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All issues Volume 23 (2016) Parasite, 23 (2016) 58 Full HTML
Open Access
Issue
Parasite
Volume 23, 2016
Article Number 58
Number of page(s) 7
DOI https://doi.org/10.1051/parasite/2016071
Published online 21 December 2016

© X.-L. Zheng et al., published by EDP Sciences, 2016

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Introduction

Eucalyptus is one of the three major fast-growing tree species worldwide, which plays important roles in reforestation and the production of timber, pulp, potential bioenergy feedstock, and other forest products [25]. In China, the cultivated area under eucalyptus covers more than 3.68 billion hectares and produces a direct economic income that exceeds 100 billion Renminbi (RMB) [33]. However, the decline of ecosystem biodiversity is very obvious with the increased cultivated area of eucalyptus and results in a sharp rise of eucalyptus insect pests [22]. The number of eucalyptus insect pest species in China has increased from 53 in 1980 to 319 in 2011 and causes direct economic losses exceeding RMB 1.125 billion annually [23].

The eucalyptus gall wasp, Leptocybe invasa Fisher & La Salle (Hymenoptera: Eulophidae), originating from Australia, is a global pest in Eucalyptus plantations [18]. A recent study based on molecular and phylogenetic analyses suggested the occurrence of geographical variability in L. invasa populations and the existence of different putative species, among them a “Chinese lineage” [20]. The wasp populations investigated in our study were not characterized from a phylogenetic point of view; we therefore cannot indicate their exact taxonomical position. Moreover, as the lineage is not a taxonomic category coded by the International Code of Zoological Nomenclature, in the present paper the wasp is cited as L. invasa. Leptocybe invasa has expanded to more than 29 countries in Asia, Europe, Africa, and the Americas [18, 35]. In China, L. invasa was first found in the Guangxi Zhuang Autonomous Region in April 2007 [30]. Subsequently, the pest has spread to Guangdong, Fujian, Hainan, Jiangxi, and Sichuan provinces [3, 29, 31, 34]. Various management strategies have been explored to control L. invasa, including chemical control [13], breeding and the selection of resistant planting stock [5, 34], and biological control [15, 16]. However, chemical control is not widely accepted due to its varying success, negative effects on biodiversity, and environmental pollution. Sylvicultural control is largely ad hoc and is unlikely to represent a viable long-term solution against an increasing number and diverse range of damaging invasive pests. Biological control is considered an attractive alternative to other control methods due to its ecological and economic benefits [4].

In Australia, parasitoids play a very important role in limiting the populations of L. invasa [8, 15]. The introduction of natural enemies from Australia has been considered an optimal way to control the eucalyptus gall wasp in epidemic areas [15, 28]. However, only a few countries have adopted this method in view of increasing evidence of attacks against non-target hosts and the resulting threat to native biodiversity [15, 28]. Recently, several L. invasa parasitoids have been found in the invaded regions, e.g., India, Israel, Turkey, Italy, Sri Lanka, Thailand, Argentina, and South Africa [7–9, 12–15, 21]. However, as mentioned above, the parasitic capacities of these parasitoids for L. invasa are different in these regions. Thus far, only Aprostocetus causalis La Salle & Wu (Hymenoptera: Eulophidae) and Quadrastichus mendeli Kim & La Salle (Hymenoptera: Eulophidae) have been reported to parasitize L. invasa in the Guangxi and Hainan provinces of China [10, 17, 32]. The number of parasitoid species of L. invasa and their parasitic capacities in the field are unknown. Therefore, it is necessary to widely investigate biological control agents for L. invasa in China.

The purpose of this study was to identify possible biological control agents for L. invasa occurring on Eucalyptus spp. In this study, we investigated the species of parasitoids present in some Chinese regions.

Materials and methods

Eucalyptus gall wasps were searched for by the typical bump-shaped galls they form on leaf midribs, petioles, and stems (Fig. 1). Branches of DH 201–2 (Eucalyptus grandis × E. tereticornis) (Myrtales: Myrtaceae), E. tereticornis Smith, E. Exserta L., and E. grandis × E. urophylla damaged by L. invasa were collected from Fujian, Guangdong, Hainan, Guangxi, Jiangxi, and Sichuan provinces from 2015 to 2016. The sampling sites and sampling times for each province are shown in Table 1. Branches were placed in a glass container filled with water to retain freshness and transferred to a sealed net cage (40 cm × 40 cm × 80 cm) at 27 ± 1 °C (the average air temperature of the sampling sites during the period of collection) with an L16:D8 photoperiod and 70–80% relative humidity to prevent the adults from escaping. The water in the glass container was replaced daily until the emergence of L. invasa and their parasitoids.

thumbnail Figure 1.

