Research Article |
Corresponding author: Jiraporn Ruangsittichai ( jiraporn.rua@mahidol.ac.th ) Academic editor: Brian Lee Fisher
© 2018 Weeyawat Jaitrong, Jiraporn Ruangsittichai.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Jaitrong W, Ruangsittichai J (2018) Two new species of the Aenictus wroughtonii species group (Hymenoptera, Formicidae, Dorylinae) from Thailand. ZooKeys 775: 103-115. https://doi.org/10.3897/zookeys.775.26893
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The Aenictus wroughtonii species group is widely distributed in Asia. The members of this group are characterised by a slender body, long legs, anterior clypeal margin with 5–10 denticles and a weakly-developed subpetiolar process. Twelve worker-based species of this group have been recorded from Asia. Herein, two new species from Thailand (Aenictus nuchiti sp. n. and Aenictus samungi sp. n.) are added to this group. A key to the Asian species of this group is provided.
Aenictus wroughtonii species group, Aenictus minutulus species group, army ant, distribution, new species, taxonomy, Thailand
The Aenictus wroughtonii species group was established by
During our survey of the Asian Aenictus, two unidentified species belonging to the A. wroughtonii group were found from Thailand. After carefully examining specimens of these two species under a stereomicroscope and comparing them with the type material of closely related species, it was concluded that both species are new to science. In the present study, the two new species are described and a key for the Asian species based on the worker caste is provided.
The holotypes and paratypes of Aenictus nuchiti sp. n. and Aenictus samungi sp. n. were pin-mounted dry specimens. The holotypes, paratypes and syntypes of seven species (A. artipus Wilson, 1964; A. biroi Forel, 1907; A. camposi Wheeler WM & Chapman, 1925; A. sagei Forel, 1901; A. stenocephalus Jaitrong & Yamane, 2010; A. vieti Jaitrong & Yamane, 2010; A. wroughtonii Forel, 1890) in the A. wroughtonii species group were examined. High-resolution images of the holotype of A. gutianshanensis Staab, 2014 available in
Multi-focused montage images were produced using NIS-Elements-D-[Sequence6*-Focused] from a series of source images taken by a Nikon Digital Sight-Ri1 camera attached to a Nikon AZ100M stereoscope. Type specimens of each species were measured for the following parts using a micrometer (accurate to 0.01 mm).
The abbreviations used for the measurements and indices are as follows:
HL Maximum head length in full-face view, measured from the anterior clypeal margin to the midpoint of a line drawn across the posterior margin of the head.
HW Maximum head width in full-face view.
ML Mesosomal length measured from the point at which the pronotum meets the cervical shield to the posterior margin of the metapleuron in profile.
PH Petiolar node height, measured in profile, the maximum vertical height of the petiole from summit to lower most part of subpetiolar process.
PL Petiole length measured from the anterior margin of the peduncle to the posteriormost point of the tergite in profile.
SL Scape length excluding the basal constriction and condylar bulb.
TL Total length, axial length of body, summed HL (including mandibles) + ML + PL + postpetiole length + gaster length.
CI Cephalic index, HW/HL × 100.
PI Petiolar index, PH/PL × 100.
SI Scape index, SL/HW × 100.
Abbreviations of the type depositories are as follows:
SKYC Seiki Yamane Collection, Japan
THNHM Natural History Museum of the National Science Museum, Thailand
The general terminology for the worker caste of the ants follows
(modified from
Greece, Iran, Israel, Turkey, Saudi Arabia, India, Sri Lanka, Southeast China, Taiwan, Vietnam, Thailand, Malay Peninsula (West Malaysia), Sumatra, Borneo (Sabah, Sarawak, and Brunei) and Philippines (Negros and Luzon) (
Aenictus arabicus Sharaf & Aldawood, 2012, A. artipus Wilson, 1964; A. biroi Forel, 1907; A. camposi Wheeler WM & Chapman, 1925; A. gutianshanensis Staab, 2014, A. nuchiti sp. n., A. rhodiensis Menozzi, 1936, A. sagei Forel, 1901; A. samungi sp. n., A. stenocephalus Jaitrong & Yamane, 2010; A. vieti Jaitrong & Yamane, 2010; A. wroughtonii Forel, 1890.
Holotype (THNHM-I-02612, THNHM), 55 paratype workers (THNHM-I-02614,
28 workers, Thailand, Chiang Mai Province, San Sai District, San Sai Luang Sub-district, near Maejo University Campus, mixed deciduous forest, collected from leaf litter, 18.92777778°N, 99.05083333°E, ca 350 m a.s.l., 15.X.2015, N. Likhitrakarn leg., Colony no. NL151015-1 (THNHM).
Holotype: HL 0.53; HW 0.40; ML 0.69; PH 0.17; PL 0.18; SL 0.41; TL 2.28; CI 75; PI 91; SI 104. Paratype workers (n = 10): HL 0.50–0.53; HW 0.38–0.43; ML 0.66–0.73; PH 0.13-0.17; PL 0.17–0.18; SL 0.40–0.43; TL 2.24–2.41; CI 77–83; PI 90-91; SI 94–104.
