Wheeler, W.M., 1929
Seifert (2003) - C. obscurior was reported to nest in cavities of bushes and trees 2 - 5 m above the ground level; it was found in dead twigs of trees such as Erythrina variegata (Okinawa), in dwarf coconuts (Brazil), galls of Acacia trees (Brazil), in a dead twig on a tree (Florida), on a Ficus tree (Israel), in the gall of a Tamarix bush (Israel), and in the cavity of a coconut high in the tree (Zanzibar).
|At a Glance||• Polygynous • Diploid male|
- 1 Identification
- 2 Distribution
- 3 Biology
- 4 Castes
- 5 Nomenclature
- 6 References
- 7 References based on Global Ant Biodiversity Informatics
Seifert (2003) - A member of the Cardiocondyla wroughtonii group. The workers of C. obscurior differ from Cardiocondyla wroughtonii by darker gaster pigmentation, shorter head, smaller postocular distance, narrower frons, wider and higher waist segments, wider spine base distance, and shorter spine length.
Keys including this Species
Distribution based on Regional Taxon Lists
Afrotropical Region: Comoros.
Indo-Australian Region: American Samoa, Fiji, Guam, Micronesia (Federated States of), New Guinea, Northern Mariana Islands.
Nearctic Region: United States.
Neotropical Region: Barbados, Bermuda, Brazil, Costa Rica, Grenada, Guadeloupe, Mexico, Netherlands Antilles.
Oriental Region: Taiwan (type locality).
Palaearctic Region: Canary Islands, Israel.
Distribution based on AntMaps
Distribution based on AntWeb specimens
Check data from AntWeb
Seifert (2003) - C. obscurior produce alate and ergatoid males (Yamauchi in lit. 3 July 2000, my own material). Average differences in chromosome numbers seem to exist but the numbers are not constant. C. wroughtonii from the Okinawa Islands had 2n = 56 chromosomes while sympatric C. obscurior had 2 n = 52 chromosomes (Yamauchi in lit., 3 July 2000). A C. obscurior sample from Gainesville/Florida had 2n = 48 (Francoeur in lit., 19 October 2000). Colonies may have more than one queen. New nests can be formed by fission.
Fuessl et al. (2018) - Cardiocondyla obscurior is characterized by a male diphenism, with winged disperser males and wingless (‘ergatoid’) fighter males (Kugler, 1983; Heinze, 2017). The latter are present in colonies year-round and compete fiercely for monopolization of mating chances with virgin queens (Kinomura &Yamauchi, 1987; Stuart et al., 1987). Under environmentally adverse conditions, colonies also produce the more peaceful, winged disperser males, the male phenotype typical for most ant species (Cremer et al., 2003). Interestingly, mating with a winged male prolongs female life span more than mating with an ergatoid male (Schrempf & Heinze, 2008). Furthermore, sperm traits show considerable variation between winged and wingless males (Schrempf et al., 2016; Metzler et al., 2018) and the two phenotypes might potentially experience different levels of sperm competition because they differ in abundance in natural nests (for preliminary data on single-mating by C. obscurior queens, see Schmidt et al., 2016).
In the present study, we investigate the proteins produced by the accessory glands of the two male phenotypes. The seminal fluid of insect males is known to contain a complex mixture of proteins with multiple functions in sperm protection, antimicrobial defence and the induction of multiple changes in female physiology (Avila et al., 2011). Our proteomic and transcriptomic study reveals that the seminal fluid and themale accessory glands of the male-diphenic ant C. obscurior contain several hundred proteins, of which many appear to differ in quantity between winged and ergatoid males. More than 20 proteins showing considerable overlap with other studies on insect seminal fluids. One example includes proteolysis regulators, such as serine proteases, carboxypeptidases and serine protease inhibitors (serpins), which all are common accessory gland proteins of insects (Ravi Ram & Wolfner, 2009; Mueller et al., 2005; Baer et al., 2009a; Xu et al., 2013; LaFlamme & Wolfner, 2013; Yu et al., 2016; Bayram et al., 2017). Although their function in C. obscurior remains to be determined,male-derived serine proteases are suggested to stimulate egg laying and other post-mating changes in the female of various insects (LaFlamme & Wolfner, 2013).
Life History Traits
- Queen number: polygynous (Cournault & Aron, 2009)
Diploid males are known to occur in this species (found in 1.5% of 67 examined nests) (Schrempf et al., 2006; Cournault & Aron, 2009).
The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.
