Literature DB >> 25834475

Nine genera of Eucnemidae (Coleoptera) new to Peru, with a key to Peruvian genera.

Varpu Vahtera1, Jyrki Muona2, Ari Linna1, Ilari E Sääksjärvi1.   

Abstract

Thirteen genera of Eucnemidae containing forty species were collected from the Iquitos region in Peru. Nine of the genera are new to the country: Rhagomicrus Fleutiaux, 1902, Adelorhagus Horn, 1890, Adelothyreus Chevrolat, 1867, Microrhagus Dejean, 1833, Dyscharachthis Blackburn, 1900, Heterotaxis Bonvouloir, 1871, Spinifornax Fleutiaux, 1926, Serrifornax Fleutiaux, 1926 and Maelodrus Fleutiaux, 1928. The previous eucnemid record from Peru contained eleven species in ten genera. Only one of the forty species caught, Entomophthalmusamericanus Bonvouloir, was previously known and described from the country. Dyscharachthis, Maelodrus and Adelorhagus are recorded from South America for the first time. Many of the collected species seem to favor white-sand forest as their habitat. Possible reasons for this are discussed. A list of eucnemids from Peru is included, containing taxa already recorded from the country and also taxa that are likely to occur there. A key to the Peruvian genera is included.

Entities:  

Keywords:  Amazon; Elateroidea; Neotropics; eucnemid; lowland; rain forest; species richness.; taxonomy; white-sand forest

Year:  2015        PMID: 25834475      PMCID: PMC4366809          DOI: 10.3897/BDJ.3.e4493

Source DB:  PubMed          Journal:  Biodivers Data J        ISSN: 1314-2828


Introduction

is a species rich (185 genera, 1700 species) mainly tropical beetle family, characterized by numerous undescribed species. Studies investigating the abundance of eucnemid beetles are rare, but the few that exist conclude that the family forms a significant portion of the beetle biodiversity in tropical forests (Hammond 1990, Penny and Arias 1982). The evolutionarily most primitive eucnemid groups live in soil as larvae, but all derived groups spend their larval time inside wood. Of these lignicolous groups only a few prefer conifers, the rest live in broad-leaved trees that are infested with white-rot. Despite their larvae living several years in a strictly lignicolous environment, eucnemids are not xylophagous per se. Instead, the few available studies investigating their gut content have shown that the larvae feed on saprotrophic fungus, not on wood (Ford and Spilman 1979, Muona 1993). Adult eucnemids feed very little, if at all, during their short lives. As is commonly the case in locations with a high diversity, the eucnemid fauna of Peru is still poorly known. Previously, only eleven species belonging to ten genera were reported from the country. In this study we investigate the diversity of eucnemid beetles in Peru as well as discuss the effect that forests growing on white-sand have on the diversity of the group.

White-sand and clay soil forests in the Peruvian Amazon

The main non-inundated lowland rain forest types in the Peruvian Amazon can be roughly divided into two groups based on the soil they grow on. “Traditional rain forests” are normally forests growing on clayey soil characterized by large trees and vines that form a shady and moist habitat for a rich flora and fauna. In contrast, forests growing on white quartz sand form nutrient-poor habitats that are not preferred by most animals because of their harshness. These forests are called varillal and chamizal in Peru (Encarnación 1985, Ruokolainen and Tuomisto 1993, and caatinga, campina and campinarana in other parts of the Amazon (see Anderson 1981). Large white-sand areas are known to occur in tropical Asia, Guyana and Brazil (Anderson 1981, MacKinnon et al. 1997) whereas in northern Peru they occur in small isolated patches, surrounded by the prevailing non-inundated rain forests growing on relatively nutrient-rich clayey ground (Räsänen et al. 1998b, Ruokolainen and Tuomisto 1993, Ruokolainen and Tuomisto 1998). In Peru, this unique white-sand forest type is characterized by slender trees and a sparse canopy and shrub layer, typically growing on small hills. In comparison to the generally dry, hot and nutrient-poor white-sand habitats, the shady and moist forests on nutrient-rich clay ground would seem like an ideal habitat for most animals. Indeed, despite several endemic and highly specialized species being reported from white-sand forests (e.g. Alvarez and Whitney 2001), the overall species richness of this habitat type has generally been considered low (MacKinnon et al. 1997, Ruokolainen and Tuomisto 1998). White-sand sites are distributed as isolated patches in the western Amazon. Their quartz-sands were formed from the Sub-Andean foreland in situ weathered sediments by aquatic recycling, sorting and re-deposition. The humid tropical climate speeded up weathering, and the Andean orogeny developing eastwards during the Neogene (25 Ma-recent) was a dynamo creating laterally migrating rivers in the Amazonian lowlands. Floodplains of different age were formed along the sequential uplift of the Andes. Minor rivers and creeks finalized the landscape to consist nowadays of sandy terrains and hills overlying the more resistant, clayish Miocene sediments, which in places forms the forest ground. White sands present the ultimate residual parts of this system, exposed as floodplains of different (depositional) age indicated by their different height, degree of denudation and a minor difference in their maturity (95-99% quartz) (Räsänen et al. 1987, Räsänen et al. 1992, Räsänen et al. 1990, Räsänen et al. 1998a).

