Skip to main content
Download PDF

Long-term dynamics of trematode infections in common birds that use farmlands as their feeding habitats

Parasites & Vectors volume 14, Article number: 383 (2021) Cite this article

Abstract

Background

The biodiversity of farmland habitats is witnessing unprecedented change, mostly in declines and simplification of assemblages that were established during centuries of the use of traditional agricultural techniques. In Central Europe, conspicuous changes are evident in populations of common farmland birds, in strong contrast to forest birds in the same region. However, there is a lack of information on longitudinal changes in trematodes that are associated with common farmland birds, despite the fact that diversity of trematodes is directly linked to the preservation of long-established food webs and habitat use adaptations of their hosts.

Methods

We analyzed the population trends of trematodes for the period 1963–2020 in six bird species that use Central European farmlands as their predominant feeding habitats. Namely, we examined Falco tinnunculus, Vanellus vanellus, winter populations of Buteo buteo, Ciconia ciconia, extravilan population of Pica pica, and Asio otus, all originating from the Czech Republic.

Results

We observed dramatic population losses of all trematode species in C. ciconia and V. vanellus; the changes were less prominent in the other examined hosts. Importantly, the declines in prevalence and intensity of infection affected all previously dominant species. These included Tylodelphys excavata and Chaunocephalus ferox in C. ciconia, Lyperosomum petiolatum in P. pica, Strigea strigis in A. otus, Neodiplostomum attenuatum and Strigea falconis in B. buteo (χ2 test P < 0.001 each), and Echinoparyphium agnatum and Uvitellina adelpha in V. vanellus (completely absent in 2011–2000). In contrast, the frequency and spectrum of isolated records of trematode species did not change to any large extent except those in V. vanellus.

Conclusions

The analysis of six unrelated common bird species that use farmlands as their feeding habitats revealed a previously unreported collapse of previously dominant trematode species. The previously dominant trematode species declined in terms of both prevalence and intensity of infection. The causes of the observed declines are unclear; of note is, however, that some of the broadly used agrochemicals, such as azole fungicides, are well known for their antihelminthic activity. Further research is needed to provide direct evidence for effects of field-realistic concentrations of azole fungicides on the survival and fitness of trematodes.

Graphical abstract

Background

Metazoan parasites are considered one of the most diverse, threatened, and under-protected animals on Earth [1]. The roles of parasites in the ecosystem remain understudied and underappreciated [2]. Moreover, only a very small number of parasite species have well-documented distributions or population sizes [1]. However, the identification of species that are at the greatest risk of extinction requires the availability of robust data, particularly the evidence of changes in diversity and/or distribution in time [3]. The rare species are not necessarily equal to threatened species. Therefore, evaluation of the conservation status of threatened taxa requires knowledge not only of the rarity of the respective species but also of the population trends or habitat deterioration. The evidence for population size reduction over a period of ≥ 10 years or ≥ 3 generations represents one of the three major criteria for the inclusion of the respective species as threatened (category Vulnerable or higher) in the International Union for Conservation of Nature (IUCN) Red List (https://www.iucnredlist.org/resources/summary-sheet). Concerning the trematode bird host species in the study area, in central Europe, the most conspicuous population changes are experienced by common farmland birds, whereas the populations of forest birds remain relatively stable or increasing [4, 5]. Longitudinal data on trematode assemblages are scarce, and the trematodes of farmland birds have never been subjected to a longitudinal study. Previous studies have addressed trematode diversity in aquatic birds that serve as definitive hosts of trematodes [4, 5] and in snail intermediate hosts [6,7,8,9,10]. The situation may differ regionally and the declines may be habitat-specific. The studies that were performed in aquatic habitats revealed that trematodes face an unprecedented decline in terms of both their abundance and species richness in Western countries, but not so in less exploited regions, such as Siberia [6,7,8,9,10,11,12]. However, some host species living in the industrialized landscapes, such as Turdus philomelos, displayed increases in the diversity of helminths during recent decades [13].

The bird species that use farmlands as their predominant feeding areas differ in their spatiotemporal distribution. These species include (1) common farmland birds, such as Falco tinnunculus and Vanellus vanellus, (2) species which utilize the farmlands nearly exclusively during the winter months, such as Buteo buteo, and (3) species that use farmlands as their main feeding habitats, such as Ciconia ciconia, extravilan (living outside the city/village limits) populations of Pica pica, and Asio otus. These species overlap only partially in their food preferences, but all their food is, in general, affected by the broad-spectrum pesticides applied to the agricultural crops [14,15,16], which therefore may affect the complex life cycles of the trematodes. During the period 1982–2005, the Czech populations of these six species experienced the following population trends: Ciconia ciconia stable, +1.9%; P. pica stable, +1.7%; A. otus declining, −4.0%; B. buteo stable, +1.4%; F. tinnunculus stable, 0.0% (but declined by 35% in 1980–2003 in Europe); and V. vanellus declining, −9.9% (also declined by 51% in 1980–2003 in Europe) [17, 18]. The studies from Russia and Central Asian countries from the 1950s, studies from Central Europe from the 1960s, and studies from other parts of Europe from the recent decades have provided trematode prevalence data from large data sets of these six bird host species (Additional file 1: Tables S1–S6). However, differences in the geographic origin of the data make it difficult to estimate prevalence trends in any of the trematodes. See, for example, the below-listed pairs of studies from different geographic regions, which reported conflicting data concerning the prevalence and species richness of trematodes in P. pica [19, 20] (Additional file 1: Table S2), B. buteo [21, 22] (Additional file 1: Table S4), or V. vanellus [23, 24] (Additional file 1: Table S6). No longitudinal studies of trematodes have been reported in any of the six species.

In the present study, we address long-term changes in component communities of trematodes in six bird species which feed over the nesting season (five species) or in winter only (one species) in open farmland habitats. We collected the source data across a time span of over half a century. The adults might harbor helminths that were acquired during migration and at their wintering grounds, and the nestlings are often fed different types of food compared to the full-grown birds. Therefore, we analyzed the component communities of first-year birds and those of adult females or males separately.

Methods

For the period 1963–2020, we examined 147 individuals of white stork C. ciconia, 169 individuals of Eurasian magpie P. pica, 242 individuals of long-eared owl A. otus, 259 individuals of common buzzard B. buteo, 1092 individuals of common kestrel F. tinnunculus, and 78 individuals of northern lapwing V. vanellus for the presence of trematodes. The examined birds were stratified according to their age to first-year birds (1Y; born in the calendar year that they were examined) and adults (birds in their second or later calendar year of life) [25, 26]. The adults were further stratified according to their sex. To enable the adult and 1Y P. pica to be merged in our analyses, we identified the sex of both adult and 1Y individuals of this species. In another species with low numbers of 1Y birds, V. vanellus, we did not keep records of the sex of the 1Y birds that we examined in the 1960s and 1970s. To analyze the changes in analyzed helminth assemblages over time, we split the obtained bird hosts into groups according to the time when they were obtained. As the availability of the respective species was not equal across the study period, the chosen time intervals were set individually for each of the six examined bird host species (Table 1). Concerning B. buteo, we examined only adult birds obtained in winter months from areas without larger forests; in winter months, B. buteo characteristically occurs in open habitats.

Table 1 Numbers of host individuals that were examined in the present study
Full size table

All the examined birds originated from the eastern and southern Czech Republic (48.7° N–49.80° N, 13.3° E–18° 30′ E). We obtained the dead birds before they were prepared for the Comenius Museum collection (Přerov, Czech Republic). The birds consisted primarily of wounded, hunted, or injured individuals, most of which were euthanized in rescue stations due to untreatable wounds. Concerning birds provided by the rescue stations, these included only individuals that were not treated with antihelminthic agents prior to being euthanized. As an exception, the examined P. pica were provided by local hunters; P. pica is listed as game according to the Decree of the Ministry of Agriculture No. 245/2002 Coll. and can be legally hunted without restriction in the period from July 1st to February 28th. Our long-term research was authorized by governmental and local authorities; our most recent permit was issued by the Ministry of the Environment of the Czech Republic on August 3, 2009 under No. 11171/ENV/09-747/620/09-ZS 25.

