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Lasius
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| Lasius Temporal range: Eocene-Present,
| |
|---|---|
| Lasius niger, type species. | |
| Scientific classification | |
| Kingdom: | Animalia |
| Phylum: | Arthropoda |
| Class: | Insecta |
| Order: | Hymenoptera |
| Family: | Formicidae |
| Subfamily: | Formicinae |
| Tribe: | Lasiini |
| Genus: | Lasius Fabricius, 1804 |
| Diversity[1] | |
| 149 species | |
| Synonyms | |
| |
Lasius is a genus of formicine ants.[2] The type species for this genus is the black garden ant, Lasius niger. Other major members, which live in drier heathland, are the cornfield ant, L. neoniger, and L. alienus. Other species include the temporary social parasites of the L. mixtus group and the hyper-social parasite Lasius fuliginosus. Lasius flavus is also a commonly seen species, building grassy hillocks in undisturbed pasture. In the Alps, these mounds – always aligned east to catch the first rays of the rising sun – have been traditionally used by goatherds as natural compasses.[citation needed] Species in the subgenus Acanthomyops, in particular L. interjectus and L. claviger, are commonly known as citronella ants due to their citronella-like smell.
Social parasitism
[edit]Several species in this genus are noted to be social parasites.[3][4][5][6] Some species such as Lasius latipes and Lasius murphyi are noted to have their mating flights in mid-late summer and invade other colonies of Lasius, primarily Lasius neoniger.[3][4][6] The queens of species Lasius orientalis and Lasius umbratus have been observed using chemical signals to invade other Lasius colonies and trick the workers to kill the residing queen, accepting the invading queen as their own.[7] Other species, such as Lasius claviger, are known to overwinter and invade colonies in the spring.[8][6]
Moisture ants
[edit]Many Lasius species, known collectively as "moisture ants" in the United States, make their nests in and around moist rotting wood as well as under rocks.[9][10] They can infest buildings, particularly foundation forms in contact with soil, becoming a minor nuisance.[11][9] They are not considered a structural threat because they only make their galleries in wood that is already decayed.[11] Some species build "cartonlike" nests in moist locations made of decayed wood fragments cemented together with honeydew and the ant's mandibular gland secretions.[10] Workers are monomorphic, 2 to 3 mm long, yellow to dark brown.[9] They are secretive, and forage mostly at night for honeydew and other sweet substances, and may also prey on small insects.[9] Winged reproductive males and females swarm in late summer and fall, which is when building infestations may be noticed.[9] They are distinguished from carpenter ants (Camponotus), another structure-infesting species, by being much smaller, and having a notch in the dorsal thorax (top of the center body division), where carpenter ants have a rounded thorax.[11][9] Widespread moisture ant species include L. alienus and L. neoniger, as well as some Acanthomyops species.[10]
Species
[edit]
- Lasius alienoflavus Bingham, 1903
- Lasius alienus (Foerster, 1850)
- Lasius americanus Emery 1893
- †Lasius anthracinus (Heer, 1867)
- Lasius aphidicola (Walsh, 1863)
- Lasius arizonicus Wheeler, 1917
- Lasius atopus Cole, 1958
- Lasius austriacus Schlick-Steiner, Steiner, Schödl & Seifert, 2003
- Lasius balcanicus Seifert, 1988
- Lasius balearicus Talavera, Espadaler & Vila, 2014
- Lasius bicornis (Foerster, 1850)
- Lasius bombycina Seifert & Galkowski, 2016
- Lasius brevicornis Emery 1893
- Lasius brevipalpus Seifert, 2020
- Lasius brunneus (Latreille, 1798)
- Lasius buccatus Stärcke, 1942
- Lasius bureni (Wing, 1968)
- Lasius californicus Wheeler, 1917
- Lasius capitatus (Kuznetsov-Ugamsky, 1927)
- Lasius carniolicus Mayr, 1861
- Lasius casevitzi Seifert & Galkowski, 2016
- †Lasius chambonensis Piton & Théobald, 1935
- Lasius chinensis Seifert, 2020
- Lasius cinereus Seifert, 1992
- Lasius citrinus Emery, 1922
- Lasius claviger (Roger, 1862)
- Lasius colei (Wing, 1968)