Materials and methods

Study site and collecting methods

The study was conducted in 1998 and 2000 in the National Reserve of Allpahuayo Mishana (NRAM, 3°57'S, 73°26'W), near the densely populated city of Iquitos (Department of Loreto, Peru). NRAM is famous for its high tropical rain forest habitat heterogeneity, high levels of endemism and extreme species richness (Gentry 1988, Sääksjärvi et al. 2004, Vásquez Martínez and Phillips 2000, Whitney and Alvarez 1998). The soil of NRAM consists of a mosaic of patches varying from white-sand (Anderson 1981, Encarnación 1985) to clay, reflecting the complex geological history and formations of the surface (Räsänen et al. 1998b). Sampling was conducted using Malaise traps in five areas containing similar kinds of non-inundated rain forest types (see Sääksjärvi et al. 2004, Sääksjärvi et al. 2006). The main aim of these field studies was to sample parasitoid wasps (see Sääksjärvi et al. 2004). In each area two traps were placed in forest growing on clayey to loamy ground (high to intermediate in nutrients) and three traps in forest patches growing on nutrient-poor white-sand soils of differing structure (representing the diversity of white-sand forests present in NRAM) in order to assure that all traps functioned independently. The resulting material was used in the current study since Malaise traps have proved efficient in collecting eucnemid beetles (Hammond 1990). The traps were emptied every second week and the specimens were preserved in 75% alcohol. Specimens were identified by JM. Part of the collected and identified material will be delivered to the Museum of Natural History, University of San Marcos, Lima, Peru where it will form part of the reference collection on Peruvian eucnemids. The rest of the material is deposited at the Finnish Museum of Natural History, Finland, where it is curated by JM. The new species will be described in connection of generic revisions of global scope. Type status: Other material. Occurrence: individualCount: 2; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM)

