Sandra Saura-Mas's research while affiliated with Autonomous University of Barcelona and other places

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Publications (9)


Boxplot of (a) basal area increment (BAI), (b) growth efficiency (basal area increment per unit of total tree leaf area, GE), (c) plot basal area, (d) tree basal area and (e) precipitation to potential evapotranspiration ratio (P/PET) as a function of species and family (Pinaceae vs. Fagaceae). The limits of boxes indicate the first and third quartiles, and the horizontal line within each box corresponds to the median. The upper whisker extends to the highest value within 1.5 × IQR (interquartile range) of the third quartile. The lower whisker extends to the lowest value within 1.5 × IQR of the first quartile. Abbreviations: Fs, Fagus sylvatica; Ph, Pinus halepensis; Pn, Pinus nigra; Ps, Pinus sylvestris; Qh, Quercus humilis; Qi, Quercus ilex
Relationship between basal area increment (BAI) and studied traits at the individual tree level. The black regression lines give the overall among‐species relationships (n = 6 species), and the coloured lines the corresponding within‐species relationships (n = 53–65 trees per species), when significant (p < 0.05). Variables were natural‐log transformed whenever required to satisfy normality assumptions. See Table S1 for definition of variable abbreviations
Relationship between growth efficiency (basal area increment per unit of total tree leaf area, GE) and studied traits at the individual tree level. The black regression lines give the overall among‐species relationships (n = 6 species), and the coloured lines the corresponding within‐species relationships (n = 53–65 trees per species), when significant (p < 0.05). Variables were natural‐log transformed whenever required to satisfy normality assumptions. See Table S1 for definition of variable abbreviations
Principal component analysis (PCA) summarizing trait variability across individual sampled trees. The first two PCA axes with the percentage of explained variance (in brackets) are shown. Variables were natural‐log transformed whenever required to satisfy the normality assumptions. See Table S1 for definition of variable abbreviations
Piecewise structural equation models relating climate (in terms of precipitation over potential evapotranspiration ratio, P/PET), forest structure (in terms of initial plot basal area), tree size (in terms of initial tree basal area) and traits (using the first and second PCA components: PCA1 and PCA2 respectively; Figure 4). Panel (a) shows the results for basal area increment (BAI) and panel (b) for growth efficiency (basal area increment per unit of total tree leaf area, GE). Arrows indicate significant links between variables. Solid and dashed lines indicate positive and negative relationships respectively. Standardized path coefficients, as well as the marginal and conditional R² values, are shown
Are leaf, stem and hydraulic traits good predictors of individual tree growth?
  • Article
  • Full-text available

September 2021

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691 Reads

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21 Citations

Functional Ecology

Functional Ecology

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Carles Batlles

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A major foundation of trait‐based ecology is that traits have an impact on individual performance. However, trait–growth relationships have not been extensively assessed in trees, especially outside tropical ecosystems. In addition, measuring traits directly related to physiological processes remains difficult and the differences between inter‐ and intraspecific relationships are seldom explored. Here, we use individual‐level data on a set of hydraulic, leaf and stem traits to assess their ability to predict basal area increment (BAI) and growth efficiency (BAI per unit of tree leaf area, GE) among and within species for six dominant tree species along a water availability gradient under Mediterranean climate (Catalonia, NE Spain). Measured traits include: leaf mass per area (LMA), leaf nitrogen concentration (N), leaf C isotopic composition (δ¹³C), the leaf water potential at turgor loss (Ptlp), stem wood density (WD) and branch‐level estimates of the Huber value (Hv), sapwood‐ and leaf‐specific hydraulic conductivity (KS and KL) and resistance to xylem embolism (P50). Trait–growth associations were generally weak, particularly for BAI and within species. High values of both growth metrics were associated with ‘conservative’ leaf and hydraulic traits. In particular, BAI was negatively associated with KL (and wood density), while GE increased with LMA, allocation to sapwood relative to leaves (Hv) and resistance to xylem embolism (P50). Climate effects on BAI and GE were indirectly mediated by changes in traits, stand structure and tree basal area. Overall, these results suggest that maintaining functionality over extended periods of time may be more important than maximum gas exchange or hydraulic capacity to achieve high radial growth under Mediterranean climates. Our study reveals that widely used ‘functional traits’ may be poor predictors of tree growth variability along environmental gradients. Moreover, trait effects (when present) do not necessarily conform to simple hypotheses based on our understanding of organ‐level processes. An improved understanding of trait coordination along common axes of variation together with a revaluation of the variables that better reflect whole‐tree performance can greatly improve our understanding of trait–growth relationships. A free Plain Language Summary can be found within the Supporting Information of this article.