- Lasius coloradensis Wheeler, 1917
- Lasius coloratus Santschi, 1937
- Lasius creightoni (Wing, 1968)
- Lasius creticus Seifert, 2020
- Lasius crinitus (Smith, 1858)
- †Lasius crispus Wilson, 1955
- Lasius crypticus Wilson, 1955
- Lasius distinguendus (Emery, 1916)
- Lasius draco Collingwood, 1982
- Lasius elevatus Bharti & Gul, 2013
- Lasius emarginatus (Olivier, 1792)
- †Lasius epicentrus Théobald, 1937
- Lasius escamole Reza, 1925
- Lasius excavatus Seifert, 2020
- Lasius fallax Wilson, 1955
- Lasius flavescens Forel, 1904
- Lasius flavoniger Seifert, 1992
- Lasius flavus (Fabricius, 1782)
- Lasius fuji Radchenko, 2005
- Lasius fuliginosus (Latreille, 1798)
- †Lasius globularis (Heer, 1849)
- †Lasius glom LaPolla & Greenwalt, 2015
- Lasius grandis Forel, 1909
- Lasius hayashi Yamauchi & Hayashida, 1970
- Lasius hikosanus Yamauchi, 1979
- Lasius himalayanus Bingham, 1903
- Lasius hirsutus Seifert, 1992
- Lasius humilis Wheeler, 1917
- Lasius illyricus Zimmermann, 1935
- †Lasius inflatus (Zhang, 1989)
- Lasius interjectus Mayr, 1866
- Lasius israelicus Seifert, 2020
- Lasius japonicus Santschi, 1941
- Lasius jensi Seifert, 1982
- Lasius kabaki Seifert, 2020
- Lasius karpinisi Seifert, 1992
- Lasius koreanus Seifert, 1992
- Lasius kritikos Seifert, 2020
- Lasius lasioides (Emery, 1869)
- Lasius latipes (Walsh, 1863)
- Lasius lawarai Seifert, 1992
- †Lasius longaevus (Heer, 1849)
- Lasius longiceps Seifert, 1988
- Lasius longicirrus Chang & He, 2002
- Lasius longipalpus Seifert, 2020
- †Lasius longipennis (Heer, 1849)
- Lasius magnus Seifert, 1992
- Lasius maltaeus Seifert, 2020
- Lasius mauretanicus Seifert, 2020
- Lasius meridionalis (Bondroit, 1920)
- Lasius mexicanus Wheeler, 1914
- Lasius mikir Collingwood, 1982
- Lasius minutus Emery, 1893
- Lasius mixtus (Nylander, 1846)
- †Lasius mordicus Zhang, 1989
- Lasius morisitai Yamauchi, 1979
- Lasius murphyi Forel, 1901
- Lasius myops Forel, 1894
- Lasius myrmidon Mei, 1998
- Lasius nearcticus Wheeler, 1906
- Lasius neglectus Van Loon, Boomsma & Andrasfalvy, 1990
- †Lasius nemorivagus Wheeler, 1915
- Lasius neoniger Emery, 1893
- Lasius nevadensis Cole, 1956
- Lasius niger (Linnaeus, 1758)
- Lasius nigrescens Stitz, 1930
- Lasius nipponensis Forel, 1912
- Lasius nitidigaster Seifert, 1996
- †Lasius oblongus Assmann, 1870
- Lasius obscuratus Stitz, 1930
- Lasius occidentalis Wheeler, 1909
- †Lasius occultatus (Heer, 1849)
- †Lasius ophthalmicus (Heer, 1849)
- Lasius orientalis Karavaiev, 1912
- Lasius pallitarsis (Provancher, 1881)
- Lasius paralienus Seifert, 1992
- †Lasius peritulus (Cockerell, 1927)
- Lasius persicus Seifert, 2020
- Lasius piliferus Seifert, 1992
- Lasius platythorax Seifert, 1991
- Lasius plumopilosus Buren, 1941
- Lasius pogonogynus Buren, 1950
- Lasius precursor Seifert, 2020
- Lasius productus Wilson, 1955
- Lasius przewalskii Ruzsky, 1915
- Lasius psammophilus Seifert, 1992
- Lasius pubescens Buren, 1942
- †Lasius pumilus Mayr, 1868
- †Lasius punctulatus Mayr, 1868
- Lasius rabaudi (Bondroit, 1917)
- Lasius reginae Faber, 1967
- Lasius sabularum (Bondroit, 1918)
- Lasius sakagamii Yamauchi & Hayashida, 1970
- Lasius schaeferi Seifert, 1992
- †Lasius schiefferdeckeri Mayr, 1868
- Lasius schulzi Seifert, 1992
- Lasius sichuense Seifert, 2020
- Lasius silvaticus Seifert, 2020
- Lasius sitiens Wilson, 1955
- Lasius sonobei Yamauchi, 1979
- Lasius spathepus Wheeler, 1910
- Lasius speculiventris Emery, 1893
- Lasius subglaber Emery, 1893
- Lasius subumbratus Viereck, 1903
- Lasius talpa Wilson, 1955
- Lasius tapinomoides Salata & Borowiec, 2018
- Lasius tebessae Seifert, 1992
- †Lasius tertiarius Zalessky, 1949
- Lasius tibialis Santschi, 1936
- †Lasius truncatus Zhang, 1989
- Lasius tunisius Seifert, 2020
- Lasius turcicus Santschi, 1921
- Lasius umbratus (Nylander, 1846)
- Lasius uzbeki Seifert, 1992
- †Lasius validus Zhang, 1989
- Lasius vestitus Wheeler, 1910
- †Lasius vetulus Dlussky, 1981
- Lasius viehmeyeri Emery, 1922
- Lasius vostochni Seifert, 2020
- Lasius wittmeri Seifert, 1992
- Lasius xerophilus MacKay & MacKay, 1994
References
[edit]- ^ Bolton, B. (2021). "Lasius". AntCat. Retrieved 31 October 2021.
