<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1794-1237</journal-id>
<journal-title><![CDATA[Revista EIA]]></journal-title>
<abbrev-journal-title><![CDATA[Revista EIA]]></abbrev-journal-title>
<issn>1794-1237</issn>
<publisher>
<publisher-name><![CDATA[Escuela de ingenieria de Antioquia]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1794-12372008000100005</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[ANNUAL AND DIURNAL CYCLES OF THE INVERSE RELATION BETWEEN PLANT TRANSPIRATION AND CARBON SEQUESTRATION]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Moreno]]></surname>
<given-names><![CDATA[Hernán Alonso]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Escuela de Ingeniería de Antioquia EIA  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>07</month>
<year>2008</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>07</month>
<year>2008</year>
</pub-date>
<numero>9</numero>
<fpage>53</fpage>
<lpage>68</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S1794-12372008000100005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S1794-12372008000100005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S1794-12372008000100005&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Understanding biogeochemical cycles and especially carbon budgets is clue to validate global change models in the present and near future. As a consequence, sinks and sources of carbon in the world are being studied. One of those sinks is the non-well known behavior of the planet vegetation which involves the processes of photosynthesis and respiration. Carbon sequestration rates are highly related to the transpiration through a molecular diffusion process occurring at the stomatal level which can be recorded by an eddy covariance micrometeorological station. This paper explores annual and diurnal cycles of latent heat (LE) and CO2 net (FC) fluxes over 6 different ecosystems. Based on the physics of the transpiration process, different time-scale analysis are performed, finding a near-linear relation between LE and CO2 net fluxes, which is stronger at the more vegetated areas. The North American monsoon season increases carbon up taking and LE-CO2 flux relation preserves at different time scales analysis (hours to days to months).]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[El conocimiento de los ciclos biogeoquímicos y, en especial, de los balances de carbono es clave para la validación de los modelos de cambio global para el presente y el futuro cercano. Como consecuencia, en el mundo se estudian las fuentes y los sumideros de carbono. Uno de esos sumideros es la vegetación del planeta, que involucra los procesos de respiración y fotosíntesis y cuyo comportamiento se empieza a estudiar. Las tasas de captura del carbono están muy ligadas a la transpiración mediante un proceso de difusión molecular en los estomas, que puede registrarse por un sistema micrometeorológico de eddy covarianza. Este artículo explora los ciclos anuales y diurnos de los flujos netos de CO2 y calor latente de seis ecosistemas diferentes. Se desarrollan diversos análisis de escala temporal, basados en la física de la transpiración, y se halla una relación cuasilineal entre los flujos netos de calor latente y CO2, más fuerte en las áreas con mayor cobertura vegetal. La temporada del monzón norteamericano incrementa la captura de carbono y la relación entre la evapotranspiración y el intercambio de gas carbónico se mantiene en las diferentes escalas temporales analizadas (horas, días, meses).]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[carbon sequestration]]></kwd>
<kwd lng="en"><![CDATA[evapotranspiration]]></kwd>
<kwd lng="en"><![CDATA[net exchange of CO2]]></kwd>
<kwd lng="en"><![CDATA[eddy covariance]]></kwd>
<kwd lng="en"><![CDATA[latent heat flux]]></kwd>
<kwd lng="en"><![CDATA[diurnal cycle]]></kwd>
<kwd lng="en"><![CDATA[annual cycle]]></kwd>
<kwd lng="en"><![CDATA[Southwestern North America]]></kwd>
<kwd lng="es"><![CDATA[fijación de carbono]]></kwd>
<kwd lng="es"><![CDATA[evapotranspiración]]></kwd>
<kwd lng="es"><![CDATA[intercambio neto de CO2]]></kwd>
<kwd lng="es"><![CDATA[eddy covarianza]]></kwd>
<kwd lng="es"><![CDATA[flujo de calor latente]]></kwd>
<kwd lng="es"><![CDATA[ciclo anual]]></kwd>
<kwd lng="es"><![CDATA[ciclo diurno]]></kwd>
