The Permian–Triassic boundary section at Baghuk Mountain, Central Iran: carbonate microfacies and depositional environment

Sections at Baghuk Mountain, 45 km NNW of Abadeh (Central Iran), have excellent exposures of fossiliferous marine Late Permian to Early Triassic sedimentary successions. Detailed bed-by-bed sampling enables the analysis of microfacies changes of three successive rock units across the Permian–Triassic boundary. The Late Permian Hambast Formation is mainly the result of biogenic carbonate production. Its carbonate microfacies is dominated by biogen-rich and bioturbated nodular limestones, indicating a well-oxygenated aphotic to dysphotic environment. The biogen-dominated carbonate factory in the Permian ceased simultaneously with the main mass extinction pulse, which is marked by a sharp contact between the Hambast-Formation and the overlaying Baghuk Member (= ‘Boundary Clay’). The clay and silt deposits of the Baghuk Member with some carbonate beds show only a few signs of bioturbation or relics of benthic communities. The Early Triassic Claraia Beds are characterised by a partly microbially induced carbonate production, which is indicated by frequent microbialite structures. The depositional environment does not provide evidence of large amplitude changes of sea level or subaerial exposure during the Permian–Triassic boundary interval. The deposition of the Baghuk Mountain sediments took place in a deep shelf environment, most of the time below the storm wave base.


Introduction
The catastrophic Late Permian mass extinction resulted in dramatic changes in biodiversity (e.g. Sepkoski 1982, 1984;Erwin 1993Erwin , 1994Stanley and Yang 1994;Erwin et al. 2002) paralleled by shifts in chemistry in the Tethys Ocean (e.g. Baud et al. 1989;Heydari et al. 2000;Korte et al. 2004a, b;Schobben et al. 2015Schobben et al. , 2017. While there is agreement on a significant increase in seawater temperatures (Joachimski et al. , 2020Sun et al. 2012;Chen et al. 2013Chen et al. , 2020Schobben et al. 2014), there is a vigorous debate, whether the Permian-Triassic (P-Tr) transition was associated with significant sea-level changes and global anoxia (e.g. Wignall and Hallam 1992;Knoll et al. 1996;Wignall and Twitchett 1996;Hallam and Wignall 1999;Berner 2006;Bond and Wignall 2010;Zhang et al. 2018;Schobben et al. 2020). Previous studies suggested that the formation of microbial communities, which occur particularly in Early Triassic successions, is either a consequence of global oceanic alkalinity changes and changes in carbonate saturation or the response of the widespread extinction of metazoans and the resulting replacement of skeletal carbonates (e.g. Baud et al. 1997Baud et al. , 2007Kershaw et al. 1999Kershaw et al. , 2002Kershaw et al. , 2007Kershaw et al. , 2011Kershaw et al. , 2012Mata and Bottjer 2012;Forel et al. 2013;Chen et al. 2014;Fang et al. 2017).
In the area south-east of Abadeh, Permian-Triassic boundary sections were described for the first time 50 years ago (Taraz 1969(Taraz , 1971(Taraz , 1973. After these pioneering studies, further monographic articles played an important role in contributing to knowledge of the most severe extinction event in the Phanerozoic (Bando 1979(Bando , 1981Taraz et al. 1981). The sections in the area around Kuh-e-Hambast (= Hambast Range) were intensively investigated to explain in detail external influences like global warming and redox conditions in the ocean. Descriptions of microfacies (e.g. Baud et al. 1997), investigations of sedimentary successions paralleled by mineralogical and geochemical studies (e.g. Heydari et al. 2000) and isotope δ 18 O studies on whole rock carbonates (e.g. Korte et al. 2004a, b) were carried out at the Hambast section.
However, studies related to the macrofossils of these sections had only been conducted for a few groups of invertebrates, for example ammonoids (Bando 1979(Bando , 1981Taraz et al. 1981;Zakharov et al. 2010). Although various groups of fossils are present in a number of horizons, no detailed analysis of the decline of Late Permian biota has been achieved. The sections of the Hambast Range in the Abadeh region consist almost exclusively of carbonates with thin shale deposits deposited at a deeper shelf (Kozur 2007).
Sections at Baghuk Mountain ( Fig. 1), which are located 45 km north-west of Abadeh (Central Iran), represent uninterrupted sedimentary successions across the P-Tr transition Leda 2020). Therefore, studies in this area are of great value for understanding the effects and possible causes of environmental changes during the transition from the Palaeozoic to the Mesozoic. These sections provide the opportunity to study the Wuchiapingian to Dienerian sedimentary succession in terms of lithology, carbonate microfacies, fossil content (particularly ammonoids, bivalves, brachiopods, conodonts, ostracods and microbial deposits) as well as stable isotopes. In the following, we present a detailed investigation of the carbonate microfacies of the Baghuk Mountain section. We aim to decipher (1) biogenic and abiogenic carbonate production in the transition from the Palaeozoic to the Mesozoic, (2) indications of redox conditions in the Late Permian successions and the extinction horizon, (3) the trigger of carbonate formation in the Early Triassic and (4) indications of large-scale sea level changes or subaerial exposure in the study area. This study contributes to the understanding of the timing of the end-Baghuk Mountain is located in Central Iran, 140 km SSEmentological perturbations. Range; 60 km SE of Abadeh). The Late Permian to Early Triassic stratigraphy in this region was first outlined by Taraz (1969Taraz ( , 1974; he divided the Permian sedimentary succession into seven units (named units 1 to 7 in ascending order) and the Early Triassic succession into five units (units a to e). The Permian units were later assigned to three formations (Taraz et al. 1981), the Surmaq, Abadeh and Hambast formations in ascending order. The rock succession in the Hambast Range can serve as a standard for the Central Iranian sections of the Permian-Triassic transition.
Studies on the 18 O/ 16 O ratio of conodont apatite and resulting temperature changes across the Permian-Triassic boundary have been achieved by Chen et al. (2020) and led to the result that the main extinction was triggered by a sudden seawater warming.
These investigations demonstrated that the Late Permian to Early Triassic succession is very similar to the classical sections near Dzhulfa (Azerbaijan) and Julfa (NW Iran). The upper part of the Late Permian carbonate succession, which is equivalent with the Paratirolites Limestone of the Julfa area Gliwa et al. 2020) extends from the Clarkina bachmanni Zone to the Clarkina hauschkei Zone (Fig. 2).
The lithological succession and the environmental conditions of sections in the Hambast Range had been thoroughly investigated, interpreted and discussed by Heydari's working group (Heydari et al. 2000. They described the argillaceous, light grey and bioturbated mudstone of the Late Permian unit 6 and the argillaceous, nodular mudstone and wackestone of unit 7 and proposed a deposition at a water depth between 100 and 200 m. According to their investigations, the latest Permian and earliest Triassic succession consists of three units in ascending order: (1) The lowermost around 1.5 m thick unit is the 'Boundary Clay' (= Baghuk Member) with shales and aggregates of dome-shaped or botryoidal crystals ('calcite  Ghaderi et al. (2014) and Baghuk Mountain after Farshid et al. (2016) and Korn et al. (2021). W = Wuchiapingian fans'), interpreted by Baud et al. (2021) as digitate stromatolites.

