Zonal and Zoogeographic Characteristic of the Ant Fauna (Hymenoptera, Formicidae) of Ukraine
One hundred fourty ant species belonging to 38 genera of 5 subfamilies are known to occur in Ukraine nowadays. All the species are attributed to 16 zoogeographic complexes that are grouped into three faunogenetic classes. Comparative zonal and zoogeographical analysis of the fauna of different geogr...
Збережено в:
| Опубліковано в: : | Вестник зоологии |
|---|---|
| Дата: | 2011 |
| Автор: | |
| Формат: | Стаття |
| Мова: | Англійська |
| Опубліковано: |
Інститут зоології ім. І.І. Шмальгаузена НАН України
2011
|
| Теми: | |
| Онлайн доступ: | https://nasplib.isofts.kiev.ua/handle/123456789/65838 |
| Теги: |
Додати тег
Немає тегів, Будьте першим, хто поставить тег для цього запису!
|
| Назва журналу: | Digital Library of Periodicals of National Academy of Sciences of Ukraine |
| Цитувати: | Zonal and Zoogeographic Characteristic of the Ant Fauna (Hymenoptera, Formicidae) of Ukraine / A.G. Radchenko // Вестник зоологии. — 2011. — Т. 45, № 6. — С. 513–522. — Бібліогр.: 26 назв. — англ. |
Репозитарії
Digital Library of Periodicals of National Academy of Sciences of Ukraine| _version_ | 1859861980954755072 |
|---|---|
| author | Radchenko, A.G. |
| author_facet | Radchenko, A.G. |
| citation_txt | Zonal and Zoogeographic Characteristic of the Ant Fauna (Hymenoptera, Formicidae) of Ukraine / A.G. Radchenko // Вестник зоологии. — 2011. — Т. 45, № 6. — С. 513–522. — Бібліогр.: 26 назв. — англ. |
| collection | DSpace DC |
| container_title | Вестник зоологии |
| description | One hundred fourty ant species belonging to 38 genera of 5 subfamilies are known to occur in Ukraine nowadays. All the species are attributed to 16 zoogeographic complexes that are grouped into three faunogenetic classes. Comparative zonal and zoogeographical analysis of the fauna of different geographical regions of Ukraine has revealed their essential heterogeneity. The ant fauna of the Forest-Steppe zone is not original. At the same time, it is not transitive between the faunae of the Forest and Steppe zones. Ant fauna of the Forest-Steppe is related to those not the Steppe but the Forests zones, and the Forest-Steppe can be included in the southern subzone of a Forest zone of t Europe.
В Украине известно 140 видов муравьев из 38 родов 5 подсемейств. Выделены 16 зоогеографических комплексов, отнесенных к трем фауногенетическим классам. Сравнительный зональный и зоогеографический анализ фаун различных физико-географических регионов Украины выявил их существенную разнородность. Показано, что фауна муравьев Лесостепи не является самобытной. В то же время, она не является переходной между фаунами лесов и степной зоны. По происхождению мирмекофауна Лесостепи связана с таковой не степной, а лесных зон, и, на основании данных о распространении муравьев, Лесостепь может быть включена в состав южной подзоны лесной зоны Европы.
|
| first_indexed | 2025-12-07T15:46:23Z |
| format | Article |
| fulltext |
UDK 595.796 (477)
ZONAL AND ZOOGEOGRAPHIC CHARACTERISTIC OF THE ANT
FAUNA (HYMENOPTERA, FORMICIDAE) OF UKRAINE
A. G. Radchenko
Schmalhausen Institute of Zoology, NAS of Ukraine,
B. Chmielnicky str., 15, Kyiv, 01601 Ukraine
E-mail: rad@izan.kiev.ua
Received 28 October 2011
Accepted 10 November 2011
Zonal and Zoogeographic Characteristic of the Ant Fauna (Hymenoptera, Formicidae) of Ukraine.
Radchenko A. G. – One hundred fourty ant species belonging to 38 genera of 5 subfamilies are known
to occur in Ukraine nowadays. All the species are attributed to 16 zoogeographic complexes that are grouped
into three faunogenetic classes. Comparative zonal and zoogeographical analysis of the fauna of differ-
ent geographical regions of Ukraine has revealed their essential heterogeneity. The ant fauna of the Forest-
Steppe zone is not original. At the same time, it is not transitive between the faunae of the Forest and
Steppe zones. Ant fauna of the Forest-Steppe is related to those not the Steppe but the Forests zones,
and the Forest-Steppe can be included in the southern subzone of a Forest zone of t Europe.
