42 results on '"Rabeling, C."'
Search Results
2. The Global Ant Genomics Alliance (GAGA)
- Author
-
Boomsma, JJ, Brady, SG, Dunn, RR, Gadau, J, Heinze, J, Keller, L, Moreau, CS, Sanders, NJ, Schrader, L, Schultz, TR, Sundström, L, Ward, PS, Wcislo, WT, Zhang, G, Abouheif, E, Adams, RMM, Aron, S, Bacci, M, Bengston, SE, Bernadou, A, Blaimer, BB, Boulay, R, Bornberg-Bauer, E, Branstetter, MG, Economo, EP, Feinerman, O, Feldhaar, H, Feldmeyer, B, Fisher, B, Foitzik, S, Frank, ET, Grasso, DA, Helanterä, H, Holman, L, Hughes, W, Jongepier, E, Kronauer, D, Kulmuni, J, Linksvayer, TA, Longino, JT, McKenzie, SK, Orivel, J, Rabeling, C, Ran, H, Rubin, BER, Seal, JN, Seifert, B, Shik, JZ, Tinaut, A, Tsutsui, ND, Tysklind, N, Vargo, E, Viljakainen, L, Wurm, Y, Xu, Y, and Yek, SH
- Subjects
Phylogenomics ,caste polymorphism ,division of labor ,ecology ,symbiosis ,life history ,evolution ,reproductive conflict ,Zoology - Published
- 2017
3. Acromyrmex fowleri: a new inquiline social parasite species of leaf-cutting ants from South America, with a discussion of social parasite biogeography in the Neotropical region
- Author
-
Rabeling, C., Messer, S., Lacau, S., do Nascimento, I. C., Bacci, Jr., M., and Delabie, J. H. C.
- Published
- 2019
- Full Text
- View/download PDF
4. The dacetine ant Strumigenys arizonica, an apparent obligate commensal of the fungus-growing ant Trachymyrmex arizonensis in southwestern North America
- Author
-
Gray, K. W., Cover, S. P., Johnson, R. A., and Rabeling, C.
- Published
- 2018
- Full Text
- View/download PDF
5. Biology of the relict fungus-farming ant Apterostigma megacephala Lattke, including descriptions of the male, gyne, and larva
- Author
-
Sosa-Calvo, J., Ješovnik, A., Lopes, C. T., Rodrigues, A., Rabeling, C., Bacci, Jr., M., Vasconcelos, H. L., and Schultz, T. R.
- Published
- 2017
- Full Text
- View/download PDF
6. Acromyrmex charruanus: a new inquiline social parasite species of leaf-cutting ants
- Author
-
Rabeling, C., Schultz, T. R., Bacci, Jr., M., and Bollazzi, M.
- Published
- 2015
- Full Text
- View/download PDF
7. Behavioral ecology and natural history of Blepharidatta brasiliensis (Formicidae, Blepharidattini)
- Author
-
Rabeling, C., Verhaagh, M., and Mueller, U. G.
- Published
- 2006
- Full Text
- View/download PDF
8. Acromyrmex fowleri Rabeling & Messer & Lacau & do Nascimento & Jr. & Delabie 2019, NEW SPECIES
- Author
-
Rabeling, C., Messer, S., Lacau, S., do Nascimento, I. C., Jr., M. Bacci, and Delabie, J. H. C.
- Subjects
Insecta ,Acromyrmex ,Arthropoda ,Animalia ,Biodiversity ,Hymenoptera ,Formicidae ,Taxonomy ,Acromyrmex fowleri - Abstract
Acromyrmex fowleri Rabeling, Messer, Lacau and Delabie, NEW SPECIES Zoobank record: http://zoobank.org/ D96C94C2-AF2D- 4543-965E���49AB99DFE6 52. Holotype, alate gyne BRAZIL, Bahia, Ilh��us, Praia do Norte, 18 km N Ilh��us; S14.6197��, W039.0607��; elevation above sea level: 0 m; collection date: 27 November 1994, 07.00 h; col. Jacques Delabie; individual was collected from the drift line of the Atlantic Ocean on the beach. Presumably alates of A. fowleri participated in a predawn nuptial flight and drowned in the sea. The holotype is deposited at the Laborat��rio de Mirmecologia, Centro de Pesquisa do Cacau, Itabuna, Bahia, Brazil (CPCD) and carries the unique specimen identifier No. ASUSIBR00000001. Description, holotype gyne Measurements: TL 7.90, WL 2.47, HL 1.30, HW 1.45, IOD 1.59, ML 0.97, FLD 0.75, SL 1.59, EL 0.37, EW 0.33, PrW 1.38, FL 1.73, PL 0.52, PW 0.57, PPL 0.50, PPW 0.92, GL 2.15, CI 110, MI 73, SI 109. A small species of Acromyrmex fungus-growing ants (WL 2.47, TL 7.90) that is immediately recognizable as a social parasite due to its smaller body size and shiny integument. Mandibles (MI 73) and appendages (FL 1.73, SI 109) long relative to head and body size, respectively. Integument smooth and shiny, in part translucent, characteristic of the inquiline syndrome. Body surface, antennal scapes, and legs (except for tarsi) sparsely covered with pale, transversally flattened, appressed setae; only tarsi covered with semi-erect setae. Color uniformly light orange brown; anepisternum, scutellum, and masticatory margin of mandibles slightly darker, reddish-brown. Head head shape subquadrate, slightly wider than long (CI 110); lateral margins parallel to each other; posterior margin with median concavity; posterior and lateral margins with numerous distinct tubercles. Mandibles long and slender in full-face view; external margins sinuate; masticatory margins with 12 teeth; apical and preapical teeth distinctly larger, followed by five small teeth that are interspersed by smaller denticles; mandible surface smooth and shiny, not striate. Palp formula 4:2, representing the plesiomorphic condition of fungus-growing ants. Posterior margin of clypeus trapezoidal, broadly inserted between frontal lobes; anterior margin of clypeus shiny and median portion concave. Unpaired median clypeal seta short (0.09 mm), semi-erect, transversally flattened, only barely projecting over the anterior clypeal margin. Frontal lobes broadly rounded, fully covering condylar bulbs in full-face view; lateral margin of frontal lobe serrated with two distinct tooth-like projections. Frontal carinae extending towards the level of the ocelli, not forming a fully shaped antennal scrobe. Preocular carina forming a straight line in lateral view and traversing the area of the antennal scrobe by onethird of the scrobe���s width behind the level of the eye. Eyes large (EL 0.37, EW 0.33) and strongly convex. The three ocelli are small and embedded in the integument. Antennae with 11 segments. Antennal scapes long (SL 1.59, SI 109) with abundant, appressed setae, surpassing the posterior margin of the head by more than one-third of its length. Mesosoma Mesosoma slender with caste-specific modifications related to wing bearing. Dorsolateral pronotal spine long, slender, and sharply pointed in dorsal view. Ventrolateral pronotal spine reduced, triangular, with blunt, rounded tip. Dorsum of mesosoma smooth and shiny. Posterior margin of scutellum concave, but not distinctly bidentate. Bulla and meatus of metapleural gland not notably modified from the condition in the host species. Propodeal spines straight, slen- der, sharply pointed, projecting away from the propodeum at a 90�� angle in lateral view. Metasoma Anterior peduncle of petiole short, about one-fourth the length of the petiolar node. Dorsum of petiolar node with a pair of irregularly shaped ridges. Postpetiole wider (PPW 0.92) than long (PPL 0.50) in dorsal view, posterior margin slightly concave. Gaster large (GL 2.15). First gastric tergite notably smooth with few broadly rounded, reduced tubercles; on median portion of anterior half tubercles form a pair of shallow, longitudinal ridges. Except for the smaller size, fore- and hindwings resemble the wings of the host species, A. rugosus. Measurements, paratype gynes (n = 25): TL 7.33���8.13, WL 2.34���2.69, HL 1.25���1.31, HW 1.38���1.47, IOD 1.53���1.61, ML 0.89���0.98, FLD 0.73���0.78, SL 1.51���1.71, EL 0.36���0.39, EW 0.33���0.37, PrW 1.23���1.44, FL 1.65���1.76, PL 0.48���0.58, PW 0.56���0.63, PPL 0.43���0.55, PPW 0.91���1.02, GL 1.90���2.22, CI 106���114, MI 69���76, SI 107���120. Paratypes 279 alate g y n e s a n d 8 4 m a l e s, ASUSIBR00000002-00000364, from three collection sites along a 40 km stretch of ���restinga��� habitat (i.e., tropical and subtropical coastal forest habitats that form on sandy, acidic, nutrient-poor soils) along the coastline with the city of Ilh��us at its center. First collection site: BRAZIL, Bahia, Ilh��us, Praia do Sul, STAC camping, 13 km south of Ilh��us; near the entrance of a subterranean nest of Acromyrmex rugosus dug in the sand about 100 m from the beach, S14.91210��, W039.02095��; elevation above sea level: 5 m; collection date: 29 October 1992; col. Jacques H. C. Delabie (1 alate gyne, ASUSIBR00000002); same as above, but 05 November 1992 (7 alate gynes and 6 males, ASUSIBR00000003-15); same as above, but 15 January 1993; col. Harold G. Fowler (1 alate gyne ASUSIBR00000016). Second collection site: BRAZIL, Bahia, Ilh��us, Praia do Norte, Barramares village, 18 km north of Ilh��us, from the drift line of the Atlantic Ocean on the beach; S14.6197��, W039.0607��; elevation above sea level: 0 m; collection date: 01 November 1993; col Jacques H. C. Delabie (1 male, ASUSIBR00000017); same as above, but 06 November 1993 (2 males, ASUSIBR00000018-19); same as above, but 14 November 1993 (3 males, ASUSIBR00000020-22); same as above, but 13 December 1993 (1 male, ASUSIBR00000023); same as above, but 08 January 1994, 18:00 h (1 male, ASUSIBR00000024); same as above, but 14 January 1994 (2 alate gynes ASUSIBR00000025-26); same as above, but 06 February 1994, 08:00 h (1 alate gyne and 1 male, ASUSIBR00000027-28); same as above, but 06 March 1994, 07:00 h (1 alate gyne, ASUSIBR00000029); same as above, but 20 March 1994, 07:00 h (1 alate gyne, ASUSIBR00000030); same as above, but 01 April 1994, 07:00 h (1 alate gyne, ASUSIBR00000031); same as above, but 02 April 1994, 07:00 h (1 male, ASUSIBR00000032); same as above, but 21 May 1994, 08:00 h (1 male, ASUSIBR00000033); same as above, but 12 June 1994, 08:00 h; col. Ivan C. do Nascimento (1 alate gyne, ASUSIBR00000034); same as above, but 12 October 1994; col. Clayton R. R. Delabie (2 alate gynes and 2 males, ASUSIBR00000035-38); same as above, but 16 October 1994, 07:00 h; col. Clayton R. R. Delabie (1 alate gyne and 4 males, ASUSIBR00000039-43); same as above, but 29 October 1994, 07:00 h; col. Jacques H. C. Delabie and Clayton R. R. Delabie (17 alate gynes and 4 males, ASUSIBR00000044-64); same as above, but 13 November 1994, 07:00-08:00 h; col. Clayton R. R. Delabie (84 alate gynes and 9 males, ASUSIBR00000066-158); same as above, but 20 November 1994, 07:00 h; col. Clayton R. R. Delabie (1 alate gyne and 1 male, ASUSIBR00000159-160); same as above, but 24 November 1994 (1 alate gyne, ASUSIBR00000161); same as above, but 27 November 1994, 07:00 h (112 alate gynes and 26 males, ASUSIBR00000162-298); same as above, but 04 December 1994, 07:00 h (4 alate gynes and 1 male, ASUSIBR00000299-303); same as above, but 18 December 1994, 06:00 h; col. Clayton R. R. Delabie (2 alate gynes and 3 males, ASUSIBR00000304-308); same as above, but 27 December 