- ^ "Genus: Lasius". AntWeb. Archived from the original on 2013-12-02. Retrieved 2012-02-05.
- ^ a b "Lasius latipes - AntWiki". www.antwiki.org. Retrieved 2024-11-23.
- ^ a b "Lasius murphyi - AntWiki". www.antwiki.org. Retrieved 2024-11-23.
- ^ "Lasius subglaber - AntWiki". www.antwiki.org. Retrieved 2024-11-23.
- ^ a b c "A Guide to Lasius Social Parasites". Stateside Ants. Retrieved 2024-11-23.
- ^ Greenfieldboyce, Nell (2025-11-17). "Why some ant colonies get tricked into killing their own queens". KPBS Public Media. Retrieved 2025-11-20.
- ^ "Lasius claviger - AntWiki". www.antwiki.org. Retrieved 2024-11-23.
- ^ a b c d e f Klotz, John H. (2010). Urban Pest Management of Ants in California. UCANR Publications, Division of Agriculture and Natural Resources, University of California. pp. 54–55. ISBN 978-1601076649.
- ^ a b c Klotz, John H. (2008). Urban Ants of North America and Europe: Identification, Biology, and Management. Cornell University Press. pp. 39–44. ISBN 978-0801474736.
- ^ a b c Antonelli, Art (2007). "Extension Bulletin 1382: Moisture Ants" (PDF). WSU Extension. Washington State University. Archived from the original (PDF) on August 13, 2012. Retrieved March 4, 2013.
External links
[edit]
Media related to Lasius at Wikimedia Commons
Lasius
View on GrokipediaTaxonomy
Classification
Lasius belongs to the family Formicidae within the order Hymenoptera, specifically placed in the subfamily Formicinae and the tribe Lasiini.[6] The genus was established by Johan Christian Fabricius in 1804, with Lasius niger (described by Carl Linnaeus in 1758) designated as the type species.[7] Significant taxonomic revisions occurred in the late 19th and early 20th centuries, notably by Auguste Forel, who expanded species descriptions and classifications, and by Carlo Emery, whose 1925 catalog synthesized Formicidae taxonomy, including Lasius groupings.[8] A 2022 phylogenetic revision by Boudinot, Borowiec, and colleagues, incorporating molecular and morphological data, proposed synonymizing all subgenera (Acanthomyops, Austrolasius, Chthonolasius, Cautolasius, Dendrolasius) under Lasius sensu stricto to reflect monophyly, replacing them with an informal species-group classification. This classification remains current as of 2025.[6][9] As of 2025, the genus comprises approximately 141 valid species.[9]Phylogenetic Relationships
A comprehensive phylogenetic analysis of the Lasiini tribe, including the genus Lasius, was conducted using a total-evidence approach integrating morphological characters and multi-locus molecular data from genes such as COI, EF1α, LW Rh, ArgK, and CAD. This study confirmed the monophyly of Lasius, resolving previous uncertainties about its internal structure and placing it within a broader Lasiini clade. Sister groups to Lasius include genera like Prenolepis, highlighting the tribe's diversification through key morphological innovations such as wideset coxae. The evolutionary origins of Lasius trace to a Holarctic radiation during the late Eocene to Oligocene, with divergence dating indicating the crown age of Lasius around 22 million years ago (early Miocene), rooted in Eurasian ancestors before transcontinental dispersal. This period facilitated adaptations to temperate environments. The genus's success in these regions is linked to ecological specializations, though behavioral details are beyond phylogenetic scope here. Recent molecular studies have uncovered significant cryptic diversity within Lasius, particularly in North America, where DNA barcoding of the COI gene revealed cryptic diversity within species complexes previously lumped under morphospecies like Lasius neoniger, leading to the description of a new species, Lasius ponderosae.[4] This integrative approach, combining barcoding with morphological and ecological data, emphasizes the role of genetic tools in delineating biodiversity and detecting invasions. Key clades within Lasius show clear separation between wood-nesting and soil-nesting lineages, reflecting early divergences in nesting ecology. The wood-nesting clade, including species like Lasius fuliginosus, forms a distinct monophyletic group adapted to arboreal or decaying wood habitats, while soil-nesting forms, such as those in the Lasius niger group, dominate open-ground environments and exhibit broader geographic ranges. These clades align with the revised species groups, providing a framework for understanding Lasius diversification.Morphology
Worker Characteristics
Workers in the genus Lasius exhibit a body length ranging from 2 to 5 mm, with most species displaying monomorphic morphology, though some show weak polymorphism where minor size variations occur among individuals within a colony.[10][11] The head is subtriangular with a straight or slightly concave posterior margin, featuring moderately sized compound eyes that provide adequate visual acuity for foraging tasks.[11] Mandibles are triangular, equipped with 7 to 12 teeth adapted for cutting vegetation and capturing small prey.[11] The antennae consist of 12 segments without a distinct club, where segments 3 through 7 are collectively shorter than segments 8 through 12.[11] The thorax, or mesosoma, has a dorsum characterized by two convex curves: the promesonotal and propodeal dorsa, with the propodeal section positioned lower than the promesonotal section and featuring a short, upwardly sloped propodeum with a longer posterior declivitous face.[11][12] The promesonotal dorsum bears well-developed pubescence, and the propodeal spiracle is approximately circular.[11] The abdomen includes a petiole with a single node and a smooth gaster, which serves as a reservoir for chemical defense; workers can expel a spray of formic acid from the acidopore at the gaster's tip to deter predators and pathogens.[13] Coloration varies across the genus, ranging from black in species like L. niger to yellow-brown in subterranean forms such as L. flavus, often accompanied by fine pubescence covering the body surface.[11]Reproductive Castes
