Literature DB >> 23653494

Checklist of the ants (Hymenoptera, Formicidae) of the Solomon Islands and a new survey of Makira Island.

Eli M Sarnat1, Benjamin Blanchard, Benoit Guénard.   

Abstract

The intent of this paper is to facilitate future research of the Solomon Islands ant fauna by providing the first comprehensively researched species inventory in over 75 years. The species list presented here includes the names of all ant species recorded from the islands that are available in the literature together with specimen records from several museum collections and new records from our 2008 Makira field expedition. All the names of described species presented are valid in accordance with the most recent Formicidae classification. In total, the checklist is composed of 237 species and subspecies (including 30 morphospecies) in 59 genera representing nine subfamilies. We report that the recent field expedition added 67 new species records to Makira and 28 new species records to the Solomon Islands. Our research recovered species occurrence records for 32 individual islands and five island groups. The five islands with the highest number of recorded species are: Makira (142 spp.), Guadalcanal (107 spp.), Malaita (70 spp.), Santa Isabel (68 spp.), and Rennell (66 spp.). Based on our results, we discuss the taxonomic composition of the archipelago's ant fauna, which islands are most in need of additional sampling, and the importance of establishing biodiversity baselines before environmental threats such as the invasive ant Wasmannia auropunctata cause irrevocable harm to the native biodiversity.

Entities:  

Keywords:  Biogeography; Formicidae; Makira Island; Pacific Islands; Solomon Islands; checklist; species distributions; taxonomy

Year:  2013        PMID: 23653494      PMCID: PMC3591739          DOI: 10.3897/zookeys.257.4156

Source DB:  PubMed          Journal:  Zookeys        ISSN: 1313-2970            Impact factor:   1.546


Introduction

The intent of this paper is to facilitate future research of the Solomon Island ant fauna and that of the larger Pacific Island region by providing the first comprehensively researched species list in over 75 years (Mann 1919; Wheeler 1935b). Reliable species lists are the foundation for biodiversity and biogeography research. This is especially true for archipelago systems such as the Solomons which serve as natural laboratories for studying the interface of geography, evolution and ecology (Diamond 1975; Diamond and Mayr 1976; Greenslade 1968; MacArthur and Wilson 1967; Mayr and Diamond 2001; Wilson 1959a; 1961). Accurate faunal lists at the archipelago level allow us to analyze biogeographic patterns at the regional scale, and faunal lists at the individual island level allow us to analyze more local scale patterns. These studies are crucial for the development of precise conservation plans that incorporate the distribution of endemic and rare taxa. Faunal lists are also necessary for recognizing biodiversity blind spots and identifying which regions and islands are most in need of additional sampling. Increasing environmental threats such as deforestation, mining, agriculture and the spread of invasive species give urgency to surveying these poorly sampled regions. In order to assess how these threats affect native biodiversity, it is important to establish baseline inventories before local populations and endemic species are driven extinct.

Geography, geology and climate

The Solomon Islands is a nation in the Southwest Pacific that is composed of seven large islands, a dozen mid-sized islands and over a thousand smaller islands (Figure 1). These islands, which comprise a total land area of 27,556 km2, are situated between the latitudes 5° and 13°S, and longitudes 155° and 169°E. The major central islands include the Shortlands, Choiseul, the New Georgias, Santa Isabel, the Russells, Guadalcanal, the Nggelas (Floridas), Malaita, Makira (San Cristóbal), and Olu Malau (Three Sisters). Rennell and Bellona are southern outlying islands situated along the northern margin of the Coral Sea Basin. Northern outlying islands include Sikaiana and the Ontong Java Atoll, which are on the southwestern edge of the Ontong Java Plateau. The eastern outlying islands of the Santa Cruz group are politically part of the Solomon Islands, but are geologically linked to the islands of Vanuatu (Kroenke and Rodda 1984).
Figure 1.

Map of the Solomon Islands. The map presents all islands and island groups for which ant species were recorded. Each island/island group from which ant species are known is labeled with the geographic name and filled darker grey. Islands for which no ant records appear in the literature are unlabeled and filled with lighter grey. Relevant historic island names from the colonial era are presented with their contemporary counterparts.

Map of the Solomon Islands. The map presents all islands and island groups for which ant species were recorded. Each island/island group from which ant species are known is labeled with the geographic name and filled darker grey. Islands for which no ant records appear in the literature are unlabeled and filled with lighter grey. Relevant historic island names from the colonial era are presented with their contemporary counterparts. The Solomons consist of a double chain of islands separating the Pacific Plate to the north from the Australian Plate to the south (Hall 2002). The islands are believed to have been formed entirely of oceanic origin, and there is no evidence that they were ever attached to continental systems or incorporated any terrains of continental origin (Kroenke and Rodda 1984). They are, in this sense, Darwinian Islands (Gillespie and Roderick 2002). According to several geologic models (Hall 2002) the Solomon Arc formed approximately 40 Ma as part of the Melanesian Arc system. It is unclear, however, when the islands emerged above sea level. PageBreakBougainville, which lies to the west, belongs politically to Papua New Guinea but is geographically part of the Solomon Islands. The next closest neighbor nation is Vanuatu, which lies southeast of the main archipelago and nearly due south of the Santa Cruz Is. The climate of the Solomon Islands is characterized as humid with a mean temperature of 27 °C (80 °F) and relatively few fluctuations of temperature or weather. The cooler and drier part of the year occurs from June through August, and the warmer and wetter season occurs from September through May. The annual rainfall is approximately 3050 mm (120 in).

