Plant, Cell and Environment 1992: Vol 15 Index

13 Pages·1992·2.6 MB·English

Plant, Cell and Environment (1992) 15
Author index
Adams III W. W. (see Demmig-Adams B.), 411. Carter J. V. (see Chu B.), 307.
Adcock M. D. (see Quick W. P.), 25. Chaves M. M. (see Quick W. P.), 25.
Allen L. H. (see Baker J. T.), 231. Chen J. M. & Black T. A. Defining leaf area index for non-flat
Amory A. M., Ford L., Pammenter & Cresswell C. F. The use of 3- leaves, 421.
amino-1,2.4-triazole to investigate the short-term effects of oxy- Chow W. S. (see Jordan B. R.), 91.
gen toxicity on carbon assimilation by Pisum sativum seedlings, Chu B., Xin Z., Li P. H. & Carter J. V. Depolymerization of corti-
655. cal microtubules is not a primary cause of chilling injury in corn
Anderson J. M. (see Jordan B. R.), 91. (Zea mays L. cv Black Mexican Sweet) suspension culture cells,
Appenroth K.-J., Augsten H. & Mohr H. Photophysiology of turion 307.
germination in Spirodela polyrhiza (L.) Schleiden. X. Role of Clarkson D. T., Jones L. H. P. & Purves J. V. Absorption ofn itrate
nitrate in the phytochrome-mediated response, 743. and ammonium ions by Lolium perenne from flowing solution
Arif I. (see Ryan P. R.), 675. cultures at low root temperatures, 99.
Amold W. M. (see Rygol J.), 11. Coley P. D. (see Kursar T. A.), 901.
Arredondo- Vega B. O. (see Band C. J.), 129. Colombo S. J. & Blumwald E. Electrical impedance of white
Ashenden T. W., Baxter R. & Rafarel C. R. An inexpensive system spruce shoots in relation to pressure-volume analysis and free
for exposing plants in the field to elevated concentrations of sugar content, 837.
CO;, 365. Comparini C. (see Pandolfini T.), 719.
Ashworth E. N., Willard T. J. & Malone S. R. The relationship Conroy S. J.. Milham P. J. & Barlow E. W. R. Effect of nitrogen
between vascular differentiation and the distribution of ice and phosphorus availability on the growth response of Eucalyp-
within Forsythia flower buds, 607. tus grandis to high CO,, 849.
Atkins R. S. (see Walsh K. B.), 849. Cooper T. A. (see Ehleringer J. R.), 301.
Augsten H. (see Appenroth K.-J.), 743. Cortes P. M. Analysis of the electrical coupling of root cells: impli-
Axelson R. D. (see Glenn E. P.), 711. cations for ion transport and the existence of an osmotic pump,
Azcon-Bieto J. (see Peftuelas J.), 485. 351.
Cresswell C. F. (see Amory A. M.), 655.
Baker J. T., Laugel F., Boote K. J. & Allen L. H., Jr. Effects of day- Crisosto G. M. (see Meinzer F. C.), 471.
time carbon dioxide concentration on dark respiration in rice, Crowe J. H. (see Hoekstra F. A.), 601.
231. Crowe L. M. (see Hoekstra F. A.), 601.
Ball E. (see Franco A. C.), 821. Cure J. D. (see Rodgers H. H.), 749.
Band C. J., Arredondo-Vega B. O., Vazquez-Duhalt R. & Greppin
H. Effect of salt-osmotic upshock on the edaphic microalga David M. (see Quick W. P.), 25.
Neochloris oleoabundans, 129. Davies W. J. (see Tardieu F.), 185.
Barlow E. W. R. (see Conroy S. J.), 849. Davies W. J. (see Tardieu F.), 193.
Baxter R. (see Ashenden T. W.), 365. Dawson T. E. (see Ehleringer J. R.), 1073.
Beevers H. (see Kwon D.-K.), 939. Day T. A. (see DeLucia E. H.), 921.
Bengough A. G. (see Gordon D. C.), 123. De GreefJ . A. (see Dedonder A.), 479.
Bergkotte M. (see Poorter H.), 221. Dedonder A., Rethy R., Fredericq H. & De Greef J. A. Phy-
Bethenod O. (see Tardieu F.), 193. tochrome-mediated changes in the ATP content of Kalanchoé
Bieleski R. L. & Liuchli A. Phosphate uptake, efflux and defi- blossfeldiana seeds, 479.
ciency in the water fern, Azolla, 665. DeLucia E. H., Day T. A. & Vogelman T. C. Ultraviolet-B and vis-
Bisson M. A. (see Yao X.), 199. ible light penetration into needles of two species of subalpine
Black R. A. (see Evans R. D.), 49. conifers during foliar development, 921.
Black T. A. (see Chen J. M.), 421. Delves A. C., Higgins A. & Gresshoff P. Shoot apex removal does
Blumwald E. (see Colombo S. J.), 837. not alter autoregulation of nodulation in soybean, 249.
Boote K. J. (see Baker J. T.), 231. Demmig-Adams B. & Adams II] W. W. Carotenoid composition in
Borland A. M. (see Maxwell C.), 37. sun and shade leaves of plants with different life forms, 411.
Bréda N. (see Epron D.), 809. Dixon M. A. (see Johnson R. W.), 947.
Briggs W. R. What remains of the Cholodny-Went theory? It’s Dreyer E. (see Epron D.), 809.
alive and well in maize, 763. Dring M. J. (see Forster R. M.), 241.
Broadmeadow M. S. J. (see Maxwell C.), 37. Dunn M. A. (see Hughes M. A.), 861.
