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Silva Lusitana

versão impressa ISSN 0870-6352

Silva Lus. vol.19 n.Especial Lisboa  2011

 

Contribution of Symbiotic Fungi to Cork Oak Colonization by Platypus cylindrus (Coleoptera: Platypodidae)

 

Maria Lurdes Inácio, Joana Henriques and Edmundo Sousa

INRB, IP – Instituto Nacional dos Recursos Biológicos. Quinta do Marquês, Av. da República, 2780-159 OEIRAS

 

Abstract

Platypus cylindrus Fab. (Coleoptera: Platypodidae) has changed its status from uncommon to pest contributing to cork oak decline. Besides its massive attacks, P. cylindrus is associated with fungi on which it depends for survival and host colonization. Isolations from beetles yielded seven genera with a potential role on insects' establishment: Acremonium, Biscogniauxia, Botryosphaeria, Gliocladium, Raffaelea, Scytalidium and Trichoderma. Raffaelea spp. were the most frequent fungi (ambrosia fungi) mainly in insect’s mycangia and gut confirming their role as primary symbionts and possibly capable of weaken the host. Similarly Biscogniauxia and Botryosphaeria genera may act to overwhelm tree defenses. The genera Scytalidium, Gliocladium andTrichoderma are known to have a degradative wood ability and play a pioneering role in host colonization. These results demonstrate the close association between P. cylindrus and its ambrosia fungi. These are mainly from the Raffaelea genus and also the auxiliary ambrosia fungi, whose presence is part of the insect's strategy for host colonization.

Key words: Ambrosia beetle; ambrosia fungi; Quercus suber, Raffaelea spp.; Ophiostomatales

 

Contribuição dos Fungos Simbiontes na Colonização do Sobreiro por Platypus cylindrus (Coleoptera: Platypodidae)

Sumário

Platypus cylindrus Fab. (Coleoptera: Platypodidae), considerado um inseto secundário, é atualmente tido como agente primário desempenhando um papel determinante no declínio do montado. Para além do ataque massivo, P. cylindrus associa-se a fungos dos quais depende para a sua sobrevivência e colonização do hospedeiro. O isolamento de fungos a partir do incesto permitiu a identificação de sete géneros potencialmente envolvidos no seu estabelecimento: Acremonium, Biscogniauxia, Botryosphaeria, Gliocladium, Raffaelea, Scytalidium eTrichoderma. Os fungos mais frequentes foram espécies do géneroRaffaelea (fungos ambrósia) principalmente associadas aos micângios e conteúdo intestinal, confirmando o seu papel como simbiontes primários, e possivelmente com capacidade para enfraquecer o hospedeiro. Do mesmo modo, os géneros Biscogniauxia e Botryosphaeria poderão atuar de forma a ultrapassar as defesas das árvores. Os géneros Scytalidium, Gliocladium eTrichoderma, conhecidos pela sua capacidade degradadora da madeira, desempenham um papel pioneiro na colonização do hospedeiro. Estes resultados demonstram a estreita associação entre P. cylindrus e os seus fungos ambrósia, principalmente do género Raffaelea, e fungos ambrósia auxiliares, cuja presença faz parte da estratégia do inseto para a colonização do hospedeiro.

Palavras-chave: Inseto ambrósia; fungos ambrósia; Quercus suber; Raffaelea spp.; Ophiostomatales

 

Introduction

Among the most successful wood-inhabiting insects are the Scolytidae and Platypodidae which cause damage of economic significance to timber and trees (CASSIER et al., 1996). Platypus cylindrus Fab., the oak pinhole borer, is the most common Platypodid beetle in southern Europe. It mainly attacks oaks (BALACKOWSKY et al., 1963) but it is also described on chestnut, beech, ash, elm and wild cherry trees (ESPAGÑOL, 1964; GRAHAM, 1967).

P. cylindrus attack is usually limited to dead or weakened trees (SEABRA 1939; BAETA-NEVES, 1950; ESPAÑOL, 1964). Sporadic attacks were also described on apparently healthy trees (BALACHOWSKY, 1949) and in Morocco this beetle is considered an important pest of cork oak (Quercus suber L.) (VILLEMENT and FRAVAL, 1993; SOUSA et al., 2005). In Portugal, since the 1980's, severe infestations were observed in apparently healthy cork oaks (SOUSA, 1992; SOUSA and DÉBOUZIE, 2002) causing widespread tree death within three months to one year and a half after the attack, depending on the host vigour and resistance (SOUSA and INÁCIO, 2005).

