20
Faciès and biostratigraphy of the Late Carboniferous/Early Permian sedimentary séquence in the Carnic Alps (Austria/ltaly) Karl KRAINER Institute for Geology and Paleontology, University of Innsbruck, Innrain 52, A-6020 Innsbruck (Austria) Karl.Krainer® uibk.ac.at Vladimir DAVYDOV Department of Geosciences, Boise State University, 1910 University Drive, Boise, Idaho 83725 (USA) [email protected] In memoriam Franz Kahler (1900-1996) KEYWORDS Peri-Tethys, Late Carboniferous, Early Permian, Carnic Alps, faciès, biostratigraphy, fusulinids, conodonts, plant fossils. Krainer K. & Davydov V. 1998. — Faciès and biostratigraphy of the Late Carboniferous/Early Permian sedimentary séquence in the Carnic Alps (Austria/ltaly), in Crasquin-Soleau S., Izart A., Vaslet D. & De Wever P. (eds), Peri-Tethys: stratigraphie cor- relations 2, Geodiversitas 20 (4) : 643-662. ABSTRACT The Late Catbonifetous/Early Permian séquence in the Carnic Alps (Austria/ltaly) is a more than 2000 m thick succession of shallow matine clastic and carbonate sedimentaty rocks. The succession unconformably overlies rhe folded Variscan basement and is divided into Bombaso Fotmation, Auernig Group, Rartendotf Group and Trogkofel Group. Auernig Group and Rattendorf Group are charactetized by clastic-catbonate cycles related to Gondwana glacioeustatic sea level changes. Catbonates contain abundant fossils throughout the séquence, biostratigtaphy is mainly based on fusulinids. Fine-grained clastic intervais contain abundant plant fossils, allowing a close corrélation with fluvial succession of the Eastern Alps (Stangnock Fotmation of the Gutktal Nappe). Fusulinids of the Carnic Alps show high similarity wirh those of the Russian Platfotm, Donets Basin and Ptedonets Trough, Southern Urals and particulatly with Central Asia. Uppermost Moscovian, Kasimovian, Gzhelian, lowermost Asselian, late Asselian, Sakmarian and Artinskian équivalents ate established and précise corrélation with sttatotype légions have been completed. Fusulinid, cono- dont and plant fossil data well coirespond with each othet. GEODIVERSITAS • 1998 • 20(4) 643

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Page 1: Faciès and biostratigraphy of the Late Carboniferous/Early ...sciencepress.mnhn.fr/sites/default/files/articles/pdf/g1998n4a5.pdf · In the Carnic Alps (southern Austria/northern

Faciès and biostratigraphy of the Late Carboniferous/Early Permian sedimentary séquence in the Carnic Alps (Austria/ltaly)

Karl KRAINER Institute for Geology and Paleontology, University of Innsbruck,

Innrain 52, A-6020 Innsbruck (Austria)

Karl.Krainer® uibk.ac.at

Vladimir DAVYDOV Department of Geosciences, Boise State University,

1910 University Drive, Boise, Idaho 83725 (USA)

[email protected]

In memoriam Franz Kahler (1900-1996)

KEYWORDS Peri-Tethys,

Late Carboniferous, Early Permian,

Carnic Alps, faciès,

biostratigraphy, fusulinids,

conodonts, plant fossils.

K r a i n e r K. & D a v y d o v V. 1 9 9 8 . — F a c i è s a n d b i o s t r a t i g r a p h y of t he La te Carboniferous/Early Permian sedimentary séquence in the Carnic Alps (Austria/ltaly), in Crasquin-Soleau S., Izart A., Vaslet D. & De Wever P. (eds), Peri-Tethys: stratigraphie cor-relations 2, Geodiversitas 20 (4) : 643-662.

A B S T R A C T

T h e Late Ca tbon i fe tous /Ear ly Permian séquence in the Carn ic Alps

(Austria/ltaly) is a more than 2000 m thick succession of shallow matine

clastic and carbonate sedimentaty rocks. The succession unconformably

overlies rhe folded Variscan basement and is d ivided in to Bombaso

Fo tma t ion , Auernig G r o u p , Rar tendot f G r o u p and Trogkofel G r o u p .

Auernig Group and Rattendorf Group are charactetized by clastic-catbonate

cycles related to Gondwana glacioeustatic sea level changes. Catbonates

contain abundant fossils throughout the séquence, biostratigtaphy is mainly

based on fusulinids. Fine-grained clastic intervais contain abundant plant

fossils, allowing a close corrélation with fluvial succession of the Eastern Alps

(Stangnock Fotmation of the Gutktal Nappe). Fusulinids of the Carnic Alps

show high similarity wirh those of the Russian Platfotm, Donets Basin and

Ptedonets Trough , Southern Urals and particulatly with Central Asia.

Uppermost Moscovian, Kasimovian, Gzhelian, lowermost Asselian, late

Asselian, Sakmarian and Artinskian équivalents ate established and précise

corrélation with sttatotype légions have been completed. Fusulinid, cono-

dont and plant fossil data well coirespond with each othet.

G E O D I V E R S I T A S • 1998 • 2 0 ( 4 ) 643

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Krainer K. & Davydov V.

MOTS CLÉS Péri-Téthys,

Carbonifère supérieur, Permien inférieur,

Alpes carniques, faciès,

biostratigraphie, fusulines,

conodontes, plantes fossiles.

R É S U M É

Faciès et biostratigraphie de la séquence sédimentaire Carbonifère supérieur!

Permien inférieur dans les Alpes carniques (Autriche/Italie). La séquence

C a r b o n i f è r e s u p é r i e u r / P e r m i e n in fé r ieur dans les Alpes ca rn iques

(Autriche/Italie) est constituée de plus de 2000 m de roches élastiques et car-

bonatées marines peu profondes. La succession recouvre en discordance le

socle varisque plissé et est subdivisée en la Formation Bombaso, les Groupes

Auernig, Rattendorf et Trogkofel. Les Groupes Auernig et Ratendorf sont

caractérisés par des cycles élastiques et carbonates produits par des variations

glacio-eustatiques (Gondwana). Les carbonates contiennent des fossiles abon­

dants tout au long de la séquence, la biostratigraphie étant principalement

fondée sur les fusulines. Les intervalles élastiques fins contiennent des fossiles

de plantes abondants, permettant une corrélation étroite avec la succession

fluviatile des Alpes orientales (Formation Stangnock de la nappe de Gurktal).

Les fusulines des Alpes carniques montrent de grande similarité avec celles de

la plate-forme russe, bassins du Donetz et Predonetz, Oural du Sud et parti­

cul ièrement Asie centrale. Des équivalents de la part ie supérieure du

Moscovien, Kasimovien, Gzhélien, de la partie inférieure de l'Assélien, de

l'Assélien supérieur, du Sakmarien et de l'Artinskien ont pu être établis et

une corrélation précise avec les régions stratotypes a été accomplie. Les don­

nées sur les fusulines, conodontes et plantes fossiles correspondent bien les

unes aux autres.

I N T R O D U C T I O N

In t he C a r n i c Alps ( sou the rn A u s t r i a / n o r t h e r n

Italy) the folded Variscan basement is unconfor -

mab ly overlain by a th ick succession of shal low

m a r i n e clastic a n d c a r b o n a t e rocks of t he Late

Carboni ferous B o m b a s o Forma t ion and Auern ig

G r o u p a n d t h e Ear ly P e r m i a n R a t t e n d o r f a n d

T r o g k o f e l G r o u p (F ig . 1) . T h è s e r o c k s w e r e

depos i ted in discrète basins formed by b lock and

wrench faulting subséquent to the Variscan o ro ­

g e n i c p h a s e w i t h i t s c l i m a x d u r i n g t h e

Westphal ian. Classic ou tc rops occur in the cen­

tral C a m i c Alps a long the Aust r ian/ I ta l ian border

(Fig. 2 ) . S e d i m e n t a r y rocks o f ail f o r m a t i o n s ,

pa r t i cu l a r l y t h e c a r b o n a t e s , c o n t a i n a b u n d a n t

fossils p r o v i d i n g t h e basis for b i o s t r a t i g r a p h i c

subdiv i s ion a n d cor ré la t ion . B ios t r a t ig raphy of

the Late Paleozoic séquence in the Ca rn ic Alps is

main ly based on fusulinids, a l though p lan t fossils

a n d c o n o d o n t s are of i m p o r t a n c e t o o . D u r i n g

the last décades major progress has been achieved

conce rn ing sedimentology, pa leonto logy and b io­

stratigraphy of this séquence (see Flugel 1980 a-b,

1 9 8 1 ; Kahler 1 9 8 3 , 1985 , 1986 , 1989; Fritz et

al. 1 9 9 0 ; Ven tu r in i 1 9 9 0 ; Kra ine r 1 9 9 2 , 1 9 9 3

a n d F o r k e 1 9 9 5 for fu r the r i n f o r m a t i o n s a n d

références). T h e présent paper gives a s u m m a r y

of the Late Carboniferous /Ear ly Permian séquen­

ce w i t h spécial emphas i s on the b ios t ra t igraphy

and corrélat ion wi th o ther régions.

