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Article

Environmental Controls on the Seasonal Variation in Gas Exchange and Water Balance in a Near-Coastal Mediterranean Pinus halepensis Forest

1
Forest Research Institute, Hellenic Agricultural Organization Demeter, 57006 Vassilika, Thessaloniki, Greece
2
Institute of Mediterranean and Forest Ecosystems, Hellenic Agricultural Organization Demeter, P. O. Box 14180, Terma Alkmanos, 11528 Ilisia, Athens, Greece
3
LSCE/IPSL, CEA-CNRS-UVSQ, Université Paris-Saclay, Orme des Merisiers, 91191 Gif-sur-Yvette, France
4
Department of Forestry & Management of the Environment & Natural Resources, Democritus University of Thrace, Pantazidou 193, 68200 Nea Orestiada, Greece
5
School of Natural Resources, University of Nebraska, 807 Hardin Hall, 3310 Holdrege Street, Lincoln, NE 68583-0968, USA
6
Chair of Environmental Meteorology, Faculty of Environment and Natural Resources, University of Freiburg, Werthmannstr. 10, D-79085 Freiburg, Germany
7
Research Center Human Biometeorology, German Meteorological Service, D-79104 Freiburg, Germany
*
Author to whom correspondence should be addressed.
Forests 2019, 10(4), 313; https://doi.org/10.3390/f10040313
Submission received: 22 February 2019 / Revised: 22 March 2019 / Accepted: 3 April 2019 / Published: 5 April 2019
(This article belongs to the Special Issue Physiological Responses to Abiotic and Biotic Stress in Forest Trees)

Abstract

:
Aleppo pine (Pinus halepensis Mill.) is widespread in most countries of the Mediterranean area. In Greece, Aleppo pine forms natural stands of high economic and ecological importance. Understanding the species’ ecophysiological traits is important in our efforts to predict its responses to ongoing climate variability and change. Therefore, the aim of this study was to assess the seasonal dynamic in Aleppo pine gas exchange and water balance on the leaf and canopy levels in response to the intra-annual variability in the abiotic environment. Specifically, we assessed needle gas exchange, water potential and δ13C ratio, as well as tree sap flow and canopy conductance in adult trees of a mature near-coastal semi-arid Aleppo pine ecosystem, over two consecutive years differing in climatic conditions, the latter being less xerothermic. Maximum photosynthesis (Amax), stomatal conductance (gs), sap flow per unit leaf area (Ql), and canopy conductance (Gs) peaked in early spring, before the start of the summer season. During summer drought, the investigated parameters were negatively affected by the increasing potential evapotranspiration (PET) rate and vapor pressure deficit (VPD). Aleppo pine displayed a water-saving, drought avoidance (isohydric) strategy via stomatal control in response to drought. The species benefited from periods of high available soil water, during the autumn and winter months, when other environmental factors were not limiting. Then, on the leaf level, air temperature had a significant effect on Amax, while on the canopy level, VPD and net radiation affected Ql. Our study demonstrates the plasticity of adult Aleppo pine in this forest ecosystem in response to the concurrent environmental conditions. These findings are important in our efforts to predict and forecast responses of the species to projected climate variability and change in the region.