Queens in Lasius species represent the reproductive female caste and are notably larger than workers, typically measuring 8–12 mm in length. Alate queens are equipped with large wings adapted for nuptial flights and possess three ocelli for enhanced vision during dispersal. A key reproductive adaptation is the presence of a spermatheca, a specialized organ that allows queens to store sperm from a single mating event for lifelong use in fertilizing eggs.[14] Males, the reproductive caste responsible for insemination, are smaller than queens, ranging from 4–7 mm in length, and exist primarily as winged alates. Their petiole is reduced compared to that of females, and the genitalia are structured for a single mating, after which males typically die. Following the nuptial flight and mating, queens shed their wings, leaving characteristic wing scars on the thorax, and become dealate. The abdomen of dealate queens becomes physogastric, greatly enlarged to accommodate developing ovaries and support high rates of egg production during colony founding. Sexual dimorphism is pronounced in Lasius, with males differing from both queens and workers in body proportions and ephemeral winged form. In parasitic species such as Lasius umbratus, queens may be ergatomorphic, morphologically resembling workers in size and appearance to facilitate infiltration of host colonies during social parasitism.[15]Distribution and Habitat
Geographic Range
The genus Lasius exhibits a primarily Holarctic native distribution, spanning Europe, northern Asia, and North America, with extensions into Mediterranean and temperate climatic zones but a notable absence from tropical regions. This range reflects the genus's adaptation to cooler, seasonal environments, where it thrives in diverse temperate ecosystems from boreal forests to grasslands.[4][16] Species richness within Lasius is highest in Europe, with numerous species documented across the continent and adjacent Mediterranean areas, compared to approximately 33 extant species in North America. These patterns underscore Europe's role as a diversity hotspot, influenced by varied topography and post-glacial recolonization, while North American assemblages show lower but significant endemism. The genus comprises around 140 valid extant species worldwide.[17][18][2] Several Lasius species have been introduced beyond their native ranges through human activities, particularly international trade and transport. Lasius niger, for instance, has established introduced populations in North America, Madagascar, and some Pacific islands, as well as urban centers worldwide, often in disturbed habitats like ports and cities. Similarly, Lasius neglectus, originally from the Middle East and Central Asia, has spread invasively across Europe and into anthropogenic sites in Asia via similar vectors, forming expansive supercolonies. Detections of cryptic L. niger-like taxa in North American urban areas.[19][20][4] Biogeographically, Lasius traces its origins to the Palearctic region, with the crown group of the tribe Lasiini emerging near the end of the Cretaceous on the Eurasian continent. Nearctic diversification occurred through repeated trans-Beringian dispersals, particularly during the Pleistocene, leading to non-reciprocal monophyly between Palearctic and Nearctic lineages and post-glacial divergences that shaped current distributions.[16]Environmental Preferences
Lasius species predominantly favor temperate climates, where they establish colonies in moist, shaded environments such as forests, meadows, and grasslands. These ants typically select nest sites in soil under stones, logs, or within shallow earthen mounds, often in rocky loam substrates that provide stability and protection from direct sunlight and desiccation.[19] Such preferences ensure consistent humidity levels essential for brood development and colony maintenance.[21] Certain Lasius species, particularly those in moist habitats like the moisture ants, construct nests in decaying wood, rotting logs, or tree stumps, capitalizing on the elevated moisture retention in these materials. These sites are common in woodlands and shaded forest edges, where soil and wood decomposition supports fungal growth and stable microclimates. Colonies generally avoid extremes of dryness, which can limit foraging and survival, though they demonstrate resilience to occasional flooding in low-lying areas.[21][22] While most Lasius taxa thrive in humid conditions, some exhibit adaptations to drier or more variable climates, such as Lasius sitiens in arid shrublands and lower montane zones of the southwestern United States. Altitudinally, the genus extends from sea level to elevations up to 2,700 meters in coniferous forests and mountain meadows, with species like Lasius nearcticus common in the Appalachian ranges. Urban adaptability further broadens their tolerance, allowing persistence in disturbed, anthropogenic landscapes alongside their native associations with vegetation-rich soils.[23][24][25]Reproduction
Mating Flights
Mating flights in the genus Lasius occur primarily during the summer months in the northern hemisphere, spanning June to August, with species-specific timing such as June to July for Lasius niger. These events are triggered by warm, humid weather conditions, often following rainfall, with optimal parameters including air temperatures around 20–25°C, soil temperatures of 18–22°C at 5–7 cm depth, relative humidity above 60%, and low wind speeds below 1.7 m/s. Synchronous eclosion of alates from multiple colonies ensures mass emergences, typically lasting 1–2 days per site and synchronizing across large areas to facilitate outbreeding.[26][27] During the nuptial flight, virgin queens and males emerge from their natal nests in the afternoon or evening, with males often outnumbering females in swarms. Queens fly relatively short distances, reaching altitudes of 7–150 m depending on the species (e.g., 7 m for Lasius alienus queens), while males patrol lower at 1 m or aggregate in leks at prominent landmarks like forest edges to pursue and intercept females. Mating occurs mid-air or on nearby vegetation, with queens typically copulating only once with a single male, acquiring sufficient sperm for lifelong egg fertilization; multiple matings are rare but documented in some populations, averaging an effective mating frequency of 1.16.[27][28] Pheromonal cues are essential for mate location, with virgin queens releasing sex attractants to draw pursuing males during the flight. Post-copulation, queens immediately undergo dealation by shedding their wings and histolyzing flight muscles, after which they disperse to seek independent nest sites for colony founding, while males perish within hours or days.[27]Colony Establishment