In the host colonization process, primary attraction of the Platypodidae was associated with certain tree volatiles like ethanol and terpenes (SHORE and MCLEAN, 1983). Analysis of the temporal evolution of P. cylindrus attacks reveals a preference for the biggest hosts (height and perimeter) mostly for those recently decorked (SOUSA and DÉBOUZIE, 1999). However, the insect preference for a host probably results from a combination of stimuli such as wood moisture, osmotic pressure, sap flow and tree leaf composition, among others (CHARARAS, 1979; SOUSA et al., 1995; YAMASAKI and FUTAI, 2008). In addition, a kairomone to P. cylindrus has been described (ALGARVIO et al., 2002; TEIXEIRA et al., 2003).

The establishment of insects on a host is the last step of the attack process. The secondary attraction begins by the appeal of insects of the same sex followed by the attraction of the other sex insects (YTSMA, 1986; ATKINSON, 2004). The high density of P. cylindrusattacks on the same tree confirms the existence of these secondary attraction mechanisms initiated by the appeal of the other males (aggregation pheromone) (ALGARVIO et al., 2002), similarly to other Platypodidae (RENWIK et al., 1977; MILLIGAN et al., 1988; TOKORO et al., 2007; KIM et al., 2009). Each male is joined to a single female whose attraction is probably mediated by sexual pheromones (ALLEGRO and DELLA BEFFA, 2001). Mated couples tunnel into the heartwood and introduce ectosymbiotic fungi into their galleries on which they and their offspring feed. These insects are so called ambrosia beetles since the larvae and adults feed mainly on the fungal mycelium lining the sinuous tunnels (BATRA, 1963; BEAVER, 1989). For the transport and maintenance of fungal inoculum, ambrosia beetles developed specialized organs – mycangia - which provide suitable conditions for fungi storage during flight and spreading of the insects (FRANCKE-GROSSMAN, 1963; CASSIER et al., 1996). The mycobiota associated with the insects allows them to be nutritionally independent of the host (KÜLNHOLZ et al., 2003). Early studies carried out on symbiosis with P. cylindrus described several fungi and yeasts that are important in insect nourishment. The main symbiotic fungus is the mitosporic Ophiostomataceae Raffaelea ambrosiae v. Arx & Hennebert, (BAKER, 1963; UCHASTNOVA, 1985; SOUSA et al., 1995). Other fungi were also identified in this association but their exact roles have yet to be fully clarified (SOUSA and INÁCIO, 2005; HENRIQUES et al., 2006). Thus, the aim of this study is to determine what fungi are carried consistently by P. cylindrus in Portuguese cork oak stands. Furthermore, their frequency and location in the insect's body was determined in order to understand the role of the main vectored fungi on the success of tree host colonization.

 

Material and methods

Collection

Twelve logs from cork oak severely infested by P. cylindrus and exhibiting decline symptoms were collected from Alentejo and Ribatejo province, two main cork producing regions of Portugal. The logs were settled in the INRB, I.P. laboratories at Oeiras and the emerged adults captured in fine mesh nets, attached to the log with a silicone joint. The samplings were repeated during 2005, 2006 and 2007.

Beetles were observed under a binocular microscope to confirm their identity. Excised mycangia from 200 insects, half males and females were mounted on microscope slides in clear lactophenol. Preparations were observed under a Olympus BX41TF microscope and the mycangial pits were counted. For scanning electron microscopy, 10 specimens of P. cylindrus (5 males, 5 females) previously ultrasound cleaned were sputter coated with gold palladium (98:2) (HENRIQUES, 2007) and examined using a JOEL 35 scanning electron microscope.

