Santonian macrofauna and nannofossils from northeast Belgium · Santonian macrofauna and...

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BULLETIN DE L’INSTITUT ROYAL DES SCIENCES NATURELLES DE BELGIQUE BULLETIN VAN HET KONINKLIJK BELGISCH INSTITUUT VOOR NATUURWETENSCHAPPEN, SCIENCES DE LA TERRE. 65: 127-137, 1995 AARDWETENSCHAPPEN, 65: 127-137, 1995 Santonian macrofauna and nannofossils from northeast Belgium by John W.M. JAGT, William James KENNEDY, Jacqueline A. BURNETT, Walter Kegel CHRISTENSEN & Annie V. DHONDT Abstract From a limited number of mine shafts in the Belgian province of Limburg (Houthalen and Zolder/Voort areas), a small fauna compris ing ammonites, belemnites and inoceramid bivalves is described. A nannofossil analysis of samples taken from the ammonites is added. This assemblage is of (late) middle to late Santonian age, and thus roughly corresponds to the ’Craie de Lonzée’ (province of Namur, Belgium) and the Aachen Formation of the Aachen-Vaals area (SE Netherlands and Germany). Key-words: Cephalopoda, Bivalvia, nannofossils, late Cretaceous, biostratigraphy. Résumé De quelques charbonnages du Limbourg belge (Houthalen et Zolder- Voort) une faunule d'ammonites, belemnites et inocérames a été étudiée. Les nannofossiles des échantillons d’ammonites ont été iden tifiés. L’assemblage est d’âge Santonien moyen (supérieur) à supérieur et peut ainsi être comparé à la “ Craie de Lonzée” (province de Namur, Belgique) et à la Formation d’Aix-la-Chapelle de la région d’Aix-la- Chapelle - Vaals (SE des Pays-Bas et Allemagne). Mots-clefs: Céphalopodes, bivalves, nannofossiles, Crétacé supérieur, biostratigraphie. Introduction During a revision of the ammonite fauna of the type Maastrichtian (K ennedy , 1987a), it was noted that the collections of the Institut royal des Sciences naturelles de Belgique at Brussels also comprised ammonite faunules of Santonian age not previously described. These limited faunas were collected during the construction of mine shafts of the former Houthalen and Zolder/Voort collie ries (Limburg, NE Belgium) (Text-fig. 1). Labels with the specimens state locality and depth below surface; other than this there are no stratigraphie details. In order to refine the dating it was decided to add data taken from belemnites and inoceramid bivalves from the same shafts and depths and to remove quantities of matrix for nanno fossil analysis. These faunas are of importance mainly in a broader context, in being roughly coeval with the “ Glauconie de Lonzée” (C hristensen , 1994; M alchus et al., 1994) of Namur province (Belgium) and (part of) the Aachen For mation as exposed in the Dutch-Belgian-German border land southwest of Aachen-Vaals (B atten et al., 1988). Material All specimens are housed in the collections of the Institut royal des Sciences naturelles de Belgique at Brussels and generally bear IG registration numbers. The figured spe cimens have been transferred and renumbered to form part of type collections. Systematic descriptions A mmonoidea Superfamily Hoplitaceae D ouvillé , 1890 Family P lacenticeratidae H yatt , 1900 Genus Placenticeras M eek , 1876 T ype species : Ammonites placenta D ekay , 1828, p. 278, by original designation of M eek (1876, p. 426). Placenticeras polyopsis (D ujardin , 1837) PI. 1, Figs. 3-6. * 1837 Ammonites polyopsis D ujardin , p. 232, pi. 17, fig. 12. 1983 Placenticeras polyopsis (Dujardin, 1837) - K enne dy & W right , p. 856, pis 86-88; text-figs. 1-4 (with full synonymy). 1987b Placenticeras polyopsis (Dujardin, 1837) - K enne dy , p. 768 (with additional synonymy). 1994 Placenticeras polyopsis (Dujardin) - W iedmann in G ischler et al., p. 238, pi. 43, figs. 10-12. T ype : Lectotype, by subsequent designation of K ennedy & W right (1983, p. 856), is the original of D ujardin

Transcript of Santonian macrofauna and nannofossils from northeast Belgium · Santonian macrofauna and...

Page 1: Santonian macrofauna and nannofossils from northeast Belgium · Santonian macrofauna and nannofossils 129 (5), borne on strong, distant, straight, prorsiradiate ribs. A pronounced

BULLETIN DE L’INSTITUT ROYAL DES SCIENCES NATURELLES DE BELGIQUE BULLETIN VAN HET KONINKLIJK BELGISCH INSTITUUT VOOR NATUURWETENSCHAPPEN,

SCIENCES DE LA TERRE. 65: 127-137, 1995 AARDWETENSCHAPPEN, 65: 127-137, 1995

Santonian macrofauna and nannofossils from northeast Belgium

by John W.M. JAGT, W illiam James KENNEDY, Jacqueline A. BURNETT,Walter Kegel CHRISTENSEN & Annie V. DHONDT

Abstract

From a limited number of mine shafts in the Belgian province of Limburg (Houthalen and Zolder/Voort areas), a small fauna compris­ing ammonites, belemnites and inoceramid bivalves is described. A nannofossil analysis of samples taken from the ammonites is added. This assemblage is of (late) middle to late Santonian age, and thus roughly corresponds to the ’Craie de Lonzée’ (province of Namur, Belgium) and the Aachen Formation of the Aachen-Vaals area (SE Netherlands and Germany).

K ey-w ords: Cephalopoda, Bivalvia, nannofossils, late Cretaceous, biostratigraphy.

Résumé

De quelques charbonnages du Limbourg belge (Houthalen et Zolder- Voort) une faunule d'ammonites, belemnites et inocérames a été étudiée. Les nannofossiles des échantillons d’ammonites ont été iden­tifiés. L’assemblage est d’âge Santonien moyen (supérieur) à supérieur et peut ainsi être comparé à la “Craie de Lonzée” (province de Namur, Belgique) et à la Formation d’Aix-la-Chapelle de la région d’Aix-la- Chapelle - Vaals (SE des Pays-Bas et Allemagne).

M ots-c lefs: Céphalopodes, bivalves, nannofossiles, Crétacé supérieur, biostratigraphie.

