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    Plan

    Plan détaillé Texte intégral Introduction Approaches to AM application in forestry practices The “reductionist” approach (controlled mycorrhization) The “holistic” approach Conclusion Bibliographie Auteurs

    The Mediterranean region under climate change

    Ce livre est recensé par

    Précédent Suivant
    Table des matières

    Sub-chapter 3.5.4. Rethinking the management of mycorrhizal soil infectivity to restore Mediterranean and tropical forest ecosystems

    Robin Duponnois, Lahcen Ouahmane, Mohamed Hafidi et Yves Prin

    p. 637-645

    Texte intégral Bibliographie References Auteurs

    Texte intégral

    Introduction

    1Desertification, one of the main causes of climate change, generally results from a variety of factors, including climatic variations and human activities. Among the man-mediated degradative activities, deforestation is considered to have a major impact by causing extinction, changes to climatic condition, desertification and the displacement of local populations (Defries et al. 2007).

    2Forest cover is an important source of protection from soil degradation and deforestation which impacts population structure, successional patterns and species diversity, generally inducing degradations in the physico-chemical and biological soil properties (Requena et al. 2001). These changes can be recorded in microbial functional capacity (microbial metabolism, biomass and composition, enzymatic activities and soil organic matter flux) which is mainly involved in soil quality and function (Chaer et al. 2009). Many studies have also shown that deforestation and soil cultivation alter soil microbial community structure (Bossio et al. 2005) and may lead to reduction in microbial biodiversity (Chaer et al. 2009).

    3Among components of soil microbiota, mycorrhizal fungi are known to be essential key components of sustainable soil-plant systems, especially in arid ecosystems (Duponnois et al. 2011). The mycorrhizal symbiosis mobilizes and transports nutrients to roots (Smith & Read, 2008), reduces water stress (Augé, 2001) and improves soil aggregation in eroded soils (Caravaca et al. 2002). It has also been reported that arbuscular mycorrhizal (AM) fungi affect the diversity of plant communities (van der Heijden et al. 1998)) and influence relationships between plants (van der Heijden et al. 1998).

    4Since trees are a primary source of protection from soil degradation, many afforestation programs have been undertaken but with generally low performance in terms of productivity and seedling survival after outplanting (Duponnois et al. 2005a). These deficiencies have usually been recorded in Mediterranean semi-arid areas known to have low bioavailable phosphate content and high phosphate retention capacities (Duponnois et al. 2011). This environmental context represents the most favourable conditions for AMF’s potential to increase plant growth without any mineral fertilizers (Rodriguez & Sanders, 2015). Unfortunately, this microbial resource has been largely neglected despite numerous studies focused on this symbiosis.

    5The native inoculum potential of AM fungi in arid and semi-arid Mediterranean ecosystems is generally limited which, in turn, prevents plant establishment and growth (Smith& Read 2008). It is necessary to apply mycorrhizal inoculation technologies or to manage native AM fungus communities to replace or reinforce the mycorrhizal potential in these degraded areas (Duponnois et al. 2011).

    Approaches to AM application in forestry practices

    6This chapter aims to describe different practical approaches to integrate the AM symbiosis in forestry practices through a “reductionist” approach (also named Controlled mycorrhization) (Inoculation of optimized AM fungal strains to improve the plant growth in unfriendly conditions) or a “holistic” approach (Suitable management of AM fungal diversity for ensuring AM fungi–dependent ecosystem services) (Rodriguez & Sanders, 2015). Each of these cultural practices will be illustrated by results from field experiments performed in Mediterranean and tropical areas.

    The “reductionist” approach (controlled mycorrhization)

    7In recent decades, considerable research has been made by using specific mycorrhizal fungal strains to enhance outplanting performances with forest tree species (Caravaca et al. 2002). Hence, numerous studies have reported the beneficial effects on plant growth resulting from AM fungal inoculation during the nursery plantation. Among all the AM fungal strains tested in these experiments, Rhizophagus irregularis has attracted great interest because of (1) its world-wide distribution, (2) its high genetic variability and variation in effects on plant growth and (3) its ability to be produced in an in vitro system.

    8Some of its impacts on the growth of different tree species in controlled conditions are reported in table 1. Most of these experiments have been performed in controlled conditions and few studies have clearly demonstrated the benefits of fungal inoculation in the field. The degree of mycorrhizal responses on a reafforestation site depends on the status of fungal colonization at planting, and the persistence of introduced fungi and other biotic and abiotic factors at the planting site (Duponnois et al. 2011).

