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Research Article
A new species of Parlatoria from China (Hemiptera, Coccomorpha, Diaspididae)
expand article infoMinmin Niu, Jinian Feng
‡ Northwest A&F University, Yangling, China
Open Access

Abstract

A new species of armoured scale insect Parlatoria menglaensis sp. n. is described and illustrated which infests leaves of Cinnamomum camphora in China. A key to the Parlatoria species occurring in China is provided.

Keywords

China, Diaspididae , Hemiptera , new species, Parlatoria

Introduction

Armoured scale insects (Hemiptera: Coccomorpha: Diaspididae) are ubiquitous sap-sucking parasites that have a worldwide distribution (Andersen 2009). Compared with other family groups of Coccoidea, the armoured scale insects have several unique characteristics. For example, they have a cecum, which has no direct connection between the stomach and the anal opening, so they do not produce sweet secretions called honeydew (Henderson 2011). Females of the armoured scale insects are immobile and firmly attached to plant leaves, stems, fruits, or roots (Chou 1982). They have an extremely simplified morphology with several fused segments (Andersen 2010). They have no wings, or legs, and the eyes and antennae are reduced (Balachowsky 1948). The Diaspididae is the largest family of the Coccoidea with 2595 species currently identified (García Morales et al. 2018).

The genus, Parlatoria Targioni Tozzetti, 1868, is a large group of Diaspididae that are members of the tribe Parlatoriini. This genus was originally established by Curtis (1843) and Aspidiotus proteus Curtis, 1843, has been subsequently designated as the type species by Leonardi. The genus currently is made up of 73 species (García Morales et al. 2018). Some species of Parlatoria, such as P. oleae (Colvée) and P. ziziphi (Lucas) are considered to be serious pests of economic plants (McKenzie 1945).

Parlatoria is distributed in both tropical and subtropical regions (García Morales et al. 2018). This genus is found predominately in southeastern Asia but has also extended its range into Australia and Africa (McKenzie 1945). Some species have been introduced in the tropics and other warm parts of the world (Takagi 1969). About 34 species of this genus have been reported from China (García Morales et al. 2018).

Recently, a new species of Parlatoria was discovered in China and is described and illustrated in this study. This discovery raises the number of species recorded in this genus to 74, of which 35 are recorded from China. A key to the Chinese species of Parlatoria is presented in this study.

Materials and methods

Plant samples infested by the new species were collected from Mengla city, Yunnan Province. Permanent slide mounts of adult females from the samples were prepared using the method described by Henderson (2011).

The illustrations of the adult female shown in Figs 1–9 were drawn from slide-mounted specimens. Fig. 1 shows an overview of the dorsal body surface on the left side and the ventral body surface on the right side, and an enlarged detail of the significant features of the body, which are not drawn in direct proportions to each other.

Slide-mounted type specimens of the new species have been deposited in the Entomological Museum, Northwest A&F University, Yangling, Shaanxi, China (NWAFU).

Taxonomy

Parlatoria Targioni Tozzetti

Parlatoria Targioni Tozzetti, 1868: 735.

Type species

Parlatoria orbicularis Targioni Tozzetti, subsequently designated by Leonardi (1899: 208).

Generic diagnosis

Female scale. Various colors, oval to elongate, with exuviae terminal, often occupying greater part of scale.

Male scale. Elongate and smaller than the female.

Adult female. Female body nearly round or broadly ovate, and the widest at metathorax or abdominal segment I. The body free segments distinct but not strongly produced, and membranous except for the pygidium. Antennae with one or two setae. Prosomatic tubercles present or absent. Anterior spiracles with disc pores, the posterior spiracles without disc pores. Derm pocket present or absent between the posterior spiracle and body margin. Peribuccal granulations present or absent. The pygidium rounded or rather triangular. Three pairs of lobes well developed, unilobate, usually notched, median lobes not yoked; marginal macroducts of pygidium, one present or absent between the median lobes, one between the median and second lobes, and also between the second and third lobes. Two or three fimbriate plates present between lobes, then extend to the whole lateral margin of the pygidium, and each with one microduct. The fourth and fifth lobes often present, sclerotized or replaced by a membraneous fimbriate plates. Submarginal dorsal ducts usually present, scattered in a broad, continuous, irregular row on each side of the abdomen. Submedian dorsal ducts present or absent. Anal opening positioned about centre of pygidium. Four or five groups of perivulvar pores present (Adapted from McKenzie 1945, Takagi 1969, Williams and Watson 1988, Henderson 2011).