FACIES

B O M B A S O F O R M A T I O N

T h e B o m b a s o Fo rma t ion consists of poor ly sort-

ed i m m a t u r e breccias a n d conglomérâ tes wh ich

are e i ther p r e d o m i n a n t l y c o m p o s e d of radiola-

rian cher t and volcanic clasts (Pramollo M e m b e r )

o r o f S i l u r i a n t o D e v o n i a n c a r b o n a t e c las t s

(Mal inf ie r H o r i z o n ) . T h i c k n e s s ranges f rom a

few meters u p to a b o u t 2 0 0 meters . T h e clasts

are der ived from the Variscan b a s e m e n t of the

upl i f ted Pa leoca rn ic C h a i n . T h e success ion of

the B o m b a s o Forma t ion generally shows a fining

upward t rend. Bioclasts of b rach iopods , cr inoids

a n d f u s u l i n i d s a re r a r e l y p r é s e n t i n d i c a t i n g

644 GEODIVERSITAS • 1998 • 2 0 ( 4 )

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Waidegger Hbhe 1961

+ Leitenkogel 1845

+

Triassic of the Gartnerkofel-Massif

Rattendorf Group and Trogkofel Group

Bombaso Formation and Auernig Group

ON

FIG. 1. — Map showing the distribution of Late Carboniferous and Early Permian sedimentary rocks in the Carnic Alps (Austria/ltaly).

Page 4: Faciès and biostratigraphy of the Late Carboniferous/Early ...sciencepress.mnhn.fr/sites/default/files/articles/pdf/g1998n4a5.pdf · In the Carnic Alps (southern Austria/northern

Krainer K. & Davydov V.

3K

IAN

Goggau L imes tone

(130 m)

_ I

L L Û -z

< AR

TIN

!

T ressdor f L imestone (10 m)

TR

OG

KO

G

RO

U

s

RIA

N

T rogkofe l L imes tone (400 m) T

RO

GK

O

GR

OU

te LU

0.

SA

KM

A

Upper Pseudoschwager ina L imes tone

(Zweikofe l Format ion ; 170 m)

RA

TT

EN

DO

RF

G

RO

UP

A S S E L I A N Grenz land Format ion

(125 m)

RA

TT

EN

DO

RF

G

RO

UP

Lower Pseudoschwager ina L imes tone

(Schul terkofe l Format ion; 160 m) RA

TT

EN

DO

RF

G

RO

UP

tn

o

oc

UJ LL

z

GIA

N Lower Pseudoschwager ina

L imes tone (Schul terkofe l Format ion; 160 m) R

AT

TE

ND

OR

F

GR

OU

P

tn

o

oc

UJ LL

z

OR

EN

BU

R

C a m i z z a Format ion (120 m)

CL

tn

o

oc

UJ LL

z

OR

EN

BU

R

Auern ig Format ion (250 m) R

OU

tn

o

oc

UJ LL

z LIA

N

Co rona Format ion (300 m) M

IG G

O

m

GZ

HE

P izzul Format ion (300 m) U

ER

I

a: K A S I M O V I A N

Meledis Format ion (120 m)

<

o U P P E R M O S T M O S C O V I A N

B o m b a s o F o r m a t i o n

V a r i s c a n B a s e m e n t

FIG. 2 . — S t r a t i g r a p h y o f t h e L a t e C a r b o n i f e r o u s a n d E a r l y

P e r m i a n s t r a t a in t h e C a r n i c A l p s .

déposi t ion in a mar ine env i ronmen t . Thèse bree-

cias a n d cong lomérâ t e s are in t e rp re t ed as mass

gravity flow deposits pr imari ly depos i ted on fan

deltas, part ly subaerially, par t ly submar ine .

A U E R N I G G R O U P

T h e B o m b a s o F o r m a t i o n is o v e r l a i n b y t h e

A u e r n i g G r o u p , w h i c h is u p t o 1.200 m th ick

a n d c o m p o s e d o f M e l e d i s - , P izzu l - , C o r o n a - ,

Auern ig- and Carnizza Format ions according to

Selli (1963) (Fig. 2 ) . T h e succession consists of

cyclic clastic a n d c a r b o n a t e rocks of a sha l low

m a r i n e e n v i r o n m e n t . M e l e d i s - , C o r o n a - a n d

Carn i zza F o r m a t i o n s p r e d o m i n a n t l y consis t of

c l a s t i c s é d i m e n t s , P i z z u l - a n d A u e r n i g

Format ions conta in substant ial quant i t ies of fos-

siliferous ca rbona te rocks. T h e m a i n lithofacies

types are a quar tz - r i ch cong lomera t e of a near-

shore e n v i r o n m e n t , frequently overlain by shale

c o n t a i n i n g a b u n d a n t a n d wel l -preserved mega-

p lan t fossils, t rough-crossbedded a n d h u m m o c k y

c rossbedded s an d s t o n e (shoreface), b i o t u r b a t e d

a n d locally fossiliferous siltstones a n d shales (off­

shore) a n d fossi l i ferous l i m e s t o n e s c o n t a i n i n g

c a l c a r e o u s a lgae {Anthracoporella spectabilis,

Archaeolithopbyllum missouriense, Epimastopora,

Eugonophyllum), fusul in ids , small foraminifers ,

e c h i n o d e r m s , b r y o z o a n s , Tubiphytes, s p h i n c t o -

zoans, sol i tary corals a n d o thers . Massive l ime­

s tones represen t algal m o u n d s {Anthracoporella

m o u n d s ; K r a i n e r 1 9 9 5 ) , i n t h e M e l e d i s

F o r m a t i o n small m o u n d s f o r m e d of a u l o p o r i d

corals are présen t (Fliigel & Kra iner 1 9 9 2 ) . In

the uppe r par t of the Auern ig G r o u p (Corona- ,

Auern ig- a n d Carnizza Format ions) thèse lithofa­

cies t y p e s f o r m p r o m i n e n t c l a s t i c - c a r b o n a t e

regress ive- t ransgress ive cycles ("Auernig cyclo-

themes") w i t h thicknesses of 10-40 m (Fig. 3) .

W i t h i n t h è s e cyc l e s c o n g l o m é r â t e s f o r m e d

d u r i n g relative sea-level lowstands a n d fossilife­

rous l imes tone was depos i ted d u r i n g per iods of

relative sea-level h i g h s t a n d s . T h e f o r m a t i o n of

thèse cycles is related to eustatic sea-level changes

c a u s e d by G o n d w a n a n g l a c i a t i o n (Massa r i &

Ventur in i 1990; Krainer 1992 , 1995) .

RATTENDORF G R O U P

T h e Ra t t endo r f G r o u p comprises a succession of

sha l low m a r i n e s é d i m e n t s o f n e a r s h o r e , i n n e r

shelf a n d outer shelf env i ronmen t s . T h e succes­

s ion is d iv ided i n t o Lower P s e u d o s c h w a g e r i n a

L i m e s t o n e ( L P L ) , G r e n z l a n d F o r m a t i o n a n d

U p p e r P s e u d o s c h w a g e r i n a L i m e s t o n e ( U P L )

(Fig. 2 ) .

T h e L P L is c o m p o s e d o f t h r e e d e p o s i t i o n a l

cycles cons i s t ing of sha l low m a r i n e l imes tones

and th in intervais of clastic s éd imen t s (Fig. 4 ) .

Clastic intervais form the base of the deposi t io­

nal succession a n d were depos i ted du r ing relative

sea-level l o w s t a n d s . D u r i n g t r ansgress ion well

bedded fossiliferous l imestones a n d massive algal

m o u n d s accumula ted . Bedded cher ty l imestones

wi th mar i in te tca la t ions are in te rp re ted to have

been d e p o s i t e d d u r i n g re la t ive sea-level h i g h ­

stands wi th water dep ths of some tens of meters .

