Abstract
Background
La Réunion Island (Mascarene Archipelago, south-western Indian Ocean) hosts a largely introduced ant fauna, shaped by historical and ongoing human-mediated introductions. Despite previous inventories, the ant fauna of the Island remains incompletely documented and updated faunistic records are needed to refine species checklists and improve knowledge of regional biodiversity. Documenting new occurrences contributes to a better understanding of species distributions, biogeographic patterns and invasion dynamics on oceanic islands, which are particularly vulnerable to biological invasions.
New information
Following recent fieldwork, we report eight new species for La Réunion Island: Brachymymex australis Forel, 1901; Cardiocondyla obscurior Wheeler, 1929; Monomorium exiguum Forel, 1894; Pheidole parva Mayr, 1865; Solenopsis globularia Smith, 1858; Solenopsis gr. pygmaea, Stigmatomma cf. zwaluwenburgi Williams, 1946; and Strumigenys membranifera Emery, 1869. All are introduced species with varying invasiveness status. This work brings the total number of ants known from La Réunion Island to 62, although the presence and identification of some species cited in literature and databases needs verification. Further collections may uncover additional introduced species in urbanised and anthropogenised habitats and native species specific to La Réunion Island or the Mascarene Islands in natural ecosystems.
Keywords: Mascarene Islands, introduced species, invasive ants, Indian Ocean islands, biodiversity inventory
Introduction
Oceanic islands are particularly sensitive to biological invasions and their ant faunas are often dominated by introduced species. Based on the most recent published sources reporting ants from La Réunion Island, a French overseas territory in the Mascarene Archipelago (Indian Ocean Blard et al. 2003, Fisher and Bolton 2016, Mévergnies et al. 2024, AntWeb 2024, AntWiki 2024), a total of 54 ant species are currently documented from the Island. Amongst them, 41 species are introduced, whereas 11 species are native (Camponotus hova Forel, 1891; Camponotus maculatus Fabricius, 1782; Hypoponera ludovicae Forel, 1892; Monomorium termitobium Forel, 1892; Plagiolepis madecassa Forel, 1892; Solenopsis mameti Donisthorpe, 1946; Syllophopsis cryptobia Santschi, 1921; Tapinoma subtile Santschi, 1911; Technomyrmex difficilis Forel, 1892; Tetramorium schaufussii Forel, 1891; and Tetramorium sikorae Forel, 1892), while two species are endemic to the Mascarene Islands (Camponotus aurosus Roger, 1863; Pristomyrmex browni Wang, 2003) (Wang 2003, Bolton 2014, Janicki et al. 2016, Guénard et al. 2017). Here, we report eight ant species recorded for the first time from La Réunion Island, based on recent field surveys and verified taxonomic identifications.
Materials and methods
Collection sites and methods
Sampling was performed at a variety of sites on La Réunion Island (Fig. 1). Collection methods included aspirator, forceps, interception traps, Winkler/Moczarski leaf litter sifting and beating tray. Ant samples were stored in ethanol (95%) before morphological identification.
Figure 1.
Localities of examined specimens. Base map derived from ESRI Satellite imagery (WGS84). Map produced by F. Jacquelin (CIRAD, 2024).
Morphological identification
Specimens were examined with a ZEISS Stemi 08 stereomicroscope and photographs taken with a DeltaPix Invenio EIII camera and the associated DeltaPix Insight software. Taxonomic identification was carried out first at the genus level following Fisher and Bolton (2016), then using the following keys to species: (Bolton 1987, Bolton 2000, Heterick 2006, Fischer and Fisher 2013, Pacheco and Mackay 2013, Ortiz-Sepulveda et al. 2019, Hamer et al. 2023). For Brachymyrmex specimens, we performed the following measurements: head width (HW), head length (HL) being the distance from the posterior margin of the frontal triangle to the vertexal margin, scape length and eye length (EL) being the maximum diameter of the compound eye and the scape length exceeding the posterior margin of the head (SLE) (Ortiz-Sepulveda et al. 2019). We then used three indices to discriminate between potential species: (i) scape index 1(SI1 = (SL/HW) × 100) (ii) scape index 2 (SI2 = (SL/HL) × 100) and (iii) scape index 3 (SI1 = EL – SLE) (Ortiz-Sepulveda et al. 2019).
