Research Article |
Corresponding author: Hirotaka Tanaka ( coccoidea@gmail.com ) Academic editor: Roger Blackman
© 2018 Hirotaka Tanaka.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Tanaka H (2018) First records of the genus Pelionella Kaydan, 2015 in East Asia, with description of a new species (Hemiptera, Coccomorpha, Pseudococcidae). ZooKeys 738: 47-58. https://doi.org/10.3897/zookeys.738.13277
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Two mealybug species (Hemiptera: Coccomorpha: Pseudococcidae), Pelionella osakaensis sp. n. and P. manifecta (Borchsenius, 1949), are described and illustrated based on adult female specimens collected in Japan, on the Japanese mugwort Artemisia indica var. maximowiczii (Nakai) H. Hara (Asteraceae). These are the first records of the occurrence of Pelionella species in East Asia. The new species is similar to P. grassiana (Goux, 1989) and P. proeminens (Goux, 1990), but differs in lacking multilocular pores with double loculi rings on the venter and in possessing dorsal cerarii and a circulus. The Japanese population of P. manifecta is morphologically slightly different from the Azerbaijani and French populations in lacking large-type oral-collar tubular ducts associated with clusters formed by multilocular pores and oral-collar ducts on ventral abdominal segments III and IV. A modified key to species of the genus Pelionella Kaydan, 2015, is provided.
Artemisia indica , Japanese mugwort, new distribution record, taxonomy
A genus of Pseudococcidae (Hemiptera: Coccomorpha), Pelionella Kaydan, 2015, was erected by
Recently, the author examined specimens of two species of Pelionella collected from Japan, and recognized among the samples the type species of the genus, Pelionella manifecta (Borchsenius, 1949), and a single specimen of an undescribed species. The former showed slight differences from western populations in some morphological character states. This paper describes or diagnoses and illustrates both species collected from Japan based on adult female morphology, and constitutes the first record of the occurrence of Pelionella species in East Asia. A modified key to species of the genus Pelionella is also given.
This new distribution record for P. manifecta, and the description of a new species of Pelionella with unique morphological features (i.e., presence of several dorsal cerarii distinctly elevated from dorsal surface) may be useful for understanding and furthering studies on the diversity, morphology, and biogeography of this genus and other related mealybug species.
Examined materials were collected by I. Takahashi, J. Imai, or K. Fujimoto in the fall (from October to November) of 2014. The adopted slide-mounting method is a slight modification of
Pelionella Kaydan, 2015: 226.
Pelionella ; Danzig & Gavrilov-Zimin, 2014: 449 (Unavailable name).
Peliococcus manifectus Borchsenius, 1949: 245.
Peliococcus manifectus Borchsenius, 1949: 245: Danzig, 2001: 125.
Peliococcus albertaccius Goux, 1990: 83.
Pelionella
manifecta
(Borchsenius, 1949);
All three adult females from Japan collected on Artemisia indica var. maximowiczii (Nakai) H. Hara (Asteraceae). Osaka-pref., Sennan City, Kansai International Airport, on: 1 adult female, 7.X.2014, coll. I. Takahashi; 1 adult female, 12.X.2014, coll. K. Fujimoto. Hyogo-pref., Kobe City, Chuo-ku, Minato-jima, Naka-machi: 1 adult female, 8.XI.2014, coll. J. Imai (
Slide-mounted specimens of Japanese populations, n = 3.Adult female. Body elongate oval, 1.7–3.1 mm long, 0.9–1.8 mm wide. Eyes on margins, each 31–44 μm in diameter. Antenna 9-segmented, 393–444 μm long; apical segment 58–60 μm long, 22–25 μm wide; with two apical setae each 36–45 μm long, and three fleshy setae 18–30 μm long. Labium 95–110 μm long, 80–88 μm wide. Circulus oval, 95–100 μm wide, situated just anterior to fold between abdominal segments III and IV. Legs well developed; hind legs: coxa 120–140 μm long; trochanter + femur 248–282 μm long; tibia + tarsus 285–306 μm long; claw 30–32 μm long; translucent pores absent. Ratio of lengths of tibia + tarsus to trochanter + femur 1.05–1.18:1; ratio of lengths of tibia to tarsus 2.0–2.41:1; ratio of length of trochanter + femur to greatest width of femur 3.22–4.10:1. Tarsal digitules hair-like, each 23–30 μm long. Claw digitules knobbed, each 25–29 μm long. Claw with well-developed denticle on plantar surface. Anterior ostioles each with a total for both lips of 15–25 trilocular pores and 2–5 setae; posterior ostioles each with a total for both lips of 24–37 trilocular pores and 4–7 setae. Anal ring 73–108 μm wide, bearing 6 setae, each seta 127–190 μm long.
