Abundance patterns of two Oropsylla (Ceratophyllidae: Siphonaptera) species on black-tailed prairie dog (Cynomys ludovicianus) hosts.

Behavioral, genetic, and immune variation within a host population may lead to aggregation of parasites whereby a small proportion of hosts harbor a majority of parasites. In situations where two or more parasite species infect the same host population there is the potential for interaction among parasites that could potentially influence patterns of aggregation through either competition or facilitation. We studied the occurrence and abundance patterns of two congeneric flea species on black-tailed prairie dog (Cynomys ludovicianus) hosts to test for interactions among parasite species. We live-trapped prairie dogs on ten sites in Boulder County, CO and collected their fleas. We found a non-random, positive association between the two flea species, Oropsylla hirsuta and O. tuberculata cynomuris; hosts with high loads of one flea species had high loads of the second species. This result suggests that there is no interspecific competition among fleas on prairie dog hosts. Host weight had a weak negative relationship to flea load and host sex did not influence flea load, though there were slight differences in flea prevalence and abundance between male and female C. ludovicianus. While genetic and behavioral variation among hosts may predispose certain individuals to infection, our results indicate apparent facilitation among flea species that may result from immune suppression or other flea-mediated factors.     

Flea (Siphonaptera) species richness in the Great Basin Desert and island biogeography theory

Numbers of flea (Siphonaptera) species (flea species richness) on individual mammals should be higher on large mammals, mammals with dense populations, and mammals with large geographic ranges, if mammals are islands for fleas. I tested the first two predictions with regressions of H. J. Egoscue's trapping data on flea species richness collected from individual mammals against mammal size and population density from the literature. Mammal size and population density did not correlate with flea species richness. Mammal geographic range did, in earlier studies. The intermediate‐sized (31 g), moderately dense (0.004 individuals/m²) Peromyscus truei (Shufeldt) had the highest richness with eight flea species on one individual. Overall, island biogeography theory does not describe the distribution of flea species on mammals in the Great Basin Desert, based on H. J. Egoscue's collections. Alternatively, epidemiological or metapopulation theories may explain flea species richness.     

Geographical variation in the 'bottom-up' control of diversity: fleas and their small mammalian hosts

Aim We searched for signs of the ‘bottom‐up’ diversity effect in the association between fleas (Siphonaptera) and their small mammalian hosts (Rodentia, Insectivora and Lagomorpha). We asked (1) whether a strong dependence of flea species richness on host species richness is characteristic for both Palaeoarctic and Nearctic realms; (2) if yes, whether the ratio of host species per flea species along the host diversity gradient is similar between the Palaeoarctic and Nearctic; and (3) whether factors other than host species richness (i.e. geographical position, climate and landscape) might better explain variation in flea species richness than host species richness. Location The study used previously published data on species richness of fleas and their small mammalian hosts from 26 Palaeoarctic and 19 Nearctic regions. Methods We regressed the number of flea species on the number of small mammal species across regions, separately for Palaeoarctic and Nearctic realms, using both non‐transformed data as well as data corrected for the confounding effects of host sampling effort and sampling area. To test whether flea species richness is determined by external factors unrelated to the host, we used stepwise multiple regressions of flea species richness against host species richness and parameters describing the geographical position, climate and relief of a region. Results When non‐transformed data were analysed, flea species richness was positively correlated with host species richness in both the Palaeoarctic and Nearctic, although the slopes of the two regressions differed significantly. After removal of the confounding effects of host sampling effort and sampling area, Palaeoarctic flea species richness remained strongly positively correlated with host species richness, whereas in the Nearctic, flea species richness appeared to be completely independent of host species richness. Results of the multiple regressions using corrected data demonstrated that in the Palaeoarctic, flea species richness was correlated with both the number of host species and the mean altitude of the region, whereas in the Nearctic, flea species richness only tended to be weakly correlated with latitude (however, this correlation turned out to be non‐significant after Bonferroni correction). Main conclusions We found evidence of bottom‐up control of flea diversity in the Palaeoarctic regions only, and not in the Nearctic. We explore several potential explanations for the different patterns observed in the two biogeographical realms, including differences in (1) levels of host specialization, (2) history of host–parasite associations and (3) landscape effects on flea diversification. We conclude that these factors combine to create different macroecological patterns in different biogeographical realms, and that diversity is not governed by the same forces everywhere.     

