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On-line version ISSN 2236-8906
Hoehnea vol.39 no.1 São Paulo Mar. 2012
Efectos del transporte de agua por el xilema en la afluencia de CO2 en el tejido leñoso de un árbol tropical, Estado del Amazonas, Brasil
Norbert KunertI,II,*; Alida Mercado CárdenasIII
IMax Planck Institute for Biogeochemistry, Department for Biogeochemical Processes, Hans Knöll Str. 10, 07745 Jena, Germany
IIInstituto Nacional de Pesquisas da Amazônia (MCT-INPA), Laboratório de Manejo Florestal, Av. Ephigênio Sales, 2239, 69011-970 Manaus, AM, Brasil
IIIMcGill University, Department of Natural Resource Sciences, Macdonald Campus, Ste-Anne-de-Bellevue, H9X3V9 Quebec,Canada
We assessed the effect of xylem sap flux on radial CO2 efflux of woody tissue of a tropical trees species growing in the Center of Manaus (Amazonas State, Brazil). An open chamber system was used to constantly measure diurnal changes in CO2 efflux over several days. Xylem sap flux was monitored additionally. We found a strong relationship between temperature and woody tissue respiration rates during night time. CO2 efflux rates were reduced up to 35% during daytime most probably due to vertical water uptake within the tree trunks. The results suggest a distinct daytime depression of the CO2 efflux compared with a night time temperature relationship. Xylem sap flux appears to be a major influence on CO2 efflux rates. The reductions in CO2 efflux will become most distinct during periods with a high evaporative demand and predictions of CO2 efflux by the temperature/flux relation are critical during these periods.
Key words: daytime depression, sap flux, temperature dependency, woody tissue respiration
Evaluamos el efecto del flujo de la savia del xilema en la afluencia del CO2 radial en tejidos leñosos de una especie de árbol tropical en el centro de Manaos (Amazonas, Brasil). Un sistema de cámara abierta fue usado constantemente para medir cambios diarios en la afluencia del CO2 durante varios días. Al mismo tiempo, se midió el flujo de la savia del xilema. Encontramos una fuerte relación entre las tazas de temperatura y la respiración del tejido leñoso durante el periodo nocturno. Las tazas de afluencia de CO2 se redujeron hasta un 35% durante el día, probablemente debido a la absorción vertical del agua dentro de los troncos. Los resultados sugieren una depresión de la afluencia del CO2 específica durante el día comparada con la relación de la temperatura durante la noche. El flujo de la savia del dilema parece tener una influencia más fuerte en las tazas de afluencia del CO2. Las reducciones en la afluencia del CO2 serán más marcadas durante periodos con una alta demanda de evaporación y las predicciones de la afluencia del CO2 dadas por la relación de temperatura/flujo son críticas durante dichos periodos.
Palabras-clave: dependencia en la temperatura, depresión diurna, flujo de savia, respiración de tejido leñoso
Woody tissue respiration plays an important role in budgeting ecosystem productivity (Chambers et al. 2004). A conventional method to estimate the CO2 efflux of wood at the ecosystem scale is by using closed dynamic chambers cinched on tree stems and measuring the increase in CO2 in the closed chamber from the tissue with an infrared gas analyzer (IRGA) over a short time period. This method provides the opportunity to sample a large number of trees within a reasonable time. The common assumption is that all the CO2 respired by the woody tissue enclosed in the chamber diffuses laterally from the stem interior into the chamber. The total CO2 efflux defusing out of the woody tissue is depending strongly on the temperature of the bark surface and/or the temperature of the conductive sap wood so that flux rates are commonly predicted using this temperature relation (Tranquillini & Schütz 1970, Edwards & Hanson 1996, Gansert et al. 2002).
However, some studies found CO2 efflux rates lower than predicted from bark surface or sap wood temperature during daytime, which suggests an inner transport of CO2 dissolved in the transpiration stream, as maybe ongoing bark photosynthesis could be excluded (Edwards & McLaughlin 1978, Kaipiainen et al. 1998, Stockfors & Linder 1998). It is assumed that a portion of the CO2 produced by the living respiring cells might dissolve in the sap and is transported vertically in the xylem along with the transpirational water uptake instead of moving laterally through the stem into the respiration chamber (Kaipiainen et al. 1998) and hence this measured CO2 efflux might not be equal to the respiration rate (Saveyn et al. 2008). Another recent study also points out the high importance of carbon re-fixation and amount of stem assimilates as significant carbon source for the whole plant carbon budget. Furthermore, bark photosynthesis did not vanish until a long-term exclusion of light (Saveyn et al. 2010). Accordingly, there is in increasing concern about the measured values of stem CO2 efflux and the possible effects caused by other processes rather than by temperature depending respiration (Saveyn et al. 2007).
