Abstract

Elatine L. contains ca. 25 small, herbaceous, annual species distributed in ephemeral waters in both hemispheres. All species are amphibious and characterized by a high degree of morphological variability. The importance of seed morphology in Elatine taxonomy has been emphasized by many authors. The degree of seed curvature and seed coat reticulation have been traditionally considered very important in recognizing individual species of this genus. Seed morphometric characteristics of 10 Elatine species, including all European native taxa, are provided on the basis of material from two or three populations of each species. A total of 24–50 seeds were studied from each population, altogether 1,260 images were used for the morphometric study. In total, six parameters were measured from SEM pictures: object surface area, profile specific perimeter (object circuit), rectangle of the object (a) length, rectangle of the object (b) width, angle of the seed curvature, and number of pits in the seed coat counted in the middle row. Our study shows that the range of morphological variation of seeds in European species of Elatine is great, both between the species and the populations. Discrimination analysis showed that all six traits significantly differentiate the populations studied (λ = 0.001, p < 0.001), and the greatest contributions were “number of pits”, “rectangle_a”, and “the angle curvature”. Multidimensional scaling based on a correlation matrix of Mahalanobis distance of the six features studied revealed the greatest similarity between the three populations of E. alsinastrum, E. macropoda, and E. hexandra. Regarding interspecific differences, a Kruskal–Wallis tests showed that, in many cases, lack of statistically significant differences between species relative to the studied seed traits. If distinction of species is only based on seeds, especially if only a few seeds are evaluated, the following species pairs can be easily confused: E. alsinastrum and E. orthosperma, E. hexandra and E. macropoda, E. campylosperma and E. hydropiper, as well and E. gussonei and E. hungarica. We found no diversity in seed coat micromorphology within pits that could have potential taxonomic importance. An identification key and descriptions of species are provided on the basis of seeds traits.

Highlights

  • Elatine L. is one of the two genera in the Elatinaceae, a family in Malpighiales (Tucker, 1986; Davis & Chase, 2004), and contains ca. 15–25 ephemeral amphibious species (Heywood et al, 2007)

  • Seeds were collected from all 10 Elatine species and from three populations each, with an exception of very rare E. brochonii and E. campylosperma, two populations, so altogether 28 populations were used for the study

  • Based on a Kruskal–Wallis tests, we found no statistically significant differences (p = 0.05) between populations studied of each European Elatine species regarding the following traits: (A) surface, (B) profile, (C) rectangle a, (D) rectangle b, (E) the angle of curvature, (F) number of pits (Table 3)

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Summary

Introduction

Elatine L. is one of the two genera in the Elatinaceae, a family in Malpighiales (Tucker, 1986; Davis & Chase, 2004), and contains ca. 15–25 ephemeral amphibious species (Heywood et al, 2007). Ten native taxa occur in Europe; Flora Europea lists seven (Cook, 1968) and Euro+Med Plantbase nine native species (Uotila, 2009b). One taxon belongs to the subgenus Potamopithys (Adanson) Seub(E. alsinastrum L.), and the other taxa are classified into subgenus Elatine Seub. Triandra mainly occur in temperate regions of the Old and New World, with the probable center of diversity in North and South America. E. ambigua is another taxon from Europe (Uotila, 2009b) It shows no substantial genetic differences in relation to E. triandra (Sramkó et al, 2016) an Asian species occurring in Europe

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