Geo.Cro.2-3-61-KB.pdf 239 � Marc A. Conrad1 and Bernard Clavel2 AB STRA CT Sediment binding crusts of Lithocodium aggregatum and associated Bacinella irregularis abound in a shallow water limestone layer, in South–East France. The sudden appearance of these crusts denotes a local, conspicuous change in an otherwise balanced, open marine depositional environment. Based on regional correlation, the layer belongs to the Lower Hauterivian, Ligatus Zone, directly dated by an assemblage of orbitolinid foraminifera, and indirectly by a specimen of ammonite. It is older than the Faraoni oceanic anoxic event (OAE), (latest Hauterivian, Angulicos- tata auct. Zone), and presumably not linked with a global climate change. Two facies are recognized: (1) Lithoco- dium bindstone, with Bacinella, other microencrusters, and fl uorescent automicrite of microbial origin; (2) fl oatstones containing numerous fragments of Lithocodium and accompanying biota. Coarse rhombohedral dolomite is locally present. Two modern analogues of microbial mediation are put forward to explain the Lithocodium event: (a) Lagoa Vermelha, in Brazil, along with anoxic, marginal marine conditions; (b) Highborne Cay, in the Bahamas, along with oxic, open marine conditions. A stack of four Upper Hauterivian parasequences is described: Parasequence 1 ends with oolitic deposits; the somewhat deeper water Parasequence 2 occurs only in the south-eastern part of the study area, towards the Subalpine depocenter; Parasequence 3 matches the layer with Lithocodium and Bacinella, of var- iable thickness (0.8 m – 11 m), resulting from syn-sedimentary tectonic activity in the area of the Vuache fault system which is a major feature; Parasequence 4 corresponds with the resumption of the normal, Urgonian carbonate fac- tory. Keywor ds: Lithocodium, Bacinella, Urgonian, automicrite, dolomite, Hauterivian, Jura, Pre-Subalpine Domain 1 71 chemin de Planta, 1223 Cologny, Switzerland; (conrad@safemail.ch) 2 24 ch. des Champs d’Amot, 74140 Messery, France A Lithocodium and Bacinella signature of a late Hauterivian, local microbial event: the Urgonian limestone in South-East France Geologia Croatica 61/2–3 239–250 6 Figs. 1 Pl. Zagreb 2008 Geologia CroaticaGeologia Croatica � 1. INTRODUCTION Lithocodium aggregatum ELLIOTT and Bacinella irregularis RADOIČIĆ are problematic, micro-encrusting calcareous or- ganisms, which are either associated or found separately in the Urgonian limestone. In the Middle East, they are impor- tant components of certain hydrocarbon bearing carbonate reservoirs. Extensive surface and subsurface studies were car- ried out to understand their habitat and depositional setting. The reader may refer to ELLIOTT (1963), BANNER et al. (1990), PASCAL (1979), KOCH et al. (2002), HILLGAERT- NER et al. (2003) and IMMENHAUSER et al. (2004, 2005). According to IMMENHAUSER et al. (2005), in Oman, the Lithocodium-Bacinella association occurs with microbial-algal foraminiferal build-ups and bindstone facies corresponding to biologically out-of-balance communities. Chemostrati gra phy shows that such intervals are coeval with the early Aptian oce- anic anoxic event OAE1a (“Livello Selli”). They alternate with intervals dominated by rudist bivalves. The infl uence of nutrient gradients on carbonate platform community structur- es is considered the most likely model for the origin of the Oman build-up episodes, (IMMENHAUSER et al. 2005, p 20). Herein, an older (Upper Hauterivian) layer containing ab- undant Lithocodium, Bacinella and other micro-encrusters, is described from the margin of the Urgonian platform, in South- Geologia Croatica Geologia Croatica 61/2–3 240 East France. The depositional setting matches a parasequence of bindstone layers, and/or the corresponding fragmented de- posits. Automicrite and idiomorphous dolomite are found, im- plying microbial mediation. Here, the sequence stratigraphy, is locally applied to the Lithocodium and Bacinella layer, and interpreted and used as a dating tool by the present authors. More generally, the much debated issue of dating the Urgo- nian limestone in South-East France and adjacent Switzerland was recently reviewed by CLAVEL et al. (2007), combining published and new biostratigraphic data from ammonites, echi- no ids, orbitolinids, Dasycladalean algae, dinocysts and cal- careous nannoplankton. 