So me f a mil ie S o f Dipt e r a f r o m be e r t r a pS 
in ba l a t o n Hig Hl a n D, Hu n g a r y
Libor Dv o ř á k
1
, k ateřina Dv o ř á k o v á
1
, Jan Má c a
2
& a ttila J. Tr á Je r
3
1 
Tři Sekery 21, c Z-35301 Mariánské Lázně, c zech r epublic; 
e-mail: lib.dvorak@seznam.cz, k.marsova@seznam.cz
2 
Na Potoce 276, c Z-39181 v eselí nad Lužnicí, c zech r epublic; 
e-mail: janxmaca@seznam.cz
3 
Sustainability Solutions r esearch Lab, University of Pannonia, 
e gyetem utca 10, H-8200 v eszprém, Hungary; 
e-mail: attilatrajer@gmail.com
a bstract – Faunistic records for 41 Diptera species from nine families (a nisopodidae,
Drosophilidae, Dryomyzidae, Heleomyzidae, Lauxaniidae, Platystomatidae, Sciomyzi-
dae, Syrphidae and Ulidiidae) collected at six sites at Felsőörs and Lovas in the
Balaton Highland, Hungary are presented. a mongst the material, the species
Drosophila suzukii (Matsumura, 1931) (Drosophilidae) and Callopistromyia annulipes
(Macquart, 1855) (Ulidiidae) belong to invasive pest species. Thermophilous species
are represented by interesting records, namely Suillia gigantea (Meigen, 1830), S. lu-
rida (Meigen, 1830), S. variegata (Loew, 1862) (all Heleomyzidae), Minettia subvittata
(Loew, 1847), Peplomyza discoidea (Meigen, 1830) (both Lauxaniidae), and Otites
lamed (Schrank, 1781) (Ulidiidae). Furthermore, the disease vector role of Phortica
variegata (Fallén, 1823) (Drosophilidae) is also discussed.
k e y w o r DS: beer traps, Diptera, faunistics, Hungary
izvleček – Ne k a J Dr UŽIN Dv o k r ILc e v IZ PIv Sk IH Pa STI Na Ba La -
To NSk e M v IŠa v JU Na Ma DŽa r Sk e M
Predstavljeni so favnistični podatki o 41 vrstah dvokrilcev iz devetih družin
(a nisopodidae, Drosophilidae, Dryomyzidae, Heleomyzidae, Lauxaniidae, Platys-
tomatidae, Sciomyzidae, Syrphidae in Ulidiidae), zbranih na šestih krajih pri vaseh
Felsőörs in Lovas na Balatonskem višavju na Madžarskem. Med temi sta vrsti
Drosophila suzukii (Matsumura, 1931) (Drosophilidae) in Callopistromyia annulipes
(Macquart, 1855) (Ulidiidae), ki sta invazivni vrsti škodljivcev. Toploljubne vrste so
93
ACTA ENTOMOLOGICA SLOVENICA
LJUBLJANA, JUNIJ 2021                  Vol. 29, øt. 1: 93–106

zastopane z zanimivimi najdbami, kot so Suillia gigantea (Meigen, 1830), S. lurida
(Meigen, 1830), S. variegata (Loew, 1862) (vse Heleomyzidae), Minettia subvittata
(Loew, 1847), Peplomyza discoidea (Meigen, 1830) (obe Lauxaniidae) in Otites
lamed (Schrank, 1781) (Ulidiidae). Poleg tega je obravnavana vloga vrste Phortica
variegata (Fallén, 1823) (Drosophilidae) kot prenašalke bolezni.
k LJUč Ne Be Se De : pivske pasti, Diptera, favnistika, Madžarska
introduction
Many Diptera species are important pests and disease vectors. w hile climate
change triggers the northward spread of mosquito (Medlock et al. 2012) and sandfly
vectors (Fischer et al. 2011), long-distance transport results in the rapid, intercontinental
spread of such invasive agricultural pest taxa as e.g., Drosophila suzukii (w alsh et al.
