Crematogaster pygmaea

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Crematogaster pygmaea
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Subfamily: Myrmicinae
Tribe: Crematogastrini
Genus: Crematogaster
Species: C. pygmaea
Binomial name
Crematogaster pygmaea
Forel, 1904

Crematogaster pygmaea casent0628114 p 1 high.jpg

A ground-nesting ant from northeastern Brazil. It is a habitat specialist in coastal and tabuleiro zones, where it forms extensive polydomous and polygynous colonies that nest in the soil. Workers forage extensively on honeydew and extrafloral nectar, and foraging continues day and night, although it is depressed at ground temperatures above 32°C. Gyne production occurs at the beginning of the rainy season, while male production starts in the dry season, some months before gyne production. (Quinet et al. 2009)


At a Glance • Polygynous  

Identification

Quinet et al. (2009) - Taxonomic conclusions are based on abundant collections and natural history observations from Fortaleza, State of Ceará, Brazil. These collections were compared directly with the types of C. pygmaea. Crematogaster pygmaea is very close to the widespread Crematogaster abstinens. Both species occur sympatrically in Fortaleza, where they are clearly distinct.

Crematogaster pygmaea and C. abstinens are uniquely characterized by the combination in the worker of (1) shiny face, (2) subquadrate dorsal face of petiole, (3) appressed tibial pilosity, (4) very wide postpetiole, (5) abundant short stiff setae on face that curve toward the median axis, and (6) complete absence of an anteroventral petiolar tooth. Crematogaster pygmaea differs from C. abstinens in shorter propodeal spines. The propodeal spines of C. pygmaea are relatively triangular in shape, not spiniform, and slightly longer than the maximum diameter of the propodeal spiracle. The propodeal spines of C. abstinens are spiniform and about twice as long as the maximum diameter of the propodeal spiracle. Another difference in the zone of sympatry is that C. abstinens has a more heavily sculptured promesonotum, particularly near the juncture of dorsal and lateral surfaces. However, in other parts of the range of C. abstinens this character is variable and approaches the condition seen in C. pygmaea. Crematogaster obscurata is also similar to these species but has a punctate face.

Distribution

NE Brazil.

Latitudinal Distribution Pattern

Latitudinal Range: -3.783333333° to -3.783333333°.

 
North
Temperate
North
Subtropical
Tropical South
Subtropical
South
Temperate

Distribution based on Regional Taxon Lists

Neotropical Region: Brazil (type locality).

Distribution based on AntMaps

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Distribution based on AntWeb specimens

Check data from AntWeb

Countries Occupied

Number of countries occupied by this species based on AntWiki Regional Taxon Lists. In general, fewer countries occupied indicates a narrower range, while more countries indicates a more widespread species.
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Estimated Abundance

Relative abundance based on number of AntMaps records per species (this species within the purple bar). Fewer records (to the left) indicates a less abundant/encountered species while more records (to the right) indicates more abundant/encountered species.
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Habitat

Quinet et al. (2009) - The state of Ceará belongs to the “caatinga” domain, a 750,000 km2 area of northeastern Brazil with a semiarid climate. Temperature varies little, with an annual average of approximately 26 C, and rainfall is low (less than 750 mm/year). Rainfall is concentrated in three consecutive months during the southern hemisphere summer (November until June). Crematogaster pygmaea occurs in two phytogeographic zones: the littoral zone stricto sensu and the adjacent savana-like formation called “tabuleiro.” The first is a narrow strip of coastal vegetation along the seashore, with dune and mangrove formations. The tabuleiro is a savanna-like formation that occurs close to the coast, on flat sandy plains of northeastern Brazil. The physiognomy of the “tabuleiro” is characterized by dense patches of trees and shrubs surrounded by a grassy cover with scattered low shrubs (Oliveira-Filho 1993). All the observed C. pygmaea colonies were found in these two zones. Colonies could be found very near the sea, in completely sandy areas with only grassy cover. Crematogaster pygmaea was never found in the “caatinga” zone, a seasonal xerophilous thorn woodland/shrubland that prevails on the semi-arid lowlands and covers most of Ceará state.

Biology

Quinet et al. (2009) - Detailed observations were made of four C. pygmaea colonies (I, II and III, IV) at sites situated on or near the campus of the State University of Ceará (3° 47' S – 38° 33' W), in Fortaleza (state of Ceará, northeastern Brazil), about 7 km from the coast. The campus itself is located in the tabuleiro zone. In the study sites the original vegetation was modified by human activities, being in the campus and Fortaleza urban areas.

