Taphonomic differentiation of Oxfordian ammonites from the Cracow Upland, Poland

Taphonomic analysis of Lower and Middle Oxfordian ammonites from the Cracow Upland, southern Poland (localities at Podłęże, Zalas, Młynka) revealed differences in ammonite preservation. The studied ammonites, usually termed as external and internal moulds, show a more complex state of preservation. In the Middle Oxfordian glauconitic marls, ammonites are preserved as internal moulds with neomorphic calcite shells showing relics of the original internal structure. In the Middle Oxfordian platy peloidal limestones, ammonites are preserved mostly as external moulds, without septal suture, however under microscope might show relics of internal whorls and septa and/or subtle differences in sediment filling phragmocone chambers. In sponge–microbial bioherms and biostromes, ammonite internal moulds have shells, which in contrast to ammonites from glauconitic marls are not strictly neomorphic ones, but originated by shell dissolution and subsequent filling of moldic porosity by calcite cement. In sponge–microbial nodular limestones, the ammonites are strongly deformed and the outer wall is usually removed by dissolution under pressure. Other important taphonomic differences include the rate of compaction (highest in platy limestones), sedimentary infillings, microborings, encrustations and preservation of siphuncular tubes. The majority of the ammonites appear to be phragmocones; aptychi in all facies are rare. Siphuncular tubes are fossilized exclusively in oppeliids, only in specimens from glauconitic marls and platy limestones, although their other taphonomic attributes are different. Tubes seem to have fossilized due to microbially mediated phosphatization that could be favoured by a set of parameters which operated rather at the scale of ammonoid carcasses: closed, poorly oxygenated conditions, and reduced pH. Taphonomic processes were controlled by the sedimentary environment (fragmentation, sedimentary filling, phosphatization of siphuncular tubes), as well as by early and late diagenesis (neomorphic transformation, dissolution, cementation, compaction) influenced by lithology.


Introduction
Research in taphonomy has increased significantly in recent years and has demonstrated its usefulness in deciphering biostratinomic (pre-burial) and diagenetic history of subfossil and fossil biota (Brett and Baird 1986;Speyer and Brett 1988;Behrensmeyer et al. 2000;Allison and Bottjer 2011, and references therein).
This paper presents results from taphonomic studies of ammonites from the main lithofacies of the Lower and Middle Oxfordian of the southern part of the Cracow (Kraków) Upland. Ammonites from analysed sediments have been termed in the biostratigraphic papers as internal and external moulds. However, detailed studies revealed that preservation of these ammonites shows more complex modes (Jurkowska 2008).

Geological setting
The studied material comes from the Lower and Middle Oxfordian rocks from the Cracow Upland, which is the southern part of the Polish Jura Chain (Fig. 1). This unit belongs to the Silesian-Cracow Monocline slightly inclined to ENE. Oxfordian limestones and marls (up to 250 m in Cracow region), including well-outcropped sponge-microbial buildups (sponge megafacies), were developed on the northern Tethyan shelf. They usually cover Callovian siliciclastics, marls and limestones. The uppermost Callovianlowermost Oxfordian interval is condensed and contains reelaborated ammonites (Gi_ zejewska and Wieczorek 1977;Matyja and Tarkowski 1981;Ogg et al. 1991;Dembicz and Praszkier 2007).

Materials and methods
The studied Lower and Middle Oxfordian ammonites come from three localities west of Cracow, namely Podłę _ ze, Młynka and Zalas (Fig. 1).
The Upper Jurassic profile begins with the Lower Oxfordian Mariae zone developed as white, marly limestones with abundant ammonites, belemnites and sponges (Gi_ zejewska and Wieczorek 1977;Hoffmann 1983). The studied ammonites are mostly from Hoffmann's (1983) collection, housed at the Institute of Geological Sciences, Jagiellonian University. They come from two levels of Middle Oxfordian glauconitic marls, at present poorly exposed. Hoffmann (1983) attributed these marls to the lower part of the Antecedens zone. Hoffmann (1983) found some biostratigraphic gaps, however according to Kin (2008) it is possible to distinguish there the Paturattensis, Ouatius and Arkelli subzones. The profile ends with the lower part of Transversarium zones represented by platy limestones (Hoffmann 1983;Kin 2008).
