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Distribution and composition of organic carbon in the Tana River Basin, (Kenya)

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Distribution and Composition of Organic Carbon

in the Tana River Basin, (Kenya).

 Rivers play an important role in the global carbon cycle, and process ~1.9 Pg C annually (Cole et al., 2007). Rivers do not merely transport carbon from the terrestrial to the oceanic environment, but also bury and process organic matter,

typically acting as a source of CO2 to the atmosphere (Devol

et al., 1987, Cole and Caraco 2001, Mayorga et al. 2005).

 Due to increased carbon emissions, it is critical to understand carbon cycling both on a global and a watershed scale. However, there are few studies which quantify carbon fluxes in tropical rivers, and data for the African continent are particularly scarce.

 In this study, we report the altitudinal and seasonal patterns in carbon pools and their stable isotope compositions in Tana River Basin (Kenya)

Introduction

Fredrick Tamooh

1,5

, Karel Van Den Meersche

4,2

, Alberto Borges

3

, Roel Merckx

1

,

Frank Dehairs

4

, Filip Meysman

2,4

& Steven Bouillon

1

(1) Katholieke Universiteit Leuven, dept. of Earth & Environmental Sciences, Belgium; E-mail : fredrick.tamooh@ees.kuleuven.be

(2)Netherlands Institute of Ecology (NIOO-CEME), Yerseke, The Netherlands (3) Unité d’Océanographie Chimique Université de Liège, Belgium (4) Department of Analytical and Environmental Chemistry, Vrije Universiteit Brussel, Belgium (5) Kenya Wildlife Services, P.O. Box 82144-80100, Mombasa, Kenya

Site and Methods

 The Tana River is the longest river system in Kenya (>1200 km), with a catchment area of ~120,000 km2

(Kitheka et al., 2005).

 The main perennial source areas of the river are Mount Kenya (up to 5199 m), the Abardares ranges in the central Highlands of Kenya, and the Nyambene Hills in Eastern Kenya.

 The basin in general experiences two rainfall seasons: long rains between March and May and short rains between October and December.

 Data from field campaigns throughout the river basin are presented from a preliminary campaign in February 2008 (Bouillon et al., 2009; end of dry season) , September to November 2009 (short rains), and June-July 2010 (end of long rains).

 Furthermore, monthly sampling was initiated in January 2009 at several locations (ongoing), and data up to March 2010 are presented here for 2 of the downstream sites (Garissa and Tana River Primate Reserve upstream of Garsen). Extensive flood plains are located between these 2 locations, flooding is irregular due to regulation of river flows by reservoirs upstream

 The samples for total suspended matter (TSM) were filtered through pre-combusted and pre-weighed,

47-mm-diameter Whatman GF/F filters, dried and re-weighed, while samples for POC and δ13C-POC were filtered

on pre-combusted 25 mm Whatman GF/F filters, acidified, dried and measured with standard techniques (EA-IRMS).

Figure 1:Location of the Tana River basin and sampling locations.

Total suspended matter and particulate organic Carbon

Results & Discussion

References

Bernardes, M. C., Martinelli, L. A., Krusche, A. V., Gudeman, J., Moreira, M., Victoria, R. L.,Ometto, J. P. H. B., Ballester, M.V. R., Aufdenkampe, A. K., Richey, J. E., and Hedges, J. I. Ecol. Appl., 14, S263–S279 (2004).

Bouillon S , Abril G, Borges AV, Dehairs F, Govers G, Hughes H.J, Merckx R, Meysman F, Nyunja J, Osburn C, & Middelburg J.J. Biogeosciences 6: 2475-2493

(2009).

Cole, J. J., Prairie, Y. T., Caraco, 5 N. F., McDowell, W. H.,

Tranvik, L. J., Striegl, R. G., Duarte, C. M., Kortelainen, P., Downing, J. A., Middelburg, J. J., and Melack , J

Ecosystems,10, 171–184, (2007).

Cole, J. J. and Caraco, N. F., Mar. Freshwater Res. 52, 101–110 (2001),

Devol, A.H., Quay, P.D., Richey, J.E. Limnology & Oceanography 32, 235–248 (1987).

Kitheka, J.U, Obiero, M., and Nthenge, P. Estuar. Coast. Shelf

Sci., 63, 455–468 (2005).

Ludwig, W., Probst, J.L., Kempe, S . Global Biogeochemical Cycles 10, 23-41 (1996).

Mayorga, E., Aufdenkampe, A. K., Masiello, C. A., Krusche, A. V., Hedges, J. I., Quay, P. D., Richey, J. E., and Brown, T. A.

Nature, 436, 538–541 (2005).