Colony I was located on the campus, in a sandy/clayey area with patches of mango or cashew trees surrounded by dense herbaceous cover. Very close to colony I and physically separated from it by an asphalt road, colony II was in a more open area. The area had rows of square beds with fodder plants separated by sandy/clayey areas covered with sparse herbaceous vegetation. Patches of mango trees, sugar cane and dense herbaceous vegetation surrounded it. Colony III was located on the campus, some 800m from colonies I and II, in an open sandy/clayey area with only herbaceous cover. Colony IV was located outside, but close to the campus, in an open area covered with dense herbaceous vegetation and patches of low shrubs surrounding sports (football) grounds.

Colony I extended over an area about 26 by 10m. It consisted of 36 nest entrances connected by nearly 104m of trails that also led the workers to plants where they explored liquid sugary food sources (nectar or honeydew). One hundred herbaceous plants were visited by ants. Nearly 50 % of them (N = 46) were Borreria verticillata G. Mey. plants (Rubiaceae) whose floral nectaries were explored by C. pygmaea workers. Some B. verticillata plants also had scale insects (Coccidae) colonies attended by ants for their honeydew production. The second and third most visited plants (N = 27 and 12 respectively) were two unknown Cyperaceae species where C. pygmaea workers attended scale insect colonies. On the remaining plants (N = 15) (Commelina sp. – Commelinaceae; Mimosa sensitiva L. – Mimosaceae; Turnera subulata Smith– Turneraceae; one unknown species of Papilionaceae; one unknown species of Cyperaceae; one species of unknown family) ants explored sugary secretions from scale insects, aphids (Aphididae), and/or extrafloral nectaries.

Colony II had roughly the same size (about 30 by 8m) and consisted of 62 nest entrances connected by nearly 75m of trail network. More than 50% of the 97 herbaceous plants visited by ants (N = 54) were T. subulata plants (white alder), a common ruderal plant in northeastern Brazil. The petiole of T. subulata leaves has two large apical extrafloral nectaries that were explored by C. pygmaea workers. The second most visited plant was B. verticillata (N = 27) whose floral nectaries and, sometimes, aphids or scale insect colonies were explored by ants. The remaining plants belonged to Asteraceae, Euphorbiaceae, Fabaceae, Plumbaginaceae and Poaceae families and had scale insect colonies attended by ants.

In each colony, one or two groups of nest entrances were disconnected from the main group. They probably represented colony disjunctions, since preliminary observations showed that the trail network of a C. pygmaea colony is an unstable structure that undergoes size and shape modifications with time. For example, during the dry season the trail network undergoes a great size reduction.

Quinet et al. 2009

In order to investigate nest architecture and composition, 72 C. pygmaea nests were excavated: 20 from colony I, in June and July 2002; 37 from colony II, in June 2003; and 25 from colony IV, in May 2006. For the nests of colony I and the first ten nest excavations of colony II, only queen number and brood presence (colony I), or number and depth of chambers per nest were recorded (colony II). More detailed observations were made with the remaining nests of colony II and those of colony IV: nest depth, number of chambers per nest, depth and size of chambers, number of queens per chamber and presence of brood in chambers. Nest excavation was carried out by digging a deep soil parallelepiped (20 x 20 x 40 cm), with the nest entrance in its center. The whole parallelepiped was carefully laid down on a plastic sheet, and then cut into thin slices with a spatula, starting from the side with the nest entrance. Depth and, when possible, size of each chamber was recorded, as well as the queen number and presence of brood. Thirteen of the 34 active nests (i.e. with at least workers) excavated in June 2003 were brought to the laboratory to count the queens and workers. Finally, the diameter of 52 nest entrances from 4 colonies (colony I, II, IV, and a fifth one) was measured in March 2003 and April 2008.

Eleven to 40% of the excavated nests were inactive, meaning that there was neither gallery nor chamber below the nest entrance, in spite of workers entering and exiting the nest entrance. Of the remaining, active, nests (i.e. with gallery, chambers, and at least workers in the chambers), almost all (92–100%) contained brood, and 47–71% contained at least one queen. Colonies were clearly polygynous, with some nests containing more than 10 queens.

