Annales des Sciences Forestières

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Rest and activity in vegetative buds of trees p. 9s

P. Champagnat

DOI: https://doi.org/10.1051/forest:19890501

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Promotion of flowering in conifers: from the simple application of a mixture of gibberellins to more integrated explanations p. 27s

M. Bonnet-Masimbert

DOI: https://doi.org/10.1051/forest:19890502

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Experimental control of flower initiation in Weigela japonica p. 34s

M. Bodson

DOI: https://doi.org/10.1051/forest:19890503

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Gibberellin A_4/7 enhances flowering of Picea glauca grafts in two consecutive years p. 37s

R.A. Cecich and D.E. Riemenschneider

DOI: https://doi.org/10.1051/forest:19890504

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Changes in endogenous cytokinins during flowering induction in Douglas fir: effect of exogenous applications p. 40s

N. Imbault, P. Doumas, C. Joseph and M. Bonnet-Masimbert

DOI: https://doi.org/10.1051/forest:19890505

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Correlative control of early stages of flower bud initiation in 'bourse' shoots of apple (Malus x domestica Borkh. cv. Golden Delicious) p. 44s

J. Escobedo and J. Crabbé

DOI: https://doi.org/10.1051/forest:19890506

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Field experiment on the effect of girdling and gibberellin application on flowering induction of 12 yr old seedlings of Douglas fir and Norway spruce p. 47s

M. Bonnet-Masimbert, G. Chanteloup, P. Delanzy and J. Coupaye

DOI: https://doi.org/10.1051/forest:19890507

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Seasonal development of female strobilus of stone pine (Pinus pinea L.) p. 51s

B. Abellanas and J.A. Pardos

DOI: https://doi.org/10.1051/forest:19890508

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Hybridization techniques and frost tolerance studies in intraspecific hybrids of Eucalyptus globulus Labill p. 54s

M.H. Almeida and A.C. Leal

DOI: https://doi.org/10.1051/forest:19890509

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Pollen-limited seed set in pods of tamarind ( Tamarindus indica L.) p. 56s

K.R. Thimmaraju, V. Bhaskar and K. Usha

DOI: https://doi.org/10.1051/forest:19890510

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Influence of the moisture content of forest tree pollen on its response to different viability tests p. 60s

J. Webber and M. Bonnet-Masimbert

DOI: https://doi.org/10.1051/forest:19890511

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Sexual reproduction in Populus I. Some physiological and biochemical events of the progamic phase p. 64s

M. Villar, M. Gaget and C. Dumas

DOI: https://doi.org/10.1051/forest:19890512

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Sexual reproduction in Populus II. Information molecules of the pollen grain p. 67s

M. Gaget, M. Villar, C. Kerhoas and C. Dumas

DOI: https://doi.org/10.1051/forest:19890513

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Physiological aspects of seed conservation p. 72s

B. Suszka

DOI: https://doi.org/10.1051/forest:19890514

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Biorhythms in conifer seed germination during extended storage p. 85s

J.P. Barnett and N.I. Mamonov

DOI: https://doi.org/10.1051/forest:19890515

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Germination and storage of recalcitrant seeds of some tropical forest tree species p. 89s

F. Corbineau and D .Côme

DOI: https://doi.org/10.1051/forest:19890516

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Storage of non-dormant hardwood seeds: new trends p. 92s

C. Muller and M. Bonnet-Masimbert

DOI: https://doi.org/10.1051/forest:19890517

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Polyamines in dormancy breaking of tree seeds p. 95s

Z. Szczotka and U. Lewandowska

DOI: https://doi.org/10.1051/forest:19890518

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An attempt at generating haploid lines of Poplar species for genetic manipulation and breeding programs p. 98s

K.E. Wolter and B.H. McCown

DOI: https://doi.org/10.1051/forest:19890519

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Physiological aspects of somatic polyembryogenesis in suspension cultures of conifers p. 101s

D.J. Durzan

DOI: https://doi.org/10.1051/forest:19890520

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Somatic embryos from callus of Salix viminalis L p. 108s

L. Grönroos, S. von Arnold and T. Ericsson

DOI: https://doi.org/10.1051/forest:19890521

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In vitro propagation of Prosopis species (P. chilensis, P. cineraria and P. juliflora) p. 110s

C.A. Batchelor, D. Yao, M.J. Koehler and P.J.C. Harris

DOI: https://doi.org/10.1051/forest:19890522

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Micropropagation of hybrid walnut trees (Juglans nigra x Juglans regia) through culture and multiplication of embryos p. 113s

D. Cornu and C. Jay-Allemand

DOI: https://doi.org/10.1051/forest:19890523

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Internal levels of plant growth regulators during in vitro culture of wild cherry (Prunus avium L.) p. 117s

P. Label, D. Cornu, B. Sotta and E. Miginiac

DOI: https://doi.org/10.1051/forest:19890524

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Morphological and physiological lesions induced by micropropagation p. 121s

A. Harbour, C.J. Atkinson, K. Oates and W.J. Davies

DOI: https://doi.org/10.1051/forest:19890525

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Polyamines and ethylene during in vitro rooting of Prunus avium L p. 124s

