European starlings: nestling condition, parasites and green nest material during the breeding season

Male European starlings (Sturnus vulgaris) intermingle fresh herbs, preferably species rich in volatile compounds, into their dry nest material. In a field study, we investigated whether these herbs affect the mite and bacteria load of the nests and the condition of the nestlings either directly or via parasite control. We examined the amount of herbs and the number of plant species males carried into their nests, the variation of volatile compounds in the headspace air of the nest boxes and mite/bacteria load of the nests throughout the season. The amount of herb material and the number of plant species, the number of substances emanated by these plants and the infestation of the nests with bacteria and mites (Dermanyssus gallinae) increased with season. In a field experiment, we exchanged natural starling nests with experimental nests with or without herbs. We found that the herbs had no effect on the mites but fewer bacteria were sampled in nests with herbs than in nests without herbs. The body mass of the fledging was not related to the season or the mite/bacteria load of the nests. However, nestlings from nests with herbs fledged with higher body mass than nestlings from nests without herbs. Both bacteria and mite load were related to nestling mortality. In nests containing no herbs, the numbers of fledglings declined significantly with the increasing mite load while the mites had no effect on the number of fledglings in nests with herbs. Thus, the nest herbs counteracted the effect of the mites. In conclusion, it seems that volatile herbs can reduce bacterial but not mite infestation of the starling nests. The positive influence of herbs on nestling growth indicates that herbs either directly (perhaps as immunostimulants) improve the condition of the nestlings and help them cope with the harmful effects of mites, or they provide a nest environment beneficial for the nestlings‘ development by the reduction of germs.     

Interacting effects of aromatic plants and female age on nest-dwelling ectoparasites and blood-sucking flies in avian nests

Some avian species incorporate aromatic plants to their nests. The "nest protection hypothesis", which posits that volatile secondary compounds contained in these plants may have antiparasite properties, has not received full support. All previous tests of this hypothesis have only considered effects on nest-dwelling ectoparasites, but not on blood-sucking flies. The "drug hypothesis" posits that aromatic plants may stimulate nestling immune system, development, or condition. We tested these hypotheses experimentally in wild blue tits, Cyanistes caeruleus, a species that adds aromatic plants to their nests. We supplemented aromatic plants to half of a sample of nests, while adding grass to the other half of nests. We quantified abundance of two groups of blood-sucking flies (blackflies and biting midges) at two different stages of the reproductive period, and abundance of three nest-dwelling ectoparasites (fleas, mites, and blowflies). Experimental supplementation of aromatic plants reduced abundance of fleas only in nests of yearling females and not in nests of older females. Blackflies and biting midges were both more numerous in nests of yearling females than in nests of older females. Mass of aromatic plants added by females was negatively related with abundance of fleas in control nests but not in experimental nests supplied with aromatic plants. Mass of plants added by females was also positively related with abundance of blackflies during the nestling stage. Finally, aromatic plants did not affect nestling growth or immune responses. We conclude that several factors such as female experience and their ability to add plants to the nest interact to explain effects of aromatic plants on different parasites.     

Green nesting material has a function in mate attraction in the European starling

The function of fresh green nest material has long been debated. It has been suggested that it reduces the number of ectoparasites in nests and on nestlings (nest protection hypothesis), or is used by males to signal condition and paternal quality (male quality hypothesis) or is used as a sexually selected ornament to attract females (courtship hypothesis). We simultaneously tested these three hypotheses in the European starling, Sturnus vulgaris, in the field. Green material was carried by male starlings only, and mainly during nest building. It was not used to reduce ectoparasites. Males nesting in nestboxes that were experimentally contaminated with ectoparasites did not carry more green nest material than males nesting in control boxes, and experimental removal and addition of green material had no effect on the number of ectoparasites on the nestlings or on their body mass. Furthermore, the amount of green material carried into a nestbox was not associated with male body mass, paternal incubation attendance or nestling food provisioning. There is two-fold experimental evidence that males use green plant material to attract mates. First, removal of greenery resulted in a significantly lower percentage of nestboxes containing a clutch than the control or addition treatment. Second, unpaired male starlings sang more and carried more greenery into a nestbox when a caged female was positioned adjacent to the nestbox than when a caged male or an empty cage was present. Paired males, when subjected to the same experimental design, did not respond.     

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.     

