Changes in intrinsic water use efficiency (iWUE) were investigated in Fagus sylvatica and Nothofagus spp. over the last century. We combined dendrochronological methods with dual-isotope analysis to investigate whether atmospheric changes enhanced iWUE of Fagus and Nothofagus and tree growth (basal area increment, BAI) along latitudinal gradients in Italy and Chile. Post-maturation phases of the trees presented different patterns in δ13C, Δ13C, δ18O, Ci (internal CO2 concentration), iWUE, and BAI. A continuous enhancement in isotope-derived iWUE was observed throughout the twentieth century, which was common to all sites and related to changes in Ca (ambient CO2 concentration) and secondarily to increases in temperature. In contrast to other studies, we observed a general increasing trend of BAI, with the exception of F. sylvatica in Aspromonte. Both iWUE and BAI were uncoupled with the estimated drought index, which is in agreement with the absence of enduring decline in tree growth. In general, δ13C and δ18O showed a weak relationship, suggesting the major influence of photosynthetic rate on Ci and δ13C, and the minor contribution of the regulation of stomatal conductance to iWUE. The substantial warming observed during the twentieth century did not result in a clear pattern of increased drought stress along these latitudinal transects, because of the variability in temporal trends of precipitation and in specific responses of populations.
Citation: Tognetti R, Lombardi F, Lasserre B, Cherubini P, Marchetti M (2014) Tree-Ring Stable Isotopes Reveal Twentieth-Century Increases in Water-Use Efficiency of Fagus sylvatica and Nothofagus spp. in Italian and Chilean Mountains. PLoS ONE9(11): e113136. https://doi.org/10.1371/journal.pone.0113136
Editor: Sylvain Delzon, INRA - University of Bordeaux, France
Received: June 25, 2014; Accepted: October 22, 2014; Published: November 14, 2014
Copyright: © 2014 Tognetti et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The authors confirm that all data underlying the findings are fully available without restriction. All relevant data are within the paper.
Funding: Financial support was provided by the project “Ciclo del carbonio ed altri gas serra in ecosistemi forestali, naturali ed artificiali dell'America Latina: analisi preliminare, studio di fattibilità e comparazione con ecosistemi italiani” (Internationalization 2008, MIUR, Italy) and “Sviluppo di modelli innovativi per il monitoraggio multiscala degli indicatori di servizi ecosistemici nelle foreste Mediterranee” (FIRB 2012, MIUR, Italy) - http://www.istruzione.it/. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
In the mid-latitudes, the emerging picture of enhanced evapotranspiration (ET) highlights the possible threat posed by increasing drought frequency to managing water resources in a greenhouse-affected climate . Extreme drought summers in Europe, throughout the twentieth century , and recent drying trends are qualitatively consistent with predictions for the coming decades . Extensive tree mortality triggered by dry and hot climatic conditions has been documented for most biomes of both Hemispheres over the past two decades . Multiple mechanisms (hydraulic failure, carbohydrate depletion and insect attack) are involved in drought-induced forest decline , which occurs not only in arid regions but also in wet forests not normally considered at drought risk   . A decrease in tree growth, in the event of prolonged drought periods might reduce the future economic value of currently productive forests , which requires the study of tree physiological adaptations  .
Variation in intrinsic water-use efficiency (iWUE) estimated as the ratio between photosynthetic rate and stomatal conductance is recorded in the variation of the carbon isotope discrimination (Δ13C) of the annual growth rings that are laid down during each growing season . Elevated atmospheric CO2 concentration (Ca) is expected to reduce stomatal openings and increase assimilation rates  , which can alter the Ca to intercellular CO2 concentration (Ci) gradient and result in increased iWUE in the long-term, which will be recorded in the variation of this Δ13C. However, the Δ13C in tree rings also responds strongly to other environmental variables, especially climatic ones, such as growing season temperature, relative humidity and precipitation . In either case, along with increases in iWUE (detected through changes in Δ13C) an increasingly faster tree growth (measured by tree-ring width converted into basal area increment, BAI) could also be observed . Nevertheless, an increase in iWUE alone is not directly translated into higher BAI, since other factors, including high temperature, recurrent drought, nutrient limitation and/or plant acclimation, may preclude tree growth. Conversely, if BAI declines while iWUE increases, any photosynthesis advantage conferred by higher CO2 concentrations should not offset warming-induced stress . The extent that rising Ca has affected long-term iWUE, and whether climate could explain deviations from expected Ca-induced growth enhancement, are still poorly understood .
 found that climate change towards more arid conditions accounted for higher iWUE in Fagus sylvatica L. forests more than the continuous increase in Ca. Drought-induced decline in the productivity of beech forests in recent decades was observed by  in the Apennines (Italy). Nevertheless, different bioclimatic regions can have opposite responses to global climatic change, and BAI of old trees showed an increasing trend over time in the Alps . Dendrochronological analysis on beech stands in Switzerland evidenced that trees near their dry distribution limit are adapted to extreme conditions already . Unusual decreases in tree growth over the last 50 years were observed in dry-mesic Patagonia . In Central Andes, Nothofagus pumilio (Poepp. & Endl.) Krasser showed reduced radial growth due to high temperatures in spring and summer, which enhanced ET . Contrasting precipitation and temperature patterns have been reported for Northern and Southern Patagonia.  observed that, in N. pumilio, the relationship between iWUE and climate was more obvious in sites with good water availability, while in drier sites the photosynthetic rate was severely limited by water deficits so that the reduction in radial growth was not compensated by the increase in iWUE.
Tissue δ13C provides an integrative record of supply and demand for CO2 . Variation in δ13C may be driven by changes in stomatal conductance (i.e., supply of CO2), or in photosynthetic rate (i.e., demand for CO2), or both. Stomatal closure, because of restrictions in water availability, generally reduces Ci, leading to an increase in δ13C. Because light limitation of photosynthesis increases Ci, δ13C can also depend on radiation . Therefore, the dependence of δ13C on the ratio Ci/Ca provides limited information about the strength of stomatal control of Ci and photosynthesis, since a change in Ci (inferred from δ13C) could be the result of a change in either stomatal conductance or photosynthesis. Tissue δ18O is not strongly influenced by photosynthetic rate, so that combined measurements of δ13C and δ18O should allow stomatal and photosynthetic effects on δ13C to be teased apart   . The relative responses of both δ13C and δ18O can be related to the sensitivity of a plant to changing evaporative conditions . In a recent study,  have assessed soil drought exposure in forest stands by calculating the stand-level increase in Δ13C of late wood from wet to dry years, which exhibited a negative linear relationship with tree species diversity in two forest types (including temperate beech), but not in others (as mountainous beech).
In this study, we used tree-ring δ13C and δ18O to investigate iWUE and tree growth changes during the twentieth century in F. sylvatica in Italy and Nothofagus spp. [N. antartica (Forster) Oerst., N. betuloides (Mirb.) Oerst., N. dombeyi (Mirb.) Oerst., and N. pumilio] in Chile. All the sampled stands were naturally occurring uneven-aged forests in national parks or protected areas that had been left unmanaged for many years, which may serve as reference for tree responses to natural disturbances. Along these two North-to-South transects, there is a substantial geographic gradient, averaged temperature and ET decreasing with increasing latitude. It was hypothesized that these Fagus and Nothofagus spp. would respond to climate by shifting from a more hydric dependence at lower latitudes to a more temperature dependence at higher latitudes. In particular, we aimed to relate the changes in Δ13C, δ13C and δ18O, and iWUE with tree growth patterns, and to test whether the beneficial effect of Ca fertilization on tree growth could compensate the negative impact of warming-drought on BAI.