Host range and distribution of small mammal fleas in South Africa,with a focus on species of medical and veterinary importance

The host range and distribution of flea species on rodents and insectivores across multiple vegetation types in South Africa were investigated. Habitat suitability for flea species considered as important vectors of disease in humans and domestic animals was modelled. Data originated from fleas that were recovered from small mammals captured at 29 localities during 2009–2013 and published literature searched for flea records. Climate‐based predictor variables, widely used in arthropod vector distribution, were selected and habitat suitability modelled for 10 flea vector species. A total of 2469 flea individuals representing 33 species and subspecies were collected from 1185 small mammals. Ten of each of the flea and rodent species are plague vectors and reservoirs, respectively. Multiple novel flea–host associations and locality records were noted. Three vector species were recorded from insectivores. Geographic distributions of flea species ranged from broad, across‐biome distributions to narrower distributions within one or two biomes. Habitat suitability models performed excellently for the majority of flea vectors and identified regions of summer and all‐year rainfall as representing suitable habitats for most vector species. Current knowledge of vector and disease ecology can benefit from similar sampling approaches that will be important not only for South Africa, but also for the sub‐region.     

Diversification of ectoparasite assemblages and climate: an example with fleas parasitic on small mammals

Aim We studied the relationships between the numbers of species and numbers of higher taxa (genera, tribes, subfamilies and families) in flea assemblages of small mammalian hosts with the aims of: (a) comparing these relationships across different regions, and (b) testing the hypothesis that flea assemblages in warmer regions diversify mainly via intrahost speciation, whereas those in colder regions diversify mainly via host switching. Location The study used previously published data on flea assemblages on small mammalian hosts from 25 different regions of the Holarctic. Methods The number of flea genera, tribes, subfamilies or families in an assemblage (host species) was plotted against the number of flea species in this assemblage for each region separately, and a power function was fitted to the resulting relationships. Then, the values of the exponent of the power function for a region were regressed against the mean annual temperature in this region, across all regions. Results The relationships between the number of flea species and the numbers of flea genera, tribes, subfamilies or families on a host species in each region were found to be well described by simple power functions. The exponent of the power function of the relationship between the number of flea species and the number of flea genera per host tended to decrease with increasing local mean annual temperature. When two apparent outliers from the trend (corresponding to regions where sampling was not performed as in other regions) were omitted from the analysis, the negative relationship between temperature and the exponent of the power function between the number of flea species and number of flea genera per host became highly significant. No relationship was found between the values of the exponents of the power functions between the number of flea species and the number of flea tribes, subfamilies or families per host, and the mean local annual temperature. Main conclusions The results suggest that the diversification of flea assemblages is associated with climatic variables. In warm regions, the greater number of congeneric species per flea assemblage, reflected by the lower exponent of the power function, may well be the outcome of intrahost speciation. This indicates that, as regional temperature increases, intrahost speciation becomes a relatively more important mode of diversification than acquisition of fleas via host switching.     

Abundance patterns and coexistence processes in communities of fleas parasitic on small mammals

The abundance of a given species in a community is likely to depend on both the total abundance and diversity of other species making up that community. A large number of co-occurring individuals or co-occurring species may decrease the abundance of any given species via diffuse competition; however, indirect interactions among many co-occurring species can have positive effects on a focal species. The existence of diffuse competition and facilitation remain difficult to demonstrate in natural communities. Here, we use data on communities of fleas ectoparasitic on small mammals from 27 distinct geographical regions to test whether the abundance of any given flea species in a community is affected by either the total abundance of all other co-occurring flea species, or the species richness and/or taxonomic diversity of the flea community. At all scales of analysis, i.e. whether we compared the same flea species on different host species, or different flea species, two consistent results emerged. First, the abundance of a given flea species correlates positively with the total abundance of all other co-occurring flea species in the community. Second, the abundance of any given flea species correlates negatively with either the species richness or taxonomic diversity of the flea community. The results do not support the existence of diffuse competition in these assemblages, because the more individuals of other flea species are present on a host population, the more individuals of the focal species are there as well. Instead, we propose explanations involving either apparent facilitation among flea species via suppression of host immune defenses, or niche filtering processes acting to restrict the taxonomic composition and abundance of flea assemblages.     

