European Journal of Taxonomy 197: 1-15
http://dx.doi.org/10.5852/ejt.2016.197
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2016 • Negrobov et al.
Research article
um:lsid:zoobank.org:pub:28A67A43-CFF6-412A-B2D8-596113B09D01
Species of the genus Chrysotus Meigen, 1824 (Diptera: Doiichopodidae)
from Japan, with descriptions of two new species
Oleg P. NEGROBOV 1 *, Tatsunori KUMAZAWA 2 , Toshihiro TAGO 3 & Viktor N. FURSOV 4
1 Voronezh State University, Universitetskaya sq., 1, Voronezh 394006, Russia.
2 Osaka Museum of Natural History, 1-23, Nagai Park, Higashi-sumiyoshi, Osaka 546-0034, Japan.
3 29-13-101, Motogou, 1-chome, Kawaguchi, Saitama, 332-0011, Japan.
4 1.1. Schmalhausen Institute of Zoology, Kyiv, Ukraine.
* Corresponding author:
[email protected]
4 Email: ufensia@gm all com
1 urn:lsid:zoobank.org:author:18FC9848-2BE3-4809-8A91-070E6C6EB8FE
2 urn:lsid:zoobank.org:author:579148A7-D61D-4D7C-BlBB-8B7573B7FAF6
3 urn:lsid:zoobank.org:author:EC82645A-5E91-4977-B0DD-6437FA3976D7
4 urn:lsid:zoobank.org:author:FFF72665-7496-4A78-A577-7C10AA998B69
Abstract. Two new species of the genus Chrysotus Meigen, 1824 are described: Ch. masunagai
Negrobov, Kumazawa, Tago sp. nov and Ch. saigusai Negrobov, Kumazawa & Tago sp. nov. Chrysotus
parilis Parent, 1926 is recorded from Japan for the first time. An identification key to all known species
of the genus Chrysotus of Japan is presented together with a tree diagram showing relationships among
them.
Keywords. Japan, Chrysotus, Doiichopodidae, new species.
Negrobov O.P., Kumazawa T., Tago T. & Fursov V.N. 2016. Species of the genus Chrysotus Meigen, 1824 (Diptera:
Doiichopodidae) from Japan, with descriptions of two new species. European Journal of Taxonomy 197: 1-15.
http://dx.doi.Org/l 0.5852/eit.2016,197
Introduction
The cosmopolitan genus Chrysotus is the largest of the subfamily Diaphorinae, including more than
440 species (Grichanov 2014; Wei et al. 2015), of which 91 occur in the Palaearctic Region (Negrobov
unpublished data). The Palaearctic species of Chrysotus were revised Negrobov and co-authors in
a series of publications (Negrobov 1980; Negrobov & Maslova 1995; Negrobov et al. 2000, 2003;
Maslova et al. 2011). In the Oriental region of China more than one hundred species of the genus
Chrysotus are known (Wei 2012; Wei et al. 2015; Liu et al. 2013, 2015).
There are few morphological differences between the species of the genus, but most species can be well
distinguished by the structure of the apex of the phallus. Negrobov et al. (2000) published the most
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European Journal of Taxonomy 197 : 1-15 ( 2016 )
recent keys of the Palaearctic species of the genus. A key, with 28 species from China, to the males of
the genus was also published by Yang et al. (2011).
Meanwhile, only a few studies on the species of the genus in Japan are available (Saigusa 2008).
Masunaga (2014) listed only 3 species: Chrysotus cilipes Meigen, 1824, Ch. nudisetus Negrobov &
Maslova, 1995 and Ch. pulchellus Kowarz, 1874. The record of Chrysotuspulchellus for Japan probably
belongs to the new species Ch. masunagai sp. nov. described herein. Recently, two species of the genus
have been recorded, Ch. tagoi Negrobov, Maslova & Fursov, 2015 and Ch. kumazawai Negrobov,
Maslova & Fursov, 2015 (Negrobov et al. 2015), but it is assumed that there are more species present in
Japan. Here, we present additional records of the genus from Japan, including two new species.
Material and methods
Specimens were collected by Dr. V.N. Fursov (Schmalhausen Institute of Zoology of the National
Academy of Sciences Ukraine) and Mr. T. Tago from Japan.