Eucalyptus tereticornis damaged by Leptocybe invasa in Guangxi.

Table 1.

Percentages of parasitization by parasitoids in Leptocybe invasa.

The emerged L. invasa adults (Fig. 2) and their parasitoids were collected daily using 50 mL plastic tubes. The percentage of parasitization for each parasitoid collected from different geographical populations was calculated as the number of emerged parasitoids (EP) divided by the sum of the total numbers of emerged gall-formers and emerged parasitoids (EGP) [15, 16].

thumbnail Figure 2.

Newly emerged female of Leptocybe invasa inserting ovipositor into the petiole of Eucalyptus grandis × E. tereticornis.

A cotton ball soaked in a 10% sucrose solution and galled eucalyptus branches were supplied to allow oviposition by the parasitoid adults. Newly emerged female wasps were reared one by one for uniparental species and in pairs for biparental species. The honey-water and galled branches were renewed daily. The rearing conditions of these parasitoids were similar to those of the host insects mentioned above. The mortality of the male and female specimens was recorded daily to evaluate the longevity of the parasitoids. The body lengths of these dead specimens were subsequently measured using image-measuring software (Leica Application Suite version 4.6.0, Leica Microsystems, Germany). Images of the parasitoid adults were taken with a Sony digital camera (DSC-HX60, Sony, Kyoto, Japan). Identification of the parasitoids was performed with keys [7, 15, 32] and confirmed by Prof. Chao-Dong Zhu and Dr. Huan-Xi Cao (Institute of Zoology, Chinese Academy of Sciences, China).

Statistical analysis was performed using SPSS 16.0 (SPSS, Chicago, IL, USA). Adult longevities and body lengths were compared using the nonparametric Mann-Whitney U test. The results were considered significant at p ≤ 0.05.

Results

Three hymenopteran parasitoid species were found in L. invasa collected from Fujian, Guangdong, Hainan, Guangxi, Jiangxi, and Sichuan provinces: Q. mendeli, A. causalis, and Megastigmus viggianii Narendran & Sureshan (Hymenoptera: Torymidae); M. viggianii is newly recorded in China (Table 1; Figs. 3–5). The percentages of parasitization by Q. mendeli were 2.96, 10.91, 9.06, 19.53, and 5.77% in Fujian, Guangdong, Hainan, Guangxi, and Sichuan provinces, respectively (Table 1). No males of this species were found, and Q. mendeli was confirmed as a uniparental species (Fig. 3). The mean longevity and body length of the females were 5.6 ± 1.2 days and 1.2 ± 0.1 mm, respectively (Table 2). The percentages of parasitization by A. causalis were 2.30, 3.13, 5.54, 3.84, and 26.38% in Guangdong, Hainan, Guangxi, Jiangxi, and Sichuan provinces, respectively (Table 1). Both sexes of A. causalis were found (Fig. 4). The longevity (U = 17.0, p = 0.000) and body length (U = 20.5, p = 0.000) of A. causalis females were significantly greater than for males (Table 2). The percentage of parasitization by M. viggianii was 24.93% in Sichuan province (Table 1). Both sexes of M. viggianii were found (Fig. 5). The life span and body length of M. viggianii females were significantly longer than those of males (U = 94.0, p = 0.000 and U = 70.0, p = 0.000, respectively) (Table 2).

thumbnail Figure 3.

(A) Dorsal view of Quadrastichus mendeli female; (B) ventral view of Q. mendeli female.

thumbnail Figure 4.

(A) Profile view of Aprostocetus causalis female; (B) profile view of A. causalis male.

thumbnail Figure 5.

(A) Dorsal view of Megastigmus viggianii female; (B) profile view of M. viggianii male.

Table 2.

Longevities and body lengths of Quadrastichus mendeli, Aprostocetus causalis, and Megastigmus viggianii adults.