History of ant collection and research in the Solomon Islands

The first ants described from the Solomon Islands were authored by Forel (1910) in a paper on Australian ants based on the collections of W.M. Froggatt and Rowland Turner. Froggatt visited the Solomon Islands to study the insects of the coconut palms, and collected at Tulagi I. and in the Russell Group. W.M. Mann (1919) provided the first and only comprehensive revision of the Solomon Island ant fauna. He spent six months on the archipelago from 19 May to 24 November 1916, and collected on the islands Guadalcanal, Makira, Malaita, Malaupaina, New Georgia, Nggela Sule, Owaraha, Rendova, Russell Is., Santa Cruz, Santa Isabel, Tulagi and Ugi. Mann reported the occurrence of 136 currently recognized species and subspecies, of which PageBreakhe described 68 from his own collections. In addition to a broad discussion of the archipelago’s ant fauna, the treatise also includes keys to Melanesian species of , , , , , , (= ), , and (= ).Additional relevant publications from Mann include descriptions of ant guests from Fiji and the Solomon Islands (Mann 1920), and accounts from his travels in the Solomon Islands (and elsewhere) in his book Ant Hill Odyssey (Mann 1948). H. Viehmeyer (1924) described a new subspecies subsp. manni (= ) from Mann’s collections at the Museum of Comparative Zoology (MCZ). H. Donisthorpe (1941) described from a worker that was on the same pin as several workers of Mann, all of which were labeled as Emery (= ). Donisthorpe attributed the close similarity of all three species to mimicry. W.M. Wheeler’s first contribution to the Solomon Island ant fauna was his description of based on specimens collected by Mann from Malaupaina (Wheeler 1918). Wheeler (1934) later published on ants collected by Maurice Willows Jr. from the Santa Cruz and Danger Islands. He listed the names and collection records of 27 currently recognized taxa, including original descriptions for two species (, ) and one subspecies (), along with the first published record of from the Solomons (Wetterer 2009). These records are combined with those of Forel and Mann in Wheeler (1935b). William Brown treated many Solomon Island taxa in his revisions (Brown 1948; 1958a; b; 1960; 1975; 1976; 1978; 1988; 1995; Willey and Brown 1983). Gressitt (1958) reported on the pest behavior of (= ) invading buildings in Malaita. According to Wilson (1962), the B.P. Bishop Museum, Honolulu, initiated a collecting program in the Solomons under the direction of Gressitt, and there is likely a considerable amount of ant material that remains unreported in the literature. Research on economically important ants involved in coconut production was an active field in the Solomons from the 1930’s through the 1960’s (Leston 1973; Lever 1933; 1961; O’Conner 1949; 1950; Phillips 1940; 1956). E.S. Brown (1959) recorded over 60 species of ants (including five new country records) collected during his work among coconut plantations in Guadalcanal and Malaita. Philip J.M. Greenslade has arguably collected more thoroughly across the Solomons than anyone since Mann. Greenslade published seven papers between 1964 and 1988 based on fieldwork he conducted in the Solomons (Greenslade 1964; 1971a; b; 1972; Greenslade and Greenslade 1970; 1971; 1977). The research focused primarily on the ecology of ants that are dominant in coconut plantations and are involved in the biological control of a coconut pest, China and the premature nutfall of coconut fruit. In addition to providing valuable ecological information on the four most dominant ant species in these plantations ( (Smith, F.), Forel, (Fabricius) and (Smith, F.)), Greenslade also PageBreakcollected a broad diversity of less economically important ant species, mainly from Mt. Austen (Guadalcanal) and Kukum—the nearby Solomon Is. Department of Agriculture farm. These specimens, most of which were deposited at the ANIC, included many new species in addition to the first records of (Taylor 1965) and (Bolton 2000) for the Solomon Islands. Interestingly, Greenslade’s (1968) work on the avifauna of the Solomon Islands was the first to apply the taxon cycle model to birds. E.O. Wilson included many species from the Solomon Islands during his revisionary work of the Melanesian ant fauna, including species currently in the genera , , and (1958a); , , , and (1958b); and (1959c); and (1959d). Wilson and Taylor (1967) added several new species records for the Solomons, including (Wheeler) and Brown (as (Brown)). Wilson and Hunt (1967) included records for the Solomons. In addition to these taxonomic studies, Wilson also included ants from the Solomons in his influential papers on the taxon cycle hypothesis (Wilson 1959a; 1961) and the theory of island biogeography (MacArthur and Wilson 1967). Wilson’s (1962) paper on the ants of Rennell and Bellona Islands examined specimens collected from three sources: a Danish Expedition (Wolff 1955); a British expedition (Bradley 1955), and a private collection made on Rennell and Bellona for several weeks during 1955, by Mr. E.S. Brown. Wilson recorded 25 species of ants in 17 genera from Rennell (including the first record of from the Solomons). He considered these to represent a large percentage of the actual ant diversity, but admitted that the lack of cryptobiotic ponerine and myrmicine species suggest that his list is incomplete. He concluded that the Rennell ant fauna is primarily composed of widespread Pacific natives that invaded the island relatively recently and are representative of ‘Stage-I’ species discussed in his taxon cycle hypothesis (Wilson 1959a; 1961). Robert Taylor, in addition to describing (Taylor 1965), also described (Taylor 1968), and ( = ) (Taylor 1979) from specimens collected by P.J.M. Greenslade on or near Mt. Austen. Rudolf Kohout’s work on added several new species records to the Solomons, introduced new synonyms and nomenclatural changes, and included the description of three new species (, , ) endemic to the Solomons (Kohout 1990; 1998; 2006). Barry Bolton described (Bolton 1975), from the Solomons, provided the replacement name of Bolton for the junior secondary homonym (= ) pulchella Mann (Bolton 1985), and added new records of dacetines in the Solomons (Bolton 2000). Bolton(1976) also described from specimens Mann (1919) mistakenly identified as André. Kugler described from a Greenslade collection made on Guadalcanal (Kugler 1994). Lattke included the Solomon Islands in his biogeographic analysis of in Southeast Asia (Lattke 2003) and described two new species ( and )from there (Lattke 2004). Lucky & Sarnat (2008) included Mann in their phylogenetic and biogeographic analysis of the gePageBreaknus. Sarnat and Moreau (2011) included species from the Solomons in their phylogenetic and biogeographic analysis of the Fijian and selected congeners from across the Pacific.

Methods

Compilation of names

In order to compile a comprehensive and accurate inventory of ant species recorded from the Solomon Islands, we researched taxonomic names that were associated with the region in the literature. We reviewed the names of all taxa that were originally described from Solomons, reviewed specimen records from Antweb.org, reviewed the species list for the Solomon Islands presented on Antwiki , searched the Formis database (Porter and Wojcik 2012) for all relevant literature containing the term ‘Solomon’, and reviewed relevant taxonomic and regional literature. We also reviewed a dataset of ca. 1,040 specimen records of identified ants collected in the Solomon Islands that are deposited at the ANIC (Australian National Insect Collection, Canberra). We used the Bolton (2012) catalog to determine the valid names of all the species on the list. The Bolton (2012) catalog does not recognize the synonymy of with , as implicitly proposed by Mackay and Mackay (2010), and the name is retained here as valid. Names were eliminated where we found evidence of misidentification or geographic inconsistencies such as geographic names erroneously considered as belonging to the Solomon Islands. We also reconciled situations in which different authors may have referred to the same species by different valid names. For example, there were instances in which we believe one author referred to a taxon using its specific name, and another author referred to the same taxon by its infraspecific name. In cases such as these, and in the absence of additional evidence, we use the infraspecific name. We also note which other names we interpret as referring to the same taxon, and which publications those names occur in. In addition to the valid names, we also use morphospecies codes to refer to presumptive species that either we or previous authors were unable to determine. The morphospecies code is ‘BP’ (The administrative code for the Solomon Islands) followed and a unique two-digit number (e.g. ‘ sp. BP01’). Bougainville is considered to belong geographically but not politically to the Solomons. As such we do not include species recorded from Bougainville that have not also been reported from at least one of islands to its east.

Survey of Makira

In addition to basing the present study on the aforementioned published records, we also include records from our own recent survey of the Solomons. Three of the authors (E.P.E., PageBreakE.M.S., J.F.) collected ants in the Solomons from 30 January to 9 February, 2008. Aside from a few collections made on Mt. Austen (Guadalcanal I.), the survey primarily focused on Makira Island (formerly San Cristóbal) where we trekked and collected from Kirakira on the coast to the interior village of Maraone, reaching a maximum elevation of 912 m. Survey methods included hand collection and litter sifting along standardized transects using Winkler extraction bags. All specimens were collected into and stored in 95% ethanol. Pinned specimens were identified using the available literature and compared to type and determined material at the United States National Museum of Natural History (USNM), Washington D.C., USA, and the Museum of Comparative Zoology (MCZC), Cambridge, Massachusetts, USA. These two collections are the primary depositories for Mann’s type material and also include type material designated by W.L. Brown, W.M. Wheeler and E.O. Wilson. We include the species records from this survey with the literature records.

Island records

Occurrence data of ant species on individual islands and island groups were compiled from the relevant literature. More detailed data with literature references for each species-island occurrence is available from the authors upon request. A map of the Solomon Islands (Figure 1) is also presented in which the name of every island and island group from which ant species have been recorded is labeled. The constituent islands comprising the listed island groups are presented in Table 1. In addition to including all taxa from Appendixes 1 and 2, we also include taxa from the 2008 survey of Makira that remain undetermined but might belong to previously described species. Inclusion of these additional taxa may weakly bias the observed species richness of Makira towards a higher value, but exclusion of these taxa would cause an even greater bias towards a lower value.
Table 1.

Island groups and their constituent islands.

Island GroupIslands
Santa Cruz Is.Anuta, Nendö (Santa Cruz), Nupani, Reef Is., Tikopia, Vanikoro
Olu Malau Is. (Three Sisters)Malaupaina
Nggela Is. (Florida Is.)Nggela Sule (Florida), Tulagi
New Georgia Is.Kolombangarav, New Georgia, Rendova, Vangunu, Vella Lavella
Reef Is.Matema
Island groups and their constituent islands.
Number of presumptive native species from Appendix 1 for each genus (arranged from greatest to least). Diverse genera with well-established subgenera are nested under the genus name and the species number of each is presented in parentheses.

Sampling analysis

We used our data compilation to estimate in a general sense how undersampled the Solomon Islands are for ants. First, we compared the species richness of individual islands in the Solomons with counts of the Fijian islands, which were the target of recent intensive sampling and taxonomic analysis (Sarnat and Economo 2012). We also compared the species richness of Makira from records before and after our 2008 survey.