Holotypes of the new species are deposited in the Osaka Museum of Natural History (OMNH, Japan) and
the Zoological Institute of the Russian Academy of Sciences (ZIN, Saint Petersburg, Russia), and some
of the paratypes are housed in the collections of the Schmalhausen Institute of Zoology of the National
Academy of Sciences Ukraine (IZU), the Osaka Museum of Natural History (OMNH, Japan) and the
Voronezh State University (VSU, Russia). We follow Cumming & Wood (2009) for the terminology.
Male terminalia were treated in 10% KOH and glycerol for observing genital structures.
Relationships among species were investigated using a tree-diagram constructed in the TNT program
(Goloboff et al. 2003). Characters were selected on the basis of their diagnostic value in the key of the
genus Chrysotus. All 20 characters were equally weighted. Character polarity was based on outgroup
comparison, with the most plesiomorphic state indicated by “0” and the apomorphic state indicated by
“1” or “2” according to Capellari (2013). The following characters were investigated:
1. Face narrower than the length between ocellar bristles or equal (0). Face wider than the length
between ocellar bristles (1).
2. Postpedicel higher than long (0). Postpedicel longer than height (1).
3. Arista subapical (0). Arista apical (1).
4. Palpus brown (0). Palpus pale (1).
5. Tower postocular setae pale (0). Tower postocular setae black (1).
6. Fore coxae dark (0). Fore coxae yellow at distal part (1).
7. Fore coxae with dark hairs (0). Fore coxae with white or yellow hairs (1).
8. Fore femur mostly dark (0). Fore femur yellow (1).
9. Mid femur dark (0). Mid femur yellow (1).
10. Basal part of hind femur dark (0). Basal part of hind femur yellow (1).
11. Hind trochanter dark (0). Hind trochanter yellow (1).
12. Hind tibia brown (0). Hind tibia yellow (1).
13. Hind femora with anteroventral hairs on entire length of femur (0). Hind femora without anteroventral
hairs on entire length of femur (1).
14. Hind tibia with short erect antero ventral hairs at lateral side, their length approximately equal to the
diameter of tibia (0). Hind tibia without short erect anteroventral hairs at lateral side (1).
15. First segment of hind tarsus with short erect hairs (0). First segment of hind tarsus without short erect
hairs (1).
16. Apical part of CuAj approximately in 2.5 times longer than dm-cu (0). Apical part of CuAj less than
in 2.5 times longer than dm-cu (1).
17. Abdomen metallic green (0). Abdomen purple or blue (1).
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NEGROBOV O.R et al., Species of Chrysotus (Dolichopodidae) from Japan
Table 1 . Morphological characters matrix of the Chrysotus species from Japan.
Morphological characters
Species
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
Ch. cilipes Meigen, 1824
0
0
0
1
0
1
1
1
1
0
1
1
0
0
0
0
0
1
2
0
Ch. laesus ( Wiedemann, 1817)
1
0
1
0
0
0
1
0
0
1
0
0
1
1
1
1
1
0
0
2
Ch. masimagai sp. nov.
0
1
0
1
0
1
0
0
1
0
1
0
0
0
0
0
0
1
2
1
Ch. midisetus Negrobov & Maslova, 1995
0
0
0
0
1
0
0
0
0
1
0
1
1
1
1
0
0
0
2
0
Ch. parilis Parent, 1926
0
0
0
1
0
1
1
1
1
0
1
1
1
1
1
0
0
1
2
1
Ch. saigusai sp. nov.
0
0
0
0
0
1
0
0
0
1
1
1
0
0
0
0
0
0
2
0
Ch. tagoi Negrobov et al. , 2015
0
0
0
0
0
1
0
1
1
0
1
1
1
0
0
0
0
0
2
0
Ch. kumazawai Negrobov et al., 2015
0
0
0
1
0
1
0
0
0
1
1
1
1
0
0
0
0
1
1
1
18. Epandrium in the basal part without small projection (0). Epandrium in the basal part with small
projection (1).
19. Apical half of surstylus with two thickened triangular bristles (0). Apical half of surstylus with one
thickened triangular bristle (1). Apical half of surstylus without thickened triangular bristles (2).
