Research Article |
Corresponding author: Adam Stroiński ( adam@miiz.waw.pl ) Academic editor: Michael Wilson
© 2021 Adam Stroiński.
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:
Stroiński A (2021) Kazukuru gen. nov. – a new Ricaniidae planthopper from Solomon Islands (Hemiptera, Fulgoromorpha). Deutsche Entomologische Zeitschrift 68(1): 165-177. https://doi.org/10.3897/dez.68.63635
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A new monotypic genus of ricaniid planthoppers (Hemiptera: Fulgoromorpha: Ricaniidae) from New Georgia Island (Solomon Islands), Kazukuru gen. nov., is described for K. zingiberis sp. nov. (type species). Habitus, female, external and internal genital structures of the new species are described and illustrated.
Fulgoroidea, Oceanian Region, New Georgia, taxonomy, morphology, eggs
The planthopper family Ricaniidae Amyot et Audinet-Serville, 1843 consists of 67 genera (2.7% of the Fulgoromorpha) and covers 437 species (3.2% of the Fulgoromorpha) (
The fauna of Ricaniidae of the Solomon Islands is not very rich. Only six genera with thirteen species and one subspecies have been recorded from the Solomon Islands. These are: Armacia hyalinata (Donovan, 1805) – Guadalcanal Is., Vella Lavella Is., A. atrofascialis
Unfortunately, the exact location is known only for some species, with others (four species) recorded only generally. All of these species belong to widely distributed genera.
The new genus described below, based on two females, is unique in family Ricaniidae and known only from a single locality.
Dry pinned specimens were used for this study.
Label information for all specimens examined is provided verbatim with each line separated by a slash (/) and each label given in square brackets.
The nomenclature of fore wing (tegmen) follows the interpretation proposed by
The SEM photographs of uncoated specimens were taken in the Laboratory of Scanning Microscopy, MIZ PAS (Warsaw), using a scanning electron microscope HITACHI S-3400N under low vacuum conditions.
Measurements were made with an ocular micrometer. The following measurements, ratios and their abbreviations were used in this study:
Total length measured (in dorsal view) from head apex to tegmina apex;
A/B width of vertex measured at anterior margin / length of vertex measured at mid-line;
C/E width of frons at upper margin / length of frons at mid-line;
D/E maximum width of frons / length of frons at mid-line;
F/B length of pronotum at mid-line / length of vertex at mid-line;
G/F length of mesonotum / length of pronotum at mid-line;
G/B+F length of mesonotum / cumulative length of vertex and pronotum at mid-line;
G/H length of mesonotum at mid-line / width of mesonotum between lateral angles;
I/J length of tegmen measured from the base to the apical margin in median portion / width of tegmen measured at the widest part.
The material studied is deposited in Bernice P. Bishop Museum, Honolulu, Hawaii, USA (
Order Hemiptera Linnaeus, 1758
Suborder Fulgoromorpha Evans, 1946
Superfamily Fulgoroidea Latreille, 1810
Family Ricaniidae Amyot & Audinet-Serville, 1843
Kazukuru zingiberis sp. nov., by present designation and monotypy.
The generic name Kazukuru refers to an extinct language once spoken in New Georgia (Solomon Islands). Kazukuru language was last recorded in the early twentieth century when its speakers were in the last stages of language shift (
The genus Kazukuru gen. nov. can be distinguished from all other genera in Ricaniidae by the following combination of characters: frons with three carinae separated at base (Figs
Head. Head with compound eyes (in dorsal view) narrower than thorax.
Vertex (Figs
Frons (Figs
Frontal disc tricarinate, all carinae (median and lateral) separated at upper margin of frons and all carinae reaching ventrad to transverse bar before frons mid-length (not extending the ‘breaking’ point of lateral margins); median carina straight, ending in thick transverse shaft; lateral carinae parallel to lateral margins, subparallel to each other, just longer than median carina and slightly extending transverse thick shaft; transverse thick shaft massive; surface of frontal disc smooth. Frontoclypeal suture straight.