Materials and Methods
Sampling was accomplished along two latitudinal transects: eight forest stands (F. sylvatica) were sampled in Italy, and five forest stands (Nothofagus spp.) were sampled in Chile (Table 1). The age (years) of trees sampled for stable isotope analyses was the following (mean ± standard errors): North-Central Italy - Pian de Cansiglio 167±17, Sasso Fratino 187±33, Val Cervara 339±15, Montedimezzo 153±4; South Italy - Gargano 193±6, Cilento 158±20, Sila 152±3, Aspromonte 156±11; Chile - Chillan 137±14, Villarrica 230±16, Torres del Paine 144±24, Omora low 203±17, Omora high 178±16. Sampling was conducted in national parks or natural reserves, under the guidance of local authorities (park authority and/or forest service). Sampling did not involve endangered or protected species and no specific permissions were required for these locations/activities.
Pian del Cansiglio is an almost pure mature F. sylvatica high stand. The landscape morphology is gently sloping with valleys, and bedrock is mainly limestone and marlstone (Cretaceous).
Sasso Fratino is a stand that has been left to natural evolution for more than seventy years. Fagus sylvatica is the prevailing tree species with an average dominant height of about 40 m. Small groups and singles trees of Abies alba Mill. eventually occur.
Val Cervara is an old-growth forest located in an amphitheater shaped valley with Cretaceous limestone bedrock and soils that can be referred to the brown group. This almost pure F. sylvatica high stand escaped logging because of difficult access .
Montedimezzo is a forest that has been un-harvested since 1950. The geology is dominated by Cretacic limestone, with greensands and clay soils prevalent. The structure of this Apennine-Corsican montane beech forest is very diverse . The F. sylvatica-dominated stand is associated with Quercus cerris L. at the lowest altitudes and sometimes mixed with other species, as Acer pseudoplatanus L., A. campestre L., A. obtusatum W. et K. and Taxus baccata L.
Gargano is an almost pure F. sylvatica stand with Ilex aquifolium L. in the understory, un-harvested since 1954. The geology is dominated by Cretacic limestone, with greensands and clay soils prevalent.
Cilento is a F. sylvatica high stand characterized by temperate climatic features (sub-continental and oceanic with mild and cool weather conditions) . The hilly landscape is mainly constituted of stratified flysch formations of Tertiary age, which is complex and chaotic sandstone sedimentation.
Sila is an uneven-aged F. sylvatica high stand, mixed with A. alba, which has been un-harvested since 1960, and occupies humid locations of the Sila plateau, alternating with forests of Pinus nigra laricio (Poir.) Maire. The geology is dominated by Cretacic limestone, with greensands and clay soils prevalent.
Aspromonte is located on a calcareous massif. Fagus sylvatica forests cover the summit of the mountains, reaching almost 2000 m a.s.l., representing the Southernmost limit of the European beech forest area. This uneven-aged F. sylvatica high stand has been unmanaged since 1900; A. alba and P. laricio are also present.
Chillan is a N. dombeyi forest stand in the Southern volcanic zone of the Andean Cordillera. This site refers to the phytogeographic transition zone between semi-arid, Mediterranean-type climate to the North and cool temperate rain forest climate to the South, a tension zone between warm and cool temperate Nothofagus forests.
Villarrica is a coigüe (N. betuloides) forest stand on the South side of Villarrica volcano. The region is characterized by a west-coast maritime climate with a mild Mediterranean influence. Throughout the region, most of the soils are derived from recently deposited volcanic ashes that overlie Pleistocene glacial topography.
Torres del Paine is a N. pumilio high forest. Much of the geology of the Paine Massif area consists of Cretaceous sedimentary rocks that have been intruded by a Miocene-aged laccolith. Orogenic and erosional processes have shaped the topography, and glacial erosion is mainly responsible for the sculpturing of the massif.
Omora “low” and Omora “high” are old-growth forest stands on the Navarino Island, about 4 km away from each other. These rainy sub-Antarctic forests are the planet's Southern-most forest ecosystems . Omora “low” is characterized by deciduous Magellanic forest, where lenga beech (N. pumilio) is the dominant tree species. Omora “high” is a pure ñirre beech (N. antarctica) stand. The climate is oceanic, while soils are composed of medium sized gravel, with a sandy-clayey matrix, showing no internal stratification.
Observed climatic data near these sites cover only a short climatic period, and the record is spatially fragmented. For this reason, we used interpolated climatic data. The meteorological data used was from the CRU TS 3.1 0.5° gridded product . Monthly minimum, mean and maximum temperatures, as well as total monthly precipitation from 1901 to 2009 were used. The coordinates of the closest grid point selected at each site are described in Table 1.
To assess water availability for tree growth, a monthly drought index (DI = P−ETo) based on precipitation sums (P) and the potential evapotranspiration (ETo), following , was calculated.
At each site, 16÷20 dominant trees were sampled, and two increment cores at breast height were collected from each tree, with large-diameter borer. Four dominant trees per site were selected and cores extracted for analyses of stable isotopes. To avoid the effect of any wood alteration and of exogenous disturbances on ring growth, only trees without abrasion scars or other visible evidence of injury were selected.
Ring widths were measured with a resolution of 0.01 mm on each of the cores, using LINTAB measurement equipment (Frank Rinn, Heidelberg, Germany) fitted with a Leica MS5 stereoscope (Leica Microsystems, Germany) and analysed with the TSAP software package. Crossdating of all the tree-ring data was verified using the Program COFECHA, which assesses the quality of crossdating and measurement accuracy of tree-ring series using the segmented time-series correlation technique . We only used the successfully crossdated cores, having a significant Gleichläufigkeit. This is a statistical measure of the year-to-year agreement between the interval trends of the chronologies, based on the sign of agreement  and Student's t test, which determines the degree of correlation between curves. With an overlap of 50 years (which is commonly used in tree-ring studies), GLK becomes significant (p<0.05) at 62% and highly significant (p<0.01) at 67%. In this study, the analysed time series were always longer than 50 years and cross-dating was considered successful if GLK was higher than 62%. The statistical significance of the GLK (GSL) was also computed. The TVBP is a Student's t-value commonly used as a statistical tool for comparing and cross-dating ring widths series. It determines the degree of correlation between curves. This method eliminates low-frequency variations in the time series, as each value is divided by the corresponding 5-year moving average. Each tree's ring-width record was standardized and then averaged with the other trees' records to obtain the mean standard chronology for the study site . The standardization procedure involves fitting the observed ring-width series to a curve or a straight line and computing an index of the observed ring widths divided by the expected value. This reduces the variance between the cores and transforms the ring widths into dimensionless index values, and computes the tree-ring chronologies' average that is not influenced by the fastest growing trees, which have large ring widths. The ARSTAN program was used to process the tree-ring data into final chronologies . To preserve the long-term fluctuations in the series, a conservative method of detrending was used. Only the negative exponential curves and/or linear regressions with negative or zero slopes were used.
Ring width was converted into tree basal area increment (BAI) according to the following standard formula:where r is the radius of the tree and n is the year of tree-ring formation. To examine the mean growth trend of the canopy trees, BAI for each year was averaged over all individuals, to remove variation in radial growth attributable to increasing circumference, and averaged on a 10-year period basis, starting from 1900 (when BAI of the 20-year period was ≥10 cm2, except for Omora sites). We worked with mean not-standardized BAI values across all trees for each year to preserve long-term cumulative effects of climatic events on tree growth.
