Carnets de Géologie / Notebooks on Geology: Memoir 2009/01 (CG2009_M01)

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Contents

[Introduction] [Stratigraphic overview] [... ammonite stratigraphy]
[Belemnite distribution] [Basin facies] [Recognition ...]
[Remarks] [Palaeontological notes] [Systematic descriptions]
[Conclusions] [Bibliographic references]
[Figures] and ... [Plates]


Mediterranean Neocomian belemnites, part 3:
Valanginian-Hauterivian belemnites

Nico M.M. Janssen

Geertekerkhof 14bis, 3511XC Utrecht (The Netherlands)

Manuscript online since March 31, 2009

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Abstract

The classical papers of Raspail (1829, 1830) and Duval-Jouve (1841) described a wide range of belemnite species, mainly from the Lower Cretaceous of the Castellane-Peyroules area (Alpes de Haute-Provence, France). The present work focuses mainly on the biostratigraphy of these previously described belemnite taxa for their stratigraphic relationships had not been determined precisely. Here, biostratigraphy is related to the lithologic successions and faunal associations (ammonites) of various outcrops in the area studied. Complementary data were obtained from the La Lagne, Les Allaves and Pas d'Escale sections (Alpes de Haute-Provence, France). And, in order to attain a better understanding of the stratigraphic distribution of Late Valanginian belemnites in condensed glauconitic deposits, these assemblages are compared with belemnites from deeper water successions in the Angles, Source de l'Asse de Moriez, Cheiron areas and those in the vicinity of La Charce and Vergol that are even deeper.

Key Words

Belemnites; Valanginian; Hauterivian; France; Peyroules.

Citation

Janssen N.M.M. (2009).- Mediterranean Neocomian belemnites, part 3: Valanginian-Hauterivian belemnites.- Carnets de Géologie / Notebooks on Geology, Brest, Memoir 2009/01 (CG2009_M01)

Résumé

Bélemnites néocomienne des régions méditerranéennes, 3ème partie : Bélemnites de l'intervalle Valanginien-Hauterivien.- Les travaux classiques mais anciens de Raspail (1829, 1830) et Duval-Jouve (1841) décrivent une grande variété d'espèces de bélemnites, provenant essentiellement du Crétacé inférieur de la région de Castellane-Peyroules (Alpes de Haute-Provence, France). Cette nouvelle contribution s'articule autour de la distribution biostratigraphique des bélemnites décrites précédemment car jusqu'à présent cet aspect avait été négligé. Le canevas biostratigraphique est calibré avec les successions lithologiques et les associations fauniques (ammonitofaune) de plusieurs affleurements dans cette région. Des données supplémentaires ont été obtenues à partir de coupes levées dans d'autres secteurs des Alpes de Haute-Provence: La Lagne, Les Allaves et Pas d'Escale. De plus, afin de mieux comprendre la distribution stratigraphique des bélemnites du Valanginien supérieur au sein de niveaux condensés glauconitiques ces associations sont comparées avec les bélemnites de milieux de dépôt plus profonds à Angles, à la Source de l'Asse de Moriez et à Cheiron, et avec celles des environs de La Charce et Vergol qui correspondent à des milieux plus profonds encore.

Mots-Clefs

Bélemnites ; Valanginien ; Hauterivien ; France ; Peyroules.


Introduction

The classical works of Raspail (1829, 1830) and Duval-Jouve (1841) were based in part on belemnites from the Castellane-Peyroules area (Fig. 1 ). Kilian & Reboul (1915) and Tomitch (1922) listed several species of belemnites from this area, and Delattre (1952) described a new species of belemnite "Hibolites rogeri n. sp.", now Adiakritobelus rogeri (Delattre). Unfortunately, the collections of Raspail and Duval-Jouve are thought to be lost (see Combémorel, 1973, p. 134), so I figure some topotypes and record their locations.

Here, the belemnite taxa are examined bed-by-bed making use of previous biostratigraphic studies and sequence stratigraphic interpretations of the successions. Their integration will lead to a better understanding of the distribution of the belemnites. Already, a provisional framework has been established in which several associations of belemnites are recognized. Future research in pelagic sediments should refine the degree of stratigraphic resolution using belemnites. Currently, in the Vocontian basin detailed stratigraphic subdivision using belemnites is available only for the Upper Valanginian. To date no detailed stratigraphic data on belemnites have been available from most of the strata of Hauterivian age there.

Stratigraphic overview

For this paper, several sections, mainly in the Peyroules area, were studied in detail. In this region the sediments of latest Valanginian and earliest Hauterivian age are glauconitic and their lithology varies considerably. Figs. 2  - 3  - 4  - 5  - 6  - 7  - 8  - 9  -10  show details of these successions and their relationships to ammonite zones (Autran, 1993; Vermeulen et alii, 1999; Vermeulen, 2002) and the distribution of belemnites. The sections encompassing the Valanginian-Hauterivian boundary are particularly rich in belemnites. Some of them show traces of reworking, rolling or physical damage. The majority of the macrofossils are cephalopods.

The following is an enumeration of the sites discussed in this study: see Figure 1  for their geographic location.

Clausson (CL), Peyroules area (Figs. 2  - 3 ): In this succession the strata that include the Valanginian-Hauterivian boundary are in a calcareous glauconitic facies. Underlying these beds disconformably are Lower Valanginian strata (the so-called Karakaschiceras-beds), that are succeeded by alternations of limestones and marls with abundant Olcostephanus guebhardi and pelecypods. These rocks are a partial lateral equivalent of the "Petite-Lumachelle" and represent the upper part of the Eristavites platycostatus Subzone. Most of the Valanginian stage is not represented in the remainder of the rock sequence, so it is possible that some of the fossils in the glauconitic strata above it are reworked (reworked ammonites are found among the phosphatic nodules). The base of this glauconitic succession is a conglomerate consisting mainly of belemnites and phosphatic ammonites. Occasionally, the basal bed of this conglomerate is a nearly monospecific layer of the belemnite Duvalia binervia (Raspail, 1829).

Ravin du Mal Bouisset (RMB), Peyroules area (Fig. 4 ): The lithologic succession of this section is comparable to the sequence at Clausson and Collet des Boules, from which it differs by the absence of a basal conglomerate. The section was figured by Autran (1993).

Collet des Boules (CB), Peyroules area (Figs. 5  - 6  - 7 ): Outcrops of this sedimentary sequence are comparable to those of the above-mentioned exposures, for the beds dated Early Valanginian are succeeded by glauconitic sediments. However, a basal glauconitic-phosphatic conglomerate is for the most part absent. In the easternmost exposure of the Collet des Boules area, the glauconitic succession is quite different (Fig. 5 ; middle and right lithological columns), for here the section is comparable to the succession exposed near La Lagne. In addition, glauconitic levels occur near the top of the Lower Hauterivian succession (Fig. 5 ), and in some beds of Late Hauterivian age (Figs. 6  - 7 ). Rocks representing the uppermost Hauterivian at Collet des Boules (Fig. 7 ) are characterized by an increase in the thickness and induration of the limestones, which form a small crest in the topography (the Pseudothurmannia-beds with possibly a few beds dated earliest Barremian). These resistant limestones are followed by sandy to marly Albian strata in an erosional relationship.

La Lagne (LLG) (Fig. 8 ): This profile is exposed south of Castellane. With the exception of some thick, glauconite-rich beds with abundant cephalopods, the limestones are often irregular, nodular, and are well exposed only in weathered profiles. Strata of latest Hauterivian to earliest Barremian age are followed by Albian sandstones and marls.

Les Allaves (ALL) (Fig. 9 ): Exposures in the area between Les Allaves and the Ravin du Carrîne are typical condensed outer-platform deposits with many variations in lithology. In contrast to the Peyroules area, strata of latest Early Valanginian to Late Valanginian age in the Les Allaves area are rich in marls with abundant echinoids and belemnites. Generally, the ammonite zones that characterize the Late Valanginian are expressed in only a few thin limestones, separated by relatively thick marls (see David, 1979; Thieuloy et alii, 1991; Bulot, 1995; Reboulet, 1996). These marls contain typical Upper Valanginian belemnite species: Duvalia gr. binervia (D. binervia, D. sp. 1), Adiakritobelus spp., and Hibolithes gr. subfusiformis Raspail, but Pseudobelus sp. appears to be rare. The beds of earliest Hauterivian age are characteristically developed in a glauconitic facies. However, glauconite is clearly less abundant than it is in the Peyroules area, while on the other hand there are many marly limestones with well-developed levels of nodules. With the exception of the base of the Crioceratites loryi Zone (C. loryi Subzone; glauconitic facies) the strata representing the upper Lower Hauterivian and Upper Hauterivian are marl-rich ("hemipelagic facies"). A striking feature is the abundant occurrence of nautilids throughout the succession.

In the sections we measured there are many small faults. So we could not compare our profiles directly with the succession depicted by Bulot (1995, fig. 32; in particular as regards the thickness of the C. loryi Subzone) and also because bed 112d (base of Acanthodiscus radiatus Biozone in Thieuloy et alii, 1991, fig. 6) could not be recognized. With these two exceptions, their bed numbers could be correlated with a fair degree of reliability. A basal conglomerate appears to be present only rarely in the Allaves area.

Pas d'Escale (PE) (Fig. 10 ): Here the lowermost Hauterivian (A. radiatus Zone) sequence is marl and limestone with abundant glauconite, phosphatic nodules and belemnites. Cephalopods are often concentrated, and occur in alternate layers of belemnites and ammonites (sorting?). The strata below these glauconitic beds are not well exposed due to recent erosion and plant growth. Apparently, specifically determinable ammonites are rare in these beds (Robert, 1994; Bulot, 1995). The bed numbers used by these authors were transferred to the extent possible. The strata at the base of the Hauterivian are more or less comparable, both in thickness and lithology, to the beds in the Les Allaves area. Notable is the occurrence of Crioceratites loryi in PE211e-f (summit of highstand). These levels correlate with the glauconitic marl above bed ALL116 (Les Allaves; Fig. 9 ). We collected the ammonite Jeannoticeras jeannoti from the glauconitic marl above bed PE213a.

The Angles Barremian Stratotype Section (ABSS): The ABSS sequence is exposed along the road to the hamlet of Angles (Thieuloy, 1979), where rocks of latest Hauterivian age yielded but few belemnites. According to Vermeulen (2002, p. 27-31) the lowest beds of this section represent the Balearites balearis Zone. Note that the first two beds (bed 1 and 1a) of this outcrop are not figured: they may represent either the B. balearis or the Plesiospitidiscus ligatus Zone. Some 80-90 limestone-marl interbeds comprise the succession up to the Hauterivian-Barremian boundary at bed 72. Most of the belemnites are Hibolithes gr. subfusiformis Raspail. In the marl above bed 73 the first typical earliest Barremian belemnite Duvalia binervia Raspail (= Duvalia silesiaca Uhlig, 1902) occurs. Hibolithes-like belemnites are still rather common in the exposures of lowermost Barremian strata but disappear in late Early Barremian times (Clément, 2000; Janssen & Fözy, 2005, p. 66).

In the Angles section data concerning the Early Hauterivian are sporadic, for the beds of this age are poorly exposed owing to an extensive cover of vegetation and scree. There is no uninterrupted succession of exposures, with the exception of the lowermost Hauterivian portion, which includes the Acanthodiscus radiatus Zone and the latest A. radiatus to earliest Crioceratites loryi zones. These upper beds are slumped; they are the top of the Angles Valanginian Hypostratotype Section (AVHS) as it crops out in the Angles section. In one of the slumped beds a very elongated, long grooved Hibolithes-like species occurs. It resembles very closely an immature Hibolithes longior (Shvetsov, 1913, Pl. III, figs. 2.d, 2.g). Similar specimens occur earlier in the A. radiatus Zone (bed 386; Pl. 2, figs. 15-16). Few belemnites were collected from the succession above the slumped beds immediately after the A. radiatus Zone. This interval consists of densely packed thick beds of limestones (apparently in the C. loryi Zone) with: H. gr. subfusiformis Raspail, Duvalia cf. dilatata binervioides? (Stoyanova-Vergilova, 1965), and D. gr. dilatata (Blainville, 1827).

Cheiron section (CHE) (Fig. 11 ): The Cheiron area is of historical importance for cephalopod research because many species have been described from this area, which is now partly covered by an artificial lake (Lac de Castillon). However, when water-levels are low, the succession of Valanginian strata is more or less continuously exposed and easily accessible. Strata of Late Valanginian and Early Hauterivian ages remain exposed along the shore of the lake and in the hills to the west of the lake. Compared to the Angles section, the Cheiron section has more complex limestones. Some minor slumped levels exist in the Late Valanginian Olcostephanus nicklesi and Criosarasinella furcillata zones and also in the Early Hauterivian Crioceratites loryi Zone. A small number of belemnites was also collected (Fig. 11 ). Interestingly, the alveolar of these belemnites is often missing, suggesting physical damage by predatation, by transportation, or a combination of both.

Late Valanginian to Early Hauterivian ammonite stratigraphy

Recently the "Kilian Group" proposed an emended standard zonation for the ammonites of the Lower Cretaceous based on intensive research over the past years (Reboulet & Hoedemaeker et alii, 2006). Many details have been published concerning the ranges of ammonites in the Lower Hauterivian glauconitic facies (Arnaud & Bulot, 1992; Autran, 1993; Bulot, 1995; Bulot et alii, 1996; Reboulet, 1996) but there are also several regarding deeper-water deposits (Angles, La Charce: Thieuloy, 1977b; Bulot et alii, 1993, 1996; Thieuloy & Bulot, 1993; Reboulet, 1996; Reboulet & Atrops, 1999). Figures 12  - 13  - 14  summarize the data from these sources and compare deep and shallow water environments with respect to the lithology and distribution of ammonites. Only some of the "important" ammonite species and genera are shown, their positioning based on a correlation of the various outcrops discussed in the above references. The combination of the stratigraphic distribution of ammonites and the associated lithology is used to make sequence stratigraphic interpretations in the several palaeogeographic domains.

Some apparent discrepancies in stratigraphic relationships seem to be present in the successions that span the transition between the Lower and Upper Hauterivian. Most probably they are caused by a misinterpretation of some ammonite index species (see Fig. 13 ). This failing seems most common in the lack of understanding of ontogenitic variation, genetic relationships and development of speciation in the genus Lyticoceras and in the species Cruasiceras cruasense Torcapel s.s. Moreover, data are sparse and inconsistent in their interpretation of index species (e.g. Balearites balearis (Nolan) s.s.) so the zonal scheme for parts of the Hauterivian is to some extent provisional.

Belemnite distribution

To create a widely applicable biozonation based on belemnites, the author chose first to determine the characteristics of the associations of the faunas as they relate to the discrete lithologic successions laid down in the several marine environments. Eventually a combination of these associations along with more detailed knowledge concerning the vertical and horizontal distribution of belemnites should lead to a well-founded biozonation. These associations will be numbered successively according to their stratigraphic position within a stage.