Geographical variation in host specificity of fleas (Siphonaptera) parasitic on small mammals: the influence of phylogeny and local environmental conditions

The evolution of host specificity remains a central issue in the study of host‐parasite relationships. Here we tackle three basic questions about host specificity using data on host use by fleas (Siphonaptera) from 21 geographical regions. First, are the host species exploited by a flea species no more than a random draw from the locally available host species, or do they form a taxonomically distinct subset? Using randomization tests, we showed that in the majority of cases, the taxonomic distinctness (measured as the average taxonomic distances among host species) of the hosts exploited by a flea is no different from that of random subsets of hosts taken from the regional pool. In the several cases where a difference was found, the taxonomic distinctness of the hosts used by a flea was almost always lower than that of the random subsets, suggesting that the parasites use hosts within a narrower taxonomic spectrum than what is available to them. Second, given the variation in host specificity among populations of the same flea species, is host specificity truly a species character? We found that host specificity measures are repeatable among different populations of the same flea species: host specificity varies significantly more among flea species than within flea species. This was true for both measures of host specificity used in the analyses: the number of host species exploited, and the index measuring the average taxonomic distinctness of the host species and its variance. Third, what causes geographical variation in host specificity among populations of the same flea species? In the vast majority of flea species, neither of our two measures of host specificity correlated with either the regional number of potential host species or their taxonomic distinctness, or the distance between the sampled region and the center of the flea's geographical range. However, in most flea species host specificity correlated with measures of the deviation in climatic conditions (precipitation and temperature) between the sampled region and the average conditions computed across the flea's entire range. Overall, these results suggest that host specificity in fleas is to a large extent phylogenetically constrained, while still strongly influenced by local environmental conditions.     

Aggregative structure is the rule in communities of fleas: null model analysis

We used null models to examine patterns of species co‐occurrences in 59 communities of fleas parasitic on small mammals from 4 biogeographic realms (Afrotropics, Nearctic, Neotropics, and Palaearctic). We compared frequencies of co‐occurrences of flea species across host species with those expected by chance, using a null model approach. We used 4 tests for non‐randomness to identify pairs of species (within a community) that demonstrate significant positive or negative co‐occurrence. The majority of flea communities were non‐randomly assembled. Patterns of flea co‐occurrences on the same host species indicated aggregation but not segregation of flea species (except for the flea community of Madagascar). Although only a small fraction of species pairs were associated significantly (264 of 10, 943 species pairs according to the most liberal criterion), most of these associations were positive (except for 2 negatively associated species pairs). Significantly associated pairs were represented mainly by non‐congeneric species. The degree of non‐randomness of the entire flea community was similar among biogeographic regions, but the strength of pair‐wise association varied geographically, being the highest in the Afrotropics and the lowest in the European region of the Palaearctic.     

喜马拉雅山南坡蚤类营养生态位的研究

对喜马拉雅山南坡地区的46种蚤的营养生态位宽度和生态位重叠进行了研究。结果表明,23种蚤只有1种宿主,其营养生态位宽度最窄(B=0),而方指双蚤的营养生态位宽度最大(B=0.6694),其次为斯氏新蚤(B=0.4968).寄生于9种小兽宿主的12种主要蚤种中,尼泊尔古蚤和后厉蚤和窄突厉蚤因其宿主动物以食虫类为主,相互间的营养生态位重叠指数最高。     

Relative susceptibility of two sweetpotato varieties to storage root damage by sweetpotato flea beetle (Coleoptera: Chrysomelidae) and wireworm (Coleoptera: Elateridae)

The feeding of soil dwelling insects on storage roots is one of the most serious management issues faced by sweetpotato, Ipomoea batatas (L.) Lam. (Convolvulaceae), growers in the southern United States. Field studies were conducted to evaluate the relative susceptibility of two commonly grown sweetpotato varieties to sweetpotato flea beetle, Chaetocnema confinis Crotch (Coleoptera: Chrysomelidae), and wireworms (Coleoptera: Elateridae, various species). The incidence and severity of sweetpotato flea beetle damage was significantly lower in the variety Covington than Beauregard in two small plot replicated studies. Surveys conducted in commercial sweetpotato fields also showed significantly less sweetpotato flea beetle damage in fields planted to Covington compared with those planted to Beauregard. There was no clear evidence of varietal effect on the incidence of wireworm damage in the study. Results indicate that the severity of wireworm damage as measured by the size of feeding scars may be less in Covington than Beauregard.     

