GEUS Bulletin no 5.pmd
GEUS Bulletin no 5.pmd GEUS Bulletin no 5.pmd
Gp Vardekløft 44 Olympen Fossilbjerget Pelion 100 50 Section 43 3 km Section 42 Fm m Bed m Bed 33 31 29 27 24 22 20 18 14 9 7 5 J34–35 1 0 0 J31? J30 J29 J27 J24–6 J22 J21 Ammonites Pectinid bivalves Terebratulid brachiopods Other bivalves Belemnoteuthid cephalopods Thalassinoides burrows J18 25 m 20 15 10 5 26 24 22 20 18 17 15 13 11 3 2 1 9 8 7 6 5 J30 faunal horizons J29 J28 J27 J26 J25 J24 J22 J21 J20 J19b J19a J18 Apertum Nordenskjoeldi Lower Callovian Calyx Ishmae Cranocephal. Variabile Upper Bathonian Fig. 2. Diagrammatic sections in weathering profile through the Fossilbjerget Formation at its type locality on the southern slopes of Fossilbjerget, central Jameson Land; section 43 is located 3 km west of section 42. Note that the beds in the two sections are numbered independently – discussion of bed numbers in the text refers to those in Section 43. Lithostratigraphy at left, standard chronostratigraphy – substages and zones – at right. Diagonal hatching: glauconitic. Numbers J18–J35: the ammonite faunal horizons recognized in Jameson Land (see Callomon 1993). The horizon of Kepplerites tenuifasciculatus is J27. Cranocephal., Cranocephaloide. GEUS Bulletin no 5.pmd 44 29-10-2004, 11:14
Table 1. Measurement of dimensions Holotype Paratype III Maximum diameter 137 mm 140 mm Septate to c. 100 mm c. 90 mm Length of bodychamber, whorl 0.70 0.75 Fractional umbilical width 0.23 0.22 at last septum Fractional umbilical width c. 0.34 c. 0.33 at aperture Primary ribs per whorl – at diameter 125–130 mm 51 57 – at diameter 85–95 mm 40 46 Ratio of secondaries:primaries 3.8 3.4 around last septum Kepplerites (tenuifasciculatus) with only occasional crushed, indeterminate Cadoceras. Description. All the available material consists of crushed internal moulds and measurements of dimensions (Table 1) are of limited value. The figured specimens are typical; both are complete adult macroconchs with strongly uncoiling seams on the last whorl. The microconchs remain unknown. The ribbing is characteristically dense and fine, the primaries rising retroradially on the umbilical wall, then swinging in a strongly forwards-directed curve on the umbilical shoulder into accentuated prorsiradiate ribbing on the whorlside, dividing into fasciculate sheaves (tenuifasciculate) of secondaries at about a third flank-height, rising uncurved to the venter, persisting with little or no loss of strength to the simple, somewhat sinuous peristome. There is no evidence of the lateral accentuation of the primaries into tubercles seen in other species of Kepplerites, especially in the younger ones and subsequently in the descendant, Kosmoceras. Inner whorls are not seen, so whether the earliest stages already have tabulate venters is not known. Comparisons. The evolution of major morphological characters in the genus Kepplerites, leading to Kosmoceras in the Middle Callovian, was very gradual. Differentiation of successive transients relies on relatively minor variations of size and ribbing, often perceptible only by the trained eye in assemblages of more than a single specimen in which the range of intraspecific variability can be assessed. Changes were not GEUS Bulletin no 5.pmd 45 29-10-2004, 11:14 continuously orthogenetic: characters could ‘progress’ and ‘regress’ with time largely independently, leading to frequent partial homoeomorphies. In descending order: 1. Kepplerites traillensis Donovan 1953 (plate 17, figs 1a, b, holotype; plate 18, figs 1a, b), faunal horizons 24–26, is similar in size, coiling and style of ribbing but significantly less densely ribbed, with only c. 31 primaries per whorl (before the onset of the modifications on the final stage of the adult bodychamber found in all the Kosmoceratidae). The type material came from mount Morris Bjerg on Traill Ø, about 5 km north-east of the coast of Kong Oscar Fjord to the south-west. It was found in isolation, both stratigraphically and faunistically, so the position of its faunal horizon in the general succession has to be deduced by correlation with the more continuous successions in Jameson Land. The closest resemblance is to the forms found also on the southern slopes of Fossilbjerget, sections 42 and 43, horizons 24–26, as minor components in faunas dominated by Cadoceras apertum (Callomon & Birkelund 1985). K. traillensis is also, among all the known faunas of Greenland, the one closest to the type-species K. keppleri (Oppel): cf. Buckman (1922, plate 289A, B, lectotype, evolute inflated variant with slightly tabulate venter); Quenstedt (1886, plate 77, figs 1–5, S. Germany); Page (1989, fig. 5.1a, b, England). The resemblance is close but may not be exact, so that both specific names are retained for the time being. It indicates, however, a close time correlation and provides the basis for the assignment of the Apertum Zone already to the Lower Callovian. 2. Kepplerites vardekloeftensis Callomon 1993 (p. 102), faunal horizon 23. The holotype (Spath 1932, plate 25, figs 2a, b, complete adult) and paratype (Spath 1932, plate 25, figs 1a, b, complete adult phragmocone) came from the calyx limestone, a prominent concretionary marker-bed in the Fossilbjerget Formation along the length of the outcrops above Neill Klinter, the line of cliffs on the west side of Hurry Inlet and traceable inland as far as Katedralen on Ugleelv (Fig. 1); level 560 m in sections of Rosenkrantz reproduced by Spath (1932, p. 126, fig. 10). The species resembles K. tenuifasciculatus in coiling, size and density of primary ribbing but the secondary ribbing is coarser and fades on the 45
- Page 1 and 2: GEOLOGICAL SURVEY OF DENMARK AND GR
- Page 3 and 4: GEUS Bulletin no 5.pmd 3 29-10-2004
- Page 5 and 6: Contents Preface . . . . . . . . .