Results

Ant records from the Solomon Islands

We present a list of nine subfamilies, 60 genera and 215 valid ant species and subspecies for the Solomon Islands based on our review of the literature and our recent collections from Makira (Appendix 1). We also present a list of 23 presumptively undescribed species that have also been recorded from the Solomons (Appendix 2). The generic composition and diversity of the Solomons is presented in Table 1. In total, our research suggests that the Solomon Islands support at least 237 unique ant taxa. The full species list with associated images and specimen data is available on Antweb.org . We excluded the following taxa from the list as they were reported from Bougainville but not from within the political boundaries of the Solomon Islands: (Emery), (Mayr), Stitz, and subsp. hiram Forel. The following taxa were reported from the Solomon Islands, but are not believed to occur there either because the records were based on misidentified material or erroneous interpretation of locality data. (Le Guillou, 1842): 316. Type locality: Tonga, Vavao. The website Antwiki.org, accessed 5 October 2012, listed this species under its Solomon Island webpage. The list was generated by extracting all species for which the Solomon Is. were listed as the type locality from the Bolton Catalog (Bolton et al. 2006). Although there are several Vavao islands in the Pacific (including in the Solomon PageBreakIs.) the original description lists the type locality as (íles des Amis), which suggests Tonga (often referred to in older literature as the ‘Friendly Islands’) is the more likely country. Moreover, the species does not appear in any of the reviewed literature as occurring in the Solomons. Roger, 1863: 139. Type locality: Sri Lanka. The first record of Roger appeared in Wilson (1962). Wilson explicitly applied Roger to the Solomons material that Wheeler (1934) referred to as subsp. bedoti Emery. In following the current classification (Bolton 2012), we accept Emery as a valid species, and apply that name to all the material from the Solomons referred to as Roger. The decision to do so is somewhat arbitrary given the current state of taxonomy for Indo-Australian , but we believe that both names refer to the same species in the Solomons. (Emery, 1900): 320. Type locality: New Guinea. Mann (1919) reported this species as occurring in the Solomon Is., but Wilson (1958b) believed Mann’s specimens belonged to (= ) Wilson. (Smith, 1857): 69. Type locality: Borneo. Mann (1919) reported this species as occurring in the Solomon Islands, but Wilson (1958a) considered Mann’s specimens to be a mixed series, part of which belong to Smith, F. and the other part to Wilson. (Linnaeus, 1758): 582. Type locality: “America meridionali.” It is presumed that specimens referred to as by Mann (1919), Wheeler (1934; 1935a) and E. S. Brown (1959) prior to Wilson’s (1959b) revision belong instead to Smith, F. Guérin-Méneville, 1844: 423. Type locality: Cuba. Forel (1910) reported this species as occurring in the Solomon Is., but it is more likely that this was a misidentification and that the specimens he examined belong to Smith, F. is not known from the Old World and was not included in Wilson (1959c). Mayr, 1866: 899. Type locality: South Africa. Forel (1910) reported this species as occurring in the Solomon Is., but it is more likely that the specimens he examined belong to the cosmopolitan tramp . (Smith, F. 1859): 137. Type locality: Indonesia, Aru I. In his introduction, Greenslade (1972) treated (= )Smith, F. as the senior synonym of var. myrmecodiae (= ) Emery. However, has been accepted as a valid species since 1903 PageBreak(Bolton 2012; Shattuck 1994). The correct name for the Solomons material would require comparison against type material for both taxa. In the meantime, our decision to use rather than reflects our belief that (1) insofar as the Solomon Is. are concerned, the use of both names refer to the same species; and (2) there is no taxonomic evidence proposed by Greenslade that Mann’s (1919) use of was misapplied. André, 1887: 294. Type locality: India. Mann (1919) misidentified a series of specimens as belonging to André that Bolton(1976) subsequently described as .We assume here that the specimens referred to as by Taylor (1976) are also .

Makira Island Survey

We collected a total of 67 described species and 30 presumptive species that are either undescribed or that we were unable to determine. Based on comparisons with type material, previously determined material and literature review, we suspect approximately 15 of the presumptive species are new to science. These taxa are included in Appendix 2. The survey added 67 new species records to Makira of taxa included in Appendixes 1 and 2, bringing the total number of species known from the island to 142. The survey also added 28 new species records to the Solomon Islands. Of these, six are previously described species (including three introduced species), and the remainder of species are included in Appendix 2.

Island records and sampling analysis

Our research recovered species occurrence records for 32 individual islands and five island groups out of the approximately 75 named small to large individual islands and approximately 12 named island groups. These occurrence records are presented in Appendix 3. The 261 taxon names include the 215 described species and subspecies from Appendix 1, the 22 presumptive undescribed species from Appendix 2, and 24 additional morphospecies that likely represent a mixture of previously described species and undescribed species. This latter group is restricted to specimens collected during the 2008 Makira survey. The five islands with the highest number of species records, listed from greatest to least, are: Makira (142 spp.), Guadalcanal (107 spp.), Malaita (71 spp.), Santa Isabel (68 spp.), and Rennell (66 spp.). Fourteen individual islands have occurrence records for between 11–38 species. Thirteen individual islands have occurrence records for between 1–8 species. The ten most widely distributed species, with the number of islands each is reported from, are: (27), (18), (17), (15), (13), (13), (13), (13), (13), (13). One hundred seven of the species and morphospecies included in Appendix 3 are only reported from single islands.

Discussion

In total, our research suggests that the Solomon Islands support at least 237 unique ant species and subspecies. The poor sampling of many islands–some of which are quite large–and the unexamined material at the ANIC suggests that the true number is likely much greater. For example, our eight days of intensive hand collection and Winkler extractions on Makira added 67 new species records to the island (including all morphospecies) and 28 new records to the archipelago. Prior to the survey, Makira Island’s 75 species records were the second highest of the entire archipelago. Choiseul Island by comparison is approximately equal in area to Makira and closer to New Guinea, but the ant fauna of the island is virtually unknown with only eleven species recorded in the literature. There are approximately as many species known from the islands of Santa Isabel and Malaita as there are from Rennell, despite the substantially larger area of the former islands and their closer proximity to other large islands within the archipelago. The difference is that although no ant specialists have thoroughly sampled Rennell, general entomologists have collected there and the ant specimens of those surveys were the subject of several faunistic reviews (Taylor 1976; Wilson 1962). Besides Makira and Rennell Islands, the only island that has been moderately sampled–thanks to the works of Mann and Greenslade–is Guadalcanal. Compared to Fijian islands of similar size, known species richness is generally much lower for individual islands within the Solomons, despite the fact that Fiji is much more isolated in the Pacific (Figure 2). This is likely due to relative sampling intensity of the two areas. Fiji has recently received intensive sampling efforts (Sarnat and Economo 2012), while richness differences among the Solomon Islands are still driven in large part by which islands were visited by W.M. Mann in 1916. For example, the 38 recorded species reported from the small island of Ugi (42 km2), where Mann resided and collected for several weeks, is a richness comparable with a similar-sized Fijian island. Several large islands not visited by Mann have almost no records (e.g. Choiseul 2,966 km2, 11 spp.; Kolombangara 704 km2, 17 spp.). Our modest survey of Makira, where we spent approximately one week of collecting time, increased known richness from 75 to 142 species. There is no doubt that such modest collecting efforts elsewhere in the archipelago would yield similar increases.
Figure 2.

The relationship between islands area and known species richness. The figure presents individual islands in the Solomon (circles) and Fijian (squares) archipelagos, illustrating the undersampling of most Solomon Islands relative to the better collected Fiji Islands. For Makira, we present known species richness before (open circle) and after (filled circle) our recent collecting expedition. Numbers: 1 Guadalcanal 2 Malaita 3 Makira 4 Choiseul 5 New Georgia 6Santa Isabel 7 Kolombangara 8 Rennell 9 Vella Lavella 10 Vangunu 11 Nendö (Santa Cruz) 12 Rendova 13 Nggela Sule 14 Shortland 15 Vanikoro 16 San Jorge 17 Russell Is. 18 Ugi 19 Savo.

