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Ant tending of Miami blue butterfly larvae (Lepidoptera: Lycaenidae): partner diversity and effects on larval performance.

The larvae of many lycaenid butterflies (Lepidoptera: Lycaenidae) interact with ants in relationships ranging from brood parasitism in ant colonies to mutualism in which both species benefit. Approximately 60% of the ant-associated lycaenid species are facultative myrmecophiles that are tended by several different ant species, usually on the larval host plant (Pierce et al. 2002). Lycaenid larvae in such relationships generally emit semiochemicals from a pair of tentacular organs and secrete a sugar-rich solution from a dorsal nectary organ to attract and retain their ant guards (Axen et al. 1996; Axen 2000; Daniels et al. 2005), which then protect the larvae from predators and parasitoids (Pierce & Mead 1981; Fiedler et al. 1996). Additionally, larvae of some lycaenid species pupate inside ant nests, where the ants presumably protect them until adult eclosion (Wagner 1995; Dejean & Beugnon 1996). Thus, these associations entail an exchange of goods and services that usually results in net benefits for both partners (Pierce et al. 1987; Cushman et al. 1994). However, there is often substantial variation in quality among potential partners in facultative, diffuse mutualistic systems that may result in negative or neutral consequences for the survival and performance of the interacting species (Bronstein 2001; Miller 2007).

Evaluating partner quality in purportedly mutualistic relationships is necessary to understand the ecological conditions and evolutionary processes that influence the outcome of the relationship (Bshary & Grutter 2002; Ness et al. 2006). A central question in research on lycaenid-ant mutualisms is how interactions with different ant species affect larval performance (Axen 2000; Fraser et al. 2001; Weeks 2003). The physiological cost of provisioning ants with a sugar-rich exocrine secretion leads to reduced growth of ant-tended larvae in some systems (Pierce et al. 1987; Baylis & Pierce 1992), but growth of ant-tended larvae in other systems is similar to or greater than that of untended larvae (Fiedler & Holldobler 1992; Cushman et al. 1994; Wagner & Del Rio 1997; Fraser et al. 2001). Because pupal mass is often correlated with adult reproductive output in Lepidoptera (Gotthard 2008), the growth consequences for larvae of ant tending could have subsequent effects on individual fitness (Elgar & Pierce 1988). Furthermore, because the relative importance of adult size and timing of adult emergence may differ between conspecific males and females (Fagerstrom & Wiklund 1982; Gotthard et al. 2000), in some lycaenid species there are sex differences in the effects of ant tending (Fiedler & Holldobler 1992). Assessing the effects of ant tending on lycaenid larvae and identifying the factors that explain variation in the interaction among and within species are central issues for furthering our understanding of these complex relationships.

Larvae of the imperiled Miami blue butterfly, Cyclargus thomasi bethunebakeri (Comstock & Huntington) (Lycaenidae: Polyommatinae), associate with several species of ants (Minno & Emmel 1993; Smith et al. 1994; Saarinen & Daniels 2006). However, we know very little about the costs and benefits of this relationship (Florida Fish and Wildlife Conservation Commission 2003; Saarinen & Daniels 2006). In addition to reporting new observations of ant tending in the wild and under laboratory conditions, our study is the first to quantify experimentally the effects of ant tending on performance of Miami blue larvae. Specifically, we observed the behavioral components of interactions between Miami blue larvae and different ant species in the field and in the laboratory and raised larvae with several ant species to assess the nature of these interactions. We then quantified the effects of ant tending and butterfly sex on larval survival, time until pupation, mass at pupation, and length of pupation with an experiment in which we raised larvae with 2 ant species and a no-ant control. We also noted the location of pupation for larvae in this experiment. The implications of our work for the conservation of wild Miami blue butterfly populations and future reintroduction efforts are discussed.