2011, Örsted & Örsted 2019). Many species, especially of a nisopodidae, Dryomyzi-
dae, Heleomyzidae, Lauxaniidae, Platystomatidae and Ulidiidae, prefer the moist,
shady habitats, because larvae most of them develop in such decaying materials as
rotten fruits and fungi or carrion, so that they play an important role in decomposition.
Sciomyzidae larvae are aquatic predators or terrestrial parasitoids of  moluscs. a l-
though most species breed in a decaying plant and fungal material, larvae of a few
species, such as D. suzukii, can also feed on fresh fruits. Drosophila species can act
as passive vectors of various pathogenic bacteria and fungi (Gilbert 1980).
The aim of the study was to study the Diptera assemblages of the Balaton highland
using simple method (beer trap) which can bring interesting results differing from
those obtained by more standard methods, such as sweeping and using Malaise or
Moericke traps.
methods
Study area. The Balaton Highland is the southern part of the Bakony Mountain
r ange which is bordered by the lake Balaton from the south. The distance of the col-
lecting sites from lake Balaton is 3 to 4 km. The bedrock is composed of Triassic-age
carbonates. There are several karst springs in the area. Mesophilous oak-forest com-
munities form the characteristic vegetation (Fig.1).
The description of the environment of the trapping sites is as follows:
a ll localities are wet and shaded, they were chosen because of preferences by
studied families.
1. a lkút spring: a cold headspring (helocren) with an associated marsh at the
north-east slope of the k ereszt hill, 47°0'31"N, 17°57'16"e . Eriophorum angustifolium
(Honck., 1782) as glacial relict species can be found in this refuge.
2. w atercourse of a lkút spring at the north slope of the k ereszt hill; the direction
of the valley is east to west, 47°0'31"N, 17°57'8"e . Carpinus betulus (L.) can be
Acta entomologica slovenica, 29 (1), 2021
94

found at this site; some orchid species are represented, however Pulmonaria officinalis
(L.) is a common herbaceous species.
3. Stream of Malom spring, site I; C. betulus, Staphylea pinnata (L.) and Acer
campestre (L.) are characteristic tree species; the direction of the valley is north to
south, 47°0'34"N, 17°56'59"e . a cold and shaded biotope in the bottom of the valley.
Asarum europaeum (L.) occurs in the undergrowth.
4. Stream of Malom spring, site II; a much more open and warmer part of the
Malom valley than the Malom I site, 47°0'41"N, 17°56'51"e . w ith a row of buildings
at the right and broad meadow at the left side of the stream; Salix species occur at the
stream coasts.
5. Stream of k irály-kút spring; this site lies at the eastern slope of a hill, on the
borderline of a forest and a cattle pasture, 47°0'18"N, 17°56'58"e . The forest is rather
mesophilic (Acer species are common trees). Planted stands of Pinus nigra (J.F.
a rnold, 1785) can be found in the higher parts of the hill on the western side of the
broad valley.
6. a ranyos spring: similar to the previous site, 47°0'12"N, 17°56'59"e . a bit more
humid – Equisetum arvense (L.) and Petasites hybridus ((L.) Gaertn. & al., 1801)
can be found there. c ows come to drink water from the spring.
In the r esult section, the localities are abbreviated by the above-mentioned six
numbers (1–6).
r espective parts of Figure 2 show the vegetation habitus pictures of a lkút spring,
stream of k irály-kút spring, stream of Malom spring and a ranyos spring.
t rapping method. w e used the fermented mixture of beer and sugar, which con-
tained about four teaspoons of sucrose (~24 g), a 1/2 can of light beer (0.25 l) and
about 1 coffee spoon of yeasts (~5-8 g). The material was inoculated with yeast. The
fermented material was filled into uncapped plastic bottles and they were hung in the
woods at head height. Traps were operated at the six sites of Felsőörs and Lovas
(about 47.00° N, 17.95° e ). a ll traps were installed in three periods. In the r esult
Libor Dvořák, Kateřina Dvořáková, Jan Máca, Attila J. Trájer: Some families of Diptera from beer traps in Balaton highland,
95
f ig. 1: Position of the studied area in c entral e urope (yellow spot) and the
localities of the trapping points in Felsőörs and Lovas.