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Figure 1. The construction of the event in the educational scene.
Figure 2. Transperformative education process.
Figure 3. Process of transformation toward the TPE paradigm.
Towards a transdisciplinary approach in the training of teachers: Creating procedures in learning and teaching in higher education

For decades we have been immersed in a constant change in our society, registered together with an increase in its degree of complexity. This greatly affects the currently prevailing educational axioms, making them obsolete, which implies, according to our hypothesis, the need for a process of revision and innovation of existing models. Our proposal starts from a bibliographic review of some existing proposals in innovation, to create a new pedagogical model based on polyhedral and transdisciplinary methodologies. At the same time, we offer a case study in a core subject of the first teacher training course at the Autonomous University of Barcelona. After the practical application of our transdisciplinary methodological theories, it has been possible to successfully collect evidence of a balanced interaction between disciplinary areas by students. The application of the innovations can become a frame of reference for higher education institutions interested in following this very important process of adaptation to social reality.


Contribution of species abundance and frequency to aboveground forest biomass along an Andean elevation gradient

January 2021

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127 Reads

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10 Citations

Forest Ecology and Management

Aims To determine whether species that contribute most to a plot’s biomass are the most abundant (high local abundance at plot scale) or the most frequent (occur the most across plots at landscape scale), or both. In the tropical Andes, these patterns may change with elevation. This study assesses the contribution to plot’s above-ground biomass (AGB) of the plant community abundance pattern –the prevalence of within-plot dominant species– and the over-occurrence of regionally frequent species, in an elevation gradient. Methods We considered all trees ≥2.5 cm DBH from 446 0.1 ha plots in an Amazonia-Andes 260–4350 m elevation cline in N Bolivia. Plot AGB was calculated as the sum of AGBs for all stems contained. We grouped plots into four bins segregated by elevation and ran a bootstrap analysis over subsets of 58 random plots per bin with 100 iterations. Simpson evenness index (ED) for all species in each plot was used as a measure for its species abundance. Values for each plot’s species frequency was calculated as the mean of all species’ in the plot mean frequencies across the bin (i.e. the fraction of plots where each species occurs). We used linear models to correlate plot AGB with (1) elevation and mean annual precipitation (MAP), and (2) ED, plot species frequency and elevation. We performed all analyses at the species, genus and family levels. Results Plot AGB was related negatively with elevation, and thus positively with MAP, and also negatively with plot ED and plot species frequency, all significant. Plot species abundance therefore contributes positively to explain the relationship with AGB along elevational gradients, while plot species frequency does so negatively (i.e. less frequent species contribute more to a plot’s AGB across elevation). AGB, for both generic and familial levels was also significantly and negatively correlated with ED, but not related with plot species frequency biomass at these taxonomic levels. Conclusions Plot AGB was mainly associated with elevation and floristic composition where species, genera and families tended to be abundant at the local (plot) scale. Species that were less frequent at the regional scale contributed with more AGB regionally, while frequency at generic and familial scales did little to explain AGB patterns. This association seems stronger at lower elevations for all taxonomic levels while decreases toward higher elevation. Our study reveals a relationship between plot structural features like C stocks –influenced by species local abundances– and the distribution of taxa across the landscape.


