Yunnan Key Laboratory for Palaeobiology, Yunnan University, 2 Cuihubei Road, 650091 Kunming, China; MEC International Joint Laboratory for Palaeobiology and Palaeoenvironment, Yunnan University, 650091 Kunming, China.
Department of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, UK; Museum of Comparative Zoology and Department of Organismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA.
Curr Biol. 2019 Jan 7;29(1):171-177.e1. doi: 10.1016/j.cub.2018.11.060. Epub 2018 Dec 27.
Pancrustaceans boast impressive diversity, abundance, and ecological impact in the biosphere throughout the Phanerozoic [1]. Molecular clock estimates suggest an early Cambrian divergence for pancrustaceans [2, 3]. Despite the wealth of Palaeozoic exceptional fossiliferous deposits [4-7], the early evolution of Pancrustacea remains elusive given the difficulty of recognizing synapomorphies between Cambrian forms and extant representatives. Although early studies suggested crustacean affinities for Cambrian bivalved euarthropods [8-11], this view has fallen out of favor by recent reappraisals of their morphology [12-16]. The best evidence for total-group pancrustaceans comes from Cambrian microfossils preserved as three-dimensional phosphatic replicates in Orsten-type assemblages [4, 17-19] or as "small carbonaceous fossils" (SCFs) [20, 21]. Although these taphonomic windows capture minute morphology enabling detailed comparisons with extant representatives, these microfossils are limited to larval stages (Orsten) or recalcitrant fragmentary remains (SCFs) restricting their phylogenetic precision [5, 12, 19, 20, 22, 23]. We employed X-ray computed tomography [24] to reveal the three-dimensionally appendage morphology of the Chengjiang bivalved euarthropod Ercaicunia multinodosa [25] from the early Cambrian of China. E. multinodosa possesses characters uniquely shared with extant crustaceans, including differentiated tritocerebral antennae and epipodite-bearing biramous trunk appendages. Similarities between E. multinodosa with clypecaridids [9], waptiids [16] and hymenocarines [11, 14] suggest that these euarthropods may also possess similarly differentiated appendages, but these details are obstructed by the limits of preservation of compacted macrofossils. E. multinodosa illuminates the early evolution of pancrustacean appendage differentiation and represents the oldest unequivocal crown-group mandibulate known from complete macrofossils [22].
泛甲壳动物在整个显生宙的生物圈中表现出令人印象深刻的多样性、丰富度和生态影响[1]。分子钟估计表明泛甲壳动物在早寒武纪就已经分化[2,3]。尽管古生代有丰富的特异化石矿床[4-7],但由于难以识别寒武纪形态与现存代表之间的同源特征,泛甲壳动物的早期进化仍然难以捉摸。尽管早期研究表明寒武纪双瓣有颚类动物具有甲壳动物亲缘关系[8-11],但最近对其形态的重新评估使这种观点不再流行[12-16]。总群泛甲壳动物的最佳证据来自寒武纪微体化石,这些微体化石以三维磷酸盐复制品的形式保存在奥斯特恩型组合中[4,17-19]或作为“小碳质化石”(SCF)[20,21]。虽然这些埋藏学窗口捕捉到了微小的形态,使我们能够与现存代表进行详细比较,但这些微体化石仅限于幼虫阶段(奥斯特恩)或难以辨认的零碎残骸(SCF),限制了它们的系统发育精度[5,12,19,20,22,23]。我们采用 X 射线计算机断层扫描[24]来揭示中国早寒武纪双瓣有颚类动物 Ercaicunia multinodosa 的三维附肢形态[25]。E. multinodosa 具有与现存甲壳动物独特共享的特征,包括分化的三叉触角和具附肢的双枝躯干附肢。E. multinodosa 与 clypecaridids[9]、waptiids[16]和 hymenocarines[11,14]之间的相似性表明,这些有颚类动物可能也具有类似分化的附肢,但这些细节被压实的大型化石的保存限制所掩盖。E. multinodosa 揭示了泛甲壳动物附肢分化的早期进化,代表了最早的、来自完整大型化石的明确的冠群蔓足类[22]。