7urn:lsid:arphahub.com:pub:743F3E25-2DA4-586E-9591-5BFF7EF2B593International Journal of MyriapodologyIJM1875-25351875-2543Pensoft Publishers10.3897/ijm.7.30641919Research ArticlesAbacionidaeBlaniulidaeCleidogonidaeEuryuridaeGlomeridaeJulidaeParajulidaePolydesmidaeSpirobolellidaeBiological InvasionsData analysis & ModellingFaunistics & DistributionIdentification keyMacroecologyPopulations & CommunitiesAtlantic OceanIndiana and OhioMaryland and DelawareNebraska and Iowa and IllinoisSouthern and South-Eastern England incl. LondonPhoretic mite associates of millipedes (Diplopoda, Julidae) in the northern Atlantic region (North America, Europe)FarfanMonica A.12KlompenHans2Acarology Laboratory, Ohio State University, Columbus, Ohio, 43212, USAUniversity of Illinois at ChicagoChicagoUnited States of AmericaDept. of Biological Sciences, Univ. Illinois at Chicago, Chicago, Illinois, 60607, USAThe Ohio State University, Museum of Biological DiversityColumbus, OhioUnited States of America
201256201276991E061AC3E-9D10-884F-5A15-FFC0B37CFFF9255299510320122252012Monica A. Farfan, Hans KlompenThis is an open access article distributed under the terms of the Creative Commons Attribution License 3.0 (CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Introduced millipede species in the family Julidae are common in the U.S. but little is known about how they interact with other organisms, such as mites. To start to determine the nature of the relationship, millipedes were sampled from across the eastern U.S.A. and the United Kingdom in 2008–2009. Sixteen morphospecies of mites (Acari: Astigmata, Mesostigmata) were collected from these millipedes, 12 of which from a total of 13 species of julid millipedes. None of these 12 species was restricted to a single host species. However, 12 of the 16 mite species collected were restricted to either the U.S.A. or the U.K. These results are consistent with locality, rather than host, specificity.
Mites evolved relationships with other arthropods between 100–300 million years ago with the diversification of both plants and arthropods in the late Mesozoic era (Southwood 1973). As more niches became available mites developed a wide variety of well-known symbiotic relationships with many arthropods (Lindquist 1975) including many species of myriapods (Maes 1983; Southcott 1987; Bloszyk et al. 2006), especially members of the class Diplopoda, the millipedes. Notably, most available studies are limited to large mites associated with relatively large, tropical species of millipedes (generally length > 3 cm). Most of these mites belong to the suborder Mesostigmata (Table 1). Second, with some exceptions (Lawrence 1939a; Evans and Sheals 1959; Kethley 1978; Ishikawa 1986; Fain 1988; Gu et al. 1991; Fain 1994; Gerdeman and Klompen 2003; Uppstrom and Klompen 2005), most studies do not report a precise identification of the millipede host (even at the generic or familial level). This, of course, makes it difficult to recollect these species or to study their ecological relationships.
Literature records of mesostigmatid mites (Acari: Mesostigmata) associated with Diplopoda. Host names are given as in the original references.
Most mites associated with small millipedes (length < 3 cm) are not Mesostigmata, but belong to the cohort Astigmata. Reported associations of astigmatid mite and millipedes are shown in Table 2. The relationships between astigmatid mites and small millipedes are suspected to be commensalistic (OConnor 2009) although little experimentation has been done to discern the exact nature of the relationship. The cohort Astigmata is characterized by having the second of the three ancestral nymphal instars, the deutonymph, highly modified for dispersal (the hypopus stage) (OConnor 2009). This instar is characterized by the absence of a mouth, a very flat venter and convex dorsum, strong sclerotization of both dorsum and venter, and modification of a number of posterior setae into a postero-ventral attachment organ. The astigmatid deutonymph is considered to be one of the best examples of a phoretic adaptation. A thorough definition of phoresy in mites is given in Houck and OConnor (1991). In broad terms, the deutonymph is a way for phoretic species to disperse from a suboptimal environment which it may not be able to escape on its own.
Literature reports of astigmatid mites (Acari: Astigmata) associated with Diplopoda. Host names are given as in the original references.