During the fieldwork about 300 specimens were collected; another 40 came from the museum collection. They were analysed on natural and cut surfaces, and 65 thin sections were analysed by binocular and petrographic microscopes. Fifteen thin sections were observed by scanning electron microscope (SEM, Hitachi S-4700). In the framework of cathodoluminescence (CL) studies of Oxfordian deposits , also five thin sections with ammonites were analysed with Carl Zeiss Jena long-distance petrographical microscope (JENAPOL 1.4/910) with a Cambridge Image Technology (CITL) 8,300 Mk III cold cathode instrument.  Matyja and Tarkowski 1981;modified and simplified). c Młynka (biostratigraphy after Głowniak and Matyja 2006). Numbers 1 to

Ammonoid preservation
Five main facies were studied in terms of ammonoid occurrence (relative abundance of specimens) and preservation style: general type of shell preservation (type of mould, type of diagenetically altered shell), sedimentary filling of shells, presence or lack of encrustations and microborings, preservation of siphuncular tube, fragmentation, compaction and other deformations. In all studied facies the majority of the ammonites appear to be phragmocones, aptychi being rare.
Glauconitic marls (Podłę _ ze) (Figs. 3,8c,d) Ammonites are abundant, represented mostly by Perisphinctidae, Oppeliidae and rare Cardioceratidae (Hoffmann 1983;Kin 2008). Ammonites attain diameters of up to 25 cm. Because the present state of outcrops is poor, and because most of the specimens studied by us from museum are devoid of surrounding deposit, some information below dealing with macroscopic features of ammonites and host deposits are taken from Hoffmann (1983). The specimens available to us were well preserved, but Hoffmann (1983) has recognized that ammonites are commonly compacted, and large forms are usually fragmented, while small ones are well preserved. Ammonites are preserved as internal moulds with neomorphic calcite shells. Sediment filling chambers is similar to the host sediment. Ammonites are associated with numerous belemnites, less commonly brachiopods, bivalves, sponges and single gastropods (Hoffmann 1983). Glauconitic marls analysed in thin sections are mostly peloidal wackestones with abundant planktonic foraminifera, visible mostly under CL microscope . Other foraminifera and sponge spicules occur rarely. Microbial crusts are absent on ammonite shells, or, if present, microbial crusts with poorly defined lamination occur on single ( Fig. 3a) or both sides of specimens. Hoffmann (1983) observed microbial encrustations, mostly on specimens from the upper part of the analysed marls. Some ammonites were also encrusted on both sides by serpulids and bryozoans. Two specimens from Hoffmann's collection are clearly corroded on one side (Fig. 3b). No microbialites were found within ammonite shells, except for well-developed dendritic microbial structures (Frutexites Maslov) recognized in two chambers of two specimens (Fig. 3c). The first chamber was partly filled with peloidal wackestone. In the second one Frutexites was embedded in matrix. About 40 % of shells contain sparfilled chambers, but rarely more than 1/4 of chambers in one phragmocone. The cement consists of three or two generations. Usually thin coating of siliceous cement occurs as the first generation. Two other generations consist of radiaxial and blocky calcite (Fig. 3f, h). Geopetal structures were also recognized.
The neomorphic calcite shells show relics of the original structure ( Fig. 3d, e, g). Double-layer shell structure unequivocally indicates that the shells were not dissolved as observed commonly in other facies, but are built by neomorphic calcite spar. Locally, the shell shows microlamination (Fig. 3g). Usually the calcite crystals building the septa differ from those in the wall (Fig. 3f), but still in some of septa there are relics of their original structure (Fig. 3g). This indicates that at least some, if not most, septa were not dissolved, but aragonite has been transformed neomorphically into calcite. Very rare and only some skeletal elements were locally dissolved, and moldic porosity was filled with micrite. Siliceous cement usually occurs as the first cement generation (if there is no sedimentary filling), but ammonite shells are very rarely, and only locally, silicified. Clear differences in wall ornamentation were observed in some ammonites. Inner surface of wall of outer whorls reveals ''smoothed'' ornamentation (Fig. 3d,e). Under CL, ammonite shells show bright redorange luminescence.