Fig. 1. Location of the 131 field sites (Dataset S1) for which this research assessed tree species replacement patterns after mortality concomitant with drought. The analysis considers forest and woodland sites across Earth's forested biomes, excluding species-rich tropical biomes (gray areas in the map). Global forest cover is based on Global Forest Watch (http://globalforestwatch.org). Biome classification (61): BorF, boreal forests/taiga; Des, deserts and xeric shrublands; MedF, Mediterranean forests, woodlands, and scrub; MnG, montane grasslands; TeBF, temperate broadleaf and mixed forests; TeCF, temperate conifer forests; TeG, temperate grasslands, savannas, and shrublands; TrG, tropical and subtropical grasslands, savannas, and shrublands. Photos exemplifying the four replacement processes considered are as follows. (A) Self-replacement; E. marginata, Northern Jarrah Forest, Australia (G.M., 2014). (B) Replacement by another tree species; Cedrus atlantica, Middle Atlas, Morocco (E.B., 2017). (C) Replacement by shrub species; Abies pinsapo, Sierra de las Nieves, Spain (E.B., 2017). (D) No replacement by woody vegetation; P. edulis, New Mexico, USA (F.L., 2012).
Fig. 2. Postdrought replacement patterns by vegetation replacement type (NR, no replacement by woody vegetation; Self, self-replacement; Shrub, replacement by shrublands; Tree, replacement by other tree species) and by tree genus. In A, each bar depicts the possible combinations of replacement by the different types (e.g., Self + Tree corresponds to sites in which self-replacement and replacement by other tree species are observed), whereas the proportion of each replacement type across all sites is depicted by the size of the gray dots. The overall proportion of sites showing a given replacement type is shown (Right). Colors depict major replacing categories in which trees (green), shrubs (violet), or lack of replacement by woody vegetation (brown) dominate. In B, outer-level colored bars show the dominant (predrought) genus and the most important replacing woody genera (NR, lack of replacement by woody vegetation; Shrub, replacement by shrub species; Tree_other, replacement by other scarcely represented tree genera: Acer, Arbutus, Austrocedrus, Betula, Carya, Dasyphyllum, Fagus, Ilex, Lomatia, Sorbus, Ulmus, Weinmannia). Inner links are directional, joinning predrought dominant genera (flat ends) and postdrought replacing genera (arrow ends). The inner links depict replacement proportions, so link width is proportional to the number of cases showing any given replacement pattern.
Fig. 5. Community bioclimatic shift as a result of forest mortality associated with drought. (Left) Relative change within the environmental space defined by precipitation regime and aridity. Environmental axes 1 and 2 encompass 82.4% of the variability of individual variables (PCA-derived axes). Each arrow represents the bioclimatic shift for a given forest site computed as the difference between the bioclimatic centroids of the dominant (predrought) and the replacing woody species weighted by the relative abundance of each species at the site. Orange and blue arrows illustrate shifts toward more xeric and more mesic communities, respectively. (Right) From A to E are examples of bioclimatic niches of the predrought dominant (blue) and postdrought replacing (red) species. Solid lines show the abundance and distribution range of each species along environmental axis 1, whereas the dotted vertical lines correspond to the species' bioclimatic optima (center of mass of the distribution).
Fig. 6. Contribution of (A) the bioclimatic characteristics of the study sites, (B) the dry bioclimatic edge of the replacing species (Rep_sp), (C) the range of the bioclimatic distribution of the replacing woody species, and (D) the successional index of the replacing species versus the dominant (predrought) species on the bioclimatic shift index. ICBS is the difference between the bioclimatic optima of the replacing woody species and the bioclimatic optima of the dominant (predrought) species along environmental axis 1 (Fig. 4). Positive ICBS values indicate shifts toward more xeric communities, whereas negative values indicate shifts toward more mesic communities. A shows a linear fit and B-D depict the component smooth functions of a generalized additive model fitted using the four variables depicted here; model R 2 = 0.612, explained deviance = 67.2%; all variables are significant at P < 0.05.
Forest and woodland replacement patterns following drought-related mortality

November 2020

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1,071 Reads

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126 Citations

Proceedings of the National Academy of Sciences

Significance Forests are experiencing growing risks of drought-induced mortality in a warming world. Yet, ecosystem dynamics following drought mortality remain unknown, representing a major limitation to our understanding of the ecological consequences of climate change. We provide an emerging picture of postdrought ecological trajectories based on field indicators of forest dynamics. Replacement patterns following mortality indicate limited short-term persistence of predrought dominant tree species, highlighting the potential for major ecosystem reorganization in the coming decades. The great variability of the observed dynamics within and among species reinforces the primary influence of drought characteristics and ecosystem legacies, modulated by land use, management, and past disturbances, on ongoing drought-related species turnover and their potential implications for future forest biodiversity and ecosystem services.