section, these periods are abbreviated as a (29. 4. 2017–16. 5. 2017), B (13.–22. 7.
2017), and c (23.–30. 8. 2017). The trapped flies were conserved in ethyl-alcohol in
plastic vials.
proceeding of the paper. a ll the material was collected by a . J. Trájer, L. Dvořák
sorted out the material. The following families were identified and commented by L.
Dvořák (a nisopodidae, Platystomatidae, Syrphidae, and Ulidiidae), k . Dvořáková
Acta entomologica slovenica, 29 (1), 2021
96
f ig. 2: v egetation habitus of four collecting sites. Photo: a . J. Trájer.

(Dryomyzidae, Heleomyzidae, Lauxaniidae, and Sciomyzidae) and J. Máca
(Drosophilidae). The voucher specimens are deposited in the private collections of
the authors who made the identification. In the Discussion, comments were made for
the species not listed in the c hecklist of the Diptera of Hungary (Papp 2001) and for
some remarkable species. w e are using the nomenclature of the portal https://fauna-
eu.org, with following exceptions: the genus Otites, family Dryomyzidae, and family
Lauxaniidae, where we comply to the newest papers of k ameneva & k orneyev
(2019), Semelbauer (2016), and Mathis & Sueyoshi (2011), repectively.
r esults
During the 2017 season, 1229 specimens of 41 species were captured of studied
families of Diptera. The number of species at localities was rather similar and varied
between 15 and 20 species (graph 1), unlike the number of species in three periods
(graph 2). 28 species were identified in the third period (=c , 23.–30. 8.), 24 in the
first period (=a , 29. 4.–16. 5.), and only 19 in the second period (=B, 13.–22. 7.).
The highest numbers of species were found in the localities and periods 2c and 6c
followed by 5a , 2B, and 4a (all more than 10 species). In contrast with this, the
most of specimens (692) were trapped in the period B, (300 in c and 237 in a ), in
individual localities and periods (graph 3), the highest numbers were identified from
3B (243 specimens), 2B (171 spec.), 2c (122 spec.), and 6B (112 spec.); the numbers
were lower than 100 specimens in other localities and periods. Nine species
(Drosophilidae and Heleomyzidae) were found in all localities, Dryomyza anilis in
Libor Dvořák, Kateřina Dvořáková, Jan Máca, Attila J. Trájer: Some families of Diptera from beer traps in Balaton highland,
97
g raph 1: Number of species at localities 1–6.

all traps. Suillia affinis has the most of specimens (280), of which 87 in one trap
(3B). Some other species from families Dryomyzidae, Drosophilidae and Heleomyzi-
dae were also caught in the mass numbers.
Acta entomologica slovenica, 29 (1), 2021
98
g raph 3: Number of specimens at localities 1–6 in the periods a , B and c .
g raph 2: Number of species at localities 1–6 in the periods a , B and c .

l ist of species
a nisopodidae
Sylvicola punctatus (Fabricius, 1787)
Material examined – 4a : 1♂, 1♀; 5a : 3♀♀.
Drosophilidae
Drosophila histrio Meigen, 1830
Material examined – 2c : 1♀; 6a : 1♂, 3♀♀.
Drosophila immigrans Sturtevant, 1921
Material examined – 2c : 2♂♂, 1♀; 3c : 1♀.
Drosophila kuntzei Duda, 1924
Material examined – 1a : 1♀; 1B: 1♀♀; 2a : 2♂♂; 2B: 22♂♂, 7♀♀; 2c : 4♂♂,
1♀; 3a : 1♂; 3B: 38♂♂, 11♀♀; 3c : 1♀; 4c : 2♂♂; 5a : 1♂, 1♀; 5B: 12♂♂, 1♀; 5c :
1♂, 1♀; 6a : 10♂♂, 2♀; 6c : 4♂♂, 6♀♀.
Drosophila melanogaster Meigen, 1830
Material examined – 1c : 1♀; 3c : 2♂♂, 9♀♀. 
Drosophila obscura Fallén, 1823
Material examined – 4a : 1♀; 6c : 3♂♂, 2♀♀.
