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1 September 2011 Host Fungi and Feeding Habits of Ciidae (Coleoptera) in a Subtropical Rainforest in Southern Brazil, with an Overview of Host Fungi of Neotropical Ciids
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Ciids or minute tree-fungus beetles (Coleoptera: Ciidae) are amongst the most abundant and speciose fungivorous beetles. They spend most of their lives in or around polypore basidiomes, which are used as a food resource and shelter by larvae and adults. The study of Neotropical ciids is incipient and there is no comprehensive work on their host fungi. The present work provides a descriptive analysis of the Ciidae fauna, its feeding habits and polypore hosts at a subtropical rainforest in São Francisco de Paula, southern Brazil. A discussion on the current knowledge of host fungi of Neotropical Ciidae is also provided. Polypore basidiomes were collected in field trips carried out monthly from Aug 2006 to Mar 2007 and kept in the laboratory for up to 3 mo, while adult beetles were continuously captured from them. Basidiomes of 376 individual fungi were collected, comprising a total of 40 species. Among these, 152 individual fungi of 33 species had ciid beetles. Twenty-one species of ciids were recognized among 233 emergent adults. Only 1 ciid species was considered monophagous, 6 were considered oligophagous, and 6 polyphagous. Eight ciid species had less than 5 occurrences, and thus could not be included in any category. There is empirical evidence, from data provided or compiled herein, indicating that some morphologically similar Ciidae species, usually comprising a species group, frequently use the same or closely related species of fungi as the host. This is the first faunistic study on Ciidae and their host fungi in the Neotropical region.

Insects, particularly dipterans and coleopterans, are the animals that most frequently utilize resources from fungi (Hanski 1989; Komonen 2003; Amat-García et al. 2004). The consumption of mycelium, basidiomes, or spores of fungi is called either fungivory or mycophagy, and may be one of the oldest feeding habits of beetles (Gillott 1982; Lawrence 1989). The specialization in using 1 or few parts of fungi has led to special adaptations of the mouthparts, ovipositor, feeding habits, and life cycle of fungivorous organisms (Lawrence 1989).

Fungi are not homogeneous resources, and nutrients may be concentrated 10 times more in the basidiomes than in the substrate on which they grow (Hsu et al. 2002). Besides being rich in proteins and carbohydrates (Gooday 1995; Hsu et al. 2002), basidiomes have large amounts of biologically important elements, such as phosphorous and nitrogen (Watkinson et al. 2006), which, for example, may accelerate the development of the larvae of beetles (Martin 1979). However, basidiomes may also contain high concentrations of toxins, such as phenols, pyrones, and heterocyclic nitrogen complexes. Therefore, there is great selective pressure for beetles to develop mechanisms to avoid intoxication against these substances while using them as food or habitat (Martin 1979).

Feeding on basidiomes may be facultative or obligatory for fungivorous beetles (Robertson et al. 2004; Grimaldi & Engel 2005). Insects that depend on fungi as food and shelter in all their developmental stages are called mycetobionts (Hammond & Lawrence 1989). Among insects, minute tree-fungus beetles in the family Ciidae are included among the most abundant and speciose mycetobionts, and currently comprise around 650 described species grouped in 42 genera (Lopes-Andrade 2008b; Lawrence & LopesAndrade 2010). They are usually gregarious, and sometimes thousands of individuals may live inside a single basidiome (Lawrence & Britton 1991). As true mycetobionts, ciids spend most of their lives in or around a basidiome, leaving it only for dispersal. Both adults and larvae build galleries inside the basidiome, and pupation also occurs there (Lawrence 1973; Costa et al. 1988). As females usually oviposit continuously for a long period, overlapping generations are usually observed (Lawrence 1973).

In the Neotropical region (sensu Morrone 2002), the study of Ciidae is incipient. There are about 150 described species in 13 genera reported in the region, and dozens of undescribed forms known from museum and institutional collections (Lawrence & Lopes-Andrade 2008; Lopes-Andrade 2008b). The present work provides a descriptive analysis of the Ciidae and their feeding habits and their polypore hosts at a subtropical rainforest in São Francisco de Paula, southern Brazil. A compilation and brief discussion on the current knowledge of host fungi of Neotropical Ciidae is also provided. This is the first faunistic study of Ciidae and their host fungi in the Neotropical region.


Study Area

This study was carried out at the National Forest of São Francisco de Paula (FLONA/SFP, 29°23′-29°27′S, 50°23′-50°27′W), located in the municipality of São Francisco de Paula, in the state of Rio Grande do Sul, southern Brazil. FLONA/SFP has remnants of subtropical rainforest (Diverio et al. 2001), which occupies 40% of its area, in addition to plantation areas of Araucaria angustifolia (Bertol.) Kuntze, Pinus spp., and Eucalyptus spp. (Dobrovolski et al. 2006). The whole area covers 1,606 ha and reaches a maximum altitude of 923 m (Diverio et al. 2001). The climate is temperate, without a dry season, and with a hot summer (“Cfa” in the Koeppen-Geiger climate classification, sensu Peel et al. 2007). All mo are rainy, with an average annual precipitation of 2,252 mm (Backes et al. 2005).

Field Collection

Field trips were carried out monthly from Aug 2006 to Mar 2007. During arbitrary walks along tracks in forest areas of FLONA/SFP, polypore basidiomes, which usually develop on dead tree trunks, were collected with a knife. Sampling of the same individual fungi in subsequent field trips was avoided by following different tracks during each field trip. Young basidiomes, which usually do not have ciids, were not collected. An individual fungus was defined as the basidiome(s) occurring on a single trunk, because it is not possible to know where an individual fungus begins and ends in the field. Therefore, the number of basidiomes sampled from different individual fungi varied. Sampling effort was quite constant, with an average of 40 individual fungi collected per field trip. After removing the basidiomes from the trunks, they were separately packed in paper towels and plastic bags to prevent escape of beetle larvae and adults.

Laboratory Work

Samples were sorted for beetles within 3 days after of field collection to avoid fungal rotting and beetle death. After the first beetle sorting, the basidiome(s) of each individual fungus was kept individually to allow newly emerged beetles to breed. Basidiomes were stored in plastic containers covered with a fine mesh cloth to keep beetles inside (Komonen 2001). Moist tissue paper was put inside the containers to prevent fungi from drying out, and the containers were partially closed (Jonsell et al. 2001; Schigle 2008).