Bruinsma J. What remains of the Cholodny-Went theory? A phan-
tom in phototropism, 765. Ehleringer J. R. & Cooper T. A. On the role of orientation in reduc-
Brzezicki L. J. (see Yao X.), 199. ing photoinhibitory damage in photosynthetic-twig desert
Bunce J. A. Stomatal conductance, photosynthesis and respiration shrubs, 301.
of temperature deciduous tree seedlings grown outdoors at an Ehleringer J. R. & Dawson T. E. Water uptake by plants: perspec-
elevated concentration of carbon dioxide, 541. tives from stable isotope composition, 1073.
Busso C. A. & Richards J. H. Diurnal variation in the temperature Ehleringer J. R. (see Flanagan L. B.), 831.
response of leaf extension of the two bunchgrass species in the Epron D., Dreyer E. & Bréda N. Photosynthesis of oak trees [Quer-
field, 855. cus petraea (Matt.) Liebl.] during drought under field condi-
tions: diurnal course of net CO, assimilation and photochemical
Cakmak I. & Marschner H. Magnesium deficiency enhances resis- efficiency of photosystem II, 809.
Ertel J., Paretzke H. G. & Ziegler H. '*’Cs penetration by contact
x Author index
exchange through isolated plant cuticles: cuticles as asymmetric Hecks B., Hejnowicz Z. & Sievers A. Spontaneous oscillations of
transport membranes, 211. extracellular electrical potentials measured on Lepidium sativum
Evans M. L. What remains of the Cholodny-Went theory? 767. L. roots, 115.
Evans R. D., Black R. A., Loescher W. H. & Fellows R. J. Osmotic Hejnowicz Z. (see Hecks B.), 115.
relations of the drought-tolerant shrub Artemisia tridentata in Henderson S. A. (see Peisker M.), 987.
response to water stress, 49. Hertel R. What remains of the Cholodny-Went theory? All, but it is
only a partial answer within the larger mechanism of tropism,
Farquhar G. D. (see Lloyd J.), 873. Tit.
Fellows R. J. (see Evans R. D.), 49. Hettiaratchi D. R. P. (see Gordon D. C.), 123.
Firn R. What remains of the Cholodny-Went theory? Which one? Higgins A. (see Delves A. C.), 249.
769. Hinckley T. M. (see Salleo S.), 491.
Flanagan L. B., Ehleringer J. R. & Marshall J. D. Differential Hoekstra F. A., Crowe J. H., Crowe L. M., van Roekel T. & Ver-
uptake of summer precipitation among co-occurring trees and meer E. Do phospholipids and sucrose determine membrane
shrubs in a pinyon-juniper woodland, 831. phase transitions in dehydrating pollen species? 601.
Ford L. (see Amory A. M.), 655. Hofmann B. (see Schafer C.), 343.
Forseth I. N. (see Kao W.-Y.), 703. Holbrook N. M. & Sinclair T. R. Water balance in the arborescent
Forster R. M. & Dring M. J. Interactions of blue light and inorganic palm, Sabal palmetto. 1. Stem structure, tissue water release
carbon supply in the control of light-saturated photosynthesis in properties and leaf epidermal structure, 393.
brown algae, 241. Holbrook N. M. & Sinclair T. R. Water balance in the arborescent
Franco A. C., Ball E. & Liittge U. Differential effects of drought palm, Sabal palmetto. Il. Transpiration and stem water storage,
and light levels on accumulation of citric and malic acids during 401.
CAM in Clusias, 821. Homann P. H. (see Muslin E. H.), 81.
Fredericq H. (see Dedonder A.), 479. Hughes M. A., Dunn M. A., Pearce R. S., White A. J. & Zhang L.
Fry B. (see Trust B. A.), 1105. An abscisic-acid-responsive, low temperature barley gene has
Fryer M. L. The antioxidant effects of thylakoid Vitamin E (a- homology with a maize phospholipid transfer protein, 861.
tocopherol), 381.
Idso S. B. & Kimball B. A. Seasonal fine-root biomass develop-
Gaal I. (see Lehoczki E.), 531. ment of sour orange trees grown in atmospheres of ambient and
Gabbrielli R. (see Pandolfini T.), 719. elevated CO, concentration, 337.
Gamalei Y. V. (see Van Bel A. J. E.), 265. lino M. What remains of the Cholodny-Went theory? Lateral auxin
Garcia-Moya E. (see Nobel P. S.), 329. translocation as a key step mediating light-gradient perception
Geng X. M. (see Laroche A.), 439. and phototropic differential growth, 773.
Gersani M. & Sachs T. Developmental correlations between roots Iwasaki N. (see Okazaki Y.), 61.
in heterogeneous environments, 463.
Glenn E. P., Watson M. C., O’Leary J. W. & Axelson R. D. Com- Jansson S. Cytokinins and tRNAs: arguments against a hypothesis
parison of salt tolerance and osmotic adjustment of low-sodium of cytokinin action, 503.
and high-sodium subspecies of the C, halophyte, Afriplex Jarvis M. C. Self-assembly of plant cell walls, 1.
canescens, 711. Johnson R. W., Dixon M. A. & Lee D. R. Water relations of the
Godwin P. B. (see Shepherd V. A.), 137. tomato during fruit growth, 947.
Godwin P. B. (see Shepherd V. A.), 152. Jones A. M. What remains of the Cholodny-Went theory? Assy-
Goldstein G. (see Meinzer F. C.), 471. metric redistribution of auxin need only occur over the distance
Gollan T., Schurr U. & Schulze E.-D. Stomatal response to drying of one cell width, 775.
soil in relation to changes in the xylem sap composition of Jones L. H. P. (see Clarkson D. T.), 99.