The relationship between islands area and known species richness. The figure presents individual islands in the Solomon (circles) and Fijian (squares) archipelagos, illustrating the undersampling of most Solomon Islands relative to the better collected Fiji Islands. For Makira, we present known species richness before (open circle) and after (filled circle) our recent collecting expedition. Numbers: 1 Guadalcanal 2 Malaita 3 Makira 4 Choiseul 5 New Georgia 6Santa Isabel 7 Kolombangara 8 Rennell 9 Vella Lavella 10 Vangunu 11 Nendö (Santa Cruz) 12 Rendova 13 Nggela Sule 14 Shortland 15 Vanikoro 16 San Jorge 17 Russell Is. 18 Ugi 19 Savo. The species list compiled from our research suggests several interesting taxonomic patterns. For example, species richness across the 51 native ant genera of the Solomons appears uneven. The 30 species represent 14% of the total native species. The nine most diverse genera (, , , , , , , ,and ) collectively contain over half of the total native species, while fifteen genera are represented by a single native species. PageBreakWhy is so strongly represented in the Solomons? These results are likely biased to some extent by idiosyncratic collecting and taxonomic study. Besides the work of Mann, and to a lesser extent Greenslade, most of the collections from the Solomons have been made by more generalist collectors, which tend to take larger, more conspicuous ants that forage on and nest in vegetation–all of which are characteristic of . Furthermore, Rudolf Kohout, who has access to the considerable collection of Solomons material at the ANIC, has devoted much of his taxonomic efforts towards revising the of the Indo-Australian region (Kohout 1990; 1998; 2006; 2012). Despite these apparent biases, it is somewhat remarkable that with a single exception, the eight distinct lineages that colonized the Solomons (as inferred from their subgeneric classifications) were unable to colonize, or at least persist PageBreakin the more eastern Pacific islands. That single exception, Wilson & Taylor,is known from the island of Rotuma which belongs politically to Fiji but is quite isolated from the Fijian archipelago and shares more geological and biological affinity with the islands of Polynesia. (9 native spp.), (7 native spp.)and (6 native spp.) are also among the most diverse ant genera in the Solomon Islands, but are either absent from or poorly represented in more easterly archipelagos. Fiji, for example, supports a single native species ( Mann), and does not support any native or species (Sarnat and Economo 2012). The Solomons are the known eastern limit for many ant genera. Out of the 51 genera native to the Solomons, the following 19 are not known to occur in the Pacific in or east of the Fijian archipelago: , , , , , , , , , , , , , , , , , , . While additional sampling may prove otherwise, the current analysis of the Solomons ant fauna does not appear to support the type of in situ single-lineage radiations that characterize much of the Fijian ant fauna to the east. Parallels to the dramatic radiations of the group (Economo and Sarnat 2012; Sarnat 2008), (Lucky and Sarnat 2008; Sarnat 2006), and the group (Sarnat and Economo 2012) are largely unknown from the Solomons. It is likely that the Solomons ant fauna is derived more from relatively frequent colonization events from nearby New Guinea than from sweepstakes colonists that diversified into largely unoccupied ecological niches as occurred in the more isolated Fijian archipelago. Unlike New Guinea and Fiji,the Solomons do not support any endemic ant genera. The importance of establishing baseline faunal inventories for the entire Solomon Island archipelago and its constituent islands is especially important when considering the growing environmental impacts resource extraction, plantation agriculture and invasive species are having on native biodiversity. Perhaps the greatest threat to native ant species in the Solomons is the spread of the Little Fire Ant (Fasi 2009). The introduction of into the Solomon Islands is believed to have occurred around 1974, possibly with the arrival of coconut nurseries (Fabres and Brown 1978; Ikin 1984; Wetterer 1997). Foucaud et al. (2010) determined that a single clonal queen genotype is shared between the Melanesian populations of from the Solomons, Vanuatu, Papua New Guinea and Australia, and suggested that the population spread by means of traditional exchange of plants and goods among Melanesian people. Although there have been reports of the ant’s effect on vertebrates in the Solomons, such as blinding dogs and attacking hatchlings of the ground-nesting Melanesian Scrubfowl ( Hartlaub) (Wetterer 1997), and also its effect on food crops and subsistence agriculture (Fasi 2009), there have yet to be any studies examining the effect of on native ant diversity in the Solomons. The potential for spread of across the entire archipelago is high (Fasi 2009), and it is likely a matter of years before all the major islands are infested. PageBreakWe hope the research presented here will help facilitate more study of the neglected Solomon Island ant fauna and aid conservation efforts before and other environmental threats cause irrevocable harm.
Table 2.

Number of presumptive native species from Appendix 1 for each genus (arranged from greatest to least). Diverse genera with well-established subgenera are nested under the genus name and the species number of each is presented in parentheses.

