Some factors affecting the extraction of soil 'available' phosphate

Soil Research ◽  
1978 ◽  
Vol 16 (3) ◽  
pp. 355
Author(s):  
GD Batten

Twenty soils from southern New South Wales were analysed for acid extractable phosphate in 1971, and again in 1977 when it was found that an increase had occurred. These same samples were also analysed using reciprocating shakers with different distances of travel. More phosphate was extracted when a shaker with a greater distance of travel was used and when more soil, but at the same soil : solution ratio, was placed in a large vessel. It is suggested that such variations in technique contribute to inter-laboratory error in soil tests for phosphate.

1981 ◽  
Vol 21 (108) ◽  
pp. 68
Author(s):  
E Seif ◽  
LN Balaam

The analysis of wheat protein data from ten homozygous genotypes grown at six locations in 4 years gave a heritability estimate of 50%, and another of 65% from a sub-set of genotypes of similar maturity. The first-order interactions, genotype x year and genotype x location, were small and nonsignificant. An examination of the variance of a genotype mean indicated that selection in regional testing programs could be based on data from as few as three trials. Laboratory error represented a large proportion of this variance, thus more than one laboratory determination will be necessary.


1997 ◽  
Vol 37 (4) ◽  
pp. 439 ◽  
Author(s):  
T. S. Andrews ◽  
C. E. Jones ◽  
R. D. B. Whalley

Summary. Four experiments were conducted to determine the effects of temperature, light and leaf extract solutions on the germination of Giant Parramatta grass [GPG, Sporobolus indicus (L.) R. Br. var. major (Buse) Baaijens] collected from a population on the North Coast of New South Wales. In the first experiment, seeds were subjected to one of a range of temperature combinations immediately after collection and again after 8 and 27 weeks. Germination was restricted to a narrow range of alternating temperatures with a peak at 35°C day/15°C night when seeds were tested immediately after collection. More seeds germinated when the samples had been stored, although germination remained depressed at constant temperatures. These data indicate that freshly collected GPG seeds are subject to primary dormancy and that few would germinate in the field immediately after seed fall. In a second experiment, seeds were buried beneath leaf litter in a pasture immediately after collection. After 7 months, the seeds were exhumed and subjected to either constant (20°C) or alternating (35/15°C) temperatures in either full light, reduced red:far-red (R : FR) light or dark treatments. Over 95% of GPG seeds germinated when subjected to alternating temperatures, regardless of light treatment. At constant temperatures, 97% of seeds germinated under full light, 59% at reduced R : FR light and <1% in dark treatments. A germination response to alternating temperatures and/or light treatments has been reported in pasture weeds and may be an adaptation to detecting gaps in the pasture canopy. Consequently, the germination of GPG in a pasture may be manipulated to some extent by altering the amount of pasture cover using grazing management, mowing and fertiliser applications. In experiment 3, leaves from a range of coastal grasses were mixed with water and the solutions were used to germinate GPG seeds. Solutions extracted from setaria (Setaria sphacelata) leaves completely inhibited GPG germination while 27% of GPG seeds germinated when imbibed with kikuyu leaf extract solution. Solution extracted from carpet grass (Axonopus affinis) leaves had the least effect on GPG germination. In experiment 4, the effects of solutions that had been leached from the leaves of either setaria or carpet grass on seed germination, and root and shoot lengths of GPG seedlings were compared. Germination was less inhibited by leachate solutions compared with the extract solutions used in experiment 3. Seedlings in setaria leachates had significantly shorter roots and shoots than both those germinated in carpet grass leachates and control seedlings. This may explain, at least in part, why carpet-grass-based pastures are readily infested with GPG while setaria-based pastures are relatively resistant to infestation. The potential for allelopathic interactions between GPG and setaria to be fully utilised to reduce the abundance of GPG in coastal New South Wales pastures is discussed.


1965 ◽  
Vol 13 (1) ◽  
pp. 47 ◽  
Author(s):  
TW Hogan

Migratory swarms of Chortoicetes terminifera established egg beds in New South Wales, South Australia, and Victoria during the autumn of 1955. Samples of eggs were taken from a number of districts in New South Wales and Victoria during the winter and the mortality rate was determined. Scelio fulgidus was the only parasite present but it was very widespread with a median percentage parasitization of 5%. Mortality from other causes had a median of 39%. Winter rainfall during 1955 was considerably above average and in some situations waterlogging of the soil in which the eggs were laid may have been one of the factors affecting survival. Low temperature seems more likely to have been the factor of importance at the higher altitudes in north-eastern Victoria where hatching was particularly poor.


1995 ◽  
Vol 17 (1) ◽  
pp. 37 ◽  
Author(s):  
MH Campbell ◽  
AM Bowman ◽  
WD Bellotti ◽  
JJ Friend ◽  
HI Nicol

In four experiments near Walgett, New South Wales, between 1987 and 1990, the establishment and survival of Astrebla lappacea, Setaria incrassata, Panicurn coloraturn var. rnakarikariense and Cenchrus ciliaris were determined when surface-sown into low, reduced or heavy stubble just before or after harvesting wheat (November or December). Despite external deleterious factors affecting three experiments, grasses established in the first six months after sowing in all experiments unde; above average rainfall. Best establishment (8 to 31 plants/m2 in the 1990 experiment) occurred in response to 166 mm in 12 rain days over a 29 day period in December-January 1990-91, followed by 10 dry days and then a further 60 mm of rain in February; plants flowered by May and thus survived winter well. Under non-flood conditions (1987, 1988 and 1990 experiments) the order of magnitude of establishment was: C. ciliaris, A. lappacea > S. incrassata > P. coloraturn. Under flood conditions (1989 experiment) establishment of S. incrassata was highest and that of A. lappacca was lowest. In the 1987 and 1988 experiments full stubble (1.5 and 3.4 t/ha) did not improve the establishment of surface-sown grasses over that on low stubble (0.1 and 1.4 tlha). In the 1989 and 1990 experiments establishment was lower on full stubble (5 and 7 tlha) than on low stubble (0.1 and 0.1 tlha) owing to, respectively, flooding and competition from volunteer wheat. After the six months establishment period grass density declined over the two to five year survival period with plants self- thinning due to interspecific competition. Allowing mature plants to seed increased plant density due to seedling recruitment under favourable climatic conditions.


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