<kwd lng="es"><![CDATA[Suroeste de Norteamérica]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="center"><font size="4" face="Verdana"><b>ANNUAL AND DIURNAL CYCLES OF THE INVERSE   RELATION BETWEEN PLANT TRANSPIRATION   AND CARBON SEQUESTRATION</b></font></p>     <p align="center">&nbsp;</p> <font face="Verdana"size="2">     <p><b> Hern&aacute;n Alonso Moreno<sup>*</sup></b></p>     <p>* Profesor Escuela de Ingenier&iacute;a de Antioquia EIA, PhD student of Hydrology, New Mexico Tech.</p>     <p> Art&iacute;culo recibido 14-I-2008. Aprobado 15-VI-2008</p>     <p> Discusi&oacute;n abierta hasta diciembre de 2008 </p> <hr size="1" /> </font>     <p><font size="3" face="Verdana"><b>  ABSTRACT</b></font></p> <font face="Verdana"size="2">     <p>  Understanding biogeochemical cycles and especially carbon budgets is clue to validate global change   models in the present and near future. As a consequence, sinks and sources of carbon in the world are being   studied. One of those sinks is the non-well known behavior of the planet vegetation which involves the   processes of photosynthesis and respiration. Carbon sequestration rates are highly related to the transpiration   through a molecular diffusion process occurring at the stomatal level which can be recorded by an eddy   covariance micrometeorological station. This paper explores annual and diurnal cycles of latent heat (LE)   and CO<sub>2</sub> net (FC) fluxes over 6 different ecosystems. Based on the physics of the transpiration process, different   time-scale analysis are performed, finding a near-linear relation between LE and CO<sub>2</sub> net fluxes, which   is stronger at the more vegetated areas. The North American monsoon season increases carbon up taking and LE-CO<sub>2</sub> flux relation preserves at different time scales analysis (hours to days to months).</p> </font>     <p>  <font size="2" face="Verdana"><b><font size="3">KEY WORDS: </font></b>carbon sequestration; evapotranspiration; net exchange of CO<sub>2</sub>; eddy covariance; latent   heat flux; diurnal cycle; annual cycle; Southwestern North America.</font></p> <font face="Verdana"size="2"> <hr size="1" /> </font>     <p>  <font size="3" face="Verdana"><b>RESUMEN</b></font></p> <font face="Verdana"size="2">     ]]></body>
<body><![CDATA[<p>  El conocimiento de los ciclos biogeoqu&iacute;micos y, en especial, de los balances de carbono es clave para   la validaci&oacute;n de los modelos de cambio global para el presente y el futuro cercano. Como consecuencia, en   el mundo se estudian las fuentes y los sumideros de carbono. Uno de esos sumideros es la vegetaci&oacute;n del   planeta, que involucra los procesos de respiraci&oacute;n y fotos&iacute;ntesis y cuyo comportamiento se empieza a estudiar.   Las tasas de captura del carbono est&aacute;n muy ligadas a la transpiraci&oacute;n mediante un proceso de difusi&oacute;n   molecular en los estomas, que puede registrarse por un sistema micrometeorol&oacute;gico de eddy covarianza. Este art&iacute;culo explora los ciclos anuales y diurnos de los flujos netos de CO<sub>2</sub> y calor latente de seis ecosistemas   diferentes. Se desarrollan diversos an&aacute;lisis de escala temporal, basados en la f&iacute;sica de la transpiraci&oacute;n,   y se halla una relaci&oacute;n cuasilineal entre los flujos netos de calor latente y CO<sub>2</sub>, m&aacute;s fuerte en las &aacute;reas con   mayor cobertura vegetal. La temporada del monz&oacute;n norteamericano incrementa la captura de carbono y la   relaci&oacute;n entre la evapotranspiraci&oacute;n y el intercambio de gas carb&oacute;nico se mantiene en las diferentes escalas temporales analizadas (horas, d&iacute;as, meses).</p> </font>     <p>  <font size="2" face="Verdana"><b><font size="3">PALABRAS CLAVE: </font></b>fijaci&oacute;n de carbono; evapotranspiraci&oacute;n; intercambio neto de CO<sub>2</sub>; eddy covarianza;   flujo de calor latente; ciclo anual; ciclo diurno; Suroeste de Norteam&eacute;rica.</font></p> <font face="Verdana"size="2"> <hr size="1" /> </font>     <p><font size="3" face="Verdana"><b>  1. INTRODUCTION</b></font></p> <font face="Verdana"size="2">     <p>  Vegetation processes respond widely different   according to seasonal, age, soil moisture and   particular ambient settings. Such response of vegetation   to the surrounding environment is a key global   change issue that scientists are investigating by using   measurements and models at short and long term   scales (Fang, Xue and Tang, 2007; Byrne, Kiely and   Leahy, 2007; Byrne et al., 2007; Litynski et al., 2006;   Chen et al., 2007; Lal, 2005; Brack, 2002; Law et   al., 2002 and Zhan and Kustas, 2001). Earlier work   suggested that annual productivity increased with   mean annual temperature and precipitation (Lieth,   1972a,b; O&rsquo;Neill and DeAngelis, 1981). Concurrently,   leaf-level studies suggested a