Discussion

Quadrastichus mendeli is one of the indigenous parasitoids parasitizing L. invasa in Australia [15], with the percentage of parasitization varying from 7.9% to 95.6%. Recently, Q. mendeli was introduced from Australia to Israel and India as a biological control agent to limit the severity of damage caused by L. invasa. The parasitoid is now successfully established in Israel and India, and the percentage of parasitization was 73% in Israel and 81.74–94.03% in India [15, 28]. However, initial efforts to establish the Q. mendeli population in quarantine facilities in South Africa and Kenya have failed [6]. Interestingly, Q. mendeli was collected from L. invasa galls on E. Camaldulensis Dehnh. in Italy beginning in 2013, although this parasitoid was never officially released [21]. Field data showed that mean parasitization percentage by Q. mendeli varied from 30.2% to 50.5% in Italy [21]. Here, we report Q. mendeli parasitizing L. invasa in China under natural conditions, although this parasitoid was never officially released in China. Although Q. mendeli is a widely distributed L. invasa parasitoid in China, the percentage of parasitization differed in these geographical populations (Table 1).

Aprostocetus causalis, a parasitoid of L. invasa in China, was described as a new species in 2014 [32]. However, the longevity of both sexes of this parasitoid in the laboratory was lower than the longevity found in a previous study carried out in Thailand [27], probably due to the different rearing method. Adults in the laboratory in Thailand were fed with a honey solution, whereas both a honey solution and galled foliage were provided in this study. Previous studies suggested that parasitization involves a high physiological cost for the parasitoid and that longevity is lower in ovipositing females [24, 26].

Megastigmus viggianii was recorded as parasitizing the bud galls of Calycopteris floribunda Lamark (Myrtales: Combretaceae) in India [19]. In 2008, this parasitoid was found parasitizing L. invasa larvae for the first time in India [11], and the percentage of parasitization varied from 14.29% to 31.82% [28]. However, M. viggianii was only found in the Sichuan site; thus, we cannot ascertain whether this parasitoid is native to China. Furthermore, M. viggianii has a multi-host-range (i.e., C. floribunda and L. invasa) compared to Q. mendeli and A. causalis. Other M. viggianii hosts have not been found in China and need further investigation.

In the field, two or three parasitoids attacked L. invasa in China with possible competition for the monopolization of host resources. The percentage of parasitization by Q. mendeli was always higher than that by A. causalis when the two parasitoids attacked the eucalyptus gall wasp in Guangdong, Hainan, and Guangxi provinces. However, the percentage of parasitization by Q. mendeli was lower than those for A. causalis and M. viggianii when the three parasitoids attacked eucalyptus gall wasps in Sichuan province. We presumed that this could be attributed to the population dynamics of Q. mendeli in Sichuan province, but this needs to be confirmed. Previous studies showed that Q. mendeli is a solitary idiobiont ectoparasitoid [15] while A. causalis and M. viggianii are solitary koinobiont endoparasitoids [32]. The competitive dynamics and mechanisms of both the ectoparasitoid (Q. mendeli) and endoparasitoids (A. causalis and/or M. viggianii) in L. invasa need to be studied.

In general, parasitoids have host-tracked their hosts either simultaneously or following invasion by the pest. For example, Ophelimus maskelli Ashmead (Hymenoptera: Eulophidae) is a leaf-gall-inducing invasive pest of several Eucalyptus species in California, while its parasitoid, Closterocerus chamaeleon Girault (Hymenoptera: Eulophidae), was also found less than 1 year after Q. maskelli [1, 2]. As Q. mendeli and M. viggianii were never released in China, their record leads us to suppose that they could shortly reach other neighboring countries around China.

Conclusion

In this study, we found that Q. mendeli, A. causalis, and M. viggianii could be used as biological control agents for L. invasa in China. However, further studies are needed on the biological characteristics, mass production and release, competitive dynamics and mechanisms of these parasitoids.

Conflict of interest

The authors declare no conflict of interest in relation with this paper.