Host associations and origin in the formation of the Caucasian fauna of fleas (Siphonaptera)

Results of analysis of the Caucasian fauna of fleas and their association with mammal and avian hosts are reported. The Caucasian fauna of potential flea hosts comprises about 130 species of mammals and about 470 species of birds. Most of the flea species in the Caucasian fauna (88 out of 155) parasitize rodents, 51 species of which are permanent hosts of different flea species; 13 flea species occur on 11 species of insectivores; 13 flea species, on 13 species of chiropterans; 14 flea species, on 20 species of carnivores. Only 2 flea species parasitize artiodactyles. 54 species of birds are permanent hosts of 23 species of fleas from 4 genera in the Caucasus. Ten types of ranges of flea species are distinguished; host associations of the Caucasian flea species from these groups are discussed. The greatest numbers of hosts from the families Cricetidae, Muridae, and Sciuridae are associated with fleas with Euro-Asian (extra-Siberian), European, Turanian, and Iranian ranges. Soricidae are known as hosts of flea species with European and Euro-Turanian ranges. Four major groups of flea taxa are represented in the Caucasian fauna. The distribution of the first group is determined by the influence of the palaeofauna of the ancient European continent in the early Cenozoic; that of the second group, by the influence of the fauna of the ancient Asian continent during the Paleogene and part of the Neogene; the third, by the influence of the fauna of southern Europe starting with the Miocene. The fourth group comprises the species which immigrated from northern Europe and Asia in the Late Neogene (2–3 mln years ago).     

Nested pattern in flea assemblages across the host's geographic range

Understanding non-random patterns in the taxonomic composition of communities occurring in insular or fragmented habitats remains a major goal of ecology. Nested subset patterns are one possible departure from random community assembly that has been reported for communities of both free-living and parasitic animals. Here, we investigate the effects of extrinsic factors on the occurrence of nestedness among the assemblages of fleas found in different populations of the same host species, using data on 25 mammalian host species. The patterns of flea species composition among host populations spanned the entire spectrum from significantly nested to significantly anti-nested. After controlling for host phylogeny, we found that across host species, the tendency for flea assemblages to approach nestedness increased with increasing host geographic range size and with decreasing latitude of the host's geographic range. This tendency also decreased with an increase in a composite variable combining data on mean January and July temperature. The number of closely-related mammalian species living in sympatry with a given host species had no influence on whether or not the structure of flea assemblages among its populations departed from randomness. We propose explanations for these results that include: the possible gradual loss of flea species as a host expands its range from its initial area of origin, the lack of specific flea faunas in narrowly-distributed host species, interspecific differences in the dispersal abilities of flea species becoming amplified in hosts with broad geographical ranges, and the effect of latitude, climate and environment on the probabilities of host-switching and extinction in fleas. Overall, our results suggest that the structure of flea assemblages in mammalian hosts may be driven by features of host biology.     

Interaction frequency across the geographical range as a determinant of host specialisation in generalist fleas

The strength of interspecific interactions varies over geographical scales, and can influence patterns of resource specialisation. Even with gene flow preventing local adaptation of a consumer to particular resources, we might expect that across its entire range, the consumer would show some specialisation for the resource types most likely to be encountered across the localities where it occurs. We tested the hypothesis that generalist fleas are more successful at exploiting small mammalian host species with which they co-occur frequently across their geographical range than host species that, though suitable, are encountered less frequently. This hypothesis was tested with data on 121 flea species compiled from field surveys across 35 regions of the Palaearctic. Using abundance (mean number of individual fleas per individual host) as a measure of flea success on a particular host species, positive correlations between flea abundance and the frequency of co-occurrence of a flea with each of its hosts amongst all regions surveyed were found in all but two of the flea species investigated, with one-fifth of these being significant. If overlap in geographical range between flea and host is used as a measure of frequency of encounters instead of the actual proportion of regions where they both occur, similar patterns are observed, though they are much weaker. In a comparative analysis across all flea species, there were significant relationships between the average abundance of fleas and average values of both measures of frequency of encounters (proportion of sites where they co-occur and range overlap), even when correcting for potential phylogenetic influences. The results suggest that for any given flea species, host species more commonly encountered throughout the spatial range of the flea are generally those on which the flea does best. Interaction frequency may be a key determinant of specialisation and abundance in host-parasite systems.     