Repositories
Collections are referred to by the following acronyms:
CAS = California Academy of Science, San Francisco, U.S.A.;
CRP = Collection of Raphaël Parnaudeau;
CTR = Collection of Thibault Ramage, Concarneau, France;
CDC = Collection of Dominique Carval, Saint-Pierre, La Réunion;
NHM = Natural History Museum of La Réunion Island;
C3P = CIRAD Pôle de Protection des Plantes, Saint-Pierre, La Réunion.
Taxon treatments
Stigmatomma zwaluwenburgi
Williams, 1946
F8FF50D5-2B70-5D30-BF17-1D0FD1599608
Materials
Type status: Other material. Occurrence: lifeStage: 1 gyne; occurrenceID: 5D3C472C-58DB-532D-AE22-FF2B4CB1C90E; Location: island: La Réunion; country: France; locality: Petite-Île; verbatimElevation: 90 m; decimalLatitude: -21.35919; decimalLongitude: 55.54150; Identification: identifiedBy: T. Ramage; D. Carval; Event: samplingProtocol: interception trap; verbatimEventDate: 22.III.2023; habitat: sugarcane field; Record Level: institutionCode: CAS
Type status: Other material. Occurrence: lifeStage: 1 gyne; occurrenceID: 6E457803-4A96-5003-8C0A-14A4B98D3BA3; Location: island: La Réunion; country: France; locality: Petite-Île; verbatimElevation: 105 m; decimalLatitude: -21.35389; decimalLongitude: 55.74056; Identification: identifiedBy: D. Carval; T. Ramage; Event: samplingProtocol: interception trap; verbatimEventDate: 22.III.2023; habitat: sugarcane field; Record Level: institutionCode: CAS
Type status: Other material. Occurrence: lifeStage: 1 gyne; occurrenceID: E4A115B6-C0A5-5FE2-977F-26C4E4CA4748; Location: island: La Réunion; country: France; locality: Petite-Île; verbatimElevation: 560 m; decimalLatitude: -21.35389; decimalLongitude: 55.74056; Identification: identifiedBy: D. Carval; T. Ramage; Event: samplingProtocol: interception trap; verbatimEventDate: 19.IV.2023; habitat: sugarcane field; Record Level: institutionCode: CAS
Type status: Other material. Occurrence: lifeStage: 1 gyne; occurrenceID: 83B7795C-8243-5C12-A94E-EFA81B7D162A; Location: island: La Réunion; country: France; locality: Petite-Île; verbatimElevation: 198 m; decimalLatitude: -21.35331; decimalLongitude: 55.54297; Identification: identifiedBy: D. Carval; T. Ramage; Event: samplingProtocol: interception trap; verbatimEventDate: 04.I.2023; habitat: sugarcane field; Record Level: institutionCode: C3P; collectionCode: MGAU05446_010
Type status: Other material. Occurrence: lifeStage: 1 gyne; occurrenceID: 2AF3E782-38BA-559B-B408-1CBB82E8D184; Location: island: La Réunion; country: France; locality: Petite-Île; verbatimElevation: 200 m; decimalLatitude: -21.35322; decimalLongitude: 55.54219; Identification: identifiedBy: D. Carval; T. Ramage; Event: samplingProtocol: interception trap; verbatimEventDate: 06.XII.2023; habitat: sugarcane field; Record Level: institutionCode: NHM
Type status: Other material. Occurrence: lifeStage: 1 gyne; occurrenceID: D4272B29-E7FE-5CB7-AAE1-DEFFC30D593F; Location: island: La Réunion; country: France; locality: Petite-Île; verbatimElevation: 198 m; decimalLatitude: -21.35331; decimalLongitude: 55.54297; Identification: identifiedBy: D. Carval; T. Ramage; Event: samplingProtocol: interception trap; verbatimEventDate: 03.I.2024; habitat: sugarcane field; Record Level: institutionCode: CAS
Type status: Other material. Occurrence: lifeStage: 1 gyne; occurrenceID: E65F5646-C6EB-5D9E-AAE8-CF9EA0078ECE; Location: island: La Réunion; country: France; locality: Petite-Île; verbatimElevation: 378 m; decimalLatitude: -21.34378; decimalLongitude: 55.54950; Identification: identifiedBy: D. Carval; T. Ramage; Event: samplingProtocol: interception trap; verbatimEventDate: 28.II.2024; habitat: sugarcane field; Record Level: institutionCode: CAS
Distribution
To our knowledge, the specimens from La Réunion are the first gynes collected for this species from the Malagasy Region. As the gyne of S. zwaluwenburgi is not known, we cannot be certain the gynes collected in Réunion Island belong to this species, but they match well with workers of S. zwaluwenburgi (Fig. 2). This species has been reported from very few places: Hawaii (Williams 1946), Christmas Island (Framenau and Thomas 2008), Fiji (Sarnat 2009) and Hong Kong (Hamer et al. 2023). The native range of this species remains a conundrum, but an east Asian origin seems likely (Ward and Fisher 2016, Hamer et al. 2023).