The pooled rings of four trees per site (10-years blocks) were examined under a microscope to ensure that no false rings were included (one core from each of the four trees with no evident growth disturbance was selected for isotope analysis). The blocks were cut using a thin sharp blade. The samples were ground with a centrifugal mill (ZM 1000, Retsch, Retsch Technology, Haan, Germany) using a mesh size of 0.5 mm to assure homogeneity . Cellulose was extracted from all samples to avoid isotope variations that are purely based on the changes in the relative abundance of individual wood constituents, differing typically in their isotope signatures. The method for cellulose extraction (modified from ) was based on a double-step digestion: the first step consisted of the treatment of wood with a solution of 5% NaOH for 2 h at 60°C, repeated twice, to remove lipids, resins, oil, tannins and hemicelluloses. In the second step, samples were washed with a solution of 7% NaClO2 and 3–4 mL of acetic acid (pH 4) for a minimum of 36 h at 60°C. Because the solution is only reacting for 10 h, it was changed daily and refilled as necessary . During this stage lignin was digested. Finally, samples were washed three to four times with boiling distilled water and dried overnight at 50°C. The δ13C values were measured by combustion and δ18O by pyrolysis of the cellulose samples in an elemental analyzer (Carlo Erba 1110, Milano, Italy) interfaced via a Conflo II Interface (Thermo Finnigan, Bremen, Germany) to a dual inlet/continuous flow isotope ratio mass spectrometer (Delta S, Thermo Finnigan, Bremen, Germany), in the continuous flow mode. Isotope ratio deviation results are presented in the common δ notation,with δ-values expressed in per mill (‰) on the international VPDB scale for carbon-13 and VSMOW scale for oxygen-18; R refers to the number ratio of 13C to 12C or 18O to 16O isotopes in the sample (‘sa’) and the reference (‘ref’), respectively.
The standard deviation for the repeated analysis of an internal standard (commercial cellulose) was <0.1% for δ13C and 0.3% for δ18O. The calibration was carried out by measurement of IAEA USGS-24 (graphite), IAEA CH7 (polyethylene) and IAEA CH3 (cellulose).
The raw δ13C chronology exhibited a decline in δ13C mainly in the twentieth century, which may be attributed to the lowering of δ13C of air through anthropogenic-related increases in CO2 concentration (the “13C Suess effect”). We removed this trend in the carbon isotope chronology using the annual records of past atmospheric δ13C obtained from ice cores .
We, thereafter, calculated Δ13C, Ci and iWUE. The Δ13C (carbon isotopic discrimination) was calculated asfollowing  and using published values for air δ13Cplant from ice core measurements, direct atmospheric measurements and inferred from C4 plants . Since Δ13C is related to Ci (intercellular CO2 concentration) and Ca (ambient CO2 concentration) by the following equation:where a (≈4.4‰) is the discrimination against 13CO2 during CO2 diffusion through stomata , b (≈27‰) is the discrimination associated with carboxylation , and given Fick's Law:where A is the net photosynthesis, measured as CO2 uptake, and gCO2 is the leaf conductance to CO2, and given that gH2O, the leaf conductance to water vapour is 1.6 gCO2, Δ13C can be finally related to the ratio A/gH2O (intrinsic water-use efficiency, iWUE)  by the following equation:we determined the Ci, using 's equation:We calculated iWUE as:
Data treatment and trend analysis
Regression analyses were used to identify significant temporal trends in δ13C, Δ13C, δ18O, Ci, iWUE and BAI of individual trees over the last century, when most trees were in their mature phase. ANCOVA was used to test for differences in past decade trends between mean mature trees δ13C, Δ13C, δ18O, Ci, iWUE and BAI at each site and the influence of Ca and climate. Differences between forest sites were tested by post hoc Bonferroni test. For correlation analyses of these variables with climate, expressed as average (10 years), annual Ca and index of aridity were calculated for the period beginning October (Italy) or April (Chile) of the previous year and ending with September (Italy) or March (Chile) of the current year. This procedure avoids relating growth to climate in the months after leaf fall when growth has ceased. Regression, ANCOVA, correlation and all the statistical calculations and analyses were conducted using the SPSS software package (SPSS Inc., Chicago, IL, USA).
Trend analysis of δ13C, Δ13C, δ18O, Ci, iWUE, BAI, and DI was investigated using the non-parametric Man-Kendall test  , which compares the relative magnitudes of the samples and provides information on whether the null hypothesis of no trend in the data can be rejected or not. The data values are evaluated as an ordered time series. Each data value is compared to all subsequent data values. The initial value of the Mann-Kendall statistic, S, is assumed to be zero (i.e., no trend; null hypothesis). If a data value from a later time period is higher than a data value from an earlier time period (i.e., a trend is detected; alternative hypothesis), S is incremented by one. On the other hand, if the data value from a later time period is lower than a data value sampled earlier, S is reduced by one. The net result of all such increments and decrements yields the final value of S. This test allows for investigating long-term trends of data without assuming any particular distribution. The rank correlation coefficient evaluates the degree of similarity between the ranks of two sets of measured data. The rank correlation provides a distribution free test of the independence and a measure of strength of dependence between two variables. The tau coefficient is defined as:where nc is the number of concordant pairs (i.e., pairs ranks with moving in the same direction), and nd is the number of discordant pairs (i.e., pairs with ranks moving in different directions), in the data set. The approach is to count the number of concordant and discordant pairs between two ordered sets. This number gives a distance between sets called symmetric difference distance. The coefficient of correlation is obtained by normalizing the symmetric difference by the total number of pairs such that it will take values between −1 and +1. The tau coefficient has the following properties: 1) If the agreement between the two rankings is perfect (i.e., the two rankings are the same) the coefficient has value 1; and 2) If the disagreement between the two rankings is perfect (i.e., one ranking is the reverse of the other) the coefficient has value −1. For all other arrangements the values lies between −1 and 1, and increasing values imply increasing agreement between the rankings. If the rankings are completely independent, the coefficient has value 0 on average.
Patterns of climate index and δ13C, Δ13C, δ18O, Ci, iWUE, and BAI
A downward trend of climate index at the end of last century, indicating increasingly drier conditions, was found for Val Cervara, Sasso Fratino and Montedimezzo (Fig. 1). However, the climate index was variable from year to year and below −25 mm only in several years (and only for Val Cervara, Gargano, Cilento and Chillan), indicating that trees were rarely subjected to severe and prolonged drought stress over the past century.
It must be pointed out that the great heterogeneity of the local environment in these mountainous areas can contribute errors to estimated values of drought index.
In general terms, similar trends in δ13C, Δ13C, δ18O, Ci and iWUE were found throughout the chronologies corresponding to F. sylvatica and Notophagus spp. trees from the different forest sites (Fig. 2). Tree rings δ13C on forest trees showed variable patterns (e.g., increasing at Torres del Paine, while decreasing at Omora high). When the atmospheric effect over plants carbon isotopic ratios is excluded, the discrimination (Δ13C) trends during the past decades showed the opposite (decreasing) trend. The more negative δ13C values resulted in higher discrimination (Δ13C) and lower iWUE. Yet, δ18O showed relatively stable patterns throughout the past century, with some increases in the last thirty years in several sites, but not in others.
Symbols with the error bars (±1 standard error, n = 4) are means of individuals per site in 10-years total values (±1 standard error n = 4). Temporal trends of Ca and atmospheric δ13C are also reported (dashed lines). Sites are referred to by symbols in the legend: Pian del Cansiglio, Sasso Fratino, Val Cervara, and Montedimezzo (North-Central Italy); Gargano, Cilento, Aspromonte, and Sila (Southern Italy); Omora low, Omora high, Torres del Paine, Villarrica, and Chillan (Chile). Site and species details are reported in Table 1. Populations are listed from North to South (Northern Hemisphere) or South to North (Southern Hemisphere).
iWUE increased throughout the 20th century, particularly in the second half, simultaneously with changes in Ca and Ci (Fig. 2). Ci ranged between 220 and 240 ppm in the forest until mid 20th century, reaching recently values as high as 270 ppm. This rise in Ci as well as in iWUE represented a significant trend, which followed the increase in Ca in the past decades.
