An evaluation of Solanum nigrum and S. physalifolium biology and management strategies to reduce nightshade fruit contamination of process pea crops
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Authors
Date
2004
Type
Thesis
Fields of Research
Abstract
The contamination of process pea (Pisum sativum L.) crops by the immature fruit of
black nightshade (Solanum nigrum L.) and hairy nightshade (S. physalifolium Rusby
var. nitidibaccatum (Bitter.) Edmonds) causes income losses to pea farmers in
Canterbury, New Zealand. This thesis investigates the questions of whether seed
dormancy, germination requirements, plant growth, reproductive phenology, or fruit
growth of either nightshade species reveal specific management practices that could
reduce the contamination of process peas by the fruit of these two weeds.
The seed dormancy status of these weeds indicated that both species are
capable of germinating to high levels (> 90%) throughout the pea sowing season when
tested at an optimum germination temperature of 20/30 °C (16/8 h). However, light
was required at this temperature regime to obtain maximum germination of S. nigrum.
The levels of germination in the dark at 20/30 °C and at 5/20 °C, and in light at 5/20 °C,
and day to 50 % germination analyses indicated that this species cycled from nondormancy
to conditional dormancy throughout the period of investigation (July to
December 2002). For S. physalifolium, light was not a germination requirement, and
dormancy inhibited germination at 5/20 °C early in the pea sowing season (July and
August). However, by October, 100% of the population was non-dormant at this test
temperature. Two field trials showed that dark cultivation did not reduce the
germination of either species.
Growth trials with S. nigrum and S. physalifolium indicated that S. physalifolium,
in a non-competitive environment, accumulated dry matter at a faster rate than
S. nigrum. However, when the two species were grown with peas there was no
difference in dry matter accumulation. Investigation of the flowering phenology and
fruit growth of both species showed that S. physalifolium flowered (509 °Cd, base
temperature (Tb) 6 °C) approximately 120 °Cd prior to S. nigrum (633 °Cd). The fruit
growth rate of S. nigrum (0.62 mm/d) was significantly faster than the growth rate of
S. physalifolium (0.36 mm/d). Because of the earlier flowering of S. physalifolium it
was estimated that for seedlings of both species emerging on the same date that
S. physalifolium could produce a fruit with a maximum diameter of 3 mm ~ 60 °Cd
before S. nigrum.
Overlaps in flowering between peas and nightshade were examined in four pea
cultivars, of varying time to maturity, sown on six dates. Solanum physalifolium had the
potential to contaminate more pea crops than S. nigrum. In particular, late sown peas
were more prone to nightshade contamination, especially late sowings using mid to
long duration pea cultivars (777-839 °Cd, Tb 4.5 °C). This comparison was supported
by factory data, which indicated that contamination of crops sown in October and
November was more common than in crops sown in August and September. Also,
cultivars sown in the later two months had an ~ 100 °Cd greater maturity value than
cultivars sown in August and September. Nightshade flowering and pea maturity
comparisons indicated that the use of the thermal time values for the flowering of
S. nigrum and S. physalifolium can be used to calculate the necessary weed free
period required from pea sowing in order to prevent the flowering of these species.
The earlier flowering of S. physalifolium indicates that this species is more likely to
contaminate pea crops than is S. nigrum. Therefore, extra attention may be required
where this species is present in process pea crops. The prevention of the flowering of
both species, by the maintenance of the appropriate weed free period following pea
sowing or crop emergence, was identified as potentially, the most useful means of
reducing nightshade contamination in peas.