We performed full-body necropsies, which included examination of the subcutaneous tissue, body cavity, esophagus, stomach, intestines, cloaca, bursa of Fabricius, liver, gall bladder, spleen, lungs, trachea, bronchus, air sacs, kidneys, and oviducts using a stereomicroscope. We fixed helminths in 70% ethanol, stained them with borax carmine, transferred them through an alcohol series to xylene, and mounted them in Canada balsam as described previously [27]. We identified the stained specimens using taxonomic keys [28,29,30,31,32], also reflecting recent reclassifications. We recorded the abundance and species richness of trematodes in each examined host individual [33]. We stored representative specimens in the Comenius Museum collections (Přerov, Czech Republic). Most of the new host–parasite records from the examined data sets were published in our previous studies, and some of the analyzed helminths were already used for molecular analyses [34,35,36,37,38,39]. The nomenclature follows the Fauna Europaea database [40] and recently published reclassifications [34, 35, 39, 41]. For details concerning the life cycles of the examined parasites, refer to Sitko et al. [42].

We calculated basic characteristics of the analyzed component communities (mean frequency of infection and helminth load) and trematode species-specific mean relative prevalence and mean intensity of infection. We referred to the most prevalent trematodes in each host as dominant. We computed rarefaction curves based on the log gamma function for computing combinatorial terms to interpolate the trematode species richness data [43]. To extrapolate the trematode species richness, and therefore to estimate the true trematode species richness of the analyzed population, we calculated the Chao-1 estimator corrected for unseen trematode species [44, 45]. We further calculated the following variables: (1) the total number of trematode species found, (2) the total number of individuals found, (3) the trematode species prevalence (the proportion of host individuals infected by trematodes), and (4) the intensity of infection (the number of trematode individuals per host calculated over all individuals that were positive for the respective trematodes). We compared the trematode species richness using the Sørensen similarity index (presence/absence-based index that assigns a greater weight to shared species than to those found in only one data set) and assessed the differences in trematode diversity between the study periods using the Shannon diversity t-test (compares Shannon H indices with a bias correction term proposed by Poole [46] of two abundance data sets assuming equal sampling conditions). We compared the prevalence of dominant trematodes in the ≤ 2000 and 2011–2020 data sets by χ2 tests, and the intensity of infection of the ≤ 2000 and 2011–2020 data sets by the Mann–Whitney rank-sum test (Shapiro–Wilk normality tests failed in all cases). In the Results section, we describe the trematode communities in more detail with regard to the host age, host sex, and year examined. However, as the resulting data were highly variable, the study was not sufficiently powered to test for possible differences at this scale. We performed all the calculations in SigmaPlot 12.0, EstimateS 9.1.0, and PAST 2.14. Data are shown as mean ± SD unless stated otherwise; data for the intensity of infection are shown as mean ± SE.

Results

Total numbers of trematodes

We collected a total of 15,549 individuals belonging to 33 species of trematodes, which represented host-species-specific component communities in C. ciconia (9751 individuals, 9 trematode species; Additional file 1: Table S7), P. pica (239 individuals, 8 trematode species; Additional file 1: Table S8), A. otus (948 individuals, 4 trematode species; Additional file 1: Table S9), B. buteo (4363 individuals, 10 trematode species; Additional file 1: Table S10), F. tinnunculus (69 individuals, 5 trematode species; Additional file 1: Table S11), and V. vanellus (179 individuals, 8 trematode species; Additional file 1: Table S12).

Changes at the level of individual host species

Trematodes in the examined host species displayed strong differences in population trends. We observed dramatic population losses of all trematode species in C. ciconia (Fig. 1), in which the number of trematode species per host individual declining from 1.2 ± 1.0 in 1963–2000 to 0.7 ± 0.7 in 2001–2010 and 0.2 ± 0.5 in 2011–2020. We observed less extensive declines in helminths in P. pica (Fig. 2) and A. otus (Fig. 3). In B. buteo, the only two characteristic trematode species were present until the period 2011–2015, declining to a third or less of their original prevalence only in recent years (Fig. 4). In this species, the number of trematode species per host individual declined from 1.0 ± 1.5 in 2011–2015 to 0.2 ± 0.5 in 2019–2020. In F. tinnunculus, the prevalence of trematodes was negligible from the very beginning of the study period (Fig. 5). In V. vanellus, we found trematodes only in host individuals examined prior to 1980, when the number of trematode species per host individual was at 0.5 ± 0.7. We did not find any trematodes in V. vanellus after that time, despite examining 33 host individuals of various sex and age during the period 1981–2020. Rarefaction analyses indicated that the trematode assemblages of five of the six birds consisted of lower numbers of trematode species when compared to those analyzed in the same study area one or more decades earlier (Figs. 1, 2, 3, 4, and 6); only the data from F. tinnunculus indicated no decline; however, the vast majority of examined F. tinnunculus were free of any trematodes already at the beginning of the study period (Fig. 5).

Fig. 1
figure1

Source data are provided in Additional file 1: Table S7

Dynamics of trematode assemblages associated with the Czech population of Ciconia ciconia. (a) The rarefaction curves (red; 95% confidence intervals in blue) of component communities in C. ciconia calculated separately for each of the four study periods (1963–2000, 2001–2010, 2011–2020). Dynamics of changes in the number of trematode species per host individual (b), the total number of trematode species found (c), and the prevalence (d) and the intensity of infection ± SE (e). The data for the prevalence and the intensity of infection are shown as a heatmap; the prevalence is shown as a percent of infected hosts, with the color green assigned to the highest prevalence of the respective trematode species and white assigned to zero prevalence. A similar color code of the heatmap was used to visualize the intensity of infection; however, the whole color code scale of the intensity of infection is based on all fields within the heatmap.

Full size image
Fig. 2
figure2

Source data are provided in Additional file 1: Table S8

Dynamics of trematode assemblages associated with the Czech extravilan population of Pica pica. (a) The rarefaction curves (red; 95% confidence intervals in blue) of component communities in P. pica calculated separately for each of the three study periods (1991–2000, 2001–2010, 2011–2020). Dynamics of changes in the number of trematode species per host individual (b), the total number of trematode species found (c), and the prevalence (d) and the intensity of infection ± SE (e). The data for the prevalence and the intensity of infection are shown as a heatmap; the prevalence is shown as a percent of infected hosts, with the color green assigned to the highest prevalence of the respective trematode species and white assigned to zero prevalence. A similar color code of the heatmap was used to visualize the intensity of infection; however, the whole color code scale of the intensity of infection is based on all fields within the heatmap.

Full size image
Fig. 3
figure3

Source data are provided in Additional file 1: Table S9

Dynamics of trematode assemblages associated with the Czech population of Asio otus. (a) The rarefaction curves (red; 95% confidence intervals in blue) of component communities in A. otus calculated separately for each of the four study periods (1963–1990, 1991–2000, 2001–2010, 2011–2020). Dynamics of changes in the number of trematode species per host individual (b), the total number of trematode species found (c), and the prevalence (d) and the intensity of infection ± SE (e). The data for the prevalence and the intensity of infection are shown as a heatmap; the prevalence is shown as a percent of infected hosts, with the color green assigned to the highest prevalence of the respective trematode species and white assigned to zero prevalence. A similar color code of the heatmap was used to visualize the intensity of infection; however, the whole color code scale of the intensity of infection is based on all fields within the heatmap.