Fusul inid-r ich l imes tone beds are présent in dif­

férent s t rat igraphie levels, part icularly at the base

and o n t o p of the clastic intervais. Fusulinids of

thèse beds are cons ide red as p a r a u t o c h t h o n o u s

assemblages, accumula ted du r ing periods of low

646 GEODIVERSITAS • 1998 • 20 (4 )

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Late Carboniferous-Early Permian of Carnic Alps

Lithology Faciès

c o n g l o m e r a t e

c o a r s e - g r a i n e d

s a n d s t o n e

f i n e - g r a i n e d

s a n d s t o n e w i t h

h u m m o c k y c r o s s b e d d i n g

s i l t s t o n e ,

b i o t u r b a t i o n

f o s s i l i f e r o u s

b e d d e d l i m e s t o n e

a n d m a s s i v e a l g a l

m o u n d s

Relative Sea-levei

low high

s i l t s t o n e ,

b i o t u r b a t i o n

fine-grained

s a n d s t o n e w i t h

h u m m o c k y c r o s s b e d d i n g

c o a r s e - g r a i n e d

s a n d s t o n e

s h a l e , p l a n t f o s s i l s

c o n g l o m e r a t e

e r o s i v e b a s e

up

per

sh

ore

face

b

each

LST

up

per

sh

ore

face

b

each

low

er

sho

refa

ce

HS

T

c

shel

(o

pen

r> CD

off

sho

i

t -

low

er

sho

refa

ce

.SI

up

per

sh

ore

face

, b

each

up

per

sh

ore

face

, b

each

LST

FIG. 3. — Idealised "Auernig-Cyclothem" from the upper part of the Auernig Group in the Garnitzenberg-Kronalpe area, Carnic Alps.

séd iment i n p u t (see H o m a n n 1969; Flûgel 1974,

1977; Buggisch et al. 1976; Forke et al. in press).

T h e Gtenz land Forma t ion is a cyclic succession,

p r edominan t ly composed of shallow mar ine clas­

t ic s é d i m e n t s (quar tz - r i ch c o n g l o m e r a t e , s and­

s t o n e a n d s i l t s t o n e ) a n d i n t e t c a l a t e d t h i n

fossiliferous c a r b o n a t e in tervais (Bu t t e r sack &

B o e c k e l m a n n 1 9 8 4 ; B o e c k e l m a n n 1 9 8 5 ) . A

caliche un i t a n d a red shale un i t w i th scattered

angu la r q u a r t z gra ins in t h e u p p e r p a r t of t he

succession indicate subaerial exposure. Fusul inids

were described from rhe th in carbonate inrercala-

t i o n s ( K a h l e r & K a h l e r 1 9 3 7 ; K a h l e r 1 9 8 5 ;

Forke 1995) . P l a n t fossils have been descr ibed

GEODIVERSITAS • 1998 • 20(4) 647

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Krainer K. & Davydov V.

f r o m a t h i n s h a l e i n t e r c a l a t i o n b y F r i t z & Boersma (1984) . T h e U p p e r P s e u d o s c h w a g e r i n a L i m e s t o n e is represenred by a cyclic succession composed p te -dominan t ly of dark-grey, th in bedded fossiliferous l imestones and intercalated th in intervais of silt-a n d sands tones a n d fine-grained, w e l l - r o u n d e d a n d w e l l - s o r t e d q u a r t z r i c h c o n g l o m e r a r e s . Limestones contain a b u n d a n t fossils, particularly calcareous algae ( H o m a n n 1972) , small foramini-fers (Fliigel 1971) , fusulinids, corals, bryozoans , brachiopods , gastropods, pelecypods and echino-d e r m fragments. Microfacies has been described by Fliigel (1968) and Buttersack & Boecke lmann ( 1 9 8 4 ) . Cycles ind ica te repeared sh i f t ing f rom nearshore to offshore e n v i r o n m e n t s in an o p e n m a r i n e shelf- lagoon wi th n o r m a l wate r circula­t ion (Fliigel 1 9 8 1 ) . C o m p a r e d ro t he L P L a n d Grenzland Format ion the l imestones are characte-rized by more diverse biota a n d microfacies rypes (Fliigel 1 9 7 1 , 1 9 8 1 ; Fliigel et al. 1971) .

TROGKOFEL G R O U P

T h e Trogkofel G r o u p is composed of approx ima-rely 4 0 0 m thick, p r e d o m i n a n t l y massive, subor-dinately bedded l imestones (Trogkofel l imesrone, Tressdorf l imes tone and Goggau l imesrone) . T h e l imestones were depos i ted in shallow, restr icted a n d o p e n m a r i n e s h e l f - l a g o o n s w i t h o n l y m i n o r b a t h y m e t r i c a l d i f f é rences . Tubiphytesl Archaeolithoporella bu i ld -ups c o m p o s e d of sedi-m e n t - b i n d i n g organisms like encrus t ing forami-n i f e r s , p h y l l o i d a l g a e , Tubiphytes, Archaeo­lithoporella a n d b r y o z o a n s f o r m e d at t he shelf edge (Fliigel 1980a, b , 1981) . Fliigel & Fliigel-Kahler (1980) described 4 6 species of calcareous a l g a e , t h e f u s u l i n i d f a u n a is r e p r e s e n t e d by 70 species (Kahler & Kahler 1980) .

B I O S T R A T I G R A P H Y

FUSULINIDS

T h e first c o m p r e h e n s i v e p a p e r o n f u s u l i n i d s f rom Lare Pa leozo ic l i m e s t o n e s o f t h e C a r n i c Alps was presenred by Schellwien (1898) . F r o m 1 9 3 2 - 1 9 9 6 F. K a h l e r (till 1 9 8 2 w i t h his wife G. Kahler) intensively s tudied the fusulinid fau-

relative sea-level low high

(shoreface) (offshore)

fine-grained sandstones

mariy limestones with mari intercalations

FIG. 4. — Stratigraphie column of the Lower Pseudoschwagerina Limestone (Rattendorf Group) from the north-western side of the Schulterkofel (type section).

n a s o f t h e B o m b a s o F o r m a t i o n , A u e r n i g , Rar t endor f and Trogkofel Groups . T h e biostrat i -graphic classification a n d subdivision of the Late

648 GEODIVERSITAS • 1998 • 20 (4 )

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Late Carboniferous-Early Petmian of Carnic Alps

Paleozoic séquence of the Ca rn ic Alps is mainly

based on the detailed investigation of fusulinids

by F. Kahler & G. Kahler. The i r data are publ i -

shed in n u m e r o u s papers , summar ies are given in

Kah le r ( 1 9 8 3 , 1 9 8 5 , 1 9 8 6 , 1 9 8 9 ) . A d d i t i o n a l

data concern ing fusulinid s t ra t igraphy have been

con t r ibu ted by Pasini ( 1 9 6 5 , 1990) a n d recently

by F o r k e ( 1 9 9 5 ) , F o r k e et al. ( in p ress ) a n d

Davydov (Davydov & Krainer, in press). W e use

t he sign * in cases of dif férence f rom or ig ina l

au thors taxonomy.

Bombaso Formation and Meledis Formation

T h e oldest fusulinid fauna of the Ca rn ic Alps is

desc r ibed f rom c a r b o n a t e rocks o n t o p of t h e

Bombaso F o r m a t i o n west of Zollnersee, consis-

t ing of Ozawainella angulata, O. kumpani a n d O.

cf. mosquensis, Fusulinella colaniae rasdorica, F.

fluxa, Beedeina* nytvica callosa, Fusulina (s.str.)

fortissima, Quasifusulinoides* mjachkovensis,

Quasifusulinoides* quasifusulinoides a n d Quasi­

fusulinoides juvenatus (Kahler 1983) . Accord ing

to Kah le r ( 1 9 8 3 ) , th is fusu l in id f auna cor res ­

p o n d s to the Fusulinella bocki zone of the Late

Myachkovian of the Russian classification.

C a r b o n a t e f r o m t h e l o w e r m o s t M e l e d i s

F o r m a t i o n o f t h e A u e r n i g G r o u p y i e l d e d a

Fusulinella, Fusulina a n d Quasifusulinoides fauna

n e a r W a i d e g g e r A l m i n d i c a t i n g l o w e r m o s t

K a s i m o v i a n C 3 A , ( K a h l e r 1 9 8 6 ) a n d a

Protriticites-ïdMna. con ta in ing P. pseudomontiparus

S W o f Z o l l n e r s e e p o i n t i n g t o l o w e r m o s t

Kasimovian A, (Kahler 1983) .

R é c e n t i nves t iga t ion y ie lded a smal l fusu l in id

assemblage from conglomérâtes of the Bombaso

F o r m a t i o n n e a r S t r a n i g e r A l p e , c o m p o s e d o f

Quasifusulinoides quasifusulinoides, Q. fallax,

Q. intermedia, Protriticites ovatus, P. cf. ovoides.

T h e compos i t ion of this assemblage is m o s t simi­

l a r t o t h a t f r o m t h e Protriticites ovatus -

Praeobsoletes burkemensis zone in t he s t t a to type

section in the M o s c o w Basin a n d occurs only in

the Peskovskaya Forma t ion of the Myachkovian

H o r i z o n o f t h e M o s c o v i a n ( D a v y d o v 1 9 9 7 ;

Davydov & Krainer, in press). A similar assem­

blage was f o u n d near t he t o p of t he B o m b a s o

F o r m a t i o n w e s t o f Z o l l n e r s e e a n d i n c l u d e s

Fusiella lancetiformis, Beedyina consobrina, B. pes-

kensis, B. pseudocylindrica, Fusulinella rara,

Quasifusulinoides pakhrensis, Q. pulchella,

Protriticites ovatus.

