ALBERT

Notes: Multiplication and spread of respresentative strains of three pathovars of Xanthomonas campestris were monitored by maceration and plating from inoculated leaves of the host and non-host plant species Oryza sativa, Poa trivialis, Brassica oleracea and Phleum pratense.Homologous interactions were characterized by higher multiplication rates and larger population increases than heterologous interactions, except for pv. oryzae which increased as much as pv. poae in leaves of Poa. Spread of heterologous pathovars was limited, but homologous pathovars were distributed throughout host leaves soon after inoculation. Pvs poae and oryzae (from Poaceae) demonstrated considerably greater population increases and higher initial multiplication rates than pv. campestris in leaves of all non-host Poaceae. Pv. poae spread further into leaves of Oryza and pv. oryzae further into leaves of Poa and Phleum than did pv. campestris. Numbers of pv. poae declined in Brassica as did those of pv. oryzae, which was localized within 2 mm of the point of inoculation.

Notes: Robinson, J. M. 1988. Does O2 photoreduction occur within chloroplasts in vivo? -Physiol. Plant. 72: 666–680.This discussion reviews evidence supporting the hypothesis that within intact chloroplasts in vivo, molecular O2 may serve as an alternative Hill oxidant (electron acceptor) on the reducing side of Photosystem I. Depending upon the availability of Hill oxidants such as NADP+ and NO−2, there is the potential within intact plastids in vivo, for photolytically derived reducing equivalents to reduce O2 to O−2 and H2O2 (the Mehler reaction). In chloroplasts of healthy tissues, the products of photosyn-thetic O2 reduction O−2 and H2O2) are rapidly removed by superoxide dismutase (EC 1.15.1.1) and L-ascorbate peroxidase (EC 1.11.1.11) to prevent toxicity. The presence of these two enzymes within chloroplasts in vivo reflects the potential for linear (non-cyclic) photosynthetic electron transport systems to draw upon molecular O2 as a terminal oxidant. In the intact plastid, O2 may act as an electron acceptor in the place of any other physiological Hill oxidant, e.g., NADP+, NO−2, and, presumably, oxidized thioredoxin. Under aerobic, physiological conditions, photo reduced ferre-doxin (Fdred), and/or reduced flavoprotein enzymes, e.g., ferredoxin:NADP+ oxidoreductase (EC 1.18.1.2), can donate electrons to O2; this reductive reaction appears to be non-enzymatic, but it is rapid. Stated from another viewpoint, O2 may serve as a Hill oxidant to support some linear electron flow when reductant supplies are in excess of reductant demands. For example, there are nitrogen assimilatory sites in the chloroplast, i.e., ferredoxin-nitrite reductase (NiR; EC 1.7.7.1) and glutamate synthase (ferredoxin) (GOGAT; EC 1.4.7.1), to which Fdred is allocated as reductant. Because NADH:nitrate reductase (NR; EC 1.6.6.1) is the rate limiting step of nitrogen assimilation, and, because NiR and GOGAT activities are in excess of NR activities by a factor of 2 or more, then an excess of unreacted Fdred could accumulate. Alternatively, the allocated Fdred would reduce the excess NiR and GOGAT sites, but the excess of reduced enzymes would not have substrates (e.g., NO−2, glutamine, and α-ketoglutarate) with which to react. Therefore, if ‘excess’ NiR and GOGAT binding sites were not employed, the available excess Fdred, and/or the reduced NiR and GOGAT proteins, would be susceptible to oxidation by O2. The resulting O2 photoreduction could account for nearly all of the observed in vivo Mehler type reactions. In vivo, apparent foliar O2 photoreduction occurs simultaneously with maximal CO2 photoassimilation, and, in high light, average rates have been determined by direct measurement to range from 10 to 40 μmol O2 consumed (mg Chl)−1 h−1. Therefore O2 reduction would support a low rate of linear (non-cyclic) electron flow which, in turn, could maintain a low, but significant rate of ATP production. However, there is not total agreement among researchers that the physiological role of O2 is that of serving as an alternative Hill oxidant in order to recycle unutilized Fdred or other photoreduced proteins. Also, there continues to be considerable controversy on whether or not O2 reduction supports significant photosynthetic phosphorylation. The total process of O2 photoreduction, and its physiological role(s), requires much more study before absolute functions can be assigned to O2 terminated, linear electron transport.〈section xml:id="abs1-1"〉〈title type="main"〉SummaryMolecular O2 possesses the physico-chemical properties that permit this molecule to serve as an alternative Hill oxidant within chloroplasts in vivo. Additionally, the physical and physiological properties within the chloroplast in vivo favor the potential for O2 to serve as an electron acceptor on the reducing side of Photosystem I. This may reflect an important ‘fail-safe mechanism’ which prevents over-reduction of linear photosynthetic electron transport chain proteins. This review has focused on the possibility that unutilized Fdred and/or other non-utilized, reduced plastid enzymes (e.g., NiR) may be electron donors to O2. It is hypothesized that this oxidation ultimately would be reflected as an in vivo Mehler reaction. However, it remains for future studies to establish without doubt, that in vivo, photoreduced chloroplast enzyme proteins can utilize O2 as a terminal electron acceptor.Further, that O2 photoreduction supports a significant level of photophosphorylation in vivo remains to be firmly established. Certainly, considerable evidence, gained with experiments utilizing isolates of intact chlo-roplasts and reconstituted chloroplast systems, supports the hypothesis that O2-terminated linear electron transport has the potential to support high rates of ATP production. However, in vivo studies e.g., with intact leaf tissues, which actually quantitate the relationship between O2 photoreduction and associated ATP production have not been conducted. These will be difficult experiments to perform, because, in vivo, it will be difficult to separate photosynthetic ATP production mediated by O2 from ATP production mediated by those other, more predominant Hill oxidants (e.g., NADP+, NO−2). Also, it continues to be a possibility that it is cyclic, and not pseudocyclic photophosphorylation that provides additional ATP to support photosynthetic cell metabolism. To establish beyond doubt that an in vivo role of the Mehler reaction is that of supplying ‘additional ATP’, remains for considerable future study.