Full size image
Fig. 4
figure4

Source data are provided in Additional file 1: Table S10

Dynamics of trematode assemblages associated with the Czech winter population of Buteo buteo. (a) The rarefaction curves (red; 95% confidence intervals in blue) of component communities in B. buteo calculated separately for each of the five study periods (1981–1990, 1991–2000, 2001–2010, 2011–2020). Dynamics of changes in the number of trematode species per host individual (b), the total number of trematode species found (c), and the prevalence (d) and the intensity of infection ± SE (e). The data for the prevalence and the intensity of infection are shown as a heatmap; the prevalence is shown as a percent of infected hosts, with the color green assigned to the highest prevalence of the respective trematode species and white assigned to zero prevalence. A similar color code of the heatmap was used to visualize the intensity of infection; however, the whole color code scale of the intensity of infection is based on all fields within the heatmap.

Full size image
Fig. 5
figure5

Source data are provided in Additional file 1: Table S11

Dynamics of trematode assemblages associated with the Czech population of Falco tinnunculus. (a) The rarefaction curves (red; 95% confidence intervals in blue) of component communities in F. tinnunculus calculated based on birds that were examined in study periods 1991–2000, 2001–2010, and 2011–2020. Dynamics of changes in the number of trematode species per host individual (b), the total number of trematode species found (c), and the prevalence (d) and the intensity of infection ± SE (e). The data for the prevalence and the intensity of infection are shown as a heatmap; the prevalence is shown as a percent of infected hosts, with the color green assigned to the highest prevalence of the respective trematode species and white assigned to zero prevalence. A similar color code of the heatmap was used to visualize the intensity of infection; however, the whole color code scale of the intensity of infection is based on all fields within the heatmap.

Full size image

Despite a sharp decrease in helminth abundance, the Chao-1 trematode species richness in C. ciconia, P. pica, B. buteo, and F. tinnunculus did not decrease (Table 2). In contrast, three of the four species were present in A. otus only prior to 1990, which translated into a sharp decline of the Chao-1 trematode species richness from 5.0 ± 2.2 in 1963–1990 to 1.0 ± 0.0 trematode species in all subsequent study periods. In V. vanellus, the Chao-1 trematode species richness reached 8.5 ± 1.3 in 1963–1980. After 1980, the examined V. vanellus did not contain any single trematode individual; therefore, the species richness for the later time periods cannot be estimated (Table 2). A comparison of diversity using the Sørensen similarity index and Shannon diversity t-test is provided in Table 2. The rarefaction analyses and the Chao-1 species richness estimator point to the fact that the overall trematode species richness of the study bird hosts changed only to a limited extent. However, this perceived stability of the study assemblages was can be explained by the isolated records of trematode species that were likely acquired from rarely exploited food sources, while the previously dominant species which were characteristic of the examined bird species declined (Fig. 7), as shown using the trematode-specific analyses below.

Table 2 Comparison of trematode species richness and diversity of the analyzed component communities in the 2010s and earlier time periods, using the Sørensen similarity index and Shannon diversity t-test
Full size table

The decrease in the diversity of component communities from the earliest to the most recent available time periods was statistically significant in four of the six examined species (see Table 2 for more detail). The exceptions were the trematodes of P. pica and F. tinnunculus (Table 2). In P. pica, there was a decline in trematode species associated with the examined host in the first study period (1991–2000), but other trematode species were newly recorded in this species only in recent years. The second species in which there were no significant dynamics in the diversity of associated trematode communities, F. tinnunculus, generally had a low number and prevalence of trematodes, and we recorded both species associated with F. tinnunculus in roughly the same prevalence and intensity of infection across all the examined time periods (Fig. 5).

Species-specific changes

In C. ciconia, two trematode species, Tylodelphys excavata and Chaunocephalus ferox, were characteristically considered dominant; the first species had 40.0% prevalence prior to 2000 and the latter species had 60.0% prevalence prior to 2000. However, their prevalence decreased in 2001–2010 and further declined in 2011–2020, when the prevalence reached 12.1% and 6.1%, representing a decline of 70% and 90% (χ2 test P < 0.001 each; Fig. 1). Despite the sharp declines in prevalence, the intensity of infection by T. excavata did not change, and reached 208 ± 61 individuals per host in the ≤ 2000 period and 127 ± 51 individuals per host in 2011–2020 (Mann–Whitney rank-sum test P > 0.05; n1 = 14, n2 = 8, T = 80, U = 44). There was a similar trend in C. ferox, the incidence of which reached 36 ± 24 individuals per host in the ≤ 2000 period and 6 ± 3 individuals per host in 2011–2020 (Mann–Whitney rank-sum test P > 0.05; n1 = 21, n2 = 4, T = 37.5, U = 27.5). Another characteristic parasite species of storks, Cathaemasia hians, was completely absent in the examined C. ciconia after 2001. Isolated records of two species, Stomylotrema pictum and Bilharziella polonica, each represented by a single individual, were the only species that were recorded for the first time in the most recent study period 2011–2020 (Fig. 1).

In P. pica, the dominant trematode species, Lyperosomum petiolatum, was characteristically found in 44.8% of examined host individuals before 2000. However, its prevalence declined in 2011–2020 by 58% to only 18.8% (χ2 test P < 0.001; Fig. 2). The intensity of infection by L. petiolatum decreased from 4.6 ± 0.6 individuals per host in the ≤ 2000 period to 2.2 ± 0.3 individuals per host in 2011–2020 (Mann–Whitney rank-sum test P = 0.007; n1 = 26, n2 = 16, T = 240.5, U = 140.5). Other trematode species were present in low prevalence, with no evidence for their decline. Isolated records of two species, Prosthogonimus ovatus and Morishitium elongatum, each found in a single host individual, were the only species that were recorded for the first time in the most recent study period 2011–2020 (Fig. 2).

In A. otus, we found only four trematode species. The dominant trematode species of adult A. otus, Strigea strigis, was characteristically found in about a third of examined host individuals before 1990. However, its prevalence gradually declined from 23.9% to just 6.6% (χ2 test P < 0.001; Fig. 3). The intensity of infection by S. strigis declined correspondingly to just one tenth of the original intensity of infection, from 27.1 ± 8.7 individuals per host in the ≤ 2000 period to 2.8 ± 0.3 individuals per host in 2011–2020 (Mann–Whitney rank-sum test p = 0.036; n1 = 22, n2 = 5, T = 36, U = 21). Three other three trematode species were present in low prevalence; we found all of them in the first study period before 1990. Other than S. strigis, we did not find any trematode species in A. otus that were examined in 1991–2020 (Fig. 3).

In B. buteo, there were two trematode species with high prevalence. These were Neodiplostomum attenuatum and Strigea falconis, which were present in 29.1% and 32.9% of examined B. buteo prior to 2000. Their prevalence remained similar until 2011–2015; the intensity of infection was generally high, showing strong fluctuations. However, the two trematode species were associated with only a fraction of the original numbers of B. buteo in its most recently examined cohort from 2019–2020, with the intensity of infection also declining to the lowest values (Fig. 4). The differences in N. attenuatum and S. falconis prevalence between the ≤ 2000 cohort and 2011–2020 cohort were statistically significant (χ2 test P < 0.001 each). There were no significant changes in the incidence of these two species. In N. attenuatum, the incidence reached 25 ± 6 individuals per host in the ≤ 2000 period and 80 ± 36 individuals per host in 2011–2020 (Mann–Whitney rank-sum test P > 0.05; n1 = 46, n2 = 11, T = 356.5, U = 215.5). In S. falconis, the incidence reached 10 ± 3 individuals per host in the ≤ 2000 period and 11 ± 4 individuals per host in 2011–2020 (Mann–Whitney rank-sum test P > 0.05; n1 = 52, n2 = 15, T = 517, U = 383). We found eight other trematode species in B. buteo; however, these were all rather isolated records, although sometimes at high intensity of infection, such as in the case of Tylodelphys circibuteonis and Echinoparyphium agnatum (Fig. 1).