C a r b o n a t e s f rom t h e basai Meled i s F o r m a t i o n

n e a r Z o l l n e r s e e a n d a t C i m a Val d i P u a r t i s

conta in fusulinids of the Protriticites pseudomon­

tiparus z o n e in its l o w e r m o s t pa r t , a n d of t h e

Montiparus paramontiparus zone in t he m i d d l e

po r t ion of this format ion . T h e Protriticites pseu­

domontiparus zone is characterized by Protriticites

globulus, Pr. pseudomontiparus, Pr. sphaericus,

Pr. rotundatus, Pr. ovoides, Pr. lamellosus a n d

Praeobsoletes burkemensis. T h è s e species are cha­

racteristic only in the Protriticites pseudomontipa­

rus - Obsolètes obsoletus z o n e o f t h e R u s s i a n

P l a t f o r m ( K r e v i a k i a n H o r i z o n ) a n d T i m a n -

P e c h o r a r é g i o n , i n t h e U r a l s , D o n e t s B a s i n ,

Cent ra l Asia, Spitsbergen a n d in the Can tab r i an

M o u n t a i n s (see Davydov & Krainer, in press).

T h e Montiparus paramontiparus subzone is cha­

racterized by the occurrence of Praeobsoletes pau-

per, P. burkemensis, Obsolètes timanicus,

O. obsoletus, Montiparus paramontiparus,

M. umbonoplicatus, M. montiparus, M. likharevi,

M. rhombiformis and M. priscus. Montiparus spe­

cies f o u n d in t h e C a r n i c Alps are w e l l - k n o w n

from m i d d l e Kas imov ian s t ra ta o f t he Russ ian

P la t fo rm ( K h a m o v n i c h e s k i a n ) , T i m a n - P e c h o r a

Bas in , t h e Ura l s ( u p p e r p a r t o f t h e O r l o v s k y i

H o r i z o n ) , C e n t r a l As ia , S p i t s b e r g e n a n d t h e

Can tab r i an M o u n t a i n s . In Cen t ra l Asia a n d the

Sou the rn Urals the Montiparus montiparus zone

is d ivided in to two subzones: the M. paramonti­

parus subzone in the lower par t a n d the M. sub-

crassulus s u b z o n e i n t h e u p p e r p a r t . T h e

assemblage recognized in the Ca rn ic Alps corres­

p o n d s to the M. paramontiparus subzone (see dis­

cussion by Davydov & Krainer) .

It should be indica ted tha t the représentatives of

the Praeobsoletes-Obsoletes l ineage in the C a r n i c

Alps appear later. In t he Russian P la t form, the

Ura ls , D o n e t s Basin a n d C e n t r a l Asia Praeob­

soletes first a p p e a r s in t h e u p p e r m o s t M y a c h ­

k o v i a n a n d r a n g e s i n t o t h e l o w e r m o s t Kas i ­

movian . Obsolètes first appears at the base of the

K a s i m o v i a n a n d is m o s t cha rac t e r i s t i c for t h e

E a r l y K a s i m o v i a n ( K r e v i a k i a n ) . O n l y r a r e ly

Obsolètes r a n g e s i n t o t h e m i d d l e K a s i m o v i a n

(Kahmovn ichesk ian ) . In t he C a r n i c Alps , s imi-

l a r l y w i t h t h e C a n t a b r i a n M o u n t a i n s a n d

GEODIVERSITAS • 1998 • 20 (4 ) 649

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Krainer K. & Davydov V.

S p i t s b e r g e n ( V i l l a et al. 1 9 9 2 ; N i l s s o n &

D a v y d o v 1 9 9 3 ) , t h e r e p r é s e n t a t i v e s o f t h e

Praeobsoletes-Obsoletes l i n e a g e a r e r a r e .

Praeobsoletes first appears only in the lowermost

K a s i m o v i a n ( K r e v i a k i a n ) a n d Obsolètes f i rs t

appears in the u p p e r m o s t Kreviakian or only in

the Khamovnichesk ian .

In the very rop of the Meledis Fo rma t ion in rhe

R C section ( R C - 1 2 b a n d R C - 1 3 ) the following

fusulinids we te ident i f ied: Ferganites ferganensis

Miklukha -Mac lay , Rauserites sp. , a n d Rauserites

rossicus (Schellwien) (Fig. 5A-E) . T h e last species

in the Russian Platform a n d the Urals characteri-

se lowermost Gzhel ian or Rechitskyi H o r i z o n of

t h e R u s s i a n P l a t f o r m ( R o s o v s k a y a 1 9 5 8 ;

Makh l ina et al. 1984; Davydov & Popov 1986) .

Ferganites ferganensis in Cent ra l Asia as well as in

S. U r a l s cha rac t e r i s e s also ear ly G z h e l i a n , an

équivalent of Amerevskyi H o r i z o n of the Russian

P l a t f o r m (F ig . 6) ( D a v y d o v & P o p o v 1 9 8 6 ;

P o p o v et al. 1 9 8 9 ) . W e sugges t t h a t t h e very

upper po r t i on of the Meledis Fo rma t ion is early

Gzhel ian in âge (Fig. 6) .

Pizzul Formation, Corona Formation, Auernig

Formation and Carnizza Formation

A c c o r d i n g t o K a h l e t ( 1 9 8 5 ) t h e P i z z u l

Formar ion (Untere kalkreiche Schichrgruppe) is

characterized by the occurrence of the following

fusulinid species: Triticites oryziformis, Rauserites*

noinskyi plicatus; Daixina alpina vetusta,

D. sokensis (s.srr.*), D. naviculaeformis, D. sakma-

rensis a n d Quasifusulina eleganta. Récent studies

of n o n - o r i e n t e d t h i n - s e c t i o n s f rom rhe Pizzul

Fo rma t ion show d o m i n a n c e of a Schagonella and

Daixina fauna. Because in Cent ra l Asia a n d sou­

thern Urals représentatives of the Daixina soken­

sis g r o u p a p p e a r ea r l i e r t h a n i n t h e R u s s i a n

Platform, a n d because of the s t ra t igraphie posi­

t i o n o f t h e P izzu l F o t m a t i o n a b o v e t h e ear ly

Gzhel ian a n d below the O r e n b u r g i a n , we believe

tha t the Pizzul Fo rma t ion has to be an équivalent

of the late Gzhel ian (s.str.).

F r o m a t h i n c a r b o n a t e b e d o f t h e C o r o n a

F o r m a t i o n at Ga rn i t zenbe rg (Mit t lere ka lka rme

S c h i c h t g r u p p e ) K a h l e r ( 1 9 8 3 ) r e p o r t e d

"Pseudofusulina multiseptata". Daixina alpina, D.

ex gr. admirabilis a n d Schagonella spp . also were

r e c e n t l y i d e n t i f i e d b y D a v y d o v . T h e spec ie s

Pseudofusulina multisepta o r i g i n a r e d f rom the

C a r n i c A lps (Sche l lwien 1 8 9 8 ) , b u t for m o r e

t h e n sixty years was used in t he l i t e ra ture as a

Late Permian Parafusulina species, reporred from

m a n y Tethyan régions. Unt i l revision and solving

of rhis t a x o n o m i c a l p r o b l e m s we use i nve r t ed

c o m m a s for this species.

In Darvas and in S. Urals Schagonella in gênerai

d o m i n a t e d in t h e m i d d l e G z h e l i a n . Daixina

admirabilis o r ig ina l ly was d e s c r i b e d f rom t h e

O r e n b u r g i a n of the Urals (Zolotova et al. 1978) ,

b u t a lso was r e p o r t e d f rom t h e la te G z h e l i a n

(s.str.) of Darvas (Davydov 1986) . Fusul in id data

f t o m P i z z u l a n d C o r o n a F o r m a t i o n s d o n o t

cons t ra in a spécifie âge. Based o n the strarigra-

ph ic posir ion of Pizzul and C o r o n a Format ions

above an équivalent of the early Gzhel ian (Upper

Meled is ) a n d be low t h e O r e n b u r g i a n A u e r n i g

F o r m a r i o n , t he âge of b o t h fo rmar ions can be

e s t i m a t e d as late G z h e l i a n (s.str.) (Amerevskyi

a n d P a v l o v o p o s a d s k y i H o r i z o n s o f R u s s i a n

Platform).