Hambast Formation
(2) The overlying unit of 1.5 m thickness is composed of packstone and grainstone with recrystallised grains, probably ooids or peloids. (3) The third Early Triassic, more than 100 m thick, unit is described as thin-bedded, bioturbated to nodular limestone with specimens of Claraia. Heydari et al. (2001) focused on the lithological succession and the δ 13 C carb as well as the δ 18 O signatures of the Hambast section. Subsequently, carbon and strontium isotope geochemistry has been carried out by other research groups (Korte et al. 2004a(Korte et al. , b, 2010Horacek et al. 2007a, b;Richoz et al. 2010;Liu et al. 2013).
Mohtat-Aghai and Vachard (2005) paid attention to the Late Permian to Early Triassic foraminifer biostratigraphy in the Hambast region. They also described various lithological features and concluded that there is a shift from an 'ammonitico rosso' facies to a facies conspicuous for the occurrence of microbialites.

Shahreza
The Permian-Triassic boundary exposure 14.5 km NNE of Shahreza (Fig. 1) shows a succession that is rather similar to the sections in the Hambast Range. The Hambast Formation at Shahreza consists primarily of nodular, often bioturbated limestones which were deposited in deep water below the storm wave. The P-T boundary interval consists of red shale, interpreted as terra rosa, which was formed during subaerial exposure (Heydari et al. 2001(Heydari et al. , 2008. The Late Permian sedimentary rocks are overlain by the Elikah Formation (named Shahreza Formation by Heydari et al. 2008Heydari et al. , 2013, which consists of grainstone, packstone and microbial mounds that may represent a shallow subtidal to intertidal facies. The microbial mounds are composed of radial fans of calcite crystals (Heydari et al. 2008). These authors suggested that the calcite deposits are formed by synsedimentary carbonate precipitation and proposed a model for the lithological change caused by increasing carbonate saturation of seawater. Baud et al. (2007) described branched, thinly laminated microbialites from Shahreza and compared them with Late Proterozoic stromatolites. The 'calcite fans' in the Shahreza section were interpreted by Richoz et al. (2010) as fans precipitated on the sea floor. The conodont zonation in the Shahreza section was outlined in combination with the signatures of δ 13 C carb (Korte et al. 2004a, b;Kozur 2007;Heydari et al. 2008;Richoz et al. 2010;Schobben et al. 2017).