The focal taxon for this study are millipedes in the family Julidae. These millipedes, are relatively small (20–40mm), are primarily distributed in the Palaearctic region, and are now found in a variety of anthropogenic habitats in temperate regions. They have also been recorded from many countries in Europe and from Canada, the Tristan da Cunha Island group in the Atlantic Ocean, Mexico, Chile, Peru, New Zealand, South Africa, and Antarctica (Blower 1985). Currently, there are 19 species known from the U.K. (Blower 1985) and 10 from the U.S. (Hoffman 1999). They are assumed to be introduced to the New World from Europe by the deposition of ballast as part of colonial-era shipping (Lindroth 1957; Blower 1985; Shear 1999). Currently, julid millipedes are found in a wide variety of man-made habitats such as residential gardens and parks. Dispersal of these millipedes within North America was, and probably continues to be, mainly through landscape management and transport of plants by humans. This history makes them an ideal test group for examining the effects of recent long range dispersal and possible founder effects.
Between March 2008 and October 2009, millipedes of the family Julidae were collected for a population genetics study. This study allows us to present preliminary data on the following questions:
1. What species are present across the eastern U.S.?
2. What mites are associated with these species?
3. Are there strong indications of host and /or locality specificity?
Host specificity in relationships between the millipedes in the family Julidae and the phoretic mite would be indicated if particular mite species are consistently associated with specific millipede host species. If mites are host specific and there was a founder effect during colonization of the New World, diversity of specific mites in the U.S. is likely to be less than in Europe. Alternately, the presence of mites on a millipede may be based on locality, not host, specificity. This assumes that mites are specific to a certain area or type of off-host habitat. In this case a wide range of hosts occurring in the preferred habitat/locality might be suitable as phoretic host. Predictions for the locality hypothesis are (1) individual mite species will be present on a number of different millipede host species but restricted to certain collection localities; (2) ‘American’, not European, mites will be present on U.S. representatives of European millipede species, and (3) there will be similar mite diversity on U.S. and European populations of the same millipede species.
Material and methodsCollection localities
Millipede specimens were collected from localities in the eastern United States from March through October in 2008 and 2009 and in the United Kingdom in April 2009. Sites in the U.S.A. were chosen to include geographic diversity and to include a number of cities used as colonial ports. While known to be found near such port cities, the current range of julid millipedes is more extensive.
Collection methods
Millipedes were collected by hand except in one instance (Whetstone Park, Columbus, OH) where litter was returned to the Ohio State University Acarology Laboratory (OSAL) for extraction by Berlese funnel. Hand collection was done from wood mulch, leaf litter, and soil. Much collecting was done at the soil/litter interface. Millipedes (with mites associates attached) were collected and placed individually into 1.5 mL vials containing 95% ethanol. Mites release their hold on immersion in alcohol, so individual host preservation is essential. Millipede and mite specimens used in this study are deposited at OSAL. Voucher numbers for representatives of all millipede host species and mite morphospecies, as well as species citations, are listed in Appendices 1 and 2.
Determinations
Millipedes were dissected and, in some cases, genitalia were slide mounted. Specimens were identified using the following keys: Blower (1985), Shear (unpublished key), and Shelley (1978, 1988, 2002). Hoffman’s checklist (1999) was used as a reference for regional distributions.
Mites were sorted to morphospecies using a 12–110× Nikon SMZ dissecting microscope, and some individuals from each morphospecies (including a diversity of hosts and/or sites) were slide-mounted for final identification using a Zeiss Axioskop compound microscope at magnifications up to 1000×. Overall, 148 mites, approximately 11% of total mites collected, were slide mounted. Astigmatid mites were identified to genus using keys by OConnor (unpublished). Specific identification proved impossible as most mite species collected appear to be undescribed. Full description of these mites is beyond the scope of this study, but we do provide some of the characters on which discrimination into morphospecies was based. This should allow evaluation of the validity of those morphospecies concepts.
Prevalence and intensity
Prevalence of the identified mites was calculated for each host species and each locality. Prevalence is defined as: (number of hosts with a particular parasite species) / (number of hosts examined) (Margolis et al. 1982). Higher prevalence results from finding a high number of hosts that were examined are found to be carrying a parasite, or phoretic, species. Additionally, the intensity (average mites per infested host) for each host species was calculated (Margolis et al. 1982). Because not all mites were mounted for identification, prevalence calculations are imperfect. A relatively high percentage of associated mites was mounted for hosts collected < 20 times, and prevalence calculations for those hosts are relatively accurate, but these numbers are minimum estimates for millipedes species where N > 20.