Helianthus annuus. 1. The concentration of cations, anions, Jordan B. R., He J., Chow W. S. & Anderson J. M. Changes in
amino acids in, and pH of, the xylem sap, 551 mRNA levels and polypeptide subunits of ribulose-1,5-bisphos-
Gollan T. (see Schurr U.), 561. phate carboxylase in response to supplementary ultraviolet-B
Gonzalez-Utor A. L. (see Sanchez-Aguayo I.), 867. radiation, 91.
Gordon D. C., Hettiaratchi D. R. P., Bengough A. G. & Young I.
M. Non-destructive analysis of root growth in porous media, Kao W.-Y. & Forseth I. N. Diurnal leaf movement, chlorophyll flu-
123. orescence and carbon assimilation in soybean grown under
Gow N. A. R. (see Morris B. M.), 645. nitrogen and water availabilities, 703.
Grantz D. A. (see Meinzer F. C.), 471. Katerji N. (see Tardieu F.), 193.
Greppin H. (see Band C. J.), 129. Keeley J. E. & Sandquist D. R. Carbon: freshwater plants, 1021.
Gresshoff P. (see Delves A. C.), 249. Kikuta S. B. (see Salleo S.), 491.
Griffiths H. Carbon isotope discrimination and the integration of Kimball B. A. (see Idso S. B.), 337.
carbon assimilation pathways in terrestrial CAM plants, 1051. Kluge M. (see Malsy S.), 519.
Griffiths H. (see Maxwell C.), 37. Koerselman-Kooij J. W. (see Wolswinkel P.), 617.
Guy R. (see Vonshak A.), 613. Kriedmann P. E. (see Lloyd J.), 873.
Kursar T. A. & Coley P. D. The consequences of delayed greening
Handley L. L. & Raven J. A. The use of natural abundance of nitro- during leaf development for light absorption and light use effi-
gen isotopes in plant physiology and ecology, 965. ciency, 901.
Harley P. C., Thomas R. B., Reynolds J. F. & Strain B. R. Mod- Kwon D.-K. & Beevers H. Growth of of Sesbana rostrata (Brem)
elling photosynthesis of cotton grown in elevated CO,, 271. with stem nodules under controlled conditions, 939.
Hartung W. (see Malsy S.), 519.
Harvey D. M. R. (see Pihakaski-Maunsbach K.), 586. Laroche A., Geng X. M. & Singh J. Differentiation of freezing tol-
He J. (see Jordan B. R.), 91. erance and vernalization responses in Cruciferae exposed to a
Author index xi
low temperature, 439.
Larsson M. Translocation of nitrogen in osmotically stressed wheat Nantawisarakul T. & Newman I. A. Growth and gravitropism of
seedlings, 447. cor roots in solution, 693.
Laskay G. (see Lehoczki E.), 531. Neufeld H. S. (see Meinzer F. C.), 471.
Liauchli A. (see Bieleski R. L.), 665. Newman I. A. (see Nantawisarakul T.), 693.
Laugel F. (see Baker J. T.), 231. Newman I. A. (see Ryan P. R.), 675.
Lee D. R. (see Johnson R. W.), 947. Nilsen E. T. The influence of water stress on leaf and stem photo-
Leegood R. C. (see Quick W. P.), 25. synthesis in Spartium junceum L., 457.
Lehoczki E., Laskay G., Gaal I. & Szigeti Z. Mode of action of Nobel P. S., Garcia-Moya E. & Quero E. High annual productivity
paraquat in leaves of paraquat-resistant Conyza canadensis (L.) of certain agaves and cacti under cultivation, 329.
Crongq., 531.
Leopold A. C. What remains of the Cholodny-Went theory? Valid Okazaki Y. & Iwasaki N. Net efflux of Cl’ during hypotonic turgor
but not universal, 777. regulation in a brackish water alga Lamprothamnium, 61.
Li P. H. (see Chu B.), 307. O'Leary J. W. (see Glenn E. P.), 711.
Lin C. H. & Lin C. H. Physiological adaptation of waxapple to O’Leary M. H., Madhavan S. & Paneth P. Physical and chemical
waterlogging, 321. basis of carbon isotope fractionation in plants, 1099.
Lin C. H. (see Lin C. H.), 321. Overall R. L. (see Reid R. J.), 507.
Lloyd J., Syvertsen J. P., Kriedmann P. E. & Farquhar G. D. Low
conductances for CO, diffusion from stomata to the sites of car- Palmer S. (see Tardieu F.), 193.
boxylation in leaves of woody species, 873. Pammenter N. W. (see Amory A. M.), 655.
Lo Gullo M. A. & Salleo S. Water storage in the wood and xylem Pandolfini T., Gabbrielli R. & Comparini C. Nickel toxicity and
cavitation in |-year-old twigs of Populus deltoides Batr., 431. peroxidase activity in seedlings of Triticum aestivum L., 719.
Lo Gullo M. A. (see Salleo S.), 491. Paneth P. (see O'Leary M. H.), 1099.
Loescher W. H. (see Evans R. D.), 49. Paretzke H. G. (see Ertel J.), 211.
Low C. S. (see Walsh K. B.), 849. Passaharino J. A. (see Quick W. P.), 25.
Liittge U. (see Franco A. C.), 821. Pearce D. W. (see Singh S.), 373.
Pearce R. S. (see Hughes M. A.), 861.