Introduction

During a revision o f the ammonite fauna o f the type M aastrichtian (K e n n e d y , 1987a), it was noted that the collections o f the Institut royal des Sciences naturelles de Belgique at Brussels also comprised ammonite faunules of Santonian age not previously described. These limited faunas were collected during the construction o f mine shafts o f the former Houthalen and Zolder/Voort collie­ries (Limburg, NE Belgium) (Text-fig. 1). Labels with the specimens state locality and depth below surface; other than this there are no stratigraphie details. In order to refine the dating it was decided to add data taken from belemnites and inoceramid bivalves from the same shafts and depths and to remove quantities of matrix for nanno­fossil analysis.

These faunas are of importance mainly in a broader context, in being roughly coeval with the “ Glauconie de Lonzée” (C h r is t e n s e n , 1994; M a l c h u s et al., 1994) of

Namur province (Belgium) and (part of) the Aachen For­mation as exposed in the Dutch-Belgian-German border­land southwest o f Aachen-Vaals (B a t t e n et al., 1988).

Material

All specimens are housed in the collections o f the Institut royal des Sciences naturelles de Belgique at Brussels and generally bear IG registration numbers. The figured spe­cimens have been transferred and renumbered to form part o f type collections.

Systematic descriptions

A m m o n o id e a

Superfamily Hoplitaceae D o u v il l é , 1890 Family P l a c e n t ic e r a t id a e H y a t t , 1900

Genus Placenticeras M e e k , 1876

T y p e s p e c ie s : Ammonites placenta D e k a y , 1828, p. 278, by original designation o f M e e k (1876, p. 426).

Placenticeras polyopsis (D u ja r d in , 1837)PI. 1, Figs. 3-6.

* 1837 Ammonites polyopsis D u ja r d in , p . 232 , pi. 17,fig . 12.

1983 Placenticeras polyopsis (D u ja rd in , 1837) - K e n n e ­d y & W r ig h t , p. 856, pis 86-88 ; tex t-fig s. 1-4 (w ith fu ll synonym y).

1987b Placenticeras polyopsis (D u ja rd in , 1837) - K e n n e ­d y , p. 768 (w ith ad d itio n al synonym y).

1994 Placenticeras polyopsis (D u ja rd in ) - W ie d m a n n in G is c h l e r et al., p. 238 , pi. 43 , figs. 10-12.

T y p e : Lectotype, by subsequent designation o f K e n n e d y

& W r ig h t (1983, p. 856), is the original o f D u ja r d in

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128 J.W .M. JAGT, W.J. KENNEDY, J.A. BURNETT, W.K. CHRISTENSEN & A.V. DHONDT

BERINGEN VOORT

* b I I ■ HOUTHALEN ^ ZOLDER

BELGIUM

AACHEN

VAALS

1 5 k m

■ LONZEE

Fig. 1 — Locality map showing locations of mine shafts and exposures/outcrops mentioned in the text.

(1837, pi. 17, fig. 12) from the “ Craie tuffau” of Tou­raine (France); its present whereabouts is unknown.

M a t e r ia l : IRSNB IG 9780 from the Hervían of the Charbonnage Houthalen, shaft 1, at a depth o f 583-585 m; three fragments. IRSNB IG 8914, Charbonnage Zol­der (Voort), shaft 2, seven fragments from a depth of 527 m. IRSNB 10378a, b, 10379 (IG 8831), from the same shaft at a depth of 581.45 m. IRSNB IG 8748, from shaft 1 at the same locality at a depth o f 582-584.30 m.

D is c u s s io n : These fragments are all rather poorly pre­served composite moulds, either fragments o f juveniles or o f body chamber. All show the characteristic strong ornament of the middle growth stages o f this species, which is discussed at length by K e n n e d y & W r ig h t (1983).

O c c u r r e n c e : Placenticeras polyopsis ranges throughout the Santonian, and is widespread in France (Aquitaine Basin, Corbières, Beausset (Var), and Touraine), north­eastern Belgium, Germany and northern Spain.

Superfamily Acanthocerataceae de G r o s s o u v r e , 1894 Family C o l l ig n o n ic e r a t id a e W r ig h t & W r ig h t , 1951

Subfamily Texanitinae C o l l ig n o n , 1948 Genus and subgenus Texanites (Texanites) S p a t h , 1932

T y p e s p e c ie s : Ammonites texanus R o e m e r , 1852, p. 31, pi. 3, fig. 1, by original designation o f S p a t h (1932, p. 379).

Texanites (Texanites) sp.PI. 1, Figs. 7, 8.

M a t e r ia l : A large com posite internal mould, and an external mould (IG 8914) o f the venter of a larger speci­men (Wh c 100 mm), Charbonnage Zolder (Voort), shaft 1, at a depth of 583-590 m. IRSNB 10377 (IG 9780), labelled “ Campanien (base)” , Houthalen (Charbonna­ges), shaft 1, at a depth o f 596.97-598 m.

D e s c r ip t io n : IRSNB 10377 is a crushed composite mould with a maximum preserved whorl height o f 60 mm. There are prominent umbilical bullae (1), clavate inner lateral (2), larger, clavate outer lateral (3), and larger, clavate inner (4) and outer ventrolateral clavi

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Santonian macrofauna and nannofossils 129

(5), borne on strong, distant, straight, prorsiradiate ribs. A pronounced groove separates the outer ventrolateral clavi from a strong, slightly undulóse siphonal keel.

D is c u s s io n : Although only fragmentary, the present m a­terial is of interest as the only known representative of the Texanitinae from the area.

Superfamily Scaphitaceae G il l , 1871 Family S c a p h it id a e G il l , 1871

Subfamily Scaphitinae G il l , 1871 Genus and subgenus Scaphites P a r k in s o n , 1811

T y p e s p e c ie s : Scaphites equalis J. S o w e r b y , 1813, p. 53, pi. 18, figs. 1-3, by subsequent designation o f M e e k (1876, p. 413).

The specimens come from Charbonnage Houthalen, shaft 1, at a depth of 575-598 m; Charbonnage Zolder (Voort), shaft 1, at a depth o f 575.8-584.3 m; same colliery, shaft 2, at a depth o f 581.45-588 m, and from Charbonnage Beringen, shaft 2, at a depth of 612 m.