As it was difficult to observe beetles outside the woody fungi, their containers were wrapped in aluminum foil and a glass vial was attached to each 1 to attract beetles to light (Jonsell et al. 2001). However, not all beetle species were attracted to light, so all fungi were dissected 3 mo later to observe whether or not there were live beetles inside them. Before being dissected, all fungi were submitted to humidity monitoring and extraction of adult beetles twice a week. For individual fungi hosting a large number of adult beetles, at least 50 beetles were collected to guarantee capture of all species. According to Schigle (2008), direct collecting on the fungus and rearing adult beetles from their basidiomes remain reliable and sensible methods of the field research. Due to the methodology used here, all host fungi records were treated as breeding records.

All fungi that had associated Ciidae were identified following the pertinent works on their taxonomy (Ryvarden & Johansen 1980; Gilbertson & Ryvarden 1986, 1987; Ryvarden 1991; Silveira & Guerrero 1991; Ryvarden & Iturriaga 2003; Ryvarden 2004). A key to the pileate polypores found in FLONA/SFP was provided by Silveira et al. (2008) based on the fungi collected for the present study, including all species except for Mycobonia flava (Sw.) Fr. (Polyporales: Boreostereaceae). Voucher specimens of the fungi were deposited at the ICN herbarium (Instituto de Biociências UFRGS). Adult ciids were identified by comparison to named specimens and literature data (Lawrence 1967, 1971; Lopes-Andrade et al. 2002; Lopes-Andrade & Lawrence 2005; Lopes-Andrade 2008b). Voucher specimens of the adult ciids were deposited at the collection of the Museu de Ciências Naturais, Fundação Zoobotânica do Rio Grande do Sul (MCNZ, Porto Alegre, RS, Brazil), and at the Lopes-Andrade Collection housed in the Universidade Federal de Viçosa (LAPC, Viçosa, MG, Brazil).

Classification of Feeding Habits

The classification of insects as specialists and generalists is based on the number of hosts utilized by each species. However, such classification is a matter of convention, because species of a major taxonomic group may show a continuum in the number of host species (Thompson 1998; Begon et al. 2006). In the case of fungivorous insects, there are divergent opinions on how many records are necessary for a given fungus species to be considered as a host (Lawrence 1973; Orledge & Reynolds 2005). Consequently, studies on feeding habits of fungivorous insects are based on different concepts of feeding specificity, and there is no single or most correct classification (Jonsell et al. 1999; Jonsell & Nordlander 2004). Here, we considered monophagous species as strict specialists (who feed in only 1 host species). When a ciid species exclusively or preferably used 1 fungus family as its host (according to Kirk et al. 2001), it was defined as oligophagous, otherwise as polyphagous (Gess & Gess 2004; Schoonhoven et al. 2005; Blüthgen & Metzner 2007). Therefore, we called oligophagous species the specialists with at least 90% of occurrence in the same fungus family. When the percentage of occurrences in a single fungus family was less than 90%, the ciid species was considered polyphagous (generalist). Here, an occurrence refers to the collection of 1 to several specimens of a ciid species in a single individual fungus. Classification of feeding habits was applied only to ciid species with at least 5 records of occurrence.


Basidiomes of 376 individual fungi were collected, comprising a total of 40 species. Among these, 152 individual fungi of 33 species (see Figs. 1–8 for a few examples) had ciid beetles. The ciid host fungi belonged to 7 families, 6 in the order Polyporales and 1 in Hymenochaetales (Table 1). Basidiomes of the following 7 fungi species were devoid of Ciidae: Abundisporus subflexibilis (Berk. & M. A. Curtis) Parmasto, Antrodiella liebmanii (Fr.) Ryvarden, Antrodiella reflexa Ryvarden & Núñez, Inonotus fulvomelleus Murrill, Junghuhnia sp. (probably J. minuta I. Lindblad & Ryvarden), Laetiporus sulphureus (Bull.) Murrill, and Polyporus ciliatus Fr. These non-host species are not listed in Tables 1 and 3. The occurrence of ciids in Mycobonia Pat., Amauroderma Murrill, Flaviporus Murrill, and Junghuhnia Corda are the first records of ciids feeding on fungi of these genera.

Twenty-one species of ciids (Table 2) were recognized, with 233 occurrence data. In several cases there was more than 1 ciid species in an individual fungus. Ten ciid species were identified to species level, 9 were determined to genus level only, and 2 species belong to 2 undescribed genera (Table 2). The following 4 ciid species (Figs. 9–12) are new country records for Brazil: Ceracis simplicicornis (Pic), Cis melliei Coquerel, Xylographus corpulentus Mellié, and X. gibbus Mellié. These 4 species were previously known only from their original descriptions. Three species-groups of Cis Latreille (named fagi, melliei and vitulus by Lawrence 1971), each with 1 species from FLONA/SFP (see Table 2), are new country records of the groups from Brazil.

Figs. 1–12.

Some host fungi (1–8) and Ciidae (9–12) collected in a subtropical rainforest in São Francisco de Paula (Rio Grande do Sul, southern Brazil): 1, Ganoderma australe; 2, Rigidoporus concrescens; 3, Fomitella supina; 4, Lenzites betulina; 5, Perenniporia martii; 6, Trametes membranacea; 7, Trichaptum sector; 8, Flaviporus subhydrophilus; 9, male of Ceracis simplicicornis, lateral view; 10, male of Cis melliei, dorsal view; 11, male of Xylographus corpulentus, lateral view; 12, male of Xylographus gibbus, lateral view.


The sampled ciid species had variable host ranges (Table 3). Scolytocis fritzplaumanni Lopes-Andrade was the only monophagous species, with all 19 occurrences in Ganoderma australe (Fr.) Pat. Six ciid species were considered oligophagous (Table 3). Among these oligophagous species, Ceracis limai Lopes-Andrade, Madureira & Zacaro and Gen.1 sp. were exclusively or mostly frequently associated with Hymenochaetaceae. The remaining oligophagous species were exclusively or mostly frequently associated with Polyporaceae. Six ciids were considered polyphagous (Table 3). Eight ciid species had less than 5 occurrences, and thus could not be included in any category (Table 3).

