Abstract

Fairy circles are striking regularly sized and spaced, bare circles surrounded by Stipagrostis grasses that occur over thousands of square kilometres in Namibia. The mechanisms explaining their origin, shape, persistence and regularity remain controversial. One hypothesis for the formation of vegetation rings is based on the centrifugal expansion of a single individual grass plant, via clonal growth and die-back in the centre. Clonality could explain FC origin, shape and long-term persistence as well as their regularity, if one clone competes with adjacent clones. Here, we show that for virtually all tested fairy circles the periphery is not exclusively made up of genetically identical grasses, but these peripheral grasses belong to more than one unrelated genet. These results do not support a clonal explanation for fairy circles. Lack of clonality implies that a biological reason for their origin, shape and regularity must emerge from competition between near neighbor individuals within each fairy circle. Such lack of clonality also suggests a mismatch between longevity of fairy circles versus their constituent plants. Furthermore, our findings of lack of clonality have implications for some models of spatial patterning of fairy circles that are based on self-organization.

Highlights

  • Fairy circles are striking regularly sized and spaced, bare circles surrounded by Stipagrostis grasses that occur over thousands of square kilometres in Namibia

  • Fairy circles (FCs) are remarkably circular and regular vegetation patterns covering an area of thousands of square kilometres in hyper-arid grasslands in Southern Africa (e.g. Namibia)[1,2,3]

  • This is correct that FCs tend to be much larger in Namibia, the mean size of FCs can be as small as 2.5 m in some areas[2]

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Summary

Introduction

Fairy circles are striking regularly sized and spaced, bare circles surrounded by Stipagrostis grasses that occur over thousands of square kilometres in Namibia The mechanisms explaining their origin, shape, persistence and regularity remain controversial. Individual plants of this species send out underground rhizomes, which, with increasing age, results in a ring of ramets (i.e. sprouts from the same clonal colony or genet) around a barren central patch, which forms as the plant centre dies[4] Such vegetation rings form and enlarge centrifugally due to competition between ramets, and as this process continues over time new ramets establish successfully only towards the periphery[4,7]. Bare centres are well known in rings and are commonly explained as being due to inter-ramet competition and resource depletion[7]

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