Figure 2.
Full-face, lateral and dorsal view of a Stigmatomma zwaluwenburgi worker (photographer: Eli M. Sarnat, CASENT0187702 https://www.antweb.org/).
Ecology
The species has been very rarely collected and its ecology is little known. As for our specimens, the type material of S. zwaluwenburgi was collected within a sugar cane field (Williams 1946). The specimens from Fiji were collected in the litter of a disturbed forest (AntWeb 2024) and Hamer et al. (2023) collected specimens from Signal Hill Gardens, an urbanised area of Hong Kong. This cryptobiotic ant is a soil-dwelling species that tolerates anthropogenised habitats.
Brachymyrmex australis
Forel, 1909
8E1CCCC5-8E08-57D2-BF59-4711DA8106D7
Materials
Type status: Other material. Occurrence: lifeStage: 4 workers; occurrenceID: CDA9844B-B8A4-5177-894F-9B8D03E3FC6C; Location: island: La Réunion; country: France; municipality: Saint-Pierre; locality: Bassin Plat; verbatimElevation: 152 m; decimalLatitude: -21.32356; decimalLongitude: 55.49042; Identification: identifiedBy: D. Carval; T. Ramage; Event: samplingProtocol: aspirator; verbatimEventDate: 27.VII.2020; habitat: living tree trunk; Record Level: institutionCode: CDC
Type status: Other material. Occurrence: lifeStage: 13 workers 6 males; occurrenceID: 0B17DC5F-6F69-5CE0-B538-C224E1A24FCF; Location: island: La Réunion; country: France; municipality: Saint-Philippe; locality: Mare Longue forest; verbatimElevation: 233 m; decimalLatitude: -21.35389; decimalLongitude: 55.74056; Identification: identifiedBy: D. Carval; T. Ramage; Event: samplingProtocol: aspirator; verbatimEventDate: 25.IV.2023; habitat: rotten wood trunk; Record Level: institutionCode: CDC
Type status: Other material. Occurrence: lifeStage: 7 workers; occurrenceID: F325AA5D-69FF-5A65-9A83-44D0B85F6E7C; Location: island: La Réunion; country: France; municipality: La Possession; locality: Crête solitude; verbatimElevation: 670 m; decimalLatitude: -21.96178; decimalLongitude: 55.36500; Identification: identifiedBy: D. Carval; T. Ramage; Event: samplingProtocol: beating tray; verbatimEventDate: 28.III.2024; habitat: shrubs; Record Level: institutionCode: CDC
Diagnosis
According to Ortiz-Sepulveda et al. (2019), B. australis is very similar to B. aphidicola Forel, 1909, but can be distinguished by scape indices 1, 2 and 3 (hereafter SI-I3). However, of our 13 specimens from the three locations, the SI1 identified none as B. australis, three as B. aphidicola and led 10 times to an uncertain classification (Table 1). Similarly, SI2 identified six specimens as B. australis, none as B. aphidicola and led seven times to an uncertain classification (Table 1). By contrast, SI3 identified all the specimens as B. australis. On La Réunion Island, this ant can be confused with Plagiolepis alluaudi Emery, 1894 from which it can be distinguished by the number of antennal segments (nine for B. aphidicola, 11 for P. alluaudi). Brachymyrmex australis can be distinguished from Brachymyrmex cordemoyi Forel, 1895 by its colouration and worker size polymorphism. Brachymyrmex australis typically exhibits a uniformly light orange colouration (Fig. 3), whereas B. cordemoyi is generally dark brown, although lighter individuals may occur. In addition, workers of B. australis are monomorphic in size, while those of B. cordemoyi show marked size polymorphism.