Maberly S. C. Carbonate ions appear to neither inhibit nor stimu- Pearcy R. W. (see Pons T. L.), 569.
late use of bicarbonate ions in photosynthesis by Ulva lactuca, Pearcy R. W. (seg Pons T. L.), 577.
250: Peisker M. & Henderson S. A. Carbon: terrestrial C, plants, 987.
McCrimmon J. N. (see Rodgers H. H.), 749. Pefiuelas J. & Azc6n-Bieto J. Changes in leaf A'*C of herbarium
McDavid C. R. (see Maxwell C.), 37. plant species during the last 3 centuries of CO, increase,
McDonald A. J. S. (see Petterson R.), 911. 485.
McDonald A. J. S. (see Sands R.), 107. Pereira J. S. (see Quick W. P.), 25.
Madhavan S. (see O'Leary M. H.), 1099. Peterson C. M. (see Rodgers H. H.), 749.
Malone S. R. (see Ashworth E. N.), 607. Petterson R. & McDonald A. J. S. Effects of elevated carbon diox-
Malsy S., van Bel A. J. E., Kluge M., Hartung W. & Ullrich C. I. ide concentration on photosynthesis and growth of small birch
Induction of crown galls by Agrobacterium tumefaciens (strain plants (Betula pendula Roth.) at optimal nutrition, 911.
C58) reverses assimilate translocation and accumulation in Pihakaski-Maunsbach K. & Harvey D. M. R. X-ray microanalyti-
Kalanchoe daigremontiana, 519. cal (EDX) investigation of potassium distributions in mesophyll
Marschner H. (see Cakmak I.), 955. cells of non-acclimated and cold-acclimated rye leaves, 586.
Marshall J. D. (see Flanagan L. B.), 831. Pilet P. E. What remains of the Cholodny-Went theory? IAA in
Martin G. J., Martin M. L. & Zhang B.-L. Site-specific natural iso- growing and gravireacting maize roots, 779.
tope fractionation of hydrogen in plant products studied by Poff K. L. What remains of the Cholodny-Went theory? Present
nuclear magnetic resonance, 1037. status, 781.
Martin M. L. (see Martin G. J.), 1037. Pons T. L., Pearcy R. W. & Seemann J. R. Photosynthesis in flash-
Masterson C., Wood C. & Thomas D. R. B-oxidation enzymes and ing light in soybean leaves grown in different conditions. 1. Pho-
the carnitine-dependent oxidation of palmitate and palmitoyl tosynthetic induction state and regulation of ribulose-|,5-bis-
CoA in mitochondria from avocado, 313. phosphate carboxylase activity, 569.
Maxwell C., Griffiths H., Borland A. M., Broadmeadow M. S. J. & Pons T. L. & Pearcy R. W. Photosynthesis in flashing light in soy-
McDavid C. R. Photoinhibitory responses of the epiphytic bean leaves grown in different conditions. II. Lightfleck utiliza-
bromeliad Guzmania monostachia during the dry season in tion efficiency, 577.
Trinidad maintain photochemical integrity under adverse condi- Poorter H. & Bergkotte M. Chemical composition of 24 wild
tions, 37. species differing in relative growth rate, 221.
Meinzer F. C., Goldstein G., Neufeld H. S., Grantz D. A. & Powell C. E. (see Ryle G. J. A.), 593.
Crisosto G. M. Hydraulic architecture of sugarcane in relation to Preston T. The measurement of stable isotope natural abundance
patterns of water use during plant development, 471. variations, 1091.
Merckx R. (see Smolders E.), 795. Purves J. V. (see Clarkson D. T.), 99.
Milham P. J. (see Conroy S. J.), 849.
Mohr H. (see Appenroth K.-J.), 743. Quero E. (see Nobel P. S.), 329.
Morris B. M., Reid B. & Gow N. A. R. Electrotaxis of zoospores of Quick W. P., Chaves M. M., Wendler R., David M., Rodrigues M.
Phytophthora palmivora at physiologically relevant field L., Passaharino J. A., Pereira J. S., Adcock M. D., Leegood R. C.
strengths, 645. & Stitt M. The effect of water stress on photosynthetic carbon
Muslin E. H. & Homann P. H. Light as a hazard for the dessicca- metabolism in four species grown under field conditions, 25.
tion-resistant ‘resurrection’ fern Polypodium polypodioides L.,
81. Rafarel C. R. (see Ashenden T. W.), 365.
xii Author index
Raven J. A. Present and potential uses of the natural abundance of cause and effect relationships in root gravitropism, 787.
stable isotopes in plant science, with illustrations from the Seemann J. R. (see Pons T. L.), 569.
marine environment, 1083. Seivers A. & Zieschang H. E. What remains of the Cholodny-Went
Raven J. A. (see Handley L. L.), 965. theory? It does not fit the growth pattern of cells during bending
Reid B. (see Morris B. M.), 645. of a root, 789.
Reid R. J. & Overall R. L. Intercellular communication in Chara: Senden M. H. M. N., Van Paassen F. J. M., Van der Meer A. J. G.
factors affecting transnodal electrical resistance and solute fac- M. & Wolterbeek H. Th. Cadmium — citric acid — xylem cell
tors, 507. wall interactions in tomato plants, 71.
Rengel Z. Disturbance of cell Ca** homeostasis as a primary trig- Shepherd V. A. & Godwin P. B. Seasonal patterns of cell-to-cell
ger of Al toxicity syndrome, 931. communication in Chara corallina Klein ex Willd. 1. Cell-to-
Rengel Z. The role of calcium in salt toxicity, 625. cell communication in vegetative lateral branches during winter
Rethy R. (see Dedonder A.), 479. and spring, 137.