Clypeus (Figs
Rostrum (Figs
Compound eyes (Figs
Antenna (Figs
Thorax. Pronotum (Figs
Mesonotum (Figs
Tegmina (Figs
Costal margin weakly arcuate, apical angle broadly rounded distad to claval angle; claval angle widely rounded; posterior margin arcuate with; postclaval margin (tornus) absent.
Costal area with dense transverse veinlets ending slightly after level of tip of clavus, in basal half about as wide as postcostal cell; subapically expanded and tapering distad.
Postcostal cell in proximal half as wide as costal area in posterior part distinctly narrower without transverse veinlets. Basal cell large, elongately rounded, about 1.5 times longer than wide.
Longitudinal veins ScP+R, MP and CuA leaving basal cell separately; veins ScP+RA and RP arising as long common stem from basal cell with first fork distad of MP and CuA forks and about level with tip of clavus; cell C1 open; first fork of MP before half of tegmen, branch MP1 touching/fused with vein ScP+R. CuA with dichotomic model of forking, first fork placed between first forks ScP+R and MP, before tip of costal area and before tip of clavus.
Tegmina with single apical line of transverse veinlets; apical cell distinctly longer than wide, median cell large, approximately trapezoidal.
Cubital cell without transverse veinlets. Clavus closed; claval veins Pcu and A1 fused just after mid-length of CuP vein; posterocubital cell at basal part and posterior part with scarce transverse veinlets; postcubital and anal cell without transverse veinlets.
Hind wings with precostal triangular cell present; ScP+R distinctly after mid-length of wing, MP not forking, single; CuA forking about middle of wing distantly before first of ScP+R before ScP+R and MP fork, slightly after half of wing; two transverse veinlets present in distal part of wing: rp-mp, mp-cua.
Protibia and profemur about same length; mesofemur slightly shorter than mesotibia; ventral margin of profemur apically with few small variable teeth (Figs
Hind legs (Figs
Basimetatarsomere longer than cumulative length of second and apical metatarsomeres, with two linear rows of partly flattened teeth; all teeth similar size, apical line with seven teeth, second row narrower, with three teeth; all teeth without setae on ventral side of teeth.
Male. Unknown.
Female terminalia
(Figs
Kazukuru zingiberis gen. et sp. nov., SEM micrographs female terminalia; 37. Abdomen and terminalia, ventral view; 38. Pregenital sternite and terminalia, ventral view; 39. Gonoplac, lateral view; 40. Posterior margin of gonoplac, ventral view; 41. Same, ventro-lateral view; 42. Teeth of posterior margin of gonoplac.
Gonoplac (Figs
Gonapophysis VIII (Fig.
Gonaphophyses IX and gonospiculum bridge well developed (as in Figs
Bursa copulatrix of two pouches connected with short ductus; first pouch elongate, with cells and sclerotised ornamentation (except dorsal part) with sclerotised plate with 5–8 small petals, but without median huge sclerite; second pouch elongate-oval, smaller than first one, without cells and without sclerotised plates.
Spermatheca (Fig.
Kazukuru zingiberis gen. et sp. nov; 49. Abdomen and terminalia, lateral view; 50. Same, dorsal view; 51. Same, ventral view; 52. Abdomen with eggs; 53. Eggs; 54. Pregenital sternite, ventral view; 55. Anal tube, dorsal view; 56. Same, lateral view; 57. Gonoplac and gonapophysis VIII with endogonocoxal process, lateral view; 58. Gonaphophyses IX and gonospiculum bridge, dorsal view; 59. Same, lateral view; 60. Spermatheca.