ResultsMillipede Collections
Twenty three species of millipedes were collected representing 9 different families (Table 3). Thirteen of these species belong to the family Julidae, the focus of this study. Six were collected in large numbers (> 100); Brachyiulus pusillus, Cylindroiulus caeruleocinctus, Cylindroiulus latestriatus, Cylindroiulus punctatus, Cylindroiulus truncorum, and Ophyiulus pilosus. Millipedes in the remaining 8 families (Abacionidae, Blaniulidae, Cleidogonidae, Euryuridae, Glomeridae, Parajulidae, Polydesmidae, and Spirobolellidae), with the exception of Blaniulidae, were collected in relatively low numbers.
Intensity (over all mite morphospecies) and prevalence (percentage by mite morphospecies) for mites associated with millipedes examined.
Family
Species
N (millipedes)
Average intensity
Rhizoglyphus A
Rhizoglyphus B
Sancassania A
Sancassania B
Schwiebea A
Schwiebea C
Schwiebea D
Schwiebea E
Schwiebea F
Schwiebea G
Schwiebea H
Thyreophagus sp.
Histiostoma sp.
Cosmolaelaps sp.
Holostapis sp.
Phaulodinychus sp.
Abacionidae
Abacion lactarium
8
3.0
13.0
13.0
Blaniulidae
Blaniulid sp.
104
2.0
2.0
2.0
2.0
2.0
Blaniulus guttulatus
93
1.2
4.0
1.0
Choneiulus palmatus
8
2.4
Nopoiulus kochii
76
1.6
Cleidogonidae
Cleidogona caroliniana
7
2.0
Euryuridae
Euryurus leachii
14
11.3
7.0
7.0
7.0
14.0
14.0
Glomeridae
Glomeris marginata
4
2.7
5.0
Julidae
Brachyiulus lusitanus
16
1.0
Brachyiulus pusillus
208
2.3
1.0
2.0
Cylindroiulus britannicus
35
2.0
3.0
3.0
3.0
3.0
Cylindroiulus caeruleocinctus
365
2.8
2.0
1.0
0.3
0.3
1.0
Cylindroiulus latestriatus
337
1.7
0.3
0.3
0.3
0.3
Cylindroiulus londinensis
2
5.0
50.0
50
Cylindroiulus punctatus
109
3.3
1.0
4.0
1.0
1.0
Cylindroiulus truncorum
171
1.9
1.0
2.0
1.0
1.0
Cylindroiulus sp.
186
2.7
1.0
2.0
1.0
Julus scandinavicus
19
3.2
5.0
5.0
Ommatoiulus sabulosus
9
2.0
11.0
Ophyiulus pilosus
373
2.6
0.3
1.0
Tachypodoiulus niger
2
5.0
50.0
Parajulidae
Uroblaniulus carolinensis
8
2.7
13.0
13.0
Polydesmidae
Polydesmus angustus
6
6.0
17.0
17.0
17.0
17.0
Polydesmus sp.
8
1.0
13.0
Spirobolellidae
Paraspirobolus lucifugus
5
2.9
20.0
40.0
Mite Collections
Representatives of 6 genera of mites were associated with millipedes collected in this study. These mites belong to two families in the cohort Astigmata; Acaridae and Histiostomatidae, and two families in the suborder Mesostigmata; Laelapidae and Uropodidae.
Astigmata
The astigmatid mites represented 13 morphospecies: Rhizoglyphus A and B (Figure 1a and 1c, respectively), Sancassania A and B (Figure 1b), Schwiebea A, C, D, E (Figures 2a, 2b, 2c, & 2d, respectively), F, G, and H (Figures 3a, 3b, & 3c, respectively), Thyreophagus (all Acaridae), and Histiostoma (Histiostomatidae). Specimens of Rhizoglyphus, Sancassania, and Schwiebea were separated into morphospecies by the shape and amount of fusion of the apodemes and the shape of the coxal fields on the venter. These characteristics were chosen because these features are unlikely to be artifacts of the slide-mounting process. The differences between the species can be subtle. Distinguishing characteristics of the morphospecies within the genera Rhizoglyphus, Sancassania,and Schwiebea are detailed in Table 4, and Figures 1–3. Figures show conoidal setae as filled-in circles and simple setae as open circles. The size of the filled-in circles in the diagram is indicative of the relative size of the conoidal setae. Broken lines indicate edges of apodemes with a greater degree of fusion. These edges appear not as distinct or “heavy” as non-fused apodemes. Apodemes and coxal fields are denoted with Roman numerals corresponding with the leg pair they are associates with (e.g., coxal fields II correspond with legs II).