    Table 1. Impact of R. irregularis on the growth of tree species in controlled conditions after different times of cultivation

    Image 10000000000002C800000279F3DB8620.jpg

    (1) (Shoot biomass of mycorrhizal plants / Shoot biomass of non mycorrhizal plants) x 100. (2) (Root biomass of mycorrhizal plants / Root biomass of non mycorrhizal plants) x 100.

    9Hence, the use of AM fungi and plants adapted to the local environmental conditions may be a prerequisite for the success of reafforestation programmes (Duponnois et al. 2005a). The potential effect of mycorrhizal inoculation with native AM fungi on the survival rates and early growth performance in the field of Mediterranean tree species (i.e. cypress, carob) has been assessed in a few studies (Manaut et al. 2015). The results showed the high potential of this approach by sustainably improving the growth and nutrient status of both tree species and also by inducing a positive soil microbial environment for nutrient cycling and environmental stress resistance (figs. 1 & 2).

    The “holistic” approach

    10It has been reported that certain shrubs react positively to the survival and growth of other neighboring plant species by creating a better environmental habitat with low stresses from high radiation and temperature as well as from soil nutrient and moisture deficiencies (Callaway & Walker, 1997) named “the nurse-plant syndrome” (Niering et al. 1963). The ecological facilitation between plant species results in the patchy distribution of the vegetation commonly observed in Mediterranean areas, especially in degraded ecosystems (Callaway & Walker, 1997).

    11Hence it has been suggested that the use of nurse plants as planting microhabitats in Mediterranean degraded ecosystems could promote the survival and development of native tree species and constitute an alternative reforestation technique compared to the standard practices (Duponnois et al. 2011). The “fertility islands” or “resource islands” (Schlesinger et al. 1996) resulting from the establishment of these nurse plants show a higher arbuscular mycorrhizal (AM) soil infectivity compared to the adjacent soil away from plant influence (Duponnois et al. 2011), which can improve plant growth and survival in arid conditions, by increasing the supply of nutrients to the plants (especially for soil P uptake) (Smith & Read, 2008), enhancing soil aggregation in eroded soils (Caravaca et al. 2002) and reducing water stress (Augé, 2001).

    12After three years’ plantation, it was reported that the association between C. atlantica and a nurse plant, L. stoechas, enhanced the growth of C. atlantica and provided better soil microbial characteristics compared to the control treatment (fig. 3) (Duponnois et al. 2011). AM mycelium network, total microbial activity, dehydrogenase activity, phosphate-solubilizing fluorescent pseudomonads and N, P nutrient uptake by C. atlantica, were significantly higher in the presence of L. stoechas. This pioneer shrub facilitated the early establishment of Cypress seedlings by improving soil microbial characteristics and AM fungus community development. Since the facilitative effect of one plant species on another increases with abiotic stress (Callaway, 1995), the benefits of this technique would be useful in reforestation programs undertaken to rehabilitate degraded areas in the Mediterranean region (Duponnois et al. 2011). Other shrub species have been identified for their potential nursing effects on Mediterranean tree species (fig. 4).

    Image 10000000000001EE000002B74D209070.jpg

    Figure 1
    Height and collar diameter of carob outplants in the field, either inoculated with AM fungi (
    ⏹) or non-inoculated (control □). An asterisk indicates a significant (P < 0.05) difference between the two treatments for a given year (From Manaut et al. 2015).

    Image 10000000000001E40000012777AF5E86.jpg

    Figure 2
    Cumulative mortality of carob outplants in the field, either inoculated with AM fungi (
    ⏹) or non-inoculated (control □) during the three years of plantation (From Manaut et al. 2015).

    Image 10000000000002590000011D87D8BB42.jpg

    Figure 3
    Time course changes in plant height (expressed in cm) of
    C. atlantica outplants growing under natural conditions in the High Atlas Mountains (Morocco), either non-inoculated (Control) (⏺) or associated with L. stoechas plants (⏹). Symbols represent means (± standard error of the mean). An asterisk indicates that the difference between the height of uninoculated C. atlantica and C. atlantica associated with L. stoechas is significant in the corresponding month according to the Newman Keul’s test (p < 0.05).