2. TALUS TO PLATFORM MARGIN TRANSECT In the northern French and Swiss Jura, the Urgonian limestone consists of two informally defi ned formations: (1) the “Urgo- nien jaune”, representing the fi rst (external) phase of the plat- form setting, dominated by heterotrophic organisms; (2) the “Urgonien blanc”, essentially made up of platform interior deposits dominated by photo-autotrophic organisms. These designations, although commonly used, do not apply to the southern Jura. The “Urgonien jaune” and its equivalents are basal Upper Hauterivian. They are made up of reefal deposits of platform margin origin. Rudists (Pachytraga) are present in an interior, but still open marine setting. Lithocodium and Bacinella are absent from the “Urgonien jaune”. The Upper Hauterivian pro parte to Lower Aptian pro parte “Urgonien blanc” (or “Urgonien s. str.”), extends from the Jura to the Subalpine Domains. As shown by CHAROL- LAIS et al. (2001), thick, prograding bioclastic deposits are present in the Pre-subalpine and Subalpine Domains, marking the installation of the platform on top of hemipelagic deposits. Vertically and laterally, they are followed by platform interior deposits with rudists (Urgonian facies s. str,) extending as far as the Swiss Cantons of Vaud and Neuchâtel. The Lithocodium and Bacinella layer which is the subject of this article,only occurs in the French Southern Jura. It is described from fi ve fi eld sections and an additional outcrop depicted in Fig. 2. Oth er locations, not dealt with herein, occur in the Valserine valley, north of Bellegarde-sur-Valserine, and on the Vuache Moun- tain, in a road cut described by BLONDEL (1990). Local cor- relations (Fig. 4) roughly run from north to south, across the still active Vuache fault system, a major tectonic feature known to be active since the Mesozoic (CHAROLLAIS et al., 1983; DONZEAU et al., 1998). 2.1. Platform talus, Pre-Subalpine Domain – Pic de l’Oeillette section Location (Figs. 1, 3) is on the road between Saint-Laurent-du- Pont and Saint-Pierre-de-Chartreuse (massif de la Chartreuse, Savoie), at Lambert coord. 868.75/5027.15. The section was initially logged by ARNAUD-VANNEAU (1980). For dating elements and correlation with the nearby Pas du Frou section, see CLAVEL et al. (2007). The echinoderm Toxaster retusus and a specimen of Plesiospitidiscus gr. ligatus (Pl. I, Fig. A), an index ammonite, was collected just below the Urgonian limestone cliff. Assemblages of orbitolinids (Pl. I) including Praedictyorbitolina busnardoi, P. claveli and P. carthusiana occur straddling the base of the Urgonian cliff. The Urgonian limestone consists of talus deposits: wackestones with echi- noderm debris, sponge spicules, Lenticulina sp. and small tex- tularids, containing increasing admixtures of diverse, transport- ed shallow water material including some oolites, bryozoan Fi gu re 1: Geological setting and Upper Hauterivian depositional environments, at the datum time shown in Fig. 3 and 4. H: hemipelagic (basin s.l.). PM: platform margin and talus, shallow water, open marine. PI: platform interior, biotically restricted, with rudists; for details see CLAVEL et al. (2007). Palinspastic section: Fig. 3. Insert covering the extent of the layer with Lithocodium and Bacinella: Fig. 4. Geologia CroaticaMarc A. Conrad and Bernard Clavel: A Lithocodium and Bacinella signature of a late Hauterivian, local microbial event... 241 2.2. Platform margin – Mont de Musièges section Location (Figs. 1, 3) is in the Southern Jura, in the Haute-Sa- voie, close to and on the SW side of the Vuache fault-line. This section has also been studied by for example CONRAD (1969), CHAROLLAIS et al. (1989) and BLANC-ALÉTRU (1995). Four parasequences are logged at Mont de Musièges, on top of fl ooding surfaces showing no evidence of exposure. In the 10 m-thick Parasequence 1, the transgressive tract contains up to 30% detrital quartz, bryozoan debris and an assemblage of foraminifera (Lenticulina sp., small textularids, small miliol- ids etc.) denoting a typically deeper water environment, below the base of the euphotic zone. Oolites prevail in the highstand tract. The 7 m-thick Parasequence 2 extends on top of a nodu- lar oolitic limestone, above a quite inconspicuous fl ooding boundary. The transgressive tract consists of weakly glauco- nitic, echinoderm lime grainstones and packstones. Here also, the faunal content, with Lenticulina sp., small textularids, small miliolids and bryozoan debris, typically stands for an open sea, deeper water environment of deposition. Chert is present in the mid-part of the tract, indicating the maximum fl ooding interval. Oolites appear higher up the section, in the highstand tract. debris, silicifi ed bivalves, annelids, corals, small gastropods, rare calcareous green algae (Piriferella paucicalcarea, a dasy- cladale, Boueina sp.), and foraminifera. Lithocodium and Ba- cinella debris are absent. Fi gu re 2: Fort de l’Ecluse Est (location Fig. 4). 