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Khan Et Al., 2023. A New SP., of Diptilomiopus
Khan Et Al., 2023. A New SP., of Diptilomiopus
https://www.mapress.com/zt/
Copyright © 2023 Magnolia Press
Article ZOOTAXA
ISSN 1175-5334 (online edition)
https://doi.org/10.11646/zootaxa.5375.1.5
http://zoobank.org/urn:lsid:zoobank.org:pub:55AA33AF-56BE-4EA9-8383-EEA56D4B902B
Abstract
The subfamily Diptilomiopinae Keifer and the genus Diptilomiopus Nalepa (Prostigmata; Eriophyoidea; Diptilomiopidae)
are recorded for the first time from Saudi Arabia with the description and illustration of a new species, D. bahaensis sp.
nov., collected from Ficus carica L. (Moraceae). Additionally, a key to diptilomiopid mite species reported from the plant
family Moraceae is provided, along with their distribution and habitus to the host plants.
Introduction
The mite family Diptilomiopidae Keifer Nalepa (Prostigmata; Eriophyoidea) includes two subfamilies;
Diptilomiopinae Keifer (tarsal empodium divided) and Rhyncaphytoptinae Roivainen (tarsal empodium entire)
(Amrine et al. 2003). These subfamilies are comprised of 35 genera (above 324 species) and 18 genera (206 species),
respectively (Craemer et al. 2017; Liu et al. 2019; Xue & Li, 2020; Varandi et al. 2022; Qin et al. 2022; Qin et al.
2023).
The genus Diptilomiopus belong to subfamily Diptilomiopinae, erected by Nalepa based on the type species,
D. javanicus (Nalepa 1916). This genus is morphologically distinct from other closely related genera by absence of
coxal seta 1b and genu segment on all legs (Amrine et al. 2003). It includes more than 100 species and most of them
have been reported from dicotyledonous host plants in the oriental region of the world (Liu et al. 2019).
The plant family Moraceae (often known as fig or mulberry family) is comprised of 38 genera and over 1100
species widely distributed over the world (The Plant List 2023). Until now, 27 species of family Diptilomiopidae
have been reported from the Moraceae plant family, of which 13 species were from Ficus spp., four from Morus
spp., and two species each from Maclura spp., Broussonetia spp., Streblus spp., and Artocarpus spp (Amrine &
de Lillo, 2011 unpublished databases). Most of the diptilomiopid mite species, reported on the host plant family
Moraceae, belong to the genus Diptilomiopus (Chakrabarti et al. 2019).
From Saudi Arabia (SA), the family Diptilmiopidae was previously known with only one species; Rhyncaphytoptus
ficifoliae Keifer reported from Ficus carica (Moraceae) (Alatawi & Halawa 2011). In the present study, a new
species; Diptilomiopus bahaensis sp. nov. is described and illustrated, collected from Ficus carica (Moraceae),
Baha, SA. Moreover, a key to all known species of the family Diptilomiopidae, their distribution and habitus with
host plant family Moraceae are provided (Table 1).
KHAN ET AL.
TABLE 1. (Continued)
Subfamily Genus Species Distribution Genus Species Relationship Reference
asperis Ghosh & Vagrant under leaf Ghosh & Chakrabarti
India Streblus asper
Chakrabarti surface 1989
racemosae (Chandrapatya Chandrapatya and
Thailand Ficus racemosa Vagrant
& Boczek) Boczek 2001
benjaminae (Boczek & Vagrant on lower Boczek and
Thailand Ficus benjamina
Chandrapatya) surface Chandrapatya 2002
cumingis Huang China Ficus cumingii Vagrant Huang 2001
Vagrant on lower Boczek &
strebli (Boczek) Thailand Streblus asper
surface Chandrapatya 1992
Diptilomiopus Vagrant on lower
sabahus Liu, Yuan & Xue Malaysia Morus unknown Liu et al. 2019
surface
Different plant foliage (leaves, twigs and branches) was snipped from the host plants and placed in polythene
bags along with paper towels and stored in the ice box. Mite specimens were collected directly from foliage under
a dissecting stereomicroscope and also by the modified washing method following Monfreda et al. (2007). The
collected specimens were cleared in lactic acid at room temperature and mounted in Keifer’s media (Amrine et al.