Study Organism

The Miami blue butterfly is a small, sexually dimorphic lycaenid formerly found in much of coastal peninsular Florida and outlying barrier islands (Smith et al. 1994; Calhoun et al. 2002; Carroll & Loye 2006). Miami blue larvae have an onisciform or sluglike shape typical of ant-tended lycaenids and have prominent ant-associated organs for communicating with and provisioning ant guards beginning in the third instar (Saarinen & Daniels 2006). The larvae elicit tending behavior from ants through chemical communication originating from a pair of eversible tentacles and, perhaps, other specialized epidermal glands (Pierce et al. 2002). Ants typically respond by rapidly antennating around the head, tentacular organs, and dorsal nectary organ of the larvae and accepting sugar-rich secretions from the latter (Saarinen & Daniels 2006). Although ants may protect Miami blue larvae against parasitoids and predators in the wild, we have not recorded parasitism or predation of any larvae despite extensive field observations.

The Miami blue butterfly is currently listed by the state of Florida as an endangered species (Florida Fish and Wildlife Conservation Commission 2003). More information on the history and current status of this species can be found in Calhoun et al. (2002), Carroll & Loye (2006), and Saarinen & Daniels (2006).

Field and Laboratory Observations of Ant Tending

Over 3 growing seasons (2006-2008), we conducted field observations of ant tending at Bahia Honda State Park (BHSP), where there is a wild population of Miami blue butterflies, as well as at 2 other sites where we introduced captive-bred larvae, Elliott Key in Biscayne National Park (BNP) and Dagny Johnson Key Largo Hammock Botanical State Park (DJSP). The introduced larvae were from a colony maintained at the University of Florida as part of the Miami blue butterfly's state-mandated management and recovery plan (Florida Fish and Wildlife Conservation Commission 2003). These larvae, and all others used in the studies we report here, originated from stock sourced from a wild population at BHSP and were raised on Caesalpinia bonduc L. (Roxb.) as the host plant. Observations at all 3 sites were opportunistic because larvae were often difficult to locate once on the host plant, were not always tended, and ants did not always immediately find recently introduced larvae. We were particularly interested in the behaviors of both ants and Miami blue larvae upon first encounter and then subsequent interactions that would indicate whether ants ignored, tended or depredated larvae.

We observed interactions between Miami blue butterfly larvae and several ant species in the laboratory. We raised dozens of larvae with the 2 focal ant species in this study, Camponotus floridanus Buckley and Linepithema humile Mayr, prior to the experimental assessment described below. For the other ant species, we raised from 2 to 4 Miami blue butterfly larvae simultaneously with a single, queenright ant colony that had no previous interactions with Miami blue butterflies. We introduced larvae to the ant colonies at the second or early third instar, observed the initial interaction to assure that the ants did not attack the larvae and replaced the host plant daily until the larvae pupated. The only 2 exceptions to this protocol were our discovery of Pheidole moerens Wheeler tending larvae after entering the laboratory without our knowledge and when we found Camponotus floridanus workers tending larvae in an outdoor flight cage.

Experimental Design and Analysis

We quantified the effects of ant tending on Miami blue larvae with an experiment in which we raised larvae from the second instar to pupation with 2 ant species, Camponotus floridanus and Linepithema humile, or in a no ant control. Camponotus floridanus is a large formicine that is the most common ant found tending Miami blue larvae in the wild, thereby making it relevant species for our study. Linepithema humile is a small, non-native dolichoderine that readily tends honeydew-producing Hemiptera and other lycaenid larvae (Agrawal & Fordyce 2000; Tillberg et al. 2007). Although we had no evidence that L. humile interacts with Miami blue larvae in the wild, this species is amenable to experimentation and in our study served as a surrogate for smaller, active ant species that we have frequently observed tending Miami blue larvae in the field (e.g., Paratrechina longicornis, P. bourbonica, Tapinoma melanocephalum).