Taxon treatments

Notes

One undescribed species was recorded from clay soil forest (Suppl. material 2). This is the first record of this genus from Peru and South America. Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species was caught in white-sand forest (Suppl. material 2). Bonvouloir, 1972 Type status: Other material. Occurrence: individualCount: 38; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) This is the only species found in our study that was previously known from Peru (Schenkling 1928). It was widespread and common in our material, present in 15 sites in both clay and white-soil forest (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 2; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species represented by two individuals was found in both forest types (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 2; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species found in both forest types (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 5; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species found from both forest types (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 3; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species found from both forest types (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 2; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species found from white-sand forest (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 4; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species found from white-sand forest (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 2; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species found from white-sand forest (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species was found from white-sand forest (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 2; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) The first record of this genus from Peru. One undescribed species was caught in both forest types (Suppl. material 2). Cobos, 1972 Type status: Other material. Taxon: higherClassification: ; genus: Cobos, 1972 was described from Tingo Maria, Rio Huallaga, a limestone mountain range area in Peru (Cobos 1972). Additional records from the Andean region are known to us, but this species was not found in our study. Type status: Other material. Occurrence: individualCount: 2; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species was caught in a white-sand site (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 5; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species found in white-sand forest (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 13; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species was caught in both forest types (Suppl. material 2). Another undescribed species is previously known from peru (JM collection). Perty, 1830 Type status: Other material. Taxon: higherClassification: ; genus: The genus was not found in our study. Previously one species, Fabricius, 1801, is reported from Peru (Schenkling 1928). Type status: Other material. Occurrence: individualCount: 2; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species was found from both forest types (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 4; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species was caught in white-sand forest (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 2; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species was caught in clayey forest (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species found in a white-sand site (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species was found in a white-sand site (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 8; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species caught in both forest types (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species was caught in a clayey forest site (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species caught in a white-sand site (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species caught in a clayey forest site (Suppl. material 2). Previously one species, (Erichson 1847), was known from Peru (Schenkling 1928). Type status: Other material. Occurrence: individualCount: 4; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species was caught in white-sand forest (Suppl. material 2). An undescribed species is previously known from Peru (JM collection). Type status: Other material. Occurrence: individualCount: 3; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species caught in white-sand forest (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 5; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species caught in white-sand forest (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 3; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species caught in both forest types (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 2; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species caught in white-sand forest (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 2; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species was caught in both forest types (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species was caught in a white-sand site (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) A single individual of an undescribed species was caught in a white-sand site (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) A single individual of an undescribed species was caught in a clayey forest site (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) A single individual of an undescribed species was caught in a clayey forest site (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 3; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species was caught in both forest types (Suppl. material 2). Fleutiaux, 1912 Type status: Other material. Taxon: higherClassification: ; genus: The genus was not found in our study. Preiviously one species, Fleutiaux, 1912, is reported from Peru (Schenkling 1928). Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) This is the first record of this genus from Peru. A single individual of an undescribed species was caught in a white-sand site (Suppl. material 2). Bonvouloir, 1871 Type status: Other material. Taxon: higherClassification: ; genus: Not found in our study, but an undescribed species is previously known from Peru (JM collection). Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) One individual caught in a white-sand site (Suppl. material 2). This genus was formerly known from the Western Pacific and Australian regions. The undescribed species found in our study exhibits all the diagnostic features of the genus: the antennae are slightly flattened, basally with faintly keeled antennomeres, the abdominal tip is deeply excavated, the lateral antennal grooves are somewhat removed from the lateral border of hypomera and become fainter caudad, and the dorsal vestiture is unevenly distributed, forming faint patterns. Berthold, 1827 Type status: Other material. Taxon: higherClassification: ; genus: We did not find this genus in our study. One species ( Cobos, 1964) is known from Peru (Cobos 1964). Type status: Other material. Occurrence: individualCount: 6; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) An undescribed species with individuals caught in both forest types was recorded in our study (Suppl. material 2). Another species, Fleutiaux 1934, is previously known from Peru (Fleutiaux 1934). Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) This is the first record of this genus from Peru. A single individual of an undescribed species was caught in a white-sand site (Suppl. material 2). Type status: Other material. Occurrence: individualCount: 1; Taxon: higherClassification: ; genus: ; Location: continent: South America; country: Peru; county: Loreto; municipality: Iquitos; locality: National Reserve of Allpahuayo Mishana (NRAM) This is the first record of this genus from Peru. A single individual of an undescribed species was caught in a white-sand site (Suppl. material 2). The genera reported either earlier or in this study are shown in bold. The key also includes genera that are still undiscovered in Peru, but likely to be found there because they are known from the surrounding region (shown in italics only).

Analysis

Since the traps were placed in two different forest types (three traps in white-sand forest and two in forest growing on clayey soil in each area), the average number of species and individuals that each trap collected was calculated. A species accumulation curve was calculated using EstimateS (Colwell 2013) in order to estimate how efficient our sampling was. The total sample size was 185 malaise trap months, which presents one of the largest insect samples ever collected in the western Amazon by Malaise trapping. The material contained 40 eucnemid species belonging to 13 genera; 39 of the species were undescribed. Nine of the collected genera have never been reported from Peru before. Two genera are new to South America as a whole (, ), and one () has only been reported there in passing in a more general context (Muona 1991, Muona 1993). The total number of individuals collected was 141. Average a trap placed in white-sand forest caught 4.5 species and 6.2 individuals whereas a trap in clay soil forest caught 3.8 species and 5.3 individuals. Many of the species were represented by only one or two individuals (the number of singletons and doubletons was 15 and 11, respectively). The species accumulation curve was far from reaching an asymptote indicating that additional sampling would yield a considerable number of new eucnemid species (Fig. 13).
Figure 13.

Local species accumulation of eucnemids in Allpahuayo Mishana, Peru (Suppl. material 1).