2003). The morphological terminology and setal notation follow Lindquist (1996). The generic key by Amrine et al.
(2003) was used for the genus identification. Different body parts were imaged by using an auto-montage software
system (Syncroscopy, Cambridge, UK) attached to a phase contrast microscope (DM2500, Leica®, Germany). All
measurements are given in micro-meters (μm). The measurements of the holotype are followed by measurements
of the paratypes as ranges between parentheses. The plant samples were identified by the Department of Botany at
College of Science, King Saud University (KSU). All collected specimens, along with the holotype and paratypes of
new species were deposited at King Saud Museum of Arthropods (KSMA), Acarology section, Department of Plant
Protection, College of Food and Agriculture Sciences, King Saud University, Riyadh, Saudi Arabia.
Results
Diagnosis. Based on the Amrine et al. 2003, and Liu et al. 2019.
Prodorsal shield typically marked by a network design; both legs with genua absent, femoral and tibial setae
absent in both legs, tarsal setae ft‘ on leg II absent, coxal setae 1b absent, setae 1a and 2a present, scapular tubercles
can be present or absent, if present then small and placed ahead of rear shield margin, scapular setae absent.
Diagnosis (Female). Prodorsal ornamentation manifest complete network of cells; central cell without median
lines; small rounded scapular tubercles located ahead of rear shield margin, ventral semi-annuali with simple round
microtubercles and ornamentation on coxae I–II with granules; tarsal empodium deeply divided (7 rayed on each
side).
Description
Female (n = 14) Body fusiform (Figures 1D, 2DL), 260 (240–280, including gnathosoma), 78 (69–85) wide, 68
(65–70) thick; dark yellow in life. Gnathosoma, 58 (56–60), projecting downwards, cheliceral stylets 64 (62–68),
pedipalp coxal setae (ep) 2 (1–2), dorsal pedipalp genual setae (d) 3 (3–4), palp tarsal ventral setae (v) 5 (4–5).
Prodorsal shield (Figure 3AD), 35 (33–38) long, 61 (58–64) wide, frontal lobe absent; prodorsal ornamentation
manifest complete network of cells; three rows of cells: 12 cells (six cells on each side) in anterior row, six cells
(three cells on each side) at center row, two cells in posterior row. A central cell without median lines, median line
connected with admedian and submedian lines by transverse lines at the anterior of 1/3 of prodorsal shield, small
rounded scapular tubercles located ahead of rear shield margin, (sc tubercle) 27 (24–27) apart; scapular setae (sc)
absent. Coxigenital region (Figure 3GF), with 6 (5–6) semiannuli between coxae and genitalia, anterolateral setae
on coxisternum І (1b) absent; coxae I and II both with granules/ ornaments, proximal setae on coxisternum І (1a) 14
(15–18), 6 (5–6) apart; proximal setae on coxisternum ІІ (2a) 45 (41–50), 24 (23–26) apart. Prosternal apodeme 5
(4–6). Leg І (Figure 3L1) 31 (30–33); length, femur 16 (15–18), basiventral femoral setae (bv) absent; genu absent;
tibia 8 (5–6), paraxial tibial setae (l‘) absent, tarsus 7 (8–11), paraxial fastigial tarsal setae long, (ft‘) 39 (36–43),
antaxial fastigial tarsal setae (ft‘‘) 43 (39–47); seta (u‘) 11 (9–12), tarsal empodium (em) 7 (6–8), deeply divided,
7 rayed on each side, tarsal solenidion (ω) 7 (6–8), knobbed. Leg ІІ (Figure 3L2), 29 (28–32), femur 16 (14–16),
basiventral femoral setae (bv) absent; genu absent; tibia 5 (4–5); tarsus 8 (7–9), setae (ft‘) absent, setae (ft‘‘) 28 (26–
31) seta (u‘) 5 (5–8) tarsal empodium (em) 8 (7–9), deeply divided, each seven rayed, tarsal solenidion (ω) 7 (6–8),
A new species of the genus Diptilomiopus Nalepa Zootaxa 5375 (1) © 2023 Magnolia Press · 97
FIGURE 2. Diptilomiopus bahaensis sp. nov. Female: DL. Dorso Lateral, Scale bars: 10 µm.
