The plant bug subfamily Phylinae in Japan, with key to genera and descriptions of eight new species (Hemiptera: Heteroptera: Miridae)
Author
Yasunaga, Tomohide
text
Zootaxa
2022
2022-02-02
5094
1
1
52
journal article
20752
10.11646/zootaxa.5094.1.1
0ec5a6ee-4a88-49c0-af24-35d1a7414124
1175-5326
5964735
72F6E1D9-E9E4-41F6-9AC0-97A249F94E68
Genus
Pityopsallus
Wagner, 1952
Diagnosis:
Pityopsallus
is distinguished from other phyline genera by the following characters, some of which (underlined) are hypothesized as autapomorphies: Dorsal silvery setae slender, almost as thick as simple setae (
Figs. 26H, O
;
28B
); labium thick, its apex sometimes reaching genital segment (
Fig. 26M
); metathoracic scent efferent system comparatively small (
Fig. 26I, N
); left paramere remarkably elongate, covering (or conforming to) apical part of phallotheca (
Fig. 28
C−D, G−L); vesica J-shaped, composed of 4–5 strap-like sclerites that are strongly twisted subapically (12C−E), usually with wide apical plate (
Fig. 28F
); apical blade of vesica tapered, notched (
Fig. 27D
); secondary gonopore completely circular, thick-rimmed (
Fig. 27E
); bursa copulatrix with weak, reduced sclerotized rings; interramal lobe of posterior wall narrow, covered with spinulate scale-like microstructures (
Fig. 27K, N
); interramal sclerite with relatively densely distributed, comb-like scaly microstructure (
Fig. 27L, O
); and ovipositor (gonapophysis I) generally slender, relatively rounded apically (
Fig. 12
G−H).
Discussion.
Pityopsallus
Wagner, 1952
(
type
species:
Psallus luridus
Reuter, 1878
, Palearctic) was proposed as a subgenus of the large Holarctic genus
Psallus
Fieber, 1858
and currently includes seventeen species. As discussed by Wyniger (2018) and evidenced by some plausible autapomorphies assumed in the above diagnosis,
Pityopsallus
is best regarded as full genus, and the relationship with
Psallus
is now posited to be only superficial.
Accordingly, the following eight new combinations are proposed for Asian (and E. Siberian) taxa; all are transferred from
Psallus
Fieber
:
Pityopsallus ermolenkoi
(Kerzhner, 1979)
n. comb.
,
Pt. hani
(Zheng & Li, 1990)
n. comb.
,
Pt. kimi
(Josifov, 1983)
n. comb.
,
Pt. laricinus
(Vinokurov, 1982)
n. comb.
,
Pt. laticeps
(Reuter, 1878)
n. comb.
,
Pt. nipponicus
(
Vinokurov, 1998
)
n. comb.
,
Pt. sachaensis
(
Vinokurov, 1998
)
n. comb.
,
Pt. yasunagai
(
Vinokurov, 1998
)
n. comb.
. A continental Chinese species listed as
Psallus (Pityopsallus) fortis
Li & Liu
in
Aukema (2018)
should be excluded from
Pityopsallus
and placed in the subgenus
Hylopsallus
(see below), based on the original description, and figured male genitalia (
Li & Liu, 2007
).
TABLE 3.
Measurements for three
Orthonotus
species.
Abbreviations—Fem: femur, L: length, Lbm: labium, Pron: pronotum, Tib: tibia; Vtx: vertex (interocular space), W: width.
Body L |
Head W |
Vtx W |
Pron W |
Max W |
Antenna L II III IV |
Lbm L |
Hind leg L Fem Tib |
Orthonotus bicoloripes
(from Russian Primorsky)
|
Male |
3.92 |
0.75 |
0.26 |
1.20 |
1.52 |
1.59 |
0.65 |
- |
- |
1.38 |
2.24 |
Male |
4.04 |
0.74 |
0.24 |
1.11 |
1.53 |
1.50 |
0.93 |
- |
- |
1.29 |
2.27 |
Female |
3.85 |
0.72 |
0.30 |
1.23 |
1.80 |
1.34 |
0.90 |
0.60 |
1.53 |
1.43 |
2.09 |
Female |
3.75 |
0.74 |
0.33 |
1.25 |
1.77 |
1.37 |
- |
- |
- |
- |
2.19 |
Orthonotus nakagawai
n. sp.
Male (N=4)
|
MAX |
3.87 |
0.80 |
0.29 |
1.20 |
1.61 |
1.52 |
0.99 |
0.69 |
1.52 |
1.53 |
2.48 |
MIN |
3.60 |
0.75 |
0.24 |
1.19 |
1.50 |
1.49 |
0.95 |
0.62 |
1.35 |
1.50 |
2.40 |
MEAN |
3.72 |
0.77 |
0.26 |
1.19 |
1.54 |
1.50 |
0.97 |
0.66 |
1.46 |
1.52 |
2.43 |
Orthonotus nakagawai
n. sp.