The North European palaeobiogeographic province extends from Ireland in the west to the Ural M ountains in the east and includes the Central European and Central Russian Subprovinces. These subprovinces are well de­fined in the Coniacian-Lower Campanian. The Central European Subprovince is characterised by the genus Go- nioteuthis and the Central Russian Province by the genus Belemnitella d'O RBiG N Y , 1840 ( C h r is t e n s e n , 1976, 1988, 1990). Belgian Limburg is part o f the Central European Subprovince as defined on belemnites.

Scaphites (Scaphites) kieslingswaldensis fisch eri R ie d e l , 1931

PI. 1, Figs. 1, 2.

1931 Scaphites bärtlingi R ied el , p. 701, pi. 79, figs. 3,4. * 1931 Scaphites fischeri R ied el , p. 704, pi. 79, figs. 5, 6.

1986 Scaphites fischeri Riedel, 1931 - K en n ed y , p. 124, fig. 40.

1991 Scaphites kieslingswaldensis fischeri Riedel, 1931 - Ken n ed y & C h r isten sen , p. 222, pi. 2, figs. 1, 2; pi. 5, fig . 2; pi. 6, figs. 2-4, 7; pi. 7, figs. 2, 4.

1993 Scaphites (Scaphites) kieslingswaldensis fischeri Riedel, 1931 - K en nedy & C h risten sen , p. 155, figs. 4f, g, m, n.

T y p e : Lectotype, designated by K e n n e d y (1986, p. 124), is the original of R ie d e l (1931, pi. 79, fig. 6).

M a t e r ia l : From the Charbonnage Houthalen, shaft 1, IRSNB 10383 (IG 9780), a single fragmentary specimen at a depth o f 583-585 m.

D is c u s s io n : The single available specimen corresponds closely to material from the lowermost Campanian of Broitzem-Braunschweig (Germany) as figured by K e n ­n e d y (1986, fig. 40); it is here recorded for the first time from the Upper Santonian/Lower Campanian o f Belgium (see below).

O c c u r r e n c e : Lower Santonian to Lower Campanian of Germany, Santonian o f Denmark and Sweden and Upper Santonian/Lower Campanian o f Belgium.

B e l e m n o id e a

The present collection comprises 109 specimens, 15 of which are complete, 26 are fragments o f the anterior end, and 68 are fragments of the middle and posterior part of the guard. All are referable to the genus Gonioteuthis B a y l e , 1878.

Family B e l e m n it e l l id a e P a v l o w , 1914 Genus Gonioteuthis B a y l e , 1878

T y p e s p e c ie s : Belemnites quadratus d e B l a in v il l e , 1827.

R e m a r k s : The evolutionary lineage o f Gonioteuthis in­cludes seven species and subspecies occurring from the M iddle Coniacian to the Lower/Upper Campanian boun­dary (Text-fig.2). This lineage was studied in great detail by the German authors E. S t o l l e y , G. E r n s t and M.-G. S c h u l z , in addition to I. J a r v is and W.K. C h r is t e n s e n (references in C h r is t e n s e n , 1991). Eleven zones have been established on the basis o f this lineage (Text-fig. 2), based mainly on the Riedel-Quotient (= length o f guard divided by depth o f pseudoalveolus; see E r n s t , 1964). E r n s t & S c h u l z (1974) introduced the term Riedel- Index, which is the depth o f the pseudoalveolus as a percentage o f the length o f the guard. The Schlankheits- Quotient (= Slenderness-Quotient) of E r n s t ( 1964) is the length of the guard divided by the dorsoventral diam eter at the alveolar end.

C h r is t e n s e n (1991) analysed the growth relationship of guard length vs the depth of the pseudoalveolus, and guard length vs the dorsoventral diam eter at the alveolar end o f a large number of samples, representing all species o f Gonioteuthis, with the exception of G. praewestfalica. He showed that the relationship o f guard length vs depth of pseudoalveolus is generally isometric. The Gonioteu­this zonation o f E r n s t (1964) is therefore valid. On the other hand, the relationship of guard length vs dorsoven­tral diam eter at the alveolar end is allometric to strongly allometric in most samples. Juvenile specimens are more slender than adults. It is therefore not valid to calculate the mean Slenderness-Quotient.

D is t r ib u t io n : Gonioteuthis is known from the upper Middle Coniacian to the Lower/Upper Campanian boun­dary. The genus had its evolutionary centre in NW Eu­rope and is recorded almost exclusively from the Central European Subprovince.

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130 J.W .M. JAGT, W.J. KENNEDY, J.A. BURNETT, W.K. CHRISTENSEN & A.V. DHONDT

G onioteuthis w estfalicagranulata (S t o l l e y , 1897) (S e e C h r is t e n s e n , 1975a, b f o r s y n o n y m y ) .

T y p e : The original o f S t o l l e y (1897, pi. 2 , fig. 16; pi. 3 , fig. 6) was designated lectotype and reillustrated by C h r is t e n s e n (1975b, pi. 10, fig. 1; text-fig. 2 A).

B i o m e t r y : Fifteen complete specimens were analysed using univariate statistical methods: these are FI 94-1/1 & 2 (2 specimens), IG 9780, Charbonnage Houthalen, shaft 1, 575- 583 m; FI 94-1/13 (2 specimens), IG 8748, Charbonnage Zolder (Voort), shaft I, 575.8-579.5 m; FI 94-1/9 (2 specimens), IG 8748, Charbonnage Zolder (Voort), shaft 1, 579.5-582 m; FI 94-1/8 (3 specimens), IG 8748, Charbonnage Zolder (Voort), shaft 1, 582-584.3 m; FI 94-1/7 (4 specimens), IG 8831, Char­bonnage Zolder (Voort), shaft 2, 581.45 m; and FI 94-1/10 (2 specimens), IG 8831, Charbonnage Zolder (Voort), shaft 2, 588 m.

