Cryptotermes colombianus a new drywood termite and distribution record of Cryptotermes in Colombia.

A new species of drywood termite (Kalotermitidae), Cryptotermes colombianus, is described and new records for Cryptotermes cylindroceps and Cryptotermes mangoldi are presented from the Caribbean coast of Colombia. Cryptotermes colombianus is described from two soldiers and genetic sequences. This unusual species differs noticeably from other regional Cryptotermes species for its weak and inconspicuous definition of the frontal and genal horns and its acute angle of the frons with respect to the vertex. Cryptotermes colombianus clustered with species from the Ethiopian and Oriental region and it is closely related to Cryptotermes havilandi. Cryptotermes cylindroceps is widely distributed along the Colombian Caribbean coast, commonly associated with dead wood in mangrove habitats. It also is commonly found in wooden furniture, constituting an important household pest. Cryptotermes mangoldi is reported from the Caribbean mainland for the first time. With these new records, there are now five Cryptotermes species for Colombia, including the pest species Cryptotermes brevis and Cryptotermes dudleyi. This new description raises the numbers of Neotropical Cryptotermes to a total of 34 species, of which 2 are fossils, 4 introduced, and 28 endemic.

Introduction

is one of the best studied and economically most significant genus of drywood termites (Krishna 1961, Chhotani 1970, Gay and Watson 1982, Lenz et al. 1985, Bacchus 1987, Constantino 1998, Scheffrahn and Křeček 1999, Korb 2009, Krishna et al. 2013). Sixty-nine species have been described with 33 distributed in the Neotropics (2 fossil, 4 introduced and 27 native species, including - nomen dubium).

has been poorly studied in Colombia, only three species have been recorded: (Walker 1853), Banks 1918, and Scheffrahn and Křeček 1999, (Gile et al. 2011). The first two species are important pests. has been introduced to the Neotropics and often appears in disturbed outdoor habitats (Scheffrahn and Křeček 1999, Constantino 2002) and whose origin was established for the Atacama Desert region of coastal northern Chile and southern Peru is widespread in the Neotropics, (Scheffrahn et al. 2009). Until this study Scheffrahn and Křeček 1999, was only known from the Dominican Republic.

Morphological identification of termite species can be difficult as diagnostic morphological markers can be rare and are often restricted to soldiers or alates. For such taxa, sequencing of gene fragments (DNAbarcoding) is now an important molecular tool widely used to elucidate phylogenetic relationships between taxa and to identify species (Inward et al. 2007a, 2007b, Legendre et al. 2008). Mitochondrial markers have been extensively used in termites, e.g. Miura et al. 2000, Lo et al. 2004, Ohkuma et al. 2004, Bergamaschi et al. 2007, Li et al. 2009, Singla et al. 2013, Hausberger et al. 2011, Scheffrahn et al. 2015. In termites, sequencing fragments of the proved to be an especially suitable marker (e.g., Legendre et al. 2008, Hausberger et al. 2011): , the standard ‘tree of life gene’, is less suitable as it does not amplify well in termites and have too low resolution to distinguish species.

cytochrome oxidase subunit II

Cytochrome oxidase subunit I

Most studies on Colombian termites have been directed towards species of economic importance as pests in agriculture and forestry (Weidner 1980, Galvis 1985, Scheffrahn et al. 1999, Scheffrahn 2010, 2011, Gutierrez et al. 2004, Medina and Pinzon-Florian 2011, Abadía et al. 2013). The total number of termite species in Colombia remains unknown, but Vargas-Niño et al. (2005) list 26 genera of from Colombia. Given that Colombia has 37 types of ecosystems (Instituto de Hidrología, Meteorología y Estudios Ambientales et al. 2007) and more than 26,000 plants (Bernal et al. 2015), 2,569 from tropical dry forests (Instituto de Investigación Alexander von Humboldt 2014), the number of termite species for Colombia is expected to be high.

The purpose of this paper is to describe a new species, , and to provide new information on the status, biology and distribution of genus in Colombia.

Materials and methods

Specimens were gathered as part of a research project on termite assemblages in the Colombian Caribbean between 2014 and 2015. Termites were collected using a standardized sampling protocol (Jones and Eggleton 2000, Hausberger and Korb 2015). Termites were also collected in structural wood from buildings and furniture. All were preserved in 100% ethanol for DNA analysis, and 80% ethanol for museum curation. Additional localities from Colombia are included in this paper, from an unpublished survey in 2009 by R. Scheffrahn.