- Page 7 and 8: (Alsen & Surlyk 2004, this volume).
- Page 9 and 10: Jurassic syn-rift sedimentation on
- Page 11 and 12: NW SE m 1000 500 0 NW SE m 1000 500
- Page 13 and 14: GEUS Bulletin no 5.pmd 13 29-10-200
- Page 15 and 16: grained than the lower parasequence
- Page 17 and 18: the Pelion Formation. The mudstone-
- Page 19 and 20: The fluviatile Bristol Elv Formatio
- Page 21 and 22: Name. After the river Bristol Elv i
- Page 23 and 24: edded, and display both sheet-like
- Page 25 and 26: N S Fig. 5. Coarse-grained sandston
- Page 27 and 28: Fig. 7. Lacustrine deposits from th
- Page 29 and 30: deposition of peat and coal. Journa
- Page 31 and 32: Maximum Middle Jurassic transgressi
- Page 33 and 34: 834 N Lycett Bjerg Barrikade Gletsc
- Page 35 and 36: SW NE Lycett Bjerg Parnas Member Be
- Page 37 and 38: Cadoceras cf. nordenskjoeldi Callom
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- Page 41 and 42: 4 C B 1 2 GEUS Bulletin no 5.pmd 41
- Page 43: Fig. 1. Sketch-map of the Jameson L
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- Page 49 and 50: 1 2 GEUS Bulletin no 5.pmd 49 29-10
- Page 51 and 52: A new Middle-Upper Jurassic success
- Page 53 and 54: 74º00'N ■■ ■■ ■■ 73º5
- Page 55 and 56: System Ma 159.4 154.1 164.4 169.2 1
- Page 57 and 58: Sedimentary structures Biota Struct
- Page 59 and 60: wards units is biogenic carbonate d
- Page 61 and 62: Fig. 7. Log panel giving a broadly
- Page 63 and 64: SPM LU to medium-grained and consis
- Page 65 and 66: and mudstone drapes reflects varyin
- Page 67 and 68: with the presence of a minor angula
- Page 69 and 70: the north-east and south-west, resp
- Page 71 and 72: elly mass-flow deposits. In: Koster
- Page 73 and 74: Jurassic dinoflagellate cyst strati
- Page 75 and 76: 74°00'N ■■ ■■ ■■ 73°5
- Page 77 and 78: Bernbjerg Formation Payer Dal Forma
- Page 79 and 80: Depositional environment. The prese
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- Page 85 and 86: Metres 30 20 10 Hold with Hope, Loc
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- Page 89 and 90: Jurassic dinoflagellate cysts from
- Page 91 and 92: Fig. 2. Sedimentological log of the
- Page 93 and 94: LITHOSTRATIGRAPHY BIOSTRATIGRAPHY F
Table 1. Measurement of dimensions<br />
Holotype Paratype III<br />
Maximum diameter 137 mm 140 mm<br />
Septate to c. 100 mm c. 90 mm<br />
Length of bodychamber, whorl 0.70 0.75<br />
Fractional umbilical width 0.23 0.22<br />
at last septum<br />
Fractional umbilical width c. 0.34 c. 0.33<br />
at aperture<br />
Primary ribs per whorl<br />
– at diameter 125–130 mm 51 57<br />
– at diameter 85–95 mm 40 46<br />
Ratio of secondaries:primaries 3.8 3.4<br />
around last septum<br />
Kepplerites (tenuifasciculatus) with only occasional<br />
crushed, indeterminate Cadoceras.<br />
Description. All the available material consists of<br />
crushed internal moulds and measurements of dimensions<br />
(Table 1) are of limited value. The figured specimens<br />
are typical; both are complete adult macroconchs<br />
with strongly uncoiling seams on the last whorl. The<br />
microconchs remain unk<strong>no</strong>wn. The ribbing is characteristically<br />
dense and fine, the primaries rising retroradially<br />
on the umbilical wall, then swinging in a<br />
strongly forwards-directed curve on the umbilical shoulder<br />
into accentuated prorsiradiate ribbing on the<br />
whorlside, dividing into fasciculate sheaves (tenuifasciculate)<br />
of secondaries at about a third flank-height,<br />
rising uncurved to the venter, persisting with little or<br />
<strong>no</strong> loss of strength to the simple, somewhat sinuous<br />
peristome. There is <strong>no</strong> evidence of the lateral accentuation<br />