Dorsum. Setae spine-like, each 5–15 μm long. Cerarii on margin somewhat prominent, slightly sclerotized, numbering 18 pairs; anal lobe cerarii each with 1–2 slender enlarged setae, each 10–22 μm long, and one or two spine-like auxiliary setae; other cerarii mostly each with two enlarged setae and several trilocular pores. Clusters of multilocular pores with double rings present on head and thorax and on abdominal segments as follows: I 9–12, II 12, III 14–15, IV 16–19, V 18–22, VI 10–15, VII 9–11, VIII 0; each cluster containing 1–7 (usually 2-3) multilocular pores with double rings, each pore 6.0–7.1 μm in diameter; a small oral-collar tubular duct, 0.5–1.8 μm wide; 1–5 large oral-collar tubular ducts, each 2.4–3.4 μm wide; and 1–3 minute discoidal pores, each 1.1–1.3 μm in diameter. Trilocular pores, each 3.2–3.9 μm in diameter, scattered throughout. Minute discoidal pores mainly restricted to within clusters.
Venter. Setae of two types: (i) slender hair-like setae, each 10–142 μm long, longest setae situated medially on head; and (ii) spine-like setae in submarginal areas, each 4–12 μm long. Apical setae of anal lobes 198–228 μm long. Multilocular disc pores with single ring, each 5.0–6.8 μm in diameter, present in 15–25 clusters on medial areas of abdominal segments III and IV; each cluster containing 1–5 (usually 2–3) multilocular disc pores surrounding a small oral-collar tubular duct; similar multilocular disc pores present also in single rows on other abdominal segments, as follows: V 7–8, VI 43–47, VII 62–69, VIII + IX 38–46. Multilocular pores with double rings, each 6.6–7.9 μm in diameter, restricted to submarginal areas of head, thorax, and abdomen, usually not arranged in clusters. Quinquelocular pores, each 3.2–5.6 μm in diameter, scattered medially on head, thorax, and medial area of abdominal segments. Trilocular pores, each 2.6–3.2 μm in diameter, scattered throughout. Minute discoidal pores, each 0.8–1.3 μm in diameter, few. Oral-collar tubular ducts of two sizes: small ducts restricted to within clusters; and large-sized ducts, each 2.1–2.9 μm wide, present on body margin and in single rows across posterior abdominal segments; also a few on head, thorax and abdominal segments II and III.
Pelionella manifecta (Borchsenius, 1949) collected in Japan. Adult female. Abbreviations: ALC, anal lobe cerarius ANT antenna DC dorsal cluster DS dorsal setae DMP Multilocular pore with double rings LG leg MP multilocular pore OCD oral-collar tubular ducts PC Penultimate cerarius QP quinquelocular pore TP trilocular pore VC ventral cluster. Scale bars: 200 µm (ANT, LG); 50 µm (ALC, PC); 10 µm for the others.
Armenia, Azerbaijan, Corsica, France, Italy, Kazakhstan, Russia (Krasnodar Territory), Sardinia, Sweden, Turkey (
The Japanese specimens of Pelionella manifecta described here differ slightly from the Azerbaijani and French material described by
In Japan, this species was collected from Kansai International Airport, one of the largest airports in the country, and from the large sea-port island of Kobe City (Minato-jima), both of which are centres of international trade. Furthermore, the species has not hitherto been recorded further east than Kazakhstan. This suggests that the species might not be truly endemic to Japan, but be a recent introduction. Studies of the detailed distribution of the species in Japan, and the current condition of the species at the sites where it was collected originally, may be important from both biological and plant-quarantine perspectives.
Comparisons of morphometric data between adult females of Japanese and Western Eurasian populations of Pelionella manifecta.
