ROGUING POTATO CROPS FOR VIRUS DISEASES

Removing virus-infected plants from plots of Majestic potatoes at Rothamsted on 2 July 1947 did not reduce the spread of leaf roll but reduced rugose mosaic (potato virus Y) to about one-fifth of that in plots rogued on 21 July or left unrogued. Roguing Arran Pilot potatoes on 16 June or 2 July reduced leaf roll to five-sixths of that in unrogued plots; roguing on 16 June reduced rugose mosaic to about half that in plots rogued on 2 July, and about a quarter of that in unrogued plots. Lifting Arran Pilot potatoes in mid-August reduced virus diseases to about two-thirds.
Roguing flattened the gradient (decrease in percentage plants diseased with increasing distance from the source of infection) with rugose mosaic, but had little effect with leaf roll. Evidently any plants prevented by roguing from contracting virus Y were near the initially infected plants.
In 1948, Majestic and King Edward potatoes at three places were rogued during 22–24 June and tubers were dug during 28–30 July and again at the end of the season. Leaf roll spread more in Majestic than in King Edward, and rugose mosaic spread more in King Edward. Roguing reduced the spread of both by about one-fifth at Rothamsted, but had no effect at Sutton Bonington. At Bretton, in the Derbyshire hills, roguing had no effect on leaf roll, but prevented the spread of rugose mosaic.
The small benefit occasionally achieved by roguing in the ware-growing districts of England does not make the practice economically worth while.     

New approaches for restricting spread of potato leafroll virus by different methods of eradicating infected plants from potato crops

Experiments were made at Invergowrie in 1984 and 1985 to compare the spread of potato leafroll virus (PLRV) after removing infected plants by three different methods; conventional roguing, desiccation with diquat, or incineration for 45–60s using a propane gas flame. Potato leaf roll 'infector' plants, grown in plots of virus-free Maris Piper seed potatoes, were artificially infested in June with aphids (Myzus persicae) from a laboratory culture, and removed from the plots after 2 or 3 wk. In both years, natural infestations of potato aphids were scarce during this period. There was no significant difference in the proportion of tubers infected with PLRV in adjacent plants after the neighbouring infector plants had been rogued by hand or desiccated with diquat, but the proportion was considerably reduced following incineration of the infector plants. In 1984, the spread of PLRV in conventionally rogued plots was also significantly reduced by a mixture of deltamethrin plus heptenophos, applied four times from 80% crop emergence, and was almost eliminated by a treatment with aldicarb granules, either at planting, or as a side-dressing 5 wk later. In 1985, delaying infector removal by 8 days in early July significantly increased the spread of PLRV to neighbouring plants from 2.3% (1 July) to 8.3% (9 July). A single application of deltamethrin plus heptenophos to infectors 1 wk before removal did not significantly decrease spread. Although incineration was quick and effective, the value of this method of eradicating infector plants in seed potato crops is limited because it failed to destroy infected tubers.     

FACTORS AFFECTING THE SPREAD OF APHID-BORNE VIRUSES IN POTATO IN EASTERN SCOTLAND

Experiments at Invergowrie, south-east Perthshire, showed that the extent of spread of potato leaf-roll and Y viruses varied from year to year and that virus Y consistently spread more than leaf roll. Most spread of Virus Y occurred before the end of June and of leaf-roll virus before the end of July. Both viruses spread slightly more in late- than in early-planted crops. When plants with leaf roll and already colonized by Myzus persicae were placed in a healthy crop of Majestic potatoes at intervals during the season, the amount of virus spread decreased rapidly with increasing age of the crop. Spread of leaf roll occurred in all of twenty-five 'seed' crops in different districts of eastern Scotland in 1955 but in only twenty out of thirty-six similar crops in 1956. Annual and regional differences in virus spread appear to reflect differences in the time at which migrant aphids reach potato crops in early summer and the rate at which infestation builds up in the crops.     

