Strumigenys lanuginosa

Strumigenys lanuginosa
Scientific classification
Kingdom:	Animalia
Phylum:	Arthropoda
Class:	Insecta
Order:	Hymenoptera
Family:	Formicidae
Subfamily:	Myrmicinae
Tribe:	Attini
Genus:	Strumigenys
Species:	S. lanuginosa
Binomial name
	Strumigenys lanuginosa; Wheeler, W.M., 1905 Specimen labels

Strumigenys lanuginosa occurs across a range of habitats, from wet and dry forests, to dry scrub, to urban gardens (Wetterer 2017). It nests in dead wood on the ground (Longino, Ants of Costa Rica).

At a Glance

• Limited invasive

Identification

Bolton (2000) - A member of the lanuginosa complex in the Strumigenys hindenburgi-group. With characters of lanuginosa-complex and instantly diagnosed by the following.

Brown 1962.

1 Upper scrobe margin with two long, freely projecting flagellate hairs, the first of these above the eye, the second apicoscrobal.

2 Mandible with a single preapical tooth that is close to the apicodorsal tooth, without a more proximal preapical tooth or denticle.

Sculpture of the first gastral tergite is variable. In most samples from Mexico and one from Costa Rica the sclerite is finely and densely striolate over its basal third, distal of which it is smooth. In most Costa Rica samples and those from Colombia and the Bahamas (where it is probably an introduction) the entire sclerite from base to apex is blanketed by the dense striolate sculpture. Apparently the two forms occur together only in Costa Rica, where the difference between them is quite striking. This may be an example of character displacement and imply that there are really two species present, but a more detailed analysis with more material will be necessary to test the hypothesis.

Apart from the diagnostic characters above, lanuginosa differs from Strumigenys vilhenai by having a broader head and shorter scapes (compare indices).

Longino (Ants of Costa Rica) - Apical fork of mandible with single intercalary tooth; mandible with single conspicuous preapical tooth near apical fork; eye composed of approximately 20 facets; basal fourth to all of first gastral tergum finely longitudinally striolate, opaque-sericeous, noncostulate portion of tergum (if any) smooth and shining; gaster covered with dense brush of flagelliform setae.

Wheeler (1905) - S. lanuginosa is closely related to Strumigenys unidentata, Strumigenys unispinulosa, Strumigenys imitator, Strumigenys louisianae, and Strumigenys fusca. It differs from the first in having perfectly straight mandibles, from the second in having the head much narrower in front, spongiform appendages on the petiole, no clavate or squamiform hairs, etc.; from the third in having a distinct tooth on the inner border of the mandibles just behind the two apical teeth; from the fourth in having the preapical mandibular spine shorter, and in lacking the club-shaped and scale-like hairs on the body; from the last in its smaller size, in having a shorter preapical spine, the head narrower in front, spongiform appendages on the petiole, etc.

Keys including this Species

Distribution

Central America, Caribbean islands and Florida. Deyrup et al. (2000) suggested this ant was introduced in Florida as it is a rare species found in mesic woods in Dade and Monroe counties. Wetterer (2017) showed the range of this species is more extensive in the Caribbean than previously thought, which he suggested makes it more likely S. lanuginosa reaches its native northern limit in Florida.

Latitudinal Distribution Pattern

Latitudinal Range: 23.133° to 4.088888889°.


North Temperate	North Subtropical	Tropical	South Subtropical	South Temperate

Source: AntMaps

Distribution based on Regional Taxon Lists

Nearctic Region: United States.
Neotropical Region: Bahamas (type locality), Colombia, Costa Rica, Cuba, Dominican Republic, Greater Antilles, Guatemala, Honduras, Mexico, Panama, Venezuela.

Distribution based on AntMaps

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.

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.

Biology

Wheeler (1905) - Described from a single worker and five females taken in and about Nassau (in the Queen's Staircase and the moat around Fort Charlotte). The females were in the act of founding their colonies. Each was found under a stone covering a nest of Tetramorium simillimum, Pheidole flavens, or Monomorium ebeninum. This fact suggests that the new species, like several other species of the genus Strumigenys, habitually forms compound nests with other ants.

Castes

Worker

Images from AntWeb


Worker. Specimen code casent0105875. Photographer Dan Kjar, uploaded by California Academy of Sciences.	Owned by USNM, Washington, DC, USA.


Worker. Specimen code casent0178644. Photographer April Nobile, uploaded by California Academy of Sciences.	Owned by MIZA, Maracay, Venezuela.


Worker. Specimen code inbiocri001281641. Photographer D. J. Cox, uploaded by California Academy of Sciences.	Owned by JTLC.

Nomenclature

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

lanuginosa. Strumigenys lanuginosa Wheeler, W.M. 1905b: 104, fig. M (w.q.) BAHAMAS. See also: Brown, 1961a: 62; Bolton, 2000: 521.

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

Description

Worker

Length 2.25 mm.