Discussion

The few studies that have sampled eucnemid diversity (Hammond 1990, Penny and Arias 1982) conclude that the group forms an important component of the beetle biodiversity in tropical forests. Major unpublished material exists from NE Australia, the Fiji Islands and the Grande Terre of New Caledonia. More exact comparisons have to wait for future analyses, but preliminary results suggest that the diversity of the Peruvian fauna is best compared with that of Australia, being somewhat higher than in Fiji and considerably higher than in New Caledonia. We have shown that by conducting a biodiversity survey in one area in the Peruvian Amazon, we were able to double the number of genera and quadruple the number of species reported from the country. However, despite our sampling being intensive and long-term (185 Malaise trap months in total), it was nowhere near sufficient to record most eucnemid species present in the sampled area. This is indicated by the species accumulation curve showing no sign of stabilizing. Also, the number of rare species remained high throughout the sampling which further indicates the presence of numerous undiscovered species (Colwell and Coddington 1994). The use of other intensive collecting methods, such as light or window trapping, would probably have resulted in a higher species richness (see Longino et al. 2002). Two of the genera reported here ( and ) have never been collected from South America before: is known from Central America (Costa Rica, unpublished; Panama, loc. class.) but the closest reported occurrences of the genus are from Western Polynesia and Australia. Furthermore, although the existence of in South America was briefly noted by Muona (1991), Muona (1993), the genus has not been properly reported from the continent before. Many of the new species obtained in this study were caught in study sites located in white-sand forest (see habitats in Figs 14, 15). This is interesting, since for most taxa the overall diversity of this habitat has been considered low (MacKinnon et al. 1997, Ruokolainen and Tuomisto 1993). The main reason that many animal groups avoid white-sand forest as their preferred habitat is its hot, dry and nutrient-poor nature. Evidently there must be something in white-sand forest conditions that attracts and favors eucnemid beetles. Given the complex structure of clay soil forest (e.g. multilayered and tall canopy, abundance of large trees, herbs, vines and epiphytes), one might have expected lignicolous beetles to be richer there than in white-sand forest. White-sand forest is characterized by a rather simple physiognomy (e.g. uniform and rather low canopy height, most tree trunks less than 20 cm in diameter, dominance of a few tree or palm species, absence of large herbs, trees and tree ferns), and a large amount of ectomychorriza (see Anderson 1981). The abundance of saprotrophic fungi could be the key factor attracting eucnemid beetles, as most eucnemid larvae are highly specialized to feed on it (Ford and Spilman 1979, Mamaev 1976, Muona and Teräväinen 2008). The harsh conditions outside the fungi-infested wood may not matter much to these saproxylic beetles that spend most of their life inside the wood.
Figure 14.

Low canopy white-sand forest (photo: I.E.Sääksjärvi).

Figure 15.

Nutrient-poor white sand exposed in Allpahuayo (photo: I.E.Sääksjärvi).

