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Journal of Paleontology, 91(6), 2017, p. 1199–1219 Copyright © 2017, The Paleontological Society 0022-3360/17/0088-0906 doi: 10.1017/jpa.2017.71


Revised Wuchiapingian conodont taxonomy and succession of South China


Dong-xun Yuan,1,2 Shu-zhong Shen,1,3 and Charles M. Henderson2 1State Key Laboratory of Palaeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences,


Nanjing 210008, China ⟨dxyuan@nigpas.ac.cn⟩; ⟨szshen@nigpas.ac.cn⟩ 2Department of Geoscience, University of Calgary, Calgary, AB, Canada, T2N 1N4 ⟨cmhender@ucalgary.ca⟩ 3Centre for Research and Education of Biological Evolution and Environment, Nanjing University, 163 Xianlin Avenue, Nanjing 210023, China


Abstract.—South China has become the most important area to establish a global stratigraphic framework of the Wuchiapingian Stage because completeWuchiapingian sequences include the GSSPs for the base and top of the stage. As the markers of the Wuchiapingian GSSP, conodonts are the most important fossil group to establish the Wuchiapingian biostratigraphic framework. However, few documents have investigated in detail the conodont biostratigraphic succession through the entire Wuchiapingian Stage. Furthermore, the conodont taxonomy of several Wuchiapingian Clarkina species is still debated. Therefore, we here review all Wuchiapingian Clarkina species from South China and figure ontogenetic growth series from juvenile to adult individuals for each valid and important species in order to revise both Wuchiapingian conodont taxonomy and the biostratigraphic succession. Based on the Penglaitan, Dukou, and Nanjiang sections, seven conodont zones (Clarkina postbitteri postbitteri, C. dukouensis, C. asymmetrica, C. leveni, C. guangyuanensis, C. transcaucasica,and C. orientalis) are recognized. The Wuchiapingian Clarkina species lineage is also reviewed to confirm the conodont biostratigraphic framework. The Guadalupian-Lopingian boundary (GLB) interval represents a sequence boundary. The time framework of the pre-Lopingian extinction interval indicates that the beginning of the end-Guadalupian regression is in the upper part of the Jinogondolella postserrata Zone, and the beginning of the early Lopingian transgression is in the lower part of the Clarkina dukouensis Zone in South China.


Introduction


Continuous marine depositional sequences of the Wuchiapingian are very limited in distribution because the global end-Guadalupian regression resulted in the emergence of much of the supercontinent Pangea. There are only a few regions along the continentalmargin and some blocks in the Paleotethys with well-developed marine Wuchiapingian sequences in theworld. South China iswell known for completeWuchiapingian sequences and theGSSPs for the base and the top of the Wuchiapingian Stage have been precisely defined by conodonts, respectively in the Penglaitan Section of Guangxi Province and in the Meishan Section of Zhejiang Province (Jin et al., 2006a, b). Thus, South China has become the most important area to establish a global stratigraphic framework of theWuchiapingian Stage. Conodonts are one of the most important fossil groups in the


Permian because all GSSPs and candidate sections for GSSPs of the Permian either have been or will be defined by conodont species, and the biostratigraphic framework in the Permian was also established based on the evolutionary lineages of conodonts (Henderson, 2017).Wuchiapingian conodonts have been widely documented from many sections in South China, including the Liangshan area in Shaanxi(Wang, 1978), theMeishan sections in Zhejiang (Wang and Wang, 1981; Zhao et al., 1981; Sheng et al., 1987; Mei et al., 2004; Zhang et al., 2009; Yuan et al., 2014a), the Xuanen, Ermen, Wufeng, Tianqiao, and Maoershan sections in Hubei (Clark and Wang, 1988; Duan, 1990; Li, 1991;


Wang andXia, 2004; Zhang et al., 2008), the Shangsi, Dukou, and Nanjiang sections in Sichuan (Li et al., 1989;Mei et al., 1994a, b), the Yangtaoshan and Yangongtang sections in Anhui (Duan, 1990), the Penglaitan, Tieqiao, and Fengshan sections in Guangxi (Mei et al., 1994b, 1998a;Wang et al., 1998;Wang, 2000, 2001, 2002; Henderson et al., 2002; Jin et al., 2006a), the Hushan region in Jiangsu (Duan, 1990), the Suoxiyu, Rencunping, Jiangya, and Matian sections in Hunan (Wang and Dong, 1991; Tian, 1993a, b; Mei and Wardlaw, 1996; Cao et al., 2013), the Qibaoshan Section in Jiangxi (Wang et al., 1997), and the Lengshuixi and Daijiagou sections in Chongqing (Yang et al., 2008; Yuan et al., 2015). However, most of the previous conodont studies focused on the Capitanian-Wuchiapingian (Guadalupian-Lopingian) boundary interval and the Wuchiapingian-Changhsingian boundary interval (e.g., Wang et al., 1997; Wang, 2000, 2001, 2002; Henderson et al., 2002; Mei et al., 2004; Jin et al., 2006a, b), or they simply described a few conodont elements (e.g., Zhao et al., 1981; Clark and Wang, 1988; Duan, 1990; Li, 1991; Wang and Dong, 1991; Wang and Xia, 2004; Yang et al., 2008). Only a few studies have investigated in detail the conodont biostratigraphic succession through the entire Wuchiapingian Stage (e.g., the Dukou and Penglaitan sections in Mei et al., 1994a, b, 1998a). Mei et al. (1994a, b, 1998a) illustrated only a few specimens for most species, which do not display the full range of character morpho- logy and ontogenetic series. The sample-population concept (Wardlaw and Collinson, 1979; Mei et al., 2004; Shen and Mei, 2010; Yuan et al., 2014a) demands the illustration of multiple


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