    Conclusion

    13These data show that the management of the mycorrhizal soil infectivity through different cultural approaches (reductionist or holistic approaches) has large potentialities to improve the performances of afforestation programmes, especially in Mediterranean and Tropical areas. This biological tool must be used according to the biological characteristics of the targeted areas (physic-chemical characteristics, biological characteristics) in order to reach sustainable objectives in forest ecosystem productivity and resistance. Hence ecological approaches at community and population scalesmust be encouraged with a view to better informed management of AM fungi in order to propose practical solutions to manage forest ecosystems in a sustainable manner.

    Image 100000000000023C000002880AC8C506.jpg

    Figure 4
    Growth responses of
    Acacia raddiana seedlings to the soil origins collected under shrub species native from Morrocan arid areas after 4 months’ culture in glasshouse conditions (Unpublished data). HL: Helianthemum lupii; ON: Ononis natrix; HS: Haloxylon scoparium; RR: Retama retama; WA: Withania adpressa; LS: Lavandula sp.: LAS: Launea sp.; CL: Cleome sp.; CT: Convolvulus trabutianus; AA: Artemisia herba alba; AS: Astericus sp.; SHC: Soil non influenced by plants.

    Bibliographie

    Des DOI sont automatiquement ajoutés aux références bibliographiques par Bilbo, l’outil d’annotation bibliographique d’OpenEdition. Ces références bibliographiques peuvent être téléchargées dans les formats APA, Chicago et MLA.