Egg description
. The eggs were extracted from the dry abdomen and observed dry. Eggs are sub-elliptical (elongate-oval), yellowish, about 640 μm long and about 300 μm wide at mid-length (Figs
The specialised area is characterised by a micropylar cap placed apically with sclerotised base with rounded spongy appearance. Surface of eggs with well developed polygonal cells with margins bearing nodules apically larger than in lower part of eggs; operculum absent. About 19 eggs were found in abdomen.
Solomon Island: Western Province, New Georgia Island.
The specific name zingiberis follows the host plant genus Zingiber Mill. on which the new species was collected. The specific name is intended as indeclinable.
For now, a single species in the genus, see diagnosis of genus.
Total length 0.85–0.86 cm.
Head. Vertex: proportion A/B = 6.00; anterior and posterior margins of vertex arcuate about same curvature; lateral margins almost straight and parallel.
Frons: proportion C/E = 1.15–1.20; proportion D/E = 1.73–1.80; upper margin weakly concave; frontoclypeal suture almost straight.
Thorax. Pronotum: proportion F/B = 5.81–6.00.
Mesonotum: proportion G/F+B = 3.50–3.87, proportion G/F = 5.81–6.00, proportion G/H = 1.0; connection between anterolateral carinae and lateral weakly visible.
Tegmina: proportion I/J = 1.71–1.77; longitudinal veins ScP with single terminal; RA with single terminal; MP with 8 terminals (MP1+2 with four terminals, MP3+4 with 4 terminals); RP with three terminals; CuA with three terminals. Hind wing. ScP+RA not forking, single, RP single; CuA with three terminals.
Female terminalia. Anal tube (in dorsal view): posterior margin medially with distinct concavity.
Colouration
(Figs
Holotype
, female: [Solomon Is.: / New Georgia Group / N. Georgia I., Munda / 1–30 m. VII-15-1959], [Ginger], [J. L. Gressitt / Collector] –
Paratype
, female: [Solomon Is.: / New Georgia Group / N. Georgia I., Munda / 1–30 m. VII-13-1959], [J. L. Gressitt / Collector] –
Solomon Island: Western Province, New Georgia Island.
Genus Zingiber Mill. (as ginger; Order: Zingiberales Griseb., family: Zingiberaceae Martinov).
The genus, described above, presents a set of unique characters that broadens our knowledge of the morphology diversity of planthoppers from the family Ricaniidae: the presence of a transverse shaft on the face and its double plane (upper part projected, lower part – below the shaft, retracted) and open cells C1 and C5 on the tegmen.
This unique set of characters within the family Ricaniidae allows the definitive description of this new species, based on only two female specimens, in a new genus, even in the absence of any male specimen. Its discovery in the future will be very interesting for completing the description with the male genitalia characteristics.
Knowledge about the host plants in relation with Ricaniidae is far from sufficient. The specimens of Kazukuru zingiberis gen. et sp. nov. were collected on ginger, Zingiber sp., a plant association not previously recorded for the family. The only other record from the family Zingiberaceae Martinov is Hedychium gardnerianum Sheppard ex Ker Gawl. (kahili ginger, wild ginger) for Scolypopa australis (Walker), a polyphagous species, recorded in New Zealand (
The current knowledge about ricaniids egg ultrastructure is very scarce and high-resolution images from a scanning electron microscope (SEM) are only known for Ricania speculum (Walker, 1851) (Rossi et al. 2014). The present description is based on the eggs extracted from the dry abdomen, which share obvious similarities with eggs of R. speculum. Both eggs have the same shape, without operculum and have developed polygonal cells on the surface. Significant differences occur however in construction of micropylar caps. Unfortunately, these differences may be due to incomplete development of immature eggs. However, differences at the base of the cap (sclerotised in Kazukuru gen. nov., porous in Ricania) and spongious-like structures are observed in both species. A comparative morphology analysis of these characters would be of great interest in the future.
I would like to thank Prof. Thierry Bourgoin, Prof. Charles Bartlett and an anonymous Reviewer for their detailed and insightful comments on the manuscript.