Experimentally broken faecal sacs affect nest bacterial environment,development and survival of spotless starling nestlings

Nestlings of most avian species produce faecal sacs, which facilitate the removal of nestlings’ excrements by parents, thereby reducing proliferation of potentially pathogenic microorganisms and/or detectability by predators and parasites. The nest microbial environment that birds experience during early life might also affect their development and thus, faecal sacs facilitating parental removal may be a strategy to decrease bacterial contamination of nests that could harm developing nestlings. Here, we tested this hypothesis by experimentally broken faecal sacs and spreading them in nests of spotless starlings Sturnus unicolor, thereby avoiding their removal by adults. In accordance with the hypothesis, experimental nests harboured higher bacterial density than control nests. Nestlings in experimental nests were of smaller size (tarsus length) and experienced lower probability of survival (predation) than those in control nests. Moreover, nestlings in experimental nests tended to suffer more from ectoparasites than those in control nests. We discuss the possible pivotal role of bacteria producing chemical volatiles that ectoparasites and predators might use to find avian nests, and that could explain our experimental results in starlings.     

Nest‐dwelling ectoparasites influence the start and duration of the first pre‐basic moult in the European starling Sturnus vulgaris

Nest‐dwelling ectoparasites represent an early stressor for birds as they impair the development of nestlings, which can adaptively respond by adjusting their growth rate to current conditions. While nest ectoparasites have long‐term effects on nesting adults, no study has examined if they also have an impact on the moult patterns of juveniles. Herein, we investigated whether the presence of ectoparasites in the nest influences the start and duration of the first pre‐basic moult in the European starling. To do so, we experimentally removed nest‐dwelling ectoparasites from a group of nests and used another group of unmanipulated (i.e. naturally infested) nests as the control. The moult began at an earlier age and lasted longer in birds from the ectoparasite‐free nests compared to their control counterparts. The timing of the moult was also affected by the hatching date (i.e. birds that fledged later had shorter moults) and the brood size (i.e. birds in larger broods started their moult at an older age). We also found evidence that the removal of nest ectoparasites influenced the condition of individuals during the course of the moult. In the control birds, we observed a decrease in hematocrit levels, but these were unaltered in the birds fledged from the ectoparasite‐free nests. Our study shows that nest‐dwelling ectoparasites adversely affected the timing of the moult and the individual condition of juvenile starlings, with possible major consequences for their subsequent life‐history events.     

Palatability of passerines to parasites: within-brood variation in nestling responses to experimental parasite removal and carotenoid supplementation

Asynchronous hatching of eggs in avian clutches produces a size hierarchy among nestlings that may lead to variation within broods in resistance to pathogens or parasites. In this study, we tested several predictions regarding variation in immunocompetence and distribution of parasites within avian broods by combining parasite removal and carotenoid supplementation treatments in nests of mountain bluebirds Sialia currucoides . Last-hatched nestlings were less likely to invest carotenoids in an induced cell-mediated immune response, suggesting they may be more susceptible to parasites; however, parasite removal disproportionately benefited middle-ranked nestlings. This supports the hypothesis that some avian ectoparasites balance host resistance against nutritional benefits by preferentially parasitizing nestlings of intermediate quality and immunocompetence. We found no evidence that males positioned last in the hatching sequence were differentially affected by ectoparasites, and, contrary to some previous studies in other passerines, last-hatched nestlings in asynchronously hatching broods were not less immunocompetent than their nest mates. In fact, junior nestlings exhibited weaker immune responses than their siblings in more synchronously hatching broods, and we suggest this may reflect environment-dependent maternal effects that warrant further investigation. Overall, our results highlight the importance of understanding the feeding and host selection behaviour of ectoparasites, as well as the fitness consequences thereof, since many predictions related to within-brood distribution of parasites require that parasites are able to discern the relative quality of available hosts.     

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.     