Table 1.
Morphological measurements (mm) on 14 Brachymyrmex specimens. According to Ortiz-Sepulveda et al. (2019): if SI1 < 94 or SI1 > 104, the Brachymyrmex specimen is classified as B. australis or B. aphidicola, respectively; if 94 ≤ SI1 ≤ 104, the classification of the specimen is considered uncertain. Similarly, if SI2 < 117 or SI2 > 135, the Brachymyrmex specimen is classified as B. australis or B. aphidicola, respectively; f 117 ≤ SI2 ≤ 135, the classification of the specimen is considered uncertain. Finally, if SI3 ≥ 0, the Brachymyrmex specimen is classified as B. australis; otherwise, it is classified as B. aphidicola. Specimen 1 was sampled at 21°19'24.8"S, 55°29'25.5"E, specimens 2–7 were sampled at 21°21'14"S, 55°44'26"E and specimens 8–13 were sampled at 20°57'42.4"S 55°21'54.6"E.
| Specimen | HL | HW | EL | SLE | SI1 | SI2 | SI3 | Classification (SI1) | Classification (SI2) | Classification (SI3) |
| 1 | 0.32 | 0.38 | 0.09 | 0.08 | 110.5 | 131.3 | 0.01 | B. aphidicola | uncertain | B. australis |
| 2 | 0.34 | 0.38 | 0.10 | 0.09 | 105.3 | 117.6 | 0.01 | B. aphidicola | uncertain | B. australis |
| 3 | 0.35 | 0.40 | 0.10 | 0.06 | 102.5 | 117.1 | 0.04 | uncertain | uncertain | B. australis |
| 4 | 0.35 | 0.39 | 0.10 | 0.06 | 102.6 | 114.3 | 0.04 | uncertain | B. australis | B. australis |
| 5 | 0.34 | 0.39 | 0.09 | 0.05 | 100.0 | 114.7 | 0.04 | uncertain | B. australis | B. australis |
| 6 | 0.34 | 0.40 | 0.10 | 0.05 | 95.0 | 111.8 | 0.05 | uncertain | B. australis | B. australis |
| 7 | 0.32 | 0.38 | 0.10 | 0.04 | 97.4 | 115.6 | 0.06 | uncertain | B. australis | B. australis |
| 8 | 0.32 | 0.41 | 0.11 | 0.08 | 100.0 | 128.1 | 0.03 | uncertain | uncertain | B. australis |
| 9 | 0.34 | 0.41 | 0.10 | 0.05 | 95.1 | 114.7 | 0.05 | uncertain | B. australis | B. australis |
| 10 | 0.32 | 0.40 | 0.10 | 0.07 | 102.5 | 128.1 | 0.03 | uncertain | uncertain | B. australis |
| 11 | 0.33 | 0.39 | 0.09 | 0.06 | 100.0 | 118.2 | 0.03 | uncertain | uncertain | B. australis |
| 12 | 0.33 | 0.37 | 0.10 | 0.07 | 105.4 | 118.2 | 0.03 | B. aphidicola | uncertain | B. australis |
| 13 | 0.33 | 0.37 | 0.08 | 0.04 | 102.7 | 115.2 | 0.04 | uncertain | B. australis | B. australis |
Figure 3.
Full-face, lateral and dorsal view of a Brachymyrmex australis worker (photographer: D. Carval).
Distribution
This species is native to South America and Central America and has been reported as introduced in Mauritius (Ortiz-Sepulveda et al. 2019, Rosas-Mejía et al. 2021).