1. Introduction

Aleppo pine (Pinus halepensis Mill.) is widespread in most countries of the Mediterranean area [1,2]. In Greece, Aleppo pine forms forests of economic importance (e.g., wood, resin, medicinal, and honey products) [1], comprising 26% of the coniferous forests in the country.
Aleppo pine can reach heights of 10–20 m, depending on the precipitation regime in the area, and has relatively shallow roots, usually not exceeding depths of 5 m [3]. The species is adapted to the xerothermic conditions (high temperatures and droughts) of the Mediterranean, due to its drought avoidance strategy of reducing stomatal conductance under water shortage [4]. This isohydric response allows Aleppo pine to limit the reduction of needle water potential and xylem cavitation, to which it is quite vulnerable [5,6]. Moreover, Aleppo pine has adapted its physiological activity to the seasonally changing climatic regime in the region. It actively grows during two periods of the growing season (spring and autumn) when temperatures are favorable and water is available. This behavior is more pronounced in the coastal regions than in continental forest sites [7]. On the other hand, extreme winter and summer temperatures and intensive summer droughts may cause growth activity to cease [8] and lead to extensive dieback and growth declines in Aleppo pine forests [9].
Improving our understanding of the driving factors that control Aleppo pine responses to climatic conditions is important for managing the species and forecasting its responses to climate variability, extremes, and change. Relationships between various physiological traits and the abiotic environment have been reported in the literature for Aleppo pine [10,11,12]. Studies have demonstrated a strong stomatal regulation in the species and coordination between foliage water potential and stomatal conductance to balance water loss [13]. However, needle and canopy stomatal responses to changes in evaporative demands, especially in combination with high temperatures remain unclear. Aleppo pine populations vary greatly in their response to extreme weather events across their distribution range [9,14]. Populations growing under the driest environments seem to be most impacted by extreme droughts and are prone to growth decline, but recover quickly. It is, however, unknown how the species will respond to the drier and hotter conditions forecasted for the Mediterranean basin under climate change [15], particularly in the eastern part [16]. Studying the seasonal dynamics of physiological traits in Aleppo pine in response to the concurrent climatic conditions will advance our understanding of the drivers that control growth and performance in the species and resilience of these forests. Few studies on the ecophysiological responses of Aleppo pine to drought regimes included Greek provenances and have focused on ecotypic variability assessed in plantations [17,18,19,20], not on adult trees of natural Aleppo pine forests. Thus, information on the ecophysiological responses of natural Aleppo pine forests in Greece is scarce.
In the present study, we assessed the seasonal dynamics of physiological traits of a mature near-coastal Aleppo pine ecosystem in Sani, Chalkidiki, northern Greece, over two consecutive years. We measured foliage gas exchange, water potential and stable carbon isotopic ratio, and tree sap flow rate and canopy conductance to characterize water balance dynamics of the species in response to climatic variability. Our specific aims were to (a) describe the seasonal variation in the physiological traits of Aleppo pine trees and (b) determine the climatic factors that control the observed seasonal trends. The combination of selected complementary techniques provides vital information from the needle to the stand level for assessing the performance of this dominant Mediterranean forest species under the prevailing climate change.

2. Materials and Methods

2.1. Site Description

The study was conducted at the peninsula of Kassandra, Chalkidiki, Greece. The experimental site is located at the Stavronikita forest (latitude: 40°06′22″ N, longitude: 23°18′80″ E, altitude 15 m.a.s.l., slope 1%, c. 300 m distance from the coast). The site is in a natural Aleppo pine (Pinus halepensis) stand with a mean tree height of 16 m, a mean diameter at breast height of 45 cm, a mean tree basal area of 0.19 m2, and a stand basal area of 23.68 m2ha−1. The understorey consists of a maquis shrub vegetation, dominated with Pistacia lentiscus L., Phyllirea media L., and Quercus coccifera L. The soil has a high pH (7.5–8.2) and, according to European soil classification, it lies at the boundary between Calcari-chromic Vertisols and Chromic Luvisols [21,22].

2.2. Environmental Conditions

The climate on site is Mediterranean (Csa), according to Köppen-Geiger’s classification, and is characterized by rainy winters and semi-arid growing seasons [23]. Micrometeorological data are available for the period 1978–1997 and from 2007 to present, from a fully automated weather station operating at a c. 50 m distance from the forest stand. Air temperature and air relative humidity (RHT2nl, Delta-T Devices Ltd., Cambridge, UK), photosynthetically active radiation (SKP215; Skye Instruments Ltd., Llandrindod Wells, UK), solar radiation (SKS1110, Skye Instruments, UK), wind speed (model 4.3515.30.000, THIES CLIMA, Göttingen, Germany), wind direction (WD4, Delta-T Devices Ltd., UK), precipitation (AR100 and RGB1, EM UK), and soil temperature at a depth of 15 cm (ST1, Delta-T Devices Ltd., UK) were continuously recorded. All parameters were data-logged on a 1-h basis (DL2e Delta-T Logger, Delta-T Devices Ltd., Cambridge, UK). Missing data due to a short-term malfunction of the meteorological station were completed after extrapolation from the respective data from the closest meteorological station of Loutra Thermis (latitude 40°30Ȳ N, longitude 23°04′ E, 30 m.a.s.l.). The filling of the missing data gaps was performed by using the double-mass curve technique [24] followed by a t-test [25]. Moreover, vapor pressure deficit (VPD) was estimated using the RayMan model [26,27], while potential stand evapotranspiration (PET) and available soil water capacity (aSWC) of the study site were calculated with the water balance model WBS3. WBS3 is a forest–hydrological model that requires daily mean values of air temperature and daily total precipitation as meteorological inputs [28] and takes into account several forest stand parameters as input, as described in detail in a previous study [29].
An aridity index (AI) [30] was selected to estimate aridity conditions prevailing at the study area. A number of aridity indices have been proposed; these indicators serve to identify, locate, or delimit regions that suffer from a deficit of water availability [31]. The aridity index is estimated as follows (Equation (1)):
AI = P/PET,
where P is precipitation (mm), which in our study is equal to rainfall, and PET is potential evapotranspiration (mm). The boundaries that define the various degrees of aridity are shown in Table S1 [32].