    Format

    Bossio, D., Girvan, M., Verchot, L., Bullimore, J., Borelli, T., Albrecht, A., … Osborn, A. (2005). Soil Microbial Community Response to Land Use Change in an Agricultural Landscape of Western Kenya. Springer Science and Business Media LLC. https://doi.org/10.1007/s00248-003-0209-6
    Callaway, R. M. (1995). Positive interactions among plants. Springer Science and Business Media LLC. https://doi.org/10.1007/bf02912621
    Callaway, R. M., & Walker, L. R. (1997). COMPETITION AND FACILITATION: A SYNTHETIC APPROACH TO INTERACTIONS IN PLANT COMMUNITIES. Wiley. https://doi.org/10.1890/0012-9658(1997)078[1958:cafasa]2.0.co;2
    Caravaca, F., Barea, J., Figueroa, D., & Roldán, A. (2002). Assessing the effectiveness of mycorrhizal inoculation and soil compost addition for enhancing reafforestation with Olea europaea subsp. sylvestris through changes in soil biological and physical parameters. Elsevier BV. https://doi.org/10.1016/s0929-1393(02)00015-x
    DeFries, R., Achard, F., Brown, S., Herold, M., Murdiyarso, D., Schlamadinger, B., & de Souza, C. , Jr. (2007). Earth observations for estimating greenhouse gas emissions from deforestation in developing countries. Elsevier BV. https://doi.org/10.1016/j.envsci.2007.01.010
    Manaut, N., Sanguin, H., Ouahmane, L., Bressan, M., Thioulouse, J., Baudoin, E., … Duponnois, R. (2015). Potentialities of ecological engineering strategy based on native arbuscular mycorrhizal community for improving afforestation programs with carob trees in degraded environments. Elsevier BV. https://doi.org/10.1016/j.ecoleng.2015.03.007
    Requena, N., Perez-Solis, E., Azcón-Aguilar C., Jeffries, P., & Barea, J.-M. (2001). Management of Indigenous Plant-Microbe Symbioses Aids Restoration of Desertified Ecosystems. American Society for Microbiology. https://doi.org/10.1128/aem.67.2.495-498.2001
    Rodriguez, A., & Sanders, I. R. (2014). The role of community and population ecology in applying mycorrhizal fungi for improved food security. Oxford University Press (OUP). https://doi.org/10.1038/ismej.2014.207
    Schlesinger, W. H., Raikes, J. A., Hartley, A. E., & Cross, A. F. (1996). On the Spatial Pattern of Soil Nutrients in Desert Ecosystems. Wiley. https://doi.org/10.2307/2265615
    Bossio, D.A., M.S. Girvan, L. Verchot, J. Bullimore, T. Borelli, A. Albrecht, K.M. Scow, A.S. Ball, J.N. Pretty, and A.M. Osborn. “Soil Microbial Community Response to Land Use Change in an Agricultural Landscape of Western Kenya”. Microbial Ecology. Springer Science and Business Media LLC, January 2005. doi:10.1007/s00248-003-0209-6.
    Callaway, Ragan M. “Positive Interactions Among Plants”. The Botanical Review. Springer Science and Business Media LLC, October 1995. doi:10.1007/bf02912621.
    Callaway, Ragan M., and Lawrence R. Walker. “COMPETITION AND FACILITATION: A SYNTHETIC APPROACH TO INTERACTIONS IN PLANT COMMUNITIES”. Ecology. Wiley, October 1997. doi:10.1890/0012-9658(1997)078[1958:cafasa]2.0.co;2.
    Caravaca, F., J.M. Barea, D. Figueroa, and A. Roldán. “Assessing the Effectiveness of Mycorrhizal Inoculation and Soil Compost Addition for Enhancing Reafforestation With Olea Europaea Subsp. Sylvestris through Changes in Soil Biological and Physical Parameters”. Applied Soil Ecology. Elsevier BV, May 2002. doi:10.1016/s0929-1393(02)00015-x.
    DeFries, Ruth, Frédéric Achard, Sandra Brown, Martin Herold, Daniel Murdiyarso, Bernhard Schlamadinger, and Carlos de Souza Jr. “Earth Observations for Estimating Greenhouse Gas Emissions from Deforestation in Developing Countries”. Environmental Science &amp;Amp; Policy. Elsevier BV, June 2007. doi:10.1016/j.envsci.2007.01.010.
    Manaut, N., H. Sanguin, L. Ouahmane, M. Bressan, J. Thioulouse, E. Baudoin, A. Galiana, M. Hafidi, Y. Prin, and R. Duponnois. “Potentialities of Ecological Engineering Strategy Based on Native Arbuscular Mycorrhizal Community for Improving Afforestation Programs With Carob Trees in Degraded Environments”. Ecological Engineering. Elsevier BV, June 2015. doi:10.1016/j.ecoleng.2015.03.007.
    Requena, Natalia, Estefania Perez-Solis, Azcón-Aguilar Concepción, Peter Jeffries, and Barea José-Miguel. “Management of Indigenous Plant-Microbe Symbioses Aids Restoration of Desertified Ecosystems”. Applied and Environmental Microbiology. American Society for Microbiology, February 2001. doi:10.1128/aem.67.2.495-498.2001.
    Rodriguez, Alia, and Ian R Sanders. “The Role of Community and Population Ecology in Applying Mycorrhizal Fungi for Improved Food Security”. The ISME Journal. Oxford University Press (OUP), October 31, 2014. doi:10.1038/ismej.2014.207.
    Schlesinger, William H., Jane A. Raikes, Anne E. Hartley, and Anne F. Cross. “On the Spatial Pattern of Soil Nutrients in Desert Ecosystems”. Ecology. Wiley, March 1996. doi:10.2307/2265615.
    Bossio, D.A., et al. “Soil Microbial Community Response to Land Use Change in an Agricultural Landscape of Western Kenya”. Microbial Ecology, vols. 49, no. 1, Springer Science and Business Media LLC, Jan. 2005, pp. 50-62. Crossref, https://doi.org/10.1007/s00248-003-0209-6.
    Callaway, Ragan M. “Positive Interactions Among Plants”. The Botanical Review, vols. 61, nos. 4, Springer Science and Business Media LLC, Oct. 1995, pp. 306-49. Crossref, https://doi.org/10.1007/bf02912621.
    Callaway, Ragan M., and Lawrence R. Walker. “COMPETITION AND FACILITATION: A SYNTHETIC APPROACH TO INTERACTIONS IN PLANT COMMUNITIES”. Ecology, vols. 78, nos. 7, Wiley, Oct. 1997, pp. 1958-65. Crossref, https://doi.org/10.1890/0012-9658(1997)078[1958:cafasa]2.0.co;2.
    Caravaca, F., et al. “Assessing the Effectiveness of Mycorrhizal Inoculation and Soil Compost Addition for Enhancing Reafforestation With Olea Europaea Subsp. Sylvestris through Changes in Soil Biological and Physical Parameters”. Applied Soil Ecology, vols. 20, nos. 2, Elsevier BV, May 2002, pp. 107-18. Crossref, https://doi.org/10.1016/s0929-1393(02)00015-x.
    DeFries, Ruth, et al. “Earth Observations for Estimating Greenhouse Gas Emissions from Deforestation in Developing Countries”. Environmental Science &amp;Amp; Policy, vols. 10, nos. 4, Elsevier BV, June 2007, pp. 385-94. Crossref, https://doi.org/10.1016/j.envsci.2007.01.010.
    Manaut, N., et al. “Potentialities of Ecological Engineering Strategy Based on Native Arbuscular Mycorrhizal Community for Improving Afforestation Programs With Carob Trees in Degraded Environments”. Ecological Engineering, vols. 79, Elsevier BV, June 2015, pp. 113-9. Crossref, https://doi.org/10.1016/j.ecoleng.2015.03.007.
    Requena, Natalia, et al. “Management of Indigenous Plant-Microbe Symbioses Aids Restoration of Desertified Ecosystems”. Applied and Environmental Microbiology, vols. 67, nos. 2, American Society for Microbiology, Feb. 2001, pp. 495-8. Crossref, https://doi.org/10.1128/aem.67.2.495-498.2001.
    Rodriguez, Alia, and Ian R Sanders. “The Role of Community and Population Ecology in Applying Mycorrhizal Fungi for Improved Food Security”. The ISME Journal, vols. 9, nos. 5, Oxford University Press (OUP), 31 Oct. 2014, pp. 1053-61. Crossref, https://doi.org/10.1038/ismej.2014.207.
    Schlesinger, William H., et al. “On the Spatial Pattern of Soil Nutrients in Desert Ecosystems”. Ecology, vols. 77, nos. 2, Wiley, Mar. 1996, pp. 364-7. Crossref, https://doi.org/10.2307/2265615.

