ALBERT

Description: During 1950, the Common Octopus (Octopus vulgaris Lamarck) was to be found along the south coast of England in greater numbers than at any time since Garstang (1900) reported on the ‘plague’ on the coasts of Devon and Cornwall in 1899–1900. In earlier papers (Rees, 1950, 1952) the distribution of the octopus in our northern waters was reviewed, and it was demonstrated that this species is an immigrant which breeds on our south coast only rarely. It reaches these coasts by being brought there as a planktonic larva by the water circulation in the English Channel and by migrations of the adult. The most important factor in controlling the movements of the adult, however, might be expected to be the water temperature in the English Channel—where the species is at the northern limit of its breeding range and might therefore be extremely sensitive to slight changes in temperature.

Description: In Britain Octopus vulgaris occurs on the Channel coast and only very rarely on other coasts. In Brittany and the Channel Islands it frequently makes its lair at low water, but on the English side of the Channel it does not come so close inshore except in abnormal years of high sea temperatures. The discovery of Octopus larvae of various sizes, from newly hatched to 6·0 mm. (mantle length), in plankton hauls taken to the north of the Channel Islands, proves that the species has a much longer planktonic life than hitherto supposed. The water circulation in the English Channel, as indicated by drift bottles, is admirably suited to the dispersal of larvae to our shores from breeding centres on the coasts of Brittany and the Channel Islands.

Description: Distributions of the species of Foraminifera (living and dead) forming the greater part of the foraminiferal faunas in marshes in Poponesset Bay, Massa- chusetts, have been studied. Eight stations were sampled bimonthly for one year (August, 1956 to September, 1957). The marsh environments vary from almost non-marine (with tidal influence) to near marine. Arenoparrella mexicana, Haplo- phragmoides hancocki, Tiphotrocha comprimata, and Trochammina macrescens de- crease with increasingly marine conditions, whereas Jadammina polystoma and Trochammina inflata increase. Other species such as Ammobaculites dilatatus, Am- motium salsum, Miliammina fusca, and Protelphidium tisburyense fluctuate inde- pendently of the degree of brackish or marine conditions. Unknown factors govern- ing micro- and macroenvironments probably play an important part in controlling distributions. Suggested factors are type of vegetation, chemical factors, pH, nutrients and food. Calcareous specimens are rapidly destroyed after death pre- sumably due either to the ability of the living form to resist acidity or to a postu- lated increase in acidity immediately below the sediment surface, more probably the latter. This destruction of the tests is of importance in the interpretation of ancient marsh environments. Many species, including the calcareous ones, had their largest living populations in June or September and their smallest in December or February. There were some exceptions such as Miliammina fusca which showed an increase in winter. The total living populations were greatest in June and lowest in December, which may be related to maximum temperature and time of greatest reduction in temperature respectively. Multiple sampling showed that distribu- tions at any one station were fairly uniform although nearby samples in different microenvironments in some cases vary considerably.