Head much narrowed in front, broadened behind, with deeply and roundly excised posterior margin and rounded posterior angles. Eyes in the middle of the sides of the head where there are also well-developed scrobes for the accommodation of the antennal scapes. Mandibles straight, linear, with parallel inner and outer borders, a little over half as long as the head, with two prominent teeth bent in at right angles at the tip, and a short but distinct tooth on the inner border just behind the tip. Clypeus triangular, equilateral, its posterior border straight, not extending over the base of the mandibles. Antennal scape about half as long as the head exclusive of the mandibles, slender at the base, but rapidly enlarging towards the tip, where it again narrows. Terminal funicular joint as long as the four basal joints taken together; first and fourth joints subequal, each somewhat longer than the second and third joints taken together. Thorax with distinct mesoepinotal constriction. Pronotum flattened, with sharp humeral angles, distinctly marginate in front and along the sides, and longitudinally carinate on the middle of its posterior half. Epinotum armed with two acute spines which are somewhat longer than broad at their bases, further apart than long, directed backward and slightly outward, and produced below as very small membranous lamina. Both the petiole and postpetiole with prominent spongiform appendages on their posterior and inferior surfaces; postpetiole half again as broad as the petiole; nodes of both semicircular from above, straight in front and convex behind; in profile the anterior slope of the petiolar node is gradual and concave. First gastric segment with spongiform appendages on its anterior and inferior border.

Mandibles smooth, subopaque. Head, thorax, petiole, and postpetiole opaque, densely punctate; thoracic dorsum somewhat rugulose. Gaster smooth and shining, first segment above opaque, with very fine longitudinal striae.

Body and appendages covered with long, delicate, flexuous, yellowish hairs, which are largely reclinate or appressed on the head, thorax, and legs, but sub-erect, very conspicuous, and abundant on the gaster. There are no club-shaped or obtuse hairs, and the curved hairs on the anterior border of the antennal scapes are inconspicuous.

Ferruginous brown; petiole, postpetiole, and gaster darker; mandibles, antennae, and legs more yellow. Mandibular teeth black.

Bolton (2000) - TL 2.3-2.6, HL 0.54-0.62, HW 0.44-0.48, CI 77-84, ML 0.31-0.39, MI 57-64, SL 0.30-0.38, SI 70-80, PW 0.27-0.32, AL 0.56-0.66.

Queen

Length 2.5-2.8 mm.

Resembling the worker very closely, except in the structure of the thorax. The basal surface of the epinotum is long, oblique, and distinctly concave. The inferior membranous lamime of the epinotal spines is more extensive. The spongiform appendages on the petiole, postpetiole, and basal gastric segment are very conspicuous. Color and pilosity as in the worker; alar insertions black.

Type Material

Described from a single worker and five females taken in and about Nassau (in the Queen's Staircase and the moat around Fort Charlotte).

Bolton (2000) - Syntype worker and queens, BAHAMAS: Nassau, v-vi.1904 (W. M. Wheeler) (American Museum of Natural History, Museum of Comparative Zoology) [examined].

References

Bolton, B. 2000. The ant tribe Dacetini. Memoirs of the American Entomological Institute. 65:1-1028. (page 521, catalogue)
Brown, W. L., Jr. 1961. The neotropical species of the ant genus Strumigenys Fr. Smith: miscellaneous concluding studies. Psyche. 68:58-69. (page 62, redescription)
Brown, W. L., Jr. 1962c. The neotropical species of the ant genus Strumigenys Fr. Smith: synopsis and keys to the species. Psyche. 69:238-267.
Deyrup, M., Davis, L. & Cover, S. 2000. Exotic ants in Florida. Transactions of the American Entomological Society 126, 293-325.
Franco, W., Ladino, N., Delabie, J.H.C., Dejean, A., Orivel, J., Fichaux, M., Groc, S., Leponce, M., Feitosa, R.M. 2019. First checklist of the ants (Hymenoptera: Formicidae) of French Guiana. Zootaxa 4674, 509–543 (doi:10.11646/zootaxa.4674.5.2).
Lubertazzi, D. 2019. The ants of Hispaniola. Bulletin of the Museum of Comparative Zoology, 162(2), 59-210 (doi:10.3099/mcz-43.1).
MacGown, J.A., Wetterer, J.K. 2013. Distribution and biological notes of Strumigenys margaritae (Hymenoptera: Formicidae: Dacetini). Terrestrial Arthropod Reviews 6, 247–255 (doi:10.1163/18749836-06001066).
Wetterer, J. K. 2017. Geographic distribution of Strumigenys lanuginosa (Hymenoptera: Formicidae). Transactions of the American Entomological Society. 143:729-733.
Wheeler, W. M. 1905c. The ants of the Bahamas, with a list of the known West Indian species. Bull. Am. Mus. Nat. Hist. 21: 79-135 (page 104, worker described)

