Experimental pyrethroid treatment underestimates the effects of ectoparasites in cavity‐nesting birds due to toxicity

Nest‐dwelling ectoparasites may result in costs for nestlings of cavity nesters in terms of compromised growth and condition before fledging. The reduction or elimination of nest ectoparasites to study their effects on avian hosts can be conducted through physical methods such as heat‐treatment or through chemical methods using insecticides. Pyrethroids are the most frequently used of the latter, although some studies have shown that they may compromise the development and future survival of birds. In this study conducted in central Spain we analysed the differences between a group of fumigated Pied Flycatcher Ficedula hypoleuca nests and a heat‐treated group, both rendered ectoparasite‐free by these treatments. We also compared these ectoparasite‐free nests with a control group with natural ectoparasite loads. Our aim was to test the possible effects of a pyrethroid‐based insecticide on reproductive success, parental care behaviours and body condition of adult females and nestlings. We also determined the effects of treatment on a biochemical biomarker, the total glutathione (tGSH) level, involved in detoxification of xenobiotics and considered the most important intracellular antioxidant. Although behavioural variables were not affected by treatment, results showed lighter 3‐day‐old chicks and shorter tarsi and wings in nestlings shortly before fledging in fumigated nests, together with depletion of tGSH levels in both females and nestlings. Fumigation with pyrethroids in ectoparasite load reduction experiments may introduce undesired systematic variability associated with toxicity, leading to underestimation of the effects of ectoparasites on avian hosts.     

Experimental manipulation of temperature reduce ectoparasites in nests of blue tits Cyanistes caeruleus

Several models predict changes in the distributions and incidences of diseases associated with climate change. However, studies that investigate how microclimatic changes may affect host–parasite relationships are scarce. Here, we experimentally increased the temperature in blue tit Cyanistes caeruleus nest boxes during their breeding season to determine its effects on the parasitic abundance (i.e. of nest‐dwelling ectoparasites, blood‐sucking flying insects and hemoparasites) in nests and the host condition of nestlings and adults. The temperature was increased using heat mats placed underneath the nest material, which resulted in an average temperature increase of 3ºC and a reduction in relative humidity of about six units. The abundance of mites Dermanyssus gallinoides and blowfly pupae Protocalliphora azurea was significantly reduced in heated nest boxes. Although not statistically significant, a lower prevalence of flea larvae Ceratophyllus gallinae was also found in heated nests. However, heat treatment did not affect hemoparasite infection of adult blue tits or the body condition of adult and nestling blue tits. In conclusion, heat treatment in blue tit nests reduced nest‐dwelling ectoparasites yet without any apparent benefit for the host.     

Behavioural responses to ectoparasites in pied flycatchers Ficedula hypoleuca: an experimental study

Nests of cavity‐nesting birds usually harbor some species of haematophagous ectoparasites that feed on the incubating adults and nestlings. Given the negative impact of ectoparasites on nestlings there will be selection on hosts to reduce parasite infestations through behavioural means. We have experimentally reduced the abundance of all ectoparasites in nests of pied flycatchers Ficedula hypoleuca to explore both whether there are changes in the frequency and duration of putative anti‐parasite behaviours by tending adults, as well as whether such anti‐parasite behaviours are able to compensate for the deleterious effects that parasites may have on nestlings. Heat treatment of nests substantially decreased the density of ectoparasites, and thereby positively affected nestling growth. The frequency and intensity of female grooming and nest sanitation behaviours during the incubation and nestling periods decreased as a consequence of the experimental reduction of ectoparasite infestation. Although nestlings begged more intensely in infested nests, the experiment had no significant effect on parental provisioning effort. Reduction of parasites resulted in larger nestlings shortly before fledging and increased fledging success. This study shows a clear effect of a complete natural nest ectoparasite fauna on parental behaviour at the nest and nestling growth in a cavity‐nesting bird. Although ectoparasites induce anti‐parasite behaviours in females, these behaviours are not able to fully remove parasite's deleterious effects on nestling growth and survival.     

