Research Article
Research Article
Nylanderia deceptrix sp. n., a new species of obligately socially parasitic formicine ant (Hymenoptera, Formicidae)
expand article infoSteven Messer, Stefan Cover§, John LaPolla|
‡ Rochester University, Rochester, United States of America
§ Harvard University, Cambridge, United States of America
| Towson University, Towson, United States of America
Open Access


Obligately socially parasitic ants are social parasites that typically lack the sterile worker caste, and depend on the host species for survival and brood care. The genus Nylanderia has over 130 described species and subspecies, none of which, until this study, were known social parasites. Here we describe the first social parasite known in the genus, Nylanderia deceptrix. Aspects of the biology of the host species, Nylanderia parvula (Mayr 1870), and N. deceptrix are examined. The data from both the host and the parasite species are combined to better understand the host-parasite relationship.


Ants, Formicinae , Nearctic, New Species, Social Parasitism


Social parasitism consists of an array of fascinating life history strategies that are expressed in several different ways among the ants (Nonacs and Tobin 1992, Bekkevold and Boomsma 2000, Buschinger 2009, Rabeling and Bacci Jr. 2010). Among the socially parasitic ants are those that are obligate social parasites. Obligately socially parasitic ants are characterized by a combination of life history traits where one ant species parasitizes another free-living ant species and relies on the host species for brood care and nourishment (Wilson 1971, Hölldobler and Wilson 1990, Buschinger 2009). For most ants the “typical” colony structure is one where there are one or more queens responsible for egg-laying and workers responsible for colony functions related to colony growth and development (Fischman et al. 2011). Conversely, obligate social parasites insert themselves into the colonies of other species, live with the host workers and possibly queen(s), and have their brood, which is usually only reproductives, reared by the host workers (Bekkevold and Boomsma 2000, Maschwitz et al. 2000). Of the over 13,000 described ant species, obligate social parasites are seemingly rare with about 80 known species displaying this life history strategy (Buschinger 1990, Mardulyn et al. 2014). The origin of socially parasitic ants has been of interest to myrmecologists for over a century. Emery’s Rule, which states social parasites tend to be closely related to their host species, was one of the earliest observations regarding the evolution of social parasitism in ants (Emery 1909). It can be expressed in either loose (likely closely related, but parasite and host are not sister taxa) or strict (parasite and host are sister taxa) forms. Examination of Emery’s Rule in the strict sense has provided evidence for sympatric speciation among obligate social parasites such as in Myrmica (Leppänen et al. 2015) and Mycoceperus (Rabeling et al. 2014).

The Nearctic Nylanderia currently consists of 14 native and 5 introduced species ranging from southern Canada to central Mexico (Kallal and LaPolla 2012). Most Nylanderia species around the world appear to nest in leaf litter and rotting wood (LaPolla et al. 2010), but there are habitat specialists in the Nearctic as well, such as the white sand nesting Nylanderia phantasma (Trager 1984) and the acorn inhabiting Nylanderia querna (Kallal and LaPolla 2012). All Nearctic Nylanderia overwinter their reproductives, which then emerge in the spring and early summer (Trager 1984, Kallal and LaPolla 2012).

Until recently Nylanderia species were all thought to display the “typical” colony life history discussed above, and social parasites were unknown. This changed, however, when one of us (SPC) discovered an unusual (only known from winged queens and wingless males), new Nylanderia species in Myles Standish State Forest in Massachusetts (USA) seemingly living in the colonies of Nylanderia parvula (Mayr 1870). This study is about that unusual Nylanderia, which we here describe as a new, obligately socially parasitic species, Nylanderia deceptrix, sp. n. Given that so little is known about obligately socially parasitic ant biology, the study of any obligately socially parasitic ant can provide valuable insights into this interesting biological phenomenon. Aspects of the biology of the host species, Nylanderia parvula (Mayr 1870), and N. deceptrix are examined with the hope of shedding light on how this example obligate social parasitism is expressed within Nylanderia.

Materials and methods

Field Site, sampling and rearing conditions: The field site for this study was Myles Standish State Forest in southeastern Massachusetts, the only known location of N. deceptrix (Fig. 1). The forest is part of the Atlantic coast pine-barrens system that stretches through the northeastern United States, including New York, New Jersey and Massachusetts (Dinerstein et al. 2015). The forest itself is open canopy, largely composed of pitch pine (Pinus rigida), bear/scrub oak (Quercus ilicifloia), and very sandy soil. Previous fieldwork had found a high density of N. parvula colonies in Myles Standish State Forest with the obligately socially parasitic species being collected from several colonies on at least three different collecting trips prior to this study.

Within Myles Standish State Forest collections were along Southeast Line Road (41°49.12'N, 70°39.75'W, elev. 31 m) a sandy horse trail, in June, July and September of 2013 and May, June, July and September of 2014. During these trips, colonies were excavated, and then collected and/or observed for data collection purposes described below.

Figure 1. 