2.3. Measurement Campaigns

Four dominant, non-neighboring Aleppo pine trees were selected for measurements and needle collection. Attention was paid to choosing healthy individuals, since infestation by the insect Marhalina hellenica (Genn.) is spread in Pinus halepensis forests of Chalkidiki. Three sun-exposed branches of the lower canopy (approximately three meters above ground) were marked and were thereafter used for measurements of gas exchange and midday water potential. After completion of each set of gas exchange measurements, the needles were sampled for carbon isotopic ratio analysis, as described below. Neighboring needles of the same branches were used for water potential measurements.
Measurements were conducted over two consecutive years on a monthly basis; gas exchange was measured from December 2007 to November 2009, while needle midday water potential was measured from January 2008 to October 2009. Needle δ13C was determined from January 2008 to May 2009 due to technical limitations.

2.4. Gas Exchange and Needle Water Potential

For gas exchange measurement, we used the Li-6400 open path infra-red gas analyzer with a Li 6400-40 fluorescence chamber (Li-Cor, Lincoln, NE, USA). Maximum photosynthesis (Amax) and stomatal conductance (gs) measurements were conducted on current year, fully expanded, and sun exposed needles between 10:00 and 13:00. The needles were carefully arranged in the 2-cm2 cuvette in a way to exclude overlapping and to fully cover the area of the cuvette and they were acclimated for c. 10 min in the chamber at a CO2 concentration of 400 ppm, under a photosynthetically active radiation (PAR) level of 1000 μmolm−2s−1 from November to March and 1500 μmolm−2s−1 from April to October. CO2 flow rate was set to 300 µmols-1 and temperature inside the chamber was controlled within the range of 17–28 °C, depending on the seasonal fluctuation of ambient air temperature.
Midday water potential (midday Ψ) measurements were conducted between 13:00 to 14:00 using a portable pressure chamber (model PMS 1003, PMS Instruments, Corvallis, OR, USA). The needles’ water potential was measured after gas exchange measurements.

2.5. Needle δ13C Signature

At the study site, new needles were fully expanded until the end of May each year. New needles (<1 year old), fully developed from the preceding May, were collected on a monthly basis from the same dominant Aleppo pine trees for the determination of the needle carbon isotopic ratio (δ13C). Samples were oven-dried at 65 °C until at a constant weight and then sent to the University of Nebraska Water Sciences Laboratory for analysis (https://watersciences.unl.edu/). Samples were finely ground and δ13C was determined using mass spectrometry. The carbon isotope ratio (δ13C) of each sample was then determined as δ13C (‰) = [(Rsample/Rstandard) − 1] × 1000, where Rsample is the 13C/12C of the sample and Rstandard is the 13C/12C ratio of the Vienna Pee Dee Belemnite (VPDB) standard.

