Growth, yield and tuber quality of Solanum tuberosum L. under supplemental ultraviolet-B radiation at different NPK levels

In many areas, decreases in the stratospheric ozone layer have resulted in an increase in ultraviolet-B (UV-B, 280-315 nm) radiation reaching the Earth's surface. The present study was conducted to evaluate the interactive effects of supplemental UV-B (sUV-B) and mineral nutrients on a tuber crop, potato (Solanum tuberosum L. var Kufri Badshah), under natural field conditions in a dry tropical environment. The nutrient treatments were the recommended dose of NPK (F(o)), 1.5 times the recommended dose of NPK (F(1)), 1.5 times the recommended dose of N (F(2)) and 1.5 times the recommended dose of K (F(3)). The response of potato plants to sUV-B varied with nutrient treatment and concentration. sUV-B adversely affected growth, yield and quality of tubers, causing an increase in reducing sugars in the tubers and thus reducing the economic value. Growth and fresh weight of tubers was maximal with sUV-B at 1.5 times recommended NPK, but the dry weight of tubers were highest with the recommended NPK dose. Reducing sugar content was lower in potato plants treated with sUV-B and the recommended NPK than with sUV-B and 1.5 times the recommended NPK. This study thus clearly shows that growing potato with 1.5 times the recommended NPK or 1.5 times the recommended dose of N/K does not alleviate the sUV-B induced changes in yield and quality of tubers compared to the recommended NPK dose.     

Comparative analysis of essential oil composition and oil containing glands in <Emphasis Type="Italic">Ocimum sanctum</Emphasis> L. (Holy basil) under ambient and supplemental level of UV-B through gas chromatography–mass spectrometry and scanning electron microscopy

Field grown plants of holy basil (Ocimum sanctum L.) were treated with biologically effective supplemental ultraviolet-B (sUV-B) radiation (ambient +1.8 kJ m⁻² day⁻¹) to evaluate its effect on specialized oil glands and quantity and quality of the essential oil. The total yield of essential oil increased significantly by 42.0% after sUV-B treatment. Gas chromatography–mass spectrometry analysis showed that most important flavor compounds β-caryophyllene, germacrene-D, ethyl linoleolate, β-elemene and camphenol increased significantly after sUV-B treatment. Moreover, the level of main compound eugenol was not affected significantly. Scanning electron microscopy analysis showed turgidity of oil glands after sUV-B exposure and it was well correlated with the higher yield of essential oil. The result is of specific interest because if other parameters remain constant, sUV-B may affect the production of the essential oil in Ocimum sanctum L.     

Impact of ambient and supplemental ultraviolet-B stress on kidney bean plants: an insight into oxidative stress management

In the present study, the response of kidney bean (Phaseolus vulgaris L. cv. Pusa Komal) plants was evaluated under three different levels of ultraviolet-B (UV-B), i.e., excluded UV-B (eUV-B), ambient UV-B (aUV-B; 5.8 kJ m^?2 day^?1), and supplemental UV-B (sUV-B; 280–315 nm; ambient?+?7.2 kJ m^?2 day^?1), under near-natural conditions. eUV-B treatment clearly demonstrated that both aUV-B and sUV-B are capable of causing significant changes in the plant’s growth, metabolism, economic yield, genome template stability, total protein, and antioxidative enzyme profiles. The experimental findings showed maximum plant height at eUV-B, but biomass accumulation was minimum. Significant reductions in quantum yield (Fv/Fm) were observed under both aUV-B and sUV-B, as compared to eUV-B. UV-B-absorbing flavonoids increased under higher UV-B exposures with consequent increments in phenylalanine ammonia lyase (PAL) activities. The final yield was significantly higher in plants grown under eUV-B, compared to those under aUV-B and sUV-B. Total protein profile through sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and analysis of isoenzymes, like superoxide dismutase (SOD), peroxidase (POX), catalase (CAT), ascorbate peroxidase (APX), guaiacol peroxidase (GPX), and glutathione reductase (GR), through native PAGE revealed major changes in the leaf proteome under aUV-B and sUV-B, depicting induction of some major stress-related proteins. The random amplified polymorphic DNA (RAPD) profile of genomic DNA also indicated a significant reduction of genome template stability under UV-B exposure. Thus, it can be inferred that more energy is diverted for inducing protection mechanisms rather than utilizing it for growth under high UV-B level.     