Baghuk Mountain
Permian-Triassic boundary beds at Baghuk Mountain were probably first studied by Ghaedi et al. (2009), who used the name Benarizeh for the section. These authors separated between three biozones, from bottom to top Pseudogastrioceras beds, Paratirolites beds and Claraia beds and correlated them with the succession known from Julfa, Shahreza and Abadeh. Ghaedi et al. (2009) illustrated a microbialite that was regarded as "algal remains".
Late Permian chondrichthyan and actinopterygian fishes from Baghuk Mountain were reported by Hampe et al. (2013). Leda et al. (2014) outlined the lithology and a brief microfacies description of one of the Baghuk Mountain sections and compared the results with sections near Julfa (NW Iran). They focused on the topmost Hambast Formation (Paratirolites Limestone equivalent), the Baghuk Member and the Claraia Beds. Leda et al. (2014) described Early Triassic 'calcite fans' similar to the ones described earlier by Heydari et al. (2008) from Kuh-e-Hambast and Foster et al. (2020) discussed the microbialites of Baghuk Mountain in a global framework.
For the microfacies, we intensely studied two sections at Baghuk Mountain, located about 100 m apart: Baghuk The excellent outcrop conditions at Baghuk Mountain enabled detailed sampling across the Permian-Triassic boundary (Fig. 4). In order to obtain a detailed picture of the various lithological features across the Permian-Triassic boundary, the samples were taken at centimetre range, i.e. with the best possible stratigraphic resolution.
The stratigraphic position of the samples is documented in alignment with the position of the extinction horizon, which is characterised by the sharp contact, visible as a sudden change from reddish nodular limestones to dark-grey shales, between the Hambast-Formation and the Baghuk Member. Samples from above the extinction horizon are marked with a plus prefix ( +), samples from below with a minus prefix (-).
-Above the Hambast Formation follows, with a sharp lithological contact, the approximately two metres thick Baghuk Member. Although this represents the youngest Changhsingian, it already belongs to the Elikah formation. The Baghuk Member reflects the sedimentological and ecological condition immediately after the main extinction pulse. The unit consists of brittle grey shales with so-called 'calcite fans' (digitate stromatolites according to Baud et al., 2021) in the upper part. These calcite structures are embedded in a matrix containing sponge remains. The 'calcite fans' are laminated and show botryoidal and leaf-shaped crystal growth.

Methods
About 140 thin sections were produced in the Museum für Naturkunde Berlin (Germany) and at the Buali-Sina University of Hamedan (Iran)to systematically study the fossil content, non-skeletal grains and sedimentary structures. Additionally more than 90 polished slabs were prepared for the morphological study of the microbialites. The thin sections were used for the microfacies analysis, including the presence and amount of biogens and taphonomic features. A detailed petrographic analysis was achieved with a polarizing microscope of the type Zeiss Axioskop 40 fit with a digital camera (Zeiss AxioCam MRc5) working with Axio Vision LE software.
Identified facies were compared with standard microfacies types (SMF) (e.g. Wilson 1975;Burchette and Wright 1992;Flügel 2013). Depositional environments of the carbonate facies were discussed based on their petrographic characteristics (Flügel 2013). Concerning nomenclature, this paper follows the definitions and descriptions of microbial limestones presented by Shapiro (2000), who used different categories to describe the microbial fabric (mega-, macro-, meso-, and microstructural). We use the term microbialite (Burne and Moore 1987) as an overall term for all microbial structures.
Semi-quantitative analyses of biogen frequencies were performed using comparison tables of Baccelle and Bosellini (1965). We used five degrees of occurrence frequency: absent, extremely rare, infrequent, moderately frequent and frequent. The degree of bioturbation was determined semi-quantitatively according to Reineck (1967), Droser and Bottjer (1986) and Taylor and Goldring (1993). We interpreted the depositional area and palaeoenvironment using the model of the Standard Facies Zone (Wilson 1975;Schlager 2002).

Hambast Formation
Microfacies HF1 -weakly bioturbated ostracod wackestone/packstone (Fig. 6a, b) Occurrence: Most common at the top of the Wuchiapingian and the base of the Changhsingian part of Hambast Formation between -9.90 m and -7.50 m.
Depending on the content of allochems, this microfacies is a mud-supported wackestone or a grain-supported packstone. In both cases it contains abundant well-preserved and also disarticulated thin-shelled ostracod valves without preferred orientation; the percentage of skeletal grains ranges from 10 to 85%. The reddish or greyish matrix is composed of microsparite; it shows diagenetic textures including pressure solution seams as well as calcite veins. Some areas of the matrix are recrystallised; others are affected by iron precipitation. Mainly equigranular, hypidiotopic crystallization fabrics replaced the microsparite matrix. Burrows of various shapes are rare; they are filled with light-grey fine-grained micrite to microsparite without biogenic components. Contacts between burrow margins and the surrounding matrix are either sharp or indistinct. Biogenic components in this facies are crinoid arm plates and other echinoderm fragments with recognisable stereom, calcispheres and radiolarians, partly dissolved fragments of ammonoids and other molluscs. Ostracod valves of sculptured and smooth-shelled species are filled with the surrounding matrix or sparitic cement; nearly all specimens have a similar size (0.5 mm length). A few euhedral mineral grains, probably pyrite and hematite, and extremely rare dark green, subangular crystals, probably chlorite, occur rarely in this microfacies.
The limestone beds possess a conspicuous nodular fabric; the nodules have rounded to irregular outlines and are composed of microsparite. They differ in the lighter colour from the surrounding marly matrix. A few nodules are bordered by pressure solution seams. The microsparite matrix has a grey to conspicuously red colour. Most of the contacts between nodules and shale matrix are indistinct, indicating a formation affected by bioturbation and diagenetic overprint (compare Flügel 2013). An interconnected burrow network is composed of irregular burrows. Biogenic components are sponge spicules, echinoderm remains with preserved stereom, bivalves, ammonoids, brachiopods, ostracods, radiolarians and . a Microfacies HF1: Ostracod wackestone/ packestone dominated by thin-shelled, well-preserved ostracods and disarticulated valves, filled with sparitic cement (o), ammonoid (a) filled with grey muddy matrix, which is grey micritic matrix and small shell fragments, disarticulated bivalve shell (b); -9.90 m. b Microfacies HF1: Ostracod wackestone/packestone with well-preserved smooth-shelled ostracod (o) in a red fine-graind matrix with preservation allowing recognition of the duplicature, echinoderm (e) fragment with stereom preservation; -9.90 m. c Microfacies HF2: Red nodular argillaceous mudstone/wackestone; micritic matrix partly recrystallised and affected by pressure solution. A well-preserved articulated brachiopod (b) filled with fine-grained matrix and filament fragments (f), lunate crinoid arm plates (c) and chlorite crystals (cl); -6.25 m. d Microfacies HF2: Weakly bioturbated red mudstone/wackestone with single rugose solitary coral Pentaphyllum (p) and a subrounded light grey lithoclast (l); -4.80 m. e Microfacies HF3: Partly recrystallised micritic matrix with pseudopeloidal texture, poorly preserved ammonoids (a) and lunate crinoid arm plats (c); -2.45 m. f Microfacies HF3: Grey, partly recrystallised micritic matrix with irregularly shaped lumps of carbonate mud (l), ostracods (o) and echinoderms (e) floating in the matrix; -1.20 m.