Land conservation map of Massachusetts (orange and green represent protected areas), with the location of Myles Standish State Forest indicated. Modified from

Whole colonies were collected in order to determine the general population size and temporal changes within colonies of N. parvula. Entire colonies were excavated using a shovel and trowel, digging in the area around active nest entrances and following active chambers until observed activity ended and no part of the colony remained. Each excavated colony was examined for the presence of obligate social parasites. A minimum of eight colonies were collected and preserved for each month (May n=12, June n=10, July n=13, and September n=19 between June 2013-September 2014) for population census analysis, and the GPS coordinates of each colony was recorded. Sampled colonies were stored in large Ziploc bags, preserved in 95% ethanol and stored in a -23°C freezer until sorting. Individual ants were separated from the soil samples manually by hand and stored in vials containing 95% ethanol in a -23°C freezer. The pupal brood from each colony was determined to species (either N. parvula or N. deceptrix) by measuring queen pupae (N. deceptrix 2.73-3.20 mm, n=31 and N. parvula 3.31-3.89 mm, n=84) and wing buds on male pupae (N. parvula is fully winged and N. deceptrix has highly reduced wing buds). Eleven colonies sampled from September 2013 were removed from analysis due to lack of whole colony collection.

Colonies taken for laboratory observation had as many individuals collected as possible via aspiration and housed temporarily in a plaster bottom nest box. In the lab live colonies were transferred to larger nest boxes composed of a nesting area and a foraging area where their food was located. The nesting area had a plaster bottom that was used to maintain moisture levels within the nest to prevent desiccation of the ants within. The colonies were fed a mixture of agar, water, egg, honey and a crushed vitamin mineral capsule. This mixture was placed inside a small cap in the foraging area and was monitored to ensure mold did not form in the food and if mold was found the food was replaced. Colonies were given 5 ml of water every 2–3 days to avoid desiccation. All gaps between tubes and the nest boxes were sealed with a silicone sealant to prevent any individuals from escaping the nest box.

Reproductive cycle: For each colony of N. parvula collected (completed as explained above for a total of n= 43) the number of individuals in each caste and developmental stage was determined: alate queens, dealate queens, males, workers, larvae (1st–4th instars) and pupae. Population census data was also compared across seasons to elucidate any temporal changes within colonies. These seasonal difference analyses included: average number of alates and average brood count.

Taxonomic description of Nylanderia deceptrix: All material examined was gathered from field sampling at Myles Standish State Forest (locality as specified above). Specimens of N. deceptrix were collected between 6 June 2013 and 16 September 2014, and preserved in 95% ethanol, and then mounted for morphological study.

Measurements were undertaken using a Leica MZ16 dissecting microscope and an ocular micrometer. Measurement terminology, abbreviations and definitions follow LaPolla et al. (2011) and Kallal and LaPolla (2012):

EL (Eye Length): maximum length of compound eye in full-face view.

GL (Gaster Length): the length of the gaster in lateral view from the anteriormost point of the first gastral segment (third abdominal segment) to the posteriormost point (in males this included through the posterior end of parameres).

HL (Head Length): the length of the head proper, excluding the mandibles; measured in full-face view from the midpoint of the anterior clypeal margin to a line drawn across the posterior margin from its highest points (to accommodate species where the posterior margin is concave).

HW (Head Width): the maximum width of the head in full-face view (in males, portion of the eyes that extends past the lateral margins of the head is included).

MMC (Mesonotal Macrosetae Count): the number of erect macrosetae on mesonotum to one side of sagittal plane.

MtMC (Metanotal Macrosetae Count): the number of erect macrosetae on metanotum to one side of sagittal plane.

MW (Mesonotal Width): the maximum width of the mesonotum in dorsal view.

PW (Pronotal Width): the maximum width of the pronotum in dorsal view.

PDH (Propodeum Height): height of the propodeum as measured in lateral view from the base of the metapleuron to the maximum height of the propodeum.

PFL (Profemur Length): the length of the profemur from its margin with the coxa to its margin with the tibia.

PFW (Profemur Width): the maximum width of the profemur.

PL (Paramere Length): the maximum length of the paramere.

PMC (Pronotal Macrosetal Count): the number of erect macrosetae on pronotum to one side of sagittal plane.

SL (Scape Length): the maximum length of the antennal scape excluding the condylar bulb.

SMC (Scape Macrosetal Count): the number of erect macrosetae on the scape visible in full frontal view.

TL (Total Length): HL+WL+GL

WL (Weber’s Length): in lateral view, the distance from the posteriormost border of the metapleural lobe to the anteriormost border of the pronotum, excluding the neck.

CI (Cephalic Index): (HW/HL) × 100

FI (Profemur Index): (FW/FL) × 100

REL (Relative Eye Index): (EL/HL) × 100

SI (Scape Index): (SL/HW) × 100

Each measurement was recorded to the nearest 0.001 mm and rounded to the nearest 0.01 mm. A total of 10 queens from six different colonies and five males from a single nest were used for the body measurement data. Color images were taken using a JVC KY-F75 digital camera and Syncroscopy Auto-Montage (v 5.0) software.