1: Rock-solid oolitic limestone, at the top of Parasequence 1; the deeper water Parasequence 2 is missing. 3: Brecciated, fossiliferous Parasequence 3, matching the layer with Lithocodium and Bacinella. Fi gu re 3: Regional correlations and palinspastic profi le, from the talus to the margin of the Urgonian platform. Locations: Fig. 1. Datum time is Upper Hauterivian pro parte, Ligatus ammonite Zone. The distinction between the “Urgonien jaune”, “Marne de la Russille” and “Urgonien blanc” units applies to the Vaud Jura Canton. The more general “Urgonien s. str.” term applies to the Southern Jura and the Pre-Subalpine Domain. For symbols, additional fi eld sections and close-up correlations in the Southern Jura see Fig. 4. Geologia Croatica Geologia Croatica 61/2–3 242 PLATE I Key ammonite and key orbitolinids Plesiospitidiscus ligatus (D’ORBIGNY) A 136.1, Pic de l’Oeillette Praedictyorbitolina busnardoi SCHROEDER et al. B 136.0-4, Pic de l’Oeillette C 136.0-3a, Pic de l’Oeillette G 6548a4, Mont de Musièges H 6548cb, Mont de Musièges. I 6548a1, Mont de Musièges M 250.1–1a, La Russille. N 250.2–2a, La Russille S MC 312a, Rocher des Hirondelles Praedictyorbitolina claveli SCHROEDER D 136.0-3b, Pic de l’Oeillette E 136.1-3a, Pic de l’Oeillette F 136.0-2a, Pic de l’Oeillette J 6549a2, Mont de Musièges K 6549a3, Mont de Musièges L 6548B, Mont de Musièges O 7041-3, La Russille P 7040-12a, La Russille Q 7040-15a, La Russille R 7040-14a, La Russille Geologia CroaticaMarc A. Conrad and Bernard Clavel: A Lithocodium and Bacinella signature of a late Hauterivian, local microbial event... 243 Geologia Croatica Geologia Croatica 61/2–3 244 Parasequence 3, only 0.8 m-thick, is visible in a small quarry, next to the D187 road (at Greenwich coord. 46.02616° N, 5.96355° E). It has a sharp boundary with the previous in- terval and consists of a knobbly limestone, free of detrital qu- artz, containing numerous Lithocodium crusts (Figs. 5, 6), act- ing as binders in a micropeloidal matrix of automicrite (see below). Transgressive deposits are absent. The accompanying biota includes subordinate amounts of Bacinella, a hetero- trophic biota including bryozoans and sponges, small textu- larids, rare dasycladalean algae and key orbitolinids (see be- low). Quite large, idiomorphic dolomite crystals are also present. The Lithocodium and Bacinella layer is dated by orbitolinids at Mont de Musièges. As at Pic de l’Oeillette, an assemblage containing Praedictyorbitolina busnardoi and P. claveli, is overlain by the fi rst specimens of P. carthusiana. Only part of the next, Parasequence 4 is shown in Figs. 3 and 4. The suc- cession starts with 3.5 m-thick, angular and very coarse grain- ed transgressive deposits, which are probably related to the adjacent Vuache fault system. Rudists occur in the highstand tract, with open sea infl uences decreasing progressively up- section. 2.3. Platform margin – Val de Fier section Location (Fig. 4) is 4 km south of Seyssel (Haute-Savoie), on the D14 road, at the entrance of a tunnel (Lambert coord. 872.76/109.40). Parasequence 2 is missing. The 3 m-thick Parasequence 3 occurs above a fl ooding surface, in sharp con- trast with the underlying, reefal oolitic grainstones belonging Fi gu re 4: Local, detailed correlations in the lower part of the “Urgonien s.str.” limestone. Considering the general palaeogeographical setting, approximately running in a SW–NE direction, the most external location is Mont de Musièges. Hence, it is placed on the left hand side in the profi le. Vuache fault system according to DONZEAU et al. (1998). Rocher des Hirondelles section: see detailed log in CONRAD (1969). Other sections: logs are taken from the author’s unpublished thesis manuscript. Geologia CroaticaMarc A. Conrad and Bernard Clavel: A Lithocodium and Bacinella signature of a late Hauterivian, local microbial event... 245 to Parasequence 1. It consists of single or multiple Lithoco- dium and Bacinella crusts, binding a wackestone containing numerous bryozoans, echinoids, pelecypods and some trans- ported ooliths. A basal transgressive layer is absent and there is no idiomorphic dolomite. Paraquence 4 is observed next, on top of a conspicuous joint, marking the fl ooding surface. Only part of it is shown in Fig.4. The transgressive tract consists of deeper water, peloi- dal packstone, typically containing Lenticulina sp. and com- mon Choffatella decipiens. Based on the literature, e.g. IM- MENHAUSER et al. (2004), the latter foraminifera indicates open marine environments, below fair-weather wave base, but within the reach of storm waves. Biotic restriction occurs much higher up in the Urgonian limestone. 