- obscurior. Cardiocondyla wroughtoni var. obscurior Wheeler, W.M. 1929g: 44 (w.q.) TAIWAN.
- Junior synonym of wroughtonii: Lin & Wu, 2003: 63.
- Subspecies of wroughtoni: Wheeler, W.M. 1930a: 98; Chapman & Capco, 1951: 84; Bolton, 1995b: 133.
- Status as species: Seifert, 2003a: 271 (redescription); Wetterer & Vargo, 2003: 417; Wetterer & Wetterer, 2004: 215; Clouse, 2007b: 230; Terayama, 2009: 179; Vonshak, et al. 2009: 41; Ellison, et al. 2012: 235; Sarnat & Economo, 2012: 74; Hita Garcia, et al. 2013: 208; Borowiec, L. 2014: 48; Ramage, 2014: 171; Bharti, Guénard, et al. 2016: 34; Wetterer, et al. 2016: 10; Deyrup, 2017: 56.
- Senior synonym of bicolor: Seifert, 2003a: 271.
- bicolor. Cardiocondyla bicolor Donisthorpe, 1930b: 366 (w.) ISRAEL.
- Status as species: Menozzi, 1933b: 93.
- Junior synonym of wroughtonii: Kugler, J. 1984: 6; Bolton, 1995b: 132; Zhou, 2001b: 86.
- Junior synonym of obscurior: Seifert, 2003a: 271.
Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Characterized by its dark color, the body and appendages being dull brown, the legs scarcely paler, the antennal clubs distinctly infuscated, the Whole gaster dark brown, except the posterior borders of the segments, which are paler.
Seifert (2003) - Small size CL 428. Head very short, CL/CW 1.108. Scape short, SL/CS 0.780. Postocular index rather large, PoOc/CL 0.435. Eyes medium-sized, EYE 0.232. Frons wide, FRS/CS 0.270, frontal carinae immediately behind FRS level parallel or slightly diverging. Anterior clypeal margin between level of frontal carinae frequently slightly notched; median occipital margin usually slightly concave; overall head shape posterior of eyes less rounded than in Cardiocondyla wroughtonii. Whole head and mesosoma without any notable rugosity. Paramedian and lateral areas of vertex with deep (sometimes shallower) foveolae of 17 - 21 mm diameter, frequently in dense honey-comb like arrangement, usually showing an inner corona of 9 mm diameter; median vertex weakly foveolate-carinulate. Whole surface of mesosoma and waist densely foveolate-reticulate, the meshes with lower diameters than ort vertex. Metanotal groove in lateral view usually with rather steep anterior and posterior slopes, occasionally shallower than in C. wroughtonii. Propodeal spines long, shorter than in C. wroughtonii, SP/CS 0.178; outer spine base distance wider than in C. wroughtonii, SPBA/CS 0.293. Petiolar peduncle in lateral aspect deviating 30° from longitudinal axis of petiole node that is often more square-shaped than in C. wroughtonii. Postpetiole as a rule more massive than in C. wroughtonii, as in this species with characteristic anteroventrolateral corners; in dorsal view, convex sides meeting concave anterior margin in distinct angle. Head, mesosoma, and waist brightly yellowish or yellowish brown, antennal club usually notably infuscated. In contrast to dark morph of C. wroughtonii, all gaster segments dark blackish brown, PigG1 98 ± 4 %.
The single specimen of this sex is dealated and headless and is perhaps immature, the body is paler and more yellowish than in the worker, except the tegulae, which are black and the gaster, which is dark brown throughout, with paler posterior borders to the segments.
Seifert (2003) - Very small size, CS 460. Head very short, CL/CW 1.122. Postocular index shorter than in Cardiocondyla wroughtonii, PoOclCL 0.423. Scape rather short, SL/CS 0.755. Median occipital margin and anterior clypeal margin between level of frontal carinae straight or slightly concave. Frontal carinae immediately caudal of FRS level diverging or subparallel. With exception of 4 - 5 longitudinal rugae on metapleuron, whole head and mesosoma without any rugosity. Paramedian area of vertex with deep, densely arranged foveolae of 18 - 22 mm diameter, showing inner coronae of 9 mm diameter. Whole surface of mesosoma and waist densely foveolate, foveolae on dorsal mesosoma similar to those on vertex, those on lateral area of mesosoma and in particular on waist with significantly lower diameters. Propodeal spines long, but shorter than in C. wroughtonii, SP/CS 0.187, ratio SPBA/SP 1.942 ± 0.138 (n = 8). Postpetiole with sharp anteroventrolateral corners; in dorsal view, its convex sides meet the concave anterior margin in a distinct corner. Head, mesosoma, and waist yellowish, small patches at wing insertions notably darker; antennal club frequently infuscate; all gaster segments on whole surface brown to dark blackish brown.
