The tectonic evolution of the Sibumasu Block during the Permian remains controversial, and Permian faunas and their paleobiogeographic affinities provide some insight into its paleogeographic and tectonic evolutionary histories. In this paper, a new brachiopod fauna dominated by Spinomartinia prolifica Waterhouse, 1981 is described from the uppermost part of the Taungnyo Group in the Zwekabin Range, eastern Myanmar. This brachiopod fauna includes 23 species and its age is well constrained as late Kungurian by the associated conodonts, i.e., Vjalovognathus nicolli Yuan et al., 2016 and Mesogondolella idahoensis (Youngquist, Hawley, and Miller, 1951), contrary to the late Sakmarian age given to the same brachiopod faunas previously reported from southern Thailand and Malaysia. Based on comprehensive comparisons of the Cisuralian brachiopod faunas and other data in different parts of the Sibumasu Block, we consider that they are better subdivided into two independent stratigraphic assemblages, i.e., the lower (earlier) Bandoproductus monticulus-Spirelytha petaliformis Assemblage of a Sakmarian to probably early Artinskian age, and the upper (younger) Spinomartinia prolifica-Retimarginifera alata Assemblage of a late Kungurian age. The former assemblage is a typical cold-water fauna, mainly composed of Gondwanan-type genera, e.g., Bandoproductus Jin and Sun, 1981, Spirelytha Fredericks, 1924, and Sulciplica Waterhouse, 1968. The latter assemblage is strongly characterized by an admixture of both Cathaysian and Gondwanan elements, as well as some genera restricted to the Cimmerian continents. Notably, the spatial distribution pattern of these two separate brachiopod assemblages varies distinctly. The Sakmarian cold-water brachiopod faunas have been found in association with glacial-marine diamictites throughout the Sibumasu Block including both the Irrawaddy and Sibuma blocks. In contrast, the Kungurian biogeographically mixed brachiopod faunas are only recorded in the Irrawaddy Block, unlike the Sibuma Block that contains a contemporaneous paleotropical Tethyan fusuline fauna. Thus, it appears likely that by the end of Cisuralian (early Permian), the Sibumasu Block comprised the Irrawaddy Block in the south with cool climatic conditions, and the Sibuma Block in the north with a temperate to warm-water environment, separated by the incipient Thai-Myanmar Mesotethys.

Permian faunal affinity in the Lhasa Block plays a critical role in reconstructing its paleogeographic evolution. Cisuralian and Guadalupian faunas have been described from the Lhasa Block, but very few Lopingian (late Permian) brachiopods have been reported so far. In this paper, a new diverse brachiopod fauna consisting of 17 species of 17 genera and an unidentifiable Orthotetoidea is described from the uppermost part of the Xiala Formation at the Aduogabu section in the central part of the Lhasa Block. The age of this fauna can be assigned to the Changhsingian (late Lopingian) as indicated by the associated foraminifers Colaniella parva (Colani, 1924) and Reichelina pulchra Miklukho-Maklay, 1954. Characteristic brachiopods include Spinomarginifera chengyaoyenensis Huang, 1932, Haydenella wenganensis (Huang, 1932), and Araxathyris cf. dilatatus Shen, He, and Zhu, 1992. They also generally suggest a Changhsingian age. Paleobiogeographically, this fauna is uniformly composed of typical Tethyan elements represented by Spinomarginifera Huang, 1932 and Haydenella Reed, 1944, and some cosmopolitan elements, but no typical cold-water taxa of Gondwanan affinity. This is in contrast to the contemporaneous brachiopod faunas from the Tethys Himalayan region that are characterized by typical cold-water taxa of Gondwanan affinity, e.g., Costiferina indica (Waagen, 1884), Retimarginifera xizangensis Shen et al., 2000, Neospirifer (Quadrospina) tibetensis Ding, 1962. Thus, it is strongly indicative that the Lhasa Block had drifted into a relatively warm-water regime during the Changhsingian. An analysis of the paleobiogeographic change of brachiopods in the Lhasa Block throughout the entire Permian further suggests that the Lhasa Block probably had rifted away from the northern peri-Gondwanan margin between the latest Cisuralian and middle Guadalupian, that is, the Neotethys Ocean had opened before middle Guadalupian.