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indistinctive shell fragments. The majority of the biogens are small, reaching a size of only 1 mm. The ammonoid conchs are widely dissolved with inner volutions filled with sparitic cement; thin-shelled ostracod valves are filled with matrix or sparitic cement. Diagenetic features are numerous pressure solution seams that generate stylonudular and stylobreccioid structures, calcite veins and microfractures. A rare feature is the occurrence of euhedral opaque mineral grains, presumably pyrite and hematite, as well as dark-green subrounded chlorite grains.
Microfacies HF3 -weakly bioturbated mudstone/ wackestone (Fig. 6e, f) Occurrence: Upper part of the Hambast Formation below the extinction horizon, particularly the top above -0.40 m. Similar facies, however, is present in the upper part of the Hambast Formation beginning at -4.40 m. This microfacies is characterised by a fine-grained micritic to microsparitic matrix, a low bioturbation degree and sparse biogenic content. At a level of -2.45 m, the matrix has a pseudopeloidal texture. The biogenic content of this facies consists of ammonoids, ostracods, crinoids and other echinoderms, radiolarians, bivalves, rare foraminifera and indistinctive shell fragments. Radiolarians of the order Entactinaria can be identified (W. Kiessling, personal comm.) as well as a single rugose coral of the genus Pentaphyllum (D. Weyer, personal comm.). The majority of biogens are poorly preserved, except from few well-preserved crinoid remains. The original aragonite of the ammonoid septa was recrystallised to calcite and the phragmocone chambers were filled with blocky cement. Ostracod valves are filled with matrix or sparite cement, which in some cases show geopetal orientation. Other shells are partially dissolved and affected by dark incrustations. Red to brown subangular lithoclasts are rare. Diagenetic features include single vertical and horizontal cracks filled with micrite and blocky cement. Irregular anastomosing pressure solution sets and bedding-parallel irregularly sutured seams with small to large amplitude are sometimes horsetail-structured. They generated stylomottled pressure solution structures (compare Flügel 2013). Iron dendrites and a few euhedral mineral grains (probably pyrite or hematite) occur frequently.
Components of these microfacies are embedded in a reddish to greyish lime mud matrix, which is partly affected by neomorphism; many widespread Fe dendrites are common. Irregular burrows are rare in this facies; they are filled with the surrounding matrix. The biogenic inventory consists of bivalves, ostracod valves and indistinct shell fragments. Thin-shelled ostracod carapaces are filled with micrite or sparitic cement. Calcite fillings in microcracks and microfractures as well as irregularly anastomosing stylolite sets are common. The heavy mineral content is composed of euhedral pyrite or hematite grains.
Microfacies BM2 -sponge wackestone with 'calcite fans' (Fig. 7b-d) Occurrence: At + 0.55 m and + 0.75 m in section C and irregularly distributed in the Baghuk Member in parallel sections.
This microfacies shows a dense accumulation of sponge spicules and the appearance of 'calcite fans', identified as digitate stromatolite by Baud et al. (2021), in a fine-grained grey to reddish micritic matrix with scattered Fe incrustations. Sponge remains of keratose demosponges occur in different morphologies; they can be identified as monoaxons and triaxons, but there is also a dominant proportion of irregular and unclassifiable remains. Various types of cement growth and cement generations accompany the 'calcite fans'; they occur in stratified and radiaxial fibrous structures, partly growing on top of each other. Diagenetic features include pressure solution seams with a brecciated structure. Individual thin calcite veins penetrate both the digitate stromatolites and the surrounding matrix.