T h e A u e r n i g F o r m a r i o n ( O b è r e k a l k r e i c h e

Sch ich tg ruppe) of G a r n i t z e n b e r g a n d Krona lpe

conta ins Boultonia europaea; Triticites schivageri-

niformis, T. perstabilis; Daixina*alpina, D.*com-

munis, D. * alpina fragilis, D. * devexa acallosa;

"Pseudofusulina multiseptata", "P. paraconcinna";

Dutkevitchia dastarensis, D. "kargalensis", D. "ruz-

hencevi"; Quasifusulina tenuissima, Q. compacta,

Q. karawankensis, Q. kaspiensis, Q. phaselus,

Q. pseudoelongata, Q. pseudolonga (Kahler 1983 ,

1985) .

T h e C a r n i z z a F o r m a t i o n ( O b è r e k a l k a r m e

S c h i c h r g r u p p e ) o f G a r n i t z e n b e r g c o n t a i n s

Daixina alpina antiqua = alpina and the subspe-

cies fragilis, a n d Dutkevitchia dastarensis.

A c c o r d i n g t o K a h l e r ( 1 9 8 6 , 1 9 8 9 ) P i z z u l

F o r m a r i o n , C o r o n a F o r m a r i o n , A u e r n i g

F o r m a t i o n a n d C a r n i z z a F o r m a t i o n a r e o f

Gzhel ian âge (Gzhel ian E).

R é c e n t s t ud i e s in t h e s o u t h e r n Ura l s , D o n e t s

Basin a n d in Cent ra l Asia (Darvas and sou the rn

Fe rgana ) s h o w e d t h a t Boultonia europaea a n d

Dutkevitchia dastarensis first appear at the basai

O t e n b u r g i a n Daixina sokensis z o n e ( D a v y d o v

1984 , 1992 ; Popov et al. 1989 ; Davydov et al.

1993) . Dutkevitchia ruzhenzevi a n d Dutkevitchia

kargalensis eve rywhere first a p p e a r on ly in t he

650 GEODIVERSITAS • 1998 • 20 (4 )

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Late Carboniferous-Early Permian of Carnic Alps

FIG. 5. — Stratigraphically significant fusulinids from the Meledis Formation (basai Auernig Group) and Lower Pseudoschwagerina Limestone (Rattendorf Group). k,Rauserites rossicus (Schellwien, 1908), tangential section, RC-13-4. B , Rausehtes sp., oblique section, RC-13-4. C - E , Ferganites aff. ferganensis (Miklukho-Maclay, 1948): C , axial section, RC-12b-9; D , tangential section, RC-12b-12; E, paraxial section, RC-12b-2. F , G , Schellwienia bornemani (Leven ef Scherbovich, 1978): F, axial section of typical spéci­men, SK-157-4; G , axial section of short spécimen, SK-157-2. H , Zigarella panjiensis (Leven ef Scherbovich, 1978), axial section of typical spécimen, SK-157-5. I, Likharevites inglorius (Bensh, 1962), axial section, SK-157-1. J - L , Schellwienia bornemani (Leven ef Scherbovich, 1978): J , axial section of spécimen with small axial fillings, SK-157-12; K, axial section of typical spécimen, SK-157-13; L , axial section of short spécimen, SK-157-9. Scale bar: 0,5 cm.

GEODIVERSITAS • 1998 • 20 (4 ) 651

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Krainer K. & Davydov V.

early Asselian, a n d we believe t h a t their occur­

rence in the O r e n b u r g i a n Auern ig Forma t ion is

misidentif ied. Therefore we place inverted c o m -

m a s w i t h b o t h o f t h è s e s p e c i e s . T h e âge o f

Auern ig and Carnizza Format ions for n o w can be

e s t i m a t e d as O r e n b u r g i a n ( é q u i v a l e n t o f

N o g o n s k i a n of Russian Platform) (Fig. 6) .

Lower Pseudoschwagerina Limestone (Schulterkofel

Formation)

F r o m t h e u p p e r m o s t p a r t o f t h e L o w e r

Pseudoschwager ina L i m e s t o n e near R u d n i g a l m

Kahler (1985) described the following fusulinid

species: Boultonia europaea; Rugosofusulina aria-

nica, R. directa, R. latioralis, R. cf. pandae,

R. praevia egregia, R. stabilis, R. stabilis longa;

Paraschwagerina cf. tinvenkiangi elongata,

Occidentoschwagerina alpina a n d "Eozellia miha-

ranoensis" (= Ultradaixina ex gr. postgallowayi).

F r o m S c h u l t e t k o f e l K a h l e r ( 1 9 8 3 ) l i s t e d

Boultonia europaea; Ruzhenzevites* parasolidus;

Rugosofusulina cf. pandae, R. serrata, R. likana,

R. praevia a n d Rugosochusenella*pseudogregaria.

In a récent paper Kahler & Krainer (1993) des­

c r i b e d a f u s u l i n i d f a u n a c o m p o s e d o f a b o u t

30 species from the upper par t of the LPL of the

Schu l te rkofe l s ec t ion . Species o f Triticites a n d

Rugosofusulina d o m i n a t e , whereas those of rare

"Daixina" {^Schellwienia), Rugosochusenella a n d

Ruzhenzevites occur. T h e Carbon i fe rous /Permian

b o u n d a r y was d r a w n at t he first appea rance of

"Pseudoschwagerina" a n d "Occidentoschwagerina

alpina" {- Ultradaixina) in the uppe r par t of the

s e c t i o n . F t o m o u r p o i n t o f v i ew, s p é c i m e n s

n a m e d as Pseudoschwagerina could no t be ident i -

fied even wi th genus n a m e , because in the tan­

g e n t i a l s e c t i o n s r e p o r t e d , t h e j u v e n a r i u m

s t ruc ture , w h i c h is m o s t i m p o r t a n t for t axono -

my, is n o t présent.

Accord ing to Forke et al. (in press) the lower par t

( d e p o s i t i o n a l S é q u e n c e 1) o f t h e L P L in t h e

Schulterkofel section, characterized by the occur­

r e n c e o f Ruzhenzevites ferganensis a n d

Ruzhenzevites parasolidus w i t h o u t species of the

g e n u s Ultradaixina, is c o r r e l a t e d w i t h t h e

Sokensis z o n e . T h e ove r ly ing p a r t ( u p p e r m o s t

par t of deposi t ional Séquence 1 u p to the t o p of

d e p o s i t i o n a l S é q u e n c e 3) c o r r e s p o n d s t o t h e

Bosbytauensis-Robusta zone . T h e C / P - b o u n d a r y

of Forke et al. lies near the base of the overlying

Grenz land Format ion .

T h e fol lowing species were ident i f ied in récent

s tudies of LPL in t he Schul terkofe l sec t ion: in

t h e v e r y l o w e r p o r t i o n o f L P L ( T S T o f

S é q u e n c e 1) w e f o u n d Daixina sokensis,

Schellwienia oblonga a n d Dutkevitchia bimorpha.

In the H S T of Séquence 1 Ultradaixina postso-

kensis a n d Schellwienia ulukensis a n d w i t h i n

Séquence 2 , Schellwienia ulukensis a n d Zigarella

elegans w e r e i den t i f i ed . M o s t i n t e r e s t i n g d a t a

were retrieved from the t o p of Séquence 3 , where

Schwagerina versabile, Schellwienia bornemani,

Zigarella panjiensis a n d Likharevites inglorius were

identified (Fig. 5 F-L).

To est imate the âge of the LPL Forma t ion we can

indicate the following: in Sou the rn Fergana a n d

Darvas Ruzhenzevites ferganensis first appea ts in

t h e m i d d l e p o r t i o n o f a n é q u i v a l e n t o f t h e

Daixina sokensis zone. (Davydov 1984; Popov et

al. 1 9 8 9 ) . Ruzhenzevites parasolidus is a m o r e

advanced species a n d in Darvas it first appears in

t he very t o p of t h e Daixina sokensis z o n e a n d

r a n g e s h i g h e r . I n S o u t h e r n a n d N o r t h e r n

Fergana this species occurs in t he Schwagerina

robusta-Ultradaixina bosbytauensis z o n e a n d

tanges higher in to the Asselian. Schellwienia ulu­

kensis in Cent ra l Asia as well as in the Sou the rn

Ura l s s e c t i o n o c c u r s o n l y in t h e Schwagerina

robusta-Ultradaixina bosbytauensis z o n e .

Schwagerina versabile in D a t v a s a n d i n t h e

S o u t h e r n Urals appears in t h e very t o p o f t he

Schwagerina robusta-Ultradaixina bosbytauensis

zone, b u t is character is t ic of the early Asselian.