Most studies regarding diurnal changes in CO2 efflux have been conducted on temperate regions and there is a lack of information dealing with trees growing in the tropics. By comparison, the approach to access the influence of internal water transfer on the CO2 diffusion out of trees stems has been applied less frequently and successfully in the tropics than in temperate regions. One study using continuous measurements with open dynamic chambers was conducted in a Schima superba Gardner & Champ. plantation, in the subtropics of southern China (Zhu et al. 2011), and another in a subtropical Combretum micranthum G. Don shrub growing in Cameroon (Levy et al. 1999). These studies generally found a positive relation between xylem sap flux and CO2 efflux, but the findings regarding the overall effect of the water transport were quite controversial compared to the results with trees from temperate and boreal forests. There was an increase of CO2 efflux of up to 9.2 and 12% with the onset of internal water transport in the Schima trees and the Combretum shrub, respectively. Whereas studies from temperate forests find a reduction of the CO2 efflux of 10-50% with the onset of the internal water transport (Gansert & Burgdorf 2005, Negisi 1975, 1982). Regarding on the difference in environmental settings, the confidence that these controversial findings apply on trees growing in the central tropics is very limited. Hence, conducting a study on a specific tree in the tropics will give us better insights on the carbon cycle of tropical trees than the existing studies. Therefore, the objectives of the present work were: (1) to assess variations from the nighttime efflux-temperature relation in a tropical tree and (2) to quantify the effect of internal water transfer on the CO2 efflux rates.
Material and methods
This study was carried out on a specimen of Hymenolobium pulcherrimum Ducke (Fabaceae) growing on a private property in the Center of Manaus, Amazonas State, Brazil in May 2011. The sample tree had its full complement of leaves during the study. The studied tree was 30.8 cm in diameter at breast height, 7.5 m high with a crown extension of 185 m2 . Only one tree was measured, due to limited available equipment and no appropriate replicate of the same tree species in the area. Microclimatic parameters were recorded with a professional weather station (PCE-FWS 20 Weather Station, PCE Inst., Durham, UK) in an open area approximately 6 m away from the sample tree. Microclimate data were stored at 30 s intervals and average was recorded every 5 minutes.
Stem respiration rates were measured with an open chamber system to assess diurnal CO2 effluxes. An infrared gas analyzer (IRGA, LI 6252 with an LI-670 flow control unit; Li-Cor, Lincoln, Nebraska, USA) was configured in differential mode similar to the method to measure leaf photosynthesis (Licor 1992). The IRGA is giving [ΔCO2] as output which is the difference between the alternately measured [CO2] of the reference air stream from a common air source and the [CO2] of the airstream flowing through the stem respiration chamber. Ambient air was drawn through an air reservoir of 2 liters to buffer CO2 and/ or H2O fluctuations. We configured the flow control unit to support a constant flow rate of 1.0 L/min. A semicylindric polyvinyl chloride (PVC) chamber (400 mL) was cinched to the trunk facing to the western side of the studied tree at 130 cm (DBH) above the ground using tie down straps. A metal bar was placed under the tie down straps on the opposite site of the chamber to reduce the pressure on the tree trunk by the tie down straps. The respiration chamber was shielded with aluminum foil to exclude thermal effects by direct sunlight or bark photosynthesis. The respiration chamber was equipped with two different thermocouple-temperature sensors. The first sensor measured the xylem temperature approximately 10 mm above the bark surface where a small radially hole (1 mm in diameter) was drilled into the tree trunk and the sensor was inserted. The second sensor was installed above the sealing of the respiration chamber to measure the stem surface temperature. IRGA and thermocouple outputs were stored every 30 seconds and the average recorded in 5 min intervals with a data logger (DL2 datalogger, Delta-T Devices LTD., Cambridge, UK).
The thermal dissipation method according to Granier (1985) was used to measure sap flux density. The sensors consisting of two cylindrical probes were inserted radially (0-20 mm below cambium) into the tree trunk, with one probe placed approximately 10-15 cm vertically above the other. The studied tree was equipped with two Granier sensors, one on the southern and one on the northern side of the trunk at 130 cm (DBH) above the ground. Sap flux sensors were at least 20 cm vertically away from the respiration chamber. After Granier (1985) the thermal influence of the heated probe on surrounding wood tissue is negligible at a distance of 10-15 cm from the source. Sensors were protected from thermal influences and water intrusion by a reflective polyethylene/paperboard box and a plastic cover. Probe output voltage was recorded every 30 seconds, and the average value stored every 5 minutes (DL2 datalogger, Delta-T Devices LTD., Cambridge, UK). Sap flux density (Js in g cm-2 h-1) was calculated from differences in voltage (ΔV) using the calibration equation determined by Granier (1987). Each night the maximal nighttime voltage (ΔVmax) was determined and used as reference voltage for that day. We assumed zero sap fluxes as nighttime vapour pressure deficits were low and the voltage courses of sensors reached equilibrium most nights suggesting refilling of internal reserves was completed. Possible controls of temperature and tree water transport on CO2 efflux were tested using linear regression analysis. We used SPSS, 15th edition (SPSS Inc., Chicago, IL, USA) for all statistical analyses.