1994, 07:00 h; col. Ivan C. do Nascimento (2 alate gynes and 2 males, ASUSIBR00000309-312); same as above, but 31 December 1994, 06:00 h; col. Clayton R. R. Delabie (1 alate gyne, ASUSIBR00000313); same as above, but 01 January 1995, 06:00 h; col. Clayton R. R. Delabie (3 alate gynes, ASUSIBR00000314-316); same as above, but 15 January 1995, 06:00 h (1 alate gyne, ASUSIBR00000317); same as above, but 19 January 1995, 07:00 h; col. Ivan C. do Nascimento (1 male, ASUSIBR00000318); same as above, but 27 January 1995 (1 male, ASUSIBR00000319); same as above, but 12 February 1995, 07:00 h (2 alate gynes, ASUSIBR00000320-321); same as above, but 26 February 1995, 06:00 h (1 alate gyne, ASUSIBR00000322); same as above, but 28 February 1995, 06:00 h (2 alate gynes and 1 male, ASUSIBR00000323-235); same as above, but 01 March 1995, 06:00 h (1 alate gyne and 1 male, ASUSIBR00000326-327); same as above, but 03 March 1995, 06:00 h (1 alate gyne and 2 males, ASUSIBR00000328-330); same as above, but 11 March 1995, 07:00 h (1 alate gyne, ASUSIBR00000331); same as above, but 17 March 1995, 07:00 h (1 alate gyne, ASUSIBR00000332); same as above, but 01 June 1995, 06:00 h (1 alate gyne and 1 male, ASUSIBR00000333-334); same as above, but 29 October 1995, 09:00 h (8 alate gynes and 8 males, ASUSIBR00000335-350); same as above, but 01 January 1996, 07:00 h (1 alate gyne, ASUSIBR00000351); same as above, but 10 February 1996, 07:00 h; col. Clayton R. R. Delabie (1 alate gyne, ASUSIBR00000352); same as above, but 20 February 1996, 08:00 h (1 alate gyne, ASUSIBR00000353); same as above, but 06 April 1996, 07:00 h (1 male, ASUSIBR00000354); same as above, but 14 July 1996 (5 alate gynes, ASUSIBR00000355-359); same as above, but 22 September 1996 (3 alate gynes, ASUSIBR00000360-362); same as above, but 26 October 1996 (2 alate gynes, ASUSIBR00000363-364). Third collection site: BRAZIL, Bahia, Ilh��us, Praia do Malhado, from the drift line of the Atlantic Ocean on the beach; S14.781��, W039.045��; elevation above sea level: 0 m; collection date: 02 November 1994; col. Ivan C. do Nascimento (1 alate gyne, ASUSIBR00000065). Description, paratype males Measurements (n = 25): TL 6.89���7.32, WL 2.25���2.47, HL 0.96���1.02, HW 1.00���1.07, IOD 1.25���1.33, ML 0.64���0.70, FLD 0.49���0.51, SL 1.31���1.45, EL 0.37���0.41, EW 0.38���0.43, PrW 1.23���1.44, FL 1.67���1.76, PL 0.37���0.44, PW 0.50���0.61, PPL 0.37���0.44, PPW 0.79���0.92, GL 2.15���2.47, CI 99���108, MI 64���71, SI 128-140. A small male (WL 2.25���2.47, TL 6.89���7.32), distinctly smaller than the male of the host species, A. rugosus. Integument smooth and shiny, thin, partly translucent. Body surface covered with few appressed, transversally flattened setae. Color uniformly pale yellow- to reddish-brown. Head Approximately as wide as long (CI 99���108); behind the level of the eyes, sides rounded and tapering towards the posterior margin of head; head size small relative to mesosoma. Mandibles long, slender, with distinct apical and preapical teeth, followed by seven to eight smaller, irregularly spaced teeth of irregular size; mandible surface smooth, shiny. Palp formula 4:2. Clypeus shape as in gyne; unpaired clypeal seta projecting over the anterior clypeal margin by two-thirds its length. Frontal lobes narrow, leaving the anterior half of the condylar bulbs exposed in full-face view. Preocular carina distinct, traversing the area of the antennal scrobe almost completely, nearly touching frontal carina. Eyes very large (EL 0.37���0.41, EW 0.38���0.43), strongly convex. Ocelli large, raised above the surface of the head; unpaired median ocellus approximately one and a half times wider than paired lateral ocelli. Antennae with 13 segments. Antennal scape long (SL 1.31���1.45) with appressed setae, surpassing the posterior margin of the head by half its length. Mesosoma Mesosoma with sex-specific modifications related to wing bearing. Anteriodorsal portion of pronotum inflated. Dorsolateral pronotal spine short, broadly triangular, and blunt in dorsal view. Ventrolateral pronotal spine absent. Dorsum of mesosoma smooth. Scutellum shape as in gyne; sculpture granulate with fine rugae. Bulla and meatus of metapleural gland small, orifice of metapleural gland tiny and round, pointing posteriorly, not notably modified from the condition in A. rugosus. Propodeal spines short, narrowly triangular, sharply pointed. Metasoma Petiole and postpetiole as in gyne. Gaster less bulbous than in host. First gastric tergite smooth, shiny, laterally with few reduced, rounded tubercles; sparsely covered with few appressed setae. Fore- and hindwings resemble the wings of its host, except for smaller size and a missing detached vein at the posterior end of the hindwing. Genitalia In toto, excluding the basal ring, parameres longer (1.04 mm) than wide (0.83 mm); apical lobe of paramere evenly rounded with less than 10 long, erect setae. In lateral view, aedeagus small (0.26 mm), ventral border of penis valve bearing 12 recurved teeth of uniform length; the anterior two and posteriormost of which are small and weakly sclerotized, whereas teeth 3-11 are distinctly larger and heavily sclerotized, as notable by the darker brown coloration. Differential diagnosis The comparative morphological analysis reveals that A. fowleri is remarkably similar to its host species, A. rugosus (Figs. 1 and 2). Notwithstanding, the gyne of A. fowleri can easily be distinguished from A. rugosus by the smaller size, the smooth and shiny integument, and the presence of appressed and transversally flattened setae (Figs. 1 and 3b). Relative to its smaller body size, A. fowleri is also characterized by longer appendages, and antennal scapes, as well as by a broader postpetiole (Fig. 1, Table 1). In the field, A. fowleri can be distinguished from its host by the significantly smaller size, the shiny appearance, the distinctly orange���brown coloration, the slowness of its movements, and the occurrence of alate females and males in some host nests throughout the year, whereas alates of A. rugosus typically occur during the rainier and warmer summer months (December���March) in coastal Bahia. The male of A. fowleri resembles the male of A. rugosus and is not gynaecomorphic (Fig. 2). Large males of A. fowleri reach the same size as small and medium size of A. rugosus males, but never reach the body size of large A. rugosus males. Despite slightly overlapping size ranges, the males of A. folweri can be distinguished from the A. rugosus males by their shiny integument, the slenderer and less bulbous gaster, the relatively longer antennal scapes, the absence of the inferior pronotal spine, the more pronounced tubercles on the first gastral tergite, and the presence of few, dorsoventrally flattened, appressed setae (Fig. 2, Table 1). The parasites��� genitalia are smaller than the hosts��� genitalia (paramere length: A. fowleri = 1.04 mm, A. rugosus = 1.66 mm), the length of the ventral aedeagal lobe is smaller in A. rugosus (A. fowleri = 0.26 mm, A. rugosus = 0.21���0.22 mm; Fig. 4). It is important to note that the aedeagus of A. rugosus bears a very large dorsal lobe that is absent from A. fowleri (Fig. 4). The ventral border of the aedeagus bears 12 teeth in A. fowleri and 12���14 teeth in A. rugosus (Fig. 4). Worker caste The worker caste is unknown and potentially nonexistent. Etymology This inquiline social parasite is named in honor of our colleague, the late Harold Gordon Fowler, in recognition of his numerous important contributions to leaf-cutting ant biology, taxonomy, biogeography, and pest management in Brazil and Paraguay. Previous studies referring to A. fowleri Acromyrmex fowleri was discovered 27 years ago and aspects of its biology were discussed in previous publications, where A. fowleri was referred to as either ��� Pseudoatta new species���, ��� Pseudoatta from Bahia ���, ��� Pseudoatta from Brazil ���, or ��� Acromyrmex new species��� (Delabie et al. 1993, Delabie et al. 2002; Schultz et al. 1998; Sumner et al. 2004; Schultz and Brady 2008; Rabeling and Bacci 2010; Soares et al. 2011; Rabeling et al. 2015). In this paper, we summarized the published and unpublished observations on the biology of A. fowleri. Key aspects of A. fowleri ���s biology and life history remain unknown and will require detailed field studies as well as conclusive behavioral experiments., Published as part of Rabeling, C., Messer, S., Lacau, S., do Nascimento, I. C., Jr., M. Bacci & Delabie, J. H. C., 2019, Acromyrmex fowleri: a new inquiline social parasite species of leaf-cutting ants from South America, with a discussion of social parasite biogeography in the Neotropical region, pp. 435-451 in Insectes Sociaux 66 on pages 445-448, DOI: 10.1007/s00040-019-00705-z, http://zenodo.org/record/3274215, {"references":["Delabie JHC, Fowler HG, Schlindwein MN (1993) Ocorrencia do parasita social Pseudoatta sp. nova em ninhos de Acromyrmex rugosus em Ilheus, Bahia: primeiro registro para os tropicos. In: IV International Symposium on Pest Ants, XI Encontro de Mirmecologia, 21 - 24 November 1993, Belo Horizonte, Brazil","Delabie JHC, do Nascimento IC, Mariano CSF (2002) Estrategias de reproducao e dispersao em formigas attines, com exemplos do sul da Bahia. In: XIX Congresso Brasileiro de Entomologia, 16 - 21 June 2002, Manaus, Brazil","Schultz TR, Bekkevold D, Boomsma JJ (1998) Acromyrmex insinuator new species: an incipient social parasite of fungus-growing ants. Insectes Soc 45: 457 - 471","Sumner S, Aanen DK, Delabie J, Boomsma JJ (2004) The evolution of social parasitism in Acromyrmex leaf-cutting ants: a test of Emery's rule. Insectes Soc 51: 37 - 42","Schultz TR, Brady SG (2008) Major evolutionary transitions in ant agriculture. Proc Natl Acad Sci USA 105: 5435 - 5440","Rabeling C, Bacci M (2010) A new workerless inquiline in the Lower Attini (Hymenoptera: Formicidae), with a discussion of social parasitism in fungus-growing ants. Syst Entomol 35: 379 - 392","Soares IMF, Della Lucia TMC, De Souza D (2011) Parasitismo social em formigas-cortadeiras. In: Della Lucia TMC (ed) Formigas- Cortadeiras: da bioecologia ao manejo. Editora da UFV, Vicosa, pp 344 - 358","Rabeling C, Schultz TR, Bacci M, Bollazzi M (2015) Acromyrmex charruanus: a new inquiline social parasite species of leaf-cutting ants. Insectes Soc 62: 335 - 349"]}