Valanginian Belemnite Association 3 (VaBA3; see Janssen & Clément, 2002): In the Vocontian basin the sedimentary record of the Late Valanginian (above the Saynoceras verrucosum Horizon) is characterized by a significant change in the composition of the belemnite faunas (Janssen & Clément, 2002). This interval, that includes the Varlheideites peregrinus to Criosarasinella furcillata zones, is comprised of sets of beds with associations dominated by Duvalia binervia (Raspail, 1829), that alternate with sets of beds without a dominant belemnite species. In the Peyroules area the binervia-bearing strata appear to be correlative with the uppermost of these intervals. There, above the binervia-bed and still in the environment that causes the deposition of condensed phosphatic and glauconitic sediments are several species of belemnites, among them: Duvalia gervaisiana (Dumas, 1876), D. variegata (Raspail, 1829; = D. hybrida (Duval-Jouve, 1841)), D. aff. variegata (Raspail, 1829), Duvalia sp. 1 (= D. vaunagensis Gayte, 1984 [-unpublished-, nom. nud.]), Pseudobelus sp. indet., Pseudobelus sp. A (in Janssen & Fözy, 2004), Hibolithes gr. subfusiformis Raspail, H. longior Shvetsov, 1913, Hibolithes sp., Vaunagites sp., and Adiakritobelus Janssen & Fözy, 2004. This genus is particularly abundant with the species: Adiakritobelus brevirostris (Raspail, 1829), A. minaret (Raspail, 1829), A. robustus (Duval-Jouve, 1841), A. rogeri (Delattre, 1952), A. brevirostris (Raspail, 1829), A. gr. rogeri (Delattre, 1952), Adiakritobelus peyroulesensis sp. nov., and Adiakritobelus (?) gayteae sp. nov. Other forms, in part juvenile and immature Mesohibolitidae, like Belemnites pistilliformis Blainville, predominate in certain levels. All these species are a part of the VaBA3 association and may occur up to the lowest levels of the A. radiatus Zone.

Hauterivian Belemnite Association 1 (new association) (HaBA1): Although still present in the glauconite-generating succession, Duvaliidae become rare, both in and above the A. radiatus beds. What may be a new species appears at this level and it is named provisionally Duvalia aff. "hybrida" (Duval-Jouve). It is most probably the ancestor of the Pseudoduvalia. Here too appear sporadically the first strongly compressed species, possibly assignable to Duvalia gr. dilatata (Blainville). Mesohibolitidae, especially Hibolithes gr. subfusiformis Raspail and some very elongate forms are the major constituents of this belemnite faunal association. Some of these very elongated forms are representatives of Belemnites pistilliformis Blainville resembling or equivalent to Vaunagites Combémorel & Gayte, 1981, while others are various ontogenetic stages of Hibolithes longior Shvetsov, 1913. This association is transitional, between association VaBA3 and the association above it, HaBA2. In the standard ammonite zonation its range encompasses the upper part of the Acanthodiscus radiatus Zone and the base of the Crioceratites loryi Zone (Fig. 15 ).

Hauterivian Belemnite Association 2 (new association) (HaBA2): The first valid representatives of Pseudobelus brevis Paquier and the genus Pseudoduvalia occur in the Jeannoticeras jeannoti Subzone. They are characteristic faunal elements of the new association (HaBA2), and occur together with typical Duvalia dilatata (Blainville). This species is common, especially in strata bridging the Lower - Upper Hauterivian boundary. Belemnites in the pelagic sediments of the Col de Rousset section, north of Die (Drôme, France; unpublished data) have comparable associations and stratigraphic relationships. The stratigraphic range of HaBA2 spans the J. jeannoti Subzone, the Lyticoceras nodosoplicatum Zone, and attains the Hauterivian-Barremian boundary. However, in the Peyroules region the belemnite data from the upper part of the localities studied are too few to define precisely the upper boundary. Nevertheless, a threefold division of this association appears feasible, based on the first occurrence (= FO) of Pseudoduvalia polygonalis (Blainville) and/or Pseudobelus brevis Paquier (HaBA2a; Fig. 15 ), the FO of true Hibolithes subfusiformis (Raspail, 1829) (HaBA2b; Fig. 15 ), and the presence or absence of P. brevis Paquier along with D. dilatata (Blainville) and Pseudoduvalia spp. (HaBA2c; Fig. 15 ). Apparently, Pseudobelus becomes extinct near the middle of the Subsaynella sayni Zone and the youngest specimens of Pseudoduvalia are found near the boundary between the P. ligatus Zone and the B. balearis Zone (Peyroules area and unpublished data from Vallon de Valbonette near Barrême, southeastern France, pers. obs.), while the range of D. dilatata (Blainville) ends at the Hauterivian - Barremian boundary. Although the upper portion of these Hauterivian strata in a hemipelagic facies is exposed poorly, it is one of the most nearly continuous exposed sections of the outer slope to pelagic deposits of the Angles Barremian Stratotype (ABSS). The main constituent of the belemnite fauna appears to be the family Mesohibolitidae.

In the ABSS the belemnite fauna in strata of Late Hauterivian age is mainly Hibolithes gr. subfusiformis Raspail and subordinate Hibolithes gr. jaculiformis (Shvetsov, 1913). The former is almost circular in cross-section while the latter is clearly elliptical. A small morph of D. dilatata binervioides (Stoyanova-Vergilova, 1965) was collected in the lower part of the B. balearis Zone (bed 9-10). This specimen shows some binervia-like characteristics that may indicate an ancestral affinity to the smaller, earliest Barremian Duvalia silesiaca Uhlig, 1902. This rather impoverished association of belemnites is characteristic of the latest Hauterivian when genera such as Pseudobelus and Pseudoduvalia became extinct. The Duvaliidae and also the Mesohibolitidae show more diversity in the earliest Barremian.

Basin facies

In the VaBA3 association the stratigraphic distribution of belemnites is based primarily on their occurrences in the Angles, Source de l'Asse de Moriez, La Charce, and Vergol areas (see Janssen & Clément, 2002). More recent data allow a more precise correlation, and suggest that the base of VaBA3 can be fixed at bed 308 (Angles) or at bed 107 (Vergol), both of which are at the upper limit of the S. verrucosum Subzone (in the "Neocomites neocomiensis Subzone" sensu Atrops & Reboulet, 1993). The interval thus bounded is characterized by abundant Hibolithes cf. jaculoides Swinnerton (see Janssen & Clément, 2002), a form that contrary to previous findings, occurs first in the uppermost levels of the S. verrucosum Horizon, but is most abundant in the "N. neocomiensis Subzone" and at the base of the Karakaschiceras pronecostatum Subzone (Fig. 15 ). It continues to occur in fluctuating abundances throughout the K. pronecostatum Subzone, the V. peregrinus Subzone up to the base of the Olcostephanus nicklesi Subzone (Fig. 16 ). And scattered occurrences have been recorded in younger strata.

Another characteristic of VaBA3 appears to be the fluctuations in the occurrences of Duvalia gr. binervia (Raspail). The early Late Valanginian (base of VaBA3) is characterized by D. binervia (Raspail) and D. aff. gervaisiana (Dumas, 1876; = Duval-Jouve, 1841, Pl. III, fig. 6). Near the boundary between the V. peregrinus and O. nicklesi Subzones these species are replaced by D. binervia (Raspail) and D. variegata (Raspail, 1829). Another species of the binervia-group (Duvalia sp. 1) appears first in the Criosarasinella furcillata Zone, and D. variegata may become extinct in the middle of the C. furcillata Zone (Fig. 16 ). Duvalia sp. 2 occurs only in the lowest beds of Hauterivian age (middle of the Acanthodiscus radiatus Zone).

Comparison of coeval stratigraphic intervals shows no significant differences between the associations of belemnites that lived in shallow and those for which the habitat was deeper water. Figure 16  shows the first and last occurrences of taxa in the several stratigraphic columns. A comparison of the occurrences of several belemnite species in the Late Valanginian deep-water sequences with those that lived in shallow water indicates that most of the genera and species of belemnites in the shallow-water basal phosphatic and glauconitic levels can be found also in the O. nicklesi and C. furcillata zones. As indicated above, in the Vocontian basin most of the data concerning belemnites from deeper water is lacking for the greater part of Hauterivian times.

Recognition of discontinuities, systems tracts and correlation of sections

Several key-horizons can be recognized in the Valanginian to Hauterivian successions. These horizons are generally erosional surfaces or discontinuities (see Cotillon, 1971, 1975; Masse & Lesbros, 1987; Autran, 1993; Bulot, 1995; Loreau & Durlet, 2000; Pasquini et alii, 2004). Also, there are sets of characteristic marker beds, such as the A. radiatus-beds, the L. nodosoplicatum-beds, and characteristic bundles of couplets (S. sayni beds; beds 106 and 107 in Fig. 6 ) or multiplets (S. mimica/P. ligatus beds, Fig. 7 ). These bundles can be correlated virtually throughout the hemipelagic-area.

A hiatus that marks an absence of sedimentation during the period of time that spans the interval between the upper limit of the Early Valanginian and a point in the Late Valanginian is apparent in the Peyroules area. There are two superimposed discontinuities, the so-called "mid Valanginian discontinuity" and the "Upper Valanginian discontinuity" (respectively DVM and DVS sensu Autran, 1993). Burrows with glauconitic infill are abundant at the top of the bed immediately below the phosphatic-glauconitic sequence. The strata of Hauterivian age include the discontinuity DZL (Autran, 1993; e.g. Fig. 17 ), the discontinuity of the C. loryi Zone, and the discontinuity DZR (Bulot, 1995; Bulot et alii, 1996) of the A. radiatus Zone. Based on sequence stratigraphic interpretations, these discontinuities are here proposed to be either related to maximum flooding surfaces (MFS), or denote the boundary between two sequences. Field observations show that many more discontinuities can be identified (Fig. 12 ), either owing to the presence of borings (bio-erosion), or of encrusting (non-deposition), or because of an abundance of phosphatic fossils and pebbles. On the other hand they can sometimes be interpreted as having been caused by "bypassing". The discontinuity at the top of the O. variegatus Subzone is especially well represented in some profiles (Collet des Boules, Fig. 3 ; Pas d'Escale, Fig. 10 ) where it is made evident by strong boring activities. Here, this discontinuity is named DZN-1 (Fig. 17 ), for it is located near the base of the L. nodosoplicatum Zone. Note that these discontinuities are less evident in the Les Allaves area. The succession there consists of stacked "condensed" transgressive system tracts with expanded prolonged highstands (sometimes including latest highstand system tracts), while lowstand system tracts are absent (Fig. 17 ).

Generally, it is possible to correlate the various sections set-by-set. The O. variegatus beds in the Peyroules area are closely comparable with successions near La Lagne and the Pas d'Escale area (Fig. 17 ). Differences in the sedimentary development of the several areas are presumably related to the amount of condensation and to the accessibility of accommodation space. Sometimes, but not necessarily, differences in the degree of condensation are reflected in the colour of the rocks, dependent on the relative percentage of glauconite. In general, all beds are condensed and transgressive systems tracts (TST) are reduced to one or a few beds of limestone that are recognizable as discrete layers. The MFS is at the top of these more calcareous sets, while the subsequent marly set is the high stand systems tract (HST and probably partially the latest HST). These marl sets are often very rich in belemnites ("marnes à bélemnites" sensu Cotillon, 1971), brachiopods or echinoids (Toxaster marls sensu David, 1979, 1980). Ammonites appear to be restricted to the TST and MSF. However, these beds may also contain abundant macrofossils of other phyla, while some limestones in the HST include abundant ammonites too. Apparently the diversity of the ammonite genera and species in these hemipelagic deposits is low, but the individuals are abundant.

Research on these sediments, their sequences and their integration with biostratigraphic information, has led to a number of correlations between basin and platform deposits (Arnaud-Vanneau et alii, 1982; Ferry & Monier, 1987; Ferry & Rubino, 1989; Ferry et alii, 1989; Magniez-Jannin, 1992) based on discontinuities and/or faunas in common. I follow a different approach (see Mancini & Tew, 1995, p. 290-291; Hoedemaeker, 1999; Janssen & Clément, 2002, fig. 4). Parts of the marly sequences in the basin interpreted as lowstand systems tracts (LST) are represented by hiatus in the hemipelagic deposits (Figs. 12  - 13  - 14  & 17 ). In both, only the MFS's are supposed to be time-equivalents. The broken lines in Fig. 17  representing the transgressive surfaces are respective sequence boundaries that are not necessarily time-equivalent but are correlative. However, the interpreted hiatuses in the deposition of the shallow-water sequences in most cases continue into the lower part of the TST's and upper part of the HST's. Moreover, condensation of the sedimentary successions laid down in shallow water is not always accompanied by the production of glauconite visible to field observation.

Remarks

In the vertical distribution of the belemnites, the most striking phenomenon seems to be the fluctuations in the respective abundances of Mesohibolitidae versus Duvaliidae. In general, Upper Berriasian to Lower Valanginian sediments are dominated by Duvaliidae ("warm"). Decrease of the Duvaliidae, in both species diversity and dominance, takes place at the boundary between the Early and Late Valanginian, the Valanginian-Hauterivian boundary and in the uppermost Hauterivian, and could, at least in part, be related to temperature changes in surface waters. In the hemipelagic deposits, Duvaliidae diversify again but do not become more abundant, in connection with the diversification of the genus Pseudoduvalia in the S. sayni Zone. However, Mesohibolitidae remain by far the most abundant of the belemnite families.

A marked change in facies takes place in the Peyroules area at the boundary between the Early and the Late Hauterivian. Though marls are already present in the latest beds of the Lower Hauterivian, hemipelagic marls in notable thickness developed mainly in Late Hauterivian times. Especially, the basal unit (S. sayni Zone) consists mainly of marly sediments, with huge quantities of belemnites, brachiopods, and at its base remains of Isocrinus peyroulensis (Loriol). Also, the boreal ammonite Simbirskites, though not known in the area under investigation, in other parts of southeastern France occurs in sediments attributed to the S. sayni beds (Thieuloy, 1977a, p. 424). Generally, these Late Hauterivian rocks include large numbers of Hibolithes but to the author's knowledge, no Hibolithes jaculoides Swinnerton, 1937, is known from the areas of this study with the sole exception of the basin deposits of earliest Late Valanginian age (Fig. 16 ). However, scattered occurrences of Hibolithes jaculoides? may exist in the lowermost Hauterivian (Les Allaves; Fig. 9 ) and in the lower Upper Hauterivian of the Peyroules area (CB108-108a, Fig. 6).