THE SPREAD OF VIRUS DISEASES TO SINGLE POTATO PLANTS BY WINGED APHIDS

Young potato plants in pots exposed in the open near plots of potatoes for limited periods at intervals during the summer, became infested with large numbers of winged aphids only during warm, calm and dry weather. Although visited by aphids during May and June, when much of the spread of viruses occurred in nearby potato crops, few of the potted plants became infected. Most potted plants became infected in July when alate aphids were leaving neighbouring potato crops. Widely different proportions of the exposed plants became infected in different years; in two of the three years, many more plants were infected with virus Y than with leaf roll virus.     

Experiments on the spread of rugose mosaic and leaf roll in potato crops in 1946

A series of experiments on the spread of potato rugose mosaic (virus Y ), and leaf roll, which has been in progress on a uniform plan since 1943, was ended in 1946. Mean values for thirteen centres in England and Wales showed that in 1946 69% of the infections with virus Y and 48 % of those with leaf-roll virus reached the tubers of Majestic potatoes by the beginning of August. There was usually little subsequent increase of rugose mosaic, but a late increase of leaf roll was associated with a relatively high initial spread. Three-quarters of the virus Y and over half the leaf-roll infections occurred within five plants distance of the source. There was no close correlation between the spread of either virus and the maximum number of Myzus persicae , either apterous forms on the plants or alate forms caught on adhesive traps, but centres with high trap catches in July and August showed pronounced late season spread of leaf roll. There were marked differences at different centres in the relative spread of the two viruses. The amount of spread and the gradients from source of infection of the two viruses are compared over the period 1943–6.     

Soil and plant water relations in a crested wheatgrass pasture: response to spring grazing by cattle

Summary Few field studies have attempted to relate effects of actual livestock grazing on soil and plant water status. The present study was initiated to determine the effects of periodic defoliations by cattle during spring on soil moisture and plant water status in a crested wheatgrass (Agropyron cristatum (L.) Gaertn. and A. desertorum (Fisch. ex Link) Schult.) pasture in central Utah. Soil moisture in the top 130 cm of the soil profile was depleted more rapidly in ungrazed plots than in grazed plots during spring and early summer. Soil moisture depletion was more rapid in grazed plots in one paddock after 1 July due to differential regrowth, but there was no difference in soil water depletion between plots in another paddock during the same period. This difference in soil water depletion between paddocks was related to a difference in date of grazing. Although more water had been extracted from the 60 cm to 130 cm depths in ungrazed plots by late September, cumulative soil moisture depletion over the entire 193 cm profile was similar in grazed and ungrazed plots. Prior to 1 July, grazing had no effect on predawn leaf water potentials as estimated by a pressure chamber technique; however, after 1 July, predawn leaf water potentials were lower for ungrazed plants. Midday leaf water potentials were lower for grazed plants before 1 July, but did not differ between grazed and ungrazed plants after 1 July. A 4- to 8-day difference in date of defoliation did not affect either predawn or midday leaf water potentials. The observed differences in water use patterns during spring and early-summer may be important in influencing growth and competitive interactions in crested wheatgrass communities that are subject to grazing by domestic livestock.     

The effects of cassava mosaic virus disease on yield and compensation in mixed stands of healthy and infected cassava