Nests had a maximum depth of nearly 30cm and each of them was formed by a single straight vertical gallery with 1 to 4 horizontal chambers. The depth of the first chamber varied depending on the number of chambers. When there were multiple chambers, the first chamber tended to be shallower. Chambers had a circular, or oval, shape with a mean thickness of 4.9 + 0.9 mm (N = 16) and a diameter of roughly 3 cm. Galleries always entered the center of a chamber from above and continued from the center of the chamber floor. Nest entrance had a mean diameter of 1.89 + 0.15 mm (N = 52) and the gallery had exactly the same diameter. It is therefore possible to describe the typical structure of a C. pygmaea nest as a straight vertical gallery, 20 cm in length and 1.9 mm in diameter, with a circular entrance 1.9 mm in diameter, and generally 3 circular or oval chambers that are 5 mm thick and 3 cm in diameter, giving a 6.9 cm3 total nest volume. Nests were measured in the rainy season, when the soil was humid. During the dry season, the soil was very hard, making it almost impossible to dig. However, a few attempts showed that the galleries and chambers were much deeper in the dry season.

Fifty queens and 4644 workers were found in the 13 nests analyzed in the laboratory, giving a queen/worker ratio of nearly 1:100.

Foraging activity of C. pygmaea was recorded during four 24 hours periods: the first in February 2000, the second in December 2000, the third in October 2001, and the fourth in September 2006. In each of the first three 24 hour recording periods, all carried out with colony I, activity was recorded at two nest entrances and on one foraging trail. In the fourth one, carried out with colony II, activity was recorded at three nest entrances and on three foraging trails. During a 24 hour period, all ants crossing a point on the selected trail(s), and all ants exiting or entering the selected nest entrances were recorded with a click counter during a 5 minute session, at 1-h intervals. Soil temperature was monitored at each recording point, for each activity measurement.

C. pygmaea forages day and night. However, foraging activity is temperature dependent since it stopped between 10:00 a.m. and midday, when soil temperature exceeded 40°C. A slight reduction of foraging activity was also observed just before dawn, when soil temperature dropped below 30°C. Foraging activity tended to peak at sunrise, when soil temperature began to rise after low night temperatures. Foraging activity is high between 24 and 32°C, above which it drops.

Reproductive phenology of C. pygmaea was investigated by excavating about ten nests of colony II and III each month, from March 2005 to March 2006. The number of queens, gynes and males found in each nest was recorded. Rainfall data were obtained from the Ceará state fundation of meteorology (FUNECE).

The mean number of queens per nest was nearly constant (+ 2 queens/nest) during most part of the year. At the beginning of the rainy season (January to March), it rose to nearly six queens per nest. Gynes were observed at the beginning of the rainy season, with a mean number reaching up to 17 gynes per nest in February. Males production began in the dry season, some three months before gyne production, and continued during the rainy season, reaching mean number of up to 9 per nest.

The presence of several reproductive females in the same nest (polygyny) is frequently observed in ants, and in most cases, nests of polygynous species contain no more than ten queens (Keller, 1993; Crozier & Pamilo, 1996). However, some species have a highly polygynous social structure characterized by a queen/worker ratio between 1:200 and 1:50. Moreover, most of the highly polygynous species so far studied are invasive/tramp species that are also characterized by lack of hostility between colonies (unicoloniality), like in Linepithema humile, Monomorium pharaonis, Tapinoma melanocephalum, or Solenopsis invicta (Passera, 1994; Tsutsui & Suarez, 2003).

This contrasts with the situation observed in C. pygmaea whose high polygynous social struture is not associated with invasive behavior. Moreover, field observations have shown that workers from different colonies interact in a hostile way (Hamidi et al., in prep.). High polygyny associated with non-invasive behavior and territoriality has also been found in Dolichoderus mariae (Laskis & Tschinkel, 2008), a North American species that shares many traits with C. pygmaea. Both are ground-dwelling species with highly polygynous and polydomous colonies whose nests are connected by an above ground trail network, and they heavily rely on sugared solutions collected from hemipteran colonies and/or nectaries. Moreover, in both species, nest location seems to be strongly related to the food source location and there is marked seasonal polydomy, with colony retraction during winter (D. mariae) or dry season (C. pygmaea) and colony expansion during spring-summer (D. mariae) or rainy season (C. pygmaea). It has been suggested that the seasonal polydomy of D. mariae represents a response to the seasonal fluctuations of food source location and abundance, allowing the ants to closely track hemipteran populations (Laskis & Tschinkel, 2008). The polydomy of C. pygmaea could also represent an adaptation to exploit dispersed and rapidly changing food sources (nectaries and hemipteran colonies).