Remarks

This genus Parlatoria, like other groups of the subfamily Aspidiotinae has an ovate body, and the second lobes are not divided into two lobules. Fringed plates are present between the lobes. Parlatoria is distinguished from other genera, especially Parlagena McKenzie, 1945, and Parlatoreopsis Lindinger, 1912, by having fringed plates across two sides of the prepygidial abdominal segments.

Parlatoria menglaensis sp. n.

Figures 1–9

Material examined

Holotype and 30 paratypes, adult female. China: Yunnan Province. Mengla city, longitude 101.57, latitude: 21.48, on Cinnamomum camphora (L.) Presl., 30.vii.2017, coll. Minmin Niu.

Description

Female scale. Adult female cover convex, circular dark green/grey; exuvia on front end. Male scale. Not recorded.

Adult female. Body elongate-ovate, the broadest in first abdominal segment or thoracic region; segmentation distinct.

Antenna composed of two stout tubercles and a seta, located midway between frontal margin and mouthparts, interantennal distance being equal to width of mouth-parts. Prosomatic tubercles absent. Anterior spiracle with 1–2 parastigmatic pores; posterior spiracle without pores. Derm pocket absent between the posterior spiracle and body margin. Submarginal duct tubercules arranged as follows: 1–2 on cephaloprothoracic sternum, 3–5 on the mesothorax, and 4–8 on the metathorax.

Pygidium rounded, with 3 pairs of well-developed lobes. The median lobes distinctly notched once on each side, the second and third usually notched once distinctly on outer side. Fourth lobes replaced by a fimbriate plate, similar to adjacent fimbriate plates in form. Fimbriate plates present throughout pygidium, mostly as long as lobes, and two between median lobes, two between the median and second, three between the second and third; pygidial marginal macroducts largest closer to median lobes, arranged as follows: absent between the median lobes, one in each interlobar space, two outside the third lobe. Submarginal dorsal ducts on prepygidium numerous, 60–70 ducts on each side. Submedian ducts absent. Ventral microducts few, scattered on pygidium. Anal opening small, positioned about centre of pygidium. Perivulvar pores present in five groups; 3–4 in the median group, laterocephalic group with four pores, and the laterocaudal group with four pores.

Figure 1–9. 

Parlatoria menglaensis sp. n., adult female. 1 body 2 antenna 3 anterior spiracle 4 posterior spiracle 5 gland tubercle 6 detail of dorsal gland duct 7 ventral microduct 8 perivulvar pore 9 pygidium.

Remarks

This species is very similar to P. machilicola (Takahashi 1933) in body shape, but differs in having (character-states on P. machilicola in brackets): (i) perivulvar pores present in five groups (perivulvar pores present in four groups); (ii) dorsal macroducts absent (dorsal macroducts present); (iii) marginal macroducts only four on each side (marginal macroducts more than four on each side).

The new species also resembles P. tsujii Tanaka, 2010, in the shape and spiracles. However, it differs from P. tsujii by the following characters (character-states on P. machilicola in brackets): (i) perivulvar pores present in five groups (perivulvar pores present in four groups); (ii) derm pocket absent (derm pocket present); (iii) marginal macroducts absent between the median lobes (marginal macroducts present between the median lobes).

Host plant

Cinnamomum camphora (L.) Presl (Lauraceae).

Etymology

The specific epithet is named after Mengla, the type locality.

Distribution

China (Yunnan).

Key to the adult females of Parlatoria Targioni Tozzetti from China

(There are records of P. ligustri Wu from China (Wu Chenfu 1935), but the information is inadequate for this key, thus it has not been included).

