A knowledge of the allometry of algal growth and respiration can be applied to biomass-size distribution models which are in turn used in the prediction of fish yield and ecosystem studies. However, the scaling exponents reported in the literature are variable. This variation may be attributed to differences in the expression of cell size and phylogeny, but could also reflect small sample size which underlie most published regressions. This thesis establishes the allometry of algal growth and respiration based on a larger sample taken from the literature, and evaluates the effects of differences in gross taxonomy and in the expression of cell size on these relations. Allometric relations based on cell carbon appear more consistent with relations from other taxa than those based on cell volume, reflecting the size dependence of algal elemental composition which does not occur in most other taxa. The allometric relation of algal respiration (R in pl O$ rm sb2 cdot cell sp{-1} cdot hr sp{-1})$ was found to be R = 0.030C$ sp{0.93}$ where C is cell carbon content in pg C$ rm cdot cell sp{-1}$. Among the 6 divisions studied (Chlorophyta, Chrysophyta, Cyanophyta, Euglenophyta, Pyrrophyta, Rhodophyta), chlorophytes, euglenophytes and rhodophytes exhibited different respiration-size relation but separate relations were not developed for each of those groups due to patterns in residuals or small sample sizes. The specific rate of algal growth ($ mu$ in divisions$ cdot$day$ sp{-1}$) also depends on size and it is found to be $ mu$ = 3.45C$ sp{-0.21}.$ All taxa studied here (Chlorophyta, Chrysophyta, Pyrrophyta) have similar scaling exponents for growth but Pyrrophyta have significantly lower growth rates than other algae of similar size.

No description available.

No description available.

Mitochondria were extracted from seedling radicles of Pima S-5 and Pima E-14 cottons and the state 3 respiration, state 4 respiration, ADP:O ratio and respiratory control (RC) ratio were measured in vitro over a range of temperatures from 6 to 18C. Mitochondria from E-14 seedlings exhibited a mean state 3 respiration rate of 13.42 μMO₂/min/gm tissue while mitochondria from S-5 seedlings showed a mean state 3 rate of 17.94 μMO₂/min/gm tissue. Mean state 4 respiration exhibited a similar trend with measurements of 73.4 μMO₂/min/gm tissue and 11.73 μMO₂/min/gm tissue for E-14 and S-5. Mitochondria from E-14 seedlings exhibited a mean ADP:O ratio of 3.73 compared to an ADP:O of 3.28 for S-5, across all assay temperatures. Mean respiratory control ratio was 1.79 for E-14 and 1.53 for S-5. These lower respiration rates of E-14 coupled with higher ADP:O ratios and RC ratios support a greater respiratory efficiency at low temperatures of this variety compared to S-5. Additionally, the E-14 mitochondrial membranes exhibited an ability to remain in a fluid state to a lower temperature than Pima S-5 mitochondrial membranes as judged by Arrhenius plots of respiration. Since mitochondrial respiration is considered to be regulated by membrane-bound enzymes, any change in membrane fluidity would conceivably affect mitochondrial enzyme activity and thus alter respiration rates. Changes in respiration rates will be reflected as a break in an Arrhenius plot. The mean break point temperature of state 3 respiration was 10.7C for E-14 and 13.4C for S-5. The mean break point temperature for state 4 respiration was 10.9C for E-14 and 13.6C for S-5. The ability of E-14 to withstand a greater degree of chilling under field conditions can be attributed, in part, to the greater fluidity of seedling mitochondrial membranes at low temperatures and concomitant conservation of respiratory energy through a lower rate of respiration. Assays of mitochondrial respiration and Arrhenius plots of mitochondrial respiration versus temperatures could be used to select cotton lines more tolerant to chilling temperatures.

Dark respiration rates of the aerial shoots of Arceuthobium tsugense, obtained by manometric and IRGA techniques, show production of C02to range between 155-300 µl CO2 g-1h-1 with evidence of seasonal variation. Experiments with 14C02 indicate that the aerial shoots are capable of some photosynthetic CO2 fixation, with 10-15% of the available 14C incorporated by the plant tissue in one hour.The portions of the o aerial shoots which are most active in C02 fixation are the young terminal regions. Biochemical characterization of the products of photosynthesis reveals that 80-90% of the incorporated 14C is ethanol soluble. Ten percent of the ethanol fraction is lipoidal in nature, the rest is H20 soluble. Ion exchange separation of the H20 soluble portion shows that 16-25% of the 14C activity is cationic, about 25% anionic, with the balance neutral. Aspartic acid, glutamic acid, and valine are present in the cationic fraction, with additional free amino acids indicated. IRGA experiments indicate an apparent photosynthetic CO2 fixation capacity of 80-90 percent of the ethanol fraction is lipoidal in nature, the rest is H20 soluble. Ion exchange separation of the H20 soluble portion shows that 16-25% of the 14C activity is cationic, about 25% anionic, with the balance neutral. Aspartic acid, glutamic acid, and valine are present in the cationic fraction, with additional free amino acids indicated. IRGA experiments indicate an apparent photosynthetic CO2 fixation capacity of 80-90 µl CO2 g-1 h-1, or 25-30% of the amount of C02 produced by respiration. The significance of these findings is discussed with respect to nutrition of the parasite.