亚麻响应盐、碱胁迫的生理特征

利用中性盐NaCl、Na₂SO₄和碱性盐NaHCO₃、Na₂CO₃混合模拟不同强度的盐、碱胁迫条件, 对亚麻(Linum usitatissimum)进行14天胁迫处理, 测定其地上部分和根生长速率、光合特征、离子平衡及有机渗透调节物质积累, 以探讨亚麻对盐、碱两种胁迫的生理响应特点。研究表明: 亚麻生长对盐、碱胁迫的响应存在差异, 在相同盐浓度下, 碱胁迫对亚麻的伤害大于盐胁迫。碱胁迫使地上部分中Na⁺浓度急剧增高, 造成叶绿体破坏、光合色素含量下降, 光合能力及碳同化能力也急剧下降。亚麻中Na⁺含量随着胁迫强度的增加而升高, 而K⁺含量呈下降趋势, 碱胁迫下的变化明显大于盐胁迫。因此, 碱胁迫导致Na⁺过度积累可能是碱胁迫对植物伤害大于盐胁迫的最主要原因。碱胁迫下Ca²⁺和Mg²⁺在根中下降明显, 可见高pH值阻碍根对Ca²⁺和Mg²⁺的吸收。Fe²⁺和Zn²⁺对渗透调节的影响不大, 因为它们的离子含量较低。盐胁迫促进阴离子(Cl^-、H₂PO₄^-和SO₄^2-)的积累来平衡大量涌入的Na⁺, 但是碱胁迫明显减少无机阴离子含量, 可能造成严重营养胁迫(如P和S不足)。亚麻在盐胁迫下积累大量可溶性糖来平衡大量的Na⁺, 但碱胁迫下积累大量有机酸来维持细胞内离子平衡和pH值稳定, 碱胁迫大量积累的有机酸也可能被分泌到根外调节根外的pH值, 这说明亚麻对两种不同胁迫的响应方式不同。研究证明高pH值会直接影响植物根系的生长发育, 影响植物矿质元素的吸收, 阻碍离子稳态重建, 有机酸代谢是亚麻碱胁迫下的关键适应机制。     

Eco-physiological responses of linseed (Linum usitatissimum) to salt and alkali stresses

AimsEffects of salt and alkali stresses (NaCl-Na₂SO₄ and NaHCO₃-Na₂CO₃) were compared on growth, photosynthesis characters, ionic balance and osmotic adjustment of linseed (Linum usitatissimum), to elucidate the mechanisms of salt and alkali stress (high pH value) damage to plants, and their physiological adaptive mechanisms to the stresses. MethodsThe experiment was carried out in an artificial greenhouse. Plants grew at approximately 700 mmol·m^-2·s^-1 photosynthetic photon flux density (PPFD) in greenhouse under photoperiod of 15 h in light and 9 h in dark. In each plastic pot (17 cm diameter) which contained 2.5 kg of washed sand, 20 linseed seeds were sown. The seedlings were exposed to stresses lasting 14 days after 2 months.Important findingsThe inhibitory effects of alkali stress on linseed growth were more remarkable than those of salt stress, indicating that alkali and salt represent two distinct forms of stress. The alkali stress increased the Na⁺ content in shoots, damaged the photosynthetic system, and highly reduced the net photosynthetic rate and C assimilation capacity. Under salinity stress, the Na⁺ content increased, the K⁺ content decreased with increasing stress. Greater changes were observed under alkali than under salt stress. Alkali stress caused the massive influx of Na⁺, which probably explained that the harmful of alkali stress on plants was stronger than that of salt stress. Under alkali stress, Ca²⁺ and Mg²⁺ decreased in roots, showing that high pH value around roots hindered the absorption of them. Fe²⁺ and Zn²⁺ had little effects on the osmotic adjustment, mainly because of they had a low ion content. Under salt stress, anion increased in order to balance the sharp increase of Na⁺. However, alkali stress made severe deficit of negative charge, broke the intracellular ionic balance and pH homeostasis, and caused a series of strain response. Our results showed that linseed enhanced the synthesis of soluble sugars to balance massive influx of Na⁺ under salt stress, but linseed enhanced the synthesis of organic acids to compensate for the shortage of inorganic anions, which might be a key pathway for the pH adjustment. In conclusion, the alkali stress (high pH value) clearly inhibited the growth, element absorption, ion homeostasis reconstruction of plants. Organic acid concentration is possibly a key adaptive factor for linseed to maintain intracellular ion balance and regulate high pH value under alkali stress.     