The BAI curve of F. sylvatica and Notophagus spp. trees showed a continuous and steep increase in the first years of the 20th century in most of the sites, before levelling off to mature levels of growth, with signals of changes in growth patterns for trees of Cilento (Southern Italy), and Torres del Paine and Villarrica (Chile) (Fig. 2). The analysis was limited to those years (20th century) for which growth suppression (before the release phase) was considered negligible in most stands of these late successional species. There were, however, exceptions to this abrupt increasing trend; more specifically, in the oldest site (Val Cervara) and in Aspromonte in Southern Italy for F. sylvatica, and in the Southernmost sites (Omora high and Omora low) for Notophagus spp. BAI showed smoother patterns over time, with values between 10 and 20 cm2 (Italian sites) or barely reaching 15 cm2 (Chilean sites) The levelling off to low BAI values marks the beginning of late successional stages. Nevertheless, a slight increase in the most recent decade was common to most sites (except for Pian del Cansiglio and Omora low).
Table 2 reports the results of trend analysis for parameters of Fig. 1 and 2, based on the Mann–Kendall test. A significant decreasing trend of DI, indicating drier conditions, was observed for Sasso Fratino, Val Cervara, Montedimezzo, and Omora sites. In general, iWUE showed significant increasing trends with strong correlation (tau values close to 1); BAI behaved similarly, with the exception of Cilento (low tau values) and Aspromonte (negative S values). Correspondingly, Δ13C showed marked decreasing trends. More uncertain were correlation coefficients for the other parameters.
The absolute averaged values for the 20th century evidenced a rather marked trend of increasing BAI with decreasing latitude in Chile, while higher variable occurred in Italy (Fig. 3) (ANCOVA, P<0.01); the old-growth forest of Val Cervara showed the lowest averaged values among the Italian sites and the highest BAI was observed in Pian del Cansiglio (Northernmost site) and Montedimezzo (ANCOVA, P<0.01). Pian del Cansiglio also showed the lowest averaged δ18O values for the Italian site, while Omora high had the lowest δ18O amongst all sites (ANCOVA, P<0.01). The latter site, which was the coldest one, showed the highest averaged δ13C and Δ13C, in absolute terms, and Ci, and the lowest iWUE amongst all sites (ANCOVA, P<0.01).
Different letters indicate significantly different values between sites (P<0.05; post hoc Boferroni test, after ANCOVA analyses). Populations are listed from North to South (Northern Hemisphere) or South to North (Southern Hemisphere).
Relations of iWUE, δ13C, δ18O and BAI with climate index, atmospheric CO2 concentration (and temperature)
The estimated iWUE was positively correlated with Ca, while the correlation with the drought index was significant and negative only for Sasso Fratino (Fig. 4). Correlations between iWUE and temperature were clear and positive for Fagus, while this was not the case for Nothofagus spp. (not shown). The calculated BAI was also positively correlated with Ca, though with varying slopes in the early decades of the 20th century (Fig. 4). Val Cervara exhibited the lowest slope among the populations of North-Central Italy. The Chilean species and populations showed a latitudinal gradient with decreasing slopes with increasing latitude. Even in the case of BAI, the relationship with the drought index was vague, with the sites clustered in some cases (North-Central Italy and Chile) and not in others (South Italy). Correlations between BAI and temperature were again positively clearer for Fagus than for Nothofagus spp., and particularly for the populations of North-Central Italy (not shown). This clustering pattern was maintained for the relationship between δ18O and Ca or the drought index (and temperature), with rather shallow slopes (not shown). Similarly, the relationship between δ13C and the drought index (or temperature) resulted in the separation among sites in the case of North-Central Italy and Chile, while this was not the case for South Italy (not shown). The relationship between δ13C and Ca was unclear, somewhat following the pattern of iWUE. Populations of North-Central Italy showed an increase of BAI with iWUE, Val Cervara showing a lower slope in comparison with all others (Fig. 4); populations of South Italy also showed a similar increase of BAI with iWUE, though levelling off at higher iWUE values, and with the exception of Aspromonte, showing a negative relationship; also in the case of Chile, the Southernmost site (Omora) showed rather shallow relationships between BAI and iWUE, the other sites exhibiting positive correlations.
Sites are referred to by symbols in the legend: Pian del Cansiglio, Sasso Fratino, Val Cervara, and Montedimezzo (North-Central Italy); Gargano, Cilento, Aspromonte, and Sila (Southern Italy); Omora low, Omora high, Torres del Paine, Villarrica, and Chillan (Chile). Site and species details are reported in Table 1. Regression coefficients are reported in Table 2.
The regression coefficients for equations describing the relationship between variables are reported in Table 3.
Correlations between δ18O and δ13C
Overall, δ18O and δ13C were positively correlated when considering pooled Chilean sites. Correlations varied between the two Italian clusters (North-Central and Southern sites), with Southern sites showing a reverse (negative) and weak relationship in comparison with North-Central sites (Fig. 5). At each site, δ18O and δ13C were poorly correlated (regressions not shown). Montedimezzo and Cilento had correlation coefficients (R2) of 0.49 and 0.30 (positive correlation), respectively. Aspromonte, Gargano, Sassofratino and Villarrica had R2 ranging from 0.21 to 0.14 (positive correlation); other populations showed rather shallow relationships (R2<0.1). The Chilean sites (and species) were fairly distinguishable from each other, with the Northernmost site (Chillan, N. dombeyi) showing the highest (more positive) and Omora high (N. antartica) the lowest (more negative) δ18O and δ13C values, N. betuloides and N. pumilio showing intermediate values. The Italian sites were also rather clearly discernible.
Populations are listed from North to South (Northern Hemisphere) or South to North (Southern Hemisphere). Symbols with the error bars (±1 standard error, n = 4) are mean values per each site. The regression equation and coefficient of correlation are also shown (P≤0.01). Site and species details are reported in Table 1.
Temporal changes in iWUE and BAI
Over the twentieth century, the iWUE increased 35.3±1.4% in the sites of Southern Italy and 39.8±1.3% in those of North-Central Italy sites (Fig. 2, 3), which is somewhat in agreement with the 44% increase reported by  in Northeastern France and with 50% increase reported by  in Northeastern Spain. Similar increases in iWUE and decreases in Δ13C have been found during the twentieth century by using historical records in tree-rings of other (temperate and boreal) Northern Hemisphere species  ; although this is not always the case . Likewise, the iWUE increased 31.6±2.0% in the Chilean sites, and all these increases in iWUE are in agreement with previous reports for the Southern Hemisphere; e.g.,  found 34% increase for Brazilian Cedrela odorata L. and 52% increase for Swietenia macrophylla King, while  found 30% increase in iWUE of mature Araucania angustifolia (Bertol.) during the second half of the past century.
The large inter-decadal variability of δ13C may have hidden long-term trends of a regulation of either Ci or Ci/Ca (Fig. 2), although a spatially uneven increase of Ci/Ca during the second half of the twentieth century points to some patchy homoeostasis in iWUE along environmental gradients. Several studies have reported widespread increases in iWUE (and decreases of Δ13C) coinciding with rising Ca over the past century  . Inter- and intra-specific differences in 13C discrimination   and variation across altitudinal and latitudinal gradients   were not pondered in this study, which warrants caution in interpreting trends in iWUE as a coherent global response to rising Ca, because of the correlation with Ca and its use as an independent factor in the iWUE calculation . The increase in iWUE across biomes without univocal effect on tree growth , indeed, raises the question of whether iWUE calculations reflect actual physiological responses to elevated Ca; hydraulic adjustment to increasing evaporative demand and nitrogen deposition affecting gas exchange may also have an impact on iWUE.
