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  • 1
    Online Resource
    Online Resource
    Cambridge :Cambridge University Press,
    Keywords: Acid-base equilibrium. ; Electronic books.
    Description / Table of Contents: A broad-ranging, authoritative and accessible review of exciting discoveries in acid-base regulation in animals and plants, together with a critical look at techniques and tools.
    Type of Medium: Online Resource
    Pages: 1 online resource (393 pages)
    Edition: 1st ed.
    ISBN: 9780511155185
    Series Statement: Society for Experimental Biology Seminar Series ; v.Series Number 68
    DDC: 571.75
    Language: English
    Note: Cover -- Half-title -- Series-title -- Title -- Copyright -- Contents -- Contributors -- Preface -- Measurement of intracellular pH: a comparison between ion-sensitive microelectrodes and fluorescent dyes -- Introduction -- Historical perspective on pHi measurement -- Weak acid and base distribution -- pH-sensitive electrodes -- Early electrodes -- Liquid ion-exchange pH-sensitive electrodes -- Using pH-sensitive microelectrodes -- pH-sensitive dyes -- Early dyes -- Fluorescent dyes -- Recent problems with dyes -- Assessing cell health -- Inhibition of transporters -- Contamination with ionophores -- Highs and lows of dyes and electrodes -- Recommendations for further reading -- Acknowledgements -- References -- pH-sensitive microelectrodes: how to use them in plant cells -- Introduction -- Technical considerations and experiences -- How to build and prepare a pH microelectrode -- Intracellular applications of the pH microelectrode -- Application of the pH microelectrode to physiological problems -- Light/dark responses of green plant cells -- Acid-base interactions -- Proton cotransport -- The proton motive force electrode -- Signal transduction -- pH regulation: the role of the H+ ATPase -- Vacuolar pH -- Extracellular applications of the pH microelectrode -- The pH of the apoplast -- The pH of the unstirred layer -- Signal transduction -- Conclusions -- References -- The use of nuclear magnetic resonance for examining pH in living systems -- Introduction -- Practical considerations -- Principles of NMR pH measurement -- NMR pH indicators -- Sources of error -- Applications in comparative physiology -- Applications in plant physiology -- Conclusions -- Acknowledgements -- References -- Invasive studies of intracellular acid-base parameters: quantitative analyses during environmental and functional stress -- Introduction. , A full set of acid-base parameters in whole-animal research -- Homogenate analyses of pHi -- Intracellular PCO2 and bicarbonate levels -- Cellular compartmentalisation -- Non-bicarbonate buffer values -- pH/bicarbonate analyses -- Interstitial pH -- Temperature and pHi -- Summary and conclusions -- Acknowledgements -- References -- Lactate, H+ and ammonia transport and distribution in rainbow trout white muscle after exhaustive exercise -- Introduction -- Methodology -- Post-exercise responses of the rainbow trout -- Problems in current understanding -- The isolated-perfused trout tail-trunk preparation -- Ammonia, H+m, and lactate distribution and transport in white muscle -- Acknowledgements -- References -- Limiting factors for acid-base regulation in fish: branchial transfer capacity versus diffusive loss of acid-base relevant… -- Introduction -- Regulatory mechanisms -- Buffering -- Adjustment of PCO2 -- Bicarbonate adjustment by ionic transfer -- Characteristics of acid-base regulation in fish -- Environmental hypercapnia -- Hyperoxia-induced and air-breathing-induced hypercapnia -- Air-breathing-induced hypercapnia -- Mechanisms and sites of transfer -- The role of the secondary circulatory system -- Ion transfer mechanisms of the secondary circulatory system -- Limitations of transfer -- Water ionic composition -- Plasma bicarbonate threshold -- Environmental Ca2+ -- Changes in transfer capacity versus diffusive loss -- Conclusion -- References -- H+-mediated control of ion channels in guard cells of higher plants -- Introduction -- Shortfalls in the Ca2+ model -- The pHi signal -- Universality of the pHi signal -- Channel sensitivity to pHe -- Origin of changes in pHi -- Is the pHi signal G-protein coupled? -- pHi interaction with [Ca2+]i -- Factors affecting pHi signal transmission -- Conclusion -- Acknowledgements -- References. , pH regulation of plants with CO2-concentrating mechanisms -- Introduction -- Diffusive entry of CO2 and acid-base regulation -- Evidence for the occurrence of CO2-concentrating mechanisms and for the inorganic carbon species entering cells during the… -- Gas exchange data -- Estimation of intracellular inorganic carbon concentrations -- Inorganic carbon species entering the cell when CO2-concentrating mechanisms are operating -- Mechanisms of CO2-concentrating mechanisms and their implications for acid-base regulation -- Crassulacean acid metabolism -- C4 pathway -- CO2-concentrating mechanisms based on active transport across membranes -- CO2-concentrating mechanisms based on active transport of inorganic carbon across membranes -- CO2-concentrating mechanisms based on HCO3- to CO2 conversion in compartments whose pH is lower than that of compartments… -- Conclusions -- Acknowledgements -- References -- Intracellular pH regulation in plants under anoxia -- Introduction -- Cytoplasmic pH changes under anoxia -- Biochemical pH regulation under anoxia -- Biophysical pH regulation under anoxia -- Conclusions -- Acknowledgements -- References -- The role of turtle shell in acid-base buffering -- Introduction -- Acid buffering by the mammalian skeleton -- The turtle shell -- Structural features of the shell -- Functional features of the shell -- Anoxic tolerance of turtles -- Acid-base consequences of prolonged anoxia -- Shell mechanism 1: export of buffer to the extracellular fluid -- Shell mechanism 2: storage of lactate within the shell -- Issues related to the results and methodologies -- In vivo versus in vitro observations -- Contribution of the shell to total lactic acid buffering -- Conclusions -- Acknowledgements -- References -- Acid-base regulation in crustaceans: the role of bicarbonate ions -- Introduction -- Aerial exposure -- Moult cycle. , Temperature -- Methodology -- Mechanisms of HCO3- transfer between body compartments -- Acknowledgements -- References -- A novel role for the gut of seawater teleosts in acid-base balance -- Introduction -- Sites for the transfer of acid-base relevant ions in fish -- The gills -- The kidney -- The skin -- The gut -- Evidence for a role of the gut in acid-base regulation in seawater teleosts -- Gut base excretion as a general feature of seawater teleosts -- Site of intestinal base secretion -- Ion transport mechanisms involved in intestinal base secretion -- Possible functions and repercussions of intestinal base secretion -- Conclusions -- Acknowledgements -- References -- pH and smooth muscle: regulation and functional effects -- Introduction -- Techniques used to measure pH in smooth muscles -- Intracellular buffering power -- pH regulation in smooth muscle -- Ureteric smooth muscle -- Recovery from an acid load -- Recovery from alkaline load -- Vascular smooth muscle -- Recovery from an acid load -- Recovery from an alkaline load -- The importance of the Na+-H+ exchanger in smooth muscle -- A comparison of the role of Na+-H+ exchange in three smooth muscles -- The effects of species, development stage and gestational state on pHi regulation -- Species -- Development -- Gestation -- Agonists and pHi -- Contraction and pHi -- Extracellular pH -- Contractile responses to pHi change -- A comparison of the effects of pHi alteration in three smooth muscles -- Uterus -- Ureter -- Stomach -- Summary and future research -- Acknowledgements -- References -- Regulation of pH in vertebrate red blood cells -- Introduction -- Methods used to measure red blood cell pH -- Theoretical considerations -- Steady-state ion distributions and red blood cell pH -- Addition of CO2 or metabolic acid to the blood. , Potential for red blood cell pH regulation via secondarily active ion transport -- Agnathans -- Gnathostome fishes -- Teleosts -- Non-teleosts -- Amphibians -- Birds and mammals -- Conclusions -- References -- Acid-base regulation in hibernation and aestivation -- Introduction: from water to air breathing -- Reduction of metabolic rate -- Respiratory acidosis -- Methods applicable to hibernation and aestivation -- Isothermal acid-base changes -- Alkalinity relative to water -- The dissociation of protein imidazole groups -- The closed system approach -- Extracellular acid-base data in hibernation -- Intermittent breathing -- Changes in relative ventilation -- Intracellular compartments -- Effects of acidosis -- Conclusions -- References -- Hepatic metabolism and pH in starvation and refeeding -- Introduction -- Hormonal action, volume change and pHi in hepatocytes -- The relevance of interactions between insulin action, cell volume and pHi in the liver -- Examples of effects of pHi on energy metabolism in hepatocytes -- Inferences about changes in pHi in the liver during the absorptive phase -- Acknowledgements -- References -- Back to basics: a plea for a fundamental reappraisal of the representation of acidity and basicity in biological solutions -- Introduction -- Theoretical considerations -- The distribution of pH and {H+} in biological solutions -- The modulation of haemocyanin-O2 affinity -- The regulation of acid-base status -- A scale for representing acid-base status -- Conclusions -- Acknowledgements -- References -- Index.