In general the belemnite associations discussed here can be compared with faunas in many discrete sedimentary and palaeogeographic settings in the Mediterranean Tethys: the Carpathian Mts. (Vašíček et alii, 1994), northeast Bulgaria (Kolarovgrad area; Stoyanova-Vergilova, 1965), Georgia (Abkhazia; Shvetsov, 1913; Kakabadze & Keleptrishvili, 1991); Gerecse Mountains (Hungaria; Janssen & Fözy, 2004), Morocco (Mutterlose & Wiedenroth, 2008), Switzerland (Châtel Saint-Denis area, Fribourg; Ooster, 1857), and the Subbetic domain of Spain (pers. obs.). Eventually, this broad dissemination will be useful for the establishment of a biostratigraphic zonation based on belemnites.

Palaeontological notes

As some readers may not be familiar with certain of the belemnites mentioned in this work, brief remarks concerning these species are added. In addition, the species introduced by Raspail (1829, 1830) and Duval-Jouve (1841) from the Peyroules area, have been revised when necessary and placed in synonymy (Table I). Synonymization here may deviate from previous interpretations (see d'Orbigny, 1840, Duval-Jouve, 1841, and Combémorel, 1973). Some new species are introduced and "unfamiliar" species are treated more extensively.

Duval-Jouve (1841, p. 6-7) reported several localities for the provenance of the material he investigated, among which are: "la plaine de Cheiron entre Castillon et Castellane" (now partially submerged by the artificial lake of Castillon), Angles, Vergons, and the "glauconitic localities": La Lagne, Chamateuil, Peyroulles (now Peyroules), etc. As several of his new species have no precisely located site of origin, it is reasonable to select one of the collecting localities to be the locus of a topotype, provided that pertinent material can still be collected.

Among the variants around Belemnites subfusiformis introduced by Duval-Jouve, the following species, assigned Adiakritobelus, are important for this work: Belemnites subfusiformis Raspail var. γ, and var. δ (= var. robustus). They are restricted to glauconitic deposits (see Duval-Jouve, 1841, p. 71; La Lagne, Peyroules, etc.). And also Belemnites Platyurus [nov.] from several localities: the Blaron-Castillon area and La Garde, Chamateuil, Robion, Escragnolle, etc. (glauconitic facies). Probably that author included some specimens of the Valanginian - Hauterivian genus Adiakritobelus (species like Adiakritobelus peyroulesensis sp. nov.) in the early Late Barremian Belemnites Platyurus from La Garde.

Systematic descriptions

Abbreviations used are in according with Granzow (2000). In addition, the following abbreviations are used: "+" = invalid: a nomen dubium, nomen nudum, or nomen nullum (= secondary typing error), and "pt" = partim.

Family Mesohibolitidae Nerodenko, 1983

Genus "Belemnites"

Belemnites pistilliformis Blainville, 1827

(Pl. 1, fig. 1 )

non + 1819 Belemnites attenuatus Faure-Biguet, p. 47-48 [=? Pseudobelus but inadequately described: nom. dub.].
pt? 1827 Belemnites pistilliformis Blainville, p. 98-99, Pl. 5, figs. 14-15, 16-17 [nom. dub.?].
non + 1828 Belemnites attenuatus Sowerby, p. 176, Pl. 589, fig. 2 [to be replaced by Belemnites minimus Miller fide Riegraf et alii, 1998, p. 64].
pt 1829 Belemnites pistilliformis Raspail, p. 327, Pl. 8, figs. 95-97 (non figs. 98-102 [= Hibolithes gr. subfusiformis Raspail]).
? + 1829 Belemnites attenuatus Raspail, p. 319-320, Pl. 8, fig. 72 [deformed specimen: nom. dub.].
pt 1829 Belemnites marginatus Raspail, p. 319, Pl. 8, figs. 73-74 [juvenile], non fig. 70 (= Hibolithes gr. jaculiformis Shvetsov, 1913).
1829 Belemnites pistilloides Raspail, p. 320, Pl. 8, fig. 75 [juvenile].
+ 1829 Belemnites gemmatus Raspail, p. 321, Pl. 8, fig. 77 [teratological specimen: nom. dub.].
? + 1829 Belemnites rostratus Raspail, p. 321, Pl. 8, fig. 78 [teratological specimen: nom. dub.].
+ 1829 Belemnites crassior Raspail, p. 327, Pl. 8, fig. 84 [nom. dub.].
+ 1829 Belemnites crassissimus Raspail, p. 327, Pl. 8, figs. 85-86 [teratological specimen: nom. dub.].
+ 1829 Belemnites aculeus Echini Raspail, p. 327-328, Pl. 8, fig. 87 [teratological specimen: nom. dub.].
pt 1841 Belemnites pistilliformis Blainville; Duval-Jouve, Pl. 8, figs. 10 (?), 13-16.
pt 1841 Belemnites subfusiformis Raspail; Duval-Jouve, Pl. 9, figs. 2, 13-14.
pt 1861 Belemnites pistilliformis Blainville; Loriol, Pl. I, fig. 2.
pt 1922 Belemnites (Aulacobelus) pistillirostris Pavlow; Tomitch, p. 7, 18, 22.
pt? + 1984 Hibolites piriformis n. sp. Gayte, Pl. I, fig. 8 [-unpublished-: nom. nud.]
+ 1997 Hibolites cf. pistiformis (Blainville); Baraboshkin & Yanin, p. 15 [nom. null.; nom. dub.].
2004 "Belemnites" pistilliformis Raspail; Janssen & Fözy, p. 37-38, Pl. II, fig. 8; Pl. III, fig. 3.

Remarks: Includes (specifically indeterminable) juvenile to immature specimens of Hibolithes spp. but also juvenile to immature specimen of the genera Vaunagites and Adiakritobelus.

Range: Essentially Late Valanginian – late Early Barremian.

Genus? species?

? 1951 Belemnites bicanaliculatus Blainville; Petkovic & Markovic, p. 23-24, Pl. I, fig. 4.

Remarks: One very small hibolitoid rostrum with faint lateral impressions, morphologically comparable with the Early - earliest Late Valanginian (S. verrucosum "Horizon") genus Mirabelobelus Janssen & Clément, 2002. It occurs in the S. sayni Zone of the Collet des Boules. A comparable specimen has been collected at the same stratigraphical interval in the Hauterivian outerslope deposits of Tornajo Mt., municipality of Lorca, southeast Spain. Superficially it resembles certain small species of the Tithonian - earliest Berriasian group of Pseudobelus (?) gr. fischeri Combémorel & Mariotti, 1990. However, this attribution is at the moment still not certain, for it might represent some small morph of a juvenile, a new, or a teratological species of the genus Hibolithes. The Serbian specimen apparently comes from Hauterivian sedimentary deposits (Petkovic & Markovic, 1951, p. 24). Probably, the species described as Belemnites (Duvalia) grasianus Duval by these authors is comparable with Duvalia cf. maioriana Stoyanova-Vergilova sensu Janssen & Fözy (2004). However, the cephalopod fauna they described (loc. cit, p. 41) appears to contain both Valanginian, Hauterivian and/or Barremian elements.

Stratigraphic occurrence: Subsaynella sayni Zone (early Late Hauterivian).

Genus Hibolithes Denys de Montfort, 1808

Hibolithes fusoides (Lamarck, 1822)

(Pl. 1, figs. 2-7 )

1822 Belemnites fusoides Lamarck, p. 592.
1918 Belemnites fusoides (Lamarck); Favre, p. 6, Pl. I, fig. 6 [= Lamarck, 1822].
? 1984 Hibolites subfusiformis (Raspail); Gayte, Pl. I, fig. 3.
1995 Pseudohibolites fusoides (Lamarck); Riegraf, p. 102.
? 2004 Hibolithes subfusiformis (Raspail); Janssen & Fözy, Pl. II, fig. 17.

Remarks: The type seems to be from Saint-Paul-Trois-Châteaux (southwest of Clansayes, Drôme, France). According to Favre (1918) the species could be one of the Hauterivian group of Belemnites (Belemnopsis) pistilliformis Blainville, I agree. Belemnites subconicus var. [b] of Lamarck is from the same locality. Forms in this variety includes specimens from the Aptian of Saint-Paul-Trois-Châteaux and an Early Jurassic species which could not have come from that area (Favre, 1918, p. 6). However, specimens A and B figured by Favre (1918, Pl. 1, figs. 1-2) are morphologically comparable to Adiakritobelus and in my opinion could with an equal degree of validity be referred to this Late Valanginian to earliest Hauterivian genus. I have no knowledge of the geology of the Saint Paul-Trois-Château area, but according to Roman (1932, p. 17-21) and the "Carte Géologique Détaillée de la France 1:50.000" (type 1922; XXX-39, map no.890, Valréas) no Aptian/Albian sedimentary rocks are exposed near St. Paul-Trois-Châteaux but only in the Clansayes area. The "marnes grises à Bélemnites" (Valanginian-Hauterivian) are exposed far to the north and east, some of them in a glauconitic, neritic facies. So, mistakes concerning the origin of this material have been made in the past, probably already in Lamarck's time. Depending on the range of morphological variation in the species, the belemnite figured by Janssen & Fözy, 2004 (Pl. II, fig. 17; apparently from the A. radiatus or C. loryi Zone) might be of this species too. At least it has the typical fusiform outline but appears to have no alveolar groove.

Geographic occurrence: Les Allaves and Peyroules area (Clausson, Collet des Boules, Alpes de Haute-Provence), Moulezan, Gard (Gayte, 1984), and possibly Hungaria.

Stratigraphic occurrence: Early Hauterivian (late A. radiatus - L. nodosoplicatum/cruasense zones).

Hibolithes cf. jaculoides Swinnerton, 1937

(Pl. 2, figs. 9-10 )

non 1829 Belemnites symmetricus Raspail, p. 324-325, Pl. 8, fig. 90 (fide Mutterlose, 1978).
non 1829 Belemnites pistilliformis Blainville; Raspail, Pl. 8, fig. 102 (fide Mutterlose, 1978).
non 1849 Belemnites subfusiformis Raspail; Quenstedt, Pl. 29, figs. 41 [= pistillifomis Raspail], 42 [= H. gr. subfusiformis Raspail], 43 [= pistilliformis Raspail] (fide Mutterlose, 1978).
pt? 1857 Belemnites pistilliformis Blainville; Ooster, Pl. 2, figs. 9-10, 11 (?).
non 1898 Belemnites jaculum Phillips; Simionescu, p. 108-109, Pl. I, figs. 5-6.
non 1913 Hibolites jaculiformis Shvetsov, p. 52, Pl. II, figs. 5-6; Pl. III, figs. 4, 11-12 (fide Mutterlose, 1978).
? 1915 Belemnites jaculum Phillips; Jekelius, p. 117, Pl. X, fig. 3.
* 1937 Hibolites jaculoides Swinnerton, p. xxv (pro Belemnites jaculum Phillips non Faure-Biguet).
pt ? 1970 Hibolites jaculoides Swinnerton; Stoyanova-Vergilova, p. 16-17, Pl. II, figs. 4-6.
pt 1978 Hibolites jaculoides s.s. Swinnerton; Mutterlose, p. 99-102, Pl. 3, figs. 1-3; Pl. 4, figs. 1-3, 5; Pl. 5, fig. 4; Pl. 6, fig. 1 (pars cum syn.).
2002 Hibolithes cf. jaculoides Swinnerton; Janssen & Clément, p. 514, 515, 521.
2002 Hibolithes sp. nov. Janssen & Clément, p. 514 (most probably juvenile specimens).

Remarks: Only few valid records of this species have been published in the Mediterranean Tethys region. Generally, it is thought to be misidentified as Hibolithes gr. subfusiformis Raspail or Belemnites pistilliformis Blainville.

Stratigraphic occurrence: Latest S. verrucosum Subzone to early O. nicklesi Zone (normal occurrence; Fig. 16) and scattered appearances in strata of earliest Hauterivian age (Les Allaves) and possibly also in the lower part of the S. sayni Zone of the Peyroules area. The oldest occurrences in the Boreal-Atlantic region are not yet resolved from a stratigraphical point of view, but it appears that the range of this species in the two palaeogeographical areas is not the same!

Geographic occurrence: In addition its well-known distribution in the Boreal-Atlantic, this species is also found in the northern margins of the Mediterranean Tethys and in parts of the Russian Platform.

Hibolithes josephinae (Honnorat-Bastide, 1890)

1890 Belemnites Josephinae nov. sp. Honnorat-Bastide, p. 465-466, figs. 1-5.
pt ? 1966 Hibolites longior Schwetzoff; Drushchits & Mikhaylova, p. 117 [Late (st) Hauterivian] (non p. 120, 121 [Early? Hauterivian]).
2004 Hibolithes cf. josephinae (Honnorat-Bastide); Janssen & Fözy, p. 44, Pl. II, fig. 15.

Remarks: This elongated cylindrical species was found in outcrops of Late Hauterivian age near La Bégude (France). In this area a succession is visible (see David, 1979) comparable to that of the sequence of Late Hauterivian age in the Peyroules area. It is quite possible that part of the Late Hauterivian group of belemnites comprised in Hibolithes longior Shvetsov should be grouped within Hibolithes josephinae (see below).

Stratigraphic occurrence: Latest S. sayni through P. ligatus Zone (Late Hauterivian).

Hibolithes longior Shvetsov, 1913

(Pl. II, figs. 1-5, 6 (?), 7, 8 (?), 11, 12 (?), 13, 14 (?), 15-17 & 18 (?) )

pt 1861 Belemnites pistilliformis Blainville; Loriol, p. 17-18, Pl. I, fig. 1.
* 1913 Hibolites longior n. sp.; Shvetsov, p. 51-52, 68, Pl. III, figs. 2a (LT fide Stoyanova-Vergilova, 1970), b/e, c/f, d/g.
1939 Hibolites longior Schwetzoff; Krymgol'ts, p. 10-11, Pl. I, fig. 7.
pt 1964 Hibolites longior Schwetzoff; Stoyanova-Vergilova, p. 138, 144 (?), 145 (pars).
pt 1966 Hibolites longior Schwetzoff; Drushchits & Mikhaylova, p. 120-121 [Early? Hauterivian] (non p. 117 [Late (st) Hauterivian]).
pt ? 1970 Hibolites longior Schwetzoff; Stoyanova-Vergilova, p. 13-14, Pl. III, figs. 1-2 (?), 3.
1984 Hibolites subfusiformis (Raspail) morphe B; Gayte, Pl. I, fig. 1.
1984 Hibolites subfusiformis (Raspail) morphe A; Gayte, Pl. I, fig. 2.
? 1984 Hibolites dumasi n. sp. morphe A Gayte, Pl. I, fig. 4 [-unpublished-: nom. nud.].
pt 1994 Hibolites longior Schwetzoff; Vašíček et alii, p. 24, 80 [Early Hauterivian].
non 1994 Hibolites longior Schwetzoff; Vašíček et alii, p. 24 (pars), 43, 80 (pars), Pl. 25, figs. 7-8 [Late Hauterivian].
1995 Pseudohibolites longior (Schwetzoff); Riegraf, p. 103.
1997 Hibolites cf. longior Schwetzoff; Baraboshkin & Yanin, p. 15 [Late Valanginian].
non 2002 Hibolites longior Schwetzoff; Topchishvili et alii, p. 64-65, Pl. VI, figs. 1-2 [latest Hauterivian; = Hibolithes sp. nov. gr. cigaretus Stoyanova-Vergilova, 1965].
2004 Hibolithes longior Shvetsov; Janssen & Fözy, p. 37, Pl. II, figs. 20-21 (pars cum syn.).

