Flowering behaviour of a New Zealand mountain grass

1965 ◽  
Vol 52 (7) ◽  
pp. 167-167 ◽  
Author(s):  
A. F. Mark
1979 ◽  
Vol 27 (5) ◽  
pp. 617 ◽  
Author(s):  
DH Greer

Clone members of each of three altitudinal populations (910-1590 m) of two ecologically important snow tussocks (Chionochloa macra and C. rigida) reciprocally transplanted to four sites (10-1590 m) in 1960 were further subdivided and re-reciprocally transplanted to the same four sites in 1974 and their subsequent growth and flowering behaviour followed over two seasons. Interpopulation differences in stature and growth rates remained distinct after the 14-year intervening period, reinforcing earlier evidence for some genetic control of these characters. In contrast, the flowering of each population at each site had converged towards that of the resident plants, which indicated some adjustment to the critical threshold temperature for flowering. Interpopulation differences in flowering behaviour could not, therefore, be strictly controlled genetically as had been previously assumed. No interpopulation differences emerged as a result of 14 years of preconditioning in diverse environments. Furthermore, the preconditioning had a negligible effect on the subsequent perfor- mance of each population in a wide range of temperature environments. Distinct differences in growth rates between a lowland coastal population of C. rigida and its alpine counterparts appear adaptive, suggesting differentiation of a lowland ecotype. The high degree of physiological plasticity inherent in all populations of snow tussock studied may have its origin in the climatically diverse post-Pleistocene period when genotypes with maximum flexibility may have been selected preferentially. Since then, probably as a result of expansion of snow tussock grasslands within the last millenium, local adaptive variants have evolved.


2017 ◽  
Vol 57 (7) ◽  
pp. 1357 ◽  
Author(s):  
C. M. Wims ◽  
C. I. Ludemann ◽  
H. Phillips ◽  
D. F. Chapman

Perennial ryegrass (Lolium perenne L.) breeding efforts have focussed on improving pasture nutritive value by altering flowering behaviour and increasing ploidy. However, the gains in farm profitability that this has delivered are not known. The flowering behaviour, botanical composition and nutritive value of pastures based on 24 perennial ryegrass cultivar–endophyte combinations released in New Zealand since 1970 were compared under grazing for 3 years in the Waikato region of New Zealand. Cultivars were grouped into the following three functional groups for data analysis: mid-season-heading diploids, late- and very late-heading diploids, and late- and very late-heading tetraploids. The first of these groups included older, ‘standard’ cultivars, while the latter two groups were dominated by cultivars released since 2002. The appearance of reproductive tillers in grazed pastures was delayed by 4–8 weeks for the late- and very late-heading cultivars, resulting in pastures that maintained a greater proportion of green leaf and had a greater metabolisable energy (ME) concentration during spring. Tetraploid pastures had a greater ME concentration than did diploid pastures, largely due to the greater ME concentration of the perennial ryegrass component of these pastures. The gains in pasture nutritive value achieved by broadening the range of perennial ryegrass functional types have the potential to deliver economic benefits in the range of NZ$54/ha.year (late-heading diploids compared with mid-heading diploids) to NZ$232/ha.year (tetraploids compared with mid-heading diploids) to New Zealand dairy farmers. Potential economic gains can be diminished by changes in pasture botanical composition both over time and between functional groups.


1999 ◽  
Vol 190 ◽  
pp. 563-566
Author(s):  
J. D. Pritchard ◽  
W. Tobin ◽  
J. V. Clausen ◽  
E. F. Guinan ◽  
E. L. Fitzpatrick ◽  
...  

Our collaboration involves groups in Denmark, the U.S.A. Spain and of course New Zealand. Combining ground-based and satellite (IUEandHST) observations we aim to determine accurate and precise stellar fundamental parameters for the components of Magellanic Cloud Eclipsing Binaries as well as the distances to these systems and hence the parent galaxies themselves. This poster presents our latest progress.


Author(s):  
Ronald S. Weinstein ◽  
N. Scott McNutt

The Type I simple cold block device was described by Bullivant and Ames in 1966 and represented the product of the first successful effort to simplify the equipment required to do sophisticated freeze-cleave techniques. Bullivant, Weinstein and Someda described the Type II device which is a modification of the Type I device and was developed as a collaborative effort at the Massachusetts General Hospital and the University of Auckland, New Zealand. The modifications reduced specimen contamination and provided controlled specimen warming for heat-etching of fracture faces. We have now tested the Mass. General Hospital version of the Type II device (called the “Type II-MGH device”) on a wide variety of biological specimens and have established temperature and pressure curves for routine heat-etching with the device.


Author(s):  
Sidney D. Kobernick ◽  
Edna A. Elfont ◽  
Neddra L. Brooks

This cytochemical study was designed to investigate early metabolic changes in the aortic wall that might lead to or accompany development of atherosclerotic plaques in rabbits. The hypothesis that the primary cellular alteration leading to plaque formation might be due to changes in either carbohydrate or lipid metabolism led to histochemical studies that showed elevation of G-6-Pase in atherosclerotic plaques of rabbit aorta. This observation initiated the present investigation to determine how early in plaque formation and in which cells this change could be observed.Male New Zealand white rabbits of approximately 2000 kg consumed normal diets or diets containing 0.25 or 1.0 gm of cholesterol per day for 10, 50 and 90 days. Aortas were injected jin situ with glutaraldehyde fixative and dissected out. The plaques were identified, isolated, minced and fixed for not more than 10 minutes. Incubation and postfixation proceeded as described by Leskes and co-workers.


1998 ◽  
Vol 36 (5) ◽  
pp. 255-262
Author(s):  
SIMPANYA ◽  
JARVIS ◽  
BAXTER

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