In contrast with other studies  , we found evidence of long-term increases in BAI (Fig. 2, 3), associated with increasing iWUE, likely because the ameliorating effects of increasing Ca on water stress. Global estimates of iWUE, inferred from the Δ13C analyses of comparable mature trees, showed a 20.5% increase and an increase in Ca of over 50 µmol mol−1 during the last 40 years, with minor differences across biomes . Several authors   suggested that changes in temperature and Ca might have accelerated tree growth over recent decades in temperate climates, though this conclusion is controversial . Although stem growth is the most sensitive component of NPP to drought, because it is low on the carbon allocation hierarchy , the documented warming   could have exerted a larger control on stem growth than precipitation in these relatively humid forest stands . Prolonged water limitation at the stand level, however, will act as major constraint on the adaptive capacity of drought-sensitive beech forests if warming continues   . Therefore, current growth trends may not translate fully into long-term increased tree density for Fagus and Nothofagus spp.   . There is already some evidence that increased variability in climate warming has had little effect on the recruitment of Nothofagus close to the tree line in the Southern Hemisphere  , which contrasts with the shift of beech populations in mountain ranges of the Northern Hemisphere .
The effect of climate
The index used here to describe soil water availability to trees cannot be assumed a priori to be indicative of soil moisture deficit, though providing straight interpretable values for correlation purposes   . Long-term trends in BAI and iWUE were uncoupled with the estimated drought index, regardless of the site (Fig. 4). This is consistent with oscillating climate patterns and minor drought cycles at these sites. Differences in soil water availability and stand structural traits among sites could also explain differences in iWUE and stable isotopes and clustering of populations . Since iWUE is function of Ci and Ca, a significant relation (from linear to asymptotic, depending on evaporative demand and water availability) between iWUE and Ca was expected (Fig. 4) . The linear correlation found for Nothofagus spp. (and to a lesser extent in populations of Southern Italy) contrasts with asymptotic-like curves as in beech of North-Central Italy, where iWUE may have not increased despite the rise in Ca .
Fagus and Nothofagus were rather sensitive to increasing Ca (Fig. 4), in the absence of climatic stress. However, our results support only in part the prediction that tree ring cellulose δ18O will necessarily increase with aridity, because significant correlations between drought index and cellulose δ18O was evident for sites of North-Central Italy (and for those of Chile, to a lesser extent), taken together, though this was not the case for sites of Southern Italy. Since no influence of marked drought periods was perceived, predictions that follow Ca effects over Ci and iWUE, together with rising temperature and related factors (e.g., length of growing season), would increase or stabilize BAI in healthy trees . The relationships between BAI and iWUE evidenced a saturation effect of tree growth in several populations. Indeed, a decrease in stomatal conductance might induce an increase in iWUE, without changing photosynthetic rate. Regardless of the cause for a reduction in stomatal conductance, an increase in iWUE would not necessarily translate into enhanced BAI .
Recently, temperate forests have shown major growth declines, high levels of mortality and delayed multi-year effects from drought and heat spells . While the available evidence is not yet conclusive, if summers become drier, trees growing on mesic sites may undergo growth reductions; whereas at their dry distribution limit, growth of Fagus and Nothofagus may collapse, inducing dieback and compromising the provision of ecosystem services. Fagus and Nothofagus have, however, high intra-specific plasticity      , probably driven by environmental factors, though with weak coordination among functional traits. In a F. sylvatica stand of Central Italy,  found an increased iWUE with decreasing soil water availability, suggesting that trees were able to adjust carbon–water balance to prevent carbon depletion, maintaining plant growth to some extent during summer.
Physiological implications of correlations between δ18O and δ13C
In populations with positive correlations between the isotopes, an increased stomatal control of Ci and photosynthesis is expected  , the slope of the relationship varying with vapour pressure deficit and the sensitivity of plants to evaporative demand . In beech, a positive relationship between δ18O and δ13C has been linked to a negative relationship of δ13C and δ18O with air moisture and stomatal conductance  , regulated by leaf transpiration. Yet, an increase in stomatal conductance might decrease evaporative enrichment in 18O by cooling the leaf and by “flushing” it with un-enriched soil-water at higher transpiration rates (Péclet effect) and increase discrimination against 13C (more negative δ13C), because CO2 supply is greater .
In most populations, conversely, δ13C and δ18O showed a weak relationship (Fig. 5), suggesting that variation in photosynthetic capacity exerted a controlling influence on Ci and δ13C, and that stomatal conductance was not suppressed during summer. Indeed, if photosynthetic capacity drives change in tree-ring δ13C, then variation in stomatal conductance can be detected from δ18O, and the two isotopes will be either negatively (water is scarce) or not correlated , with stomata showing a limited operational range of water availability. On the other hand, positive relationships between δ13C and δ18O are mainly related to stomatal limitation and photosynthetic rate is relatively unaffected, which may be expected when there is no need to reduce water loss (water is available), and stomata may operate over a wide range. However, repeated drought may reduce both the sensitivity of stomata to water stress and stomatal control of photosynthesis in F. sylvatica , metabolic impairment becoming the major limitation to photosynthesis, notwithstanding stomatal closure. Variation in internal conductance of CO2 may contribute to year-to-year differences in tree-ring δ13C, also potentially dampening the correlation between δ13C and δ18O, with change in tree-ring δ18O more strongly related to climate than δ13C .
Differences in vapour pressure deficit can modify leaf evaporative enrichment and modify cellulose δ18O without necessarily influencing stomatal conductance and its relationship with photosynthetic rate . In the conceptual model used for interpreting δ13C, δ18O is plotted against δ13C and the direction of change between conditions is considered diagnostic for interpreting δ13C signals . However, it requires that environmental influences on evaporative enrichment (i.e., source water, atmospheric vapour δ18O and vapour pressure deficits) were similar over time or that they also affect stomatal conductance. Post-assimilation fractionations/processes might alter physiological and climatic signals recorded by carbon and oxygen isotopes at the leaf level, which would be decoupled from signals stored in tree rings, adding uncertainties to the dual-isotope conceptual model  .
The global rise in CO2 and the changing climate have already influenced the gas exchange of beech forests in both Northern and Southern Hemispheres. A continuous enhancement in iWUE was observed at all the sites during the twentieth century, which was primarily related to changes in Ca. We also observed a common enhancement in BAI that, as for iWUE, was uncoupled with the estimated climate index. The combined analysis of tree rings and stable isotopes yielded insights applicable to long-term responses of these temperate forests to important drivers of global change that might have had negative (drought), or positive (CO2 fertilization), and even mixed (warming), effects on tree growth and stand ecohydrology . Increasing climatic stress will have negative impacts on the performance of drought-exposed populations.
The control over tree growth by climatic factors within a region differed across latitudinal gradients in environmental conditions, but only to a certain extent. Species- and site-specific responses to long-term environmental changes were unravelled, the dual isotope approach showing how plants were subject to different environmental influences and suggesting that variation in photosynthetic rates still exert a controlling influence on Ci. Population-specific resilience/vulnerability should be taken into account when predicting future forest dynamics under changing climatic conditions. Highly resolved stable isotope analyses would allow for the signals of dry and rainy season to be distinguished more clearly, and improve our understanding of the hydrological cycle over these forest ecosystems.