Reynolds J. F. (see Harley P. C.), 271. Shepherd V. A. & Godwin P. B. Seasonal patterns of cell-to-cell
Richards J. H. (see Busso C. A.), 855. communication in Chara corallina Klein ex Willd. II. Cell-to-
Richter H. (see Salleo S.), 491. cell communication during the development of antitherida, 151.
Ritchie R. J. Kinetics of chloride transport in the cyanobacterium Sievers A. (see Hecks B.), 115.
Synechococcus R-2 (Anacystis nidulans, S. leopoliensis) PCC Simper H. (see Schafer C.), 343.
179, 7942, 179. Sinclair T. R. (see Holbrook N. M.), 393.
Ritchie R. J. The cyanobacterium Synechococcus R-2 (Anacystis Sinclair T. R. (see Holbrook N. M.), 401.
nidulans, S. leopoliensis) PCC 7942 has a sodium-dependent Singh J. (see Laroche A.), 439.
chloride transporter, 163. Singh S., Sawhney V. K. & Pearce D. W. Temperature effects on
Rodgers H. H., Peterson C. M., McCrimmon J. N. & Cure J. D. endogenous indole-3-acetic acid levels in leaves and stamens of
Response of plant roots to elevated atmospheric carbon dioxide, the normal and male sterile ‘stamenless-2’ mutant of tomato
749. (Lycopersicon esculentum Mill.), 373.
Rodrigues M. L. (see Quick W. P.), 25. Smith F. A. (see Whittington J.), 727.
Roux S. J. What remains of the Cholodny-Went theory? Riding the Smolders E. & Merckx R. Growth and root:shoot partitioning of
transduction train to the answer, 783. spinach plants as affected by nitrogen supply, 795.
Ryan P. R., Newman I. A. & Arif I. Rapid calcium exchange for Stadenberg I. (see Sands R.), 107.
protons and potassium in cell walls of Chara, 675. Stitt M. (see Quick W. P.), 25.
Rygol J., Arnold W. M. & Zimmermann U. Zinc and salinity Strain B. R. (see Harley P. C.), 271.
effects on membrane transport in Chara connivens, 11. Streeter J. G. & Salminen S. O. Evidence supporting a non-phloem
Ryle G. J. A. & Powell C. E. The influence of elevated CO, and source of water for export of solutes in the xylem of soybean root
temperature on biomass production of continuously defoliated nodules, 735.
white clover, 593. Syvertsen J. P. (see Lloyd J.), 873.
Szigeti Z. (see Lehoczki E.), 531.
Sachs T. (see Gersani M.), 463.
Salisbury F. B. What remains of the Cholodny-Went theory? A Tardieu F., Zhang J., Katerji N., Bethenod O., Palmer S. & Davies
potential role for changing sensitivity to auxin, 785. W. J. Xyiem ABA controls the stomatal conductance of field-
Salleo S., Hinckley T. M., Kikuta S. B., Lo Gullo M. A., Weilgony grown maize subjected to compaction or soil drying, 193.
P., Yoon T.-M. & Richter H. A method for introducing xylem Tardieu F., Zhang J. & Davies W. J. What information is conveyed
emboli in situ: experiments with a field-grown tree, 491. by an ABA signal from maize roots in drying field soil, 185.
Salleo S. (see Lo Gullo M. A.), 431. Thomas D. R. (see Masterson C.), 313.
Salminen S. O. (see Streeter J. G.), 735. Thomas R. B. (see Harley P. C.), 271.
Sanchez-Aguayo I. & Gonzalez-Utor A. L. Quantitative determina- Trewavas A. J. What remains of the Cholodny-Went theory? Intro-
tion of changes induced by NaCl in vacuoles and cellar size of duction, 761.
Lycopersicon esculentum root cells, 867. Trewavas A. J. What remains of the Cholodny-Went theory? A
Sandquist D. R. (see Keeley J. E.), 1021. summing up, 793.
Sands R., McDonald A. J. S. & Stradenberg I. An evaluation of Trust B. A. & Fry B. Stable sulphur isotopes in plants, 1105.
techniques for measuring yield turgor in excised Salix leaves, Tsai Y.-Z. (see Wu F.-S.), 685.
107. Tyree M. T. (see Tyree M. T.), 633.
Sawhney V. K. (see Singh S.), 373.
Schafer C., Simper H. & Hofmann B. Glucose feeding results in Ullrich C. I. (see Malsy S.), 519.
coordinated changes of chlorophyll content, ribulose-1, 5-bis-
phosphate carboxylase-oxygenase activity and photosynthetic Van Bel A. J. E. & Gamalei Y. V. Ecophysiology of phloem load-
potential in photoautotrophic suspension cultured cells of ing in source leaves, 265.
Chenopodium rubrum, 343. van Bel A. J. E. (see Malsy S.), 519.
Schulte P. J. The units of currency for plant water status, 7. Van der Meer A. J. G. M. (see Senden M. H. M.N.), 71.
Schulze E.-D. (see Schurr U.), 551. Van Paassen F. J. M. (see Senden M. H. M.N.), 71.
Schulze E.-D. (see Schurr U.), 561. van Roekel T. (see Hoekstra F. A.), 601.
Schurr U., Gollan T. & Schulze E.-D. Stomatal response to drying Vazquez-Duhalt R. (see Band C. J.), 129.
soil in relation to changes in the xylem sap composition of Vermeer E. (see Hoekstra F. A.), 601.
