A systems approach has been developed for mitigation of risk associated with Thaumatotibia leucotreta (Meyrick) (Lepidoptera: Tortricidae), in citrus fruit exported from South Africa, as an alternative to a stand-alone cold treatment. This study was undertaken to assess compliance with inspection standards applicable to various steps within the systems approach and to determine its overall efficacy. Larval infestation of fruit was monitored weekly in fruit from 33 orchards, until the time of harvest, postpicking, and postpacking into export cartons. Significant positive regressions were recorded between infestation of fruit during the full monitoring period in the orchard and the last 4 wk before harvest, between the last 4 wk before harvest and on delivery to the packinghouse, and on delivery to the packinghouse and in the packed carton. There was an improvement in the level of compliance with each of these successive steps in the system, thus verifying that the grading and inspection thresholds were appropriately sensitive and confirmed the effectiveness of the system. The overall risk mitigation efficacy of the systems approach was calculated. The calculation included several known compounding under estimations of efficacy. Nonetheless, the proportion of fruit that could be infested with T. leucotreta after application of the systems approach was between P ≤ 5.328 × 10−6 and P ≤ 8.380 × 10−7, 6–38 times less than the proportion associated with the probit 9 ( P ≤ 3.2 × 10−5) standard for a stand-alone cold treatment, being three survivors in 100,000 at the 95% confidence level.
Some of South Africa’s citrus export markets require mandatory postharvest cold treatment of citrus fruit as a phytosanitary risk mitigation treatment for Thaumatotibia leucotreta (Meyrick) (Lepidoptera: Tortricidae). An alternative to this may be partial cold treatment as one of the final steps in a systems approach to mitigate phytosanitary risk. Consequently, the efficacy of such partial cold treatments was evaluated. It was first determined that a 2°C cold treatment was significantly more effective against fourth and fifth instars (the most cold-tolerant instars) than treatments at 3°C and 4°C for a duration of 18 d. Secondly, it was determined that 2°C for 18 d and 1°C for 16 d were similarly effective, but both treatments were significantly more effective than 1°C for 14 d. Mean mortality of fourth and fifth instars treated with 2°C for 18 d in seven replicates from four trials was 99.94%. Finally, it was determined that the inability of the majority of surviving larvae to develop to adulthood would further increase the efficacy of a 2°C for 18 d treatment to 99.96%. Inclusion of reproductive nonviability of survivors increased mortality to 99.99%.
Some of South Africa’s export markets require postharvest cold treatment of citrus fruit for phytosanitary risk mitigation for Thaumatotibia leucotreta (Meyrick) (Lepidoptera: Tortricidae) . An alternative to a standalone cold treatment may be a reduced intensity cold treatment as a step in a systems approach. For cold treatment trials, large numbers of larvae are required. Due to recent dramatic improvement of T. leucotreta control in the field, sufficient naturally infested citrus fruit are no longer available. Artificial infestation of fruit is not viable due to rapid decay of the fruit. Consequently, it is necessary to use laboratory-reared T. leucotreta larvae in artificial diet. In trials, field-collected larvae from the Eastern Cape were at least as cold-tolerant as those from other regions. Larvae in Navel oranges showed the median level of susceptibility in a range of citrus types evaluated at 6°C, and their use in trials was considered acceptable due to their greater natural susceptibility to T. leucotreta infestation. We demonstrated that larvae at high density in artificial diet were at least as cold-tolerant as larvae at lower densities. When exposed to 2°C for 18 d or longer, larvae in artificial diet as used in the trials were at least as cold-tolerant as larvae in fruit. Very few surviving larvae from fruit completed development, with no subsequent generation. Consequently, it is considered justifiable to conduct cold-treatment trials with laboratory-reared T. leucotreta larvae in artificial diet without risk of underestimating the effect of cold on feral larvae in citrus fruit.
Citrus black spot (CBS) is caused by Phyllosticta citricarpa, which is classified as a quarantine organism in certain countries whose concerns are that CBS-infected fruit may be a pathway for introduction of the pathogen. This study evaluated the reproductive capability and viability of P. citricarpa under simulated conditions in which the whole fruit, peel segments, or citrus pulp with CBS lesions were discarded. Naturally infected ‘Midknight’ Valencia orange and ‘Eureka’ lemon fruit, either treated using standard postharvest sanitation, fungicide, and wax coating treatments or untreated, were placed into cold storage for 5 weeks (oranges at 4 °C and lemons at 7 °C). Thereafter, treated and untreated fruit were incubated for a further 2 weeks at conditions conducive for CBS symptom expression and formation of pycnidia. The ability of pycnidia to secrete viable pycnidiospores after whole fruit and peel segments or peel pieces from citrus pulp were exposed to sunlight at warm temperatures (±28 °C) and ±75% relative humidity levels was then investigated. The combination of postharvest treatments and cold storage effectively controlled CBS latent infections (>83.6% control) and pycnidium formation (<1.4% of lesions formed pycnidia), and the wax coating completely inhibited pycnidiospore release in fruit and peel segments. Pycnidiospores were secreted only from lesions on untreated fruit and peel segments and at low levels (4.3–8.6%) from peel pieces from pulped treated fruit. However, spore release rapidly declined when exposed to sunlight conditions (1.4% and 0% after 2 and 3 days, respectively). The generally poor reproductive ability and viability of CBS fruit lesions on harvested fruit, particularly when exposed to sunlight conditions, supports the conclusion that citrus fruit without leaves is not an epidemiologically significant pathway for the entry, establishment, and spread of P. citricarpa.
The five-spotted fruit fly, Ceratitis quinaria (Bezzi) (Diptera: Tephritidae), is distributed in parts of eastern and western Africa, northern Africa and southern Africa (including South Africa). The species also occurs outside of Africa, in Yemen. The host range of C. quinaria is narrow, with Mangifera indica L. being the main host of commercial importance. Ceratitis quinaria was claimed to be associated with citrus in Sudan although this claim was never substantiated and there has never been any confirmed reared record of C. quinaria on citrus despite numerous surveys of citrus across Africa. In order to verify the type of association that C. quinaria has with citrus, field surveys were carried out in South Africa to determine the distribution and seasonal occurrence of C. quinaria in commercial citrus orchards and the possible natural infestation of citrus by this species. Surveys on distribution of C. quinaria across South Africa were carried out in 1999 and 2000 by trapping with Ceratitislure (containing protein hydrolysate and β-caryophyllene). The seasonal occurrence of C. quinaria in the northern areas of South Africa was determined over two years between 2015 and 2017 by trapping with Enriched Ginger Oil (EGO), a male lure containing α-copaene. In the same trapping period, citrus and other fruit were sampled to determine infestation by C. quinaria. Additionally between 2009 and 2018, citrus fruit was sampled from the trees and ground in other commercial and non-commercial areas in the north of South Africa. All fruit samples collected were incubated for at least five weeks to allow rearing of flies to the pupal and adult stages. Trapping surveys conducted between 1999 and 2000 showed the presence of C. quinaria only in the northern areas of South Africa. Catches of C. quinaria males in EGO-baited traps were low in commercial citrus orchards (peak of catches being lower than 0.05 flies/trap/day). Catches of C. quinaria were mainly recorded outside of the citrus ripening period. No C. quinaria was reared from any of the citrus fruit sampled, even in those areas where the presence of the species was demonstrated by catches in EGO-baited traps. The fruit surveys therefore demonstrated the absence of natural infestation of citrus with C. quinaria in South Africa and supported existing biological information that citrus is not a host for C. quinaria.