Identification

Taxonomic keys from Scheffrahn and Křeček (1999) were used to determine species. The specimens of the new species could not be identified with this key. Hence, it was sequenced together with specimens from all samples, except , for genetic species identification. In addition, eleven other species and were used for comparison (Table 1). Fragments of the mitochondrial gene cytochrome oxidase subunit II (; total length ~740 bp), 12S rRNA (~385 bp) and 16S rRNA (total length ~480bp) were used and sequenced as described in Hausberger et al. (2011). DNA sequences were aligned with MEGA 6.0. (Tamura et al. 2013) and a Bayesian inference phylogeny was created with MrBayes 3.2.1. (Ronquist and Huelsenbeck 2003) (107 generations, 50% discarded as burn-in). The resultant tree was visualized using FigTree version 1.4.2 (http://tree.bio.ed.ac.uk/software/figtree/). Additionally, we also used MEGA 6.0. to calculate p-distance between species.

Table 1.

GenBank accession numbers of the mitochondrial genes.

Species	GenBank ID
	COII	12S rRNA	16S rRNA
Blatta orientalis	DQ874267.1	-	-
Cryptotermes cavifrons	FN377806.1	-	-
Cryptotermes colombianus	KU510330	KX267100	KX267099
Cryptotermes cylindroceps	KU510331	-	-
Cryptotermes declivis	HQ012042.1	-	-
Cryptotermes domesticus	AF189085.1	-	-
Cryptotermes dudleyi	FN377808.1	-	-
Cryptotermes havilandi	FN377809.1	-	-
Cryptotermes longicollis	FN377810.1	-	-
Cryptotermes primus	AF189090.1	-	-
Cryptotermes queenslandis	AF189092.1	-	-
Cryptotermes secundus	AF189093.1	-	-
Cryptotermes simulatus	AF189094.1	-	-
Cryptotermes tropicalis	AF189095.1	-	-

Imaging and measurements

Specimens were suspended in Sagrotan® Hand Sanitizer and images were taken with a Nikon SMZ25 stereomicroscope coupled to a Nikon Model DS-Fi2 digital camera. The software Helicon Focus® was used to stack pictures. Morphological definitions and measurements were done following Roonwal (1969), Gay and Watson (1982) and Scheffrahn and Křeček (1999).

Deposit

Voucher specimens are held at Freiburg University. The holotype, dealated morphotype and pseudergates from type colony of will be deposited in the Natural History Museum of the Alexander von Humboldt Institute of Bogotá (MIAvH) and Paratype soldier in the collection of the American Museum of Natural PageBreakHistory, New York. Specimens of will be part of the collection of the Department of Chemistry and Biology at the University del Norte, Barranquilla, Colombia. Other Colombian material is housed in the University of Florida Termite Collection in Davie, Florida.

Systematics

Family Froggatt, 1897 Genus Banks, 1906

sp. n.

http://zoobank.org/9D27B3AE-E8A0-4512-8A1E-D9E54A88A46C

Fig. 1

Figure 1.

Cryptotermes sp. n. Dealated imago: Head in dorsal (A) and lateral view (B). Soldier: Head in dorsal (C), lateral (D), oblique (E), and frontal view (F). Scale bar: 0.5 mm.

Description.

Dealated (Fig. 1A–B). General color brown. Frons pale brown, vertex brown. Pronotum and abdominal tergites brown. Antennae pale brown. Labrum pale brown. Femora brown, tibiae pale brown. Abdominal sternites pale brown and very pale brown laterally. Head suboval; cranial sutures fine, but distinct. Eyes moderately large, non-protruding, and oval. Ocelli moderately large, oval, and touching eyes. Antenna with 6 and 8 articles but incomplete, with formulae 2>3<4=5=6. Pronotum wider than long, usually with distinctive midline mark. Arolia present. Measurements are reported in Table 2.

Table 2.

Measurements (in mm) of sp. n. dealated imago.