South China has become the most important area to establish a global stratigraphic framework of the Wuchiapingian Stage because complete Wuchiapingian 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.

This paper describes a unique deepwater brachiopod fauna from the upper part of the Talung Formation at the Dongpan Section, southern Guangxi, South China. This brachiopod fauna includes 10 species belonging to 10 genera. New taxa are Anidanthus mucronata n. sp., Dongpanoproductus elegans n. gen. and sp., Costatumulus dongpanensis n. sp., and Spinomarginifera semicircridge n. sp. This fauna is characterized by small, thin-shelled species with high abundance and low diversity, and therefore is different in generic and species composition from the coeval faunas of the Late Permian limestone facies in South China. The brachiopod fauna can be safely assigned to the latest Changhsingian as indicated by the presence of abundant Paracrurithyris pigmaea, the immediately underlying radiolarian Neoalbaillella optima Zone of late Changhsingian age, and the overlying ammonoid Ophiceras sp. cf. O. tingi Tien of the lowest Triassic. This fauna is most likely to have lived in a deepwater environment as indicated by coexistence with the radiolarian Latentifistularia, small thin-shelled brachiopods, and the dominance of silica-bearing mudstone.

A fusuline fauna consisting of 9 species of 4 genera from the Xiala Formation of the Mujiucuo section, Xainza County, Tibet, China is described. The fusuline fauna is dominated by Nankinella and Chusenella and indicates a Midian (Late Guadalupian) age. The earliest record of fusuline fauna during the Midian in the Lhasa Block suggests that the block rifted later than the Qiangtang Block to the north and the Baoshan and Tengchong blocks to the east, all of which yield much earlier fusuline faunas of Yakhtashian (Artinskian) age, but had drifted away from Gondwana to a relatively warm temperate zone in the Late Guadalupian (Middle Permian).

Members of the Lyttoniidae Waagen, 1883 (Lyttonioidea Waagen, 1883, Brachiopoda) are characterized by numerous peculiarities, including their disproportionately inequivalve, rudimentary articulatory apparatus and asymmetrically developed muscle scars. The ventral valve of lyttonioids usually possesses a posterior flap and complementary septal apparatus and the dorsal valve has corresponding lobes and slits to fit around the ventral septa (Noetling, 1905; Fredericks, 1926; Wanner, 1935; Williams, 1953; Grant, 1976; Williams et al., 2000). Externally, the Lyttoniidae have been previously described as being smooth or having some growth banding, lines, or disturbances only (Cooper and Grant, 1974; Williams et al., 2000). Spines were previously reported by Sarytcheva (1964), but subsequently not confirmed by Cooper and Grant (1974, p. 387) and Williams et al. (2000). Radial ornamentation has never been reported prior to this study. In 2002, two specimens with Linoproductus-like costellae and Old-hamina-like septal apparatus were found by one of the authors (CLR) from the Middle Permian Xiala Formation at the Xinji Section in the Xainza area (89–91°E, 30–31°N) in northern Tibet (Fig. 1.1, 1.2) during 1:250,000 mapping. We consider that the present specimens represent another distinct phylogenetic branch within the Lyttoniidae, although only two specimens were found. Further collecting is currently impossible because of the inaccessibility of the remote area in northern Tibet. In this paper we aim to propose a new subfamily of Lyttoniidae based on the specimens found from northern Tibet.

Eleven athyridoid species are described and other related species are revised from the Lopingian (late Permian) of South China and Transcaucasia in southern Azerbaijan and northern Iran. The family Comelicaniidae Merla, 1930 is adopted. It includes six subfamilies, of which Araxathyriinae is proposed as a new subfamily. Comparisons of species based on detailed internal structures indicate that some previously commonly recorded species from South China and Transcaucasia actually belong to different genera. Araxathyris coexisted in the two regions. Comelicania, Gruntallina, Janiceps, Transcaucasathyris, and Comelicothyris are only found in the southern Alps, Hungary, and/or Transcaucasia; whereas Tongzithyris and Rectambitus are restricted to South China. Other new taxa are Transcaucasathyris n. gen., Araxathyris sinensis n. sp., Rectambitus xui n. sp., and R. spondomarginata n. sp.