We conducted 2 trials in which we randomly assigned 3 larvae to each of 4 replicate shoebox-style trays in each of the 3 ant treatments (total of 72 larvae). We placed new groups of ants in each tray between trials. Larvae were from eggs laid by multiple females in the captive colony and were all the same age in each of the 2 trials. We replaced the host plant daily and manually transferred larvae from the old to the new cuttings. Each tray contained an ant harborage comprising a 90-mm diameter Petri dish containing a layer of dental plaster that we wetted occasionally to maintain humidity and covered with dark paper. For the C. floridanus treatment, we placed 50 workers in each tray, and for the L. humile treatment we placed 100 workers and 1 queen in each tray. These ants had been maintained in captivity for approximately 6 months prior to the experiment and were allowed a week to acclimate to the tray before we introduced the Miami blue larvae. To assure that malnourishment would not affect the ants' interactions with the Miami blue larvae, we provisioned ants with water, 10% sucrose solution, and cut mealworms (larvae of Tenebrio sp.); these were also provided to the control trays. We coated the sides of the trays with a fluoropolymer resin slippery barrier (Insect-a-Slip, BioQuip Products, Rancho Dominguez, CA) to contain the ants but, even with this preventative measure, a small number of Miami blue larvae escaped during our experiments.

We monitored the presence of all larvae each day. Upon pupation, we recorded the location of the pupae, measured their mass with a digital analytic balance accurate to 0.01mg (Denver Instruments SI-215D), and kept them in individual vials in the laboratory under fairly constant temperature and humidity until adult emergence (2428 C with 40-50% relative humidity). We measured the wing chord length (mm) and recorded the sex of each adult. Thus, our response variables for statistical analyses were age at pupation, location of pupation, pupal mass, length of pupation, and adult wing chord. From these data we calculated 2 additional response variables--the proportion of time spent in the pupal and larval stadia (length of pupation divided by age at pupation) and total time as an immature (age at pupation plus length of pupation)--to increase our understanding of the potential effects of ants on larval development of Miami blue butterflies.

We conducted correlation analysis to test for relationships between the measures of larval performance to elucidate patterns in developmental strategies of Miami blue larvae. We analyzed differences among ant treatments in the location of pupation with Fisher's exact test. To assess the influence of ant treatment and sex on larval performance, we conducted linear mixed-effects analyses in which we tested the effects of ant treatment and sex (both fixed effects) on age at pupation, pupal mass, length of pupation, and the 2 compound variables described above. All models contained a nested random effect of tray within trial to account for variance due to differences between the 2 experimental trials or among groups of the same ant species. All analyses were conducted in the R language and environment for statistical computing (R Development Core Team 2009) and followed protocols for model specification and interpretation described by Pinheiro & Bates (2002) and Faraway (2006).


Field and Laboratory Observations of Ant Tending

We observed 8 ant species tending Miami blue larvae in the field, including observations at the natural population in Bahia Honda State Park and the reintroduction sites in Biscayne National Park and Dagny Johnson Key Largo Hammock Botanical State Park (Tables 1 and 2). Saarinen & Daniels (2006) reported 1 additional species, Forelius pruinosus, tending Miami blue larvae but we have not since observed this interaction. We most frequently observed 2 Camponotus species, C. floridanus and C. planatus, tending both wild and recently introduced larvae. Additionally, at both reintroduction sites, Pseudomyrmex gracilis was common and tended recently released larvae.

Experimental Assessment of Ant Effects

We collected data on age at pupation, location of pupation, pupal mass, length of pupation, and wing chord from 64 Miami blues. Of the original 72 larvae, 5 escaped from the ant trays and were excluded from further study and 3 individuals did not successfully eclose from the pupal stage so could only be included in some analyses. Pupal mass and wing chord were highly positively correlated (r = 0.69, t = 7.31, df = 59, P < 0.0001), and so we used pupal mass as a measure of size for our analyses. There was no correlation between age at pupation and pupal mass (r = -0.14, t = -1.13, df = 62, P = 0.26), but pupal mass was positively correlated with length of pupation (r = 0.31, t = 2.54, df = 62, P = 0.014) and age at pupation was negatively correlated with length of pupation (r = 0.49, t = -4.42, df = 62, P < 0.0001).