Schellwienia bornemani, Zigarella panjiensis a n d

Likharevites inglorius in C e n t r a l Asia a n d t h e

Sou the rn Urals are k n o w n only from the Asselian

( B e n s h 1 9 6 2 ; L e v e n & S c h e r b o v i c h 1 9 7 8 ;

Davydov 1984; Popov et al. 1989) (see corréla­

t ion char t , Fig. 6) .

Based o n ail this da ta we can suggest the follo­

w i n g . T h e T S T ( t r a n s g r e s s i v e Sys tems t r a c t ;

Fig. 4) of Séquence 1 of LPL can be correlated

wi th the u p p e r m o s t par t of the Daixina sokensis

z o n e . T h e H S T ( h i g h s t a n d Sys tems t r a c t ) o f

Séquence 1 can be correlated wi th the lower por­

t ion of the Schwagerina robusta-Ultradaixina bos­

bytauensis z o n e o r w i t h t h e Ultradaixina

postsokensis z o n e o f t h e S o u t h e r n U r a l s a n d

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Late Carboniferous-Early Permian of Carnic Alps

D a r v a s . M o s r p a r t of S é q u e n c e 2 (excepr t h e H S T ) convent ional ly can be correlated wi th the m i d d l e p o r t i o n o f t h e Schwagerina robusta-Ultradaixina bosbytauensis z o n e o r w i t h t h e Ultradaixina bosbytauensis zone of the S o u t h e t n Urals and Darvas . T h e H S T of Séquence 2 a n d L S T ( l o w s t a n d S y s t e m s t r a c t ) a n d T S T o f Séquence 3 should be correlared wirh the upper por t ion of the Schwagerina robusta-Ultradaixina bosbytauensis zone or wi th rhe Ultradaixina post-gallowayi zone of the Sou the rn Urals a n d Darvas . T h e H S T of Séquence 3 very probably is Early Asselian in âge. T h e lasr conclus ion is based on rhe following: in Darvas , the Sou thern Urals a n d in the D o n e t s Basin the acme-zone ( m a x i m u m of occurrences) fot Ultradaixina is in the upper por­t i o n ( b u t n o t u p p e r m o s t ) o f t he Schwagerina robusta-Ultradaixina bosbytauensis zone . In t he very uppe r p o r t i o n of this zone Ultradaixina is rare a n d pe thaps extinct, and absolutely absent in the Asselian. Similarly in the Schulterkofel sec­t ion the a c m e - z o n e for t he Ultradaixina is the H S T of Séquence 2 and the L S T of Séquence 3 . In the T S T of Séquence 3 Ultradaixina is extre-mely rare a n d absolutely no Ultradaixina is pré­sen t in t h e H S T of S é q u e n c e 3 . Schellwienia bornemani and Zigarella panjiensis originally were described from the midd le Asselian of Darvas . In r h e S o u t h e t n U r a l s t h e y o c c u r in t h e ea r ly -midd le Asselian. Likharevites inglorius in Darvas , N o r t h e r n F e r g a n a , t h e S o u t h e r n U r a l s a n d Predoners Trough was found in the ear ly-middle Asse l ian ( B e n s h 1 9 6 2 ; Leven & S c h e r b o v i c h 1978; Davydov 1990; Davydov et al. 1993) . So, occurrences of Schellwienia bornemani, Zigarella panjiensis a n d Likharevites inglorius s u g g e s t Asselian âge for the H S T of Séquence 3 of the Lower Pseudoschwagerina Limestone .

Grenzland Formation F t o m l imestones of the Grenz land Forma t ion at Rudnigsa t te l Kahler (1985) repor ted the occur­rence of Quasifusulina cf. compacta, Q. eleganta, Q. kaspiensis, "Darvasites contractus", Zigarella

pseudopointeli, Sphaeroschwagerina carniolica, Pseudoschwagerina extensa a n d Sphaeroschwage­rina sphaerica. F r o m the type sec t ion near R a t t e n d o r f e r A l m , Kahler & Kahler (1937) described Pseudoschwa­

gerina aequalis, Ps. extensa a n d Sphaeroschwa­gerina* confinii, f r o m t h e e a s t e r n s i d e o f S c h u l t e r k o f e l , Pseudoschwagerina turbida a n d Sphaeroschwagerina * carniolica. Based o n the o c c u r r e n c e of Pseudoschwagerina aequalis, Sphaeroschwagerina* confinii a n d Sphaeroschwagerina* carniolica K a h l e r ( 1 9 8 6 ) d a t e d t h e G r e n z l a n d F o r m a r i o n as m i d d l e Asselian.

Forke (1995) descr ibed Sphaeroschwagerina glo-merosa f r o m t h e G r e n z l a n d F o r m a t i o n n e a r Rudnigsat te l . M o s t of t h e species of G r e n z l a n d F o r m a t i o n , except Quasifusulina species, are k n o w n from the m i d d l e as w e l l as f r o m t h e l a t e A s s e l i a n . Sphaeroschwagerina glomerosa indicates on ly late Asselian âge. Base on this we can suggest midd le -late Assel ian âge for the G r e n z l a n d F o r m a t i o n (see Fig. 6) .

Upper Pseudoschwagerina Limestone F r o m t h e t y p e s e c t i o n o f t h e U p p e r P s e u d o s c h w a g e r i n a L i m e s t o n e at Z o t t a c h k o p f Kahler described the following fusulinid species: Boultonia willsi, Pseudofusulina regularis, McCloudia* haydeni, Darvasites contractus, Schwagerina "krtowf, Pseudoschwagerina pulchra, Biwaella inopinata a n d Rugosochusenella paragre-garia. Red l imestones at T t o g h ô h e a n d at p o i n t 2 0 1 6 (according to Kahler be longing to the Trogkofel L i m e s r o n e , a f t e r F o r k e t o t h e U p p e r P s e u d o s c h w a g e r i n a L i m e s t o n e ) c o n t a i n a r ich fusul in id fauna. Kahler ( 1 9 8 3 , 1985) r e p o r t e d t h e f o l l o w i n g s p e c i e s : Boultonia willsi, Quasifusulina nimia, Q. pseudoelongata, Q. tenuissima, Q. cf. kaspiensis, " Chusenella cheni", "Ch. chihsiaensis", "Ch. rabatei", Schwagerina* moelleri, Schw.*paraconfusa, Eoparafusulina* " tschernyschewi', Robustoschwagerina geyeri, R. schellwieni, Paraschwagerina inflata longa, Sphaeroschwagerina * carniolica, S. * lata, S. * pul­chra, Zellia heritschi, Z. galatea. A c c o r d i n g to Fo rke ( 1 9 9 5 ) t h e red l imes tones con ta in the following stratigraphically i m p o r t a n t s p e c i e s : Zellia heritschi, Robustoschwagerina schellwieni, R. geyeri, Paraschwagerina inflata, Schwagerina moelleri, Schwagerina cf. verneuili

GEODIVERSITAS • 1998 • 20 (4 ) 653

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Krainer K. & Davydov V.

FIG. 6. — Corrélation chart for the Late Carboniferous and Early Permian.

654 GEODIVERSITAS • 1998 • 20

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Late Carboniferous-Early Permian of Carnic

GEODIVERSITAS • 1998 • 20 (4 )

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Krainer K. & Davydov V.

a n d Pseudofusulinoid.es pusillus. F o r k e ( 1 9 9 5 )

dates rhe U p p e r Pseudoschwager ina Limesrone as

Sakmar i an (Robustoschwagerina geyeri zone a n d

Zellia heritschi zone) .

Trogkofel Group

Af te r K a h l e r & K a h l e r ( 1 9 8 0 ) t h e f u s u l i n i d

fauna of the Trogkofel G r o u p consisrs ma in ly of

species of the gênera Triticites, Darvasites, Pseudo-

fusulinoides, Pseudofusulina, " Praeparafusulina",

Pamirina a n d Minojapanella. T h e y d e s c r i b e d

a b o u t seventy species. S t ra t ig raphica l ly i m p o r ­

tan t index fossils are Schwagerina* moelleri, cha-

r a c t e r i s t i c f o r t h e l o w e r p a r t ( T r o g k o f e l

l imesrone) , "Parafusulina lutuginf typical for the

T r e s s d o r f l i m e s t o n e , a n d t h e Chalaroschwa-

gerina* vulgaris-gtoup t o g e t h e t w i t h Pamirina

darvasica in the Goggau l imestone . True parafu-

sulinids a n d Misellina species are lacking.

