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Atypical behavior of a black fly species connects cavity-nesting birds with generalist blood parasites in an arid area of Spain



The feeding behavior of bloodsucking insects determines the transmission, distribution, host spectrum and evolution of blood parasites in the wild. Conventional wisdom suggests that some vector groups (e.g. black flies, family Simuliidae) are consistently exophagous daytime biters. We aimed to understand more about the exceptions to this pattern by combining targeted trapping and molecular identification of parasites in vectors.


In this study, we collected black flies in nest boxes used by European rollers Coracias garrulus in southeastern Spain. We molecularly analyzed 434 individual insects, identifying the black fly species caught in the nest boxes, their potential vertebrate blood meals, and the haemosporidian parasite lineages that they carried.


Only one black fly species, Simulium rubzovianum, appeared to enter the nest boxes of rollers. Among the trapped specimens, 15% contained vertebrate DNA, which always belonged to rollers, even though only half of those specimens were visibly engorged. Furthermore, 15% of all black flies contained Leucocytozoon lineages, indicating previous feeding on avian hosts but probably not on infected adult rollers. The known vertebrate hosts of the recorded Leucocytozoon lineages suggested that large and/or abundant birds are their hosts. Particularly represented were cavity-nesting species breeding in the vicinity, such as pigeons, corvids and owls. Open-nesting species such as thrushes and birds of prey were also represented.


Our data strongly suggest that S. rubzovianum bites uninfected roller nestlings and infected individuals of other species, potentially incubating adults, inside nest boxes and natural cavities. This simuliid does not appear to have a strong preference for specific host clades. Contrary to the general pattern for the group, and possibly enhanced by the harsh environmental conditions in the study area, this black fly appeared to intensively use and may even have a preference for confined spaces such as cavities for feeding and resting. Preferences of vectors for atypical microhabitat niches where hosts are less mobile may enable social and within-family transmission and parasite speciation in the long term. At the same time, a lack of host preference in concentrated multispecies communities can lead to host switches. Both processes may be underappreciated driving forces in the evolution of avian blood parasites.

Graphical abstract


Vector-borne parasites exert major selection forces on their hosts, but the distribution of the former crucially depends on the behavior and habitat choice of the transmitting organisms [1]. Understanding the feeding behavior of potential vectors can be informative both about short-term processes relevant to health and conservation, such as increased virulence in weakened and atypical hosts, and about long-term coevolutionary processes [2,3,4,5]. However, studies of the natural foraging behavior of insect vectors in the field are often constrained by their size and mobility. Thus, parasites present in vectors can be used as handy markers of host-parasite interactions, as they can inform simultaneously about the current members of exchange networks and the potential for rare evolutionary events such as host shifts [6].

Black flies (Diptera, Simuliidae) are one of the main groups of bloodsucking dipteran vectors, with members of the family transmitting haemosporidian parasites, trypanosomes and filarial nematodes [7]. Compared to other bloodsucking dipterans transmitting human diseases, black flies have been less investigated and may be harder to study. The feeding ecology of black flies is not well understood because colonies of very few species have been established in laboratories and feeding behavior is almost never performed in captivity. Adult black flies are commonly trapped using CO2-baited traps [8,9,10,11,12]. Valuable information complementary to that obtained with classic methods can be gathered by investigating the wide spectrum of habitat niches and hosts that attract different black fly species. Alternative approaches to black fly trapping, such as net-scooping and use of living hosts as bait, have been used [8, 9, 13,14,15]. Black flies seem to prefer either common and/or large hosts [14, 16]. Black fly species are distinguishable as either mammalophilic or ornithophilic, but blood meals of engorged black flies in Scandinavia suggest species-specific preferences for different bird host groups [17]. At the same time, the host species composition and parasite loads of black flies in central Europe suggest lack of host specificity for some ornithophilic black fly species but a preference for specific habitat niches, e.g. the upper forest canopy [14, 18]. Correspondingly, habitat and nest height explain the prevalence of black fly-transmitted Leucocytozoon lineages observed in host bird assemblages, while cavity nesting increases the probability of high Leucocytozoon prevalence in bird hosts [19].

It is important to note that bird hosts live in complex environments that offer many microhabitat niches. Habitat preferences of vectors can lead them to have more frequent contact with certain host species, e.g. open-nesting birds breeding high in the canopy such as raptors, corvids and thrushes, or cavity-nesting birds such as diverse passerines and owls [14, 20]. Thus, the specificities of black fly behavior may lead to separate parasite-exchange networks between species sharing similar niches within a given habitat. Vectors can potentially enhance parasitic host-switching rates by increasing the incidence of spillover between niche-sharing host species. This process may select for adaptability of parasites to novel host groups and blood environments, and eventually also lead to the establishment of new predominant host-parasite relationships and a consequent increase in co-speciation rates [21, 22]. However, the differences in vector behavior and the dominating vector species in most microhabitats are still largely unknown even in the best studied areas of the world.

