Photosynthetic gas exchange and the stable isotope composition of leaf water: comparison of a xylem-tapping mistletoe and its host

Photosynthetic gas exchange and the stable isotopic composition of foliage water were measured for a xylem tapping mistletoe, Phoradendron juniperinum, and its host tree, Juniperus osteosperma, growing in southern Utah. The observed isotopic composition of water extracted from foliage was compared to predictions of the Craig-Gordon model of isotopic enrichment at evaporative sites within leaves. Assimilation rates of juniper were higher and stomatal conductance was lower than the values observed for the mistletoe. This resulted in lower intercellular/ ambient CO₂ values in the juniper tree relative to its mistletoe parasite. For mistletoe, the observed foliage water hydrogen and oxygen isotopic enrichment was less than that predicted by the model. In juniper, foliage water hydrogen isotopic enrichment was also lower than that predicted by the evaporative enrichment model. In contrast, the oxygen isotopic enrichment in juniper foliage water was slightly greater than that predicted for the evaporative sites within leaves. Hydrogen isotopic enrichment in mistletoe foliage shows systematic variation with stem segment, being highest near the tips of the youngest stems and decreasing toward the base of the mistletoe, where isotopic composition is close to that of stem water in the host tree. In a correlated pattern, mid-day stomatal conductance declined abruptly in mistletoe foliage of increasing age.     

The osmoregulatory role of the filter-chamber in relation to phloem-feeding in Eurymela distincta (Cicadelloidea, Homoptera)

ABSTRACT. The cicadelloid leaf-hoppers, Eurymela distincta (Signoret) and Eurymela fenestrata (Le Pelletier & Serville), feed on the phloem sap of Eucalyptus spp. The osmotic pressure profile of haemolymph and gut fluids is consistent with a filtration mechanism based on passive osmosis. This is responsible for shunting water rapidly from foregut to hindgut in the relatively simple filter chamber. The osmotic gradient which drives the system is probably produced by active secretion of sodium and potassium into the Malpighian tubules and posterior midgut. Although the osmotic pressures in all parts of the system are higher, the mechanism is probably similar to that previously described for xylem-feeding cicadas.
The major haemolymph cations are sodium and magnesium and the concentrations of sodium and magnesium in the urine are higher than potassium. A variety of storage granules in the midgut contain calcium, phosphorus (as phosphate), ferric iron, zinc, magnesium, manganese and copper.     

The Effect of Temperature on the Initiation of Leaf Primordia in Developing Potato Sprouts

Kirk, W W., Davies, H. V. and Marshall, B. 1985. The effectof temperature on the initiation of leaf primordia in developingpotato sprouts.—J. exp. Bot. 36: 1634–1643. Initiation of leaf primordia in potato sprouted out of soilin light was an asymptotic function of thermal time and thebase temperature for the process was 3.6 °C. The parametervalues of the asymptotic function were universal for cv. MarisPiper. The estimated rate of leaf primordium initiation decreasedlinearly from 0.033 leaf pnmordia (K day)^–1 when abouteight leaf primordia were present to zero after a maximum numberof 24 leaf primordia had been initiated. The decrease in rateof development with increasing number of primordia may be dueto depletion of mother tuber resources. The transition of theapex from a vegetative to a reproductive state was not the factorlimiting the initiation of additional leaf primordia. Key words: Potato, Solanum tuberosum L., leaf primordia initiation, temperature, thermal time, development     

Ovule abortion in white clover (Trifolium repens L.)

Plants of white clover ( Trifolium repens L.) cv. Olwen were grown in an open glasshouse maintained at a mean temperature of 20^oC and ovule growth and seed production measured. Differences in the rate of growth of ovules within ovaries were observed as early as 2 days after pollination. Ovules reached a maximum size after 8 days with the smallest only half the size of the largest. After 8 days, the smallest ovules became flaccid and shrivelled. Ovule position within the ovary had little effect on the frequency of seed set and although there was an apparently higher probability that central ovules produced a seed than those nearer the peduncle or style this was not statistically significant. Inflorescence position and floret position on the inflorescence had a significant effect on the number of seeds per floret and seed weight; the first formed inflorescences and the first florets to be pollinated on each inflorescence had more seeds per floret and heavier seeds and fewer florets with no seed than later pollinated florets. There were also differences between florets within the same whorl. The role of a number of factors which may influence floret site utilisation are discussed.