2.4. Platform margin – Perte de la Valserine section Location (Fig. 4) is 1.7 km NNW of Bellegarde-sur-Valserine (Ain), at (Lambert coord. 868.87/131.50). Parasequence 1 is observed on the Valserine river bed and therefore remains in- accessible. The lack of Parasequence 2 can therefore only be inferred from nearby locations. The 6 m-thick Parasequence 3 consists of very numerous, angular fragments of Lithoco- dium crusts (Fig. 7), which are embedded in fl oatstones also containing encrusting bryozoans, numerous oyster and echi- noid debris, including spines, microgastropods, and diverse foraminifera, Coptocampylodon lineolatus (incertae sedis), and common specimens of Pseudoactinoporella fragilis, a dasy- cladalean alga. Idiomorphous dolomite is present (Fig. 7) and a few, probably reworked ooliths are scattered in the sediment. Fi gu re 5: LC: Lithocodium aggregatum crust, sediment-binding. FAM: fl uorescent pelletal automicrite. F: fl oatstone containing numerous lithoclasts of automicrite. Upper Hauterivian, Mont de Musièges (Haute- Savoie), sample Conrad 84, normal transmitted light. Fi gu re 6: A: Lithocodium aggregatum crust, binding a pelletal automicrite; lithoclasts of pene-contemporaneously reworked automicrite; normal transmitted light. B: epifl uorescence image of the same view. The automicrite fl uoresces considerably, indicating the presence of primary organic matter. In contrast, the secondary, blocky calcite cement fi lling cavities in the Lithocodium crusts remains dark. Also the Lithocodium crust is fl uores- cent, supporting a calcimicrobial origin. Upper Hauterivian, Mont de Musièges (Haute-Savoie), sample Conrad 84. Fi gu re 7: Lithocodium aggregatum fl oatstone. F: dolomitized matrix containing numerous fragments of Lithocodium. L: large fragment of Lithocodium crust. D: large dolomite crystal. Upper Hauterivian, Perte de la Valserine (Ain), sample Conrad 631, normal transmitted light. Geologia Croatica Geologia Croatica 61/2–3 246 A single, inconspicuous level of Lithocodium and Bacinella bindstone is present in the mid part of the interval. The pieces of Lithocodium are interpreted as having originated from bind- stone deposits forming hard substrates, which were fragment- ed and re-deposited in an allomicrite. In contrast to the Mont de Musièges and Val de Fier sec- tions, normal marine biota such as bryozoan micro-encrusters and sponges are absent from the next, Parasequence 4 depos- its. The transgressive tract begins abruptly with a 3 m-thick, low energy and burrowed wackestone, containing angular rud- ist debris, foraminifera and ostracods. Rudist biostromes (Ur- gonian facies s. str.) are located up-section, in the highstand tract. 2.5. Platform margin – Boge sur Confort section Location (Fig. 4) is 5 km north of Bellegarde-sur-Valserine, on the D16 road (Lambert coord. 870.3/134.5). Here also, Pa- rasequence 2 is missing. The 11 m-thick Parasequence 3 rests directly on an oolitic grainstone belonging to the top of Para- sequence 1. As at Perte de la Valserine, it contains numerous, angular pieces of Lithocodium, with Bacinella, bryozoans, scat tered corals debris, foraminifera including rare orbitolinids, and some dasycladalean algae. The transgressive tract dis- plays a rather inconspicuous upward shoaling trend, fi rst with a basal fl oatstone including Lenticulina sp., grading to grain- stones containing an increasing number of dasycladalean al- gae such as Pseudoactinoporella fragilis. Both bindstone lay- ers was dolomite are apparently missing. As at Perte de la Valserine, an open sea biota is absent from the overlying Parasequence 4. The basal, slightly deeper water transgressive tract consists of a wackestone containing some transported ooliths. Rudist biostromes occur up-section, in the highstand tract. 2.6. Platform margin – Rocher des Hirondelles section Location (Figs. 1, 3) is 15 km north of Bellegarde-sur-Valser- ine, on the D991 road (Lambert coord. 