Ecology
This species has been found under stones and in rotten wood and epiphytes (Ortiz-Sepulveda et al. 2019). B. australis nests underground, in organic litter (Wild 2007) or in rotting tree trunks
Pheidole parva
Mayr, 1865
920A7FF5-F591-50CD-B5F7-F65FA322125E
Materials
Type status: Other material. Occurrence: individualCount: 10 workers; occurrenceID: 4ABBD950-E963-59C3-8D54-B3AC14F968DB; Location: island: La Réunion; country: France; municipality: Saint-Pierre; locality: Front de mer; verbatimElevation: 6 m; decimalLatitude: -21.34389; decimalLongitude: 55.47389; Identification: identifiedBy: D. Carval; Event: samplingProtocol: pincers; verbatimEventDate: 03.I.2024; habitat: beach front; Record Level: collectionCode: CDC
Type status: Other material. Occurrence: individualCount: 3 minor workers, 1 major worker; occurrenceID: 58F1D2AB-A268-59E6-A570-BAC64EA6DDCC; Location: island: La Réunion; country: France; municipality: Saint-Pierre; locality: Front de mer; verbatimElevation: 6 m; decimalLatitude: -21.34389; decimalLongitude: 55.47389; Identification: identifiedBy: D. Carval; Event: samplingProtocol: pincers; verbatimEventDate: 03.I.2024; habitat: beach front; Record Level: collectionCode: CDC
Diagnosis
Pheidole parva can be distinguished from the other Pheidole species present in La Réunion Island (Pheidole megacephala (Fabricius, 1793) by its smaller size, the fact that both minors and majors are prominently sculptured, head of majors more elongate and with a broadly V-shaped posterior emargination and postpetiole without a large convex ventral process (Fischer and Fisher 2013) (Figs 4, 5). In Mauritius, two other introduced Pheidole species are reported (Pheidole fervens Smith, 1858 and Pheidole indica Mayr, 1879) and it would not be surprising if they are found on La Réunion Island as well (Fischer and Fisher 2013).
Figure 4.
Full-face, lateral and dorsal view of a Pheidole parva major worker (photographer: April Nobile, CASENT0055997 from https://www.antweb.org/).
Figure 5.
Full-face, lateral and dorsal view of a Pheidole parva minor worker (photographer: April Nobile, CASENT0055998 from https://www.antweb.org/).
Distribution
This species is native to the Indomalaya Region and has been reported as introduced in Japan, Mauritius, Rodrigues, Seychelles, Oman and Saudi Arabia. It has also been reported from indoor locations in Germany and Austria.
Ecology
This invasive species is well adapted to human environments, such as ports and urban beachfronts. This ant forages or nests in various habitats such as soil, litter, under stones, in root mats, rotten logs or the bark of live trees. This species likely invades new areas through human commerce, especially maritime commerce (Fischer and Fisher 2013).
Strumigenys membranifera
Emery, 1869
87211A88-FD99-5F42-B690-1722DB0CD5B5
Materials
Type status: Other material. Occurrence: individualCount: 3 workers; occurrenceID: 5C397122-D41A-59C2-9B64-B12DBAB58E7B; Taxon: genus: Strumigenys; specificEpithet: membranifera; scientificNameAuthorship: Emery, 1869; Location: island: La Réunion; country: France; municipality: Saint-André; locality: Front de mer; verbatimElevation: 21 m; decimalLatitude: -20.97917; decimalLongitude: 55.68361; Identification: identifiedBy: T. Ramage; Event: verbatimEventDate: 10.XII.2023; habitat: beach front; Record Level: collectionID: CRP
Diagnosis
This species can be confused with the four other Strumigenys species present in La Réunion Island (Strumigenys emmae (Emery, 1890), Strumigenys ludovici (Forel, 1904), Strumigenys nepalensis (De Andrade, 1994), Strumigenys rogeri Emery, 1890). S. membranifera can be differentiated from S. emmae and S. rogeri by its distinctive mandibular shape. In S. membranifera, the mandibles are triangular and short, featuring numerous teeth along the inner margin (Fig. 6). In contrast, S. rogeri displays elongated and slender mandibles, while S. emmae exhibits sickle-shaped mandibles, both of which possess apical and pre-apical teeth. It differs from S. nepalensis by the number of antennal segments (six for S. membranifera, four for S. nepalensis). Finally, S. membranifera has shorter mandibles with fewer teeth (< 20) and a more rounded head, while S. ludovici has longer mandibles with more than 25 teeth and a more elongate head than S. membranifera.