The effects of cassava mosaic virus disease (CMD) on yield in fully and partly infected stands of cassava were investigated in field trials in Uganda in 1990-91 and 1991-92. Three cultivars (Ebwanateraka, Bao and Bukalasa 1 l), each at three levels of cutting infection (O%, 50% and 100%) and harvested 510 and 15 months after planting (MAP) were used in a randomised block design with split-split plots and four replicates. Moreover, yield and growth data for individual infected and uninfected plants were considered in relation to the health status of their nearest neighbours. In each experiment, fresh tuberous root yields of plants from 100% infected plots gave sigdicantly lower yields than those from 0% or 50% infected plots at each harvest date and the losses were greatest in cv. Bao. Yields of plants from 0% and 50% plots for each of the three cultivars were not significantly different, 10 and 15 MAP. The loss in yield differed between cultivars and harvest dates. Fresh stem, leaf and root yields and the number of tuberous roots were influenced by the health status of the plants harvested and that of their nearest neighbours. Uninfected plants surrounded by infected ones had more roots and heavier total fresh root, stem and leaf weights than those surrounded by uninfected ones. Overall, 26% and 42% compensation was recorded in 1990-91 and 1991-92, respectively. The effects of CMD on cassava production and of compensation in mixed stands of infected and uninfected plants are discussed, especially in relation to control strategies such as roguing.     

Experiments on the Spread of Potato Virus X Between Plants in Contact

Experiments on the spread of five strains of potato virus X were made with seven potato varieties and with tomato plants both under glass and in the field. Spread by leaf contact between healthy and infected plants was confirmed, and it was also found that spread could occur between plants whose only contact was below ground.
The rate of spread was much greater in tomato than in potato plants, and virulent strains of the virus, which achieve a high concentration in infected plants, spread more rapidly than avirulent strains. In only one experiment with potatoes did more than 10% of the healthy potato plants exposed to infection become infected during one season.
Datura stramonium and tomato plants became infected when growing in soil containing sap or residues from X -infected plants.
It was common in the field for potato plants whose foliage gave no reaction for virus X at the end of the season to yield a mixed progeny of healthy and infected tubers. Such infections are thought to result from underground spread.
Attempts to transmit virus X from infected to healthy potatoes by means of Rhizoctonia solani failed. No examples of infection were found except when healthy plants came into direct contact with sources of the virus.     

THE INFLUENCE OF PLANTING DATE AND MANURING ON THE INCIDENCE OF VIRUS DISEASES IN POTATO CROPS

Field experiments with Majestic potatoes were made over six years at Rothamsted to test the effects of varying date of planting and manuring on the yield of tubers and the incidence of the aphid-transmitted leaf roll and Y (rugose mosaic) viruses. Yield was increased by early planting, and by all the manures, especially dung. Early planting also usually increased the incidence of virus disease. Different manures had different effects on disease incidence; the average results from all comparisons showed the largest increase in incidence of both viruses from the use of dung; sulphate of ammonia increased the incidence of leaf roll, and muriate of potash that of rugose mosaic. Counts in two years showed that aphid populations were highest on the earlier planted potatoes, and were increased by dung, sulphate of ammonia and superphosphate, but were reduced by muriate of potash.     

Cost-Effective Control of Plant Disease When Epidemiological Knowledge Is Incomplete: Modelling Bahia Bark Scaling of Citrus

A spatially-explicit, stochastic model is developed for Bahia bark scaling, a threat to citrus production in north-eastern Brazil, and is used to assess epidemiological principles underlying the cost-effectiveness of disease control strategies. The model is fitted via Markov chain Monte Carlo with data augmentation to snapshots of disease spread derived from a previously-reported multi-year experiment. Goodness-of-fit tests strongly supported the fit of the model, even though the detailed etiology of the disease is unknown and was not explicitly included in the model. Key epidemiological parameters including the infection rate, incubation period and scale of dispersal are estimated from the spread data. This allows us to scale-up the experimental results to predict the effect of the level of initial inoculum on disease progression in a typically-sized citrus grove. The efficacies of two cultural control measures are assessed: altering the spacing of host plants, and roguing symptomatic trees. Reducing planting density can slow disease spread significantly if the distance between hosts is sufficiently large. However, low density groves have fewer plants per hectare. The optimum density of productive plants is therefore recovered at an intermediate host spacing. Roguing, even when detection of symptomatic plants is imperfect, can lead to very effective control. However, scouting for disease symptoms incurs a cost. We use the model to balance the cost of scouting against the number of plants lost to disease, and show how to determine a roguing schedule that optimises profit. The trade-offs underlying the two optima we identify—the optimal host spacing and the optimal roguing schedule—are applicable to many pathosystems. Our work demonstrates how a carefully parameterised mathematical model can be used to find these optima. It also illustrates how mathematical models can be used in even this most challenging of situations in which the underlying epidemiology is ill-understood.     