 

Fungal isolation and identification

A total of 100 insects per year were aseptically dissected with iris scissors to obtain their mycangia, intestine and parts of the exoskeleton (elytra). All the pieces were surface sterilized with a sodium hypochlorite solution (1%) for 1 min and rinsed with sterilized distilled water. They were plated into 9 cm diameter Petri dishes with malt extract agar (MEA, Difco, USA) added with 500mg/l of streptomycin (Sigma-Aldrich, USA), a large spectrum antibiotic, and MEA added with 500 mg/l of cycloheximide (Sigma-Aldrich, USA), inhibitory to most fungi except those belonging to the genus Ophiostoma (HARRINGTON, 1981; HAWKSWORTH et al., 1995). Some yeasts, however, and species of filamentous fungi, including Penicillium, also may grow on these media (HARRINGTON, 1992). Cultures were incubated at 25±1ºC in darkness. Pure cultures of each fungus were obtained and grouped according to their macroscopic characteristics. Fungal identification at the genus level was based on cultural and morphological features in accordance to BATRA (1967), ELLIS (1971, 1976), KIFFER and MORELET (1997) and BARNETT and HUNTER (1998). Fungi were scored as either present or absent on a Petri dish, regardless on the number of colonies of each fungi on the plate.

 

Statistical analysis

Results were analyzed through analysis of variance (ANOVA) after the angular transformation in to arcsin√x of the fungi frequencies expressed in percentage.  Significant means were compared through a LSD test. In all cases p < 0.001. The analyses were made using the software Statistica 6.0 (Statsoft).

 

Results

Specialized organs for transporting fungi

Observations of adults confirmed the presence of mycangia, ovoid in shape, located in both sexes on the flat middle upper part of the prothorax. This cuticular plate was perforated by numerous pits and the male has a less developed mycangium with 15±11 integumentary pits (min = 0; max = 53) separated by the straight cuticular line. In P. cylindrus females, 370±26 cavities were observed (min = 326; max = 406) (Figure 1A-D). In both sexes, perforations were apparently filled with the same type of fungal structures. On a specimen, a growing mycelium expanding on the cuticular surface and protruding from the perforations was observed (Figure 1E).

 

Figure 1 - Scanning electron micrographs of Platypus cylindrus adults. A. Male. B. Male mycangia. C. Female. D. Female mycangia. E. Growing mycelium and spores on female mycangia cavities

 

Fungal isolation and identification

Out of the 300 insects observed (142 males and 158 females), 258 yielded at least one fungal isolate in any insect's body location. From this 86% that contained fungi, 116 were male and 142 were female. Fungi belonging to seven genera were obtained: Acremonium, Biscogniauxia, Botryosphaeria, Gliocladium, Raffaelea, Scytalidium and Trichoderma. More than one species was isolated from the genera Gliocladium, Raffaelea and Trichoderma. Phoretic, intestinal and mycangial fungi obtained from individual P. cylindrus are summarized in Table 1.

 

Table 1 - Fungal isolates from the intestinal content (Ic), mycangia (My) and exoskeleton (Ex) of Platypus cylindrus males (M) and females (F)

 

The mycobiota obtained from individual P. cylindrus did not significantly differ in the three years of fungal isolation (F2.123 = 0.2255; p = 0.7985).

Although females may transport large amounts of fungal propagules, in terms of frequency of vectored fungi there were no statistically significant differences between males and females (F1.124 = 0.0708; p = 0.7906). Therefore, results for both sexes were pooled.  

The ophiostomatoid Raffaeleagenus was the most frequently isolated, in particular from the mycangia and the intestinal content. Different putative species of Raffaelea were obtained but their identification requires a multigene phylogeny and will be the subject of a future work.

The second most frequent genera was Botryosphaeria which together with Raffaelea species scored more than 90% of presence in the gut and in mycangia of the insects (Figure 2).

 

Figure 2- Genera of fungi (%) isolated from the intestine, mycangia and exoskeleton of Platypus cylindrus

 

The proportions of fungi found in mycangia and in the intestine versus phoretic on the exoskeleton were significantly different (F2.123 = 16.5784;p < 0.001). Besides Botryosphaeria sp. several non-ophiostomatoid fungi were isolated mainly from exoskeleton surfaces. In the mycangia these fungi were the rarest and the insects’ gut showed lower diversity of fungi. Species of Biscogniauxia, Gliocladium and Trichoderma genera were found in all the insect organs. Scytalidium sp. and Acremonium sp. were not found in the intestinal content.