874.0/144.7). A de- tailed account of the section was fi rst published by CONRAD (1969). For later developments, reference is made to CLAVEL et al. (2007). At the time of writing, the original thin section material was unfortunately missing, and therefore the follow- ing brief account is based on the literature. The level of inter- est (Parasequence 3) is 4–5 m-thick, occurring on top of an oolitic packstone belonging to Parasequence 1. Evidence of deeper water, transgressive deposits is missing. Lithocodium crusts suddenly appear in a basal grainstone also including some reworked ooliths. A Lithocodium bindstone occurs high- er up, but without dolomite. Bryozoans, microgastropods and dasycladalean algae are present throughout the interval. At Rocher des Hirondelles, the Lithocodium and Bacinel- la layer is dated by orbitolinids. Here also, a rich assemblage including Praedictyorbitolina busnardoi and P. claveli is fol- lowed, up-section, by the fi rst specimens of P. carthusiana. Only part of the overlying Parasequence 4 is shown in Figs. 3 and 4. The succession begins abruptly with an exception- ally thick (52 m), transgressive sequence of grain- and lime rudstones, containing unaltered, angular debris represetnaing an open marine, shallow water biota. Presumably, these are scarp deposits related to the past presence of an active fault belonging to Vuache system. Up-section, in the Angulicos- tata ammonite Zone (Uppermost Hauterivian), they are fol- lowed by highstand deposits containing rudists. 2.7. Platform margin – La Russille and other NW Switzerland sections Location (Fig. 1) is 7 km east of Vallorbe (Canton Vaud), on the road between Montcherand and Lignerolle, at Latitude 46.73° N, 6.48° E. The section (Fig. 3) is of historical interest. For a review, see for example CONRAD & MASSE (1989), BLANC-ALETRU (1995) and CLAVEL et al. (2007). Also at La Russille, a rich assemblage of orbitolinids including Prae- dictyorbitolina busnardoi and P. claveli straddles the “Urgo- nien jaune”, the improperly called “Marne de la Russille” (a narrow argillaceous interval of regional extent) and the “Ur- gonien blanc”. The fi rst specimens of P. carthusiana occur 3 m above the base of the “Urgonien blanc”. The Lithocodium and Bacinella deposits are missing at La Russille and elsewhere in the Swiss Cantons of Vaud and Neuchâtel. A study comprising a number of mineralogical ana- lyses was carried out by BLANC-ALETRU (1995) in this area, in an effort to understand the signifi cance of several uncon- formities observed in the “Urgonien jaune”, the “Marne de la Russille” and the “Urgonien blanc”. At La Russille and Val- lorbe, the “Urgonien jaune” consists of a bioclastic, partly oolitic shallow water limestone capped by coral biostromes. After BLANC-ALETRU (1995, fi g. 84, 141), at Vallorbe, dol- omite unexpectedly occurs at the top of the “Urgonien jaune”, while carbonate dissolution is present, and kaolinite is the leading clay mineral, in the overlying, transgressive “Marne de la Russille”. Here, these signals of terrestrial exposure are tentatively correlated with Parasequence 3, elsewhere form- ing the Lithocodium and Bacinella layer. 3. PALEONTOLOGICAL AGE DETERMINATION AND CORRELATION In the Southern Jura, at Mont de Musièges and Rocher des Hirondelles, the Lithocodium and Bacinella layer is dated by an assemblage of three species of orbitolinids, combining part of the Praedictyorbitolina busnardoi and P. claveli concurrent range zone, a few metres below the appearance of P. carthu- siana. P. busnardoi (Pl. I) is Upper Hauterivian pro parte, (Say- ni to near the topof the Ligatus ammonite Zones); P. claveli (Pl. I) is Upper Hauterivian to Lower Barremian pro parte, (Sayni to Nicklesi pro parte); P. carthusiana (CLAVEL et al., 2007, pl. 3) is Upper Hauterivian pro parte to Lower Barre- mian pro parte, (top of the Ligatus to the base of the Caillau- dianus). At Pic de l’Oeillette, in the Pre-Subalpine Domain, this assemblage occurs in talus deposits, directly dated by a specimen of Plesiospitidiscus gr. ligatus, an index ammonite (Pl. I). In the Swiss Canton of Vaud Jura, the same assemblage of orbitolinids straddles a narrow argillaceous interval (im- properly called the “Marne de la Russille”), separating the “Ur gonien jaune” from the “Urgonien blanc”. In the same ge- neral area, at La Sarraz – Les Buis, the upper part of the “Ur- Geologia CroaticaMarc A. Conrad and Bernard Clavel: A Lithocodium and Bacinella signature of a late Hauterivian, local microbial event... 