Remarks: The material of Shvetsov [Schwetzoff] is from the "Calcaire à Duvalia bipartita, Duv. polygonalis, Hoplites amblygonius, etc." from Abkhasia (western Georgia). At first these cephalopods were thought to indicate a Valanginian and Hauterivian age. However, subsequently this limestone was considered to represent only the Late Hauterivian (Eristavi, 1961; Drushchits & Mikhaylova, 1966). The belemnites in it: Duvalia bipartita (= Pseudobelus (gr.) brevis Paquier) and Duvalia polygonalis (=? Pseudoduvalia trabiformis) would indeed indicate "mid" Hauterivian beds. Either Hibolithes longior has a fairly long stratigraphic range, or two or more species are involved (see above). Clearly, H. longior occurs in strata of earliest Hauterivian age and, as can be judged from the synonymy, I prefer to restrict the species to the latest (?) Valanginian - earliest Hauterivian interval. Individuals from strata of Late Hauterivian age are referred to one of these three species: Hibolithes gr. subfusiformis Raspail, Hibolithes josephinae (Honnorat-Bastide) or Hibolithes gr. cigaretus Stoyanova-Vergilova. The specimen listed as Hibolithes longior? differs from the type in that the alveolar groove is shorter. These variants are most probably within the limits of intra-specific variation. Hibolithes longior clearly differs from Hibolithes subfusiformis (Raspail) and Hibolithes subfusiformis Raspail. Juvenile specimens of H. longior s.s. are much more elongated and show (generally) a marked, longer alveolar groove than the questionable variant does. Juvenile specimens of H. subfusiformis Raspail are of the Belemnites pistilliformis-type and show no, or at most a very faint, alveolar groove. Like most species of Hibolithes, excluding H. subfusiformis (Raspail) with its spindle-like rostrum, the rostrum is hastate and during ontogeny this feature becomes more and more pronounced. Hibolithes (gr.) cigaretus appears more robust than the relative slender H. longior, is much less elongated, and has a pronounced rather long alveolar groove. H. josephinae is an elongated rather slender, well rounded (in cross-section) belemnite, with a long but faint alveolar groove.

Stratigraphic distribution: Latest Valanginian (?) – earliest Hauterivian.

Hibolithes sp. 1

(Pl. 1, figs. 12-13)

? 1849 Belemnites pistilliformis Blainville; Quenstedt, Pl. 29, fig. 44.

Remarks: A relative short fusiform rostrum with a well developed alveolar groove and a pointed to mucronate apex. All cross-sections show rounded outlines. Whether it is a new species or a teratological specimen of H. gr. subfusiformis Raspail is not known at the moment (see below). Superficially it shows some morphological similarities to Rhopaloteuthis-like species. Unfortunately, the provenance of Quenstedt's specimen is uncertain. However, it is indicated to have come from the Castellane area.

Stratigraphic occurrence: Earliest S. sayni Zone (early Late Hauterivian).

Hibolithes sp. (gr. subfusiformis Raspail)

(Pl. 1, figs. 8-11, 18-19)

? 1800 "bélemnite en massue" Sage, Pl. II, fig. 3.
+ 1829 Belemnites rugosus Raspail, p. 322-323, Pl. 8, fig. 89 [nom. dub.].
pt 1841 "deformed Belemnites subfusiformis" Raspail; Duval-Jouve, Pl. 10, figs. 11-24.
1913 Hibolites sp. Shvetsov, p. 53, 68, Pl. II, fig. 3.

Remarks: Teratologic specimens of H. gr. subfusiformis Raspail are common. Apparently, predatation (synecological; see Mietchen et alii, 2005) and accumulation (environmentally induced stress) was relatively high, especially in the hemipelagic deposits.

Stratigraphic occurrence: These teratological morphs occur throughout the sedimentary rocks but appear to be especially abundant near the boundary between the Early and Late Hauterivian.

Hibolithes subfusiformis (Raspail, 1829)

(Pl. 1, figs. 14-17)

1829 Belemnites subfusiformis Raspail, p. 325, Pl. 8, fig. 93.
pt 1841 Belemnites subfusiformis Raspail; Duval-Jouve, Pl. 9, figs. 3 (?), 7, 11.
non 2004 Hibolithes subfusiformis (Raspail); Janssen & Fözy, Pl. II, fig. 17 (pars cum syn.).

Remarks: Only morpho-typical specimens are included, i.e. specimens with a true spindle-like (subfusiform) outline. Specimens with fusiform (lanceolate or hastate) morphs are referred to H. gr. subfusiformis Raspail or to Hibolithes fusoides (Lamarck, 1822).

Stratigraphic occurrence: S. sayni through earliest P. ligatus zones (Late Hauterivian).

Hibolithes gr. subfusiformis Raspail
(= pars Belemnites jaculum Phillips, non Faure-Biguet, 1819 nec Swinnerton, 1937)

(Pl. 1, figs. 20-21)

+ 1819 Belemnites clava Faure-Biguet, p. 48-49 [nom. dub.].
? + 1819 Belemnites index Faure-Biguet, p. 50 [nom. dub.].
+ 1819 Belemnites striatus Faure-Biguet, p. 53-54 [nom. dub.].
+ 1829 Belemnites praemorsus Raspail, p. 325-326, Pl. 6, fig. 27 [teratological specimen: nom. dub.].
1829 Belemnites symmetricus Raspail, p. 324-325, Pl. 8, fig. 90 [nom. obl.].
+ 1829 Belemnites pistilliformis Raspail, p. 327, Pl. 8, figs. 98-102.
pt 1841 Belemnites pistilliformis Blainville; Duval-Jouve, Pl. 8, figs. 11-12.
pt 1841 Belemnites subfusiformis Raspail; Duval-Jouve, Pl. 9, figs. 1, 8-9, 12.
pt 1841 "deformed Belemnites subfusiformis" Raspail; Duval-Jouve, Pl. 10, figs. 25-26.
1886 Belemnites inopinatus n. sp. Rothpletz, p. 168, Pl. XIV, figs. 17-17.a.
? 1984 Hibolites dumasi n. sp. morphe B Gayte, Pl. I, fig. 4 [-unpublished-: nom. nud.].
2004 Hibolithes subfusiformis (Raspail); Janssen & Fözy, Pl. II, fig. 17 (pars cum syn.).

Remarks: This group includes species like Hibolithes symmetricus (Raspail, 1829), and probably Hibolithes dumasi Gayte, 1984 [-unpublished-: nom. nud.], Hibolithes subfusiformis Raspail, among others. Also see remarks in Janssen & Fözy (2004, p. 42-43).

Stratigraphic occurrence: This group of belemnites appears first in the Early Hauterivian and disappears in the earliest Barremian (Nicklesi pulchella/Kotetišvilia nicklesi zones).

Genus Vaunagites Combémorel & Gayte, 1981

Remarks: In my opinion Belemnites pistilliformis Blainville, 1827, and Vaunagites pistilliformis Combémorel & Gayte, 1981, should be considered discrete species. However, part of Blainville's specimens could be referred to the genus Vaunagites, but all of those figured are apical parts only (see Belemnites pistilliformis Blainville).

Stratigraphic occurrence: Latest Valanginian through earliest Hauterivian (early A. radiatus Zone only). A closely related group occurs in the C. loryi Zone, however, most probably these are related to Hibolithes longior Shvetsov.

Vaunagites sp.

pt ? 1827 Belemnites pistilliformis Blainville, p. 98-99, non Pl. 5, figs. 14-15 nec figs. 16-17.
1981 Vaunagites pistilliformis (Blainville); Combémorel & Gayte, p. 107-108, Pl. 1, figs. 1-4, 8-9 (pars cum syn.).

Remarks: Incomplete and immature specimens are virtually inseparable from immature H. gr. subfusiformis Raspail or Belemnites pistilliformis Blainville. In general, Vaunagites is distinguishable because it has a very elongated rounded rostrum with no, or virtually no alveolar groove.

Stratigraphic occurrence: Teschenites callidiscus Subzone (see Gayte, 1984) through A. radiatus Zone (Combémorel & Gayte, 1981); latest Valanginian to earliest Hauterivian. This species seems to be rare or could not be recognized in our material, and is included in Belemnites pistilliformis Blainville. Here, it appears to be present only in the "middle" of the A. radiatus Zone.

Genus Adiakritobelus Janssen & Fözy, 2004

Remarks: A genus that partially replaces the invalid (manuscript name) genus Combemorelites Gayte, 1984 [-unpublished-: nom. nud.; see Janssen & Fözy, 2004, p. 35-36]. The species are characterized by mature growth-stages that show either a hibolitoid outer-morphology or a mesohibolitoid outer-morphology. Hibolitoid-morphs display mainly rounded to slightly depressed cross-sections. Most mesohibolitoid-morphs are more strongly depressed in cross-section. Juvenile to immature specimens are in general hibolitoid. The alveolar areas are generally rounded in cross-section but may show a tendency toward becoming subquadrangular. The alveolus occupies from one-third to two-third of the length of the rostrum. However, in some species it is shorter and the alveolar cavity is always shallow with respect to the length of the alveolus. The position of the alveolar-line shifts between a central and a dorsal position but is generally on the dorsal side. Some species show a poorly defined to clearly flattened area in the ventral region. The apical area is always depressed, while the apex may be obtuse, pointed or even very elongated. The rostrum varies: subfusiform, fusiform or elongated. The splitting surface shows a slit more or less comparable with that of the Late Barremian - Early Aptian genus Mesohibolites s.s., and curves forwards, i.e. towards the alveolar opening, in an arcuate curve. Lateral lines, when visible, appear to be comparable to those of Hibolithes. They run parallel approximately from the alveolar opening to the apex. Exceptionally, three parallel lines can be seen. Mature specimens often have a mucronate apex.

Species included: Hibolitoid-morphs include Adiakritobelus robustus (Duval-Jouve, 1841; = Combemorelites mariae Gayte, 1984 [-unpublished-: nom. nud.]), Adiakritobelus rogeri (Delattre, 1952), and Adiakritobelus gayteae sp. nov. (pro Hibolites piriformis Gayte, 1984 [-unpublished-: nom. nud.]), while mesohibolitoid-morphs include Adiakritobelus brevirostris (Raspail, 1829), Adiakritobelus minaret (Raspail, 1829), and Adiakritobelus peyroulesensis sp. nov. (see Table II for differences between the species).

Stratigraphic occurrence: Late Valanginian (V. peregrinus Zone) to earliest Hauterivian (early A. radiatus Zone only). However, in the upper part of the K. pronecostatum Subzone and the base of the V. peregrinus Subzone, teratological? (Pl. 3, figs. 1-2) specimens occur that most probably represent the ancestor of this genus.

Adiakritobelus brevirostris (Raspail, 1829)

(Pl. 3, figs. 3-8)

* 1829 Belemnites brevirostris Raspail, p. 321-322, Pl. 8, fig. 80 [HT by MT].
1829 Belemnites navicula Raspail, p. 321, Pl. 8, fig. 79 [immature].
? 1829 Belemnites oblongus Raspail, p. 322, Pl. 8, fig. 82.

Remarks: Specimens of this species came from the glauconitic beds (Valanginian-Hauterivian) near La Lagne (east of Castellane).

Stratigraphic occurrence: This species is present in the phosphatic conglomerate, at the base of the glauconitic sediments that characterize the Valanginian-Hauterivian boundary in the Peyroules area. In the deeper water deposits of the Vocontian Basin it occurs from the V. peregrinus Zone up to the base of the C. furcillata Zone (e.g. beds 338a-b to 363 of the Angles Valanginian Hypostratotype section (= AVHS)).

Adiakritobelus minaret (Raspail, 1829)

(Pl. 3, figs. 9-16)

* 1829 Belemnites minaret nob. Raspail, p. 324, Pl. 8, fig. 94 [HT by MT].
1829 Belemnites fusus Raspail, p. 322, Pl. 8, fig. 81 [immature].
? 1858 Belemnites minaret Raspail; Pictet & Loriol, p. 7-8, Pl. I bis, fig. 8.
pt 1915 Belemnites minaret Raspail; Kilian & Reboul, p. 26

Remarks: The type specimen is from the glauconitic (Valanginian-Hauterivian) beds near La Lagne (east of Castellane). See Table II, for its distinction from other species.

Stratigraphic occurrence: The phosphatic conglomerate at the base of the glauconitic sediments that characterize the Valanginian-Hauterivian boundary in the Peyroules area. In the deeper-water deposits its range is rather short. It occurs from bed 346a through bed 358-359 (upper part of the O. nicklesi Zone) of the AVHS.

Adiakritobelus peyroulesensis sp. nov.

(Pl. 4, figs. 1-2 (HT), 3-4 (paratype), 5-6 (see Ooster, 1863, Pl. A, fig. 3), 7-10; Pl. 9, figs. 5-6)

1841 Belemnites subfusiformis Raspail var. γ Duval-Jouve, Pl. 9, fig. 10.
pt 1841 Belemnites Platyurus Duval-Jouve, p. 73-74 [the locality La Garde], non Pl. 11, figs. 1-4.
pt 1863 Belemnites semicanaliculatus Blainville, variété Ooster, p. 3-4, Pl. A, figs. 2, 3 (?), 4.
? 1897 Belemnites beskidensis Neumayr & Uhlig; Roman, p. 123.
? 1897 Belemnites (Hibolites) beskidensis Uhlig; Roman, p. 129.
? 1922 Belemnites Beskidensis Uhlig; Tomitch, p. 14.
? 1922 Belemnites cf. gladiiformis Uhlig; Tomitch, p. 14.

Derivation of name: Named after the geographical area of the community of Peyroules (Alpes de Haute-Provence, France).

Holotype: RGM 214.798 (Pl. 4, figs. 1-2).

Types: RGM 214.798 [HT, mature], RGM 214.787 (immature) and RGM 214.995 (juvenile).

Type stratum: Latest Valanginian - earliest Hauterivian glauconite bed CB79 (Collet des Boules).

