ALBERT

Description: This chapter discusses the Maillard reaction. Results of the many investigations into the mechanism of the Maillard reaction support one of two main theories. The first assumes the formation of glycosylamines that undergo the Amadori (or, for ketoses, the Heyns) rearrangement. The 1-amino-l-deoxyketose derivative (or 2-amino-2-de- oxyaldose derivative) formed may be dehydrated and cyclized to form furan derivatives, or it may enolize. In either case, intermediates that are readily transformed into brown compounds are formed. A third possibility is for the deoxy sugar derivative to react with more amino acid to form colored products. The many workers who have supported this mechanism found also that optimum conditions for occurrence of the Maillard reaction are (1) fairly low water content, (2) a pH of 7 to 10, and (3) a high temperature. Nevertheless, some reaction occurs under conditions far removed from these, but in the absence of moisture there is no reaction. The formation of an acyclic Schiff base as an initial step is not very likely, since replacement of the aldose by salicylaldehyde caused only a very small loss of amino groups. The second theory of the mechanism of the browning reaction is of recent origin and maintains that the browning reaction and the Maillard reaction are separate and distinct. Browning, according to this school of thought, is due to the effect of pH on the sugar and can occur over a wide range of pH, whereas the Maillard reaction proceeds only in alkaline media.

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.

Description: Fourteen instances of whales entangled in submarine cables are reported. Ten entanglements occured off the Pacific coast of Central and South America. Six cases occured in about 500 fathoms, with 620 fathoms the maximum depth reported. Five entanglements occured in the period, Februray-March-April. All whales positively identified were sperm whales. The submarine cable was generally wrapped around jaw and often around the flukes and fins. The cable was rarely broken but always badly mauled. The entanglements often occured near former repairs where there is a chance for extra slack cable on the bottom. Two photographs of a sperm whale entangled in a cable and one photograph of a whale-jaw entangled in a cable are presented. It is concluded that sperm whales often swim alog the sea floor in depths as grat as 620 fathoms. It is suggested that the whales become entangled while swimming along with their jaw plowing through the sediment in search of food. It is possible that the whales attack tangled masses of slack cable mistaking them for items of food.

Description: Baltic sediments have been studied by Behrens, Munthe, Kiippers, Spethmann, Apstein, Sjostedt, Pratje and the writer. The following types of sediments have been observed: varved and non-varved late-glacial clays, gray and black, post-glacial muds, and sands. The organic content of late-glacial clays ordinarily is less than 1.3 per cent, and of post-glacial muds more than 3 per cent. Sediments containing intermediate quantities are scarce. This can be explained as a result of the changed balance between organic and inorganic sedimentation when the glacial period ended; the abundance of fresh detritus then suddenly ceased and inorganic sedimentation became very much slower than before; consequently, the relative amount of organic detritus increased. As most of the material was not subjected to biological analysis, it has not been possible to distinguish different ages among post-glacial sediments. Extremely fine-grained sediments occur in the Baltic. Non-varved late-glacial clays have medians from 0.40 to 0.62 micron, and post-glacial muds collected in the Baltic proper have medians from 0.58 to 1.6 microns. Non-varved late-glacial clays have a uniform composition over a wide area. The percentage of colloidal clay in total clay is about 5 per cent higher in post-glacial muds, showing that these sediments have been more exposed to weathering. This is attributed to the slower rate of settling and also the chemical and biological processes taking place within them as a result of the high content of organic matter. It is shown that Baltic water is under-saturated with respect to calcium carbonate. Yet carbonates do occur in the bottom deposits. In both late-glacial and post-glacial sediments, the carbonate content is ascribed to limestone detritus from deposits on the shores of and on the islands of the Baltic. The highest carbonate content, more than 40 per cent, was found in the southern part of the Gulf of Bothnia, on the bottom of which Silurian limestone is known to occur.