In Lasius ants, colony establishment primarily occurs through claustral founding, where a newly fertilized queen seals herself in a small underground chamber shortly after her mating flight, relying solely on her body reserves to rear the first brood without foraging or external aid. This strategy minimizes predation risk during the vulnerable initial phase, as the queen histolyzes her flight muscles and mobilizes stored lipids and proteins to produce eggs and nourish developing larvae. The first workers, known as nanitics, typically emerge after 4-6 weeks, marking the transition to a functional workforce that begins foraging and nest expansion.[29] The brood development process unfolds in distinct stages under claustral conditions. Eggs, laid in clusters by the queen, hatch into larvae after approximately 14-16 days at optimal temperatures around 25-27°C, though durations can extend to 20 days or more at lower temperatures or higher latitudes. Larvae, which are legless and require constant care, develop over 2-3 weeks and are fed a diet consisting primarily of trophic eggs produced by the queen—nutrient-rich eggs that serve as food rather than developing into adults. Pupae form next, with the larvae spinning silken cocoons; this stage lasts 10-14 days, culminating in the eclosion of the first workers. These timelines vary with temperature and queen condition, with total development from egg to adult worker ranging from 35-70 days depending on environmental factors.[30][31] Dependent founding is rare in the genus Lasius but occurs in certain socially parasitic species through usurpation of host colonies. In these cases, ergatoid or specialized queens infiltrate an established nest of a closely related Lasius species, such as Lasius niger for Lasius umbratus or Lasius neoniger for Lasius claviger, eliminating or supplanting the resident queen to commandeer the host workers for rearing their own brood. This temporary parasitism allows the invading queen to bypass the energy-intensive claustral phase, though it is limited to specific taxa like Lasius umbratus and Lasius claviger.[32] Once established, Lasius colonies grow steadily, achieving maturity in 1-3 years with populations exceeding 10,000 workers in many species, such as Lasius niger. Mature colonies in some taxa, including L. niger and L. fuliginosus, often adopt polydomy, distributing the workforce across multiple interconnected nests to enhance resource exploitation and defense.[19][33]Behavior
Foraging Strategies
Lasius ants exhibit an omnivorous diet, with honeydew from tended aphids serving as the primary carbohydrate source, supplemented by predation on small insects for protein, scavenging of carrion, collection of plant nectar, and occasional harvesting of seeds.[34][35][36] Workers stimulate honeydew production by gently stroking aphids with their antennae, a behavior that underscores the mutualistic relationship central to their foraging economy, while direct predation on aphids occurs rarely and typically involves non-productive individuals.[35] This diverse intake allows colonies to balance nutritional needs, with carbohydrates fueling general activity and proteins supporting brood development. Foraging is coordinated through chemical communication, where workers deposit trail pheromones such as (Z)-9-hexadecenal to mark paths to food sources, enabling efficient navigation and recruitment of nestmates.[37] In species like Lasius niger, mass recruitment events are triggered by large or abundant prey items or high-quality food sources, where foragers deposit up to 43% more pheromones on high-value sucrose sources compared to dilute ones.[38] This group-mass recruitment strategy enhances colony exploitation of ephemeral resources, with trails often reinforced near food to concentrate efforts. Most Lasius species, including L. niger, display predominantly nocturnal foraging patterns, with peak activity during nighttime to avoid daytime heat and competition while benefiting from cooler temperatures that reduce desiccation risk.[19] In contrast, subterranean species such as Lasius flavus conduct foraging primarily underground, targeting root-feeding aphids in soil without surface excursions.[39] Territorial defense is integral to these strategies, as workers aggressively confront and repel rival ants from aphid colonies, a behavior intensified in urban settings where L. niger exhibits heightened aggression to secure honeydew supplies.[40]Nest Construction