Experimental addition of greenery reduces flea loads in nests of a non-greenery using species, the tree swallow Tachycineta bicolor

Several bird species, including cavity-nesters such as European starlings Sturnus vulgaris , add to their nests green sprigs of plants such as yarrow Achillea millefolium that are rich in volatile compounds. In this field study on another cavity-nester, tree swallows Tachycineta bicolor , we tested whether yarrow reduced ectoparasite loads (the nest protection hypothesis), stimulated nestling immune systems (the drug hypothesis), or had other consequences for nestling growth or parental reproductive success (predicted by both preceding hypotheses). Tree swallows do not naturally add greenery to their nests, and thus offer several advantages in testing for effects of greenery independent of other potentially confounding explanations for the behaviour. We placed fresh yarrow in 23 swallow nests on the day the first egg was laid, replenishing every two days until clutch completion (=three times), and at 44 control nests, nesting material was simply touched. At 12 days of age, we measured nestling body size and mass, and took blood smears to do differential white blood cell counts. We subsequently determined the number and proportion of young fledging from nests and the number of fleas remaining after fledging. Higher humidity was associated with higher flea numbers whereas number of feathers in the nest was not. Our most significant finding was that an average of 773 fleas Ceratophyllus idius was found in control nests, versus 419 in yarrow nests. Possibly, parents compensate for blood that nestlings lose to ectoparasites by increasing food delivery, because we detected no differences between treatments in nestling mass, nestling leukocyte profiles, or proportion of young fledging, or relative to flea numbers. Our results provide no support for the drug hypothesis and strong support for the nest protection hypothesis.     

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.     

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.     

The price of insulation: costs and benefits of feather delivery to nests for male tree swallows Tachycineta bicolor

Many species of birds line their nests with feathers, and it has been hypothesized that this functions to provide a thermally stable microenvironment for the development of eggs and nestlings. Feathers in the nest may also function as a mechanism for parasite control, providing a physical barrier that protects nestlings from ectoparasites. We tested these hypotheses by performing a feather removal and addition experiment in tree swallows Tachycineta bicolor, a species well‐known for lining their nests with feathers. While we found no evidence that quantity of feathers in nests influenced the ability of females to produce and incubate eggs, offspring in well‐feathered nests had longer flight feathers and were structurally larger just prior to fledging that those in nests with fewer feathers. Furthermore, we also demonstrated a positive correlation between feathers and the abundance of larval blow flies Protocalliphora spp. in nests, a result opposite to that predicted by the anti‐parasite hypothesis. While our study provides strong support for the insulation hypothesis, we also discuss the possibility that devoting time to feather gathering may result in males losing paternity in their nests, although manipulative studies will be necessary to fully evaluate this idea.     

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.     

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.     

Aromatic plants in blue tit Cyanistes caeruleus nests: no negative effect on blood-sucking Protocalliphora blow fly larvae

Nesting birds use several behavioural or physiological defence mechanisms against parasites. On Corsica, female blue tits Cyanistes caeruleus incorporate fresh fragments of a limited number of aromatic plants in the nest cup, from the end of nest construction until fledging. Some of these plants negatively affect bacterial growth and host location by blood-sucking mosquitoes in laboratory conditions. In natural populations, Corsican blue tit chicks are exposed to the highest levels of blood-sucking ectoparasitic blow flies Protocalliphora spp. reported in Europe. These ectoparasites can have severe negative effects on chick development and survival probabilities, especially when food constraints are elevated. Here we investigated in several natural Corsican blue tit populations the hypothesis that aromatic plants brought to the nest have anti-blow fly effects during the chick-rearing stage. We predicted that: 1) the amount of aromatic plants should be negatively related to blow fly infestation intensity across nests, 2) experimental addition of aromatic plants in nests should reduce blow fly infestation intensity, and 3) nestlings should be in better physical condition in nests where aromatic plants were experimentally added. No significant relation was found between amount of aromatic plants in nests and blow fly infestation intensity. Experimental addition of aromatic plants did not reduce blow fly infestation intensity and did not affect the chick phenotypic parameters we measured. We conclude that aromatic plants in blue tit nests are not used as a defence against ectoparasitic Protocalliphora blow flies in our study population.     

Experimental evidence for host preference in a tick parasitizing songbird nestlings