Climatic and fire determinants of early life-history stages in the Mediterranean shrub Cistus albidus

February 2020

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28 Reads

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3 Citations

Journal of Plant Ecology

Aims Cistus albidus reproductive traits have been studied on typical Mediterranean shrublands along a water availability gradient in Northeastern Iberian Peninsula. Germination of this species is known to be highly favoured by fire. Moreover, Mediterranean species are particularly dependent on water availability. Therefore, we establish the hypothesis that in addition to fire disturbance, seedling recruitment in this Mediterranean seeder will be improved in drought-induced episodes resulting in generalized canopy die-off. Methods Individuals of several populations of C. albidus were collected and the size, weight and number of fruits and seeds were measured. Germination tests were also carried out on five pre-germination treatments: seeds’ exposure to heat shock, imbibition, two cycles of imbibition/desiccation and the combination of heat shock and imbibition and imbibition/desiccation cycles. Moreover, the number of seedlings after a drought event was surveyed in the field and correlated with canopy die-off. Important findings Our study shows the variability of the C. albidus reproductive traits, such as germination rate or fruit production, along the water availability gradient. This variability resulted in a decrease in fruit production but an increase in successful germination under drier conditions. Cistus albidus seeds increased germination with heat, demonstrating their ability to successfully establish after fire. However, recruitment was not exclusively fire dependent since seedling establishment was higher under C. albidus canopies that had collapsed after the extreme drought. Finally, adult density increased C. albidus die-off and mortality, as well as seedling establishment. These results suggest that this species exhibits a trade-off between different reproductive outcomes (i.e. seed production vs. viability), which in turn is determined by climate. This study also provides evidence of how intra-specific competition, climate, particularly drought events and fire disturbance, can determine the success of key early stages of the life history of a common, representative Mediterranean fire-prone seeder shrub.


Effects of the invasive crayfish Procambarus clarkii on growth and development of Pelophylax perezi tadpoles in field conditions

August 2019

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189 Reads

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4 Citations

Animal Biodiversity and Conservation

Introduced predatory aquatic invertebrates may contribute to the global decline of amphibians as their larval are extremely vulnerable to predators. The objective of this study was to examine the effects of the predatory invasive crayfish Procambarus clarkii on the growth and development of native Iberian green frog tadpoles, Pelophylax perezi, in field conditions. We hypothesized that P. clarkii might affect P. perezi development by (a) inducing a delay in its metamorphosis and (b) reducing survival and mass of metamorphs. The experiment was developed in two ponds (with and without P. clarkii’s presence) in the Natural Park of Aiguamolls de l’Empordà (NE of the Iberian Peninsula). For each pond, groups of 10 tadpoles were randomly assigned to 15 cylindrical field enclosures. These enclosures avoided direct contact (i.e. predation) between both species. Our results suggest that, in field conditions, the presence of P. clarkii accelerates metamorphosis of P. perezi tadpoles. The higher growth rate of P. perezi through shorter larval periods could be the result of behavioural plasticity in response to the strong pressure imposed by P. clarkii. This conclusion would be in accordance with the hypothesis that phenotypic plasticity plays an important role in the conservation of P. perezi in front of biological invasions.