Virus content of seed potato stocks produced in a unique seed potato production scheme

Western Australia has a unique seed potato production scheme which has remained virtually unchanged for more than 60 years, consisting of summer plantings of predominantly one cultivar in wind-exposed coastal swamplands. No rotation is used and the scheme relies on natural winter flooding and 'grazing' by sheep to eliminate unharvested tubers. Stocks are recycled every year with only limited inputs of pathogen-tested seed tubers in recent times. Virus spread in the crop is controlled by selecting large tubers for planting, roguing, aphicide application and growing season inspections. Potato viruses X and S were commonly detected in old seed stocks produced by this scheme attaining 100% infection in some. Both viruses were less frequently found in newly introduced seed stocks. By contrast, potato virus Y was never detected and potato leaf roll virus rarely found.     

The use of menazon seed dressing to decrease spread of virus yellows in sugar-beet root crops

Menazon, an organophosphorus insecticide (only slightly toxic to mammals), applied to sugar-beet seed, decreased the proportion of seedlings infested with aphids during May and early June and the number of aphids per plant during June and early July to one-third of that in the control plots. It also checked the spread of virus yellows. Of eight field trials in 1965, 1966 and 1967 in which more than 10% of the plants in plots not treated with insecticide had yellows, menazon seed dressing increased sugar yield by about 8 cwt per acre. Spraying with demeton-methyl when ‘a spray warning’ was issued in the area gave a similar increase, and had no further effect on plots sown with menazon-treated seed. Menazon-dressed sugar-beet seed is recommended in regions where yellows is usually prevalent, or where there is reason to expect a large aphid infestation.     

The Influence of the Application of Mineral Fertilizers with the Biopreparation Supresivit ( Trichoderma Harzianum ) on the Health and the Yield of Different Crops

The biopreparation Supresivit based on spores from the fungus Trichoderma harzianum was applied as a dressing mixed with mineral fertilizers: NPK, LAV (ammonium nitrate with limestone) and DASA (ammonium nitrate and ammonium sulphate). Our experimental plots with spring barley, winter wheat, winter oil rape, maize and potatoes were fertilized with the mixtures of the biopreparation (1 g, 0.5 g and 0.1 g per 1 kg of fertilizer). There were two check variants, the first variant without any fertilization and without biopreparation, the second with fertilizer and without biopreparation. We observed the infestation of plants with pathogenic fungi and yield parameters. In our experiments it was indicated that Trichoderma harzianum suppresses pathogenic fungi at the concentration 0,5 g of Supresivit per 1 kg of the fertilizer and higher ones. The plants from treated plots had lower infestation - decreasing about 5-15% superficial infestation: tan spot of barley - yellow leaf spot on cereals and leaf blotch of barley, winter wheat - leaf spot of wheat, tan spot of wheat, take-all etc., winter oil-seed rape - black leg and collar rot, potatoes - blight fungus etc. Simultaneously the effect on higher yields was observed.     

