Literature DB >> 22859894

A new species of Pseudaulacaspis MacGillivray, 1921 from China (Hemiptera, Coccoidea, Diaspididae) with a key to Chinese species.

Jiu-Feng Wei1, Ji-Nian Feng.   

Abstract

A new species of armored scale, Pseudaulacaspis zhenyuanensis Wei & Feng, sp. n. is described and illustrated from specimens collected on Spermadictyon suaveolens in China. A key to armored scale species known from China is provided.

Entities:  

Keywords:  Diaspididae; Hemiptera; armored scale; new species; taxonomy

Year:  2012        PMID: 22859894      PMCID: PMC3406451          DOI: 10.3897/zookeys.210.3122

Source DB:  PubMed          Journal:  Zookeys        ISSN: 1313-2970            Impact factor:   1.546


Introduction

The Coccoidea is one of the four superfamilies of the monophyletic suborder Seternorrhyncha belongs to the Hemiptera (Gullan and Cook 2007), with at least 30 families and around 8000 species (Andersen 2010). The family Diaspididae is the largest family of the Coccoidea with more than 2400 dispidid species currently known (Ben-dov 2012). The higher classification within the family is uncertain but two of the major PageBreaksubfamilies are the Aspidiotinae and the Diaspidinae, and most species can be assigned to one or the other (Miller and Davidson 2005) The genus was established by MacGillivray (1921) for Targioni Tozzetti, 1886 was belongs to subfamily Diaspidinae. When he described it, he referred to it 9 nominal species, which are now considered to represent only 2 species. Since then, many additional species were described and added to by other authors (Chen 1983; Ferris 1953, 1955; Hu 1986; Takagi 1956, 1961, 1966, 1970, 1985; Tang 1986, 1988; Williams and Watson 1988; Hodgson and Lagowska 2011). This genus is large with 68 species (Hodgson and Lagowska 2011) which is a widespread and polyphaous genus infesting a large number of plant (Borchsenius 1966) and occurs in most of zoogeographical regions except Antarctica. Up until now, 32 species have been described from China. In the present paper, a new species sp. n.is described and illustrated, bringing the number of recognized species in this genus to 69, of which 33 are recorded from China. And a key to species from China is included.

Materials and methods

The morphological terms for Diaspididae follow those of Henderson (2011). The illustrations of the adult female are drawn from slide-mounted specimens, which depict the dorsum on the left and venter on the right. Enlargements of important characters are shown around the edges of the main illustration. All measurements are given in micrometers (μm). Measurements were made using the measurement tools NIT-Elements D. The abbreviations L1, L2, L3 and L4 stand for median and second to fourth pygidial lobes. All specimens are deposited in the Entomological Museum, Northwest A & F University, Yangling, Shaanxi, China (NWAFU).

Taxonomy

MacGillivray, 1921 http://species-id.net/wiki/Pseudaulacaspis Pseudaulacaspis MacGillivray, 1921: 305. Type species:

Generic diagnosis.

Female scale. White, suborbicular or long pyriform. Exuviae terminal. Male scale. Same colour as female scale, elongate. Adult female. Body shape varied, fusiform, olivary or elongate; derm membraneous except for the marginal of pygidium; mesothorax, metathorax, and abdominal segments I-III produced laterally. Cephalothorax. Antennae each with a seta. Anterior spiracles each usually with a cluster of trilocular pores, posterior spiracle eachPageBreak associate with or without trilocular pores. Pygidium. With 2 or 3 pairs of lobes. Median lobes (L1) well-developed, much larger than lobules of lateral lobes, zygotic basally, with a distinct pair of marginal setae between lobes. In general, L1 divide into two types: bark-type, individuals occur on bark and prominent median lobes; leaf-type, those on leaves and sunken into the pygidium. Second lobes (L2) much smaller than the L1, bilobed, divided into inner lobule and outer lobule, outer lobule usually smaller than inner, in some species much reduced. Third lobes (L3) smaller than L2, bilobed or represented by serrations along the body margin in some species. Gland spines. Gland spines developed, usually single on abdominal segments VI-VIII, becoming shorter into conical on anterior segments which called gland tubercles. Ducts. Dorsum with 2-barred ducts, forming submedial and submarginal rows on abdominal and pygidium, usually as same size as marginal macroducts. Ventral microductsscattered. Anal opening. Anal opening close to the base of or situated about the centre of the pygidium. Perivulvar pores quinquelocular, in five groups.

Remarks.

This genus is very closely related to Signoret, 1868 and Cockerell, 1893 in feature of pygidial lobes and dorsal ducts present on pygidium and abdomen, but can differ from these genus: presence of a pair of setae between the median lobes in , but absent in and . Wei & Feng sp. n. urn:lsid:zoobank.org:act:AB75F5D8-7BDF-42D4-9DA9-13F4DFD1D43F http://species-id.net/wiki/Pseudaulacaspis_zhenyuanensis Figures 1–8
Figures 1–8.