247 gonien jaune” is dated Upper Hauterivian by signifi cant as- semblages of dinocysts and calcareous nannofossils (CLAVEL et al., 2007). As for the dasycladalean algae, at Val de Fier, the layer with Lithocodium and Bacinella contains the typically Hau- terivian Dissocladella hauteriviana. At Mont de Musièges, a sample taken 3 m above the bindstone layer contains Suppil- uliumaella corbarica. The species is Upper Hauterivian pro parte, (Sayni and Ligatus ammonite Zones), (CLAVEL et al., 2007). Based on these observations, the level with Lithoco- dium and Bacinella must be assigned to the Ligatus Zone which represents the mid part of the Upper Hauterivian. The layer with Lithocodium and Bacinella is in between the Valanginian Weissert OAE and the latest Hauterivian (up- per part of the Angulicostata auct. Zone), Faraoni OAE (for reference see for example BAUDIN & al., 2006). Hence, it seems unrelated to a large-scale, signifi cant oceanographic event, and/or global climate change. It is more indicative of being a consequence of locally abnormal conditions, such as those resulting from a sudden infl ux of key nutrients, perhaps of nearby terrestrial origin. 4. SEQUENCE STRATIGRAPHY Defi nitions introduced by SCHLAGER (2004, 2005) are used here. Based on bio- and lithofacies analyses, at least four units are present in the study interval (Figs. 3, 4). They are bounded by fl ooding surfaces, with no evidence of exposure, corres- pond ing to Type-3 sequence boundaries. Still, these deposi- tional parasequences, as described below, are succinctly com- pared to the subdivisions elaborated by CLAVEL et al. (1995), using the Exxon terminology. Parasequence 1 presents the onset of the Urgonian deposits. It is up to 18 m-thick, on top of a clear-cut fl ooding surface, followed by a conspicuous, quartz -bearing transgressive tract. The highstand tract, almost entirely oolitic, is capped by coral biostromes at Val de Fier. Using the terminology introduced by CLAVEL et al. (1995), Parasequence 1 corresponds to the Ha5 sequence lowstand tract, covering, for example the upper part of the “Urgonien jaune” at La Russille, in the Vaud Jura Canton. The 7 m-thick Parasequence 2 was logged only at Mont de Musièges, in the southeastern-most part of the area, in the direction of the Subalpine depocenter. The depositional envi- ronment is markedly deeper than in the previous interval, with oolites appearing only near the top of the highstand tract. As shown by Fig. 3, the base fl ooding surface of Parasequence 2 is tentatively correlated with an argillaceous, hemipelagic in- terval at Pic de l’Oeillette, in the Pre-Subalpine Domain. At Mont de Musièges, the Parasequence 2 corresponds to the Ha5 transgressive tract, and the Ha5 highstand tract pro parte. The bindstone and/or fl oatstone layer with Lithocodium and Bacinella matches Parasequence 3, abruptly interrupting Parasequence 2 at Mont de Musièges and, elsewhere, Parase- quence 1. The thickness varies considerably, reaching an 11 m maximum measured at Boge sur Confort, in the area of the Vuache fault system. The base of Parasequence 3, taken as a datum, is considered as corresponding to a local, “instantane- ous” M (microbial) carbonate factory event. It is tentatively correlated with the transgressive base of the improperly called “Marne de la Russille”, in the Vaud Jura Canton. Alternative- ly, the top of the layer with Bacinella and Lithocodium may be locally diachronous and since masked by the rapid deposi- tion of bioclastic debris. At Rocher des Hirondelles, Parase- quence 3 corresponds to part of the Ha5 highstand tract. Finally, Parasequence 4 corresponds to the onset of the Urgonian T (tropical) and photozoan carbonate factory, an im- portant event of regional extent, traceable as far as the Pre- Subalpine Domain (Fig. 3) and beyond, at the base of the Urgo- nian cliff. At Val de Fier, a 12 m-thick, deeper water trans gressive tract occurs on top of a conspicuous fl ooding surface. At Mont de Musièges and Rocher des Hirondelles, the transgressive succession consists of thick, angular, often coarse grained de- posits the presence of which is interpreted as being linked to submarine escarpments of tectonic origin. In same area, cor- responding to the Vuache fault system, more or less coeval deposits witness the impressive effect of such syn-sedimen- tary activity with, for example, highly heterogeneous chan- nel-fi lls at Bellegarde-sur-Valserine. At La Russille (Canton Vaud Jura), the Parasequence 4 transgressive tract corresponds to the Ha6 lowstand tract. 5. INTERPRETATION OF THE LAYER WITH LITHOCODIUM AND BACINELLA The layer was initially interpreted by CONRAD (1969) as a marine facies corresponding to the back fl ank of oolite shoals. In a draft version of the present article, the coarse, rhombohe- dral dolomite accompanying the Lithocodium crusts was con- sidered as supporting the Dorag depositional model. This mod- el (BADIOZAMANI, 1973) calls for dolomite precipitation in the marine and fresh water mixing zones, for example in the vicinity of islands subject to heavy rains. Actually, although possible, the Dorag model is rather unlikely. It is highly con- troversial (for a review, see MOORE, 2001) and still requires well-documented examples for support. 