1. Introduction
The papaya mealybug,
Paracoccus marginatus Williams and Granara de Willink (Hemiptera: Pseudococcidae), is native to Central America and since the 1990s. It has spread rapidly in mainly tropical areas of the Caribbean, islands in the Indian and Pacific Oceans, Africa and southern Asia, and transmitted throughout most provinces of southern China; till now it distributed in a total of 62 countries
[1-4]. Ahmed et al. (2015) conducted a genetic analysis on samples of
P. marginatus collected across Asian (Cambodia, China, India, Indonesia, Malaysia and Thailand) and African countries; and revealed that there was only one haplotype (a group of alleles in an organism that are inherited together from a single parent) reflecting the very recent invasion of
P. marginatus in Asia[
5,
6]. Papaya mealybug is an economic insect which is estimated causing more than 75% economic damage and income loss of more than USD 3009 per ha at the farm level in Keniya[
7]. It has a wide range of hosts and has recorded damage to 189 genera in 58 families. The main economic crops include papaya, mango, custard apple, emblica, acerola, jackfruit, banana, guava, pomegranate, Indian date, sapodilla, and cassava[
1,
4]. The nymphs and adult females insert its stylet into the epidermis of the leaf or the skin of fruit or stem and feeds on the plant sap. At the same time, it injects a toxic substance into the plant which results in chlorosis, distortion, stunting, early leaf and fruit fall, the production of honeydew, sooty mould and possibly the death of the plant, resulted in huge economic losses[
1,
6]. In addition, it is one of the vectors of
Piper yellow mottle virus[
8]. The insect can spread long-distance along with entering and exiting fruits, vegetables, ornamental plants, etc., and has been listed as a quarantine pest by the United States, Canada, Australia, the European Union and other countries. As a result, phytosanitary measures including pest risk analysis, inspection, treatment, and eradication are needed to be carry out to prevent its spread and to reduce the economic losses[
1,
6,
9].
Control measures have been developed for quarantine disinfestation and field controlling, including chemical (fumigation, spraying/dipping pesticide) and physical (irradiation, cold, heat, mechanical clean) treatments on consignments or during processing, cleaning and disinfection of facilities, tools and machinery, and field temperature control[
6,
10,
11]. Currently, cold treatment and methyl bromide fumigation is a common measure to disinfest regulated pests founded in fresh commodities, but the fumigant is restricted in use excepted quarantine and pre-shipment uses because it depletes ozone layers; alternative measure should be developed[
12,
13]. Irradiation treatment has many advantages such as highly penetration in the commodities, prevention of development and reproduction effectively, no residues, and no negative effects that could endanger consumers[
14,
15]. It is an optimum alternative to methyl bromide fumigation treatment in disinfesting insect pests of fruits and vegetables to overcome quarantine barriers in trade[
16,
17]. Phytosanitary irradiation (PI) treatment measure has been developed and used in international trade since the establishment of the International Standard on Phytosanitary Treatment (ISPM) No.18 (
Guidelines/
Requirements for the use of irradiation as a phytosanitary measure) by the secretariat of the International Plant Protection Convention (IPPC) in 2003 and revised in 2023, and the international shipment trials on irradiated mangoes (at 250 Gy) between Australia and New Zealand in 2004
[16-18]. In the meanwhile, the schedule and standards are essential for the application of PI treatment; there are two phytosanitary treatment (PT) standards for mealybugs (PT 19 and 45) have been established by IPPC[
19,
20]; more PT standards on mealybugs species are urgently needed to push forward the listed topic: 2017-012 (
Irradiation treatment for all stages of the family Pseudococcidae (
generic)) for drafting, consultation and adoption, since mealybugs are the second most important regulated pests besides fruit flies on fruits and vegetables[
1,
21,
22].
For the PI treatment of papaya mealybug, Seth et al. (2016) found that the radiotolerance grows with increasing stages and times in the dose-response tests; gamma radiation in the LD
99.9 (99.9% mortality or prevention at 95% confidence level (CL)) of 165 and 258 Gy, which was estimated by the linear regression on dose-percent mortality data, induced lethality in developing stages, and sterility in adults, respectively[
23]. Unfortunately, LD
99.9968 prevention of F
1 neonates was neither estimated nor validated by the large-scale confirmatory tests, which is essential for the development of ISPMs according to ISPM 28 (
Phytosanitary treatments for regulated pests)
[19.20,24]. Therefore, normalized dose-response and large-scale confirmatory tests are required to determine the phytosanitary treatment dose for
P. marginatus gravid females, and to develop a treatment schedule, national standard, and IPPC PT standard (annex to ISPM 28) based on the outcomes of this study.
4. Discussion
During this research, radiotolerance for the 2-, 4-, and 6-d-old eggs and gravid female (containing immature eggs) of
P. marginatus were tested by comparing the number of eggs (
Table 1), and the ability to develop into 1st instar nymphs after exposure to X-rays irradiation at the dose of 15 to 105 Gy with intervals of 15 Gy; whereas preventing egg-hatching (mortality of egg including eggs laid by irradiated females) was used as the criteria for efficacy evaluation. The dose-mortality data was analyzed by two-way ANOVA (
Table 2), probit and LDR test (
Table 3, 4), and overlapping test on fiducial intervals of LD
90, LD
99, and LD
99.9968 afterwards. As a result, the 2-, 4-, and 6-d-old eggs present very closed radiotolerance, but they are significantly more sensitive than the immature eggs in the ANOVA and LDR test at LD
90 (
Table 2, 3 and 4); whereas there is no significant difference in LD
99.9968. This result agrees with the relative radiotolerance of
D. lepelleyi eggs irradiated by X-ray irradiation, in which the immature eggs seem more tolerant that 1-, 2-, and 3-d-old eggs[
26]. This also indicate that the egg developed well in the body of female of papaya mealybug. However, the radiotolerance grows with the developing ages of egg[
14] for other mealybugs, for instance,
Ps.
comstocki Kuwana[
36] and
Ps. baliteus[
15] in which 0-d-old eggs (immature eggs in the body of gravid females) were significantly more sensitive to radiation than 2-, 4-, and 6-day-old eggs.
