Mj. Hedley et Ns. Bolan, DEVELOPMENTS IN SOME ASPECTS OF REACTIVE PHOSPHATE ROCK RESEARCH AND USE IN NEW-ZEALAND, Australian journal of experimental agriculture, 37(8), 1997, pp. 861-884
There has been over 50 years of use and research into the agronomic ef
fectiveness of reactive phosphate rocks (RPR) directly applied to New
Zealand pastures. In recent years RPR-carrying fertilisers made up abo
ut 16% of phosphatic fertiliser sales in the North Island of New Zeala
nd. Most is applied, as maintenance fertiliser, to hill country sheep
and beef farms. Use has been recommended on soils with pH <6 and in an
nual rainfall regimes >800 mm. This is based on the poor performance o
f Sechura phosphate rock in summer dry areas receiving <750 mm of rain
fall annually. Phosphate rocks that have more than 30% of their total
phosphate soluble in 2% citric acid have been classed as 'reactive' an
d suitable for direct application. More recent research indicates that
extraction with 2% formic acid, or a dissolution test performed in a
simulated soil solution at a fixed pH, will provide improved measures
of RPR quality. Field trials, undertaken by the New Zealand Ministry o
f Agriculture and Fisheries [MAF; now AgResearch Crown Research Instit
ute (CRI)] and others, to evaluate the relative agronomic effectivenes
s of RPR versus soluble P fertilisers in adequate to marginally P-defi
cient soils have proven to be a painstaking task. Long periods (3-6 ye
ars) of fertiliser withdrawal were required for pasture growth on some
soils to become significantly responsive to applied P. Only then did
differences between P sources become significant. This problem has enc
ouraged efforts to relate measurements of the extent of RPR dissolutio
n in soils to their agronomic effectiveness. Three main modelling appr
oaches have been used to achieve this objective: Kirk and Nye (1986a,
1986b, 1986c); Sinclair et al. (1993a); and Watkinson (1994b). These m
odels are reviewed and their explanation of RPR dissolution in mowing
trials tested. Components of each model have then been combined to pro
duce models to predict the agronomic effectiveness of RPR. The develop
ment of P tests for soils receiving RPR-containing fertilisers is revi
ewed. Separate Olsen P test-yield response calibration curves are requ
ired for soils fertilised with soluble P fertilisers and soils fertili
sed with sparingly soluble P sources or soluble P in the presence of h
eavy lime applications. Whereas alkaline P tests such as Olsen or Colw
ell underestimate the amount of plant-available P in these soils, acid
P tests such as Bray I are likely to overestimate the available P. Te
sts involving cation and anion exchange resin membranes appear to be m
ore appropriate for soils with unknown histories of soluble P and RPR
use and may permit the use of single calibration curves. Trends observ
ed in Olsen P soil test values, from farms on the North Island of New
Zealand that have a history (3-15 years) of RPR use are presented. A p
redictive dissolution model is used to explain these trends but it is
evident that spatial and temporal variation in soil test results on fa
rmers' paddocks will be a major constraint to the precision to which t
his or similar models may be used. The model, however, may provide the
basis for sound advice on the strategic use of RPR for direct applica
tion to New Zealand pasture soils. It may prove useful in explaining t
he variation in RPR effectiveness in a wider range of climates and soi
ls.