This study investigates respiration rate of potatoes (Solanum tuberosum L.) under real and experimental storage conditions. Real storage conditions were obtained by building a small-scale storage facility equipped with two independent storage bins including all controls. Each bin was filled with 2.5 metric tons of potatoes and these were stored for five months. Temperature, relative humidity, air flowrate and other operational parameters were collected. Also, mass loss and CO2 analyses were performed. / A heat and moisture balance was applied to quantify heat and moisture rates produced by potatoes and were converted to respiration rates as CO 2 produced (ml.kg-1.h-1). Evaporation rates were also determined (g.kg-1.h -1). The balance was mainly applied on data collected from specific periods in which steady conditions were imposed; heaters and humidifiers were turned off and fans were operated to circulate air at a given flowrate for more than 8 h/day over a two month period. Respiration rates were determined as rates of heat produced (W) with stability and acceptable accuracy for a relatively large facility. Respiration rates were converted to CO2 production (ml.kg-1.h-1), and these agreed fairly with ranges reported in the literature. Simultaneously, respiration rates were measured by in-store CO2 analysis, and later they were measured under laboratory conditions using a closed gas analysis system. Comparing these with rates obtained by the heat and moisture balance, the later were slightly higher. Mass losses were also obtained by both weight losses and moisture balance; results from the two methods were quite similar and comparable with those reported in the literature. / Under experimental conditions, respiration rates were measured for healthy, diseased and sprouted tubers using a gas analysis method. This experiment demonstrated the need for a more extensive investigation of disease development and its relation to respiration rates, and the need for a faster and more convenient gas analysis system. (Abstract shortened by UMI.)

Bibliography: p. 171-181. / xxiii, 181 leaves : ill. ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / The comparision of the pond and field plants suggests both species are eminently more suited to static water regime where adaptations by the plant can be made effectively to help with the problem of oxygen transport. The results also suggest that plants experience a variable and static water regime differently. / Thesis (Ph.D.), University of Adelaide, Dept. of Botany, 1999

Germination, respiration, and photosynthesis in seeds of dwarf mistletoe (Arcenthobium) were studied. The effects of 1 hour soakings of seeds in aqueous solutions of 1, 2, or 3% H2O2 or 1, 2, 3, 4, or 5% Chlorox on germination of seeds were tested. Germination rates for seeds from three consecutive years (1975-1977) were obtained. Germination rates varied widely. This variance transcended subtle changes in treatment. Pretreatment of seeds with Chlorox resulted in significantly lower germination rates than those of the control. Chlorophyll concentrations were determined for seeds and aerial shoot tissue of four species. Seeds of A. douglasii had the highest chlorophyll concentration (0.39 mg/g fresh weight) while seeds of A. tsugense had the lowest concentration (0.25 mg/g fresh weight). Net O2 uptake by seeds of A. campylopodum in dark and in light was measured by manometric and polarographic methods. The mean values were 353 μl O2 g-1 h-1 in the dark and 201 O2 g-1 h-1 in the light. The difference between these rates is apparently due to O2 evolution during photosynthesis. In light the seeds can fix 43% of the CO2 produced by respiration. Experiments in which seeds were exposed to 14CO2 in light confirmed that the seeds are able to fix CO2. Extraction of seeds with ethanol showed that 97-99% of the incorporated 14C was ethanol soluble. Ten to sixteen percent of the ethanol fraction was chloroform soluble while the rest was H2o soluble. Ion exchange separation of the H2o phase showed that 11-25% of 14C activity was cationic, 15-29% anionic, and 53-67% neutral.

No description available.

Respiration rates of developing muskmelon (Cucumis melo L.) seeds were determined polarographically using a Clark-type O₂ electrode (Hansatech LD2). Seeds were obtained from fruits harvested 20, 30, 40, and 50 days after anthesis (DAA). Respiration (O₂ uptake) was measured for fresh intact seeds and fresh dissected seeds. The respiration rate of intact seeds declined from a maximum of 2.28 μmol O₂/min/g DWT at 20 DAA to a minimum of 0.16 μmol O₂/min/g DWT at 50 DAA. Dissecting intact seeds into embryo, testae, and perisperm tissues increased the respiration rate of 20 DAA seeds to 3.12 μmol O₂/min/g DWT but had no effect on more mature seeds. Respiration rate was highly correlated with seed relative growth rate and water content. Respiration rate was not consistently changed after incubation in water. This indicates that respiration rate is not directly controlled by subtle variations in water content. Rather, seed respiration rate is directly linked with turgor-driven, expansive growth and relative growth rate. Fifty-DAA seeds from dry storage were imbibed on water saturated blotters, and respiration rates of whole seeds, decoated seeds, and embryos were compared. Respiration during imbibition was not significantly inhibited by the testae or perisperm tissue. In addition, 50-DAA dried, imbibed seeds were subjected to reduced O₂ concentrations ranging from 3.5 kPa partial pressure O₂ (pO₂) to 21 kPa pO₂. Respiration was not limited by O₂ until pO₂ was reduced to approximately 5 kPa, indicating a high affinity for O₂. Gas chromatography revealed that pO₂ in the seed cavity of muskmelon fruits ranged from 12.5 to 8 kPa. Fifty-DAA seeds from dry storage were imbibed on polyethylene glycol (PEG), mannitol, or NaCl ranging from -0.5 to -2.5 MPa water-potential or on abscisic acid (ABA) solutions ranging in concentration from 10 to 50 μM. Respiration and solution water-potential were measured at 10-hr intervals. At 10 hr of imbibition, each type of osmoticum and ABA stimulated respiration to values greater than for seeds imbibed in pure water. Beyond 10 hr, respiration rates were variable. / Master of Science