20. Phallus with two lateral processes at apex (0). Phallus with one lateral process at apex (1). Phallus
without lateral processes at apex (2).
Results
Taxonomic descriptions
Class Hexapoda Blanville, 1816
Order Diptera Linnaeus, 1758
Family Dolichopodidae Latreille, 1809
Genus Chrysotus Meigen, 1824
We found the following six species in the collection of Mr. T. Tago and of the Schmalhausen Institute of
Zoology of National Academy of Sciences Ukraine, including a species new to Japan and two species
new to science.
Chrysotus cilipes Meigen, 1824
Material examined
JAPAN: 9 Saitama Prefecture, Misato City, Edogawa river bank, 9 Aug. 2008, 15 May 2010, leg.
T. Tago.
Distribution
Western Europe, Abchazia, Afghanistan, Armenia, Azerbaijan, China, Japan, Kazakhstan, Korea,
Mongolia, Turkey, Ukraine and Russia (Leningrad, Novgorod, Pskov, Moscow, Voronezh, Adygea,
Kabardino-Balkaria, Krasnodar, Rostov, Tomsk, Altai, Krasnoyarsk, Baikal, Transbaikalia, Yakutia,
Amur, Maritime Territory). There are a few records of the species in Japan (Negrobov et al. 2008;
Masunaga 2014).
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European Journal of Taxonomy 197 : 1-15 ( 2016 )
Chrysotus laesus (Wiedemann, 1817)
Material examined
JAPAN: 29 SS, Honshu, Aichi Prefecture, Nagoya, Nagakute-cho Park, 23-30 May 1999, leg. V. Fursov.
Distribution
Western Europe, Armenia, Georgia, Japan and Russia (Karelia, Saint Petersburg, Pskov, Yaroslavl,
Moscow, Ryasan, Bashkiria, Tatarstan, Kursk, Lipetsk, Voronezh, Krasnodar, Adygea, North Caucasus,
Orenburg, Omsk, Tomsk, Altai, Krasnoyarsk, Irkutsk, Buryatia, Yakutia, Amur).
Chrysotus nudisetus Negrobov & Maslova, 1995
Chrysotus sp. 3t - Tago 2010: 44.
Material examined
JAPAN: 1 S, Saitama Prefecture, Misato City, Edogawa river bank, 9 Aug. 2008, leg. T. Tago; 1 S,
Chiba Prefecture, Nagareyama City, Ichinoya, 30 Sep. 2008, leg. T. Tago; 1 Saitama Prefecture,
Hidalca City, Yokote, 12 Jul. 2009, leg. T. Tago; 1 S, Saitama Prefecture, Ootaki, Chichibu City,
Mameyakibashi, 7 Aug. 2010, leg. T. Tago.
Distribution
Japan and Russia: Sakhalin, Primorye, Khabarovsk, Magadan, Chukotka. The species was described
from Japan and the Far East of Russia by Negrobov & Maslova (1995).
Chrysotus parilis Parent, 1926
Material examined
JAPAN: Saitama Prefecture, Misato City, Edogawa river bank, 9 Aug. 2008 (3 SS, 2 $ $), 13 Oct. 2008
(1 S), 15 May 2010 (2 <SS), leg. T. Tago; 1 Honshu, Ibaraki Prefecture, Tsukuba, Yawara, rice fields,
16 Jul. 1997, leg.V. Fursov; 1 S, Honshu Aichi Prefecture, Nagoya, Nagakute-cho Park, 23-30 May
1999, leg. V. Fursov.
Distribution
China, Japan. The species originally described from China is here recorded for the first time from Japan.
Chrysotus masunagai Negrobov, Kumazawa & Tago, sp. nov.
urn:lsid:zoobank.org:act:CA904F5D-F488-4B95-B043-0D598C014071
Figs 1, 5A
Chrysotus sp. 2t - Tago 2010: 43.
Diagnosis
Face narrow; postpedicel small; lower postocular setae white; fore coxa with black hairs; femora mostly
yellow; mid tibia with 2 anterodorsal and 2 posterodorsal setae; hind femur and with long setae, hind
tibia with short hairs; phallus with two lateral processes on tip.