Ornithophilic simuliids are the essential vectors of avian haemosporidian parasites of the genus Leucocytozoon [22]. Members of this genus have been recently shown to have the higherst rates of co-speciation and host switching among blood parasites, but the vector behaviors which may lead to these patterns remain to be revealed [23]. A great diversity of genetic Leucocytozoon lineages has been described and systematized in recent years, along with the vertebrate hosts in which they occur [12, 24]. This allows Leucocytozoon lineages to be used as natural markers for the feeding preferences and foraging habitats of black flies in which they are molecularly detected [6, 14].

In this study, we aimed to explore the feeding behavior of black flies to assess whether they are really mainly exophagous feeders. For this, we studied the system formed by European rollers, Coracias garrulus (hereafter ‘rollers’) breeding in nest boxes, and the black flies visiting them. We also studied which Leucocytozoon lineage composition they carry. Many black fly species suck blood from hosts of different taxonomic orders. Therefore, our hypothesis was that cavity-feeding black flies will bear parasites of most host species breeding locally in nest boxes and possibly also in the nest box surroundings. Since microhabitats such as cavities and burrows may demand particular behavioral or morphological adaptations, and since black flies are generally outdoors (exophilic) biters, we predicted that only few species might forage on cavity-nesting birds [7]. The samples were collected in an arid area in southern Spain, where the breeding habitat for black fly larvae—running water—is scarce and frequently brackish. Harsh environmental conditions can make nest boxes an attractive, relatively humid microhabitat, and thus they could become an important reservoir of black fly diversity [25]. In contrast to most other local birds, rollers are exclusive cavity breeders and are the most common cavity breeders in the study area. Black flies were collected in the framework of a long-term project on host-parasite interactions of cavity-nesting birds.


Study area

The study area and specimen collection methods largely correspond to those of a previous study [26]. In brief, the samples were collected in a 50-km2 area in the Tabernas Desert (Almería, southeastern Spain; 37°05′N, 2°21′W). The landscape mostly consists of patches of shrubby vegetation and olive and almond groves interspersed among dry watercourses and ravines. Inhabited farms are scarce and scattered along the study area. The climate is temperate, semiarid Mediterranean with a strong water deficit during the long, hot summer months (June–September), when the absolute maximum monthly temperature is higher than 40 °C and the monthly average maximum daily temperature remains above 30 °C. The average annual temperature is 18 °C, with mild inter-annual oscillations of 3–4 °C and significant intra-annual fluctuations. The mean annual rainfall is ca. 230 mm with high inter-annual and intra-annual variability [27].

The bird community can be divided into open-nesting species (small passerines, and some species of doves and pigeons) and cavity-nesting ones. The latter breed mainly in natural cavities in dry ravines (i.e. ramblas, temporary stream channels with steep sandstone banks) and human-made constructions [28]. Among the cavity-nesting species in the study area are the common kestrel (Falco tinnunculus), jackdaw (Corvus monedula), Eurasian hoopoe (Upupa epops), rock pigeon (Columba livia), little owl (Athene noctua) and Eurasian scops owl (Otus scops). The European roller and rock pigeon are, by far, the most abundant ones. As a result of a long-term nest box scheme which started in 2005, most rollers breed in wooden nest boxes (height × length × width, 310 × 232 × 230 mm; entrance diameter, 60 mm; with a removable upper lid to allow nest monitoring) installed on eucalyptus trees, sandstone banks and isolated and deserted country houses [29, 30]. Rollers are migratory birds wintering in Africa and arriving at the breeding grounds in the study area at the end of April, when resident, secondary cavity-nesting birds are already settled. Eggs (mean clutch size = 4.23) are incubated by both sexes for ca. 21 days [31] and hatching is distinctly asynchronous. Rollers rear a single brood per year with fledglings leaving the nest approximately 22–25 days after hatching in the studied population.

Simulium trapping

Simulium spp. specimens were trapped using sticky traps placed in nest boxes (n = 36) occupied by rollers between 6 June and 23 July 2018, i.e. during the nestling stage when roller chicks were between 13–14 and 21–22 days old. We followed the method described by Tomás et al. [32] (i.e. using Petri dishes smeared with body gel oil as a non-attractant glue) but replaced the Petri dishes with white vegetal paper (175.5 cm2) that was fixed by thumbtacks on the inner side of the upper lid. The sticky paper was replaced every 4 days to avoid desiccation; two traps were placed per nest and trapping occurred for 8 consecutive days. Additionally, Simulium were opportunistically caught at the nests by hand during routine visits, and all specimens were preserved in 95% ethanol and frozen until identification. The thorax and the abdomen of engorged black flies were separated and analyzed independently.

Morphological identification of black flies

From the total black flies captured during 2018 a subsample of 68 were used for the combined analysis of morphological and molecular identification. Individuals were identified based on descriptions given in the keys of Belqat et al. [33] and Rivosecchi et al. [34]. Morphological identification was facilitated by examining preparations of specimen genitalia mounted on slides.