Diagram of the coxal fields and coxal apodemes of aRhizoglyphus A bRhizoglyphus B and cSancassania B.
https://binary.pensoft.net/fig/12570
Diagram of the coxal fields and coxal apodemes of aSchwiebea A bSchwiebea C cSchwiebea D and d Schwiebea E.
https://binary.pensoft.net/fig/12571
Diagram of the coxal fields and coxal apodemes of aSchwiebea F bSchwiebea G and c Schwiebea H.
https://binary.pensoft.net/fig/12572
Comparative characters for Schwiebea (Acari, Astigmata, Acaridae) species associated with millipedes (Diplopoda).
Schwiebea A (Fig. 2A)
Schwiebea C (Fig. 2B)
Schwiebea D (Fig. 2C)
Schwiebea E (Fig. 2D)
Schwiebea F (Fig. 3A)
Schwiebea G (Fig. 3B)
Schwiebea H (Fig. 3C)
Coxal fields II
oval, well-developed
quadrilateral; apodemes straight, well-developed
oval, widened distally, mostly well-developed
quadrilateral; coxal fields I & II contiguous, well-developed
quadrilateral; anterior apodemes II end in distinct curve medially
quadrilateral; fields I & II contiguous, well-developed
oval, well-developed
Posterior edge of coxal fields II
convex, poorly developed medially
concave, poorly developed
convex, poorly developed medially
straight, horizontal, well-developed
slightly concave, quadrilateral edge poorly developed
straight, horizontal, well-developed
median section of posterior curve poorly developed
Anterior edge of coxal fields III
roughly concave, well-developed
concave, poorly developed
slightly concave, well-developed
straight, horizontal, well-developed
slightly concave, poorly developed
straight, horizontal, well-developed
slightly concave at lateral edges, well-developed
Coxal fields III
rounded medially
rounded medially
rounded medially, almost touching
triangular, separated medially
triangular, not touching
connected, quadrilateral
triangular, not touching
Coxal fields IV
triangular
triangular
triangular
deltoid
triangular
deltoid; acutely tapering medially
arrow-shaped
Apodemes III & IV
well-developed
poorly developed
anterior III and median ventral apodemes well-developed; others poorly developed
well-developed
poorly developed
well-developed
mostly well-developed
Median ventral apodemes III
not fused
not fused
almost fused
fused
not fused
not present
not fused, poorly developed
Median ventral apodemes IV
fused, extending to genital opening
not fused, extending to genital opening
fused, terminates half-way to genital opening
fused, extending to genital opening
not fused, extending to genital opening
fused, extending to genital opening
fused, terminates half-way to genital opening
Conoidal setae on coxal field I
medium
medium
large
small
large
very small
very small
Mesostigmata
Mites in the families Laelapidae and Uropodidae were determined to genus. Two genera of laelapids were identified as Cosmolaelaps and Holostaspis, the uropodid as Phaulodinychus.
Julidae - mite associations
Nearly all mite specimens collected from julid millipedes were astigmatid deutonymphs. Morphospecies of Schwiebea were the most commonly collected from these millipedes (Table 3). Rhizoglyphus A was collected from the highest number of julid species in this study (n = 9). This was followed by Histiostoma sp. (n = 6). Thyreophagus specimens were found on Ommatoiulus sabulosus and Cylindroiulus britannicus only. Schwiebea D, E, and G and Phaulodinychus sp. were also collected from one julid host species only. Phaulodinychus sp. was collected only once on a julid millipede, Cylindroiulus latestriatus. There were no laelapid mites collected from julid millipedes.
Cylindroiulus caeruleocinctus had five species of mite associates which was the highest diversity among julids. Tachypodoiulus niger and Ommatoiulus sabulosus had the fewest associate species (one species each).
Prevalences were found to range from 0.27%–50.0% (minimum estimates). Notable are the associations of Schwiebea H on Tachypodoiulus niger (N=2), and Rhizoglyphus A and Histiostoma sp. on Cylindroiulus londinensis (N= 2), each with the highest prevalence of 50.0%. The lowest prevalence was calculated for Rhizoglyphus Aon Ommatoiulus pilosus (0.27%) (but see comments in Material and Methods). Intensity also tends to be low. The average intensities for the six most common julid species ranged from 1.66–3.32 mites per host with an average of 2.43. This is probably close to the average intensity for all Julidae.
