 mmol CO₂ g dry wt.^-1· h^-1) was similar to that of P. fastigiata f. gracilis (0.17 mmol. O₂ g dry wt.^-1· h^-1; 0.14 mmol CO₂ g dry wt. ^-1· h^-1). Light saturation occurred between 150 and 250 μE · m^-2· s^-1 for H. harveyanus and between 75 and 150 μE · m^-2· s^-1 for P. fastigiata f. gracilis; photon flux densities required for compensation were 6.4 and 9.2 μE · m^-2· s^-1, respectively. Photoinhibition was not observed for either species. The light-saturated, submersed net photosynthetic performances of both species varied significantly with temperature. Greatest photosynthetic rates were obtained at 23° C for H. harveyanus and at 18° C for P. fastigiata f. gracilis. Under emersed conditions, the maximal net photosynthetic rate and the photon flux densities required for saturation were greater for H. harveyanus (0.08 mmol CO₂ g dry wt.^-1· h^-1; 260 to 700 μE · m^-2· s^-1) than for P. fastigiata f. gracilis (0.02 mmol CO₂g dry wt.^-1· h^-1; 72 to 125 μE · m^-2· s^-1). However, for both species, emersed photosynthetic rates were much lower (14–44%) than those obtained under submersed conditions. Desiccation negatively influenced emersed photosynthesis, of both species, but H. harveyanus thalli contained more water when fully hydrated and lost water more slowly during dehydration, thus suggesting greater photosynthetic potential during field conditions of emersion.