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  • 2
    ISSN: 1432-1793
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Seasonal variations and the effect of reproductive development on resource acquisition by two intertidal fucoid species, the iteroparous Fucus serratus L. and the semelparous Himanthalia elongata (L.) S. F. Gray were examined. The oxygen-exchange characteristics of vegetative apical tissue of both non-fertile and fertile plants and receptacle tissue were compared at monthly intervals throughout reproductive development. Respiratory rates in non-fertile F. serratus varied seasonally between 1.5 and 8.0 μmol g−1 fresh wt h−1; in fertile plants the receptacle had a significantly lower respiratory rate than the vegetative tissue. The respiratory rate of the vegetative button of fertile H. elongata displayed less seasonal variation and was lower than that of the receptacle, which varied from a maximum of 9.5 μmol g−1 fresh wt h−1 at receptacle initiation in October to a minimum of 2.0 μmol g−1 fresh wt h−1 in February. The maximum photosynthetic rate (P max) of non-fertile plants of both species did not vary in a distinct seasonal manner (∼60 μmol g−1 fresh wt h−1 for F. serratus and ∼12 μmol g−1 fresh wt h−1 for H. elongata). In fertile plants, the P max of the receptacle tissue was (∼50% lower in F. serratus, and at its peak three times higher in H. elongata, than that of vegetative tissue. The stable carbon-isotope ratio (δ13C) did not differ between different tissue types in F. serratus, but values did vary seasonally, being less negative in the summer than in the winter (−13.5‰ compared to −18‰). The receptacle tissue of H. elongata also displayed a distinct seasonal variation in δ13C values (−12‰ in summer, −16‰ in winter), whilst the δ13C of the vegetative button did not vary seasonally. The rate of uptake of inorganic nitrogen by the vegetative thallus was lower in H. elongata than in F. serratus. The receptacle tissue of F. serratus had lower uptake rates than the vegetative tissue, whilst the uptake rate by H. elongata receptacle tissue was higher than that of the vegetative button.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 6 (1971), S. 89-107 
    ISSN: 1432-1424
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary The effects of various inhibitors on photosynthesis, respiration, and active influx of K and Cl in light and dark inHydrodictyon africanum is reported. The inhibitors used were arsenate (uncouples electron-transport phosphorylations), dicyclohexylcarbodiimide (energy-transfer inhibitor in electron-transport phosphorylation), quinacrine (uncouples photophosphorylation and inhibits oxidative phosphorylation), and ethionine (traps adenylates as S-adenosyl ethionine). The action of these inhibitors, and of those previously used onHydrodictyon africanum, suggests that K influx requires ATP, while Cl influx requires some earlier manifestation of the ATP synthesizing process. Possible reasons for the greater sensitivity of K influx than of CO2 fixation to treatments which interfere with photophosphorylation are discussed.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Plant Physiology 30 (1979), S. 289-311 
    ISSN: 0066-4294
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 415 (2002), S. 375-377 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Higher plants can be divided into two groups — C3 and C4 — according to which biochemical route they use to produce their food from water and carbon dioxide (the numbers simply refer to carbon atoms in the initial photosynthetic product). Over 85% of higher plants ...
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science, Ltd
    Plant, cell & environment 26 (2003), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Many macroalgae have significant spatial differentiation involving higher rate resource use at a site than of acquisition of that resource from the environment at that site. Long-distance symplasmic transport of solutes occurs in some large green algae where the solutes are moved in streaming cytoplasm. In some large brown algae there is evidence of long-distance symplasmic transport of organic C and other solutes. Structural and physiological data suggest that while the transport in ‘sieve tubes’ of Macrocystis might be by a Munch pressure flow mechanism the transport in many other brown algae is less likely to be by this mechanism. Less is known of long-distance symplasmic transport in red algae. In terrestrial bryophytes transpiration occurs and in some liverworts and many mosses (but not in hornworts) there are files of dead cells in their tissues which may, and in some cases certainly, function in long-distance apoplasmic water transport. The hydraulic conductivity of these conduits is poorly characterized. Long-distance symplasmic transport in some mosses have been characterized both structurally and physiologically, but in other mosses and in liverworts the evidence is only structural. Most of these symplasmic transport pathways seem to have a high resistance to flow.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd.