Univariate analysis

Character N X SD CV OR

L 15 60.1 3.8 6.4 52.0-64.9

RQ 15 9.2 2.4 25.8 6.4-15.0

RI 15 11.4 2.8 24.3 6.7-15.7

SQ 15 6.1 0.8 13.8 5.1- 7.5

L/MLD 13 6.2 1.0 15.6 4.9- 8.5

MLD/LDAE 13 1.1 0.1 5.5

cn1©

N = number of specimens; X = mean value; SD = standard deviation; CV = coefficient of variation; OR = observed range; L = length of guard; RQ = Riedel-Quotient; RI = Riedel-Index; SQ = Slenderness-Quotient; MLD = maximum lateral diameter; LDAE = lateral diameter at alveolar end.

wLUCDKCO

ZONATION

N W -GE RM ANY( 1 )

GO NI OTE UTH IS

Z O N E S( 2 )

S A M P L E S OF G O N I O T E U T H I S

Tai-------LAGER-DORF

731MISBURG/HÖ VER

7ïïl-------OTHERAREAS

( 6 ) RIEOEL-QUOTIENT20 18 16 14 12 10 8 6 4

g rac ilis /m u cro n a ta Zone (RQ = Í 4.5)

con ica/g rac ilis Zone

G quadrata gracilis

RQ =4.5

RQ =4.7(RQ = 4.0-4.5) RQ =4.5 RQ=4.5

RQ=4.2

I I

¡ I<oœUi«Ïo

p ap illo sa ZoneRQ =4.2RQ = 3.8

RQ =4.1

RQ = 3.8RQ = 3.9

senonensis Zone G. quadrataquad ra ta (RQ = i4 .0 )

RQ = 4.0RQ = 3.9

r q =3.7RQ =4.5

m ean value and observed range of the R led e l-Q u o tien t

RQ = 4.2

p ilu la /sen o n en sis ZoneRQ = 3.8

RQ = 4.2

C(0aa33o

pilula Zone RQ=4.2 RQ=3.9

lin g u a /q u a d ra ta ZoneRQ=4.1 RQ=4.3

(RQ = 4 0 -5 .0 ) RQ = 3.9 RQ = 4.0 RQ=4.9

g ran u la taq u ad ra ta Zone G. g ranulata- (RQ = 5 .o -6 .0 ) quad ra ta

RQ = 5.5 RQ = 5.1

M arsup ites/g ranu lata Zone G. g ranu la ta (RQ =6.0-7.0) RQ = 6.5

U intacrinus/granulata Zone (RQ =7.0-8.0) RQ = 6.9RQ = 8.1

Z O

<CO

w estfalicagranulata Zone G .w estfalica­granulata (RQ = 8 .0 -9 .5 ) RQ = 8.8 RQ = 9.0

cordiform is/westfalica Zone G. w estfalica ( RQ=9.5-11.5) RQ=11.0 RQ= 10.0

w e s t f a l i c a ( r q =>11.5) RQ =13.0undulatoplicatus Zone

Z => < praew estfa lica Zone G. w estfalica praew estfalica RQ=13.0

involutus Zone Koeneni Zoneo

o . deform is Zone

Fig. 2 — Zonation of the Coniacian-Lower Campanian of NW Germany (Braunschweig-Hannover area), Gonioteuthis zones, and the mean value and observed range of the Riedel-Quotient of samples of Gonioteuthis from Lägerdorf, Misburg/Höver (Hannover) and other areas (Braunschweig and Essen). Modified from C h r i s t e n s e n (1988).

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Santonian macrofauna and nannofossils 131

D is c u s s io n : According to E r n s t (1964, 1968) samples ofG. westfalicagranulata have a mean Riedel-Quotient of 8.0-9.5 (Text-fig. 2). The mean value o f this index of the present sample is 9.2, and it can thus be referred to this species.

E r n s t (1968) analysed two samples o f G. westfalica­granulata from NW Germany; these samples have a mean Riedel-Quotient o f 9.0, and the observed range is c. 5.5-15.0. The observed range of the Riedel-Quotient of the Belgian sample is 6.4-15.0, which is closely similar to the samples from NW Germany.

E r n s t (1964, fig. 12) did not indicate the mean Slen­derness-Quotient o f samples o f G. westfalicagranulata from NW Germany. He showed, however, that the mean Slenderness-Quotient o f G. westfalica varied from 6.4- 6.9, and the mean Slenderness-Quotient o f G. granulata is about 5.7. The present sample has a mean Slenderness- Quotient o f 6.1, implying that the specimens are stouter than G. westfalica and more slender than G. granulata. In this respect, the Belgian sample may be referred to G. westfalicagranulata as well.

As noted above, calculating the mean Slenderness- Quotient should be discarded, because the relationship o f the length o f the guard v.v dorsoventral diam eter is generally allometric to strongly allometric. Nevertheless, the mean Slenderness-Quotient has been calculated for the present sample in order to compare it with samples from NW Germany ( E r n s t , 1 9 6 4 ) . All specimens from NE Belgium are adult. If juvenile and adolescent speci­mens had been available, the mean Slenderness-Quotient would have been slightly larger. However, this would not have affected the above conclusion.

To summarise, the present sample is assigned to G. westfalicagranulata on the basis o f the means o f Riedel- Quotient and Slenderness-Quotient, in addition to the observed range of Riedel-Quotient. The sample exhibits a variation with respect to Riedel-Quotient, which does not differ in any significant respect with coeval samples from NW Germany.

D is t r ib u t io n : Gonioteuthis westfalicagranulata occurs in the upper M iddle Santonian westfalicagranulata Zone ( E r n s t , 1964, 1968) (= rogalae/westfalicagranulata Zone o f Lägerdorf; E r n s t & S c h u l z , 1974; S c h u l z et al., 1984).

M iddle Santonian belemnite faunas

Four belemnitellid genera occur in the M iddle Santonian: Actinocam ax M il l e r , 1823, Gonioteuthis, Belemnelloca- max N a id in , 1964 and Belemnitella (see C h r is t e n s e n , 1988, 1990). In NW Europe, Actinocam ax is restricted to a single species, A. verus M il l e r , 1823, Gonioteuthis to two species, G. westfalica ( S c h l ü t e r , 1876) and G. westfalicagranulata, Belemnellocamax to one group, B. ex gr. grossouvrei ( J a n e t , 1891) and Belemnitella to a single species, B. propinqua (M o b e r g , 1885).

The belemnite fauna of Belgian Limburg comprises but a single species, G. westfalicagranulata. The absence

of A. verus is enigmatic and may be due to collection failure, because this species occurs commonly in the Santonian near-shore “ Glauconie de Lonzée” ( C h r is ­t e n s e n , 1994) and in the upper M iddle Santonian marls at Eriksdal in Scania, Sweden ( C h r is t e n s e n , 1986). The absence o f B. ex gr. grossouvrei may be explained by its overall rarity. Belemnitella propinqua occurs mainly on the Russian Platform and in southern Scandinavia. Out­side this area, only three specimens have been recorded from southern England ( C h r is t e n s e n , 1991). Its absence in Limburg may be explained by its overall rarity in the Central European Subprovince.