(paratype). HL 0.92; HW 01.06; ML 1.55; PH 0.53; PL 0.53; SL 0.64; TL 5.31; CI 114; PI 100; SI 61.
(Holotype and paratypes; Fig.
Head, antennal scapes, pronotum, petiole, postpetiole, gaster, femora and tibiae of legs entirely or extensively smooth and shiny. Antennal flagellum densely punctate; mesothorax and propodeum with dense punctures; metapleuron partly or extensively smooth.
Body with relatively sparse standing hairs mixed with sparse short hairs over surface; longest pronotal hair 0.10–0.13 mm long. Head, mesonotum, propodeum and gaster dark brown; pronotum, waist, antennae and legs reddish brown.
(Paratype, Fig.
Entire body smooth and shiny, with relatively dense standing hairs; hairs slightly shorter on pronotum than on head, mandible and antennal scape; longest pronotal hair 0.08 mm long. Head dark brown; lateral and ventral faces of head and mandible reddish brown; scapes and legs yellowish brown. Mesosoma with ground colour reddish brown; lateral faces of pronotum and mesonotum, entire mesopleura and propodeal declivity dark brown. Petiole with ground colour reddish brown; lower portion of petiole, posterior slope of petiole and subpetiolar process dark brown; gaster with ground colour dark brown; lateral faces of second tergite reddish brown.
The species is named after Mr Supachai Nuchit (Royal Forest Department, Thailand) who kindly helped us with ant collecting at Pa Omkoi National Forest, Chiang Mai Province.
Northern Thailand (Chiang Mai Province).
Aenictus nuchiti sp. n. is most similar to A. biroi, A. camposi, A. gutianshanensis and A. vieti in having dense punctures on the mesosoma and an angulate propodeal junction. However, A. nuchiti is much smaller than the latter four (TL 2.24–2.41 mm, HW 0.38–0.43 mm in A. nuchiti; TL > 2.6 mm, HW > 0.43 mm in the latter four). It has a short antennal scape that reaches only two-thirds the head length (in contrast, reaching or extending beyond the posterolateral corners of the head in the latter four). This species can be distinguished from A. gutianshanensis and A. vieti by the configuration of the subpetiolar process (ventral outline roundly convex and without anterior angle in A. nuchiti; ventral outline with anterior angle in A. biroi, A. gutianshanensis and A. vieti). Aenictus nuchiti is similar to A. biroi and A. camposi in the unarmed subpetiolar process. In A. nuchiti, however, the body size is much smaller than that of A. biroi and the head is clearly longer than broad in A. nuchiti (almost as long as broad in A. biroi). The body colour is dark brown in A. nuchiti, whereas it is entirely yellow in A. camposi. The propodeal declivity is broader and widely rounded above in A. nuchiti but is narrow and tapers distinctly above in A. camposi.
Holotype (THNHM-I-02615, THNHM) and 15 paratype workers (THNHM-I-02616,
One worker, Thailand, Tak Province, Near Myanmar border, Tung Yai [Thung Yai] W.S., 23.V.1999, W. Jaitrong leg. (THNHM).
Holotype: HL 0.41; HW 0.31; ML 0.53; PH 0.17; PL 0.12; SL 0.20; TL 1.75; CI 76; PI 143; SI 63. Paratypes (n = 11): HL 0.40–0.43; HW 0.31–0.33; ML 0.51–0.53; PH 0.17–0.18; PL 0.12–0.13; SL 0.20–0.23; TL1.72–1.78; CI 76–80; PI 138–143; SI 63–70.
(holotype and paratypes; Fig.
Head, antennal scape, promesonotum, propodeal dorsum, petiole, postpetiole, gaster, femora and tibiae of legs entirely or extensively smooth and shiny; mesopleuron, metapleuron and lateral face of propodeum superficially reticulate. Antennal flagellum densely finely punctate.
Body with relatively sparse standing hairs mixed with sparse short hairs over surface; longest pronotal hair 0.07–0.08 mm long. Head, mesosoma, waist, gaster, antennae and legs yellowish brown; mandible dark brown.
The species is named after Mr Yuthana Samung (Faculty of Tropical Medicine, Mahidol University, Thailand) who kindly helped us in taking pictures of Thai ants, including the two new species discovered in the present study.
Western Thailand (Tak Province).