First-year birds of F. tinnunculus were free of any trematodes; adult F. tinnunculus were rarely infected by five species of trematodes, which did not display any seasonal trends. We found the highest prevalence of infections in 2001–2005; there were no species that would newly emerge in the study periods after 2006 (Fig. 5).

In V. vanellus, we recorded eight species of trematodes in the first study period prior to 1980. The V. vanellus trematodes were dominated by Echinoparyphium aconiatum (prevalence 12.3%, intensity of infection 11 ± 5 individuals per host) and Uvitellina adelpha (prevalence 8.8%, intensity of infection 1.2 ± 0.2 individuals per host). After 1980, all examined V. vanellus were free of any trematodes (Fig. 6).

Fig. 6
figure6

Source data are provided in Additional file 1: Table S12

Dynamics of trematode assemblages associated with the Czech population of Vanellus vanellus. (a) The rarefaction curves (red line; 95% confidence intervals in blue) of component communities in V. vanellus calculated only for the first sampling period (1963–1980), as there were no species acquired in later time periods (1981–2000, 2001–2020). Dynamics of changes in the number of trematode species per host individual (b), the total number of trematode species found (c), and the prevalence (d) and the intensity of infection ± SE (e). The data for the prevalence and the intensity of infection are shown as a heatmap; the prevalence is shown as a percent of infected hosts, with the color green assigned to the highest prevalence of the respective trematode species and white assigned to zero prevalence. A similar color code of the heatmap was used to visualize the intensity of infection; however, the entire color code scale of the intensity of infection is based on all fields within the heatmap.

Full size image

Discussion

The present study provides another important piece of evidence of the simplification of helminth communities. The data complement our previous study on wetland birds [12] by showing that trematode species that have dominated the component communities in various birds that use farmlands as their feeding habitats have experienced massive declines, and in some cases they have completely vanished from the analyzed bird host populations. These changes have affected in particular the previously dominant trematode species that had been characteristic of the examined host bird species (Fig. 7).

Fig. 7
figure7

Overview of changes in the prevalence of previously dominant trematode species found in 2000 or earlier as compared to the period 2011–2020. The prevalence in the two respective time periods and the decline in prevalence of the respective dominant species are indicated. The prevalence is shown as a percent of infected hosts, with the color green assigned to the highest prevalence of the respective trematode species and white assigned to zero prevalence. All the observed declines in prevalence were found to be significant (χ2 test P < 0.001 each); the declines in trematodes of V. vanellus were not tested. Using the same logic, the figure shows the intensity of infection by the previously dominant trematode species in the two respective time periods and the change in the intensity of infection of the respective dominant species. The color code used follows similar logic as that for the prevalence. All the observed changes in the intensity of infection were tested by the Mann–Whitney rank-sum test, which revealed that only the differences in the intensity of infection by Lyperosomum petiolatum and Strigea strigis were significant (P < 0.05 each); the changes in the intensity of infection in V. vanellus were not tested

Full size image

We assumed that the population changes in common farmland birds could be associated with changes in the assemblages of trematodes, as their presence is directly linked to the preservation of long-established food webs and habitat use adaptations of their hosts [47,48,49]. The most prominent changes were, indeed, associated with the trematodes of host species, which experienced a strong population decline (V. vanellus). However, strong effects were also found in bird species, which recently shifted their feeding strategies and correspondingly shifted the spectrum of captured prey (C. ciconia) [17, 18]. In contrast, the species richness and diversity of trematodes of some other species (F. tinnunculus) changed very little throughout the study period, and displayed only fluctuations. These fluctuations may reflect generally low prevalence of the F. tinnunculus trematodes, which means that very large cohorts of F. tinnunculus would need to be examined to provide a definitive answer on whether these fluctuations were artifacts, or whether they reflected real changes in the F. tinnunculus trematode assemblages (Fig. 5). The association between changes in trematode prevalence and changes in feeding strategies of their host birds points to the fact that a large part of observed changes could likely be determined by changes in the composition of intermediate host assemblages and prey preferences of the birds [50,51,52]. However, the declines in trematodes were widespread, involved multiple bird orders, and involved both common and rare trematode species. In particular, the changes affected the previously dominant trematode species of the birds that use farmlands as their feeding habitats. In contrast, with the exception of V. vanellus, the frequency and spectrum of isolated records of trematode species did not change to any large extent. This is likely related to the random nature of their acquisition from rarely exploited food sources, particularly from food sources associated with wetlands, as many of these trematodes use various wetland snails as their intermediate hosts.

We recently reported similar or even stronger declines in trematodes in freshwater aquatic birds [12]. The changes identified in birds that use farmlands as their feeding habitats differed from those identified previously in freshwater aquatic birds, particularly in Anas platyrhynchos. The component communities of A. platyrhynchos faced simplification and dominance by only a few surviving species. The two other previously examined freshwater aquatic birds, Fulica atra and Chroicocephalus ridibundus, displayed a mixed response, with severe declines in previously dominant species and overall simplification of the trematode component communities [12].

All the available data are only observational; therefore, the causes of observed declines are unclear. In C. ciconia, the changes could be related to a decline in the contribution of wetland organisms to the diet of this host species. The increasing contribution of anthropogenic sources of diet also could play a role [53, 54]. Besides the changes in feeding habits, the decline in trematode prevalence and intensity of infection could be related to the changes in farm management and land use since the 1950s, including agricultural intensification and landscape simplification [55]. The common agricultural policy of the European Union and the collectivism practiced in the eastern part of Europe further accelerated the loss of uncultivated elements, such as hedgerows, woodlots, and ditches [56], resulting in a decline in farmland landscape biodiversity [57,58,59].

An important but under-researched factor is the broad use of azole fungicides in agriculture, which has shaped communities of various non-target organisms [60,61,62]. Some of the azole fungicides, such as carbendazim, are among the most frequently used agrochemicals worldwide, despite having already been banned in the USA and the European Union [63]. The use of azole fungicides is directly linked to the abundance of helminths, as the same compounds belong to the most effective antiparasitic treatments. In veterinary medicine, albendazole or mebendazole are commonly used for this purpose [64,65,66,67]; however, many other azole compounds display antihelminthic activity of similar extent due to their shared mechanism of action that is based on the binding to β-tubulin in microtubules [68].

The diversity and abundance of parasites generally decreases with human-induced habitat disturbance [69,70,71,72,73]. The disruption of spatiotemporal relationships within host assemblages likely facilitated a decline in species richness of trematode assemblages. Surprisingly, we only rarely identified severe intensity of infection of the respective trematodes, and we found no outbreaks of trematode species. This corresponds to the fact that the loss of diversity was accompanied by a decline in the intensity of infection. The decline in the intensity of infection affected the trematode assemblages of V. vanellus, A. otus, and B. buteo most severely; in all three species, the intensity of infection declined by more than one order of magnitude. Infection intensity also declined several times in C. ciconia and P. pica, and maintained the same level only in F. tinnunculus, where it was very low throughout the study period. The trematode biodiversity loss was rather gradual, and included the decline in both the prevalence and the intensity of infection in the respective trematode species. The diversity of the trematode assemblages differed strongly among four of the six bird host species examined when comparing the assemblages in 1963–2000 with those examined in 2011–2020; the exceptions were P. pica and F. tinnunculus. In general, we observed a simplification of the trematode assemblages; in three of the six analyzed host species, some or all the trematode species were present prior to 2000 but not in the 2011–2020 period. However, there was no such change in F. tinnunculus, and both lost and newly acquired species were present in C. ciconia and P. pica (Table 2).