Material: From Angles, RGM 214.765 (ANG373-381) and unregistered material; Cheiron, RGM 560.587 (CHE377a2top); Clausson, RGM 214.789a-793e, 214.794, 214.799, 214.870-872, 214.880, 214.884, 214.891-896, 214.904-906, 214.921-922, 214.927, 214.934, 214.937, 214.994-996, 215.000, 288.371, 288.373, 288.375 (CL095); Collet des Boules, RGM 214.787 (CB078), RGM 214.788, 214.791a-c, 214.795-798, 214.800, 214.845, 214.852-854; La Charce RGM 214.766 (LC166-167); Ravin du Mal Bouisset, RGM 560.526, 560.536-538 (RMB097); Vergol, RGM 214.755 (VGL163-164, latest O. nicklesi Zone), 214.756 (VGL167b-168), 214.757-758 (VGL170), 214.759 (VGL172b) all C. furcillata Zone, 214.760 (VGL185, T. callidiscus Subzone), 214.767-768 (VGL169-169a1, C. furcillata Zone).

Description: Very elongated rostrum, due to the stretched apical area. Rostrum is more or less spindle-like in immature specimens, while in mature specimens the maximum diameter of the cross-section is near the beginning of the elongate, conical alveolus. The alveolar groove is long, the alveolar cavity short, the beginning of the alveolus is centrally placed. Apical area initially depressed, flattened dorso-ventrally but towards the apex it becomes more and more rounded. The alveolar part is rounded to angular. These characteristics results in a mesohibolitoid type of rostrum.

Remarks: The mesohibolitoid types like Adiakritobelus brevirostris (Raspail) and Adiakritobelus minaret (Raspail) differ from the new species due to their more obtuse outer morphology and shorter overall rostrum.

Stratigraphic distribution: Only a few specimens were collected from the AVHS and Cheiron sites, where they appear to be restricted to the latest Valanginian. However, in other successions (Vergol, La Charce) the species first occurs in the sediments that characterize the uppermost part of the O. nicklesi Zone. Most commonly, it is associated with the glauconitic deposits in the Peyroules area. It appears to range from to the top of the O. nicklesi Zone to the base of the T. callidiscus Subzone, being most abundant in the C. furcillata Subzone of the deeper-water deposits.

Adiakritobelus robustus (Duval-Jouve, 1841)

(Pl. 5, figs. 1-6, 7-8 (cf.), 9-10, 11-13 (cf.); Pl. 9, figs. 1-2 [NT])

1841 Belemnites subfusiformis Raspail var. δ, robustus Duval-Jouve, p. 69, Pl. 9, figs. 5-6.
1922 Belemnites (cf.) Fallauxi Uhlig; Tomitch, p. 14.
+ 1984 Combemorelites mariae n. sp. Gayte, p. 101-102, Pl. 2, figs. 4-5 [-unpublished-: nom. nud.].
1993 Hibolithes subfusiformis var. robustus (Duval-Jouve); Autran, p. 57, 66.
2004 Adiakritobelus n. gen., n. sp. Janssen & Fözy, Pl. II, figs. 11-12.

Remarks: Duval-Jouve (1841, p. 71) noted that these belemnites occur only in the glauconitic deposits, among others, in the Peyroules area. The material presented here shows various ontogentic stages.

Stratigraphic occurrence: In the phosphatic conglomerate at the base of the glauconitic strata that characterize the Valanginian-Hauterivian boundary in the Peyroules area, and in the early A. radiatus Zone of the Les Allaves area. A specimen from Angles is from bed 393 (A. radiatus beds; Pl. 5, figs. 7-8). It is restricted to the earliest Hauterivian. The Hungarian specimen figured by Janssen & Fözy (2004) occurred either in uppermost Valanginian or lowermost Hauterivian sedimentary rocks.

Geographical occurrence: France, Hungary (Janssen & Fözy, 2004), and Spain (Tornajo, see Pl. 5, figs. 11-13).

Adiakritobelus rogeri (Delattre, 1952)

(Pl. 6, figs. 1-4, 5-6 (immature), 7-8 (juvenile); Pl. 9, figs. 3-4)

? + 1829 Belemnites rimosus Raspail, p. 318-319, Pl. 8, fig. 68 [teratological specimen: nom. dub.].
1952 Hibolites rogeri n. sp. Delattre, p. 42-43, Pl. II.a, figs. 1-3.
1984 Combemorelites rogeri (Delattre); Gayte, p. 102-104, Pl. 2, figs. 6-9  [-unpublished-: comb. nud.].
1989 Hibolites cigaretus Stoyanova-Vergilova; Michalík & Vašíček, Pl. 3, fig.1.
1993 Hibolites rogeri Delattre; Autran, p. 57, 73.
1994 Hibolites cigaretus Stoyanova-Vergilova; Vašíček et alii, p. 79, Pl. 25, figs. 3-4 [= Michalík & Vašíček, 1989].
1995 Pseudohibolites rogeri (Delattre); Riegraf, p. 105.

Remarks: Type specimens are from the Peyroules area.

Stratigraphical occurrence: In the phosphatic conglomerate, at the base of the glauconitic sediments that characterize the Valanginian-Hauterivian boundary in the Peyroules area. In the AVHS it is found in the beds 362 to 387 (C. furcillata through early A. radiatus Zone).

Adiakritobelus (?) gayteae sp. nov.

(Pl. 6, figs. 9-10)

pt 1965 Hibolites aff. obtusirostris (Pavlow); Stoyanova-Vergilova, p. 153-154, Pl. II, fig. 1 (non, cum syn.).
pt ? + 1984 Hibolites piriformis n. sp. Gayte, p. 94-96, Pl. 1, figs. 6-7, 8 (non?) (cum syn.) [-unpublished-: nom. nud.].

Derivation of name: Named after Dominique Gayte.

Holotype: RGM 214.909 (Pl. 6, figs. 9-10).

Type stratum: Uppermost Valanginian - lowermost Hauterivian glauconite bed CL095 (Clausson).

Description: Rostrum hibolitoid with a characteristic flattened ventral side, better developed and more visible in mature or gerontic specimens (see HT). The apex is mucronate and the maximum width of the rostrum is close to the apex. As a result the overall aspect is that of a rostrum which tapers down to the alveolar opening. The alveolar area is round, due to the absence of the flattened ventral side and generally a well-marked but narrow alveolar groove is visible. The alveolus is shallow and may attain about half the length of the alveolar groove, but is generally much shorter. Immature rostra have a hibolitoid appearance, with a ventral flattening less pronounced than that of mature specimens and a mucron is absent. The juvenile stages are virtually impossible to distinguish from Belemnites pistilliformis Blainville.

Material: Clausson, RGM 214.875, 214.900, 214.909, 214.915, 214.940, 288.363, 288.364 (CL095); La Lagne RGM 288.720 (LLG102), 288.725 (LLG098); Les Allaves RGM 560.513 (ALL113-114), 560.514 (ALL113-114).

Remarks: The species is most probably related to Adiakritobelus rather than to Hibolithes. It was described as having been collected from the A. radiatus beds of Clarensac (Gard, France) in the manuscript of Gayte (1984).

Stratigraphic occurrence: Late (?) C. furcillata (latest Valanginian) - earliest A. radiatus Zone (earliest Hauterivian).

Adiakritobelus spp.

pt 1841 "deformed Belemnites subfusiformis" Raspail; Duval-Jouve, Pl. 10, figs. 1-8, 9-10 (?) [teratological].
1842 Belemnites semicanaliculatus d'Orbigny; Matheron, p. 37 (?), 38-39, 259.
? 1858 Belemnites platyurus Duval-Jouve; Ducret, p. 161.
? 1863 Belemnites semicanaliculatus Blainville, variété Ooster, p. 3-4, Pl. A. fig. 1 (=? gr. rogeri Delattre).
1872 Belemnites minaret Raspail; Rouville, p. 729-730.
1876 Belemnites Minaret Raspail; Dumas, p. 316-317, 369.
1878 Belemnites minaret Raspail; Escher von der Linth, p. 41, 159.
1880 Belemnites minaret Raspail; Sarran d'Allard, p. 337, 338.
1887 Hastites (Hibolites) minaret Raspail; Mayer-Eymar, p. 76, 78.
1892 Belemnites cf. Fallauxi Uhlig; Nicklès, p. 40, 47-48, 50.
1892 Belemnites cf. minaret Raspail; Nicklès, p. 40, 47-48, 51.
1912 Belemnopsis cf. minaret Raspail; Blayac, p. 170.
1919 Belemnites semicanaliculatus Blainville; Rodighiero, p. 57.
1922 Hibolites Minaret Raspail; Fallot, p. 121.
? 1922 Belemnites Carpaticus Uhlig; Tomitch, p. 14 [or? H. longior Shvetsov].
1923 Mesohibolites minaret Raspail; Fallot & Termier, p. 82.
1925 Belemnites minaret Raspail; Eder, p. 35.
1936 Mesohibolites aff. minaretiformis Schwetzoff; Breistroffer, p. 136.
1956 Belemnites cf. fallauxi Uhlig; Dupuy de Lôme & Sánchez Lozano, p. 216.
1956 Mesohibolites minaret Raspail; Dupuy de Lôme & Sánchez Lozano, p. 216.
1960 Mesohibolites minaret Raspail; Vyalov et alii, p. 11.
1961 Mesohibolites minaret Raspail; Trigueros Molina & Navarro Alvargonzález, p. 14.

Remark: This is a list of the belemnites that for the most part have been attributed erroneously to the Barremian genus Mesohibolites. Based on the published lists of faunas that accompanied these species, most probably they can be referred to the Valanginian-Hauterivian genus Adiakritobelus. However, specific attribution seems to be impossible. They include specimens recorded by various researchers in Valanginian-Hauterivian successions in the whole of the western Mediterranean area.

Family Duvaliidae Pavlow, 1914

Genus Duvalia Bayle, 1878

Duvalia binervia (Raspail, 1829)

(Pl. 7, figs. 1-6, 7-8 (gr.), 9-10 (gr.); Pl. 9, figs. 7-8 [NT])

* 1829 Belemnites binervius Raspail, p. 304-305, Pl. 6, fig. 6 [HT by MT].
1829 Belemnites distans Raspail, p. 305-306, Pl. 6, fig. 7.
1829 Belemnites truncatus Raspail, p. 305, Pl. 6, fig. 9.
1829 Belemnites elegans Raspail, p. 306, Pl. 6, fig. 10.
? 1829 Belemnites linearis Raspail, p. 306, Pl. 6, fig. 11.
pt 1841 Belemnites hybridus Duval-Jouve, Pl. 3, figs. 3-4 (gerontic), 5 (gerontic? or teratological?), 9-12, 14-16 (?).
non 1879 Belemnites Œhlerti Hermite, p. 317-318, Pl. IV, figs. 6-7.

Remarks: The material (Pl. 9, figs. 7-8; RGM 560.594) from strata of Late Valanginian age near Cheiron (bed CHE345, O. nicklesi (Sub)Zone, Valanginian), is chosen to be topotypical. Juvenile to immature specimens of Duvalia oehlerti (Hermite) are comparable to D. binervia but mature species of D. oehlerti are larger, more elongated with a well developed alveolus.

Stratigraphic occurrence: Latest Early Valanginian ("N. neocomiensis" beds sensu Atrops & Reboulet, 1993, in the S. verrucosum Subzone) through earliest Hauterivian (early A. radiatus Zone).

Duvalia dilatata (Blainville, 1827)

pt 1827 Belemnites dilatatus Blainville, p. 99-100, Pl. 5, fig. 18 [LT] (non Pl. 3, fig. 13; = early/mid Jura species).
+ 1829 Belemnites triquetor Raspail, Pl. 7, fig. 46 [teratological specimen: nom. dub.].
+ 1829 Belemnites amorphus Raspail, Pl. 7, fig. 49 [nom. nud.].
1829 Belemnites emarginatus Raspail, Pl. 7, figs. 50-51.
1829 Belemnites mitraeformis Raspail, Pl. 7, fig. 52.
+ 1829 Belemnites mitra Raspail, Pl. 7, fig. 53 [teratological specimen: nom. dub.].
+ 1829 Belemnites difformis Raspail, Pl. 7, fig. 54 [teratological specimen: nom. dub.].
1829 Belemnites apiculatus Raspail, Pl. 7, fig. 56.
1829 Belemnites sinuatus Raspail, Pl. 7, figs. 59-60.
1829 Belemnites spathulatus Raspail, Pl. 7, fig. 61.
1829 Belemnites complanatus Raspail, Pl. 7, figs. 63-64.
1829 Belemnites angustus Raspail, Pl. 7, fig. 66 [juvenile].
pt ? 1830 Heteromorphi Raspail, Pl. 2, fig. 19.
pt 1841 Belemnites dilatatus Blainville; Duval-Jouve, Pl. 4, figs. 2, 4-6 (?).
1861 Belemnites dilatatus Blainville; Loriol, p. 18-19, Pl. I, fig. 3.

Remarks: Specimens of this species appear especially abundant in the sequences around the Early-Late Hauterivian.

Stratigraphic occurrence: (Latest A. radiatus?)/C. loryi through P. ohmi Zone (Early Hauterivian to latest Hauterivian).

Duvalia gervaisiana (Dumas, 1876)

(Pl. 8, figs. 3-4)

+ 1872 Belemnites Gervaisianus Rouville, p. 729, 730 [nom. nud.].
pt 1876 Belemnites Gervaisianus Dumas, p. 369, Pl. 1, figs. 2-3 (type missing fide Gayte, 1984, p. 113).
? 1907 Duvalia crimica nov. sp. Karakash, p. 20, Pl. 1, fig. 8.
1984 Duvalia gervaisiana (Dumas); Gayte, p. 112-114, Pl. 3, fig. 2.

Remarks: Compared to Duvalia binervia (Raspail) this species shows a much larger, much more elongate rostrum and a well-marked, relatively deep alveolus. The constriction in the alveolar area is scarcely visible or nearly absent. Juvenile to immature specimens also have this characteristic and thus can be distinguished from the more slender and well-constricted juvenile and immature binervia-specimens. Moreover, apparently characteristically, the alveolar area is initially bent slightly to the ventral side. The alveolar groove is well developed but relatively short. Compared to Duvalia dilatata (Blainville) the species appears stouter, i.e. less compressed and is more regular in outline in mature stages, and lacks a well-marked constriction in juvenile and immature specimens. Furthermore its stratigraphic distribution is discrete, preceding that of the Duvalia dilatata-group.

Stratigraphic occurrence: The uppermost Valanginian (?) - lowermost Hauterivian glauconitic deposits at Clausson. According to Gayte (1984), it is known only from the lowermost Hauterivian A. radiatus beds in the Gard (south of France). It probably occurs in the Crimea (Biassala) too.

Duvalia aff. hybrida (Duval-Jouve, 1841)

(Pl. 8, figs. 17-18)

? 1965 Duvalia hybrida (Duval-Jouve); Stoyanova-Vergilova, p. 190-191, text-fig. F, Pl. VIII, fig. 5 (? or Pseudoduvalia polygonalis (Blainville)).

Remarks: Probably ancestral to the genus Pseudoduvalia. It represents one of the last of the group of species related to the Late Valanginian - earliest Hauterivian Duvalia binervia (Raspail).