Molecular identification of black flies, host blood and haemoparasites

Sample and data analyses were performed as described previously [14]. Briefly, DNA of single black flies was extracted from complete specimens or separated abdomen and thorax (in engorged black flies) using overnight digestion in 490 µl of QIAGEN ATL lysis buffer and 10 µl of Proteinase K followed by a standard phenol–chloroform protocol. DNA was quantified using a NanoDrop spectrophotometer (Thermo Fisher Scientific, Waltham, MA). A modified Hotshot technique was used for the DNA extraction of each individual of the subsample for morphological identification [35]. Samples were screened with three separate polymerase chain reaction (PCR) assays: (i) black fly species was determined for a subsample of 126 individuals with conserved primers targeting the cytochrome c oxidase subunit 1 DNA region (LCO1490, 5′-GGT CAA CAA ATC ATA AAG ATA TTG G-3′; and HCO2198, 5′-TAA ACT TCA GGG TGA CCA AAA AAT CA-3′) [36]; (ii) presence of vertebrate host DNA was tested for a subsample of 176 individuals with conserved primers targeting the vertebrate cytochrome b (L14841, 5′-AAA AAG CTT CCA TCC AAC ATC TCA GCA TGA TGA AA-3′; and H15149, 5′-AAA CTG CAG CCC CTC AGA ATG ATA TTT GTC CTC A-3′) [37]; and (iii) presence of haemosporidian lineages within the black fly individuals was established for a subsample of 434 individuals with a nested PCR following Pérez-Rodríguez et al. [38], using the primer pair Plas1 (5′-GAG AAT TAT GGA GTG GAT GGT G-3′) and HaemNR3 (5′-ATA GAA AGA TAA GAA ATA CCA TTC-3′) for the first PCR and the internal primers 3760F (5′-GAG TGG ATG GTG TTT TAG AT-3′) and HaemJR4 (5′-GAA ATA CCA TTC TGG AAC AAT ATG-3′) for the second PCR. This nested PCR primer protocol amplifies the cytochrome b gene of all haemosporidian genera, including Leucocytozoon lineages that are less well detected with other nested PCR protocols, e.g. Leucocytozoon of raptors [24; personal observation]. A Leucocytozoon-infected sample from an adult roller was additionally amplified to ensure that the used nested PCR protocol can detect roller-infecting haemosporidian lineages. PCR products were run on 2% agarose gels. Amplicons were purified with ExoSAP (Thermo Fisher Scientific) and bidirectionally sequenced on an ABI 3730 Analyzer (Applied Biosystems, Waltham, MA) with the BigDye Terminator v1.1 cycle sequencing kit (Thermo Fisher Scientific) using the respective two primers. Raw sequences were edited and aligned in Geneious 8.1.9 ( and compared with sequences on GenBank or, in the case of 3760F/HaemJR4, with sequences on the MalAvi database, as of 28 July 2020 [24].


A total of 515 black flies (range 0–199 per nest) were collected by sticky traps in nest boxes occupied by rollers during 2018. Black flies were captured in 29 out of 36 roller nest boxes (prevalence = 0.81; confidence interval 95% = 0.64–0.92; mean intensity ± SE = 17.8 ± 6.95). Of these, 13 individuals were visibly engorged. Two additional black flies were captured manually in one roller and one scops owl nest box.

Morphological identification

Morphological identification of the subset of 68 black fly individuals revealed the presence of a single morphospecies: Simulium rubzovianum. All morphologically inspected individuals caught in nest boxes were females.

Molecular identification of black flies, host blood and haemoparasites

Black flies species barcoding of the subset of 68 individuals morphologically identified and a subset of 126 individuals identified only by molecular barcoding revealed that all of them belonged to the species S. rubzovianum. Barcoding of all individuals clustered together in the neighbor joining tree (not shown).

Barcoding of 176 black flies for vertebrate DNA showed that 26 specimens contained DNA of rollers, C. garrulus, and one further sample of a manually caught black fly in a scops owl nest box contained DNA of this bird species. Only 12 of the 26 specimens with roller DNA were visibly engorged. In two engorged black flies, vertebrate DNA could be identified both from the thorax and abdomen, in 11 cases (including one black fly with scops owl DNA) only from the abdomen, and in two cases of apparently engorged individuals no vertebrate DNA could be amplified.

Haemosporidian barcoding of a subset of 434 black flies from 21 nests revealed that 63 individuals contained one Leucocytozoon lineage while three others contained two lineages of Leucocytozoon which could be identified (Fig. 1; Table 1). This corresponded to 15.2% (confidence interval 95% = 11.96–18.94%) overall Leucocytozoon prevalence in the collected black flies.

Fig. 1
figure 1

Number of Simulium rubzovianum caught at separate nest boxes inhabited by Eurasian rollers Coracias garrulus including number of specimens in which Leucocytozoon was detected (grey, n = 66). The figure is based on a subset of 434 black fly individuals caught in 21 nests

Table 1 Haemosporidian lineages found in black flies from nest boxes of European rollers in southeastern Spain

Only in two instances were both parasite and avian DNA present in black flies—in one case scops owl DNA was found together with DNA of the Leucocytozoon lineage OTSCO01. In another specimen, roller DNA was present along with DNA of lineage COLIV04.

