Mortimore, R.N., Wood, C.J. & Gallois, R.W. 2001. British Upper Cretaceous Stratigraphy. Geological Conservation Review Series, No. 23, JNCC, Peterborough. The original source material for these web pages has been made available by the JNCC under the Open Government Licence 3.0. Full details in the JNCC Open Data Policy
Catton Grove Chalk Pit, Norwich, Norfolk
Introduction
Catton Grove Chalk Pit (also known as 'Campling's Pit') is a small quarry surrounded by a housing estate, situated to the east of the Sprowston Road, in the Catton area of Norwich
The Catton Sponge Bed marks the boundary between two of the zones of the northern European Upper Campanian belemnite zonal scheme that now replaces the traditional Belemnitella mucronata Zone. It is a level of major macrofaunal change, which particularly affects the brachiopods, molluscs and echinoids. It marks the entry of certain benthic foraminiferal species that range up to and, in some cases, above the Campanian–Maastrichtian boundary, and is tfius of particular relevance to the interpretation of the microfaunal biostratigraphy of the Chalk successions in the southern North Sea Basin. It reflects a European-wide regressive phase, which elsewhere is expressed either by a hardground or by a change in lithofacies to shallow-water sponge-rich siliceous marls with a high-diversity macrofauna.
Description
The previously exposed section at Catton Grove Chalk Pit has been backfilled, but the Catton Sponge Bed and the overlying basal Beeston Chalk, at the top of the pit, have been deliberately covered by soil and turfed within a semi-circular retaining wall of gabions, in order to preserve it.
Lithostratigraphy
In the 1960s, this pit exposed c. 10 m of the highest part of the Weybourne Chalk Formation, terminating in the Catton Sponge Bed; and overlain by the basal 1.8 m of the Beeston Chalk (Peake and Hancock, 1961, fig. 6). Those workers recorded six flint bands below the Caton Sponge Bed, and one band of huge flints up to 0.45 m thick above it. They noted that an additional 22 ft (6.7 m) of section had previously been visible down to a flint that formed the floor of the pit. When this flint, probably the thick semi-tabular flint T of the stratotype Weybourne Chalk succession (Peake and Hancock, 1961, fig. 5), was broken through, the lower part of the pit rapidly flooded and had to be backfilled. Wood (1988, fig. 7) recognized some additional flints, and published a revised log.
The Caton Sponge Bed was named by Peake and Hancock (1961) to describe the 'hard yellow bed'or 'sponge bed' of the earlier literature that had been recorded in the chalk pits at Caxton, and which Rowe (in manuscript) and Brydone (1938) regarded as marking a level of significant faunal change in the Chalk of Norfolk. Peake and Hancock's Canon Sponge Bed comprises two closely spaced beds of iron-stained, indurated chalk capped by hardgrounds (cf. Wood, 1988, p. 62, fig. 7), rather than the single hardground recorded by them. The two hardgrounds were designated hardgrounds I and II by Wood (1988, fig. 7), the higher (the Catton Sponge Bed proper of previous workers) being taken as the boundary between his topmost (Weybourne3) subdivision of the Weybourne Chalk and the succeeding Beeston Chalk. Hardground I is patchily and relatively poorly indurated, but is capped by a well-defined, planar erosion surface. The Canon Sponge Bed (Hardground II) contains a rich assemblage of hexactinellid sponges, in limonitic preservation, together with moulds of originally aragonite-shelled bivalves and gastropods reminiscent of the reussianum fauna from the Hitch Wood Hardground of the Upper Turonian Chalk Rock. It is locally strongly indurated, and also terminates in a clearly defined erosion surface. This is overlain by soft glauconitized chalk pebbles and a concentration of large, reworked belemnites, which forms an excellent example of a so-called 'belemnite battlefield'. The Sponge Bed is penetrated by an extensive Thalassinoides burrow system, which in places contains belemnites 'piped down' from the overlying concentration. The huge flint A of the Peake and Hancock notation in the basal part of the Beeston Chalk is a section through a giant ring flint; it is underlain by chalk containing large pieces of shell of inoceramid bivalves, and is followed by weakly indurated chalk without an obvious erosion surface, which was designated by Wood (1988) as Hardground III.
Biostratigraphy
The section falls within the traditional Belemnitella mucronata macrofossil Zone, which covers the entire Upper Campanian Substage (
Records of ammonites (Nostoceras (Bostrychoceras) polyplocum (Roemer), Baculites sp. and Menuites portlocki (Sharpe)) can safely be inferred to have come from the Sponge Bed. However, other ammonites from the 'Norwich Chalk' in museum collections, particularly those preserved as glauconitized composite moulds, probably came from less well indurated ammonite-bearing horizons in the Beeston and Paramoudra Chalk. The non-ammonite molluscan fauna is largely undescribed, but includes species of the gastropod genera Periaulax and Planolateralus. The rich hexactinellid sponge fauna (details in Reid, 1968) is dominated by Leptophragma striatopunctata (Schrammen) with, in addition to another five species, Aphrocallistes cylindrodactylus Schrammen and Lepidospongia rugosa Schlüter. The latter two species also occur in the coeval strata in Northern Ireland.