    Plant, cell & environment 22 (1999), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Submerged aquatic macrophytes growing in water where free CO2 is unavailable (above pH 8·2) must use mechanisms to supply external dissolved inorganic carbon in a form available to chloroplasts (CO2). Active transport of HCO3– across the plasmalemma has not been proven to be widespread in aquatic macrophytes and catalytic conversion of HCO3– to CO2 is the usual supply mechanism in submerged macrophytes. The interaction of leaf form and function in this respect was investigated in the linear, submerged leaves of Ranunculus penicillatus (Dumort.) Bab ssp. pseudofluitans (Syme) S.Webster. Viable protoplasts were isolated using a mixture of cell wall degrading enzymes optimized for this species. Protoplast viabilities greater than 80% after 5 h of isolation were achieved. Photosynthetic rates of isolated protoplasts were comparable with that of intact plant tissue. Results of carbon isotopic disequilibrium experiments showed that CO2 was the preferred species of dissolved inorganic carbon for photosynthesis by protoplasts and that HCO3– which predominates in the plant’s natural environment mainly contributes by supplying CO2 outside the cells.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 22 (1999), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: There is approximately 50 times more inorganic carbon in the global ocean than in the atmosphere. On time scales of decades to millions of years, the interaction between these two geophysical fluids determines atmospheric CO2 levels. During glacial periods, for example, the ocean serves as the major sink for atmospheric CO2, while during glacial–interglacial transitions, it is a source of CO2 to the atmosphere. The mechanisms responsible for determining the sign of the net exchange of CO2 between the ocean and the atmosphere remain unresolved. There is evidence that during glacial periods, phytoplankton primary productivity increased, leading to an enhanced sedimentation of particulate organic carbon into the ocean interior. The stimulation of primary production in glacial episodes can be correlated with increased inputs of nutrients limiting productivity, especially aeolian iron. Iron directly enhances primary production in high nutrient (nitrate and phosphate) regions of the ocean, of which the Southern Ocean is the most important. This trace element can also enhance nitrogen fixation, and thereby indirectly stimulate primary production throughout the low nutrient regions of the central ocean basins. While the export flux of organic carbon to the ocean interior was enhanced during glacial periods, this process does not fully account for the sequestration of atmospheric CO2. Heterotrophic oxidation of the newly formed organic carbon, forming weak acids, would have hydrolyzed CaCO3 in the sediments, increasing thereby oceanic alkalinity which, in turn, would have promoted the drawdown of atmospheric CO2. This latter mechanism is consistent with the stable carbon isotope pattern derived from air trapped in ice cores. The oceans have also played a major role as a sink for up to 30% of the anthropogenic CO2 produced during the industrial revolution. In large part this is due to CO2 solution in the surface ocean; however, some, poorly quantified fraction is a result of increased new production due to anthropogenic inputs of combined N, P and Fe. Based on ‘circulation as usual’, models predict that future anthropogenic CO2 inputs to the atmosphere will, in part, continue to be sequestered in the ocean. Human intervention (large-scale Fe fertilization; direct CO2 burial in the deep ocean) could increase carbon sequestration in the oceans, but could also result in unpredicted environmental perturbations. Changes in the oceanic thermohaline circulation as a result of global climate change would greatly alter the predictions of C sequestration that are possible on a ‘circulation as usual’ basis.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 9 (1986), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract The patterns of naturally growing ion currents associated with horizontally growing roots of Trifolium repens L. seedlings were measured in a simple low-salt bathing medium using a highly sensitive vibrating electrode. Current consistently enters the main elongation zone of the root and leaves from mature, elongated tissue. This current enters and leaves with densities of ca. 4.0–11.0 mA m−2 and 4.0 mA m−2, respectively. Current was also delected entering the zone of emerging root hairs and also the root-hair tips themselves.These results are a further example of the involvement of self-generated electrical fields in plant developmental processes. Possible, secondary rhizosphere-associated effects of the extracellular loop of the developmental current are also suggested.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 20 (1997), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: A testable mechanism of CO2 accumulation in photolithotrophs, originally suggested by Pronina & Semenenko, is quantitatively analysed. The mechanism involves (as does the most widely accepted hypothesis) the delivery of HCO3− to the compartment containing Rubisco. It differs in proposing subsequent HCO3− entry (by passive uniport) to the thylakoid lumen, followed by carbonic anhydrase activity in the lumen; uncatalysed conversion of HCO3− to CO2, even at the low pH of the lumen, is at least 300 times too slow to account for the rate of inorganic C acquisition. Carbonic anhydrase converts the HCO3− to CO2 at the lower pH maintained in the illuminated thylakoid lumen by the light-driven H+ pump, generating CO2 at 10 times or more the thylakoid HCO3− concentration. Efflux of this CO2 can suppress Rubisco oxygenase activity and stimulate carboxylase activity in the stroma. This mechanism differs from the widely accepted hypotheses in the required location of carbonic anhydrase, i.e. in the thylakoid lumen rather than the stroma or pyrenoid, and in the need for HCO3− influx to thylakoids. The capacity for anion (assayed as Cl−) entry by passive uniport reported for thylakoid membranes is adequate for the proposed mechanism; if the Cl− channel does not transport HCO3−, HCO3− entry could be by combination of the Cl− channel with a Cl− HCO3− antiporter. This mechanism is particularly appropriate for organisms which lack overt accumulation of total inorganic C in cells, but which nevertheless have the gas exchange characteristics of an organism with a CO2-concentrating mechanism.
    Type of Medium: Electronic Resource
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