Among the 8 ciid species without an attributed feeding habit, 3 showed a tendency to oligophagy: Cis sp.3 (comptus group) and Cis diadematus Mellié, each with 3 occurrences only in Polyporaceae species; and Cis kawanabei Lopes-Andrade, with 4 occurrences in Rigidoporus spp. (Meripilaceae). Three non-categorized ciid species showed a tendency to polyphagy: Cis sp. 5 (fagi group) with 3 occurrences, each in a fungus of a different host family; Cis melliei with 3 occurrences in hosts of 2 families; and Ceracis sp.3 with 2 occurrences, each in a host from different families. No tendency could be traced for X. gibbus because it was captured only once. The last non-categorized ciid species, Gen.2 sp., occurred in only 1 host fungus, Perenniporia martii (Berk.) Ryvarden (with 4 occurrences).








Ciidae of FLONA/SFP

The Ciidae found at FLONA/SFP are characteristic of a Neotropical fauna, and the species, species-groups, and most genera are, for instance, quite distinct from those of the Andean region (see Lopes-Andrade 2010 for a brief discussion on the composition of the Andean Ciidae fauna). Among the new records from Brazil, C. simplicicornis belongs to the furcifer species-group, together with the common Neotropical species Ceracis cornifer (Mellié) and Ceracis furcifer Mellié. It was previously known only from the type locality in Buenos Aires, Argentina (Pic 1916). Cis melliei belongs to the melliei species-group, which comprises also Cis crinitus Lawrence, Cis rotundulus Lawrence, Cis ursulinus Casey, Cis hirsutus Casey, and Cis hirtellus Jacquelin-Duval, the latter 2 being possible synonyms (Lawrence 1971). All species of the melliei species-group are rarely collected, and few specimens are available in collections for most of them. Xylographus corpulentus and X. gibbus were formerly known only from Peru and Colombia, respectively. However, both have been collected in several localities in southeastern, northeastern, and northern Brazil, but the specimens from São Francisco de Paula are the first collected in southern Brazil (C.L.A., unpublished data). Each of these 2 species of Xylographus Mellié may indeed constitute a species-complex, rather than a single species.

Ceracis bicornis Mellié, Cis testaceimembris (Pic), and Cis kawanabei Lopes-Andrade are species frequently collected in Brazil (C.L.A., unpublished data). The former belongs to the cucullatus species-group, and the latter 2 belong to the taurus species-group together with Cis sp.1. However, all these species are widespread and polymorphic, and each may constitute a species-complex, instead of a single species.

Cis diadematus was previously known only from its original description, from Bahia, Brazil (Mellié 1849). In fact, it does not fit the generic limits of Cis and will be transferred to a new genus in a work already in preparation (C.L.A., unpublished data). Cis sp.3 possibly belongs to the comptus species-group, which comprises species of broad geographic distribution in the Neotropics (Lopes-Andrade et al. 2003; de Almeida & Lopes Andrade 2004) and several Nearctic and Palearctic species (Lawrence 1971; Krolik 2002). Cis sp.4 belongs to the tricornis species-group, which is mostly Neotropical (Lawrence 1971).






Ceracis sp.1 is morphologically similar to Ceracis multipunctatus (Mellié), a northern Neotropical species that also occurs in Alabama and Florida (USA). Ceracis sp.2 is morphologically similar to Ceracis powelli Lawrence, a species from southern Arizona (USA) and northern Mexico (Lawrence 1967). Ceracis limai is not frequently collected, and specimens found in FLONA/SFP are the first known from southern Brazil. Ceracis sp.3 is a small species without secondary sexual characters in males, and of unknown morphological affinities in the Neotropical region. It somewhat resembles females of species of the furcatus species-group, such as Ceracis variabilis Mellié.

Scolytocis fritzplaumanni was described during the elaboration of this work, based partially on the specimens collected at FLONA/SFP (Lopes-Andrade 2008b). The species seems to be restricted to southern Brazil and is 1 of 3 species of Xylographellini found in the country (LopesAndrade 2008b).

The genus assignment of the Strigocis sp. from FLONA/SFP is a matter of discussion. The specimens have a suturai flange diverging near the elytral apex and the apex of each protibia bears a row of spines, a combination of features regarded as diagnostic for Strigocis Dury (Lawrence 1971; Lopes-Andrade 2011). The species named Gen.1 sp. and Gen.2 sp. belong to 2 undescribed Neotropical genera, each with a small number of species previously collected in northern and southeastern Brazil (C.L.A., unpublished data). It will certainly take several years to adequately describe the species of FLONA/SFP. The high proportion of undescribed forms, in relation to the described species, had been expected, because Neotropical species of the family have not been studied well until recently.

Host Fungi and Feeding Habits

Among the fungi recorded as ciid hosts for the first time, Amauroderma is a pantropical genus (Ryvarden 1991) and Mycobonia is distributed only in the Neotropical region (Corner 1984). Junghuhnia and Flaviporus may also be found in temperate regions (Ginns 1980; Gilbertson & Ryvarden 1986), but currently there is no available information on their use as hosts by ciids. The records of 5 ciid species in Pycnoporus sanguineus (L.) Murrill, a common species throughout the Neotropical region, is worth mentioning. This fungus belongs to the trametoid group and, as the other species of the genus, their basidiomes have a high concentration of cinnabarins, a group of toxic substances with antibiotic action (Smânia et al. 1998; Oliveira et al. 2007). The high toxicity of these fungi would be expected to function as a barrier for their consumption by insects, and therefore it would be expected that few beetle species could use them as a food resource; which is supported by documented reports. So far, only species of the Ceracis furcifer species-group have been collected in Pycnoporus P. Karst. fungi (Lawrence 1973; Gumier-Costa et al. 2003). However, some insects are known to be resistant to the chemicals of their hosts (see Schoonhoven et al. 2005 for plant examples). The use of Pyc. sanguineus by 5 ciid species (see Table 3) suggests that insect resistance may also be possible against antibiotic constituents in fungi. Both Ganoderma australe (Fr.) Pat. and Pyc. sanguineus hosted the same number of ciid species at FLONA/SFP, although 59 occurrences of ciids were recorded from the former species, 1 of the commonest bracket fungi in the study area, and only 15 occurrences were recorded from Pyc. sanguineus.