The known host groups for the identified Leucocytozoon lineages were doves and pigeons (28 cases, including one co-infection), corvids (28 cases), diurnal raptors (15 cases), thrushes (13 cases, including one co-infection), sparrows (7 cases), owls (4 cases, including one co-infection), finches (3 cases) and tits and warblers (2 cases each). In all three cases of mixed infections, the co-infecting lineages appeared to be typical of the same host group—STAL1 and OTSCO09 are typical of owls, AEMO02 and COLPAL04 are typical of pigeons [39], and TUMER01 and NEVE01 are thrush parasites [40]. Three of the most represented Leucocytozoon lineages (AEMO02, COCOR12, COLIV04), comprising 26 of the 69 lineage occurrences, are generalist Leucocytozoon parasites which have been shown to infect host species from different avian orders (Table 1).


To our knowledge, this is one of the first studies of a local black fly fauna that utilizes the specific niche constituted by nest boxes, which potentially corresponds to the use of natural tree and rock cavities [7, 20, 41]. Additionally, the data on the Leucocytozoon lineages found in these potential vectors in southeastern Spain indicate their natural host spectrum, feeding habitat range and preferences.

Cavity use and feeding habits of black flies

Based on morphological and molecular identification, S. rubzovianum was the only species of black fly found in this study in the nest boxes of European rollers in southern Spain.

The general rule is that simuliids are daytime exophagous, i.e. outdoors biters. Most species are reluctant to feed even in large enclosed rooms, making them particularly hard to maintain in laboratory colonies [7]. Although some exceptions have been reported that suggest that feeding by simuliids on small mammals in burrows or on cavity-nesting birds does occur [41,42,43], endophagous feeding of simuliids in dark, confined and narrow spaces has not been documented. After feeding, simuliids have decreased mobility and often rest in places where they are unlikely to be found, e.g. tree crowns, or confined spaces such as within leaf litter, on nest branches, in crevices and potentially burrows [7, 14]. This impedes making a distinction between “feeding and resting in the nest box” and “feeding around the nest box and resting inside”.

However, several of our observations may help us to clarify whether the black flies were actually feeding in the nest boxes: (i) all morphologically inspected individuals caught in the nest boxes were females, which suggests that black flies enter nest boxes specifically to feed and not solely to rest or seek shelter, as the latter would equally apply to males; (ii) black flies trapped in nest boxes occupied by rollers had Leucocytozoon lineages specific to other co-existing bird species. However, in no case did we find black flies that contained blood of these species, which suggests that these flies had previously fed, and after completing the gonotrophic cycle, entered the nest boxes for their next meal; (iii) all 12 freshly engorged specimens trapped in nest boxes with roller nestlings had roller blood. European rollers are standard hosts of two morphospecies of Leucocytozoon—Leucocytozoon eurystomi and Leucocytozoon bennetti—with the prevalence of the latter exceeding 50% in some avian populations [6]. Previous studies based on smear screening found ca. 30% prevalence of Leucocytozoon in adults of a focal roller population [44]. This was probably an underestimate of the infected adults since microscopic examination can have low sensitivity [45]. In fact, the prevalence of Leucocytozoon in adult rollers from the study area estimated by molecular techniques is ca. 90% (Veiga et al., in preparation). Therefore, at least some blood meals originating from adult breeding rollers should carry detectable Leucocytozoon DNA. However, only in one case did the engorged black fly also contain Leucocytozoon DNA, and even in this case the lineage was typical of pigeons and corvids. In the other cases, the blood meal could have come from uninfected adults or, more probably, from nestlings, since blood of young nestlings is much less likely to contain parasite DNA. Revisiting the same feeding sites and even boxes by black flies and other vectors may commonly lead to quasi-vertical transmission of parasites—from adults to offspring via the vector—thus creating a prevalence structure based on host families [46]. Support for such patterns of infection has been found in other hosts of Leucocytozoon [47, 48]. However, engorged black fly vectors would need two sufficiently long time windows to bite and transmit parasites previously ingested from incubating adults: (i) several days or weeks to lay eggs at a water body and develop infective sporozoites in the salivary glands; and (ii) a window when nestlings have not fledged and can be bitten. This would be followed by a prepatent period before the development of blood stages in nestlings, which typically takes more than 10 days for Leucocytozoon [6]. This makes the presence of Leucocytozoon blood stages in 2- to 3-week-old nestlings less probable.