(a) Quartile coefficient of dispersion of the studied traits across all measurements of the study; (b) variance partitioning across different ecological levels of organization. ‘Within’ denotes variance between individuals of the same population. Traits are ordered (left to right) from higher to lower total variation in (a), and from higher to lower percentage variation within species in (b). LMA, leaf mass per area; N, leaf nitrogen concentration; δ¹³C, leaf carbon isotope composition; WD, wood density; Hv, Huber value, sapwood to leaf area ratio; KL, leaf‐specific xylem hydraulic conductivity; KS, stem‐specific xylem hydraulic conductivity; P50, pressure causing 50% xylem embolism; Ptlp, leaf water potential at turgor loss point.
Relationship between water availability (in terms of the precipitation to potential evapotranspiration ratio, P : PET) and (a) leaf mass per area, (b) leaf nitrogen concentration, (c) leaf carbon isotope composition, (d) wood density, (e) Huber value, sapwood to leaf area ratio, (f) leaf‐specific xylem hydraulic conductivity, (g) stem‐specific xylem hydraulic conductivity, (h) pressure causing 50% xylem embolism and (i) leaf water potential at turgor loss point. The black regression lines give the overall cross‐species relationships, and the coloured lines give the corresponding within‐species relationships, when significant (P < 0.05). Variables were loge‐transformed whenever required to satisfy normality assumptions. LMA, leaf mass per area; N, leaf nitrogen concentration; δ¹³C, leaf carbon isotope composition; WD, wood density; Hv, Huber value, sapwood to leaf area ratio; KL, leaf‐specific xylem hydraulic conductivity; KS, stem‐specific xylem hydraulic conductivity; P50, pressure causing 50% xylem embolism; Ptlp, leaf water potential at turgor loss point. [Correction added after online publication 8 February 2019: the units for LMA on the y‐axis of panel (a) have been corrected.]
(a–g) Trait correlation networks across species (n = 6) (a) and for each studied species separately (b–g). Solid black and grey dashed edges show positive and negative correlations, respectively. Correlation strength is represented by edge thickness. Only significant correlations are shown (P < 0.05). Traits identified by red circles show the highest centrality value in terms of weighted degree (the sum of all the significant coefficients of correlation of a node). All traits were loge‐transformed before analysis. LMA, leaf mass per area; N, leaf nitrogen concentration; δ¹³C, leaf carbon isotope composition; WD, wood density; Hv, Huber value, sapwood to leaf area ratio; KL, leaf‐specific xylem hydraulic conductivity; KS, stem‐specific xylem hydraulic conductivity; P50, pressure causing 50% xylem embolism; Ptlp, leaf water potential at turgor loss point.
Adjustments and coordination of hydraulic, leaf and stem traits along a water availability gradient

February 2019

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653 Reads

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198 Citations

Trait variability in space and time allows plants to adjust to changing environmental conditions. However, we know little about how this variability is distributed and coordinated at different organizational levels. For six dominant tree species in northeastern Spain (three Fagaceae and three Pinaceae) we quantified the inter‐ and intraspecific variability of a set of traits along a water availability gradient. We measured leaf mass per area (LMA), leaf nitrogen (N) concentration, carbon isotope composition in leaves (δ¹³C), stem wood density, the Huber value (Hv, the ratio of cross‐sectional sapwood area to leaf area), sapwood‐specific and leaf‐specific stem hydraulic conductivity, vulnerability to xylem embolism (P50) and the turgor loss point (Ptlp). Differences between families explained the largest amount of variability for most traits, although intraspecific variability was also relevant. Species occupying wetter sites showed higher N, P50 and Ptlp, and lower LMA, δ¹³C and Hv. However, when trait relationships with water availability were assessed within species they held only for Hv and Ptlp. Overall, our results indicate that intraspecific adjustments along the water availability gradient relied primarily on changes in resource allocation between sapwood and leaf area and in leaf water relations.