Morphological features | Measurements of Japanese specimens (n = 3) | Measurements of Azerbaijani and French specimens (from Kaydan, 2015) (n = 5) |
---|---|---|
General morphological features | ||
Length of body | 1.7–3.1 mm | 1.36–1.88 mm |
Width of body | 0.9–1.8 mm | 0.86–1.10 mm |
Width of eyes | 31–44 µm | 47.5–60.0 µm |
Lendth of antenna (total) | 393–444 µm | 410–425 µm |
Length of antenna’s apical segment | 58–60 µm | 60 µm |
Width of antenna’s apical segment | 22–25 µm | 20–28 µm |
Length of antenna’s apical setae | 36–45 µm | 27–45 µm |
Length of fleshly setae on antenna’s apical segment | 18–30 µm | 25–33 µm |
Length of labium | 95–110 µm | 135–140 µm |
Width of labium | 80–88 µm | 95 µm |
Width of circulus | 95–100 µm | 65–85 µm |
Length of hind coxa | 120–140 µm | 155–175 µm |
Length of hind trochanter and femur | 248–282 µm | 240–260 µm |
Length of hing tibia and tarsus | 285–306 µm | 260–280 µm |
Length of hind claw | 30–32 µm | 25–30 µm |
Ratio of lengths of hind tibia + tarsus to hind trochanter + femur | 1.05–1.18:1 | 1.07–1.23:1 |
Ratio of lengths of hind tibia to hind tarsus | 2.0–2.41:1 | 2.16–2.41:1 |
Ratio of length of hind trochanter + femur to greatest width of hind femur | 3.22–4.10:1 | 3.42–4.0:1 |
Length of hind tarsal digitules | 23–30 µm | 20–23 µm |
Length of hind claw digitules | 25–29 µm | 20–25 µm |
Morphological features on Dorsum | ||
The number of triolocular pores on anterior ostiole | 15–25 | 21–30 |
The number of setae on anterior ostiole | 2–5 | 2–4 |
The number of triolocular pores on posterior ostiole | 24–37 | 32–40 |
The number of setae on posterior ostiole | 4–7 | 2–4 |
Width of anal ring | 73–108 µm | 85–110 µm |
Lenth of anal ring setae | 127–190 µm | 115–145 µm |
Length of anal lobe cerarian setae | 10–22 µm | 17–23 µm |
The number of auxiliary setae on anal lobes | 1–2 | 3–4 |
Length of dorsal setae | 5–15 µm | 7.5–15 µm |
The number of multilocular pore with double rings in clusters | 1–7 | 2–6 |
Width of multilocular pores with double rings in clusters | 6.0–7.1 µm | 7.5–10.0 µm |
Width of small oral collar tubular ducts in clusters | 0.5–1.8 µm | 3.0–4.0 µm |
Width of large oral collar tubular ducts in clusters | 2.4–3.4 µm | 4.0–5.0 µm |
The number of minute discoidal pores in clusters | 1–3 | 1–4 |
Width of minute discoidal pores in clusters | 1.1–1.3 µm | 2 µm |
The number of dorsal clusters in abdominal segment I. | 9–12 | 9–11 |
The number of dorsal clusters in abdominal segment II. | 12 | 10 |
The number of dorsal clusters in abdominal segment III. | 14–15 | 11–13 |
The number of dorsal clusters in abdominal segment IV. | 16–19 | 11–15 |
The number of dorsal clusters in abdominal segment V. | 18–22 | 12 |
The number of dorsal clusters in abdominal segment VI. | 10–15 | 8–11 |
The number of dorsal clusters in abdominal segment VII. | 9–11 | 10–14 |
Width of triolocular pores | 3.2–3.9 µm | 3–5 µm |
Morphological features on Venter | ||
Length of slender hair-like setae | 10–142 µm | 15–88 µm |
Length of spine-like setae | 4–12 µm | 10.0–12.5 µm |
Length of apical setae on anal lobes | 198–228 µm | 145–185 µm |
Width of multilocular pores with double rings | 6.6–7.9 µm | 7.5–10.0 µm |
Witdth of multilociular pores with single ring | 5.0–6.8 µm | 7.5–10.0 µm |
The number of clusters on abdominal segments III-IV | 15–25 | 10–14 |
The number of multilocular pores on abdominal segment V. | 7–8 | 2–3 |
The number of multilocular pores on abdominal segment VI. | 43–47 | 14–18 |
The number of multilocular pores on abdominal segment VII. | 62–69 | 34–40 |
The number of multilocular pores on abdominal segments VIII+IX. | 38–46 | 20–23 |
Width of quinquelocular pores | 3.2–5.6 µm | 5.0–7.5 µm |
Width of triolocular pores | 2.6–3.2 µm | 2–3 µm |
Width of minute discoidal pores | 0.8–1.3 µm | 2 µm |
Adult ♀. Japan, Osaka-pref., Sennan City, Kansai International Airport, 12.X.2014, host plant: Artemisia indica var. maximowiczii, coll. K. Fujimoto. (
Eighteen pairs of cerarii present on body margin. Several slightly elevated dorsal cerarii also present on dorsal surface. Clusters of multilocular pores with double rings present on dorsum; each cluster contains 1–2 multilocular pores with double rings, 0–1 small oral-collar tubular ducts, 0–2 large oral-collar tubular ducts, and 0–3 minute discoidal pores. Multilocular pores with double rings and clusters of multilocular disc pores with single ring and oral-collar tubular ducts absent on venter. Circulus oval, present on posterior part of third abdominal segment of venter. Translucent pores absent on hind legs.