Results and discussion
The maximum and minimum CO2 efflux we found was around 6.5 (day time) and 4.0 (night time) µmol m-2 s-1. These values are corresponding well with results from other studies from various trees. Levy et al. (1999) reported efflux rates between 6.0 (day time) and 3.5 (night time) µmol m-2 s-1 in a Combretum micranthum G. Don shrub in Cameroon, whereas maximum values of 9.9 µmol m-2 s-1 are also known for Schima superba Gardner & Champ. trees in the subtropics of southern China (Zhu et al. 2011). The maximum sap flux density (Js) of 10 g cm2 h-1 was relatively low but within the range found for neotropical tree species (Kunert et al. 2010). Stem CO2 efflux, sap flux density, stem surface temperature and air temperature followed similar diurnal patterns (figures 1a to 1c). CO2 efflux increased with increasing surface temperature, air temperature and sap flux density at day time, but decreased with increasing xylem temperature at night time (figures 1a and 1b). On the first view, this is imposing a positive correlation of CO2 efflux with surface temperature, ambient air temperature and a negative correlation with xylem temperature. The positive relationship between surface/air temperature and CO2 efflux would follow the common theory that an increase in temperature causes an increase in cellular respiration and diffusion coefficient and a decrease in the solubility of CO2 in the xylem water (McGuire et al. 2007). On the other hand, the decrease in xylem temperature should have exactly the opposite effect of lower cellular respiration and higher CO2 solubility during the day. The reduced xylem temperature increases most probably by a cooling effect with the onset of the transpirational water uptake and showed a relatively low amplitude of 0.52 ºC difference between night and day time. In contrast, the surface temperature was coupled to the diurnal changes in air temperature and was defined by much higher amplitude between day and night time which was up to 1.19 ºC. Thus, we observed that the correlation between surface/air temperature and CO2 efflux was less clear during the day and significant reduction of CO2 efflux took place during daytime relative to night-time rates (figure 2).
CO2 efflux peaked with maximum surface temperature (figure 1a). Despite the higher temperatures during the day than night time, a clear daytime depression was present when CO2 efflux was normalized to 20 ºC (figure 2). Similar results were found in a beech and oak tree, where the temperature adjusted CO2 efflux showed a very pronounced day time depression (Saveyn et al. 2007). CO2 efflux was significantly reduced with the onset of sap flux in the morning. This effect is more obvious on days with high sap flux rates (e.g. second day, figure 2). The increase in CO2 efflux under high sap flux rates was less temperature related in the morning (figure 3, 6h05min-12h) than the decrease under already lower sap flux rates in the afternoon and evening (figure 3, 13h-18h). Assuming that the experimental set up could exclude most of the bark photosynthesis, the reduction in CO2 efflux rate must be caused by the internal water transfer. This reduction was accounting up to a 35% of the CO2 efflux compared to values predicted by a simple night time temperature relation (figure 4). Similar values were found in beech trees in a temperate forest in Japan, where CO2 efflux rates were reduced about 10-40% on days with high sap flux rate (Gansert & Burgdorf 2005) and up to 50% in pine and oak trees (Negesi 1975, 1982).
We conclude that the prediction of CO2 efflux of wood tissue by the temperature/flux relation is critical and that simple temperature functions are insufficient to predict stem respiration on ecosystem scales. The results suggest a distinct daytime depression of the CO2 efflux compared with a night time temperature relationship. Xylem sap flux density appears to be a major influence on CO2 efflux rates. The reductions in CO2 efflux will become most distinct during periods with a high evaporative demand. Values based on day or night time measurements will be either under-or overestimated, respectively, especially on days with high evaporative demand.
We want to thank Susanne Trumbore for a valuable discussion on the design of this study. We would also like to thank two anonymous reviewers for their valuable comments on an earlier version of the manuscript.