One worker and one female from Eisei, Formosa.
Seifert (2003) - Three investigated gynes from the Museum of Comparative Zoology collection, labelled by Wheeler “Kagi, Formosa 11.1.1927 R.Takahashi Wm. M. Wheeler\ Cotypes\ var. obscurior Wheeler” fully match the conception of C. obscurior presented here but cannot be considered as genuine type material. These gynes were the basis of a second description, published on 7 March 1 930 (Wheeler 1930). Wheeler's first description, published on 22 October 1929, was based upon one worker and a headless dealate queen collected at Eisei / Formosa (Wheeler 1929). These specimens were not available from MCZ Cambridge and are believed to be lost.
- Bressan, J.M.A., Benz, M., Oettler, J., Heinze, J.Ã., Hartenstein, V., Sprecher, S.G. 2015. A map of brain neuropils and fiber systems in the ant Cardiocondyla obscurior. Frontiers in Neuroanatomy 8, art. 166 (doi:10.3389/fnana.2014.00166).
- Cournault, L., Aron, S. 2009. Diploid males, diploid sperm production, and triploid females in the ant Tapinoma erraticum. Naturwissenschaften 96: 1393–1400 (doi:10.1007/s00114-009-0590-1).
- Cremer, S.; Heinze, J. 2003. Stress grows wings: environmental induction of winged dispersal males in Cardiocondyla ants. Curr. Biol. 13: 219-223 (page 219, see also)
- Du, Y., Schrempf, A. & Heinze, J. 2007. Environmental determination of the male morph in the ant Cardiocondyla obscurior (Hymenoptera: Formicidae). Eur. J. Entomol. 104: 243–246.
- Fuessl, M., C. G. Santos, K. Hartfelder, A. Schrempf, and J. Heinze. 2018. Accessory gland proteins of males in the male-diphenic ant Cardiocondyla obscurior. Physiological Entomology. 43:276-284. doi:10.1111/phen.12257
- Giehr, J., Grasse, A.V., Cremer, S., Heinze, J., Schrempf, A. 2017. Ant queens increase their reproductive efforts after pathogen infection. Royal Society Open Science 4, 170547 (doi:10.1098/RSOS.170547).
- Gratiashvili, N., Kuschel, L., Heinze, J. 2020. Morphometry and colony structure of ants of the genus Cardiocondyla (Hymenoptera: Formicidae) from Georgia. Zoology in the Middle East 66, 347–356 (doi:10.1080/09397140.2020.1835216).
- Habenstein, J., Amini, E., Grübel, K., el Jundi, B., Rössler, W. 2020. The brain of ants: Neuronal organization and visual projections. Journal of Comparative Neurology 2020: 1–28 (doi:10.1002/CNE.24934).
- Heinze, J. 2019. Emeryia, Xenometra, zoserka: it's a boy, again! The misleading morphology of Cardiocondyla male ants. Insectes Sociaux 67, 139–146 (doi:10.1007/s00040-019-00737-5).
- Heinze, J., Trindl, A., Seifert, B., Khin Ma Ma, Maung, W. 2020. First records of Cardiocondyla ants from Myanmar. Asian Myrmecology 12, e012005 (doi:10.20362/am.012005).
- Klein, A., Schultner, E., Lowak, H., Schrader, L., Heinze, J., Holman, L., Oettler, J. 2016. Evolution of social insect polyphenism facilitated by the sex differentiation cascade. PLoS Genetics 12(3): e1005952 ( DOI 10.1371/journal.pgen.1005952).
- Liu, C., Fischer, G., Hita Garcia, F., Yamane, S., Liu, Q., Peng, Y.Q., Economo, E.P., Guénard, B., Pierce, N.E. 2020. Ants of the Hengduan Mountains: a new altitudinal survey and updated checklist for Yunnan Province highlight an understudied insect biodiversity hotspot. ZooKeys 978, 1–171 (doi:10.3897/zookeys.978.55767).
- Meurgey, F. 2020. Challenging the Wallacean shortfall: A total assessment of insect diversity on Guadeloupe (French West Indies), a checklist and bibliography. Insecta Mundi 786: 1–183.