The male’s 9th gastral sternite and penis valve were dissected under a Leica MZ16 dissecting microscope. The male’s gaster was placed in a potassium hydroxide (KOH) solution to dissolve/weaken any connective tissues and then the sternite and penis valve were separated from the gaster. The sternite and penis valves were dyed with double stain, slide mounted in glycerin and drawn using an ocular grid with a Leica DM2500 light microscope.

Prevalence of host species and parasitism rate: Nest entrance density for N. parvula was determined by counting the number of nest entrances found within four 50 m × 0.5 m transects and dividing the number found by the area (Kaspari et al. 2000, Abbott 2005, Braschler 2005). Transects were laid out along the edge of the trail that served as the study site. Once counted, a nest entrance was marked by a flag to ensure that a nest entrance was not counted twice in the same transect. One of the 50 m transects intersected with a trail, as a result the length of the transect that was intersecting the trail was excluded, resulting in two smaller transects measuring 14 m × 0.5 m and 25 m × 0.5 m.

The parasitism rate of N. deceptrix was determined by excavating 356 N. parvula colonies over the course of two collecting seasons (as stated above). In excavating to determine if N. deceptrix was present, a colony was excavated using a shovel and the sand containing the colony was visually inspected for N. deceptrix. The number of host colonies containing N. deceptrix (n=9) was then divided by the total number of N. parvula nests excavated (n=356) to calculate the parasitism rate.

Flight and dispersal: Morphological calculations for forewing length and Weber’s length were made and compared against each other. The forewing length (FWL) (maximum length of the forewing from mesosomal attachment to wingtip) and Weber’s length (WL) were measured for N. deceptrix (n=22) and the following other Nearctic Nylanderia species that are known to fly: Nylanderia arenivaga (Wheeler 1905) (n=1), Nylanderia austroccidua (Trager 1984) (n=1), Nylanderia concinna (Trager 1984) (n=3), Nylanderia faisonensis (Forel 1922) (n=9), N. parvula (n=20), N. phantasma (n=1), N. querna (n=5), Nylanderia terricola (Buckley 1866) (n=1), Nylanderia vividula (Nylander 1846) (n=13), and Nylanderia wojciki (Trager 1984) (n=10). For N. deceptrix and N. parvula the measurements converted to a ratio (FWL:WL), and a Student’s t-test was used to determine if there was a significant difference between the proportionate size of forewings to Weber’s length between the two species. This was done specifically to see if the wings of N. deceptrix were proportionally smaller than the wings of N. parvula, and potentially link reduced wing size to their dispersal method. All species measurements were plotted on a scatter plot for comparison.

To determine whether or not N. deceptrix queens could fly (males are wingless), individual queens were tested by allowing them to walk to the tip of a pencil to see if they would fly off (Rabeling and Bacci Jr. 2010). Additionally queens were dropped to see if they would fly once put into free-fall. The pencil test was conducted with five individuals with five trials each and the drop test on two individuals with two trials each.

Aggression behavior: Pairings for aggression tests consisted of the following combinations (all workers are of N. parvula; parasitized refers to coming from a colony that had N. deceptrix queens within it): not parasitized colony worker-foreign not parasitized colony worker (control) (n=6), parasitized colony worker-not parasitized colony worker (n=5), N. deceptrix queen-not parasitized colony worker (n=2), N. deceptrix queen-not parasitized colony N. parvula queen (n=16), parasitized colony worker-parasitized colony worker (n=3), and N. deceptrix queen-foreign parasitized colony worker (n=2). Assessment of the aggression level followed a slightly modified scale used by Abbott (2005): 1=antennation then tolerance; 2=prolonged antennation (>5 seconds) followed by tolerance; 3=rapid flight or brief gaster flexion for chemical defense; 4=brief aggression consisting of biting legs, antennae, or other body parts followed by avoidance and flight; 5=prolonged fight between individuals, potentially to the death. The number of trials for each combination varied based on the available number of individuals/colony at the time of testing.

Introduction tests were also conducted to observe behaviors at the colony level in response to foreign individuals being introduced. Introduced individuals were placed into the foraging area of colonies (see Fig. 2) and observed. Combinations for the introduction tests consisted of the following (all workers are of N. parvula): not parasitized nest worker-foreign not parasitized nest (control) (n=5), N. deceptrix queen-foreign parasitized nest (n=3), parasitized nest worker-foreign parasitized nest (n=3), N. deceptrix queen-not parasitized nest (n=4), parasitized nest worker-not parasitized nest (n=5), and not parasitized nest worker-parasitized nest (n=4). The introduction tests were scored on the same scale as the aggression tests. These tests allowed for any behaviors that occur within or around the nest to be observed that may have been missed due to the inability to see within the nest during field observations (Heinze 1989, Johnson 1994).

Figures 2–11. 

