Summary• Few studies have investigated plant-plant interactions involving hyperaccumulator plants. Here, we investigated the effect of selenium (Se) hyperaccumulation on neighboring plants.• Soil and litter Se concentrations were determined around the hyperaccumulators Astragalus bisulcatus and Stanleya pinnata and around the nonhyperaccumulators Medicago sativa and Helianthus pumilus. We also compared surrounding vegetative cover, species composition and Se concentration in two plant species (Artemisia ludoviciana and Symphyotrichum ericoides) growing either close to or far from Se hyperaccumulators. Then, Arabidopsis thaliana germination and growth were compared on soils collected next to the hyperaccumulators and the nonhyperaccumulators.• Soil collected around hyperaccumulators contained more Se (up to 266 mg Se kg )1 ) than soil collected around nonhyperaccumulators. Vegetative ground cover was 10% lower around Se hyperaccumulators compared with nonhyper-

Hyperaccumulators are plants that accumulate toxic elements to extraordinary levels. Selenium (Se) hyperaccumulators can contain 0.1-1.5% of their dry weight as Se, levels toxic to most other organisms. In this review we summarise what is known about the ecological functions and implications of Se (hyper)accumulation by plants. Selenium promotes hyperaccumulator growth and also offers a plant several ecological advantages through negative effects on Se-sensitive partners. High tissue Se levels reduce herbivory and pathogen infection, and high-Se litter deposition can inhibit neighbouring plants. There is no evidence for a cost of hyperaccumulation in terms of reproductive functions or pollinator visitation. Hyperaccumulators offer a niche for Se-tolerant herbivores, pollinators, microbes and neighbouring plants. They may even facilitate these partners through Se enrichment: neighbouring plants with elevated Se levels enjoy enhanced growth and reduced herbivory. Through combined negative and positive effects on ecological partners, Se hyperaccumulators likely affect local plant, microbial and animal species composition and richness, favouring Se-tolerant species at different trophic levels. By locally concentrating Se and altering its chemical form, Se hyperaccumulators likely play an important role in Se entry into, and Se cycling through, seleniferous ecosystems. These findings are of significance since they provide insight into the ecological reverberations of Se hyperaccumulation, and shed light on the possible selection pressures that have led to the evolution of this fascinating phenomenon. Better ecological insight will also help in the management of seleniferous areas and the agricultural production of Se-rich crops for phytoremediation or biofortification.

SummaryStanleya pinnata not only hyperaccumulates selenium (Se) to 0.5% of its dry weight, but also exhibits higher tissue Se-to-sulfur (S) ratios than other species and its surroundings.To investigate the mechanisms underlying this Se enrichment, we compared S. pinnata with the nonhyperaccumulators S. elata and Brassica juncea for selenate uptake in long-(9 d) and short-term (1 h) assays, using different concentrations of selenate and competitor sulfate. Different sulfate pre-treatments (0, 0.5, 5 mM, 3 d) were also tested for effects on selenate uptake and sulfate transporters' expression.Relative to nonhyperaccumulators, S. pinnata showed higher rates of root and shoot Se accumulation and less competitive inhibition by sulfate or by high-S pretreatment. The selenate uptake rate for S. pinnata (1 h) was three-to four-fold higher than for nonhyperaccumulators, and not significantly affected by 100-fold excess sulfate, which reduced selenate uptake by 100% in S. elata and 40% in B. juncea. Real-time reverse transcription PCR indicated constitutive upregulation in S. pinnata of sulfate transporters SULTR1;2 (root influx) and SULTR2;1 (translocation), but reduced SULTR1;1 expression (root influx).In S. pinnata, selenate uptake and translocation rates are constitutively elevated and relatively sulfate-independent. Underlying mechanisms likely include overexpression of SULTR1;2 and SULTR2;1, which may additionally have evolved enhanced specificity for selenate over sulfate.

Enhanced soil Se levels around hyperaccumulators can facilitate growth of Se-tolerant plant species through reduced herbivory and enhanced growth. This study is the first to show facilitation via enrichment with a nonessential element. It is interesting that Se enrichment of hyperaccumulator neighbors may affect competition in two ways, by reducing growth of Se-sensitive neighbors while facilitating Se-tolerant neighbors. Via these competitive and facilitating effects, Se hyperaccumulators may affect plant community composition and, consequently, higher trophic levels.

The S. pinnata species complex has a range of physiological properties making it an attractive system to study the evolution of Se hyperaccumulation. Beyond the basic scientific value of understanding the evolution of this fascinating trait, we can potentially use S. pinnata or its genes for environmental cleanup and/or nutrient-enhanced dietary material.