How to comparing the relative radiotolerance in different insect stages/ages had once been discussed by Zhan et al. (2020)[
11], the statistical methods including probit analysis, CI overlapping, relative median potency, and ANOVA; the 95% CI of the LDR at LD
99 had been recommended for comparing the significance of tolerance in phytosanitary treatments. In this investigation, no significant radiotolerance difference was found for the 2-, 4-, and 6-d-old eggs by all above measures except for LDR test at LD
90 (
Table 3, 6-d-old eggs are significantly tolerant than 4-d-old eggs); whereas, 0-d-old eggs showed significantly more resistant than produced eggs when comparing in ANOVA (
Table 2) and LDR test at LD
90 (
Table 3 and 4) may due to the lack of the 100% mortality data for the 0- and 6-d-old eggs. The dose-probit line for 0-d-old egg showed steeper (possess of a larger slope of 0,034 vs. 0.026-0.028) than other lines and they crossed at probit 8.20 and probit 9 (
Figure 2), resulted in no significant tolerance difference in LD
99 and LD
99.9968. However, during the probit analysis, all the 95% CIs overlapped means there is no significant radiotolerance difference among all testing eggs; and this may due to the larger CIs ranges in produced eggs caused by the larger experimental errors. In a word, there is none significant radiotolerance exist among the eggs when the probit-9 mortality was used as the criterion for efficacy evaluation.
Additionally, the estimated LD
99.9968 value for produced eggs (
Table 3) will be increased by 4.22 to 5.33-fold with a large rang of CI If the dose was logarithmic transformed during the probit analysis; and the calculation for adult female suspended due to heterogeneity factor exceeding 100 [
32]. The results are in agreement with that for PI treatment of the cacao mealybug
Planococcus lilacinus Cockerell[
27]. Therefore, the traditional logarithmic transformation of radiation dose is unsuitable for dose-response data analysis in this investigation.
It is very important and reasonable to conduct the dose-response tests (i.e., predict the treatment intensity of large-scale confirmatory trials) in order to develop a technical schedule or standard for PI treatment of papaya mealybug[
15,
18,
24]. In order to facilitate the application of PI technology, we prefer to choose the effect of radiation on preventing the emergence of 2nd instar nymphs as the end-point of efficacy evaluation, rather than neonate (1st instar nymphs) from the irradiated females, even though the oviparous mealybugs that they lay eggs, because it is difficult to find out all eggs or neonates lurking in the female's abdomen before irradiation treatment[
19,
20,
27,
37,
38]. Additionally, very high radiation doses are required to prevent hatching of ready-to-hatch eggs; for instance, the minimum dose to prevent egg-hatch of
Pl. minor Maskell is different from 7–14-d-old old and un-oviposited eggs (in the abdomen of females); they are > 250 Gy and 150 Gy, respectively[
39].
The target dose used in the large-scale testing was always obtained from the probit analysis on the most tolerant stage(s) that may present on commodity, which is the gravid females for mealybugs and scale insects, for instance the PI treatment of
Aonidiella aurantia Maskell[
40],
Aspidiotus destructor Signoret[
41,
42],
Hemiberlesia lataniae Signoret[
43],
Pl. citri Risso and
Pl.
ficus Signoret[
44],
Pl. lilacinus[
27],
Ps. baliteus[
15], and
Ps. jackbeardsleyi Gimpel & Miller[
37,
38]. For
P. marginatus, however, probit-9 value was 176.7 Gy (160.7 – 198.9 Gy, 95% CL) for gravid females, and 143.8 – 272.1 Gy for produced eggs (
Table 3), then, 165 Gy was used as the target dose for the confirmatory tests. No F
1 generation neonate developed from an estimation of 60,386 gravid females and their immature eggs (≥1.5 billion) on sprouting potatoes irradiated at monitored doses of 146.8 to 185.0 Gy (
Table 5), indicating the estimated dose for probit-9 efficacy was validated. In the meantime, the largest radiation dose of 185 Gy monitored in the confirmatory tests, which is also larger than or equal to the estimated mean values of probit-9 for the late females (176.7 Gy), 2-d-old eggs (178.5 Gy), 4-d-old eggs (182.9 Gy), and 6-d-old eggs (185.2 Gy) in
Table 3, could be recommended as the phytosanitary treatment doses for commodity internationally[
14,
20,
21,
45].
For PI studies on oviparous mealybugs, preventing egg-hatching of the F
1 genera-tion could be used as the efficacy criterion, thereby using eggs to replace females in the dose-response tests to determine the relative tolerance and estimate the probit-9 mortality value [
15,
26]. During the life cycle of mealybugs, immature eggs in the body of adult females are the connector between adults and F
1 generation eggs (for oviparous reproduction type) or neonates (deuterotokous ovoviviparous reproduction type). Gravid female is the most radiotolerance stage and should be used as the target stage to be tested in the PI researches according to ISPM 18 and 28[
4,
14,
17], then, the produced eggs, same as
D. lepelleyi[
27] and
Ps. baliteus[
15], can be used as alternative to gravid females for the dose-response testing.