Phosphatized siphonal tubes were recognized in 15 specimens of oppeliids from Podłę _ ze and Młynka. They were attached to the wall or fragmented (Fig. 8c). SEM observations of seven tubes (including those from Młynka) revealed hollow globules (bacterial structures?) within and on the outer surface of three tubes (Jurkowska 2008) (Fig. 8d). Energy-dispersive spectroscopy (EDS) analyses revealed that tubes are composed of francolite (calcium phosphate).
Platy limestones (Młynka) (Figs. 4,8a,b) Ammonites are represented mostly by Perisphinctidae and rare Taramelliceratidae (Głowniak and Matyja 2006). Ammonites attain diameters up to 100 cm. Based on macroscopic observations of the outer surface of ammonites (easily extracted from the host sediment), they appear to be preserved as external moulds, because the skeletal elements, wall and septal suture are absent (Fig. 4a). However, observations of cut specimens and thin sections indicate that some ammonites revealed relics of walls of inner whorls (Fig. 4b) and even suture line. These relicscalcite cement filling dissolved skeletal element-are not well recognizable as in sponge-microbial limestones. More detailed microscopic studies are required to estimate the abundance of shell relics. Moreover, subtle differences in sediment filling phragmocone chambers indicate the previous location of skeletal elements in some specimens (Fig. 4d). Sediment filling-peloidal wackestone to packstone with fine bioclasts-shows similarities to the host sediment, or grains are slightly smaller (Fig. 4c, d).
No empty chambers or chambers filled only with calcite spar were observed.
Most of ammonites appear to occur parallel to bedding. Chaotic concentrations of small ammonites (up to 5 cm) or their remains (also fragmented larger forms) were observed locally (Fig. 4f). However, no reelaborated (sensu Fernández-López 2007, i.e. exhumed and displaced) ammonites were recognized. Ammonites from platy limestones show the highest degree of compaction (Fig. 4e). Some ammonites are visible within the rock only because of the fossilized siphuncular tubes (Fig. 8a). Similarly, as in glauconitic marls, phosphatized siphuncular tubes occur only in the specimens from the family Oppeliidae. They are common, non-fragmented or fragmented and scattered within the chamber. Most of siphuncular tubes are compressed, with crack along the middle part (Fig. 8b), but some are still round in the transverse section.
In contrast to the Lower Oxfordian grey marls, the marly intercalations within platy limestones do not contain ammonites; however, sampling from these marls is difficult.
Sponge-microbial bioherms and biostromes (Młynka, Zalas) (Fig. 5) Ammonites are dominated by the perisphinctids, which attain diameters of 2-20 cm. Domination of small forms may be a sampling effect: finding large ammonites is more difficult in hard rocks than in platy limestones or marls. The top parts of some bioherms are covered by accumulations of small (up to 3 cm) ammonites (Hoffmann and Matyszkiewicz 1989). Macroscopic observations of rock slabs and analysis of thin sections revealed the presence of abraded and fragmented ammonites (Fig. 5b). Such ammonites are relatively rare within biostromes in Zalas, but more common in bioherms and particularly associated with them detrital limestones in Młynka, where ammonite fragments occur mostly within clasts of eroded bioherms.