1 Perivulvar pores absent P. pseudaspidiotus (Lindinger)
Perivulvar pores present in 4 or 5 groups 2
2 A marginal macroduct absent between the median lobes 3
A marginal macroduct present between the median lobes 4
3 Perivulvar pores absent in the median group P. machilicola (Takahashi)
Perivulvar pores present in the median group P. menglaensis sp. n.
4 Puparium of adult female black; with 1 peculiar, large and ear-like lobe on each side margin of head region about opposite anterior spiracles P. ziziphi (Lucas)
Puparium of adult female variable in color, but not black; on margin without ear-like lobes or lobes very small on each side of head region about opposite of anterior spiracles 5
5 Pygidium with 2 pairs of well-developed lobes, the 3rd quite small, but sclerotized P. cupressi (Ferris)
Pygidium with 3 or more pairs of well-developed lobes 6
6 Anterior spiracles without disc pores P. mytilaspiformis Green
Anterior spiracles with disc pores 7
7 Derm pockets present between each posterior spiracle and body margin 8
Derm pockets absent between each posterior spiracle and body margin 13
8 Fourth lobes definitely present, not closely resembling adjacent plates 9
Fourth lobes absent, replaced by a membranous, plate-like process, smaller than the adjacent plates P. proteus (Curtis)
9 Four plates present between third lobe and fourth lobe P. pinicola Tang
Three plates present between third lobe and fourth lobe 10
10 Eyespots modified to form a stout spur P. crotonis (Douglas)
Eyespots various, flat, irregular or absent 11
11 Peribuccal granulations absent P. camelliae (Comstock)
Peribuccal granulations present 12
12 Pygidial lobes almost equal in size; perivulvar pores always in 4 groups P. pini Tang
Pygidial lobes of different sizes, the third pair smallest; perivulvar pores sometimes present in 5 groups P. theae (Cockerell)
13 Pygidium normally with four plates present between third lobe and fourth lobe 14
Pygidium with three plates present between third lobe and fourth lobe 17
14 Peribuccal granulations present 15
Peribuccal granulations absent P. multipora McKenzie
15 Dorsal ducts present on submedian area on abdominal segments I-III P. yanyuanensis Tang
Dorsal ducts absent from submedian area on abdominal segments I-III 16
16 Median lobes usually with a deep lateral notch and no medial notch (rarely with a small medial notch) P. oleae (Colvée)
Median lobes with deep lateral and medial notches P. bambusae Tang
17 Fourth lobes definitely present, not closely resembling adjacent plates 18
Fourth lobes replaced by a membranous, plate-like process, smaller than the adjacent plates 27
18 Lobes with outer margins normally notched 19
Lobes with outer margins minutely toothed P. yunnanensis Ferris
19 Lobes with outer margins with more than one notch 20
Lobes with outer margins with a single notch 22
20 Plates reduced 21
Plates well developed, fimbriate P. desolator McKe nzie
21 Dorsal median macroducts present on pygidium within frame formed by perivulvar pores P. cinerea (Doane & Hadden)
Dorsal median macroducts absent on pygidium within frame formed by perivulvar pores P. fluggeae Hall
22 Peribuccal granulations present 23
Peribuccal granulations absent 24
23 Submedian dorsal macroducts absent; Eyespot modified to form rounded elevation P. machili Takahashi
Submedian dorsal macroducts present on abdominal segments IV–V; Eyespot absent or inconspicuous P. cinnamomicola Tang
24 Median pygidial lobes deeply notched on outer and inner margins 25
Median pygidial lobes deeply notched only on outer margins 26
25 Perivulvar pores absent in the median group, antero- and posterolateral groups confluent on each side; submedian dorsal macroducts present on abdominal segments I-III P. emeiensis Tang
Perivulvar pores absent or a single one present in the median group, 6 to 8 in the anterolateral group, and 6 to 8 in the posterolateral group; submedian dorsal macroducts absent P. pergandii (Comstock)
26 Fourth lobes represented by small sclerotized spurs P. ghanii Hall & Williams
Fourth lobes well developed P. reedia Zhang, Feng & Liu
27 Peribuccal granulations absent 28
Peribuccal granulations present 30
28 Anterior spiracle with 1–3 disc pores 29
Anterior spiracle with 6–15 disc pores P. stigmadisculosa Bellio
29 Plates tapering apically to a point P. lithocarpi Takahashi
Plates well fimbriated P. acalcarata McKenzie
30 Perivulvar pores present in the median group, with 5 groups P. piniphila Tang
Perivulvar pores absent in the median group 31
31 Prosomatic tubercles rounded P. arengae Takagi
Prosomatic tubercles pointed apically, inconspicuous or absent 32
32 Posterolateral groups of perivulvar pores with 2–3 pores each P. hydnocarpus Hu
Posterolateral groups of perivulvar pores with more than 6 pores each 33
33 Gland tubercles: 1 to 3 prespiraculars, 3 to 4 anterior spiraculars, 3 to 5 mesothoracics, 4 metathoracics, and 4 first abdominals; submarginal dorsal ducts containing 18 to 22 on each side P. liriopicola Tang
Gland tubercles: 1 to 7 prespiraculars, 4 to 10 anterior spiraculars, 14 to 16 mesothoracics, 8 to 16 metathoracics, and 5 to 8 first abdominals; submarginal dorsal ducts containing 35 to 47 on each side P. keteleericola Tang & Chu

