ALBERT

Notes: The object of this study was to determine the effect of closing date and date of harvest for conservation (accumulation period), on dry-matter (DM) yield and forage quality of annual pasture in Western Australia. The field study comprised 48 plots, 2 m × 2 m, sown with either annual ryegrass (Lolium rigidum Gaud.) or Italian ryegrass (L. multiflorum Lam.), and mixed with subterranean clover (Trifolium subterraneum L.). Defoliation of swards until the end of winter was at the three leaves tiller–1 stage. In spring, once stem nodal development had commenced, swards were defoliated every 3–4 weeks. Swards were defoliated either twice with three leaves tiller–1 (accumulation period 1 commenced on 15 August); twice with three leaves tiller–1 and then once after 4 weeks (accumulation period 2 commenced on 11 September); twice with three leaves tiller–1 and then twice after 4-week intervals (accumulation period 3 commenced on 9 October) or; twice with 3 leaves tiller–1 and then twice after 4-week intervals and then once after 3 weeks (accumulation period 4 commenced on 30 October). From the commencement of the accumulation period, tiller density, DM yield and forage quality were determined weekly for up to 10 weeks.There was a positive quadratic association between DM yield and days after the commencement of the accumulation period. Yields were maximized from accumulation period 1 with 5·3, 6·6 and 9·5 t DM ha–1, and growth rates were 140, 128 and 145 kg DM ha–1 d–1, for Wimmera annual ryegrass and Richmond and Concord cultivars of Italian ryegrass respectively. In contrast, in vitro dry-matter digestibility (IVDMD) and crude protein (CP) content were negatively associated with days after the commencement of the accumulation period, and initial values were greater than 0·80 and 180 g kg DM–1 for IVDMD and CP content respectively. The rate of decline in IVDMD d–1 for Wimmera annual ryegrass was 0·005, 0·019 and 0·012 d–1 for accumulation periods 1, 2 and 3, respectively, while for Italian ryegrass cultivars Richmond was 0·015, 0·011, 0·02 and 0·012 d–1 and Concord was 0·014, 0·009, 0·013 and 0·01 d–1, for the 4 accumulation periods respectively.It is recommended that annual and Italian ryegrass pastures be harvested between 10% and 20% inflorescence emergence when IVDMD will exceed 0·70 regardless of cultivar and/or defoliation practice prior to the commencement of the accumulation period.

Notes: The effect of defoliation on the vegetative, early reproductive and inflorescence stages of tiller development, changes in the dry-matter yield of leaf, stem and inflorescence and the associated changes in forage quality was determined on plants of annual ryegrass (Lolium rigidum Gaud.) and Italian ryegrass (L. multiflorum Lam.). The field study comprised seventy-two plots of 1 m × 2 m, sown with one annual ryegrass and seven Italian ryegrass cultivars with a range of heading dates from early to late; defoliation commenced 6 weeks after germination. During the vegetative stage of growth, plots were defoliated when the tillers had three fully expanded leaves (three-leaf stage). During the early reproductive stage of growth, to simulate a cut for silage, plots were defoliated 6–7 weeks after 0·10 of the tillers displayed nodal development. The subsequent regrowth was defoliated every 3 weeks.Assessments of changes in tiller density, yield and quality were made in the growth cycle that followed three contrasting cutting treatments during the winter–spring period (from 10 July). In treatment 1, this growth cycle (following closing-up before a subsequent conservation cut) commenced on 7 August following two defoliations each taken when the tillers were at the three-leaf stage. In treatment 2, the growth cycle commenced on 16 October following: for early-maturing cultivars, two cuts at the three-leaf stage, a cut for silage and an additional regrowth cut; for medium-maturing cultivars three cuts at the three-leaf stage and a cut for silage; and late-maturing cultivars, five cuts at the three-leaf stage. In treatment 3, defoliation up to 16 October was as for treatment 2, but the growth cycle studied started on 27 November following two additional regrowth cuts for early- and medium-maturing cultivars and cut for silage for the late-maturing cultivars.Tiller development for all cultivars was classified into three stages; vegetative, early reproductive and inflorescence. In treatment 1, in vitro dry-matter digestibility (IVDMD) and crude protein (CP) content were negatively associated with maturation of tillers. IVDMD ranged from 0·85 to 0·60 and CP ranged from 200 to less than 100 g kg–1 dry matter (DM) during the vegetative and inflorescence stages respectively. This large reduction in forage quality was due to an increase in the proportion of stem, inflorescence and dead material, combined with a reduction in the IVDMD and CP content of the stem. A high level of forage quality was retained for longer with later-maturing cultivars, and/or when vegetative tillers were initiated from the defoliation of early reproductive tillers (treatments 2 and 3). However, 15 weeks after the closing-up date in treatment 1, defoliation significantly reduced the density of inflorescences with means (±pooled s.e_m.) of 1560, 1178 and 299 ± 108 tillers m–2, and DM yield of inflorescence with means of 3·0, 0·6 and 0·1 ± 0·15 t ha–1 for treatments 1, 2 and 3 respectively.This study supports the recommendation that annual and Italian ryegrass cultivars should be classified according to maturity date based on the onset of inflorescence emergence, and that the judicious defoliation of early reproductive tillers can be used to promote the initiation of new vegetative tillers which in turn will retain forage quality for longer.