Lasius nests are predominantly subterranean, excavated from soil or occasionally wood, forming complex multi-chambered structures that include dedicated brood chambers for larval development and areas for food storage. These nests consist of interconnected galleries and chambers, with typical dimensions featuring chamber heights of approximately 5.5–5.9 mm and widths around 12 mm, occupying about 30% of the total nest volume in mature setups. Workers shape and deposit excavated soil particles into cohesive pellets, often using a sand-clay mixture, to build pillars and roofs that support the architecture, guided by stigmergic cues such as pheromones that enhance deposition on existing structures.[41] Nest expansion occurs through ongoing excavation by workers, who regulate nest size in direct proportion to colony population growth, ensuring sufficient space as the number of individuals increases. In species like Lasius neglectus, mature colonies develop polydomous networks, comprising multiple interconnected nests linked by persistent trails that facilitate worker movement and resource transport without delving into foraging specifics. This modular growth involves adding new shafts and chambers, with digging rates adjusting based on environmental factors like soil moisture and composition. Defense of the nest relies on behavioral and chemical mechanisms, with workers acting as entrance guards to patrol openings and aggressively confront intruders through biting and recruitment. Formic acid, produced by the ants, serves as a key chemical barrier, sprayed to repel threats and acting as an alarm pheromone that mobilizes colony members for collective defense. In established colonies, the queen remains a stationary egg-layer in a central, protected chamber, relying entirely on workers for all construction, expansion, and maintenance activities.[42]Social Parasitism
Parasitic Mechanisms
In the genus Lasius, social parasitism primarily manifests through temporary strategies during colony foundation, where newly mated queens of parasitic species infiltrate established colonies of host species, typically congeneric ones such as Lasius niger or Lasius japonicus. These queens employ aggressive tactics to eliminate the resident queen, often by direct physical attack, allowing them to appropriate the host's workforce for rearing their own brood without the energetic demands of independent claustral founding. This process relies on the parasite queen's ability to evade initial host aggression through behavioral stealth and rapid integration, enabling her offspring—workers, queens, and males—to be raised by host workers until the parasitic colony achieves independence and expels or outcompetes the hosts.[43] Permanent social parasitism in Lasius lacks true slave-making (dulosis), where parasites actively raid and enslave brood from other colonies, a trait more common in genera like Formica or Polyergus. Instead, some species exhibit dependency without raiding, relying on sustained exploitation of host colonies through chemical mimicry of the host's cuticular hydrocarbons to prevent rejection and maintain acceptance within the mixed society. Parasitic queens and their progeny blend chemically with hosts, facilitating long-term brood care by host workers, though most retain a reduced worker caste. This mimicry evolves as a deceptive strategy to exploit host recognition systems, allowing parasites to persist in host nests.[43] Inquilinism represents an extreme form of permanent parasitism in ants generally, characterized by workerless parasites that produce only sexuals and depend entirely on host workers for all brood care, foraging, and nest maintenance. While rare in Lasius, species in subgenera like Chthonolasius show elements of high dependency, where queens integrate into host colonies post-nuptial flight and lay eggs reared solely by hosts, with minimal or no parasitic workers emerging. This total dependency evolves in isolated lineages, rendering the parasites incapable of independent survival.[44] The evolution of these parasitic mechanisms in over 20 Lasius species is driven by the high costs associated with claustral colony founding, where independent queens must provision and rear initial workers in isolation without external aid, facing risks of starvation, predation, and disease. Temporary parasitism has arisen at least twice in the genus's phylogeny, often reversing back to independent founding, while permanent forms emerge from further degeneration of worker production, favored in environments where host availability reduces the selective pressure for self-sufficiency. These adaptations highlight how social parasitism circumvents founding bottlenecks, promoting diversification within the genus.[45][46]Notable Parasites
Lasius reginae serves as a prominent example of a temporary social parasite in Europe, targeting hosts such as Lasius alienus. The queen infiltrates the host colony through aggressive usurpation, typically by throttling the resident queen to death, enabling her to lay eggs that are reared by the host workers until the parasite's own workforce emerges.[47][48] In North America, Lasius latipes represents an occasional parasitic species on Lasius neoniger, the cornfield ant, particularly in open or moist habitats. The parasite queen gains acceptance by mimicking the host's chemical cues, relying on host workers for brood care during initial colony establishment before producing her own offspring.[49][50] Lasius fuliginosus is another key temporary parasite that establishes in nests of Lasius umbratus across Europe, which itself parasitizes Lasius niger; this forms a chain where the queen exploits the intermediate host colony for workforce support post-infiltration, often without producing workers in the early stages.[51] Social parasitism in Lasius exhibits strong intra-generic host specificity, with parasitic success heavily dependent on chemical integration, such as matching cuticular hydrocarbon profiles to evade host aggression and facilitate mimicry.[52]Ecology
Interspecies Interactions