The main elements of C. pygmaea nests are consistent with the nest architecture generally observed in ant species that excavate nests in soil, i.e. vertical tunnels connecting horizontal chambers (Tschinkel, 2003). However, compared to other ant species with subterranean nests, C. pygmaea nests are small and very simple, the average nest being no more than a single 20 cm straight vertical gallery connecting three small horizontal chambers, at least during the rainy season. Most ant species whose subterranean nest architecture has been investigated have much more complex nests, like in Pogonomyrmex badius, Solenopsis invicta, Prenolepis imparis or Formica pallidefulva (Tschinkel, 2003). Pogonomyrmex badius, whose deep nests (up to 3.5 m) may contain four or five vertical tunnels connecting up to 150 chambers, is one of the best known examples of such complex nests (Tschinkel, 2004). The smaller and shallower nests of Formica pallidefulva with its multiple branching tunnels are another example (Mikheyev & Tschinkel, 2004). Although formed by a single shallow conical chamber, the nests of Dolichoderus mariae are much larger, with a 930 cm3 mean volume (Laskis & Tschinkel, 2008), than those of C. pygmaea that are only about 7 cm3 in volume. The simple architecture of C. pygmaea nests could be related to the need to have a flexible colony structure, with nests and trail networks able to track food sources that frequently change location.

In conclusion, the high polygyny found in C. pygmaea, combined with other prominent features (noninvasive behavior, high polydomy, strong worker/queen dimorphism, ground-nesting habits, simple nest architecture), make this species a particularly interesting model to investigate the selective pressures that allowed the evolution and the maintenance of a social structure in which workers rear genetically distant brood.

Castes

In this and other species (e.g. Crematogaster biroi and Crematogaster schimmeri) belonging to subgenus Orthocrema, a third caste exists that is intermediate in size, weight and morphology between winged queens and workers. These individuals are numerically few in the colonies, and lay many unfertilized eggs that are mostly eaten by larvae. Histology confirmed the lack of a spermatheca, hence sexual reproduction is impossible. Using scanning electron microscopy and ovarian dissections, Peeters et al. (2013) showed that this third caste is a patchwork of queen-like and worker-like traits. It is a soldier caste with a specialized trophic function. These soldiers are produced seasonally in C. pygmaea, not in Crematogaster schimmeri.

Comparison of all three female castes as well as males in C. pygmaea, showing the large size differences. Photo by Christian Peeters
Dorsal SEMs of thorax of three castes (Q: queen, S: soldier; W: worker)'. Note different sizes and degrees of fusion of flight sclerites. Photo by Johan Billen


Worker

Images from AntWeb

Crematogaster pygmaea casent0904523 h 1 high.jpgCrematogaster pygmaea casent0904523 p 1 high.jpgCrematogaster pygmaea casent0904523 d 1 high.jpgCrematogaster pygmaea casent0904523 l 1 high.jpg
Type of unpublished name: Crematogaster pygmaea divergensWorker. Specimen code casent0904523. Photographer Z. Lieberman, uploaded by California Academy of Sciences. Owned by MSNG, Genoa, Italy.
Crematogaster pygmaea casent0906661 h 1 high.jpgCrematogaster pygmaea casent0906661 p 1 high.jpgCrematogaster pygmaea casent0906661 d 1 high.jpgCrematogaster pygmaea casent0906661 l 1 high.jpg
Worker. Specimen code casent0906661. Photographer Estella Ortega, uploaded by California Academy of Sciences. Owned by CAS, San Francisco, CA, USA.
Crematogaster pygmaea casent0906662 h 1 high.jpgCrematogaster pygmaea casent0906662 p 1 high.jpgCrematogaster pygmaea casent0906662 d 1 high.jpgCrematogaster pygmaea casent0906662 l 1 high.jpg
Worker. Specimen code casent0906662. Photographer Estella Ortega, uploaded by California Academy of Sciences. Owned by CAS, San Francisco, CA, USA.

Queen

Images from AntWeb

Crematogaster pygmaea casent0906663 h 1 high.jpgCrematogaster pygmaea casent0906663 p 1 high.jpgCrematogaster pygmaea casent0906663 p 2 high.jpgCrematogaster pygmaea casent0906663 d 1 high.jpgCrematogaster pygmaea casent0906663 l 1 high.jpg
Queen (alate/dealate). Specimen code casent0906663. Photographer Estella Ortega, uploaded by California Academy of Sciences. Owned by CAS, San Francisco, CA, USA.
Crematogaster pygmaea jtlc000003537 h 1 high.jpgCrematogaster pygmaea jtlc000003537 p 1 high.jpg
Queen (alate/dealate). Specimen code jtlc000003537. Photographer J. Longino, uploaded by University of Utah. Owned by JTLC.