2.6. Tree Sap Flow and Canopy Stomatal Conductance

Xylem sap flux was monitored using the thermal dissipation method [33,34]. In July 2008, 2-cm long Granier-type sensors and measurements were taken until early November 2009. Probe pairs were inserted radially into the stem of five dominant Aleppo pine trees averaging 43.5 cm diameter at breast height (DBH) with a vertical separation between the probes of approximately 12.0 cm. Probes were installed in the outer sapwood of the north-facing side of the stem and both probes and stems were insulated to minimize natural temperature gradients.
The temperature difference between the Granier-type probes was recorded at 10 second intervals and stored as 15 min averages on a data logger (CR10X Campbell Scientific, Logan, UT, USA) and used to obtain sap flux density by means of the equation derived empirically by Granier [33]. The daily maximum temperature difference was used as an estimate of the temperature difference under zero flow conditions. This variable was approximately constant over the study period (average coefficient of variation ± SE = 1.24% ± 0.04%).
Natural temperature gradients in the stem can interfere with sap flow measurements. These were measured over 60 days, but as values were consistently <5.2% of the sap flow signal, no corrections were applied [35].
The thickness of active sapwood was estimated using an allometric relationship obtained from a close by Aleppo pine site (in Peukochori, Chalkidiki; Radoglou K, unpublished data). For this purpose, 20 wood slices were used to estimate sapwood and heartwood areas. The equation best fitted to our data (r2 = 0.999) was As = 0.077 × (DBH1.9905), where As stands for sapwood area (in m2) and DBH for diameter at breast height (in m). Allometric relationships were also applied to estimate total tree leaf area [36] and used to calculate sap flow per unit leaf area (Ql; kgm−2day−1).
Canopy stomatal conductance (Gs; mms−1) was derived from sap flow measurements as described by [37].
Mean daily values of Ql and Gs corresponding to days with mean daily values of VPD <0.1 kPa were excluded [38].

2.7. Statistical Analysis

Statistical analysis was performed with SPSS 23.0 (IBM Corp., SPSS for Windows, NY, USA) and OriginPro 8.0 (OriginLab Corp., Northampton, MA, USA). Relationships between physiological traits, as well as between physiological and single or combined environmental parameters, were examined using linear and non-linear regression analyses and coefficients of determination (adjusted R2). The physiological traits tested were Amax, gs, Ψmid, needle δ13C, Ql, and Gs, while the respective environmental parameters were rainfall, air relative humidity, VPD, mean, maximum and minimum air temperature (Tmean, Tmax and Tmin, respectively), PET, net radiation, daytime net radiation, and aSWC of the actual day the physiological parameters were measured, or averaged over (a) the respective month, (b) the preceding month, (c) one week prior to measurements, and (d) two weeks prior to measurements. For the regression model between Ql, VPD, and net radiation, mean hourly values for the wetter period (November to March of each study year, when data were available) were considered after excluding the ones corresponding to VPD <0.1 KPa. For all analyses, the environmental parameter(s) having an insignificant effect on each regression model (p > 0.05) were excluded from the model. When the combined effect of more than one environmental parameter on physiological traits was tested, only the independent environmental parameters were entered into the regression model. All tested significant regression models are presented in Table S2. The regression models with the highest adjusted R2 and the highest significance level are presented in figures. The level of significance of each relationship (p < 0.05, p < 0.01, p < 0.001) is given in the respective plot.

3. Results

3.1. Climatic Conditions

The seasonal fluctuation of Tmean cumulative precipitation, mean aSWC, and mean VPD during the two-year study is presented in Figure 1. On average, 2009 was characterized by a combination of both higher average air temperatures and rainfall relative to 2008, resulting in lower VPD, higher aSWC, and higher aridity index (less xerothermic conditions) in 2009 compared to 2008 and to averages from the previous decade (Table 1).