Mechanisms of host preference in ectoparasites are important to the understanding of host‐parasite interactions. Since ectoparasites negatively affect the condition of their hosts, while the hosts’ condition itself may affect the parasites’ choice, separating the factors that drive host preference from parasite impact asks for experiments. We combined the data of two choice experiments to investigate the preference of the nidicolous tick Ixodes arboricola when exposed to the nestlings of a passerine bird (Parus major). In the first experiment, in which complete broods at hatching were exposed to an ecologically relevant number of ticks, the relationship between tick loads and nestlings’ developmental status was characterized by a distribution with the highest tick loads on the more developed nestlings. Host preference became more apparent at a smaller brood size, suggesting a role for host density. In a second experiment we evaluated host choice in a pairwise choice experiment, exposing pairs of siblings with contrasting developmental status to eight ticks. In the first and the second pair, a median developed nestling was linked with the most developed and the least developed nestling, respectively. Seventy‐two h after tick exposure we measured the innate constitutive humoral immunity and haematocrit. No differences were found in innate immunity, but the least developed nestlings had on average a lower haematocrit than the median and most developed nestlings. Significantly fewer ticks attached on the least developed nestling compared to the median nestling, and this difference was more pronounced when the innate immunity of the median developed nestling was higher. No difference in tick load was found among the median and best developed nestlings. The linkage between host preference and host physiological condition provide further insight in the mechanisms driving ectoparasite aggregation, which is important for the population dynamics of host, ticks and tick‐transmitted pathogens.     

The nest defence by the red‐backed shrike Lanius collurio – support for the vulnerability hypothesis

The majority of altricial bird species defend their brood against predators more intensively in nestlings rather than eggs stage. Several hypotheses have been proposed to explain this difference. The majority of existing experimental studies have recorded a gradually increasing intensity of nest defence supporting the reproductive value hypothesis. We have compared nest defence in two nesting stages of the red‐backed shrike against two predators of adult birds and against two predators of nests. While the nests with nestlings were defended by parents against three out of four predators, nests with eggs were almost not defended at all. This rapid change in parent nest defence supports rather the vulnerability hypothesis, predicting that the threat to nests with nestlings increases rapidly after hatching, as they became more conspicuous due to their begging and parental provisioning. Unlike most of the species tested previously, the red‐backed shrike uses very vigorous mobbing towards predators. We suggest that the occurrence of this active mobbing (strikes, including physical contact) is a good proxy of the current threat to the nest.     

Behavioral responses of nesting female dark‐eyed juncos Junco hyemalis to hetero‐ and conspecific passerine preen oils

Several studies have suggested a greater role for olfactory cues in avian social interactions than previously recognized, but few have explicitly investigated the effect of odor on parental behavior. We present results from a preliminary study in which we applied hetero‐ and conspecific preen gland secretions, which are known to contain volatile compounds, to the nests and eggs of incubating female dark‐eyed juncos Junco hyemalis. The responses to these two conditions were compared to the responses of females whose nests were treated with their own preen oil as a control condition, and to females whose nests were treated with the vehicle only. We found that females significantly reduced incubation bout length, a form of parental care, in response to alien secretions, more so if they came from a heterospecific than a conspecific. Females did not reduce incubation bout length in response to their own preen oil or to a vehicle‐only control. These results suggest that odors in the nest may influence avian parental care. However, the behavioral change was only temporary and had no effect on later hatching success. In our study population, brood parasitism by brown‐headed cowbirds is common, but resulting nest abandonment is rare; juncos are frequently able to successfully breed even with cowbird nestlings in their nests. Thus, we suggest that more extreme behavioral responses to alien odor, such as nest abandonment or egg ejection, may not be adaptive and should not be expected.     

Nest size predicts the effect of food supplementation to magpie nestlings on their immunocompetence: an experimental test of nest size indicating parental ability

Post-mating sexually selected signals are expected to indicateparental quality. The good parent model assumes that expressionof the sexual character positively reflects parental ability,resulting in a potential link between the exaggeration of thecharacter and nestling-fitness traits. We tested this predictionin a population of a monogamous passerine, the magpie (Picapica), for which nest size is known to act as a post-matingsexually selected signal. We provided a food supplement to halfof the magpie nestlings in each nest, keeping the other halfas control nestlings. We found that food-supplemented nestlingsexperienced a significantly higher T-cell-mediated immune responseand a tendency to an increased condition index. In accordancewith the good parent model, we found that nest size was positivelyrelated to T-cell mediated immune response for control magpie,whereas this relationship was nonexistent in food-supplementednestlings. In addition, the difference in T-cell mediated immuneresponse between food-supplemented and control nestlings ofthe same nest was principally explained by nest size. Basedon our results, we discuss that magpie pairs with large nestsprovided their nestlings with higher quality food as comparedto pairs with smaller nests, nest size thereby being an indicatorof parental ability. To our knowledge, this is the first studyshowing a link between a post-mating sexually selected signaland nestling immunocompetence, a trait closely related to fitnessin birds.     

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.