To cite this article: J. M. De Ruiter (1999) Yield and quality of malting barley (Hordeum vulgare
L. Valetta') in response to irrigation and nitrogen fertilisation, New Zealand Journal of Crop and
Horticultural Science, 27:4, 307-317, DOI: 10.1080/01140671.1999.9514110
To link to this article: http://dx.doi.org/10.1080/01140671.1999.9514110
New Zealand Journal of Crop and Horticultural Science, 1999, Vol. 27: 307-317
0014-0671/99/2704-0307
$7.00 The Royal Society of New Zealand 1999
307
J. M. DE RUITER
New Zealand Institute for Crop & Food
Research Limited
Canterbury Agricultural Science Centre
Private Bag 4704
Christchurch, New Zealand
email: deruiterj@crop.cri.nz
H99011
Received 4 March 1999; accepted 15 October 1999
INTRODUCTION
Consistency of grain quality is important in the
malting industry. Batches of seed with comparable
germination characteristics are desirable so that
adjustments can be made during malting to reduce
the impact of variable or substandard grain. Ideal
grain has a high mean weight (>40 g/1000 kernels)
with nitrogen (N) concentrations between 1.5 and
1.95%. Variation in grain quality can occur between
seasons and within farms as a result of paddock
management or local environmental effects. N
fertiliser and irrigation are the only practical ways
for growers to manage the quality of grain. Variation
in protein quality, (D-hordein composition), for
example, has been shown to vary according to N
fertiliser treatment and cultivar (Howard et al. 1996),
and this variation may be best accounted for by
available water/available N ratios early in growth
(Dalai et al. 1997). Variable grain size and N content
may also have deleterious effects on the quality of
malted grain for brewing. Heterogeneous malt
occurs when modification (degree of breakdown of
endosperm structure) in individual kernels proceeds
at different rates or when individual kernels are
undermodified (Edney 1996). Processing difficulties
may be averted by appropriate crop management in
308
309
Plant measurements
Yield components
Crop grain yield was determined on 1 m2 duplicate
samples from each plot at maturity. Grain was
threshed using a Kurt Pelz stationary thresher and
representative 250 g subsamples saved for thousand
grain weight analysis and kernel size distribution.
Total above ground biomass was determined on
0.1 m2 (2 rows x 33.3 cm row) quadrats at weekly
intervals beginning 3 weeks after emergence. All
plant material was dried in a forced-draught oven at
80C for 48 h before weighing.
Grain size distribution (main stems and tillers)
Permanent 0.1 m2 quadrats were located in all plots
and five plants were selected with main stems
identified during early stem elongation. Individual
kernels at known spike positions for main stem and
tiller ears were weighed and the distribution pattern
along the rachis was determined for each floret
position from base to spike tip. Remaining kernels
in the quadrat were passed over a set of screens to
determine the overall mean weight distribution in six
size classesthree above and three below the
standard screen dimensions (2.36 mm). In addition,
the size distribution was verified on samples from
the 1 m2 yield harvest. Three independent
subsamples of grain (100 g each) were analysed for
each plot and passed over the standard screens with
slot dimensions of <2.00, >2.00, >2.10, >2.36, >2.50,
and >2.76 mm, respectively for the standard size
classes of <5.0, >5.0, >5.5, >6, >6.5, and >7.
Grain quality
Grain subsamples from 1 m2 quadrats were prepared
for N analysis by grinding in a Cyclotec 1095 mill
(1 mm screen). N concentration was determined by
micro-Kjeldahl analysis on oven-dry samples. Grain
was dressed and sieved over a standard 6A screen
(2.36 mm slot) in preparation for malt analysis.
Grain not passing the screen was micro-malted according to Haslemore et al. (1985). Malt samples
were mashed by a modified IoB procedure (Slack et
al. 1986). Wort p-glucan concentration was determined on the mashing liquor by a FIA-calcofluor
procedure (Haslemore et al. 1990). Derived indicators of maltability were % fine extract, % coarse
extract, and fine-coarse difference. Physical indicators of grain modification of grain during steeping
was determined by % water uptake and malting loss
(calculated as the percent dry matter loss before kilning). A N index, indicating the relative lability of
310
nitrogenous components during malting, was determined as the proportion of the grain N remaining in
the mashing liquor relative to the concentration in
the grain sample. N index is indicative of the potential N solubility in the grain sample for malting but
it also depends on the initial amount of grain protein, and the degree of modification through proteolytic activity during malting.
Uniformity trial and statistical analysis
The positioning of the rain shelter cover meant that
water treatments were not fully randomised across
the trial area. Therefore, variance components for all
variables within and outside the shelter were tested
to determine: (1) whether above ground effects as a
result of rain shelter position were significant; and
(2) if there was a systematic pattern in pre-sowing
soil NO3 levels that could be used as a covariate to
test fertiliser responses.
A uniformity trial was conducted on 25
September to determine NO3-N levels by sampling
soil to a depth of 20 cm in a 2 x 3 m centre grid
pattern within the rain shelter. Sampling was
repeated both inside and outside the shelter on 4
October. Soil nitrate was determined by water
extraction followed by direct measurement with a
nitrate electrode using a known-addition method.