- Published
- 2019
- Full Text
- View/download PDF
9. Evolution, systematics, and natural history of a new genus of cryptobiotic fungus‐growing ants.
- Author
-
SOSA‐CALVO, J. E. F. F. R. E. Y., SCHULTZ, T. E. D. R., JEŠOVNIK, A. N. A., DAHAN, R. O. M. A. I. N. A., and RABELING, C. H. R. I. S. T. I. A. N.
- Subjects
FUNGUS ants ,INSECT phylogeny ,INSECT evolution ,FORAGING behavior ,INSECT-fungus relationships ,TRACHYMYRMEX ,CRYPTOZOA ,ANIMAL behavior - Abstract
Abstract: Xerolitor, a new, monotypic genus of fungus‐growing ants, is described to accommodate the phylogenetically isolated, relict species Mycetosoritis explicatus Kempf. We also diagnose the male and the larva of Xerolitor explicatus (Kempf) comb.n. and report ecological observations for the species, including nest architecture and foraging behaviour. Xerolitor explicatus comb.n. inhabits the dry habitats of the Brazilian Cerrado and the Bolivian and Paraguayan Gran Chaco. Bayesian multilocus phylogenetic analyses indicate that X. explicatus comb.n. is, contrary to some prior hypotheses, a member of the ‘higher’ fungus‐growing ants and the sister taxon of the genus Sericomyrmex Mayr. Results from phylogenetic analyses of the fungal cultivar grown by X. explicatus comb.n. in Paraguay, as well as the presence of gongylidia, indicate that the fungal mutualist is a member of the clade of higher fungal cultivar species and that it is probably the same species cultivated by some Trachymyrmex Forel and Sericomyrmex species. [ABSTRACT FROM AUTHOR]
- Published
- 2018
- Full Text
- View/download PDF
10. Comparative Study of Nest Architecture and Colony Structure of the Fungus-Growing Ants,Mycocepurus goeldiiandM. smithii
- Author
-
Rabeling, C., primary, Verhaagh, M., additional, and Engels, W., additional
- Published
- 2007
- Full Text
- View/download PDF
11. Comparative study of nest architecture and colony structure of the fungus-growing ants, Mycocepurus goeldii and M. smithii.
- Author
-
Rabeling, C., Verhaagh, M., and Engels, W.
- Published
- 2007
- Full Text
- View/download PDF
12. The coevolution of fungus-ant agriculture.
- Author
-
Schultz TR, Sosa-Calvo J, Kweskin MP, Lloyd MW, Dentinger B, Kooij PW, Vellinga EC, Rehner SA, Rodrigues A, Montoya QV, Fernández-Marín H, Ješovnik A, Niskanen T, Liimatainen K, Leal-Dutra CA, Solomon SE, Gerardo NM, Currie CR, Bacci M Jr, Vasconcelos HL, Rabeling C, Faircloth BC, and Doyle VP
- Subjects
- Animals, Agriculture, Domestication, Photosynthesis, Phylogeny, South America, Ants microbiology, Ants genetics, Biological Coevolution, Fungi genetics, Fungi classification, Symbiosis
- Abstract
Fungus-farming ants cultivate multiple lineages of fungi for food, but, because fungal cultivar relationships are largely unresolved, the history of fungus-ant coevolution remains poorly known. We designed probes targeting >2000 gene regions to generate a dated evolutionary tree for 475 fungi and combined it with a similarly generated tree for 276 ants. We found that fungus-ant agriculture originated ~66 million years ago when the end-of-Cretaceous asteroid impact temporarily interrupted photosynthesis, causing global mass extinctions but favoring the proliferation of fungi. Subsequently, ~27 million years ago, one ancestral fungal cultivar population became domesticated, i.e., obligately mutualistic, when seasonally dry habitats expanded in South America, likely isolating the cultivar population from its free-living, wet forest-dwelling conspecifics. By revealing these and other major transitions in fungus-ant coevolution, our results clarify the historical processes that shaped a model system for nonhuman agriculture.
- Published
- 2024
- Full Text
- View/download PDF
13. Four new inquiline social parasite species in the dolichoderine ant genus Tapinoma (Hymenoptera, Formicidae).
- Author
-
Cover SP and Rabeling C
- Abstract
Four new inquiline social parasites are described in the dolichoderine ant genus Tapinoma from the Nearctic region, and keys are provided for queens and males of the Nearctic Tapinoma species. The new social parasite species represent the first inquiline species in the genus Tapinoma and the first confirmed inquilines known from the ant subfamily Dolichoderinae. The four new species appear to be workerless inquilines that exploit a single host, Tapinomasessile (Say), and they represent at least two distinct life history syndromes. Tapinomaincognitum Cover & Rabeling, sp. nov . is highly derived morphologically and is a host-queen-tolerant inquiline. In contrast, T.inflatiscapus Cover & Rabeling, sp. nov. shows a lesser degree of morphological modification and appears to be a host-queen-intolerant social parasite. The life history of T.pulchellum Cover & Rabeling, sp. nov. is presently unknown, but its close similarity to T.incognitum suggests that it is also a host-queen-tolerant inquiline. The life history of T.shattucki Cover & Rabeling, sp. nov. is still uncertain. Our findings provide novel insights into the complex biology of ant inquiline life history syndromes., Competing Interests: The authors have declared that no competing interests exist., (Stefan P. Cover, Christian Rabeling.)
- Published
- 2024
- Full Text
- View/download PDF
14. The rediscovery of the putative ant social parasite Manica parasitica syn. nov. (Hymenoptera: Formicidae) reveals an unexpected endoparasite syndrome.
- Author
-
Prebus M, Georgiev BB, van de Kamp T, Hamann E, Baker I, and Rabeling C
- Subjects
- Animals, Host-Parasite Interactions, Social Behavior, Reproduction, Ants, Parasites
- Abstract
Parasitism is ubiquitous across the tree of life, and parasites comprise approximately half of all animal species. Social insect colonies attract many pathogens, endo- and ectoparasites, and are exploited by social parasites, which usurp the social environment of their hosts for survival and reproduction. Exploitation by parasites and pathogens versus social parasites may cause similar behavioural and morphological modifications of the host. Ants possess two overlapping syndromes: the endo- and social parasite syndromes. We rediscovered two populations of the putative social parasite Manica parasitica in the Sierra Nevada, and tested the hypothesis that M. parasitica is an independently evolving social parasite . We evaluated traits used to discriminate M. parasitica from its host Manica bradleyi, and examined the morphology of M. parasitica in the context of ant parasitic syndromes. We find that M. parasitica is not a social parasite. Instead, M. parasitica represents cestode-infected M. bradleyi . We propose that M. parasitica should be regarded as a junior synonym of M. bradleyi . Our results emphasize that an integrative approach is essential for unravelling the complex life histories of social insects and their symbionts.