S. Biondi and N. Bagni

DOI: https://doi.org/10.1051/forest:19890526

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Rooting of stem cuttings of Populus x euramericana under different water potentials p. 127s

S. Puri and F.B. Thompson

DOI: https://doi.org/10.1051/forest:19890527

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Embryogenèse somatique chez trois espèces de chênes méditerranéens p. 130s

C. Féraud-Kelier, M. El Maâtaoui, O. Gouin and H. Espagnac

DOI: https://doi.org/10.1051/forest:19890528

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Walnut somatic embryogenesis: physiological and histological aspects p. 133s

D. Cornu

DOI: https://doi.org/10.1051/forest:19890529

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A micropropagation system for Eucalyptus dunnii × Eucalyptus sp p. 136s

M. Fantini Jr. and M.E. Cortezzi Graça

DOI: https://doi.org/10.1051/forest:19890530

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Micropropagation of Eucalyptus dunnii Maid p. 140s

M.E. Cortezzi Graça and S. Mendes

DOI: https://doi.org/10.1051/forest:19890531

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Comportement in vitro d'embryons zygotiques de chêne liège (Quercus suber L.) excisés à divers stades de leur développement p. 145s

M. El Maâtaoui and H. Espagnac

DOI: https://doi.org/10.1051/forest:19890532

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Walnut (Juglans regia L.) micropropagation p. 149s

M.A. Revilla, J. Majada and R. Rodriguez

DOI: https://doi.org/10.1051/forest:19890533

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In vitro propagation of several Betula species representing various ploidy levels p. 152s

E. Särkilahti

DOI: https://doi.org/10.1051/forest:19890534

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In vitro propagation of interspecific hybrids in Alnus p. 155s

H. Sbay, J. Guillot, P. Danthu and D. Prat

DOI: https://doi.org/10.1051/forest:19890535

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Micropropagation of Araucaria columnaris Hook p. 158s

L. Sehgal, O.P. Sehgal and P.K. Khosla

DOI: https://doi.org/10.1051/forest:19890536

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Micropropagation of Eucalyptus viminalis Labill p. 161s

M. Wiecheteck, M.E. Cortezzi Graga and A.J. de Araújo

DOI: https://doi.org/10.1051/forest:19890537

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Micropropagation of Paulownia taiwaniana from mature tissues p. 165s

J.C. Yang, S.H. Chang and C.K. Ho

DOI: https://doi.org/10.1051/forest:19890538

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Optimizing growth of conifer seedlings in vitro p. 168s

G. Flygh, R. Grönroos and S. von Arnold

DOI: https://doi.org/10.1051/forest:19890539

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The effect of phase change on annual growth increment in eastern larch (Larix laricina (Du Roi) K. Koch) p. 171s

M. Greenwood

DOI: https://doi.org/10.1051/forest:19890540

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Réflexion sur les modalités d'appréciation du rajeunissement in vitro chez le Sequoia sempervirens p. 178s

Y. Arnaud, Y. Fouret, C. Larrieu, H. Tranvan, A. Franclet and E. Miginiac

DOI: https://doi.org/10.1051/forest:19890541

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Rejuvenation of a 100 yr old giant sequoia (Sequoiadendron giganteum Buchholz) through in vitro meristem culture p. 183s

O. Monteuuis and M.C. Bon

DOI: https://doi.org/10.1051/forest:19890542

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Effects of sustained subculture on apparent rejuvenation of the apple rootstock M.9 in vitro and in vivo p. 187s

C.A. Webster and O.P. Jones

DOI: https://doi.org/10.1051/forest:19890543

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Polyphenolic and enzymatic characterization of ageing and rejuvenation of hybrid walnut trees (Juglans nigra x Juglans regia): relationship to growth p. 190s

C. Jay-Allemand, A. Drouet, A. Ouaras and D. Cornu

DOI: https://doi.org/10.1051/forest:19890544

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Some architectural aspects of tree ageing p. 194s

D. Barthelemy, C. Edelin and F. Hallé

DOI: https://doi.org/10.1051/forest:19890545

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Crown architecture in relation to productivity of Populus clones in the Pacific Northwest, U.S.A p. 199s

R. Ceulemans, T.M. Hinckley, P.E. Heilman, J.G. Isebrands and R.F. Stettler

DOI: https://doi.org/10.1051/forest:19890546

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Mathematical analysis and comparison of growth fluctua- tions of the aerial system of young Terminalia superba Englers et Diels (Combretaceae) p. 202s

P. Maillard, M. Jacques, E. Miginiac and B. Millet

DOI: https://doi.org/10.1051/forest:19890547

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Variations in expression of episodic growth by in vitro- cultured shoots of oak (Quercus robur L.) p. 206s

J.M. Favre and B.Juncker

DOI: https://doi.org/10.1051/forest:19890548

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Effect of a feedback control by early secondary xylem formation on the outcome of competition between leafy shoots in apple (Malus x domestica Borkh.) p. 209s

A. Jebari and J. Crabbé

DOI: https://doi.org/10.1051/forest:19890549

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Concurrence des rameaux latéraux vis-à-vis de la pousse terminale chez le frêne (Fraxinus excelsior L.) : relation avec les défauts de branchaison et de fourchaison p. 213s

