A B S T R A C T Greenhouse gas emissions have significantly altered global climate, and will continue to do so in the future. Increases in the frequency, duration, and/or severity of drought and heat stress associated with climate change could fundamentally alter the composition, structure, and biogeography of forests in many regions. Of particular concern are potential increases in tree mortality associated with climateinduced physiological stress and interactions with other climate-mediated processes such as insect outbreaks and wildfire. Despite this risk, existing projections of tree mortality are based on models that lack functionally realistic mortality mechanisms, and there has been no attempt to track observations of climate-driven tree mortality globally. Here we present the first global assessment of recent tree mortality attributed to drought and heat stress. Although episodic mortality occurs in the absence of climate change, studies compiled here suggest that at least some of the world's forested ecosystems already may be responding to climate change and raise concern that forests may become increasingly vulnerable to higher background tree mortality rates and die-off in response to future warming and drought, even in environments that are not normally considered water-limited. This further suggests risks to ecosystem services, including the loss of sequestered forest carbon and associated atmospheric feedbacks. Our review also identifies key information gaps and scientific uncertainties that currently hinder our ability to predict tree mortality in response to climate change and emphasizes the need for a globally coordinated observation system. Overall, our review reveals the potential for amplified tree mortality due to drought and heat in forests worldwide.Published by Elsevier B.V.

After a millenarian history of overexploitation, most forests in the Mediterranean Basin have disappeared, leaving many degraded landscapes that have been recolonized by early successional shrub‐dominated communities. Common reforestation techniques treat these shrubs as competitors against newly planted tree seedlings; thus shrubs are cleared before tree plantation. However, empirical studies and theory governing plant– plant interactions suggest that, in stress‐prone Mediterranean environments, shrubs can have a net positive effect on recruitment of other species. Between 1997 and 2001, we carried out experimental reforestations in the Sierra Nevada Protected Area (southeast Spain) with the aim of comparing the survival and growth of seedlings planted in open areas (the current reforestation technique) with seedlings planted under the canopy of preexisting shrub species. Over 18 000 seedlings of 11 woody species were planted under 16 different nurse shrubs throughout a broad geographical area. We sought to explore variation in the sign and magnitude of interactions along spatial gradients defined by altitude and aspect. In the present work, we report the results of a meta‐analysis conducted with seedling survival and growth data for the first summer following planting, the most critical period for reforestation success in Mediterranean areas. The facilitative effect was consistent in all environmental situations explored (grand mean effect size d+ = 0.89 for survival and 0.27 for growth). However, there were differences in the magnitude of the interaction, depending on the seedling species planted as well as the nurse shrub species involved. Additionally, nurse shrubs had a stronger facilitative effect on seedling survival and growth at low altitudes and sunny, drier slopes than at high altitudes or shady, wetter slopes. Facilitation in the dry years proved higher than in the one wet year. Our results show that pioneer shrubs facilitate the establishment of woody, late‐successional Mediterranean species and thus can positively affect reforestation success in many different ecological settings.

Summary 1We analyse the factors controlling seedling establishment of Scots pine at its southernmost geographical limit (southern Spain), by monitoring emergence, survival and growth for up to 4 years in the microhabitats to which seeds are dispersed. Naturally established seedlings were monitored in two mountain ranges, and experimental sowings were performed both in woodlands and in adjacent successional shrublands into which the forest could expand. 2 Emergence was high in all microhabitats, although it was highest under the canopy of shrubs. Overall survival was low, with c . 90% of seedlings dying in the first growing season ( c . 98% after several growing seasons). Survival differed among microhabitats, being highest under shrubs and extremely low (or zero) under pines or in bare soil. 3 Seedling growth was the highest in areas of bare soil, intermediate under shrubs, and very low under pines. 4 Establishment under pines was prevented by both mortality and poor performance, and good performance cannot counteract high mortality in the open. Shrubs, however, acted as nurse plants, buffering summer drought without reducing radiation to levels critical for growth, and protecting seedlings from ungulate trampling, hail and frost heave. 5 Patterns of recruitment were similar for woodland stands and successional shrublands. In addition, patterns of survival for naturally established seedlings were similar to those of seedlings originating from experimental sowings. 6 Juveniles were positively associated with shrubs but negatively with bare soil or areas below pine canopies. The facilitative effect of shrubs on seedling survival therefore changes the spatial pattern of recruitment from that determined by germination. 7 Overall, processes controlling seedling establishment in these southern Scots pine forests differ sharply from those operating in its main distribution area. The comparison among contrasting geographical ranges may contribute to an understanding of the role of environmental conditions in the balance between competition and facilitation, and assist in forecasting plant regeneration responses to global climate change.

Common techniques currently used for afforestation in the Mediterranean basin consider the pre‐existing vegetation (mainly shrubs) as a source of competition for trees, and consequently it is generally eliminated before planting. Nevertheless, it has been demonstrated that woody plants can facilitate the establishment of understory seedlings in environments that, like the Mediterranean area, are characterized by a pronounced dry season. In this study, we experimentally analyze the usefulness of shrubs as nurse plants for afforestation of two native conifers, Pinus sylvestris L. (Scots pine) and Pinus nigra Arnold (black pine). Two‐year‐old seedlings were planted in four microhabitats: (1) open interspaces without vegetation (which is the usual method used in afforestation programs), (2) under individuals of Salvia lavandulifolia, (3) under the north side of spiny shrubs, and (4) under the south side of spiny shrubs. Pine survival was remarkably higher when planted under individuals of the shrub S. lavandulifolia (54.8% for Scots pine, 81.9% for black pine) compared with open areas (21.5% for Scots pine, 56.8% for black pine; chi square, p < 0.05). The survival of both pines was also higher when planted on the north side of spiny shrubs, although the survival on the south side was similar to that found in open areas. In addition, pine growth was not inhibited when planted in association with shrubs. This pattern appears to result from the combination of abiotic conditions imposed by the presence of a nurse shrub, which leads to improvement in seedling water status and therefore reduced summer mortality by drought. The results show that the use of shrubs as nurse plants is a technique that offers both economic and ecological advantages, in terms of savings in labor and plant material and reduced and even negligible impact on the pre‐existing vegetation.

Plants interact with the environment by sensing “non-self” molecules called elicitors derived from pathogens or other sources. These molecules bind to specific receptors located in the plasma membrane and trigger defense responses leading to protection against pathogens. In particular, it has been shown that cell wall and storage polysaccharides from green, brown and red seaweeds (marine macroalgae) corresponding to ulvans, alginates, fucans, laminarin and carrageenans can trigger defense responses in plants enhancing protection against pathogens. In addition, oligosaccharides obtained by depolymerization of seaweed polysaccharides also induce protection against viral, fungal and bacterial infections in plants. In particular, most seaweed polysaccharides and derived oligosaccharides trigger an initial oxidative burst at local level and the activation of salicylic (SA), jasmonic acid (JA) and/or ethylene signaling pathways at systemic level. The activation of these signaling pathways leads to an increased expression of genes encoding: (i) Pathogenesis-Related (PR) proteins with antifungal and antibacterial activities; (ii) defense enzymes such as pheylalanine ammonia lyase (PAL) and lipoxygenase (LOX) which determine accumulation of phenylpropanoid compounds (PPCs) and oxylipins with antiviral, antifugal and antibacterial activities and iii) enzymes involved in synthesis of terpenes, terpenoids and/or alkaloids having antimicrobial activities. Thus, seaweed polysaccharides and their derived oligosaccharides induced the accumulation of proteins and compounds with antimicrobial activities that determine, at least in part, the enhanced protection against pathogens in plants.