Several saprobes fungi of the genera Alternaria, Aspergillus, Geotrichum, Paecylomyces and Penicillium were frequently isolated as well as species of Streptomyces and Mucorales but they fall outside the scope of this paper.

 

Discussion

In this study Platypus cylindrus was found to transport several fungi, out of which the most frequent was the ophiostomatoid species of RaffaeleaRaffaelea ambrosiae was considered the main ambrosia fungi and several authors reported this species as the principal symbiont of the oak pinhole borer (BAKER, 1963; ARX and HENNEBERT, 1965; SOUSA et al., 1995). However, and according to more recent work, P. cylindrus is associated with other Raffaelea species namely R. montetyi, an ambrosia fungus that decays wood (MORELET, 1998; INÁCIO et al., 2008), and R. canadensis (INÁCIO et al., 2008). The Ophiostomatales are economically important sapstaining fungi that occur worldwide on hardwoods. Moreover, some species of Raffaelea that are closely associated with ambrosia insects cause serious outbreaks in healthy trees (KUBONO and ITO, 2002; MURATA et al., 2005; FRAEDRICH et al., 2008; KIM et al., 2009; HARRINGTON et al., 2010).

P. cylindrus, although a wood borer, is not a wood feeder. Our results clearly show that adults feed on fungi, mainly on Raffaelea species thus confirming them as the primary ambrosia fungi. Botryosphaeria sp. is also very frequent in all the isolations, even from the intestine. This genus comprises the widespread and virulent species, B. corticola (ALVES et al., 2004; LUQUE et al., 2008; LINALDEDDU et al., 2009). The ingested thick-walled spores may pass through the gut unchanged and germinate on the walls of the galleries, but the hyphae are digested by the beetles and their larvae, hence providing a richer source of protein than wood (BEAVER, 1989).

Aside from these two most frequent fungi, others were isolated either from the exoskeleton or from the mycangia. Although these fungi may be significant components of the insect fungal flora, they were usually considered to be weed fungi with no more than a commensal relationship with the insects (HARRINGTON, 2005). Nevertheless, Biscogniauxia sp. and specifically B. mediterranea (HENRIQUES, 2007), the causal agent of cork oak charcoal canker (COLLADO et al., 2001; LINALDEDDU et al., 2010), was consistently present in all the insect organs, even if in small fractions. Given both its epizoic and endozoic dispersal by the insect, it could be hypothesized that P. cylindrus contributes to the spreading of its spores in cork oak stands. Likewise, Acremonium sp. and in particular A. crotocinigenum has shown to be pathogenic towards cork oak seedlings (INÁCIO et al., 2010a).

The association of P. cylindrus with cosmopolitan fungi is well documented by others (BAKER, 1963; CASSIER et al., 1996; SOUSA et al., 1997). In the present study, they were consistently isolated from the exoskeleton and mycangia, even after an accurate and thorough disinfection by fractional sterilization (FRANCKE-GROSMANN, 1956) to avoid saprobes growth (data not shown). It is possible that they might play a role in the insect-fungi interaction and thus in the establishment of the insect. It has been emphasized that these secondary symbionts may act as wood degrading agents to facilitate galleries excavation. Gliocladium sp., Trichoderma sp. and Scytalidium sp., as producers of lignocellulolytic enzymes might have this pioneer role (KIFFER and MORELET, 1997; SZAKACS and TENGERDY, 1997; MADDAU et al., 2009; INÁCIO et al., 2010b). Moreover, species of Trichoderma and Gliocladium are known for their antagonistic activity and may possibly control fungal growth inside the galleries (HENRIQUES, 2007).

The increase of P. cylindrus attacks in Portuguese cork oak stands suggests that behaviour changes may have happened and new strategies of host colonization may have arisen. The identification of chemical attractants such as kairomones and aggregation pheromones and possibly sexual pheromones mediating P. cylindrus attraction to host explains the massive attacks of the insect (ALGARVIO et al., 2002; TEIXEIRA et al., 2003; HENRIQUES et al., 2010). Our studies confirmed the phoretic transportation of fungi on the exoskeleton surfaces and the intimate association with fungi housed in the insect’s mycangia. The final role of the ambrosia fungi, which is the base of this insect-fungi interaction, is the nourishment of the larvae and adults. In fact, a more restrict range of fungi was found associated with P. cylindrus feeding habits. Future work will be carried out in order to identify the several fungal species isolated within each genus.