Most larvae (45 of 64) pupated under the paper that shaded the Petri dish harborages regardless of ant presence or identity, but the frequency of pupal location was non-random among the 3 ant treatments (Fisher's exact test P = 0.029). Five of 22 larvae raised with C. floridanus pupated inside the Petri dish with the ants, whereas no larvae from either the L. humile or no ant treatments pupated in that location

We present summarized values of the performance parameters measured in Table 3 and the results of all statistical analyses of the effects of larval sex and ant treatment on larval performance in Table 4. There was no significant effect of ant treatment on any of the measures of larval performance, although the analysis suggested that larvae raised with C. floridanus may have a shorter length of pupation relative to the time spent in the larval stadium. Male larvae pupated at a significantly smaller mass than females but females tended to complete pupation faster.

Although we did not quantify the frequency of tending behaviors in this study, both C. floridanus and L. humile regularly tended Miami blue butterfly larvae throughout the course of the experiment. We rarely found untended larvae, particularly in the later instars, with either ant species. The interactions conformed to the common behavioral pattern of the larvae everting their tentacular organs and secreting from the dorsal nectary organs, followed by the ants antennating the larvae and consuming the nectar. However, upon disturbance associated with maintaining the experiment, L. humile usually abandoned the larvae whereas C. floridanus showed typical defensive behaviors such as running around larvae, tapping on the host plant or other surfaces with their mandibles, and antennating the air with open mandibles.


Relationships between lycaenid butterfly larvae and ants range dramatically in the effects on the interacting species. Previous studies have suggested that some ant species may depredate Miami blue butterfly larvae or may opportunistically tend larvae without providing protection against predators or other benefits (Saarinen & Daniels 2006). However, through both field observations and laboratory trials, we recorded a universal tending response among ants consistent with a mutualistic interaction. Indeed, including the observations we report here, a total of 17 ant species have been observed tending Miami blue larvae either in wild populations, in reintroduction sites following releases of captive raised larvae or in the laboratory (Saarinen & Daniels 2006; Carroll & Loye 2006). We have not observed any depredation of Miami blue larvae by ants in the field, and laboratory trials suggest that even ant species identified by Saarinen & Daniels (2006) as potential predators in fact tend larvae in ways consistent with a mutualistic interaction. These results are notable for the large number of potential ant partners, the consistency of behaviors toward larvae among distantly related ant taxa and the nearly complete lack of obviously antagonistic interactions.

Despite the high diversity of potential ant partners, our observations suggest that only a small subset of ant species accounts for the vast majority of interactions with Miami blue butterfly larvae in the field. Previous studies have reported that ant species in the genus Camponotus most commonly tended larvae (Minno & Emmel 1993; Carroll & Loye 2006; Saarinen & Daniels 2006), and we most commonly found C. floridanus and C. planatus associated with wild and recently released larvae. Notably, this pattern was consistent across 3 sites (BHSP, BNP, and DJSP) that likely differ dramatically in ant community composition (Deyrup et al. 1988). There are at least 4 likely explanations for the apparent reciprocal affinity between Miami blue larvae and Camponotus. First, Camponotus commonly forage on nickerbean for plant exudates, honeydew-producing Hemiptera, and insect prey even in sites where Miami blues do not occur, so frequent tending could be opportunistic association resulting from high rate of encounters compared to other potential ant partners. Second, after discovering Miami blue larvae, even those tended by other ant species, Camponotus may competitively exclude other ants from interacting with them through constant tending and defense. Third, following initial contact, the Miami blue larvae may allocate more resources to retaining Camponotus compared to other ant species because Camponotus are higher quality defenders. Finally, Camponotus are quite large and active and therefore researchers may be more likely to find larvae tended by these ants.

Larvae of some facultatively ant-tended lycaenid species pupate inside ant nests (e.g., Wagner 1995), but this has not been previously reported for the Miami blue butterfly. We found that a higher than expected number of larvae pupated in the ant harborages in the laboratory when tended by C. floridanus and no larvae pupated in that location when kept with L. humile or raised without ants, suggesting that this aspect

of the relationship may have been overlooked. Clearly, future studies are required to elucidate the precise mechanisms that account for the persistent and geographically widespread association between Camponotus species, particularly C. floridanus and C. planatus (and possibly C. inequaelis), and Miami blue larvae.