No.	Measurements in mm (n=1) from 1 colony
1	Head length with labrum	1.27
2	Head length to postclypeus	1.08
3	Head width, maximum at eyes	0.86
4	Eye diameter, maximun	0.30
5	Eye to head base, minimum	0.16
6	Ocellus diameter	0.08
7	Pronotum, maximum width	0.90
8	Pronotum, maximum length	0.73
9	Total length without wings	4.60
10	Total length with wings	–
11	Fore wing length to suture	–
12	Fore wing, maximun width	–

Soldier. (Fig. 1C–F). Head in dorsal view with frontal flange and front horns very dark; 3/4 of anterior vertex almost black chestnut, grading to chestnut brown; PageBreakposterior it turns ferruginous orange to pale yellow (Figure 1C). Head in lateral view with anterodorsal region almost black, which grades steeply to chestnut brown then to pale yellow under eye spot and occipital foramen (Figure 1D). Mandibles chestnut brown. Anterior margin of pronotum chestnut brown posterior margin pale yellow (Fig. 1E–F).

Head in dorsal view abruptly truncated in front; frontal flange forming a rim surrounding a few undulations on frons. Head widest behind flange, gradually narrowing toward the occiput (Figure 1C). Frontal flange coalesces with frontal horn and postclypeus to form pentagonal rim occupying the entire frontal view. In lateral view, margin of frons and occiput from acute ca. 60 degree angle (Fig. 1D–E). Vertex widely striated PageBreakwith several robust undulations; frontal horns very broad and shallow; genal horns reduced to tiny protrusions anterior to antennal sockets. Mandibles short humped and slightly bended forward, right mandible tip under tip of left mandible, tips are under labrum in frontal view. Labrum short, hyaline and tongue-shaped. Anteclypeus white; postclypeus trapezoidal with undulating rugosity. Eye spots large, narrowly elliptical. Antenna moniliform between 10 and 12 articles, formula variable 2> 3 = 4 = 5 <6. Legs with three apical spurs on each tibia, formula 3:3:3. Pronotum slightly incised in front, slightly narrower than head capsule. Measurements are reported in Table 4.

Table 4.

Measurements (in mm) of sp. n. soldier.

No.	Measurements in mm, n=2 from 1 colony	(Holotype)	(Paratype)	Mean
1	Head length to tip of mandibles	1.54	1.38	1.46
2	Head length to frontal horns	1.33	1.23	1.28
3	Frontal flange width	1.32	1.22	1.27
4	Frontal horns, outside span	1.32	1.22	1.27
5	Head width, maximum	1.32	1.22	1.27
6	Head height, excluding postmentum	1.01	0.88	0.94
7	Pronotum, maximum width	1.16	1.14	1.15
8	Pronotum, maximum length	0.82	0.77	0.79
9	Left mandible length, tip to ventral condyle	–	–	–
10	Total length	4.18	3.95	4.07

Genetic characterization.

Thirteen COII mtDNA sequences were aligned for species using as an outgroup. Information from NCBI is largely limited to COII (see Suppl. material 1), hence we could not include comparative analysis for nuclear and mitochondrial 12S and 16S rRNA genes. Note, COII is very informative to identify termite species (Hausberger et al. 2011).

The COII tree topology for revealed two major clusters, one group composed of eastern Australian species (53% bootstrap value) and the other comprising clusters of Northwest Australian-Papuan (98% bootstrap value), Ethiopian-Oriental (65% bootstrap value) and Neotropical species (100% bootstrap value) (Figure 2). is located on a separate basal branch within the Ethiopian–Oriental cluster. Based on additional sequence comparisons, its closest relative among the studied species is (p-distance = 0.148) (Table 3).

Figure 2.

Tree topology and branch lengths inferred with MRBAYES from COII sequence data (Bootstrap values above branches). Origin (O), unknown (?) and established introductions from other regions or land masses (I): , , , , , , .

Neartic=

Neotropic=

Ethiopian=

Paleartic=

Oriental=

Australian=

Papuan=

Table 3.

Estimates of Evolutionary Divergence between Sequences (p-distance between species).

	Species	1	2	3	4	5	6	7	8	9	10	11	12	13
1	Cryptotermes cavifrons
2	Cryptotermes longicollis	0.030
3	Cryptotermes cylindroceps	0.157	0.165
4	Cryptotermes primus	0.174	0.186	0.184
5	Cryptotermes tropicalis	0.158	0.172	0.167	0.096
6	Cryptotermes queenslandis	0.167	0.177	0.162	0.130	0.117
7	Cryptotermes simulatus	0.165	0.188	0.160	0.137	0.132	0.064
8	Cryptotermes secundus	0.174	0.183	0.179	0.179	0.163	0.153	0.165
9	Cryptotermes dudleyi	0.200	0.202	0.188	0.209	0.190	0.188	0.205	0.137
10	Cryptotermes havilandi	0.150	0.160	0.167	0.160	0.137	0.151	0.167	0.170	0.183
11	Cryptotermes domesticus	0.165	0.172	0.190	0.160	0.146	0.174	0.177	0.188	0.216	0.113
12	Cryptotermes declivis	0.169	0.176	0.183	0.167	0.150	0.181	0.177	0.176	0.203	0.108	0.059
13	Cryptotermes colombianus	0.183	0.186	0.167	0.172	0.160	0.169	0.162	0.186	0.202	0.148	0.150	0.160
14	Blatta orientalis	0.287	0.296	0.257	0.247	0.256	0.256	0.254	0.270	0.285	0.264	0.237	0.249	0.278