Limitations

A limitation of the present study is that it relied on an opportunistic sampling design, where the carcasses of five of the six examined species consisted solely of wounded or injured individuals, and therefore may not necessarily represent the helminths that would be present in birds of good health. Further, we cannot exclude the possibility that trematode species with low prevalence might escape detection in any of the study periods due to limited number of examined host individuals. However, the purpose of the study was to illustrate the overall longitudinal trends in trematode component communities, not to provide a complete list of species that infected the examined host species. Although the present study is based on one of the largest data sets of host individuals among the studies of bird trematodes, it still suffers from issues associated with limited sample size. The sampling effort affects not only trematode richness, but also prevalence, intensity, and some of the diversity indices. Especially at low prevalence, intensity estimates can be skewed when sample size is small. We also cannot exclude the possibility that the observed population trends may differ from those that would be experienced in other regions with better-preserved farmland habitats. As we have shown in Additional file 1: Tables S1–S6 [19,20,21,22,23,24, 36, 37, 74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107], there are strong differences in the prevalence of trematodes among different regions within host distribution ranges. However, the present study, which was based on definitive hosts, confirmed the declines in trematodes reported in previous longitudinal studies on the diversity of trematodes in intermediate hosts in other regions [6,7,8,9,10].

Conclusions

The analysis of six unrelated common bird species that use farmlands as their feeding habitats revealed a previously unreported collapse of formerly dominant trematode species. These trematode species declined in terms of both prevalence and intensity of infection. In contrast, isolated records of a broad range of other trematode species continued to be detected throughout the study period, which is likely related to occasional use of a broad spectrum of food sources. However, the collapse of host–parasite networks in common bird species that use farmlands as their feeding habitats points to yet unknown factors that underlie such dramatic changes. As we observed most of the declines in recent decades, we speculate that the use of recently developed agrochemicals, perhaps the azole fungicides, also known as anthelminthic agents, may be responsible for the unprecedented decline in the farmland trematodes.

Availability of data and materials

Representative specimens of the helminths analyzed in this study are available in the collections of the Comenius Museum in Přerov. All data are available in the main text or additional materials.

Abbreviations

1Y:

First-year birds

IUCN:

International Union for Conservation of Nature

References

  1. 1.

    Carlson J, Hopkins S, Bell KC, Doña J, Godfrey SS, Kwak ML, Lafferty KD, Moir ML, Speer KA, Strona G, Torchin M, Wood CL. A global parasite conservation plan. Biol Conserv. 2020;250:108596.

    Article  Google Scholar 

  2. 2.

    Dougherty ER, Carlson CJ, Bueno VM, Burgio KR, Cizauskas CA, Clements CF, Seidel DP, Harris NC. Paradigms for parasite conservation. Conserv Biol. 2016;30:724–33.

    PubMed  Article  PubMed Central  Google Scholar 

  3. 3.

    Costello MJ, May RM, Stork NE. Can we name Earths species before they go extinct? Science. 2013;339:413–6.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  4. 4.

    Reif J, Voříšek P, Šťastný K, Bejček V, Petr J. Population increase of forest birds in the Czech Republic between 1982 and 2003. Bird Study. 2007;54:248–55.

    Article  Google Scholar 

  5. 5.

    Reif J, Storch D, Voříšek P, Šťastný K, Bejček V. Bird-habitat associations predict population trends in central European forest and farmland birds. Biodiv Conserv. 2008;17:3307–19.

    Article  Google Scholar 

  6. 6.

    Keas BE, Blankespoor HD. The prevalence of cercariae from Stagnicola emarginata (Lymnaeidae) over 50 years in northern Michigan. J Parasitol. 1997;83:536–40.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  7. 7.

    Faltýnková A, Haas W. Larval trematodes in freshwater molluscs from the Elbe to Danube rivers (Southeast Germany): before and today. Parasitol Res. 2006;99:572–82.

    PubMed  Article  PubMed Central  Google Scholar 

  8. 8.

    Serbina EA. Characteristics of the seasonal development of Schistogonimus rarus (Trematoda: Prosthogonimidae). An essay on quantitative estimation of the trematode in the ecosystem of the Malye Chany lake (south of Western Siberia). Parazitologiia. 2008;42:53–65 (in Russian).

    CAS  PubMed  PubMed Central  Google Scholar 

  9. 9.

    Serbina EA. Cercariae Opisthorchis felineus and Metorchis bilis from first intermediate hosts for the first time in basin of Chany lake (Novosibirsk region, Russia) is found. Russian J Parasitol. 2016;37:421–9 (in Russian).

    Article  Google Scholar 

  10. 10.

    Serbina EA. The effect of trematode parthenites on the individual fecundity of Bithynia troscheli (Prosobranchia: Bithyniidae). Acta Parasitol. 2015;60:40–9.

    Google Scholar 

  11. 11.

    Serbina EA, Bonina OM. Dynamics of foci of bird notocotylidosis in the ecosystem of Lake Chany (Western Siberia) in the last 80 years. Russian J Parasitol. 2015;3:29–36 (in Russian).

    Google Scholar 

  12. 12.

    Sitko J, Heneberg P. Systemic collapse of a host-parasite trematode network associated with wetland birds in Europe. Parasitol Res. 2020;119:935–45.

    PubMed  Article  PubMed Central  Google Scholar 

  13. 13.

    Sitko J, Heneberg P. Emerging helminthiases of song thrush (Turdus philomelos) in central Europe. Parasitol Res. 2020;119:4123–34.

    PubMed  Article  PubMed Central  Google Scholar 

  14. 14.

    Hallmann CA, Foppen RPB, van Turnhout CAM, de Kroon H, Jongejans E. Declines in insectivorous birds are associated with high neonicotinoid concentrations. Nature. 2014;511:341–3.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  15. 15.

    Badry A, Schenke D, Treu G, Krone O. Linking landscape composition and biological factors with exposure levels of rodenticides and agrochemicals in avian apex predators from Germany. Environ Res. 2021;193:110602.

    CAS  PubMed  Article  Google Scholar 

  16. 16.

    Christensen TK, Lassen P, Elmeros M. High exposure rates of anticoagulant rodenticides in predatory bird species in intensively managed landscapes in Denmark. Arch Environ Contam Toxicol. 2012;63:437–44.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  17. 17.

    Reif J, Voříšek P, Šťastný K. Bejček V Population trends of birds in the Czech Republic during 1982–2005. Sylvia. 2006;42:22–37.

    Google Scholar 

  18. 18.

    Voříšek P. Trends of common farmland birds in Europe. Prague: ČSO; 2006. http://oldcso.birdlife.cz/index.php?ID=1320. Accessed 28 Sep 2020.

  19. 19.

    Koubek P, Vojtek J. Příspěvek k poznání helmintofany našich havranovitých (Corvidae). Folia Fac Sci Nat Univ Purkyn Brun, Biol. 1973;40:71–101.

    Google Scholar 

  20. 20.

    Rutkowska M. A study of the helminth fauna of Corvidae in Poland. Acta Parasitol Pol. 1973;21:183–237.

    Google Scholar 

  21. 21.

    Škarda J. The helminthofauna of some wild birds in Czechoslovakia. Acta Univ Agricult Brno. 1964;12:269–93 (in Czech).

    Google Scholar 

  22. 22.

    Vaidova SM. Helminths of birds of Azerbaijan. Baku: Elm; 1978. (in Russian).

    Google Scholar 

  23. 23.

    Macko JK. Die Plattwürmer des Kiebitzes (Vanellus vanellus L.) in der Ostslowakei. Biologia. 1959;15:523–30.

    Google Scholar 

  24. 24.