Drosophila phalerata Meigen, 1830
Material examined – 1B: 1♂; 2a : 9♂♂, 4♀♀; 2B: 20♂♂, 11♀♀; 2c : 2♂♂, 5♀♀;
3a : 1♀; 3B: 32♂♂, 22♀♀; 3c : 2♀♀; 4a : 7♂♂, 1♀; 4c : 2♀♀; 5a : 2♂♂; 5B: 24♂♂,
7♀♀; 6a : 4♂♂, 2♀♀.
Drosophila simulans Sturtevant, 1919
Material examined – 3c : 1♂, 5♀♀; 6c : 1♀.
Drosophila subobscura c ollin in Gordon, 1936
Material examined – 1a : 4♂♂, 1♀; 2a : 1♂; 3a : 2♂♂; 3c : 1♂, 3♀♀; 4a : 2♀♀;
4c : 1♂; 5a : 1♂, 3♀♀; 6a : 1♂, 1♀; 6c : 1♀.
a west-Palaearctic species with a globally increasing range due to international
transport of goods. It is habitat-tolerant, occurring at forest edges, wetlands, bushes
etc., also in gardens, houses and canning factories, where it supports spreading of de-
cay; it can develop in the sap flow of injured trees as well as in decaying fruit.
Drosophila suzukii (Matsumura, 1931)
Material examined – 1c : 1♀; 4c : 1♂. 
The a sian cherry fly, which infests ripening cherries and other soft-skin fruits, is
native roughly to the south-eastern half of a sia. r ecently – mostly after the onset of
Libor Dvořák, Kateřina Dvořáková, Jan Máca, Attila J. Trájer: Some families of Diptera from beer traps in Balaton highland,
99

this millenium – it has invaded e urope (also reached Turkey, Nw Iran and Morocco),
North and South a merica, k enya, and some oceanic islands such as Hawaii, French
Polynesia, Madeira, a zores and r éunion (c alabria et al. 2012, c habert et al. 2012,
Poyet et al. 2014, Örsted & Örsted 2019). D. suzukii causes severe economic losses
(c ini et al. 2012). In Hungary, it was first recorded in the year 2012 from the locality
Táska, some 10 km to the south of Balaton lake (k iss et al. 2013); several Hungarian
localities are known at present.
Drosophila testacea von r oser, 1840
Material examined – 1a : 1♀; 1B: 1♀; 1c : 1♂; 2a : 3♂♂, 1♀; 2B: 20♂♂, 11♀♀;
2c : 4♂♂, 9♀♀; 3a : 1♂; 3B: 10♂♂, 4♀♀; 4a : 1♀; 4c : 1♂; 5a : 1♀; 5B: 4♂♂; 6a :
2♂♂; 6c : 3♂♂.
Drosophila transversa Fallén, 18230
Material examined – 2B: 1♀; 2c : 1♂; 3B: 1♂, 1♀; 4c : 1♀.
Drosophila unimaculata Strobl, 1893
Material examined – 3a : 2♂♂; 3B: 2♀♀. 
Hirtodrosophila confusa (Stæger, 1844)
Material examined – 3B: 3♀♀; 5a : 1♂, 1♀; 5B: 1♀; 5c : 1♂.
Leucophenga maculata (Dufour, 1839)
Material examined – 5B: 1♂, 2♀♀; 5c : 1♂; 6a : 1♀; 6c : 1♂.
Phortica variegata (Fallén, 1823)
Material examined – 4a : 1♀.
w est-Palaearctic species, recently introduced to North a merica. It is an intermediate
host of the nematode Thelazia callipaeda (r ailliet and Henry, 1910) under natural
conditions (o tranto et al. 2006a). This zoophilic fruit fly can be collected in the
highest number during July to a ugust in e urope (o tranto et al. 2006b). Larvae of the
nematode are transmitted by secretophagous flies into the conjunctival sac and sur-
rounding tissues of wild and domestic mammals, as well as humans (reviewed in
o tranto & Traversa 2005). Thelaziasis occurred originally in southeast a sia (e.g.,
y ang et al. 2006; k rishnachary et al. 2014; k osin et al. 1989); more than thirty years
ago it was first observed in e urope and now it has been recorded from many e uropean
countries including Hungary (o tranto & Dutto 2008, do v ale et al. 2020).