- Published
- 2023
- Full Text
- View/download PDF
15. Biogeography and evolution of social parasitism in Australian Myrmecia bulldog ants revealed by phylogenomics.
- Author
-
Mera-Rodríguez D, Jourdan H, Ward PS, Shattuck S, Cover SP, Wilson EO, and Rabeling C
- Subjects
- Animals, Phylogeny, Australia, Symbiosis, New Caledonia, Biological Evolution, Bayes Theorem, Ants genetics
- Abstract
Studying the historical biogeography and life history transitions from eusocial colony life to social parasitism contributes to our understanding of the evolutionary mechanisms generating biodiversity in eusocial insects. The ants in the genus Myrmecia are a well-suited system for testing evolutionary hypotheses about how their species diversity was assembled through time because the genus is endemic to Australia with the single exception of the species M. apicalis inhabiting the Pacific Island of New Caledonia, and because at least one social parasite species exists in the genus. However, the evolutionary mechanisms underlying the disjunct biogeographic distribution of M. apicalis and the life history transition(s) to social parasitism remain unexplored. To study the biogeographic origin of the isolated, oceanic species M. apicalis and to reveal the origin and evolution of social parasitism in the genus, we reconstructed a comprehensive phylogeny of the ant subfamily Myrmeciinae. We utilized Ultra Conserved Elements (UCEs) as molecular markers to generate a molecular genetic dataset consisting of 2,287 loci per taxon on average for 66 out of the 93 known Myrmecia species as well as for the sister lineage Nothomyrmecia macrops and selected outgroups. Our time-calibrated phylogeny inferred that: (i) stem Myrmeciinae originated during the Paleocene ∼ 58 Ma ago; (ii) the current disjunct biogeographic distribution of M. apicalis was driven by long-distance dispersal from Australia to New Caledonia during the Miocene ∼ 14 Ma ago; (iii) the single social parasite species, M. inquilina, evolved directly from one of the two known host species, M. nigriceps, in sympatry via the intraspecific route of social parasite evolution; and (iv) 5 of the 9 previously established taxonomic species groups are non-monophyletic. We suggest minor changes to reconcile the molecular phylogenetic results with the taxonomic classification. Our study enhances our understanding of the evolution and biogeography of Australian bulldog ants, contributes to our knowledge about the evolution of social parasitism in ants, and provides a solid phylogenetic foundation for future inquiries into the biology, taxonomy, and classification of Myrmeciinae., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2023
- Full Text
- View/download PDF
16. Multi-queen breeding is associated with the origin of inquiline social parasitism in ants.
- Author
-
Dahan RA and Rabeling C
- Subjects
- Animals, Biological Evolution, Host-Parasite Interactions, Phylogeny, Social Behavior, Symbiosis, Ants parasitology, Parasites
- Abstract
Social parasites exploit the brood care behavior of their hosts to raise their own offspring. Social parasites are common among eusocial Hymenoptera and exhibit a wide range of distinct life history traits in ants, bees, and wasps. In ants, obligate inquiline social parasites are workerless (or nearly-so) species that engage in lifelong interactions with their hosts, taking advantage of the existing host worker forces to reproduce and exploit host colonies' resources. Inquiline social parasites are phylogenetically diverse with approximately 100 known species that evolved at least 40 times independently in ants. Importantly, ant inquilines tend to be closely related to their hosts, an observation referred to as 'Emery's Rule'. Polygyny, the presence of multiple egg-laying queens, was repeatedly suggested to be associated with the origin of inquiline social parasitism, either by providing the opportunity for reproductive cheating, thereby facilitating the origin of social parasite species, and/or by making polygynous species more vulnerable to social parasitism via the acceptance of additional egg-laying queens in their colonies. Although the association between host polygyny and the evolution of social parasitism has been repeatedly discussed in the literature, it has not been statistically tested in a phylogenetic framework across the ants. Here, we conduct a meta-analysis of ant social structure and social parasitism, testing for an association between polygyny and inquiline social parasitism with a phylogenetic correction for independent evolutionary events. We find an imperfect but significant over-representation of polygynous species among hosts of inquiline social parasites, suggesting that while polygyny is not required for the maintenance of inquiline social parasitism, it (or factors associated with it) may favor the origin of socially parasitic behavior. Our results are consistent with an intra-specific origin model for the evolution of inquiline social parasites by sympatric speciation but cannot exclude the alternative, inter-specific allopatric speciation model. The diversity of social parasite behaviors and host colony structures further supports the notion that inquiline social parasites evolved in parallel across unrelated ant genera in the formicoid clade via independent evolutionary pathways., (© 2022. The Author(s).)
- Published
- 2022
- Full Text
- View/download PDF
17. Ant phylogenomics reveals a natural selection hotspot preceding the origin of complex eusociality.
- Author
-
Romiguier J, Borowiec ML, Weyna A, Helleu Q, Loire E, La Mendola C, Rabeling C, Fisher BL, Ward PS, and Keller L
- Subjects
- Animals, Phylogeny, Reproduction genetics, Selection, Genetic, Social Behavior, Ants genetics
- Abstract
The evolution of eusociality has allowed ants to become one of the most conspicuous and ecologically dominant groups of organisms in the world. A large majority of the current ∼14,000 ant species belong to the formicoids,
1 a clade of nine subfamilies that exhibit the most extreme forms of reproductive division of labor, large colony size,2 worker polymorphism,3 and extended queen longevity.4 The eight remaining non-formicoid subfamilies are less well studied, with few genomes having been sequenced so far and unclear phylogenetic relationships.5 By sequencing 65 genomes, we provide a robust phylogeny of the 17 ant subfamilies, retrieving high support to the controversial leptanillomorph clade (Leptanillinae and Martialinae) as the sister group to all other extant ants. Moreover, our genomic analyses revealed that the emergence of the formicoids was accompanied by an elevated number of positive selection events. Importantly, the top three gene functions under selection are linked to key features of complex eusociality, with histone acetylation being implicated in caste differentiation, gene silencing by RNA in worker sterility, and autophagy in longevity. These results show that the key pathways associated with eusociality have been under strong selection during the Cretaceous, suggesting that the molecular foundations of complex eusociality may have evolved rapidly in less than 20 Ma., Competing Interests: Declaration of interests The authors declare no competing interests., (Copyright © 2022 Elsevier Inc. All rights reserved.)- Published
- 2022
- Full Text
- View/download PDF
18. Decay of homologous chromosome pairs and discovery of males in the thelytokous fungus-growing ant Mycocepurus smithii.
- Author
-
Barros LAC, Rabeling C, Teixeira GA, Dos Santos Ferreira Mariano C, Delabie JHC, and de Aguiar HJAC
- Subjects
- Animals, Brazil, Female, Fungi genetics, Humans, Karyotype, Male, Parthenogenesis genetics, Ants genetics
- Abstract
The prevalent mode of reproduction among ants is arrhenotokous parthenogenesis where unfertilized eggs give rise to haploid males and fertilized eggs develop into diploid females. Some ant species are capable of thelytokous parthenogenesis, a type of asexual reproduction where females develop from unfertilized diploid eggs. Thelytoky is well-documented in more than 20 ant species. Cytogenetic data are available for six species demonstrating that some thelytokous ant species are capable of producing males occasionally as well as maintaining their chromosome numbers and proper chromosome pairings. Mycocepurus smithii is a thelytokous fungus-growing ant species that inhabits large parts of Central and South America. Cytogenetic data are unavailable for M. smithii and male individuals were never documented for this species, although the presence of males is expected because genetic recombination was observed in a few sexually reproducing populations in Brazil and haploid sperm was documented from the spermathecae of M. smithii queens. This study aims at comparatively studying asexual and sexual populations of M. smithii using classical and molecular cytogenetic methods to test whether karyotype configuration is modified according to the mode of reproduction in M. smithii. Moreover, we report the discovery of M. smithii males from a sexually reproducing population in the Brazilian state Pará, diagnose the male of M. smithii, and morphologically characterize their spermatozoa. Karyotypic variation was observed within the asexual population (2n = 9, 10, or 11), whereas the chromosome number was fixed in the sexual population (2n = 14, n = 7). Identical karyotypes were maintained within individual M. smithii colonies and karyotype variation was only observed between colonies. In asexual individuals, the karyomorphs showed a decay of homologous chromosome pairs, especially in individuals with the karyomorph 2n = 11, which is potentially caused by relaxed natural selection on proper chromosome pairing. In contrast, females in the sexual population showed proper homologous chromosome pairings. In individuals of both asexual and sexual populations, we find that heterochromatin was localized in centromeric regions and on the short arms of the chromosomes, GC-rich regions were associated with heterochromatic regions, and 18S rDNA genes were located on the largest chromosome pair. This comparative cytogenetic analysis contributes to our understanding about the cytological mechanisms associated with thelytokous parthenogenesis in ants and suggests the decay of chromosome structure in the absence of meiosis and genetic recombination., (© 2022. The Author(s).)
- Published
- 2022
- Full Text
- View/download PDF
19. The maintenance of polymorphism in an ancient social supergene.
- Author
-
Purcell J, Lagunas-Robles G, Rabeling C, Borowiec ML, and Brelsford A
- Subjects
- Alleles, Animals, Evolution, Molecular, Haplotypes, Male, Polymorphism, Single Nucleotide, Sex Chromosomes, Ants genetics
- Abstract
Supergenes, regions of the genome with suppressed recombination between sets of functional mutations, contribute to the evolution of complex phenotypes in diverse systems. Excluding sex chromosomes, most supergenes discovered so far appear to be young, being found in one species or a few closely related species. Here, we investigate how a chromosome harbouring an ancient supergene has evolved over about 30 million years (Ma). The Formica supergene underlies variation in colony queen number in at least five species. We expand previous analyses of sequence divergence on this chromosome to encompass about 90 species spanning the Formica phylogeny. Within the nonrecombining region, the gene knockout contains 22 single nucleotide polymorphisms (SNPs) that are consistently differentiated between two alternative supergene haplotypes in divergent European Formica species, and we show that these same SNPs are present in most Formica clades. In these clades, including an early diverging Nearctic Formica clade, individuals with alternative genotypes at knockout also have higher differentiation in other portions of this chromosome. We identify hotspots of SNPs along this chromosome that are present in multiple Formica clades to detect genes that may have contributed to the emergence and maintenance of the genetic polymorphism. Finally, we infer three gene duplications on one haplotype, based on apparent heterozygosity within these genes in the genomes of haploid males. This study strengthens the evidence that this supergene originated early in the evolution of Formica and that just a few loci in this large region of suppressed recombination retain strongly differentiated alleles across contemporary Formica lineages., (© 2021 John Wiley & Sons Ltd.)