We acknowledge the help of Claudia Cocozza, Emanuele Conte, Andrea Andreoli, and Anibal Pauchard. We thank CONAF (Chile) for assistance in site selection. The research is linked to activities conducted within the COST FP1106 (STReESS - Studying Tree Responses to extreme Events: a SynthesiS) and COST ES1203 (SENSFOR - Enhancing the resilience capacity of SENSitive mountain FORest ecosystems under environmental change). The authors would like to thank the reviewers for their comments that help improve the manuscript.
Conceived and designed the experiments: RT FL BL MM. Performed the experiments: RT FL BL MM. Analyzed the data: RT FL BL PC. Contributed reagents/materials/analysis tools: RT FL BL PC MM. Wrote the paper: RT FL BL PC MM.
- 1. Douville H, Ribes A, Decharme B, Alkama R, Sheffield J (2012) Anthropogenic influence on multidecadal changes in reconstructed global evapotranspiration. Nature Climate Change 3: 59–62.
- 2. Kress A, Saurer M, Siegwolf RTW, Frank DC, Esper J, et al. (2010) A 350 year drought reconstruction from Alpine tree ring stable isotopes,. Global Biogeochemical Cycles 24: GB2011.
- 3. Dai A (2011) Characteristics and trends in various forms of the Palmer Drought Severity Index during 1900–2008. Journal of Geophysical Research 116: D12115.
- 4. Allen CD, Macalady AK, Chenchouni H, Bachelet D, McDowell N, et al. (2010) A global overview of drought and heat induced tree mortality reveals emerging climate change risks for forests. Forest Ecology and Management 259: 660–684.
- 5. McDowell NG, Beerling DJ, Breshears DD, Fisher RA, Raffa KF, et al. (2011) The interdependence of mechanisms underlying climate-driven vegetation mortality. Trends in Ecology and Evolution 26: 523–532.
- 6. Suarez ML, Ghermandi L, Kitzberger T (2004) Factors predisposing episodic drought-induced tree mortality in Nothofagus: site, climatic sensitivity and growth trends. Journal of Ecology 92: 954–966.
- 7. Anderegg WRL, Berry JA, Field CB (2012) Linking definitions, mechanisms, and modeling of drought-induced tree death. Trends in Plant Science 17: 693–700.
- 8. Choat B, Jansen S, Brodribb TJ, Cochard H, Delzon S, et al. (2012) Global convergence in the vulnerability of forests to drought. Nature 491: 752–755.
- 9. Hanewinkel M, Cullmann DA, Schelhaas M-J, Nabuurs G-J, Zimmermann NE (2012) Climate change may cause severe loss in the economic value of European forest land. Nature Climate Change 3: 203–207.
- 10. Andreu-Hayles L, Planells O, Gutiérrez E, Muntan E, Helle G, et al. (2011) Long tree-ring chronologies reveal 20th century increases in water-use efficiency but no enhancement of tree growth at five Iberian pine forests. Global Change Biology 17: 2095–2112.
- 11. Gagen M, Finsinger W, Wagner-Cremer F, McCarroll D, Loader NJ, et al. (2011) Evidence of changing intrinsic water-use efficiency under rising atmospheric CO2 concentrations in Boreal Fennoscandia from subfossil leaves and tree ring δ13C ratios. Global Change Biology 17: 1064–1072.
- 12. Duquesnay A, Bréda N, Stievenard M, Dupouey JL (1998) Changes of tree-ring δ13C and water-use efficiency of beech (Fagus sylvatica L.) in north-eastern France during the past century. Plant, Cell and Environment 21: 565–572.
- 13. Tognetti R, Longobucco A, Miglietta F, Raschi A (1999) Water relations, stomatal response and transpiration of Quercus pubescens trees during summer in a Mediterranean carbon dioxide spring. Tree Physiology 19: 261–270.
- 14. Tognetti R, Johnson JD, Michelozzi M, Raschi A (1998) Response of foliar metabolism in mature trees of Quercus pubescens and Quercus ilex to long-term elevated CO2. Environmental and Experimental Botany 39: 233–245.
- 15. Switsur R, Waterhouse J (1998) Stable isotopes in tree ring cellulose. In: Griffiths H, editor. Stable Isotopes: Integration of Biological, Ecological and Geochemical Processes. Oxford: BIOS Scientific Publishers Ltd. pp. 303–321.
- 16. Peñuelas J, Canadell JG, Ogaya R (2011) Increased water-use efficiency during the 20th century did not translate into enhanced tree growth. Global Ecology and Biogeography 20: 597–608.
- 17. Silva LCR, Anand M, Leithead MD (2010) Recent widespread tree growth decline despite increasing atmospheric CO2. PLoS ONE 5: e11543.
- 18. Linares JC, Camarero JJ (2012) From pattern to process: linking intrinsic water-use efficiency to drought-induced forest decline. Global Change Biology 18: 1000–1015.
- 19. Peñuelas J, Hunt JM, Ogaya R, Jump AS (2008) Twentieth century changes of tree-ring δ13C at the southern range-edge of Fagus sylvatica: increasing water use efficiency does not avoid the growth decline induced by warming at low altitudes. Global Change Biology 14: 1076–1088.
- 20. Piovesan G, Biondi F, Di Filippo A, Alessandrini A, Maugeri M (2008) Drought-driven growth reduction in old beech (Fagus sylvatica L.) forests of the central Apennines, Italy. Global Change Biology 14: 1265–1281.
- 21. Di Filippo A, Biondi F, Maugeri M, Schirone B, Piovesan G (2012) Bioclimate and growth history affect beech lifespan in the Italian Alps and Apennines. Global Change Biology 18: 960–972.
- 22. Weber P, Bugmann H, Pluess AR, Walthert L, Rigling A (2013) Drought response and changing mean sensitivity of European beech close to the dry distribution limit. Trees 27: 171–181.
- 23. Villalba R, Lara A, Masiokas MH, Urrutia R, Luckman BH, et al. (2012) Unusual Southern Hemisphere tree growth patterns induced by changes in the Southern Annular Mode. Nature Geoscience 5: 793–798.
- 24. Lara A, Aravena JC, Wolodarsky-Franke A, Villalba R, Luckman B, et al. (2001) Dendroclimatology of high-elevation Nothofagus pumilio forests in the central Andes of Chile. Canadian Journal of Forestry Research 31: 925–936.
- 25. Srur AM, Villalba R, Villagra PE, Hertel D (2008) Influences of climatic and CO2 concentration changes on radial growth of Nothofagus pumilio in Patagonia. Revista Chilena de Historia Natural 81: 239–256.
- 26. Farquhar GD, O'Leary MH, Berry JA (1982) On the relationship between carbon isotope discrimination and the intercellular carbon dioxide concentration in leaves. Australian Journal of Plant Physiology 9: 121–137.
- 27. Leavitt SW, Long A (1986) Stable-carbon isotope variability in tree foliage and wood. Ecology 67: 1002–1010.
- 28. Barbour MM, Walcroft AS, Farquhar GD (2002) Seasonal variation in δ13C and δ18O of cellulose from growth rings of Pinus radiata. Plant, Cell and Environment 25: 1483–1499.
- 29. Ripullone F, Guerrieri MR, Saurer M, Siegwolf R, Jäggi M, et al. (2009) Testing a dual isotope model to track carbon and water gas exchanges in a Mediterranean forest. iForest 2: 59–66.
- 30. Barnard HR, Brooks JR, Bond BJ (2012) Applying the dual-isotope conceptual model to interpret physiological trends under controlled conditions. Tree Physiology 32: 1183–1198.