Acknowledgements

Funding for this work was provided by the Research Foundation Flanders (FWO-Vlaanderen, project G.0651.09 and travel grants to F.T., K.v.d.M., and S.B), and ERC-StG 24002 (AFRIVAL, http://ees.kuleuven.be/ project/afrival/). We are grateful to Olivier Hamerlynck and Kenya Water Resource Authority for sharing discharge data

Conclusions

 A consistent downstream increase in TSM was

observed during all three sampling campaigns.

 TSM values were similar for the 2008 and 2010 datasets (p>0.05), but significantly higher during the short rains campaign in 2009.

 The altitudinal distribution of POC concentrations shows similar trends as those in TSM, i.e. a

consistent downstream increase during all

sampling campaigns (p<0.01).

 POC for 2008, 2009 & 2010 differed significantly (p<0.05).

 δ13C-POC increased downstream during all three sampling

campaigns (p<0.01), and were predominantly of terrestrial origin as reflected by generally high POC/Chl a ratios. This trend thus reflects an increasing contribution of C4-derived carbon downstream. However, different years were not significantly different (p>0.05)

 TSM & % POC followed the classical inverse relationship (Bernardes et al., 2004) for all years sampled i.e. dilution of % POC with increase in TSM (p<0.01).

 The % POC/TSM relationship fits well with NEWS2 Model based on Ludwig et al. (1996) data.

Seasonal variation in organic composition

 DOC concentration was higher in wet season (2009) & increased downstream.

 δ13C-DOC increased downstream during the two

sampling campaigns (p<0.01) suggesting C4 plant contribution, but were divergent in high altitudes

 As expected, TSM & POC were highly episodic and highest in periods with high discharge

 Both TSM & POC maxima preceded peak discharge, particularly at TRPR station as observed previously by Kitheka et al. (2005). This suggests release of relatively mobile sediments during initial peak discharge.

 Seasonal patterns in δ13C-POC signatures at both stations coincided closely, with δ13C increasing

markedly during periods of high discharge (-23 to -21 ‰), and decreasing towards predominantly C3 signatures toward the end of dry periods. This suggests that high sediment mobilization during rains occurs mostly in areas with significant grassland cover (C4).

 TSM and POC delivery is episodic during peak discharge, and mostly mobilized at intermediate altitudes

 In the lower section of the Tana River, POC mainly originates from areas with a significant contribution by C4 plant species during high discharge, while

during low discharge POC is

predominantly derived from C3 plant species. Monthly station 4000 3000 2000 1000 0 10000 1000 100 10 1 Altitude (m) T S M ( m g /L ) 2008 2009 2010

Figure 2: Altitudinal profile of TSM Figure 3: Altitudinal profile of POC

4000 3000 2000 1000 0 -20 -22 -24 -26 -28 -30 -32 Altitude (m) δ 1 3 C -P O C ( ) 2008 2009 2010

Figure 4: Altitudinal profile of δ13C-POC Figure 5: Relation Between POC % and TSM

10000 1000 100 10 1 100 10 1 TSM (mg/L) P O C ( % ) 2008 2009 2010 10000.0 1000.0 100.0 10.0 1.0 0.1 100 10 1 TSM (mg/l) P O C ( % ) Tana River NEWS2 Model

Figure 6: Comparison of Organic Carbon Export with NEWS2 Model 3500 3000 2500 2000 1500 1000 500 0 40000 30000 20000 10000 0 Altitude (m) P O C /C h l a ( µ g g ) 2008 2009 2010

Figure 7: Altitudinal profile of POC/Chl a Ratio

4000 3000 2000 1000 0 100.0 10.0 1.0 0.1 Altitude (m) P O C ( m g /L ) 2008 2009 2010 M F J D N O S A J J M A M F J 500 400 300 200 100 0 5000 4000 3000 2000 1000 0 Month (2009-2010) D is c h a rg e ( m 3 /s ) T S M ( m g /L ) Discharge Garissa TRPR

Figure 9: Altitudinal profile of δ13C-DOC

Figure 8: Altitudinal Profile of DOC

M F J D N O S A J J M A M F J 500 400 300 200 100 0 -21 -22 -23 -24 -25 -26 -27 -28 -29 Month (2009-2010) D is c h a rg e ( m 3 /s ) δ 1 3 C -P O C ( ) Discharge Garissa TRPR

Figure 10: Discharge Superimposed with TSM Figure 11: Discharge Superimposed with δ13C-POC

4000 3000 2000 1000 0 7 6 5 4 3 2 1 0 Altitude (m) D O C (m g /l ) 2008 2009 3500 3000 2500 2000 1500 1000 500 0 -21 -22 -23 -24 -25 -26 -27 -28 Altitude (m) δ C 1 3 -D O C ( ) 2008 2009

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