5.1. Epifl uorescence tests In the layer with Lithocodium and Bacinella, the binding-trap- ping mechanism is primarily performed by Lithocodium crusts, Bacinella, and other micro-encrusters denoting an open ma- rine habitat, and by fi ne-grained, organo-mineralic deposits conceivably generated by microbes. Six epifl uorescence tests were carried out in thin section, to check for the presence, at Mont de Musièges, of automicrite containing residual organ- ic matter. The tests were carried out by B. Van der Kooij, at the Department of Sedimentology and Marine Geology Vrije Universiteit, Amsterdam. A Zeiss epifl uorescence microscope was used mounted with an Hg vapour light and a bypass fi l- ters for the green wavelength. Both the automicrite matrix and the Lithocodium crusts are brightly luminescent (Fig. 6), in- dicating a high organic content. In contrast, the secondary, granular mosaic calcites fi lling up the pore spaces, are non lu- minescent, and hence devoid of organic material. 5.2. The microbial mediation, anoxic conditions model A possible interpretation of the Lithocodium and Bacinella deposit is the sudden development, next to an otherwise nor- Geologia Croatica Geologia Croatica 61/2–3 248 mal, open marine environment, of anoxic conditions, leading to the formation of microbial mats and bacterially-driven, epi- genetic dolomite. In such an unbalanced environment, Lith- ocodium and Bacinella were possibly acting as low-trophic, opportunistic calcifi ers, at work in semi-enclosed pools. A pos- sible modern analogue is the Lagoa Vermelha, a moderately hypersaline, high pH and anoxic lagoon located 90 km east of Rio de Janeiro, where dolomite precipitation occurs. Experi- ments carried out by WARTHMANN et al. (2000), on a par- ticular strain of sulphate-reducing bacteria found in the Lagoa Vermelha, indicate that bacterial sulphate reduction can induce the precipitation of signifi cant amounts of metastable, nonstoi- chiometric dolomite which, in the fossil record, may evolve as the central nucleus of larger, rhombohedral dolomite crystals. A disadvantage of the Lagoa Vermelha model is that apart from the automicrite, clearly of microbial origin, the layer with Lithocodium and Bacinella contains no indices of meso- or eutrophic conditions, such as an impoverished biota with Tri- loculina sp., or euhaline assemblages with charophytes, brack- ish molluscs and ostracods. In contrast, the Lithocodium crusts are accompanied by numerous, freshly broken and unaltered fragments of a typically stenohaline biota. 5.3. The microbial mediation, oxic conditions model Another possible model is based on Highborne Cay, in the Ba- hamas, where stromatolite build-ups and micritic crusts are presently forming and trapping oolites in open marine envi- ronments of normal salinity. The location is at the back of a fringing algal reef (REID et al., 2000 and references therein). Cyanobacteria are the primary producers in this eco-system. According to BAUMGARTNER et al. (2006), sulfate-reduc- ing bacteria (SRB), although traditionally viewed as restricted to anoxic zones, can tolerate oxygen. Certain SRB strains not only survive in the oxic zone of microbial mats, but even ex- hibit some of their highest rates of sulfate reduction during oxic conditions. Although it is yet to be confi rmed, dolomite precipitation does not seem to occur at Highborne Cay, whilst epigenetic dolomite is locally found in the layer with Lithocodium and Bacinella. The origin of organogenic dolomites has been the object of a number of studies. Among several processes, anaer- obic methane oxidation favours dolomite formation. In the study area, fi ne mud, and syngenetic dolostones are missing in the Urgonian limestone. However, besides the layer with Lithocodium and Bacinella, coarse rhombohedral, epigenetic dolomite, although rare, is also found higher up in the forma- tion. Such an occurrence was described by CONRAD (1969, p. 24 and fi g. 7), from a Barremian limestone with rudists, in the Subalpine Domain. Pervasive dolomitization occurs near the top of a small sequence, right below beach deposits over- lain by mm-thick coal seams. Lithocodium and Bacinella are missing in this case. 5.4. Distribution of Lithocodium and Bacinella