Nylanderia deceptrix (queen USNMENT00755074; male 4, 5USNMENT00755083; male 6–11USNMENT00755073): 2 queen in lateral view 3 queen head in full-frontal view 4 male in lateral view 5 male head in full-frontal view 6–9 male genitalia in dorsal, lateral, and ventral view, and ventral view close-up of digitus and cuspis 10 male 9th sternite 11 penis valve (ectal view).


Nylanderia deceptrix sp. n.

Figs 2, 3 (queen); 4–11 (male)


queen, USA. Massachusetts: Plymouth County: Myles Standish State Forest; Southeast Line Road; 41°49.12'N, 70°39.75'W; elev. 31 m; in N. parvula nest; 06 June 2013 (S. Messer) (MCZC); 10 paratype queens and 7 paratype males same locality information as holotype except different collection dates (MCZC and USNM).


Queen: smallest of Nearctic Nylanderia (TL less than 3.5 mm); mesosoma color mottled with areas of lighter and darker brown to yellowish-brown; Male: very small, nonfunctional wings present.

QUEEN. Measurements (n=10): TL: 2.91–3.40; HW: 0.55–0.63; HL: 0.58–0.69; EL: 0.22–0.24; SL: 0.73–0.78; MW: 0.52–0.57; PW: 0.55–0.67; WL: 0.99–1.07; GL: 1.24–1.69; PDH: 0.35–0.42; PFL: 0.67–0.72; PFW: 0.15–0.17; SMC: 0–3; PMC: 4–5; MMC: 21–27; MtMC: 3–4.

Indices: CI: 92–97; REL: 33–37; SI: 121–130; FI: 21–24.

Overall brown to yellowish-brown; head and gaster darker brown with generally lighter mesosoma; mesosoma color mottled with areas of lighter and darker brown to yellowish-brown; antennae, mandibles and legs yellow; body covered with dense pubescence; macrosetae dark brown but usually with lighter yellowish-brown tips. Eyes bulge slightly beyond head outline in full-frontal view; three prominent ocelli present. Scapes long; yellow; exceed posterior margin of the head by the length of first 3 funicular segments; scapes with dense pubescence and sometimes with up to three short standing macrosetae, but often with none. Head with abundant macrosetae and layer of pubescence; slightly longer than broad; becoming slightly wider at posterior of head. Mesosoma covered with erect macrosetae and pubescence; most macrosetae on mesonotum and metanotum show strong curvature. Gaster covered in pubescence and a large cluster of macrosetae on first gastral tergite.

MALE. Measurements (n=5): TL: 1.91–2.05; HW: 0.45–0.46; HL: 0.48–0.53; EL: 0.17–0.18; SL:0.57–0.59; MW: 0.28–0.32; PW: 0.37–0.39; WL: 0.66–0.69; GL: 0.74–0.88; PDH: 0.24–0.26; PFL: 0.52–0.54; PFW: 0.11–0.13; PL: 0.20–0.24; SMC: 0; PMC: 0; MMC: 7–12; MtMC: 1–2.

Indices: CI: 88–97; REL: 34–36; SI: 125–127; FI: 22–25.

Overall color brown to brownish-yellow; head and gaster darker brown with generally lighter mesosoma; antennae, mandibles, legs, and parameres yellow; body covered with dense pubescence; macrosetae dark brown but usually with lighter yellowish-brown tips; cuticular surface dull, covered in a dense layer of appressed setae. Head longer than broad; eyes large and bulging beyond head outline in full-frontal view; three prominent ocelli present; scapes long, exceeding posterior margin of the head by length of first 3 funicular segments; scapes absent of macrosetae and with a dense layer of pubescence; clypeus roughly rectangular, with anterior margin emarginated; mandible broad, with 4 teeth; all but apical tooth are weakly developed; apical tooth distinct, curves in toward body midline. Mesosoma relatively small; very small nonfunctional wings present; mesosoma covered in pubescence, with erect setae of varying lengths dorsally and on legs. Pronotum collar-like; mesonotum offset from pronotum at sulcus; mesonotum rises sharply above height of pronotum; mesonotum flat dorsally with many erect setae of varying lengths; marcosetae on mesonotum and metanotum show strong curvature of about 90°; propodeum indistinct from remainder of mesosoma, but with steep declivity; petiole short, triangular, upright, with posterior face only slightly longer than anterior face. Gaster with a dense layer of pubescence and erect setae; parameres especially setose; parameres roughly triangular, turning slightly mesad posteriorly; long setae extend off of parameres; cuspi small and tubular, reaching digiti dorsally; digiti weakly anvil-shaped, with poorly developed point directed ventrally; volsellar lobes flat, slightly indented relative to digital margin.


The species epithet deceptrix (Latin = deceiver) is attributed to the parasitic lifestyle, deceiving the host to allow cohabitation.