Kahler (1986) da ted the Trogkofel l imes tone as

Sakmarian (Tastubian-Ster l i tamakian) due to the

occurrence of Robustoschwagerina schellwieni and

Pseudoschwagerina lata. T h e Tressdorf l imestone,

c o n t a i n i n g "Praeparafusulina lutugini" is classi-

f ied as E a r l y A r t i n s k i a n ( B u r c h e v ) , a n d t h e

G o g g a u l i m e s t o n e , w h i c h c o n t a i n s Chalaro-

schwagerina* vulgaris a n d Pamirina, is da ted as

L a t e A t t i n s k i a n ( I r g i n ) . A c c o r d i n g t o F o r k e

( 1 9 9 5 ) t h e T r o g k o f e l l i m e s t o n e is L a t e

Sakmar ian to Eatly At t insk ian in âge.

I t s h o u l d b e n o t e d , t h a t S a k m a r i a n a n d

Ar t insk ian fusulinids of the Urals can no t occur

in t h e T e t h y a n s e c t i o n , as t h e C a r n i c A l p s ,

because b e g i n n i n g in t he ear ly S a k m a r i a n t h e

Boréal province was comple te ly isolated from the

T e t h y a n p rov inces . N o n e A r t i n s k i a n fusu l in id

species of the Urals are k n o w n from Tethys sédi­

men t s , b u t those listed, we believe, are identified

e r roneous ly . For th i s r eason "Praeparafusulina

lutugini" takes i nve r t ed c o m m a s a n d ind ica tes

taxonomical misidentif icat ion.

W e c a n n o t e s t i m a t e t h e âge o f t h e Trogkofe l

l imesrone based on ly o n fusul inids for now. It

could be Sakmat i an as well as early Ar t insk ian .

B e c a u s e t h e G o g g a u L i m e s t o n e c o n t a i n s

Chalaroschwagerina vulgaris a n d Pamirina darva­

sica, w h i c h in D a r v a s c h a r a c t e r i s e s t h e l a t e

Y a k h t a s h i a n (Ea r ly A r t i n s k i a n ) ( L e v e n et al.

1992) , we can convent ional ly es t imate the âge of

t h e T r e s s d o r f l i m e s t o n e as e a r l y A r t i n s k i a n

(Fig. 6) .

T h e fol lowing p rob l ems for fusul inid biosrrari-

graphy shou ld be addressed immedia te ly :

- p r éc i s e f u s u l i n i d b i o s t r a t i g r a p h y o f P izzu l ,

Corona , Auern ig a n d Carnizza Format ions ;

- complè te charactet ist ic of C / P b o u n d a r y beds

a n d be t t e r cr i ter ia for t he C / P b o u n d a r y pos i ­

t ion;

- âge of Grenz land Format ion ;

- fusulinid biost ra t igraphy a n d succession of the

Trogkofel Limestone;

- r e s tudy of t he Tres sdor f a n d G o g g a u L i m e ­

stones.

CONODONTS

T h e occur rence of c o n o d o n t s in Late Paleozoic

carbonates of the Ca rn ic Alps was first n o t ed by

Fliigel et al. (1971) from the Ra t t endo r f G r o u p

a n d B o e c k e l m a n n ( 1 9 8 3 ) f r o m t h e A u e r n i g

G r o u p (discoveries of individual c o n o d o n r frag­

ments , wh ich have n o s t ra t igtaphic impor tance ) .

Forke (1995) descr ibed a c o n o d o n t fauna from

red l imestones of the U p p e r Pseudoschwager ina

Limesrone. T h e c o n o d o n t fauna is c o m p o s e d of

t h e f o l l o w i n g s p e c i e s : Aethotaxis advena,

Hindeodus minutus, Mesogondolella cf. bisselli,

Diplognathodus expansus?, Sweetognathus inorna-

tus a n d Sweetognathus aff. whitei.

In c e n t r a l a n d w e s t e r n U S A S. inornatus a n d

S. aff. whitei appea r in t he Late W o l f c a m p i a n .

S. inornatus belongs to the Sweetognathus whitei-

Mesogondolella bisselli z o n e . I n t h e U t a l s ,

Sweetognathus inornatus a p p e a r s i n t h e

Ster l i tamakian (Late Sakmarian) a n d ranges in to

the A t t i n s k i a n . Sweetognathus whitei is k n o w n

only in Aktastian (Early Artinskian) (Chernykh &

R e s h e t k o v a 1 9 8 7 ; C h e r n y k h & C h u v a s h o v

1 9 9 3 ) . Sweetognathus whitei in t h e Trogkofe l

G r o u p is represented by incomplè te atypical spé­

c i m e n s ( i den r i f i ed w i t h "af f in i ty" s i g n ) . T h e

appearance of Sweetognathus inornatus and S. aff.

whitei t o g e t h e r w i t h Robustoschwagerina a n d

Zellia, b u t w i t h o u t typical A t t in sk ian fusul inid

faunas (Pamirina, Chalaroschwagerina) in t h e

Carnic Alps, indicates at this t ime Sakmarian âge.

A c c o r d i n g to Forke (1995) the U p p e t P s e u d o ­

s c h w a g e r i n a L i m e s r o n e is o f S a k m a r i a n âge

656 GEODIVERSITAS • 1998 • 20 (4 )

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Late Carboniferotis-Early Permian of Catnic Alps

(based o n the occurrence of Robustoschwagerina

geyeri a n d Zellia heritschî). Forke (1995) in his

p a p e r p r é s e n t s c o r r é l a t i o n c h a r t s o f t h e

R a t t e n d o r f a n d Trogkofel G r o u p w i t h sect ions

f r o m t h e U r a l s , D a r v a s , N - C h i n a , S - C h i n a ,

Japan and USA.

FOSSIL FLORA

Plan t fossils were r e p o r t e d f rom the B o m b a s o

F o r m a t i o n a n d A u e r n i g G r o u p m o r e t h a n

100 years ago. Hôfer seems to be the first w h o

c o l l e c t e d p l a n t fossils in 1 8 6 9 in t h e M o n t e

C o r o n a / K r o n a l p e and Casera Fo r /Ofena lm area.

T h e spéc imens were d e t e r m i n e d a n d descr ibed

by U n g e r ( 1 8 6 9 ) , t h e t a p h o f l o r a list c o n t a i n s

19 taxa.

T h e dé te rmina t ions of Unger (1869) were later

r e v i s e d b y R e i c h a r d t ( 1 9 3 7 ) a n d F r i t z &

Boersma (1982) .

Taphoflora lists from the M o n t e C o r o n a section

( C o r o n a F o r m a t i o n ) have b e e n p u b l i s h e d by

Stache (1874) , Schellwien (1892) , Frech (1894)

and Geyer (1897) .

F r o m t h e local i t ies C a s o n d i Lanza (?Meledis

Format ion) a n d M o n t e Pizzul (type locality for

the Pizzul Fo rma t ion ) p lan t fossils were descri­

b e d by T o m m a s i ( 1 8 8 9 ) , Bozz i ( 1 8 9 0 ) a n d

Vinassa D e Regny & Gor t an i (1905) .

Later, n u m e r o u s n e w locali t ies of p l a n t fossils

w i t h i n t he A u e r n i g G r o u p were d iscovered by

Kahler, Me tz a n d others in the Auernig , Nassfeld

a n d Schul terkofe l areas. T h e p l a n t fossils were

descr ibed by Re i cha rd t ( 1 9 3 3 ) a n d Kie lhauser

(1937) , a first s u m m a r y on the fossil flora of the

Auern ig G r o u p inc lud ing 25 taxa was given by

Reichardt (1937) a n d j o n g m a n s (1938) .

J o n g m a n s ( 1 9 3 8 ) c l a s s i f i ed t h e f lo ra o f t h e

A u e r n i g G r o u p as W e s t p h a l i a n D (= E a r l y

S t e p h a n i a n ) a n d W e s t p h a l i a n E (= L a t e

S tephanian) . H e also po in ted ou t tha t w i th in the

Auernig G r o u p the Schulterkofel flora represents

the youngest flora.

Berger ( i 9 6 0 ) repor ted 30 taxa from n e w locali­

t i e s , m o s t o f t h e m w i t h i n t h e B o m b a s o

F o r m a t i o n a n d l o w e r m o s t p a r t of t he A u e r n i g

G r o u p . H e c l a s s i f i e d t h e foss i l f l o r a as

Westphal ian D . Plant fossils have also been des­

c r i b e d f rom several n e w in t e rva i s w i t h i n t h e

u p p e r m o s t C o r o n a - , A u e r n i g - a n d C a r n i z z a

Format ions . (Kahler et al. 1933 ; Kahler & Prey

1963 ; Fenninger & Schon laub 1972; Francavilla

1974) .

F r i t z & B o e r s m a ( s i n c e 1 9 8 0 ) a n d F r i t z &

Krainer (since 1993) systematically invest igated

the fossil flora of the B o m b a s o F o r m a t i o n a n d

A u e r n i g G r o u p f rom m o r e t h a n 3 0 local i t ies .

