Asterococcus muratae (Kuwana)

Chris J. Hodgson & Douglas J. Williams, 2016, (Hemiptera: Sternorrhyncha, Coccomorpha) with particular reference to species from the Afrotropical, western Palaearctic and western Oriental Regions, with the revival of Antecerococcus Green and description of a new genus and fifteen new species, and with ten new synonomies, Zootaxa 4091 (1), pp. 1-175: 138-139

publication ID

http://doi.org/10.11646/zootaxa.4091.1.1

publication LSID

lsid:zoobank.org:pub:urn:lsid:zoobank.org:pub:76D13D36-682E-4E91-AC91-693CA9D3D465

persistent identifier

http://treatment.plazi.org/id/03F2FF48-81A2-0DB4-24B6-AC32FC8EFB39

treatment provided by

Plazi

scientific name

Asterococcus muratae (Kuwana)
status

 

Asterococcus muratae (Kuwana)  

Cerococcus muratae Kuwana 1907: 180   .

Solenophora muratae   ; Cockerell 1909: 55. Change of combination. Solenococcus muratae   ; Sanders 1909: 36. Change of combination Asterococcus pyri Borchsenius 1960: 118–120   . Synonymy by Lambdin 1983: 298. Asterococcus muratae   ; Borchsenius 1960: 128. Change of combination.

Type details. Asterococcus muratae   , JAPAN, Tokyo, on Viburnum odoratissimum   ( Caprifoliaceae   ), 16.iv. 1906, S.I. Kuwana. Depository: IAES, Japan: holotype adf. [USNM: possesses 3 slides, 1 labelled paratype by Lambdin and other 2 labelled as cotype but, although locality and date are correct, all three are off grape not Vibernum (Miller, pers. comm.).]

Type details. Asterococcus pyri   , GEORGIA, Abkhazie, on Pyrus   sp. ( Rosaceae   ), 23.x. 1934, A. Shorkin. Depository: ZIAS: holotype adf (ZIAS also has 8 non-type slides).

Material studied. JAPAN, Yokohama, on Viburnum   sp. ( Caprifoliaceae   ), 26.ix. 1954, Takahashi (BMNH): 3 / 4 adff (g).

Comment. This species was redescribed by Lambdin (1983). Based on the material here studied, additional details to his description are: (i) the anteroventral sclerotizations on the anal lobes are absent; (ii) the structure of the multilocular disc-pores looks normal (Lambdin illustrates two rings of loculi); (iii) the anterior line of multilocular disc-pores is medial on the metathorax and these pores have fewer loculi; (iv) Lambdin describes the 8 -shaped pores on the dorsum of the cephalothorax as being in transverse lines but they appeared to be randomly distributed to us; (v) the transverse bands of 8 -shaped pores dorsally on the abdomen appear to be in three bands as follows: a broad band on segment III or IV (but Borchsenius (1960) shows this as two bands), possibly no band on IV or V, but narrow bands on VI and VII; (vi) the larger tubular ducts appear to be on segment VI, and (vii) each transverse band of multilocular disc-pores has a gap between the submarginal group and the medial band.

Based on the figure of A. pyri   (= A. muratae   ) in Borchsenius (1960), the adult female is characterised by the following combination of character-states: (i) eight-shaped pores on dorsum of head and thorax very sparse and smaller than those in transverse bands across abdomen; (ii) slightly larger 8 -shaped pores on abdomen in three or four transverse bands, possibly on segments IV, V, VII and VIII; (iii) cribriform plates absent; (iv) tubular ducts on dorsum of two sizes, narrow ducts sparse medially but becoming more abundant around margins; broader ducts restricted to medially on abdominal segments (v) tubular ducts on venter absent medially; (vi) posterior stigmatic bands bifurcated; (vii) each stigmatic band very broad near spiracles, each band narrowing near margin; (viii) 8 - shaped pores of two sizes on venter, both forming a broad marginal band but with smaller pores towards outside of band; (ix) multilocular disc-pores present across abdominal segments II –VII, absent on metathorax; (ix) leg stubs present, and (x) loculate pores near antennae abundant.