Among the oligophagous species, only 2, C. limai and Gen.1 sp., were found mostly or exclusively in Hymenochaetaceae. The other oligophagous species were mostly associated with Polyporaceae. It is interesting to note that none of the oligophagous ciids were mostly associated with the other 5 Polyporales families, which means that fungi of these families were most frequently explored by polyphagous and monophagous species. Gen.2 sp. had all of its 4 occurrences in Perenniporia martii and future records may confirm that the species is monophagous.

Considering the patchy distribution of the hosts of Ciidae, the existence of strong selection against specialization, particularly monophagy, can be expected to be operating. Such a feeding habit would only be sustainable if the host were a reliably present species amenable to be used efficiently as a resource. The only monophagous species found in FLONA/SFP was S. fritzplaumanni, and it occurred in the most frequent and perennial fungus, G. australe. The specialization in closely related hosts (oligophagy), rather than in a single host species, would be the most advantageous strategy, because these hosts would be more efficiently located, and variations in population dynamics of a single fungus species would not affect the availability of resources to such ciid species. Several studies suggest that oligophagous insects tend to use closely related hosts as resources (Jonsell & Nordlander 2004; Schoonhoven et al. 2005; Bangert et al. 2006; Blüthgen & Metzner 2007). This pattern may be applied to oligophagous ciids, as in the case of C. limai, which occurred only in species of Phellinus Quél, except for 1 occurrence in R. ulmarius. In such cases, the oligophagous species should have the capability of detecting volatiles common to closely related host fungi, and a physiological mechanism to allow breeding in these hosts. However, the factors determining host use by ciids are not clearly elucidated (Guevara et al. 2000). It has already been suggested that host fungi have volatile compounds that attract insects (Jonsson et al. 1997; Jonsell et al. 2003; Orledge & Reynolds 2005), and it has already been shown that ciid species have distinct responses to several fungal volatiles (Thakeow et al. 2008). Graf (2008) also showed that the consistency of the basidiome is important for host selection.

The available surveys or compilations on the host fungi of Ciidae are for the Nearctic and Palearctic faunas (e.g. Paviour-Smith 1960; Lawrence 1973; Reibnitz 1999). In these works, most of the ciid species were shown to be polyphagous, several were oligophagous, and a few species were truly monophagous. Lawrence (1973) suggested that the degree of host specificity would be greater in tropical forests than in temperate and subtropical regions, but he did not suggest possible explanations for this pattern. Future studies should concentrate on tropical and subtropical climate areas in order to evaluate the degree of specialization of Ciidae and its correlation to latitude and/or climate.

Host Fungi of Neotropical Ciidae

The oldest information available was provided by Mellié (1849) who cited Pyc. sanguineus as the host for C. furcifer in Izabal, Guatemala, and by Coquerel (1849) who cited Rigidoporus lineatus (Pers.) Ryvarden (Meripilaceae) as the host for Cis melliei at Fort-de-France, Martinique. Interestingly, Cis melliei was found in FLONA/SFP and had 3 occurrences, each from a different host fungus, 2 Hymenochaetaceae and 1 Steccherinaceae (Table 3). Future records from both locations may show that the species is polyphagous, or that there are regional differences in host-use for this species.

Lawrence (1971) listed the host fungi for Nearctic populations of several Neotropical-Nearctic Cis species, as follows: Cis castlei (Dury) mainly in Bjerkandera adusta (Willd.) P. Karst. and Trichaptum biforme (Fr.) Ryvarden; Cis cayensis Lawrence mainly in Inonotus porrectus Murrill (doubtful identification, see Lawrence 1971), Phellinus robiniae (Murrill) A. Ames, and Hexagonia hydnoides (Sw.) M. Fidalgo; Cis creberrimus Mellié in several hosts, which indicates polyphagous feeding habits; Cis crinitus Lawrence, with few records but occurring mainly in H. hydnoides, Coriolopsis caperata (Berk.) Murrill, and Lopharia papyrina (Mont.) Boidin; Cis hirsutus Casey mainly in H. hydnoides, Fomes fasciatus (Sw.) Cooke, and Ganoderma zonatum Murrill; Cis subfuscus Gorham in Trametes hirsuta (Wulfen) Pilát, Panellus stipticus (Bull.) P. Karst., Lenzites elegans (Spreng.) Pat., and Pyc. sanguineus. Cis delicatulus (Jacquelin-Duval), of the tricornis species-group, was originally found in Trametes membranaceae (Sw.) Kreisel (Jacquelin-Duval 1857) and has 1 record in Trametes villosa (Sw.) Kreisel (Navarrete-Heredia & Burgos-Solorio 2000). Interestingly, the Cis sp.4 from FLONA/SFP, which also belongs to the tricornis species-group, had 80% of its occurrences in the former fungus and 1 occurrence in the latter. Jacquelin-Duval (1857) also cited that Cis hirtellus Jacquelin-Duval was collected in “boletus ungulatus”, which possibly corresponds to Fomitopsis pinicola (Sw.) P. Karst. Cis fluzai de Almeida & Lopes-Andrade was originally found in Pyc. sanguineus (de Almeida & Lopes-Andrade 2004), where occasionally species of the comptus speciesgroup, such as Cis subfuscus, are found. Notably, the only species of the comptus species-group found in FLONA/SFP, Cis sp.3, had 1 record in Pyc. sanguineus and the other 2 occurrences were on different species of the same fungus family. Cis chinensis Lawrence, an Asian species introduced in Brazil (Lopes-Andrade 2008a), was observed breeding in Schizophyllum commune Fr. and other unidentified fungi together with Ennearthron victori Lopes-Andrade & Zacaro. Finally, it is worth mentioning that although these previous host records for Cis species seem to be numerous, the data is scanty considering that Cis is the most speciose genus of the Neotropical region, with about 70 described species.