Figure 6.
Full-face, lateral and dorsal view of a Strumigenys membranifera worker (photographer: Michele Esposito, CASENT0023769 from https://www.antweb.org/).
Distribution
Besides S. emmae and S. rogeri, this species is one of the most widespread dacetine ants in the world (Wetterer 2011). This highly invasive species is considered native to several countries of Africa, although phylogenetic analyses place the origin of S. membranifera in the Indomalay Region (Booher et al. 2021). This species is widespread worldwide and reported as introduced in South America, United States of America, Europe, Asia, Oceania and the Malagasy Region.
Ecology
As with other dacetines, S. membranifera is a predatory species that primarily feeds on springtails (Collembola) and other minuscule soil arthropods (Wilson 1953). Typically dwelling within soil and leaf litter, S. membranifera seldom ventures openly above ground for foraging purposes (Wetterer 2011). Thanks to minuscule teeth on pliers-like mandibles, S. membranifera can clamp down on and securely hold prey (Wetterer 2011).
Cardiocondyla obscurior
Wheeler, 1929
52D5F8EE-EAA6-5F3F-82CE-7EFFB67D2F42
Materials
Type status: Other material. Occurrence: individualCount: 6 workers; occurrenceID: A023853A-0DCE-51C1-8985-EA38D88E9595; Taxon: genus: Cardiocondyla; specificEpithet: obscurior; scientificNameAuthorship: Wheeler, 1929; Location: island: La Réunion; country: France; municipality: Saint-Pierre; locality: Front de mer; verbatimElevation: 8 m; decimalLatitude: -21.34389; decimalLongitude: 55.47917; Identification: identifiedBy: D. Carval; Event: samplingProtocol: pincers; verbatimEventDate: 06.VI.2024; habitat: beach front; Record Level: collectionID: CDC
Diagnosis
This species closely resembles Cardiocondyla wroughtonii (Forel, 1890), which has been reported from La Réunion Island. Workers of C. obscurior (Fig. 7) differ from C. wroughtonii in having a darker gaster, a shorter head, a reduced postocular distance, a narrower frons, broader and higher waist segments, a greater distance between the bases of the propodeal spines and shorter propodeal spines (Seifert 2002).
Figure 7.
Full-face, lateral and dorsal view of a Cardiocondyla obscurior worker (photographer: Eli M. Sarnat, CASENT0171038 from https://www.antweb.org/ ) .
Distribution
This species is native to the Indomalaya Region and has been reported as introduced in many locations, such as Brazil (Meurer et al. 2015), Venezuela (Guénard et al. 2017, Janicki et al. 2016), France and Belgium (Blatrix et al. 2018), Spain (Sánchez-García and Espadaler 2015) and Kenya (Garcia et al. 2013).
Ecology
Cardiocondyla obscurior has been reported from a variety of disturbed and undisturbed habitats, such as urban areas, grasslands, agricultural areas and forest margins (Seifert 2002). Nests are typically located in cavities of bushes and trees, but the species has also been found in plant galls and dead twigs.
Monomorium exiguum
Forel, 1894
97E72725-28AC-537E-A01A-3FDEC062BE1A
Materials
Type status: Other material. Occurrence: individualCount: 1 worker; occurrenceID: 536F5F1A-9029-58A4-A5F4-FF17AF2C0BE5; Taxon: genus: Monomorium; specificEpithet: exiguum; scientificNameAuthorship: Forel 1894; Location: island: La Réunion; country: France; municipality: Petite Île; verbatimElevation: 378 m; decimalLatitude: -21.34378; decimalLongitude: 55.54950; Identification: identifiedBy: D. Carval; Event: samplingProtocol: interception trap; verbatimEventDate: 19.XII.2023; habitat: sugarcane field; Record Level: collectionID: CDC
Diagnosis
Amongst the 20 Monomorium species reported in the Malagasy Region (Fisher and Bolton 2016), M. exiguum is easily distinguished by its 11-segmented antennae (M. monomorium species group), a metanotal groove weakly impressed, an elongated propodeum and a petiolar node that is conical and dorsally tapered (Heterick 2006) (Fig. 8). All other Monomorium species reported from La Réunion Island have 12-segmented antennae (Monomorium floricola (Jerdon, 1851), Monomorium pharaonis (Linnaeus, 1758), Monomorium subopacum (Smith, 1858) and Monomorium termitobium (Forel, 1892)). This species displays great variability in colour, from yellow pale to brown (Heterick 2006), but our specimen was a pale orange similar to that found in M. exiguum flavescens (Forel, 1916), now considered as a junior synonym of M. exiguum (Bolton 2014).