Etymology
The species is named after the famous dipterologist Dr. Kazuhiro Masunaga from Japan.
4
NEGROBOV O.R et al., Species of Chrysotus (Dolichopodidae) from Japan
Material examined
Holotype
JAPAN: 1 3, Ibaraki Prefecture, Tsukuba, Yawara, 16 Jun. 1997, leg. V. Fursov (ZIN, Russia).
Paratypes
JAPAN: 1 3, labeled, Saitama Prefecture, Misato City, Edogawa river bank, 13 Oct. 2008, leg. T. Tago;
4 S3, same data, 28 Apr. 2012, leg. T. Tago; 1 3, same data, 15 May 2010, leg. T. Tago (OMNH, 2
paratypes VSU).
Description
Male
Measurements. Body length: 1.3-1.4 mm, wing length: 1.4-1.5 mm
Head. Frons green with purple tinge, without pollen. Face narrow, its width narrower than the width
between ocellar bristles in lower part. Frons green at the top, with pollinosity at the bottom. Antenna
black, postpedicel small, triangular, length 1.3 times greater than height. Arista subapical, with short
hairs. Fength of arista more than two times longer than length of postpedicel. Proboscis and palpus
brown with black hairs without pollen. Power postocular setae pale.
Fig. 1 . Chrysotus masunagai Negrobov, Kumazawa & Tago sp. nov., 3, paratype, coll. 28 Apr. 2012.
A. Hypopygium, lateral view. B. Apex of surstylus, lateral view. C. Antenna. D. Apex of phallus, lateral
view. E. Cerci, lateral view.
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European Journal of Taxonomy 197 : 1-15 ( 2016 )
Thorax. Metallic green, scutum with bronze tinge and without pollen. Pleura with pollen, propleuron
with 1-2 setae. 5 pairs of strong dorsocentral setae. Acrostichal setae long, irregular 6-7 pairs, arranged
in two rows. Scutellum with 2 long and 2 short lateral setae.
Leg. Fore coxa yellowish brown, mid and hind coxa dark; femora mostly yellow, except dorsal surfaces
of fore femur, middle part of the mid femur and apical third part of the hind femur dark; fore and mid
tibiae yellow, hind tibia dark; tarsi yellow except hind tarsus and apical parts of fore and mid tarsus dark.
All coxae with dark hairs and setae. Fore femur with long white anteroventral hairs, length approximately
equal to the width of femur. Fore tibia with 1 anterodorsal seta and short posteroventral hairs. Ratio of
fore tibia and tarsus (from 1 to 5) 2.6: 1.5: 0.6: 0.5: 0.3: 0.4. Mid femur with a short preapical seta. Mid
tibia with 2 anterodorsal and 2 short posterodorsal setae. Ratio of mid tibia and tarsus (from 1 to 5) 3.4:
1.6: 0.8: 0.6: 0.4: 0.3. Hind femur with several long preapical setae and short anteroventral hairs on
entire length femur. Hind tibia with 3-4 short anterodorsal setae and short erect anteroventral hairs, its
length approximately equal to the diameter of tibia. First segment of hind tarsus with short erect hairs.
Ratio of hind tibia and tarsus (from 1 to 5) 3.7: 1.2: 1.0: 0.6: 0.4: 0.3.
Wing. Hyaline with dark veins; R 4+5 and M 1+0 parallel at apex. Length of costal section between R 4+5 and
M 1+0 more than 2 times longer than that between R 0+3 and R 4+5 ; m-cu distinctly shorter than apical part
of CuA ] . Halter and cilia on lower calypter yellow.
Abdomen. Metallic green, grey pollinose laterally, covered with black hairs. Epandrium oval in the
basal part of the oval; apical part of surstylus bent. Apex of phallus with two short lateral processes, left
process is rounded. Cercus with brown hairs, top of the left side with long processes.
Female
Unknown.
Addition to the key
In the key to the Palearctic species of Chrysotus (Negrobov et al. 2000), the new species Chrysotus
masunagai sp. nov. runs to Chrysotus verralli Parent, 1923 and can be distinguished from the latter by
following characters:
45. Femora almost yellow; dorsal side of fore femur, middle part of the mid femur and apical part
of the hind femur dark. Hind trochanter yellow .