Acknowledgments

We are grateful to two anonymous reviewers and the Editor-in-Chief for their valuable comments on this manuscript, and thank Chu-Jiang Wei and Hua-Feng Zhang (Department of Fujian Forestry Pest Management, Fujian Province), Jing Chen (Department of Luoding Forestry Pest Management, Guangdong Province), Tang Shi and Bing Sun (Department of Danzhou Forestry Pest Management, Hainan Province), Kai Lin (Guangxi University), Fan-Yu Zeng (Department of Nankang Forestry Pest Management, Jiangxi Province), and Wen-Xia Teng (Department of Panzhihua Forestry Pest Management, Sichuan Province) for their assistance during the field investigation. Many thanks also to John La Salle (CSIRO, Australia) for his valuable comments on identification of parasitoids, and Chao-Dong Zhu and Huan-Xi Cao (Institute of Zoology, Chinese Academy of Sciences, China) for their assistance in identification of parasitoids. The research was financially supported by the National Natural Science Foundation of China (31300549 and 31560212) and the Scientific Research Foundation of Guangxi University (XBZ160068).

References

  1. Burks RA, Mottern JL, Pownall NG, Waterworth R, Paine TD. 2015. First record of Closterocerus chamaeleon, parasitoid of the eucalyptus gall wasp Ophelimus maskelli (Hymenoptera: Chalcidoidea: Eulophidae), in the New World. ZooKeys, 504, 149–152. [CrossRef] [Google Scholar]
  2. Burks RA, Mottern JL, Waterworth R, Paine TD. 2015. First report of the eucalyptus gall wasp, Ophelimus maskelli (Hymenoptera: Eulophidae), an invasive pest on Eucalyptus, from the Western Hemisphere. Zootaxa, 3926, 448–450. [CrossRef] [PubMed] [Google Scholar]
  3. Chen YS, Liao ZM, Tu XY. 2015. Study on resistance of different Eucalyptus varieties to Leptocybe invasa in southern Jiangxi. Northern Horticulture, (11), 106–109. (in Chinese with English abstract). [Google Scholar]
  4. De Clercq P, Mason PG, Babendreier D. 2011. Benefits and risks of exotic biological control agents. BioControl, 56, 681–698. [CrossRef] [Google Scholar]
  5. Dittrich-Schröder G, Wingfield MJ, Hurley BP, Slippers B. 2012. Diversity in Eucalyptus susceptibility to the gall-forming wasp Leptocybe invasa. Agricultural and Forest Entomology, 14, 419–427. [CrossRef] [Google Scholar]
  6. Dittrich-Schröder G, Harney M, Neser S, Joffe T, Bush S, Hurley BP, Wingfield MJ, Slippers B. 2014. Biology and host preference of Selitrichodes neseri: a potential biological control agent of the eucalyptus gall wasp, Leptocybe invasa. Biological Control, 78, 33–41. [CrossRef] [Google Scholar]
  7. Doğanlar M. 2015. Diagnosis of Megastigmus spp. (Hymenoptera: Torymidae) reared from galls of Leptocybe invasa Fisher & La Salle 2004 (Hymenoptera: Eulophidae) on Eucalyptus spp. (Myrtaceae), with description of a new species from South Africa. Entomofauna Zeitschrift für Entomologie, 36, 561–580. [Google Scholar]
  8. Doğanlar M, Hassan E. 2010. Review of Australian species of Megastigmus (Hymenoptera: Torymidae) associated with Eucalyptus, with descriptions of new species. Australian Journal of Basic and Applied Sciences, 4, 5059–5120. [Google Scholar]
  9. Doğanlar M, Zaché B, Wilcken CF. 2013. A new species of Megastigmus (Hymenoptera: Torymidae: Megastigminae) from Brazil. Florida Entomologist, 96, 196–199. [CrossRef] [Google Scholar]
  10. Feng MX, Cao HX, Hao HH, Wang W, Chen LS. 2016. A new record species of Quadrastichus (Hymenoptera: Eulophidae) from China. Chinese Journal of Tropical Crops, 37, 582–585. (in Chinese with English abstract) [Google Scholar]
  11. Gupta A, Poorani J. 2008. New distribution and host records of Chalcidoidea (Insecta: Hymenoptera) from various parts of India. Check List, 4, 410–414. [CrossRef] [Google Scholar]