mechanism for optimal   stomatal variation that regulates the relationship between   water loss through assimilation in response to   the environment (Cowan, 1977). The net ecosystem   exchange (NEE) of CO<sub>2</sub> between the biosphere and   atmosphere is the balance between fluxes associated   with photosynthetic assimilation by the foliage (gross   ecosystem production) and respiratory effluxes from   autotrophs (Ra) and heterotrophs (Rh). Differences in   annual NEE between locations might be attributable   to disturbance history, climate, nutrition, biome type   and physiological differences associated with age   (Law et al., 2002; Schulze et al., 1999). Environmental   conditions may influence photosynthetic uptake and   autotrophic and heterotrophic respiration differently.   Research in European forests showed that there was   no correlation between GEP and latitude, but annual   ecosystem respiration increased with latitude, in spite of decrease in mean annual temperature.</p>     <p>  Transpiration is the evaporation of excess of   water from aerial parts of plants especially leaves   but also stems, flowers, and fruits. Transpiration is a   side effect of the plant needing to open its stomata   in order to obtain carbon dioxide gas from the air   for photosynthesis. Transpiration also cools plants   and enables mass flow of mineral nutrients from   roots to shoots. Mass flow is caused by the decrease   in hydrostatic (water) pressure in the upper parts of   the plants due to the diffusion of water out of stomata   into the atmosphere. The rate of transpiration is   directly related to whether the stomata are open or   closed. The amount of water lost by a plant depends   on its size, along with the surrounding light intensity,   temperature, humidity, wind speed, and soil water   supply. The reason that an increase in temperature   will cause an increase in transpiration rate is because   an increase in temperature will cause more water to   evaporate from the cell walls. This will increase the   water potential gradient between the leaf interior and   the outside air causing water to leave the leaf more   quickly, thereby increasing the rate of transpiration. The transpiration ratio is the ratio of the mass of water   transpired to the mass of dry matter produced; the   transpiration ratio of crops tends to fall between 200   and 1000, for instance, crop plants transpire 200 to   1000 kg of water for every kg of dry matter produced (Martin, Leonard and Stamp, 1976).</p>     <p>  The carbon budget of a tree (or any plant)   can be expressed much like a balance in terms of the uptake of CO<sub>2</sub> a plant can do:</p>     <p>  Income = carbohydrates manufactured in photosynthesis</p>     <p>Expenditures = carbohydrates used in growth and   maintenance (construction and maintenance respiration)</p>     <p>Balance = carbohydrates stored (so-called nonstructural   carbohydrates and other storage compounds)</p>     <p>The carbon balance of a tree is very much   related to its health and vigour and to its interactions with other organisms. A general equation for photosynthesis is:</p>     ]]></body>
<body><![CDATA[<center>   <img src="img/revistas/eia/n9/n9a05ecu1.gif" /> </center>     <p>A highly simplified summary of the respiration process is:</p>     <center>   <img src="img/revistas/eia/n9/n9a05ecu2.gif" /> </center>     <p>It is characterized by light dependent oxygen consumption and the release of carbon dioxide.</p>     <p>  The objective of this paper is exploring diurnal   and annual cycles of the latent heat and CO<sub>2</sub> fluxes   and temporal scale effects on the molecular carbon   dioxide and water vapor diffusion and exchange   processes at 6 different ecosystems in Southwestern North America.</p> </font>     <p><font size="3" face="Verdana"><b>  2. DATA AND METHODOLOGY</b></font></p> <font face="Verdana"size="2">     <p>  Data were collected from AmeriFlux web page   free downloads: http://cdiac.esd.ornl.gov/programs/   ameriflux/data_system/aamer.html, for 6 sites inside   the American Monsoon Area. The geographic range   of sites varies in latitude from 29.95&deg;N - 35.4&deg;N and   97.99&deg;W -111.77&deg;W in Texas and Arizona American   states. Automated micrometeorological measurements   of CO<sub>2</sub> net flux (FC), latent (LE), sensible (H)   and ground heat fluxes (G), air and soil temperature   (Ta, Ts), wind speed and direction (W-S) and soil   moisture (SWC) were taken over different vegetation   landcovers. Experimental sites are monotypic   ecosystems representative of regional vegetation.   <a href="img/revistas/eia/n9/n9a05fig1.gif" target="_blank">Figure 1</a> and <a href="img/revistas/eia/n9/n9a05tab1.gif" target="_blank">table 1</a> describe the location and major   features of each site. Carbon, water vapor, and   energy fluxes were estimated with the eddy covariance   technique from towers above the vegetation   canopies. Flux systems comprised three axis sonic   anemometers that measured wind-speed and virtual   temperature, infrared gas analyzers that measured   concentrations of water vapor and CO<sub>2</sub>. Fluxes were   averaged half-hourly.</p>      <p><font size="3" face="Verdana"><b>3. RESULTS AND DISCUSSION</b></font></p> <font face="Verdana"size="2">     <p><b>  CO<sub>2</sub> AND LATENT HEAT FLUXES ABOVE THE CANOPY</b></p>     <p>  Averaged 30 minutes CO<sub>2</sub> and latent heat   fluxes time series above the canopy for all the ecosystems   are showed in <a href="img/revistas/eia/n9/n9a05fig2.gif" target="_blank">figure 2</a> at the same time period of   Jul 1st - July 7th 2006 (7 daily cycles). Except by Santa   Rita (30 % areal mesquite) and Kendall (graslands),   general behavior reflects a considerable increase in   the downward CO<sub>2</sub> flux (negative flux) with the upward   increase of the latent heat flux in the daytime   around noon, showing vegetal activity through diffusion   processes of transpiration. Data from Santa Rita   and Kendall illustrate an increasing behavior in the   upward CO<sub>2</sub> flux with an increase in the latent heat   flux, showing a convection (free and/or forced) effect   which transports CO<sub>2</sub> away along with the flux of LE from the soil or poorly vegetated area.</p>     ]]></body>
<body><![CDATA[<p><b>  ANNUAL CYCLES</b></p>     <p>  To have a seasonal view of the data, probability   distributions of the monthly quartiles were plotted   using box-plots for each climatic station using daily   averaged data. Each horizontal line inside the box   shows the median of the distribution which gives an   idea of the data asymmetry. Annual cycle for Santa   Rita is showed in <a href="img/revistas/eia/n9/n9a05fig3.gif" target="_blank">figure 3</a>. Particular behaviors can be   seen from each station. However, a whole pattern is   described by the global radiation seasonal variation   with extreme values in the days of the summer and   winter Northern Hemisphere solstices. In whole,   latent heat and CO<sub>2</sub> fluxes have a unimodal behavior   with maximum/minimum values in the summer season,   mostly in August-September showing a slight lag   with the net radiation peak rate. Increase in net radiation,   soil moisture, and high activity vegetation make   CO<sub>2</sub> downward flux or net ecosystem exchange (NEE)   to be in average 2 to 4 times larger in the monsoon   season than in other months of the year, whereas LE   could be as large as 10 times compared with the winter   months. This explains formation of big cloudy systems   which positively feedbacks the wet season. Such rates   are obviously higher for the cases of the ponderosa forest   and mesquite vegetation, which can be explained   by the large vegetation activity in the summer season.   Soil water content may be a controlling variable that   shows a tendency of peak in summer at some stations   and probably another peak at the ripening and melting   phase of snow at the beginning of spring.</p>     <p><b>DAILY CYCLES</b></p>     <p>  Daily cycles are becoming important in the   scientific community, among other reasons, due to the   possibility of having daily estimates of hydro-meteorological   variables from instantaneous measurements   (i.e. remote sensing images). Thereby, an analysis of   the diurnal cycle may offer important information   about the phase, amplitude, and influence of the radiation   cycle and biophysical activity at that environment.   <a href="img/revistas/eia/n9/n9a05fig4a.gif" target="_blank">Figure 4a</a> and <a href="img/revistas/eia/n9/n9a05fig4b.gif" target="_blank">4b</a> illustrate the averaged daily cycles of   CO<sub>2</sub> and latent heat fluxes for the six study sites. From   <a href="img/revistas/eia/n9/n9a05fig4a.gif" target="_blank">figure 4a</a>, phase of the maximum values are found to   be between 11 a.m. and 1 p.m. according with the   diurnal cycle of global radiation on the planet. A sine   or cosine fitting process could be performed with the   phase highly determined by solar zenith angle and a   slight offset given by the mechanism of the transpiration   process. High standard deviation from the main   quartiles is found at noon or