Fig. 1. (A) Location of the study site. (B) Standardized precipitation-evapotranspiration index (SPEI) for years 1951-2013, calculated using a time scale of 12 months. Negative values (black) indicate water deficit (i.e. drought periods) while positive ones (grey) indicate water surplus relative to reference climatic conditions. Each SPEI value is calculated from the data of the last 12 months. (C) Difference between historical (1951-2000) and current (2009-13) mean monthly temperature and precipitation. Arrows indicate the two sampling dates (drought in April 2012 and post-rain in February 2013). Climatic data correspond to Zaragoza Airport, 90 km west of the Valcuerna study site. Source: Agencia Española de Meteorología (AEMET), Ministerio de Agricultura, Alimentación y Medio Ambiente, Gobierno de España. 
Fig. 2. Changes between drought (April 2012) and post-rain (February 2013) periods of non-structural carbohydrate (NSC) and soluble sugar (SS) concentrations of the different species in stems and roots of plants with leaf loss and in undefoliated plants. Bold lines correspond to average values for all nine species (for detailed information for each species see Supplementary Data Fig. S1). The + and − symbols indicate a significant increase or decrease (P < 0.001), respectively, between periods, overall considering undefoliated plants and plants with leaf loss. **Significant difference (P < 0.001) between undefoliated plants and plants with leaf loss, overall considering drought and post-rain periods; ns, no significant difference (see Table 3 for the respective model results). 
Fig. 3. Mean percentage of green canopy during the drought (April 2012) and post-rain (February 2013) periods of plants of the different species. Values were obtained for the plants that were sampled in the post-rain period (N = 10 for each dieback state category). Error bars indicate s.e. *P < 0.05, **P < 0.01 (drought versus post-rain periods). Differences between undefoliated plants and those with leaf loss (dieback) were always significant (P < 0.01). 
Non-structural carbohydrate dynamics associated with drought-induced die-off in woody species of a shrubland community

April 2018

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372 Reads

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31 Citations

Annals of Botany

Background and aims: The relationship between plant carbon economy and drought responses of co-occurring woody species can be assessed by comparing carbohydrate (C) dynamics following drought and rain periods, relating these dynamics to species' functional traits. We studied nine woody species coexisting in a continental Mediterranean shrubland that experienced severe drought effects followed by rain. Methods: We measured total non-structural carbohydrates (NSC) and soluble sugars (SS) in roots and stems during drought and after an autumn rain pulse in plants exhibiting leaf loss and in undefoliated ones. We explored whether their dynamics were related to foliage recovery and functional traits (height [H], specific leaf area [SLA], wood density [WD]). Key results: During drought, NSC concentrations were overall lower in stems and roots of plants experiencing leaf loss, while SS decreases were smaller. Roots had higher NSC concentrations than stems. After the rain, NSC concentrations continued to decrease, while SS increased. Green foliage recovered after rain, particularly in plants previously experiencing higher leaf loss, independently of NSC concentrations during drought. Species with lower WD tended to have more SS during drought and lower SS increases after rain. In low-WD species, plants with severe leaf loss had lower NSC relative to undefoliated ones. No significant relationship was found between H or SLA and C content or dynamics. Conclusions: Our community-level study reveals that, while responses were species-specific, C stocks overall diminished in plants affected by prolonged drought and did not increase after a pulse of seasonal rain. Dynamics were faster for SS than NSC. We found limited depletion of SS, consistent with their role in basal metabolic, transport and signalling functions. In a scenario of increased drought under climate change, NSC stocks in woody plants are expected to decrease differentially in coexisting species, with potential implications for their adaptive abilities and community dynamics.


Environmental stress effects on reproduction and sexual dimorphism in the gynodioecious species Silene acaulis

December 2017

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41 Reads

Environmental and Experimental Botany

In gynodioecious species, hermaphrodite plants invest both in seed and pollen production, whereas female plants only produce fruits. For both sexes to coexist, such unbalanced investment is expected to translate in some kind of reproductive compensation, particularly under severe nutrient shortage or environmental stress. This study investigates 1) whether females of the gynodioecious boreo-alpine plant Silene acaulis show any overall compensation in fitness components; 2) the existence of sexual dimorphism in flowers that favor different modes in each sex; 3) whether environmental severity, characterized by means of a Species Distribution Model, strength these patterns. Flower size, fruit and seed production, and germination success were recorded in six populations across the Pyrenees and the Alps. Fruit set was significantly higher in female (59%) than in hermaphrodite plants (17%), and female organs (ovary and style) were larger in female than in hermaphrodite plants, but female flowers were smaller. Contrary to expectations, environment severity was not related with most of the biological traits studied and only germination was associated to environmental gradients. These results confirm that fruit production plays an important role as a compensatory strategy between sexes and, consequently, may favor the presence of both sexes in a gynodioecious species.