Falsocis brasiliensis Lopes-Andrade was collected only in Hymenochaete luteobadia (Fr.) Höhn. & Litsch., wrongly identified as Phellinus sp. by Lopes-Andrade (2007) but belonging to the same fungus family, Hymenochaetaceae. Porculus grossus Lawrence was most frequently found in Rigidoporus Murrill basidiomes (R. concrescens (Mont.) Rajchenb., R. lignosus (Klotzsch) Imazeki, and unidentified Rigidoporus spp.); the other 2 host records for the species, Trametes corrugata (Pers.) Bres. and Ganoderma sp., were possibly incidental (Lawrence 1987; NavarreteHeredia & Burgos-Solorio 2000). Porculus grossus is a common species in the Neotropical region, and several host fungi suitable for it were collected in the present survey. However, this beetle was not found in FLONA/SFP. Few species occupied Rigidoporus basidiomes in FLONA/SFP, 5 of them were polyphagous (C. bicornis, C. limai, Ceracis sp.1, Ceracis sp.2, and Cis sp.1), whereas Cis kawanabei was the only beetle that occurred exclusively in Rigidoporus.

Species of Phellinocis Lopes-Andrade & Lawrence are usually found in Phellinus (LopesAndrade & Lawrence 2005). Phellinocis erwini Lopes-Andrade & Lawrence was collected mainly in basidiomes of Phellinus gilvus (Schwein.) Pat. in Panama, whereas Phellinocis thayerae LopesAndrade & Lawrence was most frequently found in Phellinus nilgheriensis (Mont.) G. Cunn. in the same country. However, both ciid species were also less frequently collected in unidentified Phellinus spp., and Phellinocis thayerae had 2 records in P. gilvus and a single record in Phylloporia pectinata (Klotzsch) Ryvarden. There are no published data on the host fungi of Phellinocis romualdoi Lopes-Andrade & Lawrence, but the species is usually collected in basidiomes of unidentified Hymenochaetaceae in southeastern, northeastern, and northern Brazil (C.L.A., unpublished data). It is worth mentioning that no Phellinocis were found in FLONA/SFP, although several suitable host fungi for them were collected. The genus has 2 described species from the northern Neotropical region, and only 1 species, Phellinocis romualdoi, from the southern Neotropics. The southernmost record of Phellinocis romualdoi is from Lavras, Minas Gerais (21fi01_553.gif14′S) (Lopes-Andrade & Lawrence 2005), about 1,000 km north of FLONA/SFP.

Data on host fungi of the New World Ceracis Mellié are based mainly on records for Nearctic populations of Neotropical-Nearctic species (Lawrence 1967), as follows (in part): Ceracis curtus (Mellié) in Fomes fasciatus and H. hydnoides; Ceracis nigropunctatus Lawrence mainly in H. hydnoides and Trametes hirsuta; Ceracis pullulus mainly in P. gilvus, H. hydnoides, and G. zonatum; Ceracis punctulatus Casey in P. gilvus and less frequently in several other fungi; and Ceracis quadricornis Gorham mainly in Coriolopsis occidentalis (Klotzsch) Murrill, Trametes spp. and H. hydnoides. Ceracis similis Horn was collected in Ganoderma lobatum (Schwein.) G.F. Atk. in Mexico (Navarrete-Heredia 1987). Ceracis castaneipennis Mellié was found in Trichaptum sector (Ehrenb.) Kreisel in Cuba, and the enigmatic Ceracis taurulus Jacquelin-Duval was taken in Trametes membranaceae (Jacquelin-Duval 1857). The Nearctic Ceracis monocerus Lawrence, a member of the furcifer species-group, is usually collected in Pyc. sanguineus (Lawrence 1967), as well as morphologically similar Neotropical species of the same species-group, such as C. cornifer and C. furcifer (Lawrence 1973; Gumier-Costa et al. 2003). Ceracis simplicicornis in FLONA/SFP had 90% of its occurrences in Pyc. sanguineus, confirming the general pattern of host-use by the species in the group. Ceracis multipunctatus (Mellié) was mostly found in G. zonatum and Fomitella supina (Sw.) Murrill (Lawrence 1967). A morphologically similar species from FLONA/ SFP, Ceracis sp.1, was observed mostly in G. australe (64.5%). Specimens included in the type series of C. limai (singularis species-group) were collected in unidentified Phellinus and Ganoderma in southern Brazil (Lopes-Andrade et al. 2002). However, the species is most frequently collected in basidiomes of Phellinus spp. (C.L.A., unpublished data), in a similar pattern as found in FLONA/SFP (more than 93% of the occurrences in Phellinus spp.). The closely related Ceracis singularis (Dury), from North America, is also found in Phellinus spp., mainly in P. gilvus (Lawrence 1967). It is worth mentioning that no other species of Ceracis from FLONA/SFP was found in Phellinus.

The Neotropical species of Scolytocis Blair (Xylographellini) are most frequently found in Ganoderma spp., Rigidoporus spp., and Phellinus spp. basidiomes (Lopes-Andrade 2008b). However, a few records provide identification of hosts to species level, as follows: Scolytocis kiskeyensis LopesAndrade in Fomes fasciatus (but also in an unidentified Ganoderma); Scolytocis lawrencei Lopes-Andrade in R. lineatus, R. microporus (Fr.), and Earliella scabrosa (Pers.) Gilb. & Ryvarden (and in Rigidoporus sp.); and Scolytocis panamensis Lopes-Andrade in Fomes pseudosenex (Murrill) Sacc. & Trotter (and in Phellinus sp.). The identified host fungus of Scolytocis fritzplaumanni, G. australe, observed in São Francisco de Paula and cited by Lopes-Andrade (2008b) corresponds exactly to the host records provided for the species in the present work. Lopes-Andrade (2008b) also cited an unidentified Ganoderma from Guaratuba as host for the species, which could possibly be G. australe in a very advanced decaying stage.


The present work shows that most of the data previously available on host fungi of Neotropical Ciidae were scattered, provided by different authors during more than a century and a half. The data provided here on the host fungi of the Ciidae of FLONA/SFP are based on the first comprehensive survey of host fungi of a Neotropical Ciidae fauna, and a first step in elucidating the patterns of host-use and host-specialization of Neotropical Ciidae.