There is a major macrofaunal change at the Sponge Bed, which especially affects the brachiopods, bivalves and echinoids. This was first noted by Rowe (in manuscript) and independently confirmed by Brydone (1922, 1938) (see review by Wood, 1988, pp. 19–39). Both workers compared this faunal change in the inland sections with the difference in faunal content between the (Weybourne) and (Beeston) Chalk successions to the west and east of Sheringham respectively. The rhynchonellid brachiopod Cretirhynchia woodwardi Pettitt, characteristic of the Weybourne Chalk, disappears abruptly at the top of the Sponge Bed, while the terebratulid Carneithyris carnea (J. Sowerby) and the rhynchonellids Cretirhynchia arcuata Pettitt and C. norvicensis Pettitt, all of which occur sporadically in the Weybourne Chalk, become abundant and represented by large-sized individuals in the Beeston Chalk. The large limacean bivalve Plagiostoma marrotianum (d'Orbigny) and the pectinacean Mimachlamys mantelliana (d'Orbigny) are apparently restricted to the pre-Sponge Bed succession. There is a striking change in the echinoids across the Weybourne Chalk–Beeston Chalk boundary, from an assemblage characterized by Cardiotaxis heberti Cotteau, Micraster glyphus Schltiter and M. stolleyi Lambert (the 'Epiaster' of both Rowe and Brydone) to one characterized by Cardiaster cordiformis (S. Woodward) ('Cardiaster ananchytis') and Galerites roemeri (Desor), with only extremely rare Micraster.
There is an important change in the microfauna (ostracods and foraminifera) across the same boundary. Two very long-ranging species of the ostracod genus Cytherelloidea cut out a short distance above the Sponge Bed, with other taxa entering at this level and continuing into the Maastrichtian strata (I. Slipper, pers. comm., 1998). Swiecicki (1980) recorded the extinction of some long-ranging benthic foraminiferal taxa, notably Globorotalites micheliana (d'Orbigny) at the Sponge Bed, and noted the abrupt entry of Bolivina incrassata Reuss, Eponides beisseli Schijfsma, Globorotalites hiltermanni Kaever, Neoflabellina praereticulata Hiltermann and Reussella szajnochae szajnochae (Grzybowski). These are species that range up to and, in some cases, above the Campanian–Maastrichtian boundary. There is also a significant drop in the planktonic foraminiferal content, in both numbers and diversity, at this level. The turnover in the benthic foraminifera constitutes a significant bio-event, potentially applicable to the interpretation of offshore wells, near the top of the UKB18 or Bolivinoides decoratus Interval Zone (cf. Hart et al., 1989, p. 314, figs 7.16, 7.25). This higher part of the UKB18 Zone, given a separate subzonal status (B3iv) by Swiecicki (1980) (
Interpretation
South of Norwich, Hardground I and the Canon Sponge Bed were revealed in a trench in the now degraded Halfway House Chalk Pit
The Catton hardgrounds were formerly also seen in intermittent foreshore exposures at Sheringham, where the old Lifeboat House
Hardground I and the Catton Sponge Bed correlate with the North Antrim Hardgrounds of Northern Ireland, which comprise two closely spaced hardgrounds, the lower one weakly, and the higher strongly, hardened and glauconitized. The higher hardground is similarly succeeded by chalks with fragmented inoceramid shell and giant ring flints (Fletcher, 1977; Fletcher and Wood, 1978). Towards the depositional margins and over structural highs, the North Antrim Hardgrounds become even more indurated and more strongly mineralized. The Catton Sponge Bed and the North Antrim Hardgrounds reflect the polyplocum' regression in northern Germany (Niebuhr, 1995; Niebuhr et al., 1997), where it is marked by evidence of significant shallowing, including a high-diversity macrofauna with many baculitid ammonites, and the development of siliceous spongiferous marls (opoka facies), following marl-chalk rhythmites. This inter-regional regressive event, which can now be identified by correlative hardgrounds in Belgium and the Netherlands (Christensen, 1999) is interpreted as a sea-level lowstand, associated with a sequence boundary (Niebuhr et al., 1997).
Conclusions
Catton Grove Chalk Pit is the type section and only remaining exposure of the Catton Sponge Bed, the other exposure on the foreshore at Sheringham having been permanently covered by the construction of a slipway. It forms the boundary between two of the belemnite zones of the standard northern European belemnite zonal scheme (