Lasius ants engage in mutualistic relationships with aphids, where workers tend colonies of hemipteran insects such as Aphis fabae to harvest honeydew, a sugar-rich excretion produced by aphids feeding on plant phloem sap. This interaction provides Lasius species, including L. niger, with a reliable carbohydrate source that supports larger colony sizes and higher worker densities compared to non-tending colonies. In exchange, Lasius ants defend aphids against predators and parasitoids, resulting in increased aphid survival and abundance on tended plants. For instance, L. niger workers aggressively remove ladybird beetles and other natural enemies, though this protection can indirectly increase plant damage by allowing aphid populations to proliferate unchecked. Recent studies show L. flavus protects eggs of root aphids like Anoecia zirnitsi from predators, increasing their viability.[53] Lasius species exhibit antagonistic interactions with other ant genera through territorial conflicts, particularly with Formica and Solenopsis. L. niger workers display heightened aggression in group encounters, attacking intruders more frequently when supported by nestmates, which helps maintain foraging boundaries against competing species like Formica polyctena. Experimental introductions of Formica species on islands have reduced Lasius colony densities through competitive exclusion and direct combat. Similarly, boundary skirmishes with Solenopsis invicta often follow a linear mortality pattern, where larger colonies dominate and eliminate smaller ones via raids. Beyond inter-ant antagonism, Lasius ants are opportunistic predators of small invertebrates, including tick eggs and other arthropods. L. alienus workers remove up to 68% of dewaxed eggs from species like Rhipicephalus bursa and Hyalomma excavatum within 24 hours, with predation rates dropping for waxed eggs due to the protective coating; this behavior meets the ants' protein needs by targeting accessible prey. Lasius ants are susceptible to entomopathogenic fungi and nematodes, prompting defensive grooming behaviors. L. flavus experiences significant mortality from Beauveria bassiana exposure, with survival rates decreasing by over 50% compared to controls, though L. platythorax shows no behavioral self-medication like altered foraging to avoid infection. Mermithid nematodes infect L. alienus at high rates, altering host morphology and behavior to facilitate transmission, while L. brunneus workers carry nematodes externally at frequencies up to 43.5%. In response, Lasius ants employ autogrooming to remove pathogens, though this behavior paradoxically decreases in L. flavus and L. platythorax post-exposure to B. bassiana, potentially exacerbating infection; allogrooming and trophallaxis occur rarely, with fewer than 0.1 events per observation period. Interactions with plants include seed dispersal and occasional herbivory or damage. Certain Lasius species, such as L. niger, participate in myrmecochory by transporting elaiosome-bearing seeds in temperate forests, removing them from parent plants and improving germination rates through burial in nutrient-rich nest soil. L. flavus mounds alter soil properties, increasing pH and base cations, which favors certain plant growth but can inhibit others via indirect root stress from excavation. While primarily aphid-dependent, Lasius workers occasionally feed on plant sap at wounds or roots, contributing to minor herbivory on temperate species like Veronica, though this is less significant than their predatory impacts.Ecosystem Roles
Lasius ants play a significant role in soil aeration through their extensive nest excavation activities. Species such as Lasius neoniger construct complex tunnel networks extending up to one meter deep, which enhance soil porosity and oxygen availability for plant roots, while also facilitating water infiltration and reducing soil compaction.[54] Similarly, Lasius flavus mounds alter soil physical properties, promoting better drainage and aeration in grassland ecosystems.[55] These processes contribute to nutrient cycling by redistributing organic matter and biomass; for instance, Lasius spp. activities increase soil total available nitrogen by approximately 17%, supporting plant growth and overall ecosystem productivity.[56] In terms of biodiversity support, Lasius ants serve as a key prey resource for various predators, including birds and insects, particularly during nuptial flights when winged alates emerge en masse.[57] Their nests also influence soil microarthropod communities, creating heterogeneous microhabitats that, despite reducing detritivore abundance like Collembola and Oribatida, foster specialized myrmecophilous species and overall community structure in urban and grassland settings.[58] Regarding aphid interactions, Lasius tending provides indirect benefits to host plants by deterring other herbivores; for example, Lasius fuliginosus reduces leaf herbivory on oak trees (Quercus liaotungensis) by up to 2.3% at the whole-tree scale, outweighing aphid-induced damage in certain contexts and enhancing plant biomass production.[59][60] The invasive species Lasius neglectus forms expansive supercolonies across Europe and Asia, originating from Asia Minor and spreading rapidly since the 1990s through human-mediated transport.[61] These supercolonies exhibit high aggression toward native ants, effectively excluding them from core areas and drastically reducing local ant diversity and broader invertebrate communities in urban and disturbed habitats.[62][63] Over 200 sites have been documented, with ecological impacts including the displacement of native species and alteration of ground-nesting arthropod assemblages.[64] Lasius species are valuable indicator taxa for ecological monitoring due to their sensitivity to habitat fragmentation and disturbance. Their nest density and community composition decline in fragmented landscapes, reflecting changes in soil quality and connectivity; for instance, Lasius niger and Lasius flavus presence correlates with improved soil nutrients and rehabilitation progress in restored sites.[55] In temperate ecosystems, shifts in Lasius abundance signal fragmentation effects, aiding assessments of biodiversity loss and ecosystem health.[65]Species Diversity
Subgenera