Citations (7)


... The heightened environmental stress experienced by evergreen species (i.e., lower soil fertility) resulted in stronger trait integration compared to deciduous species (Dwyer andLaughlin, 2017, He et al. 2021), potentially limiting the diversity of trait combinations among evergreen species (Delhaye, et al. 2020). The traits disparity and the inconsistent trend in the trait-rate relationship between leaf habits might partially account for the limited correlation between functional traits and growth rates, particularly in mixed forests characterized by complex trait-environment interactions (Paine, et al. 2015, Rosas, et al. 2021, Vargas, et al. 2021, Browne, et al. 2022, Feng, et al. 2022. ...

Reference:

Interactions between leaf traits and environmental factors help explain the growth of evergreen and deciduous species in a subtropical forest
Are leaf, stem and hydraulic traits good predictors of individual tree growth?
Functional Ecology

Functional Ecology

... In addition to that, elevation gradient result in variations in climatic variables (temperature and precipitation) which indirectly affect the distribution of biomass. Furthermore, the variance in species composition, variety, structure, and primary productivity along the elevation gradient can generally be predicted using these climate variables (Sandoya et al., 2021). ...

Contribution of species abundance and frequency to aboveground forest biomass along an Andean elevation gradient
  • Citing Article
  • January 2021

Forest Ecology and Management

... Seeds were manually removed from fruits, and empty seeds were separated by density using a wind tunnel, followed by inspection under a magnifier to remove visibly damaged seeds. All seeds were stored in cellulose bags in a dark chamber at 20 °C for optimal storage conditions (Luna et al., 2007;Saura-Mas et al., 2020). There is evidence that seed mass varies along environmental gradients (Cochrane et al., 2014), and that seed mass influences germination response to heat shock and heat resistance among species of post-fire seeders (Hanley et al., 2003;Liyanage and Ooi, 2017), and within populations of Cistus species (Tavşanoğlu and Çatav, 2012). ...

Climatic and fire determinants of early life-history stages in the Mediterranean shrub Cistus albidus
  • Citing Article
  • February 2020

Journal of Plant Ecology

... Wide-spread spruce (Picea abies L.) mortality occurred in Germany [11], Slovakia [12], and the southern part of European Russia [13]. The main causes of mortality in those areas are considered to be multi-year low precipitation and root-zone drying [2,14,15]. ...

Forest and woodland replacement patterns following drought-related mortality

Proceedings of the National Academy of Sciences

... In the last decade, studies on the behavior of amphibian tadpoles exposed to multiple stressors suggested not only behavioral shifts but also morphological and physiological modifications (Üveges et al. 2019;Saura-Mas and Benejam 2019). Ecotoxicological studies address several biological traits to determine the toxicity of single or complex chemical mixtures on amphibians (Robles-Mendoza et al. 2011;Cuzziol Boccioni et al. 2020). ...

Effects of the invasive crayfish Procambarus clarkii on growth and development of Pelophylax perezi tadpoles in field conditions

Animal Biodiversity and Conservation

... This would undoubtedly add complexities to the understanding of plant ecological strategy as well as the prediction of distribution and dynamics of vegetation. Intra-specific variation of hydraulic traits along climate gradients is increasingly documented in the literature (Laughlin et al., 2020;Rosas et al., 2019;Skelton et al., 2019), yet it remains unclear if decoupling between traits and climate is common across species. ...

Adjustments and coordination of hydraulic, leaf and stem traits along a water availability gradient
New Phytologist

New Phytologist

... Some exploratory research has been conducted on this topic. Lloret et al. [45] found that species characterized by low WD have lower concentrations of nonstructural carbohydrates. Kiaei [46] found positive correlations between ironwood WD and one type of extractive compound, 1,2-benzendicarboxylic. ...

Non-structural carbohydrate dynamics associated with drought-induced die-off in woody species of a shrubland community

Annals of Botany