Stratigraphic occurrence: Latest A. radiatus through C. loryi Zone (earliest Hauterivian).

Duvalia maioriana Stoyanova-Vergilova, 1965

(Pl. 7, figs. 15-16, 17-18 (imm.); Pl. 8, figs. 19-20)

? 1951 Belemnites (Duvalia) grasianus Duval-Jouve; Petkovic & Markovic, p. 23, Pl. I, fig. 1.
? 1965 Duvalia dilatata majoriana subsp. nov. Stoyanova-Vergilova, Pl. VI, figs. 1-2.
pt ? 1965 Duvalia binervia (Raspail); Stoyanova-Vergilova, Pl. V, fig. 4 (?).
1995 Duvalia dilatata majoriana Stoyanova-Vergilova; Riegraf, p. 111 (recte maioriana).
2004 Duvalia cf. maioriana Stoyanova-Vergilova; Janssen & Fözy, Pl. II, figs. 6-7, 18-19 (but only a part of the species in their synonymy).

Remarks: Only three free specimens were collected from the sections investigated here. They are from the glauconitic beds in the Clausson area (the westernmost of the sections studied, see Fig. 2 ). Most probably they come from strata in that area dated latest Early Hauterivian. At the moment the species is not yet well understood. For instance, it seems to show a wide variation with respect to its alveolar groove and has a relative deep alveolus. Its outline is much more regular than those of mature morphs of D. dilatata and D. dilatata binervioides. It occurs over a broad geographical area (Bulgaria, France, Hungary, Morocco, Serbia, and Spain). An immature specimen from the Río Argos (Spain) is figured on Pl. 7, figs. 17-18.

Stratigraphic occurrence: In the L. nodosoplicatum through S. sayni / P. ligatus zones (latest Early to early Late Hauterivian).

Duvalia sp. 1

(Pl. 7, figs. 19-20 (imm.?))

+ 1984 Duvalia valnagensis n. sp. Gayte, p. 109-111, Pl. 3, figs. 3-4 [-unpublished-: nom. nud.].
+ 1998 Duvalia vaunagensis [Gayte)]; Riegraf et alii, p. 264 [nomen correctum; nom. nud.].

Remarks: This species is one of the Duvalia gr. binervia (Raspail) offshoots. But both immature and mature specimens can be distinguished quite easily from Duvalia binervia for the species has a very pronounced dorsally bended knick in the alveolar region. Otherwise juvenile to immature specimens are much like binervia-morphs. As the material from the investigated sections is too sparse, the species is listed here only with an open nomenclature.

Stratigraphic occurrence: Latest C. furcillata (Late Valanginian) through early A. radiatus Zone (earliest Hauterivian). Gayte (1984) mentions its being from the T. callidiscus beds of the Gard.

Duvalia sp. 2

+ 1984 Duvalia clapiti n. sp. Gayte, p. 111-112, Pl. 3, figs. 5-8 [-unpublished-: nom. nud.].

Remarks: As Gayte (1984) indicated in her manuscript, these belemnites appear to be intermediate between the binervia- and dilatata-groups.

Stratigraphic occurrence: According to Gayte (1984) it is from the T. callidiscus beds of the Gard (top of the C. furcillata Zone; latest Valanginian).

Duvalia sp. 3

(Pl. 7, figs. 21-24)

Remarks: This species is one of the Duvalia binervia (Raspail) group. It differs in that it appears to be more elongated and has a well-defined alveolus in most of the available material. The alveolar area is more or less comparable to that of Duvalia sp. 2, so it may be related to, or a variation of that species. But it appears to be more dilated than Duvalia sp. 2. Only few specimens could be collected, in the same beds as Duvalia sp. 2.

Stratigraphic occurrence: Latest C. furcillata (late T. callidiscus beds at Cheiron) through mid A. radiatus Zone (Les Allaves), besides in the glauconitic deposits at Clausson (CL095).

Duvalia sp. 4

(Pl. 8, figs. 5-6)

? pt 1841 Belemnites hybridus Duval-Jouve, Pl. III, figs. 7-8.

Remarks: Most probably this form is one of the larger morphs of the variations around Duvalia gr. binervia (Raspail). Like Duvalia variegata (Raspail) it has a tendency towards the Hauterivian dilatata-group (perhaps close to D. maioriana) or Duvalia sp. 2. The well-compressed rostrum tapers downward with the apex (almost mucronate) more or less in the middle. Only two specimens were collected, both on the west side of the Clausson area. One is only an apical part, but has the characteristic tapering aspect. In lateral view the ventral side bends much more rapidly, but still relatively gradually, towards the apex as compared to the less pronounced curvature of the dorsal side, but together they give the rostrum the typical tapering aspect. The remains of an alveolar groove are visible and a large alveolar opening appears to be present. The alveolar cavity begins well before the alveolar groove starts. This species is not known from the literature, nor has it been collected in other sections.

Stratigraphic occurrence: In the glauconitic deposits at Clausson. Due to the paucity of this species the only information available is that it was found in the uppermost Valanginian - Lower Hauterivian glauconitic deposits at Clausson.

Duvalia variegata (Raspail, 1829)

(Pl. 7, figs. 11-12 [NT], 13-14)

1829 Belemnites variegatus Raspail, p. 311, Pl. 7, fig. 55, Pl. 6, fig. 32 (median section).
? 1829 Belemnites formosus Raspail, p. 311, Pl. 7, fig. 58.
non 1829 Belemnites pseudo-formosus Raspail, p. 315, Pl. 8, fig. 83 [=? teratological Mesohibolitidae].
pt 1841 Belemnites hybridus Duval-Jouve, p. 51-54 (pars), Pl. 3, figs. 1 (?; juv.), 2 [forme typique: HT] (non Pl. 3, figs. 3-4 (= D. binervia (Raspail)), nec fig. 5 [= D. binervia (Raspail) ger.? or ter.?], nec fig. 6 [= D. aff. gervaisiana (Dumas) in Janssen & Clément, 2002], nec? figs. 7-8 [ter.? or Duvalia sp. 4 nov.?], nec figs. 9-16 [= D. binervia].
[note: Duval-Jouve (1841, loc. cit. p. 10) indicates this specimen is from the "marnes à Belemnites dilatatus" (thus from the Hauterivian; ergo part of the material could be assigned to Pd. gr. polygonalis or D. cf. maioriana)], while on p. 53 he says: "cette espèce se trouve exclusivement dans la couche chloriteuse, qui est la plus basse de l'étage à Bélemnites, ..." (this would be a typical observation regarding location in the glauconitic deposits)].
1973 Duvalia hybrida (Duval-Jouve); Combémorel, p. 148-149, Pl. 4, figs. 2-3.
non ? 1984 Duvalia binervia morph. hybrida (Duval-Jouve); Gayte, Pl. 4, figs. 8-12.
1994 Duvalia hybrida (Duval-Jouve); Vašíček et alii, p. 87, Pl. 29, figs. 10-12.
non 1997 Duvalia hybrida (Duval-Jouve); Janssen, p. 20-21, Pl. 4, fig. 5 (pars cum syn.).

Remarks: A topotype has been selected (Pl. 7, figs. 11-12 (RGM 288.637)) from the glauconitic bed CL095. A second, less mature specimen also came from the same stratum (Pl. 7, figs. 13-14) at Clausson. This species is often placed in synonymy with Duvalia binervia (Raspail). Herein, Belemnites hybridus Duval-Jouve is believed to be a junior synonym of Belemnites variegatus Raspail. Duvalia variegata shows no apparent constriction in the alveolar region and it has a relative deep alveolus and a well developed alveolar groove. Juvenile to immature specimens might be confused, but "full-grown" specimens are much bigger and approach mature Duvalia gr. dilatata (Blainville) in appearance. However, in general D. gr. dilatata is much more regular in outline, while mature specimens of D. variegata have a most irregular outline with various bulges on the dorsal and ventral sides (note that this irregular aspect of the outline in Duvalia is a characteristic of gerontic specimens). However, some groups or species tend to be more bulgy than others, and especially among the D. gr. dilatata and in D. binervia this feature occurs commonly.

Stratigraphic occurrence: Latest V. peregrinus or earliest O. nicklesi through mid C. furcillata Subzone.

Genus Pseudoduvalia Naef, 1922

Pseudoduvalia polygonalis (Blainville, 1827)

(Pl. 8, figs. 7-10, 14-16)

1827 Belemnites polygonalis Blainville, p. 121-122, Pl. 5, fig. 11.
1830 Tetragonolobi Raspail, p. 87, Pl. 4, figs. 1-7.
pt 1830 Tetragoni Raspail, p. 87, Pl. 4, figs. 8-9, 10 (?).
1841 Belemnites isoscelis Duval-Jouve, Pl. 1, figs. 9-16.
1841 Belemnites urnula Duval-Jouve, Pl. 2, figs. 1-5, 6 (?), 7.
pt 1841 Belemnites sicyoides Duval-Jouve, Pl. 2, figs. 16-17.

Remarks: Apparently, the most common species of the Pseudoduvalia, it varies widely in morphology. Its range appears to include the whole of the Mediterranean Tethys. Based on morphologic resemblances, this species is most probably derived from Duvalia aff. "hybrida (Duval-Jouve)".

Stratigraphic occurrence: J. jeannoti Subzone through latest P. ligatus or early B. balearis Zone (late Early Hauterivian - early Late Hauterivian).

Pseudoduvalia rafaeli? (Stoyanova-Vergilova, 1965)

(Pl. 8, figs. 11-13)

+ 1964 Duvalia rafaelii sp. nov. Stoyanova-Vergilova, p. 138 [nom. nud.].
+ 1964 Duvalia rafaeli sp. nov. Stoyanova-Vergilova, p. 146 [nom. nud.].
* 1965 Duvalia rafaeli sp. nov. Stoyanova-Vergilova, p. 201-202, text-figs. N-O, Pl. 2, figs. 3, 4 [HT], 5-6.
+ 1970 Duvalia ravaeli Stoyanova-Vergilova; Stoyanova-Vergilova, Pl. XXXIII, fig. 8.
1995 Duvalia rafaeli Stoyanova-Vergilova; Riegraf, p. 111.
1998 Duvalia rafaeli Stoyanova-Vergilova; Riegraf et alii, p. 264.
2004 Pseudoduvalia rafaeli (Stoyanova-Vergilova); Janssen & Fözy, p. 39, Pl. II, fig. 1 (cum syn.).

Remarks: Most probably a rare species. However, it may be a morph of Pd. polygonalis.

Stratigraphic occurrence: Latest (?) L. nodosoplicatum, latest L. cruasense beds, or earliest S. sayni Zone (latest Early Hauterivian or earliest Late Hauterivian).

Pseudoduvalia trabiformis (Duval-Jouve, 1841)

pt 1830 Tetragoni Raspail, p. 87, Pl. 4, figs. 11-13.
1841 Belemnites trabiformis Duval-Jouve, Pl. 2, figs. 8 (?), 9-12, 13-14 (?).
pt 1841 Belemnites sicyoides Duval-Jouve, Pl. 2, fig. 15.

Remarks: Clearly less numerous and less widely dispersed geographically than Pd. polygonalis (Blainville).

Stratigraphic occurrence: Mid S. sayni Zone through P. ligatus Zone (Late Hauterivian).

Genus Pseudobelus Blainville, 1827

Pseudobelus brevis Paquier, 1900

non 1827 Pseudobelus bipartitus Blainville, p. 113, Pl. 5, fig. 19.
+ 1829 Belemnites contortus Raspail, p. 326-327, Pl. 6, figs. 28-29 [deformed specimen: nom. dub.].
+ 1830 Belemnites bipartitus Deshayes, p. 128 [nom. dub.].
1830 Belemnitae bisulci Raspail, p. 88, Pl. 2, figs. 20-21.
pt 1841 Belemnites bipartitus Blainville; Duval-Jouve, Pl. 1, figs. 3, 5 [LT fide Vašíček, 1978], 6.
1900 Pseudobelus bipartitus Blainville mut. brevis Paquier, p. 486-487, ii (palaeontological appendix).
+ 1963 Pseudobelus bipartitus var. minor Paquier; Flandrin, p. 18 [nom. nud.; nom. dub.].

Remarks: Apparently the lastest taxon, and one of the smallest species of Pseudobelus.

Stratigraphic occurrence: Latest J. jeannoti Subzone through S. sayni Zone (late Early Hauterivian – early Late Hauterivian).

Pseudobelus sp. A

1861 Belemnites bipartitus (Catullo), Blainville; Loriol, p. 20, Pl. I, fig. 4.
1978 Pseudobelus aff. brevis Paquier; Bordea et alii, p. 85, Pl. I, fig. 11.
2004 Pseudobelus sp. Janssen & Fözy, p. 36-37, Pl. III, figs. 16-19 (with remarks and synonymy).

Remarks: This species precedes Pseudobelus brevis Paquier and succeeds Pseudobelus jantikensis? Nerodenko, 1986. It differs from Pb. brevis by its more elongated and more slender rostrum. Pb. jantikensis? appears to be more robust. It is obvious that juvenile and incomplete specimens (in general) can not be identified to a specific species. For further remarks see Janssen & Fözy (2004, p. 36-37).

Stratigraphic occurrence: C. furcillata through C. loryi Zone; latest Valanginian – earliest Hauterivian.

The species are stored at the Museum of Natural History "Naturalis", Leiden (The Netherlands). The storage numbers are: RGM 214.701-214.753, RGM 214.755-214.826, RGM 214.828, RGM 214.830-214.832, RGM 214.835, RGM 214.837-214.952, RGM 214.959-214.980, RGM 214.987-215.000, RGM 288.001-288.377, RGM 288.401-288.679, RGM 288.701-288.781, RGM 288.792-288.900, RGM 560.501-560.926, RGM 561.019-561.502. A few specimens are not registered.

Conclusions

(1) An important change in the composition of the belemnite fauna takes place at both the genus and species levels in earliest Hauterivian times at the boundary between VaBA3 and HaBA1. The vertical distribution of Late Valanginian taxa from the succession deposited in the deep water of the Vocontian basin are compared with those found in the condensed glauconitic beds that comprise the boundary between the Valanginian and Hauterivian stages in the Peyroules area. They show that latest Valanginian (in part reworked) and earliest Hauterivian species are abundant in the basal glauconitic deposits.

(2) A second, less significant change on the species level; and in the radiation of duvalid types of belemnites, takes place in the late Early Hauterivian; at the change from HaBA1, an interval of low diversity, to HaBA2.

(3) During late Early to Late Hauterivian times the composition of the belemnite fauna is more uniform. This period can be divided into three units (HaBA2a, HaBA2b and HaBA2c; Fig. 15). These units are distinguished according to the FO or absence of certain species. Since these characterizing species have a wide palaeogeographic distribution, they may be used to establish a biochronological zonation based on belemnites (but see (4)).

