Stratigraphic occurrences and vegetational patterns of Pennsylvanian pteridosperms in Euramerican coal swamps

The vegetation of many Euramerican coal swamps is known from coal-ball peats in the tropical rainy zone across the paleocontinent of Laurussia in the Upper Carboniferous. The stratigraphic occurrences of coal balls in Europe (lower Westphalian) and in North America (upper Westphalian and lower Stephanian) are largely complementary and a revised correlation chart is given. Quantitative analyses of the vegetation from these autochthonous peats are combined with coal palynology to determine on overview of swamp vegetation patterns during the Westphalian and early Stephanian. In comparison to the dominance and great diversity of pteridosperms in the Upper Carboniferous compression floras, seed ferns were minor to subdominant elements in the coal-ball peats. The quantitative composition of organ assemblages of the principal pteridosperms is given with stratigraphic occurrences of Medullosa and Sutcliffia (Medullosaceae), Heterangium, Lyginopteris, Microspermopteris, and Schopfiastrum (Lyginopteridaceaea) and Callistophyton (Callistophytaceae). The major peat contributors among pteridosperms are Lyginopteris (?90%) in the Westphalian A and Medullosa (?95%) in the Westphalian D and Stephanian. Lyginopteris became extinct in the early Westphalian B and Medullosa became abundant during the Westphalian C–D transition and a subdominant in the Stephanian contributing 13–21% of the permineralized peats. Paleoecological interpretations indicate that medullosan trees were most abundant but patchy in distribution in drier swamp stages with enriched nutrients and near major channels in swamps during the Westphalian D. It is suggested that the swamp pteridosperms are probably quite similar to or identical with some of the representatives in the more diverse compression floras. The evolution and diversity noted in swamp pteridosperms are considered principally the product of adjacent lowland communities which repeatedly introduced seeds into the wetlands. The swamp pteridosperms exhibit the greatest fluctuation in abundance (biomass) from site to site in the same coal, probably the highest level of diversity and the only steady pattern of increase in importance during the Late Carboniferous with the possible exception of the Westphalian B–C interval. The close relationships inferred between swamp pteridosperms and their lowland seed sources are also compatible with the frequent association of tree ferns and seed ferns during the Westphalian D and in the Stephanian when these two kinds of frond-bearing trees formed most of the vegetation in both lowland and swamp environments.     

Diel vertical migration in Mesocyclops edax: implications for predation rate estimates

The diel migration patterns of Mesocyclops edax and its preyin a small lake were followed in two studies separated by approximatelyone year. Gut contents of the predators were examined and selectivityindices calculated at each depth at 0100 h during 1980. Thethree principal zooplankton prey found in the guts of M. edaxwere Keratella, Kellicottia, and Bosmina. The predator and allthree major prey species exhibited unique and different dielvertical distribution and migration patterns. The complex natureof the spatio-temporal variation in prey density to which M.edax is exposed, demonstrates the dangers of using selectivityindices without knowledge of the distribution patterns of bothpredator and prey. An increase in vertebrate predation pressurefrom one year to the next is thought to be responsible for anincrease in the abundance of small zooplankton species, thedisappearance of two out of three of the large zooplankton species,and the onset of a pronounced nocturnal migration pattern inthe third large species. ¹Present address: Biology Department, Williams Hall #31, LehighUniversity, Bethlehem, PA 18015, USA     

Stereospecific activity of 1-O-alkyl-2-O-acetyl-sn-glycero-3-phosphocholine and comparison of analogs in the degranulation of platelets and neutrophils

1-O-Hexadecyl-2-O-acetyl-$\text{sn}$-glycero-3-phosphocholine (platelet activating factor) stimulated the degranulation of rabbit platelets and human neutrophils, whereas the enantiomer, 3-O-hexadecyl-2-O-acetyl-$\text{sn}$-glycero-1-phosphocholine, was inactive. The analogs compared had the following relative potencies in degranulating platelets and neutrophils: 1-O-hexadecyl-2-O-acetyl-$\text{sn}$-glycero-3-phosphocholine > 1-O-hexadecyl-2-O-ethyl-$\text{sn}$-glycero-3-phosphocholine >$\text{rac}$-1-O-octadecyl-2-O-ethylglycero-3-phosphocholine = 1-O-hexadecyl-2-O-methyl-$\text{sn}$-glycero-3-phosphocholine >$\text{rac}$-1-O-dodecyl-2-O-ethyl-glycero-3-phosphocholine. The deacetylated compound, 1-O-hexadecyl-2-lyso-$\text{sn}$-glycero-3-phosphocholine, and 1-O-hexadecyl-2,2-dimethylpropanediol-3-phosphocholine were inactive. The active analogs selectively desensitized the response to each other in the neutrophils. It is suggested that these compounds may activate cells through interaction with a stereospecific receptor.     