- Published
- 2021
- Full Text
- View/download PDF
20. The evolution of social parasitism in Formica ants revealed by a global phylogeny.
- Author
-
Borowiec ML, Cover SP, and Rabeling C
- Subjects
- Aggression physiology, Animals, Ants genetics, Biological Evolution, Cooperative Behavior, DNA, Mitochondrial genetics, Host-Parasite Interactions, Parasites genetics, Phylogeny, Species Specificity, Behavior, Animal physiology, Social Behavior, Symbiosis physiology
- Abstract
Studying the behavioral and life history transitions from a cooperative, eusocial life history to exploitative social parasitism allows for deciphering the conditions under which changes in behavior and social organization lead to diversification. The Holarctic ant genus Formica is ideally suited for studying the evolution of social parasitism because half of its 172 species are confirmed or suspected social parasites, which includes all three major classes of social parasitism known in ants. However, the life history transitions associated with the evolution of social parasitism in this genus are largely unexplored. To test competing hypotheses regarding the origins and evolution of social parasitism, we reconstructed a global phylogeny of Formica ants. The genus originated in the Old World ∼30 Ma ago and dispersed multiple times to the New World and back. Within Formica , obligate dependent colony-founding behavior arose once from a facultatively polygynous common ancestor practicing independent and facultative dependent colony foundation. Temporary social parasitism likely preceded or arose concurrently with obligate dependent colony founding, and dulotic social parasitism evolved once within the obligate dependent colony-founding clade. Permanent social parasitism evolved twice from temporary social parasitic ancestors that rarely practiced colony budding, demonstrating that obligate social parasitism can originate from a facultative parasitic background in socially polymorphic organisms. In contrast to permanently socially parasitic ants in other genera, the high parasite diversity in Formica likely originated via allopatric speciation, highlighting the diversity of convergent evolutionary trajectories resulting in nearly identical parasitic life history syndromes., Competing Interests: The authors declare no competing interest., (Copyright © 2021 the Author(s). Published by PNAS.)
- Published
- 2021
- Full Text
- View/download PDF
21. Publisher Correction: Relaxed selection underlies genome erosion in socially parasitic ant species.
- Author
-
Schrader L, Pan H, Bollazzi M, Schiøtt M, Larabee FJ, Bi X, Deng Y, Zhang G, Boomsma JJ, and Rabeling C
- Published
- 2021
- Full Text
- View/download PDF
22. Relaxed selection underlies genome erosion in socially parasitic ant species.
- Author
-
Schrader L, Pan H, Bollazzi M, Schiøtt M, Larabee FJ, Bi X, Deng Y, Zhang G, Boomsma JJ, and Rabeling C
- Subjects
- Animals, Ants classification, Ants physiology, Evolution, Molecular, Female, Gene Rearrangement genetics, Genomics methods, Host-Parasite Interactions, Insect Proteins classification, Insect Proteins genetics, Male, Parasites classification, Parasites physiology, Phylogeny, Receptors, Odorant classification, Receptors, Odorant genetics, Species Specificity, Ants genetics, Genome, Insect genetics, Parasites genetics, Social Behavior
- Abstract
Inquiline ants are highly specialized and obligate social parasites that infiltrate and exploit colonies of closely related species. They have evolved many times convergently, are often evolutionarily young lineages, and are almost invariably rare. Focusing on the leaf-cutting ant genus Acromyrmex, we compared genomes of three inquiline social parasites with their free-living, closely-related hosts. The social parasite genomes show distinct signatures of erosion compared to the host lineages, as a consequence of relaxed selective constraints on traits associated with cooperative ant colony life and of inquilines having very small effective population sizes. We find parallel gene losses, particularly in olfactory receptors, consistent with inquiline species having highly reduced social behavioral repertoires. Many of the genomic changes that we uncover resemble those observed in the genomes of obligate non-social parasites and intracellular endosymbionts that branched off into highly specialized, host-dependent niches.
- Published
- 2021
- Full Text
- View/download PDF
23. Comprehensive phylogeny of Myrmecocystus honey ants highlights cryptic diversity and infers evolution during aridification of the American Southwest.
- Author
-
van Elst T, Eriksson TH, Gadau J, Johnson RA, Rabeling C, Taylor JE, and Borowiec ML
- Subjects
- Animals, Bayes Theorem, Conserved Sequence genetics, Desert Climate, Genetic Loci, Honey, Humans, Likelihood Functions, Southwestern United States, Species Specificity, Time Factors, Ants classification, Biodiversity, Phylogeny
- Abstract
The New World ant genus Myrmecocystus Wesmael, 1838 (Formicidae: Formicinae: Lasiini) is endemic to arid and semi-arid habitats of the western United States and Mexico. Several intriguing life history traits have been described for the genus, the best-known of which are replete workers, that store liquified food in their largely expanded crops and are colloquially referred to as "honeypots". Despite their interesting biology and ecological importance for arid ecosystems, the evolutionary history of Myrmecocystus ants is largely unknown and the current taxonomy presents an unsatisfactory systematic framework. We use ultraconserved elements to infer the evolutionary history of Myrmecocystus ants and provide a comprehensive, dated phylogenetic framework that clarifies the molecular systematics within the genus with high statistical support, reveals cryptic diversity, and reconstructs ancestral foraging activity. Using maximum likelihood, Bayesian and species tree approaches on a data set of 134 ingroup specimens (including samples from natural history collections and type material), we recover largely identical topologies that leave the position of only few clades uncertain and cover the intra- and interspecific variation of 28 of the 29 described and six undescribed species. In addition to traditional support values, such as bootstrap and posterior probability, we quantify genealogical concordance to estimate the effects of conflicting evolutionary histories on phylogenetic inference. Our analyses reveal that the current taxonomic classification of the genus is inconsistent with the molecular phylogenetic inference, and we identify cryptic diversity in seven species. Divergence dating suggests that the split between Myrmecocystus and its sister taxon Lasius occurred in the early Miocene. Crown group Myrmecocystus started diversifying about 14.08 Ma ago when the gradual aridification of the southwestern United States and northern Mexico led to formation of the American deserts and to adaptive radiations of many desert taxa., (Copyright © 2020. Published by Elsevier Inc.)
- Published
- 2021
- Full Text
- View/download PDF
24. Evolution: Shape-Shifting Social Parasites.
- Author
-
Parker J and Rabeling C
- Subjects
- Animals, Madagascar, Phenotype, Ants, Parasites
- Abstract
Ants exploit differences in body surface chemistry to distinguish nestmates from colony intruders. Socially parasitic ants in Madagascar have convergently evolved morphological similarities to host worker anatomy, implying that body shape may also be surveilled. Studies of tactile behaviors in ant societies are now needed., (Copyright © 2020 Elsevier Inc. All rights reserved.)
- Published
- 2020
- Full Text
- View/download PDF
25. Two new species of socially parasitic Nylanderia ants from the southeastern United States.
- Author
-
Messer SJ, Cover SP, and Rabeling C
- Abstract
In ants, social parasitism is an umbrella term describing a variety of life-history strategies, where a parasitic species depends entirely on a free-living species, for part of or its entire life-cycle, for either colony founding, survival, and/or reproduction. The highly specialized inquiline social parasites are fully dependent on their hosts for their entire lifecycles. Most inquiline species are tolerant of the host queen in the parasitized colony, forgo producing a worker caste, and invest solely in the production of sexual offspring. In general, inquilines are rare, and their geographic distribution is limited, making it difficult to study them. Inquiline populations appear to be small, cryptic, and they are perhaps ephemeral. Thus, information about their natural history is often fragmentary or non-existent but is necessary for understanding the socially parasitic life history syndrome in more detail. Here, we describe two new species of inquiline social parasites, Nylanderia deyrupi sp. nov. and Nylanderia parasitica sp. nov. , from the southeastern United States, parasitizing Nylanderia wojciki and Nylanderia faisonensis , respectively. The formicine genus Nylanderia is large and globally distributed, but until the recent description of Nylanderia deceptrix , social parasites were unknown from this genus. In addition to describing the new social parasite species, we summarize the fragmentary information known about their biology, present a key to both the queens and the males of the Nylanderia social parasites, and discuss the morphology of the social parasites in the context of the inquiline syndrome., (Steven J. Messer, Stefan P. Cover, Christian Rabeling.)
- Published
- 2020
- Full Text
- View/download PDF
26. Compositional heterogeneity and outgroup choice influence the internal phylogeny of the ants.
- Author
-
Borowiec ML, Rabeling C, Brady SG, Fisher BL, Schultz TR, and Ward PS
- Subjects
- Animals, Ants genetics, Bayes Theorem, Computer Simulation, Likelihood Functions, Time Factors, Ants classification, Phylogeny
- Abstract
Knowledge of the internal phylogeny and evolutionary history of ants (Formicidae), the world's most species-rich clade of eusocial organisms, has dramatically improved since the advent of molecular phylogenetics. A number of relationships at the subfamily level, however, remain uncertain. Key unresolved issues include placement of the root of the ant tree of life and the relationships among the so-called poneroid subfamilies. Here we assemble a new data set to attempt a resolution of these two problems and carry out divergence dating, focusing on the age of the root node of crown Formicidae. For the phylogenetic analyses we included data from 110 ant species, including the key species Martialis heureka. We focused taxon sampling on non-formicoid lineages of ants to gain insight about deep nodes in the ant phylogeny. For divergence dating we retained a subset of 62 extant taxa and 42 fossils in order to approximate diversified sampling in the context of the fossilized birth-death process. We sequenced 11 nuclear gene fragments for a total of ∼7.5 kb and investigated the DNA sequence data for the presence of among-taxon compositional heterogeneity, a property known to mislead phylogenetic inference, and for its potential to affect the rooting of the ant phylogeny. We found sequences of the Leptanillinae and several outgroup taxa to be rich in adenine and thymine (51% average AT content) compared to the remaining ants (45% average). To investigate whether this heterogeneity could bias phylogenetic inference we performed outgroup removal experiments, analysis of compositionally homogeneous sites, and a simulation study. We found that compositional heterogeneity indeed appears to affect the placement of the root of the ant tree but has limited impact on more recent nodes. Our findings have implications for outgroup choice in phylogenetics, which should be made not only on the basis of close relationship to the ingroup, but should also take into account sequence divergence and other properties relative to the ingroup. We put forward a hypothesis regarding the rooting of the ant phylogeny, in which Martialis and the Leptanillinae together constitute a clade that is sister to all other ants. After correcting for compositional heterogeneity this emerges as the best-supported hypothesis of relationships at deep nodes in the ant tree. The results of our divergence dating under the fossilized birth-death process and diversified sampling suggest that the crown Formicidae originated during the Albian or Aptian ages of the Lower Cretaceous (103-124 Ma). In addition, we found support for monophyletic poneroids comprising the subfamilies Agroecomyrmecinae, Amblyoponinae, Apomyrminae, Paraponerinae, Ponerinae, and Proceratiinae, and well-supported relationships among these subfamilies except for the placement of Proceratiinae and (Amblyoponinae + Apomyrminae). Our phylogeny also highlights the non-monophyly of several ant genera, including Protanilla and Leptanilla in the Leptanillinae, Proceratium in the Proceratiinae, and Cryptopone, Euponera, and Mesoponera within the Ponerinae., (Copyright © 2019 Elsevier Inc. All rights reserved.)