Figure 8.
Full-face, lateral and dorsal view of a Monomorium exiguum worker (photographer: Erin Prado, CASENT0217367 from https://www.antweb.org/).
Distribution
This species is native to the Afrotropical Region, where it is widely distributed in sub-Saharan Africa, including Madagascar (AntWeb 2024) and the Arabian Peninsula (Aldawood and Sharaf 2009). It has been reported as introduced on the Socotra Archipelago (Sharaf et al. 2018), in the Balearic Islands (Gómez and Espadaler 2006) and in Crete (Borowiec et al. 2023). This is the first report of this species in the Mascarene Islands.
Ecology
Monomorium exiguum appears adapted to numerous types of habitats. In the Arabian Peninsula, it has been found in humid soil, in leaf litter, under rocks and under the bark of trees (Sharaf et al. 2018). Interestingly, it has been found inside the galleries of a Camponotus species (Sharaf et al. 2018) and inside the galleries of a termite nest (Sharaf et al. 2017). In the Province of Tolaria in Madagascar, M. exiguum has been found to be the most abundant Monomorium species in leaf litter samples (Heterick 2006). In Benin, one specimen was found in a mango orchard with no specification of the microhabitat (Taylor et al. 2018). In La Réunion Island, the specimen was found in a sugarcane field.
Solenopsis globularia
Smith, 185
AF4641EB-FE59-5018-836B-5DC883E17CEA
Materials
Type status: Other material. Occurrence: individualCount: 2 workers; occurrenceID: 1A1DDE49-A486-54B8-9D37-2FF4A2287845; Taxon: genus: Solenopsis; specificEpithet: globularia; scientificNameAuthorship: Smith, 1858; Location: island: La Réunion; country: France; municipality: Etang-Salé; locality: Piton Reinette; verbatimElevation: 53 m; decimalLatitude: -21.27444; decimalLongitude: 55.34750; Identification: identifiedBy: D. Carval, T. Ramage; Event: samplingProtocol: aspirator; verbatimEventDate: 25.IV.2023; habitat: litter; Record Level: collectionID: CDC
Type status: Other material. Occurrence: individualCount: 2 workers; occurrenceID: 3BF9971A-F882-5C5A-A268-CB6838C68BEB; Taxon: genus: Solenopsis; specificEpithet: globularia; scientificNameAuthorship: Smith, 1858; Location: island: La Réunion; country: France; municipality: Etang-Salé; locality: Beach front; verbatimElevation: 11 m; decimalLatitude: -21.26250; decimalLongitude: 55.33278; Identification: identifiedBy: D. Carval, T. Ramage; Event: samplingProtocol: aspirator; verbatimEventDate: 25.IV.2023; habitat: beach front; Record Level: collectionID: CDC
Diagnosis
This species can be confused with the two other Solenopsis species (Solenopsis geminata (Fabricius, 1804) and Solenopsis mameti Donisthorpe, 1946) as well as with the three Cardiocondyla species reported from La Réunion Island: Cardiocondyla emeryi Forel, 1881, Cardiocondyla itsukii and Cardiocondyla wroughtonii (Forel, 1890). It differs from other Solenopsis by its enlarged postpetiole and from Cardiocondyla species by its 2-segmented antennal club and the absence of propodeal spines (Fig. 9).
Figure 9.
Full-face, lateral and dorsal view of a Solenopsis globularia worker (photographer: April Nobile, CASENT0173279 from https://www.antweb.org/).
Distribution
This introduced species is native to south-eastern regions of the United States, Caribbean, Central America and South America. It has been introduced to several African countries and islands, as well as the Philippines and Oceania (French Polynesia, Galápagos, Hawaii) (Pacheco and Mackay 2013).
