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Use of δ13C for soil CO2 efflux partitioning in a beech temperate forest and a rain tropical forest

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HAL Id: hal-01032070

https://hal.archives-ouvertes.fr/hal-01032070

Submitted on 6 Jun 2020

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Use of δ 13C for soil CO2 efflux partitioning in a beech temperate forest and a rain tropical forest

Bernard Longdoz, Daniel Epron, Jerome Ngao, Stéphane Ponton, Damien Bonal, Valérie Le Dantec

To cite this version:

Bernard Longdoz, Daniel Epron, Jerome Ngao, Stéphane Ponton, Damien Bonal, et al.. Use of δ13C

for soil CO2 efflux partitioning in a beech temperate forest and a rain tropical forest. 33. European

Geosciences Union General Assembly, Apr 2006, Vienne, Austria. 1 p. �hal-01032070�

(2)

LICOR Li LICOR Li--62006200

Gas sampling chamber

Soil CO

2

efflux is the main respiration flux in the terrestrial ecosystems. Because of its high dependence on temperature and water content and important carbon stock in the soil, it plays an important role in the perturbations of the global carbon cycle due to climatic change.

13

C (stable isotope of the carbon) can be used as a tracer to achieve a better understanding and modelling of the processes involve in soil respiration (identification and quantification of these processes, determination of the relative importance of the different soil CO

2

sources). In this context, the aim of this study was first to measure the δ

13

C (ratio

13

C/

12

C ) at different stages of soil respiration to evaluate the discriminations (modification of δ

13

C value during a carbon transformation or transfer) and then to compare δ

13

C of soil CO

2

efflux coming from trenched (zone without living roots) sand control plots to separate the heterotrophic and autotrophic components of Rs.

Use of

Use of δ δ δ δ δ δ δ δ 13 13 C for soil CO C for soil CO 2 2 efflux partitioning in a efflux partitioning in a beech temperate forest and a rain tropical forest beech temperate forest and a rain tropical forest

1.Objectives

2.Sites

LONGDOZ B.

1

([email protected]), EPRON D.

1

, NGAO J.

4

, PONTON S.

2

, BONAL D.

2

, LE DANTEC V.

3

1UMR Ecologie et Ecophysiologie Forestières, INRA-Université HP Nancy (France); 2UMR Ecologie des Forêts de Guyane, INRA Kourou (Guyane Française); 3Centre d’Etude Spatial de la Biosphère, Université PS,Toulouse (France); 4Dipartemente di Scienze Ambientali Seconda Universita di Napoli (Italy)

N E W

S

HESSE, France (

HESSE, France (CarboEurope CarboEurope & & Fluxnet Fluxnet site) site)

Age: 37 years 37 years

Mean annual air Temp.: 9.2°C Mean annual Precip.: 820 mm Soil type: luvisol/stagnic luvisol (FAO)

LAI: 7- 7 -4 m 4 m

22

m m

--22

Temperate oceanic climate

Species: 90% Beech

Height: 18m 18m

Age : 14 years LAI : 8-5 m

2

m

-2

Species: Beech, Hornbeam, Oak Height : 8m Hesse

Hesse 1 ( 1 (H1 H1): ):

Hesse 2 (H2):

Nancy Nancy HesseHesse

PARACOU, French Guyana

Paracou

Mean annual air Temp.: 25.8°C Mean annual Precip.: 2875 mm

Soil type:

ferralitic (FAO)

Tropical climate

LAI: 7 m

2

m

-2

Mixed forest:

180 species ha

-1

Height: 35 m

3.Material and Methods

P)

• Measurement of δ

13

C for CO

2

efflux (soil Keeling plot):

• Measurement of δ

13

C for dry matter of fine roots, soil organic matter (SOM) and litter:

• Measurement of δ

13

C for CO

2

coming from fine roots, SOM and litter :

• Measurement of δ

13

C for soil air CO

2

Soil respiration system Core sampling, soil components (roots-S0M-litter separation), passage of dry samples in

the mass spectrometer

Core sampling, soil components separation, air sampling during incubation (use of gas sampling chamber, Fig. 3.1.), passage of the samples in the mass spectrometer

Tubes (closed at the top and pierced at the bottom) inserted

permanently in the soil (Fig. 3.2.), sampling of gas in these tubes (use of gas sampling chamber), passage of the samples in the mass

spectrometer

Fig. 3.2.

4.Results and discussion

Results of δ

13

C for different sites (H1, H2, Paracou) and different campaigns (March, May, September, October) with Blue = dry matter; Green = CO

2

from incubation; White δ

13

C(soil CO

2

) = CO

2

from soil air; Red δ

13

C(KP) = soil Keeling plot

A. Control plots:

Lit = litter; LR = living roots; SOM = soil organic matter Fig. 3.1.

accumulation of CO

2

coming from soil in the soil respiration system (Fig. 3.1.), air sampling in the system at different CO

2

concentration, passage of the gas samples in the mass spectrometer, Keeling plot (Fig 3.3.)

Fig. 3.3.

Systematic (all campaigns, all soil components) positive discrimination during the CO

2

production ( δ δ δ δ

13

C incubation - δ δ δ δ

13

C dry matter, 3‰ in mean) Systematic (all campaigns, all soil components) negative discrimination during the CO

2

diffusion toward surface (CO

2

efflux - incubation ,-5‰ in mean) Logically the value of soil air δ

13

C is quasi-systematically between the incubation δ

13

C of the different soil components

accumulation δ13C of CO2efflux

5.Conclusion • Better quantification of discrimination is needed to improve the results of soil respiration process studies using

13

C

• Use of

13

C don’t give significant results for soil CO

2

efflux partitioning between potential sources (roots, SOM, litter) Comparison between soil air δ

13

C measured on trenched plots ( δ

TP

, no living roots) and control plots ( δ

S

) A. Trenched plots:

Except in one case, no significant difference between δ

TP

and δ

S

• δ

13

C of living root and SOM are too close

•The discriminations during respiration process (that are not well quantified) seem to be larger than the difference studied ( δ

TP

- δ

S

)

Possible causes:

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