Nest excavation does not reduce harmful effects of ectoparasitism: an experiment with a woodpecker, the northern flicker Colaptes auratus

It has been hypothesized that it is adaptive for birds to build new nests annually in order to avoid the accumulation of ectoparasites. Previous studies on costs of ectoparasitism have focused on cavity nesters in nestboxes while largely ignoring reproductive consequences in natural tree cavity nests, the context where nest selection strategies presumably evolved. To see whether ectoparasitism could be a driving selective force in the evolution of nest excavation in a woodpecker, I experimentally fumigated a subset of freshly excavated cavities and a subset of reused cavities of the northern flicker Colaptes auratus and compared reproductive performance with a set of control nests. The main ectoparasite of nestlings, a blood-sucking fly Carnus hemapterus , may have appeared one or two days earlier in reused nests but there was no difference between fresh and reused nests in intensities of flies one week post-hatching. Prevalence of parasitism reached 100% in both reused and freshly-excavated control nests in the second week. Nestlings from control nests had lower body mass residuals than those from fumigated nests after 15 d and fledged at a lower weight, suggesting that ectoparasitism by C. hemapterus was costly. However, fresh nest construction was no benefit, likely because the high dispersal ability of the ectoparasite meant all nests were colonized rapidly. Parents did not adjust provisioning effort according to parasitism as delivery rates did not differ between control and fumigated nests but delivery rates increased with brood size.     

The presence of kleptoparasitic fledglings is associated with a reduced breeding success in the host family in the barn owl

Fledgling birds sometimes abandon their own nest and move to neighboring nests where they are fed by host parents. This behaviour, referred to as ‘nest‐switching’, is well known in precocial birds that are mobile soon after hatching and can easily reach foster nests. In contrast, due to the difficulty of observing nest‐switching in territorial altricial birds, the causes and consequences of moving to others’ nests are poorly known in this group of birds. Nest‐switchers can be adopted by the foster parents or they can steal food from the host parents meant for their offspring, a form of kleptoparasitism, which may result in reduced breeding success of the host nest. In Israel, 12 barn owl fledglings left their natal nests and were found in 9 host nests out of 111 monitored nests (8.1%). Nest‐switchers that fledged earlier in the breeding season flew shorter distances to reach host nests probably because the density of nests with younger nestlings is higher early in the season. The number of host nestlings fledged and the percentage of nestlings fledged was lower in host nests than in nests without switchers. The occasional nest‐switchers were always older than host nestlings (respectively 80 and 50 days of age, on average) and host parents fledged fewer young when nest‐switchers occupied host nests with younger nestlings. This suggests that nest‐switchers are kleptoparasites because the presence of the older alien fledglings is associated with a lower breeding success of the host parents.     

Green plants in starling nests: effects on nestlings

European starlings, Sturnus vulgaris, intermingle fresh herbs, especially species rich in volatile compounds, with their otherwise dry nest material. In this field study we investigated whether these herbs reduce ectoparasites and thereby protect nestlings (the nest protection hypothesis). We also considered whether volatile compounds in herbs improve the condition of nestlings (the drug hypothesis). As measures of condition we used body mass, haematocrit levels and immunological parameters. We replaced 148 natural starling nests with artificial ones: half contained herbs and half (controls) contained grass. The ectoparasite loads (mites, lice, fleas) in herb and control nests were indistinguishable. However, nestlings in herb nests weighed more and had higher haematocrit levels at fledging than nestlings in control nests. Fledging success was similar in herb and control nests, but more yearlings from herb nests were identified in the colony the year after hatching. The response of the immune system when challenged with phytohaemagglutinin did not differ in nestlings from herb and control nests. Nestlings from herb nests had more basophils and fewer lymphocytes in their blood than those from control nests, while the eosinophil and heterophil counts did not differ. We conclude that herbs do not reduce the number of ectoparasites, but they improve the condition of nestlings, perhaps by stimulating elements of the immune system that help them to cope better with the harmful activities of ectoparasites. Copyright 2000 The Association for the Study of Animal Behaviour.     

Nest‐site selection and productivity of Vesper Sparrows breeding in grazed habitats

