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CARBON DIOXIDE AND WATER VAPOR FLUXES IN TWO CONTRASTING MANGROVE ECOSYSTEMS IN NORTHWEST MEXICO ABSTRACT SEASONAL CO 2 AND WATER VAPOR FLUXES DYNAMIC HEADLINES References Alongi, D. M. (2014). Carbon cycling and storage in mangrove forests. Annual review of marine science, 6, 195-219. Barr, J. G., Engel, V., Fuentes, J. D., Zieman, J. C., O'Halloran, T. L., Smith, T. J., & Anderson, G. H. (2010). Controls on mangrove forestatmosphere carbon dioxide exchanges in western Everglades National Park. Journal of Geophysical Research: Biogeosciences (20052012), 115(G2). Feller, I. C., Lovelock, C. E., Berger, U., McKee, K. L., Joye, S. B., & Ball, M. C. (2010). Biocomplexity in mangrove ecosystems. Annual Review of Marine Science, 2, 395-417. Giri, C., Ochieng, E., Tieszen, L. L., Zhu, Z., Singh, A., Loveland, T., ... & Duke, N. (2011). Status and distribution of mangrove forests of the world using earth observation satellite data. Global Ecology and Biogeography, 20(1), 154-159. Figure 1 .Localization of monitoring sites El Sargento Estuary (PE) and Tóbari Bay (DE), coastal mangroves in northwestern México. ACKNOWLEDGEMENTS We wish to acknowledge to Masuly Guadalupe Vega-Puga for the support with image and data processing. We also want to thank to Miguel Agustín Rivera-Díaz for helping with GIS skills and equipment installation as well as Carlos Alfredo Robles-Zazueta for the support provided on fieldwork. Financial support is recognized to CONACYT (Ciencia Básica, CB180704-T) given to Rodríguez Julio C. Vargas-Terminel Martha L. 1 ; Rodríguez Julio C. 2 ; Yépez Enrico A. 1 ; Watts Christopher J. 2 , Garatuza-Payán Jaime 1 . 1 Instituto Tecnológico de Sonora, 5 de febrero 818 sur, Col. Centro, C.P. 85000, Ciudad Obregón, Sonora, México. 2 Universidad de Sonora, Blvd. Luis Encinas y Rosales S/N, Col. Centro, C.P. 83000 Hermosillo Sonora, México. Corresponding author: Martha L. Vargas-Terminel; [email protected]. . MANGROVE FLUX SITES IN SONORA Figure 2. Representative mangrove species at monitoring sites. a) Avicennia germinans b) Laguncularia racemosa. c) Rhizophora mangle. Figure 3. Water level (a) and conductivity (b) data logger. c) b) a) b) a) c) Mangroves are biocomplex ecosystems due to diverse functional processes related to abiotic factors such salinity, tides, continental nutrient loads and disturbance, which control net ecosystem production (NEP). However, the relative importance of these factors controlling NEP is poorly understood because we lack of information on how fluxes and C pools vary at different scales in these ecosystems. The goal was to characterize CO 2 (NEE) and water vapor (ET) flux dynamics from January- November of 2014 in contrasting mangrove ecosystems: a preserved site (PE) and a site influenced by agriculture from the Yaqui Valley in southern Sonora (DE). Eddy covariance systems were used to determine NEE and water vapor fluxes on four defined periods: winter, spring, summer and autumn. NEE and ET patterns were different during dry and wet seasons, showing contrasts between sites. Over the winter, daily mean NEE on PE was -1.60 μmolCO 2 m -2 s -1 , meanwhile DE was -0.04 μmol CO 2 m -2 s -1 ; higher respiratory rates dominating on DE corresponds with the peak discharge season of nutrient loads from agricultural canals. During spring NEE for DE and PE were -2.09 and -4.23 μmolCO 2 m -2 s -1 , respectively. This suggests that during this period of higher radiation, photosynthetic activity was the dominant flux. In contrast, during summer values were lower than spring since PE presented -0.64 μmol CO 2 m -2 s -1 and DE-0.63 μmol CO 2 m -2 s -1 . During the autumn season NEE for PE and DE were -2.59 and-1.54μmol CO 2 m -2 s -1 .Mean daily ET values for PE ranged between 2.52 to 6.34 mm and for DE were 2.44 to 3.56 mm. Differences on NEE and ET patterns are modulated by temperature and solar radiation. The next stages of this research will evaluate the variability of salinity, nutrient loads and hydroperiod of these transitional ecosystems. b) Month/Site Water temperature (°C) Salinity (ppt) Water level (m) March El Sargento estuary Tóbari Bay July El Sargento estuary Tóbari Bay 18.59 20.96 26.31 30.01 28.20 (34.65-26.37) 33.03 (30.55-35021) 27.16 (27.48-26.37) 28.01 (28.66-27.26) -0.60 -0.69 0.15 0.13 Figure 4. Eddy covariance systems: a) El Sargento Estuary and b) Tóbari Bay. a) b) Figure 6. Diurnal behavior of NEE and LE for PE (a) and DE (b) . Patterns on DE show a similar trend through January, April and July with no drastical changes. However, PE presents a significant contrast o diurnal behavior comparing with DE, a marked amplitude on NEE and LE during above the three months shown. (PE) Figure 7. 8-day Ocean Net Primary Production (mg C m- 2 d- 1 ) from MODIS during October 2013 (a) and January 2014 (b) for the coast of Sonora. (DE) a) b) NEE and LE patterns were different during wet and dry seasons. Although, PE presents a higher productivity than DE over the study period there´s a contrast on LE flux which is higher on PE than DE. Higher respiration activity on daily on NEE values during winter for DE suggest a relationship with the peak of nutrients loads discharged by agricultural canals to the bay. a) b) Figure 5. Daily values showing the seasonal trends of NEE , LE and radiation at (PE) and (DE) during study period. Daily NEE fluctuations suggesrtthe presence of photosynthetic and respiration processeses showing contrast on sites increasing with the presence of higher radiation. Table 1. Contrast on water level, water temperature and salinity average values during March and July, 2014 for PE and DE.