Scaptodrosophila deflexa (Duda, 1924)
Material examined – 1a : 1♀; 1B: 1♂.
Dryomyzidae
Dryomyza anilis Fallén, 1820
Acta entomologica slovenica, 29 (1), 2021
100

Material examined – 1a : 1♂; 1B: 9♂♂, 5♀♀; 1c : 3♀♀; 2a : 3♂♂, 14♀♀; 2B:
6♂♂, 9♀♀; 2c : 8♂♂, 14♀♀; 3a : 4♂♂, 2♀♀; 3 B: 7♂♂, 5♀♀; 3c : 1♂, 1♀; 4a :
5♂♂, 3♀♀; 4B: 11♂♂, 9♀♀; 4c : 11♂♂, 4♀♀; 5a : 3♂♂, 4♀♀; 5B: 7♂♂, 3♀♀;
5c : 2♂♂, 1♀; 6a : 3♂♂, 1♀; 6B: 10♂♂, 12♀♀; 6c : 10♂♂, 7♀♀.
Dryope flaveola (Fabricius, 1794)
Material examined – 2a : 1♂; 2c : 1♂; 4a : 1♂; 6B: 2♂♂; 6c : 3♂♂, 1♀.
Heleomyzidae
Suillia affinis (Meigen, 1830)
Material examined – 1B: 1♂, 2♀♀; 1c : 3♂♂, 4♀♀; 2a : 1♂, 1♀; 2B: 23♂♂,
7♀♀; 2c : 31♂♂, 13♀; 3a : 1♀; 3 B: 47♂♂, 40♀♀; 4B: 22♂♂, 11♀♀; 4c : 5♂♂,
1♀; 5a : 1♂; 5B: 6♂♂, 6♀♀; 5c : 1♂; 6a : 5♂♂, 6♀♀; 6B: 24♂♂, 9♀♀; 6c : 6♂♂,
3♀♀.
Suillia bicolor (Zetterstedt, 1838)
Material examined – 3 c : 1♀.
Suillia gigantea (Meigen, 1830)
Material examined – 1B: 2♀♀; 1c : 1♀; 2a : 1♂; 2B: 14♂♂, 13♀♀; 2c : 4♂♂,
2♀♀; 3 B: 6♂♂, 7♀♀; 3c : 1♂, 1♀; 4B: 3♂♂, 4♀♀; 4c : 1♀; 5a : 2♂♂, 1♀; 5B: 1♂;
5c : 3♂♂, 2♀♀; 6a : 25♂♂, 3♀♀; 6B: 15♂♂, 17♀♀; 6c : 4♂♂.
Thermophilous species, common in Hungary in suitable conditions.
Suillia lurida (Meigen, 1830)
Material examined – 6B: 1♂, 1♀.
Larvae develop in garlic, onion, and other related plants, they are ranked as not
important agriculture pests.
Suillia pallida (Fallén, 1820)
Material examined – 2c : 1♂, 2♀♀; 6B: 2♂♂, 5♀♀; 6c : 1♂.
Suillia ustulata (Meigen, 1830)
Material examined – 2c : 1♂.
This species is known from several e uropean countries, but it is collected only in-
dividually; the larvae develop in dead alder stems.
Suillia variegata (Loew, 1862)
Material examined – 1a : 1♂; 1c : 6♂♂, 1♀; 2B: 1♂, 2♀♀; 2c : 6♂♂, 5♀♀; 3 B:
3♂♂, 4♀♀; 4B: 1♂, 2♀♀; 5B: 1♂; 5c : 4♂♂, 2♀♀; 6B: 1♀; 6c : 4♂♂, 2♀♀.
Thermophilous species, common in Hungary in suitable conditions.
Tephrochlamys flavipes (Zetterstedt, 1838)
Material examined – 6c : 1♂.