Slide-mounted specimen.Adult female. Body elongate oval, 1.7 mm long, 0.9 mm wide. Eyes submarginal, each 30–32 μm in diameter. Antenna 9-segmented, 363–387 μm long; apical segment 53–57 μm long, 20–25 μm wide; with two apical setae each 30–38 μm long, and three fleshy setae each 20–30 μm long. Labium 103 μm long, 68 μm wide. Circulus oval, approx. 74 μm wide, situated on posterior part of third abdominal segment. Legs well developed; posterior legs: coxa 82–85 μm long; trochanter + femur 248–250 μm long; tibia + tarsus 275–278 μm long; claw 30–34 μm long. Translucent pores absent. Ratio of lengths of hind tibia + tarsus to trochanter + femur 1.1:1; ratio of lengths of tibia to tarsus 1.4–1.5:1; ratio of length of trochanter + femur to greatest width of femur 3.0:1. Tarsal digitules hair-like, each 20–31μm long. Claw digitules knobbed, each 28 μm long. Claw with well-developed denticle on plantar surface. Anterior ostioles with a total for both lips of 26 to 30 trilocular pores and 2–3 setae; posterior ostioles with a total for both lips of 33–36 trilocular pores and 5–6 setae. Anal ring 85 μm wide, bearing 6 setae, each seta 103–125 μm long.
Dorsum. Cerarii on margins slightly prominent but with no sclerotization, numbering 18 pairs; anal lobe cerarii each with 2–3 slender enlarged setae, each 11–21 μm long, and 2–3 spine-like auxiliary setae; other cerarii on margins each with 2–3 slender enlarged setae and several trilocular pores. Several dorsal cerarii present on dorsal surfaces as shown in Figure
Venter. Setae of two types: (i) hair-like setae, each 14–81 μm long, longest present on medial area of posterior abdominal segments; and (ii) spine-like setae, each 5–10 μm long, present in submarginal areas. Apical setae of anal lobes each 162–169 μm long. Multilocular disc pores, each 5.5–6.5 μm in diameter, present in bands on abdominal segments as follows: IV 4, V 0, VI 28, VII 34, VIII + IX 29. Quinquelocular pores, each 3.5–4.5 μm in diameter, scattered medially on head, thorax, and first four abdominal segments. Trilocular pores, each 2.8–3.2 μm in diameter, scattered throughout. Minute discoidal pores, each 1.0–1.2 μm in diameter, few in number. Oral-collar tubular ducts of 1size, each 1.9–2.1 μm wide, mostly present in bands across posterior abdominal segments and on medial areas of thoracic segments; a few ducts present in submarginal areas.
Pelionella osakaensis sp. n. adult female (holotype). ALC, anal lobe cerarius ANT antenna DC dorsal cluster DS dorsal setae LG leg MP multilocular pore OCD oral-collar tubular ducts QP quinquelocular pore PC Penultimate cerarius TP trilocular pore. Scale bars: 200 µm (ANT, LG); 50 µm (ALC, PC); 10 µm for the others.
The species is named after the prefecture in Japan where it was collected.
Pelionella osakaensis sp. n. is quite similar to P. grassiana (Goux, 1989) and P. proeminens (Goux, 1990) in having clusters containing one or two multilocular pores with double rings on dorsum and more than 16 pairs of cerarii. However, P. osakaensis differs from the latter species in having a circulus on the posterior part of the third abdominal segment, several slight elevated dorsal cerarii, and in lacking translucent pores on hind legs. Although the presence or absence of a circulus can be variable within a mealybug species, it may be a useful, readily observable diagnostic character for P. osakaensis given the current status of classification of Pelionella species. Pelionella osakaensis is also similar to P. stellarocheae (Goux, 1990) in lacking translucent pores on hind legs and in having smaller number of multilocular pores with double rings in each cluster on dorsum; however, it clearly differs from P. stellarocheae in having 18 pairs of cerarii plus dorsal cerarii. The presence of dorsal cerarii is one of the important features of P. osakaensis, although it may appear to conflict with the generic definition of Pelionella proposed by
Pelionella osakaensis has only been collected from the site of Kansai International Airport, one of the largest airports in Japan, so it is possible that it is not endemic. A more detailed distributional study of the species and the current population level and distribution of the species at the airport may be important in relation to plant-quarantine measures.