close to, due to the zenith   angle seasonal variability or cloudiness during some   days. From <a href="img/revistas/eia/n9/n9a05fig4b.gif" target="_blank">figure 4.b</a>, according to the latent heat flux   diurnal cycle, CO<sub>2</sub> flux shows a negative peak between   10 a.m. and 12 m. of each day. Such lag with respect   to LE could be showing the optimal temperature effect   for photosynthesis. However, flux rates are pretty   similar during these three hours of the day. Again a   sine wave could be fitted to this graph. The largest   rates of CO<sub>2</sub> downward fluxes are accomplished at   Flagstaff Unmanaged, Flagstaff Managed and Freeman   Ranch. At these places, net ecosystem exchange   at noon could be 5 times larger than in the afternoon, night or early morning.</p>     <p><b>  CO<sub>2</sub> AND LATENT HEAT FLUX RELATIONSHIP   TIME-SCALE DEPENDENCE</b></p>     <p><b>  30 minutes time series</b></p>     <p>  Latent heat flux and net ecosystem exchange   are related through the carbon and energy balance   equations. Specifically, this paper tries to answer the   question: How much of the CO<sub>2</sub> net flux variability is   explained by the latent heat flux at each site? Such   exploration could lead us to identify an easy but   strong relationship between the carbon fluxes and   any other climatic or environmental measured variable.   Hypothetically, if the surface under the eddy   covariance station is well vegetated, diffusion process   of the water vapor transpiration and CO<sub>2</sub> incorporation   should have a strong negative correlation.   <a href="img/revistas/eia/n9/n9a05fig5.gif" target="_blank">Figure 5</a> shows such correlations with a significance   statistical test. Bars with the small black circle on top   mean enough statistical significance to consider valid   the correlation. The statistical test uses a matrix of   critical values p for testing the hypothesis of no correlation.   Each p-value is the probability of getting a   correlation as large as the observed value by random   chance, when the true correlation is zero. If P(i,j) is   small, less than the significance level &alpha;=0.05, then the correlation R(i,j) is significant.</p>     <p>  <a href="img/revistas/eia/n9/n9a05tab2.gif" target="_blank">Table 2 </a>summarizes the hypothesis test for the   significance, p&lt;&alpha;, for the correlation coefficient on   each of the time series with the CO<sub>2</sub> flux (&alpha;=0.05). At   this time scale, almost all the correlations are more   significant than the purely random process with a probability of 95 %.</p>     <p>  Valuable information may be extracted from   the linear correlations. Both, Rn, LE and PAR have the   strongest influence on the NEE process at this time   scale. In fact, latent heat flux shows slightly higher   correlations with CO<sub>2</sub> flux (FC), showing that it is   probably the dominant predictive variable, mainly   at vegetated landcovers, with correlations ranging   between ~ -0.6 to ~ -0.8. Complementarily, LE depends   on other variables as net radiation, sensible heat flux, ground heat flux.</p>     <p>  <a href="img/revistas/eia/n9/n9a05fig6.gif" target="_blank">Figure 6</a> shows an attempt to relate averaged   net FC to LE at the 30 minutes time scale at all the   sites. It is evident that steeper slopes and better fittings   occur in the most vegetated zones (ponderosa   forest and mesquite at Flagstaff unmanaged, Flagstaff   managed and Freeman Ranch). Equations in <a href="img/revistas/eia/n9/n9a05tab3.gif" target="_blank">table 3</a>  show the fitting process and correlation coefficient   for each site. The largest net primary production and   the largest carbon sequestration should be occurring   given the vegetation presence. Comparing the slopes and assuming a very similar proportion between net   ecosystem exchange and net primary production we   could say that forest is capturing carbon at a rate of   approximately 3 times greater than the grasslands or   bare soil at Santa Rita, Kendall or the Flagstaff land   cover after the fire (wildfire).</p>      ]]></body>