ABSTRACT Livestock grazing in the shortgrass steppe of the Intermountain region of British Columbia may have a negative impact on ground‐nesting birds, but evidence of such an impact is lacking. We examined nest‐site selection and productivity of ground‐nesting Vesper Sparrows (Pooecetes gramineus) across sites with different grazing histories. From 2006 to 2008, we monitored Vesper Sparrow nests and measured vegetation characteristics known to be affected by grazing within nest patches. We used an information‐theoretic approach to test the relative importance of grazing‐affected vegetation variables as predictors of nest‐site selection, nest survival, and nestling condition. Vesper Sparrows selected nest sites with greater cover of late‐seral grass species that decrease in occurrence in response to grazing (i.e., “decreasers”) than was available in random patches in the same territories. Daily nest survival was also lower for nests surrounded by shorter vegetation (odds ratio = 1.12). However, “decreaser” cover was not associated with either of the two indices of productivity measured (daily nest survival probability and nestling condition). In addition, vegetation height, although an important driver of success, was not linked with nest‐site selection, and no vegetation‐cover variable was positively associated with productivity, despite nest concealment being central to our predictions. This suggests that predation risk for nests in areas with shorter vegetation was being elevated through some factor unrelated to concealment. Our results show that grazing reduced both the availability of suitable habitat for and nesting success of Vesper Sparrows, indicating that grazing could pose a threat to population persistence at a broader scale and could potentially contribute to observed declines. Additional research is needed to determine if grazing guidelines in the Intermountain region of British Columbia should be amended, better enforced, or both to prevent regional declines in populations of ground‐nesting grassland birds.     

Evaluation of disruptive camouflage of avian cup‐nests

Parent birds employ various strategies to protect their offspring against nest predators. Two well‐researched anti‐nest‐predation strategies involve visual concealment of the nest by way of parental camouflage and egg camouflage. By contrast, camouflage of nest structures is relatively under‐researched, particularly in the case of cup‐nests in trees and bushes. We explored how birds camouflage cup‐nests in nature. Specifically, we tested Hansell’s hypothesis that birds use externally applied pale and white objects such as spider cocoons and lichens to achieve cup‐nest camouflage. To test Hansell’s hypothesis, three complementary experiments were performed: (1) an in situ nest predation experiment; (2) a photo‐based visual search experiment; and (3) contrast analyses using PAT‐GEOM software in IMAGEJ. White paper and chalk spots were used to mimic white objects used by birds in nature. Whereas predation rates in Experiment 1 were not affected by white spots, location rates in Experiment 2 were lower for natural nests with white spots than without white spots. Experiment 3 demonstrated that white spots significantly increased the contrast between different visual elements of nests. It was concluded that white objects can potentially camouflage nests against some nest predators, and that any improved camouflage was probably achieved via disruptive camouflage.     

Aromatic plants in nests of the blue tit <Emphasis Type="Italic">Cyanistes caeruleus</Emphasis> protect chicks from bacteria

Several bird species add fresh fragments of plants which are rich in volatile secondary compounds to their nests. It has been suggested, although never tested, that birds use fresh plants to limit the growth of nest microorganisms. On Corsica, blue tits (Cyanistes caeruleus) incorporate fresh fragments of aromatic plants into their nests. These plants do not reduce infestation by nest ectoparasites, but have been shown to improve growth and condition of chicks at fledging. To understand the mechanisms underlying such benefits, we experimentally tested the effects of these plants on the bacteria living on blue tits. Aromatic plants significantly affected the structure of bacterial communities, in particular reducing bacterial richness on nestlings. In addition, in this population where there is a strong association between bacterial density and infestation by blood-sucking Protocalliphora blow fly larvae, these plants reduced bacterial density on the most infested chicks. Aromatic plants had no significant effect on the bacteria living on adult blue tits. This study provides the first evidence that fresh plants brought to the nests by adult birds limit bacterial richness and density on their chicks.     

Short‐ and long‐term costs of reproduction in a migratory songbird

Costs of reproduction represent a common life‐history trade‐off. Critical to understanding these costs in migratory species is the ability to track individuals across successive stages of the annual cycle. We assessed the effects of total number of offspring fledged and date of breeding completion on pre‐migratory body condition, the schedule of moult and annual survival in a migratory songbird, the Savannah Sparrow Passerculus sandwichensis. Between 2008 and 2010, moult was delayed for individuals that finished breeding later in the breeding period and resulted in reduced lean tissue mass during the pre‐migratory period, suggesting an indirect trade‐off between the timing of breeding completion and condition just prior to migration. Lean tissue mass decreased as the number of offspring fledged increased in 2009, a particularly cool and wet year, illustrating a direct trade‐off between reproductive effort and condition just prior to migration in years when weather is poor. However, using a 17‐year dataset from the same population, we found that parents that fledged young late in the breeding period had the highest survival and that number of offspring fledged did not affect survival, suggesting that individuals do not experience long‐term trade‐offs between reproduction and survival. Taken together, our results suggest that adult Savannah Sparrows pay short‐term costs of reproduction, but that longer‐term costs are mitigated by individual quality, perhaps through individual variation in resource acquisition.     