Furthermore, there is empirical evidence, from the present work and data compiled herein, indicating that some morphologically similar ciids, usually comprising a species-group, frequently use the same fungus species or closely related species as host. Evolutionary and ecological processes certainly determine host-use by ciids. Further studies should analyze the co-occurrence of ciid species in a host to evaluate the possibility of competitive exclusion and to explain regional patterns of host-use by ciids. Also, future work should focus on the phylogenetic analyses of ciids to make possible a comparison to phylogenetic hypotheses of their host fungi.


This project was partially financed by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) and by the Graduate Program in Ecology of the Federal University of Rio Grande do Sul (grant to L.V.G.P.). C.L.A. was supported by Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG: PPP 21/2008, CRA - APQ-00049-09; PPM 03/2010, CRA PPM-00017-10), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq: post-doctoral fellowship n° 151800/2007-3, from Nov 2007 to Oct 2008; PROTAX 52/2010 n° 562229/2010-8), and the Graduate Program in Entomology of the Federal University of Viçosa. L.A.M. was financed by CNPq (post-doctoral fellowship, process n° 150639/2009-0). The recognition of Gen.2 sp. as not belonging to Xylographus and the identification of the true Xylographus species were possible only after a careful comparison and study of the specimens by Vivian E. Sandoval-Gómez, who also kindly corrected the abstract in Spanish. We thank Tatiana B. Gibertoni for the identification of Hymenochaete luteobadia, host fungus of Falsocis brasiliensis.



E. C. Amat-García , G. D. Amat-García , and L. G. Henaom 2004. Diversidad taxonómica y ecológica de la entomofauna micófaga en un bosque altoandino de la cordillera oriental de Colombia. Ecología 28: 223–231. Google Scholar


A. Backes , F. L. Prates , and M. G. Viola 2005. Produção de serapilheira em Floresta Ombrófila Mista, em São Francisco de Paula, Rio Grande do Sul, Brasil. Acta Bot. Bras. 19: 155–160. Google Scholar


R. K. Bangert , R. J. Turek , B. Rehill , G. M. Wimp , J. A. Schweitzer , G. J. Allan , J. K. Bailey , G. D. Martinsen , P. Keim , R. L. Lindroth , and T. G. Whitham 2006. A genetic similarity rule determines arthropod community structure. Mol. Ecol. 15: 1379–1391. Google Scholar


M. Begon , C. R. Townsend , and J. L. Harper 2006. Ecologia: de individuos a ecossistemas, 4 ed. Artmed, Porto Alegre. Google Scholar


N. Bluthgen , and A. Metzner 2007. Contrasting leaf age preferences of specialist and generalist stick insects (Phasmida). Oikos 116: 1853–1862. Google Scholar


C. Coquerel 1849. Observations entomologiques sur divers Coléoptères recueillis aux Antilles. Ann. Soc. Entomol. Fr. 7(2): 441–454. Google Scholar


E. J. H. Corner 1984. Ad Polyporaceas II & III. Beih. Nova Hedwigia 78: 1–222. Google Scholar


C. Costa , S. A. Vanin , and S. A. Casari-Chen 1988. Larvas de Coleoptera do Brasil. Museu de Zoologia da Universidade de São Paulo, São Paulo. Google Scholar


S. D. P. De Almeida , and C. Lopes-Andrade 2004. Two new Brazilian species of Cis Latreille, 1796 (Coleoptera: Tenebrionoidea: Ciidae). Zootaxa 717:1–10. Google Scholar


V. T. Diverio , A. Stranz , and T. L. Dutra 2001. Uso de imagens Landsat no mapeamento de Araucaria angustifolia no Estado do Rio Grande do Sul, pp. 1579–1581. IN Anais X Simpósio Brasileiro de Sensoriamento Remoto. UNISINOS, Foz do Iguaçu, São Leopoldo. Google Scholar


R. Dobrovolski , R. Both , I. P. Coelho , J. F. B. Stolz , G. Schüssler , G. G. Rodrigues , T. Guerra , and S. M. Hartz 2006. Levantamento de áreas prioritárias para a conservação da Floresta Nacional de São Francisco de Paula (RS, Brasil) e seu entorno. Rev. Bras. Biociências 4: 7–14. Google Scholar


S. K. Gess , and F. W. Gess 2004. A comparative overview of flower visiting by non-apis bees in the semiarid to arid areas of Southern Africa. J. Kansas Ent. Soc. 77: 602–618. Google Scholar


R. L. Gilbertson , and L. Ryvarden 1986. North America Polypores (1). Fungiflora, Oslo. Google Scholar


R. L. Gilbertson , and L. Ryvarden 1987. North America Polypores (2). Fungiflora, Oslo. Google Scholar


C. Gillott 1982. Entomology. Plenum Press, New York. Google Scholar


J. Ginns 1980. The genus Flaviporus Murrill (Polyporaceae). Can. J. Bot. 58: 1578–1590. Google Scholar


G. M. Gooday 1995. Cell walls, pp. 43–62 In N. A. R. Gow , and G. M. Gad [eds.], The Growing Fungus. Chapman & Hall, London. Google Scholar


L. V. Graf 2008. Interação trófica entre Coleoptera e basidiomas de Polyporales e Hymenochaetales (Fungi: Basidiomycota). Dissertation, Graduate Program in Ecology, Federal University of Rio Grande do Sul, Porto Alegre. 68 pp. Google Scholar


D. Grimaldi , and M. S. Engel 2005. Evolution of the Insects. Cambridge University Press, New York. 755 pp. Google Scholar


R. Guevara , A. D. M. Rayner , and S. E. Reynolds 2000. Orientation of specialist and generalist fungivorous ciid beetles to host and non-host odours. Phys. Entomol. 25: 288–295. Google Scholar


F. Gumier-Costa , C. Lopes-Andrade , and A. A. Zacaro 2003. Association of Ceracis cornifer (Mellié) (Coleoptera: Ciidae) with the bracket fungus Pycnoporus sanguineus (Basidiomycetes: Polyporaceae). Neotropical Entomol. 32: 359–360. Google Scholar