Notes: Over a large part of the photoperiod, light energy absorbed by upper canopy leaves saturates photosynthesis and exceeds the energetic requirements for light-saturated linear electron flow through photosystem II (JPSII), so that photoinhibition results. From a theoretical consideration of the response of light-saturated photosynthesis to elevated atmospheric CO2 partial pressure (pCO2) it may be predicted that, where light-saturated photosynthesis is Rubisco-limited, an increase in pCO2 will stimulate JPSII. Therefore, the proportion of absorbed quanta dissipated photochemically will increase and the potential for photoinhibition of photosynthesis will decrease. This was tested by measuring modulated chlorophyll a fluorescence from Quercus myrtifolia Willd. growing in the field in open-top chambers, at either current ambient or elevated (ambient + 35 Pa) pCO2 on Merritt Island, Florida, USA. During spring and summer, light-saturated photosynthesis at current ambient pCO2 was Rubisco-limited. Consistent with theoretical prediction, JPSII was increased and photoinhibition decreased by elevated pCO2 in spring. In the summer, when growth had largely ceased, an acclimatory decrease in the maximum Ribulose 1,5 bisphosphate saturated carboxylation capacity (Vc max) removed the stimulation of JPSII seen in the spring, and photoinhibition was increased in elevated pCO2. It is concluded that, for Q. myrtifolia growing in the field, the effects of elevated pCO2 on JPSII and photoinhibition will reflect seasonal differences in photosynthetic acclimation to elevated pCO2 in a predictable manner.

Notes: For most studies involving the response of plants to future concentrations of atmospheric carbon dioxide (CO2), a current concentration of 360–370 μatm is assumed, based on recent data obtained from the Mauna Loa observatory. In the present study, average seasonal diurnal values of ambient CO2 obtained at ground level from three global locations (Australia, Japan and the USA) indicated that the average CO2 (at canopy height) can vary from over 500 μatm at night to 350 μatm during the day with average 24-h values ranging from 390 to 465 μatm. At all sites sampled, ambient CO2 rose to a maximum value during the pre-dawn period (03.00–06.00 hours); at sunrise, CO2 remained elevated for several hours before declining to a steady-state concentration between 350 and 400 μatm by mid-morning (08.00–10.00 hours). Responses of plant growth to simulations of the observed variation of in situ CO2 were compared to growth at a constant CO2 concentration in controlled environment chambers. Three diurnal patterns were used (constant 370 μatm CO2, constant 370 during the day (07.00–19.00 hours), high CO2 (500 μatm) at night; or, high CO2 (500 μatm) at night and during the early morning (07.00–09.00 hours) decreasing to 370 μatm by 10.00 hours). Three plant species − soybean (Glycine max, L (Merr.), velvetleaf (Abutilon theophrasti L.) and tomato (Lycopersicon esculentum L.) − were grown in each of these environments. For soybean, high night-time CO2 resulted in a significant increase in net assimilation rate (NAR), plant growth, leaf area and biomass relative to a constant ambient value of CO2 by 29 days after sowing. Significant increases in NAR for all three species, and significant increases in leaf area, growth and total biomass for two of the three C3 species tested (velvetleaf and soybean) were also observed after 29 days post sowing for the high night/early morning diurnal pattern of CO2. Data from these experiments suggest that the ambient CO2 concentration experienced by some plants is higher than the Mauna Loa average, and that growth of some agricultural species at in situ CO2 levels can differ significantly from the constant CO2 value used as a control in many CO2 experiments. This suggests that a reassessment of control conditions used to quantify the response of plants to future, elevated CO2 may be required.