Helianthus annuus. Il. Stomatal sensitivity to abscisic imported Vogelman T. C. (see DeLucia E. H.), 921.
from the xylem sap, 561. von Caemmerer S. Carbon isotope discrimination in C,-C, inter-
Schurr U., (see Schurr U.), 551. mediates, 1063.
Schwenke H. & Wagner E. A new concept in root exudation, 289. Vonshak A. & Guy R. Photoadaptation, photoinhibition and pro-
Scott T. K. What remains of the Cholodny-Went theory? Some ductivity in the blue-green alga, Spirulina plantensis grown out-
Author index xiii
doors, 613. Xin Z. (see Chu B.), 307.
Wagner E. (see Schwenke H.), 289.
Walsh K. B., Atkins R. S. & Low C. S. Vascular anatomy of faba- Yakir D. Variations in the natural abundance of oxygen-18 and
ceous nodules of determinate growth, 849. deuterium in plant carbohydrates, 1005.
Watson M. C. (see Glenn E. P.), 711. Yang S. & Tyree M. T. A theoretical model of hydraulic conduc-
Wayne R. What remains of the Cholodny-Went theory? While tivity recovery from embolism with comparison to experimental
there is probable cause to take it to court, there is not a prepon- data on Acer saccharum, 633.
derance of evidence to throw it out, 791. Yao X., Bisson M. A. & Brzezicki L. J. ATP-driven proton pump-
Weilgony P. (see Salleo S.), 491. ing in two species of Chara differing in salt tolerance, 199.
Wendler R. (see Quick W. P.), 25. Yoon T.-M. (see Salleo S.), 491.
White A. J. (see Hughes M. A.), 861. Young I. M. (see Gordon D. C.), 123.
Whittington J. & Smith F. A. Calcium-salinity interactions affect
ion transport in Chara corallina, 727.
Willard T. J. (see Ashworth E. N.), 607. Zhang B.-L. (see Martin G. J.), 1037.
Wolswinkel P. & Koerselman-Kooij J. W. Effect of a pretreatment Zhang J. (see Tardieu F.), 185.
of seed coats with a low osmolality solution on subsequent [S E) Zhang J. (see Tardieu F, ), 193.
sucrose transport into attached empty ovules of pea, 617. Zhang L.(see Hughes M. A.), 861.
Wolterbeek H. Th. (see Senden M. H. M.N.), 71. Ziegler H. (see Ertel J.), 211.
Wood C. (see Masterson C.), 313. Zieschang H. E. (see Seivers A.), 789.
Wu F.-S. & Tsai Y.-Z. Evacuolation and enucleation of mesophyll Zimmermann U. (see Rygol J.), 11.
protoplasts in self-generating percoll gradients, 685.

Plant, Cell and Environment (1992) 15
Subject index
ABA, 185, 193, 307. C,, 1021:
Abies lasiocarpa, 921. plants, 987.
Abscisic acid, 561, 861: '4C assimilate flow, 519.
import, 561. Cabbage palm, 393, 401.
Acer rubrum, 541. Cadmium, 71.
Acer saccharinum, 541. Calcium, 561, 625, 675, 693, 727:
Acer saccharum, 633. homeostasis, 931.
Acid growth, 675. Calmodulin, 931.
Action potentials, 137. CAM, 821, 1021.
Agave mapisaga, 329. Capacitance, 401.
Agave salmiana, 329. Carbohydrates, 1005, 1037.
Agropyron desertorum, 855. Carbon:
Air seeding, 491. budget, 283;
a-tocopherol, 381. dioxide, 231, 337;
Aluminium toxicity, 931. isotope:
Amino acids, 99, 551, 1037. discrimination, 485, 873, 987, 1051, 1063;
Aminotriazole, 655. fractionation, 1099;
Ammonium, 675: partitioning, 25.
assimilation, 965. Carotenoids, 411.
Anastomosis, 849. Cation content, 711.
Annonaceae, 901. Cavitation, 491.
Antioxidants, 381, 955: cDNA, 861.
systems, 655. Cell:
Apoplastic phloem loading, 265. composition, 129;
Applied electrical field, 645. suspension culture, 343;
Aquatic plants, 1021. volume, 867;
Arecaceae, 393, 401. wall, 1, 675.
Aridlands, 831. Cellulose, 1, 1005.
Artemisia tridentata, 49. Cell-cell communication, 137, 151.
Asteraceae, 49, 301. Chara, 199, 675.
Asymmetry, 211. Chara buckellii, 199.
Atmospheric carbon dioxide concentration, 485, 541. Chara connivens Salzmann, 11.
ATP, 479. Chara corallina, 137, 151, 199, 507, 727.
Atrazine resistance, 531. Characeae, 11, 61, 151, 199.
Atriplex canescene ssp.: Charophyte, 61, 507.
canescens, 711; Chemical composition, 221.
linearis, 711; Chenopodiaceae, 711, 795.
macropoda, 711. Chenopodium rubrum, 343.
Avocado pear, 313. Cherry, 211.
Azolla mexicana, 665. Chilling, 307.
Chirality, 1037.
Ballotini, 123. Chlorophyll, 901.
Barley, 861. destruction, 955.
Basket willow, 491. fluorescence, 809.
B-oxidation (enzyme location), 313. Chlorophyll a fluorescence, 703.
Betula pendula, 911. Chlorophyta, 255.
Bicarbonate assimilation, 1021. Chloroplast:
Big Sagebrush, 49. development, 901;
Biomass, 613. partial pressure of CO,, 873.
Birch, 911. Citric acid, 71.
Blue light, 241. Citrus aurantium, 337.
Blue-green algae, 613. Citrus limon, 873.