Insecticidal control of aphids and the spread of potato leafroll virus in potato crops in eastern Scotland

Field experiments were carried out in eastern Scotland in 1976-78 to test the ability of granular insecticides, applied to soil at planting, and of insecticide sprays applied to the foliage, to control aphids and spread of potato leafroll virus (PLRV) in potatoes. The three years provided contrasting opportunities for virus spread. In 1976, the main vector of PLRV, Myzus persicae, arrived in early June and multiplied rapidly in untreated plots, and PLRV spread extensively. In 1977, M. persicae arrived 4–6 wk later than in 1976 and most spread of PLRV, which was less than in 1976, occurred after the end of July. In 1978, few M. persicae were recorded but the potato aphid, Macrosiphum euphorbiae, arrived early and very large populations developed in untreated plots. However, little spread of PLRV occurred in 1978, supporting other evidence that M. euphorbiae is an inefficient vector of PLRV in field conditions. In each year, granular insecticides decreased PLRV spread to a quarter or less of that in control plots. Thiofanox gave somewhat better and longer-lasting control of aphid populations than disulfoton, especially of M. persicae, but did not give greater control of PLRV spread. Application of three (1976) or five (1977) sprays of demeton-S-methyl to plots treated with granular insecticides further improved the control of M. euphorbiae but had less or no effect on M. persicae, especially where organophosphorus resistant aphids (R1 strain) were found. These supplementary sprays of insecticide did not further improve the control of PLRV but, in 1978, four sprays of demephion or pirimicarb to plots not treated with granular insecticide decreased PLRV spread. These data, together with previous findings, indicate that the amount of virus spread depends on the date of arrival and rate of multiplication of M. persicae in relation to the timing and effectiveness of removal of PLRV sources in crops. It is concluded that in Scotland insecticide granules should be used routinely only in crops of the highest grade of seed potato. Their use for other grades need be considered only in years following mild winters, when aphids can be expected to enter crops earlier and in larger numbers.     

Vertical dispersal of the two-spotted spider mite Tetranychus urticae, and the predatory mite Phytoseiulus persimilis on dwarf hops

1 The pattern of dispersion within plants of the two-spotted spider mite, Tetranychus urticae, and its predator, the phytoseiid Phytoseiulus persimilis, was studied on the dwarf hop variety First Gold from May to September in 1997 and 1998. 2 Spider mite populations developed on the lower leaves initially but, by late July, as the numbers of mites increased, most were found towards the top of plants. From early August, the numbers of spider mites decreased most rapidly on the upper parts of plants. 3 Where P. persimilis was released, the predator maintained the numbers of T. urticae below those found on non-release plots throughout the season. 4 By early August, the predator’s pattern of dispersion was similar to that of the pest. 5 Predators spread to non-release plots by 20 June in 1997 and 24 July in 1998 and eventually became more numerous than on the plots where they had been released.     

Effects of infection with narcissus mosaic, narcissus yellow stripe and tobacco rattle viruses on the growth and flowering of narcissus cv. 'Minister Talma'

Three plots were planted with similar-sized narcissus bulbs: healthy; infected with narcissus mosaic virus (NMV); and infected with narcissus yellow stripe + tobacco rattle virus (NYSV+TRV). No effects of infection were observed on flower number, diameter, paracorolla length or flower dry weight, but the flower stalks were shorter in the infected plants. NMV-infected plants produced slightly blemished flowers, and 74% of the NYSV + TRV-infected flowers were of poor quality. Virus infection delayed leaf growth and loss of bulb dry weight early in the season and senescence in July. NYSV+TRV-infected plants were more affected than NMV-infected plants. However, maximum leaf area was similar for all plants. The maximum plant dry weight and the final weight of the bulb were not significantly affected by infection, but small differences, which could be cumulative in successive years would not have been detected. Differences in net assimilation rate, if any, were small.     

Construction of Plant Expression Vectors and Identification of Transgenic Potato Plants

Potato virus X (PVX), potato virus Y (PVY) and potato leaf roll virus (PLRV) infection in potato may result in the loss of centrification of seed potatoes and affect the quality and yield of potatoes in agricultural production. The authors cloned coat protein (cp) genes of PVX, PVY and PLRV and constructed two kinds of plant expression vector which contain PVX and PVY or PVY and PLRV cp genes. Three major commercial cultivars of potato and one cultivar of tobacco were transformed via Agrobacterium tumefaciens mediated procedure. Transgenic plants were confirmed by PCR analysis. Transgenic tobacco plants containing both PVX and PVY cp genes were significantly resistant to PVX and PVY infection via mechanical inoculation.     

