1
Soil depth: 0-5 cm Soil depth: 5-10 cm a b a ab a ab ab b No 3 - (mg.l -1 ) Sole Acacia Sole Eucalyptus Acacia mixed with Eucalyptus Eucalyptus mixed with Acacia Monospecific tree plantation Mixed tree plantation 8 6 4 2 0 8 6 4 2 0 Morocco Tunisia Algeria Institutes involved in the research projects : Soil biota, symbiotic and rhizospheric microorganisms N & P biogeochimical cycles and C sequestration in soils Agronomic & environmental diagnosis, and sustainability assessment N & P utilisation efficiency in plants, and candidate genes The field activities (WP1 and WP5 in fig 2) includes agronomic experiments and participatory research in reference agroecosystems with a wide range of agroclimatical and socioecological situations (e.g. fig 3 and 4). Figure 3. A, Zaï cultivation for cowpea associated to sorghum in Burkina Faso; B, Common-bean associated to maize in rotation with rainfed rice in Madagascar ; C, Wheat associated with chickpea or faba bean (not shown) in South of France ; D, Acacia-hevea in Brazil. Figure 5. Increasing N 2- dependent growth of legume in a low-P soil would generate physico-chemical and biotic mechanismes to enhance P bioavailability in the nodulated-root rhizospĥere, and generate a virtual cycle of N&P fertility. 7A A multidisciplinary research strategy for legume contributions in the biogeochemical cycles of N, P and C in agricultural and forestry systems under Mediterranean and Tropical climates Drevon Jean-Jacques, Blavet Didier, Bouillet Jean-Pierre & Hinsinger Philippe Figure 2. The interdisciplinary strategy for Fabatropimed. Figure 4. Localisation of field sites for nodular diagnosis on Common bean in the agro-ecosystem of Aïn Temouchent in Algeria (from C. Benadis). Figure 1. Network of reference agrosystems with legumes. pO2 CO 2 O 2 H 2 H + HCO 3 - PO4 - C + absorption exsorption pH eH Phytate influx efflux Figure 6. A, In the rhizosphere, water-extractable P was higher for chickpea than for durum wheat in a P-poor luvisol of France, and intercropping increased water-extractable P for wheat (Betencourt et al. 2012 – Soil Biol. Biochem.); B, Acacia introduction in Eucalyptus plantations decreased phosphorus availability (not shown) but increased nitrate availability in Congo. Figure 7. A, Phytate-solubilising rhizobia were isolated from faba-bean nodules in South of France, as confirmed subsequently with liquid culture and phytase gene (from O. Domergue); B, localisation by in situ RT-PCR of β propeler bacterial gene on the surface of root hairs, and C, in the root tip of nodulated faba-bean in hydroaeroponic culture (Maougal et al. Planta, 2014). 7B Figure 8. A, Recombinant inbred lines of common-bean contrasting in phosphorus use efficiency for symbiotic nitrogen fixation ; B, Localisation by in situ RT-PCR in common-bean nodules of plant gene of phospho enol P phosphatase (Bargaz et al., J Exp Bot, 2013), and (not shown) Fructose biP phosphatase, phytase (Lazali et al. Planta, 2014) Algeria : ENSAA Algiers, Universities of Constantine & Oran; Brazil : Embrapa, University of Sao Paulo ; Burkina-Faso : INERA, University of Ouagadougou ; Congo : CRDPI ; France : CIRAD, INRA, IRD, Montpellier SupAgro, ESA-Angers, AFAF, Arvalis, BioCivam11 ; Madagascar : FOFIFA, GSDM, University of Madagascar, TAFA; Morroco : IAV Rabat, University of Marrakesh; Tunisia : INRAT, University of Tunis. 8B South of France Madagascar Congo Brasil Burkina-Faso http://intens-fix.cirad.fr & http://www6.inra.fr/fabatropimed & http://www6.montpellier.inra.fr/systerra-perfcom_eng/ Since 2008, the Eco&Sols mixed research unit has been coordinating the PerfCom, Intens&Fix and Fabatropimed projects with Agropolis Fondation, ANR Systerra and EU Averoes supports, for studying and promoting the association or rotation of N 2 -fixing legumes in a diversity of agricultural and foresty systems (fig 1) . 3 A 3 C 3 D 3 B 6 A 0.0 0.2 0.4 H 2 O – P (mg kg -1 ) wheat chickpea Chickpea intercropped with wheat Weath intercropped with chickpea sole wheat sole chickpea bulk soil b a c d d 6 B 8A Hydroaeroponic exp The exchange of N, P and C between soils, legumes and atmosphere are conceptualized as biogeochemical models and provide working hypotheses (fig 5). These are tested in the field or in controlled conditions (pots, rhizotrons). The results obtained (e.g. fig 6) allow comparisons of the hypotheses with the facts and help to identify efficient farming practices. In the laboratory, the projects include the study of the role in the cycles of C, N and P of microorganisms (bacteria like rhizobia, mycorrhiza ..) that are present in the symbiotic nitrogen-fixing nodules (e.g. fig 7A) and in the rhizosphere of legumes (e.g. fig 7 B and C) For a given legume, some genotypes are more tolerant than others to low P conditions (eg. Fig 8a). The study of these genotypes and their symbiotic nodules (eg. Fig 8B) indicates genes that might promote such tolerance. 7C

Since 2008, the Eco&Sols mixed PerfCom, Intens&Fix and ... · 4). Figure 3. A, Zaï cultivation for cowpea associated to sorghum in Burkina Faso; B, Common-bean associated to maize