Notes: Summary Phagocytosis by polymorphonuclear leukocytes triggers a burst of oxidative metabolism resulting in hydrogen peroxide and superoxide production, and these active oxygen species function in the killing of microorganisms. A new cytochemical technique, based on a manganese dependent diaminobenzidine oxidation, has been developed to detect superoxide in these cells. It has been shown that superoxide generation is associated with the plasma membrane in cells activated by particulate (zymosan) and nonparticulate (phorbol myristate acetate) stimuli. This membraned activity is maintained during invagination such that reduced oxygen is generated within the endocytic vacuoles. Reaction product is absent from unstimulated cells; additionally, formation of precipitate is blocked by omission of Mn++, low temperature, glutaraldehyde prefixation, and the presence of superoxide dismutase in the incubation medium.

Notes: Summary Normal skeletal and cardiac striated muscle from adult rats was incubated for the cytochemical detection of acid phosphatase activity with cerium as the capture metal. Results from these experiments show that normal striated muscle has a greater number of acid phosphatase-positive structures, which are presumed to be lysosomes, than has been indicated by several previous cytochemical studies.

Notes: Summary Forty communities were assembled through the controlled inoculation of algae, protozoans and a rotifer according to either of 2 distinct introduction schedules. These introduction schedules were constructed such that species reinvaded on average either every 6 or 8 w. Ten of the 20 beakers experiencing each invasion schedule contained 300 ml of media; the remaining beakers in each invasion category contained 100 ml of media. Species richness consistently increased throughout the initial 4 w and 7 w of the experiment for the low and high invasion rate beakers, respectively. The numbers of species in the low rate beakers were uncorrelated with time during the last half of the experiment; however, species richness gradually declined during this period in the high rate beakers. The extinction rate is shown to be disproportionately higher for large organisms in the small microcosms. Such “selective extinction” is consistent with the MacArthur-Wilson equilibrium model.

Notes: Summary An investigation of the larval dragonfly fauna associated with the plant, Sagittaria platyphylla, was conducted in a small pond. Despite the presence of several larval anisopteran species in the pond, only Pachydiplax longipennis larvae were found on Sagittaria plants. A study of the microspatial distribution of P. longipennis larvae on S. platyphylla indicated that larvae use the various regions of a plant in a highly non-random fashion. Larvae show a strong preference for the leaf axil area. A generalized predator, the bluegill sunfish (Lepomis macrochirus), was allowed to selectively eat either of two larvae placed in various plant regions. This experiment indicated that larvae in a leaf axil area were significantly less susceptible to bluegill predation than larvae positioned in other plant regions. The microspatial distribution of starved larvae revealed that larvae with high hunger levels occupied the leaf axil area significantly less than well fed larvae, suggesting 1) larvae do not use these regions as feeding sites, and 2) high hunger levels may induce a behavioral shift in habitat use, with starved larvae forced into areas of high predation risk by the need to fulfill nutritional requirements.

Notes: Summary The effect of variation in group size on age-specific survivorship and fecundity rates were examined in a population of wedge-capped capuchin monkeys Cebus olivaceus during a 10 year study. Life tables were constructed separately for four large (≥15 individuals) and four small groups (〈15 individuals). Female reproductive success, and its relative contribution to population growth, was much higher in large groups, primarily through higher age-specific fecundity. Age-specific survivorship was similar in groups of different sizes. The reproductive success of the single breeding male in a group was much higher in large than small groups. Compared to small groups, breeding males in large groups had a longer breeding tenure, and access to greater numbers of reproductive females with a higher average fecundity. Differences in female reproductive success apparently resulted from variation in access to monopolizable fruit trees. Large groups predictably displaced small groups during intergroup encounters. Group rank depended on the number of males resident in groups. The large number of non-breeding males in large groups results from their longer average residency time. I explain the longer residency of males in large groups by the higher average reproductive success of breeding males in these groups.