Spatial and temporal variations in biological diversity are critical in understanding the role of biogeographical regulation (if any) on mass extinctions. An analysis based on a latest database of the stratigraphic ranges of 89 Permian brachiopod families, 422 genera, and 2059 species within the Boreal, Paleoequatorial, and Gondwanan Realms in the Asian–western Pacific region suggests two discrete mass extinctions, each possibly with different causes. Using species/family rarefaction analysis, we constructed diversity curves for late Artinskian–Kungurian, Roadian–Wordian, Capitanian, and Wuchiapingian intervals for filtering out uneven sampling intensities. The end-Changhsingian (latest Permian) extinction eliminated 87–90% of genera and 94–96% of species of Brachiopoda. The timing of the end-Changhsingian extinction of brachiopods in the carbonate settings of South China and southern Tibet indicates that brachiopods suffered a rapid extinction within a short interval just below the Permian/Triassic boundary.

In comparison, the end-Guadalupian/late Guadalupian extinction is less profound and varies temporally in different realms. Brachiopods in the western Pacific sector of the Boreal Realm nearly disappeared by the end-Guadalupian but experienced a relatively long-term press extinction spanning the entire Guadalupian in the Gondwanan Realm. The end-Guadalupian brachiopod diversity fall is not well reflected at the timescale used here in the Paleoequatorial Realm because the life-depleted early Wuchiapingian was overlapped by a rapid radiation phase in the late Wuchiapingian. The Guadalupian fall appears to be related to the dramatic reduction of habitat area for the brachiopods, which itself is associated with the withdrawal of seawater from continental Pangea and the closure of the Sino-Mongolian seaway by the end-Guadalupian.

Studies of the end-Permian mass extinction have suggested a variety of patterns from a single catastrophic event to multiple phases. But most of these analyses have been based on fossil distributions from single localities. Although single sections may simplify the interpretation of species diversity, they are susceptible to bias from stratigraphic incompleteness and facies control of preservation. Here we use a data set of 1450 species from 18 fossiliferous sections in different paleoenvironmental settings across South China and the northern peri-Gondwanan region, and integrate it with high-precision geochronologic data to evaluate the rapidity of the largest Phanerozoic mass extinction. To reduce the Signor-Lipps effect, we applied constrained optimization (CONOP) to search for an optimal sequence of first and last occurrence datums for all species and generate a composite biodiversity pattern based on multiple sections. This analysis indicates that an abrupt extinction of 62% of species took place within 200 Kyr. The onset of the sudden extinction is around 252.3 Ma, just below Bed 25 at the Meishan section. Taxon turnover and diversification rates suggest a deterioration of the living conditions nearly 1.2 Myr before the sudden extinction. The magnitude of the extinction was such that there was no immediate biotic recovery. Prior suggestions of highly variable, multi-phased extinction patterns reflect the impact of the Signor-Lipps effect and facies-dependent occurrences, and are not supported following appropriate statistical treatment of this larger data set.

The Qiangtang Metamorphic Belt (QMB) was considered to have either formed in situ by amalgmation of the North and South Qiangtang blocks or been underthrust from the Jinsha suture and exhumed in the interior of a single ‘Qiangtang Block’. A new Sphaeroschwagerina fusuline fauna discovered in the Raggyorcaka Lake area supports the interpretation that the North and South Qiangtang blocks were separated by a wide ocean during Asselian (Early Permian) time, indicating that the QMB was formed by the suturing of the Palaeotethys Ocean along the Longmu Co-Shuanghu suture.