An experimental demonstration that house finches add cigarette butts in response to ectoparasites

Urban species encounter resources that are uncommon in nature, such as materials found in city waste. Many studies have shown that these can be harmful to wildlife. In Mexico City, house finches bring cigarette butts to their nests, which reduces the amount of ectoparasites, but also induces genotoxic damage in chicks and parents. Yet, the reason for this behaviour is unknown. One possibility is that birds extract the cellulose fibres from discarded butts simply because they resemble feathers. Alternatively, disassembled cigarette butts may be brought to the nests because they repel ectoparasites. Here we tested the latter hypothesis by assessing whether house finches Carpodacus mexicanus increase the amount of cigarette butts in their nests in response to a raise in ectoparasite load. When present, fibres from butts are concentrated in the nest lining. By taking it away, we simultaneously removed most of the butt material and collected the bulk of the tick population infesting each nest, as these parasites cluster in the lining. We removed the bedding of nests when chicks had recently hatched, and randomly assigned each nests to one of the following treatments: 1) addition of live ticks, 2) addition of dead ticks and 3) simulation of tick addition. Females in the live ticks’ treatment added more butt fibres to their nests than parents in control treatments. Additionally, the amount of butt fibres in the original lining also predicted the amount of fibres added after the manipulation. It seems that the tendency to bring to the nest cigarette butts is at least partially a response to current, and perhaps also past, parasite load.     

Environmental conditions but not nest composition affect reproductive success in an urban bird

Adjusting the composition of their nests, breeding birds can influence the environmental conditions that eggs and offspring experience. Birds often use feathers to build nests, presumably due to their insulating properties. The amount of feathers in nests is often associated with increased nestling survival and body condition. However, it is unclear whether these putative beneficial effects of adding feathers to nests are relevant in a wide range of environmental conditions. Here, we combine data on weather conditions and feathers in nests (i.e., nest composition) to investigate their relative contribution to reproductive success in the Eurasian tree sparrow (Passer montanus). Specifically, we investigate whether the effect of weather conditions on breeding success is modulated by the amount of feathers added to the nest. We found a strong negative effect of rainfall on the number of nestlings that successfully fledged per breeding attempt, but this negative effect was not mitigated by the amount of feathers in nests. We also found that the amount of feathers in nests varied along the breeding season, with nests containing more feathers early in the breeding season, when temperatures were lower. Despite considerable variation in nest composition, our results do not suggest an important role of feathers in nests protecting eggs or nestling tree sparrows against fluctuations in environmental conditions.     

A pre‐breeding immune challenge delays reproduction in the female dark‐eyed junco Junco hyemalis

Precise timing of life‐history transitions in predictably changing environments is hypothesized to aid in individual survival and reproductive success, by appropriately matching an animal's physiology and behavior with prevailing environmental conditions. Therefore, it is imperative for individuals to time energetically costly life‐history stages (i.e. reproduction) so they overlap with seasonal peaks in food abundance and quality. Female lifetime reproductive fitness is affected by several factors that influence energy balance, including arrival date, timing of egg production, and energetic condition. Therefore, any extra energetic costs during reproduction may negatively affect timing of egg production, and ultimately a female's fitness. For example, mounting an immunological response elicits a high energetic cost, and this transfer of resources towards cell and immune system maintenance could have direct negative effects on reproductive timing. In order to determine whether an immune challenge delays onset of breeding (i.e. egg production), we administered either a humoral immune challenge (keyhole limpet hemocyanin (KLH)) (treatment) or physiological saline (control) to free‐living female dark‐eyed juncos Junco hyemalis in the period immediately prior to egg‐laying (～4 weeks). We found that KLH‐injected females artificially delayed clutch initiation when compared to control females. These data help to refine our understanding of how free‐living birds allocate resources between reproduction and self‐maintenance processes during the critical pre‐laying period of the annual cycle.     