    Smogorzhevskaya LA. Helminth parasites of waterfowl and marsh birds from the fauna of the Ukraine. Kiev: Naukova Dumka; 1976. (in Russian).

    Google Scholar 

  25. 25.

    Jenni L, Winkler R. Moult and ageing of European passerines. London: Helm; 2020.

    Google Scholar 

  26. 26.

    Hájek V. Určování stáří a pohlaví nepěvců. Přerov: Okresní vlastivědné museum J. A. Komenského; 1984.

  27. 27.

    Sitko J, Heneberg P. Composition, structure and pattern of helminth assemblages associated with central European herons (Ardeidae). Parasitol Int. 2015;64:100–12.

    PubMed  Article  PubMed Central  Google Scholar 

  28. 28.

    Yamaguti S. Systema Helminthum: the digenetic trematodes of vertebrates, vol. 1. New York: Interscience Publishers; 1958.

    Google Scholar 

  29. 29.

    Schell SC. Handbook of trematodes of North America north of Mexico. Idaho: University of Idaho Press; 1985.

    Google Scholar 

  30. 30.

    Gibson DI, Jones A, Bray RA. Keys to the Trematoda, vol. I. New York: CAB International; 2002.

    Book  Google Scholar 

  31. 31.

    Gibson DI, Jones A, Bray RA. Keys to the Trematoda, vol. 2. New York: CAB International; 2005.

    Google Scholar 

  32. 32.

    Gibson DI, Jones A, Bray RA. Keys to the Trematoda, vol. 3. New York: CAB International; 2008.

    Google Scholar 

  33. 33.

    Colwell RK. Biodiversity: concepts, patterns and measurement. In: Levin SA, editor. The Princeton guide to ecology. Princeton: Princeton University Press; 2009. p. 257–63.

    Chapter  Google Scholar 

  34. 34.

    Heneberg P, Sitko J, Těšínský M, Rząd I, Bizos J. Central European Strigeidae Railliet, 1919 (Trematoda: Strigeidida): molecular and comparative morphological analysis suggests the reclassification of Parastrigea robusta Szidat, 1928 into Strigea Abildgaard, 1790. Parasitol Int. 2018;67:688–701.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  35. 35.

    Heneberg P, Sitko J, Těšínský M. Paraphyly of Conodiplostomum Dubois, 1937. Parasitol Int. 2020;76:102033.

  36. 36.

    Sitko J, Heneberg P. Composition, structure and pattern of helminth assemblages associated with central European storks (Ciconiidae). Parasitol Int. 2015;64:130–4.

    PubMed  Article  PubMed Central  Google Scholar 

  37. 37.

    Sitko J. Trematodes of birds of prey (Falconiformes) in Czech Republic. Helminthologia. 1998;35:131–46.

    Google Scholar 

  38. 38.

    Okulewicz A, Sitko J. Parasitic helminthes – probable cause of death of birds. Helminthologia. 2012;49:241–6.

    Article  Google Scholar 

  39. 39.

    Heneberg P, Sitko J. Cryptic speciation among Tylodelphys spp.: the major helminth pathogens of fish and amphibians. Parasitol Res. 2021;120:1687–97.

  40. 40.

    de Jong Y, Verbeek M, Michelsen V, de Place BP, Los W, Steeman F, et al. Fauna Europaea—all European animal species on the web. Biodivers Data J. 2014;2:e4034.

  41. 41.

    Sitko J, Bizos J, Sherrard-Smith E, Stanton DWG, Komorová P, Heneberg P. Integrative taxonomy of European parasitic flatworms of the genus Metorchis Looss, 1899 (Trematoda: Opisthorchiidae). Parasitol Int. 2016;65:258–67.

    PubMed  Article  PubMed Central  Google Scholar 

  42. 42.

    Sitko J, Faltýnková A, Scholz T. Checklist of the trematodes (Digenea) of birds. Prague: Academia; 2006.

    Google Scholar 

  43. 43.

    Willis AD. Rarefaction, alpha diversity, and statistics. Front Microbiol. 2019;10:2407.

    PubMed  PubMed Central  Article  Google Scholar 

  44. 44.

    Chao A. Estimating the population size for capture-recapture data with unequal catchability. Biometrics. 1987;43:783–91.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  45. 45.

    Chao A, Chazdon RL, Colwell RK, Shen T-J. A new statistical approach for assessing compositional similarity based on incidence and abundance data. Ecol Lett. 2005;8:148–59.

    Article  Google Scholar 

  46. 46.

    Poole RW. An introduction to quantitative ecology. New York: McGraw-Hill; 1974.

    Google Scholar 

  47. 47.

    Galaktionov KV, Dobrovolskij AA. The trematode life cycle as a system of adaptations. In: Fried B, Graczyk TK, editors. The biology and evolution of trematodes. Dordrecht: Springer; 2003. p. 215–317.

    Chapter  Google Scholar 

  48. 48.

    Esch GW, Curtis LA, Barger MA. A perspective on the ecology of trematode communities in snails. Parasitology. 2001;123(Suppl):S57-75.

    PubMed  Article  PubMed Central  Google Scholar 

  49. 49.

    Hechinger RF, Lafferty KD. Host diversity begets parasite diversity: bird final hosts and trematodes in snail intermediate hosts. Proc Biol Sci. 2005;272:1059–66.

    PubMed  PubMed Central  Google Scholar 

  50. 50.

    Skirnisson K. Association of helminth infections and food consumption in common eiders Somateria mollissima in Iceland. J Sea Res. 2015;104:41–50.

    Article  Google Scholar 

  51. 51.

    Strona G. Past, present and future of host-parasite co-extinctions. Int J Parasitol: Parasites Wildl. 2015;4:431–41.

    Google Scholar 

  52. 52.

    Kołodziej-Sobocińska M. Factors affecting the spread of parasites in populations of wild European terrestrial mammals. Mammal Res. 2019;64:301–18.

    Article  Google Scholar 

  53. 53.

    Rahman ML, Tarrant S, McCollin D, Ollerton J. The conservation value of restored landfill sites in the East Midlands, UK for supporting bird communities. Biodiv Conserv. 2011;20:1879–93.

    Article  Google Scholar 

  54. 54.

    Orlowski G, Karg J, Jerzak L, Bocheński M, Profus P, Książkiewicz-Parulska Z, Zub K, Ekner-Grzyb A, Czarnecka J. Linking land cover satellite data with dietary variation and reproductive output in an opportunistic forager: Arable land use can boost an ontogenetic trophic bottleneck in the White Stork Ciconia ciconia. Sci Tot Environ. 2019;646:491–502.

    CAS  Article  Google Scholar 

  55. 55.

    Meeus JHA. The transformation of agricultural landscapes in Western Europe. Milieu. 1990;6:225–36.

    Google Scholar 

  56. 56.

    Pain D, Pienkowski MW. Farming and birds in Europe. London: Academic Press; 1997.

    Google Scholar 

  57. 57.

    Robinson RA, Sutherland WJ. Post war changes in arable farming and biodiversity in Great Britain. J Appl Ecol. 2002;39:157–76.

    Article  Google Scholar 

  58. 58.

    Butet A, Michel N, Rantier Y, Comor V, Hubert-Moy L, Nabucet J, Delettre Y. Responses of common buzzard (Buteo buteo) and Eurasian kestrel (Falco tinnunculus) to land use changes in agricultural landscapes of Western France. Agricult Ecosyst Environ. 2010;138:152–9.

    Article  Google Scholar 

  59. 59.

    Szép T, Nagy K, Nagy Z, Halmo G. Population trends of common breeding and wintering birds in Hungary, decline of longdistance migrant and farmland birds during 1999–2012. Ornis Hung. 2012;20:13–63.

    Article  Google Scholar 

  60. 60.