FIGURE 3. Diptilomiopus bahaensis sp. nov. Female: AD. prodorsal shield; CF. coxigenital area; EM. empodium; IG. internal
genitalia; L1. leg І; L2. leg II; Scale bars: 5 µm for AD, CF, L1, L2; 2.5 µm for EM, and IG.
Key to species of the family Diptilomiopidae associated with the plant family Moraceae
A new species of the genus Diptilomiopus Nalepa Zootaxa 5375 (1) © 2023 Magnolia Press · 99
- Central cell without median lines. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
19. Each branch of empodium multi-rayed . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D. broussonetus Liu, Yuan, & Xue
- Each branch of empodium 5-6 rayed. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
20. Leg tarsal seta (ft’, ft’’) divided . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D. sabahus Liu, Yuan, & Xue
- Leg tarsal seta (ft’, ft’’) simple. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D. ficivorus Sarkar
21. Coxal area smooth . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
- Coxal area granulated/punctate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
22. Second row of mid shield with 5 cells; genital area with few granules. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D. cumingis Huang
- Second row of mid shield with 3 cells; genital area entirely smooth. . . . . . . . . . . . . . . . . . . . . . . D. asperis Gosh & Chakrabarti
23. Genital shield entirely smooth. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D. benjaminae (Boczek & Chandrapatya)
- Genital shield granulated. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
24. Dorsal annulai smooth. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
- Dorsal annulai with pointed micortubercles. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
25. Only coxae I granulated, . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D. racemosae (Chandrapatya & Boczek)
- Both coxae granulated . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D. bahaensis sp. nov. Alatawi & Khan
26. Setae h1 absent; empodium 6 rayed. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D. indogangeticus Chakrabarti, Sur, & Sarkar
- Setae h1 present; empodium 8 rayed. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D. ficus Attiah
27. All coxal setae present. . . . . . . . . . . . . . . . . . . . . . . . .Genus Asetadiptacus . . . . . . . . . . . . . . . . . . . . . . . . . A. emiliae Carmona
- Coxal setae 1b absent. . . . . . . . . . . . . . . . . . . . . . . . .Genus Vimola. . . . . . . . . . . . . . . . . . . . . V. artocarpae (Mohanasundaram)
Ecological notes
Twenty-eight species (including the new species), belonging to eleven genera of Diptilomiopidae, associated
with six genera of Moraceae (Table 1). These diptilomiopid mite species are mainly reported from India, China,
Thailand, Malaysia, Portugal, USA, Egypt, and Saudi Arabia (Amrine & de Lillo unpublished databases).
Among the two subfamilies i.e. Rhyncaphytoptinae and Diptilomiopinae, two genera Rhyncaphytoptus and
Diptilomiopus, respectively, were diversely reported on wide variety of Moraceae host plants (Chakrabarti et
al. 2019). Rhyncaphytoptus ficifoliae is abundantly recorded from different regions of the world, infesting Ficus
carica. However, twelve species belonging to the genus Diptilomiopus were infesting four plant genera i.e. Ficus,
Streblus, Morus, and Broussonetia (Amrine & de Lillo unpublished databases). The geographic distribution and
host association essentially depicts the importance of the Diptilomiopus species.
Acknowledgments
We would like to express sincere thanks to Dr. J.W. Amrine Jr (West Virginia University Morgantown, USA), Dr.
Carlos Holger Wenzel Flechtmann (University of São Paulo, Brazil), and Dr. Xiao-Feng Xue (Nanjing Agriculture
University, China) for providing literature. We are also grateful to the two anonymous reviewers for their invaluable
suggestions.
Funding
The authors would like to extend their sincere appreciation for funding this research work through project number
(RSPD2023R807), King Saud University, Riyadh Saudi Arabia.
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