Impact of ultraviolet-B radiation on photosynthetic capacity,antioxidative potential and metabolites in Solanum tuberosum L. under varying levels of soil NPK

The impact of supplemental ultraviolet-B (sUV-B; 280–315 nm; +7.2 kJ m^?2 d^?1) radiation was studied on various physiological parameters, antioxidative potential and metabolites of Solanum tuberosum L. cv. Kufri Badshah plants under varying levels of soil NPK. The N, P and K treatments were: the recommended dose of N, P and K; 1.5 times the recommended dose of N, P and K; 1.5 times the recommended dose of N and 1.5 times the recommended dose of K. The recommended NPK level provided maximum protection to photosynthetic assimilation under sUV-B radiation, while stomatal conductance was best at 1.5 times the recommended NPK. Carbon dioxide assimilation declined maximally at 1.5 times the recommended N/K under sUV-B radiation. Plants grown at the recommended NPK and 1.5 times the recommended NPK levels showed higher superoxide dismutase, peroxidase and ascorbate peroxidase activities under sUV-B radiation compared to 1.5 times the recommended N/K levels. sUV-B significantly increased total phenolics and flavonoids in plants at the recommended and 1.5 times the recommended NPK, while flavonoids declined at 1.5 times the recommended N. This study clearly showed that NPK amendment provided maximum protection to photosynthetic assimilation of potato plants under sUV-B radiation, activating the antioxidative defense system as well as flavonoids. NPK at 1.5 times the recommended dose, however, did not cause any additional benefit to photosynthetic carbon fixation; hence the recommended dose of NPK is found to be the best suited dose of fertilizer under ambient as well as sUV-B regime.     

Investigation of protein expression in magnetic field-treated human glioma cells

We previously reported phenotypic changes in human breast cancer cells following low-level magnetic field (MF) exposure. Here proteomic methods were used to investigate the biochemical effect of MF exposure in SF767 human glioma cells. Protein alterations were studied after exposure to 1.2 microTesla (microT) MF [12 milliGauss (mG), 60 Hertz (Hz)] +/- epidermal growth factor (EGF). SF767 cells were exposed for 3 h to sham conditions (<0.2 microT ambient field strength) or 1.2 microT MF (+/-EGF; 10 ng/ml). Solubilized protein fractions (sham; 1.2 microT; sham + EGF; 1.2 microT + EGF) were loaded for electrophoresis by 2D-PAGE and stained using a colloidal Coomassie blue technique to resolve and characterize the proteins. Protein patterns were compared across groups via Student's t-test using PDQUEST software. Cell profiles revealed significant alterations in the spot density of a subset of treated cells. Automated spot excision and processing was performed prior to peptide mass fingerprinting proteins of interest. Fifty-seven proteins from the detectable pool were identified and/or found to differ significantly across treatment groups. The mean abundance of 10 identified proteins was altered following 1.2 microT exposure. In the presence of EGF six proteins were altered after low magnetic field treatment by increasing (4) or decreasing (2) in abundance. The results suggest that the analysis of differentially expressed proteins in SF767 cells may be useful as biomarkers for biological changes caused by exposure to magnetic fields.     

Fast exact algorithms for the closest string and substring problems with application to the planted (L, d)-motif model

We present two parameterized algorithms for the closest string problem. The first runs in O(nL + nd · 17.97d) time for DNA strings and in O(nL + nd · 61.86d) time for protein strings, where n is the number of input strings, L is the length of each input string, and d is the given upper bound on the number of mismatches between the center string and each input string. The second runs in O(nL + nd · 13.92d) time for DNA strings and in O(nL + nd · 47.21d) time for protein strings. We then extend the first algorithm to a new parameterized algorithm for the closest substring problem that runs in O((n - 1)m2(L + d · 17.97d · m[log2(d+1)])) time for DNA strings and in O((n - 1)m2(L + d · 61.86d · m[log2(d+1)])) time for protein strings, where n is the number of input strings, L is the length of the center substring, L - 1 + m is the maximum length of a single input string, and d is the given upper bound on the number of mismatches between the center substring and at least one substring of each input string. All the algorithms significantly improve the previous bests. To verify experimentally the theoretical improvements in the time complexity, we implement our algorithm in C and apply the resulting program to the planted (L, d)-motif problem proposed by Pevzner and Sze in 2000. We compare our program with the previously best exact program for the problem, namely PMSPrune (designed by Davila et al. in 2007). Our experimental data show that our program runs faster for practical cases and also for several challenging cases. Our algorithm uses less memory too.     

Bronchial reactivity of healthy subjects: 18-20 h postexposure to ozone.