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Page 1: CARBON DIOXIDE AND WATER VAPOR FLUXES IN TWO … · CARBON DIOXIDE AND WATER VAPOR FLUXES IN TWO CONTRASTING MANGROVE ECOSYSTEMS IN NORTHWEST MEXICO ABSTRACT SEASONAL CO 2 AND WATER

CARBON DIOXIDE AND WATER VAPOR FLUXES IN TWO CONTRASTING MANGROVE ECOSYSTEMS IN NORTHWEST MEXICO

ABSTRACT SEASONAL CO2 AND WATER VAPOR FLUXES DYNAMIC

HEADLINES

References

Alongi, D. M. (2014). Carbon cycling and storage in mangrove forests. Annual review of marine science, 6, 195-219.

Barr, J. G., Engel, V., Fuentes, J. D., Zieman, J. C., O'Halloran, T. L., Smith, T. J., & Anderson, G. H. (2010). Controls on mangrove forest‐atmosphere carbon dioxide exchanges in western Everglades

National Park. Journal of Geophysical Research: Biogeosciences (2005–2012), 115(G2).

Feller, I. C., Lovelock, C. E., Berger, U., McKee, K. L., Joye, S. B., & Ball, M. C. (2010). Biocomplexity in mangrove ecosystems. Annual Review of Marine Science, 2, 395-417.

Giri, C., Ochieng, E., Tieszen, L. L., Zhu, Z., Singh, A., Loveland, T., ... & Duke, N. (2011). Status and distribution of mangrove forests of the world using earth observation satellite data. Global Ecology and

Biogeography, 20(1), 154-159.

Figure 1 .Localization of monitoring sites El Sargento Estuary (PE) and Tóbari Bay (DE), coastal

mangroves in northwestern México.

ACKNOWLEDGEMENTS We wish to acknowledge to Masuly Guadalupe Vega-Puga for the support with image and data processing. We also want to thank to Miguel Agustín Rivera-Díaz for helping with GIS skills and equipment installation as well as Carlos Alfredo Robles-Zazueta for the support provided on fieldwork. Financial support is recognized to CONACYT (Ciencia Básica, CB180704-T) given to Rodríguez Julio C.

Vargas-Terminel Martha L.1; Rodríguez Julio C.2; Yépez Enrico A.1; Watts Christopher J.2, Garatuza-Payán Jaime1.