(4) The belemnite faunal associations and changes in their succession can be used to establish a zonation in the western part of the Mediterranean Tethys. However, due to the condensed and incomplete nature of the stratigraphic sequences under investigation, more data from deeper water environments are needed to establish a meaningful biozonation.

(5) Except in strata of the earliest Late Valanginian age, there is no indication of the presence of Hibolithes jaculoides Swinnerton in the Hauterivian rocks of the southern margins of the Vocontian Basin, except for possible scattered occurrences in the middle of the A. radiatus Zone of Les Allaves and lower part of the S. sayni Zone in the Peyroules area.

Acknowledgement

The contributions of the following persons are highly appreciated. They furthered my progress completing this work. Dick van Straaten (Utrecht) is thanked for computer technical aid especially with the figures and plates. Both Florentin Maurasse's and Nestor Sander's structural and linguistic corrections are highly appreciated. Bruno Granier's patience, reviews of M. Company (Granada) and J. Mutterlose (Bochum), and photos made by Willem Bont (Amsterdam) are all highly pleasing contributions to this work. In the field I was aided by Jaap Klein, Vinkeveen; Stéphane Bodin, Neuchâtel; Jean Vermeulen, Barrême, and some of the issues presented here were clarified by discussions with Paul Floor (Zwolle, The Netherlands). Unless otherwise stated all interpretations and conclusions are entirely those of the author.

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Tables

sections origin range remarks
species junior synonym
I. Belemnitae petalopsides (leaf-like belemnites)
Duvalia emericii pileus Cheiron area
affinis
Duvalia binervia distans Cheiron area Neocomiensis Subzone to base Radiatus Zone topotype Pl.9, figs. 7-8 (CHE345, Nicklesi Zone)
acinaformis
truncatus
Duvalia elegans juvenile specimens of either D. emericii or D. binervia
Duvalia linearis
II. Belemnitae blachesii (belemnites from Blasches area, N of Castellane)
of no importance for this work Blaches Jurassic-Neocomian
III. Belemnitae blieuxii (belemnites from Blieux area, W of Castellane)
of no importance for this work Blieux Aptian Neohibolites
IV(III). Belemnitae dilatatii (dilatated belemnites)
apiculatus Thorène Hauterivian (except for the earliest part) Duvalia dilatata (Blainville, 1827)
complantus
apiculatus Robion
emarginatus Blaches, Gréolières
teratologic; nom. dub. mitra no locality
difformis
triqueter Gréolières
? teratologic mitraeformis
sinuatus no locality
spathulus La Lagne
Duvalia convexus no locality Hauterivian = ? Duvalia grasiana (Duval-Jouve, 1841)
Barremian - Aptian = ? Duvalia maioriana Stoyanova-Vergilova, 1965
Duvalia variegata  formosus Gréolières Late Valanginian
no locality Pl. 7, figs. 11-12 (Clausson, CL095)
juvenile augustus La Lagne Hauterivian Duvalia gr. lata (Blainville, 1827)
pisciformis Late Valanginian - Hauterivian Duvalia gr. lata (Blainville, 1827) or D. gr. binervia
teratologic; nom. dub. persona tonsoria no locality
immature ? bifurcatus Gréolières
Duvalia sp. 1 ?  delphinus La Lagne Valanginian - Hauterivian Duvalia gr. binervia
ellipsoides no locality Late Valanginian ? Duvalia gr. binervia
V(IV). Belemnitae vermiculati (moulded [weathered] belemnites), not treated in this work
nomen dubium? honorati Sisteron Berriasian - Valanginian? = ? Duvalia gr. lata (Blainville, 1827)
VI(V). Belemnitae chamateulii (sordidi)
nomen dubium attenuatus Chamateuil Late Hauterivian - early Late Barremian Belemnites pistilliformis Blainville
incurvatus Mesohibolitidae undet.
marginatus juvenile Mesohibolitidae 
pistilloides
teratologic; nom. dub. rimosus
nomen dubium depressus Conohibolites
VII(VI). Belemnitae peronii (hideous belemnites)
Adiakritolebus brevirostris La Lagne and Gréolières Late Valanginian
Adiakritolebus minaret fusus immature
navicula
??? oblongus Adiakritolebus?
nomen dubium gemmatus juv.; ter.
rostratus Adiakritolebus
gibbosus
rugosus ??? Hibolithes gr. subfusiformis Raspail
VIII(VII). Belemnitae claviformis
Adiakritolebus minaret La Lagne Late Valanginian no Mesohibolites!
collective species pistilliformis Late Valanginian - Early Barremian Belemnites pistilliformis Blainville
crassior
crassissimus
teratologic; nom. dub. acuteus echini
contortus Hibolithes gr. subfusiformis Raspail
praemorsus

Table 1: Division of belemnites after Raspail (1829, 1830). Indicated are valid species, invalid species, synonyms, origin of material, approximate stratigraphical range, and some remarks.

Description / Species robustus rogeri peyroulensis brevirostris minaret gayteae
Morph hibolitoid ± + - - - ±
mesohibolitoid - - + + + -
subfusiform - - + + - -
elongated - ± + - - -
fusiform ± + - + - -
Groove 1/4 ± - - - - -
1/3 + ± ± - - ±
1/2 ± ± + + + ±
2/3 - - + + + -
Relative depths of the alveolus very shallow - - + + + ±
shallow + ± - - - ±
intermediate depth - ± - - - -
deep - - - - - -
Apex obtused ± ± - - ± +
pointed ± + - + ± -
elongated - - + - - -
Alveolus rounded + + ± - ± ±
subquadrangular - - ± + ± ±
Alveolar line dorsal + + - + ? ?
central - - + - ? ?
Ventrally flattened ± - ± - - +
Range Pronecostatum - - - - - -
Peregrinus - - - + - -
Nicklesi - - + ++ ++ -
Furcillata - + ++ + + ?
Callidiscus ? + + - - +
Radiatus (base) + + ? - - +

Table 2: Short-key to Adiakritobelus-species. Key: ? unknown; -- not present; ± uncommon; + present.


Figures


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Figure 1: Geographical situation of localities mentioned in the Castellane area (Alpes de Haute-Provence, southeast France). The positions of the main areas of investigation and of some areas with a historical significance are shown.

Key: ANG = Angles (see Thieuloy, 1979, p. 18-20); CB = Collet des Boules; CH = Chamateuil; CHE = Cheiron; CL = Clausson; LGR = La Garde; LLG = La Lagne; RMB = Ravin de Mal Bouisset; SAM = Source de l'Asse de Moriez (see also Thieuloy, 1979, p. 19). The following localities (mentioned by Raspail, 1829) are not on the map: Lates (department of Var; 5-6 km east of Peyroules), plateau of Gréolières (east of Castellane, between Castellane and Roquestron, department of Var). Other areas not indicated on the map: PE = Pas d'Escale is near Majastres, approximately 8-10 km northwest of Blieux and ALL = Les Allaves, is approximately 25 km west of Castellane.


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Figure 2: Correlation of sections in the Clausson region (CL; Peyroules area), showing the variations in lithology and thickness of the glauconitic sediments of Early Hauterivian age. Note the absence of a phosphatic basal conglomerate in some sections, and especially the variation in beds CL096 to 097d. The sections figured are sited in approximate accordance with their geographic position, from west to south-east. Note the extreme condensation in the western section which is but 100 m from the first east-side column. The changes in the eastern columns occur over a distance of about 50 m. Vertical scale graduations = 1 m.


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Figure 3: Belemnite distribution in the Clausson area (Peyroules), beds CL095 - CL104a. Three columns are figured, approximately 300 metres apart (see Fig. 2  for comparison of distances) showing bed-numbers, their correlation, and their lithology. The distribution of the belemnites in these columns (with data from the columns depicted in Fig. 2  added) is given on the right, along with ammonite- (sub)zones, and belemnite associations. Key in Figs. 2  and 4 . Scale bar graduations = 1 m. The following species were collected as free material below the base of the glauconitic succession: Duvalia gr. dilatata (Blainville), Duvalia cf. maioriana (Stoyanova-Vergilova) or Duvalia sp. 2 (= D. clapiti Gayte [-unpublished-: nom. nud.]), Duvalia aff. "hybrida (Duval-Jouve)", and Duvalia sp. 4.


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Figure 4: Valanginian-Hauterivian in the Ravin du Mal Bouisset (RMB) near Clausson area (see Fig. 1 ). Indicated are (sub-)stages, ammonite zones, bed-numbers, lithology and belemnite distribution. Scale bar indicated (1 m interval). Key: R/L? = Acanthodiscus radiatus or Crioceratites loryi Zone, for explanation of other ammonite zone abbreviations (see Fig. 2  for key). Scale bar graduations = 1 m.


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Figure 5: Correlation of three field-sections in the Collet des Boules: beds CB078 to CB100/103?. Lithology (see Figs. 2  and 4  for key), bed-numbers, belemnite distribution, ammonite (sub-)zones, and belemnite associations are shown. Scale bar graduations = 1 m. Key: A. = Adiakritobelus, Bel. = Belemnites, D. = Duvalia, H. = Hibolithes, Pd. = Pseudoduvalia.


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Figure 6: Correlation of five field-sections in the Collet des Boules area: beds CB101 to CB109/110, all within approximately 100 meters of each other. Indicated are lithology (key in Fig. 2 ), bed-numbers, belemnite distribution, bed-numbers sensu Vermeulen, 2002 (beds 115-118 on right), ammonite zones, sequences, and belemnite associations. Black arrow indicates position of (first?) occurrence of Subsaynella sayni (after Vermeulen, 2002). Key: Bel. = Belemnites, D. = Duvalia, Gen. = Genus, H. = Hibolithes, Pb. = Pseudobelus, Pd. = Pseudoduvalia. Red star indicates occurrence of Isocrinus peyroulensis (Loriol). Scale bar graduations = 1 m.


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Figure 7: Late Hauterivian sequences in the Collet des Boules (beds CB108-134) with bed-numbers, lithology (key in Fig. 2 ), belemnite ranges, sequences, and ammonite (sub)zones. Abbreviations used: Bel. = Belemnites; D. = Duvalia; H. = Hibolithes; Pd. = Pseudoduvalia. Bed numbers after Bulot (1995, beds: 40 to 49), Vermeulen et alii, 1999, Vermeulen, 2002 (beds 122 to 130), pers. obs. (beds: CB108 to CB134). Note that Bulot (1995) indicated Balearites sp. to occur in bed 45 (= 119). Scale bar graduations = 1 m.


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Figure 8: Valanginian-Hauterivian section in the La Lagne area. Indicated are stage, ammonite (sub)zones, bed-numbers, lithology and belemnite distribution. Key to lithology and abbreviations in Figs. 2  and 4 . Scale bar graduations = 1 m.


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Figure 9: Comparison of lithology and belemnite distribution in strata of Valanginian–Hauterivian age in the Les Allaves area (between Les Allaves profile and the Ravin du Carrîne (southwest of Les Allaves). In columns to the left of the seven profiles are stages, ammonite zones (modified after: Thieuloy et alii, 1991; Bulot, 1995; pers. obs.) and bed-numbers (modified after Bulot, 1995). Abbreviations used: Ad. = Adiakritobelus; B. = Belemnites; Bux. = Leopoldia buxtorfi Subzone sensu Arnaud & Bulot, 1992; Cas = Breistrofferella castellanensis Subzone; D. = Duvalia; H. = Hibolithes; Pb. = Pseudobelus; Pd. = Pseudoduvalia; Valang. = Valanginian. See Figs. 2  and 4  for key to lithology and abbreviations. Scale bar graduations = 1 m.


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Figure 10: Lower Hauterivian sequence in the Pas d'Escale area. Indicated on the left are stages, ammonite (sub)zones, bed-numbers (modified after Robert, 1994; Bulot, 1995), and lithology, belemnite distribution and zonation on right. For abbreviations see Figs. 2  and 4 . Free specimens from glauconitic beds include: Duvalia sp. 1 (?) and Adiakritobelus rogeri (Delattre, 1952). Scale bar graduations = 1 m.


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Figure 11: Valanginian-Hauterivian boundary and lowermost Hauterivian beds in the Cheiron section. Bed-numbers according to their equivalents in the Angles Valanginian Hypostratotype. Indicated are: stages, ammonite zonation (zones and subzones), bed-numbers, lithology (key in Fig. 2 ), sequences (Va6 (p.p.), Ha0 (new sequence), and Ha1), and belemnite distribution (from Cheiron and Angles both). Key: A. = Adiakritobelus, D. = Duvalia, H. = Hibolithes. Small triangle indicates occurrence of Pygope. Scale bar graduations = 1 m.


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Figure 12: Correlation of ammonite distribution in Lower Hauterivian deep-water deposits (Vocontian Basin: La Charce, bed-numbers after Bulot (243-294) and Reboulet (182-242); Angles (375-401)) and shallow depositional areas (glauconitic platform deposits of Peyroules and platform "type section" of Carajuan, see Arnaud & Bulot, 1992). Some stratigraphically important ammonite species and genera are indicated (after Bulot, 1995; Bulot et alii, 1996; Reboulet, 1996; Vermeulen, 2002). Bed-numbers refer to calcareous beds only. Abbreviations used: Acanthod. = Acanthodiscus; Breistrof. = Breistrofferella; Call. = Teschenites callidiscus Subzone; C. = Crioceratites; Furc. = Criosarasinella furcillata Zone; L. = Lyticoceras; O. = Olcostephanus; S. = Subsaynella. Key in Figs. 2  and 4 .


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Figure 13: Correlation of ammonite distribution in Lower Hauterivian deep-water deposits (Vocontian Basin; La Charce section, bed-numbers after Bulot (292-329a) and Reboulet (241-275); Vergons section after Bulot, 1995) and shallow depositional areas. Ammonite data after Bulot, 1995, Bulot et alii, 1996, Reboulet, 1996, Reboulet & Atrops, 1999, and Vermeulen, 2002. A correlation is indicated to the platform "type section" of Carajuan (Arnaud & Bulot, 1992). Bed-numbers refer to calcareous beds only. Sequences (Ha 3, etc. modified after Arnaud & Bulot, 1992). Cruasiceras? sp. and/or Lyticoceras sp. nov. (in Bulot et alii, 1996) could be conspecific with Lyticoceras kiliani Reboulet & Atrops, 1999. Abbreviations used: Cru. = Cruasiceras; Cru. = Lyticoceras cruasense Subzone; L. = Lyticoceras; n.f.d. = no further data; O. = Olcostephanus; S. = Subsaynella. Key in Figs. 2  and 4 .