3.2. Seasonal Patterns of Gas Exchange, Needle Water Potential, and δ13C Composition

Gas exchange rates were high at the beginning of April in both years of measurements (Figure 2a,b). In 2008, a second pick in gas exchange was recorded in early July, before the summer drought was intensified, whereas in 2009 a second pick was evident in early October, after the completion of the drought season.
The combined effects of daytime net radiation and Tmean on sampling dates largely explains the variation in Amax between October and March (Radj2 = 0.62, p < 0.05; Figure 3). The particularly low Amax values observed in October and November 2008, compared to the same period in 2009, could be due to the substantially lower air temperatures of the former period compared to the latter. Tmean ranged from 8.5 to 15.5 °C in October–November measuring days of 2008 vs. 19.6 to 21.7 °C in 2009, while the Tmin of the preceding nights was, similarly, lower in these measuring days of 2008 (5.4–11.2 °C) vs. 2009 (15.7–18.4 °C).On the other hand, the higher Tmean, increased aSWC, and decreased VPD during October–December of 2009, compared to the same period in 2008, resulted in a substantial increase in gas exchange, which reached values comparable to those observed during the spring in Aleppo pine. The strong and significant relationship between Amax and gs (Radj2 = 0.59, p < 0.01; Figure 4a) indicated a close stomatal regulation of photosynthesis during the study period.
The δ13C ratio and midday Ψ of the current year needles displayed seasonal variability (Figure 2c,d) that was more pronounced in 2008 than 2009, consistent with the observed lower VPD and higher aSWC in 2009 vs. 2008 (Figure 1; Table 1). A significant negative linear relationship was recorded between δ13C and Ψ (Radj2 = 0.38, p < 0.05; Figure 4b), with the highest δ13C and the lowest midday Ψ values reported in August. Among all tested environmental parameters, the average VPD over two weeks period prior to sampling had the strongest effect on the δ13C ratio of the needles (Radj2 = 0.64, p < 0.001; Figure 4a). The PET of the day of measurements was found to be the strongest predictor of midday Ψ (Radj2 = 0.72, p < 0.001; Figure 5b).

3.3. Seasonal Patterns of Sap Flow and Canopy Conductance

In 2009, maximum Ql values were reached early in the growing season, when mean daily aSWC was still quite high (Figure 6a). Comparison with the same period in 2008 was not possible, since sap flow measurements were initiated in July 2008. In addition, datalogger malfunctioning resulted in missing values in April 2009, thus, not allowing comparison with the gas exchange maximum values in April. During the dry months, from July to September of both study years, similar declining trends were apparent in Ql, with higher overall rates in less xerothermic 2009 compared to 2008 (Figure 6a). Ql increased in October 2008, with the increase in aSWC, from 13% (in the second half of September) to 49% (first half of October), while mean daily values of VPD and net radiation were still not limiting. Ql declined until December 2008, before increasing again to reach maximum values in March 2009 (Figure 6a), when VPD started to increase and aSWC was still very high (>85%). The combined effect of net radiation and VPD during the wet season (November–March) of the study period largely explained the variation in Ql (Radj2 = 0.64, p < 0.001; Figure 7). Thus, when water availability was not a limiting factor, Ql was mainly controlled by VPD and net radiation.
To investigate the causes of the drought-induced decrease in Ql, canopy stomatal conductance (Gs) was derived from Ql. The seasonal pattern of Gs was strongly controlled by PET (Radj2 = 0.69, p < 0.001; Figure 8a) and VPD (R2 = 0.62, p < 0.001; Figure 8c) of the respective period, indicating increased stomatal control as drought progressed. Gs was also strongly related to aSWC (Radj2 = 0.72, p < 0.001; Figure 8b) and tracked its seasonal changes, which explains the high values in October and December 2008, as well as in January 2009 (Figure 6b).