In o c e r a m id b iv a l v e s

Superfamily Pteriacea Family I n o c e r a m id a e Z it t e l , 1881 (ICZN 4 7 3 )

The collections of the Institut royal des Sciences naturel­les de Belgique include the following poorly preserved inoceramid material, from the mine shafts discussed he­rein:— Charbonnage Houthalen, shaft 1 (IG 9 7 8 0 )

5 8 3 -5 8 5 m Cordiceramus brancoiformis (S e it z , 19 6 1 )Platyceramus cf. cycloides (W e g n e r , 1905)

— Charbonnage Zolder, shaft 1 (IG 8 7 4 8 )5 7 9 .5 -5 8 2 m Endocostea baltica (J. B ö h m , 1 9 0 7 )

— Charbonnage Zolder, shaft 2 (IG 8 8 3 1 )5 8 1 .4 5 m Endocostea aff. baltica.

The stratigraphie range of Cordiceramus brancoiformis is Middle - Upper Santonian in Germany (S e it z , 1 9 6 7 ; T r ö g e r , 1 9 8 7 ); Platyceramus cycloides is known through­out the Santonian and also from the Lower Campanian ( T r ö g e r , 1 9 8 7 ). The oldest Endocostea baltica specimens recorded by S e it z (1 9 6 7 ) and T r ö g e r (1 9 8 7 ) are from the Upper Santonian, but the species reaches throughout the Campanian and possibly into the Maastrichtian (D h o n d t , 1 9 9 3 ). These ranges agree well with the belemnite and ammonite/nannofossil ages.

N a n n o f o s s il s

Nine calcareous sandstone samples were analysed for nanno­fossils. Due to the high sand content of the material (sample descriptions appear below), nannofossil slides were prepared in the following way: each sample was rinsed, placed into a beaker with distilled water, and subjected to ultrasonic vibration for a few minutes, until break-down of the sample was effected. The suspension was stirred, the coarse (sandy) fraction allowed to settle for a few seconds, and the uppermost (nannofossil-bear- ing) part of the suspension pipetted onto a glass coverslip on a hotplate. The suspension was allowed to dry. The sediment on the coverslip was then remobilised with a drop of distilled water, and the sediment smeared evenly and more thinly across the coverslip with a flat-sided toothpick. The smear was then dried and mounted on a glass slide, using Norland Optical Adhesive, for examination.

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132 J.W .M . JAGT, W.J. KENNEDY, J.A. BURNETT, W.K. CHRISTENSEN & A.V. DHONDT

^ a a C,Ss» 20 b ggfsNF ABUNDANCE

C ( m o n - 1-10/fieId of view F«w - 1-2/10 fields of view Rare - 1/11-100 fields of view . » absent T ■ questionable

TAXA (IN ALPHABETICAL ORDER)

A c . scotusA b . octoradiataA h . r e g u l a r i aAm. b r o o k a i i (large fora)dr. c y m b i fo r m isB l . e l l i p t i c u mB l . sp.Bra. b i g e l o v i iB r o . e norm i aB r o . p a r c a espansaB to . a ig n a taC a. c f . C a . o b a c u ru aC a. obscurusC a. o v a l i sC h . ampb i p o a aC h. b i f a r l u aC h. litterariusC h. a y n q u a d 'r ip e r fo r a tu aC h. t e t r a g o n o t b y r u a lC o. e x ig u u mC o. a ig n u mC r e . c o n ic u sCr e . a t r i a t u aC r i . e h r e n b e r g i iC jc . m a r g e r e l i iCyc. r o t a c l y p e a t aC y l . b ia r c u aD i . i g u o tu aE i . e x im lu aR I . g o r k a eE i . parallelusE i . turriseiffeliiC a. o b l iq u u mG e. c o r o o a d v e n t iaHa. circumradiatusH e. a o c e p aB e . trabeculatusfa. m a g n i f i c u aL i t h a . g r i l l i i a . a .L i t h r . carniolensis L o . a r m i l l a L u . a r c u a t u s L u . c a y e u x i iL u . m a le fo r m ia (long fora) L u . m a le fo r m ia (abort fora) H an. p e m m a to id e a M ar. f u r c a t u a a.s.H ie r , b e l g i c u sH i e r , d e c o r a t u sH ie r , h e l i c o i d e u sM ie r . u n d o s u sH ic u . c o n c a v aH ic u . c u b i f o r n i sN lc u . s ta u r o p h o r aH ic u . s t r a a t i c aH a nnocouua r e g u l a r i aN an n o co n u a sp. (x-sectiou)O c. cf. O c. multiplusP I . f i b u l i f o r m i sP l . t cf. Z y . s ig m o id e aP r . b u k r y iP r . c l . P r . g r a n d i sP r . c r e t a c e aP r . p o n t i c u l aP r . s p in o s a (medium fora)P r . a p in o e a (large fora)P r . a t o v e r i (AI. g o th ic u m Re c . compactus Re i . anthophorus R ep . p a r v id e n ta tu m R e t . a n g u a ! i f o r a t a R e t . c r e n u l a t a R h . a n g u s tu s R b . i n f i n i t u s !

p l e b e i u s r e n i f o r m i ss p l e n d e n sc r e n u l a t u s f o a a i l i a h o r t i c u a co m p a c ta i n t e g r a

R b .

R b .Ro.

S t .

S t .S t .S t .

cruxlaffitteim i e l n i c e n s i sc o p t e n a i a lecclesiasticag a b a lu sm in im u so r io n a tu am a ta lo s a (medium fora)m a ta lo s a (small fora)b a r n e s a efo a a a c i n c t amauivitaeq u a d r i r a d i a t ab i p e r f o r a t u sd ip lo g ra m m u serectusn o e l i a e

00 —

■ esMa « ~

009>m -o • J = 5 • *¿ s

?n Ë i n ■io «o «i sr

sii

Im

3 N ' nS ín O «i «o eo

m io

R R .C C R . . R

C C F

F C F F F R

R RF F . R

R . R R

R F R . R R

. F F F F F R RF C R R R F C C F . R R F F . R F F

F FF .

The nannofossil assemblages in all of the samples are diverse (a total o f 100 taxa were identified), but preserva­tion is generally poor to moderate, although this did not affect the identification of any taxa. Etching o f calcite is typically predominant in sediments of this nature, where the sand has aided percolation o f acidic pore-waters.