Nylanderia deceptrix can be identified from other Nearctic species because it has the smallest queens of all Nearctic Nylanderia, ranging between 2.91–3.40 mm (Trager 1984, Kallal and LaPolla 2012). Compared to other Nearctic species with no macrosetae on the scape such as N. parvula and Nylanderia trageri (Kallal and LaPolla 2012), N. deceptrix is the only species with queens showing bicoloration, with the head and gaster being darker in color than the mesosoma. Additionally the queens have a mottled coloration on the mesosoma with areas of darker brown and yellow-brown. Nylanderia deceptrix males are currently the only Nearctic Nylanderia to display highly reduced wings. The male parameres display dense and very long macrosetae compared to those of other Nearctic species. The digitus displays a narrower area towards the base of the structure that expands towards the tip and ends with a narrow point. The end of the digitus also has distinct foveolate (pitted) sculpturing. The head of both the queen and the male are worker-like in overall appearance (except for the presence of distinct, large ocelli; never strongly developed in workers), and are longer than wide, whereas Nylanderia reproductives, especially queens, typically have wider than long heads. Additionally, Nylanderia queens usually have heads covered in dense pubescence, and this is not the case in N. deceptrix.

Prevalence of host species and parasitism rate

Across the seven transects, the average N. parvula nest entrance density was 2.35 nest entrances/m2 (SD=0.15), ranging from 1.64–2.64 nest entrances/m2 for the individual transects. Transect 1 was excluded from all calculations because of inexperience in locating nest entrances and insufficient surveying effort resulting in a density 81.3% less than the average across all other transects.

In total, 356 N. parvula colonies were excavated and checked for the presence of N. deceptrix. Of those 356 colonies, nine had N. deceptrix present, resulting in a parasitism rate of 2.53%. The number of N. deceptrix queens found in a single colony ranged from 1–8 per colony. Nylanderia deceptrix males were only found in one of the nine parasitized colonies, and contained a total of nine males. Nylanderia deceptrix brood were found in two of the nine parasitized colonies. One colony contained only a single N. deceptrix queen pupa. The range for N. parvula pupal length was 3.31–3.89 mm (n=84) and the range for N. deceptrix pupal length was 2.73–3.20 mm (n=30). On the other end of the spectrum one colony contained 74 N. deceptrix queen pupae and 4 N. deceptrix male pupae (male N. deceptrix pupae could be determined by highly reduced wing buds and the presence of genitalia).

Reproductive cycle

All colonies that were found to have dealate queens (n=17) only possessed one queen and we are taking this as evidence of monogyny in N. parvula. A total of 43 colonies were excavated and used for population census data collection. Among the 43 colonies, the average number of adult N. parvula reproductives (alate queens and males) found in colonies was: 15.4 (±23.3) for May, 0 for June, 6.1 (±4.1) for July, and 20.4 (±11.77) for September (Fig. 12). Compared to the number of alates, the total brood (larvae and pupae combined) within colonies shows the opposite trend (Figs 12, 13). Counts were low in May (37 ±134.2) and September (15.8 ±209.6), moderate in July (177.6 ±65.2), and at the highest in June (722.7 ±116.1). Nylanderia parvula reproductive pupae were only found in July, and N. deceptrix reproductive pupae were only observed in July as well.

Figure 12. 

Box-and-Whisker plot of within colony N. parvula alate reproductive counts from May, June, July and September.

Figure 13. 

Box-and-Whisker plot of within colony N. parvula brood counts from May, June, July and September.

Flight and dispersal

Forewing length (FWL) measurements were used along with Weber’s Length to determine a ratio of forewing to Weber’s length to examine if the wings of N. deceptrix were smaller in proportion to N. parvula. The FWL:WL for N. parvula ranged from 2.27–2.59, with an average of 2.47 (±0.018), and for N. deceptrix the ration ranged from 2.07–2.31, averaging 2.18 (±0.014). Comparing the averages using a Student’s t-test, the difference between the two was significant (P<0.00001, t=12.59 for a two-tailed test), meaning the wings of N. deceptrix were smaller in proportion to Weber’s length compared to N. parvula. When examining the scatter plot of Weber’s length to forewing length of all the Nylanderia species used (see material and methods for list), N. deceptrix falls well below the trendline created from the data of the other species (Fig. 14). The R2 value of the trendline was significant with a P-value<0.00001 (F=98.12), indicating a true relationship between forewing length and Weber’s length for the non-obligately socially parasitic Nearctic Nylanderia species.

Figure 14. 

Scatter plot displaying mesosoma length (=Weber’s length) to forewing length and trendline fitting non-parasitic Nearctic Nylanderia: N. arenivaga, N. austroccidua, N. concinna, N. faisonensis, N. parvula, N. phantasma, N. querna, N. terricola, N. vividula, and N. wojciki (diamonds) with added N. deceptrix data (squares, not part of trendline data).

Both N. deceptrix and N. parvula queens were allowed to climb to the top of a pencil to see if they would use it as a location to take off and fly from. Five N. parvula queens were tested and each of them flew off of the pencil tip within two trials, however, none of the five N. deceptrix flew off of the pencil tip after five trials for each individual. In the lab, attempts at dropping two N. deceptrix queens over a white surface to provoke flight while freefalling were conducted, but neither of them flew. As N. deceptrix individuals were hard to collect and maintain in a laboratory setting; only two drop trials were done per individual to avoid harming or losing individuals.


