Changes in Holocene (Flandrian) relative sea levels and coastal geomorphology in the lower Cree valley and estuary, SW Scotland, are inferred from detailed morphological and stratigraphical investigations. A graph of relative sea level changes is proposed for the area. Rising relative sea levels during the early Holocene were interrupted at c. 8300–8600 14C years B.P.(c. 9400–9900 calibrated years B.P.), when an extensive estuarine surface was reached at c. −1 m O.D., after which a fluctuating rise culminated at c. 6100–6500 14C B.P. (c. 7000–7500 calibrated years B.P.) in a prominent shoreline and associated estuarine surface measured at 7·7–10·3 m O.D. A subsequent fall in relative sea level was followed by a rise to a shoreline at 7·8–10·1 m O.D., exceeding or reoccupying the earlier shoreline over much of the area after c. 5000 14C B.P. (c. 5,800 calibrated years B.P.), before relative sea level fell to a later shoreline, reached after c. 2900 14C B.P. (c. 3100 calibrated years B.P.) at 5·5–8·0 m O.D., following which relative sea levels fell, ultimately reaching present levels. During these changes, a particular feature of the coastline was the development of a number of barrier systems. The relative sea level changes identified are compared with changes elsewhere in SW Scotland and their wider context is briefly considered.

The Eocene sparid fauna (Teleostei: Percoidei) from Monte Bolca, Italy and from the London Clay, U.K. is revised based on re-examination of the type material and phylogenetic analyses of primarily osteological data. Two phylogenetic analyses, one of the Eocene taxa and a combined analysis of fossil and extant taxa, were performed. The addition of fossils to the extant data greatly increased numbers of most parsimonious trees, destabilising and obscuring basal relationships within the Sparidae. Combination of the data from fossil and extant data also affected relationships among the fossil taxa, changing some from those recovered using fossil data alone and destabilising others. Successive approximations character weighting supported the inclusion of the Eocene taxa within a monophyletic Sparidae. The genus Sparnodus, as previously conceived, is paraphyletic and is partitioned to remove the paraphyly. Five monotypic genera are recognised, including three new genera, Abromasta, Ellaserrata and Pseudosparnodus. Inclusion of the fossils in the phylogenetic analysis implies a minimum age of origin for the Sparidae of 55 Ma with most Recent sparid fauna in place no later than the Miocene, and provides further evidence that the diversification of feeding strategies occurred early on in the evolutionary history of the group.

A new crustacean, Castracollis wilsonae is described from a loose block of the Early Devonian Rhynie chert, found in the vicinity of Rhynie, Aberdeenshire, Scotland. It differs markedly from Lepidocaris rhyniensis, Scourfield 1926, the only other crustacean found in the Rhynie chert.

The material comprises complete individuals up to 8 mm long and fragmentary remains. The head is normally damaged and detached from the body, and damage to the anterior of the trunk suggests the specimens are exuviae. The head appears domed with a labrum, robust mandibles, and long biramous antennae. A few specimens exhibit a probable detached cephalo-thoracicshield. The trunk is multi-segmented, comprising similar ring-like somites. The thorax variably comprises up to 26 segments. The anterior 11 segments possess similar long, phyllopodous appendages, the remainder variably possess 10 to 15 phyllopodous appendages with a disposition of one per somite. The abdomen comprises up to 28 apodous segments. The posterior of the body comprises a telson with two furcal rami.

The crustacean is most probably a calmanostracan branchiopod. It occurs associated with Lepidocaris, charophytes, cyanobacteria and coprolites within a ‘clotted’ chert texture, indicating subaqueous deposition, most probably in a temporary freshwater pool in an area of surficial hydrothermal activity.

In late Ordovician and early Silurian times, the Girvan district lay in a shelf marinesetting on the margin of Laurentia, on the northern side of the Iapetus Ocean. The Lower Palaeozoic rocks of the Girvan district, and their shelly and graptolitic fossil fauna, were systematically described by Lapworth in 1882 and have formed an important research resource ever since. They provide valuable evidence for the depositional environment and geological setting of Girvan during the early Palaeozoic, in both regional and wider contexts, and demonstrate the long-recognised close affinity with contemporaneous Laurentian faunas. However, by late Ordovician and into Silurian times, the earlier Iapetus oceanic barrier to faunal migration had largely gone and there is good correlation between contemporaneous marine fauna throughout the British Isles and Scandinavia. Despite much recent research in the area, including resurvey work by the British Geological Survey, no comprehensive review of Silurian lithostratigraphy at Girvan has been published since the revision by Cocks and Toghill in 1973. The present review of the Silurian rocks addresses this need and complements the recently published (Fortey et al. 2000) revision of the underlying Ordovician rocks, thus bringing the entire Girvan Lower Palaeozoic succession up to modern standards of nomenclature.

The litho- and biostratigraphical subdivisions of the Tremadocian-Arenigian succession of the southern Montagne Noire are hereby revised. The Lower Ordovician diversity patterns are estimated through statistical analysis of 27 families, 64 genera and 132 species of trilobites across nine interval zones; from bottom to top: the Proteuloma geinitzi, Shumardia (Conophrys) pusilla, Euloma filacovi, Taihungshania miqueli, Taihungshania shui landyranensis, Colpocoryphe maynardensis, Neseuretus (Neseuretus) arenosus, Apatokephalus incisus and Hangchungolithus primitivus zones. Maximum trilobite diversity occurred within the E. filacovi and A. incisus zones, alternating with two sharp declines (S. (C.) pusilla and T.shui landyranensis zones), in both cases drastically related to transgressive-regressive trends. Trilobites attained their highest diversity in muddy outer-platform settings, decreasing in fine-grained sandstones and siltstones of shoreface environments, where trilobites could still be numerically abundant. Four major trilobite turnovers are recognised at the bottom of the P. geinitzi, S.(C.)pusilla, E. filacovi and T. shui landyranensis zones, in which survivors from previous intervals are not reported at specific level, and important generic replacements took place. Despite the relative incompleteness of the Lower Ordovician trilobite record, envisaged after analysing the high proportion of monotypic taxa and discontinuous ranges of some families, the trilobite record is representative enough to estimate diversity patterns, although a better understanding of the palaeoenvironmental control will greatly enhance biodiversity resolution.