Pseudaulacaspis zhenyuanensis Wei & Feng, sp. n., adult female: 1 habitus 2 antennae 3 anterior spiracle 4 gland tubercles 5 detail of gland macroduct 6 detail of the duct in the head on the dorsum 7 detail of pygidium 8 pygidium.

Material examined.

Holotype: adult female:CHINA:Guizhou Prov., Zhenyuan County, 13. viii. 1996, Zeng (NWAFU). Paratypes: 2 adult females: same data as the holotype (NWAFU).

Description

, n=3. Adult female. Appearance in life not recorded. Slide-mounted adult female 1755-1910 μm long (holotype 1910 μm long); 930-970 μm wide (holotype 931 μm wide), body outline fusiform, derm membranous except for pygidium. Normally widest at metathorax and abdominal segment I, lateral abdominal lobes well-developed, with large gland spines on the margin of prepygidial and pygidial segments. Cephalothorax. Antennae each with 1 long fleshy seta, distance between antennae is 111 µm. Anterior spiracle each with 12-31 trilocular pores in a cluster, posterior spiracle each with 11-17 trilocular pores. Pygidial Lobes. With 3 pairs of lobes; L1 well-developed, zygotic basally, protruding from pygidial margin, with small serrations along both margins, with a pair of setae between lobes; L2 bilobate, inner lobule rounded, much larger than outer lobule; L3 bilobate, slightly smaller than L2, inner lobule rounded, outer lobule margin serrate; L4 represented by serrations along the body margin. Gland spines. Large, arranged singly on pygidial segments VI-VIII but with 2 on segment V, 4-5 on segment IV, 5-6 on segment III, 5 on segment II, anterior spines smallest (on segPageBreakPageBreakment II). Gland tubercle present submarginally, with 2 on prothorax, 9-11 on mesothorax, 5-6 on metathorax, 6 on segment I. Ducts. Marginal macroducts, 2-barrel-shaped, 1 present between L1 and L2, 2 on segment VI, 1 on segment V. Dorsal macroducts on pygidium about same size as marginal macroducts, becoming slightly smaller on anterior abdomen, 2-barrel-shaped, arranged segmentally in submedian and submarginal rows; submedian: 3-6 on segment I, 4-5 on II, 4-6 on III, 7-13 on IV, 3-4 on V; submarginal: 11-14 on I, 11-12 on II, 10-11 on III, 10-11 on IV, 8-9 on V. Dorsal ducts scattered on margin of thorax, smaller than those on abdomen, 2-barrel-shaped, with 8 or 9 on prothorax, 15-17 on mesothorax, 14 or 15 on metathorax. Dorsal ducts on head as big as ventral microducts, very smaller than dorsal ducts present on thorax, scattered distribution. Ventral microductsscattered, numerous on head and with several microducts on submargin of pygidium and prothorax and submedian of abdomen, meso- and metathorax. Anal opening, small, 15-17µm in diameter, positioned 214 µm from posterior margin. Perivulvar pores in 5 groups, 31-37 in the median group, 33-44 in the anterolaterally and 45-48 in the posterolaterally.

Diagnosis.

This species is similar to (Cockerell, 1896) in body shape and the number of pygidial lobes, but can be distinguished by the following features (those for in brackets): 1) dorsal macroducts absent on abdominal segment VI (present); 2) L1 prominent the pygidium (sunken into the pygidium). Host: .

Etymology.

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

Distribution.