The aggression tests between workers, the pairing of both N. parvula workers from not parasitized colonies had an average score of 2.5 (n=6, range 1–3), from one parasitized and one not parasitized colony averaged 4.4 (n=5, range 3–5), and from both parasitized colonies averaged 2.67 (n=3, range 1–4) (here colony is always referring to N. parvula colonies). Pairings with an N. deceptrix queen and a N. parvula worker from a not parasitized colony had an average of 5 (n=2), and with a N. parvula worker from a parasitized colony averaged 1 (n=2). Also, the average aggression between a N. deceptrix queen and a N. parvula queen was 1.88 (n=16, range 1–3). Introduction tests placing a N. parvula worker from a parasitized colony into another parasitized colony had an average score of 3.33 (n=3, range 2–5), and introducing a N. deceptrix queen to an already parasitized colony averaged 2.33 (n=3, range 1–5). Two of the three N. deceptrix introductions into an already parasitized colony resulted in acceptance of the queen into the new colony (score=1), while the third was attacked and rejected (score=5). When taking N. deceptrix queens or parasitized colony workers and introducing them to not parasitized colonies, the average score was 5 for each case (n=4 and 5, respectively). Similarly, workers from not parasitized colonies introduced to a parasitized colony resulted in an average score of 4.75 (n=4). The final set of introductions involved taking a N. parvula worker from a not parasitized colony and introducing her to another not parasitized colony. The resulting average score for that case was 4.8 (n=5, range 4–5). See Table 1 for all the aggression and introduction test average scores.

Table 1.

Average Aggression scores (see text for details) for aggression and introduction tests (n=sample size). W/W-Colony = N. parvula worker to N. parvula worker; Dec/W-Colony = N. deceptrix queen to N. parvula worker; Dec/Queen = N. deceptrix queen to N. parvula queen.

W/W-Colony (N) Dec/W-Colony (N) Dec/Queen (N)
Parasitized to Parasitized
Solo Aggression 2.67 (3) 1 (2) ---
Introduction Test 3.33 (3) 2.33 (3) ---
Parasitized to Not Parasitized
Solo Aggression 4.4 (5) 5 (2) 1.88 (16)
Introduction Test 5 (5) 5 (4) ---
Not Parasitized to Not Parasitized
Solo Aggression 2.5 (6) --- ---
Introduction Test 4.8 (5) --- ---
Not Parasitized to Parasitized
Introduction Test 4.75 (4) --- ---


The data collected about the biology and natural history of N. deceptrix indicates it is an obligate social parasite of N. parvula. Nylanderia deceptrix has not been observed to produce a worker caste (we observed no features among the thousands of N. parvula workers examined that would indicate N. deceptrix workers were present; i.e. all conformed to the expected worker morphology of N. parvula), it is functionally polygynous, host-queen tolerant, and has only been found within colonies of N. parvula. The intermediate size of N. deceptrix queens between that of N. parvula workers and queens is a morphological indication of its obligate social parasite status, as obligately socially parasitic ants are smaller than their host queens (Buschinger 2009). They are also often the size of their host workers but that is not the case with N. deceptrix. The males of N. deceptrix have highly reduced wings and cannot fly, a trait seen in several obligate social parasites such as Anergates atratulus (Schenck, 1852), Pheidole inquilina (Wheeler, 1903), Plagiolepis xene (Stärcke, 1936), and Pogonomyrmex colei (Snelling, 1981).

Nylanderia deceptrix seems to have a much more restricted range than its host and resides in an area with a high density of host colonies, traits that appear to be common among obligately socially parasitic species (Heinze 1989, Nonacs and Tobin 1992, Savolainen and Vepsäläinen 2003). The likelihood of a restricted range is enhanced by the fact N. deceptrix queens either have very poor flight capability, or do not fly at all, coupled with the fact that males have very small, non-functional wings. The incidence of colonies parasitized with N. deceptrix supports this as well, since all the colonies were clustered in close proximity to one another. The presumed poor flight capability coupled with the observed clustering of parasitized colonies leads us to suspect that N. deceptrix disperses by walking to nearby host colonies.

Once at a host colony, the data presented here suggest it is difficult for N. deceptrix to become established in a N. parvula colony if that colony does not already possess N. deceptrix queens. Our aggression data shows that N. parvula workers act very aggressively towards any individual (N. parvula worker or N. deceptrix queens) from a colony already parasitized with N. deceptrix. Comparatively, N. parvula displays lower aggression towards N. parvula workers from colonies not parasitized with N. deceptrix. Our data suggest that N. parvula can detect some kind of cue that indicates whether a N. parvula worker has had contact with N. deceptrix, resulting in the observed higher level of aggression. The reason for this high aggression towards individuals from parasitized colonies is still unknown, but it could be the result of N. deceptrix actually having a significant fitness cost to the N. parvula colonies. However, our data was not able to identify any significant fitness cost to N. parvula colonies.