Libor Dvořák, Kateřina Dvořáková, Jan Máca, Attila J. Trájer: Some families of Diptera from beer traps in Balaton highland,
101

l auxaniidae
Meiosimyza decempunctata (Fallén, 1820)
Material examined – 1c : 1♂, 1♀; 2B: 1♂, 1♀; 2c : 3♀♀; 3c : 1♀; 4B: 1♂, 1♀;
4c : 1♂; 5B: 1♀; 5c : 2♂♂, 1♀; 6B: 5♂♂, 7♀♀; 6c : 1♀.
Meiosimyza rorida (Fallén, 1820)
Material examined – 5c : 3♀♀; 6c : 1♂.
Minettia subvittata (Loew, 1847)
Material examined – 1B: 2♂♂.
Thermophilous species, common in Hungary in suitable conditions.
Peplomyza discoidea (Meigen, 1830)
Material examined – 2B: 1♂.
Thermophilous species, common in Hungary in suitable conditions.
Pseudolyciella sp.
Material examined – 1c : 1♀.
There are three species of the genus Pseudolyciella known from Hungary, all
identifiable according to the male terminalia only. However, there are crosses between
these taxa and also according to the wing shape morphometric analyses it is probable
that the genus Pseudolyciella includes only one morphoplastic species (Semelbauer
2016).
Tricholauxania praeusta (Fallén, 1820)
Material examined – 5c : 1♂.
platystomatidae
Platystoma seminatione (Fabricius, 1775)
Material examined – 1a : 7♂♂, 3♀♀.
Sciomyzidae
Euthycera chaerophylli (Fabricius, 1798)
Material examined – 1c : 1♀; 2c : 1♂.
Syrphidae
Volucella inflata (Fabricius, 1794)
Material examined – 4a : 2♀♀; 5a : 1♀.
u lidiidae
Callopistromyia annulipes (Macquart, 1855)
Material examined – 1a : 1♀.
This species was not included in the checklist of Papp (2001), its first records
from Hungary were published by k ameneva & Pekarsky (2016). It is an invasive
Acta entomologica slovenica, 29 (1), 2021
102

species in e urope, first published from e urope by Merz (2007). For the present dis-
tribution see e. g., Dvořák et al. (2019).
Otites lamed (Schrank, 1781)
Material examined – 1a : 1♀.
Otites levigata (Loew, 1873)
Material examined – 2a : 19♂♂, 4♀♀; 4a : 2♂♂, 1♀. 
a species known mainly from south-eastern e urope – in a relatively small area
bordered by Italy, Slovakia, and Bulgaria. 
Otites ornata (Meigen, 1826)
= O. bacescui (Gheorghiu, 1987)
Material examined – 4a : 3♂♂, 1♀; 5a : 4♂♂, 1♀.
a south e uropean species occurring from France to Bulgaria. This species was
not included to the Hungarian checklist (Papp 2001), although k ameneva (1997) re-
ported the material from Hungary. w e confirm the occurrence for Hungary.
Otites ruficeps (Fabricius, 1805)
= O. formosa (Panzer, 1798)
Material examined – 2a : 1♂; 3a : 1♂; 6a : 1♂.
Discussion
Many of studied species are psychrophilous or rather psychrophilous, so that they
can occur more often at the beginning and the end of season, which explains the
smaller number of species in the middle of the season. Moreover, in a ugust, the
summer and autumn aspects meet. The mass occurrence of some species in the middle
of the season can be explained by their retreatment to the shaded valleys during the
hottest time of the year.
The beer traps are catching different species spectrum than other traps or sweeping,
as we found in previous surveys (for example Dvořáková 2008, Dvořák et al. 2019).
It is not always clear why this is the case. For example, regular high incidence of
mycetophagous Suillia species is surprising. a dults, in contrast with larvae, probably
prefer fermenting juice. More detailed comparison of various types of traps would
require special research in terrain or meta-research of published results. 
Conclusions
During the survey using beer traps in Balaton highlands in 2017, altogether 41
Diptera species from nine families were identified: a nisopodidae (one species),
Drosophilidae (16 species), Dryomyzidae (two species), Heleomyzidae (eight species),
Lauxaniidae (six species), Platystomatidae (one species), Sciomyzidae (one species),
Syrphidae (one species), and Ulidiidae (five species).