Use of the smith degradation in the study of the branching pattern in the complex-type carbohydrate units of glycoproteins

The site of substitution of the peripheral branches on the core mannose-residues in the complex-type carbohydrate units of glycoproteins has been studied by Smith degradation. By using glycopeptides of known structure, it is shown that the site of attachment of the (1→4)-linked, third branch to the mannose core in tri- and tetra-antennary structures may be conveniently demonstrated by this technique. A critical factor was found to be the concentration of acid used for cleavage of the periodate-oxidized product. This finding could explain discrepancies concerning the previously published structures of fetuin glycopeptides. The technique was applied for study of the branching pattern in human transferrin, porcine thyroglobulin, and rat plasma and brain glycoproteins. The results support the concept that, in glycoproteins from most sources, the third (1→4)-linked branch is attached to the (1→3)-linked mannose residue of the core portion in the complex-type structures. An indication for a novel type of branching pattern in human transferrin was, however, also obtained.     

Induction of tyrosine aminotransferase by pyridoxine in Drosophila hydei

Salivary glands incubated in various concentrations of pyridoxine (Vitamin B₆) show increasing tyrosine aminotransferase (TAT) activity at concentrations up to 10^–5 M and then decreasing activity up to 10^–2 M but in all cases the activity is greater than that of the controls. This increase in activity is demonstrable for up to 6 h, the longest period tested, and is dependent on the synthesis of new mRNA. A similar increase in TAT activity is observed in salivary glands subjected to heat shock. Antibodies prepared against purified tyrosine aminotransferase precipitate a peptide of the same molecular weight (40 KD) as that induced by pyridoxine.     

Mouse DNA methylase: methylation of native DNA.

An improved method of purification of DNA methylase from Krebs II ascites cells is reported. The enzyme sediments at 8.3 S on glycerol-gradients and a major band on SDS polyacrylamide gel electrophoresis has a molecular weight of 184 000. Aggregation occurs at low salt and this may interfere with enzymic activity. The preferred double stranded DNA substrate is that rendered partially unmethylated by an in vitro repair mechanism or by isolation from methionine starved cells. Methylation of native partially methylated DNA is favoured under conditions of low salt and high temperature; conditions which encourage 'breathing' of the DNA. Methylation of native, unmethylated DNA also involves breathing but results in formation of a salt resistant tight binding complex between the enzyme and the DNA.     

Optimum interaction of sterol side chains with phosphatidylcholine.

The specificity of the interaction between the cholesterol side chain and egg phosphatidylcholine was precisely defined by examining the effect of three new analogues of cholesterol with modified side chains on the ordering of two steroid spin labels in liposomes. The complete side chain of cholesterol was shown to be required for maximum ordering. Sterols with side chains shorter or longer than cholesterol caused significantly less ordering.     

Presence of two forms of fumarase (fumarate hydratase E.C. 4.2.1.2) in mammalian cells: Immunological characterization and genetic analysis in somatic cell hybrids. Confirmation of the assignment of a gene necessary for the enzyme expression to human chromosome 1

Two major forms of fumarate hydratase have been resolved in extracts prepared from a wide variety of mammalian cells by electrophoresis. Fractionation experiments with human and mouse cells suggest that one form (the slower migrating) is localized in the mitochondria, whereas the other form is predominant in the cytoplasm. Analysis of the segregation of the enzyme forms in human-mouse somatic cell hybrids indicates that a gene(s) necessary for the expression of both forms can be assigned to human chromosome 1 (confirmation of a previous assignment by van Someren et al., 1974). Electrophoretic analysis suggests that the two forms may be interrelated. Furthermore, they both exhibit identical reactivity toward anti-fumarate hydratase antiserum. It is suggested that a modification of one form may occur in vivo and that the modification may be important in determining the intracellular localization of the enzyme.