Conversely, when an individual from a colony containing N. deceptrix encounters an individual from a different colony that also contains N. deceptrix, the aggression that results is noticeably lower. This suggests that N. deceptrix is influencing the amount of aggressive behavior displayed by N. parvula. This decrease in aggression could also be responsible for acceptance of N. deceptrix queens from one colony into another foreign colony already containing N. deceptrix. Although the mechanism and cause of acceptance for foreign N. deceptrix queens has not been determined, it seems likely that a contributing cause is a general decrease in aggression, a disruption in recognizing foreign individuals, or N. deceptrix having the ability to somehow not be recognized as a foreign individual. Overall the parasitism rate of N. deceptrix within N. parvula colonies was seemingly low at 2.5%, but it is comparable to that of several other obligate social parasites. Examples include: Acromyrmex charruanus at 2% (Rabeling et al. 2015), Leptothorax wilsoni at 1.9% (Heinze 1989), and Cataglyphis hannae at less than 1% (Agosti 1994). But not all obligate social parasites have such low parasitism rates. Study of Vollenhovia nipponica found it in over 56% of the host colonies sampled (Kinomura and Yamauchi 1992).

Our field and lab observations confirm that Nylanderia deceptrix is an obligate social parasite, the first known within the genus. An important next step will be to examine the phylogenetic position of N. deceptrix among the Nearctic Nylanderia, especially to see how closely related or not it is to N. parvula and to test whether or not a strict or loose sense Emery’s Rule applies in this example of obligate social parasitism.


We would like to thank Ken Gooch (Mass. DCR) for the initial permission to collect and work in Myles Standish State Forest. We also extend thanks to the staff of Myles Standish State Forest for their help during our study. Christian Rabeling and James Trager both provided excellent suggestions and comments that greatly improved the manuscript. This study was supported in part by the National Science Foundation under grant DEB-0743542 awarded to JSL and awards from the Towson University Graduate Student Association to SJM.