Genus (Subgenus)Native spp.%Total
Polyrhachis3014
Polyrhachis (Myrma)(7)
Polyrhachis (Cyrtomyrma)(5)
Polyrhachis (Chariomyrma)(4)
Polyrhachis (Hedomyrma)(4)
Polyrhachis (Myrmhopla)(3)
Polyrhachis (Myrmatopa)(2)
Polyrhachis (Myrmothrinax)(1)
Polyrhachis (Hirtomyrma)(1)
Pheidole157
Camponotus147
Camponotus (Colobopsis)(5)
Tetramorium115
Vollenhovia115
Pachycondyla94
Strumigenys94
Crematogaster73
Crematogaster (Crematogaster)(5)
Crematogaster (Orthocrema)(2)
Gnamptogenys63
Cryptopone52
Hypoponera52
Myrmecina52
Nylanderia52
Ponera52
Acropyga42
Cerapachys42
Eurhopalothrix42
Leptogenys42
Myopias42
Odontomachus42
Anochetus31
Rogeria31
Adelomyrmex21
Arnoldius21
Cardiocondyla21
Carebara21
Colobostruma21
Iridomyrmex21
Podomyrma21
Prionopelta21
Pristomyrmex21
Proceratium21
Rhytidoponera21
Solenopsis21
Stigmatomma21
Turneria21
Amblyopone1<1
Anonychomyrma1<1
Discothyrea1<1
Lordomyrma1<1
Monomorium1<1
Myopopone1<1
Oecophylla1<1
Opisthopsis1<1
Paraparatrechina1<1
Philidris1<1
Platythyrea1<1
Probolomyrmex1<1
Stereomyrmex1<1
Tapinoma1<1
Tetraponera1<1
TaxonAuthorYearReference
Amblyoponinae
Amblyopone australisErichson, 1842: 26119193, 8, 9, 13, 17, 38, 81
Myopopone castanea(Smith, F. 1860): 10519193, 8, 9, 13, 17, 21, 81
Prionopelta majusculaEmery, 1897b: 595200860, 81
Prionopelta opacaEmery, 1897b: 596197634, 60, 79, 81
Stigmatomma celata(Mann, 1919): 27919193, 8, 13, 17, 21, 34, 38, 81
Stigmatomma gnomaTaylor, 1979: 829197838, 81
Cerapachyinae
Cerapachys inconspicuusEmery, 1901: 15319193, 8, 9, 18, 20, 34
Cerapachys pawaMann, 1919: 27719193, 8, 20, 32
Cerapachys terricolaMann, 1919: 27719193, 8, 32, 79
Dolichoderinae
Anonychomyrma dimorpha(Viehmeyer, 1912): 719193, 8, 9, 79
Arnoldius pusillus(Mayr, 1876): 83195915
Iridomyrmex anceps(Roger, 1863a): 16419193, 6, 8, 15, 36, 81
Iridomyrmex pallidusForel, 1901: 22196381
Iridomyrmex rufoniger(Lowne, 1865): 27919193, 8
Ochetellus glaber*(Mayr, 1862): 705200979
Philidris myrmecodiae(Emery, 1887): 24919193, 6, 8, 15, 16, 291, 301, 681, 341, 361, 79
Tapinoma (Micromyrma) indicum timidumSantschi, 1928195915
Tapinoma melanocephalum*(Fabricius, 1793): 35319346, 8, 15, 18, 34, 36, 73, 81
Tapinoma minutumMayr, 1862: 703196726
Technomyrmex albipes*(Smith, F. 1861): 3819101, 3, 8, 15, 18, 34, 36, 56, 79, 81
Technomyrmex vitiensisMann, 1921: 473200879
Turneria dahliiForel, 1901: 17195918, 34, 42, 81
Turneria pacificaMann, 1919: 36119193, 42, 81
Ectatomminae
Gnamptogenys albiclava(Mann, 1919): 28319193, 8, 11, 17, 54
Gnamptogenys crenaticeps(Mann, 1919): 28519193, 8, 11, 17, 54, 79
Gnamptogenys lucida(Mann, 1919): 28519193, 8, 11, 17, 54
Gnamptogenys malaensis(Mann, 1919): 28119193, 8, 11, 17, 54, 79
Gnamptogenys preciosaLattke, 2004: 66200454, 81
Gnamptogenys solomonensisLattke, 2004: 66200454, 81
Rhytidoponera araneoides(Le Guillou, 1842): 31719101, 3, 14, 17, 79, 81
Rhytidoponera chalybaeaEmery, 1901b: 51195915
Formicinae
Acropyga acutiventrisRoger, 1862: 24319193, 8, 53, 79, 81
Acropyga lautaMann, 1919: 36519193, 8, 53, 79, 81
Acropyga oceanicaEmery, 1900: 333200879
Acropyga pallida(Donisthorpe, 1938): 598196581
Anoplolepis gracilipes*Smith, F. 1857: 5519193, 6, 8, 15, 15, 18, 29, 30, 68, 34, 36, 81
Brachymyrmex obscurior*Forel, 1893: 345197634, 79
Camponotus (Myrmamblys) bedotiEmery, 1893: 19619193, 6, 8, 15, 182, 342, 362
Camponotus chloroticusEmery, 1897b: 574195915
Camponotus elysiiMann, 1919: 37219193, 8
Camponotus guppyiMann, 1919: 37019193, 8
Camponotus loaMann, 1919: 37319193, 8
Camponotus loa belliMann, 1919: 37519193, 8
Camponotus novaehollandiaeMayr, 1870: 93919193
Nylanderia bourbonica*(Forel, 1886): 210195915, 34, 36, 81
Nylanderia braueri glabrior(Forel, 1902): 490195481
Nylanderia dichroaWheeler 1934: 18119346, 8, 81
Nylanderia manniDonisthorpe, 1941: 41194172, 15, 36
Nylanderia obscura bismarckensis(Forel, 1901): 2619193, 6, 8
Nylanderia stigmaticaMann, 1919: 36719193, 8, 62, 79, 81
Nylanderia vaga*(Forel, 1901): 2619346, 8, 18, 26, 34, 36, 79, 81
Nylanderia vividula*(Nylander, 1846): 90019193, 15, 79
Oecophylla smaragdina subnitidaEmery 1892: 56519101, 3, 6, 8, 153, 163, 293, 303, 683, 363, 793, 813
Opisthopsis manniWheeler, W.M. 1918: 36119182, 3, 8, 15
Paraparatrechina minutula(Forel, 1901): 2519193, 8, 15, 34, 79, 81
Paratrechina longicornis*(Latreille, 1802): 11319193, 8, 15, 34, 79, 81
Plagiolepis alluaudi*Emery, 1894: 71195915
Polyrhachis (Myrma) andromacheRoger, 1863b: 8195934, 18, 345, 79
Polyrhachis (Hedomyrma) annaeMann, 1919: 37719193, 6, 8, 15, 18, 34
Polyrhachis (Chariomyrma) arcuata acutinotaForel, 1901: 3119346
Polyrhachis (Hedomyrma) campbelliMann, 1919: 37619193, 8, 79
Polyrhachis (Myrmothrinax) dahliiForel, 1901: 3019193, 8, 9, 64
Polyrhachis (Cyrtomyrma) emeryanaMann, 1919: 39019193, 8, 55
Polyrhachis (Cyrtomyrma) fulakoraMann, 1919: 38919193, 8, 15, 55
Polyrhachis (Hedomyrma) geminataMann, 1919: 37619193, 8, 79
Polyrhachis greensladeiKohout, 1990: 503199074
Polyrhachis (Myrma) ithonaSmith, F., 1860: 9919346, 8
Polyrhachis (Cyrtomyrma) johnsoniMann, 1919: 39019193, 8, 55
Polyrhachis (Chariomyrma) kaipiMann, 1919: 38219193, 6, 8, 79
Polyrhachis (Myrma) labella brunneipesWheeler, 193419346, 8
Polyrhachis (Myrma) litigiosaEmery, 1897b: 58119193, 8, 79
Polyrhachis (Myrma) malaensisMann, 1919: 38619193, 8
Polyrhachis nofraBolton, 1975: 9197531
Polyrhachis (Myrmatopa) osaeMann, 1919: 38419193, 6, 8, 9, 15
Polyrhachis pacificaKohout, 2006: 140200655
Polyrhachis (Chariomyrma) rereMann, 1919: 38119193, 6, 8, 15
Polyrhachis (Myrmhopla) saevissima argenteaMayr, 1862: 8219193, 8, 9
Polyrhachis (Myrma) salomoForel, 1910: 8719101, 3, 8, 15
Polyrhachis (Hedomyrma) santschiiMann, 1919: 37519193, 8
Polyrhachis setosaKohout, 2006: 141200655
Polyrhachis (Myrma) similisViehmeyer, 1912: 819193, 8
Polyrhachis (Cyrtomyrma) ugiensisMann, 1919: 38919193, 8, 55, 79
Polyrhachis (Myrmatopa) ulyssesForel, 1910: 9119101, 3, 8
Polyrhachis (Cyrtomyrma) undulataKohout, 2006: 142200655, 79
Polyrhachis (Myrmhopla) wheeleriMann, 1919: 38719193, 8, 9
Myrmicinae
Cardiocondyla kagutsuchi*Terayama, 1999: 100200979
Cardiocondyla nivalisMann, 1919: 31719193, 8, 34, 36
Cardiocondyla nuda(Mayr, 1866): 508195915, 34, 36, 51, 59
Carebara atoma(Emery, 1900): 32819193, 8, 34, 36, 79
Carebara viehmeyeri(Mann, 1919): 33119193, 8, 79
Colobostruma foliaceaEmery, 1897a: 573200048, 81
Crematogaster (Crematogaster) abruptaMann, 1919: 32019358, 15, 61
Crematogaster (Crematogaster) elysiiMann, 1919: 31919358, 3, 61
Crematogaster (Crematogaster) foxiMann, 1919: 32119358, 3, 61
Crematogaster (Crematogaster) nesiotisMann, 1919: 32219358, 3, 61
Crematogaster (Crematogaster) obnigraMann, 1919: 32319193, 15, 61
Crematogaster (Orthocrema) scitaForel, 1902: 409195915
Crematogaster (Orthocrema) wheeleriMann, 1919: 31819358, 3, 61
Eurhopalothrix brevicornis(Emery, 1897a): 572197736, 80, 28, 82
Eurhopalothrix greensladeiTaylor, 1968: 342196828, 82
Eurhopalothrix isabellae(Mann, 1919): 35719193, 8, 22, 80, 28, 82
Eurhopalothrix procera(Emery, 1897a): 57219193, 8, 22, 28, 79, 81, 82
Lordomyrma epinotalis(Mann, 1919): 34319193, 8, 34, 58, 79
Monomorium australicumForel, 1907:2019193, 8, 15, 34, 36
Monomorium destructor*(Jerdon, 1851): 105195918, 34
Monomorium floricola*(Jerdon, 1851): 107195915, 34, 36, 41, 79, 81
Monomorium pharaonis*(Linnaeus, 1758): 58019193, 8, 15, 34, 41, 81
Myrmecina modestaMann, 1919: 33519193, 8, 346
Myrmecina modesta subarmataMann, 1919: 33719193, 8