The electrode response was calibrated with known
standards in aqueous solutions. These extracts were
RESULTS
Uniformity analysis
There were no systematic trends in soil nitrate-N (020 cm depth) concentrations within the rain shelter
on the first sampling date (mean 3.0 1.0 kg/ha). In
a second sampling, 1 week later, inside- and outsideshelter effects were also found to be not significant.
Soil N (nitrate extracted in water) to a depth 20 cm
Table 1 Soil fertility variables for 20 cm layers sampled on 16 October in the rain shelter. Nitrate and ammonium
were extracted in 2M KC1.
Depth
(cm)
Microbial
biomass C
(ugC/g)
Microbial
biomass N
(UgN/g)
Organic C
(%)
Total N
(%)
Nitrate
(HgN/g)
Ammonium
(HgN/g)
0-20
20-40
40-60
265
234
213
29.8
15.4
3.3
2.4
1.3
0.6
0.20
7.4
4.3
2.7
5.2
5.8
5.3
Table 2 Mean rainfall, irrigation, and calculated crop water use for {Hordeum vulgare ' Valetta')
in drought treatments, from 15 November to maturity (defined as time at disappearance of green
stem and attainment of stable kernel weight).
Treatment
Full drought
Early drought
Late drought
Rain-fed
Irrigated
Rain (mm)
Irrigation (mm)
17
17
17
62.1
89.3
17
260.5
68.6
5.1
291.6
124.4
241.1
186.2
150.5
345.1
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Table 3 Grain yield, yield component, and grain nitrogen (N) concentration for barley (Hordeum vulgare 'Valetta')
for drought and N treatment means. All measurements were made on 24 January (89 days after emergence). (TKW =
thousand kernel weight.)
Treatment
Drought treatment
Full drought
Early drought
Late drought
Rain-fed
Irrigated
Biomass
(t/ha)
Grain yield
(t/ha)
Grain number
per m2
TKW
(g/1000)
Grain N
(%)
LSD(P<0.05);d.f.=19
8.6
10.8
8.9
7.5
12.0
1.3
4.1
4.9
5.1
3.9
5.7
0.60
10 954
11 258
12 651
9 487
13 160
1 386
37.2
43.4
37.7
40.7
43.8
2.02
1.62
1.64
1.54
1.66
1.64
0.1 OX
Nitrogen treatment
ON
1 x50
2x50
3x50
LSD(P<0.05);d.f.=19
6.9
9.1
11.6
10.8
1.2
3.7
4.5
5.1
5.4
0.53
9 294
10 853
12 631
13 231
1 240
40.1
41.2
40.1
40.9
1.81
1.39
1.58
1.65
1.87
0.09(-
312
10
15
20
Kernel position
25
10
15
20
Kernel position
25
10
Fig. 1 Mean kernel weight of malting barley {Hordeum vulgare 'Valetta') at the indicated positions from the rachis
base for: A, main stem ( = full drought, A = early drought, = late drought, = rain-fed, and O = fully irrigated);
and B, tiller ears.
kernel weight only explained 18% of the yield
variation. A significant proportion of this variation
could be accounted for by water treatment effects
(Table 3). Full drought and late drought significantly
reduced grain size compared to treatments with less
water stress late in the season.
Grain number/m2 ranged from 7312 (rain-fed, 0
N) to 15 896 for the fully irrigated high N treatment
(data not shown). N and water interactions were not
significant (P > 0.05). N treatment significantly
affected grain number in all water treatments (Table
3). The effect of N was particularly strong when
water was in good supply (fully irrigated and early
drought treatment). Differences between the early
and late drought treatments were only apparent in
low N treatments. Therefore, the effect of water
stress on floret set only occurred when N was
limiting.
Kernel weight
The maximum kernel weight was achieved in all
water treatments by 40 days after anthesis. N effects
on the pattern of grain size development were
minimal but the responses to water treatment were
more pronounced. The pattern of kernel mass along
the axis of the main stems (Fig. 1 A) and tillers (Fig.
IB) showed consistent responses to drought
treatment. The early drought and fully irrigated
treatments showed similar patterns, and late drought/
rain-fed/full drought treatments were also similar.
Kernel weights were progressively smaller from
kernel position 10 to the spike tip, with the smallest
grains occurring at the basipetal end of the spike. The
range of kernel weight/spike on the main stem was
1.18-1.42 gcomparedwithO.77-0.98 g/tillerspike.
<5.0
>5.0
>5
313
>5.0
>5.0
>7
Fig. 2 Cumulative kernel weight distributions for malting barley (Hordeum vulgare 'Valetta') at maturity for: A,
nitrogen (N) treatment means ( = 0 N (control), A = 50 kg N/ha, = 2 x 50 kg N/ha, and = 3 x 50 kg N/ha); and
B, drought treatment; means ( = full drought, = early drought, = late drought, = rain-fed, and O = fully
irrigated). Least significant difference (5%) between means are only shown for significant treatment effects.