Aenictus samungi sp. n. can be easily distinguished from the other members of the A. wroughtonii species group by the following characteristics: smallest species of the group (HW 0.31–0.33 mm in A. samungi; HW > 3.7 mm in other members); petiole shorter than high (as long as or longer than high in other members); promesonotum with almost flat or straight dorsal outline (convex and sloping gradually to metanotal groove in other members); antennal scape short only just reaching mid-length of the head (at least two-thirds of the head length or beyond the posterolateral corner of the head in other members). Both Aenictus nuchiti sp. n. and A. samungi sp. n. have small bodies and short antennae, but can be easily separated from each other by the different conditions of the propodeum (Figs
1 | Antennal scapes short, when laid back only attaining mid-length or two-thirds of the head length | 2 |
– | Antennal scape long, when laid back attaining or extending beyond the posterolateral corner of the head | 4 |
2 | HW 0.31–0.33 mm; antennal scape attaining only mid-length of the head; petiole excluding subpetiolar process shorter than high (Thailand) | A. samungi sp. n. |
– | HW > 0.37 mm; antennal scape attaining two-thirds of the head length; petiole excluding subpetiolar process longer than high | 3 |
3 | Propodeal junction rounded; lateral faces of the petiole and postpetiole superficially reticulate; subpetiolar process present, its anteroventral corner angulate; postpetiole slightly longer than the petiole (Saudi Arabia) | A. arabicus |
– | Propodeal junction angulate; lateral faces of the petiole and postpetiole entirely smooth and shiny; subpetiolar process convex dorsally, anteroventrally not angulate; postpetiole slightly shorter than the petiole (Thailand) | A. nuchiti sp. n. |
4 | Propodeal junction rounded | 5 |
– | Propodeal junction angulate | 9 |
5 | Subpetiolar process almost absent, anteroventrally not angulate (India) | A. wroughtonii |
– | Subpetiolar process weakly developed; its anteroventral corner angulate | 6 |
6 | Entire pronotum and petiole sculptured (punctate or reticulate) (China) | A. gutianshanensis |
– | Pronotum and petiole largely smooth and shiny | 7 |
7 |
HW 1.00–1.04 mm ( |
A. rhodiensis |
– | HW < 0.60 mm; posterior margin of head almost straight or convex | 8 |
8 | Scape short; SI 100 or less; body hairy; the longest pronotal hair 0.23–0.25 mm; subpetiolar process very low, with ventral outline almost straight (India, Nepal, Afghanistan) | A. sagei |
– | Scape long; SI 130–140; body with sparse hairs; the longest pronotal hair approximately 0.15–0.18 mm; subpetiolar process with ventral outline slightly convex (China, Vietnam, Thailand) | A. artipus |
9 | Ventral outline of subpetiolar process convex, anteroventrally not angulate | 10 |
– | Ventral outline of subpetiolar process convex or almost straight; its anteroventral corner angulate | 11 |
10 | Declivity of propodeum narrower, seen from back strongly tapering above; petiole longer than high (PI 84–86); body smaller with TL 2.6–2.7 mm; antenna longer with SI 122–135 (Thailand, Indonesia, Malaysia, Philippines) | A. camposi |
– | Declivity of propodeum broader and more rounded above; petiole almost as long as high (PI 95–100); body larger with TL 3.1–3.2 mm; antenna shorter with SI 114–118 (Sri Lanka) | A. biroi |
11 | Ventral outline of subpetiolar process strongly convex in anterior half; mesonotum partly and propodeum almost entirely densely sculptured; pronotum clearly demarcated from mesonotum by a shallow transverse groove (Taiwan, Vietnam and Thailand) | A. vieti |
– | Ventral outline of subpetiolar process almost straight; entire mesonotum and propodeum smooth and shiny, with at most superficial sculpture; pronotum only weakly demarcated from mesonotum (Thailand) | A. stenocephalus |
These two new species are also similar to members of the Aenictus minutulus species group (A. changmaianus Terayama & Kubota, 1993, A. minutulus Terayama & Yamane, 1989, A. minimus Jaitrong & Hashimoto, 2012) in general appearance and by having a short petiole, short antennal scapes (reaching only to mid-length of the head) and subtriangular mandibles (masticatory margin with a large apical tooth, medium-sized subapical and basal teeth and 2–6 denticles between them) (Jaitrong and Hashimoto 2012). However, herein, both species were treated as members of the A. wroughtonii group because they have a serrate anterior clypeal margin, the most important characteristic that separates the A. wroughtonii group from the A. minutulus group (anterior clypeal margin without denticles in the A. minutulus group) (see the key for the species groups of Aenictus in
Aenictus nuchiti sp. n. is a rare species. The type series was collected from a bivouac under a large rotting log in a dry dipterocarp forest (Fig.
Aenictus samungi sp. n. is also a rare species and is known only from the type locality (ca 1100 m a.s.l.). The type series was collected from a foraging column on a forest path in a dry evergreen forest (Fig.
We thank Mr Supachai Nuchit (Royal Forest Department, Thailand) who kindly helped us with ant collecting at Pa Omkoi National Forest. We also thank Mr Yuthana Samung (Mahidol University, Thailand) and Mr Kochakorn Moonsatan (National Science Museum, Thailand) who kindly helped us with taking pictures of Thai ant specimens, including the two new species discovered in this study. We also thank Dr Natdanai Likhitrakarn (Maejo University, Thailand) who donated some specimens of Aenictus nuchiti. The present study was supported by the National Science and Technology Development Agency (Funding contract number FDA-CO2561-5851-TH).