Genetics of the ability of Phyllotreta nemorum larvae to survive in an atypical host plant, Barbarea vulgaris ssp. arcuata

A polymorphism in host plant exploitation has been discovered in the flea beetle, Phyllotreta nemorum L. (Coleoptera: Chrysomelidae: Alticinae) where one resistant population is able to use Barbarea vulgaris R.Br. ssp. arcuata (Opiz.) Simkovics (Brassicaceae) as a host plant while a susceptible population is not. Crosses (F1, F2, and backcrosses) between the two flea beetle populations were made, and survival of the progeny on B. v. ssp. arcuata was measured. The ability of P. nemorum larvae to survive in this plant species depended on the presence of major, dominant genes (R-genes). The two most abundant R-genes in the resistant flea beetle population were X- and Y-linked, respectively. The use of B. v. ssp. arcuata as a natural host plant by the resistant population of P. nemorum seems to be an extension of the host plant range of the species. The role of sex-linked genes in the evolution of host range is discussed.     

Plague management of prairie dog colonies: degree and duration of deltamethrin flea control

Plague is a flea‐borne disease of mammalian hosts. On the grasslands of western North America, plague stifles populations of Cynomys spp. prairie dogs (PDs). To manage plague, PD burrows are treated with 0.05% deltamethrin dust that can suppress flea numbers and plague transmission. Here, we evaluate the degree and duration of deltamethrin flea control with three PD species at six sites across four U.S. states. Data were simultaneously collected at paired plots. Burrows from one randomly assigned member of each pair were treated with deltamethrin; non‐treated plots served as experimental baselines. Flea control was strong ≤two months after treatment, remained moderate one year later, and was statistically detectable for up to two years at some sites. Flea abundance was lower in plots with higher rates of deltamethrin application. After burrow treatments, flea abundance increased over time, reaching >one per PD within 255 to 352 days. Nevertheless, annual treatments of burrows with deltamethrin provided PDs with substantial protection against plague. Even so, deltamethrin should be further evaluated and combined with other tools under an integrated approach to plague management. Integrated plague management should help to conserve PDs and species that associate with them, including the endangered black‐footed ferret (Mustela nigripes).     

Australia’s vanishing fleas (Insecta: Siphonaptera): a case study in methods for the assessment and conservation of threatened flea species

While invertebrate conservation is attracting increased funding and interest, research remains heavily skewed towards ‘flagship’ insect groups like bees and butterflies. This has resulted in a knowledge gap relating to less popular but equally imperilled groups like fleas. Methods for the risk assessment of host specific parasites were used to determine the conservation status of all host specific flea species distributed in Australia. The results indicated one species apparently extinct, two critically endangered, two endangered, and three vulnerable. Based on these results, novel methods for the conservation of threatened fleas are outlined, including the concepts of holistic conservation and the cryptic loss effect.     

Fleas of Small Mammals on Reunion Island: Diversity,Distribution and Epidemiological Consequences

The diversity and geographical distribution of fleas parasitizing small mammals have been poorly investigated on Indian Ocean islands with the exception of Madagascar where endemic plague has stimulated extensive research on these arthropod vectors. In the context of an emerging flea-borne murine typhus outbreak that occurred recently in Reunion Island, we explored fleas'' diversity, distribution and host specificity on Reunion Island. Small mammal hosts belonging to five introduced species were trapped from November 2012 to November 2013 along two altitudinal transects, one on the windward eastern and one on the leeward western sides of the island. A total of 960 animals were trapped, and 286 fleas were morphologically and molecularly identified. Four species were reported: (i) two cosmopolitan Xenopsylla species which appeared by far as the prominent species, X. cheopis and X. brasiliensis; (ii) fewer fleas belonging to Echidnophaga gallinacea and Leptopsylla segnis. Rattus rattus was found to be the most abundant host species in our sample, and also the most parasitized host, predominantly by X. cheopis. A marked decrease in flea abundance was observed during the cool-dry season, which indicates seasonal fluctuation in infestation. Importantly, our data reveal that flea abundance was strongly biased on the island, with 81% of all collected fleas coming from the western dry side and no Xenopsylla flea collected on almost four hundred rodents trapped along the windward humid eastern side. The possible consequences of this sharp spatio-temporal pattern are discussed in terms of flea-borne disease risks in Reunion Island, particularly with regard to plague and the currently emerging murine typhus outbreak.     