  12. Hernández CM, Aquino DA, Cuello EM, Andorno AV, Botto EN. 2015. First record of Megastigmus zebrinus Grissell (Hymenoptera: Torymidae) from Argentina associated with galls of Leptocybe invasa (Hymenoptera: Eulophidae). Revista de la Sociedad Entomológica Argentina, 74, 75–77. [Google Scholar]
  13. Javaregowda J, Prabhu ST, Patil RS. 2010. Evaluation of botanicals and synthetic insecticides against eucalyptus gall wasp, Leptocybe invasa (Eulophidae: Hymenoptera). Karnataka Journal of Agricultural Sciences, 23, 200–202. [Google Scholar]
  14. Kelly J, La Salle J, Harney M, Dittrich-Schröder G, Hurley B. 2012. Selitrichodes neseri n. sp., a new parasitoid of the eucalyptus gall wasp Leptocybe invasa Fisher and La Salle (Hymenoptera: Eulophidae: Tetrastichinae). Zootaxa, 3333, 50–57. [Google Scholar]
  15. Kim I, Mendel Z, Protasov A, Blumeberg D, La Salle J. 2008. Taxonomy, biology and efficacy of two Australian parasitoids of the eucalyptus gall wasp, Leptocybe invasa Fischer & La Salle (Hymenoptera: Eulophidae: Tetrastichinae). Zootaxa, 1910, 1–20. [Google Scholar]
  16. Kulkarni H, Kumari NK, Vastrad AS, Basavanagoud K. 2010. Release and recovery of parasitoids in eucalyptus against gall wasp, Leptocybe invasa (Hymenoptera: Eulophidae) under green house. Karnataka Journal of Agricultural Sciences, 23, 91–92. [Google Scholar]
  17. Li DW, Wu YJ, Jiang XJ, Chang MS, Huang HY, Qin YL. 2010. Aprostocetus sp. a parasitoid on the Leptocybe invasa. China Forestry Science and Technology, 24, 52–54. (in Chinese with English abstract). [Google Scholar]
  18. Mendel Z, Protasov A, Fisher N, La Salle J. 2004. Taxonomy and biology of Leptocybe invasa gen. & sp. n. (Hymenoptera: Eulophidae), an invasive gall inducer on Eucalyptus. Austral Entomology, 43, 101–113. [Google Scholar]
  19. Narendran TC, Sureshan PM. 1988. A contribution to our knowledge of Torymidae of India (Hymenoptera: Chalcidoidea). Bollettino del Laboratorio di Entomologia Agraria Filippo Silvestri, 45, 37–47. [Google Scholar]
  20. Nugnes F, Gebiola M, Monti MM, Gualtieri L, Giorgini M, Wang JG, Bernardo U. 2015. Genetic diversity of the invasive gall wasp Leptocybe invasa (Hymenoptera: Eulophidae) and of its Rickettsia endosymbiont, and associated sex-ratio differences. PLoS One, 10, e0124660. [CrossRef] [PubMed] [Google Scholar]
  21. Nugnes F, Gebiola M, Gualtieri L, Russo E, Sasso R, Bernardo U. 2016. When exotic biocontrol agents travel without passport: first record of Quadrastichus mendeli, parasitoid of the blue-gum chalcid Leptocybe invasa, in Italy. Bulletin of Insectology, 69, 85–91. [Google Scholar]
  22. Paine TD, Steinbauer MJ, Lawson SA. 2011. Native and exotic pests of Eucalyptus: a worldwide perspective. Annual Review of Entomology, 56, 181–201. [CrossRef] [PubMed] [Google Scholar]
  23. Pang ZH. 2013. Current situation and development in trend of Eucalypts pest in China. Journal of Guangxi Academy of Sciences, 29, 192–206. (in Chinese with English abstract). [Google Scholar]
  24. Protasov A, Blumberg D, Brand D, La Salle J, Mendel Z. 2007. Biological control of the eucalyptus gall wasp Ophelimus maskelli (Ashmead): Taxonomy and biology of the parasitoid species Closterocerus chamaeleon (Girault), with information on its establishment in Israel. Biological control, 42, 196–206. [Google Scholar]
  25. Rejmánek M, Richardson DM. 2011. Eucalypts, in Encyclopedia of Biological Invasions. Simberloff D, Rejmánek M, Editors. University of California Press: Berkeley, USA. p. 203–209. [Google Scholar]
  26. Rizzo MC, Verde GL, Rizzo R, Caleca V. 2015. Risk assessment of non-target effects of Closterocerus chamaeleon Girault parasitoid of the eucalypt gall maker Ophelimus maskelli Ashmead (Hymenoptera: Eulophidae). Phytoparasitica, 43, 407–415. [CrossRef] [Google Scholar]