In most facultative ant-lycaenid mutualisms, the primary direct cost for the lycaenid larvae is metabolic expense required to produce sugary secretions for ant defenders (Pierce et al. 1987; Daniels et al. 2005). Because the secretions are induced by ant tending (Agrawal & Fordyce 2000), we might expect to find reduced larval growth rate or pupal mass in ant-tended larvae. In our experimental assessment of ant effects on performance of Miami blue butterfly larvae, both C. floridanus and L. humile almost constantly tended larvae and we frequently observed both species consuming secretions from the dorsal nectary organ. Carroll & Loye (2006) found that Camponotus sp. raised with Miami blue larvae lived longer than ants raised without any food source, demonstrating that larval secretions are nutritionally valuable for tending ants. However, contrary to theoretical predictions and the results of studies in similar ant-lycaenid systems, we found no effect of ant presence on any of our measurements of larval performance. It is possible that these secretions are less metabolically expensive than some studies have suggested or that ants tend larvae even when they receive only small nutritional rewards (Fiedler & Saam 1995). Alternatively, larvae may compensate for metabolic expenses of provisioning ants by feeding more efficiently when tended (Fiedler & Holldobler 1992; Wagner & del Rio 1997). If the latter is true for Miami blue butterfly larvae, we may have found no effect of ant association on larval performance because increased growth of tended larvae offset the costs of the sugary secretions. Regardless of the specific mechanism, it appears that the net costs of ant tending for Miami blue butterflies do not substantially affect their larval development compared to untended conspecific larvae.

The primary benefit of ant association for lycaenid larvae is defense against natural enemies (Atsatt 1981; Pierce & Mead 1981; Weeks 2003). We did not test this important aspect of the relationship for Miami blue butterfly larvae in this study, nor have we observed ants actively protecting larvae against attack by predators or parasitoids in the wild. However, in the laboratory C. floridanus displayed strong defensive behaviors (e.g., rapidly circling larvae, recruiting nearby workers and lunging at forceps) when disturbed, particularly when we moved Miami blue butterfly larvae to new host plant. The large size of this ant species and nearly constant tending may serve as a visual deterrent to potential attackers. Although L. humile workers assiduously tended Miami blue larvae in our experiment, they are substantially smaller than C. floridanus and did not show such a strong defensive response; instead, they usually ran away from the larvae and source of disturbance. Despite these qualitative observations, it is important to emphasize that we have no definitive evidence from this study that C. floridanus are more effective defenders of Miami blue butterfly larvae than small-bodied ant species. Given the apparently small physiological costs for Miami blue larvae of associating with ants, any predator or parasitoid deterrence provided by ant defenders could substantially increase their probability of survival to the adult stage.

Male and female Lepidoptera larvae may have divergent developmental strategies, and may therefore exhibit variation in behaviors, such as foraging or prolonging the larval period that represent trade-offs between growth and mortality (Gotthard 2008). In lycaenid larvae, such differences could result in sex-specific interactions with ants, particularly in species for which timing of adult emergence and adult size have different effects on the relative reproductive success of males and females (Elgar & Pierce 1988). Indeed, Fiedler & Holldobler (1992) found that Polyommatus icarus males benefited from ant association through increased pupal mass, but ant tending appeared to be energetically costly for females. This species has a strongly protandrous mating system with frequent male-male competition for access to females (Lundgren 1977), so it is reasonable that male larvae would interact with ants to optimize adult size as long as the costs to development time were not too great. Similarly, Baylis & Pierce (1992) found that male Jalmenus evagoras lost less mass from secretions for ants during the nonfeeding, prepupal instar. By contrast, studies on other lycaenid species have found no sex-related differences in ant association (e.g., Fraser et al. 2001). It is worth noting that most experiments testing lycaenid larval performance with and without ants have not recognized sex as a potentially important predictor of the interaction and its effects. We found that male and female Miami blue larvae differed in some performance parameters, but the sex x ant treatment term did not explain a significant amount of variation in any of the analyses. As such, our results suggest that Miami blue larvae did not have sex-specific costs or benefits of interacting with ants, at least under our experimental conditions.