- Published
- 2019
- Full Text
- View/download PDF
27. Convergent evolution of complex structures for ant-bacterial defensive symbiosis in fungus-farming ants.
- Author
-
Li H, Sosa-Calvo J, Horn HA, Pupo MT, Clardy J, Rabeling C, Schultz TR, and Currie CR
- Subjects
- Animals, Phylogeny, Actinobacteria physiology, Ants microbiology, Biological Evolution, Fungi physiology, Host-Pathogen Interactions, Symbiosis
- Abstract
Evolutionary adaptations for maintaining beneficial microbes are hallmarks of mutualistic evolution. Fungus-farming "attine" ant species have complex cuticular modifications and specialized glands that house and nourish antibiotic-producing Actinobacteria symbionts, which in turn protect their hosts' fungus gardens from pathogens. Here we reconstruct ant-Actinobacteria evolutionary history across the full range of variation within subtribe Attina by combining dated phylogenomic and ultramorphological analyses. Ancestral-state analyses indicate the ant-Actinobacteria symbiosis arose early in attine-ant evolution, a conclusion consistent with direct observations of Actinobacteria on fossil ants in Oligo-Miocene amber. qPCR indicates that the dominant ant-associated Actinobacteria belong to the genus Pseudonocardia Tracing the evolutionary trajectories of Pseudonocardia -maintaining mechanisms across attine ants reveals a continuum of adaptations. In Myrmicocrypta species, which retain many ancestral morphological and behavioral traits, Pseudonocardia occur in specific locations on the legs and antennae, unassociated with any specialized structures. In contrast, specialized cuticular structures, including crypts and tubercles, evolved at least three times in derived attine-ant lineages. Conspicuous caste differences in Pseudonocardia -maintaining structures, in which specialized structures are present in worker ants and queens but reduced or lost in males, are consistent with vertical Pseudonocardia transmission. Although the majority of attine ants are associated with Pseudonocardia , there have been multiple losses of bacterial symbionts and bacteria-maintaining structures in different lineages over evolutionary time. The early origin of ant- Pseudonocardia mutualism and the multiple evolutionary convergences on strikingly similar anatomical adaptations for maintaining bacterial symbionts indicate that Pseudonocardia have played a critical role in the evolution of ant fungiculture., Competing Interests: The authors declare no conflict of interest.
- Published
- 2018
- Full Text
- View/download PDF
28. An ant genus-group (Prenolepis) illuminates the biogeography and drivers of insect diversification in the Indo-Pacific.
- Author
-
Matos-Maraví P, Clouse RM, Sarnat EM, Economo EP, LaPolla JS, Borovanska M, Rabeling C, Czekanski-Moir J, Latumahina F, Wilson EO, and Janda M
- Subjects
- Animals, Ants, Asia, Australia, Calibration, Fossils, Geography, Indonesia, New Guinea, Phylogeny, Species Specificity, Time Factors, Biodiversity, Phylogeography
- Abstract
The Malay Archipelago and the tropical South Pacific (hereafter the Indo-Pacific region) are considered biodiversity hotspots, yet a general understanding of the origins and diversification of species-rich groups in the region remains elusive. We aimed to test hypotheses for the evolutionary processes driving insect species diversity in the Indo-Pacific using a higher-level and comprehensive phylogenetic hypothesis for an ant clade consisting of seven genera. We estimated divergence times and reconstructed the biogeographical history of ant species in the Prenolepis genus-group (Formicidae: Formicinae: Lasiini). We used a fossil-calibrated phylogeny to infer ancestral geographical ranges utilizing a biogeographic model that includes founder-event speciation. Ancestral state reconstructions of the ants' ecological preferences, and diversification rates were estimated for selected Indo-Pacific clades. Overall, we report that faunal interchange between Asia and Australia has occurred since at least 20-25 Ma, and early dispersal to the Fijian Basin happened during the early and mid-Miocene (ca. 10-20 Ma). Differences in diversification rates across Indo-Pacific clades may be related to ecological preference breadth, which in turn may have facilitated geographical range expansions. Ancient dispersal routes suggested by our results agree with the palaeogeography of the region. For this particular group of ants, the rapid orogenesis in New Guinea and possibly subsequent ecological shifts may have promoted their rapid diversification and widespread distribution across the Indo-Pacific., (Copyright © 2018 Elsevier Inc. All rights reserved.)
- Published
- 2018
- Full Text
- View/download PDF
29. Biogeography of mutualistic fungi cultivated by leafcutter ants.
- Author
-
Mueller UG, Ishak HD, Bruschi SM, Smith CC, Herman JJ, Solomon SE, Mikheyev AS, Rabeling C, Scott JJ, Cooper M, Rodrigues A, Ortiz A, Brandão CRF, Lattke JE, Pagnocca FC, Rehner SA, Schultz TR, Vasconcelos HL, Adams RMM, Bollazzi M, Clark RM, Himler AG, LaPolla JS, Leal IR, Johnson RA, Roces F, Sosa-Calvo J, Wirth R, and Bacci M Jr
- Subjects
- Animals, Ants classification, Central America, Genetic Markers, Genetics, Population, Genotype, Microsatellite Repeats, North America, Phylogeny, Phylogeography, South America, Symbiosis, Agaricales genetics, Ants microbiology, Biological Coevolution
- Abstract
Leafcutter ants propagate co-evolving fungi for food. The nearly 50 species of leafcutter ants (Atta, Acromyrmex) range from Argentina to the United States, with the greatest species diversity in southern South America. We elucidate the biogeography of fungi cultivated by leafcutter ants using DNA sequence and microsatellite-marker analyses of 474 cultivars collected across the leafcutter range. Fungal cultivars belong to two clades (Clade-A and Clade-B). The dominant and widespread Clade-A cultivars form three genotype clusters, with their relative prevalence corresponding to southern South America, northern South America, Central and North America. Admixture between Clade-A populations supports genetic exchange within a single species, Leucocoprinus gongylophorus. Some leafcutter species that cut grass as fungicultural substrate are specialized to cultivate Clade-B fungi, whereas leafcutters preferring dicot plants appear specialized on Clade-A fungi. Cultivar sharing between sympatric leafcutter species occurs frequently such that cultivars of Atta are not distinct from those of Acromyrmex. Leafcutters specialized on Clade-B fungi occur only in South America. Diversity of Clade-A fungi is greatest in South America, but minimal in Central and North America. Maximum cultivar diversity in South America is predicted by the Kusnezov-Fowler hypothesis that leafcutter ants originated in subtropical South America and only dicot-specialized leafcutter ants migrated out of South America, but the cultivar diversity becomes also compatible with a recently proposed hypothesis of a Central American origin by postulating that leafcutter ants acquired novel cultivars many times from other nonleafcutter fungus-growing ants during their migrations from Central America across South America. We evaluate these biogeographic hypotheses in the light of estimated dates for the origins of leafcutter ants and their cultivars., (© 2017 John Wiley & Sons Ltd.)
- Published
- 2017
- Full Text
- View/download PDF
30. Lenomyrmex hoelldobleri : a new ant species discovered in the stomach of the dendrobatid poison frog, Oophaga sylvatica (Funkhouser).
- Author
-
Rabeling C, Sosa-Calvo J, O'Connell LA, Coloma LA, and Fernández F
- Abstract
The ant genus Lenomyrmex was recently discovered and described from mid to high elevation rainforests in southern Central and northwestern South America. Lenomyrmex currently consists of six described species, which are only rarely collected. Here, we add a new species, Lenomyrmex hoelldobleri sp. n. , which was discovered in a stomach content sample of the dendrobatid frog, Oophaga sylvatica , from northwestern Ecuador. Lenomyrmex hoelldobleri can be distinguished from other species in the genus by the presence of a well-developed petiolar node, whereas in all other species the node of the petiole is ill-defined. In addition to the shape of the petiolar node, Lenomyrmex hoelldobleri can be distinguished from the morphologically similar Lenomyrmex costatus by (i) the presence of the metanotal suture, (ii) the direction of the striae on dorsum of propodeum (concentrically transverse in Lenomyrmex hoelldobleri , longitudinal in Lenomyrmex costatus ), (iii) the finely striate dorsum of postpetiole, (iv) its larger size, and (v) distinctly darker coloration. We also describe the gyne of Lenomyrmex foveolatus . This collection record from northwestern Ecuador extends the geographic distribution of Lenomyrmex foveolatus 400 km south from its previous record in Colombia. A revised taxonomic key to the workers and gynes of all described Lenomyrmex species is provided. We discuss the taxonomic relationship of Lenomyrmex hoelldobleri to other species in the genus and its biology based on the limited information that is currently available. Finally, we briefly discuss the feeding ecology of dendrobatid poison frogs in the context of providing a valuable source of rarely collected and cryptic new ant species.