- 31. Saurer M, Aellen K, Siegwolf R (1997) Correlating δ13C and δ18O in cellulose of trees. Plant, Cell and Environment 20: 1543–1550.
- 32. Grossiord C, Granier A, Ratcliffe S, Bouriaud O, Bruelheide H, et al. (2014) Tree diversity does not always improve resistance of forest ecosystems to drought. Proceedings of the National Academy of Sciences 111: 14812–14815.
- 33. Lombardi F, Lasserre B, Tognetti R, Marchetti M (2008) Deadwood in relation to stand management and forest type in Central Apennines (Molise, Italy). Ecosystems 11: 882–894.
- 34. Piovesan G, Biondi F, Bernabei M, Di Filippo A, Schirone B (2005) Spatial and altitudinal bioclimatic zones of the Italian peninsula identified from a beech (Fagus sylvatica L.) tree-ring network. Acta Oecologica 27: 197–210.
- 35. Marchetti M, Tognetti R, Lombardi F, Chiavetta U, Palumbo G, et al. (2010) Ecological portrayal of old-growth forests and persistent woodlands in the Cilento and Vallo di Diano National Park (southern Italy). Plant Biosystems 144: 130–147.
- 36. Lombardi F, Cocozza C, Lasserre B, Tognetti R, Marchetti M (2011) Dendrochronological assessment of the time since death of dead wood in an old growth Magellan's beech forest, Navarino Island (Chile). Austral Ecology 36: 329–340.
- 37. Harris I, Jones PD, Osborn TJ, Lister DH (2014) Updated high-resolution grids of monthly climatic observations. International Journal of Climatology 34: 623–642.
- 38. Hargraeves GH, Samani ZA (1982) Estimating potential evapotranspiration. Journal of Irrigation and Drainage Division 108: 225–230.
- 39. Holmes RL (1983) Computer-assisted quality control in tree ring dating and measurement. Tree-Ring Bulletin 43: 69–78.
- 40. Kaennel M, Schweingruber FH (1995) Multilingual Glossary of Dendrochronology. Terms and Definitions in English, Spanish, Italian, Portuguese, and Russian. Bern: Haupt.
- 41. Fritts H (1976) Tree Rings and Climate. Academic Press: New York.
- 42. Cook ER, Briffa K, Shiyatov S, Mazepa V (1990) Tree-ring standardization and growth-trend estimation. In: Cook ER, Kairiukstis L, editors. Methods of Dendrochronology. Amsterdam: Kluwer. pp. l04–132.
- 43. Borella S, Leuenberger M, Saurer M, Siegwolf R (1998) Reducing uncertainties in δ13C analysis of tree rings: poolings, milling and cellulose extraction. Journal of Geophysical Research 103: 19519–19526.
- 44. Loader NJ, Robertson I, Barker AC, Switsur VR, Waterhouse JS (1997) An improved technique for the batch processing of small whole wood samples to α-cellulose. Chemical Geology 136: 313–317.
- 45. Battipaglia G, Jäggi M, Saurer M, Siegwolf RTW, Cotrufo MF (2008) Climatic sensitivity of δ18O in the wood and cellulose of tree rings: results from a mixed stand of Acer pseudoplatanus L. and Fagus sylvatica L. Palaeogeography Palaeoclimatology, Palaeoecology 261: 193–202.
- 46. Francey RJ, Allison CE, Etheridge DM, Trudinger CM, Enting IG, et al. (1999) A 1000-year high precision record of δ13C in atmospheric CO2. Tellus Series B 51: 170–193.
- 47. McCarroll D, Loader NJ (2004) Stable isotopes in tree rings. Quaternary Science Reviews 23: 771–801.
- 48. O'Leary M (1981) Carbon isotope fractionation in plants. Phytochemistry 20: 553–567.
- 49. Farquhar GD, Richards RA (1984) Isotopic composition of plant carbon correlates with water-use efficiency of wheat genotypes. Australian Journal of Plant Physiology 11: 539–552.
- 50. Osmond CB, Björkman O, Anderson DJ (1980) Physiological Processes in Plant Ecology. Toward a Synthesis with Atriplex. New York: Springer.
- 51. Francey RJ, Farquhar GD (1982) An explanation of 13C/12C variations in tree rings. Nature 297: 28–31.
- 52. Mann H (1945) Nonparametric tests against trend. Econometrica 13: 245–259.
- 53. Kendall M (1976) Rank Correlation Methods. 4th edn. London: Griffin.
- 54. Feng X (1999) Trends in intrinsic water-use efficiency of natural trees for the past 100–200 years: a response to atmospheric CO2 concentrations. Geochimica et Cosmochimica Acta 63: 1891–1903.
- 55. Marshall JD, Monserud RA (1996) Homeostatic gas-exchange parameters inferred from 13C/12C in tree rings of conifers. Oecologia 105: 13–21.
- 56. Hietz P, Wanek W, Dunisch O (2005) Long-term trends in cellulose delta C-13 and water-use efficiency of tropical Cedrela and Swietenia from Brazil. Tree Physiology 25: 745–752.
- 57. Silva LCR, Anand M, Oliveira JM, Pillar VD (2009) Past century changes in Araucaria angustifolia (Bertol.) Kuntze water use efficiency and growth in forest and grassland ecosystems of southern Brazil: implications for forest expansion. Global Change Biology 15: 2387–2396.
- 58. Anderson WT, Sternberg LSL, Pinzon MC, Gann-Troxler T, Childers DL, et al. (2005) Carbon isotopic composition of cypress trees from South Florida and changing hydrologic conditions. Dendrochronologia 23: 1–10.
- 59. Nock CA, Baker PJ, Wanek W, Leis A, Grabner M, et al. (2011) Long-term increases in intrinsic water-use efficiency do not lead to increased stem growth in a tropical monsoon forest in western Thailand. Global Change Biology 17: 1049–1063.
- 60. Körner C, Farquhar GD, Wong SC (1991) Carbon isotope discrimination by plants follows latitudinal and altitudinal trends. Oecologia 88: 30–40.
- 61. Silva LCR, Anand M (2012) Probing for the influence of atmospheric CO2 and climate change on forest ecosystems across biomes. Global Ecology and Biogeography 22: 83–92.
- 62. Silva LCR, Horwath WR (2013) Explaining global increases in water use efficiency: why have we overestimated responses to rising atmospheric CO2 in natural forest ecosystems? PLoS ONE 8: e53089.
- 63. Barber VA, Juday GP, Finney BP (2000) Reduced growth of Alaskan white spruce in the twentieth century from temperature-induced drought stress. Nature 405: 668–673.
- 64. Linares JC, Delgado-Huertas A, Camarero JJ, Merino J, Carreira JA (2009) Competition and drought limit the response of water-use efficiency to rising atmospheric carbon dioxide in the Mediterranean fir Abies pinsapo. Oecologia 161: 611–624.
- 65. Salzer MW, Hughes MK, Bunn AG, Kipfmueller KF (2009) Recent unprecedented treering growth in bristlecone pine at the highest elevations and possible causes. Proceedings of the National Academy of Sciences USA 106: 20348–20353.
- 66. McMahon SM, Parker GG, Miller DR (2010) Evidence for a recent increase in forest growth. Proceedings of the National Academy of Sciences USA 107: 3611–3615.
- 67. Chapin FS, Schulze ED, Mooney HA (1990) The ecology and economics of storage in plants. Annual Review of Ecology and Systematics 21: 423–447.
- 68. Giorgi F, Lionello P (2008) Climate change projections for the Mediterranean region. Global Planetary Change 63: 90–104.