References based on Global Ant Biodiversity Informatics

Achury R., and A.V. Suarez. 2017. Richness and composition of ground-dwelling ants in tropical rainforest and surrounding landscapes in the Colombian Inter-Andean valley. Neotropical Entomology https://doi.org/10.1007/s13744-017-0565-4
Ahuatzin D. A., E. J. Corro, A. Aguirre Jaimes, J. E. Valenzuela Gonzalez, R. Machado Feitosa, M. Cezar Ribeiro, J. Carlos Lopez Acosta, R. Coates, W. Dattilo. 2019. Forest cover drives leaf litter ant diversity in primary rainforest remnants within human-modified tropical landscapes. Biodiversity and Conservation 28(5): 1091-1107.
Basset Y., L. Cizek, P. Cuenoud, R. K. Didham, F. Guilhaumon, O. Missa, V. Novotny, F. Odegaards, T. Roslin, J. Schmidl et al. 2012. Arthropod diversity in a tropical forest. Science 338(6113): 1481-1484.
Bolton, B. 2000. The Ant Tribe Dacetini. Memoirs of the American Entomological Institute 65
Brown W. L. Jr. 1962. The neotropical species of the ant genus Strumigenys Fr. Smith: synopsis and keys to the species. Psyche (Cambridge) 69: 238-267.
Dattilo W. et al. 2019. MEXICO ANTS: incidence and abundance along the Nearctic-Neotropical interface. Ecology https://doi.org/10.1002/ecy.2944
Donoso D. A. 2014. Assembly mechanisms shaping tropical litter ant communities. Ecography 37 doi: 10.1111/j.1600-0587.2013.00253.x
Fernandes, P.R. XXXX. Los hormigas del suelo en Mexico: Diversidad, distribucion e importancia (Hymenoptera: Formicidae).
Fernández, F. and S. Sendoya. 2004. Lista de las hormigas neotropicales. Biota Colombiana Volume 5, Number 1.
Fontanla Rizo J.L. 1997. Lista preliminar de las hormigas de Cuba. Cocuyo 6: 18-21.
Fontenla J. L., and J. Alfonso-Simonetti. 2018. Classification of Cuban ants (Hymenoptera: Formicidae) into functional groups. Poeyana Revista Cubana de Zoologia 506: 21-30.
Fontenla Rizo J. L. 1993. Mirmecofauna de Isla de la Juventud y de algunos cayos del archipielago cubano. Poeyana. Instituto de Ecologia y Sistematica, Academia de Ciencias de Cuba 444:1-7.
Fontenla Rizo J. L. 1997. Lista preliminar de las hormigas de Cuba (Hymenoptera: Formicidae). Cocuyo 6: 18-21.
Franco W., N. Ladino, J. H. C. Delabie, A. Dejean, J. Orivel, M. Fichaux, S. Groc, M. Leponce, and R. M. Feitosa. 2019. First checklist of the ants (Hymenoptera: Formicidae) of French Guiana. Zootaxa 4674(5): 509-543.
Groc S., J. H. C. Delabie, F. Fernandez, M. Leponce, J. Orivel, R. Silvestre, Heraldo L. Vasconcelos, and A. Dejean. 2013. Leaf-litter ant communities (Hymenoptera: Formicidae) in a pristine Guianese rainforest: stable functional structure versus high species turnover. Myrmecological News 19: 43-51.
Groc S., J. Orivel, A. Dejean, J. Martin, M. Etienne, B. Corbara, and J. H. C. Delabie. 2009. Baseline study of the leaf-litter ant fauna in a French Guianese forest. Insect Conservation and Diversity 2: 183-193.
Kaspari M., D. Donoso, J. A. Lucas, T. Zumbusch, and A. D. Kay. 2012. Using nutritional ecology to predict community structure: a field test in Neotropical ants. Ecosphere 3(11): art.93.
Kempf, W.W. 1972. Catalago abreviado das formigas da regiao Neotropical (Hym. Formicidae) Studia Entomologica 15(1-4).
Levings S. C. 1983. Seasonal, annual, and among-site variation in the ground ant community of a deciduous tropical forest: some causes of patchy species distributions. Ecological Monographs 53(4): 435-455.
Longino J. T. 2013. Ants of Nicargua. Consulted on 18 Jan 2013. https://sites.google.com/site/longinollama/reports/ants-of-nicaragua
Longino J. T. L., and M. G. Branstetter. 2018. The truncated bell: an enigmatic but pervasive elevational diversity pattern in Middle American ants. Ecography 41: 1-12.
Longino J. T., J. Coddington, and R. K. Colwell. 2002. The ant fauna of a tropical rain forest: estimating species richness three different ways. Ecology 83: 689-702.
Longino J. et al. ADMAC project. Accessed on March 24th 2017 at https://sites.google.com/site/admacsite/
Mirmecofauna de la reserva ecologica de San Felipe Bacalar
Silva T. S. R., and R. M. Feitosa. 2019. Using controlled vocabularies in anatomical terminology: A case study with Strumigenys (Hymenoptera: Formicidae). Arthropod Structure and Development 52: 1-26.
Smith M. A., W. Hallwachs, D. H. Janzen. 2014. Diversity and phylogenetic community structure of ants along a Costa Rican elevational gradient. Ecography 37(8): 720-731.
Vásquez-Bolaños M. 2011. Lista de especies de hormigas (Hymenoptera: Formicidae) para México. Dugesiana 18: 95-133
Wetterer J. K. 2017. Geographic distribution of Strumigenys lanuginosa (Hymenoptera: Formicidae). Transactions of the American Entomological Society, 143(4):729-733.