Brassica, 685. Citrus paradisi, 873.
Brassicaceae, 115 Climate change, 541.
Bromeliad, 25. Clusia, 821.
Brown algae, 241. Cl, 163, 179:
Br, 179. efflux, 61.
Bubble dissolution, 633. CO), 337:
Buffering capacity, 551. assimilation, 271;
Bunchgrasses, 855. concentrating mechanisms, 1083;
concentration, 987;
C,-C, intermediates, 1063. diffusion, 1083:
xvi Subject index
conductance, 873; Energy metabolism, 479.
enrichment, 365, 749, 843; Enucleation, 685.
isotopes, 1083; Environmental:
losses from bundle sheath cells, 987; effects, 1005;
uptake, 329. stress, 1051.
CO,*, 255. Enzyme-linked immunosorbent assay, 373.
Codon usage, 503. Epidermal conductance, 393.
Cold acclimation, 585, 861. Epidermis, 921.
Compatible solutes, 49. Epiphyte, 25.
Competitive inhibition, 179. Ethane production, 531.
Compositae, 531, 551, 561. Eucalyptus, 25:
Conductivity recovery, 633. grandis, 843.
Construction costs, 221. Evacuolation, 685.
Contact exchange, 211. Exponential nutrient addition, 795.
Continuous defoliation, 593. Exposure chamber, 365.
Continuous flow-IRMS, 1091. Extracellular potential (root), 115.
Conyza canadensis, 531. Exudation pulses, 289.
Corn, 307, 693.
Correlative inhibition, 463. Fabaceae, 455, 703, 849.
Coryphoideae, 393, 401. Fern physiology, 665.
Cotton, 271. Fibre optic microprobe, 921.
Crassulaceae, 479. Fluorescence induction, 531.
Crassulacean acid metabolism, 1051. Fluorescent probes, 151.
Cress, 115. Foliage, 921.
Cruciferae, 439. Food webs, 1083.
'37Cs penetration, 211. Forsythia, 607.
Culture conditions, 939. Forsythia x intermedia, 607.
Cyanobacteria, 163, 179, 503. Fourwing saltbush, 711.
Cytokinin, 503. Free sugars, 837.
'8¢/'°C ratios, 831. Freezing:
damage, 585;
Deficiency, 665. injury, 607;
Defoliation, 855. tolerance, 439.
Delayed greening, 901. FTIR, 601.
Dentrification, 965.
Desert, 301: Gadolinium, 289.
alga, 129. Gas chromatography-mass spectrometry, 373.
Desiccation, 601.
Deuterium, 1005, 1037. Gene expression, 91.
Diazotrophy, 965. Germination, 743.
DNA restriction, 439. Glacial CO, drawdown, 1083.
Donnan, 675. Global change, 337.
Drought, 809: Glycine max (L.) Merr., 249, 569, 577, 703, 735, 749.
tolerance, 49. Gossypium hirsutum L., 271.
Dry matter, 947: Grafting, 249.
partitioning, 911. Gramineae, 99, 585, 855.
Dry season, 25. Grapefruit, 873.
Dual batch inlet, 1091. Gravitropism, 693.
D/H, 1073: Great duckweed, 743.
ratios, 831. Greenhouse effect, 337, 485.
Ground water, 1073.
Ecophysiology, 265. Growth, 593, 911:
Efflux, 665. rate (root), 115;
Elasticity, 7. substances, 625.
Electrical: Guaiacol peroxidases, 719.
impedance, 837;
oscillations (root), 115. Halophytes, 711.
Electrochemical equilibria, 163. HCO,, 255.
Electrogenic pump, 351. Helianthus, 25:
Electron microscopy, 585. annuus L., 551, 561.
Elevated: Heliotropism, 703.
CO,, 593, 911; Herbaria, 485.
temperature, 593. Heterogenous environments, 463.
Ellipsoidal distribution, 421. High light stress, 411.
Embolism, 633. Hordeum vulgare L., 861.
Endodermis, 849. Hormone-dependent phloem induction, 519.
Subject index
Horseweed, 531. Macadamia integrifolia, 873.
Hydraulic conductivity, 11,471, 491. Macroalgae, 255.
Hydrogen: Magnesium nutrition, 955.
isotope, 1073; Maize, 185, 193.
peroxide, 655. Male sterility, 373.
Hymenoclea salsola, 301. Malus domestica, 541.
Malvaceae, 271.
Indole-3-acetic acid, 373. Mannan, |.
Infra-red, 123. Membrane potential, 163, 351.
Inhibitors, 163. Mesophyll protoplasts, 685.
Inorganic carbon, 241, 255. Metabolism, 1105.
Interspecific variation, 221. Metabolite pools, 1051.
Ion: Microalga, 129.
channels, 289; Microbody, 313.
exchange, 71; Microtubules, 307.
transport, 61; Mitochondria, 685.
uptake, 351. Mitochondrion, 313.
Ionic composition, 551. Mitosis, 625.
Irradiance, 987. Model, 987.
Isolated cuticles, 211. Modelling, 7, 271.
Isotope: Monoterpenes, 1037.
fractionation, 965, 1021, 1005, 1099; Mutant, 373.
heterogeneity, 1005;
ratio mass spectrometry (IRMS), 1091. Natural abundance, 965, 1083.
Isotopic heterogeneity, 1005. Na‘, 163:
and Li*-stimulation, 179.
Kalanchoé blossfeldiana, 479. Needle anatomy, 921.
Km, 179. Neochloris oleoabundans, 129.
Ni**, 719.
