Cleal, C.J., Thomas, B.A., Batten, D.J. & Collinson, M.E. 2001. Mesozoic and Tertiary Palaeobotany of Great Britain. Geological Conservation Review Series No. 22, JNCC, Peterborough, ISBN 1 86107 489 1. 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

Scalby Ness

[TA 037 911]

Introduction

The plant beds of the Scalby Formation contain an important flora, well known for its outstanding examples of ginkgoalean remains. The most significant is Ginkgo buttonii, here at its type locality. It is a good example of a 'living fossil', being closely similar to the only extant species, Ginkgo biloba, the maidenhair tree. The Scalby Ness site is also the type locality for six other species of plant fossils.

Fossil plants have been collected, studied and described from this locality from the earliest days of investigations on the Yorkshire Jurassic flora. W.C. Williamson collected specimens of Ginkgo from here and these were illustrated in Lindley and Hutton's Fossil Flora of Great Britain (1831–1837). Subsequent studies have been carried out by Phillips (1875), Black (1929), Harris (1946b, 1948, 1961a, 1964, 1969, 1979a; Harris et al., 1974) and Morgans (1999).

Description

Stratigraphy

The Scalby plant beds are part of the Scalby Formation (Bathonian), which overlies the thick marine Scarborough Formation (Figure 3.50). The exact age of the Scalby Formation has been debated for many years although Hogg (1993) recently dated it as late Bathonian, discus Zone on the basis of a sparse dinoflagellate cyst assemblage. It is fluvio-deltaic in origin although the actual type of depositional environment has been the subject of much discussion and disagreement. The lower division, the Moor Grit Member, consists of foreset deposits of a pro-grading delta front, channel fills of a braided river system and a deltaic distributary system. The upper division, the Long Nab Member, comprises delta-top deposits, a meander belt complex crossing an alluvial plain, and a saline-influenced delta plain system with smaller sinuous channels, some of which may have been tidal (Nami and Leeder, 1978; Leeder and Nami, 1979).

The plant fossils are found just above the base of the Long Nab Member at a number of places in the immediate vicinity of Scalby Ness where the gentle seaward dip brings these silty shales to the base of the cliff (Table 3.7). They constitute the Scalby Plant Bed. Nearby at Scalby Wyke the plant bed is a few metres from the base of the Long Nab Member and exposed on the shore under flat sandstone reefs. It is full of waterworn fragments suggesting that it is a drifted plant bed in a channel inflll. In contrast, the Plant Bed at Scalby Ness is full of plants at various levels in what is interpreted as a river channel. The fragmentary nature of the plant remains and the fact that they are spread along the bedding planes indicate that they have drifted (Black, 1929). However, the fact that most of the fossils are well preserved indicates that they were not carried very far before becoming trapped in the river sediments.

Palaeobotany

Fifteen species are known from Scalby Ness

(Table 3.7) The locations of the plant beds identified by T.M. Harris (in manuscript) at Scalby Ness.

[GR added 2023]
Scalby Ness Plant Bed 54°18'14" 0°24'18" [TA 03885 90982]
Scalby Ness Ginkgo Bed in beach 54°18'20" 0°24'17" [TA 03899 91168]
Scalby Ness Brown Ginkgo Bed 54°18'21" 0°24'30" [TA 03663 91194]
Scalby Wyke Black's Bed E 54°19'2" 0°24'50" [TA 03273 92453]
Scalby Wyke Drifted Bed 54°19'0" 0°25'0" [TA 03094 92387]
Scalby Wyke Black's Bed G 54°18'57" 0°25'0" [TA 03096 92294]
Scalby Wyke Otozamites Bed 54°18'21" 0°24'36" [TA 03555 91191]
Scalby Beck, sand above black clay 54°18'13" 0°24'36" [TA 03561 90944]
Scalby Beck, black clay
Scalbv Beck sandy laver 54°18'14" 0°24'35" [TA 03578 90975]

(Table 3.1); (Figure 3.51), (Figure 3.52), (Figure 3.53), (Figure 3.54). Although this is poor in comparison to the floras from the Cloughton Formation, it is particularly interesting and important because of the abundance of ginkgoalean remains. There are well-preserved leaves with cuticles of Ginkgo and Baiera, together with cuticle fragments of Pseudotorellia. Ginkgo huttonii (here in its type locality; (Figure 3.51)) has a fairly thick cuticle with well-developed papillae surrounding the stomata, which together suggest a xerophytic habitat for the plants. There are also the very occasional seeds, bud scales and male cones, which have been attributed to G. huttonii.

Other species that are relatively common are Coniopteris bella (Figure 3.52), Zamia gigas, Otozamites graphicus and Czekanowskia blackii (here at its type locality; (Figure 3.53)). There are also the interesting conifers Cyparissidium blackii (foliage), Pityanthus scalbiensis (male cone) and Scarburgia hillii (female cone), this being the type locality for the last two.

Morgans (1999) has recently described charcoalified fragments of conifer wood from meandering channel sandstones comprising the overlying Long Nab Member as Cedroxylon spp. and Cupressinoxylon spp..

Interpretation

This is one of the classic sites for Mesozoic ginkgophytes. The well-preserved leaves here, referred to G. huttonii, bear a striking similarity to those of the living G. biloba. More significant, however, are the closely associated seeds and pollen organs that compare well with those of the living tree. Not all fossil ginkgoaleans are quite so similar to the modern form (Hori et al., 1997). It is clear that there was a considerable diversity in this group in the Mesozoic Era. Nevertheless, the fossils from the Scalby Ness Ginkgo Bed strongly support the idea of Ginkgo biloba being a 'living fossil'.

Harris (1979a) took Cyparissidium blackii, Pityanthus scalbiensis and Scarburgia hillii to be parts of one plant species, which he assigned to the extant Southern Hemisphere family Podocarpaceae. This suggests a cosmopolitan history for the family, as also inferred from the widespread distribution of podocarp-like pollen grains in Mesozoic and Tertiary deposits of the Northern Hemisphere, particularly in Russia. The cone is much larger and more developed than those of living podocarps, which suggests that the modern cones, which often comprise just one or two cone scales, are probably reduced.

The presence of well-preserved plant organs shows that they were not carried far, if at all, before becoming trapped in the sediment. Consistent with this interpretation are the associations of Ginkgo leaves with what are probably the seeds and pollen organs of the plant, and the conifer Cyparrisidium blackii with its male fructification Pityanthus scalbiensis and its female cone Scarburgia hillii. These characters of the assemblage are consistent with the idea that a delta marsh flora is represented, as suggested by Hemingway (1974). In contrast, the water-worn fragments that dominate the nearby Scalby Wyke plant bed suggest that it is a bed of drifted plants that settled with fine clastic sediments in an abandoned channel.

Conclusions

The main significance of the plant bed lies in the abundance of ginkgoalean remains. It is the type locality for Ginkgo huttonii and the seeds, scales and male cones referable to this species. Although some 170 Ma old, these fossils are very similar to the living maidenhair tree, Ginkgo biloba. Much has also been learned about the evolutionary history of the Podocarpaceae from the shoots and cones collected here.

References