Myrmecina transversaEmery, 1897a: 582200879
Pheidole belliMann, 1919: 30619193, 8
Pheidole eratoMann, 1919: 30719193, 8
Pheidole fusculaEmery, 1900: 32519193, 8
Pheidole isisMann, 1919: 31119193, 8
Pheidole isis takiMann, 1919: 31419193, 8, 79
Pheidole megacephala*(Fabricius, 1793): 361191017, 6, 8, 15, 26, 30, 34, 81
Pheidole mendanaiMann, 1919: 31119193, 8
Pheidole nindiMann, 1919: 31419193, 8, 34, 36, 79
Pheidole oceanicaMayr, 1866: 51019193, 8, 15, 18, 34, 36, 79
Pheidole philemonForel, 1910: 44 19101, 3, 8, 15, 79
Pheidole sexspinosaMayr, 1870: 97719193, 8, 34, 36, 79
Pheidole sexspinosa fuscescensEmery, 1900: 32319193, 8, 18
Pheidole umbonataMayr, 1870: 97819193, 8, 15, 18, 34, 36
Podomyrma basalis salomoMann, 1919: 33319193, 8
Podomyrma basalis woodfordiMann, 1919: 33419193, 8
Pristomyrmex levigatusEmery, 1897a: 58319193, 52, 79
Pristomyrmex obesusMann, 1919: 33919193, 8, 80, 52
Rogeria megastigmaticaKugler, C. 1994: 35199445, 79
Rogeria stigmaticaEmery, 1897: 58919193, 8, 34, 45
Romblonella elysii(Mann, 1919): 34619193, 8, 44
Solenopsis geminata*(Fabricius, 1804): 423197736
Solenopsis papuanaEmery, 1900: 33019193, 79
Solenopsis pawaensisMann, 1919: 32919193, 79
Stereomyrmex dispar(Wheeler, W.M. 1934): 17519346, 18, 34, 44
Strumigenys chyzeriEmery, 1897a: 57619193, 48, 79
Strumigenys decollataMann, 1919: 35319193, 8, 12, 48
Strumigenys emmae*Emery, 1890: 70197634, 36, 48, 81
Strumigenys euryceraEmery, 1897a: 581200048, 81
Strumigenys frivaldszkyiEmery, 1897: 580197634, 48, 79
Strumigenys godeffroyi*Mayr, 1866: 51619193, 15, 34, 36, 47, 48, 79
Strumigenys karawajewi(Brown, 1948): 44197634, 46, 48, 79, 81
Strumigenys membranifera*(Emery, 1869): 24200048, 36, 81
Strumigenys mocsaryi(Emery, 1897a): 580200048
Strumigenys rogeri*Emery, 1890: 68200048
Strumigenys szalayiEmery, 1897: 578200048, 79
Strumigenys undrasBolton, 2000: 752200048
Strumigenys yaleopleuraBrown, 1988: 41200048
Tetramorium antennatum(Mann, 1919): 35019193
Tetramorium aspersum(Smith, F. 1865): 7219193, 6, 8, 35, 79
Tetramorium bicarinatum*(Nylander, 1846): 1061191938, 68, 88, 158, 348, 35, 36
Tetramorium carinatum(Smith, F. 1859): 14819193, 8
Tetramorium insolens(Smith, F., 1861)19346, 8, 18, 34, 35
Tetramorium lanuginosum*Mayr, 1870: 97619358, 69
Tetramorium mayri(Mann, 1919: 351)19193, 8, 79
Tetramorium melanogynaMann, 1919: 34519193, 8, 79
Tetramorium mutatumBolton, 1985: 24719193, 8, 69
Tetramorium pacificumMayr, 1870: 97619346, 8, 18, 34, 35
Tetramorium salomoMann, 1919: 34419358, 35, 79
Tetramorium simillimum*(Smith, F. 1851): 118195915, 34, 35, 36, 79
Tetramorium tonganumMayr, 1870: 97619193, 8, 15, 18, 34, 35
Tetramorium vombisBolton, 1976: 358198539, 349, 69
Vollenhovia dentataMann, 1919: 32519193, 8, 24, 79
Vollenhovia dentata marginataMann, 1919: 32719193, 8, 24
Vollenhovia elysiiMann, 1919: 32719193, 8, 24
Vollenhovia foveacepsMann, 1919: 32819193, 8, 24
Vollenhovia loboiiMann, 1919: 32419193, 8, 24
Vollenhovia oblonga(Smith, F. 1861): 46195918, 34, 43
Vollenhovia oblonga pedestris(Smith, F. 1860): 10719193, 8, 15, 79
Vollenhovia subtilisEmery, 1887: 45419193, 8
Wasmannia auropunctata*(Roger, 1863a): 183198440, 75, 76, 77, 79
Ponerinae
Anochetus catoForel, 1901: 619193, 8, 17, 19, 79, 81
Anochetus graeffeiMayr, 1870: 96119193, 8, 15, 17, 19, 34, 36, 65, 79, 81
Anochetus isolatusMann, 1919: 30219193, 8, 17, 19, 34, 37, 65, 79, 81
Cryptopone butteliForel, 1913: 9196581
Cryptopone crassicornis(Emery, 1897): 533196581
Cryptopone fusciceps(Emery, 1900): 32119193, 4, 8, 14, 17, 81
Cryptopone testacea(Emery, 1893): cclxxv19193, 4, 8, 14, 17, 32, 81
Hypoponera biroi(Emery, 1900): 7195917, 34
Hypoponera confinis(Roger, 1860): 284195917
Hypoponera pallidula(Emery, 1900): 32019193, 8, 9
Hypoponera papuana(Emery, 1900): 31919193, 8, 79
Hypoponera pruinosa(Emery, 1900): 31919193, 8, 9, 14, 17, 34, 79
Hypoponera punctatissima*(Roger, 1859): 246197634, 79
Hypoponera ragusai*(Forel, 1899): 2819193, 8, 14, 17, 36
Hypoponera sororcula(Wilson, 1958a): 338195814, 17
Leptogenys diminuta(Smith, F. 1857): 6919193, 8, 17, 79
Leptogenys foreliMann, 1919: 29719193, 8, 13, 17, 1810, 3410
Leptogenys oresbiaWilson, 1958b: 1311958311, 13, 17
Leptogenys truncataMann, 1919: 2619193, 17
Odontomachus malignusSmith, F. 1859: 14419193, 17, 1812, 19, 33, 3412, 63, 81
Odontomachus rufithoraxEmery, 1911: 53419193, 17, 19, 33, 81
Odontomachus saevissimus(Smith, F. 1858)195915, 33, 81
Odontomachus simillimus(Smith, F. 1858): 801910113, 314, 614, 814, 1514, 17, 18, 19, 26, 34, 36, 79, 81
Pachycondyla acutaEmery, 1900195814, 17
Pachycondyla aequalis(Mann, 1919): 28919193, 8, 14, 17, 79
Pachycondyla croceicornis(Emery, 1900): 31519193, 14, 17, 36, 79
Pachycondyla darwinii(Forel, 1893): 460195917
Pachycondyla exarataEmery, 1901b: 15619193, 8
Pachycondyla manni(Viehmeyer, 1924): 228192471, 14, 17
Pachycondyla melancholicaSmith, F. 1865: 7119193
Pachycondyla papuana(Viehmeyer, 1914): 60819193, 9
Pachycondyla sheldoni(Mann, 1919): 29219193, 8, 14, 17
Pachycondyla stigma*(Fabricius, 1804): 40019193, 8, 9, 15, 17, 18, 34, 79
Platythyrea parallela(Smith, F., 1859): 14319193, 9, 17
Ponera clavicornisEmery, 1900: 31719193, 8, 10, 25, 3415, 81
Ponera incerta(Wheeler, W.M. 1933): 18195917, 25, 81
Ponera swezeyi(Wheeler, W.M. 1933): 16200979
Ponera szaboiWilson, 1957: 371197634
Ponera tenuis(Emery, 1900): 321196581
Proceratiinae
Discothyrea clavicornisEmery, 1897b: 59319193, 8, 9, 17, 81
Probolomyrmex salomonisTaylor, 1965: 358196523, 66, 81
Proceratium austronesicumDe Andrade, in Baroni Urbani and De Andrade 2003: 313200350, 81
Proceratium papuanumEmery, 1897b: 592200350, 81
Pseudomyrmecinae
Tetraponera laeviceps(Smith, F. 1859): 14519193, 8, 49
TaxonNotesYearReference
Adelomyrmex sp. BP02nr. hirsutus200879
Adelomyrmex sp. BP03as “Adelomyrmex (Arctomyrmex) sp.”197634
Arnoldius sp. BP01as “nr. flavus195915
Camponotus sp. BP02nr. guppyi200879
Camponotus sp. BP05nr. elysii200879
Camponotus sp. BP06as “Camponotus (Colobopsis) sp. A”197634
Camponotus sp. BP07as “Camponotus (Colobopsis) sp. B”197634
Camponotus sp. BP08as “Camponotus (Colobopsis) sp. C”197634
Camponotus sp. BP09as “Camponotus (Colobopsis) spp. (2)”195918,34
Camponotus sp. BP10as “Camponotus (Colobopsis) spp. (2)”195918,34
Cerapachys sp. BP01as “Cerapachys? (Syscia) sp. 1”195918,34
Colobostruma sp. BP01nr. foliacea200879
Cryptopone sp. BP01nr. testacea200879
Myopias sp. BP01200879
Myopias sp. BP02200879
Myopias sp. BP03200879
Myopias sp. BP04as “Myopias cf. tenuis198339
Myrmecina sp. BP01200879
Myrmecina sp. BP03200879
Pheidole sp. BP02200879
Pheidole sp. BP12nr. mendanai200879
Pheidole sp. BP13as “Pheidole (Pheidolacanthinus) sp.”197634
Platythyrea sp. BP01as “Platythyrea sp.”197634
Polyrhachis sp. BP01Polyrhachis (Myrmhopla) nr. bismarckensis 200879
Polyrhachis sp. BP03as “Polyrhachis (Chariomyrma) sp.”197634
Rogeria sp. BP01nr. stigmatica200879
Strumigenys sp. BP05nr. mocsaryi200879
Vollenhovia sp. BP01nr. elysii200879
Vollenhovia sp. BP02nr. loboii200879
Vollenhovia sp. BP03as “Vollenhovia sp.”197634
TaxonAnutaBellonaChoiseulGuadalcanalKolombangaraMakiraMalaitaMalaupainaMatemaMbanikaNew GeorgiaNEW GEORGIA IS.NGGELA IS.Nggela SuleNupaniOLU MALAU IS.Ontong Java Is.OwarahaREEF IS.RendovaRennellRussell Is.San JorgeSanta CatalinaSanta CruzSANTA CRUZ IS.Santa IsabelSavoShortlandSikaianaTikopiaTulagiUgiVangunuVanikoroVella LavellaSOLOMON IS.Total
Acropyga
Acropyga acutiventrisxxxxxxx7