Laminaria digitata, 241. Nicotiana, 685.
Lamprothamnium succinctum, 61. Nitrate, 447, 561, 743:
Lauraceae, 313. reductase activity, 447.
Leaf: Nitrate-ammonium-absorption, 99.
angle, 901; Nitrogen, 271, 447, 843:
area index, 329, 421; fixation, 249;
canopy, 577; productivity, 795;
development, 901; transport, 736;
extension, 855; use efficiency, 703, 873.
growth, 107, 855;
rehydration, 431;
shape, 421; N, fixation, 593, 939.
water potential, 185, 193. Nodule permeability, 849.
Legume nodule, 849. Non-photochemical quenching, 25.
Leguminosae, 569, 577, 849. Nutrient availability, 463, 569, 577.
Lemnaceae, 743. Nutrition, 665, 911.
Lemon, 873.
Lepidium sativum L., 115. Oak, 809.
Ligand exchange, 71. Oleaceae, 607.
Light: Open-top chamber, 365.
absorption, 901; Opuntia amyclea, 329.
climate, 569, 577; Opuntia ficusindica, 329.
gaps, 901; Organic acid accumulation, 821.
penetration, 921; Osmoregulation, 129.
use efficiency, 901. Osmotic:
Lightfleck utilization, 577. adjustment, 711;
Light-stimulated recovery of functional activity, 531. potential, 837;
Linolenic acid (content), 601. stress, 447.
Lipid oxidation, 381. Oxygen isotope, 1073.
Lolium perenne, 99. Oxygen-18, 1005.
Long-distance transport, 519. '$0/'°0, 1073.
Low temperature, 861. Ozone depletion, 921.
LSU and SSU polypedtide subunits, 91.
Lupinus, 25. Palaeoecology, 1051.
Lycopersicon esculentum Mill., 373, 867. Paimae, 393.
Paraquat, 955:
Macadamia, 873. resistence, 531.
xviii Subject index
Parasitic angiosperm, 283. Pseudoroegneria spicata, 855.
Partitioning, 795. Pyrus communis, 211,
Pea, 617.
Peach, 873. Quantum yield, 301.
Pear, 211. Quercus petraea, 809.
Pectin, 1. Quercus prinus, 541,
Percoll gradient, 685. Quercus robur, 541.
Persea americana L., 313.
pH, 551, 561, 693. Rainforest, 901.
Phaeophyceae, 241. Regulation, 343.
Phaseolus vulgaris L., 955. Relative growth, 795:
Phloem transport, 617. rate, 221.
Phosphate transport, 665. Resistance, 955,
Phosphatidylcholine, 601. Respiration, 231, 283, 541.
Phosphoenolpyruvate carboxylase, 987. Respiratory CO, recycling, 821.
Phospholipid transfer protein, 861. Resurrection fern, 81.
Phosphorus, 843. Rhizodermis exudation, 289.
Photoadaptation, 613. Rhizosphere, 645.
Photoinhibition, 37, 81, 301, 703, 809. Rhodamine 123, 685.
Photomixotrophy, 343. Ribulose- 1 ,5-bisphosphate carboxylase/oxygenase, 91, 569, 987.
Photorespiration, 655. Rice, 231.
Photosynthesis, 25, 241, 255, 271, 283, 343, 541, 613, 809, 821, RNA polymerase, 439.
873, 911, 1005: RNA transcripts, 91.
in flashing light, 569, 577; Root, 351, 665:
model, 1063. architecture, 749;
Photosynthetic: cells, 867;
apparatus, 411; exudation, 289;
capacity, 343; fraction, 99;
induction state, 569, 577. growth, 123, 337, 693:
Photo-oxidation, 381, 955. and electrical oscillations, 115;
Phylogeny, 1051. inhibition, 463;
Physical impedance, 123. micromorphology, 749;
Phytochrome control, 479. temperature, 99.
Phytochrome-mediated, 743. Root-to-root communication, 551.
Phytophthora palmivora, 645. Root-to-shoot communication, 561.
Picea engelmannii, 921. Rosaceae, 211, 873.
Picea glauca, 837. rRNA, 439.
Pinyon-juniper woodlands, 831. Rye, 585.
Pisum sativum, 91, 123, 463, 617.
Plant, 1005: Sabal palmetto, 393, 401.
metabolism, 1037; Saccharum spp., 471.
pathogenesis, 645; Salicaceae, 491.
root, 645; Salinity, 129, 727, 867:
water, 1005. tolerance, 711.
Plasma membrane, 625. Salix viminalis, 107, 491.
Plasmin membrane, 931. Salt:
Plasmodesmata, 137, 507. stress, 11, 199;
Pollen species, 601. toxicity, 625.
Pollution, 1105. Sample gas preparation, 1091.
Polypodiacaeae, 81. Secale cereale, 585.
Polypodium polypodioides, 81. Second messengers, 625, 931.
Poplar, 431. Seed:
Populus deltoides, 431. coat, 617;
Post illumination CO, fixation, 577. development, 617;
Potassium, 351: germination, 479.
concentration, 585. Selected ion monitoring, 373.
Pressure: Self-assembly, 1.
cell, 123; Senecio douglasii, 301.
collar, 491. Sesbania rostrata, 939.
Pressure-volume curves, 393. Shade, 569, 577.
Productivity, 329, 613. Single-file pore, 11.
Proteaceae, 873. Sink strength, 617.
Proton efflux, 675. SNIF-NMR, 1037.
Proton transport, 199. Sodium fluxes, 727.
Prunus cerasus, 211. Soil:
Prunus persica, 873. compaction, 185, 193;