1 Instituto Tecnológico de Sonora, 5 de febrero 818 sur, Col. Centro, C.P. 85000, Ciudad Obregón, Sonora, México. 2 Universidad de Sonora, Blvd. Luis Encinas y Rosales S/N, Col. Centro, C.P. 83000 Hermosillo Sonora, México.

Corresponding author: Martha L. Vargas-Terminel; [email protected]. .

MANGROVE FLUX SITES IN SONORA

Figure 2. Representative mangrove species at monitoring sites. a) Avicennia germinans

b) Laguncularia racemosa. c) Rhizophora mangle.

c)

f)

g)

Figure 3. Water level (a) and conductivity (b) data logger.

c)

b)

a)

b)

a)

c)

Mangroves are biocomplex ecosystems due to diverse functional processes related to abiotic factors such salinity, tides, continental nutrient loads and disturbance, which control net ecosystem production (NEP). However, the relative importance of these factors controlling NEP is poorly understood because we lack of information on how fluxes and C pools vary at different scales in these ecosystems. The goal was to characterize CO2 (NEE) and water vapor (ET) flux dynamics from January-November of 2014 in contrasting mangrove ecosystems: a preserved site (PE) and a site influenced by agriculture from the Yaqui Valley in southern Sonora (DE). Eddy covariance systems were used to determine NEE and water vapor fluxes on four defined periods: winter, spring, summer and autumn. NEE and ET patterns were different during dry and wet seasons, showing contrasts between sites. Over the winter, daily mean NEE on PE was -1.60 μmolCO2 m-2 s-1, meanwhile DE was -0.04 μmol CO2 m-2 s-1; higher respiratory rates dominating on DE corresponds with the peak discharge season of nutrient loads from agricultural canals. During spring NEE for DE and PE were -2.09 and -4.23 μmolCO2 m-2 s-1, respectively. This suggests that during this period of higher radiation, photosynthetic activity was the dominant flux. In contrast, during summer values were lower than spring since PE presented -0.64 μmol CO2m-2 s-1 and DE-0.63 μmol CO2 m-2 s-1. During the autumn season NEE for PE and DE were -2.59 and-1.54μmol CO2 m-2 s-1.Mean daily ET values for PE ranged between 2.52 to 6.34 mm and for DE were 2.44 to 3.56 mm. Differences on NEE and ET patterns are modulated by temperature and solar radiation. The next stages of this research will evaluate the variability of salinity, nutrient loads and hydroperiod of these transitional ecosystems.

b)

Month/Site Water

temperature

(°C)

Salinity

(ppt)

Water level

(m)

March

El Sargento estuary

Tóbari Bay

July

El Sargento estuary

Tóbari Bay

18.59

20.96

26.31

30.01

28.20 (34.65-26.37)

33.03 (30.55-35021)

27.16 (27.48-26.37)

28.01 (28.66-27.26)

-0.60

-0.69

0.15

0.13

Figure 4. Eddy covariance systems: a) El Sargento Estuary and b) Tóbari Bay.

a)

b)

Figure 6. Diurnal behavior of NEE and LE for PE (a) and DE (b) . Patterns on DE show a similar trend through January,

April and July with no drastical changes. However, PE presents a significant

contrast o diurnal behavior comparing with DE, a marked amplitude on NEE and LE during above the three months shown.

(PE)

Figure 7. 8-day Ocean Net Primary Production (mg C m-2 d-1 ) from MODIS

during October 2013 (a) and January 2014 (b) for the coast of Sonora.

(DE)

a)

b)

NEE and LE patterns were different during wet and dry seasons. Although, PE presents a higher productivity than DE over the study period there´s a contrast on LE flux which is higher on PE than DE. Higher respiration activity on daily on NEE values during winter for DE suggest a relationship with the peak of nutrients loads discharged by agricultural canals to the bay.

a)

b)

Figure 5. Daily values showing the seasonal trends of NEE , LE and radiation at (PE) and (DE) during study period. Daily NEE

fluctuations suggesrtthe presence of photosynthetic and respiration processeses showing contrast on sites increasing

with the presence of higher radiation.

Table 1. Contrast on water level, water temperature and salinity average values during March and July, 2014 for PE and DE.