Acropyga lautaxxxxxxx7
Acropyga oceanicax1
Acropyga pallidax1
Adelomyrmex
Adelomyrmex sp. BP02*x1
Adelomyrmex sp. BP03*xx2
Amblyopone
Amblyopone australisxxxx3
Anochetus
Anochetus catoxxxxxxxxxxxx11
Anochetus graeffeixxxxxxxxxxxxxx13
Anochetus isolatusxxxxxxxxx8
Anonychomyrma
Anonychomyrma dimorphaxxxx3
Anoplolepis
Anoplolepis gracilipesxxxxxxxxxxxxxxxxxx18
Arnoldius
Arnoldius sp. BP01x1
Arnoldius pusillusx1
Brachymyrmex0
Brachymyrmex obscuriorxxx3
Camponotus
Camponotus bedotixxxxxxxxxxxxxxxxx17
Camponotus chloroticusxx2
Camponotus elysiixxx3
Camponotus guppyix1
Camponotus loaxxxxxxxxxx10
Camponotus loa bellixx2
Camponotus novaehollandiaexxxx4
Camponotus sp. BP01x1
Camponotus sp. BP02*x1
Camponotus sp. BP04x1
Camponotus sp. BP05*x1
Camponotus sp. BP06*x1
Camponotus sp. BP07*x1
Camponotus sp. BP08*xx2
Camponotus sp. BP09*x1
Camponotus sp. BP10*x1
Cardiocondyla
Cardiocondyla kagutsuchix1
Cardiocondyla nivalisxxxxxxxx8
Cardiocondyla nudaxxxxx5
Carebara
Carebara atomaxxxxx5
Carebara viehmeyerix1
Cerapachys
Cerapachys inconspicuusxxx2
Cerapachys pawaxx1
Cerapachys terricolaxxxxxxx6
Cerapachys sp. BP01*x1
Colobostruma
Colobostruma foliaceaxxxxxx6
Colobostruma sp. BP01*x1
Crematogaster
Crematogaster abruptaxxx3
Crematogaster elysiixx2
Crematogaster foxix1
Crematogaster nesiotisx1
Crematogaster obnigraxx2
Crematogaster scitax1
Crematogaster wheelerix1
Cryptopone
Cryptopone buttelix1
Cryptopone crassicornisx1
Cryptopone fuscicepsxxxxxx5
Cryptopone testaceaxxxxxxxxx8
Cryptopone sp. BP01*x1
Dilobocondyla
Dilobocondyla sp. BP01x1
Discothyrea
Discothyrea clavicornisxxxxxxxxx8
Eurhopalothrix
Eurhopalothrix brevicornisxxxxxx5
Eurhopalothrix greensladeix1
Eurhopalothrix isabellaexxxx4
Eurhopalothrix proceraxxxxxxxxxxxxxx14
Gnamptogenys
Gnamptogenys albiclavaxxx2
Gnamptogenys crenaticepsxxx2
Gnamptogenys lucidaxx1
Gnamptogenys malaensisxxxxxxxxx8
Gnamptogenys preciosax1
Gnamptogenys solomonensisxxx3
Gnamptogenys sp. BP03x1
Hypoponera
Hypoponera biroixx1
Hypoponera confinisx0
Hypoponera pallidulaxxx2
Hypoponera papuanaxxxxxx5
Hypoponera pruinosaxxxxxxxxxxxx11
Hypoponera punctatissimaxx2
Hypoponera ragusaixxx2
Hypoponera sororculax0
Hypoponera sp. BP01x1
Hypoponera sp. BP06x1
Hypoponera sp. BP07x1
Hypoponera sp. BP08x1
Iridomyrmex
Iridomyrmex ancepsxxxxxxxxxxx11
Iridomyrmex pallidusx1
Iridomyrmex rufonigerx1
Leptogenys
Leptogenys diminutaxxxxx4
Leptogenys forelixxxxx4
Leptogenys oresbiaxx1
Leptogenys truncataxxx2
Lordomyrma
Lordomyrma epinotalisxxxxxxx7
Monomorium
Monomorium australicumxxxxx5
Monomorium destructorx1
Monomorium floricolaxxxxxxxx8
Monomorium pharaonisxxxxx5
Myopias
Myopias sp. BP01*x1
Myopias sp. BP02*x1
Myopias sp. BP03*x1
Myopias sp. BP04*xx2
Myopopone
Myopopone castaneaxxxxxxxxxxxxxx13
Myrmecina
Myrmecina modestaxxxxxxxx8
Myrmecina subarmatax1
Myrmecina
Myrmecina transversax1
Myrmecina sp. BP01*x1
Myrmecina sp. BP03*x1
Nylanderia
Nylanderia bourbonicaxxx3
Nylanderia braueri glabriorxxxx4
Nylanderia dichroaxxxxxxxxx9
Nylanderia mannix1
Nylanderia bismarckensisxxx3
Nylanderia stigmaticaxxxxxxx7
Nylanderia vagaxxxxxxxxxxxxxxx15
Nylanderia vividulaxxx3
Ochetellus
Ochetellus glaberx1
Odontomachus
Odontomachus malignusxxxxxxx6
Odontomachus rufithoraxxxxxx4
Odontomachus saevissimusxxx2
Odontomachus simillimusxxxxxxxxxxxxxxxxxxxxxxxxxxxx27
Oecophylla
Oecophylla subnitidaxxxxxxxxxxxxx13
Opisthopsis0
Opisthopsis mannixxxxxx6
Pachycondyla
Pachycondyla acutaxx1
Pachycondyla aequalisxxxxx4
Pachycondyla croceicornisxxxx3
Pachycondyla darwiniix0
Pachycondyla exarataxxx3
Pachycondyla mannixxx2
Pachycondyla melancholica x1
Pachycondyla papuanaxxx2
Pachycondyla sheldonixx1
Pachycondyla stigmaxxxxxxxxxxxxxx13
Pachycondyla sp. BP01x1
Paraparatrechina
Paraparatrechina minutulaxxxxxx6
Paratrechina
Paratrechina longicornisxxxxxxxxxx10
Pheidole
Pheidole bellix1
Pheidole eratox1
Pheidole fusculax1
Pheidole isisx1
Pheidole takix1
Pheidole megacephalaxxxxxxxxx8
Pheidole mendanaix1
Pheidole nindixxxx4
Pheidole oceanicaxxxxxxxxxxx11
Pheidole philemonxxxxxxxx7
Pheidole sexspinosaxxxxxxxxxx10
Pheidole fuscescensxx2
Pheidole umbonataxxxxxx6
Pheidole sp. BP02*x1
Pheidole sp. BP09x1
Pheidole sp. BP10x1
Pheidole sp. BP11x1
Pheidole sp. BP12*x1
Pheidole sp. BP13*x1
Philidris
Philidris myrmecodiaexxxxxxxxxxxxx13
Plagiolepis
Plagiolepis alluaudix1
Platythyrea
Platythyrea parallelaxxx2
Platythyrea sp. BP01*x1
Podomyrma
Podomyrma salomoxxxx4
Podomyrma woodfordixx2
Polyrhachis
Polyrhachis andromachex1
Polyrhachis annaexxxxxxxxxx10
Polyrhachis acutinotax1
Polyrhachis argenteaxxxx3
Polyrhachis brunneipesxx1
Polyrhachis campbellixx2
Polyrhachis dahliixxxxxxxxx8
Polyrhachis emeryanax1
Polyrhachis fulakoraxx2
Polyrhachis geminataxxx3
Polyrhachis greensladeixx2
Polyrhachis ithonaxx2
Polyrhachis johnsonixxxx4
Polyrhachis kaipixxxx4
Polyrhachis litigiosaxx2
Polyrhachis malaensisx1
Polyrhachis nofrax1
Polyrhachis osaexxxx3
Polyrhachis pacificax1
Polyrhachis rerexxx3
Polyrhachis salomoxxxx3
Polyrhachis santschiixx2
Polyrhachis setosax1
Polyrhachis similisxxxxxxxxx9
Polyrhachis ugiensisxxx3
Polyrhachis ulyssesxxxx3
Polyrhachis undulataxx2
Polyrhachis wheelerixx2
Polyrhachis sp. BP01x1
Polyrhachis sp. BP03x1
Polyrhachis sp. BP04x1
Ponera
Ponera clavicornisxxxxxxxxxxxx12
Ponera incertaxxxxxxxx7
Ponera swezeyix1
Ponera szaboixx2
Ponera tenuisx1
Ponera sp. BP01x1
Ponera sp. BP02x1
Prionopelta
Prionopelta majusculaxxx3
Prionopelta opacaxxxxxxxxxxx11
Pristomyrmex
Pristomyrmex levigatusxxx3
Pristomyrmex obesusxxxxxxxxxx10
Probolomyrmex
Probolomyrmex salomonisxxx2
Proceratium
Proceratium austronesicumx1
Proceratium papuanumxxxx4
Rhytidoponera
Rhytidoponera araneoidesxxxxxxxxxxx10
Rhytidoponera chalybaeax1
Rogeria
Rogeria megastigmaticaxx2
Rogeria stigmaticaxxxx4
Rogeria sp. BP01*x1
Romblonella
Romblonella elysiixxxxx5
Solenopsis
Solenopsis geminatax1
Solenopsis papuanax1
Solenopsis pawaensisxxx3
Stereomyrmex
Stereomyrmex disparx1
Stigmatomma
Stigmatomma celataxxxxxxxxxxx10
Stigmatomma gnomax1
Strumigenys
Strumigenys chyzerixxxxxxxxx9
Strumigenys decollatax1
Strumigenys emmaexxxxxx6
Strumigenys euryceraxxxxx5
Strumigenys frivaldszkyixx2
Strumigenys godeffroyixxxxxxxxxxxx11
Strumigenys karawajewixxxxxx5
Strumigenys membraniferaxxxx4
Strumigenys mocsaryixxxx4
Strumigenys rogerix1
Strumigenys szalayixxxxx5
Strumigenys undrasx1
Strumigenys yaleopleuraxxxxx5
Strumigenys sp. BP05x1
Strumigenys sp. BP06x1
Tapinoma
Tapinoma melanocephalumxxxxxxxxx9
Tapinoma minutumx0
Tapinoma timidumx1
Technomyrmex
Technomyrmex albipesxxxxxxxxxxxxx12
Technomyrmex vitiensisxx2
Technomyrmex sp. BP01x1
Tetramorium
Tetramorium antennatumxx2
Tetramorium aspersumxxxxxxx7
Tetramorium bicarinatumxxxxxxx7
Tetramorium carinatumxxxxxxxxx9
Tetramorium insolensxxxxxx6
Tetramorium lanuginosumxx2
Tetramorium mayrix1
Tetramorium melanogynaxxxx4
Tetramorium mutatumx1
Tetramorium pacificumxx2
Tetramorium salomoxxx3
Tetramorium simillimumxxxx4
Tetramorium tonganumxxxxx5
Tetramorium vombisx1
Tetraponera
Tetraponera laevicepsxxx3
Turneria
Turneria dahliixxxx4
Turneria pacificaxxx3
Vollenhovia
Vollenhovia dentataxxx2
Vollenhovia marginataxxx2
Vollenhovia elysiixxx2
Vollenhovia foveacepsxx1
Vollenhovia loboiixx1
Vollenhovia oblongaxxxxxx6
Vollenhovia pedestrisxxxxxxx7
Vollenhovia subtilisxx2
Vollenhovia sp. BP01*x1
Vollenhovia sp. BP02*x1
Vollenhovia sp. BP03*x1
Wasmannia
Wasmannia auropunctatax1
Total83211107171427129721840432843548101666182432376812211213832760217
  6 in total