N. Le Goff and F. Ningre

DOI: https://doi.org/10.1051/forest:19890550

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Some aspects of bud activity and branch formation in young oak p. 217s

R. Harmer

DOI: https://doi.org/10.1051/forest:19890551

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Physiological correlations and bud dormancy in the apple tree (Malus domestica Borkh.) p. 220s

O. Bailly and J.C. Mauget

DOI: https://doi.org/10.1051/forest:19890552

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Evolution au cours du repos hivernal de l'aptitude au débourrement, à l'allongement et à la ramification de bourgeons isolés de Douglas p. 223s

M. Jacques, M. Bonnet-Masimbert, D. Cornu and E. Miginiac

DOI: https://doi.org/10.1051/forest:19890553

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The role of photoperiod and temperature in the induction and the release of dormancy in Pinus sylvestris L. seedlings p. 228s

I. Dormling

DOI: https://doi.org/10.1051/forest:19890554

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Dormancy and spring burst of lateral buds on stems of low-pruned mulberry (Morus alba L.) p. 233s

T. Suzuki, M. Kitano and K. Kohno

DOI: https://doi.org/10.1051/forest:19890555

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Influence de la durée de l'exposition en jours courts sur la dormance des bourgeons de Gleditsia triacanthos L p. 236s

G.J. Aillaud, A. Al Ibrahem and P. Neville

DOI: https://doi.org/10.1051/forest:19890556

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Greenhouse production of nectarines for early harvest in France: a cultivation system with shallow rest or no rest p. 242s

P. Balandier and R. Rageau

DOI: https://doi.org/10.1051/forest:19890557

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Evaluation of some markers of vigor in seedlings of Douglas fir (Pseudotsuga menziesii (Mirb.) Franco) p. 246s

J.B. Zaerr, V.D. Hipkins and K. Forry

DOI: https://doi.org/10.1051/forest:19890558

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Comparative growth analysis of five first year establishment poplar clones (Populus sp.) grown under a short-rotation intensive culture system p. 250s

F. Mau and I. Impens

DOI: https://doi.org/10.1051/forest:19890559

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Study of endogenous plant growth substances in Douglas fir I. Cytokinin analysis p. 256s

N. Imbault, P. Doumas, C. Joseph and M. Bonnet-Masimbert

DOI: https://doi.org/10.1051/forest:19890560

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Study of endogenous plant growth substances in Douglas fir II. Gibberellin analysis p. 259s

P. Doumas, J. Bianco and M. Bonnet-Masimbert

DOI: https://doi.org/10.1051/forest:19890561

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Old colchicine-induced polyploid materials of Betula pendula Roth and Betula pubescens Ehrh p. 264s

K. Pieninkeroinen and T. Valanne

DOI: https://doi.org/10.1051/forest:19890562

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Control of xylogenesis within the whole tree p. 267s

R. Aloni

DOI: https://doi.org/10.1051/forest:19890563

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Some aspects of phytohormonal participation in the control of cambial activity and xylogenesis in tree stems p. 273s

S.Lachaud

DOI: https://doi.org/10.1051/forest:19890564

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Factors affecting the direction of growth of tree roots p. 277s

M.P. Coutts

DOI: https://doi.org/10.1051/forest:19890565

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Analysis and simulation of the architecture of a growing root system: application to a comparative study of several tree seedlings p. 288s

M. Colin-Belgrand, L. Pages, E. Dreyer and H.Joannes

DOI: https://doi.org/10.1051/forest:19890566

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Effect of coppicing on hybrid poplar fine root dynamics p. 294s

M. Bédéneau and D. Auclair

DOI: https://doi.org/10.1051/forest:19890567

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Growth relationships between root and shoot in walnut seedlings (Juglans regia L.) p. 297s

J.S. Frossard, A. Charron and A. Lacointe

DOI: https://doi.org/10.1051/forest:19890568

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Fine root growth in a sweet chestnut (Castanea sativa Mill.) coppice p. 301s

P. Montpied

DOI: https://doi.org/10.1051/forest:19890569

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A new data processing system for root growth and ramifi- cation analysis: description of methods p. 305s

M. Colin-Belgrand, H. Joannes, E. Dreyer and L. Pages

DOI: https://doi.org/10.1051/forest:19890570

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Aeration of the root system in Alnus glutinosa L. Gaertn p. 310s

P. Schröder

DOI: https://doi.org/10.1051/forest:19890571

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Current focuses in woody plant water relations and drought resistance p. 317s

T.M. Hinckley and R. Ceulemans

DOI: https://doi.org/10.1051/forest:19890572

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Evapotranspiration measurements in a Mediterranean forest stand by means of ecophysiological and microclimatic techniques p. 325s

R. Valentini, G.E. Scarascia-Mugnozza and M. Sabatti

DOI: https://doi.org/10.1051/forest:19890573

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Cavitation in trees and the hydraulic sufficiency of woody stems p. 330s

M. Tyree

DOI: https://doi.org/10.1051/forest:19890574

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The use of ultrasonic detectors for water stress determination in fruit trees p. 338s

H.G.Jones, K.H. Higgs and A. Bergamini

DOI: https://doi.org/10.1051/forest:19890575

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Detection of cavitation events upon freezing and thawing of water in stems using ultrasound techniques p. 342s