 

References

ALGARVIO, R., TEIXEIRA, C., BARATA, E., PICKETT, J., CASAS-NOVAS, P., FIGUEIREDO, D., 2002. Identification of a putative aggregation pheromone from males Platypus cylindrus (Coleoptera: Platypodidae). In Proceedings of the 19th Annual Meeting International Society of Chemical Ecology, Univ. Hamburg, Germany: 151.         [ Links ]

ALLEGRO, G., DELLA BEFFA, G., 2001. Un nuovo problema entomologico per la pioppicoltura italiana: Platypus mutatus (Chapuis) (Coleoptera, Platypodidae). Sherwood – Foresti ed Alberi Oggi 66: 31-34.         [ Links ]

ALVES, A., LUQUE, J., PHILLIPS, A., 2004. Botryosphaeria corticola sp. nov. on Quercus species, with notes and description of Botryosphaeria stevensii and its anamorph, Diplodia mutila. Mycologia 96: 598-613.         [ Links ]

ARX, VON, H., HENNEBERT, G.L., 1965. Deux champignons ambrosia. Mycopathol. Mycol. Appl. 25: 309-315.         [ Links ]

ATKINSON, T.H., 2004. Ambrosia Beetles. Platypus spp. (Insecta: Coleoptera: Platypodidae) Univ. Florida, Gainsville, FL. (available on line at http://edis.ifas.ufl.edu/IN331, accessed 22.10.2010).         [ Links ]

BAETA-NEVES, C., 1950. Introdução à Entomologia Florestal Portuguesa. A Serra e o Homem. Lisboa.

BAKER, J.M., 1963. Ambrosia beetle and their fungi, with particular reference to Platypus cylindrus Fab. Symp. Soc. General Microbiol. 13: 323-354.         [ Links ]

BALACHOWSKY, A.S., 1949. Faune de France: coléoptères scolytides. Lechevalier Ed., Paris, 320 pp.         [ Links ]

BALACHOWSKY, A.S., CHEVALIER, M., CUILLE, J., GRISON, P., HOFFMANN, A., JOURDHEUIL, P., LABEYRIE, V., REMAUDIERE, G., STEFFAN, J.R., TOUZEAU, J., VILARDEBO, A., 1963. Famille des Platypodidae. In Balachowsky AS (Ed.), Entomologie appliquée à l'agriculture". Tome II. Coleoptères. Ed. Masson et Cie, Paris, pp. 1289-1291.         [ Links ]

BARNETT, H.L., HUNTER, B.B., 1998. Illustrated Genera of Imperfect Fungi. APS Press, Minnesota, USA, 218 pp.         [ Links ]

BATRA, L.R., 1963. Ecology of ambrosia fungi and their dissemination by beetles. Trans. Kansas Acad. Sci. 66: 213–236.         [ Links ]

BATRA, L.R., 1967. Ambrosia fungi: A taxonomic revision and nutritional studies of some species. Mycologia 59: 976–1017.         [ Links ]

BEAVER, R.A., 1989. Insect-fungus relationships in the bark and ambrosia beetles. In Wilding N, Collins, NM, Hammond, PM, Webber, JF (Eds.), Insect-Fungus Interactions. Academic Press, London, pp. 121-143.         [ Links ]

CASSIER, P., LÉVIEUX, J., MORELET, M., ROUGON, D., 1996. The Mycangia of Platypus cylindrus Fab. and P. oxyurus Dufour (Coleoptera: Platypodidae). Structure and associated fungi. J. Insect Physiol. 42: 171-179.         [ Links ]

CHARARAS, C., 1979. Écophysiologie des insectes parasites des forêts. Chararas C. (Ed.), Paris, 297 pp.         [ Links ]