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    Auteurs

    • Robin Duponnois

      IRD, France
      Microbiologist, IRD, Montpellier, France
      robin.duponnois@ird.fr

    • Lahcen Ouahmane

      Cadi Ayyad University of Marrakech, Morocco
      Microbiologist – ecologist, Université Cadi Ayyad de Marrakech, Morocco
      l.ouahmane@uca.ac.ma

    • Mohamed Hafidi

      Cadi Ayyad University of Marrakech, Morocco
      Soil scientist – ecologist, Université Cadi Ayyad de Marrakech, Morocco
      hafidi.ucam@gmail.com

    • Yves Prin

      CIRAD, France
      Microbiologist, LSTM, CIRAD, Montpellier, France
      yves.prin@cirad.fr

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    Duponnois, R., Ouahmane, L., Hafidi, M., & Prin, Y. (2016). Sub-chapter 3.5.4. Rethinking the management of mycorrhizal soil infectivity to restore Mediterranean and tropical forest ecosystems. In J.-P. Moatti & S. Thiébault (éds.), The Mediterranean region under climate change. Marseille: IRD Éditions. https://doi.org/10.4000/books.irdeditions.24051
    Duponnois, Robin, Lahcen Ouahmane, Mohamed Hafidi, et Yves Prin. « Sub-Chapter 3.5.4. Rethinking the Management of Mycorrhizal Soil Infectivity to Restore Mediterranean and Tropical Forest Ecosystems ». In The Mediterranean Region under Climate Change, édité par Jean-Paul Moatti et Stéphane Thiébault. Marseille: IRD Éditions, 2016. doi:10.4000/books.irdeditions.24051.
    Duponnois, Robin, et al. « Sub-Chapter 3.5.4. Rethinking the Management of Mycorrhizal Soil Infectivity to Restore Mediterranean and Tropical Forest Ecosystems ». The Mediterranean Region under Climate Change, édité par Jean-Paul Moatti et Stéphane Thiébault, IRD Éditions, 2016, https://doi.org/10.4000/books.irdeditions.24051.

    Référence numérique du livre

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    Moatti, J.-P., & Thiébault, S. (éds.). (2016). The Mediterranean region under climate change. Marseille: IRD Éditions. https://doi.org/10.4000/books.irdeditions.22908
    Moatti, Jean-Paul, et Stéphane Thiébault, éd. The Mediterranean Region under Climate Change. Marseille: IRD Éditions, 2016. doi:10.4000/books.irdeditions.22908.
    Moatti, Jean-Paul, et Stéphane Thiébault, éditeurs. The Mediterranean Region under Climate Change. IRD Éditions, 2016, https://doi.org/10.4000/books.irdeditions.22908.
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