Another explanation for the high eucnemid diversity in white-sand forest stems from the geological history of the white-sands. White-sand forests in the geologically more stable Central and Eastern Amazon may have been more persistent and extensive than the geologically recently formed and isolated white-sand patches in the western Amazon (Anderson 1981). Although scattered at present, the forests growing on white-sand in the western Amazon may have been open to colonization from more widely distributed white-sand forests in the Central and Eastern Amazon, serving as refugiae for species specialized to this forest type. Moreover, although the species richness in one white-sand patch may be low overall, the heterogeneity of forest types growing on white-sand patches makes the diversity extremely high between different patches. Their differences are regulated by the formation and depth of the impermeable spodic horizon (Klemola 2003) affecting the moisture conditions in the soil. The thickest impermeable horizons have been formed against the Miocene clayish sediments and it is possible that allochthonous material has been enriched in them. Although the quartz-sands are highly nutrient-poor, they occasionally contain small amounts of clay, the capacity of which to release mineral nutrients (Ca2+. Mg2+, Na+ and K+) into the system is 2,5 – 5 times less than in the Miocene sediments of the region and five times higher than in the thoroughly weathered clays in the Eastern Amazonia, Guyana Shield (Linna et al. 1998). Though eucnemid species are mostly characterized by having a relatively small body size, there are also large-sized taxa, of which e.g. the genus occurs in the Brazilian Amazon. Interestingly, all the species collected in this study are small, 2-8 mm in length. This may just be a matter of low sampling efficiency or alternatively it may reflect the fact that white-sand forest trees are commonly thin (most tree trunks less than 20 cm in diameter). The latter alternative cannot be the sole explanation, however, since clay soil forest also had only small eucnemids despite the presence of large trees. Species accumulation data Data type: EstimateS results File: oo_35345.xlsx Eucnemid specimens by traps Data type: occurences Brief description: Data showing the number of specimens / species collected by each trap. File: oo_36842.xlsx
1Antennomeres 9-11 elongated, 8 clearly shorter and narrower than 9 2
Antennomeres 9-11 not enlarged, 8 about as long and wide as 9 3
2Antennomeres 9-11 serrate or pectinate in males, females larger than 15 mm Phlegon
Antennomeres 9-11 neither serrate nor pectinate, females smaller than 15 mm Ceratogonys
3Hypomera with basally closed lateral antennal grooves forming deep basal pockets for reception of antennae (Fig. 1), male protarsomere 1 without a sex comb 4
Hypomera either simple (Fig. 2), or with notosternal antennal grooves (Fig. 3), or with basally open evenly deep lateral antennal grooves (Fig. 4) in which case the male protarsomere 1 has a basal sex comb (Fig. 5) 7
4Clypeus very wide and short, distance between the antennal insertion points 6-10 times the distance from the lower edge of the antennal insertion point to the edge Bossionus
Clypeus much narrower, the width at most 4.5 times the height 5
5Hypomera with pit-like hairy excretory organs (Fig. 6) Idiotarsus
Hypomera without such structures 6
6Head simple, frons and clypeus without keels Entomosatopus
Frons and/or clypeus with sharp keels Dyscharachthis
7Lateral pronotal ridge minutely serrate (Fig. 7), hypomera usually with notosternal antennal grooves (Fig. 3), male protarsomere 1 usually with an apical sex comb (Fig. 8) 8
Lateral pronotal ridge smooth 15
8Elytral suture forming a beak before the apex in lateral view (Fig. 9) Arrhipis
Elytral apex evenly curved to end in lateral view 9
9Combined length of antennomeres 2 and 3 less than the length of 4 Entomophthalmus
Combined length of antennomeres 2 and 3 always distinctly greater than the length of 4 10
10Metacoxal plates approximately parallel-sided (Fig. 10) 11
Metacoxal plates distinctly wider close to the insertion point of the trochanter than on the sides (Fig. 11) 14
11Antennal grooves parallel-sided, always well defined, body parallel-sided, antennae feebly serrate, often elongated Rhagomicrus
Antennal grooves either entirely absent or widening caudad, poorly delimited 12
12Antennomeres dentate, body uniformly yellow Adelorhagus
Antennomeres 4-10 serrate or pectinate, dorsum dark or bicoloured 13
13Pronotum unusually large compared to the rest of the body, body front-heavy in appearance, pronotum black, elytra sometimes with pale spots Adelothyreus
Dorsum black, pronotum and elytral longitudinal stripes yellow Weyrauchiella
14Width of the frons between antennal sockets less than half the distance between the eyes, usually distinctly less, body usually black or dark brown, male protarsomere 1 with an apical sex comb Microrhagus
Width of the frons between antennal sockets at least half the distance between the eyes, usually distinctly more, body evenly yellowish brown, male protarsomere 1 without any spine comb Golbachia
15Hypomera without medially defined antennal grooves (Fig. 2) 16
Hypomera with medially sharply defined basally open lateral antennal grooves (Fig. 4) 21
16Mandibles slender Monrosina
Mandibles stout with a secondary basal tooth 17
17Meso- and metatibiae without spine combs on lateral surfaces, male protarsomere 1 simple 18
Meso- and metatibiae with spine combs, male protarsomere 1 with a basal sex comb (Fig. 5) 19
18Antennomeres 3-10 deeply serrate or flabellate Calyptocerus
Antennomeres 3-10 tubular, neither serrate nor flabellate Paraxylophilus
19Frons usually conspicuously flattened, antennomeres 6-10 slightly enlarged and flattened, 6 always longer and usually wider than 5, 3-10 not serrate Nematodes
Frons convex, antennomere 5 usually similar in size to 6, antennomeres 3-10 dentate, serrate or tubular, protibiae with simple apexes 20
20Dorsum shiny or very shiny, at most densely punctate, brownish Plesiofornax
Dorsum extremely dull, very densely and strongly rugose, black Gagatellus
21Elytral epipleura grooved, smooth and shiny basally Serrifornax
Elytral epipleura even, not grooved in front 22
22Abdominal tip excavated, bifid Maelodrus
Abdominal tip pointed or rounded 23
23Antennal grooves large in volume, wider than rest of hypomera Macraulacus
Antennal grooves much narrower than rest of hypomera (Fig. 4) 24
24Elytra with sharply marked, punctate striae (Fig. 12) parallel-sided in shape Heterotaxis
Elytral striae faint, never punctate, elytra rarely parallel-sided in shape 25
25Claws with basal teeth Fornax
Claws simple Dromaeolus

The genera reported either earlier or in this study are shown in bold. The key also includes genera that are still undiscovered in Peru, but likely to be found there because they are known from the surrounding region (shown in italics only).

  3 in total

1.  Tree species richness of upper Amazonian forests.

Authors:  A H Gentry
Journal:  Proc Natl Acad Sci U S A       Date:  1988-01       Impact factor: 11.205

2.  Fluvial perturbance in the Western Amazon basin: regulation by long-term sub-andean tectonics.

Authors:  M E Räsänen; J S Salo; R J Kalliola
Journal:  Science       Date:  1987-12-04       Impact factor: 47.728

3.  Estimating terrestrial biodiversity through extrapolation.

Authors:  R K Colwell; J A Coddington
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1994-07-29       Impact factor: 6.237

  3 in total

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