Large Lithocodium-Bacinella build-ups, such as those inter- bedded with rudist banks in the Aptian of the Middle East, are lacking in South-East France. These organisms occur in the “Urgonien blanc” (or “Urgonien s. s.”) in the following man- ner: (1) in the partly dolomitized layer dealt with in this article, Lithocodium crusts are found either alone or accompanied by other micro-encrusters including Bacinella; (2) Bacinella on- coids, up to several cm-large, are coated by Lithocodium; they commonly occur in non-dolomitic fl oatstones which are asso- ciated with, but separate from rudist boundstones, in platform interior deposits; similar oncoids were studied by VÉDRINE et al. (2000) in the Oxfordian of the Swiss Jura. Accord ing to these authors, the Bacinella-Lithocodium association charac- terizes lagoonal environments with oligotrophic conditions, in normal-marine waters; (3) Bacinella alone (Lithocodium missing) commonly occupies primary cavities in rudist bio- stromes; (4) in the Subalpine Domain, dolomitized lithoclasts formed by questionable Lithocodium debris, occasionally form a minor component of thick grainstones, forming sand waves on the margin of the platform. If related to the type (1) above, these lithoclasts may indicate small scale exposures of the plat- form, between the shoreline and the shelf break, followed by the erosion and re-sedimentation of temporary, in situ bind- stone deposits. With reference to the above, observations made by other authors confi rm that Lithocodium aggregatum and Bacinella irregularis are taxonomically distinct organisms. As for Litho- codium, its origin remained controversial for decades. Recent- ly CHERCHI & SCHROEDER (2006) have shown that it can- not be a loftusiacean foraminifera. Instead it is considered as representing a colony of calcifi ed cyanobacteria. This inter- pretation is supported by our observation showing that the dark Lithocodium crusts have a high organic content. 6. CONCLUSIONS The layer with Lithocodium aggregatum and Bacinella irreg- ularis is found in the Southern Jura, in the lower part of the “Urgonien s.s.” formation. Two variants occur: (1) bindstones containing fl uorescent automicrite and epigenetic dolomite; (2) much thicker fl oatstones containing, inter alia, numerous fragments of Lithocodium crusts. By analogy with the modern Lagoa Vermelha, in Brazil, one interpretation calls for a sud- den, local anoxic episode of microbial carbonate and dolomite precipitation, interrupting the normal marine carbonate fac- tory. Another model calls for an analogy with the Highborne Cay area, in the Bahamas, where stromatolite build-ups and micritic crusts are presently forming, in an open marine envi- ronment of normal salinity. Litho- and biofacies analyses show that the depositional setting, during the earliest development of the “Urgonien s. s.” carbonate platform, consists of a stack of four, upward shoal- ing depositional parasequences, bounded by fl ooding surfac- es. Parasequence 1 represents the initial onset of the “Urgon- ien s. s.”. Parasequence 2 occurs in the south-eastern-most part of the area, in the direction of the subalpine depocenter. Par- asequence 3 matches the layer with Lithocodium and Ba- cinella, abruptly interrupting Parasequence 2 or Parasequence 1, depending on location. Wide thickness variations (0.8–11 m) are interpreted as resulting from simultaneous tectonic ac- tivity, in the area of the currently still active Vuache fault sys- Geologia CroaticaMarc A. Conrad and Bernard Clavel: A Lithocodium and Bacinella signature of a late Hauterivian, local microbial event... 249 tem. Parasequence 4, fi nally, corresponds to the resumption of the normal, Urgonian carbonate factory. The Lithocodium and Bacinella event is of Upper Hauterivian age, in the Liga- tus ammonite Zone. Dating elements are provided, directly, by an assemblage of three species of orbitolinids and, indi- rectly, by an index ammonite found in the Pre-subalpine Do- main. Based on these elements, the Lithocodium and Bacinella event is correlated with platform talus deposits, in the Pre - subalpine Domain, and with the improperly called “Marne de la Russille”, in the Swiss Jura. It is signifi cantly older than the latest Hauterivian Faraoni anoxic event (OAE) and unlikely to be linked with global climate change. ACKNOWLEDGEMENT The authors wish to thank Wolfgang Schlager (Vrije University, Am- sterdam) and Geraint W. 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Manuscript received January 8, 2008 Revised manuscript accepted June 16, 2008