Non-julid millipede collections
Schwiebea C was collected from the highest number of non-julid hosts (n = 5). Polydesmus angustus was associated with 4 morphospecies of Schwiebea, all collected from one host individual. Histiostoma sp. and three species of Schwiebea have been collected from the combined specimens in the family Blaniulidae. The two taxa collected from Uroblaniulus carolinenesis and Paraspirobolus lucifugus were Histiostoma sp. and Schwiebea C. Abacion lactarium was the only species, julid or non-julid, to have Rhizoglyphus B as an associate. The euryurid Euryurus leachii was the only millipede host to have mite associates in the family Laelapidae. Representatives of two genera, Cosmolaelaps and Holostaspis,were collected. Consistent with the general association pattern of Laelapidae, these mites were collected as adults, not deutonymphs. Additionally, a considerable number of deutonymphs of the uropodine Phaulodinychus sp. were collected from this millipede. Euryurus leachii was the millipede with the highest intensity (11.27) and the largest number of mite species among the non-julids with five mite morphospecies.
The prevalence of mites found on non-julid millipedes was generally high. This may be associated with the fact that the numbers of non-julids collected were relatively low, with the exception of blaniulids. For example, 50.0% of the Glomeris marginata (N = 4) carried Schwiebea E. Blaniulids were collected most commonly, and showed prevalences between 0.94–3.77% for their mite associates Schwiebea D, E, and F, and Histiostoma sp.
Mite taxa and telation to locality
Only four mite species were collected from localities in both the U.S.A. and in the U.K., Rhizoglyphus A, Schwiebea C, Schwiebea F, and Histiostoma sp. (Table 5). Mite taxa that were found exclusively in the U.S.A. are Rhizoglyphus B, Sancassania A, Sancassania B, Schwiebea D, Cosmoglyphus sp., Holostapis sp. and Phaulodinychus sp. Taxa found only in the U.K. Schwiebea A, Schwiebea E, Schwiebea G, Schwiebea H, and Thyreophagus sp. The highest diversity of mite taxa by locality was found in Cornwall, U.K. Only one mite taxon each was collected in Chicago, IL, Columbus, OH, and Lakewood, OH.
Prevalence (percentage) of mites on millipedes (all species combined) by collecting locality.
Locality
N (millipedes)
Rhizoglyphus A
Rhizoglyphus B
Sancassania A
Sancassania B
Schwiebea A
Schwiebea C
Schwiebea D
Schwiebea E
Schwiebea F
Schwiebea G
Schwiebea H
Thyreophagus sp.
Histiostoma sp.
Cosmolaelaps sp.
Holostapis sp.
Phaulodinychus sp.
North Kingstown, RI
175
1
3
1
1
2
Chicago, IL
452
1
Lakewood, OH
61
2
Cleveland, OH
119
2
1
Delaware, OH
23
9
4
4
Columbus, OH
1054
1
Southern Ohio
7
14
29
33
Baltimore, MD
102
8
1
3
2
Charlotte, NC
161
1
1
1
1
Fort Mill, SC
15
7
7
7
Cornwall, UK
59
2
2
2
2
2
2
2
2
Eden Project, UK
56
2
4
2
2
5
Slough, UK
27
7
19
7
4
4
4
4
Of the seven millipede species collected in both the U.S.A. and the U.K. only Cylindroiulus caeruleocinctus had the same mite associates in both countries, Rhizoglyphus A and Histiostoma sp. (Table 5). Mite associates of the other six species of millipedes did not appear in both countries on the same julid host species.
Discussion
The current study does not suggest strong host specificity of mite species for julid hosts. The only species that were collected from only one host, Rhizoglyphus B, Cosmolaelaps sp. and Holostaspis sp. are rare, and (so far) exclusively associated with non-julid hosts. This result supports the view of OConnor (1998) who noted that acarids are (1) often associates of a wide variety of hosts and (2) are often cosmopolitan. There is precedent for this in terms of millipede-associated Mesostigmata. While most Heterozerconidae are associated with large millipedes, one genus, Amheterozercon (Fain 1989), is associated with snakes and amphisbaenids (Flechtmann and Johnston 1990). Similarly, most Paramegistidae are associates of carabid beetles or millipedes, except for the genus Ophiomegistus (Banks 1914) which is associated with skinks and snakes (Klompen and Austin 2005). These records suggest that these mites may favor a host with a specific type of locomotion, general distance from the ground, or habitat preference, at best a modified host specificity.