- Published
- 2016
- Full Text
- View/download PDF
31. Reciprocal genomic evolution in the ant-fungus agricultural symbiosis.
- Author
-
Nygaard S, Hu H, Li C, Schiøtt M, Chen Z, Yang Z, Xie Q, Ma C, Deng Y, Dikow RB, Rabeling C, Nash DR, Wcislo WT, Brady SG, Schultz TR, Zhang G, and Boomsma JJ
- Subjects
- Animals, Calibration, Carbohydrate Metabolism genetics, Chitin metabolism, Crops, Agricultural genetics, Domestication, Genome, Insect, Genome, Plant, Phylogeny, Sequence Analysis, DNA, Time Factors, Agriculture, Ants genetics, Evolution, Molecular, Fungi genetics, Genome, Symbiosis genetics
- Abstract
The attine ant-fungus agricultural symbiosis evolved over tens of millions of years, producing complex societies with industrial-scale farming analogous to that of humans. Here we document reciprocal shifts in the genomes and transcriptomes of seven fungus-farming ant species and their fungal cultivars. We show that ant subsistence farming probably originated in the early Tertiary (55-60 MYA), followed by further transitions to the farming of fully domesticated cultivars and leaf-cutting, both arising earlier than previously estimated. Evolutionary modifications in the ants include unprecedented rates of genome-wide structural rearrangement, early loss of arginine biosynthesis and positive selection on chitinase pathways. Modifications of fungal cultivars include loss of a key ligninase domain, changes in chitin synthesis and a reduction in carbohydrate-degrading enzymes as the ants gradually transitioned to functional herbivory. In contrast to human farming, increasing dependence on a single cultivar lineage appears to have been essential to the origin of industrial-scale ant agriculture.
- Published
- 2016
- Full Text
- View/download PDF
32. Breaking out of biogeographical modules: range expansion and taxon cycles in the hyperdiverse ant genus Pheidole .
- Author
-
Economo EP, Sarnat EM, Janda M, Clouse R, Klimov PB, Fischer G, Blanchard BD, Ramirez LN, Andersen AN, Berman M, Guénard B, Lucky A, Rabeling C, Wilson EO, and Knowles LL
- Abstract
Aim: We sought to reconstruct the biogeographical structure and dynamics of a hyperdiverse ant genus, Pheidole, and to test several predictions of the taxon cycle hypothesis. Using large datasets on Pheidole geographical distributions and phylogeny, we (1) inferred patterns of biogeographical modularity (clusters of areas with similar faunal composition), (2) tested whether species in open habitats are more likely to be expanding their range beyond module boundaries, and (3) tested whether there is a bias of lineage flow from high- to low-diversity areas., Location: The Old World., Methods: We compiled and jointly analysed a comprehensive database of Pheidole geographical distributions, the ecological affinities of different species, and a multilocus phylogeny of the Old World radiation. We used network modularity methods to infer biogeographical structure in the genus and comparative methods to evaluate the hypotheses., Results: The network analysis identified eight biogeographical modules, and a suite of species with anomalous ranges that are statistically more likely to occur in open habitat, supporting the hypothesis that open habitats promote range expansion. Phylogenetic analysis shows evidence for a cascade pattern of colonization from Asia to New Guinea to the Pacific, but no 'upstream' colonization in the reverse direction., Main Conclusions: The distributions of Pheidole lineages in the Old World are highly modular, with modules generally corresponding to biogeographical regions inferred in other groups of organisms. However, some lineages have expanded their ranges across module boundaries, and these species are more likely to be adapted to open habitats rather than interior forest. In addition, there is a cascade pattern of dispersal from higher to lower diversity areas during these range expansions. Our findings are consistent with the taxon cycle hypothesis, although they do not rule out alternative interpretations.
- Published
- 2015
- Full Text
- View/download PDF
33. Molecular phylogeny of Indo-Pacific carpenter ants (Hymenoptera: Formicidae, Camponotus) reveals waves of dispersal and colonization from diverse source areas.
- Author
-
Clouse RM, Janda M, Blanchard B, Sharma P, Hoffmann BD, Andersen AN, Czekanski-Moir JE, Krushelnycky P, Rabeling C, Wilson EO, Economo EP, Sarnat EM, General DM, Alpert GD, and Wheeler WC
- Abstract
Ants that resemble Camponotus maculatus (Fabricius, 1782) present an opportunity to test the hypothesis that the origin of the Pacific island fauna was primarily New Guinea, the Philippines, and the Indo-Malay archipelago (collectively known as Malesia). We sequenced two mitochondrial and four nuclear markers from 146 specimens from Pacific islands, Australia, and Malesia. We also added 211 specimens representing a larger worldwide sample and performed a series of phylogenetic analyses and ancestral area reconstructions. Results indicate that the Pacific members of this group comprise several robust clades that have distinctly different biogeographical histories, and they suggest an important role for Australia as a source of Pacific colonizations. Malesian areas were recovered mostly in derived positions, and one lineage appears to be Neotropical. Phylogenetic hypotheses indicate that the orange, pan-Pacific form commonly identified as C. chloroticus Emery 1897 actually consists of two distantly related lineages. Also, the lineage on Hawai'i, which has been called C. variegatus (Smith, 1858), appears to be closely related to C. tortuganus Emery, 1895 in Florida and other lineages in the New World. In Micronesia and Polynesia the C. chloroticus-like species support predictions of the taxon-cycle hypothesis and could be candidates for human-mediated dispersal., (© The Willi Hennig Society 2014.)
- Published
- 2015
- Full Text
- View/download PDF
34. A social parasite evolved reproductive isolation from its fungus-growing ant host in sympatry.
- Author
-
Rabeling C, Schultz TR, Pierce NE, and Bacci M Jr
- Subjects
- Animals, Ants genetics, Ants physiology, Cell Nucleus genetics, Food Chain, Fungi growth & development, Mitochondrial Proteins genetics, Molecular Sequence Data, Phylogeny, Sequence Analysis, DNA, Social Behavior, Sympatry, Ants parasitology, Genetic Speciation, Host-Parasite Interactions, Insect Proteins genetics, Reproductive Isolation
- Abstract
Inquiline social parasitic ant species exploit colonies of other ant species mainly by producing sexual offspring that are raised by the host. Ant social parasites and their hosts are often close relatives (Emery's rule), and two main hypotheses compete to explain the parasites' evolutionary origins: (1) the interspecific hypothesis proposes an allopatric speciation scenario for the parasite, whereas (2) the intraspecific hypothesis postulates that the parasite evolves directly from its host in sympatry [1-10]. Evidence in support of the intraspecific hypothesis has been accumulating for ants [3, 5, 7, 9-12], but sympatric speciation remains controversial as a general speciation mechanism for inquiline parasites. Here we use molecular phylogenetics to assess whether the socially parasitic fungus-growing ant Mycocepurus castrator speciated from its host Mycocepurus goeldii in sympatry. Based on differing patterns of relationship in mitochondrial and individual nuclear genes, we conclude that host and parasite occupy a temporal window in which lineage sorting has taken place in the mitochondrial genes but not yet in the nuclear alleles. We infer that the host originated first and that the parasite originated subsequently from a subset of the host species' populations, providing empirical support for the hypothesis that inquiline parasites can evolve reproductive isolation while living sympatrically with their hosts., (Copyright © 2014 Elsevier Ltd. All rights reserved.)
- Published
- 2014
- Full Text
- View/download PDF
35. A Brazilian population of the asexual fungus-growing ant Mycocepurus smithii (Formicidae, Myrmicinae, Attini) cultivates fungal symbionts with gongylidia-like structures.
- Author
-
Masiulionis VE, Rabeling C, De Fine Licht HH, Schultz T, Bacci M Jr, Bezerra CM, and Pagnocca FC
- Subjects
- Agaricales cytology, Agaricales genetics, Animals, Bayes Theorem, Likelihood Functions, Phylogeny, Reproduction, Asexual, Symbiosis, Agaricales growth & development, Ants physiology, Behavior, Animal
- Abstract
Attine ants cultivate fungi as their most important food source and in turn the fungus is nourished, protected against harmful microorganisms, and dispersed by the ants. This symbiosis evolved approximately 50-60 million years ago in the late Paleocene or early Eocene, and since its origin attine ants have acquired a variety of fungal mutualists in the Leucocoprineae and the distantly related Pterulaceae. The most specialized symbiotic interaction is referred to as "higher agriculture" and includes leafcutter ant agriculture in which the ants cultivate the single species Leucoagaricus gongylophorus. Higher agriculture fungal cultivars are characterized by specialized hyphal tip swellings, so-called gongylidia, which are considered a unique, derived morphological adaptation of higher attine fungi thought to be absent in lower attine fungi. Rare reports of gongylidia-like structures in fungus gardens of lower attines exist, but it was never tested whether these represent rare switches of lower attines to L. gonglyphorus cultivars or whether lower attine cultivars occasionally produce gongylidia. Here we describe the occurrence of gongylidia-like structures in fungus gardens of the asexual lower attine ant Mycocepurus smithii. To test whether M. smithii cultivates leafcutter ant fungi or whether lower attine cultivars produce gongylidia, we identified the M. smithii fungus utilizing molecular and morphological methods. Results shows that the gongylidia-like structures of M. smithii gardens are morphologically similar to gongylidia of higher attine fungus gardens and can only be distinguished by their slightly smaller size. A molecular phylogenetic analysis of the fungal ITS sequence indicates that the gongylidia-bearing M. smithii cultivar belongs to the so-called "Clade 1"of lower Attini cultivars. Given that M. smithii is capable of cultivating a morphologically and genetically diverse array of fungal symbionts, we discuss whether asexuality of the ant host maybe correlated with low partner fidelity and active symbiont choice between fungus and ant mutualists.
- Published
- 2014
- Full Text
- View/download PDF
36. Cyatta abscondita: taxonomy, evolution, and natural history of a new fungus-farming ant genus from Brazil.
- Author
-
Sosa-Calvo J, Schultz TR, Brandão CR, Klingenberg C, Feitosa RM, Rabeling C, Bacci M Jr, Lopes CT, and Vasconcelos HL
- Subjects
- Animals, Ants anatomy & histology, Ants genetics, Biological Evolution, Brazil, Female, Genes, Insect, Geography, Male, Molecular Sequence Data, Nesting Behavior, Phylogeny, Ants classification
- Abstract
Cyatta abscondita, a new genus and species of fungus-farming ant from Brazil, is described based on morphological study of more than 20 workers, two dealate gynes, one male, and two larvae. Ecological field data are summarized, including natural history, nest architecture, and foraging behavior. Phylogenetic analyses of DNA sequence data from four nuclear genes indicate that Cyatta abscondita is the distant sister taxon of the genus Kalathomyrmex, and that together they comprise the sister group of the remaining neoattine ants, an informal clade that includes the conspicuous and well-known leaf-cutter ants. Morphologically, Cyatta abscondita shares very few obvious character states with Kalathomyrmex. It does, however, possess a number of striking morphological features unique within the fungus-farming tribe Attini. It also shares morphological character states with taxa that span the ancestral node of the Attini. The morphology, behavior, and other biological characters of Cyatta abscondita are potentially informative about plesiomorphic character states within the fungus-farming ants and about the early evolution of ant agriculture.