. Ch. masunagai Negrobov, Kumazawa, Tago sp. nov.
- Femora dark. Hind trochanter black. England. Ch. verralli Parent, 1923
Chrysotus saigusai Negrobov, Kumazawa & Tago sp. nov.
urn: lsid: zoobank, org: act: D4B29EE A-1EF 5 -4210-A3 83-94EFE3ED3 5E A
Figs 2, 5B
Chrysotus sp. It - Tago 2010: 43.
Diagnosis
Face narrow, width in lower part less than distance between ocellar bristles; antenna black; postpedicel
transverse-oval, with a triangular tip; lower postocular setae white; fore coxa with black hairs; femora
mainly green-brown; mid tibia with 2 anterodorsal and 2 posterodorsal setae; hind femur with long
setae, hind tibia with short hairs; phallus with two lateral processes on tip.
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NEGROBOV O.R et al., Species of Chrysotus (Dolichopodidae) from Japan
Etymology
The species is named after the famous dipterologist Dr. Toyohei Saigusa from Japan.
Material examined
Holotype
JAPAN: 3, Honshu, Aichi Prefecture, Kasugai, Univ. Experim. Farm, on grass near ponds, 19 Jun.
2004, leg. V. Fursov (ZIN).
Paratypes
JAPAN: 4 33, same data as holotype, leg. V. Fursov; 5 33, Honshu, Nagoya, Higashiyama Park,
oak forest, 2 May 1999, leg. V. Fursov; 14 33, Honshu, Nagoya, Higashiyama Park, oak forest,
11 Aug. 1999, leg. V. Fursov; 1 3, Ibaraki Prefecture, Tsukuba, Sakuragaoka, swept grass near forest,
26 Apr. 1997, leg. V. Fursov; 2 33, Ibaraki Prefecture, Tsukuba, Sakuragaoka, 3 May 1997, leg.
V. Fursov; 2 33, Ibaraki Prefecture, Tsukuba, Sakuragaoka, 5 May 1997, leg. V. Fursov; 2 33, Ibaraki
Prefecture, Tsukuba, Yaware, near rice fields, 17 Jun. 1997, leg. V. Fursov; 4 33, Ibaraki Prefecture,
Tsukuba, Yaware, 25 Jun. 1997, leg. V. Fursov; 2 33, Ibaraki Prefecture, Tsukuba, Hanare, near rice
fields, 14 Jun. 1997, leg. V. Fursov; 2 33, Honshu, Nagoya, Midori-ku, Odalca Green Park, 5 May
1999, leg. V. Fursov; 1 3, Honshu, Nagoya, Nissin-shi, 5 Apr. 1999, leg. V. Fursov (IZU, VSU, ZIN);
Fig. 2. Chrysotus saigusai Negrobov, Kumazawa & Tago sp. nov., 3, paratype, coll. 8 Jul. 2012.
A. Hypopygium, lateral view. B. Hypopygium, ventral view. C. Antenna. D. Apex of phallus, lateral
view. E. Cerci, ventral view.
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European Journal of Taxonomy 197 : 1-15 ( 2016 )
1 Tochigi Prefecture, Kanuma City, Shimokasuo, 8 Jul. 2012, leg. T. Tago; 1 3, Saitama Prefecture,
Saitama City, Akigase Park, Sakura wood, 1 Oct. 2011, leg. T. Tago (OMNH, Japan); 1 S, Kuril Islands,
island Kunashir, Alekhine, 8-12 Aug. 1984, leg. Kirejtshulc (ZIN).
Description
Male
Measurements. Body length: 1.2-1.3 mm, wing length: 1.2—1.3 in in
Head. Frons green with purple tinge, without pollen. Face narrow, its width narrower than the width
between ocellar bristles in lower part. Frons green at the top, with pollinosity on the bottom. Antenna
black, postpedicel small, a right-angled triangular, its length about equal to its height. Arista subapical,
with short hairs. Length of arista approximately five times longer than length of postpedicel. Proboscis
and palpus brown with black hairs without pollen. Lower postocular setae pale.