A. Raschi, G.E. Scarascia- Mugnozza, R. Valentini and C. Vazzana

DOI: https://doi.org/10.1051/forest:19890576

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Ultrasound acoustic emission in water-stressed plants of Picea abies Karst p. 346s

M. Borghetti, A. Raschi and J. Grace

DOI: https://doi.org/10.1051/forest:19890577

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Hourly and daily variations of xylem sapflow in sweet chestnut coppices using a thermal measurement method p. 350s

V. Bobay and B. Saugier

DOI: https://doi.org/10.1051/forest:19890578

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Diurnal evolution of water flow and potential in an individual spruce: experimental and theoretical study p. 353s

P. Cruiziat, A. Granier, J.P. Claustres and D. Lachaize

DOI: https://doi.org/10.1051/forest:19890579

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Variation of hydraulic conductance of some adult conifers under natural conditions p. 357s

A. Granier, N. Breda, J.P. Claustres and F. Colin

DOI: https://doi.org/10.1051/forest:19890580

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Water movement and its resistance in young trees of Cryptomeria japonica p. 361s

H. Yahata

DOI: https://doi.org/10.1051/forest:19890581

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Effects of water deficit on leaf growth and initiation in fast-growing tree species p. 366s

J.C. Metcalfe, W.J. Davies and J.S. Pereira

DOI: https://doi.org/10.1051/forest:19890582

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Importance of water consumption for calcium nutrition of trees p. 369s

A. Vigouroux, C. Bussi and J.F. Berger

DOI: https://doi.org/10.1051/forest:19890583

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Water relation characteristics and photosynthesis of saline-stressed seedlings of non-halophyte species p. 372s

T. Suzaki, H. Yahata and H. Shigenaga

DOI: https://doi.org/10.1051/forest:19890584

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Effects of saline stress on Eucalyptus seedlings p. 376s

R.A. Fathi and D. Prat

DOI: https://doi.org/10.1051/forest:19890585

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Effect of water stress on potassium distribution in young seedlings of maritime pine (Pinus pinaster Ait.) p. 379s

A. Nguyen and A. Lamant

DOI: https://doi.org/10.1051/forest:19890586

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Drought resistance of two Douglas fir species (Pseudo- tsuga menziesii (Mirb.) Franco and Pseudotsuga macro- carpa (Torr.) Mayr.): relative importance of water use efficiency and root growth potential p. 384s

G. Aussenac, P. Grieu and J.M. Guehl

DOI: https://doi.org/10.1051/forest:19890587

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Variations in seed and seedling responses to water stress in three provenances of Eucalyptus camaldulensis Dehnh p. 388s

A. Gibson and E.P. Bachelard

DOI: https://doi.org/10.1051/forest:19890588

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Control of gas exchange: evidence for root-shoot communication on drying soil p. 393s

T. Gollan, W.J. Davies, U. Schurr and J. Zhang

DOI: https://doi.org/10.1051/forest:19890589

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Responses of photosynthesis and stomatal conductance to atmospheric humidity in some mediterranean Abies species p. 401s

J.M. Guehi, J. Bouachrine, R. Zimmermann and E. Dreyer

DOI: https://doi.org/10.1051/forest:19890590

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Effects of exogenous ABA on photosynthesis and stomatal conductance of cut twigs from oak seedlings p. 406s

E. Dreyer and I. Scuiller

DOI: https://doi.org/10.1051/forest:19890591

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Effects of long-term water stress on net photosynthesis, growth and water-use efficiency of conifers in the field p. 401s

K. Gross

DOI: https://doi.org/10.1051/forest:19890592

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CO₂ response curves can be measured with a field-portable closed-loop photosynthesis system p. 416s

D.K. McDermitt, J.M. Norman, J.T. Davis, T.M. Ball, T.J. Arkebauer, J.M. Welles and S.R. Roerner

DOI: https://doi.org/10.1051/forest:19890593

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In situ measurement of leaf water use efficiency of lilac (Syringa vulgaris): comparison with crop plants p. 421s

O. Bethenod, J. Pilarski and P. Quetin

DOI: https://doi.org/10.1051/forest:19890594

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Variability of stomatal conductance in the crown of a maritime pine (Pinus pinaster Ait.) p. 426s

D. Loustau, F. El Hadj Moussa, M. Sartore and M. Guedon

DOI: https://doi.org/10.1051/forest:19890595

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Variation of stomatal resistance with leaf age in Quercus petraea: effect on the soil-water balance of an oak forest p. 429s

J. Nizinski, D. Morand and B. Saugier

DOI: https://doi.org/10.1051/forest:19890596

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CO₂ assimilation in young Prosopis plants p. 433s

M. Pinto

DOI: https://doi.org/10.1051/forest:19890597

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Field studies of leaf gas exchanges in oil palm tree (Elaeis guineensis Jacq.) p. 439s

E. Dufrene and B. Saugier

DOI: https://doi.org/10.1051/forest:19890598

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Environmental control of CO₂ assimilation rate and leaf conductance in two species of the tropical rain forest of French Guiana (Jacaranda copaia D. Don and Eperua falcata Aubl.) p. 443s