COLLADO, J., PLATAS, G., PELÁEZ, F., 2001. Identification of an endophytic Nodulisporium sp. from Quercus ilex in central Spain as the anamorph of Biscogniauxia mediterranea by rDNA sequence analysis and effect of different ecological factors on distribution of the fungus. Mycologia 93: 875-886.         [ Links ]

ELLIS, M.B., 1971. Dematiaceous Hyphomycetes. CAB, England, 609 pp.         [ Links ]

ELLIS, M.B., 1976. More Dematiaceous Hyphomycetes. CAB, England, 507 pp.         [ Links ]

ESPAÑOL, F., 1964. Los Platipodidos de Cataluña (Col. Phytophagoidea). Bol. Ser. Plagas For. 7: 115-117.         [ Links ]

FRAEDRICH, S.W., HARRINGTON, T.C., RABAGLIA, R.J., ULYSHEN, M.D., MAYFIELD, A.E., HANULA, J.L., EICKWORT, J.M., MILLER, D.R., 2008. A fungal symbiont of the redbay ambrosia beetle causes a lethal wilt in redbay and other Lauraceae in the southeastern United States. Plant Dis. 92: 215–224.         [ Links ]

FRANCKE-GROSMANN, H., 1956. Hautdrüsen als Träger der Pilzsymbiose bei Ambrosiakäfern. Z. Morphol. Öekol. Tiere 45: 275-308.         [ Links ]

FRANCKE-GROSMANN, H., 1963. Some New Aspects in Forest Entomology. Ann. Rev. Entomol. 8: 415-438.         [ Links ]

GRAHAM, K., 1967. Fungal-insect mutualism in trees and timber. Ann. Rev. Entomol. 12: 105-126.         [ Links ]

HARRINGTON, T.C., 1981. Cycloheximide sensitivity as a taxonomic character in Ceratocystis. Mycologia 73: 1123-1129.         [ Links ]

HARRINGTON, T.C., 1992. Leptographium. In Singleton LL, Mihail, JD, Rush, CM (Eds.), Methods for Research on Soilborne Phytopathogenic Fungi. APS Press, St. Paul, Minnesota, pp. 129–133.         [ Links ]

HARRINGTON, T.C., 2005. Ecology and evolution of mycophagous bark beetles and their fungal partners. In Vega FE, Blackwell, M. (Eds.), Insect-Fungal Associations: Ecology and Evolution. Oxford University Press, Inc. New York, pp. 257–292.         [ Links ]

HARRINGTON, T.C., AGHAYEVA, D.A., FRAEDRICH, S.W., 2010. New combinations in Raffaelea, Ambrosiella and Hyalorhinocladiella, and four new species from the red-bay ambrosia beetle, Xyleborus glabratus. Mycotaxon 111: 337–361.         [ Links ]

HAWKSWORTH, D.L., KIRK, P.M., SUTTON, B.C., PEGLER, D.N., 1995. Ainsworth & Bisby's Dictionary of the Fungi. CAB International, England, 616 pp.         [ Links ]

HENRIQUES, J., 2007. Fungos associados a Platypus cylindrus Fab. (Coleoptera: Platypodidae e sua relação com o declínio do sobreiro em Portugal. Dissertação de mestrado, Universidade de Évora, Évora, Portugal,188 pp.         [ Links ]

HENRIQUES, J., INÁCIO, M.L., PIRES, S., SOUSA, E., 2010. Platypus cylindrus Fab. (Coleoptera: Platypodidae) control strategies. IOBC/wprs Bulletin 57: 103-106.         [ Links ]

HENRIQUES, J., INÁCIO, M.L., SOUSA, E., 2006. Ambrosia fungi in the insect-fungi symbiosis in relation to cork oak decline. Rev. Iberoam. Micol. 23: 185-188.         [ Links ]

INÁCIO, M.L., HENRIQUES, J., GUIMARÃES, L., AZINHEIRA, H., LIMA, A., SOUSA E., 2010a. The symbiotic fungus Acremonium crotocinigenum causes canker on cork oak. In Actas do VI Congresso da Sociedade Portuguesa de Fitopatologia. Univ. Évora, Évora, Portugal: 191.