  • Abbott KL (2005) Supercolonies of the invasive yellow crazy ant, Anoplolepis gracilipes, on an oceanic island: Forager activity patterns, density and biomass. Insectes Sociaux 52: 266–273. doi: 10.1007/s00040-005-0800-6
  • Agosti D (1994) A new inquiline ant (Hymenoptera: Formicidae) in Cataglyphis and its phylogenetic relationship. Journal of Natural History 28: 913–919. doi: 10.1080/00222939400770481
  • Bekkevold D, Boomsma JJ (2000) Evolutionary transition to a semelparous life history in the socially parasitic ant Acromyrmex insinuator. Journal of Evolutionary Biology 13: 615–623. doi: 10.1046/j.1420-9101.2000.00201.x
  • Braschler BM (2005) Effects of experimental small-scale grassland fragmentation on the population dynamics of invertebrates, 1–166.
  • Buckley SB (1866) Descriptions of new species of North American Formicidae. Proceedings of the Entomological Society of Philadelphia 6: 152–172.
  • Buschinger A (1990) Sympatric speciation and radiative evolution of socially parasitic ants – heretic hypotheses and their factual background. Zeitschrift für Zoologische Systematik und Evolutionsforschung 28: 241–260. doi: 10.1111/j.1439-0469.1990.tb00379.x
  • Buschinger A (2009) Social parasitism among ants: a review (Hymenoptera: Formicidae). Myrmecological News 12: 219–235.
  • Cole AC (1954) Studies of New Mexico ants. VII. The genus Pogonomyrmex with synonomy and a description of a new species (Hymenoptera: Formicidae). Journal of the Tennessee Academy of Science 29: 115–121.
  • Douglas A, Brown Jr. WL (1959) Myrmecia inquilina new species: the first parasite among the lower ants. Insectes Sociaux 6: 13–19. doi: 10.1007/BF02223789
  • Emery C (1909) Über den Ursprung der dulotischen, parasitischen und myrmekophilen Ameisen. Biologisches Centralblatt 29: 352–362.
  • Forel A (1922) Glanures myrmécologiques en 1922. Revue Suisse de Zoologie 30: 87–102. doi: 10.5962/bhl.part.144519
  • Haskins CP, Haskins F (1964) Notes on the biology and social behavior of Myrmecia inquilina. The only known Myrmeciine social parasite. Insectes Sociaux 11: 267–282. doi: 10.1007/BF02222677
  • Heinze J (1989) Leptothorax wilsoni n. sp., a new parasitic ant from eastern North America (Hymenoptera: Formicidae). Psyche 96: 49–61. doi: 10.1155/1989/15931
  • Johnson RA (1994) Distribution and natural history of the workerless inquiline ant Pogonomyrmex anergismus Cole (Hymenoptera: Formicidae). Psyche 101: 257–262. doi: 10.1155/1994/73940
  • Kallal RJ, LaPolla JS (2012) Monograph of Nylanderia (Hymenoptera: Formicidae) of the World, Part II: Nylanderia in the Nearctic. Zootaxa 3508: 1–64.
  • Kaspari M, O’Donnell S, Kercher J (2000) Energy, Density, and Constraints to Species Richness: Ant Assemblages along a Productivity Gradient. The American Naturalist 155: 280–293. doi: 10.1086/303313
  • Kinomura K, Yamauchi K (1992) A new workerless socially parasitic species of the genus Vollenhovia (Hymenoptera: Formicidae) from Japan. Japanese Journal of Entomology 60: 203–206.
  • LaPolla JS, Brady SG, Shattuck SO (2010) Phylogeny and taxonomy of the Prenolepis genus-group of ants (Hymenoptera: Formicidae). Systematic Entomology 35: 118–131. doi: 10.1111/j.1365-3113.2009.00492.x
  • LaPolla JS, Brady SG, Shattuck SO (2011) Monograph of Nylanderia (Hymenoptera: Formicidae) of the world: an introduction to the systematics and biology of the genus. Zootaxa 3110: 1–9.
  • Leppänen J, Seppä P, Vepsäläinen K, Savolainen R (2015) Genetic divergence between the sympatric queen morphs of the ant Myrmica rubra. Molecular Ecology 24: 2463–2476. doi: 10.1111/mec.13170
  • Mardulyn P, Thurin N, Piou V, Grumiau L, Aron S (2014) Dispersal in the inquiline social parasite ant Plagiolepis xene. Insectes Sociaux 61: 197–202. doi: 10.1007/s00040-014-0345-7
  • Maschwitz U, Dorow WHO, Buschinger A, Kalytta G (2000) Social parasitism involving ants of different subfamilies: Polyrhachis lama (Formicidae) an obligatory inquiline of Diacamma sp. (Ponerinae) in Java. Insectes Sociaux 47: 27–35. doi: 10.1007/s000400050005
  • Mayr G (1870) Neue Formiciden. Verhandlungen der Kaiserlich-Koniglichen Zoologisch-Botanischen Gesellschaft in Wien 20: 939–996.
  • Nonacs P, Tobin JE (1992) Selfish larvae: development and the evolution of parasitic behavior in the Hymenoptera. Evolution 46: 1605–1620. doi: 10.2307/2410019
  • Nylander W (1846) Adnotationes in monographiam formicarum borealium Europae. Acta Societatis Scientiarum Fennicae 2: 875–944.
  • Rabeling C, Bacci Jr. M (2010) A new workerless inquiline in the Lower Attini (Hymenoptera: Formicidae), with a discussion of social parasitism in fungus-growing ants. Systematic Entomology 35: 379–392. doi: 10.1111/j.1365-3113.2010.00533.x
  • Rabeling C, Schultz TR, Pierce NE, Bacci Jr. M (2014) A social parasite evolved reproductive isolation from its fungus-growing ant host in sympatry. Current Biology 24: 2047–2052. doi: 10.1016/j.cub.2014.07.048
  • Rabeling C, Schultz TR, Bacci Jr. M, Bollazzi M (2015) Acromyrmex charruanus: a new social parasite species of leaf-cutting ants. Insectes Sociaux 62: 335–349. doi: 10.1007/s00040-015-0406-6
  • Savolainen R, Vepsäläinen K (2003) Sympatric speciation through intraspecific social parasitism. Proceedings of the National Academy of Sciences 100: 7169–7174. doi: 10.1073/pnas.1036825100
  • Schenck CF (1852) Beschreibung nassauischer Ameisenarten. Jahrbuch des Vereins für Naturkunde im Herzogthum Nassau. Wiesbaden 8: 1–149.
  • Snelling RR (1981) The taxonomy and distribution of some North American Pogonomyrmex and descriptions of two new species (Hymenoptera: Formicidae). Bulletin of the Southern California Academy of Sciences 80: 97–112.
  • Stärcke A (1936) Retouches sur quelques fourmis d’Europe. I. Plagiolepis xene n. sp. et Pl. vindobonensis Lomnicki. Entomologische Berichten (Amsterdam) 9: 277–279.
  • Sumner S, Hughes WHO, Pedersen JS, Boomsma JJ (2004) Ant parasite queens revert to mating singly. Nature 428: 35–36. doi: 10.1038/428035a
  • Trager JC (1984) A revision of the genus Paratrechina (Hymenoptera: Formicidae) of the Continental United States. Sociobiology 9: 1–162.
  • Wheeler WM (1903) Some new gynandromorphous ants, with a review of the previously recorded cases. Bulletin of the American Museum of Natural History 19: 653–683
  • Wheeler WM (1905) An annotated list of the ants of New Jersey. Bulletin of the American Museum of Natural History 21: 371–403.
  • Wilson EO (1971) The insect societies. Belknap Press, Cambridge, MA, 548 pp.
login to comment