Description of the previously unknown morphs of Periphyllus koelreuteriae (Takahashi) (Hemiptera, Aphididae: Chaitophorinae)
Author
Junkiert, Łukasz
Author
Wieczorek, Karina
text
Zootaxa
2019
2019-04-12
4585
1
360
368
journal article
27321
10.11646/zootaxa.4585.2.9
5184aeb0-8e12-477d-92a7-61460b951e7a
1175-5326
2637406
92B6F908-8ED0-460A-A605-419CFFF53D7F
Periphyllus koelreuteriae
(Takahashi, 1919)
(
Figs 1–3
;
Table 1
)
Chaitophorinella koelreuteriae
Takahashi, 1919a
: 275
Re-description of apterous viviparous female
(based on five specimens) (
Fig. 1
;
Table 1
).
Colour
. In life not recorded, but colour of apterae in spring generations reported in the literature as variably pigmented (generally dark or green by
Essig and Abernathy (1952)
; black or yellow by
Blackman and Eastop (2018))
. In mounted specimens: head, legs, sclerites and siphunculi dusky. Antennae dusky, only basal part of ANT III slightly paler.
Morphological characters
. Body oval (
Fig 1a
). Frons flat. Head with 6–7 pairs of fine, pointed setae, which are
0.08–0.22 mm
long. ANT 6-segmented (
Fig. 1b
), long, reaching ABD SEGM III, 0.61–0.64 × BL. ANT IV slightly longer than ANT V; ANT V always shorter than ANT VI; PT 2.72–3.11 × BASE; other antennal ratios: VI:III 0.84–0.93, V:III 0.50–0.51, IV:III 0.52–0.58. ANT I with 6–7 setae, ANT II with 4 setae, ANT III with 16–17 setae, ANT IV with 6–9 setae, ANT V with 2–6 setae, BASE with 2 setae. PT with 2–3 apical setae. ANT setae fine, pointed, up to
0.14 mm
long. LS ANT III 3.50–4.50 × BD III. Rostrum reaching middle coxae. ARS with 4 accessory setae (
Fig 1c
), 0.25–0.29 × ANT III and 0.81–0.86 × HT II. Legs setose, with numerous stout, pointed setae, which are
0.04–0.25 mm
long. Distal part of hind tibiae with few rows of short spinules; empodial setae spatulate; first tarsal chaetotaxy 5:5:5 (
Fig. 1d
). Abdominal tergites membranous, with large marginal and spinal sclerites, pleural sclerites very small, irregularly placed. 2–3 pale, pointed setae arising from marginal and spinal abdominal tergites, pleural sclerites with 1 setae each. Abdominal setae
0.05–0.34 mm
long. Siphunculi truncate with 1–3 rows of reticulations and well developed flange (
Fig. 1e
). Cauda broadly rounded, with 8 setae (
Fig. 1f
).
FIGURE 1.
Periphyllus koelreuteriae
—apterous viviparous female: (a) general view, (b) antenna, (c) apical segment of rostrum, (d) hind tarsus, (e) siphunculus, (f) cauda.
Description of oviparous female
(based on six specimens) (
Fig. 2
;
Table 1
).
Colour
. In life: unknown, in mounted specimens: head, legs, sclerites and siphunculi dusky. Antennae dusky, 2/3 length of ANT III slightly paler.
Morphological characters.
Body oval, segments VII–VIII of abdomen strongly elongated (
Fig. 2a
). Frons flat. Head with 6–7 pairs of fine, pointed setae, which are
0.12–0.22 mm
long. ANT 6-segmented (
Fig. 2b
), long, reaching abdominal segment III, 0.44–0.48 × BL. ANT IV slightly longer than ANT V; ANT V always shorter than ANT VI; PT 2.2–2.5 × BASE; other antennal ratios: VI:III 0.73–0.75, V:III 0.42–0.51, IV:III 0.46–0.57. ANT I with 3–4 setae, ANT II with 4 setae, ANT III with 11–16 setae, ANT IV with 5–8 setae, ANT V with 3–5 setae, BASE with 2 setae, PT with 2–3 apical setae. ANT setae fine, pointed, up to
0.17 mm
long. LS ANT III 4.25 × BD III. Rostrum reaching middle coxae. ARS with 4 accessory setae (
Fig. 2c
), 0.28–0.35 × ANT III and 0.86–0.90 × HT II. Legs setose, with numerous stout, pointed setae, which are
0.06–0.20 mm
long. Hind tibiae with numerous (79–85) rounded pseudosensoria, distributed on the whole length of tibiae. Distal part of hind tibiae with few rows of short spinules; empodial setae spatulate; first tarsal chaetotaxy 5:5:5 (
Fig. 2d
). Abdominal tergites membranous, tergites I–VI with large, oval marginal sclerites, clearly visible spinal sclerites and inconspicuous pleural sclerites. Abdominal setae
0.10–0.30 mm
long; marginal sclerites with 2–7 setae, spinal sclerites with 2 setae. Siphunculi truncate, with 4–5 rows of reticulations and well developed flange (
Fig. 2e
). Cauda broadly rounded, with 8 setae (
Fig. 2f
).