Chambers, J.Q., Tribuzy, E.S., Toledo, L.C., Crispim, B.F., Higuchi, N., dos Santos, J., Araújo, A.C., Kruijt, B., Nobre, A.D. & Trumbore, S.E. 2004. Respiration from a tropical forest ecosystem: Partitioning of sources and low carbon use efficiency. Ecological Applications 14:72-88. [ Links ]
Edwards, N.T. & Hanson, P.J. 1996. Stem respiration in a closed-canopy upland oak forest. Tree Physiology 16:433-439. [ Links ]
Edwards, N.T. & McLaughlin, S.B. 1978. Temperatureindependent diel variations of respiration rates in Quercus alba and Liriodendron tulipifera. Oikos 31:200-206. [ Links ]
Gansert, D., Backes, K., Ozaki, T. & Kakubari, Y. 2002. Seasonal variation of branch respiration of a treeline forming (Betula ermanii Cham.) and a montane (Fagus crenata Blume) deciduous broad-leaved tree species on Mt. Fuji, Japan. Flora - Morphology, Distribution, Functional Ecology of Plants 197:186-202. [ Links ]
Gansert, D. & Burgdorf, M. 2005. Effects of xylem sap flow on carbon dioxide efflux from stems of birch (Betula pendula Roth). Flora - Morphology, Distribution, Functional Ecology of Plants 200:444-455. [ Links ]
Granier, A. 1985. A new method of sap flow measurement in tree stems. Annals of Forest Science 42:193-200. [ Links ]
Granier, A. 1987. Evaluation of transpiration in a Douglasfir stand by means of sap flow measurements. Tree Physiology 3:309-320. [ Links ]
Kaipiainen, L.K., Sofronova, G.I., Hari, P. & Yalynskaya, E.E. 1998. The role of xylem in CO2 exchange in Pinus sylvestris woody stems. Russian Journal of Plant Physiology 45:500-505. [ Links ]
Kunert, N., Schwendenmann, L. & Hölscher, D. 2010. Seasonal dynamics of tree sap flux and water use in nine species in Panamanian forest plantations. Agricultural and Forest Meteorology 150:411-419. [ Links ]
Levy, P.E., Meir, P., Allen, S.J. & Jarvis, P.G. 1999. The effect of aqueous transport of CO2 in xylem sap on gas exchange in woody plants. Tree Physiology 19:53-58. [ Links ]
Licor. 1992. LI-670 flow control unit instruction manual, LI-COR Inc., Lincoln, Nebraska, USA. [ Links ]
McGuire, M.A., Cerasoli, S. & Teskey, R.O. 2007. CO2 fluxes and respiration of branch segments of sycamore (Platanus occidentalis L.) examined at different sap velocities, branch diameters, and temperatures. Journal of Experimental Botany 58:2159-2168. [ Links ]
Negisi, K. 1975. Diurnal fluctuation of CO2 release from the stem bark of standing young Pinus densiflora trees. Journal of the Japanese Forestry Society 57:375-383. [ Links ]
Negisi, K. 1982. Diurnal fluctuations of the stem bark respiration in relationship to the wood temperature in standing young Pinus densiflora, Chamaecyparis obtusa and Quercus myrsinaefolia trees. Journal of the Japanese Forestry Society 64:315-319. [ Links ]
Saveyn, A., Steppe, K. & Lemeur, R. 2007. Daytime depression in tree stem CO2 efflux rates: is it caused by low stem turgor pressure? Annals of Botany 99:477-485. [ Links ]
Saveyn, A., Steppe, K., McGuite, M.A., Lemeur, R. & Teskey, R.O. 2008. Stem respiration and carbon dioxide efflux of young Popolus deltoids trees in relation to temperature and xylem carbon dioxide concentration. Oecologia, 154:637-649. [ Links ]
Saveyn, A., Steppe, K., Umbierna, N. & Dawson, T.E. 2010. Woody tissue photosynthesis and its contribution to trunk growth and bud development in young plants. Plant, Cell and Environment 33:1949-1958. [ Links ]
Stockfors, J. & Linder, S. 1998. Effect of nitrogen on the seasonal course of growth and maintenance respiration in stems of Norway spruce trees. Tree Physiology 18:155-166. [ Links ]
Tranquillini, W. & Schütz, W. 1970. Über die Rindenatmung einiger Bäume an der Waldgrenze. Centralblatt für das Gesamte Forstwesen 87:42-60. [ Links ]
Zhu, L.W., Zhao P., Cai, X.A., Zeng, X.P., Ni, G.Y., Zhang, J.Y., Zou, L.L., Mei, T.T. & Yu, M.H. 2011. Effects of sap velocity on the daytime increase of stem CO2 efflux from stems of Schima superba trees. Trees 26:535-542. [ Links ]
Received: 1.03.2012; accepted: 13.03.2012