Neither is there strong overlap of the mite fauna of specific julid millipedes collected both in the U.S.A. and the U.K., another prediction of the host specificity hypothesis. Only one millipede species (Cosmolaelaps caeruleocinctus) carried the same mite species in both the U.S.A. and the U.K. In a comparison of mite associates found on millipedes and the locality in which they were found (Table 5), 12 of the 16 taxa were collected in either the U.S.A. or the U.K. Only four were collected from both countries. This is an indication that the mites are most likely not associated with specific hosts but, instead, are favoring hosts associated with specific habitats.
An unusual finding regarding mite associates was the collection of a species in the genus Thyreophagus collected in the U. K. Past reports of Thyreophagus sp. are mostly from the U.S.A. Thyreophagus is a mite thought to be associated only with subcortical insects (OConnor 1982) with often high host specificity (OConnor 1984). This is very different from the lifestyles of the other acarids collected in this study that seem to be very general in their host choice. Ommatoiulus sabulosus and Cylindroiulus britannicus were the hosts of this mite. They were collected from an outdoor garden and a greenhouse/conservatory in Cornwall, U.K., sites which were a good distance from each other. A further survey of ground arthropods in Cornwall could help clarify the degree of specificity of this genus in the area.
Acknowledgements
Thanks to Helen J. Read, and the British Myriapod and Isopod Group for their help in the collection of specimens, and to Barry OConnor for permission to use his unpublished keys to Astigmatid genera. Thanks to John W. Wenzel, currently Carnegie Mellon University, and Andrew P. Michel, OSU Department of Entomology, for their kind review of earlier drafts of this publication.
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Pt 2. The family Diplogyniidae (Mesostigmata-Trigynaspida).81: 13-29.Appendix 1
Voucher numbers for millipede hosts.
Millipede species
Author, year
Accession number
Abacion lactarium
(Say, 1821)
N/A
Blaniulus guttulatus
(Fabricius, 1789)
OSAL0100704 ♂
Brachyiulus lusitanus
Verhoeff, 1898
OSAL0100959 ♂
*OSAL006951 ♂
Brachyiulus pusillus
(Leach, 1815)
OSAL0100593 ♂
Choneiulus palmatus
(Nemec, 1895)
OSAL0100811 ♂
Cleidogona caroliniana
Causey, 1957
OSAL0100283 ♂
Cylindroiulus britannicus
(Verhoeff, 1891)
OSAL0100455 ♀
OSAL0100394 ♂
*OSAL006949 ♀
*OSAL006950 ♂
Cylindroiulus caeruleocinctus
(Wood, 1864)
OSAL0100759 ♂
*OSAL006948 ♂
Cylindroiulus latestriatus
(Curtis, 1845)
OSAL0100650 ♂
*OSAL006947 ♂
Cylindroiulus londinensis
(Leach, 1815)
OSAL0100375 ♂
*OSAL006955 ♂
Cylindroiulus punctatus
(Leach, 1815)
OSAL0100417 ♂
Cylindroiulus truncorum
(Silvestri, 1896)
OSAL0100935 ♀
OSAL0100536 ♂
*OSAL006952 ♂
Euryurus leachii
(Gray, 1832)
OSAL0100840 ♂
Glomeris marginata
(Villers, 1789)
OSAL0100376 ♂
Julus scandinavicus
Latzel, 1884
OSAL0100358 ♂
Nopoiulus kochii
(Gervais, 1836)
OSAL0100282 ♂
Ommatoiulus sabulosus
(Linné, 1815)
OSAL0100403 ♂
Ophyiulus pilosus
(Newport, 1843)
OSAL0100423 ♀
OSAL0100613 ♂
*OSAL006954 ♀
*OSAL006953 ♂
Paraspirobolus lucifugus
(Gervais, 1836)
OSAL0100386 ♂
Polydesmus angustus
(Latzel 1884)
OSAL0100439 ♂
Tachypodoiulus niger
(Leach, 1815)
OSAL0100384 ♂
Uroblaniulus carolinensis
Causey, 1953
OSAL0100882 ♂
* denotes slide of genitalia
Appendix 2
Voucher numbers for associated mite morphospecies.