  27. Sangtongpraow B, Charernsom K. 2012. Longevity and developmental time of Aprostocetus sp. (Hymenoptera: Eulophidae), the local parasitoid of Leptocybe invasa Fisher & La Salle (Hymenoptera: Eulophidae). International Symposium of BioPesticides and Ecotoxicological Network (2nd IS – BioPEN), 24–25 September, Maruay Garden Hotel, Bangkok, Thailand. [Google Scholar]
  28. Shylesha AN. 2008. Classical biological control of eucalyptus gall wasp Leptocybe invasa Fisher & La Salle. Final Project Report on the Management of Emerging Pests Eucalyptus, [online] URL: http://www.dcpulppaper.org/gifs/report63.pdf. [Google Scholar]
  29. Tang C, Wang XJ, Wan FH, Ren SX, Peng ZQ. 2008. The blue gum chalcid, Leptocybe invasa, invaded Hainan Province. Chinese Journal of Applied Entomology, 45, 967–971. (in Chinese with English abstract). [Google Scholar]
  30. Wu YJ, Jiang XJ, Li DW, Luo JT, Zhou GF, Chang MS, Yang ZQ. 2009. Leptocybe invasa, a new invasive forest pest making galls on twigs and leaves of eucalyptus trees in China. Scientia Silvae Sinicae, 45, 161–163. (in Chinese with English abstract). [Google Scholar]
  31. Xu JX, Ren H, Zhao DY, Lin MS, Qiu HX, Zhong TK, Chen MR, Huang MY, Chen RP. 2008. Study on the population regularity and spatial distribution pattern of Leptocybe invasa at eucalyptus. Guangdong Forestry Science and Technology, 24, 50–57. (in Chinese with English abstract). [Google Scholar]
  32. Yang MM, Lin YC, Wu YJ, Fisher N, Saimanee T, Sangtongpraow B, Zhu CD, Chiu WCH, La Salle J. 2014. Two new Aprostocetus species (Hymenoptera: Eulophidae: Tetrastichinae), fortuitous parasitoids of invasive eulophid gall inducers (Tetrastichinae) on Eucalyptus and Erythrina. Zootaxa, 3846, 261–272. [CrossRef] [PubMed] [Google Scholar]
  33. Yang MS, Xie YJ, Liu JF. 2011. Three decades of Chinese eucalyptus. China Forestry Press: Beijing, China. (in Chinese). [Google Scholar]
  34. Zhang HF, Kang WT, Chen SL, Tang XH, Lin XQ. 2012. Study on the relationship between eucalyptus clones and the damage degrees caused by Leptocybe invasa Fisher & La Salle. Journal of Fujian College of Forestry, 32, 345–349. (in Chinese with English abstract). [Google Scholar]
  35. Zheng XL, Li J, Yang ZD, Xian ZH, Wei JG, Lei CL, Wang XP, Lu W. 2014. A review of invasive biology, prevalence and management of Leptocybe invasa Fisher & La Salle (Hymenoptera: Eulophidae: Tetrastichinae). African Entomology, 22, 68–79. [CrossRef] [Google Scholar]

Cite this article as: Zheng X-L, Huang Z-Y, Dong D, Guo C-H, Li J, Yang Z-D, Yang X-H & Lu W: Parasitoids of the eucalyptus gall wasp Leptocybe invasa (Hymenoptera: Eulophidae) in China. Parasite, 2016, 23, 58.

All Tables

Table 1.

Percentages of parasitization by parasitoids in Leptocybe invasa.

In the text
Table 2.

Longevities and body lengths of Quadrastichus mendeli, Aprostocetus causalis, and Megastigmus viggianii adults.

In the text

All Figures

thumbnail Figure 1.

Eucalyptus tereticornis damaged by Leptocybe invasa in Guangxi.
In the text
thumbnail Figure 2.

Newly emerged female of Leptocybe invasa inserting ovipositor into the petiole of Eucalyptus grandis × E. tereticornis.
In the text
thumbnail Figure 3.

(A) Dorsal view of Quadrastichus mendeli female; (B) ventral view of Q. mendeli female.
In the text
thumbnail Figure 4.

(A) Profile view of Aprostocetus causalis female; (B) profile view of A. causalis male.
In the text
thumbnail Figure 5.

(A) Dorsal view of Megastigmus viggianii female; (B) profile view of M. viggianii male.
In the text

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