Temporal photosynthetic carbon isotope signatures revealed in a tree ring through 13CO2 pulse-labelling

Using a combined method of pulse-labelling trees and analysing detailed distribution of ¹³C tracer within tree rings, we studied how photo-assimilates incorporated on a given day are then distributed in a tree ring. A branch of a 4-year-old Cryptomeria japonica D.Don tree growing in Tsukuba, Japan was pulse-labelled with non-radioactive ¹³CO₂ on two occasions: 29 May 2001 and 18 September 2001. Two discs were cut from the stem on 4 March 2002, one immediately under and the other 0.5 m below the branch and put through high-resolution δ ¹³C analysis. δ ¹³C peaks were observed in both the earlywood and latewood of the concerned tree ring, corresponding to each pulse-labelling date. The earlywood peaks was broader than the latewood peaks, possibly reflecting seasonal variation of the width of wood developing zone. Half-widths of the peaks were measured and used as indicators for the potential time resolution of tree-ring isotope analysis. The half-widths of the peaks indicated a time resolution no finer than 8.7–28 and 33–42 d in the early and latewood, respectively. Holocellulose extraction yielded only a slight change to the shape of the δ ¹³C peaks. ¹³C tracer pulse-labelled in May and September reached tangentially different locations in the lower disc, suggesting a seasonal change in the pathway of carbohydrates. Local consumption of spring assimilates and long-distance downward transport of autumn assimilates were also suggested.     

Trilobite taphonomy and ecology in Upper Ordovician carbonate buildups in Dalarna, Sweden

A major ecological grouping of the trilobites in the Upper Ordovician Boda Limestone buildups in Dalarna is outlined, based primarily on the modes of occurrences in the Jutjärn quarry. The so-called pockets are analysed with regard to their trilobite contents and distribution within a carbonate buildup. The pockets are of two general types. One consists of narrow opened fissures along bedding planes. The matrix of these may contain either of the peculiar blind Isocolus sjoegreni or Ityophorus undulatus , both of which appear to have been cavernous species, possibly belonging to the Bathyuracea (or Leiostegiacea). In addition, small proetids used the fissures for moulting. The other kind of pocket is a cavity largely filled with sediment from the surface of the buildup. The size is considerable, in rare cases up to many tens of cubic metres. Although the buildups housed about 90 trilobite species, each of these pockets is dominated by one or two out of seven large species. Of these, six are illaenids, the seventh the illaenid-like cheirurid Holotrachelus punctillosus. Usually only pygidia and cranidia are found. These species may have lived gregariously around the rims of the cavities. The remaining species, about 85% of the trilobite fauna, appear to have lived on the surface of the buildups. The largest group is the proetids with some 20 species (in addition to those known from pockets). Cheirurinids and lichids contribute with some 15 species each, and there are six odontopleurids. The distinctness of the 'community' is indicated by the circumstance that only three species are shared with contemporaneous level-bottom faunas in Sweden.     

The occurrence and properties of dihydrofolate reductase in pea seedlings

Dihydrofolate reductase (E.C. 1.5.1.3 [EC] ) was found in pea seedlingsand was partially purified by treatments with ammonium sulfate,protamine sulfate and by DEAE-cellulose column chromatography.Some properties of the enzyme were investigated. Optimum pHfor the reaction was 6.5. In the enzyme reaction, FAH₂ and NADPH₂were specifically required. MICHAELIS constants for FAH₂ andNADPH₂ were 4.3x10^–6 M and 4.0x10^–5 M, respectively.Folate antagonists such as aminopterin, methotrexate and pyrimethaminewere potent inhibitors of this enzyme. Enzyme activity was almostcompletely inhibited at a concentration of 10^–7 M of aminopterinand methotrexate and 10^–6 M of pyrimethamine. Growth of germinating pea seeds was inhibited by aminopterin,methotrexate and pyrimethamine, and it recovered significantlywith a tetrahydro-derivative of folate, CF, but not with dihydrofolicor folic acid. These results suggest that growth inhibitionof pea seedlings by these antagonists is due to inhibition ofdihydrofolate reductase in seedlings. ¹Studies on the enzymatic synthesis and metabolism of folatecoenzymes in plants IV. (For the previous paper, Part III, seeReference (21)) . Part of this paper was presented at the AnnualMeeting of the Agricultural Chemical Society of Japan held atTokyo on April 4, 1967 (Received October 8, 1969; )     

The role of a glyoxylate-glycolate system in chloroplasts of higher plants

Photoreduction of glyoxylate and oxidation of glycolate wereinvestigated using unwashed chloroplasts from spinach leaves.A glyoxylateglycolate system operated in light and under aerobicconditions. Accompanying the photoreduction of glyoxylate andthe oxidation of glycolate, was the disappearance of inorganicphosphate. Photoreduction of oxalate was also observed in illuminatedchloroplasts. The reaction rate was, however, much lower thanthat for the photoreduction of glyoxylate. (Received August 4, 1969; )     

Prospective Neural Areas and Their Morphogenetic Movements during Neural Plate Formation of Xenopus Embryos. I. Development of Vegetal Half Embryos and Chimera Embryos