Description of alate male
(based on four specimens) (
Fig. 3
;
Table 1
).
Colour
. In life: unknown, in mounted specimens: head, antennae, pronotum, sclerites, siphunculi and genitalia dusky. Legs dusky with basal part of femur and middle part of tibia slightly paler.
Morphological characters.
Body elongated. Frons flat. Head with 7 pairs of long fine, pointed setae, which are
0.15–0.17 mm
long (
Fig. 3a
). ANT 6-segmented (
Fig. 3b
), long, reaching abdominal segment III, 0.76–0.82 × BL. ANT IV slightly longer than ANT V; ANT V always shorter than ANT VI; PT 3.63 × BASE; other antennal ratios: VI:III 0.71–0.82, V:III 0.43–0.48, IV:III 0.61–0.64. ANT I with 7–8 setae, ANT II with 3–5 setae, ANT III with 10–19 setae, ANT IV with 8–12 setae, ANT V with 4–6 setae, BASE with 2 setae, PT with 2–3 apical setae. ANT setae fine, pointed, up to
0.13 mm
long. LS ANT III 3.25 × BD III. The whole surface of ANT III–V covered by rounded, secondary rhinaria: ANT III with 64–86 rhinaria, ANT IV with 30–42 rhinaria, ANT V with 12–18 rhinaria. Rostrum reaching fore coxae. ARS with 4 accessory setae (
Fig. 3c
), 0.17–0.20 × ANT III and 0.81–0.86 × HT II. Legs setose, with numerous stout, pointed setae, which are
0.05–0.23 mm
long. Distal part of hind tibiae with rows of short spinules; empodial setae spatulate; first tarsal chaetotaxy 5:5:5 (
Fig. 3d
). Fore wings with normal venation (
Fig. 3e
). Abdominal tergites membranous, with large fused spinal sclerites, pleural sclerites very small, irregularly placed, marginal sclerites oval. Abdominal setae
0.10–0.35 mm
long; marginal sclerites with 2–3 setae, pleural sclerites with 1 setae each, spinal sclerites with 4 setae (
Fig. 3f
). Siphunculi truncate, reticulated, except basal part, with developed flange (
Fig.
3g
). Cauda broadly rounded, with 8 setae (
Fig. 3h
). Genitalia well developed, strongly sclerotized with roundish, lobate parameres, covered by numerous spine-like setae. Basal parts of phallus slightly extended, tongue-shaped, with numerous short spinules (
Fig.
3i
).
Life cycle.
P
.
koelreuteriae
is a holocyclic species and its life cycle was studied in detail by
Liu
et al
. (1999a)
and
Lin
et al
. (2001b)
in
Taiwan
. Specifically, the sexual generation appeared in winter with eggs as the overwintering form. The oviparous females appeared in the period when the foliage began to fall off the host plants (December to February), whereas the males and eggs were found from mid-January to early February. The highest population density was found in the lower layer and the lowest density in the upper layer of the canopy of the host trees. Both winged and wingless viviparous females were found in the field throughout the year, except from July to September, when the aphid population was extremely low. The aestivating forms occurred from March to June and reached their peak from April to May. These morph were probably present during the whole summer, what is in line with the phenology of host tree and in accordance with the biology of other species of the genus
Periphyllus
(
Essig & Abernathy 1952
;
Wieczorek
et al
. 2017
). Such a shift in the life cycle is also typical in the warm, humid subtropical climate in the Ta-Keng area of
Taichung
in
Taiwan
, where the aphids were studied. In this area, the highest temperature of the year occurs in July and August, while the lowest temperature occurs in January and February. Numerous experimental studies have shown that the temperature has the greatest effect on the development, longevity and reproduction of the various morphs of this species (
Liu
et al
. 1999b
;
Kuo
et al
. 2001
;
Lin
et al
. 2001a
,
b
,
2002
; Ding Xu
et al
. 2015;
Jing
et al
. 2015
). By contrast, the life cycle of
P
.
koelreuteriae
in the condition of the temperate climate of
Tiencin
, northeast
China
(present study) was typical for aphids, with the sexual generation being observed from mid-October to mid-November.
Host plants.
Koelreuteria
is a small genus of flowering plants of the family
Sapindaceae
, which is native to southern and eastern Asia.