4. Discussion

The seasonal variation in key physiological traits as impacted by the environmental conditions were investigated in a mature near-coastal Aleppo pine forest in Sani, Chalkidiki, northern Greece. The study site is characterized by semi-arid growing seasons (mean aridity index of April to October during the last decade was 0.38) and compared to other Mediterranean Aleppo pine forests, it falls within the average rainfall range but has relatively high mean air temperatures (Table S3). Assessments were conducted during two consecutive years (2008 and 2009) differing in climatic conditions. The latter was characterized by considerably higher water availability, while the former was comparable or even drier than the last decade’s average (Figure 1; Table 1). This enabled monitoring of the ecophysiological responses of Aleppo pine under a wider range of climatic conditions. Within this frame, the effects of key environmental parameters on the gas exchange and water balance of Pinus halepensis were tested.
Aleppo pine exhibited a bimodal pattern of Amax which peaked twice in each year, when conditions were favorable (Figure 2a), corresponding with the species growth activity in the spring and autumn [6]. Stomatal regulation over Amax was observed throughout the year (Figure 4a), which appeared to respond to the limiting environmental factors. During the xerothermic summer conditions, PET exceeded that of aSWC and caused a decline in midday Ψ to values comparable to those reported in adult Aleppo pine trees (c. −2.6 MPa) [6]. As a result, gs also declined, thus limiting Amax (Figure 2a,b), in line with the isohydric water-saving strategy of Aleppo pine [4,8,39]. This reduction of gs is probably a response to minimize conductivity loss. Similar midday Ψ levels caused a c. 30% loss of conductivity in Aleppo pine seedlings subjected to drought [4], indicating its relatively high vulnerability to xylem embolism [6].
Air temperature and net radiation appear to be key controllers of Amax during the period of October to March (Figure 3). High Amax rates were reached during the warm days of October–November 2009, but not during the substantially colder measuring days between October 2008 and March 2009 (Figure 2a). It has similarly been reported [40] that the decrease of night temperatures below 10 °C, accompanied by a photoperiod below 12 h, results in low photosynthetic rates in seedlings of Pinus strobus during autumn. The Amax of Mediterranean pines was also found to be controlled by the preceding night temperatures and internal factors during autumn and winter months [41], as well as by extreme preceding summer droughts [10]. Any photoinhibition effects on Amax during the colder months of 2008 can be excluded since Fv/Fm values remained high (above 0.84; data not shown) and the air temperature was not low enough to account for such a response [42].
The quite xerothermic summer of 2008 resulted in a low midday Ψ (Figure 2d) that was reflected in the δ13C isotopic ratio (Figure 2c), which increased linearly with decreasing midday Ψ (Figure 4b). This has been observed in other forest species during water deficits [43], owing to decreased Rubisco discrimination against 13C under stomatal closure due to abiotic stresses [44]. Midday Ψ was found to immediately respond to short-term changes in air evaporative demand, as similarly shown by [11], since current day evapotranspiration explains 72% of its variation (p < 0.001; Figure 5b). On the contrary, the air vapor pressure deficit over the last two weeks strongly affected the needle δ13C (R2 adj = 0.64, p < 0.001, Figure 5a), while this effect was less pronounced when shorter or longer time intervals were examined (Table S2). Foliar δ13C being affected by recent environmental conditions has been previously reported [29,45] and may apply for Aleppo pine as well, as the isotopic signature of recently produced assimilates could be detected quicker in a conifer that maintains an active C metabolism through most of the year.
Sap flow per unit leaf area (Ql) showed a seasonal water saving pattern, with maximum values in early spring and a gradual decline as summer drought progressed (Figure 6a) and stomatal control increased (Figure 2b) to prevent water loss. A second peak in Ql occurred in autumn 2008 (Figure 6a) associated with aSWC increase (from 13% in the last half of September to 49% in the first half of October). It is also evident that, when water availability was not a limiting factor, Ql was mainly controlled by VPD and net radiation (Figure 7). Our results indicate that, in accordance to the findings from other Mediterranean type ecosystems [37,46], interannual variability in sap flow of Aleppo pines can be substantial, to avoid periods of prolonged drought and high transpirational demands.
Consistent with the patterns of leaf-level responses and sap flow, canopy conductance (Gs) decreased during the summer drought months (Figure 6b) being strongly affected by the gradual increases in PET, VPD (Figure 8a,c) and air temperature (Table S2), as similarly reported in numerous other studies [37,47]. As PET increased, midday Ψ decreased (Figure 5b) and gs followed the same pattern to prevent conductivity losses [48]. On the other hand, gs responded positively when water availability increased (Figure 8b), possibly due a gradual refill of previously cavitated tracheids [49].
The studied Aleppo pine stand exhibited plasticity to environmental conditions and showed the ability to recover from the effects induced by drought when climatic factors were improved. A similar response is reported for Aleppo pine growth when precipitation is increased [9]. However, during the period of increased water availability (October to March), varying patterns may be observed on the leaf and on the canopy level, responding to different parameters that seem to have a limiting effect. Thus, photosynthesis at the level of the lower canopy was greatly affected by air temperature and net radiation and increased when temperature was optimal (in October–November 2009), while sap flow and conductance at the canopy level responded positively to the favorable VPD, net radiation, and evapotranspiration during the same period of both years.
The results of the present study demonstrate the potential of this dominant Mediterranean forest tree species, to overcome the adverse conditions during summer droughts and to take advantage of more favorable water regimes occurring in early spring and occasionally also during autumn and winter, if other environmental parameters are not limiting, in a semi-arid ecosystem in Chalkidiki, Greece. Furthermore, some light is shed on the environmental controls over key physiological traits at the leaf and the canopy level.