Ecology
According to Wetterer (2019), this intermediate-sized invasive species behaves more like a small fire ant rather than a thief ant. This species forages on the ground and may be collected at bait traps and nests under rocks and logs (Pacheco and Mackay 2013).
Solenopsis pygmaea
Forel, 1901
450672E2-7C36-5B50-9D06-049175C3DBAA
Materials
Type status: Other material. Occurrence: individualCount: 2 workers; occurrenceID: 6E4F2A93-F0F2-57C7-9F2C-B45D4DE20128; Location: island: La Réunion; country: France; municipality: La Possession; locality: Crête Ti Bon Dieu; verbatimElevation: 534 m; decimalLatitude: -20.92444; decimalLongitude: 55.38833; Identification: identifiedBy: D. Carval, T. Ramage; Event: samplingProtocol: pincers; verbatimEventDate: 29.III.2024; habitat: rotten wood trunk; Record Level: collectionID: CDC
Type status: Other material. Occurrence: individualCount: 3 workers; occurrenceID: BA968C8F-B8D4-5609-B8FB-A44F1F6CCEE1; Location: island: La Réunion; country: France; municipality: La Possession; locality: Crête Ti Bon Dieu; verbatimElevation: 534 m; decimalLatitude: -20.92444; decimalLongitude: 55.38833; Identification: identifiedBy: D. Carval, T. Ramage; Event: samplingProtocol: Winkler-Moczarski; verbatimEventDate: 29.III.2024; habitat: rotten wood trunk; Record Level: collectionID: CDC
Diagnosis
This species is easily distinguishable from the three other Solenopsis species reported from La Réunion Island (Fig. 10). Firstly, this thief ant species is significantly smaller than S. geminata (Fabricius, 1804) and S. globularia with a total length < 1.2 mm. The second thief ant species present on the Island, S mameti, exhibits uniformly dark body colouration, while Solenopsis gr pygmaea is concolorous pale yellow.
Figure 10.
Full-face, lateral and dorsal view of a Solenopsis gr. pygmaea worker (photographer: Michele Esposito, CASENT0923738 from https://www.antweb.org/).
Distribution
To date, the identification to species has not been confirmed. This species has been compared to Afrotropical and Australasian Solenopsis, but does not match any species. This Solenopsis seems to have an affinity with the neotropical Solenopsis, confirmed by the barcoding of the Mauritius specimens that share a BIN (BOLD:AAC3883) with specimens from Bahamas, Costa Rica, Puerto Rico and Suriname. This Solenopsis was likely introduced to the Mascarene Islands, despite the fact that it was found in a natural habitat on La Réunion Island.
Ecology
This species has been found nesting in rotten wood and litter. As with other thief ants, this species probably has lestobiotic and cryptic habits (Pacheco and Mackay 2013).
Discussion
With the discovery of these eight new reported species, the total number of ant species documented on La Réunion Island now stands at 62 (AntWeb 2024, Mévergnies et al. 2024). These surveys suggest that other introduced species may remain undiscovered on the Island. Similar to past invasions, we can theorise that introductions are associated with maritime or air cargo. These introductions might also arise from the movement of plant materials or soil substrates by travellers. Meanwhile, the total number of species recorded on Mauritius Island is 78, including 11 species endemic to the Island or the Mascarene Islands (AntWeb 2024). Only two endemic species of the Mascarene Islands (Camponotus aurosus and Pristomyrmex browni) are reported from La Réunion Island, despite its significantly larger area of preserved primary forests compared to Mauritius. Therefore, further studies are needed in both urbanised and human-impacted environments to identify more introduced species, as well as in natural habitats to discover species endemic to La Réunion Island or the Mascarene Islands. Finally, the origin of the new reported species should be investigated using molecular techniques, such as COI barcoding.
Supplementary Material
Acknowledgements
We thank Flavia Esteves for help on the identification of Stigmatomma cf. zwaluwenburgi. This work was carried out as part of the CIRAD DPP SADur agronomical research programme. This programme is co-funded by the European Union, the French State and La Réunion Region. Europe is committed to La Réunion through the ERDF (grant 2024- 1248-583 005756), for which La Réunion Region is the managing authority. This work was also carried out as part of the Sustainable Territories project funded by the French Overseas Ministry.
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