Spread of potato leafroll virus is decreased from plants of potato clones in which virus accumulation is restricted

Tubers of eight potato clones infected with potato leafroll luteovirus (PLRV) were planted as ‘infectors’ in a field crop grown, at Invergowrie, of virus-free potato cv. Maris Piper in 1989. The mean PLRV contents of the infector clones, determined by enzyme-linked immunosorbent assay (ELISA) of leaf tissue, ranged from c. 65 to 2400 ng/g leaf. Myzus persicae colonised the crop shortly after shoot emergence in late May and established large populations on all plants, exceeding 2000/plant by 27 June. Aphid infestations were controlled on 30 June by insecticide sprays. Aphid-borne spread of PLRV from plants of the infector clones was assessed in August by ELISA of foliage samples from the neighbouring Maris Piper ‘receptors’. Up to 89% infection occurred in receptor plots containing infector clones with high concentrations of PLRV. Spread was least (as little as 6%) in plots containing infectors in which PLRV concentrations were low. Primary PLRV infection in guard areas of the crop away from infectors was 4%. Some receptor plants became infected where no leaf contact was established with the infectors, suggesting that some virus spread may have been initiated by aphids walking across the soil.     

EXPERIMENTS ON THE COLONIZATION OF POTATO PLANTS BY APTEROUS AND BY ALATE APHIDS IN RELATION TO THE SPREAD OF VIRUS DISEASES

Batches of potato plants in pots were placed in the field for limited periods among plants infected with potato virus Y and leaf roll virus. Some of the potted plants were surrounded by sticky boards which prevented apterous aphids from reaching them. Almost as many plants within the boards as without became infected, indicating that most of the spread of virus was by winged aphids.
Apterae were probably responsible for spreading the viruses throughout a hill after one or more stems were infected. They may carry infection to neighbouring plants, but most of these will have been infected already by alatae.
The number of plants contracting infection was unaffected by watering.     

Patterns of spread of the non-persistently transmitted bean yellow mosaic virus and the persistently transmitted subterranean clover red leaf virus in Vicia faba

Patterns of spread of two aphid borne viruses, the non-persistently transmitted bean yellow mosaic virus (BYMV) and the persistently transmitted subterranean clover red leaf virus (SCRLV), were compared simultaneously in field plots of Vicia faba minor grown in a Mediterranean climate (winter-spring growing season, and dry summer). Spread from a primary source was mapped following the artificial introduction of virus alone, or virus with vector, at the centre of the plots. BYMV spread rapidly from the virus source whether or not vectors were introduced with the virus. By contrast, SCRLV spread from the source only when plants were also artificially infested with the vector Aulacorthum solani. An attempt was made to evaluate the importance of secondary spread of both viruses by assessing the degree of clumping of infected plants that occurred outside the primary sites of virus introduction. BYMV-infected plants were clumped in each treatment irrespective of whether the virus was introduced alone or with vector, as well as in control plots. Clumping of SCRLV occurred only when the vectors were introduced on virus source plants at the beginning of the experiment. Times of spread were determined both by exposing trap plants at 4-weekly intervals throughout the 30 month trial period, and by analysing the rates of spread in experimental plots between June and November in one growing season. Both viruses spread in the spring when vectors were flying, but negligible spread of the viruses was observed in the autumn despite aphid flight activity. Times of flight of the four main aphid vector species were continuously monitored with yellow water traps. A major spring and a minor autumn flight peak were observed for Aphis craccivora, Macrosiphum euphorbiae, Aulacorthum solani and Myzus persicae. Aphid flights occurred predominantly in weeks when the mean temperature was in the range 13–17°C. Rainfall above 7 mm per week appeared to affect flights only when mean weekly temperatures were outside the range 13–17°C.