Exposure of humans to ambient levels of ozone (O(3)) causes inflammatory changes within lung tissues. These changes have been reported for the "initial" (1- to 3-h) and "late" (18- to 20-h) postexposure periods. We hypothesized that at the late period, when protein and cellular markers of inflammation at the airway surface remain abnormal and the integrity of the epithelial barrier is compromised, bronchial reactivity would be increased. To test this, we measured airway responsiveness to cumulative doses of methacholine (MCh) aerosol in healthy subjects 19+/-1 h after a single exposure to O(3) (130 min at ambient levels between 120 and 240 parts/billion and alternate periods of rest and moderate exercise) or filtered air. Exposures were conducted at two temperatures: mild (22 degrees C) and moderate (30 degrees C). At the late period, bronchial reactivity to MCh increased, i.e., interpolated dose of MCh leading to a 50% fall in specific airway conductance (PC(50)) was less after O(3) than after filtered air. PC(50) for O(3) at 22 degrees C was 27 mg/ml (20% less than the PC(50) after filtered air), and for O(3) at 30 degrees C it was 19 mg/ml (70% less than the PC(50) after filtered air). The forced expiratory volume in 1 s (FEV(1)) at the late time point after O(3) was slightly but significantly reduced (2.3%) from the preexposure level. There was no relationship found between the functional changes observed early after exposure to O(3) and subsequent changes in bronchial reactivity or FEV(1) at the late time point. These results suggest that bronchial reactivity is significantly altered approximately 1 day after O(3); this injury may contribute to the respiratory morbidity that is observed 1-2 days after an episode of ambient air pollution.     

Effects of superoxide anions on red cell deformability and membrane proteins.

The effect of superoxide anions (O2-) on red blood cells (RBC) deformability and membrane proteins was investigated using hypoxanthine-xanthine oxidase system. Exposure of RBC to O2- caused a marked decrease in RBC deformability with a concomitant increase in cell volume and shape changes. The RBC exposed to O2- also displayed pronounced degradation of membrane proteins such as band 3 protein and spectrin; new bands of low molecular weight products appeared as the original membrane proteins tended to diminish, without the appearance of high molecular weight products. Since the membrane proteins are involved in processes regulating membrane properties such as permeability and viscoelasticity, the decreased deformability induced by O2- may be attributable to changes in membrane proteins. Interestingly, resealed ghosts exposed to O2- did not show any significant change in membrane proteins, which suggests the existence of further generation of O2- and subsequent production of other active oxygen species mediated by O2(-)-initiated autoxidation of hemoglobin in intact RBC. Furthermore, electrophoretic analysis suggested that active oxygens increased the endogenous proteolytic susceptibility of RBC. In conclusion, a close linkage was suggested between RBC deformability and the membrane proteins.     

Rapid temperature-induced changes in the fatty acid composition of certain lipids in developing linseed and soya-bean cotyledons.

A change in ambient temperature caused marked alterations, over a 24h period, in the proportions of the unsaturated C18 fatty acids in 3-sn-phosphatidylcholine and 1,2-diacyglycerols during the development of soya-bean and linseed cotyledons. The molar proportion of oleate increased when the temperature was increased whereas that of linoleate or linolenate, depending on the species, increased when the temperature was lowered. Concomitant changes in the composition of 3-sn-phosphatidylethanolamine and triacylglycerols were small.     

Dietary emu oil supplementation suppresses 5-fluorouracil chemotherapy-induced inflammation, osteoclast formation, and bone loss

Cancer chemotherapy can cause osteopenia or osteoporosis, and yet the underlying mechanisms remain unclear, and currently, no preventative treatments are available. This study investigated damaging effects of 5-fluorouracil (5-FU) on histological, cellular, and molecular changes in the tibial metaphysis and potential protective benefits of emu oil (EO), which is known to possess a potent anti-inflammatory property. Female dark agouti rats were gavaged orally with EO or water (1 ml·day(-1)·rat(-1)) for 1 wk before a single ip injection of 5-FU (150 mg/kg) or saline (Sal) was given. The treatment groups were H(2)O + Sal, H(2)O + 5-FU, EO + 5-FU, and EO + Sal. Oral gavage was given throughout the whole period up to 1 day before euthanasia (days 3, 4, and 5 post-5-FU). Histological analysis showed that H(2)O + 5-FU significantly reduced heights of primary spongiosa on days 3 and 5 and trabecular bone volume of secondary spongiosa on days 3 and 4. It reduced density of osteoblasts slightly and caused an increase in the density of osteoclasts on trabecular bone surface on day 4. EO supplementation prevented reduction of osteoblasts and induction of osteoclasts and bone loss caused by 5-FU. Gene expression studies confirmed an inhibitory effect of EO on osteoclasts since it suppressed 5-FU-induced expression of proinflammatory and osteoclastogenic cytokine TNFα, osteoclast marker receptor activator of nuclear factor-κB, and osteoclast-associated receptor. Therefore, this study demonstrated that EO can counter 5-FU chemotherapy-induced inflammation in bone, preserve osteoblasts, suppress osteoclast formation, and potentially be useful in preventing 5-FU chemotherapy-induced bone loss.     