of the primaries into tubercles seen in other<br />
species of Kepplerites, especially in the younger ones<br />
and subsequently in the descendant, Kosmoceras. Inner<br />
whorls are <strong>no</strong>t seen, so whether the earliest stages<br />
already have tabulate venters is <strong>no</strong>t k<strong>no</strong>wn.<br />
Comparisons. The evolution of major morphological<br />
characters in the genus Kepplerites, leading to Kosmoceras<br />
in the Middle Callovian, was very gradual.<br />
Differentiation of successive transients relies on relatively<br />
mi<strong>no</strong>r variations of size and ribbing, often perceptible<br />
only by the trained eye in assemblages of more<br />
than a single specimen in which the range of intraspecific<br />
variability can be assessed. Changes were <strong>no</strong>t<br />
<strong>GEUS</strong> <strong>Bulletin</strong> <strong>no</strong> <strong>5.pmd</strong> 45<br />
29-10-2004, 11:14<br />
continuously orthogenetic: characters could ‘progress’<br />
and ‘regress’ with time largely independently, leading<br />
to frequent partial homoeomorphies.<br />
In descending order:<br />
1. Kepplerites traillensis Do<strong>no</strong>van 1953 (plate 17, figs<br />
1a, b, holotype; plate 18, figs 1a, b), faunal horizons<br />
24–26, is similar in size, coiling and style of<br />
ribbing but significantly less densely ribbed, with<br />
only c. 31 primaries per whorl (before the onset of<br />
the modifications on the final stage of the adult<br />
bodychamber found in all the Kosmoceratidae). The<br />
type material came from mount Morris Bjerg on<br />
Traill Ø, about 5 km <strong>no</strong>rth-east of the coast of Kong<br />
Oscar Fjord to the south-west. It was found in isolation,<br />
both stratigraphically and faunistically, so the<br />
position of its faunal horizon in the general succession<br />
has to be deduced by correlation with the more<br />
continuous successions in Jameson Land. The closest<br />
resemblance is to the forms found also on the<br />
southern slopes of Fossilbjerget, sections 42 and<br />
43, horizons 24–26, as mi<strong>no</strong>r components in faunas<br />
dominated by Cadoceras apertum (Callomon<br />
& Birkelund 1985).<br />
K. traillensis is also, among all the k<strong>no</strong>wn faunas<br />
of Greenland, the one closest to the type-species<br />
K. keppleri (Oppel): cf. Buckman (1922, plate<br />
289A, B, lectotype, evolute inflated variant with<br />
slightly tabulate venter); Quenstedt (1886, plate 77,<br />
figs 1–5, S. Germany); Page (1989, fig. 5.1a, b, England).<br />
The resemblance is close but may <strong>no</strong>t be<br />
exact, so that both specific names are retained for<br />
the time being. It indicates, however, a close time<br />
correlation and provides the basis for the assignment<br />
of the Apertum Zone already to the Lower<br />
Callovian.<br />
2. Kepplerites vardekloeftensis Callomon 1993 (p. 102),<br />
faunal horizon 23. The holotype (Spath 1932, plate<br />
25, figs 2a, b, complete adult) and paratype (Spath<br />
1932, plate 25, figs 1a, b, complete adult phragmocone)<br />
came from the calyx limestone, a prominent<br />
concretionary marker-bed in the Fossilbjerget Formation<br />
along the length of the outcrops above Neill<br />
Klinter, the line of cliffs on the west side of Hurry<br />
Inlet and traceable inland as far as Katedralen on<br />
Ugleelv (Fig. 1); level 560 m in sections of Rosenkrantz<br />
reproduced by Spath (1932, p. 126, fig. 10).<br />
The species resembles K. tenuifasciculatus in coiling,<br />
size and density of primary ribbing but the<br />
secondary ribbing is coarser and fades on the<br />
45