Female (N=3)
|
MAX |
3.80 |
0.75 |
0.30 |
1.32 |
1.79 |
1.19 |
0.89 |
0.62 |
1.49 |
1.47 |
2.25 |
MIN |
3.60 |
0.74 |
0.29 |
1.23 |
1.70 |
1.13 |
0.77 |
0.57 |
1.40 |
1.40 |
2.16 |
MEAN |
3.71 |
0.75 |
0.29 |
1.28 |
1.75 |
1.17 |
0.85 |
0.60 |
1.45 |
1.43 |
2.20 |
Orthonotus takaii
n. sp.
Male (N=4)
|
MAX |
3.58 |
0.75 |
0.29 |
1.20 |
1.68 |
1.29 |
1.02 |
0.63 |
1.35 |
1.35 |
2.10 |
MIN |
3.26 |
0.74 |
0.24 |
1.16 |
1.44 |
1.17 |
0.83 |
0.60 |
1.29 |
1.16 |
1.92 |
MEAN |
3.38 |
0.74 |
0.26 |
1.19 |
1.55 |
1.25 |
0.90 |
0.61 |
1.32 |
1.29 |
2.02 |
Orthonotus takaii
n. sp.
Female (N=3)
|
MAX |
3.58 |
0.74 |
0.32 |
1.34 |
1.85 |
1.13 |
0.84 |
0.63 |
1.41 |
1.35 |
2.03 |
MIN |
3.19 |
0.69 |
0.30 |
1.25 |
1.71 |
1.05 |
0.75 |
0.60 |
1.35 |
1.32 |
1.95 |
MEAN |
3.40 |
0.71 |
0.31 |
1.29 |
1.77 |
1.08 |
0.79 |
0.62 |
1.38 |
1.34 |
2.00 |
Within the
Pityopsallus
congeners, two monophyletic species-groups are recognized. The first group of species, including the
type
species of the genus
P. luridus
, is characterized by the moderate size, long labium whose apex exceeds the metacoxa and sometimes reaches the genital segment (
Fig. 21M
), the elongate and broadened left paramere (
Fig. 28C, D, H
, I−L), and the presence of the wide subapical plate on the vesica (
Fig. 28F
). The species of the second group share the relatively small size, shorter labium that is not exceeding apex of metacoxa (
Fig. 26N
), narrowed, caudally pointed left paramere (
Figs. 12A
,
28
J−K), and reduced subapical plate on the vesica (
Figs. 12
C−E, 27C−D, I).
Almost all the members of
Pityopsallus
are associated with
Pinaceae
conifers (
Yasunaga, 2001d
;
Wyniger, 2004
); however,
P. kimi
(Josifov, 1983)
is known to inhabit willows (
Salix
spp.
,
Salicaceae
) (
Kerzhner 1988
;
Vinokurov, 1998
) and
P. hani
was found from wheat (
Triticum
sp.
,
Poaceae
) and
Pyrus
sp. (Rosaceae)
. In
Japan
, six conifer inhabiting
Pityopsallus
members, including two undescribed species, have hitherto been recognized. The following key would be useful to identify the Japanese congeners.
Key to Japanese species of
Pityopsallus
1. Labium very long, its apex easily surpassing apex of metacoxa, reaching abdominal sterna VII–IX (cf.
Fig. 26M
); metatarsomere III as long as or slightly longer than I+II; sensory lobe of left paramere conspicuously developed, protruding posteriad (cf.
Fig. 28
C−D)...................................................................................... 2
– Apex of labium not exceeding apex of metacoxa; meta-tarsomere III shorter than I+II; left paramere moderately or sharply protruding posteriad (
Fig. 28
J−K)........................................................................ 4
2. Meso and metafemur with clear, fuscous, large spots ventrally; restricted to
Abies
spp.
....................
P. nipponicus
– Ventral spots on meso and metafemur small and obscure; on other conifers....................................... 3
3. Dorsum generally dark brown; ventral surface of metafemur with a row of small, obscure spots mesially; on
Pinus pumila
at alpine zones in
Hokkaido
.....................................................................
P. ermolenkoi
– Dorsum somber pale brown to brown; ventral surface of metafemur with obscure spots only on apical region; on
Larix kaempferi
..................................................................................
P. yasunagai
4. Vertex narrow (0.36 times as wide as head across eyes); labium shorter than basal width of pronotum (currently known only by a male
holotype
specimen).................................................................
P. sakuraii
n. sp.
– Male vertex wider (> 0.38 times as wide as head across eyes); labium about as long as or longer than basal width of pronotum ................................................................................................... 5
5. Metatibia almost equal in length to basal width of pronotum; each claw smooth; in
Japan
currently known only from Chishima Islands (Kunashiri and Etorofu)...................................................................
P. vittatus
–
Metatibia longer than basal width of pronotum; claws of pro- and metalegs minutely notched (
Fig. 26D, F
); central and
northern Honshu
(
Nagano and Tochigi
)..............................................................
P. maeharai
n. sp
.