Microfacies BM3 -weakly bioturbated marly siltstone with grey marly nodules
Occurrence: Middle part of the Baghuk Member.
Within the reddish marly matrix of siltstone, the biogenic assemblage is composed of few ammonoids, thin-shelled ostracods and indistinctive shell fragments. The biogenic content of grey marly nodules is made up of sponge spicules, consisting of monoaxons, triaxons, irregular and non-allocate specimens. Few burrows are filled with dark brown micrite, unlike the surrounding matrix. The matrix is affected by small, widespread Fe-dendrites.

Claraia Beds
Microfacies CB1: Laminated wackestone/mudstone with calcite spheres (Fig. 8a) Occurrence: Base of the Claraia Beds at + 2.45 m and + 5.45 m. This facies is characterised by greyish to brown mudstone or wackestone with sparry, neomorphic components. The laminated fabric consists of millimetre-thick lamellae, which differ in their internal composition. Slightly thicker lamellae consist of closely spaced sparry spheres, which vary in size and morphology ranging from irregular to euhedral. In some beds, the calcite spheres are normally graded and cause layers separated by different grain size. Fine-grained components are formed by individual calcite crystals. Coarser components are accumulations of several individual calcite grains or single grains. The lowest layer is separated from the lime mud matrix by the bedding of parallel pressure solution seams. Biogens are rare and consist of few micritefilled ostracod valves and small shell fragments. Swarms of pressure solution seams cross the matrix. Some horsetail structures and calcite veins are visible.
The microfacies shows wispy to broad lamination that is characterised by a colour change form light grey to darker grey. The matrix is fine-crystalline micrite without any grain size change. Some parts of the matrix are recrystallised. Diagenetic features are calcite veins and single stylolites.
The laminated mudstone was deposited in a low-energy environment with quiet water conditions below storm wave base in a restricted marine area.
This facies is a burrowed wackestone with domal, dishshaped microbial overgrowth on bivalve and ammonoid shells. The thin section from + 13.95 m contains a large ammonoid conch as well as thin bivalve shells with layered microbial overgrowth. The aragonitic ammonoid shell is completely neomorphosed; the initial whorls as well as part of the outer chambers are filled with blocky sparite; other parts of the   .1 mm). a Microfacies CB1 Greyish to brown mudstone to wackestone with calcite spheres (e) and recrystallised, restored components (c), laminated fabric of millimetre-thick laminae that differ in their internal composition, fine-grained components formed by single calcite crystals, coarser components are accumulations of several single calcite (arrow) grains or single grains; + 5.45 m. b Microfacies CB2: Laminated mudstone without any biogens, matrix partly recrystallised; + 48.00 m. c Microfacies CB3: Burrowed wackestone with microbial overgrowth. An ammo-noid conch (a) with phragmocone filled with blocky sparite and body chamber filled with micritic matrix, thin bivalve shells (b) with layered microbial overgrowth (m) and numerous gastropod shells (g); + 13.95 m. d Microfacies CB3: detail of c) with brownish bivalve shells (b) and small gastropods (g), single sponge spicules (s) float in the matrix; + 13.95 m. e Microfacies CB4: red sponge wackestone with small, thin, densely packed sponge spicules, various morphologies of keratose demosponge remains (monoaxons and triaxons) (s) in micritic matrix, furthermore gastropods (g), bivalves (b) and ostracods (o), burrows partly recrystallised; + 10.50 m. f Microfacies CB4: sponge wackestone with widespread sponge remains (s); + 14.80 m Microfacies CB4 -sponge wackestone/packstone (Fig. 8e, f) Occurrence: Claraia Beds between + 10.50 m and + 13.60 m. This facies is characterised by a reddish fine-grained micritic matrix with a dense accumulation of sponge spicules with various morphological features (keratose demosponges); the sponge spicules are monoaxons and triaxons and a dominant proportion of irregular and nonallocateable remains. The sponge remains range, in their morphology, from small, thin densely packed spicules to big, broad and widespread clusters. The amorphous silica of the spicules has been completely replaced by calcite, so that they are preserved as calcite pseudomorphs .
The microbialites at Baghuk Mountain are diverse in scale, external morphology and internal structure (Fig. 9). Three macroscopic morphotypes are distinguished here: (1) dome-shaped, conical and/or bulbous in shape with protuberance on top and round to ellipsoid form, (2) planar and lens-to dome-shaped with protuberance on top and (3) clubshaped and mushroom-shaped, inverted conical structures with dished upper surface. Common mesostructures are dendrolite (dendritic), stromatolite (laminated), thrombolite (clotted) or leiolite (structureless, aphanitic). Club-shaped microbialites were regularly growing on bivalve or ammonoid shells as solitary structures or small communities. Thin section investigation reveals that various microbialites are accompanied with keratose demosponges.