Thorax. Metallic green, scutum with bronze tinge and without pollen. Pleura with pollen, propleuron
with 1-2 setae. 5 pairs of strong dorsocentral setae. Acrostichal setae long, irregular 6-7 pairs, arranged
in two rows. Scutellum with 2 long and 2 short lateral setae.
Leg. All coxae dark; femora mostly dark, except apical part of fore femur, apical and basal part of
mid femur and basal part of hind femur yellow; trochanters yellow or yellowish-brown; fore and mid
tibiae yellow, hind tibia yellowish-brown; most part of mid and hind tarsi yellow, basal parts hind
tarsus yellowish-brown. Coxae with dark hairs and setae. Fore femur with 3 long preapical setae. Fore
tibia with 1 anterodorsal seta and short posteroventral hairs. Fore tarsus with short hairs. Ratio of fore
tibia and tarsus (from 1 to 5) 2.8: 1.7: 0.7: 0.5: 0.4: 0.5. Mid femora with 3 short preapical setae and
short anteroventral hairs. Mid tibia with 2 anterodorsal and 2 short posterodorsal setae. Ratio of mid
tibia and tarsus (from 1 to 5) 3.8: 2.1: 1.0: 0.7: 0.5: 0.4. Hind femora with 4 long preapical setae and
short anteroventral hairs on entire length of femur. Hind tibia with 4 short anterodorsal, 3 posterdorsal
setae and short erect anteroventral hairs, their length approximately equal to the diameter of tibia. First
segment of hind tarsus with short erect hairs. Ratio of hind tibia and tarsus (from 1 to 5) 4.4: 1.5: 1.2:
0.7: 0.5: 0.4.
Wing. Hyaline with dark veins; R 4+5 and M 1+0 slightly divergent at apex. Length of costal section between
R 4+5 and M 1+0 about twice longer than that between R 0+3 and R 4+5 ; m-cu distinctly shorter than apical part
of CuA r Halter and cilia on lower calypter yellow.
Abdomen. Metallic green, pollinose laterally, covered with black hairs. Epandrium oval in the basal part
with the small projection; apical tip of surstylus bent. Phallus with two lateral processes at apex. Cercus
oval with black hairs.
Female
Unknown.
Addition to the key
In the key to the Palearctic species of Chrysotus (Negrobov et al. 2000), the new species Chrysotus
saigusai Negrobov, Kumazawa & Tago sp. nov. runs to Chrysotus defensus Negrobov & Maslova, 2000
and can be distinguished from the latter by the following characters:
58. Basal part of hind femur and hind trochanter black. The phallus before the apex with two long
dorsal processes. Caucasus. Ch. defensus Negrobov & Maslova, 2000
- Basal part of hind femur and hind trochanter yellow. The phallus before the apex with short lateral
processes. Ch. saigusai Negrobov, Kumazawa & Tago sp. nov.
8
NEGROBOV O.R et al.. Species of Chrysotus (Dolichopodidae) from Japan
Key to the males of Japanese Chrysotus
1. Femora mostly dark-green or brown.2
- Femora mostly yellow.5
2. Postocular setae black (Fig. 3A-C) . Ch. nudisetus Negrobov & Maslova, 1995
- Postocular setae pale .3
Fig. 3. A-C. Chrysotus nudisetus Negrobov & Maslova, 1995, S, paratype, Russia (Sakhalin).
A. Hypopygium, lateral view. B. Surstylus, ventral view. C. Apex of phallus, lateral view. —
D-E. Chrysotus laesus (Wiedemann, 1817), Russia (European part). D. Hypopygium, lateral view.
E. Phallus, lateral view. — F-G. Chrysotus kumazawai Negrobov, Maslova & Fursov, 2015, S, paratype,
coll. 20 Jul. 1997 by V. Fursov. F. Hypopygium, lateral view. G. Apex of phallus, lateral view.
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European Journal of Taxonomy 197 : 1-15 ( 2016 )
3. Face wide, more than 2 times wider than the length between ocellar bristles. Thorax and abdomen
with purple tingle. Postpedicel large, approximately 2 times wider than long (Fig. 3D-E).
. Ch. laesus (Wiedemann, 1817)
- Face narrow, narrower than the length between ocellar bristles. Thorax and abdomen green.