The genus Lasius comprises over 140 species worldwide, primarily distributed across the Holarctic region, with ongoing taxonomic revisions revealing cryptic diversity through integrative approaches like quantitative morphology and molecular data.[2] These revisions have led to splits in previously recognized species complexes, increasing the documented count beyond 100, though subgeneric boundaries remain debated due to phylogenetic paraphyly in some lineages.[3][6] The nominotypical subgenus Lasius s.str. includes more than 50 species, predominantly soil-nesting black ants characterized by large compound eyes, above-ground foraging, and elongated maxillary palps adapted for generalist predation and scavenging. These ants are primarily Palearctic in distribution, with species like L. niger forming extensive polydomous colonies in temperate grasslands and forests. Recent revisions using numeric morphology-based alpha-taxonomy (NUMOBAT) have identified 56 valid Palaearctic species in this subgenus, including several newly described forms from cryptic sibling species. The subgenus Chthonolasius, known as moisture ants, consists of wood-nesting species that inhabit damp, decaying timber in forested environments, with workers featuring moderately large eyes and a preference for humid microhabitats.[3] This group has a Holarctic distribution but is particularly diverse in North America, where species like L. umbratus exploit moist rot pockets in logs and stumps for nesting.[18] Colonies often exhibit above-ground foraging trails and are adapted to high-moisture conditions, contributing to decomposition processes.[18] Acanthomyops, comprising yellowish cornfield ants, is distinguished by small eyes, subterranean nesting habits, and a tendency for temporary social parasitism during colony founding, with workers releasing a citronella-like odor when disturbed.[3] Primarily Nearctic, this subgenus includes around 10-15 species, such as L. claviger, which nest in open fields and grasslands, often under stones or in soil.[18] Parasitism is common, with queens infiltrating host colonies of other Lasius species to raise initial broods.[3] The subgenus Dendrolasius features fewer species, estimated at 5-10, specialized for arboreal nesting in tree hollows and branches, with workers showing adaptations for climbing and tending tree-dwelling hemipterans.[66] This group is largely restricted to East Asia, including species from the Russian Far East and Japan, where they form smaller colonies in temperate woodlands.[66] Taxonomic reviews highlight their distinct morphology, such as reduced scapes and pubescence, separating them from soil-dwelling relatives.[3] The subgenus Cautolasius includes about 7 species, primarily Holarctic, characterized by small eyes and often social parasitic lifestyles, with workers adapted to subterranean or wood-nesting in moist environments.[67] Austrolasius is a small subgenus with few species restricted to Australasia, featuring adaptations to temperate and subtropical habitats, distinct from the Holarctic groups.[2] Donisthorpea comprises rare, socially parasitic species, mostly in the Palearctic, known for inquilinism in host colonies of other Lasius subgenera.[2]Key Species
Lasius niger, commonly known as the black garden ant, is one of the most widespread and adaptable species within the genus, thriving in diverse environments including urban settings where it adjusts foraging patterns and colony growth in response to abiotic stressors like temperature and humidity.[68] This species exhibits remarkable flexibility in habitat use, ranging from soil to arboreal tiers, enabling it to colonize anthropogenic landscapes effectively.[69] Mature colonies can support over 10,000 workers, facilitating robust social organization and resource exploitation.[70] Lasius flavus, the yellow meadow ant, is predominantly European and specializes in subterranean lifestyles, constructing mound nests in grasslands while relying heavily on root-dwelling aphids for nutrition through mutualistic farming.[71] These ants protect aphid eggs during winter hibernation, enhancing the aphids' survival against predators and pathogens, which in turn sustains the colony's carbohydrate and protein intake.[72] Their mound-building alters soil properties and influences local plant communities by favoring grasses over herbs.[73] Lasius neoniger, referred to as the cornfield ant, is a prominent North American species known for its mound-building behavior, creating conspicuous nests in open fields and disturbed areas that can disrupt managed landscapes like golf courses.[74] As a native yet abundant forager, it demonstrates potential as a nuisance in agricultural and recreational settings due to its polydomous colony structure and competitive foraging, though it remains ecologically integrated in grasslands.[75] Lasius neglectus stands out as an invasive species capable of forming expansive supercolonies, characterized by unicoloniality where multiple queens and nests interconnect without aggression, leading to reduced genetic diversity and high worker relatedness across vast populations. This social structure enhances its invasive success by promoting polygyny and resource sharing, displacing native ants in introduced ranges across Europe and Asia.[76] Lasius nearcticus, known as the moisture ant, prefers nesting in decaying wood and damp soils within forested or wooded areas, forming small colonies under logs, stones, or leaf litter in moist environments.[77] Its affinity for high-moisture sites makes it a structural pest in buildings, where it infests rotting wooden elements, potentially exacerbating damage in humid conditions.References
- https://www.antwiki.org/wiki/Lasius
- https://www.antwiki.org/wiki/Checklist_of_Lasius_species
- https://www.antwiki.org/wiki/Lasius_niger
- https://www.antwiki.org/wiki/Lasius_nearcticus
- https://www.antwiki.org/wiki/Lasius_flavus
- https://www.antwiki.org/wiki/Social_Parasitism
- https://www.antwiki.org/wiki/Lasius_reginae
- https://www.antwiki.org/wiki/Lasius_latipes
- https://www.antwiki.org/wiki/Lasius_fuliginosus
- https://app.sib.[illinois](/page/Illinois).edu/suarez/local/suarez/uploads/2020/01/Belcher_etal2016AmEnt.pdf