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Page 1: Since 2008, the Eco&Sols mixed PerfCom, Intens&Fix and ... · 4). Figure 3. A, Zaï cultivation for cowpea associated to sorghum in Burkina Faso; B, Common-bean associated to maize

Soil depth: 0-5 cm

Soil depth: 5-10 cm

a b

a ab

a ab ab b

No3-

(mg.l-1)

Sole Acacia

Sole Eucalyptus

Acacia mixed with Eucalyptus

Eucalyptus mixed with Acacia

Monospecific tree plantation

Mixed tree plantation

8 6 4 2 0 8 6 4 2 0

Morocco Tunisia Algeria

Institutes involved in the research projects :

Soil biota, symbiotic and rhizospheric microorganisms

N & P biogeochimical cycles and C sequestration in soils

Agronomic & environmental diagnosis, and sustainability assessment

N & P utilisation efficiency in plants, and candidate genes

The field activities (WP1 and WP5 in fig 2) includes agronomic experiments and participatory research in reference agroecosystems with a wide range of agroclimatical and socioecological situations (e.g. fig 3 and 4).

Figure 3. A, Zaï cultivation for cowpea associated to sorghum in Burkina Faso; B, Common-bean associated to maize in rotation with rainfed rice in Madagascar ; C, Wheat associated with chickpea or faba bean (not shown) in South of France ; D, Acacia-hevea in Brazil.

Figure 5. Increasing N2-dependent growth of legume in a low-P soil would generate physico-chemical and biotic mechanismes to enhance P bioavailability in the nodulated-root rhizospĥere, and generate a virtual cycle of N&P fertility.

7A

A multidisciplinary research strategy for legume contributions in the biogeochemical cycles of N, P and C in agricultural and forestry systems

under Mediterranean and Tropical climates Drevon Jean-Jacques, Blavet Didier, Bouillet Jean-Pierre & Hinsinger Philippe

Figure 2. The interdisciplinary strategy for Fabatropimed.

Figure 4. Localisation of field sites for nodular diagnosis on Common bean in the agro-ecosystem of Aïn Temouchent in Algeria (from C. Benadis).

Figure 1. Network of reference agrosystems with legumes.

pO2 CO2

O2

H2

H+ HCO3-

PO4- C+ absorption

exsorption

pH eH

Phytate

influx efflux

Figure 6. A, In the rhizosphere, water-extractable P was higher for chickpea than for durum wheat in a P-poor luvisol of France, and intercropping increased water-extractable P for wheat (Betencourt et al. 2012 – Soil Biol. Biochem.); B, Acacia introduction in Eucalyptus plantations decreased phosphorus availability (not shown) but increased nitrate availability in Congo.

Figure 7. A, Phytate-solubilising rhizobia were isolated from faba-bean nodules in South of France, as confirmed subsequently with liquid culture and phytase gene (from O. Domergue); B, localisation by in situ RT-PCR of β propeler bacterial gene on the surface of root hairs, and C, in the root tip of nodulated faba-bean in hydroaeroponic culture (Maougal et al. Planta, 2014).

7B

Figure 8. A, Recombinant inbred lines of common-bean contrasting in phosphorus use efficiency for symbiotic nitrogen fixation ; B, Localisation by in situ RT-PCR in common-bean nodules of plant gene of phospho enol P phosphatase (Bargaz et al., J Exp Bot, 2013), and (not shown) Fructose biP phosphatase, phytase (Lazali et al. Planta, 2014)

Algeria : ENSAA Algiers, Universities of Constantine & Oran; Brazil : Embrapa, University of Sao Paulo ; Burkina-Faso : INERA, University of Ouagadougou ; Congo : CRDPI ; France : CIRAD, INRA, IRD, Montpellier SupAgro, ESA-Angers, AFAF, Arvalis, BioCivam11 ; Madagascar : FOFIFA, GSDM, University of Madagascar, TAFA; Morroco : IAV Rabat, University of Marrakesh; Tunisia : INRAT, University of Tunis.

8B

South of France

Madagascar

Congo Brasil

Burkina-Faso

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Since 2008, the Eco&Sols mixed research unit has been coordinating the PerfCom, Intens&Fix and Fabatropimed projects with Agropolis Fondation, ANR Systerra and EU Averoes supports, for studying and promoting the association or rotation of N2-fixing legumes in a diversity of agricultural and foresty systems (fig 1) .

3 A

3 C 3 D

3 B

6 A

0.0

0.2

0.4

H2O – P (mg kg-1) wheat

chickpea

Chickpea intercropped with wheat

Weath intercropped with chickpea

sole wheat

sole chickpea

bulk soil

b a c

d d

6 B

8A

Hydroaeroponic exp

The exchange of N, P and C between soils, legumes and atmosphere are conceptualized as biogeochemical models and provide working hypotheses (fig 5). These are tested in the field or in controlled conditions (pots, rhizotrons). The results obtained (e.g. fig 6) allow comparisons of the hypotheses with the facts and help to identify efficient farming practices.

In the laboratory, the projects include the study of the role in the cycles of C, N and P of microorganisms (bacteria like rhizobia, mycorrhiza ..) that are present in the symbiotic nitrogen-fixing nodules (e.g. fig 7A) and in the rhizosphere of legumes (e.g. fig 7 B and C)

For a given legume, some genotypes are more tolerant than others to low P conditions (eg. Fig 8a). The study of these genotypes and their symbiotic nodules (eg. Fig 8B) indicates genes that might promote such tolerance.

7C