- Published
- 2013
- Full Text
- View/download PDF
37. Thelytokous parthenogenesis in eusocial Hymenoptera.
- Author
-
Rabeling C and Kronauer DJ
- Subjects
- Animals, Apomixis, Hymenoptera cytology, Hymenoptera genetics, Parthenogenesis, Biological Evolution, Hymenoptera physiology
- Abstract
Female parthenogenesis, or thelytoky, is particularly common in solitary Hymenoptera. Only more recently has it become clear that many eusocial species also regularly reproduce thelytokously, and here we provide a comprehensive overview. Especially in ants, thelytoky underlies a variety of idiosyncratic life histories with unique evolutionary and ecological consequences. In all eusocial species studied, thelytoky probably has a nuclear genetic basis and the underlying cytological mechanism retains high levels of heterozygosity. This is in striking contrast to many solitary wasps, in which thelytoky is often induced by cytoplasmic bacteria and results in an immediate loss of heterozygosity. These differences are likely related to differences in haplodiploid sex determination mechanisms, which in eusocial species usually require heterozygosity for female development. At the same time, haplodiploidy might account for important preadaptations that can help explain the apparent ease with which Hymenoptera transition between sexual and asexual reproduction.
- Published
- 2013
- Full Text
- View/download PDF
38. Cryptic sexual populations account for genetic diversity and ecological success in a widely distributed, asexual fungus-growing ant.
- Author
-
Rabeling C, Gonzales O, Schultz TR, Bacci M Jr, Garcia MV, Verhaagh M, Ishak HD, and Mueller UG
- Subjects
- Animals, Ants microbiology, Base Sequence, Biological Evolution, DNA, Mitochondrial genetics, Ecosystem, Female, Genetic Variation, Genetics, Population, Genome, Insect, Latin America, Male, Parthenogenesis genetics, Parthenogenesis physiology, Phylogeography, Reproduction genetics, Reproduction physiology, Reproduction, Asexual genetics, Reproduction, Asexual physiology, Ants genetics, Ants physiology
- Abstract
Sex and recombination are central processes in life generating genetic diversity. Organisms that rely on asexual propagation risk extinction due to the loss of genetic diversity and the inability to adapt to changing environmental conditions. The fungus-growing ant species Mycocepurus smithii was thought to be obligately asexual because only parthenogenetic populations have been collected from widely separated geographic localities. Nonetheless, M. smithii is ecologically successful, with the most extensive distribution and the highest population densities of any fungus-growing ant. Here we report that M. smithii actually consists of a mosaic of asexual and sexual populations that are nonrandomly distributed geographically. The sexual populations cluster along the Rio Amazonas and the Rio Negro and appear to be the source of independently evolved and widely distributed asexual lineages, or clones. Either apomixis or automixis with central fusion and low recombination rates is inferred to be the cytogenetic mechanism underlying parthenogenesis in M. smithii. Males appear to be entirely absent from asexual populations, but their existence in sexual populations is indicated by the presence of sperm in the reproductive tracts of queens. A phylogenetic analysis of the genus suggests that M. smithii is monophyletic, rendering a hybrid origin of asexuality unlikely. Instead, a mitochondrial phylogeny of sexual and asexual populations suggests multiple independent origins of asexual reproduction, and a divergence-dating analysis indicates that M. smithii evolved 0.5-1.65 million years ago. Understanding the evolutionary origin and maintenance of asexual reproduction in this species contributes to a general understanding of the adaptive significance of sex.
- Published
- 2011
- Full Text
- View/download PDF
39. Thelytokous parthenogenesis in the fungus-gardening ant Mycocepurus smithii (Hymenoptera: Formicidae).
- Author
-
Rabeling C, Lino-Neto J, Cappellari SC, Dos-Santos IA, Mueller UG, and Bacci M Jr
- Subjects
- Animals, Behavior, Animal, Ants physiology, Parthenogenesis
- Abstract
The general prevalence of sexual reproduction over asexual reproduction among organisms testifies to the evolutionary benefits of recombination, such as accelerated adaptation to changing environments and elimination of deleterious mutations. Documented instances of asexual reproduction in groups otherwise dominated by sexual reproduction challenge evolutionary biologists to understand the special circumstances that might confer an advantage to asexual reproductive strategies. Here we report one such instance of asexual reproduction in the ants. We present evidence for obligate thelytoky in the asexual fungus-gardening ant, Mycocepurus smithii, in which queens produce female offspring from unfertilized eggs, workers are sterile, and males appear to be completely absent. Obligate thelytoky is implicated by reproductive physiology of queens, lack of males, absence of mating behavior, and natural history observations. An obligate thelytoky hypothesis is further supported by the absence of evidence indicating sexual reproduction or genetic recombination across the species' extensive distribution range (Mexico-Argentina). Potential conflicting evidence for sexual reproduction in this species derives from three Mycocepurus males reported in the literature, previously regarded as possible males of M. smithii. However, we show here that these specimens represent males of the congeneric species M. obsoletus, and not males of M. smithii. Mycocepurus smithii is unique among ants and among eusocial Hymenoptera, in that males seem to be completely absent and only queens (and not workers) produce diploid offspring via thelytoky. Because colonies consisting only of females can be propagated consecutively in the laboratory, M. smithii could be an adequate study organism a) to test hypotheses of the population-genetic advantages and disadvantages of asexual reproduction in a social organism and b) inform kin conflict theory.For a Portuguese translation of the abstract, please see Abstract S1.
- Published
- 2009
- Full Text
- View/download PDF
40. Coevolution between attine ants and actinomycete bacteria: a reevaluation.
- Author
-
Mueller UG, Dash D, Rabeling C, and Rodrigues A
- Subjects
- Actinobacteria classification, Actinobacteria metabolism, Actinomycetales classification, Actinomycetales genetics, Actinomycetales metabolism, Animals, Ants classification, Ants metabolism, Ants microbiology, Female, Genetic Variation, Mycobacterium classification, Mycobacterium genetics, Phylogeny, Social Behavior, Symbiosis genetics, Actinobacteria genetics, Ants genetics, Evolution, Molecular
- Abstract
We reassess the coevolution between actinomycete bacteria and fungus-gardening (attine) ants. Actinomycete bacteria are of special interest because they are metabolic mutualists of diverse organisms (e.g., in nitrogen-fixation or antibiotic production) and because Pseudonocardia actinomycetes are thought to serve disease-suppressing functions in attine gardens. Phylogenetic information from culture-dependent and culture-independent microbial surveys reveals (1) close affinities between free-living and ant-associated Pseudonocardia, and (2) essentially no topological correspondence between ant and Pseudonocardia phylogenies, indicating frequent bacterial acquisition from environmental sources. Identity of ant-associated Pseudonocardia and isolates from soil and plants implicates these environments as sources from which attine ants acquire Pseudonocardia. Close relatives of Atta leafcutter ants have abundant Pseudonocardia, but Pseudonocardia in Atta is rare and appears at the level of environmental contamination. In contrast, actinomycete bacteria in the genera Mycobacterium and Microbacterium can be readily isolated from gardens and starter-cultures of Atta. The accumulated phylogenetic evidence is inconsistent with prevailing views of specific coevolution between Pseudonocardia, attine ants, and garden diseases. Because of frequent acquisition, current models of Pseudonocardia-disease coevolution now need to be revised. The effectiveness of Pseudonocardia antibiotics may not derive from advantages in the coevolutionary arms race with specialized garden diseases, as currently believed, but from frequent recruitment of effective microbes from environmental sources. Indeed, the exposed integumental structures that support actinomycete growth on attine ants argue for a morphological design facilitating bacterial recruitment. We review the accumulated evidence that attine ants have undergone modifications in association with actinomycete bacteria, but we find insufficient support for the reverse, modifications of the bacteria resulting from the interaction with attine ants. The defining feature of coevolution--reciprocal modification--therefore remains to be established for the attine ant-actinomycete mutualism.
- Published
- 2008
- Full Text
- View/download PDF
41. Newly discovered sister lineage sheds light on early ant evolution.
- Author
-
Rabeling C, Brown JM, and Verhaagh M
- Subjects
- Animals, Ants anatomy & histology, Base Sequence, Female, Genes, Insect, Male, Molecular Sequence Data, Ants classification, Ants genetics, Phylogeny
- Abstract
Ants are the world's most conspicuous and important eusocial insects and their diversity, abundance, and extreme behavioral specializations make them a model system for several disciplines within the biological sciences. Here, we report the discovery of a new ant that appears to represent the sister lineage to all extant ants (Hymenoptera: Formicidae). The phylogenetic position of this cryptic predator from the soils of the Amazon rainforest was inferred from several nuclear genes, sequenced from a single leg. Martialis heureka (gen. et sp. nov.) also constitutes the sole representative of a new, morphologically distinct subfamily of ants, the Martialinae (subfam. nov.). Our analyses have reduced the likelihood of long-branch attraction artifacts that have troubled previous phylogenetic studies of early-diverging ants and therefore solidify the emerging view that the most basal extant ant lineages are cryptic, hypogaeic foragers. On the basis of morphological and phylogenetic evidence we suggest that these specialized subterranean predators are the sole surviving representatives of a highly divergent lineage that arose near the dawn of ant diversification and have persisted in ecologically stable environments like tropical soils over great spans of time.
- Published
- 2008
- Full Text
- View/download PDF
42. A breakthrough innovation in animal evolution.
- Author
-
Mueller UG and Rabeling C
- Subjects
- Animals, Behavior, Animal, Ecosystem, Fungi growth & development, Ants genetics, Biological Evolution
- Published
- 2008
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.