China (Guizhou). Pseudaulacaspis zhenyuanensis Wei & Feng, sp. n., adult female: 1 habitus 2 antennae 3 anterior spiracle 4 gland tubercles 5 detail of gland macroduct 6 detail of the duct in the head on the dorsum 7 detail of pygidium 8 pygidium.
1Trilocular pores absent near each anterior spiraclePseudaulacaspis manni (Green & Mann, 1907)
Trilocular pores present near each anterior spiracle2
2Body slender, both side nearly parallelPseudaulacaspis dendrobii Kuwana & Muramatsu, 1931
Body nonslender3
3Body suborbicular or oval4
Body long ovate or furiform8
4Trilocular pores present near each anterior spiracle, absent near each posterior spiracle5
Trilocular pores present near anterior spiracle and posterior spiracle7
5With 2 pairs of lobes on pygidiumPseudaulacaspis canarium Hu, 1986
With 3 pairs of lobes on pygidium6
6The eggs white or salmon; with 1 pairs of gland spines between L3 and the traces of L4, each bifurcatePseudaulacaspis pentagona (Targioni Tozzetti, 1886)
The eggs always salmon; with 2 pairs of gland spines between L3 and the traces of L4, each pointedPseudaulacaspis prunicola (Maskell, 1895)
7Perivular pores in 6 groupsPseudaulacaspis mirabilis Hu, 1986
Perivular pores in 5 groupsPseudaulacaspis ficicola Tang, 1986
8Anterior spiracle and posterior spiracle both with trilocular pores9
Anterior spiracle with trilocular pores, posterior spiracle without trilocular pores14
9Dorsal macroducts absent on submarginal and submedial area of abdominal segment VI10
Dorsal macroducts present on submarginal or submedial area of abdominal segment VI11
10Submarginal and submedial macroducts present on abdominal segment IPseudaulacaspis zhenyuanensis sp. n.
Submarginal and submedial macroducts absent on abdominal segment IPseudaulacaspis ulmicola Tang & Li, 1988
11Dorsal macroducts absent on submarginal and submedial area of abdominal segment II12
Dorsal macroducts present on submarginal or submedial area of abdominal segment II13
12Antennae 6 segments in first instarPseudaulacaspis centreesa (Ferris, 1953)
Antennae 5 segments in first instarPseudaulacaspis eucalypticola Tang, 1986
13Dorsal macroducts present on submedial area of abdominal segment VI; anal opening situated at the base of pygidiumPseudaulacaspis momi (Kuwana, 1931)
Dorsal macroducts present between submarginal or submediaal area of abdominal segment VI; anal opening situated on the centre of pygidiumPseudaulacaspis loncerae Tang, 1986
14Dorsal macroducts present on submarginal or submedial area of abdominal segment VI15
Dorsal macroducts absent on submarginal and submedial area of abdominal segment VI23
15Dorsal macroducts present on submarginal and submedial area of abdominal segment VI16
Dorsal macroducts only present on submedial area of abdominal segment VI18
16L2 bilobate, each with a pair of short basal sclerosesPseudaulacaspis sasakawai Takagi, 1970
L2 bilobate, without basal scleroses17
17With 9-11 trilocular pores near each anterior spiraclePseudaulacaspis camelliae (Chen, 1983)
With more than 25 trilocular pores near each anterior spiraclePseudaulacaspis latisoma (Chen, 1983)
18Dorsal macroducts present on submarginal or submedial area of abdominal segment I19
Dorsal macroducts absent on submarginal or submedial area of abdominal segment I20
19L3 not obvious, anal opening situated on the centre of pygidiumPseudaulacaspis takahashii (Ferris, 1955)
L3 bilobate, anal opening situated at the base of 2/5 of pygidiumPseudaulacaspis chinensis (Cockerell, 1896)
20L3 bilobate21
L3 not obvious, present by a prominence22
21L1 protruding from pygidial marginPseudaulacaspis cockerelli (Cooley, 1897)
L1 sunk into apex of pygidiumPseudaulacaspis kentiae (Kuwana, 1931)
22Only 1 submedial macroduct present on abdominal segment VIPseudaulacaspis eugeniae (Maskell, 1892)
With 2 submedial macroducts present on abdominal segment VIPseudaulacaspis ericacea (Ferris, 1953)
23Submarginal macroducts present on abdominal segment II, submedial macroducts absent on abdominal segment II24
Submarginal and submedial macroducts both present on abdominal segment II26
24Submedial macroducts absent on abdominal segment IIIPseudaulacaspis subcorticalis (Green, 1905)
Submedial macroducts present on abdominal segment III25
25With more than 30 trilocular pores near each anterior spiraclePseudaulacaspis poloosta (Ferris, 1953)
With 20 or fewer trilocular pores near each anterior spiraclePseudaulacaspis megaloba (Green, 1899)
26L3 obvious, bilobate27
L3 not obvious, present by a shallow prominence28
27With 2-4 trilocular pores near each anterior spiraclePseudaulacaspis subrhombica (Chen, 1983)
With 11-14 trilocular pores near each anterior spiraclePseudaulacaspis frutescens (Hu, 1986)
28With 10 or fewer trilocular pores near each anterior spiracle29
With more than 15 trilocular pores near each anterior spiracle31
29L1 protruding from pygidial margin, only with 2 trilocular pores near each anterior spiraclePseudaulacaspis taiwana (Takahashi, 1935)
L1 sunk into apex of pygidium, with more than 4 trilocular pores near each anterior spiracle30
30The terminal of L3 arc-shaped, smoothly, with 4-8 trilocular pores near each anterior spiraclePseudaulacaspis abbrideliae (Chen, 1983)
The terminal of L3 serration, with more than 4 trilocular pores near each anterior spiraclePseudaulacaspis brideliae (Takahashi, 1933)
31Gland tubercles present on prothorax, dorsal ducts present on head, smaller than those present on pygidium and abdomenPseudaulacaspis syzygicola (Tang, 1986)
Gland tubercles absent on prothorax, dorsal ducts absent on head32
32L2 small, bilobulate, with 17-20 submedial macroduct in totalPseudaulacaspis kuishiuensis (Kuwana, 1909)
L2 very small, the outer lobule at times almost obsolete, with 4-11 submedial macroduct in totalPseudaulacaspis celtis (Kuwana, 1928)
  1 in total

1.  A phylogenetic analysis of armored scale insects (Hemiptera: Diaspididae), based upon nuclear, mitochondrial, and endosymbiont gene sequences.

Authors:  Jeremy C Andersen; Jin Wu; Matthew E Gruwell; Rodger Gwiazdowski; Sharlene E Santana; Natalie M Feliciano; Geoffrey E Morse; Benjamin B Normark
Journal:  Mol Phylogenet Evol       Date:  2010-05-10       Impact factor: 4.286

  1 in total

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