    Zubrod JP, Bundschuh M, Arts G, Brühl CA, Imfeld G, Knäbel A, et al. Fungicides: an overlooked pesticide class? Environ Sci Technol. 2019;53:3347–65.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  61. 61.

    Heneberg P, Svoboda J, Pech P. Claustral colony founding does not prevent sensitivity to the detrimental effects of azole fungicides on the fecundity of ants. J Environ Manag. 2021;280:111740.

    CAS  Article  Google Scholar 

  62. 62.

    Mussen EC, Lopez JE, Peng CYS. Effects of selected fungicides on growth and development of larval honey bees, Apis mellifera L. (Hymenoptera: Apidae). Environ Entomol 2004;33:1151–4.

  63. 63.

    Singh S, Singh N, Kumar V, Datta S, Wani AB, Singh D, Singh K, Singh J. Toxicity, monitoring and biodegradation of the fungicide carbendazim. Environ Chem Lett. 2016;14:317–29.

    CAS  Article  Google Scholar 

  64. 64.

    Hemphill A, Stadelmann B, Scholl S, Müller J, Spiliotis M, Müller N, Gottstein B, Siles-Lucas M. Echinococcus metacestodes as laboratory models for the screening of drugs against cestodes and trematodes. Parasitology. 2010;137:569–87.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  65. 65.

    Keiser J. In vitro and in vivo trematode models for chemotherapeutic studies. Parasitology. 2010;137:589–603.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  66. 66.

    Pakharukova MY, Pakharukov YV, Mordvinov VA. Effects of miconazole/clotrimazole and praziquantel combinations against the liver fluke Opisthorchis felineus in vivo and in vitro. Parasitol Res. 2018;117:2327–31.

    PubMed  Article  PubMed Central  Google Scholar 

  67. 67.

    Vale N, Gouveia MJ, Gärtner F. Current and novel therapies against helminthic infections: The potential of antioxidants combined with drugs. Biomolecules. 2020;10:350.

    CAS  PubMed Central  Article  Google Scholar 

  68. 68.

    Crawford LM, Franco DA. Animal drugs and human health. Boca Raton: CRC Press; 1994.

    Google Scholar 

  69. 69.

    Hudson PJ, Dobson AP, Lafferty KD. Is a healthy ecosystem one that is rich in parasites? Trends Ecol Evol. 2006;21:381–5.

    PubMed  Article  PubMed Central  Google Scholar 

  70. 70.

    Aguirre-Macedo ML, Vidal-Martínez VM, Lafferty KD. Trematode communities in snails can indicate impact and recovery from hurricanes in a tropical coastal lagoon. Int J Parasitol. 2011;41:1403–8.

    PubMed  Article  PubMed Central  Google Scholar 

  71. 71.

    Wood CL, Lafferty KD. Biodiversity and disease: a synthesis of ecological perspectives on Lyme disease transmission. Trends Ecol Evol. 2013;28:239–47.

    PubMed  Article  PubMed Central  Google Scholar 

  72. 72.

    Rząd I, Sitko J, Sałamantin R, Wysocki D. Helminth community structure study on urban and forest blackbird (Turdus merula L.) populations in relation to seasonal bird migration on the south Baltic Sea coast (NW Poland). Helminthologia. 2014;51:117–29.

  73. 73.

    Wood CL, Lafferty KD, DeLeo G, Young HS, Hudson PJ, Kuris AM. Does biodiversity protect humans against infectious disease? Ecology. 2014;95:817–32.

    PubMed  Article  PubMed Central  Google Scholar 

  74. 74.

    Kurashvili BE. Helminths of game birds of Georgia. Moscow: Izd Akad Nauk SSSR; 1957.

    Google Scholar 

  75. 75.

    Sultanov MA. The Helminths of Domestic and Game Birds in Uzbekistan. Tashkent: Izd AN Uzbek SSR; 1963. (in Russian).

    Google Scholar 

  76. 76.

    Macko JK. Die Fauna der Plathelminthes des Storches Ciconia ciconia L. Folia Parasitol. 1961;8:283–94.

    Google Scholar 

  77. 77.

    Gundlach JL. Contribution to the helminthofauna of storks (Ciconia ciconia L. and C. nigra L.) originating from the Lublin Palatinate. Acta Parasitol Pol. 1969;16:83–9.

  78. 78.

    Schuster R, Schaffer T, Shimalov V. Die Helminthenfauna einheimischer Weiβstörche (Ciconia ciconia). Berl Münch Tierärztl Wschr. 2002;115:435–9.

    Google Scholar 

  79. 79.

    Girişgin AO, Birlik S, Senlik B, Yildirimhan HS. Intestinal helminths of the white stork (Ciconia ciconia Linnaeus, 1758) from an inter-route site in Turkey. Acta Vet Hung. 2017;65:221–33.

    PubMed  Article  PubMed Central  Google Scholar 

  80. 80.

    Stoimenov K. [Contribution to the helminthofauna of the magpie (Pica pica L.) in northeastern Bulgaria]. Izvest Tsentr Khelmint Lab. 1962;7:161–7.

  81. 81.

    Borgsteede FHM, Okulewicz A, Okulewicz J. A study of the helminth fauna of birds belonging to the Passeriformes in the Netherlands. Acta Parasitol. 2000;45:14–21.

    Google Scholar 

  82. 82.

    Halajian A, Eslami A, Mobedi I, Amin O, Mariaux J, Mansoori J, Tavakol S. Gastrointestinal helminths of magpies (Pica pica), rooks (Corvus frugilegus) and carrion crows (Corvus corone) in Mazandaran province, north of Iran. Iranian J Parasitol. 2011;6:38–44.

    CAS  Google Scholar 

  83. 83.

    Girişgin AO, Alasonyalilar Demirer A, Büyükcangaz E, Khider M, Birlik S, Ipek V. Postmortem findings on a group of Pica pica (Passeriformes: Corvidae). Ankara Üniv Vet Fak Derg. 2019;66:155–61.

    Google Scholar 

  84. 84.

    Furmaga S. The helminth fauna of predatory birds (Accipitres et Striges) of the environment of Lublin. Acta Parasitol Pol. 1957;5:215–87.

    Google Scholar 

  85. 85.

    Kutzer E, Frey H, Nöbauer H. Zur Parasitenfauna österreichischer Eulenvögel (Strigiformes). Angew Parasitol. 1982;23:190–7.

    CAS  PubMed  PubMed Central  Google Scholar 

  86. 86.

    Taft SJ, Suchow K, Van Horn M. Helminths from some Minnesota and Wisconsin raptors. J Helminthol Soc Wash. 1993;60:260–3.

    Google Scholar 

  87. 87.

    Lierz M, Göbel T, Schuster R. Untersuchungen zum Vorkommen von Parasiten bei einheimischen Greifvögeln und Eulen. Berl Münch Tierärztl Wschr. 2002;115:43–52.

    CAS  Google Scholar 

  88. 88.

    Borgsteede FHM, Okulewicz A, Zoun PEF, Okulewicz J. The helminth fauna of birds of prey (Accipitriformes, Falconiformes and Strigiformes) in the Netherlands. Acta Parasitol. 2003;48:200–7.

    Google Scholar 

  89. 89.

    Sanmartín ML, Álvarez F, Barreiro G, Leiro J. Helminth fauna of Falconiform and Strigiform birds of prey in Galicia. Northwest Spain Parasitol Res. 2004;92:255–63.

    PubMed  Article  PubMed Central  Google Scholar 

  90. 90.

    Ferrer D, Molina R, Castellà J, Kinsella JM. Parasitic helminths in the digestive tract of six species of owls (Strigiformes) in Spain. Vet J. 2004;167:181–5.

    PubMed  Article  PubMed Central  Google Scholar 

  91. 91.