R. Huc and J.M. Guehl

DOI: https://doi.org/10.1051/forest:19890599

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Gas exchange and water relations of evergreen and deciduous tropical savanna trees p. 448s

G. Goldstein, F. Rada, P. Rundel', A. Azocar and A. Orozco

DOI: https://doi.org/10.1051/forest:198905ART0100

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Ecophysiology of 8 woody multipurpose species from semiarid northeastern Mexico p. 454s

H. Stienen, M.P. Smits, N. Reid, J. Landa and J.H.A. Boerboom

DOI: https://doi.org/10.1051/forest:198905ART0101

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Effects of soil temperature on gas exchange and mor- phological structure of shoot and root in 1 yr old Scots pine (Pinus sylvestris L.) seedlings p. 459s

J. Lippu and P. Puttonen

DOI: https://doi.org/10.1051/forest:198905ART0102

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The effects of transplanting stress on photosynthesis, stomatal conductance and leaf water potential in Cedrus atlantica Manetti seedlings: role of root regeneration p. 464s

J.M. Guehl, G. Aussenac and P. Kaushal

DOI: https://doi.org/10.1051/forest:198905ART0103

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A comparison of the photosynthetic radiation response of Scots pine shoots in direct and diffuse radiation p. 496s

P. Oker-Blom, H. Smolander and T. Lahti

DOI: https://doi.org/10.1051/forest:198905ART0104

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The effect of nitrogen content on the photosynthesis of Scots pine needles and shoots p. 473s

H. Smolander and P. Oker-Blom

DOI: https://doi.org/10.1051/forest:198905ART0105

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Photosynthesis and leaf longevity in alder, birch and ash seedlings grown under different nitrogen levels p. 476s

T. Koike and M. Sanada

DOI: https://doi.org/10.1051/forest:198905ART0106

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Photosynthetic response of poplar leaves under varying quantum flux density p. 479s

J.P. Gaudillère

DOI: https://doi.org/10.1051/forest:198905ART0107

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Seasonal variations in photosynthetic activity of spruces as determined by chlorophyll fluorescence p. 483s

H.K. Lichtenthaler, U. Rinderle and M. Haitz

DOI: https://doi.org/10.1051/forest:198905ART0108

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Ontogenetic changes in leaf development and photosynthesis of Prunus serotina seedlings p. 490s

S.B. Horsley and K.W. Gottschalk

DOI: https://doi.org/10.1051/forest:198905ART0109

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Leaf number, water stress and carbon nutrition effects on poplar leaf growth p. 493s

J.P. Gaudillère

DOI: https://doi.org/10.1051/forest:198905ART0110

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Influence of light conditions on the predetermination of foliar characteristics in Betula alleghaniensis Britton p. 497s

M. Labrecque, P. Bellefleur, J.P. Simon and S. Popovich

DOI: https://doi.org/10.1051/forest:198905ART0111

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Primary productivity of a Hevea forest in the Ivory Coast p. 502s

B.A. Monteny

DOI: https://doi.org/10.1051/forest:198905ART0112

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Effect of doubling atmospheric CO₂ concentration on growth, dry matter distribution and CO₂ exchange of 2 yr old sweet chestnut trees (Castanea sativa Mill.) p. 506s

M. Mousseau and H.Z. Enoch

DOI: https://doi.org/10.1051/forest:198905ART0113

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A model of light interception and carbon balance for a sweet chestnut coppice (Castanea sativa Mill.) p. 509s

L. Mordacq and B. Saugier

DOI: https://doi.org/10.1051/forest:198905ART0114

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Photosynthesis and growth of present New Zealand forest trees relate to ancient climates p. 512s

B.J. Hawkins and G.B. Sweet

DOI: https://doi.org/10.1051/forest:198905ART0115

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Dynamics of light interception, leaf area and biomass production in Populus clones in the establishment year p. 515s

G.E. Scarascia-Mugnozza, J.G. Isebrands, T.M. Hinckley and R.F. Stettler

DOI: https://doi.org/10.1051/forest:198905ART0116

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Modelling the coppice stand structure: an ecophysiological approach p. 519s

G.E. Scarascia-Mugnozza, R. Valentini, E. Giordano and A. Del Lungo

DOI: https://doi.org/10.1051/forest:198905ART0117

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PAR conversion efficiencies of a tropical rain forest p. 523s

R.J. Luxmoore and J.G. Saldarriaga

DOI: https://doi.org/10.1051/forest:198905ART0118

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Aboveground biomass production in an irrigation and fer- tilization field experiment with Eucalyptus globulus p. 526s

C. Araújo, J.S. Pereira, L. Leal, M. Tomé, J. Flower-Ellis and T. Ericsson

DOI: https://doi.org/10.1051/forest:198905ART0119

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Diurnal and seasonal fluctuations in the bark respiration of standing Quercus acutissima trees in Nakaizu, Japan p. 529s

Y. Kakubari

DOI: https://doi.org/10.1051/forest:198905ART0120

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Components of woody-tissue respiration in Abies amabilis p. 532s

D.G. Sprugel

DOI: https://doi.org/10.1051/forest:198905ART0121

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Physiological responses to air pollutants p. 536s