The numerical zonation scheme o f S is s in g h ( 1 9 7 7 ) , modified and summarised by P e r c h - N ie l s e n ( 1 9 8 5 ) , was applied to the assemblages in order to assign biostrati- graphical zones. These are summarised below. The stage age-assignments, shown in brackets, are those derived from S is s in g h and P e r c h - N ie l s e n . Table 1 shows the taxa recorded from each sample and the nannofossil zone assigned on the basis o f the assemblage. A complete taxonomic list appears below.

— Charbonnage Houthalen, shaft 1583-585 m (sample 2): CC16 (late Santonian)583-585 m (sample 4): CC16 (late Santonian),

possibly C C I7 (Santonian/Cam panian)

596.97-598 m (sample 8): CC16 (late Santonian)

— Charbonnage Zolder (Voort), shaft 1 582-584.3 m (sample 7): CC 15 (late early

Santonian), possibly C C I6 (late Santonian)

585-590 m (sample 5): C C I6 (late Santonian)

— Charbonnage Zolder (Voort), shaft 2572 m 572 m

581.45 m581.45 m

(sample 1): CC 16 (late Santonian) (sample 3): CC 16 (late Santonian,

possibly CC 17 (Santonian/Cam panian)

(sample 6): CC 16 (late Santonian) (sample 9): CC 16 (late Santonian)

Sample descriptions

— Charbonnage HouthalenShaft 1, 583-585 m (sample 2): indurated, medium- dark grey, calcareous sandstone.Shaft 1, 583-585 m (sample 4): relatively soft, cohe­sive, dark grey, clayey calcareous sandstone.Shaft 1, 596.97-598 m (sample 8): relatively soft, cohesive, dark green (Cu ?)/black, calcareous sand­stone.

— Charbonnage Zolder (Voort)Shaft 1, 582-584.3 m (sample 7): as sample 4.Shaft 1, 585-590 m (sample 5): as sample 8.Shaft 2, 572 m (sample 1): soft, non-cohesive, dark grey, clayey sandstone.Shaft 2, 572 m (sample 3): as above.Shaft 2, 581.45 m (sample 6): as above.Shaft 2, 581.45 m (sample 9): as above.

Table 1.Nannofossil stratigraphical distribution.

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Santonian macrofauna and nannofossils 133

Nannofossil taxonomic list

Acuturris scotus ( R is a t t i, 1 9 7 3 ) W in d & W is e in W is e & W in d , 1 9 7 7

Ahmuellerella octoradiata ( G o r k a , 1 9 5 7 ) R e i n h a r d t , 1 9 6 6

A. regularis ( G o r k a , 1 9 5 7 ) V e r b e e k , 19 7 7 Amphizygus brooksii B u k r y , 1 9 6 9 Arkhangelskiella cymbiformis V e k s h i n a , 1 9 5 9 Biscutum ellipticum ( G o r k a , 1 9 5 7 ) G r ü n in G r ü n &

A l l e m a n n , 197 5 Biscutum sp . [ s im ila r to B. ellipticum b u t m u c h la rg e r ] Braarudosphaera bigelowii ( G r a n & B r a a r u d , 1 9 3 5 )

D e f l a n d r e , 1 9 4 7 Broinsonia enormis ( S h u m e n k o , 1 9 6 8 ) M a n i v i t , 1971B. parca expansa W is e & W a t k in s in W is e , 198 3B. signata ( N o e l , 1 9 6 9 ) N o e l , 1 9 7 0Calculites obscurus (D e f l a n d r e , 1 9 5 9 ) P r in s & S is ­

s in g h in S is s in g h , 197 7C. cf. obscurus [ s im ila r to C. obscurus b u t s m a l le r a n d

w ith m u c h lo w e r b ir e f r in g e n c e ]C. ovalis (S t r a d n e r , 1 9 6 3 ) P r in s & S is s in g h in S is ­

s in g h , 19 7 7Chiastozygus amphipons ( B r a m l e t t e & M a r t i n i , 1 9 6 4 )

G a r t n e r , 1 96 8 C. bifarius B u k r y , 1 9 6 9 C. litterarius ( G o r k a , 1 9 5 7 ) M a n i v i t , 1971 C. synquadriperforatus B u k r y , 1 9 6 9 C. tetrágono thy ru si H i lL , 1 9 7 6 Corollithion exiguum S t r a d n e r , 1961 C. signum S t r a d n e r , 1 9 6 3Cretarhabdus conicus B r a m l e t t e & M a r t i n i , 1 9 6 4 C. striatus ( S t r a d n e r , 1 9 6 3 ) B l a c k , 1973 Cribrosphaerella ehrenbergii ( A r k h a n g e l s k y , 1 9 1 2 )

D e f l a n d r e in P iv e t e a u , 1 9 5 2 Cyclagelosphaera margerelii N o e l , 19 6 5 C. rotaclypeata B u k r y , 1 9 6 9 Cylindralithus biarcus B u k r y , 1 9 6 9 Discorhabdus ignotus ( G o r k a , 1 9 5 7 ) P e r c h - N i e l s e n ,

1 9 6 8Eiffelii thus eximius ( S t o v e r , 1 9 6 6 ) P e r c h - N i e l s e n , 19 6 8 E. gorkae R e i n h a r d t , 1965 E. parallelus P e r c h - N i e l s e n , 1973 E. turriseiffelii ( D e f l a n d r e , 1 9 5 4 ) R e i n h a r d t , 1 9 6 5 ,

B u k r y , 1 9 6 9Gartnerago obliquum ( S t r a d n e r , 1 9 6 3 ) R e i n h a r d t , 1 9 7 0 Gephyrorhabdus coronadventis ( R e i n h a r d t , 1 9 6 6 ) H i l l ,

19 7 6Haqius circumradiatus ( S t o v e r , 1 9 6 6 ) R o t h , 197 8 Helicolithus anceps ( G o r k a , 1 9 5 7 ) N o e l , 1 9 7 0H. trabeculatus ( G o r k a , 1 9 5 7 ) V e r b e e k , 197 7 Kamptnerius magnificus D e f l a n d r e , 1 9 5 9 Lithastrinus grillii S t r a d n e r , 1 9 6 2 Lithraphidites carniolensis D e f l a n d r e , 19 5 9 Loxolithus armilla ( B l a c k in B l a c k & B a r n e s , 1 9 5 9 )