Proteomic profiling of ClpXP substrates after DNA damage reveals extensive instability within SOS regulon

ClpXP, a bacterial AAA+ protease, controls intracellular levels of many stress-response proteins. To investigate substrate profile changes caused by a specific environmental stress, quantitative mass spectrometry (SILAC) was used to analyze proteins trapped by ClpXP(trap) before and after DNA damage. The abundance of half of the trapped proteins changed more than 3-fold after damage. Overrepresented substrates included the DNA-repair proteins RecN and UvrA. Among SOS-response proteins, 25% were ClpXP substrates and, importantly, nearly all of the highly induced regulon members were rapidly degraded. Other proteins, including the stress regulator sigma(S), were underrepresented in ClpXP(trap) after DNA damage; overproduction experiments suggest that simple substrate competition does not account for this reduced recognition. We conclude that damage-response proteins are an unusually rapidly degraded family and that ClpXP has substantial capacity to process the influx of newly synthesized substrates while maintaining the ability to degrade its other substrates in an environmentally responsive manner.     

Effects of elevated carbon dioxide and ozone on the phytochemistry of aspen and performance of an herbivore

The purpose of this study was to assess the independent and interactive effects of CO(2), O(3), and plant genotype on the foliar quality of a deciduous tree and the performance of a herbivorous insect. Two trembling aspen (Populus tremuloides Michaux) genotypes differing in response to CO(2) and O(3) were grown at the Aspen FACE (Free Air CO(2) Enrichment) site located in northern Wisconsin, USA. Trees were exposed to one of four atmospheric treatments: ambient air (control), elevated carbon dioxide (+CO(2); 560 microl/l), elevated ozone (+O(3); ambient x1.5), and elevated CO(2)+O(3). We measured the effects of CO(2) and O(3) on aspen phytochemistry and on performance of forest tent caterpillar (Malacosoma disstria Hübner) larvae. CO(2) and O(3) treatments influenced foliar quality for both genotypes, with the most notable effects being that elevated CO(2) reduced nitrogen and increased tremulacin levels, whereas elevated O(3) increased early season nitrogen and reduced tremulacin levels, relative to controls. With respect to insects, the +CO(2) treatment had little or no effect on larval performance. Larval performance improved in the +O(3) treatment, but this response was negated by the addition of elevated CO(2) (i.e., +CO(2)+O(3) treatment). We conclude that tent caterpillars will have the greatest impact on aspen under current CO(2) and high O(3) levels, due to increases in insect performance and decreases in tree growth, whereas tent caterpillars will have the least impact on aspen under high CO(2) and low O(3) levels, due to moderate changes in insect performance and increases in tree growth.     

Protein damage and degradation by oxygen radicals. I. general aspects

Aggregation, fragmentation, amino acid modification, and proteolytic susceptibility have been studied following exposure of 17 proteins to oxygen radicals. The hydroxyl radical (.OH) produced covalently bound protein aggregates, but few or no fragmentation products. Extensive changes in net electrical charge (both + and -) were observed. Tryptophan was rapidly lost with .OH exposure, and significant production of bityrosine biphenol occurred. When incubated with cell-free extracts of human and rabbit erythrocytes, rabbit reticulocytes, or Escherichia coli, most .OH-modified proteins were proteolytically degraded up to 50 times faster than untreated proteins. The exceptions were alpha-casein and globin, which were rapidly degraded without .OH modification. ATP did not stimulate the degradation of .OH-modified proteins, but alpha-casein was more rapidly degraded. Leupeptin had little effect under any condition, and degradation was maximal at pH 7.8. The data indicate that proteins which have been denatured by .OH can be recognized and degraded rapidly and selectively by intracellular proteolytic systems. In both red blood cells and E. coli, the degradation appears to be conducted by soluble, ATP-independent (nonlysosomal) proteolytic enzymes. In contrast with the above results, superoxide (O2-) did not cause aggregation or fragmentation, tryptophan loss, or bityrosine production. The combination of .OH + O2- (+O2), which may mimic biological exposure to oxygen radicals, induced charge changes, tryptophan loss, and bityrosine production. The pattern of such changes was similar to that seen with .OH alone, although the extent was generally less severe. In contrast with .OH alone, however, .OH + O2- (+O2) caused extensive protein fragmentation and little or no aggregation. More than 98% of the protein fragments had molecular weights greater than 5000 and formed clusters of ionic and hydrophobic bonds which could be dispersed by denaturing agents. The results indicate a general sensitivity of proteins to oxygen radicals. Oxidative modification can involve direct fragmentation or may provide denatured substrates for intracellular proteolysis.     