G. Halbwachs

DOI: https://doi.org/10.1051/forest:198905ART0122

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Interactions of ozone and pathogens on the surface structure of Norway spruce needles p. 543s

K. Ojanperä and S. Huttunen

DOI: https://doi.org/10.1051/forest:198905ART0123

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Etude des surfaces foliaires des arbres dépérissants p. 547s

J.P. Garrec, C. Kerfourn and E. Laitat

DOI: https://doi.org/10.1051/forest:198905ART0124

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Studies on Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst.) needle cuticles p. 553s

S. Huttunen, M. Turunen and J. Reinikainen

DOI: https://doi.org/10.1051/forest:198905ART0125

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Ionic interactions between precipitation and leaf cuticles p. 557s

T. Scherbatskoy

DOI: https://doi.org/10.1051/forest:198905ART0126

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Effects of polyaromatic hydrocarbons on the forest ecosystem and woody plants p. 561s

M. Berteigne, C. Rose, J. Gérard and P. Dizengremel

DOI: https://doi.org/10.1051/forest:198905ART0127

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Light-quality and -quantity effects on monoterpene-medi- ated photo-bleaching of conifer needles p. 565s

J. Franzen, K. Gross, M. Bonzon and E. Wagner

DOI: https://doi.org/10.1051/forest:198905ART0128

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A delayed effect of ozone fumigation on photosynthesis of Norway spruce p. 568s

D. Eamus, J.D. Barnes, L. Mortensen, H. Ro-Poulsen and A.W. Davison

DOI: https://doi.org/10.1051/forest:198905ART0129

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Changes of partitioning and increased root lengths of spruce and beech exposed to ambient pollution concentrations in southern England p. 573s

G. Taylor, M.C. Dobson and P.H. Freer-Smith

DOI: https://doi.org/10.1051/forest:198905ART0130

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The influence of acid mist upon transpiration, shoot water potential and pressure—volume curves of red spruce seedlings p. 577s

D. Eamus, I. Leith and D. Fowler

DOI: https://doi.org/10.1051/forest:198905ART0131

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Ozone fumigation of Norway spruce at timberline p. 581s

W.M. Havranek, G. Wieser and M. Bodner

DOI: https://doi.org/10.1051/forest:198905ART0132

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Direct effects of acidic wet deposition on photosynthesis and stomatal conductance of two Populus clones (P. cv. Beaupré and P. cv. Robusta) p. 586s

C. Martens, K. Landuydt and I. Impens

DOI: https://doi.org/10.1051/forest:198905ART0133

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Apoplast: a sensitive site for assessing some biochemical effects of O₃ or SO₂ in Norway spruce needles p. 590s

G. Ogier, F.J. Castillo and H. Greppin

DOI: https://doi.org/10.1051/forest:198905ART0134

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Response of shoot growth and gas exchange of Picea abies clones to rain acidity and the addition of ions p. 595s

P. Van Elsacker and I. Impens

DOI: https://doi.org/10.1051/forest:198905ART0135

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Effects of sulfuric acid and nitrogen deposition on mineral nutrition of Picea abies (L.) Karst p. 599s

B.U. Schneider, M. Kaupenjohann and W. Zech

DOI: https://doi.org/10.1051/forest:198905ART0136

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Physiological responses to low temperature p. 604s

O. Junttila

DOI: https://doi.org/10.1051/forest:198905ART0137

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Winter moisture content and frost-crack occurrence in oak trees (Quercus petraea Liebl. and Q. robur L.) p. 614s

B. Cinotti

DOI: https://doi.org/10.1051/forest:198905ART0138

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Assessment of the effects of below-zero temperatures on photosynthesis and chlorophyll a fluorescence in leaf discs of Eucalyptus globulus p. 617s

L.F. Serrano, M.M. Chaves, M.H. Almeida and J.S. Pereira

DOI: https://doi.org/10.1051/forest:198905ART0139

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The development of winter hardiness of pine and spruce seedlings in a simulated acid rain experiment p. 621s

J. Reinikainen and S. Huttunen

DOI: https://doi.org/10.1051/forest:198905ART0140

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The effects of summer exposure to ozone on the frost hardiness after the vegetation period of Norway and Sitka spruce seedlings p. 624s

P. W. Lucas

DOI: https://doi.org/10.1051/forest:198905ART0141

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Carbon and nitrogen allocation in trees p. 631s

R.E. Dickson

DOI: https://doi.org/10.1051/forest:198905ART0142

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Biochemical aspects of inorganic nitrogen assimilation by woody plants p. 648s

G.R. Stewart, J. Pearson, J.L. Kershaw and E.C.M. Clough

DOI: https://doi.org/10.1051/forest:198905ART0143

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Nitrogen recycling in the apple (Malus domestica Borkh.) p. 654s

J.S. Titus

DOI: https://doi.org/10.1051/forest:198905ART0144

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Partitioning of assimilated nitrogen in beech (Fagus sylvatica) p. 660s

F. Martin and M. Ben Driss Amraoui

DOI: https://doi.org/10.1051/forest:198905ART0145

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Comparative study of nitrogen assimilation in woodland species p. 663s