Libor Dvořák, Kateřina Dvořáková, Jan Máca, Attila J. Trájer: Some families of Diptera from beer traps in Balaton highland,
103

c ommon and widespread species prevailed in the material. a mong others, we
caught several thermophilous species, as Suillia gigantea, S. variegata (Heleomyzidae),
Minettia subvittata, Peplomyza discoidea (Lauxaniidae) and Otites lamed (Ulidi-
idae).
The species Callopistromyia annulipes (Ulidiidae) and Drosophila suzukii
(Drosophilidae) are imported invasive fly species. The second one, as well as Suillia
lurida (Heleomyzidae), are ranked as agriculture pests.
Some species of Drosophila (e. g. D. immigrans, D. melanogaster, D. subobscura)
are noxious in the food industry.
o ne species, Phortica variegata, is a species of medical importance.
a cknowledgement
w e would like to say thank to Szabolcs v arga (University of Pannonia, Hungary)
for his technical assistance.
The research presented in this article also was carried out with the support of the
Nk FIH-872 project of the Hungarian National r esearch, Development and Innovation
o ffice.
r eferences
Calabria, g ., J. máca, g . bächli, l . Serra, m. pascual, 2012: First records of the
potential pest species Drosophila suzukii (Diptera: Drosophilidae) in e urope.
Journal of applied Entomology, 136(1-2): 139-147.
Chabert, S., r . a llemand, m. poyet, p. e slin, p. g ilbert, 2012: a bility of e uropean
parasitoids (Hymenoptera) to control a new invasive a siatic pest, Drosophila
suzukii. Biol. Control, 63: 40-47.
Cini, a ., C. ioriatti, g . a nfora, 2012: a review of the invasion of Drosophila
suzukii in e urope and a draft research agenda for integrated pest management.
Bulletin of Insectology, 65(1): 149-160.
Dvořák, l ., J.-p. Haenni, K. Dvořáková, e .p. Kameneva, r . mariychuk, p.
manko, J. o boňa, V.a . Korneyev, 2019: Some insects from beer traps in
westernmost Ukraine. Ukrainska Entomofaunistyka, 10(2): 1-6.
Dvořáková, K., 2008: Heleomyzidae and Lauxaniidae (Diptera: Brachycera: a ca-
lyptrata) trapped in the c zech r epublic with syrup and fermented fruit. Linzer
biologische Beiträge, 40, 507-515.
f ischer, D., p. moeller, S. m. t homas, t . J. n aucke, C. beierkuhnlein, 2011:
c ombining climatic projections and dispersal ability: a method for estimating
the responses of sandfly vector species to climate change. PLoS neglected tropical
diseases, 5(11), e1407.
g ilbert, D. g ., 1980: Dispersal of yeasts and bacteria by Drosophila in a temperate
forest. Oecologia, 46(1), 135-137.
Acta entomologica slovenica, 29 (1), 2021
104

Kameneva, e . p., 1997: a preliminary review of the Otites formosa species-group
(Diptera, Ulidiidae, o titinae). Russian Entomological Journal, (1996) 5(1-4):
125-133.
Kameneva, e . p., V. a . Korneyev, 2019: New nomenclatural changes in the genus
Otites Latreille, 1804 (Diptera: Ulidiidae: o titinae). Ukrainska Entomofaunistyka,
10(2) : 23-30.
Kameneva, e . p., o . pekarsky, 2016: First record of Nearctic invader, the peacock
fly Callopistromyia annulipes Macquart (Diptera: Ulidiidae: o titinae: Myenni-
dini) from Hungary. Ukrainska Entomofaunistyka, 7: 38.
Kiss, b ., g . l engyel, Z. n agy, Z. Karpati, 2013: a pettyesszarnyu muslica
(Drosophila suzukii) elso Magyarorszagi elofordulasa. Növenyvédelmi Tudo-
manyos Napok (Budapest), 49: 97-99. 
Kosin, e ., m. l . Kosman, a . a . Depary, 1989: First case of human thelaziasis in
Indonesia. The Southeast Asian Journal of tropical Medicine and public Health,
20(2): 233-236.