Seasonal dynamics of a flea number (Siphonaptera) on the common shrew (Sorex araneus) in the north part of the Novgorod oblast

In the course of 5-year stationary investigations of the common shrew Sorex araneus in the north part of the Novgorod oblast, 12 flea species have been recorded on this host. Among them, Palaeopsylla soricis and Doratopsilla dasycnema are specific parasites of small insectivores, including the common shrew. Hystrichopsylla talpae is a polyxenous species, parasitizing both rodents and insectivores. Other 9 flea species are not common parasites of S. araneus and apparently have come to this host from other mammal species inhabiting the forest biotopes in the area of investigation. P. soricis and D. dasycnema have similar phenology of parasitism. These fleas appear in spring (April), are present during summer and autumn and disappear in winter. During a year, the abundance of these species shows three pikes, which correspond to three generations: spring (April), summer (June-July) and autumn (September-October) generation. The first species dominates in spring (April-May) and in the autumn-winter period, while the second species predominates in summer. These two species comprise over 90% of total number of fleas collected and determine general dynamics of the flea number on the shrews; during the year the flea number has a sinusoidal increasing from spring to autumn and minimum in winter.     

Deconstructing spatial patterns in species composition of ectoparasite communities: the relative contribution of host composition,environmental variables and geography

Aim We determined whether dissimilarity in species composition between parasite communities depends on geographic distance, environmental dissimilarity or host faunal dissimilarity, for different subsets of parasite species with different levels of host specificity. Location Communities of fleas parasitic on small mammals from 28 different regions of the Palaearctic. Method Dissimilarities in both parasite and host species composition were computed between each pair of regions using the Bray–Curtis index. Geographic distances between regions were also calculated, as were measures of environmental dissimilarity consisting of the pairwise Euclidean distances between regions derived from elevation, vegetation and climatic variables. The 136 flea species included in the dataset were divided into highly host‐specific species (using 1–2 host species per region, on average), moderately host‐specific species (2.2–4 hosts per region) and generalist species (>4 hosts per region). The relative influence of geographic distance, host faunal dissimilarity and environmental dissimilarity on dissimilarity of flea species composition among all regions was analysed for the entire set of flea species as well as for the three above subsets using multiple regressions on distance matrices. Results When including all flea species, dissimilarity in flea species composition was affected by all three independent variables, although the pure effect of dissimilarity in host species composition was the strongest. Results were different when the subsets of fleas differing in host specificity were treated separately. In particular, dissimilarity in species composition of highly host‐specific fleas increased solely with environmental dissimilarity, whereas dissimilarity for both moderately specific and non‐specific fleas increased with both geographic distance and dissimilarity in host species composition. Main conclusions Host specificity seems to dictate which of the three factors considered is most likely to affect the dissimilarity between flea communities. Counter‐intuitively, environmental dissimilarity played a key role in determining dissimilarity in species composition of highly host‐specific fleas, possibly because, although their presence in a region relies on the occurrence of particular host species, their abundance is itself mostly determined by climatic conditions. Our results show that deconstructing communities into subsets of species with different traits can make it easier to uncover the mechanisms shaping geographic patterns of diversity.     

Spatial variation in species diversity and composition of flea assemblages in small mammalian hosts: geographical distance or faunal similarity?

Aim Spatial variation in the diversity of fleas parasitic on small mammals was examined to answer three questions. (1) Is the diversity of flea assemblages repeatable among populations of the same host species? (2) Does similarity in the composition of flea assemblages among populations of the same host species decay with geographical distance, with decreasing similarity in the composition of local host faunas, or with both? (3) Does the diversity of flea assemblages correlate with climatic variables? Location The study used previously published data on 69 species of small mammals and their fleas from 24 different regions of the Holarctic. Methods The diversity of flea assemblages was measured as both species richness and the average taxonomic distinctness of their component species. Similarity between flea assemblages was measured using both the Jaccard and Morisita–Horn indices, whereas similarity in the composition of host faunas between regions (host ‘faunal’ distance) was quantified using the Jaccard index. Where appropriate, a correction was made for the potentially confounding influence of phylogeny using the independent contrasts method. Results Flea species richness varied less within than among host species, and is thus a repeatable host species character; the same was not true of the taxonomic distinctness of flea assemblages. In almost all host species found in at least five regions, similarity in flea assemblages decreased with increases in either or both geographical and faunal distance. In most host species, the diversity of flea assemblages correlated with one or more climatic variable, in particular mean winter temperature. Main conclusions Spatial variation in flea diversity among populations of the same mammal species is constrained by the fact that it appears to be a species character, but is also driven by local climatic conditions. The results highlight how ecological processes interact with co‐evolutionary history to determine local parasite biodiversity.