Ammonites strongly embedded in hard limestone are internal moulds with shells preserved by calcite cement (no clear evidence for the presence of pseudosparite) filling moldic porosity (moldic shell) (Fig. 5c). Thinning of shell whorls occur locally (Fig. 5e). Ammonite shells are dull in CL view. Ammonites are commonly encrusted by microbialites, mostly micropeloidal or peloidal-agglutinated laminated crusts, and by nubecularid foraminifera (Fig. 5c), serpulids, T. lapilloides and rarely bryozoans. External wall may contain abundant microborings (Fig. 5d). Apart from microbialites, sedimentary matrix within sponge-microbial limestones is peloidal-bioclastic packstone to grainstone. Similar sediment, and microbialites, occur within phragmocone chambers. The calcite cement within some inner ammonite chambers clearly differs from those occurring in glauconitic marls, because only blocky spar occurs (Fig. 5a), and siliceous cement is rare. Shells completely filled only with cement were not found, and empty chambers occur sporadically (Fig. 5f).
Sponge-microbial nodular limestones (Zalas) (Fig. 6) Ammonites are represented mostly by Perisphinctidae, and attain diameters up to 12 cm. Creamy-reddish nodules commonly developed around sponges, and ammonites are surrounded by more marly and more reddish sediment (Fig. 6a). Ammonites are preserved as internal moulds with diagenetically altered shell. Commonly, some parts of walls and septa, particularly external wall, are removed (dissolved), thinned or disturbed (continuously or not) ( Fig. 6b-d). Surrounding sediment matrix contains more bioclasts than sediment within ammonite chambers. Microbialites occur both on ammonites and within shell chambers.

Discussion
Ammonoid occurrences and their preservation traits were controlled by both palaeoecological and taphonomic processes. Differences in relative abundance, taxonomy and size between the Lower and Middle Oxfordian ammonites are palaeobiogeographical results of ammonite temporal incursions from Boreal and Mediterranean Provinces into the area of the Polish epicratonic basin (e.g. Głowniak 2006). Abundant occurrence of ammonite shells and complete, non-hollow concretionary internal moulds in the Lower Oxfordian grey marls are related to sedimentological condensation. This phenomenon is linked with a well-known global crisis in carbonate sedimentation during the Late Callovian and Early Oxfordian. In the Cracow region this condensation persisted locally until the lower part of the Middle Oxfordian, which was possibly related to synsedimentary tectonics  . As discussed below, differential preservation of the studied specimens from five facies reflects mainly various parameters of the depositional environment: type and rate of sedimentation, hydrodynamics, oxygenation, microbial activity, timing of dissolution and cementation. These parameters are controlled biostratinomically, as well as by early and late diagenetic processes (Fig. 8).

Preservation of ammonite shells
Moderately low sedimentation rate of platy limestones, and particularly of grey marls, as well as slow cementation resulted in complete sedimentary filling of ammonite shells, without empty chambers or chambers filled only with cement. Domination of external moulds and high compaction of ammonites from platy limestones indicate slow cementation (cf. Seilacher et al. 1976). Ichnological analysis of platy limestones, including those from Młynka, revealed trace fossils typical for soft bottom, as well as those produced by late burrowers in firm sediment (Hoffmann and Uchman 1992). Local concentrations of small ammonites and/or fragments of large ammonites suggest high-energy events. Early partial dissolution of shells might made them more vulnerable to fragmentation even by poor currents or burrowing organisms. According to Hoffmann and Uchman (1992), trace fossils preserved in platy limestones were produced by deep-burrowing organisms, whereas shallower burrows were obliterated by intensive infaunal activity at the near-bottom layer. Shell fragments can also represent so-called kitchen middens (cf. Radwańska and Radwański 2004). Differences in sediment filling (even subtle) in some ammonites from platy limestones indicate that dissolution of walls of inner whorls occurred after sedimentary filling. Sedimentary differences are more commonly recognizable between whorls than between phragmocone chambers. In such specimens, septa have been dissolved earlier, in preburial stage, forming in result hollow phragmocones (shells without septa; sensu Seilacher et al. 1976).