An experimental test of predator–parasite interaction in a passerine bird

Experimental studies incorporating multiple trophic levels are scarce but of increasing interest for understanding ecological communities. Here we investigated interactive effects of perceived predation risk and parasite pressure on life‐history traits in a hole‐nesting bird, and the effects of predation risk on parasite success. In a 3 × 2 experimental design we increased perceived predation risk for breeding great tits Parus major via simulations of either nest‐predators (woodpeckers) or post‐fledging predators (sparrowhawks) close to nests, and used a non‐predatory species (song thrush) as a control. Concurrently, half of the nests in each treatment were either infested with ectoparasites, or kept parasite‐free. Regarding the predation risk – parasite interaction, exposure to nest‐predators tended to lower wing and sternum growth rates of nestlings in the absence, but not the presence, of parasites. In the presence of parasites, exposure to a post‐fledging, but not to a nest‐predator, led to significantly reduced wing growth. Mass and tarsus length were not affected by predator exposure, but ectoparasites had slight positive effects on mass gain. In the last third of the nestling period, overall nestling size was significantly smaller when exposed to a post‐fledging predator than to a nest‐predator, but neither differed from the control. Parental feeding rates were not affected by the treatments, but parents became less selective towards food items under either predation risk. Hen‐flea population sizes (adult or larvae) in nests were not affected by predation risk treatment of hosts. In summary, we found some evidence for an interactive effect of predation risk and parasite pressure on nestling growth. The complexity of the interaction, combined with certain inconsistencies of the effects and potential statistical artifacts, prevent however a straightforward interpretation of the results. The insights from the study are useful for designing additional experiments to further investigate the complexity of predator–parasite interactions in wild populations.     

Factors associated with nest survival of Black‐throated Sparrows,desert‐breeding nest‐site generalists

Black‐throated Sparrows (Amphispiza bilineata) are common breeding birds throughout the desert regions of North America and can be considered nest‐site generalists. Information about how spatial (e.g., vegetation) and temporal factors influence nest survival of these sparrows is lacking throughout their range. Our objective was to examine the spatial and temporal factors associated with nest survival of Black‐throated Sparrows at the nest and nest‐patch scales in the predator‐rich environment of the northern Chihuahuan Desert of New Mexico. We used a logistic‐exposure model fit within a Bayesian framework to model the daily survival probability of Black‐throated Sparrow nests. Predation was the leading cause of nest failure, accounting for 86% of failed nests. We found evidence of negative associations between nest survival and both vegetative cover above nests and shrub density within 5 m of nests. We found no support for other habitat covariates, but did find strong evidence that daily survival rate was higher earlier in the breeding season and during the egg‐laying stage. A decline in nest survival later in the breeding period may be due to increased predator activity due to warmer ambient temperatures, whereas lower survival during the incubation and nestling stages could be a result of increased activity at nests. A generalist approach to nest‐site selection may be an adaptive response to the presence of a diverse assemblage of nest predators that results in the reduced influence of spatial factors on nest survival for Black‐throated Sparrows.     

A review of available methods and description of a new method for eliminating ectoparasites from bird nests

Bird nests offer an ideal situation to manipulate ectoparasites and study how they impact hosts. Several methods are available to eliminate parasites from nests and each has its own suite of advantages and disadvantages. For example, recent toxicity research has revealed that some commonly used insecticides may not be suitable for use in experiments with nestlings. This highlights the need for investigators to control for the effects of methods used to eliminate nest parasites within experimental designs. Methods that can be used across treatment groups are also often needed to study the effects of variation in parasite intensity. To aid investigators in deciding which method(s) to use, we provide a comprehensive review of available methods for eliminating nest ectoparasites and also describe a new heat gun method. We tested the effectiveness of the heat‐gun method with nests of Barn Swallows (Hirundo rustica) to which 100 nest mites were added and then quantified the number of surviving mites and other naturally occurring arthropods. We found that fully heated nests had significantly fewer mites and other arthropods than partially heated or control nests. Use of the heat gun had no negative effects on nestling growth or mortality rates. In studies of avian nest ectoparasites, investigators need to consider methods that can be used across treatment groups to ensure that unaccounted for toxicity effects are not influencing results and leading to underestimation of the often subtle effects of ectoparasites on birds.     