- Miyakawa, M.O., Miyakawa, H. 2018. Induction and evaluation of inbreeding crosses using the ant, Vollenhovia Emeryi. Journal of Visualized Experiments (140), e58521 (doi:10.3791/58521).
- Park, J., Xi, H., Park, J. 2021. Complete mitochondrial genome of the acrobat ant Crematogaster teranishii Santschi, 1930 (Formicidae; Hymenoptera). Mitochondrial DNA Part B 6, 593–595 (doi:10.1080/23802359.2021.1875922).
- Ramalho, M.de O., Kim, Z., Wang, S., Moreau, C.S. 2021. Wolbachia Across Social Insects: Patterns and Implications. Annals of the Entomological Society of America 114, 206–218 (doi:10.1093/aesa/saaa053).
- Schrader, L., Kim, J.W. et al. 2014. Transposable element islands facilitate adaptation to novel environments in an invasive species. Nature Communications 5:5495 (doi:10.1038/ncomms6495).
- Schrempf, A., Aron, S., Heinze, J. 2006. Sex determination and inbreeding depression in an ant with regular sib-mating. Heredity 97:75–80
- Seifert, B. 2003a. The ant genus Cardiocondyla (Insecta: Hymenoptera: Formicidae) - a taxonomic revision of the C. elegans, C. bulgarica, C. batesii, C. nuda, C. shuckardi, C. stambuloffii, C. wroughtonii, C. emeryi, and C. minutior species groups. Ann. (page 271, Raised to species and senior synonym of bicolor)
- Trigos-Peral, G., Abril, S., Angulo, E. 2020. Behavioral responses to numerical differences when two invasive ants meet: the case of Lasius neglectus and Linepithema humile. Biological Invasions (doi:10.1007/s10530-020-02412-4).
- Wheeler, W. M. 1929h. Ants collected by Professor F. Silvestri in Formosa, the Malay Peninsula and the Philippines. Boll. Lab. Zool. Gen. Agrar. R. Sc. Super. Agric. 24: 27-64 (page 44, worker, queen described)
References based on Global Ant Biodiversity Informatics
- Branstetter M. G. and L. Sáenz. 2012. Las hormigas (Hymenoptera: Formicidae) de Guatemala. Pp. 221-268 in: Cano E. B. and J. C. Schuster. (eds.) 2012. Biodiversidad de Guatemala. Volumen 2. Guatemala: Universidad del Valle de Guatemala, iv + 328 pp
- Chapman, J. W., and Capco, S. R. 1951. Check list of the ants (Hymenoptera: Formicidae) of Asia. Monogr. Inst. Sci. Technol. Manila 1: 1-327
- Guénard B., and R. R. Dunn. 2012. A checklist of the ants of China. Zootaxa 3558: 1-77.
- HUANG Jian-hua, ZHOU Shan-yi. 2006. A Checklist of Family Formicidae of China - Myrmicinae (Part I) (Insecta: Hymenoptera). Journal of Guangxi Normal University. Natural science edition 24: 87-94.
- Li Z.h. 2006. List of Chinese Insects. Volume 4. Sun Yat-sen University Press
- Seifert B. 2003. The ant genus Cardiocondyla (Insecta: Hymenoptera: Formicidae) - a taxonomic revision of the C. elegans, C. bulgarica, C. batesii, C. nuda, C. shuckardi, C. stambuloffii, C. wroughtonii, C. emeryi, and C. minutior species groups. Annalen des Naturhistorischen Museums in Wien. B, Botanik, Zoologie 104: 203-338.
- Terayama M. 2009. A synopsis of the family Formicidae of Taiwan (Insecta: Hymenoptera). Research Bulletin of Kanto Gakuen University. Liberal Arts 17:81-266.
- Terayama Mamoru. 2009. A synopsis of the family Formicidae of Taiwan (Insecta, Hymenoptera). The Research Bulletin of Kanto Gakuen University 17: 81-266.
- Terayama, M. 2009. A synopsis of the family Formicidae of Taiwan (Insecta; Hymenoptera). The Research Bulletin of Kanto Gakuen University 17: 81-266.
- Wheeler W. M. 1929. Ants collected by Professor F. Silvestri in Formosa, the Malay Peninsula and the Philippines. Bollettino del Laboratorio di Zoologia Generale e Agraria della Reale Scuola Superiore d'Agricoltura. Portici 24: 27-64.
- Wheeler W. M. 1930. Formosan ants collected by Dr. R. Takahashi. Proceedings of the New England Zoological Club 11: 93-106.