N o e l , 196 5Lucianorhabdus arcuatus F o r c h h e i m e r , 1 9 7 2 L. cayeuxii D e f l a n d r e , 19 5 9 L. maleformis R e i n h a r d t , 1 9 6 6

Manivitella pemmatoidea ( D e f l a n d r e in M a n iv it , 1965) T h ie r s t e in , 1971

M arthasterites furcatus (D e f l a n d r e , 1954) D e f l a n d r e , 1959, B u k r y , 1969

M icrorhabdulus belgicus H a y e & T o w e , 1963 M. decoratus D e f l a n d r e , 1959 M. helicoideus D e f l a n d r e , 1959 M. undosus P e r c h - N ie l s e n , 1973 M icula concava (S t r a d n e r in M a r t in i & S t r a d n e r ,

1960) B u k r y , 1969, V e r b e e k , 1976 M. cubiformis F o r c h h e im e r , 1972 M. staurophora ( G a r d e t , 1955) S t r a d n e r , 1963 (= M .

decussata V e k s h in a , 1959)M. swástica (sensu P r in s , 1977) S t r a d n e r & S t e in m e t z ,

1984Nannoconus regularis D é r è S & ACHERITÉGUY, 1980 Octolithus cf. O. multiplus ( P e r c h - N i e l s e n , 1973) R o ­

m e i n , 1979 [similar to O. multiplus but sm aller and with only six blocks visible]

Placozygus fibuliform is ( R e in h a r d t , 1964) H o f f m a n n , 197Ó

P. cf. Zygodiscus sigmoides B r a m l e t t e & S u l l iv a n , 1961 [possibly a predecessor o f Z. sigmoides]

Prediscosphaera bukryi P e r c h - N ie l s e n , 1973 P. cretacea ( A r k h a n g e l s k y , 1912) G a r t n e r , 1968 P. grandis P e r c h -N ie l s e n , 1979 P. cf. P. grandis [similar to P. grandis but smaller]P. ponticula B u k r y , 1969, P e r c h - N ie l s e n , 1984 P. spinosa ( B r a m l e t t e & M a r t in i, 1964) G a r t n e r ,

1968P. stoveri ( P e r c h - N ie l s e n , 1968) S h a f ik & S t r a d n e r ,

1971Quadrum gothicum ( D e f l a n d r e , 1959) P r in s & P e r c h -

N ie l s e n in M a n iv it et al., 1977 Rectapontis compactus ( B u k r y , 1969) V a r o l & J a k u -

b o w s k i , 1989Reinhardtites anthophorus ( D e f l a n d r e , 1959) P e r c h -

N ie l s e n , 1968 Repagulum parvidentatum (D e f l a n d r e & F e r t in D e ­

f l a n d r e , 1954) F o r c h h e im e r , 1972 Retecapsa angustiforata B l a c k , 1971 R. crenulata ( B r a m l e t t e & M a r t in i , 1964) G r ü n in

G r ü n & A l l e m a n n , 1975 Rhagodiscus angustus (S t r a d n e r , 1963) R e in h a r d t ,

1971R. infinitus ( W o r s l e y , 1971) A p p l e g a t e et al. in C o ­

v in g t o n & W is e , 1987 R. plebeius P e r c h - N ie l s e n , 1968 R. reniformis P e r c h - N ie l s e n , 1973 R. splendens (D e f l a n d r e , 1953) V e r b e e k , 1977 Rotelapillus crenulatus (S t o v e r , 1966) P e r c h - N ie l s e n ,

1984Scapholithus fossilis D e f l a n d r e , 1954 Sollasites horticus (S t r a d n e r et al. in S t r a d n e r & A d a -

m ik e r , 1966) ¿ e p e k & H a y , 1969 Staurolithites compacta integra ( B u k r y , 1969)S. crux (D e f l a n d r e & F e r t in D e f l a n d r e , 1954) C a r a -

t in i , 1963 S. laffittei C a r a t in i , 1963

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134 J.W .M. JAGT, W.J. KENNEDY, J.A. BURNETT, W.K. CHRISTENSEN & A.V. DHONDT

S. mielnicensis ( G o r k a , 1957) P e r c h - N ie l s e n , 1968, C r u x in L o r d , 1982

Tetrapodorhabdus coptensisl B l a c k , 1971 Thiersteinia ecclesiastica W is e & W a t k in s in W is e ,

1983Tranolithus gabalus S t o v e r , 1966T. minimus ( B u k r y , 1969) P e r c h - N ie l s e n , 1984T. orionatus ( R e in h a r d t , 1966a) R e in h a r d t , 1966b (= T.

phacelosus S t o v e r , 1966)Vagalapilla matalosa (S t o v e r , 1966) T h ie r s t e in , 1973 Watznaueria barnesae (B l a c k in B l a c k & B a r n e s ,

1959) P e r c h - N ie l s e n , 1968 W. fossacincta ( B l a c k , 1 9 7 1 ) B o w n in B o w n & C o o p e r ,

1989W. manivitae B u k r y , 1973 W. quadriradiata B u k r y , 1969 Zeugrhabdotus biperforatus (G a r t n e r , 1968)Z. diplogrammus ( D e f l a n d r e in D e f l a n d r e & F e r t ,

1954)Z. erectus (D e f l a n d r e , 1954) R e in h a r d t , 1965 Z. noeliae R o o d et al., 1971

