Interactions among species determine local-scale diversity, but local interactions are thought to have minor effects at larger scales. However, quantitative comparisons of the importance of biotic interactions relative to other drivers are rarely made at larger scales. Using a data set spanning 78 sites and five continents, we assessed the relative importance of biotic interactions and climate in determining plant diversity in alpine ecosystems dominated by nurse-plant cushion species. Climate variables related with water balance showed the highest correlation with richness at the global scale. Strikingly, although the effect of cushion species on diversity was lower than that of climate, its contribution was still substantial. In particular, cushion species enhanced species richness more in systems with inherently impoverished local diversity. Nurse species appear to act as a 'safety net' sustaining diversity under harsh conditions, demonstrating that climate and species interactions should be integrated when predicting future biodiversity effects of climate change.
Lysenko 91,92 | Armin Macanović 93 | Parastoo Mahdavi 94 | Peter Manning 35 | Corrado Marcenò 13 | Vassiliy Martynenko 95 | Maurizio Mencuccini 96 | Vanessa Minden 97 | Jesper Erenskjold Moeslund 54 | Marco Moretti 98 | Jonas V. Müller 99 | Abstract Aims: Vegetation-plot records provide information on the presence and cover or abundance of plants co-occurring in the same community. Vegetation-plot data are spread across research groups, environmental agencies and biodiversity research centers and, thus, are rarely accessible at continental or global scales. Here we present the sPlot database, which collates vegetation plots worldwide to allow for the exploration of global patterns in taxonomic, functional and phylogenetic diversity at the plant community level.Results: sPlot version 2.1 contains records from 1,121,244 vegetation plots, which comprise 23,586,216 records of plant species and their relative cover or abundance in plots collected worldwide between 1885 and 2015. We complemented the information for each plot by retrieving climate and soil conditions and the biogeographic context (e.g., biomes) from external sources, and by calculating community-weighted means and variances of traits using gap-filled data from the global plant trait database TRY. Moreover, we created a phylogenetic tree for 50,167 out of the 54,519 species identified in the plots. We present the first maps of global patterns of community richness and community-weighted means of key traits. Conclusions: The availability of vegetation plot data in sPlot offers new avenues for vegetation analysis at the global scale. K E Y W O R D S biodiversity, community ecology, ecoinformatics, functional diversity, global scale, macroecology, phylogenetic diversity, plot database, sPlot, taxonomic diversity, vascular plant, vegetation relevé 166 |
Biotic interactions can shape phylogenetic community structure (PCS). However, we do not know how the asymmetric effects of foundation species on communities extend to effects on PCS. We assessed PCS of alpine plant communities around the world, both within cushion plant foundation species and adjacent open ground, and compared the effects of foundation species and climate on alpha (within-microsite), beta (between open and cushion) and gamma (open and cushion combined) PCS. In the open, alpha PCS shifted from highly related to distantly related with increasing potential productivity. However, we found no relationship between gamma PCS and climate, due to divergence in phylogenetic composition between cushion and open sub-communities in severe environments, as demonstrated by increasing phylo-beta diversity. Thus, foundation species functioned as micro-refugia by facilitating less stress-tolerant lineages in severe environments, erasing a global productivity - phylogenetic diversity relationship that would go undetected without accounting for this important biotic interaction.
Conservation biology aims at identifying areas of rich biodiversity. Currently recognized global biodiversity hotspots are spatially too coarse for conservation management and identification of hotspots at a finer scale is needed. This might be achieved by identification of areas of endemism. Here, we identify areas of endemism in Iran, a major component of the Irano-Anatolian biodiversity hotspot, and address their ecological correlates. Using the extremely diverse sunflower family (Asteraceae) as our model system, five consensus areas of endemism were identified using the approach of endemicity analysis. Both endemic richness and degree of endemicity were positively related to topographic complexity and elevational range. The proportion of endemic taxa at a certain elevation (percent endemism) was not congruent with the proportion of total surface area at this elevation, but was higher in mountain ranges. While the distribution of endemic richness (i.e., number of endemic taxa) along an elevational gradient was hump-shaped peaking at mid-elevations, the percentage of endemism gradually increased with elevation. Patterns of endemic richness as well as areas of endemism identify mountain ranges as main centres of endemism, which is likely due to high environmental heterogeneity and strong geographic isolation among and within mountain ranges. The herein identified areas can form the basis for defining areas with conservation priority in this global biodiversity hotspot.
Iran is a mountainous country. Zagros and Alborz mountains reach altitudes of more than 4,000 m. Alpine regions are above timber-line, which is not easy to recognize, since aridity is prominent in most regions. The alpine zone in Alborz lies between 3,000 and 4,000 m, the nival zone is above 4,000 m, locally varying by some hundred meters. A first evaluation of vascular flora shows that 682 species belonging to 193 genera and 39 families are known from the alpine zone of Iran. The alpine zone is commonly characterized by many species of hemicryptophytes and thorny cushions. Species numbers decline very strongly with increasing altitude. In this paper biogeographical patterns of the alpine flora of Iran have been discussed and distribution maps of 44 species are illustrated. New data indicate a transitional situation of the Iranian mountains between Anatolia/ Caucasus and the Hindu Kush, but with a strong own element with high endemism and remarkable relict species. Ca. 58% of the alpine flora of Iran are endemic and subendemic. The Zagros Mountains harbor high endemism which justify considering this area as a separate floristic province. Based on the evaluation of published data from 682 known alpine species ca. 160 species have been known only by one record, 110 species by 2-3 records and 87 endemic species have been known only based on the type location. These plants need a strong conservation and protection management since the fragile ecosystems are often very restricted, small and very isolated, nonetheless grazing and overgrazing are still common threats.
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