Hambast Formation
The microfacies analysis of the top 10 m of the Late Permian Hambast-Formation enables a reconstruction of the latest Wuchiapingian and Changhsingian carbonate environment of the time before the main extinction pulse. Both the biogenic content and the degree of bioturbation provide information about the likely oxygen supply to the seafloor (Fig. 10, 11).
The sediments of the Wuchiapingian-Changhsingian boundary interval (-9.90 m to -7.50 m) contain mostly benthic organisms and show little evidence of bioturbation. Radiolarians, echinoderms and cephalopods indicate a fully marine, normal saline environment. The high proportion of non-oriented ostracods and the bimodal ratio of complete shells and single disarticulated valves may indicate deposition in an episodic high-energy environment. Similar timeequivalent deposits with mass occurrences of ostracods are already known from Ali Bashi near Julfa in NW Iran (Baud 2008;Leda et al. 2014).
The Changhsingian record from our sampled sections contains mainly benthic organisms, occurring in ostracod packstone, non-fossiliferous mudstone and sparse to moderately bioturbated mudstone to wackestone. They reflect a mixed benthic and pelagic assemblage (ammonoids, ostracods, foraminifers, echinoderms, radiolarians, bivalves, sponges). A nodular mudstone to wackestone facies is present between -7.55 m and -5.95 m. It is the most common lithology in the upper part of the Hambast Formation and has already been described from several Late Permian sections in Central Iran (e.g. Taraz et al. 1981;Heydari et al. 2000Mohtat-Aghai and Vachard 2005;Leda et al. 2014) as well as from time equivalent sections in the Julfa area (e.g. Stepanov et al. 1969;Teichert et al. 1973;Leda et al. 2014;Gliwa et al. 2020). The biogenic content of a mixed benthic and pelagic community speaks for a well-oxygenated environment. In contrast to Taraz et al. (1981), who proposed a lagoonal environment for these deposits, we agree with Heydari et al. (2000),  and Leda et al. (2014) and Gliwa et al. (2020), who interpreted the depositional environment as deep shelf setting below the storm wave base.
This nodular facies resembles the so-called Griotte Limestone of the Devonian and Carboniferous (e.g. Tucker 1974;Wendt and Aigner 1985;Baud and Richoz 2019) and the Jurassic Alpine-Mediterranean Ammonitico Rosso facies, which describe reddish to grey, nodular pelagic limestone formations with abundant ammonoids (e.g. Aubouin 1964; Garrison and Fischer 1969;Jenkyns 1991;Cecca et al. 1992;Mohtat Aghai et al. 2009). Mohtat Aghai et al. (2009) associated this facies with a decrease of CaCO 3 sedimentation and reduced oceanic circulation. Noble and Howells (1974) and Jenkyns (1991) postulated that the formation of the nodules is an early diagenetic process. Jenkyns (1991) suggested a rhythmic formation of the nodules based on dissolution of aragonite, leading to high carbonate concentrations at the sediment-water interface. According to this interpretation, the nodules were cemented directly below the sediment surface; they might have grown from skeletal calcite and micrite intraclasts, which acted as nuclei. Mamet and Préat (2006) discussed three formation scenarios for the red pigmentation of this facies. They concluded that the red colour is induced by oxidising iron microbes in a poorly oxygenated environment. In contrast, , Kozur (2007) and Leda et al. (2014) postulated that the reddish nodular limestone originated in a well-oxygenated environment, indicated by the specific biogenic content (e.g. ostracods) as well as the high bioturbation activity.
No evidence for discontinuity surfaces was seen throughout the entire Late Permian succession and therefore no break in sedimentation or deposition is recorded. Typical indicators like hardgrounds are missing.
The biogenic content and bioturbation of the Hambast Formation show a change from a predominantly benthic community with ostracods and echinoderms and only a few pelagic organisms (ammonoids and radiolarians) to a balanced mixed benthic and pelagic community (Fig. 10).
Ostracods and undifferentiated shell fragments are generally the most common bioclasts in the upper part of the Hambast Formation. The radiolarians show frequency fluctuations throughout the Changhsingian samples; they have already been described from time-equivalent strata of the Canadian Arctic and South China (Beauchamp and Baud 2002;Isozaki et al. 2007). Radiolarians are frequent in the interval between -9.90 m and -5.95 m and less common between -5.95 m and -2.00 m. In the topmost two metres of the Hambast Formation, they occur  Fig. 9a; + 8.55 m. d Thin section of planar microbialites growing on bivalve shells; the surrounding matrix contains a high accumulation of sponge spicules; + 8.70 m almost continuously in mass occurrences. Beauchamp and Baud (2002) suggested a collapse of biogenic silica production and a disappearance of radiolarians, caused by an assumed rapid warming during the last Permian. Temperature changes as well as redox and alkalinity changes together with nutrient deficiency were considered as possible causes for the reduction of carbonatestabilising benthic/nektonic and silicic silica-stabilising plankton (Isozaki et al. 2007). The occurrence of the pelagic community terminates 0.05 m below the extinction horizon; only ostracod valves and a mass occurrence of small ammonoids are recorded here.
The degree of bioturbation varies constantly between sparse and moderate in the upper part of the Hambast Formation ( Fig. 11) with decreasing bioturbation and biogenic content immediately below the extinction horizon. Burrows are usually isolated and overlaps are rare. Using the index by Droser and Bottjer (1986), 10-40% of the sediment is affected by bioturbation. As the investigated succession of the Hambast Formation is characterised by rich benthic and pelagic assemblages and frequent bioturbation, we suggests a well-oxygenated environment for this interval.

