Plant Science & Landscape Architecture Theses and Dissertations

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    The kinetics and quantum yield of photophosphorylation in Anacystis nidulans (Richt.) Drouet
    (1972) Owens, Olga v. H.; Krauss, Robert W.; Plant Physiology; Digital Repository at the University of Maryland; University of Maryland (College Park, MD)
    The active metabolite, ATP, serves not only as a high energy intermediate but also as a controller of some enzymatic reactions. In plant cells, the larger part of the ATP is formed by photophosphorylation. In this paper the rates, the quantum yields, and the wavelength dependencies of photophosphorylation in the blue-green alga Anacystis nidulans are reported. A fluorometric method for determination of enzymatically produced NADPH from ATP was adapted for use on cell extracts. In the light, the ATP level was 0.15 to 0.25 µmoles/mg chl. In the dark, the ATP level was 70% of that in light. In both darkness and anaerobosis, the level was 20%. A return to the light restored the ATP level from both conditions. Dark, anaerobic cells were exposed to measured irradiancies of 710 nm and 620 nm. The rate of ATP formation was measured within the first few seconds and found to be directly proportional to absorbed intensity. Saturation of the rates occurred at an intensity one-tenth the optimum for oxygen production. Quantum requirements of 6-8 were similar for each of the two wavelengths. The system II inhibitor DCMU, had a greater effect at 620 nm that at 710 nm indicating an involvement of system II in photophosphorylation only at 620 nm. At low intensities and over long time periods white light failed to produce a saturating steady-state level of ATP indicating a simultaneous consumption of ATP. Measurements in short dark periods following marginal illumination showed consumption of ATP to be 2 to 4 times greater that production in weak light. Thus, the quantum requirement can be calculated to be 2. ATP formation, therefore, is not the limit ing factor in co2 fixation. The evidence is the high quantum yield of photophosphorylation and the unsaturation of co2 fixation at intensities at which ATP synthesis is saturated.
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    A Revision of North American Melanthium L. (Liliaceae)
    (1978) Bodkin, Norlyn Lee; Reveal, James L.; Botany; Digital Repository at the University of Maryland; University of Maryland (College Park, Md)
    Melanthium L. (Liliaceae ) is a genus of perhaps eight species with the four species of North America distributed from central Iowa eastward to southern New York, south to northern Florida and eastern Texas. The type species , M. -virginicum L., is found over this entire range growing commonly in swamps , marshes and bogs. Melanthium latifolium Desr. , found mostly on rich wooded slopes, and M. parviflorum (Michx.) S. Wats. located at higher elevations, occur mainly in the mid-Appalachian mountains. Melanthium woodii (Robbins ex Wood) Bodkin, comb. nov., is known from rich deciduous slopes of the Ozark Plateaus where it is very local and rare, and from five small disjunct populations in three eastern states. The major decision made in this treatment is the maintenance of Melanthium as distinct from the heterogeneous genus Veratrum L. on the basis of leaf size and shape, inflorescence, features of the tepalular glands and claws, adnation of stamens to tepals and general habit of the plants. The numerous synonyms associated with the name Melanthium are treated and either included under that genus , or excluded and assign d to their proper genera. The four (tentatively) Asian species, all of southwestern China , are not discussed due to a paucity of recent material.
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    Net Productivity of Emergent Vegetation at Horn Point Salt Marsh
    (1975) Cahoon, Donald Richard; Stevenson, John C.; Botany; Digital Repository at the University of Maryland; University of Maryland (College Park, Md)
    Analyses of monthly standing crop, daily rates of production, and variations in yearly productivity for 5 production for the Spartina patens/Distichlis spicata mixture were conducted over two consecutive growing seasons for a Chesapeake Bay brackish marsh. Regression models for plant height and dry weight biomass were generated for all that the relationship between height and dry weight within each species is the same for all seasons of the year except in the species Spartina alterniflora and Phragmites australis. Positive correlation coefficients ranged from .27 for S. alterniflora to .96 for P. australis with the other species having intermediate value. Overall, production at Horn Point is lower than most other values in the literature with the 2-year average for S. alterniflora (676 g/m2) being 1/2 the average for the Atlantic Coast but the 2-year average for S. patens (628 g/m2) being slightly higher than its Atlantic Coast average. On a square meter basis, the primary producers rank in the following order of importance for the two year average of standing crop: Typha angustifolia (985 g/m2), Phragmites australis (892 g/m2), S. alterniflora/Amaranthus cannabinus (676 g/m2), S. patens/D. spicata (628 g/m2), and Hibiscus moscheutos (531 g/m2). However, the most important zones in terms of areally weighted production (in metric tons) for 1973 at Horn Point Marsh are the S. patens/D. spicata (7.61), H. mocheutos (5.07), S. alterniflora/A. cannabinus (3.22), P. australis (0.659), and T. angustifolia/H. moscheutos (0.644). In the brackish marsh (S. patens/D. spicata) exclosure experiments demonstrated that almost 100% of the net primary production (NPP) passes through the detritus food chain but in the contiguous fresh marsh (H. moscheutos) 37% of the NPP is utilized by the grazing food chain. Underground production for S. patens/D. spicata was determined by an experimental approach involving transplantations of underground material and a dry weight shoot:root ratio of 1:16 was determined over a twelve month period. An efficiency rate for conversion of visible solar radiation to plant production in 1974 ranged from 0.11% for H. moscheutos in the Typha/Hibiscus zone to 1.12% for the Typha angustifolia/Hibiscus moscheutos mixture.
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    A Study of the Soils Derived from Serpetinite and Associated Rocks in Maryland
    (1978) Rabenhorst, Martin Capell; Foss, John E.; Agronomy; Digital Repository at the University of Maryland; University of Maryland (College Park, Md)
    Approximately 25,000 acres have been mapped as serpentinite-derived soils in Maryland. While fertility studies have been done in serpentine areas, little work has been undertaken concerning the genesis of these soils. The objectives of this study were: 1) characterize the properties of soils formed from serpentinite and associated mafic rocks; 2) apply the results of the characterization study to an understanding of the genesis of these soils; and 3) examine the mapping and classification of serpentine soils with reference to geologic mapping. In a reconnaissance effort, 48 sites were sampled and analyzed for extractable Mg, Ca, P, and K and for pH. From field observations and these data, seven locations were selected for profile descriptions and detailed sampling. Physical, chemical , and mineralogical analyses were conducted on these samples. All serpentine profiles showed weak to moderate expression of argillic horizons and as a result of high Mg saturation, are classified as Alfisols. Argillic horizons in the non-serpentine profiles were strongly developed. Serpentine minerals were generally abundant in the > 0.2 μm fractions of serpentinite-derived soils. These weather to form expansible 2:1 minerals in the finer fractions. Vermiculite and smectite were important in both serpentine and non-serpentine profiles. The presence of quartz, mica, and feldspar in the surface horizons of all profiles indicate that eolian additions have occurred in many counties in the Maryland Piedmont. Comparison of soil mapping with geologic mapping has revealed large acreages of serpentine soil units mapped over non-serpentine mafic rock . This demonstrates the need to better utilize available geologic information in soil mapping. Serpentinitic mineral families are not currently recognized in any soil series in Maryland. Three of the four serpentine profiles, however, contained high levels of serpentine minerals. There is, therefore, a need to recognize serpentinitic soil families in Maryland in order to better differentiate between soils formed from serpentinite or from non-serpentine mafic rocks.