Phylogeny and phylogeography of the is debated (Chhotani 1970, Gay and Watson 1982, Bacchus 1987, Thompson et al. 2000, Scheffrahn and Křeček 2009). Bourguignon et al. (2014) proposed that evolved at the cusp of Gondwana dissolution with originating after the separation of land masses. The current distribution of species can be explained with transoPageBreakPageBreakceanic dispersal via drift wood (Scheffrahn et al. 2009, Bourguignon et al. 2016) and more recently through human introductions during colonization and trade (Li et al. 2009, Scheffrahn et al. 2009, Evans 2011). The geographic pattern on the phylogeny with regional specific clades may also indicative for some continent specific radiations. The origin of is unclear, it may have arrived in Colombia via infested drift wood. Data presented here are not conclusive. More genetic analyses, including different populations, are needed to reveal the origin of and track the evolutionary history and dispersal of species.

Material examined.

Type-locality: Colombia, Magdalena: Santa Marta, Tayrona National Park, Gayraca Bay, , tropical dry forest, 23 June 2015.

Holotype-colony: Colombia. Magdalena Santa Marta Tayrona National Park, Gayraca Bay, 23.VI.2015 (collected by R. Casalla) in a piece of dry wood on soil, at elevation of 12 m a.s.l (), sample COLPT1LII-56: 2 soldiers, 1 dealated, 23 pseudergates; 3 for DNA isolation. Holotype: Soldier from the previous sample (COLPT1LII-56), it will be deposited at the Arthropod Collection of the Natural History Museum of the Alexander von Humboldt Institute of Bogotá, Colombia (MIAvH). Paratypes from sample COLPT1LII-56: 1 soldier, 1 reproductive dealate. Paratypes will be deposited as follows: 1 soldier will be deposited at the American Museum of Natural History New York, United States, 1 dealated at MIAvH. Pseudergates will be part of the collection of the Department of Chemistry and Biology at the University del Norte, Barranquilla, Colombia. All measurements for dealated reproductive, holotype and paratype soldiers are reported in Tables 2, 4.

Diagnosis.

The diminutive frontal and genal horns and the truncated frons and converging genal margins of the head capsule (in dorsal view) distinguish the soldier from all other Neotropical congeners.

Etymology.

Named for its country of origin, Colombia.

Discussion

We extend the distribution of to Colombia and we herein report for the first time, along the Caribbean coast (Figure 3). We found in infested drywood trunks of Glírícidia sepium, , , and , which are often used for wooden artefacts, furniture and as structural material (Figure 4). Along the coast, was common in dead branches and trunks of the black mangrove, . In line transects that covered a total of 500m × 2m, accounted for 24 % of all termite encounters (N = 241) (Casalla and Korb, unpublished data). also occurred up to 100 km inland (Figure 3). Hence, can be considered an economically important pest to this part of the Caribbean. was only known from the Dominican Republic (Scheffrahn and Křeček 1999). In 2009, R. Scheffrahn found three samples from two localities near Santa Marta, Colombia (Figure 4).

Figure 3.

Distribution of the genus in Colombia. not shown, but widespread.

Figure 4.

Window frame damaged by (A), workers (white-reddish) (pseudergates sensu lato) and neotenic reproductives (brownish) (B), soldier of (C). Scale bar: 1 mm

Genetically, clustered with the other Neotropical endemics, and (100% bootstrap value) (Figure 2). Our data provided strong branch support at the regional level, but more resolution from different species are needed to attain a well-corroborated phylogeny of the .

With these new records, there are now five species recorded for Colombia: , , , and . Further PageBreakstudies on the diversity of termites will determine if there are more in northern and western Colombia, especially at the pacific coast which has important mangroves areas.