J. Pearson, E.C.M. Clough and J.L. Kershaw

DOI: https://doi.org/10.1051/forest:198905ART0146

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Effect of nitrogen supply on growth and internal nitrogen cycling within deciduous trees p. 666s

P. Millard

DOI: https://doi.org/10.1051/forest:198905ART0147

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Nitrate utilization and nitrogen status in English woodland communities p. 669s

E.C.M. Clough, J. Pearson and G. R. Stewart

DOI: https://doi.org/10.1051/forest:198905ART0148

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How the absolute growth rate of poplar adapts to the light-NO ^-₃-dosage p. 673s

G.A. Pieters

DOI: https://doi.org/10.1051/forest:198905ART0149

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Allocation of dry matter in Eucalyptus grandis seedlings in response to nitrogen supply p. 680s

R.N. Cromer and P.G. Jarvis

DOI: https://doi.org/10.1051/forest:198905ART0150

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H⁺-pumping activities of plasma membrane and tonoplast from Quercus rubra roots p. 684s

A. Lamant, R. Devilder and P. Seillac

DOI: https://doi.org/10.1051/forest:198905ART0151

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Effect of phosphate fertilization on trace element nutrition of Pinus pinaster grown in a sandy acid soil p. 690s

E. Saur

DOI: https://doi.org/10.1051/forest:198905ART0152

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Croissance juvénile du chêne rouge sur des sols carbonatés à des profondeurs variables p. 694s

J. Timbal and J. Gelpe

DOI: https://doi.org/10.1051/forest:198905ART0153

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Physiology and metabolism of ectomycorrhizae p. 697s

C. Bledsoe, D. Brown, M. Coleman, W. Littke, P. Rygiewicz, U. Sangwanit, S. Rogers and J. Ammirati

DOI: https://doi.org/10.1051/forest:198905ART0154

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The role of glutamine synthetase, glutamate synthase and glutamate dehydrogenase in ammonia assimilation by the mycorrhizal fungus Pisolithus tinctorius p. 706s

J.L. Kershaw and G.R. Stewart

DOI: https://doi.org/10.1051/forest:198905ART0155

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Growth, mineral nutrient content and nitrogen metabo- lism in Laccaria laccata-inoculated and non-inoculated Douglas fir seedlings during their growth period p. 711s

M. Chalot, B. Botton and J. Banvoy

DOI: https://doi.org/10.1051/forest:198905ART0156

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Carbon and phosphorus relations in mycorrhizal and non-mycorrhizal pine seedlings p. 715s

J.V.D. Rousseau and C.P.P. Reid

DOI: https://doi.org/10.1051/forest:198905ART0157

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Changing electrophoretic patterns of glutamate dehydro- genases and aspartate aminotransferases in a few tree species under the influence of ectomycorrhization p. 718s

B. Botton, M. Chalot and B. Dell

DOI: https://doi.org/10.1051/forest:198905ART0158

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Changes in pathways for carbon and nitrogen assimilation in spruce roots under mycorrhization p. 721s

C. Namysl, M. Chalot, B. Dell, P. Dizengremel, B. Botton and F. Le Tacon

DOI: https://doi.org/10.1051/forest:198905ART0159

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Assessment of the contributions of glycolysis and the pentose phosphate pathway to glucose respiration in ectomycorrhizas and non-mycorrhizal roots of spruce (Picea abies L. Karsten) p. 724s

I. Bilger, V. Guillot, F. Martin and F. Le Tacon

DOI: https://doi.org/10.1051/forest:198905ART0160

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Production and characterization of exocellular proteases in ectomycorrhizal fungi p. 728s

K. El-Badaoui and B. Botton

DOI: https://doi.org/10.1051/forest:198905ART0161

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Effect of phytotoxic solutions on the respiration of mycorrhizal and non-mycorrhizal spruce roots (Picea abies L. Karst.) p. 731s

F. Pellissier and L. Trosset

DOI: https://doi.org/10.1051/forest:198905ART0162

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Cytokinin activity in Citrus seedlings colonized by mycorrhizal fungi p. 734s

R.K. Dixon

DOI: https://doi.org/10.1051/forest:198905ART0163

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Amplification of root—fungus interface in ectomycorrhizae by Hartig net architecture p. 737s

I. Kottke and F. Oberwinkler

DOI: https://doi.org/10.1051/forest:198905ART0164

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Experimental study of pine ectomycorrhizae: ectomycorrhizal organization after girdling of the hypocotyl p. 741s

J. Lei and J. Dexheimer

DOI: https://doi.org/10.1051/forest:198905ART0165

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Interrelationship between vitality of ectomycorrhizae and occurrence of microfungi p. 745s

T. Ritter, G. Weber, I. Haug, I. Kottke and F. Oberwinkler

DOI: https://doi.org/10.1051/forest:198905ART0166

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Effect of soil temperature upon the root growth and mycorrhizal formation of white spruce (Picea glauca (Moench) Voss) seedlings grown in controlled environments p. 750s

L. Husted and D.P. Lavender

DOI: https://doi.org/10.1051/forest:198905ART0167

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Ultrastructural and biochemical changes at the preinfection stage of mycorrhizal formation by two isolates of Pisolithus tinctorius p. 754s