Male

Images from AntWeb

Crematogaster pygmaea casent0906664 h 1 high.jpgCrematogaster pygmaea casent0906664 d 1 high.jpgCrematogaster pygmaea casent0906664 p 1 high.jpgCrematogaster pygmaea casent0906664 p 2 high.jpgCrematogaster pygmaea casent0906664 p 3 high.jpgCrematogaster pygmaea casent0906664 l 1 high.jpg
Male (alate). Specimen code casent0906664. Photographer Estella Ortega, uploaded by California Academy of Sciences. Owned by CAS, San Francisco, CA, USA.

Nomenclature

The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.

  • pygmaea. Crematogaster pygmaea Forel, 1904c: 37 (w.) BRAZIL (Ceará).
    • Type-material: syntype workers (number not stated).
    • Type-locality: Brazil: Ceará (Diaz da Rocha).
    • Type-depository: MHNG.
    • Quinet, et al. 2009: 47 (q.).
    • Combination in C. (Orthocrema): Emery, 1922e: 135.
    • Subspecies of brevispinosa: Forel, 1909a: 259.
    • Junior synonym of abstinens: Longino, 2003a: 30.
    • Status as species: Forel, 1912f: 215; Emery, 1922e: 135; Borgmeier, 1927c: 96; Kempf, 1972a: 88; Bolton, 1995b: 160; Quinet, et al. 2009: 45 (redescription).
    • Distribution: Brazil.

Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.

Description

Worker

Quinet et al. (2009) - HL (head length; perpendicular distance from line tangent to rearmost points of vertex margin to line tangent to anteriormost projections of clypeus, in full face view) 0.565, HW (head width; maximum width of head in face view, including eyes if they project beyond the sides of the head) 0.604, SL (scape length; length of scape shaft from apex to basal flange, not including basal condyle and neck) 0.436, EL (eye length, measured along maximum diameter) 0.174, WL (Weber's length; viewing mesosoma in lateral profile, distance from approximate inflection point, where downward sloping pronotum curves into anteriorly projecting neck, to posteroventral propodeal lobes) 0.609, SPL (propodeal spine length; measured from tip of propodeal spine to closest point on outer rim of propodeal spiracle) 0.076, PTH (petiole height; viewed in lateral profile, perpendicular distance from ventral margin to highest point of posterolateral tubercles) 0.124, PTL (petiole length; viewed in lateral profile and measured in same plane as anterodorsal face, distance from inflection point marking juncture of posterolateral lobes and cylindrical posterior portion of segment to anterior inflection point where petiole curves up to condyle) 0.217, PTW (petiole width; maximum width of petiole in dorsal view) 0.217, PPL (postpetiole length; viewed dorsally, perpendicular distance from narrowest point of peduncle joining postpetiolar node and helcium, to line tangent to posteriormost lobes) 0.155, PPW (postpetiole width; maximum width of postpetiole, in same view as and perpendicular to postpetiole length) 0.201.

Queen

Quinet et al. (2009) - HL 0.998, HW 1.330, SL 0.671, EL 0.364, WL 2.402, PTH 0.399, PTL 0.538, PTW 0.574, PPL 0.431, PPW 0.643.

Type Material

Quinet et al. (2009) - Syntype worker: Brazil, Ceará (Diaz da Rocha) Musee d'Histoire Naturelle Genève (examined).

References

References based on Global Ant Biodiversity Informatics

  • Forel A. 1912. Formicides néotropiques. Part III. 3me sous-famille Myrmicinae (suite). Genres Cremastogaster et Pheidole. Mémoires de la Société Entomologique de Belgique. 19: 211-237.
  • Kempf, W.W. 1972. Catalago abreviado das formigas da regiao Neotropical (Hym. Formicidae) Studia Entomologica 15(1-4).
  • Quinet Y., R. Hamid, M. X. Ruiz-Gonzalez, J. C. de Biseau, and J. T. Longino. 2009. Crematogaster pygmaea (Hymenoptera: Formicidae, Myrmicinae), a highly polygynous and polydomous Crematogaster from northeastern Brazil. Zootaxa 2075: 45-54.