Ammonites from glauconitic marls (Podłę _ ze) show differences in terms of compaction. The well-preserved, poorly compacted specimens from the museum collection indicate early lithification producing concretionary moulds. Some ''closed'' chambers remained empty until filled by cement during subsequent diagenetic stages. The presence of microbial crusts on some ammonites, as well as Frutexites structures within some chambers, suggest that lithification, at least partially, was microbially mediated. Frutexites microbial structure is known from deep-water stromatolites or cryptic habitats (Böhm and Brachert 1993). Changes in the rate of sedimentary accumulation and lithification may be inferred by the presence of strongly flattened ammonites too (Hoffmann 1983). Low rate of sedimentation of glauconite marls apart from stratigraphic condensation (Hoffmann 1983) is supported by the occurrence of microbial crusts and corrosion observed on one side of some ammonite shells. On the other hand, encrustations on both sides of some ammonites imply changes in hydrodynamics or activity of burrowing organisms. Because the museum ammonite collection from Podłę _ ze contains mainly well-preserved specimens, deciphering of depositional dynamics is not possible without precise sampling in new outcrops.
Microbial contribution to formation and early cementation of bioherms and biostromes (Młynka, Zalas) resulted in other ammonite taphonomic attributes in comparison with glauconitic marls. Although poorly compacted, the ammonites from sponge-microbial limestones can be deformed due to diagenetic dissolution. In particular, ammonites from sponge-microbial nodular limestones are strongly deformed and the external shell wall is commonly removed by dissolution under pressure. Late(?) diagenetic dissolution under pressure is also responsible for formation of nodules around ammonite shells and sponges. Nodular appearance of some sponge-microbial limestones, their reddish coloration and taphonomic features of ammonites may be related to diagenetic processes due to tectonics.
Ammonites from grey marls are poorly compacted, but numerous specimens show continuous and discontinuous deformations. The lack of ammonites in marly intercalations within platy limestones can be due to a decrease of carbonate production and enhanced clay input during a transient sea-level fall (cf. Pittet et al. 2000) or alternatively due to dissolution of aragonitic shells before infilling by sediment (e.g. Wright et al. 2003). Limestone-marl alternations may reflect differential diagenesis: aragonite dissolution in marly interlayers and cementation in limestone beds (e.g. Westphal et al. 2008). To decipher the environmental control or diagenetic overprint on fossil record, more extensive sampling from thin marly intercalations is required to make quantitative estimations of originally calcitic and aragonitic fossils.
Only ammonites from glauconitic marls contain neomorphic shells, i.e. shells which were not dissolved, but only affected by transformation from aragonite to calcite and recrystallization. These shells are hard to recognize macroscopically, therefore ammonites from these deposits were called moulds (Hoffmann 1983). Due to differences in original microstructures, as well as in the thickness of wall and septa, their original internal structure is better recognizable within wall than septa. The problem arises whether the calcite crystals in septa are pseudosparite or calcite cement. We suppose that most of skeletons were diagenetically transformed to neomorphic calcite, but it cannot be excluded that some skeletal parts, particularly septa, were preferentially dissolved. By contrast ''diagenetic shells'' of ammonites from other facies are built by calcite sparite cement, without evidence for neomorphic transformation. The means by which neomorphic shells occur only in glauconitic marls remain unclear. Some authors noticed that aragonitic or neomorphic calcite shells of ammonites are preserved when encrusted by stromatolites (Pallini et al. 2003(Pallini et al. -2004Myczyński and Jach 2009), which is the case of only some of ammonites from Podłę _ ze. Our observations revealed that using the term ''external mould'' may pose problems without thin-section analysis. Ammonites that, based on macroscopic observations, are termed as ''external moulds'' (walls and suture line not visible) may reveal under a microscope relics of diagenetically altered shells: external wall, wall of the inner whorls and/or septa. Due to common similarities in external and internal shell ornamentation, ammonites termed as external moulds can in fact reflect the ornamentation of the inner shell surface. A diagenetically altered shell either can be a neomorphic shell (aragonite transformed to calcite, relics of the original structure present) or is built by calcite Fig. 8 Phosphatized siphuncular tubes from Młynka (a, b) and Podłę _ ze (c, d). a Oppeliid shell with siphuncular tube attached to the outer wall (not preserved). b Compressed siphuncular tube with longitudinal crack along the middle part. c Thin-section image with fragmented siphuncular tubes. Note neomorphic wall (left) built by pseudosparite with double layer structure. d SEM image of siphuncular tube with globular (bacterial?) structures cement filling moldic porosity (moldic shell) resulting from dissolution of the shell. In literature when the term ''internal mould'' is used it is commonly done without information on whether a diagenetically altered shell (or its relic) occurs or not. Also, if the term ''neomorphic shell'' is used, it is not clear whether the shell is the result of neomorphism, or the shell was dissolved and moldic porosity was subsequently filled with calcite cement; For example, Olóriz et al. (2004) alternatively used the terms ''inner mould with neomorphic shell'' and ''inner mould with epigenetic shell''. This latter term is used even when one can suppose that the shell is built rather by calcite cement and not by neomorphic (pseudosparite) calcite (see Olóriz et al. 2004, pl. 2, fig. E). Some ammonites have been described in literature as ''internal moulds with occasionally preserved epigenized shells'' (Caracuel et al. 2000, p. 361).