Review 1.  Arthropods on islands: colonization, speciation, and conservation.

Authors:  Rosemary G Gillespie; George K Roderick
Journal:  Annu Rev Entomol       Date:  2002       Impact factor: 19.686

2.  Revisiting the ants of Melanesia and the taxon cycle: historical and human-mediated invasions of a tropical archipelago.

Authors:  Evan P Economo; Eli M Sarnat
Journal:  Am Nat       Date:  2012-05-24       Impact factor: 3.926

3.  Species-area relation for birds of the Solomon Archipelago.

Authors:  J M Diamond; E Mayr
Journal:  Proc Natl Acad Sci U S A       Date:  1976-01       Impact factor: 11.205

4.  Biogeography and morphological evolution in a Pacific island ant radiation.

Authors:  Eli M Sarnat; Corrie S Moreau
Journal:  Mol Ecol       Date:  2010-11-08       Impact factor: 6.185

5.  Worldwide invasion by the little fire ant: routes of introduction and eco-evolutionary pathways.

Authors:  Julien Foucaud; Jérôme Orivel; Anne Loiseau; Jacques H C Delabie; Hervé Jourdan; Djoël Konghouleux; Merav Vonshak; Maurice Tindo; Jean-Luc Mercier; Dominique Fresneau; Jean-Bruno Mikissa; Terry McGlynn; Alexander S Mikheyev; Jan Oettler; Arnaud Estoup
Journal:  Evol Appl       Date:  2010-02-02       Impact factor: 5.183

6.  A revision of Malagasy species of Anochetus mayr and Odontomachus latreille (Hymenoptera: Formicidae).

Authors:  Brian L Fisher; M Alex Smith
Journal:  PLoS One       Date:  2008-05-28       Impact factor: 3.240

  6 in total
  1 in total

1.  Ants of Ambon Island - diversity survey and checklist.

Authors:  Fransina Latumahina; Michaela Borovanska; Nugroho Susetya Putra; Milan Janda
Journal:  Zookeys       Date:  2015-01-19       Impact factor: 1.546

  1 in total

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