Plant stinging hairs have fascinated humans for time immemorial. True stinging hairs are highly specialized plant structures that are able to inject a physiologically active liquid into the skin and can be differentiated from irritant hairs (causing mechanical damage only). Stinging hairs can be classified into two basic types: Urtica-type stinging hairs with the classical “hypodermic syringe” mechanism expelling only liquid, and Tragia-type stinging hairs expelling a liquid together with a sharp crystal. In total, there are some 650 plant species with stinging hairs across five remotely related plant families (i.e., belonging to different plant orders). The family Urticaceae (order Rosales) includes a total of ca. 150 stinging representatives, amongst them the well-known stinging nettles (genus Urtica). There are also some 200 stinging species in Loasaceae (order Cornales), ca. 250 stinging species in Euphorbiaceae (order Malphigiales), a handful of species in Namaceae (order Boraginales), and one in Caricaceae (order Brassicales). Stinging hairs are commonly found on most aerial parts of the plants, especially the stem and leaves, but sometimes also on flowers and fruits. The ecological role of stinging hairs in plants seems to be essentially defense against mammalian herbivores, while they appear to be essentially inefficient against invertebrate pests. Stinging plants are therefore frequent pasture weeds across different taxa and geographical zones. Stinging hairs are usually combined with additional chemical and/or mechanical defenses in plants and are not a standalone mechanism. The physiological effects of stinging hairs on humans vary widely between stinging plants and range from a slight itch, skin rash (urticaria), and oedema to sharp pain and even serious neurological disorders such as neuropathy. Numerous studies have attempted to elucidate the chemical basis of the physiological effects. Since the middle of the 20th century, neurotransmitters (acetylcholine, histamine, serotonin) have been repeatedly detected in stinging hairs of Urticaceae, but recent analyses of Loasaceae stinging hair fluids revealed high variability in their composition and content of neurotransmitters. These substances can explain some of the physiological effects of stinging hairs, but fail to completely explain neuropathic effects, pointing to some yet unidentified neurotoxin. Inorganic ions (e.g., potassium) are detected in stinging hairs and could have synergistic effects. Very recently, ultrastable miniproteins dubbed “gympietides” have been reported from two species of Dendrocnide, arguably the most violently stinging plant. Gympietides are shown to be highly neurotoxic, providing a convincing explanation for Dendrocnide toxicity. For the roughly 648 remaining stinging plant species, similarly convincing data on toxicity are still lacking.

Trichome biomineralization is widespread in plants but detailed chemical patterns and a possible influence of soil chemistry are poorly known. We explored this issue by investigating trichome biomineralization in 36 species of Mediterranean Brassicaceae from ultramafic and calcareous soils. Our aims were to chemically characterize biomineralization of different taxa, including metallophytes, under natural conditions and to investigate whether divergent Ca, Mg, Si and P-levels in the soil are reflected in trichome biomineralization and whether the elevated heavy metal concentrations lead to their integration into the mineralized cell walls. Forty-two samples were collected in the wild while a total of 6 taxa were brought into cultivation and grown in ultramafic, calcareous and standard potting soils in order to investigate an effect of soil composition on biomineralization. The sampling included numerous known hyperaccumulators of Ni. EDX microanalysis showed CaCO₃ to be the dominant biomineral, often associated with considerable proportions of Mg—independent of soil type and wild versus cultivated samples. Across 6 of the 9 genera studied, trichome tips were mineralized with calcium phosphate, in Bornmuellera emarginata the P to Ca-ratio was close to that of pure apatite-calcium phosphate (Ca₅(PO₄)₃OH). A few samples also showed biomineralization with Si, either only at the trichome tips or all over the trichome. Additionally, we found traces of Mn co-localized with calcium phosphate in Bornmuellera emarginata and traces of Ni were detected in trichomes of the Ni-hyperaccumulator Odontarrhena chalcidica. Our data from wild and cultivated plants could not confirm any major effect of soil chemistry on the chemistry of trichome biominerals. Hyperaccumulation of Ni in the plants is not mirrored in high levels of Ni in the trichomes, nor do we find large amounts of Mn. A comparison based on plants from cultivation (normal, calcareous and serpentine soils, Mg:Ca-ratios ca 1:2 to 1:20) shows at best a very weak reflection of different Mg:Ca-ratios in the mineralized trichomes. The plants studied seem to be able to maintain highly conserved biomineralization patterns across a wide range of soil chemistries.