500
<D
100
150
Fig. 3 Relationships indicating responses for malting barley (Hordeum vulgare 'Valetta') to total applied nitrogen
(N) fertiliser and water treatments for: A, wort (3-glucan; B, wort N; and C, N index. Water treatments A-E are: =
full drought, = early drought, = late drought, D = rain-fed, and O = fully irrigated respectively. R2 = coefficient
of determination for regression.
Grain nitrogen
All grain was within accepted specification (<2% N)
for malting even in the high fertiliser N treatments,
(Table 3). Grain N concentrations varied from 1.39
to 1.85%. The effect of level of N application was
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Wort /3-glucan
Treatments that favoured a shortened grain filling
period (Treatments A and C: Fig. 3A) had the highest
levels of wort P-glucan. Wort (3-glucan contents
were high in the full drought (A) and late drought
treatments (C), and low in the rain-fed (D) and fully
irrigated treatments (E) (Fig. 3A).
Nitrogen index
Nitrogen solubility index (N index) was the only
malting quality variable with a significant water and
N interaction (Table 4). A statistical model
incorporating the interactive effects of water and N
was strongly significant and accounted for 88% of
the variation in N index (Figure 3B). Wort P-glucan
and wort N levels were also significantly influenced
by N and water treatment, but the interaction was not
significant.
High N application in the fully irrigated treatment
had the ideal N index, whereas in all other water
treatments the ideal N index values occurred at lower
N application rates. An exception occurred in the full
drought treatment in which N index values were less
than optimal regardless of N application.
There were few consistent trends in the fine and
coarse extract levels. However, the extent of modification, as indicated by the fine-coarse difference
values, showed that timing of drought effects was
significant (Table 4). There was a significant linear
Table 4 Water and nitrogen (N) effects on barley (Hordeum vulgare 'Valetta') malt quality variables and indicators
of malt modification (WULin = linear response to seasonal crop water use; N Lin = linear response to total N fertiliser
applied; the N lin x water interaction for N index was significant at P < 0.01; NS = not significant).
Treatment effects
Uptake (%)
Malting loss (%)
Grain N (%)
Wort (3-glucan (mg/litre)
Wort N (%)
N index
Fine (F) extract (%)
Coarse (C) extract (%)
F/C difference (%)
Water, WULin
N, NLin.
Water x N
NS,NS,0.001, P<
0.001, P<
0.001, P<
0.001, P<
NS,NS,NS,-
NS
P<0.05
NS
NS
NS
P < 0.05/NS
NS
NS
NS
P<
P<
P<
P<
0.001
0.001
0.001
0.001
315
WortN
Wort N levels are indicative of high levels of
solubilised protein during mashing. While it is
desirable to have moderate levels of amino N and
soluble protein for yeast metabolism, excessive
levels are generally detrimental to quality. There
were significant responses of wort N content to N
fertiliser in water treatments that imposed late stress
on the crops. In these situations, N treatment may
result in higher levels of non-protein N in the wort,
which is generally considered detrimental to quality.
316
Nitrogen index
Higher N applications tended to decrease the solubility index (residual N in the wort relative to premalted N content). A high level of N remaining in
the wort is indicative of high levels of metabolised
cell wall protein or high levels of non-protein N
(amino and inorganic N). N resisting hydrolysis
during malting has significant effects on quality of
malt for further processing. A measure of N level in
the wort in relation to the initial concentration of N
in the grain provides a useful indicator of substandard malt. N indices around 40% are generally acceptable but lower values are preferable and are
indicative of improved quality. Wort-N concentration generally increased with fertiliser N application
and the N index showed a marked decline. Fertiliser
N application had a probable effect on the soluble
protein and non-protein N levels.
Under conditions of heat stress, higher protein
modification has been observed compared to controls (Savin et al. 1997b), indicating greater lability
of protein during malting. Free amino N in the wort
was not quantified in our experiment. However,
Savin et al. (1997b) suggest that stress during grain
filling increases wort amino N and reduces the N
index value. This is a result consistent with the
present study, given the reduced index values in the
late (grain filling) water stress treatment.
CONCLUSIONS
Nitrogen fertiliser level had a strong influence on the
N content of grain although no treatment caused N
concentrations that would have resulted in reject
quality (>2%) grain. This occurred irrespective of the
soil water status during growth. Grain quality was
acceptable for malting on the basis of N content even
in the high N treatments and with drought during
grain filling. This suggested that the crops were not
stressed to a point where grain size development was
severely restricted. Kernel size was not influenced
by N treatment however drought did influence the
patter of size distribution in main stem and tiller ears.
Water and N treatment had significant effects on
the N index values, a result that was significant in
terms of management for optimum quality. The
interaction of water and N treatment was significant
for N index, whereas the main effects alone were
significant for N and water treatment for the wort
quality indicators (P-glucan and wort N). N
application tended to exacerbate the levels of Pglucan and wort N thereby producing poorer quality
ACKNOWLEDGMENTS
I thank Richard Gillespie for managing the irrigation
treatments in the rain shelter. The assistance of Daniel
Coe, Craig Davies, Rachel Munro, Maryann Robson, and
Sarah Sinton with data collection is much appreciated.
This work was funded by the New Zealand Foundation
for Research, Science and Technology.
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