Discussion

Parlatoria menglaensis sp. n. is a pest in urban areas of China. Its primary host plant is Cinnamomum camphora (L.) Presl (Lauraceae), which grows south of the Yangtze River in China. This plant is also found in southern Japan, Korea, and Vietnam, and has been introduced to many other countries, including Australia and the United States. Currently, P. menglaensis sp. n. has only been identified in China, but it could eventually spread to the previously mentioned countries where its potential host plants occur.

Acknowledgements

We are grateful to Prof. William H. Reissig from Cornell University (New York, USA) for language revision of the manuscript. The work is supported by the National Natural Science Foundation of China (No. 31472022 and No. 31772502).

References

  • Andersen JC (2009) A phylogenetic analysis of armored scale insects, based upon nuclear, mitochondrial, and endosymbiont gene sequences. University of Massachusetts Amherst, 66 pp.
  • Andersen JC, Wu J, Gruwell ME, Morse GE, Santana S, Feliciano N, Gwiazdowski RA, Normark BB (2010) A phylogenetic analysis of armored scale insects, based up on nuclear, mitochondrial, and endosymbiont gene sequences. Molecular Phylogenetics and Evolution 57: 992–1003. https://doi.org/10.1016/j.ympev.2010.05.002
  • Balachowsky AS (1948) Les cochenilles de France, d’Europe, du nord de l’Afrique et du bassin Méditerranéen. IV. Monographie des Coccoïdea, classification – Diaspidinae (Premïère partie). Actualités Scientifigues et Industrielles 1054: 243–394.
  • Bellio G (1929) Note su Diaspinae dell’ estremo oriente con descrizione di nuove specie (Homoptera: Coccidae). Bollettino del R. Istituto Superior Agraria Laboratorio di Zoologia Generale e Agraria 22: 219–243.
  • Chou I (1982) Monograph of the Diaspididae of China. Vol. 1. Shanxi Publication House of Science & Technology Shanxi, 195 pp.
  • Cockerell TDA (1896) Some coccidae found by Mr. Alex Craw in the course of his quarantine work at San Francisco. United States Department of Agriculture, Division of Entomology, Technical Series 4: 42–46.
  • Colvée P (1880) Ensayo sobre una nueva enfermedad del olivo, producida por una nueva especie del género Aspidiotus. Gaceta Agrícola del Ministerio de Fomento 14: 21–41.
  • Comstock JH (1881) Report of the Entomologist. Report of the Commissioner of Agriculture, United States Department of Agriculture 1880/1881: 276–349.
  • Comstock JH (1883) Second report on scale insects, including a monograph of the sub-family Diaspinae of the family Coccidae and a list, with notes of the other species of scale insects found in North America. Department of Entomology Report, Cornell University Agricultural Experiment Station 2: 47–142.
  • Curtis J (1843) The small brown scale, Aspidiotus proteus, Nobis. Gardeners’ Chronicle 39: 676.
  • Ferris GF (1953) Report upon scale insects collected in China (Homoptera: Coccoidea). Part IV. (Contribution No. 84). Microentomology 18: 59–84.
  • García Morales M, Denno B, Miller DR, Miller GL, Ben-Dov Y, Hardy NB (2018) ScaleNet: A Literature based model of scale insect biology and systematics. http://scalenet.info