INÁCIO, M.L., HENRIQUES, J., LIMA, A., SOUSA, E., 2008. Fungi of Raffaelea genus (Ascomycota: Ophiostomatales) associated to Platypus cylindrus (Coleoptera: Platypodidae) in Portugal. Rev. de Ciências Agrárias 31: 96-104.         [ Links ]

INÁCIO, M.L., HENRIQUES, J., SOUSA, E., 2010b. Mycobiota associated with Platypus cylindrus Fab. (Coleoptera: Platypodidae) on cork oak in Portugal. IOBC/wprs Bulletin 57: 87-95.         [ Links ]

KIFFER, E., MORELET, M., 1997. Les Deutèromycetes – classification et clés d´identification génériques. INRA Editions,Paris, 306 pp.         [ Links ]

KIM, K.H., CHOI, Y.J., SEO, S.T., SHIN, H.D., 2009. Raffaelea quercus-mongolicae sp. nov. associated with Platypus koryoensis on oak in Korea. Mycotaxon 110: 189–197.         [ Links ]

KUBONO, T., ITO, S., 2002. Raffaelea quercivora sp. nov. associated with mass mortality of Japanese oak, and the ambrosia beetle (Platypus quercivorus). Mycoscience 43: 255-260.         [ Links ]

KÜLNHOLZ, S., BORDEN, J.H., UZONOVIC, A., 2003. Secondary ambrosia beetles in apparently healthy trees: Adaptations, potential causes and suggested research. Integrated Pest Management Reviews 6: 209-219.         [ Links ]

LINALDEDDU, B.T., SIRCA, C., SPANO, D., FRANCESCHINI, A., 2009. Physiological responses of cork oak and holm oak to infection by fungal pathogens involved in oak decline. For. Path. 39: 232–238.         [ Links ]

LINALDEDDU, B.T., SIRCA, C., SPANO, D., FRANCESCHINI, A., 2010. Variation of endophytic cork oak-associated fungal communities in relation to plant health and water stress. Forest Pathology, 2010, on line early, doi: 10.1111/j.1439-0329. 2010.00652.x.         [ Links ]

LUQUE, J., PERA, J., PARLADÉ, J., 2008. Evaluation of fungicides for the control of Botryosphaeria corticola on cork oak in Catalania (NE Spain). For. Path. 38: 147-155.         [ Links ]

MADDAU, L., CABRAS, A., FRANCESCHINI, A., LINALDEDDU, B.T., CROBU, S., ROGGIO, T., PAGNOZZI, D., 2009. Occurrence and characterization of peptaibols fromTrichoderma citrinoviride, an endophytic fungus of cork oak, using electrospray ionization quadrupole time-of-flight mass spectrometry. Microbiology 155: 3371–3381.         [ Links ]

MILLIGAN, R.H., OSBORNE, G.O., YTSMA, G., 1988. Evidence for an aggregation pheromone in Platypus gracilis (Coleoptera: Platypodidae). J. Appl. Entomol. 106: 20-24.         [ Links ]

MORELET, M., 1998. Une espèce nouvelle de Raffaelea, isolée de Platypus cylindrus, coléoptère xylomycétophage des chênes. Extrait des Annales de la Société des Sciences Naturelles et d’Archeologie de Toulon et du Var 50: 185-193.

MURATA, M., YAMADA, T., ITO, S., 2005. Changes in water status in seedlings of six species in the Fagaceae after inoculation with Raffaelea quercivora Kubono et Shin-Ito. J. For. Res. 10: 251–255.         [ Links ]

RENWICK, J.A., VITÉ, J.P., BILLINGS, R.F., 1977. Aggregation pheromones in the ambrosia beetle Platypus flavicornis. Naturwissenschaften 64: 226.         [ Links ]

SEABRA, A.F., 1939. Contribuição para a história de Entomologia em Portugal. Publicações D.G.S.F.A. 6: 1-20.         [ Links ]

SHORE, T.L., MCLEAN, J.A., 1983. Attraction of Platypus wilsoni Swaine (Coleoptera: Platypodidae) to traps baited with sulcatol, ethanol and a-pinene. Can. For. Serv. Bi-Mon. Res. Notes 3: 24-25.         [ Links ]