Investigation of supplemental ultraviolet-B-induced changes in antioxidative defense system and leaf proteome in radish (Raphanus sativus L. cv Truthful): an insight to plant response under high oxidative stress

Impact of supplemental UV-B (sUV-B) has been investigated on photosynthetic pigments, antioxidative enzymes, metabolites, and protein profiling of radish plants under realistic field conditions. Exposure of sUV-B leads to oxidative damage in plants. However, plants possess a number of UV-protection mechanisms including a stimulation of antioxidant defense system. It caused alteration in reactive oxygen species metabolism primarily by decreasing catalase activity vis-à-vis enhanced activities of other enzymatic (superoxide dismutase, ascorbate peroxidase, and glutathione reductase) and non-enzymatic (ascorbic acid) antioxidants. Qualitative analysis of samples also showed significant reductions in photosynthetic pigments and protein content. After sUV-B exposure, protein profile showed differences mainly at eight points—126.8, 84.8, 71.9, 61.5, 47.8, 40.6, 38.9, and 17.5 kDa, whereas protein(s) of 38.9 kDa showed increment. Results of the present investigation clearly showed the adverse effect of sUV-B on total biomass at final harvest.     

Does the presence of a seawater gill morphology induced by dietary salt loading affect Cl(-) uptake and acid-base regulation in freshwater rainbow trout Oncorhynchus mykiss

The goal of this study was to determine the effect of the changes in gill morphology induced by dietary salt feeding on several aspects of gill function in rainbow trout Oncorhynchus mykiss maintained in fresh water with specific emphasis on Cl(-) uptake (J(IN)Cl(-)) and acid-base regulation. The addition of 11% NaCl to the diet caused J(IN)Cl(-) to be reduced by c. 45% from 214·4 ± 26·7 to 117·3 ± 17·4 μmol kg(-1) h(-1) (mean ± s.e.). Rates of Cl(-) efflux (J(OUT)Cl(-)), net Cl(-) flux (J(NET)Cl(-)), J(NET) Na(+) and plasma levels of Na(+) or Cl(-) were unaffected by salt feeding. On the basis of significant effect of the salt diet on decreasing the maximal uptake rate of Cl(-)(J(MAX)Cl(-)), it would appear that internal salt loading caused a decrease in the number of functional ion transport proteins involved in Cl(-) uptake (e.g. Cl(-) -HCO(3)(-) exchangers) and decreased the transporting capacity of existing proteins. The acid-base regulating capacity of control fish and salt-loaded fish was assessed by monitoring arterial blood acid-base status [partial pressure of CO(2) (PCO(2)), pH and HCO(3)(-)] during exposure to external hypercapnia (nominally 7·5 mm Hg). Both groups of fish exhibited typical compensatory responses to sustained hypercapnia consisting of the gradual accumulation of plasma HCO(3) (-) and thus metabolic restoration within 24 h of the initial respiratory acidosis elicited by hypercapnia. Overall, the results demonstrate that while Cl(-) uptake capacity is reduced in salt-fed fish, there is no associated alteration in acid-base regulating capability.     

Trend in ambient ozone and an attempt to detect its effect on biota in forest ecosystem. Step I of Lithuanian studies

The presented study aimed to explore the relationships between ambient ozone (O3) and tree defoliation, specific diversity, and abundance of soil microarthropods, stream macroinvertebrates, and small mammals (mainly rodents) in order to test the hypothesis that changes in the considered objects of the forest ecosystem could be related to changes in ambient O3, concentration of which is below critical level. The observations were carried out from 1994 at three integrated monitoring stations. The obtained data revealed that only peak O3 concentrations (from 125-215 microg x m(-3)) had significant effect on changes in the considered components of forest biota.