Krishnachary, p. S., V. g . Shankarappa, r . r ajarathna, m. Shanthappa, 2014:
Human ocular thelaziasis in k arnataka. Indian Journal of Ophthalmology, 62(7):
822.
mathis, W. n ., m. Sueyoshi, 2011: w orld c atalog and c onspectus on the Family
Dryomyzidae (Diptera: Schizophora). MYIA, 12: 207-233.
medlock, J. m., K. m. Hansford, f . Schaffner, V. Versteirt, g . Hendrickx, H.
Zeller, W. V. bortel, 2012: a review of the invasive mosquitoes in e urope:
ecology, public health risks, and control options. Vector-borne and zoonotic dis-
eases, 12(6): 435-447.
merz, b., 2007: Callopistromyia annulipes (Macquart, 1855), a Nearctic species of
Ulidiidae (Diptera), new for the Palaearctic r egion. Studia Dipterologica, 14(1):
161-165.
Örsted, i. V., m. Örsted, 2019: Species distribution models of the Spotted w ing
Drosophila (Drosophila suzukii, Diptera: Drosophilidae) in its native and invasive
range reveal an ecological niche shift. Journal of applied Ecology, 56: 423-435.
o tranto, D., m. Dutto, 2008: Human thelaziasis, e urope. Emerging infectious dis-
eases, 14(4): 647.
o tranto, D., C. Cantacessi, g . t estini, r . p l ia, 2006a: Phortica variegata as an
intermediate host of Thelazia callipaeda under natural conditions: evidence for
pathogen transmission by a male arthropod vector. International Journal for
Parasitology, 36(10-11): 1167-1173.
o tranto, D., e . brianti, C. Cantacessi, r . p. l ia, J. máca, 2006b: The zoophilic
fruitfly Phortica variegata: morphology, ecology and biological niche. Medical
and veterinary Entomology, 20(4): 358-364.
o tranto, D., D. t raversa, 2005: Thelazia eyeworm: an original endo-and ecto-par-
asitic nematode. Trends in Parasitology, 21(1): 1-4.
papp, l . (ed.) 2001: c hecklist of the Diptera of Hungary. Hungarian Natural History
Museum, Budapest, 550 pp.
Libor Dvořák, Kateřina Dvořáková, Jan Máca, Attila J. Trájer: Some families of Diptera from beer traps in Balaton highland,
105

poyet, m., p. e slin, m. Héraude, V. l e r oux, g . prévost, p. g ibert, o . Chabrerie,
2014: Invasive host for invasive pest: when the a siatic cherry fly (Drosophila
suzukii) meets the a merican black cherry (Prunus serotina) in e urope. Agricul-
tural and Forest Entomology, 16(3): 251-259.
Semelbauer, m., 2016: Fauna Slovenska 4, Lauxaniidae – tieňovkovité (Diptera,
c yclorrhapha). VEDA, Slovak Academy of Science, Bratislava, 185 pp. (in Slovak)
do Vale, b., a . p. l opes, m. da Conceição f ontes, m. Silvestre, l . Cardoso, a .
C. Coelho, 2020: Systematic review on infection and disease caused by Thelazia
callipaeda in e urope: 2001–2020. Parasite, 27: 52. https://doi.org/10.1051/par-
asite/2020048.
y ang, y . J., t . H. l iag, S. H. l in, H. C. Chen, S. C. l ai, 2006: Human thelaziasis
occurrence in Taiwan. Clinical and experimental Optometry, 89(1): 40-44.
Walsh, D. b., m. p. bolda, r . e . g oodhue, a . J. Dreves, J. l ee, D. J. bruck, V.
m. Walton, S. D. o ’n eal, f . g . Zalom, 2011: Drosophila suzukii (Diptera:
Drosophilidae): invasive pest of ripening soft fruit expanding its geographic
range and damage potential. Journal of Integrated Pest Management, 2(1): G1-
G7.
Received / Prejeto: 5. 3. 2021
Acta entomologica slovenica, 29 (1), 2021
106