The state-mandated management plan for the Miami blue butterfly identified examining the relationship between larvae and ants as one of the research goals to inform conservation efforts (Florida Fish and Wildlife Conservation Commission 2003). Saarinen & Daniels (2006) generated further interest in the implications of this relationship for protecting the Miami blue by suggesting that some ant species, particularly the nonnative Solenopsis invicta and Pseudomyrmex gracilis, could be predators of Miami blue larvae. Indeed, non-native ants can disrupt coevolved mutualistic interactions through competition with native ants or failure to provide the benefits to partner species (Ness & Bronstein 2004). The ant fauna of the Florida Keys contains numerous nonnative species, including some that are extremely invasive and have been implicated as major predators of arthropods (Deyrup et al. 1988; Deyrup et al. 2000). However, we found a universal tending response toward Miami blue larvae and very little antagonism across a wide range of ant species, including those previously identified as potential predators. This is a similar result to studies on honeydew-producing Hemiptera that have generally mutualistic relationships with ants, including non-native species (Helms & Vinson 2003; Mondor & Addicott 2007). Different ant species may not have equivalent effects on Miami blue larvae but, based on our observations, we doubt that many ant species regularly depredate larvae. We suggest that ants may be important for protecting larvae from natural enemies, but the identity of the ant attendants may not be particularly important for other measures of larval performance. Furthermore, because the 2 ant species that most commonly tend larvae in the wild and show a strong defensive response, C. floridanus and C. planatus, are common throughout southern Florida, it is likely that at least 1 of these species would be present at any potential reintroduction site. Our results suggest that the facultative and diffuse interactions between ants and Miami blue larvae are unlikely to be the most important determinant of conservation success for the imperiled butterfly.


We thank E. V Saarinen and 2 anonymous reviewers for helpful comments on a previous version of this paper. Research for this study was conducted under Florida Fish and Wildlife Conservation Commission permit WX02525f. Funding for this work was provided by the Florida Fish and Wildlife Conservation Commission, E. O. Dunn Foundation, U.S. Fish and Wildlife Service and the National Fish and Wildlife Foundation; additionally, M. D. Trager was funded by a National Science Foundation Graduate Research Fellowship. The opinions expressed herein are solely those of the authors and do not represent the position of any of these funding sources.


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(1.) Department of Entomology and Nematology, University of Florida, Gainesville, FL 32611

(2.) McGuire Center for Lepidoptera and Biodiversity, Florida Museum of Natural History, University of Florida, Gainesville, FL 32611

Ant taxa Interaction Sites and observers

Subfamily Pseudomyrmicinae
 Pseudomrymex gracilis P DJSP (2), BNP (2)

Subfamily Myrmicinae
 Crematogaster cf. ashmeadi S BHSP (1,2)
 Monomorium floricola u BHSP (1,2)

Subfamily Dolichoderinae
 Forelius pruinosus S ENP (1), BHSP (1)
 Tapinoma melanocephalum S BHSP (1,2)

Subfamily Formicinae
 Camponotus floridanus S BHSP (1,2), BNP (2),
 ENP (1)
 Camponotus inaequalis KWNWR (3)
 Camponotus planatus S DJSP (2), BNP (2),
 BHSP (1)
 Paratrechina bourbonica pS BHSP (2)
 Paratrechina longicornis pS BHSP (2), KWNWR (3)

Interaction status suggested by Saarinen & Daniels (2006):
P = potential predator, pS = potential symbiont (i.e.,
potential mutualist), S = symbiont (i.e., mutualist),
u = unknown. 1 = observations reported by Saarinen &
Daniels (2006); 2 = new observations by the authors; 3 = new
observations by P. Cannon (pers. comm.).