All these arguments suggest that nestlings are the likely donors of uninfected roller blood meals and that the sampled S. rubzovianum individuals had indeed foraged in the confined darkness of the nest box. It should be noted that under the scenario of family-based social transmission, the closest interactions are between parents and offspring and thus most transmission events may occur before young fledge. This would select for short prepatent periods, followed by a peak in infection intensity allowing for some extra transmission between siblings. Such a short prepatent period may account for the black fly that contained both roller and parasite DNA, which was collected in the nest box with the oldest nestlings of the study, which were very close to their fledging age. However, since the lineage found has been cited for pigeons and corvids, it is more likely that this black fly previously fed on pigeons and then on an uninfected roller. A further specimen engorged with infected scops owl blood (in this case with a Leucocytozoon lineage found in Strigiformes) was caught in a nest box during a regular incubation check, also suggesting that it fed in the box shortly before it was caught. Specific studies on the development of parasitemia over the lifetime of hosts and on the lineages of Leucocytozoon found in rollers are needed to highlight the potential vectorial role of black flies in our roller population.

While it seems very likely that S. rubzovianum feeds in nest boxes and even in natural cavities, this type of behavior does not necessarily apply to all ornithophilic species. Previous studies found Simulium (Eusimulium) petricolum to be another ornithophilic simuliid species present in this type of habitat and entering nest boxes [44]; however, we could not find any evidence that S. petricolum used nest boxes as foraging or resting sites in 2018. Other black fly species reported using nest boxes, in the Czech Republic, are Simulium (Nevermannia) vernum and Simulium (Eusimulium) angustipes [20]. This study [20] confirmed Eusimulium and Nevermannia as the two main ornithophilic subgenera of black flies in Europe and further suggested that more species of Eusimulium are prone to exploit cavities as a microhabitat niche. At this point, we cannot conclude whether S. rubzovianum is the only, or the most frequent, black fly species present in the dry river beds of our study area, or whether it is the only species attracted to nest boxes or to roller olfactory cues. To be able to make a clearer distinction between the locally available vector fauna and actual users of a given microhabitat, we would recommend simultaneous trapping inside and outside of the microhabitat. With regard to simuliids, this calls for less established and unorthodox methods of catching vectors such as sticky traps or scoop netting [7, 14, 17]. Nonetheless, for such trapping methods, attractants are also necessary and bird-inhabited cavities may be among the most obvious attractants, which simultaneously lead to a higher diversity of potential avian hosts in this habitat [30].

Leucocytozoon lineage composition and host preference

The composition of Leucocytozoon lineages found in the black flies trapped in nest boxes is also informative of their host range and foraging habitat. Lineages known from doves, pigeons, corvids and owls were well represented in the present study. Some known sources of these parasites are other secondary inhabitants of cavities present in this habitat—rock pigeons C. livia, jackdaws C. monedula and little owls A. noctua. Indeed, roller nest boxes installed on cliffs and on farms are often very close to cavities, whether artificial or natural, used by these species [30]. However, none of the parasite-bearing black flies contained DNA of these hosts. This suggests that black flies feed on infected hosts of these species, whether in other cavities or in the open. Only after spending sufficient time for complete blood digestion, egg development, and search and return from an oviposition site, do they enter cavities again, likely in search of new hosts. For parasites of colonial host species, this may lead to less structured transmission than outlined above (e.g. quasi-vertical) and allow exchange between families of different colony members, which may belong to the same or to different host species.

It should be noted that the presence of some Leucocytozoon lineages in S. rubzovianum does not prove that this species is their competent vector. As outlined above, Leucocytozoon transmission between rollers in the area remains elusive. Since rollers are Afro-Palearctic migrants, transmission of their Leucocytozoon parasites may occur predominantly in Africa, rather than at the breeding grounds, but reasons for the latter remain to be identified. Transmission experiments show that most well-studied Leucocytozoon species develop in diverse black fly species [6, p. 80 and references therein]. Therefore, the ecology of black fly vectors may be a greater limitation for the transmission of different Leucocytozoon species than incompatibility with the vector. Factors such as vector species-specific interactions with Wolbachia symbionts and microhabitat preferences may strongly determine which vector individuals transmit which parasites between which hosts and where [49]. Further studies with more comprehensive sampling strategies are needed to elucidate such details of the host-vector-parasite exchange networks.

Despite a strong bias towards hole-nesting species, some of the lineages found in this study are only known from thrushes, diurnal raptors and warblers, whose representatives in southeastern Spain only breed in open nests. Additionally, black flies in this habitat have been found to be more common and abundant in nest boxes on trees than on cliffs [50]. Therefore, similarly to other black fly species, S. rubzovianum may be attracted to wooded areas and feed both on open- and cavity-nesting species, thus utilizing the full range of microhabitats where avian hosts can be easily attacked. The propensity to feed naturally in closed spaces makes S. rubzovianum a good candidate for breeding in laboratory conditions, if its broad habitat tolerance also extends to mating and ovipositing [7]. It remains open whether the apparent common use of holes by this species is due to an actual preference for this microhabitat or is driven by the harsh climatic conditions of the area. Given the overall avifauna of the habitat where rollers breed, the composition of Leucocytozoon lineages shows representation of host species which are either abundant or relatively large bodied, thus confirming a pattern that has been established at other locations [8, 14].