Postpedicel small, approximately as long as wide.4
4. Postpedicel triangular apically. Surstylus approximately 1.5 times longer than cercus.
Apicoventral epandrial lobe well developed, broad oval, without excavation .
. Ch. saigusai Negrobov, Kumazawa & Tago sp. nov.
- Postpedicel oval apically. Surstylus approximately equal to cercus. Apicoventral epandrial lobe not
developed, with excavation at apex (Fig. 3F-G).
. Ch. kumazawai Negrobov, Maslova & Fursov, 2015
5. Fore coxae with black hairs.6
- Fore coxae with white hairs.7
Fig. 4. A-B. Chrysotus tagoi Negrobov, Maslova & Fursov, 2015, paratype, Japan (Honshu, Ibaraki
Pref., Tsulcuba), coll. 16. Jul. 1997 by V. Fursov. A. Hypopygium, lateral view. B. Apex of phallus, lateral
view. — C-D. Chrysotusparilis Parent, 1926, Russia (Primorje). C. Hypopygium, lateral view. D. Apex
of phallus, lateral view. — E-F. Chrysotus cilipes Meigen, 1824, Russia (Primorje). E. Hypopygium,
lateral view. F. Apex of phallus, lateral view.
10
NEGROBOV O.R et al.. Species of Chrysotus (Dolichopodidae) from Japan
6. Postpedicel longer than wide. Dorsal part of fore femora, middle femora in the middle part
and apical third of hind femora dark. Phallus with oval process at apex on the left side .
. Ch. masunagai Negrobov, Kumazawa, Tago sp. nov.
- Postpedicel small, approximately as long as wide. Hind femora with dark spot at apex, the rest of
femora yellow. Phallus with claw-shaped process at apex on the left side (Fig. 4A-B) .
. Ch. tagoi Negrobov, Maslova & Fursov, 2015
7. Hind tibia without long erect hairs. Hind tibia at apex without group of ventral hairs. Postpedicel
large, triangular at apex (Fig. 4C-D). Ch. parilis Parent, 1926
- Hind tibiae and hind tarsi with long erect hairs, longer than tibia width. Hind tibia at apex with
group of ventral hairs. Postpedicel small, oval apically (Fig. 4E-F). Ch. cilipes Meigen, 1824
Cladistic analyses
According to Capellari (2013), the absence of a small projection in the basal part of the epandrium
represents the plesiomorphic character state. The combination of this character state with such character
states as pale palpus, dark fore coxae, yellow hind tibia with short erect anteroventral hairs and short
erect hairs on the first segment of hind tarsus separate the group of Ch. saigusai and Ch. tagoi from all
other Japanese Chrysotus (Fig. 6). The species Ch. saigusai can be separated from Ch. tagoi by having
anteroventral hairs on the entire length of find femora and mostly dark fore femora.
The presence of the epandrial projection is the typical character states of the species Ch. cilipes ,
Ch. parilis and Ch. masunagai sp. nov., they are, however, included in the group with Ch. saigusai
A B
Fig. 5. Male habitus, lateral view. A. Chrysotus masunagai Negrobov, Kumazawa & Tago sp. nov.,
paratype, coll. 15 May 2010. B. Chrysotus saigusai Negrobov, Kumazawa & Tago sp. nov., S, paratype,
coll. 8 Jul. 2012.
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European Journal of Taxonomy 197 : 1-15 ( 2016 )
sp. nov. and Ch. tagoi on the basis of the characters of face width, position of arista, cooler of postocular
bristles, fore coxa, hind trochanter and morphology of CuAj. Concerning the distinctive characters of the
group including Ch. cilipes , Ch. parilis and Ch. masunagai sp. nov., in addition to the above mentioned,
the following character states can be ascribed: yellow middle femora and dark basal part of hind femur.
The morphological similarity between Ch. cilipes and Ch. parilis is sufficiently significant, while the
relationship with Ch. masunagai sp. nov. is unstable.
The species Ch. laesus , Ch. nudisetus and Ch. kumazawai compose the group with the least stable
internal connections. Their association is based on the similarity of color of fore, middle and hind
femora and the absence of the anteroventral hairs on entire length of hind femur.