- 69. Villalba R, Lara A, Boninsegna JA, Masiokas M, Delgado S, et al. (2003) Large-scale temperature changes across the southern Andes: 20th-century variations in the context of the past 400 years. Climatic Change 59: 177–232.
- 70. Lara A, Villalba R, Wolodarsky-Franke A, Aravena JC, Luckman BH, et al. (2005) Spatial and temporal variation in Nothofagus pumilio growth at tree line along its latitudinal range (35°40′–55°S) in the Chilean Andes. Journal of Biogeography 32: 879–893.
- 71. Gutierréz E (1988) Dendroecological study of Fagus sylvatica L. in the Montseny Mountains (Spain). Acta Oecologica-Oecologia Plantarum 9: 301–309.
- 72. Villalba R, Boninsegna JA, Veblen TT, Schmelter A, Rubulis S (1997) Recent trends in tree-ring records from high elevation sites in the Andes of Northern Patagonia. Climatic Change 36: 425–454.
- 73. Dittmar C, Zech W, Elling W (2003) Growth variations of common beech (Fagus sylvatica L.) under different climatic and environmental conditions in Europe - a dendroecological study. Forest Ecology and Management 173: 63–78.
- 74. Bascietto M, Cherubini P, Scarascia-Mugnozza G (2004) Tree rings from a European beech forest chronosequence are useful for detecting growth trends and carbon sequestration. Canadian Journal of Forest Research 34: 481–492.
- 75. Cullen LE, Stewart GH, Duncan RP, Palmer JG (2001) Disturbance and climate warming influences in New Zealand Nothofagus tree-line population dynamics. Journal of Ecology 89: 1061–1071.
- 76. Daniels LD, Veblen TT (2004) Spatiotemporal influences of climate on altitudinal treeline in northern Patagonia. Ecology 85: 1284–1296.
- 77. Holtmeier FK, Broll G (2005) Sensitivity and response of northern hemisphere altitudinal and polar treelines to environmental change at landscape and local scales. Global Ecology and Biogeography 14: 395–410.
- 78. Eilmann B, Rigling A (2012) Tree-growth analyses to estimate tree species' drought tolerance. Tree Physiology 32: 178–187.
- 79. Rigling A, Bigler C, Eilmann B, Feldmeyer-Christe E, Gimmi U, et al. (2013) Driving factors of a vegetation shift from Scots pine to pubescent oak in dry Alpine forests. Global Change Biology 19: 229–240.
- 80. Härdtle W, Niemeyer T, Assmann T, Baiboks S, Fichtner A, et al. (2013) Long-term trends in tree-ring width and isotope signatures (δ13C, δ15N) of Fagus sylvatica L. on soils with contrasting water supply. Ecosystems 16: 1413–1428.
- 81. Li JB, Cook ER, D'Arrigo R, Chen FH, Gou XH, et al. (2008) Common tree growth anomalies over the northeastern Tibetan Plateau during the last six centuries: implications for regional moisture change. Global Change Biology 14: 2096–2107.
- 82. Granda E, Rossatto DR, Camarero JJ, Voltas J, Valladares F (2014) Growth and carbon isotopes of Mediterranean trees reveal contrasting responses to increased carbon dioxide and drought. Oecologia 174: 307–317.
- 83. Ciais P, Reichstein M, Viovy N, Granier A, Ogée J, et al. (2005) Europe-wide reduction in primary productivity caused by the heat and drought in 2003. Nature 437: 529–533.
- 84. Borghetti M, Leonardi S, Raschi A, Snyderman D, Tognetti R (1993) Ecotypic variation of xylem embolism, phenological traits, growth parameters and allozyme characteristics in Fagus sylvatica. Functional Ecology 7: 713–720.
- 85. Tognetti R, Johnson JD, Michelozzi M (1995) The response of European beech (Fagus sylvatica L.) seedlings from two Italian populations to drought and recovery. Trees 9: 348–354.
- 86. Tognetti R, Minotta G, Pinzauti S, Michelozzi M, Borghetti M (1998) Acclimation to changing light conditions of long-term shade-grown beech (Fagus sylvatica L.) seedlings of different geographic origins. Trees 12: 326–333.
- 87. Premoli AC, Raffaele E, Mathiasen P (2007) Morphological and phenological differences in Nothofagus pumilio from contrasting elevations: evidence from a common garden. Austral Ecology 32: 515–523.
- 88. Fajardo A, Piper FI (2011) Intraspecific trait variation and covariation in a widespread tree species (Nothofagus pumilio) in southern Chile. New Phytologist 189: 259–271.
- 89. Richardson SJ, Allen RB, Buxton RP, Easdale TA, Hurst JM, et al. (2013) Intraspecific relationships among wood density, leaf structural traits and environment in four co-occurring species of Nothofagus in New Zealand. PLoS ONE 8: e58878.
- 90. Scartazza A, Moscatello S, Matteucci G, Battistelli A, Brugnoli E (2013) Seasonal and inter-annual dynamics of growth, non-structural carbohydrates and C stable isotopes in a Mediterranean beech forest. Tree Physiology 33: 730–742.
- 91. Cullen LE, Adams MA, Anderson MJ, Grierson PF (2008) Analyses of δ13C and δ18O in tree rings of Callitris columellaris provide evidence of a change in stomatal control of photosynthesis in response to regional changes in climate. Tree Physiology 28: 1525–1533.
- 92. Tognetti R, Lombardi F, Lasserre B, Battipaglia G, Saurer M, et al. (2012) Tree-ring responses in Araucaria araucana to two major eruptions of Lonquimay Volcano (Chile). Trees 26: 1805–1819.
- 93. Keitel C, Matzarakis A, Rennenberg H, Gessler A (2006) Carbon isotopic composition and oxygen isotopic enrichment in phloem and total leaf organic matter of European beech (Fagus sylvatica L.) along a climate gradient. Plant, Cell and Environment 29: 1492–1507.
- 94. Grams TEE, Kozovits AR, Haberle K-H, Matyssek R, Dawson TE (2007) Combining δ13C and δ18O analysis to unravel competition, CO2 and O3 effects on the physiological performance of different-aged trees. Plant Cell and Environment 30: 1023–1034.
- 95. Barbour MM (2007) Stable oxygen isotope composition of plant tissue: a review. Functional Plant Biology 34: 83–94.
- 96. Scheidegger Y, Saurer M, Bahn M, Siegwolf RTW (2000) Linking stable oxygen and carbon isotopes with stomatal conductance and photosynthetic capacity: a conceptual model. Oecologia 125: 350–357.
- 97. Tognetti R, Michelozzi M, Borghetti M (1994) Response to light of shade-grown beech seedlings subjected to different watering regimes. Tree Physiology 14: 751–758.
- 98. Roden JS, Farquhar GD (2012) A controlled test of the dual-isotope approach for the interpretation of stable carbon and oxygen isotope ratio variation in tree rings. Tree Physiology 32: 490–503.
- 99. Gessler A, Ferrio JP, Hommel R, Treydte K, Werner RA, et al. (2014) Stable isotopes in tree rings: towards a mechanistic understanding of isotope fractionation and mixing processes from the leaves to the wood. Tree Physiolgy in press.
- 100. Song X, Farquhar GD, Gessler A, Barbour MM (2014) Turnover time of the non-structural carbohydrate pool influences δ18O of leaf cellulose. Plant, Cell and Environment in press.
- 101. Schollaen K, Heinrich I, Neuwirth B, Krusic PJ, D'Arrigo RD, et al. (2013) Multiple tree-ring chronologies (ring width, δ13C and δ18O) reveal dry and rainy season signals of rainfall in Indonesia. Quaternary Science Reviews 73: 170–181.