The term ''external mould'' should be applied to such replicas where the sediment filled the void after dissolution of the shell. If relics of the shell occur, or there are differences in sediment filling reflecting the position of inner whorls and septa, they can suggest that the mould in fact reflects inner shell ornamentation and the shell was dissolved in subsequent stages.
Difficulties with estimation of the type of mould are also due to the fact that some ammonites may be composite moulds; i.e. during burial diagenesis, external shell ornamentation is overprinted on the internal infillings (mould) (Macchioni 2000, p. 337). More studies are necessary to reveal whether some studied ammonites show such preservation.
Summarizing, the terms ''internal moulds'' and ''external moulds'' are commonly used in general to mean underlying the presence or lack of suture line and/or wall. However, literature review indicates that both terms are used also for ammonites with a more complex state of preservation. Thin-section observations are required to reveal whether the relics of shells are preserved. Such observations may provide information on whether the filling of the shell occurred before dissolution of septa and inner whorls (which may be marked only by subtle differences in filling material), or after their dissolution. Moreover, shells may be preserved as neomorphic shells or by calcite cement filling cavity resulting from shell dissolution (moldic shell).
Phosphatization of siphuncular tubes is interpreted as microbially mediated even though globular structures interpreted as bacteria were recognized only in a few tubes observed under SEM. Similar phosphatic spheroidal microbial structures were recognized for example in phosphatized soft tissue of horseshoe crabs (Briggs et al. 2005, fig. 4) or fish (Wilby and Briggs 1997, fig. 1; Briggs 2003, fig. 7).
Laboratory experiments have shown that phosphatization of soft tissues is favoured by closed, anoxic conditions, where the drop in pH induced by decay is sustained long enough to inhibit precipitation of CaCO 3 (Briggs andKear 1993, 1994). Such conditions can be reached by fast burial or overgrowth by microbial mats. The carcass itself may provide sufficient phosphorus for limited phosphatization of soft tissues, as revealed in experiments on shrimps (Briggs andKear 1993, 1994). Briggs and Wilby (1996) and Wilby et al. (1996) showed that microbial mats played an important role in the phosphatization of soft tissues. Microbial mats may act as a barrier to diffusion of dissolved phosphorus, thus promoting apatite precipitation in a closed system. Microbial crusts were recognized on ammonites in glauconitic marls. Additionally, Frutexites structures observed in two ammonites suggest that microbes might have contributed to early cementation of the marly matrix. Microbialites are not known however from platy limestones. Spectacular, spheroidal, nannobacteria-like globules were recognized within carbonate matrix in both glauconitic marls and platy limestones. However, they were observed also in grey marls, as well as in other material studied by us, and are interpreted as sample etching artefacts . Microbial mats promote closed microenvironment, thus phosphatization, but soft-tissue fossilization is a dynamic process, controlled by more than one set of sedimentary and geochemical parameters, and moreover may act on a very local scale such as animal carcasses .