SOUSA, E., 1992. Alguns dos factores responsáveis pelo declínio do montado de sobro na Herdade da Chaminé. In Actas do 2º Encontro sobre os Montados de Sobro e Azinho, Évora, pp. 324-335.         [ Links ]

SOUSA, E., DEBOUZIE, D., 1999. Spatio-temporal distribution of Platypus cylindrus F. attacks in cork oak stands in Portugal. IOBC/ wprs Bull. 22: 47-58.         [ Links ]

SOUSA, E., DEBOUZIE, D., 2002. Contribution à la bioecologie de Platypus cylindrus F. au Portugal. IOBC/ wprs Bull. 25: 75-83.         [ Links ]

SOUSA, E., DEBOUZIE, D., PEREIRA, H., 1995. Le rôle de l'insecte Platypus cylindrus F. (Coleoptera, Platypodidae) dans le processus de dépérissement des peuplements de chêne-liège au Portugal. IOBC/ wprs Bull. 18: 24-37.         [ Links ]

SOUSA, E., INÁCIO, M.L., 2005. New Aspects of Platypus cylindrus Fab. (Coleoptera: Platypodidae): Life History on Cork Oak Stands in Portugal. In Lieutier F, Ghaioule, D. (Eds.), Entomological Research in Mediterranean Forest Ecosystems, INRA Editions, pp. 147-168.         [ Links ]

SOUSA, E., INÁCIO, M.L., EL ANTRY, S., BAKRY, M., KADIRI, Z.A., 2005. Comparaison de la bio-écologie de l'insecte Platypus cylindrus Fab. (Col., Platypodidae) dans les subéraies portugaises et marocaines. IOBC/ wprs Bull 28: 137-144.         [ Links ]

SOUSA, E., TOMAZ, I.L., MONIZ, F.A., BASTO, S., 1997. La répartition spatiale des champignons associés à Platypus cylindrus Fab. (Coleoptera: Platypodidae). Phytopath. Medit. 36: 145-153.         [ Links ]

SZAKACS, G., TENGERDY, R.P., 1997. Lignocellulotytic enzyme production on pretreated poplar wood by filamentous fungi. World Journal of Microbiology & Biotechnology 13: 487-490.         [ Links ]

TEIXEIRA, C., ALGARVIO, R.M., CASAS-NOVAS, P., BARATA, E.N., 2003. Actividade biológica de análogos de três componentes da putativa feromona de agregação de Platypus cylindrus (Coleoptera: Platypodidae). In Actas V Congresso Nacional de Etologia. Universidade do Algarve, Faro, 29.         [ Links ]

TOKORO, M., KOBAYASHI, M., SAITO S., KINUURA, H., NAKASHIMA, T., SHODA-KAGAYA, E., KASHIWAGI, T., TEBAYASHI, S., KIM, C.S., MORI, K., 2007. Novel aggregation pheromone, (1S,4R)-p-menth-2-en-1-ol, of the ambrosia beetle, Platypus quercivorus (Coleoptera: Platypodidae). Bull. For. For. Prod. Res. Inst. 6: 49–57.         [ Links ]

UCHASTNOVA, L.N., 1985. The Complex of fungi associated with the galleries of Platypus cylindriformis (Coleoptera, Platypodidae) and Xyleborus monographus (Coleoptera, Scolytidae). Biol. Nauki. 2: 47-50.         [ Links ]

VILLEMANT, C., FRAVAL, A., 1993. La faune entomologique du chêne-liège en forêt de la Mamora (Maroc). Ecol. Mediterr. 19: 89-98.         [ Links ]

YAMASAKI, M., FUTAI, K., 2008. Host selection by Platypus quercivorus (Murayama) (Coleoptera: Platypodidae) before and after flying to trees. Appl. Entomol. Zool. 43: 249–257.         [ Links ]

YTSMA, G., 1986. Inducing attack by male Platypus (Col.: Platypodidae) on wood billets in the laboratory. J. Appl. Entomol. 102: 210-212.         [ Links ]

 

Acknowledgements

We thank Doctor Maria Costa Ferreira (INRB, I.P.) for reviewing the manuscript and Octávio Chaveiro for the technical assistance in SEM photos. This research was supported in part by a grant from the Fundação para a Ciência e a Tecnologia BD/26033/2005.