The effects of force‐fledging and premature fledging on the survival of nestling songbirds

Despite the broad consensus that force‐fledging of nestling songbirds lowers their probability of survival and therefore should be generally avoided by researchers, that presumption has not been tested. We used radiotelemetry to monitor the survival of fledglings of Ovenbirds Seiurus aurocapilla and Golden‐winged Warblers Vermivora chrysoptera that we unintentionally force‐fledged (i.e. nestlings left the nest in response to our research activities at typical fledging age), that fledged prematurely (i.e. nestlings left the nest earlier than typical fledging age), and that fledged independently of our activities. Force‐fledged Ovenbirds experienced significantly higher survival than those that fledged independent of our activities, and prematurely fledged Ovenbirds had a similarly high survival to those that force‐fledged at typical fledging age. We observed a similar, though not statistically significant, pattern in Golden‐winged Warbler fledgling survival. Our results suggest that investigator‐induced force‐fledging of nestlings, even when deemed premature, does not necessarily result in reduced fledgling survival in these species. Instead, our results suggest that a propensity or ability to fledge in response to disturbance may be a predictor of a higher probability of fledgling survival.     

Ectoparasitism and the role of green nesting material in the European starling

Summary The use of green nesting material is widespred among birds. Recent evidence suggests that birds use secondary chemicals contained in green plants to control ectoparasites. We manipulated green nesting material and ectoparasites of European starlings (Sturnus vulgaris) to test two hypotheses: (1) ectoparasites adversely affect prefledging survival and morphometrics or postfledging survival, and (2) green nesting material ameliorates the effects of ectoparasites. We recorded fat score, numbers of scabs, tarsal length, body mass, and hematocrit level on each nestling 17 days after hatching. We also fitted each nestling with unique patagial tags and resighted the starlings for 6–8 weeks after fledging to estimate survival and sighting rates. Nests devoid of green nesting material and dusted with the insecticide, carbaryl, had fewer high ectoparasite infestations, and nestlings had significantly lower scab scores, and significantly higher body masses than nestlings in undusted boxes. However, there was no difference in postfledging survival between birds from carbaryl-treated and undusted nests. There also was no difference in prefledging survival and morphometrics or postfledging survival between nestlings from boxes with and without green nesting material. These results do not support the hypothesis that starlings use green nesting material to control nest ectoparasites. We suggest an alternative hypothesis; green nesting material is used for mate selection or pairbonding in the starling.     

Ectoparasites of terrestrial vertebrates inhabiting the Georgia Barrier Islands, USA: an inventory and preliminary biogeographical analysis

Aim To document ectoparasitic arthropods of terrestrial vertebrates inhabiting barrier islands and to offer preliminary interpretations. Location The coast of Georgia, USA, with most data presented for St Catherines, Sapelo, Jekyll, and Cumberland islands. Methods Ectoparasites were collected and identified from hundreds of live‐trapped mammals, birds, and reptiles. Ticks and louse‐flies were also collected by dragging or flagging a white cloth through vegetation. Some ectoparasites were recovered from host nests or roosting sites. Literature records and specimen records from the US National Tick Collection supplemented these data. Results Inventories of ectoparasite species recovered from vertebrates on each island are provided. Many new records and a small number of undescribed species are reported. Main conclusions Compared with most ectoparasite faunas associated with the same host species on the adjacent mainland, ectoparasite species diversity on the barrier islands is depauperate. Possible reasons for this phenomenon are discussed including ecological, geological, and vicariant factors. Tick faunas do not appear to be depauperate on the islands probably because immature stages attach to visiting or migrating birds. Some host‐ectoparasite associations that we recorded are atypical for mainland faunas. This trend has also been recorded in some previous surveys of insular ectoparasites and may be related to vacant ectoparasite niches on some islands.     

Observation of plugging behaviour reveals entrance‐guarding schedule of morphologically specialized caste in Colobopsis nipponicus

The success of social insects is often attributed to the specialized morphologies and behaviours of workers. One of the most elaborate specializations in ant species is the workers’ plugging behaviour, in which their uniquely shaped heads are used for nest defence. These species generally nest in tree cavities. Without morphologically specialized workers (major workers) plugging the nest entrance, nests are easily attacked and replaced by conspecific and heterospecific cavity‐dwelling ants and other predators. Therefore, major workers are expected to defend the nest at all times. However, empirical evidence on the social time investment for nest defence is still lacking. Here, we investigated how major workers of Colobopsis nipponicus achieve nest defence (plugging behaviour) in terms of their work schedule. Our results showed that the nests had more major workers than entrances. The observation of artificial plastic nests over 6 days in the laboratory revealed that the nest entrance was guarded almost continuously by multiple major workers. The entrance‐guarding schedule was not equally divided among major workers, and there were no clear shift patterns in the timing of changeovers. We highlight the importance of investigating the time investment of workers to fully understand the defence strategies of this morphologically specialized caste.