Baghuk Member
The facies of the approximately two metres thick event interval represent the deposition conditions immediately after the main extinction pulse. In general, the Baghuk Member is separated from the carbonate-dominated Hambast-Formation by a sharp lithological contact caused by interrupted carbonate production. Limestone beds occur only occasionally in the Baghuk Member (Fig. 5). This facies was likely deposited in a low-energy environment with calm water conditions below the storm wave base (Mohtat Aghai et al. 2009;Leda et al. 2014).
Section C contains 'calcite fans' embedded in a matrix full of sponge spicules (at + 0.55 m and + 0.75 m). Timeequivalent structures are known from the Hambast sections and were first named 'colonial limestones' by Taraz  (1981) and later named'calcite fans ' by . Very similar calcite precipitates were already described, apart from sections in Central Iran, from Turkey and Armenia (Baud et al. 2007;Kershaw et al. 2012;Heindel et al. 2015;Friesenbichler 2016;Friesenbichler et al. 2018). Kershaw et al. (2012) interpreted such 'calcite fans' in the Hambast Range as crystal fans that grew on thinly laminated stromatolites. Recently, Baud et al. (2021) interpreted them as digitate stromatolites. The 'calcite fan' formation was interpreted to have been caused by the dissolution of Ca 2+ and HCO 3 − in seawater, which led to carbonate precipitation or degassing of CO 2 and consequently to a decrease in oceanic carbonate solubility (Woods et al. 1999(Woods et al. , 2007Pruss and Bottjer 2004;Pruss et al. 2006). Woods et al. (1999) proposed a model in which a mixture of deep, anoxic, highly alkaline water and surface water favours the formation of seafloor cements and that this mixing leads to CO 2 degassing and carbonate supersaturation with CaCO 3 .
The study by Friesenbichler (2016) of sections in Armenia dealt with the growth conditions of similar 'calcite fans' and their relationship to the surrounding sediment, as well as with the relationship between the occurrence of 'calcite fans' and sponges. She interpreted the asymmetric growth of the 'calcite fans' as being caused by steady bottom currents; this led to the assumption that they were formed on the sediment and not in the sediment (Friesenbichler 2016;Friesenbichler et al. 2018). In contrast, Heindel et al. (2015) preferred the displacement growth of crystals, which pushed away the surrounding sediment. This type of growth was neither found in the Armenian sections studied by Friesenbichler (2016) nor at Baghuk Mountain. Friesenbichler (2016) and Friesenbichler et al. (2018) assumed that 'calcite fans' grew before the sponge remains deposited. The sponge spicules fit to the crystal margins; they used the available space between the crystals and adapted their morphology.
Compared to the underlying Hambast-Formation, the biogenic content of the Baghuk Member is extremely low. Only in section C, few ammonoids, ostracods, echinoderms and bivalves were found at + 0.02 m, whereas sponges are conspicuously frequent. Bioturbation is also extremely sparse in the first few centimetres and disappears in the Baghuk Member.

Claraia Beds
The Early Triassic Claraia Beds begin above the Baghuk Member with a laminated wackestone that contains abundant calcite aggregates. This type of wackestone, which occurs at + 2.45 m and + 5.45 m (Fig. 8a), was already described by Richoz et al. (2010) from the Zal section and by Leda et al. (2014) from Ali Bashi in NW Iran. Both articles described them as seafloor cement crusts of sparse calcite spheres. The origin of these calcite spheres is still unknown; they are somewhat similar to those of tew same age found in deep water limestone from Oman ). The moderately bioturbated mudstone above is characteristic for sedimentation conditions below the storm wave base. At + 8.00 m the first microbial structures appear as overgrowth on ammonoid and bivalve shells; presumably the shells were used as a hard substrate for the growth of the microbial structures. Microbialites occur in a number of beds (at + 7 to + 10 m, + 14 m and + 19.70 m) in Baghuk Mountain Section C (Fig. 5).
Early Triassic microbial deposits have been described from many regions and with varying morphological richness, but the environmental conditions for the growth of these structures are not yet fully understood. Various  hypotheses involving geochemical changes in seawater leading to carbonate factory alteration or atmospheric changes have already been postulated (e.g. Baud et al. 1997Baud et al. , 2007Kershaw et al. 1999;Riding 2000;Kershaw et al. 2002Kershaw et al. , 2007Kershaw et al. , 2011Kershaw et al. , 2012Ezaki et al. 2003Ezaki et al. , 2008Pruss et al. 2006;Richoz et al. 2010;Yang et al. 2011;Tian et al. 2014;Zheng et al. 2016;Fang et al. 2017;Wu et al. 2017). Taraz et al. (1981) were the first to mention stromatolitic deposits in Early Triassic sections near Abadeh and interpreted them as thrombolites. These authors suggested a calm intertidal or subtidal depositional milieu for the stromatolite formation.
Apparently, all microbialites at Baghuk Mountain are accompanied by sponge spicules, which have been identified as keratose demosponges. Between the microbial horizons, wackestone to packstone with sponge spicules also occur without any microbial structure. This spiculite microfacies is typical of basal or deeper shelf environments (Flügel 2013, p. 682). Leda et al. (2014) described a sponge packstone in the Julfa sections (NW Iran) and postulated a deep carbonate shelf.
The biogenic content of the Early Triassic deposits immediately above the Baghuk Member is extremely low. The first occurrence of ostracods was recorded at + 3.60 m. Up to + 8.00 m only rare gastropods, ostracods and echinoderms occur, followed by mass occurrences of sponge spicules between + 9.00 m and + 10.00 m. In the Early Triassic interval from + 13.60 m to + 13.95 m sponges, foraminifers, ammonoids, ostracods, gastropods and echinoderms have their first co-occurrences.
The first sign of bioturbation is recorded at + 3.60 m (Fig. 11). Bioturbation occurs only in facies with microbial growth, whereas facies with individual micro-organisms do not contain bioturbation.