  • Green EE (1899) The Coccidae of Ceylon, Part II. Dulau London, 105–169.
  • Hall WJ, Williams DJ (1962) New Diaspididae (Homoptera: Coccoidea) from the Indo-Malayan region. Bulletin of the British Museum (Natural History) Entomology 13: 21–43.
  • Henderson RC (2011) Diaspididae (Insecta: Hemiptera: Coccoidea). Fauna of New Zealand 66. Manaaki Whenua Press, Lincoln, Canterbury, 275 pp.
  • Hu J (1986) Studies on scale insects in the Hainan Island of China (Part I). Contributions from Shanghai Institute of Entomology 6: 213–227.
  • Leonardi G (1899) Sistema delle “Parlatoriae” nota preventiva. Mariani Florence, 203–209.
  • Lindinger L (1905) Zwei neue Schildläuse aus Asien. Insecten Börse 22: 131–132.
  • Lindinger L (1912) Die Schildläuse (Coccidae) Europas, Nordafrikas und Vorder-Asiens, einschliesslich der Azoren, der Kanaren und Madeiras. Ulmer, Stuttgart, 388 pp.
  • Lucas H (1853) [Coccus ziziphi]. Annales de la Société Entomologique de France 1: 28–29.
  • McKenzie HL (1945) A revision of Parlatoria and closely allied genera (Homoptera: Coccoidea: Diaspididae). Microentomology 10: 47–121.
  • McKenzie HL (1960) Taxonomic position of Parlatoria virescens Maskell, and descriptions of related species (Homoptera: Coccoidea: Diaspididae). Scale studies pt. 14. Bulletin of the California Department of Agriculture 49: 204–211.
  • Takagi S (1969) Diaspididae of Taiwan based on material collected in connection with the Japan-U.S. Co-operative Science Programme, 1965 (Homoptera: Coccoidea). Part I. Insecta Matsumurana 32: 1–110.
  • Takahashi R (1933) Observations on the Coccidae of Formosa. III. Report. Government Research Institute. Department of Agriculture. Formosa 60: 1–64.
  • Takahashi R (1935) Observations on the Coccidae of Formosa. V. Report Department of Agriculture Government Research Institute, Formosa 66: 1–37.
  • Tanaka H (2010) A New Species of the Genus Parlatoria (Hemiptera, Diaspididae) from Japan. Japanese Journal of Systematic Entomology 16(2): 179–183.
  • Tang FT (1984) The scale insects of horticulture and forests of China. Shanxi Agricultural University Press Research Publication 2: 1–115.
  • Tang FT, Chu CY (1983) Three new species of Diaspididae from Keteleeria evelyniana in vicinity of Kunming, Yunnan. Acta Zootaxonomica Sinica 8: 301–306.
  • Targioni Tozzetti A (1868) Introduzione alla seconda memoria per gli studi sulle cocciniglie, e catalogo dei generi e delle specie della famiglia dei coccidi. Atti della Società italiana di scienze naturali 11: 721–738.
  • Williams DJ, Watson GW (1988) The Scale Insects of the Tropical South Pacific Region. Pt. 1: The Armoured Scales (Diaspididae). CAB International Wallingford, 290 pp.
  • Wu Chenfu F (1935) Catalogus Insectorum Sinensium (catalogue of Chinese insects). Volume II. The Fan Memorial Institute of Biology, Peiping, China, 639 pp.
  • Zhang FP, Feng JN, Liu XW (2006) A new species and a new record of Parlatoria from China (Hemiptera: Diaspididae). Acta Zootaxonomica Sinica 31(4): 832–834.
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