<body><![CDATA[<p><b>Daily scale</b></p>     <p>  Averaging 30 minutes fluxes to daily scale we   will observe if relations preserve or even if others   appear. <a href="img/revistas/eia/n9/n9a05tab4.gif" target="_blank">Table 4</a> shows the hypothesis test among CO<sub>2</sub>   flux and any other variable. Now, many variables go   out of the significant correlation, but still latent heat   flux and net radiation have the maximum values at   the highly vegetated stations. <a href="img/revistas/eia/n9/n9a05fig7.gif" target="_blank">Figure 7</a> shows that   the 30 min-scale linear tendency found at Santa Rita   and Kendall is almost totally lost at the daily scale,   which proofs that the effect of averaging fluxes could   bring to misinterpretations of the fluxes occurring   at finer time scales. Again it is evident that steeper   slopes and better fittings occur in the most vegetated   zones. Equations in <a href="img/revistas/eia/n9/n9a05tab5.gif" target="_blank">table 5</a> show the fitting process   and correlation coefficient for each site. Comparing   the slopes and assuming a very similar proportion   between net ecosystem exchange and net primary   production we could say that the forest are having downward fluxes (uptake of carbon) in umol.w-1s-1 in   average 6 times larger than the grasslands or bare   soil at Santa Rita, Kendall or the Flagstaff land cover   after fire (wildfire) at the daily time scale.</p>      <p>  <a href="img/revistas/eia/n9/n9a05fig8.gif" target="_blank">Figure 8</a> as well as <a href="img/revistas/eia/n9/n9a05tab6.gif" target="_blank">table 6</a> illustrate the same   procedure for the time series aggregated at the   monthly scale. Basically, the most significant variables   in determining CO<sub>2</sub> fluxes are net radiation and latent   heat flux. Going back again at the CO<sub>2</sub> vs LE figures,   slope relationship between the forest and mesquite   vs grasslands and bare soils show that rates of carbon   uptake for photosynthesis, in average 2 times larger,   are found in the most vegetated environments. As   expected, an increase in the net radiation and soil   water content in the monsoon season leads to an   increase in the rate of evapotranspiration and, as a   consequence, in the net CO<sub>2</sub> exchange ecosystem.</p>      <p><font size="3" face="Verdana"><b>4. CONCLUSIONS</b></font></p> <font face="Verdana"size="2">     <p>  Highly vegetated areas show higher influence   of the diffusion transpiration process on the CO<sub>2</sub>   downward rates establishing a high negative correlation   between the latent heat and the net ecosystem exchange.</p>     <p>  Poorly vegetated zones exhibit smaller negative   correlations and convection processes of CO<sub>2</sub>   involved with the upward latent heat fluxes which   makes less efficient the process of carbon up taking by the few vegetation landcover.</p>     <p>  Latent heat and CO<sub>2</sub> fluxes have a unimodal   behavior with maximum values at the summer season,   mostly in August-September showing a slight lag   with the net radiation peak rate. Large net radiation,   soil moisture, and activity vegetation make CO<sub>2</sub> 30   minutes averaged downward flux or net ecosystem   exchange (NEE), to be in average 2 to 4 times higher   in the monsoon season than in other months of the   year, whereas LE could be as large as 10 times compared   with the values for other months. This explains   formation of big cloudy monsoon systems. Such rates   are obviously higher for the cases of the ponderosa forest and mesquite vegetation.</p>     <p>  CO<sub>2</sub> flux diurnal cycle shows a negative peak   between 10 a.m. and 12 m. each day. Such lag with   respect to LE could be related to the optimal temperature   for photosynthesis. The largest rates of CO<sub>2</sub>   fluxes are accomplished at Flagstaff Unmanaged,   Flagstaff Managed and Freeman Ranch. At these   places, net ecosystem exchange at 10 a.m. could be   5 times larger than in the afternoon, night or early morning.</p>     <p>  At almost all the explored time scales LE explains   more than 50 % of the variability of the NEE   in the studied highly vegetated zones. At the 30 minutes   time scale a nice straight line could be adjusted   between CO<sub>2</sub> flux and latent heat flux at forests and   other highly vegetated places since transpiration   increases. The net uptake of carbon for the photosynthetic   processes (&mu;mol.m-2.s-1) could be at least 3   times greater than that found in grasslands, wildfire, or bare soil landcover.</p>     <p>The effect of aggregating time series to larger   time-scales is smoothing values but the most important correlations preserve.</p>     ]]></body>
<body><![CDATA[<p>  At daily and monthly scales evapotranspiration   and CO<sub>2</sub> net flux could also be controlled by the net   radiation, which has a direct influence on PAR, latent   heat flux, and soil moisture, which at time could be   controlling LE especially in the monsoon season.   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