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Figure 14: Correlation of ammonite distribution in Late Hauterivian deep-water deposits (Vocontian Basin). La Charce (bed-numbers after Bulot et alii, 1993: 327-368; note that bed-numbers between sections depicted on p. 49 and 51 are not comparable, e.g. bed 342-364 on p. 49 = bed 340-359 on p. 51), Vergons (after Bulot et alii, 1993, Bulot, 1995), and shallow water deposits (glauconitic platform deposits of Peyroules and "type section" of Carajuan, Arnaud & Bulot, 1992). Bed-numbers refer to calcareous beds only. Sequences modified after Arnaud & Bulot, 1992. Some stratigraphically important ammonite species and genera are indicated after: Bulot et alii, 1993, 1996; Bulot, 1995; Vermeulen, 2002. Light bluish area indicates possible occurrence of Subsaynella begudensis (indicated as Subsaynella sayni in Bulot et alii, 1993). The interval between beds 329a and 359 appears to correlate with two sequences in the platform deposits. Abbreviations used: B. = S. begudensis; M. = S. mimica; Pl. = Plesiospitidiscus; S. = Subsaynella. Key in Figs. 2  and 4 .


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Figure 15: Distribution of belemnites in Late Valanginian to Hauterivian age strata in the investigated areas. Ammonite zonation modified after Reboulet et alii, 2006 (ammonite zones between "" are not yet accepted). Belemnite associations after Janssen & Clément, 2002; Janssen & Fözy, 2004, and data presented herein. Possible zonal belemnite species are in red. More abundant occurrences are indicated by thicker lines. Broken lines indicate approximate range of species. Abbreviations used: AZ = Ammonite zones; Biass. = Karakaschiceras biassalensis; "Buxt." = Leopoldia buxtorfi Horizon sensu Arnaud & Bulot, 1992; Camp. = Busnardoites campylotoxus; Cast. = Breistrofferella castellanensis; Cru? = beds with Cruasiceras? sp. (in Bulot et alii, 1993); Cru. = Lyticoceras cruasense; "Kili." = Lyticoceras kiliani sensu Reboulet & Atrops, 1999; "Mi/Be." = Subsaynella mimica resp. Subsaynella begudensis Horizon sensu Vermeulen et alii, 1999; "Neoc." = Neocomites neocomiensis Horizon sensu Atrops & Reboulet, 1993; "Nodo." = Lyticoceras nodosoplicatum Subzone sensu Reboulet & Atrops, 1999; Platy. = Eristavites platycostatus; Var. = Olcostephanus variegatus; Verr. = Saynoceras verrucosum.


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Figure 16: Vergol area: a Late Valanginian succession. Note that the slumps below bed 174 and above 169b are not to scale. Bed numbers correlated with those of beds 339-376 at Angles, are shown, along with lithology, sequences, and ammonite zonations (based on correlations). The FO, LO, or single occurrences of belemnite species are indicated. Key in Figs. 2  and 4 . Scale bar graduations = 1 m.


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Figure 17: Correlation of Lower Hauterivian sedimentary rocks. Arrow indicates position of Valanginian-Hauterivian boundary. Abbreviations: ALL = Les Allaves; CB = Collet des Boules; CL = Clausson; Nic. = Olcostephanus nicklesi Zone; PE = Pas d'Escale. Lithology, sequences, ammonite (sub)zones, belemnite associations (VaBA-3, HaBA1, and HaBA2a), and discontinuities (DVS, DZR, DZL, and DZN) are depicted. See text for explanation. Keys to lithology and abbreviations in Figs. 2  and 4 . Scale bar graduations = 1 m.


Planches


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Plate 1 (Valanginian-Hauterivian; Hibolithes):
Fig. 1.
- Belemnites pistilliformis Blainville, RGM 288.898, ALL121, Lyticoceras nodosplicatum Zone.
Figs. 2-3.- Hibolithes fusoides (Lamarck, 1822), RGM 288.483, CL099top, Lyticoceras nodosplicatum Zone.
Figs. 4-5.- Hibolithes fusoides (Lamarck, 1822), RGM 214.809, Clausson (west), free specimen.
Figs. 6-7.- Hibolithes fusoides (Lamarck, 1822), RGM 214.810, Clausson (west), free specimen.
Figs. 8-9.- Hibolithes sp. (ter.), RGM 288.296a, CB107-107a, Subsaynella sayni Zone.
Figs. 10-11.- Hibolithes sp. (ter.), RGM 288.296b, CB107-107a, Subsaynella sayni Zone.
Figs. 12-13.- Hibolithes sp. 1, RGM 288.295, CB106-107, Subsaynella sayni Zone.
Figs. 14-15.- Hibolithes subfusiformis (Raspail, 1829), RGM 288.764, La Bâtie, LB113-114, "Subsyanella mimica" Subzone.
Figs. 16-17.- Hibolithes subfusiformis (Raspail, 1829), RGM 288.307a, CB107a-108, Subsaynella sayni Zone.
Figs. 17-19.- Hibolithes sp. (ter.), RGM 288.481, CL097-098, top Acanthodiscus radiatus/base Crioceratites loryi Zone.
Figs. 20-21.- Hibolithes gr. subfusiformis Raspail, RGM 288.333, CB104a-105, Lyticoceras cruasense Zone.


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Plate 2 (Valanginian-Hauterivian; Hibolithes):
Figs. 1-2.
- Hibolithes longior Shvetsov, 1913, RGM 288.328, CB079, V/H boundary.
Figs. 3-4.- Hibolithes longior Shvetsov, 1913, RGM 288.835, ALL116, top Acanthodiscus radiatus Zone ("Leopoldia buxtorfi Subzone").
Figs. 5-6.- Hibolithes longior? Shvetsov, 1913, RGM 288.467, CL096, Acanthodiscus radiatus Zone.
Figs. 7-8.- Hibolithes longior Shvetsov, 1913, RGM 288.474, CL097c-d, Crioceratites loryi Zone.
Figs. 9-10.- Hibolithes jaculoides Swinnerton, 1937, RGM 560.599, Cheiron, Karakaschiceras pronecostatum Subzone.
Figs. 11-12.- Hibolithes longior? Shvetsov, 1913 (juv.), RGM 288.352, CB079, V/H boundary.
Figs. 13-14.- Hibolithes longior? Shvetsov, 1913, RGM 288.332, CB085-087, Crioceratites loryi Zone.
Figs. 15-16.- Hibolithes longior? Shvetsov, 1913, RGM 288.331, CB085-087, Crioceratites loryi Zone.
Figs. 17-18.- Hibolithes longior Shvetsov, 1913, RGM 560.609, Angles, ANG386, Acanthodiscus radiatus Zone.


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Plate 3 (Valanginian-Hauterivian; Adiakritobelus):
Figs. 1-2.
- Adiakritobelus? sp. (ter.), RGM 214.706, Angles, ANG337-338, Varlheideites peregrinus Subzone. 
Fig. 1a.- Cross-section in alveolar opening.
Figs. 3-4.- Adiakritobelus brevirostris (Raspail, 1829), RGM 214.714, Vergol, VGL149e-150, Olcostephanus nicklesi Subzone.
Figs. 5-6.- Adiakritobelus brevirostris (Raspail, 1829), RGM 214.731, Vergol, VGL154b-155, Olcostephanus nicklesi Subzone.
Figs. 7-8.- Adiakritobelus brevirostris (Raspail, 1829), RGM 214.780, CL095, V/H boundary.
Fig. 7a.- Cross-section in alveolar opening.
Figs. 9-10.- Adiakritobelus minaret (Raspail, 1829), RGM 214.990, CL095, V/H boundary.
Figs. 11-12.- Adiakritobelus minaret (Raspail, 1829), RGM 214.741, Angles, ANG358-359, Olcostephanus nicklesi Subzone.
Fig. 11a.- Cross-section in alveolar opening.
Fig. 11b.- Cross-section near maximum outline.
Figs. 13-14.- Adiakritobelus minaret (Raspail, 1829), RGM 214.715, Vergol, VGL154-158, Olcostephanus nicklesi Subzone.
Fig. 13a.- Cross-section in alveolar opening.
Fig. 13b.- Cross-section in apical part.
Figs. 15-16.- Adiakritobelus minaret (Raspail, 1829), RGM 214.782, CB079, V/H boundary.
Figs. 17-18.- Adiakritobelus? sp., RGM 214.850, CL095, V/H-boundary.


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Plate 4 (Valanginian-Hauterivian; Adiakritobelus):
Figs. 1-2.
- Adiakritobelus peyroulesensis sp. nov. holotype, RGM 214.798, CB079, V/H boundary.
Fig. 1a.- Cross-section in alveolar opening.
Fig. 1b.- Cross-section near end of alveolar groove.
Figs. 3-4.- Adiakritobelus peyroulesensis sp. nov. paratype, RGM 214.787, CB078, V/H boundary.
Figs. 5-6.- Adiakritobelus peyroulesensis sp. nov. topotype, RGM 214.796, CB079, V/H boundary.
Fig. 5a.- Cross-section in alveolar opening.
Fig. 5b.- Cross-section near maximum diameter.
Fig. 5c.- Cross-section in apical part
Figs. 7-8.- Adiakritobelus peyroulesensis sp. nov. topotype, RGM 214.758, Vergol, VGL170, Criosarasinella furcillata Zone.
Figs. 9-10.- Adiakritobelus cf. peyroulesensis sp. nov. topotype, RGM 214.895, CL095, V/H boundary.


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Plate 5 (Valanginian-Hauterivian; Adiakritobelus):
Figs. 1-2.
- Adiakritobelus robustus (Duval-Jouve, 1841) topotype, RGM 214.803, CL095, V/H boundary.
Figs. 3-4.- Adiakritobelus robustus (Duval-Jouve, 1841) topotype, RGM 214.913, CL095, V/H boundary.
Figs. 5-6.- Adiakritobelus robustus (Duval-Jouve, 1841), RGM 214.804, LLG102, V/H-boundary.
Figs. 7-8.- Adiakritobelus cf. robustus (Duval-Jouve, 1841), RGM 214.778, Angles, ANG393, Acanthodiscus radiatus Zone.
Fig. 7a.- Cross-section in alveolar part.
Figs. 9-10.- Adiakritobelus robustus (Duval-Jouve, 1841) (imm.) topotype, RGM 214.989, CB079, V/H boundary.
Figs. 11-13.- Adiakritobelus cf. robustus? (Duval-Jouve, 1841), RGM 361.675, Tornajo (southeastern Spain), B130 (-131), late Teschenites callidiscus (?) Subzone.


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Plate 6 (Valanginian-Hauterivian; Adiakritobelus):
Figs. 1-2.
- Adiakritobelus rogeri (Delattre, 1952) topotype, RGM 214.926, CL095, V/H boundary.
Figs. 3-4.- Adiakritobelus rogeri (Delattre, 1952) topotype, RGM 214.897, CL095, V/H boundary.
Figs. 5-6.- Adiakritobelus rogeri (Delattre, 1952) imm. topotype, RGM 214.910, CL095, V/H boundary.
Figs. 7-8.- Adiakritobelus sp. (gr. rogeri (Delattre, 1952)) (juv.), RGM 214.963, Vergol, VGL119-124, Karakaschiceras pronecostatum Subzone.
Figs. 9-10.- Adiakritobelus (?) gayteae sp. nov. holotype, RGM 214.909, CL095, V/H boundary.


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Plate 7 (Valanginian-Hauterivian; Duvalia):
Figs. 1-2.
- Duvalia binervia (Raspail, 1829) gerontic, RGM 288.571, CL095, V/H boundary.
Figs. 3-4.- Duvalia binervia (Raspail, 1829) topotype, RGM 560.593, CHE361-362, Criosarasinella furcillata Zone.
Figs. 5-6.- Duvalia binervia (Raspail, 1829) juv./imm. topotype, RGM 560.588, CHE342-a, Olcostephanus nicklesi Subzone.
Figs. 7-8.- Duvalia sp. juv. (gr. binervia? (Raspail, 1829)), RGM 288.343, CB085, Crioceratites loryi Zone.
Figs. 9-10.- Duvalia gr. binervia (Raspail, 1829), RGM 288.526, CL095, V/H boundary.
Figs. 11-12.- Duvalia variegata (Raspail, 1829) gerontic topotype, RGM 288.637, CL095, V/H boundary.
Figs. 13-14.- Duvalia variegata (Raspail, 1829) topotype, RGM 288.636, CL095, V/H-boundary.
Figs. 15-16.- Duvalia maioriana Stoyanova-Vergilova, 1965, RGM 288.648, Clausson (west), free specimen.
Figs. 17-18.- Duvalia maioriana Stoyanova-Vergilova, 1965, RGM 345.565, Río Argos (Spain), A43-44, Lyticoceras nodosoplicatum Zone.
Figs. 19-20.- ?Duvalia sp. 1 (imm.), RGM 288.599, CL095, V/H boundary.
Figs. 21-22.- Duvalia sp. 3 (gr. binervia (Raspail, 1829)), RGM 288.584, CL095, V/H boundary.
Figs. 23-24.- Duvalia sp. 3 (gr. binervia (Raspail, 1829)), RGM 560.590, CHE378mid, Acanthodiscus radiatus Zone.


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Plate 8 (Valanginian-Hauterivian; Duvalia):
Figs. 1-2.- Pseudoduvalia? sp. (ter.?), RGM 288.679, CL095, Clausson (west).
Figs. 3-4.- Duvalia gervaisiana (Dumas, 1876), RGM 288.613, CL095, V/H boundary.
Figs. 5-6.- Duvalia sp. 4, RGM 288.645, CL095, Clausson (west). Arrow indicates initiation of alveolar groove.
Figs. 7-8.- Pseudoduvalia polygonalis (Blainville, 1827), RGM 288.677, CL102-104?, Lyticoceras nodosoplicatum? Zone.
Figs. 9-10.- Pseudoduvalia polygonalis (Blainville, 1827), RGM 288.654, CL106-107, Subsaynella sayni Zone.
Figs. 11-13.- Pseudoduvalia rafaeli? (Stoyanova-Vergilova, 1965), RGM 288.777, La Bâtie, Subsaynella sayni Zone (free specimen).
Figs. 14-16.- Pseudoduvalia polygonalis (Blainville, 1827), RGM 288.348, CB091, Jeannoticeras jeannoti Subzone.
Figs. 17-18.- Duvalia aff. "hybrida (Duval-Jouve, 1841)", RGM 288.347, CB087, Crioceratites loryi Zone.
Figs. 19-20.- Duvalia maioriana Stoyanova-Vergilova, 1965, RGM 288.649, Clausson (west), free specimen.


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Plate 9:
Figs. 1-2.
- Adiakritobelus robustus (Duval-Jouve, 1841) topotype, RGM 288.357, CL095, V/H-boundary.
Figs. 3-4.- Adiakritobelus rogeri (Delattre, 1952) topotype, RGM 214.998, CL095, V/H-boundary.
Figs. 5-6.- Adiakritobelus peyroulesensis sp. nov. topotype, RGM 215.000, CL095, V/H-boundary.
Figs. 7-8.- Duvalia binervia (Raspail, 1829) topotype, RGM 560.594, CHE345, Olcostephanus nicklesi Subzone.