Discussion
Sea-level changes across the Permian-Triassic boundary  postulated a significant sea-level drop at the end of the Permian for sections near Abadeh, followed by a rapid rise in the Early Triassic. The Early Triassic carbonates were there interpreted as shallow water deposits. Our microfacies analysis of the Baghuk Mountain sections show that the depositional environment of the entire section across the Permian-Triassic boundary shows no evidence of large-scale sea level changes or even subaerial exposure. With a few exceptions, the deposition probably took place on a deep shelf below the storm wave base. Richoz et al. (2010) and Leda et al. (2014) already identified such conditions in sections near Julfa (NW Iran). The Late Permian Hambast Formation including the Paratirolites Limestone equivalent at Baghuk Mountain is characterised by a typical deep shelf facies with benthic and pelagic assemblages. We agree with other authors that the Late Permian nodular facies were deposited in a deep shelf below the storm wave base (Heydari et al. 2000Leda et al. 2014).
The marly facies of the Baghuk Member also does not show any indications for a sea-level drop, such as vadose meteoric cement types or palaeokarst. Sections in Julfa (NW-Iran) show a similar conditions without sedimentological evidence of large-scale sea-level changes at the Permian-Triassic boundary like other sections (Richoz et al. 2010).
Early Triassic microorganisms can provide an indication of shallowing after the extinction event. This coincides with the occurrence of large bivalves in chaotic position (mixed convex up and down) in some of the strata 8-9 m above the extinxtion horizon at Baghuk Mountain (Fig. 9d). These possible storm beds, which occur in immediate vicinity of microbiatites, may indicate episodic shallowing.
Carbonate production and ocean chemistry At Baghuk Mountain, the biogen-dominated Permian carbonate factory was interrupted at the time of the end-Permian mass extinction, which is indicated by a sharp contact between the Hambast Formation and the Baghuk Member. The Baghuk Member is characterised by clay and/or silt deposits and few carbonate horizons. The synsedimentary carbonate precipitations were interpreted to be caused by a transition from biochemical to inorganic chemical carbonate production . Heydari et al. (2008) postulated that a decrease in oceanic pH and an increase in seafloor carbonate saturation causes the change in carbonate production. This geochemical change is also supported by boron isotope records from sections in the Dolomites, indicating an acidification event at the extinction horizon (Jurikova et al. 2020). Furthermore, Heydari et al. (2008) recorded a mineralogical change from primary calcite in the Late Permian to aragonite after the mass extinction event and during the Early Triassic.

Conclusions
The investigation of the lithology and microfacies of the Permian-Triassic boundary section at Baghuk Mountain (Central Iran) led to the following results: -In line with neighbouring sections near Shahreza and Abadeh, the sections of Baghuk Mountain consist of three lithostratigraphic units, in ascending order the Late Permian Hambast-Formation, the Baghuk Member of the latest Permian and the Early Triassic Claraia Beds. The latter two compose the Elikah Formation. -The main Permian-Triassic extinction pulse has a position at the sharp lithological contact between the carbonate-dominated Hambast Formation and the shale and 1 3 marl-dominated Baghuk Member. It exactly coincides with the decease of the Late Permian carbonate factory. -Changes in microfacies across the Permian-Triassic boundary in sections at Baghuk Mountain provide evidence for a change from Late Permian skeletal carbonate production to to a non-skeletal carbonate production in the Early Triassic. -The upper ten metres of the Hambast Formation up to the Baghuk Member are strongly influenced by bioturbation, which suggests a well-oxygenated environment. The Baghuk Member shows no indications for bioturbation or relicts of benthic communities. -In the Early Triassic, carbonate production was episodically induced by microbes and led to the formation of microbialites. The frequency of these microbial structures in the study area is remarkable. -The carbonate deposition at Baghuk Mountain suggests a deep shelf environment, mostly below storm wave base. There is no evidence for a large scale sea-level change or subaerial exposure during the Permian-Triassic succession at Baghuk Mountain. During the Early Triassic, occasional shallowing led to tempestitic deposition of biogenes such as Claraia valves.

Conflict of Interest
The authors declare that they have no conflict of interest.
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