5. Conclusions

By assessing the ecophysiological responses of the studied Aleppo pine forest in Northern Greece within a range of varying climatic conditions during a two year period, different but complementary patterns were revealed. During xerothermic periods, a typical isohydric behavior was exhibited by Aleppo pine; Amax, Ql and gs declined through stomatal control to limit Ψ reduction and loss of conductivity. However, in periods when water availability was not a limiting factor, the species was able to maximize its carbon gain if other controlling parameters, such as air temperature and net radiation, simultaneously ensured a favorable environmental regime. In conclusion, a high plasticity of the Pinus halepensis at the studied forest site to concurrent environmental conditions is indicated. Continuing studies are needed across Aleppo pine locations in the Mediterranean, particularly at its eastern part which is expected to be more prone to climate change, to improve our understanding of the species responses to ongoing climate variability.

Supplementary Materials

The following are available online at https://www.mdpi.com/1999-4907/10/4/313/s1, Table S1: Classification of aridity index (AI) categories; Table S2: Significant regression models describing the relationship between physiological and single or combined environmental parameters over different time intervals. The adjusted R2 values and the levels of significance are presented. The models in bold are the most significant ones with the highest adjusted R2, explaining the variation in the respective physiological parameter, which are presented in figures; Table S3: Characterization of the study site, in comparison to other Aleppo pine sites of Mediterranean countries.

Author Contributions

Conceptualization, M.N.F. and E.K.; Formal analysis, M.N.F., E.K. and S.A.P.; Investigation, M.N.F. and E.K.; Methodology, M.N.F. and E.K.; Project administration, K.R. and T.A.; Resources, K.R. and T.A.; Validation, M.N.F., E.K. and S.A.P.; Writing—original draft, M.N.F. and E.K.; Writing—review & editing, M.N.F., E.K., S.A.P., K.R., T.A. and A.M.

Funding

This research was funded by the General Secretariat for Research and Technology, Greece, grant number 05NON-EU-230 and the FoResMit LIFE14 CCM/IT/000905 project.

Acknowledgments

We wish to thank Gavriil Spyroglou and Nikolaos Fyllas for the biometrical characterization of the site, as well as George Halyvopoulos and Grigoris Morakis for their contribution in field measurements.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