References

B a t t e n , D.J., D u p a g n e - K i e v i t s , J. & L i s t e r , J.K., 1988. Paly- nology of the Upper Cretaceous Aachen Formation of northeast Belgium. In: S t r e e l , M. & B l e s s , M.J.M. (Editors), The Chalk District of the Euregio Meuse-Rhine. Selected papers on Upper Cretaceous deposits. Natuurhistorisch Museum Maastricht/La­boratoires de Paléontologie de l’Université d’État à Liège, pp. 95-103.Bayle, E., 1878. Fossils principaux des terrains de la France. Explication de la Carte géologique de la France, 4(1), Atlas, 79 pis.B l a c k , M., 1971. The systematics of coccoliths in relation to the palaeontological record. In: F u n n e l l , E.M. & R i e d e l , W .R . (Editors), The micropalaeontology of oceans. Cambridge Uni­versity Press, pp. 611-624.B l a in v i l l e , H.M.D. d e , 1827. Mémoire sur les Belemnites, considérées zoologiquement et géologiquement. Levrault, Pa­ris, 136 pp.B ö h m , J., 1907. Ueber Inoceramus Cripsi Mant. Zeitschrift der deutschen geologischen Gesellschaft, 59: 113, 114. B r a m l e t t e , M.H. & M a r t i n i , E., 1964. The great change in calcareous nannoplankton fossils between the Maestrichtian and Danian. Micropaleontology, 10: 291-322.B u k r y , D., 1969. Upper Cretaceous coccoliths from Texas and Europe. University o f Kansas Paleontological Contributions, 51: 1-79.C h r i s t e n s e n , W.K., 1975a. Upper Cretaceous belemnites from the Kristianstad area in Scania. Fossils and Strata, 7: 1-69. C h r i s t e n s e n , W.K., 1975b. Designation of lectotypes for Go­nioteuthis westfalicagranulata and G. granulataquadrata. Pa- läontologische Zeitschrift, 49: 126-134.C h r i s t e n s e n , W.K., 1976. Palaeobiogeography of Late Creta­ceous belemnites of Europe. Paläontologische Zeitschrift, 50: 113-129.C h r i s t e n s e n , W.K., 1986. Upper Cretaceous belemnites from

Discussion

O f the cephalopods, only the belem nites yield a precise age assignment, viz. westfalicagranulata Zone sensu ger­m ánico (= upper part o f middle Santonian). The am m o­nites have been additionally dated by nannofossils, which generally indicate a late Santonian age, with some o f the material being o f late early Santonian and latest Santo- nian/earliest Campanian date.

Ammonite biozonation o f the Santonian is still com pa­ratively crude; one o f the species recognised amongst the material from Houthalen and Zolder/Voort, Placenticeras polyopsis, ranges throughout the Santonian, while the texanitid is specifically indeterminate and thus precludes comparison with occurrences elsewhere. Lithologically, the single specimen referred to Scaphites kieslingswal­densis fischeri from H outhalen-shaft 1, at a depth of 583- 585 m, differs from the other ammonites recorded from the same depth. It is possible that the occurrence of this species marks the Santonian/Campanian boundary at Houthalen (see also nannofossil data, sample 4).

the Vomb Trough in Scania, Sweden. Sveriges geologiska Undersökning, Ca 57: 1-57.C h r i s t e n s e n , W.K., 1988. Upper Cretaceous belemnites of Europe: state of the art. In: S t r e e l , M. & B l e s s , M.J.M. (Editors), The Chalk District of the Euregio Meuse-Rhine. Natuurhistorisch Museum Maastricht/Laboratoires de Paléon­tologie de l’Université d’Etat, Liège, pp. 5-16.C h r i s t e n s e n , W.K., 1990. Upper Cretaceous belemnite strati­graphy of Europe. Cretaceous Research, 11: 371-386. C h r i s t e n s e n , W.K., 1991. Belemnites from the Coniacian to Lower Campanian chalks of Norfolk and southern England. Palaeontology, 34: 695-749.C h r i s t e n s e n , W.K., 1994. Upper Cretaceous belemnites from Lonzée (SE Belgium) and their stratigraphical significance. Bulletin de l ’Institut royal des Sciences naturelles de Belgique, Sciences de la Terre, 64: 151-158.C o l l i g n o n , M., 1948. Ammonites néocrétacées du Menabe (Madagascar). I. Les Texanitidae. Annales géologiques du Ser­vice des Mines de Madagascar, 13: 49-107 [1-63]; 14: 7-101 [64-120],D e f l a n d r e , G., 1959. Sur les nannofossiles calcaires et leur systématique. Revue de Micropaléontologie, 2: 127-152. D e f l a n d r e , G. & F e r t , C., 1954. Observations sur les coccoli- thophoridés actuels et fossiles en microscopie ordinaire et électronique. Annales de Paléontologie, 40: 115-176.D h o n d t , A. V., 1993. Upper Cretaceous bivalves from Tercis, Landes, SW France. Bulletin de l ’Institut royal des Sciences naturelles de Belgique, Sciences de la Terre, 63: 211-259. D o u v i l l é , H., 1890. Sur la classification des Cératites de la Craie. Bulletin de la Société géologique de France, (3) 18: 275- 292.D u j a r d i n , F., 1837. Mémoire sur les couches du sol en Tou­raine et description des coquilles de la craie et des faluns. Mémoires de la Société géologique de France, (1)2: 211-311.

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Santonian macrofauna and nannofossils 135

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poda (1853-1857)” . Monograph o f the Palaeontographical Society, 104: 1-40.

Typescript submitted: 15.3.1993 Revised typescript received: 1.10.1994

John W.M. J a g t Dienst KCO

Natuurhistorisch Museum Maastricht

Postbus 882 NL-6200 AW Maastricht,

The Netherlands

William James K e n n e d y

Geological Collections Oxford University Museum

Parks Road Oxford OX1 3PW, U.K.

Jacqueline A. B u r n e t t Micropalaeontology Unit,

Research School of Geological and Geophysical Sciences

Birkbeck College & University College London

Gower Street London WC1E6BT, U.K.

Walter Kegel C h r is t e n s e n Geologisk Museum Oster Voldgade 5-7

DK-1350 Copenhagen K. Denmark

Annie V. D h o n d t Dept, of Palaeontology

Koninklijk Belgisch Instituut voor Natuurwetenschappen

Vautierstraat 29 B-1040 Brussels, Belgium

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Santonian macrofauna and nannofossils 137

Pl a te 1

Figs. 1 ,2 — Scaphites (Scaphites) kieslingswaldensis fischeri Riedel, 1931, IRSNB 10383, from the Charbonnage Houthalen, shaft 1, at a depth of 583-585 m, x 1.

Figs. 3-6 — Placenticeras polyopsis (Dujardin, 1837). 3,4 - IRSNB 10378a, from Charbonnage Zolder (Voort), shaft 2, at a depth of 581.45 m, x 1. 5, 6 - IRSNB 10378b, from Charbonnage Zolder (Voort), shaft 2, at a depth of 581.45 m, x 1.

Figs. 7, 8 — Texanites (Texanites) sp. IRSNB 10377, from Charbonnage Zolder (Voort), shaft 1, at a depth of 583-590 m, x 1.

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