So far, no Leucocytozoon lineages have been molecularly described from roller samples that might allow identification of the morphospecies infecting this host group. Several of the most common lineages found in our study are known to infect pigeons as well as corvids and raptors. This very wide range of hosts across the avian phylogeny might encompass rollers and make them potential hosts of these generalist lineages. It remains to be shown if this is really the case and whether infection of distant host groups leads to differences in the morphology of Leucocytozoon generalist lineages. To achieve this aim, it is highly recommended to make blood smears when collecting avian blood samples for DNA analyses.


Insights into the behavior and ecology of vectors are scarce although they are both indispensable and key to understanding the transmission dynamics of parasites, and their consequences for host populations and multi-host assemblages [22]. The differential use of some niches within a given habitat by some vectors may be additionally elucidated by analyzing host networks and using unconventional sampling methods. Our study utilized a habitat (i.e. nest boxes) supplementation programme, combined with microhabitat-targeted trapping and extensive knowledge of bird-haemosporidian associations, carefully curated by devoted colleagues in recent years [24]. This powerful combination of factors shows that in arid habitats a sole vector species may connect hosts of different microhabitat niches by feeding and potentially transmitting numerous lineages both inside and outside of breeding cavities. Most details about habitat and host specializations of vectors remain to be revealed and the use of parasites as biological markers can be a potent approach to achieving these aims [6].

Availability of data and materials

All data supporting the conclusions of this article are included in the article.


  1. Schmid-Hempel P. Evolutionary parasitology. The integrated study of infections, immunology, ecology, and genetics. Oxford: Oxford University Press; 2011.

    Google Scholar 

  2. Van Riper C, Van Riper SG, Goff ML, Laird M. The epizootiology and ecological significance of malaria in Hawaiian land birds. Ecol Monogr. 1986;56:327–44.

    Article  Google Scholar 

  3. Václav R, Valera F. Host preference of a haematophagous avian ectoparasite: a micronutrient supplementation experiment to test an evolutionary trade-off. Biol J Linn Soc. 2018;125:171–83.

    Article  Google Scholar 

  4. Veiga J, De Oña P, Salazar B, Valera F. Defining host range: host–parasite compatibility during the non-infective phase of the parasite also matters. Parasitology. 2019;146:234–40.

    Article  PubMed  Google Scholar 

  5. Kilpatrick AM, Kramer LD, Jones MJ, Marra PP, Daszak P. West Nile virus epidemics in North America are driven by shifts in mosquito feeding behavior. PLoS Biol. 2006;4:e82.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  6. Valkiūnas G. Avian malarial parasites and other Haemosporidia. Boca Raton: CRC Press; 2005.

    Google Scholar 

  7. Crosskey RW. The natural history of black flies. Chichester: Wiley; 1990.

    Google Scholar 

  8. Malmqvist B, Strasevicius D, Adler PH. Catches of bloodsucking black flies (Diptera: Simuliidae) tell different stories depending on sampling method. Entomol Fenn. 2007;18:110–6.

    Google Scholar 

  9. Synek P, Munclinger P, Albrecht T, Votypka J. Avian haemosporidians in haematophagous insects in the Czech Republic. Parasitol Res. 2013;112:839–45.

    Article  PubMed  Google Scholar 

  10. Verocai GG, Nelson KJ, Callahan RT, Wekesa JW, Hassan HK, Hoberg EP. A cryptic species of Onchocerca (Nematoda: Onchocercidae) in black flies (Simulium spp.) from southern California, USA. Parasites Vectors. 2018;11:1–11.

    Article  CAS  Google Scholar 

  11. Ignjatović-Ćupina A, Zgomba M, Vujanović L, Konjević A, Marinković D, Petrić D. An outbreak of Simulium erythrocephalum (De Geer, 1776) in the region of Novi Sad (Serbia) in 2006. Acta Entomol Serbica, Supplement. 2006;11:97–114.

    Google Scholar 

  12. Murdock CC, Adler PH, Frank J, Perkins SL. Molecular analyses on host-seeking black flies (Diptera: Simuliidae) reveal a diverse assemblage of Leucocytozoon (Apicomplexa: Haemospororida) parasites in an alpine ecosystem. Parasites Vectors. 2015;8:343.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Bennett GF. On some ornithophilic blood-sucking diptera in Algonquin Park, Ontario, Canada. Can J Zool. 1960;38:377–89.

    Article  Google Scholar 

  14. Chakarov N, Kampen H, Wiegmann A, Werner D, Bensch S. Blood parasites in vectors reveal a united black fly community in the upper canopy. Parasites Vectors. 2020;13:309.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Ruiz-Arrondo I, Garza-Hernández JA, Reyes-Villanueva F, Lucientes-Curdi J, Rodríguez-Pérez MA. Human-landing rate, gonotrophic cycle length, survivorship, and public health importance of Simulium erythrocephalum in Zaragoza, northeastern Spain. Parasites Vectors. 2017;10:1–9.

    Article  Google Scholar 

  16. Malmqvist B, Strasevicius D, Hellgren O, Adler PH, Bensch S. Vertebrate host specificity of wild-caught black flies revealed by mitochondrial DNA in blood. Proc R Soc Lond Ser B-Biol Sci. 2004;271:S152–5.