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Figure 1. Daily values of: (a) Mean air temperature (Tmean) and rainfall and (b) available soil water capacity (aSWC) and vapor pressure deficit (VPD) during the study period.
Figure 1. Daily values of: (a) Mean air temperature (Tmean) and rainfall and (b) available soil water capacity (aSWC) and vapor pressure deficit (VPD) during the study period.
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Figure 2. Seasonal pattern of monthly (a) maximum photosynthesis (Amax), (b) stomatal conductance (gs), (c) δ13C ratio, and (d) midday water potential (Ψ) during two consecutive years (2008 and 2009). n = 4 trees ± SE.
Figure 2. Seasonal pattern of monthly (a) maximum photosynthesis (Amax), (b) stomatal conductance (gs), (c) δ13C ratio, and (d) midday water potential (Ψ) during two consecutive years (2008 and 2009). n = 4 trees ± SE.
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Figure 3. Regression model describing the combined effect of net radiation [kWm−2] and mean air temperature [°C] on needle Amax during the period October–March. Mean daily values of net radiation and air temperature corresponding to the days of Amax measurements were used. For net radiation, only daytime values were used. RSPV stands for regression standardized predicted value. The confidence levels of the models are depicted by grey upper and lower bands.
Figure 3. Regression model describing the combined effect of net radiation [kWm−2] and mean air temperature [°C] on needle Amax during the period October–March. Mean daily values of net radiation and air temperature corresponding to the days of Amax measurements were used. For net radiation, only daytime values were used. RSPV stands for regression standardized predicted value. The confidence levels of the models are depicted by grey upper and lower bands.
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Figure 4. Regression models describing the relationship between needle (a) Amax and gs and (b) δ13C and midday Ψ. The confidence levels of the models are depicted by grey upper and lower bands.
Figure 4. Regression models describing the relationship between needle (a) Amax and gs and (b) δ13C and midday Ψ. The confidence levels of the models are depicted by grey upper and lower bands.
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Figure 5. Regression models describing the relationship between (a) needle δ13C and mean vapor pressure deficit (VPD) averaged over the preceding two weeks prior to measurements and (b) needle midday Ψ and potential stand evapotranspiration (PET) of the current day of measurements. The confidence levels of the models are depicted by grey upper and lower bands.
Figure 5. Regression models describing the relationship between (a) needle δ13C and mean vapor pressure deficit (VPD) averaged over the preceding two weeks prior to measurements and (b) needle midday Ψ and potential stand evapotranspiration (PET) of the current day of measurements. The confidence levels of the models are depicted by grey upper and lower bands.
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Figure 6. Seasonal patterns of mean monthly values of: (a) Sap flow per unit leaf area Ql and (b) canopy stomatal conductance (Gs) measured over two consecutive years (2008 and 2009). n = 5 trees ± SE.
Figure 6. Seasonal patterns of mean monthly values of: (a) Sap flow per unit leaf area Ql and (b) canopy stomatal conductance (Gs) measured over two consecutive years (2008 and 2009). n = 5 trees ± SE.
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Figure 7. Regression model describing the combined effect of vapor pressure deficit (VPD) [kPa] and net radiation [kWm−2] on Ql. Mean hourly values of VPD and net radiation corresponding to the days’ sap flow was monitored during the wet period (November to March) were used. RSPV stands for regression standardized predicted value.
Figure 7. Regression model describing the combined effect of vapor pressure deficit (VPD) [kPa] and net radiation [kWm−2] on Ql. Mean hourly values of VPD and net radiation corresponding to the days’ sap flow was monitored during the wet period (November to March) were used. RSPV stands for regression standardized predicted value.
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Figure 8. Regression models describing the relationship between mean monthly canopy stomatal conductance (Gs) and (a) potential stand evapotranspiration (PET), (b) available soil water capacity (aSWC), and (c) vapor pressure deficit (VPD). The confidence levels of the models are depicted by grey upper and lower bands.
Figure 8. Regression models describing the relationship between mean monthly canopy stomatal conductance (Gs) and (a) potential stand evapotranspiration (PET), (b) available soil water capacity (aSWC), and (c) vapor pressure deficit (VPD). The confidence levels of the models are depicted by grey upper and lower bands.
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Table 1. Annual cumulative rainfall and mean annual aridity index, aSWC and VPD during the study years and the previous decade.
Table 1. Annual cumulative rainfall and mean annual aridity index, aSWC and VPD during the study years and the previous decade.
PeriodRainfall (mm)Aridity IndexaSWC (%)VPD (KPa)
2008542.10.7736.90.55
2009680.21.1646.60.46
2008–2017544.90.8437.50.48

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Fotelli, M.N.; Korakaki, E.; Paparrizos, S.A.; Radoglou, K.; Awada, T.; Matzarakis, A. Environmental Controls on the Seasonal Variation in Gas Exchange and Water Balance in a Near-Coastal Mediterranean Pinus halepensis Forest. Forests 2019, 10, 313. https://doi.org/10.3390/f10040313

AMA Style

Fotelli MN, Korakaki E, Paparrizos SA, Radoglou K, Awada T, Matzarakis A. Environmental Controls on the Seasonal Variation in Gas Exchange and Water Balance in a Near-Coastal Mediterranean Pinus halepensis Forest. Forests. 2019; 10(4):313. https://doi.org/10.3390/f10040313

Chicago/Turabian Style

Fotelli, Mariangela N., Evangelia Korakaki, Spyridon A. Paparrizos, Kalliopi Radoglou, Tala Awada, and Andreas Matzarakis. 2019. "Environmental Controls on the Seasonal Variation in Gas Exchange and Water Balance in a Near-Coastal Mediterranean Pinus halepensis Forest" Forests 10, no. 4: 313. https://doi.org/10.3390/f10040313

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