Cryptotermes colombianus
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Ordo: Isoptera
Familia: Kalotermitidae
Genus: Cryptotermes
Name
Cryptotermes colombianus Casalla & Scheffrahn & Korb, 2016 sp. n. – Wikispecies link – ZooBank link – Pensoft Profile
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.
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 | – |
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 with 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.
Genetic characterization
Thirteen COII mtDNA sequences were aligned for Cryptotermes species using Blatta orientalis 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[1]).
The COII tree topology for Cryptotermes 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). Cryptotermes colombianus 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 Cryptotermes havilandi (p-distance = 0.148) (Table 3).
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 |
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 |
Material examined
Type-locality: Colombia, Magdalena: Santa Marta, Tayrona National Park, Gayraca Bay, 11°18.84'N; 74°6.34'W, 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 (11°18.84'N; 74°6.34'W), 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 Cryptotermes colombianus soldier from all other Neotropical congeners.
Etymology
Named for its country of origin, Colombia.
Original Description
- Casalla, R; Scheffrahn, R; Korb, J; 2016: Cryptotermes colombianus a new drywood termite and distribution record of Cryptotermes in Colombia ZooKeys, (596): 39-52. doi
Images
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Other References
- ↑ Hausberger B, Kimpel D, Neer A, Korb J (2011) Uncovering cryptic species diversity of a termite community in a West African savanna. Molecular Phylogenetics and Evolution 61: 964–969. doi: 10.1016/j.ympev.2011.08.015
- ↑ Chhotani O (1970) Taxonomy, zoogeography and phylogeny of the genus Cryptotermes (Isoptera: Kalotermitidae) from the Oriental region. Memoirs of the Zoological Survey of India 15: 1–81.
- ↑ Gay F, Watson J (1982) the genus Cryptotermes in Australia (Isoptera: Kalotermitidae). Australian Journal of Zoology Supplementary Series 88: 1–64. doi: 10.1071/AJZS088
- ↑ Bacchus S (1987) A taxonomic and biometric study of the genus Cryptotermes (Isoptera: Kalotermitidae). Tropical Pest Bulletin No. 7. Tropical Development and Research Institute, London, U.K., 91 pp.
- ↑ Thompson G, Miller L, Lenz M, Crozier R (2000) Phylogenetic analysis and trait evolution in Australian lineages of drywood termites (Isoptera, Kalotermitidae). Molecular Phylogenetics and Evolution 17: 419–429. doi: 10.1006/mpev.2000.0852
- ↑ Bourguignon T, Lo N, Cameron S, Šobotník J, Hayashi Y, Shigenobu S, Watanabe D, Roisin Y, Miura T, Evans T (2014) The evolutionary history of termites as inferred from 66 mitochondrial genomes. Molecular Biology and Evolution 32: 406–421. doi: 10.1093/molbev/msu308
- ↑ 7.0 7.1 Scheffrahn R, Křeček J, Ripa R, Luppichini P (2009) Endemic origin and vast anthropogenic dispersal of the West Indian drywood termite. Biological invasions 11: 787–799. doi: 10.1007/s10530-008-9293-3
- ↑ Bourguignon T, Lo N, Šobotník J, Sillam-Dussès D, Roisin Y, Evans T (2016) Oceanic dispersal, vicariance and human introduction shaped the modern distribution of the termites Reticulitermes, Heterotermes and Coptotermes. Proceedings of the Royal Society B: Biological Sciences 283: 1829. doi: 10.1098/rspb.2016.0179
- ↑ Li H, Ye W, Su N, Kanzaki N (2009) Phylogeography of Coptotermes gestroi and Coptotermes formosanus (Isoptera: Rhinotermitidae) in Taiwan. Annals of the Entomological Society of America 102: 684–693. doi: 10.1603/008.102.0413
- ↑ Evans T (2011) Invasive termites. In: Bignell D Roisin Y Lo N (Eds) Biology of Termites: A Modern Synthesis. Springer SBM, Dordrecht, The Netherlands, 519–562.