Notes: The purpose of this study was to test for direct inhibition of rice canopy apparent respiration by elevated atmospheric carbon dioxide concentration ([CO2]) across a range of short-term air temperature treatments. Rice (cv. IR-72) was grown in eight naturally sunlit, semiclosed, plant growth chambers at daytime [CO2] treatments of 350 and 700 μmol mol−1. Short-term night-time air temperature treatments ranged from 21 to 40 °C. Whole canopy respiration, expressed on a ground area basis (Rd), was measured at night by periodically venting the chambers with ambient air. This night-time chamber venting and resealing procedure produced a range of increasing chamber [CO2] which we used to test for potential inhibitory effects of rising [CO2] on Rd. A nitrous oxide leak detection system was used to correct Rd measurements for chamber leakage rate (L) and also to determine if apparent reductions in night-time Rd with rising [CO2] could be completely accounted for by L. The L was affected by both CO2 concentration gradient between the chamber and ambient air and the inherent leakiness of each individual chamber. Nevertheless, after correcting Rd for L, we detected a rapid and reversible, direct inhibition of Rd with rising chamber [CO2] for air temperatures above 21 °C. This effect was larger for the 350 compared with the 700 μmol mol−1 daytime [CO2] treatment and was also increased with increasing short-term air temperature treatments. However, little difference in Rd was found between the two daytime [CO2] treatments when night-time [CO2] was at the respective daytime [CO2]. These results suggest that naturally occurring diurnal changes in both ambient [CO2] and air temperature can affect Rd. Because naturally occurring diurnal changes in both [CO2] and air temperature can be expected in a future higher CO2 world, short-term direct effects of these environmental variables on rice Rd can also be expected.

Notes: Borrelia hermsii, a spirochaete responsible for relapsing fever in humans, grows to high density in the bloodstream and causes thrombocytopenia. We show here that B. hermsii binds to human platelets. Extended culture in bacteriological medium resulted in both diminished infectivity in vivo and diminished platelet binding in vitro. Platelet binding was promoted by the platelet integrin αIIbβ3: the bacterium bound to purified integrin αIIbβ3, and bacterial binding to platelets was diminished by αIIbβ3 antagonists or by a genetic defect in this integrin. Integrin αIIbβ3 undergoes a conformational change upon platelet activation, and bacteria bound more efficiently to activated rather than resting platelets. Nevertheless, B. hermsii bound at detectable levels to preparations of resting platelets. The bacterium did not recognize a point mutant of αIIbβ3 that cannot acquire an active conformation. Rather, B. hermsii was capable of triggering platelet and integrin αIIbβ3 activation, as indicated by the expression of the platelet activation marker P-selectin and integrin αIIbβ3 in its active conformation. The degree of platelet activation varied depending upon bacterial strain and growth conditions. Prostacyclin I2, an inhibitor of platelet activation, diminished bacterial attachment, indicating that activation enhanced bacterial binding. Thus, B. hermsii signals the host cell to activate a critical receptor for the bacterium, thereby promoting high-level bacterial attachment.

Notes: Sex is an obligate step in the life cycle of the malaria parasite and occurs in the midgut of the mosquito vector. With both Plasmodium falciparum and Plasmodium berghei, the tryptophan metabolite xanthurenic acid induces the release of motile male gametes from red blood cells (exflagellation), a prerequisite for fertilization. The addition of cGMP or phosphodiesterase inhibitors to cultures of mature gametocytes has also been shown to stimulate exflagellation. Here, we demonstrate that there is a guanylyl cyclase activity associated with mature P. falciparum gametocyte membrane preparations, which is dependent on the presence of Mg2+/Mn2+ but is inhibited by Ca2+. Significantly, this activity is increased on addition of xanthurenic acid. In contrast, a xanthurenic acid precursor (3-hydroxykynurenine), which is not an inducer of exflagellation, does not induce this guanylyl cyclase activity. These results therefore suggest that xanthurenic acid-induced exflagellation may be mediated by activation of the parasite cGMP signalling pathway.