Discussion
The genus Chrysotus is paraphyletic or possibly polyphyletic within the subfamily Diaphorinae
(Capellari & Amorim 2012). Bickel (2010) considers species of Chrysotus as various small-size
Diaphorinae species, mostly with inadequate description. Knowledge on the phylogenetic relationships
of the genus is poor. Therefore, it is important to investigate phylogenetic relationships of Chrysotus
species using both morphological and biogeographical data.
Similarity
0.0 0.4 0.8 1.2 1.6 2.0 2.4 2.8 3.2
_i_i_i_i_i_i_i_i_i_
- Ch. cilipes
- Ch. parilis
- Ch. masunaga
- Ch.saigusai
- Ch. tagoi
- Ch. iaesus
- Ch. nudisetus
- Ch. kumazawai
Fig. 6. Consensus cladistic tree of 6 equally parsimonious trees obtained from 20 morphological
characters for the Chrysotus Meigen, 1824 species from Japan.
12
NEGROBOV O.R et al. , Species of Chrysotus (Dolichopodidae) from Japan
Eight species of the genus Chrysotus have been reported from the studied country and four of them are
endemic, while the others have trans-Palearctic ( Ch. cilipes , Ch. laesus, Ch. parilis) and East-Palearctic
(Ch. nudisetus) distributions.
The present cladistic analysis was made in two ways. When we consider the characteristics used in the
Palearctic keys of the genus, we were considering the possible relationship between the endemic and
trans-Palearctic species, thus inserting the endemic species in the general scheme.
The morphology of the genus Chrysotus is relatively variable, and the most important diagnostic
characters are the morphology of the apical part of the phallus, the color of the legs and the form of the
postpedicel. It should be noted that the use of the full list of characteristics does not allow for allocating
the endemic species in a separate cluster on any of the cladistic trees.
The cladistic analysis was carried out on the basis of a different combination of characters. It allowed
for the identification of groups of characters that separate the Japanese endemic species from the trans-
Palearctic species. This group of characters includes color of coxae and trochanter, ratio of apical
part of CuAj and dm-cu, the presence of erect hairs at hind tibia and the first segment of hind tarsus
and morphology of hypopygium. Most of the cladistic trees that were based on this combination of
characters demonstrated the allocation of two clusters comprising pairwise Ch. masunagai sp. nov. -
Ch. kumazawai and Ch. saigusai sp. nov. - Ch. tagoi. However, other stable regularities should also be
noted, which is shown in a number of cladistic trees. The clusters of endemic species often have been
associated with Palearctic species. So Ch. masunagai sp. nov. - Ch. kumazawai have been associated
with Ch. parilis and Ch. saigusai sp. nov- Ch. tagoi have been associated with Ch. cilipes. None of the
combinations of characters showed a clear allocation of these endemic species.
Most of the characteristics, including head morphology and color of legs, which are used for the diagnosis
of the Palearctic species, cannot be used for the Japanese species. Thus, further study of the phylogenic
relationships of Chrysotus species should be carried out, using a wider range of species, including both
trans-Palearctic and endemic species.
Acknowledgements
We express our gratitude to Dr. L. Wei for information about the species of the genus Chrysotus in
China, to the assistant of Voronezh University M. Chursina for the parsimony analysis of the species and
head of the Laboratory Olga Selivanova for creating the figures. We express our gratitude to Dr. Martin
Drake for making available the species of Chrysotus from England. The work was supported by the
Russian Foundation for Basic Research, grant No. 14-04-00264-a.
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Manuscript received: 4 December 2015
Manuscript accepted: 5 February 2016
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NEGROBOV O.R et al.. Species of Chrysotus (Dolichopodidae) from Japan
Published on: 17 May 2016
Topic editor: Koen Martens
Desk editor: Kristiaan Hoedemakers
Printed versions of all papers are also deposited in the libraries of the institutes that are members of the
EJT consortium: Museum national d’Histoire naturelle, Paris, France; Botanic Garden Meise, Belgium;
Royal Museum for Central Africa, Tervuren, Belgium; Natural History Museum, London, United
Kingdom; Royal Belgian Institute of Natural Sciences, Brussels, Belgium; Natural History Museum of
Denmark, Copenhagen, Denmark.
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