1 | Clusters on dorsum each with only 1 size of oral-collar tubular duct; multilocular pores with double rings around cluster without larger oral-collar tubular ducts | 2 |
– | Clusters on dorsum each with 2 sizes of oral-collar tubular ducts, with smaller ducts in center of each cluster and larger ducts and multilocular pores with double rings around cluster (very rarely multilocular pores with double rings few on dorsum but ducts still in clusters, i.e., P. glandulifer (Borchsenius) and P. tritubulata (Kiritchenko) | 3 |
2 | With 3–6 (generally fewer than 5) multilocular pores with double rings in each cluster on thorax and head; each anal lobe cerarius with 4 enlarged cerarian setae | P. balteata (Green, 1928) |
– | With 4–8 (generally more than 5) multilocular pores with double rings in each cluster on thorax and head; each anal lobe cerarius with only 2 enlarged setae and 2 smaller auxiliary setae | P. cycliger (Leonardi, 1908) |
3 | Circulus present | 4 |
– | Circulus absent | 10 |
4 | Quinquelocular pores numerous on venter; marginal cerarii numbering 13–18 pairs | 5 |
– | Quinquelocular pores absent or, if a few present, mainly around mouthparts; fewer than 8 pairs marginal cerarii | 9 |
5 | Each dorsal cluster with 0–4 multilocular pores with double rings and 0–3 large oral-collar tubular ducts | 6 |
– | Each dorsal cluster with 2–16 multilocular pores with double rings, and 2–13 large oral-collar tubular ducts | 7 |
6 | Clusters on dorsum few (3–5 in total); each cluster normally without multilocular pores with double rings but with 1–3 large oral-collar tubular ducts around a central smaller duct | P. tritubulata (Kiritchenko, 1940) |
– | Clusters abundant throughout dorsum, each cluster with 1–3 multilocular pores with double ring, 0–3 large oral-collar tubular ducts and 0–1 small oral-collar tubular duct | 8 |
7 | Each cluster with 5–16 (usually 8–10) multilocular pores with double rings, 5–13 large oral-collar tubular ducts, and 7–9 minute discoidal pores; quinquelocular pores extremely sparse on venter | P. multipora Kaydan, 2015 |
– | Each cluster with 1–7 (usually 2–4) multilocular pores with double rings, 1–5 large oral-collar tubular ducts, and 1–4 minute discoidal pores; quinquelocular pores common on venter | P. manifecta (Borchsenius, 1949) |
8 | Dorsal cerarii absent. Cerarii numbering 13 pairs | P. stellarocheae (Goux, 1990) |
– | Dorsal cerarii present. Cerarii numbering 18 pairs | P. osakaensis sp. n. |
9 | Multilocular pores with double rings on dorsum generally absent; if present, very few, restricted to posterior abdominal segments; each cluster with 0 or 2 (usually 0) multilocular pores with double rings, 1–4 large oral-collar tubular ducts, and 2–4 minute discoidal pores | P. glandulifer (Borchsenius, 1949) |
– | Multilocular pores with double rings present in clusters on dorsum, each cluster with 2–5 (usually 3) multilocular disc pores, 2–5 large oral-collar tubular ducts, and 2–4 minute discoidal pores | P. kansui Kaydan, 2015 |
10 | Marginal cerarii numbering 14–18 pairs; multilocular disc pores restricted to abdominal segments VI–VIII | 11 |
– | Marginal cerarii numbering fewer than 4 pairs; multilocular disc pores present on abdominal segments IV–VIII | P. sablia (Goux, 1989) |
11 | Clusters on dorsum common and in distinct rows on each segment; femur without translucent pores | P. grassiana (Goux, 1989) |
– | Clusters on dorsum sparsely distributed on each segment, not forming distinct rows; femur with translucent pores | P. proeminens (Goux, 1989) |
The author thanks Dr. M. Bora Kaydan (Cukorova University, Adana, Turkey) for his kind comments and suggestions about the identity of the mealybug species here described and Dr. Takumasa Kondo (Corporación Colombiana de Investigación Agropecuaria (CORPOICA), Colombia) for reviewing an earlier version of the manuscript.