Development of animal cap-less Xenopus gastrulae was examined. In vegetal halves from which the animal cap was removed 0.6 mm above the blastopore, an apparently normal array of craniocaudal structures developed. Histological examination showed differentiation of central nervous system (CNS) structures in the cap-less embryos, but differentiation of sensory organs, such as a lens and ear vesicle in only a few embryos. Only the dorsal midline of the embryos was covered with epidermis, and its lateral-ventral areas consisted of bare endoderm and mesoderm. The development of animal cap was also investigated by exchanging the animal cap of X. laevis embryos with that of X. borealis embryos, which can be distinguished by quinacrine fluorescence staining. The central nervous system of chimera embryos consisted mainly of X. laevis cells stained homogeneously with quinacrine but a small number of punctately-stained X. borealis cells was in the anterior tip of the forebrain. Cells of the lens and ear vesicle were punctately stained. More than two-thirds of the epidermal area consisted of punctately-stained cells and only the dorsal midline of the posterior head- and trunk-epidermis consisted of homogeneously-stained cells.
Areas of the prospective central nervous system and their movement during embryogenesis of Xenopus are discussed.     

Reflections on the Limits of Science and Technology

SYNOPSIS. Exuberance over insights gained in the infant fieldof genetics early this centuryled scientists to extrapolatebeyond their data to heredity of behavioral traits in people.Oneof the direct consequences was the incarceration of Americansand Canadians of Japanese ancestry during World War II as enemyaliens. Drawing on this personal experience of the misapplicationof science, I describe the process of scientific indoctrinationand blindness to the limitations of this way of knowing. Thisled to my attempt to demystify science through the electronicmedia. Only recently have I come to understand that two assumptionsthat impelled me to use television in the first place are wrong.The first was that with access to more information about science,the general public would be in a position of making better informeddecisions on issues involving science and technology. The problemis that we are overwhelmed with information and most peoplelack the ability to distinguish meaningful "signal" (i.e., credibleinformation) from background "noise" (i.e., garbage). We believein phantoms created by the acceptance of anything because itexists as print or television programs. My second assumption had been that we need a mechanism to doan in-depth "cost/benefit" analysis of new technologies beforethey are actually made available. But history reveals that thebenefits of new technologies are immediate and obvious whilethe costs are usually hidden and completely unpredictable. But in the rush to exploit new scientific insights we ignorethe fact that science must lookat nature in isolated bits andpieces. Knowledge gained in fragments does not yield an understandingof the greater context from which the pieces are taken. Witheach new discovery, we itch to apply it, forgetting how muchwe have yet to learn. Our attempts to manipulate nature areoften illusions of control created by our ability to overpowernature by brute strength. In the area of genetic engineering,this could be truly disastrous.     

Ontogenetic change of distributional patterns of pore systems in Cythere species and its phylogenetic significance

Species of Cythere (Ostracoda, Crustacea) have about one hundred normal pore systems on each valve of the carapace. These can be classified into five types on the basis of morphological features. They were examined in the light of intraspecific variation and interspecific difference. Each of the five pore systems has its own mode of ontogenetic increase in number. Comparison among fourteen Cythere species shows that the distributional patterns are completely identical in the A-3 stage, but that they are classified into four and eight groups in the A-2 and A-1 stages, respectively. In the adult stage the pattern becomes diversified among the fourteen species, though homologous relationships are still recognized between different species. The similarity and difference of the pore patterns, which are traceable until the last ontogenetic stage, can be used to determine phylogenetic relationships. These findings were applied to the reconstruction of phylogeny of the eleven living and three extinct species of Cythere. □ Crustacea. Ostracoda , Cythere, Ontogeny. Phylogeny, pore system, pore canal. speciation, laroal morphology.     

Fractal Analysis of Plant Root Systems

The morphology of root systems of crop plants was analysed byfractal geometry using an image processing system. Results indicatethat these root systems have a fractal structure (D; 1.48     

Stimulation of Spermatid Phosphofructokinase by Fructose 2,6-Bisphosphate from Rat Testes

Effect of fructose 2, 6-bisphosphate on 6-phosphofructokinase (ATP: D-fructose-6-phosphate 1-phosphotransferase, EC 2.7.1.11) in spermatid extract from rat testes was studied. Fructose 2, 6-bisphosphate stimulated the enzyme greatly by increasing its affinity for fructose 6-phosphate and relieving the inhibition by ATP. Fructose 2, 6-bisphosphate (0.8 μM) was required for 50% activation of 6-phosphofructokinase (PFK). In addition, fructose 2, 6-bisphosphate, AMP and fructose 6-phosphate acted cooperatively to stimulate the activity of PFK. This stimulation may play an important role in the regulation of glycolysis in spermatids of rat testes.     

Respiration of Sea Urchin Spermatozoa in the Presence of a Synthetic Jelly Coat Peptide and Ionophores

Sperm respiration and motility of the sea urchin Hemicentrotus pulcherrimus were studied at pH 6.8 in the presence of a synthetic jelly peptide (Gly-Phe-Asp-Leu-Asn-Gly-Gly-Gly-Val-Gly) and monovalent cationic ionophores. The synthetic peptide stimulated sperm respiration and motility to the level of that found in normal sea water (pH 8.2) with half-maximal stimulation at approximately 100 pM. Monensin and valinomycin also stimulated sperm respiration with half-maximal effects at 7 μM and 0.7 μM, respectively. The stimulation of sperm respiration by the peptide and monensin was dependent on external Na⁺, but was not dependent on the osmolarity of the suspending medium. Approximately 50 mM Na⁺ was required for half-maximal respiratory responses to the peptide and monensin.