P. M. Hammond , and J. F. Lawrence 1989. Mycophagy in insects: a summary, pp. 275–324 In N. Wilding , N. M. Collins , P. M. Hammond and J. F. Weber [eds.], Insect-Fungus Interactions. 14th Symp. Royal Entomol. Soc. London. Academic Press, London. Google Scholar


I. Hanski 1989. Fungivory: fungi, insects and ecology, pp. 24–68 In N. Wilding , N. M. Collins , P. M. Hammond and J. F. Weber [eds.], Insect-Fungus Interactions. 14th Symp. Royal Entomol. Soc. London. Academic Press, London. Google Scholar


T. Hsu , L. Shiao , C. Hsieh , and D. Chang 2002. A comparison of the chemical composition and bioactive ingredients of the Chinese medicinal mushroom DongChongXiaCao, its counterfeit and mimic, and fermented mycelium of Cordyceps sinensis. Food Chem. 78: 463–469. Google Scholar


P. N. C. Jacquelin-Duval 1857. Ordre des Coléoptères Lin., pp. 137–328 In R. Sagra [ed.], Histoire Physique, Politique, et Naturelle de l'Ile de Cuba. Tome 7. Bertrand, Paris. Google Scholar


M. Jonsell , and G. Nordlander 2004. Host selection patterns in insect breeding in bracket fungi. Ecol. Entomol. 29: 697–705. Google Scholar


M. Jonsell , G. Nordlander , and B. Ehnström 2001. Substrate association of insects breeding in fruiting bodies of wood-decaying fungi. Ecol. Bull. 49: 173–194. Google Scholar


M. Jonsell , G. Nordlander , and M. Jonsson 1999. Colonization patterns of insects breeding in wooddecaying fungi. J. Insect Conserv. 3: 145–161. Google Scholar


M. Jonsell , M. Schroeder , and T. Larsson 2003. The saproxylic beetle Bolitophagus reticulatus: its frequency in managed forests, attraction to volatiles and flight period. Ecography 26: 421–428. Google Scholar


M. Jonsson , G. Nordlander , and M. Jonsell 1997. Pheromones affecting flying beetles colonizing the polypores Fomes fomentarius and Fomitopsis pinicola. Entomol. Fenn. 8: 162–165. Google Scholar


P. M. Kirk , P. F. Cannon , J. C. David and J. A. Stalpers 2001. Ainsworth & Bisby's Dictionary of the Fungi. 9 ed. CABI Bioscience, Wallingford. 650 pp. Google Scholar


A. Komonen 2001. Structure of insect communities inhabiting old-growth forest specialist bracket fungi. Ecol. Entomol. 26(1): 63–75. Google Scholar


A. Komonen 2003. Hotspots of insect diversity in Boreal forests. Cons. Biol. 17: 976–981. Google Scholar


R. Królik 2002. Cis tauriensis n. sp. from Turkey (Coleoptera: Ciidae). Genus 13(2): 197–202. Google Scholar


J. F. Lawrence 1967. Delimitation of the genus Ceracis (Coleoptera: Ciidae) with a revision of North American species. Bull. Mus. Comp. Zool. 136: 91– 143. Google Scholar


J. F. Lawrence 1971. Revision of the North American Ciidae (Coleoptera). Bull. Mus. Comp. Zool. 142: 419–522. Google Scholar


J. F. Lawrence 1973. Host preference in ciid beetles (Coleoptera: Ciidae) inhabiting the fruiting bodies of basidiomycetes in North America. Bull. Mus. Comp. Zool. 145: 163–212. Google Scholar


J. F. Lawrence 1987. A new genus of Ciidae (Coleoptera, Tenebrionoidea) from the Neotropical region. Rev. Bras. Entomol. 31(1): 41–47. Google Scholar


J. F. Lawrence 1989. Mycophagy in the Coleoptera: Feeding Strategies and Morphological Adaptations, pp. 1–23 In N. Wilding , N. M. Collins , P. M. Hammond and J. F. Weber [eds.], Insect-Fungus Interactions. 14th Symp. Royal Entomol. Soc. London. Academic Press, London. Google Scholar


J. F. Lawrence , and E. B. Britton 1991. Coleoptera (Beetles), pp. 543–683 In CSIRO [ed.], The Insects of Australia, 2 ed. Melbourne Univ. Press, Carlton. Google Scholar


J. F. Lawrence , and C. Lopes-Andrade 2008. Ciidae Species Listing In J. Hallan [ed.], Biology Catalog. Texas A&M University, Accessed on October 2010. Google Scholar


J. F. Lawrence , and C. Lopes-Andrade 2010. Ciidae Leach in Samouelle 1819, pp. 504–514 In R. G. Beutel , and R. A. B. Leschen [eds.], Handbook of Zool. Vol. IV Arthropoda: Insecta. Part 39. Coleoptera, Vol. 2: Morphol. and System. (Elateroidea, Bostrichiformia, Cucujiformia partim). Walter de Gruyter, Berlin, New York. Google Scholar


C. Lopes-Andrade 2007. Notes on Falsocis Pic (Coleoptera: Tenebrionoidea: Ciidae), with the description of an endangered Brazilian species. Zootaxa 1544: 41–58. Google Scholar


C. Lopes-Andrade 2008a. The first record of Cis chinensis Lawrence from Brazil, with the delimitation of the Cis multidentatus species-group (Coleoptera: Ciidae). Zootaxa 1755: 35–46. Google Scholar


C. Lopes-Andrade 2008b. An essay on the tribe Xylographellini (Coleoptera: Tenebrionoidea: Ciidae). Zootaxa 1832: 1–110. Google Scholar


C. Lopes-Andrade 2010. Two new species of Cis Latreille (Coleoptera: Ciidae) from Chile. Zootaxa 2441: 53–62. Google Scholar


C. Lopes-Andrade 2011. The first Strigocis Dury (Coleoptera, Ciidae) from the southern Neotropical region and a provisional key to world species. Zookeys 81: 27–37. Google Scholar


C. Lopes-Andrade F. Gumier-Costa , and A. A. Zacaro 2003. Cis leoi, a new species of Ciidae (Coleoptera: Tenebrionoidea) from the Neotropical Region. Zootaxa 161: 1–7. Google Scholar