The uppermost 5–15 m of the Douling Formation in the southern Hunan area, South China, yields a diverse fauna comprised of ammonoids, bivalves, and brachiopods. The brachiopods reported in this paper consist of 51 species in 34 genera and are dominated by the Lopingian (Late Permian) species associated with a few species persisting from the underlying Maokouan (Late Guadalupian). This fauna is of earliest Wuchiapingian in age as precisely constrained by the associated conodont Clarkina postbitteri postbitteri and the Guadalupian-type ammonoid fauna of the Roadoceras-Doulingoceras Zone in the brachiopod horizon. The discovery of the Lopingian species-dominated brachiopod fauna in the earliest Wuchiapingian in southern Hunan suggests a much less pronounced effect of the pre-Lopingian crisis (end-Guadalupian mass extinction) than the end-Changhsingian mass extinction in terms of brachiopods, a contemporaneous onset of the Lopingian recovery/radiation during the pre-Lopingian crisis period, and taxonomic selectivity of the pre-Lopingian crisis in terms of different fossil groups. New taxa are Echinauris doulingensis n. sp., Pararigbyella quadrilobata n. gen. and n. sp. and P. doulingensis n. gen. and n. sp.

Late Permian gastropod fauna in the Mt. Everest (Qomolangma) region, southern Tibet (Xizang), China is poorly known. This paper describes a small gastropod fauna collected by one of the authors (SSZ) from the upper part of the Qubuerga Formation at the Qubu section. The section is located at about 30 km north of Mt. Everest (Fig. 1). Although a limited number of specimens is available, the fauna is more diverse than all previously reported gastropod faunas (e.g., Yu, 1975) from southern Tibet. Description of the gastropod fauna in the Mt. Everest region adds significant data for understanding the distribution of gastropods during the Late Permian and the paleobiogeographic relationship between the Himalayan and Tethyan regions.

Twelve brachiopod species are described from the Cisuralian (Early Permian) Kungurian horizon of a large limestone block in the Middle Jurassic accretionary complex at Hatahoko in the Mino Belt, central Japan. Most species of the Hatahoko fauna are known from the Kungurian to lowest Guadalupian (Middle Permian) of West Texas, U.S.A. The Kungurian age is also indicated by the associated conodonts in the same limestone block. The Hatahoko brachiopod fauna, as well as some other previously-reported Guadalupian brachiopod faunas, exhibits a very strong paleobiogeographical affinity with the faunas in West Texas, U.S.A. Therefore it can be interpreted as a fauna which inhabited reef-seamount complexes close to North America in the mid-equatorial region of the Panthalassa in the late Early Permian, rifted westwards thousands of kilometers, and finally accreted onto the Japanese Island when the Western Pacific Plate subducted beneath the Eurasian Plate during the Jurassic.

An abundant and diverse Late Griesbachian (Early Induan) Wordieoceras-dominated cephalopod fauna occurs in the lower part of the Daye Formation at the Wenjiangsi section, Guiding County, Guizhou Province, South China. The cephalopod fauna consists of 17 species belonging to 10 genera, including two nautiloid species and 15 ammonoid species representing the families Ophiceratidae, Proptychitidae, Meekoceratidae, and Khangsariidae. One genus and five species are new: Vishnuites wenjiangsiensis, Pseudovishnuites guidingensis, Wordieoceras guizhouensis, Gyrophiceras subplicatum, and Hubeitoceras? Wangi.

Seminiferous tubule tissues from goat fetal testis were treated using four methods. One of the treatments, with 0.1% collagenase for 15 min and then with an enzyme mixture (containing 0.25% trypsin, 10 μg/ml DNase I, 0.04% EDTA) for 5 min showed ideal cell dispersal after centrifugation and washing. The in vitro culture of the cells separated with a different medium system showed that mulberry-shaped male germ-line stem cell (mGSC) clusters and a single layer of Sertoli cells appeared as the original generation in 120 h. The mGSC clusters developed in suspension and were distributed in different locations from the Sertoli cells in the plate. The cells in the marginal area of incompletely digested mGSCs clusters, and the single cells from them, were obviously homogenized after culture for 5 days in a fibre cell feeding layer from fetal mice (MEF feeding layer), whereas identically treated mGSCs clusters co-cultured with Sertoli cells in the same culture system did not displayed clear homogenization in marginal cells of the clusters. Also, the first generation of mGSC clusters co-cultured with Sertoli cells could form the same morphological properties with the original generation; cells in clusters were tight and mGSCs divided more slowly than those in the MEF feeding layer.