Abstract

Identification of relevant taxonomic and evolutionary units is a recurrent issue in the fossil record, and all the more for ancient fossils devoid of modern equivalents such as conodonts. Extensive morphological variation has often led to the description of numerous species, subspecies or morphotypes, which may correspond to end-member morphologies reached through ontogeny. The platform elements of the Late Devonian conodont speciesIcriodus alternatuswere characterized by rows of denticles coming into occlusion between opposite elements; each element grew by the incremental addition of lamellae and by the addition of successive triads during ontogeny. During the late Frasnian and the early Famennian, the important morphological variation within this species led to the description of three subspecies. An extensive sample of early FamennianIcriodus alternatuswas quantified using 2D biometric measurements and denticle counts on 2D pictures, showing that the subspecies mainly differed in their size range but not in their general morphology. A 3D morphometric analysis was further performed on a subsample to characterize the shape of the ontogenetically older part of the elements. During ontogeny, early valleys between denticles tended to be filled, and the asymmetry between the inner and outer side of the element increased. These ontogenetic trends are responsible for the morphologies formerly described as the subspeciesIc. alt. mawsonaeandIc. alt. helmsi. Slight discrepancies between temporal ranges of the subspecies may be achieved through variations in range of size reached by the elements as a response to environmental changes. Disparity along ontogeny seems to follow an “hourglass model” suggesting a shift from relatively loose developmental constraints to a pattern of growth modulated by functional constraints during occlusion.

Highlights

  • Conodonts are long extinct animals known from the Cambrian to the end-Triassic, without modern equivalent

  • The present study aims at quantifying the morphological variation within the most abundant Icriodus species at that time, Icriodus alternatus Branson and Mehl 1934, based on material from the Buschteich section (Thuringia, Germany) (Fig. 1)

  • The altitude h at the summit A can be obtained as h = 2S/a. According to these formulas, the height of md1 can be approximated as the altitude of a triangle defined by the tip of the denticle and the two valleys surrounding it along a same line (Suppl. material 3: Fig. S1), the sides of the triangles being calculated as the corresponding inter-landmark distances

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Summary

Introduction

Conodonts are long extinct animals known from the Cambrian to the end-Triassic, without modern equivalent These early vertebrates were an important part of the nektonic fauna increasing in richness through the Paleozoic era (Purnell 1995). Anterior elements formed a trapping structure, whereas posterior platform elements processed food items (Aldridge et al 1987, Purnell and Donoghue 1997). These elements functioned in occlusion between right and left elements and displayed a complex morphology, sometimes even allowing a molar-like occlusion (Donoghue and Purnell 1999). The morphological complexity of the posterior platform elements, together with their rapid temporal evolution made, them efficient stratigraphic tools for the Paleozoic and Triassic eras

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