P lan t fossils are f o u n d in ail fo rma t ions of the

Auern ig G r o u p , f rom mos t localities t he strat i ­

g r a p h i e p o s i t i o n w i t h i n t he s e c t i o n is exac t ly

k n o w n .

F r o m ai l l o c a l i t i e s 1 0 5 t a x a a r e d e s c r i b e d

( E q u i s e t o p h y t a 2 6 t a x a , L y c o p h y t a 12 t a x a ,

F i l i cophyta , P t e r i d o s p e r m a e a n d P t e r i d o p h y l l a

5 7 t axa , C o r d a i t o s p e r m a e 9 t axa ; C o n i f e r a e

1 t axon , see Fri tz et al. 1 9 9 0 ; F t i tz & Kra iner

1993 , 1994, 1995) .

F r o m the G t e n z l a n d F o r m a t i o n t he occur rence

of p l a n t fossils ( n o d é t e r m i n a t i o n s ) has b e e n

n o t e d by severa l a u t h o r s (Felser et al. 1 9 5 6 ;

Felser & K a h l e r 1 9 6 3 ; K a h l e r & Prey 1 9 6 3 ;

Flùgel 197A). He rzog (1984) discovered a p lan t

fossil bear ing interval and collected a flora which

w a s d e t e r m i n e d a n d d e s c r i b e d b y F r i t z &

Boersma (1984) a n d Fritz et al. ( 1 9 9 0 ) . So far

k n o w n this local i ty is t he on ly o n e w i t h i n t he

R a t t e n d o r f G r o u p a n d thus the younges t fossil

flora of the Late Paleozoic séquence in the Carn ic

Alps.

FLORA OF T H E B O M B A S O F O R M A T I O N

From the Bombaso Format ion 3 localities conta i ­

n ing p lan t fossils are k n o w n (Tomri tsch 1, 2 a n d

6) . T h e lowermost locality (Tomri tsch 6) is cha-

racter ized by t he occu r r ence of Sphenophyllum

oblongifolium, Linopteris neuropteroid.es,

Neuropteris ovata, Neuropteris scheuchzeri a n d

o t h e r s (Fr i tz & K r a i n e r 1 9 9 5 ) . A c c o r d i n g t o

Wagner (1984) N. scheuchzeri is a guideform of

the C a n t a b r i a n {Odontopteris cantabrica zone ) .

T h i s corrélat ion qui te precisely corresponds wi th

fusu l in id d a t a , w h i c h sugges ts for C a n t a b r i a n

U p p e r m o s t Moscovian a n d Early Kasimovian âge

( G i n k e l 1 9 7 1 ; R a u s e r - C h e r n o u s o v a &

Scherbovich 1974) .

FLORA OF T H E AUERNIG G R O U P

From the Auern ig G r o u p p lan t fossils are k n o w n

from m a n y hor izons wi th in ail format ions . T h e

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Krainer K. & Davydov V.

l o w e r m o s t h o r i z o n c o n t a i n i n g p l a n t fossils is f r o m p e r h a p s t h e b a s a i p a r t o f t h e M e l e d i s F o r m a t i o n ( local i t ies T o m r i t s c h 3 , Z o l l n e r s e e a n d S t ran ige r A l m ) . T h e fossil assemblages of rhese localiries are characterized by the a b u n d a n -ce o f Linopteris neuropteroid.es. T h e présence of Sphenophyllum angustifolium, S. oblongifolium, Callipteridium pteridium, Odontopteris brardii a n d Pecopteris species of the g r o u p P. arborescence -P. schlotheimii indicates S tephan ian âge (early to midd le S tephan ian C according to the megaflora zona t ion of W a g n e r 1984) . However , there is a cont rad ic t ion berween fusulinid a n d floral da t ing of the lower Meledis Fo rma t ion . Based on fusuli­n i d s t h e lower M e l e d i s F o r m a t i o n is Ear ly to M i d d l e K a s i m o v i a n in âge a n d s h o u l d cor res ­p o n d a t l eas t w i t h t h e u p p e r p o r t i o n o f t h e C a n t a b r i a n , S t e p h a n i a n A a n d p e r h a p s S t ephan ian B (Wagner & W i n k l e r - P r i n s 1 9 8 5 ; D a v y d o v 1 9 9 0 ) . O n l y rhe u p p e r m o s r Me led i s Formar ion , wh ich conta ins early Gzhel ian fusuli­nids , could cor respond wi th S tephanian C . T h e âge of the Meledis Format ion in the Tomri tsch 3, Zo l lne r see a n d S t ran iger A l m localiries s h o u l d also be dated by fusulinids.

T h e u p p e r m o s t p o r t i o n of the A u e t n i g G t o u p con ta in ing p lan t fossils lies w i th in the u p p e t par t o f t h e C a r n i z z a F o r m a t i o n ( l o c a l i t y S c h u l t e r k o f e l ) . F r o m t h i s l o c a l i t y F r i t z & Boersma ( 1 9 8 1 , 1983) Fritz et al. (1990) descri­bed a flora composed of 30 taxa, characterized by the occurrence of Callipteridium gigas, C. pteri­dium, Odontopteris alpina, O. brardii, Pecopteris feminaeformis a n d i n d e x f o s s i l s f o r L a t e Srephanian âge: Aphlebia elongata, Pseudomario-pteris busquetii a n d Sphenophyllum alatifolium [Sphenophyllum angustifolium zone, Stephanian C according to W a g n e r 1984) .

FLORA OF T H E G R E N Z L A N D F O R M A T I O N

T h e flora of the Grenz land F o r m a t i o n conta ins 16 species inc lud ing Annularia sphenophylloides, A. stellata, Sphenophyllum cf. angustifolium, Callipteris conferta, Odontopteris brardii, Pecopteris feminaeformis and P. schlotheimii. T h e o c c u r r e n c e o f Callipteris conferta a n d Spheno­phyllum cf. angustifolium indicates Early Permian â g e {Callipteris conferta z o n e a c c o r d i n g to W a g n e r 1984) .

Typical guideforms of the Lobatopteris lamuriana z o n e (Bar rue l ian) a n d Alethopteris zeilleri zone ( S t e p h a n i a n B) h a v e n o t b e e n d i s c o v e r e d till now. A c c o r d i n g to t h e p l a n t fossi ls t h e B o m b a s o F o r m a t i o n is o f C a n t a b t i a n âge , t h e A u e r n i g G r o u p conta ins rypical guideforms of Srephanian C , a n d rhe Grenz land Forma t ion is characterized by a flora of Early Permian âge (see Table Ca rn ic Alps, this vo lume) . Based o n D o n e t s Basin data ( D a v y d o v 1990) S t e p h a n i a n A c o r r e s p o n d s to the midd le and perhaps par t of late Kasimovian, S tephanian B cor responds to the late Kasimovian a n d S tephanian C to the mos t parr of Gzhel ian . A u r u n i a n begins from the Schwagerina robusta-Ultradaixina bosbytauensis z o n e o f t h e O r e n b u r g i a n a n d also co t responds to the whole Asselian (Fig. 6) .

T h e flora of rhe B o m b a s o F o r m a t i o n , A u e t n i g G r o u p , a n d Grenz l and Formar ion is well dared by fusul inids . Fluvial séquences of t he Eas t e tn Alps ( S t a n g n o c k F o r m a t i o n , G u t k t a l N a p p e ) , wh ich conta in a similar assemblage of p lan t fos­sils r a n g i n g f fom rhe Odontopteris cantabrica zone ro the Callipteris conferta zone , can be well c o r r e l a t e d w i t h t h e m a r i n e s é q u e n c e o f t h e C a i n i c A l p s ( B o m b a s o F o t m a t i o n - G r e n z l a n d Forma t ion ) .

Acknowledgements K. K. wishes to t h a n k the Austr ian Academy of S c i e n c e s ( C o m m i s s i o n for S t r a r i g r a p h y ) for f inanc ia l s u p p o r t of field w o r k in rhe C a r n i c Alps . B o t h a u t h o t s t h a n k D o r a Gal legos from B o i s e S t a t e U n i v e r s i t y for c o r r e c t i o n o f t h e English. T h e Permian Research Ins t i tu te at Boise State Univers i ty p rov ided s u p p o r t for th in -sec -t ion prépara t ion a n d s tudy of fusulinid biostrat i­g r a p h y . W e a re v e r y g r a t e f u l t o A l a i n I z a r t (Nancy) a n d Danie l Vachard (Lille) for reviewing rhe m a n u s c r i p r a n d m a k i n g helpful c o m m e n t s and suggestions.

R E F E R E N C E S

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Submitted for publication on 1 January 1997; accepted on 15 December 1997.

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