F. Lapeyrie, J. Lei, N. Malajczuk and J. Dexheimer

DOI: https://doi.org/10.1051/forest:198905ART0168

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Succession of mycorrhizae: a matter of tree age or stand age? p. 758s

D. Blasius and F. Oberwinkler

DOI: https://doi.org/10.1051/forest:198905ART0169

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Experimental weathering of mica by mycorrhizal and non-mycorrhizal beech and pine p. 762s

C. Leyval and J. Berthelin

DOI: https://doi.org/10.1051/forest:198905ART0170

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Interactions between root symbionts, root pathogens and actinorhizal plants p. 765s

A. Akkermans, D. Hahn and F. Zoon

DOI: https://doi.org/10.1051/forest:198905ART0171

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Comparison of nitrogenase and nitrate reductase activities in two nitrogen-fixing tree species: black alder (Alnus glutinosa) and black locust (Robinia pseudoacacia) p. 772s

G. Pizelle, S. Benamar, F. Boutekrabt and G. Thiéry

DOI: https://doi.org/10.1051/forest:198905ART0172

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Occurrence of foliar nitrate reductase activity not induced by nitrate in symbiotic nitrogen-fed black alder (Alnus glutinosa) p. 777s

S. Benamar, G. Pizelle and G. Thiéry

DOI: https://doi.org/10.1051/forest:198905ART0173

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Influence of the form of nitrogen nutrition on foliar nitrate reductase activity in young black locust ( Robinia pseudoacacia L.) p. 782s

F. Boutekrabt and G. Pizelle

DOI: https://doi.org/10.1051/forest:198905ART0174

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Phloem loading and unloading p. 786s

S. Delrot and J.L. Bonnemain

DOI: https://doi.org/10.1051/forest:198905ART0175

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Autophagic response of higher plant cells to a prolonged period of sucrose deprivation p. 797s

R. Bligny, C. Roby, A. Dorne and R. Douce

DOI: https://doi.org/10.1051/forest:198905ART0176

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Factors modulating superoxide dismutase activity in needles of spruce trees (Picea abies L.) p. 807s

A. Polle, B. Krings and H. Rennenberg

DOI: https://doi.org/10.1051/forest:198905ART0177

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Extraction and study of enzymes linked to malate metabolism in tree leaves p. 811s

D. Gerant, A. Citerne, C. Fabert and P. Dizengremel

DOI: https://doi.org/10.1051/forest:198905ART0178

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Comparison between the structure and function of chloroplasts at different levels of willow canopy during a growing season p. 815s

E. Vapaavuori, A. Nurmi, H. Vuorinen and T. Kangas

DOI: https://doi.org/10.1051/forest:198905ART0179

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Carbon partitioning: fructose 2,6-bisphosphate content as an indicator of specific changes in carbohydrate metabolism in needles from class II spruce trees p. 819s

W. Einig and R. Hampp

DOI: https://doi.org/10.1051/forest:198905ART0180

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Effects of the period of glyphosate treatment on oak seedlings: phenological and physiotogical aspects p. 824s

C. Fabert, H. Frochot and P. Dizengremel

DOI: https://doi.org/10.1051/forest:198905ART0181

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Compartmentation of storage compounds in peach leaves p. 828s

J.P. Gaudillère, A. Moing, A. Lamant, M. Brison and J. Schaeffer

DOI: https://doi.org/10.1051/forest:198905ART0182

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Assimilate allocation and carbon reserves in Juglans regia L. seedlings p. 832s

A. Lacointe

DOI: https://doi.org/10.1051/forest:198905ART0183

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Light-dependent changes in the glutathione content of Norway spruce (Picea abies (L.) Karst.) p. 837s

R. Schupp and H. Rennenberg

DOI: https://doi.org/10.1051/forest:198905ART0184

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Compatible solutes in different organs of mangrove trees p. 842s

M. Popp and J. Polania

DOI: https://doi.org/10.1051/forest:198905ART0185

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Variations de la teneur en glucides de l'érable à sucre p. 845s

J.P. Renaud and Y. Mauffette

DOI: https://doi.org/10.1051/forest:198905ART0186

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Molecular structure and biochemical properties of lignins in relation to possible self-organization of lignin networks p. 848s

B. Monties

DOI: https://doi.org/10.1051/forest:198905ART0187

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A new method for the histochemical localization of laccase in Rhus verniciflua Stokes p. 856s

M.R. Li

DOI: https://doi.org/10.1051/forest:198905ART0188

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Excretion of laccase by sycamore (Acer pseudoplatanus L.) cambial cells: effect of copper deficiency, reversible removal of type 2 Cu ²⁺ p. 860s

J. Quinton-Tulloch, J. Gaillard, J. Jordanov, R. Bligny and R. Douce

DOI: https://doi.org/10.1051/forest:198905ART0189

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Effects of decline and/or air pollution on the terpene metabolism of Picea abies needles p. 864s

A. Saint-Guily

DOI: https://doi.org/10.1051/forest:198905ART0190

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Hypoxylon mammatum toxins: possible involvement in canker development on aspen p. 868s

I. Genetet, J. Pinon, B. Bodo and S. Rebuffat

DOI: https://doi.org/10.1051/forest:198905ART0191

• PDF (171.8 KB)