Ant taxa Interaction status

Subfamily Pseudomyrmicinae
 Pseudomyrmex ejectus
 Pseudomyrmex gracilis P

Subfamily Myrmicinae
 Pheidole moerens
 Solenopsis invicta P

Subfamily Dolichoderinae
 Dorymyrmex bureni
 Linepithema humile
 Tapinoma melanocephalum S

Subfamily Formicinae
 Brachymyrmex patagonicus
 Camponotus floridanus S

Interaction status suggested by Saarinen & Daniels (2006):
P = potential predator, pS = potential symbiont (i.e., mutualist),
S = symbiont (i.e., mutualist), u = unknown.


 Age Pupal Length of
 at pupation (d) mass (mg) pupation (d)

Ant treatment
C. floridanus 19.09 [+ or -] 60.52 [+ or -] 8.73 [+ or -]
(n = 22) 0.31 1.56 0.13
L. humile 18.81 [+ or -] 58.11 [+ or -] 8.76 [+ or -]
(n = 21) 0.44 2.23 0.19
No ants 18.57 [+ or -] 62.06 [+ or -] 9.0 [+ or -]
(n = 21) 0.44 2.23 0.19

Male 18.51 [+ or -] 58.92 [+ or -] 9.10 [+ or -]
(n = 39) 0.36 1.86 0.15
Female 19.32 [+ or -] 62.27 [+ or -] 8.56 [+ or -]
(n = 25) 0.28 1.45 0.12
All 18.83 [+ or -] 60.23 [+ or -] 8.82 [+ or -]
(n = 64) 0.18 0.92 0.079

 Time Length
 as immature (d) pup./Age at pup.

Ant treatment
C. floridanus 27.82 [+ or -] 0.460 [+ or -]
(n = 22) 0.27 0.013
L. humile 27.57 [+ or -] 0.471 [+ or -]
(n = 21) 0.39 0.019
No ants 27.57 [+ or -] 0.489 [+ or -]
(n = 21) 0.39 0.019

Male 27.51 [+ or -] 0.490 [+ or -]
(n = 39) 0.32 0.015
Female 27.88 [+ or -] 0.446 [+ or -]
(n = 25) 0.25 0.012
All 27.66 [+ or -] 0.473 [+ or -]
(n = 64) 0.16 0.008


Response Predictor F-value (df) P-value
variables variables

Age at Ant treatment 2.15 (2, 51) 0.13
pupation Sex 0.41 (1, 51) 0.53
 Ant treatment * Sex 0.23 (2, 51) 0.8
 Trial [sigma] = 1.16; Tray
 in Trial [sigma] = 0.10
Pupal Ant treatment 1.68 (2, 51) 0.2
mass Sex 8.91 (1, 51) 0.0043
 Ant treatment * Sex 0.18 (2, 51) 0.84
 Trial [sigma] = 0.0021; Tray
 in Trial [sigma] = 3.57 *
Length of Ant treatment 1.40 (2, 51) 0.26
pupation Sex 3.60 (1, 51) 0.063
 Ant treatment * Sex 0.76 (2, 51) 0.47
 Trial [sigma] = 0.27; Tray in
 Trial [sigma] = 4.91 *
Time as Ant treatment 0.57 (2, 51) 0.57
immature Sex 0.17 (1, 51) 0.68
 Ant treatment * Sex 0.2 0.82
 Trial [sigma] = 0.87; Tray in
 Trial [sigma] = 0.089
Length of Ant treatment 2.90 (2, 51) 0.064

Age at Sex 3.14 (1, 51) 0.082
pupation Ant treatment * Sex 0.81 (2, 51) 0.45
 Trial [sigma] = 0.045; Tray
 in Trial [sigma] = 1.79 *
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Article Details
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Author:Trager, Matthew D.; Daniels, Jaret C.
Publication:Florida Entomologist
Article Type:Report
Geographic Code:1USA
Date:Sep 1, 2009
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