It is unclear why phosphatization of siphuncular tubes occurs only in some representatives of the Oppeliidae family, although analysed ammonites from Młynka and Podłę _ ze show different taphonomic features, indicating different (at larger scale) depositional environments. Possible explanations for this taxonomic control include particular microenvironment within flattened, oxyconic shells of oppeliids or anatomical structure of their siphuncular tube, which-together with other factors-increased the chance for phosphatization. An additional explanation is that phosphatization occurred when carcasses were laid on the bottom during particular favourable environmental events (taphonomic window).

Taphonomic differentiation 79
Suggestions for further studies More detailed taphonomic studies of ammonites as well as their host sediment may provide useful data on the depositional dynamics of the studied facies: changes in hydrodynamic energy, rate of sedimentation and associated environmental parameters. They may also allow estimation of the changes in sea water chemistry versus sedimentary environment and the influence on ammonite taphonomy. Taphonomic studies of ammonites-commonly reelaborated-from the uppermost Callovian and lowermost Oxfordian (not studied here) might provide a new tool in the interpretation of sedimentary and diagenetical history during different ammonite zones. It is worth underlining that preliminary observations of thin sections of ammonite shells from the condensed uppermost Callovian red marls (Zalas) revealed that they are built by neomorphic calcite sparite. This mode of preservation was observed in present studies only in ammonites from the Middle Oxfordian glauconitic marls.
Observations of ammonite shells under CL microscope indicate on additional tool in study of diagenesis of the ammonite-bearing facies. Different diagenetic history of the discussed facies is supported by CL observations of foraminifera , and preliminary observations of ammonites (Jurkowska 2008). Abundant tests of planktonic foraminifera Globuligerina oxfordiana and most benthic forms from glauconitic marls, when observed in a CL microscope, show (like the studied ammonites) bright red-orange luminescence. In contrast, foraminifera and ammonite shells from sponge-microbial limestones and platy limestones (foraminifera observed only) are mostly dull in CL view. Courville and Collin (2002) concluded from their work on taphonomic sequences that a similar taphonomic approach, especially analysis of ammonites, may be applied for other condensed sections at the Middle-Upper Jurassic boundary around the Tethyan margins, including Poland. Such taphonomic analysis should be necessarily performed together with biostratigraphic studies of ammonites.
2. Only in glauconitic marls do inner ammonite moulds have preserved neomorphic calcite shells. In grey marls, and sponge-microbial limestones, ammonite inner moulds contain ''diagenetic'' shell built by calcite cement filling moldic porosity. Ammonites from platy limestones reveal a more complex state of preservation. Usually they show features typical for external mould: walls of whorls and septa appear to be absent based on macroscopic observations. However, analysis of thin sections indicates that some of them have relics of wall and septa. Subtle differences in sediment filling indicate that sedimentary filling occurred, in some ammonites, before dissolution of inner whorls and even septa. Slow lithification of platy limestones influenced the strong shell dissolution and the highest degree of compaction of ammonites. 3. Phosphatized siphuncular tubes occur only in glauconitic marls and platy limestones, despite differences in other taphonomic attributes of ammonites. Microbially mediated phosphatization was possibly favoured by closed, anoxic conditions and a drop in pH. Such a taphonomic phosphatization window occurred rather at the scale of ammonite carcasses and appears to be taxonomically controlled, because phosphatized tubes occur exclusively in specimens of the family Oppeliidae. 4. Taphonomic attributes of ammonites were controlled by sedimentary environment (type and rate of sedimentation, hydrodynamics, oxygenation, microbial activity, timing of dissolution and cementation), resulting in lithology that influenced early and late diagenesis. 5. Our results show that ammonites from the studied rocks, described in the literature as external and internal moulds, represent a more complex state of preservation. Further studies of ammonite taphonomy, particularly on ammonites from the condensed uppermost Callovian-lowermost Oxfordian sequences of the Cracow region, may be a useful tool for sequence stratigraphy.