    Article  Google Scholar 

  17. Hellgren O, Bensch S, Malmqvist B. Bird hosts, blood parasites and their vectors—associations uncovered by molecular analyses of black fly blood meals. Mol Ecol. 2008;17:1605–13.

    Article  CAS  PubMed  Google Scholar 

  18. Černý O, Votýpka J, Svobodová M. Spatial feeding preferences of ornithophilic mosquitoes, black flies and biting midges. Med Vet Entomol. 2011;25:104–8.

    Article  PubMed  Google Scholar 

  19. Lutz HL, Hochachka WM, Engel JI, Bell JA, Tkach VV, Bates JM, et al. Parasite prevalence corresponds to host life history in a diverse assemblage of Afrotropical birds and haemosporidian parasites. PLoS ONE. 2015.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Synek P, Popelková A, Koubínová D, Šťastný K, Langrová I, Votýpka J, et al. Haemosporidian infections in the Tengmalm’s owl (Aegolius funereus) and potential insect vectors of their transmission. Parasitol Res. 2016;115:291–8.

    Article  PubMed  Google Scholar 

  21. Takken W, Verhulst NO. Host preferences of blood-feeding mosquitoes. Annu Rev Entomol. 2013;58:433–53.

    Article  CAS  PubMed  Google Scholar 

  22. Santiago-Alarcon D, Palinauskas V, Schaefer HM. Diptera vectors of avian haemosporidian parasites: untangling parasite life cycles and their taxonomy. Biol Rev. 2012;87:928–64.

    Article  PubMed  Google Scholar 

  23. Alcala N, Jenkins T, Christe P, Vuilleumier S. Host shift and cospeciation rate estimation from co-phylogenies. Ecol Lett. 2017;20:1014–24.

    Article  PubMed  Google Scholar 

  24. Bensch S, Hellgren O, Pérez-Tris J. MalAvi: a public database of malaria parasites and related haemosporidians in avian hosts based on mitochondrial cytochrome b lineages. Mol Ecol Resour. 2009;9:1353–8.

    Article  PubMed  Google Scholar 

  25. Castaño-Vázquez F, Merino S, Cuezva S, Sánchez-Moral S. Nest gasses as a potential attraction cue for biting flying insects and other ectoparasites of cavity nesting birds. Front Ecol Evol. 2020;8:258.

    Article  Google Scholar 

  26. Veiga J, Martínez-de la Puente J, Václav R, Figuerola J, Valera F. Culicoides paolae and C. circumscriptus as potential vectors of avian haemosporidians in an arid ecosystem. Parasites Vectors. 2018;11:524.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Lázaro R, Rodrigo F, Gutiérrez L, Domingo F, Puigdefábregas J. Analysis of a thirty year rainfall record (1967–1997) from semi-arid SE Spain: a plant ecological perspective. J Arid Environ. 2001;48:373–95.

    Article  Google Scholar 

  28. Valera F, Díaz-Paniagua C, Garrido-García JA, Manrique J, Pleguezuelos JM, Suárez F. History and adaptation stories of the vertebrate fauna of southern Spain’s semi-arid habitats. J Arid Environ. 2011;75:1342–51.

    Article  Google Scholar 

  29. Václav R, Valera F, Martínez T. Social information in nest colonisation and occupancy in a long-lived, solitary breeding bird. Oecologia. 2011;165:617–27.

    Article  PubMed  Google Scholar 

  30. Valera F, Václav R, Calero-Torralbo MÁ, Martínez T, Veiga J. Natural cavity restoration as an alternative to nest box supplementation. Restor Ecol. 2019;27:220–7.

    Article  Google Scholar 

  31. Avilés JM, Sánchez JM, Sánchez A, Parejo D. Breeding biology of the roller Coracias garrulus in farming areas of the southwest Iberian Peninsula. Bird Stud. 1999;46:217–23.

    Article  Google Scholar 

  32. Tomas G, Merino S, La Puente JMD, Moreno J, Morales J, Lobato E. A simple trapping method to estimate abundances of blood-sucking flying insects in avian nests. Anim Behav. 2008;75:723–9.

    Article  Google Scholar 

  33. Belqat B, Dakki M. Identification keys of the black flies (Diptera: Simuliidae) of Morocco. Zool Baet. 2004;15:77–137.

    Google Scholar 

  34. Rivosecchi L, Maiolini B, Addonisio M. I Ditteri Simulidi: nuove chiavi dicotomiche per l'identificazione delle specie italiane con brevi note bio-tassonomiche. Museo tridentino di scienze naturali; 2007.

  35. Ruiz-Arrondo I, Hernández-Triana LM, Ignjatović-Ćupina A, Nikolova N, Garza-Hernández JA, Rodríguez-Pérez MA, et al. DNA barcoding of black flies (Diptera: Simuliidae) as a tool for species identification and detection of hidden diversity in the eastern regions of Spain. Parasites Vectors. 2018;11:1–7.

    Article  CAS  Google Scholar 

  36. Folmer O, Black W, Lutz R, Vrijenhoek R. DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Mol Mar Biol Biotechnol. 1994;3:294–9.