Koelreuteria
spp. grows easily in average, dry to medium, well-drained soil in full sun and adapts to a wide range of soils. Moreover, it tolerates drought and many urban air pollutants (
Gilman & Watson 1993
). Therefore, is significant the shade trees of the green areas and parks in its native range in
China
,
Korea
and
Japan
and its use as a medicinal plant in
China
(
Yang
et al
. 2018
). Although the Golden Rain Tree,
K
.
paniculata
, is treated as the main host plant for
P
.
koelreuteriae
(Holman 2010)
, the species is also associated with other representatives of this genus, including
K. elegans
(Seem.) A.C. Sm.
, which is endemic to
Taiwan
(
Taiwan
, Ta- Keng area of
Taichung
Liu
et al
. 1999a
), or
K. bipinnata
, which is native to southern
China
(
Jing
et al
. 2015
). Because
P
.
koelreuteriae
seriously affects the growth of its host-plants, not only by causing new leaf deformities and curly leaves, but also by inducing its own leaves to have sooty mould, it is known as one of the most damaging pests of the ornamental trees of this genus (
Ping
et al
. 2004
).
FIGURE 2.
Periphyllus koelreuteriae
—oviparous female: (a) general view, (b) antenna, (c) apical segment of rostrum, (d) hind tibia with pseudosensoria and tarsus, (e) siphunculus, (f) cauda.
FIGURE 3.
Periphyllus koelreuteriae
—alate male: (a) head, (b) antenna, (c) apical segment of rostrum, (d) hind tarsus, (e) fore wing, (f) abdomen, (g) siphunculus, (h) cauda, (i) genitalia.
Distribution.
China
, Chaozhou (
Wu 1935
);
China
,
Shanghai
(
Ping
et al
. 2004
);
China
, Changzhou (
Wang
et al
. 2018
);
China
,
Beijing
(BMNH coll., London,
UK
);
China
,
Tiencin
(present study);
Taiwan
, Ta-Keng area of
Taichung
(
Liu
et al
. 1999a
);
South Korea
(
Paik 1972
);
Japan
,
Tokyo
(
Takahashi 1919a
);
Japan
,
Tokyo
, Morioka,
Aomori
(
Shinji 1927
,
1941
) (
Fig. 4
).
FIGURE 4.
Distribution of
Periphyllus koelreuteriae
.
TABLE 1.
Measurements (in mm) of autumn generations of apterous viviparous females, oviparous females and males of
Periphyllus koelreuteriae
.
Apterous viviparous female |
Oviparous female |
Alate male |
Number of specimens |
5 |
6 |
4 |
Body length |
2.3–2.57 |
2.88–3.81 |
2.47–2.67 |
Maximal width of body |
1.17–1.32 |
1.10–1.52 |
0.85–0.87 |
Length of antennae |
1.42–1.67 |
1.39–1.69 |
2.05 |
Length of antennal segment III |
0.44–0.51 |
0.45–0.56 |
0.62–0.73 |
Length of antennal segment IV |
0.23–0.30 |
0.21–0.32 |
0.40–0.45 |
Length of antennal segment V |
0.22–0.26 |
0.19–0.29 |
0.30–0.32 |
Length of antennal segment VIa base |
0.09–0.11 |
0.10–0.12 |
0.11 |
Length of antennal segment VIb p.t. |
0.28–0.30 |
0.22–0.30 |
0.40–0.41 |
Length of seta antennal segment III |
0.14–0.18 |
0.11–0.18 |
0.13 |
Length of apical segment of rostrum |
0.13 |
0.13–0.20 |
0.13 |
Length of hind femora |
0.72–0.85 |
0.56–0.87 |
0.85–1.00 |
Length of hind tibiae |
1.07–1.25 |
0.95–1.22 |
1.27–1.55 |
Length of hind tarsi segm. II |
0.15–0.16 |
0.15–0.22 |
0.15–0.16 |
Length of siphunculi |
0.14–0.15 |
0.12–0.17 |
0.12–0.14 |
Maximal width of siphunculi |
0.21–0.23 |
0.12–0.17 |
0.15–0.17 |
Length of cauda |
0.18–0.20 |
0.17–0.19 |
0.14–0.17 |
It is highly possible that
P. koelreuteriae
occurs more widely in countries where
Koelreuteria
spp. is grown, as it is a significant ornamental plant.
Remarks.
Among the 13 species of the East Asian
Periphyllus
, the sexuales are only known for four of them (
Blackman & Eastop 2018
). Therefore, for now, it is impossible to compare and key the oviparous females or males of these species of the genus
Periphyllus
from the mentioned area. Apterous viviparae of
P. koelreuteriae
were first found by the authors on the
K. paniculata
that were growing on the campus of Nankai University,
Tiencin
,
China
in
July 2010
. In
October and November 2010
, Dr Kai Dang simultaneously collected apterous viviparous females and sexuales from this same tree, which confirmed that the described morphs belong to
P. koelreuteriae
. In mounted specimens, the spring and autumn generations of apterous viviparous females, are broadly similar in body colouration and sclerotization of dorsal abdominal tergites.