    Rząd I, Sitko J, Wysocki D, Stępniewski K. Digenean trematodes from six species of birds (Passeriformes, Piciformes and Strigiformes) from north-western Poland. Wiad Parazytol. 2011;57:271–6.

    Google Scholar 

  92. 92.

    Santoro M, Mattiucci S, Nascetti G, Kinsella JM, Di Prisco F, Troisi S, D’Alessio N, Veneziano V, Aznar FJ. Helminth communities of owls (Strigiformes) indicate strong biological and ecological differences from birds of prey (Accipitriformes and Falconiformes) in Southern Italy. PLoS ONE. 2012;7:e53375.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  93. 93.

    Komorová P, Sitko J, Špakulová M, Hurníková Z. Intestinal and liver flukes of birds of prey (Accipitriformes, Falconiformes, Strigiformes) from Slovakia: uniform or diverse compound? Parasitol Res. 2016;115:2837–44.

    PubMed  Article  PubMed Central  Google Scholar 

  94. 94.

    Komorová P, Sitko J, Špakulová M, Hurníková Z, Salamantin R, Chovancová G. New data on helminth fauna of birds of prey (Falconiformes, Accipitriformes, Strigiformes) in the Slovak Republic. Helminthologia. 2017;54:314–21.

    Article  Google Scholar 

  95. 95.

    Kutzer E, Frey H, Kotremba J. Zur Parasitenfauna österreichischer Greifvögel (Falconiformes). Angew Parasitologie. 1980;21:183–205.

    CAS  Google Scholar 

  96. 96.

    Illescas Gomez MP, Rodriguez Osorio M, Aranda MF. Parasitation of falconiform, strigiform and passeriform (Corvidae) birds by helminths in Spain. Res Rev Parasitol. 1993;53:129–35.

    Google Scholar 

  97. 97.

    Krone O. Endoparasites in free-ranging birds of prey in Germany. In: Lumeij JT, Remple JD, Redig PT, Lierz M, Cooper JE, editors. Raptor biomedicine III. Lake Worth: Zoological Education Network; 2000. p. 101–16.

    Google Scholar 

  98. 98.

    Ferrer D, Molina R, Adelantado C, Kinsella JM. Helminths isolated from the digestive tract of diurnal raptors in Catalonia. Spain Vet Rec. 2004;154:17–20.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  99. 99.

    Papazahariadou M, Diakou A, Papadopoulos E, Georgopoulou I, Komnenou A, Antoniadou-Sotiriadou K. Parasites of the digestive tract in free-ranging birds in Greece. J Nat Hist. 2008;42:381–98.

    Article  Google Scholar 

  100. 100.

    Santoro M, Tripepi M, Kinsella JM, Panebianco A, Mattiucci S. Helminth infestation in birds of prey (Accipitriformes and Falconiformes) in Southern Italy. Vet J. 2010;186:119–22.

    PubMed  Article  PubMed Central  Google Scholar 

  101. 101.

    Santoro M, Kinsella JM, Galiero G, Uberti B, Aznar FJ. Helminth community structure in birds of prey (Accipitriformes and Falconiformes in Southern Italy. J Parasitol. 2012;98:22–9.

    PubMed  Article  PubMed Central  Google Scholar 

  102. 102.

    Tezel M, Girişgin AO, Birlik S, Yildirimhan HS, Şenlik B. Helminths of the digestive tract in Buteo buteo (Falconiformes: Falconidae) in Bursa Province of Northwest Turkey. Turk J Zool. 2015;39:323–7.

    CAS  Article  Google Scholar 

  103. 103.

    Kobyshev NM, Markov GS, Ryzhikov KM. Ecological analysis of parasite fauna in numerous species of falcon-like birds from Lower Volga region. Parasites and Parasitosis in Animals and Humans. Kiev: Naukova dumka; 1975. p. 25–38.

    Google Scholar 

  104. 104.

    Mohammad MK. Helminth parasites of the kestrel Falco tinnunculus L. 1758 in Iraq. Bull Iraq nat Hist Mus. 1999;9:123–9.

  105. 105.

    Antunes AFN. Pesquisa de helmintes gastrointestinais em quarto espécies de aves de rapina na zona centro de Portugal: Buteo buteo, Falco tinnunculus, Tyto alba e Athene noctua. MIMV Thesis. Lisboa: Fac Med Vet, Univ Lisboa; 2016.

  106. 106.

    Bykhovskaya-Pavlovskaya IE. Fauna of trematodes of birds in west Siberia and its dynamics. Parazitologicheskiy Sbornik. 1953;15:5–117 (in Russian).

    Google Scholar 

  107. 107.

    Hintzen J, Thielebein J, Daugschies A, Schmäschke R. Trematodes from the Northern Lapwing, Vanellus vanellus (Charadriidae), from Central Germany. Parasitol Res. 2017;116:661–6.

    PubMed  Article  Google Scholar 

Download references

Acknowledgements

We thank Petr Orel, the head of the Bartošovice rescue station, for his excellent long-term cooperation, which allowed the acquisition of the majority of birds examined in the present study. We thank the governmental and local authorities for providing the necessary permissions to conduct this long-term research. We also thank the landlords, gamekeepers and the staff of local rescue stations for providing us with carcasses of untreatable birds.

Funding

The study was supported by the Ministry of Culture of the Czech Republic project DE07P04OMG007.

Author information

Affiliations

  1. Comenius Museum, Moravian Ornithological Station, Přerov, Czech Republic

    Jiljí Sitko

  2. Charles University, Third Faculty of Medicine, Prague, Czech Republic

    Petr Heneberg

Authors
  1. Jiljí Sitko
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Petr Heneberg
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

JS and PH conceived the study, JS collected the data, PH analyzed the data and wrote the manuscript. Both authors read and approved the final manuscript.

Corresponding author

Correspondence to Petr Heneberg.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

On behalf of both authors, the corresponding author states that there is no conflict of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Table S1.

Previous records of trematodes from Ciconia ciconia. Table S2. Previous records of trematodes from Pica pica. Table S3. Previous records of trematodes from Asio otus. Table S4. Previous records of trematodes from Buteo buteo. Table S5. Previous records of trematodes from Falco tinnunculus. Table S6. Previous records of trematodes from Vanellus vanellus. Table S7. Raw data. Listed are all examined C. ciconia host individuals together with the abundance of all trematode species found. Indicated are the age and sex of analyzed hosts, as well as the year when the respective host individual was acquired. Table S8. Raw data. Listed are all examined P. pica host individuals together with the abundance of all trematode species found. Indicated are the age and sex of analyzed hosts, as well as the year when the respective host individual was acquired. Table S9. Raw data. Listed are all examined A. otus host individuals together with the abundance of all trematode species found. Indicated are the age and sex of analyzed hosts, as well as the year when the respective host individual was acquired. Table S10. Raw data. Listed are all examined B. buteo host individuals together with the abundance of all trematode species found. Indicated are the age and sex of analyzed hosts, as well as the year when the respective host individual was acquired. Table S11. Raw data. Listed are all examined F. tinnunculus host individuals together with the abundance of all trematode species found. Indicated are the age and sex of analyzed hosts, as well as the year when the respective host individual was acquired. Table S12. Raw data. Listed are all examined V. vanellus host individuals together with the abundance of all trematode species found. Indicated are the age and sex of analyzed hosts, as well as the year when the respective host individual was acquired.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Sitko, J., Heneberg, P. Long-term dynamics of trematode infections in common birds that use farmlands as their feeding habitats. Parasites Vectors 14, 383 (2021). https://doi.org/10.1186/s13071-021-04876-2

Download citation

Keywords

  • Agricultural landscapes
  • Common farmland birds
  • Biodiversity decline
  • Helminths
  • Population dynamics
  • Trematoda

Parasites & Vectors

ISSN: 1756-3305

Contact us