    CAS  PubMed  Google Scholar 

  37. Kocher TD, Thomas WK, Meyer A, Edwards SV, Pääbo S, Villablanca FX, et al. Dynamics of mitochondrial DNA evolution in animals: amplification and sequencing with conserved primers. Proc Natl Acad Sci USA. 1989;86:6196–200.

    Article  CAS  PubMed  Google Scholar 

  38. Pérez-Rodríguez A, de la Puente J, Onrubia A, Pérez-Tris J. Molecular characterization of haemosporidian parasites from kites of the genus Milvus (Aves: Accipitridae). Int J Parasitol. 2013;43:381–7.

    Article  PubMed  CAS  Google Scholar 

  39. Schumm YR, Bakaloudis D, Barboutis C, Cecere JG, Eraud C, Fischer D, et al. Prevalence and genetic diversity of avian haemosporidian parasites in wild bird species of the order Columbiformes. Parasitol Res. 2021.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Harl J, Himmel T, Valkiūnas G, Ilgūnas M, Bakonyi T, Weissenböck H. Geographic and host distribution of haemosporidian parasite lineages from birds of the family Turdidae. Malar J. 2020;19:1–35.

    Article  Google Scholar 

  41. Martínez-de la Puente J, Merino S, Lobato E, Rivero-de Aguilar J, del Cerro S, Ruiz-de-Castaneda R, et al. Does weather affect biting fly abundance in avian nests? J Avian Biol. 2009;40:653–7.

    Article  Google Scholar 

  42. Usova Z. On the places of concealment of black flies (Diptera, Simuliidae) in the Karelian ASSR. Entomol Obozr. 1963;42:316–9.

    Google Scholar 

  43. Adler PH, McCreadie JW. Black flies (Simuliidae). Medical and veterinary entomology. Elsevier; 2019. p. 237–59.

    Chapter  Google Scholar 

  44. Václav R, Betáková T, Švančarová P, Pérez-Serrano J, Criado-Fornelio Á, Škorvanová L, et al. Nest ecology of blood parasites in the European roller and its ectoparasitic carnid fly. Exp Parasitol. 2016;165:71–80.

    Article  PubMed  Google Scholar 

  45. Richard FA, Sehgal RNM, Jones HI, Smith TB. A comparative analysis of PCR-based detection methods for avian malaria. J Parasitol. 2002;88:819–22.

    Article  CAS  PubMed  Google Scholar 

  46. Ebert D. The epidemiology and evolution of symbionts with mixed-mode transmission. Annu Rev Ecol Evol Syst. 2013;44:623–43.

    Article  Google Scholar 

  47. Chakarov N, Linke B, Boerner M, Goesmann A, Kruger O, Hoffman JI. Apparent vector-mediated parent-to-offspring transmission in an avian malaria-like parasite. Mol Ecol. 2015;24:1355–63.

    Article  PubMed  Google Scholar 

  48. Ashford RW, Wyllie I, Newton I. Leucocytozoon toddi in British sparrowhawks Accipiter nisus: observations on the dynamics of infection. J Nat Hist. 1990;24:1101–7.

    Article  Google Scholar 

  49. Woodford L, Bianco G, Ivanova Y, Dale M, Elmer K, Rae F, et al. Vector species-specific association between natural Wolbachia infections and avian malaria in black fly populations. Sci Rep. 2018;8:1–11.

    Article  CAS  Google Scholar 

  50. Veiga J, Valera F. Nest box location determines the exposure of the host to ectoparasites. Avian Conserv Ecol. 2020.

    Article  Google Scholar 

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We thank Stanislav Kolencik, Francisco Castaño, Teresa Martínez, Maite Amat and Miguel Ángel Calero for their help with the fieldwork. We are grateful to Prisca Viehoefer, Bielefeld University, Germany for assistance with the sequencing. We would like to thank Staffan Bensch for assembling and curating the MalAvi database, which is indispensable for studies like ours. We would also like to thank the two anonymous referees for their useful and constructive suggestions.


Open Access funding enabled and organized by Projekt DEAL. This work was partially funded by the German Science Foundation (DFG) as part of the SFB TRR 212 (project number 316099922 - NC3). the German Research Foundation (DFG) as part of the SFB TRR 212 FV received financial support from projects CGL2014-55969 and PGC2018-097426-B-C22 (Spanish Ministry of Universities; Spanish State Research Agency; FEDER Program, European Union). JV was funded by a predoctoral grant (BES-2015-075951) of the Spanish Ministry of Science and Innovation.

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JV, IRA, FV gathered the samples. NC and IRA performed the molecular analyses of the samples. All the authors wrote, read and approved the final manuscript.

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Correspondence to Nayden Chakarov.

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Chakarov, N., Veiga, J., Ruiz-Arrondo, I. et al. Atypical behavior of a black fly species connects cavity-nesting birds with generalist blood parasites in an arid area of Spain. Parasites Vectors 14, 298 (2021).

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