C. Lopes-Andrade and J. F. Lawrence 2005. Phellinocis, a new genus of Neotropical Ciidae (Coleoptera: Tenebrionoidea). Zootaxa 1034: 43–60. Google Scholar


C. Lopes-Andrade M. S. Madureira, and A. A. Zacaro 2002. Delimitation of the Ceracis singularis group (Coleoptera: Tenebrionoidea: Ciidae), with the description of a new Neotropical species. Dugesiana 9(2): 59–63. Google Scholar


M. M. Martin 1979. Biochemical implications of insect mycophagy. Biol. Rev. 54: 1–21. Google Scholar


J. Mellié 1849. Monographie de l'ancien genre Cis des auteurs. Ann. Soc. Entomol. Fr. 6(2): 205–274, 313–396. Google Scholar


J. J. Morrone 2002. Biogeographical regions under track and cladistic scrutiny. J. Biogeogr. 29: 149– 152. Google Scholar


J. L. Navarrete-Heredia 1987. Ceracis similis Horn (Coleoptera: Ciidae) asociado a Ganoderma lobatum (Schw.) Atk (Basidiomycetes: Polyporaceae). Folia Entomol. Mexicana 72: 161–162. Google Scholar


J. L. Navarrete-Heredia , and A. Burgos-Solorio 2000. Ciidae (Coleoptera), pp. 413–420 In J. E. Llorente-Bousquets , E. González-Soriano and N. Papavero [eds.], Biodiversidad, Taxonomía y Biogeografía de Artrópodos de México: hacia una síntesis de su conocimiento. Volumen IL Universidad Nacional Autónoma de Mexico, Mexico, D.F. Google Scholar


L. F. C. Olpveira M. Le Hyaric , M. M. Berg , M. V. Almeida , and H. G. M. Edwards 2007. Raman spectroscopic characterization of cinnabarin produced by the fungus Pycnoporus sanguineus (Fr.) Murr. J. Raman Spectrosc. 38: 1628–1632. Google Scholar


G. M. Orledge , and S. E. Reynolds 2005. Fungivore host-use groups from cluster analysis: patterns of utilisation of fungal fruiting bodies by ciid beetles. Ecol. Entomol. 30: 620–641. Google Scholar


K. Paviour-Smith 1960. The fruiting-bodies of macrofungi as habitats for beetles of the family Ciidae (Coleoptera). Oikos 11: 43–71. Google Scholar


M. C. Peel B. L. Finlayson, and T. A. McMahon 2007. Updated world map of the Koppen-Geiger climate classification. Hydrol. Earth Syst. Sc. 11: 1633–1644. Google Scholar


M. Pic 1916. Diagnoses specifiques. Mel. Exot.-Ent. Moulins 17: 8–20. Google Scholar


J. Reibnitz 1999. Verbreitung und Lebensräume der Baumschwammfresser Südwestdeutschlands (Coleoptera: Cisidae). Mitt. Entomol. V. Stuttgart 34: 2– 75. Google Scholar


J. A. Robertson , J. V. McHugh , and M. F. Whiting 2004. A molecular phylogenetic analysis of the pleasing fungus beetles (Coleoptera: Erotylidae): evolution of colour patterns, gregariousness and mycophagy. Syst. Entomol. 29: 173–187. Google Scholar


L. Ryvarden 1991. Genera of Polypores: Nomenclature and taxonomy. Synopsis Fungorum (5). Fungiflora, Oslo. Google Scholar


L. Ryvarden 2004. Neotropical Polypores I. Introduction: Ganodermataceae & Hymenochaetaceae . Synopsis Fungorum (19). Fungiflora, Oslo. Google Scholar


L. Ryvarden , and T. Iturriaga 2003. Studies in Neotropical polypores: new polypores from Venezuela. Mycologia 95: 1066–1077. Google Scholar


L. Ryvarden , and I. Johansen 1980. A preliminary Polypore Flora of East Africa. Fungiflora, Oslo. Google Scholar


D. S. Schigle 2008. Collecting and rearing fungivorous Coleoptera. Rev. d'Ecologie 63: 7–12. Google Scholar


L. M. Schoonhoven , J. A. Van Loon , and M. Dicke 2005. Insect-plant Biology: from Physiology to Evolution. Oxford University Press, London. Google Scholar


R. M. B. Silveira and R. T. Da Guerrero 1991. Aphyllophorales poliporoides (Basidiomycetes) do Parque Nacional de Aparados da Serra, Rio Grande do Sul. Bol. Inst. Biociências 48: 1–127. Google Scholar


R. M. B. Silveira , M. A. Reck , L. V. Graf , and F. Nogueira-de-Sá 2008. Polypores from a Brazilian pine forest in Southern Brazil: pileate species. Hoehnea 35(4): 619–630. Google Scholar


E. F. A. Smânia , S. A. Júnior , and C. Loguercio-Leite 1998. Cinnabarin synthesis by Pycnoporus sanguineus strains and antimicrobial activity against bacteria from food products. Rev. Microbiol. 29(4): 317–320. Google Scholar


P. Thakeow , S. Angeli , B. Weissbecker , and S. Schütz 2008. Antennal and behavioral responses of Cis boleti to fungal odor of Trametes gibbosa. Chem. Senses 33(4): 379–387. Google Scholar


J. N. Thompson 1998. The evolution of diet breadth: monophagy and polyphagy in swallowtail butterflies. J. Evol. Biol. 11: 563–578. Google Scholar


S. Watkinson , D. Bebber , P. Darrah , M. Frocker , M. Tlalka , and L. Boddy 2006. The role of wood decay fungi in the carbon and nitrogen dynamics of the forest floor, pp. 151–181 In G. M. Gad [ed.], Fungi in Biogeochemical Cycles. Cambridge University Press, Cambridge. Google Scholar
Letícia V. Graf-Peters, Cristiano Lopes-Andrade, Rosa Mara B. da Silveira, Luciano de A. Moura, Mateus A. Reck, and Flávia Nogueira de Sá "Host Fungi and Feeding Habits of Ciidae (Coleoptera) in a Subtropical Rainforest in Southern Brazil, with an Overview of Host Fungi of Neotropical Ciids," Florida Entomologist 94(3), 553-566, (1 September 2011).
Published: 1 September 2011

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