Ke y wo r d s: ants, Formicidae, fauna, zoogeography, Ukraine, Europe.
Çîíàëüíàÿ è çîîãåîãðàôè÷åñêàÿ õàðàêòåðèñòèêà ìèðìåêîôàóíû (Hymenoptera, Formicidae) Óêðàèíû.
Ðàä÷åíêî À. Ã. –  Óêðàèíå èçâåñòíî 140 âèäîâ ìóðàâüåâ èç 38 ðîäîâ 5 ïîäñåìåéñòâ. Âûäåëåíû
16 çîîãåîãðàôè÷åñêèõ êîìïëåêñîâ, îòíåñåííûõ ê òðåì ôàóíîãåíåòè÷åñêèì êëàññàì. Ñðàâíèòåëüíûé
çîíàëüíûé è çîîãåîãðàôè÷åñêèé àíàëèç ôàóí ðàçëè÷íûõ ôèçèêî-ãåîãðàôè÷åñêèõ ðåãèîíîâ
Óêðàèíû âûÿâèë èõ ñóùåñòâåííóþ ðàçíîðîäíîñòü. Ïîêàçàíî, ÷òî ôàóíà ìóðàâüåâ Ëåñîñòåïè íå
ÿâëÿåòñÿ ñàìîáûòíîé. Â òî æå âðåìÿ, îíà íå ÿâëÿåòñÿ ïåðåõîäíîé ìåæäó ôàóíàìè ëåñîâ è ñòåï-
íîé çîíû. Ïî ïðîèñõîæäåíèþ ìèðìåêîôàóíà Ëåñîñòåïè ñâÿçàíà ñ òàêîâîé íå ñòåïíîé, à ëåñíûõ
çîí, è, íà îñíîâàíèè äàííûõ î ðàñïðîñòðàíåíèè ìóðàâüåâ, Ëåñîñòåïü ìîæåò áûòü âêëþ÷åíà â ñîñòàâ
þæíîé ïîäçîíû ëåñíîé çîíû Åâðîïû.
Êëþ÷åâûå ñ ëîâ à: ìóðàâüè, Formicidae, ôàóíà, çîîãåîãðàôèÿ, Óêðàèíà, Åâðîïà.
Introduction
In Ukraine 140 species of ants from 38 genera of 5 subfamilies are known at present. Among them, 5 occa-
sionally introduced species (Hypoponera punctatissima (Roger), Linepithema humile (Mayr), Brachymyrmex heeri
Forel, Paratrechina vividula (Nylander) and Monomorium pharaonis (Linnaeus)) are indoor species, living in
houses, greenhouses, etc. All of the above mentioned species are not included in the following zonal and zoo-
geographical analysis. Thus, the ant fauna of Ukraine includes 135 native species.
Zonal-geographical analysis of the fauna
The richness of ant fauna of Ukraine is emphasized by comparing it with the fau-
nas of adjacent regions. For example, 62 species are known in Belarus, 103 in Poland,
108 in Slovakia, 104 in Czech Republic, 120 in Hungary, and 105 in Romania ant species.
Even in the vast and diverse territory of European Russia (excluding the Northern
Caucasus, bordering between Europe and Asia along the Kuma-Manych Depression) only
131 ant species are found (Arnoldi, Dlussky, 1978; Blinov, 1984, 1985; Czechowski et
al., 2002; Radchenko et al., 2003, 2004, 2005; Markó et al., 2006; Werner, Wiezik, 2007;
Csősz et al., 2011; see also Radchenko, 2007 b).
Vestnik zoologii, 45(6): 513—522, 2011 Ýêîëîãèÿ
Ukraine is located within different physiographic zones: the East European Plain,
which includes zones of mixed forests (Polissya), deciduous forests (including the
Carpathian lowland), Wood-and-Steppe and Steppe zones, the Carpathian mountain coun-
try and the Crimean Mountains, including subtropics of the southern coast of the
Crimea. Earlier authors (Marinich et al., 1982) did not separate a zone of deciduous forests,
but now there are more and more evidences for such zoning, proposed by Marinich (2003).
Such a variety of conditions led to the richness of the ant fauna and also to the signifi-
cant differences in allocation of species and faunistic complexes.
Species richness of different natural zones generally corresponds to the generic one:
14 genera and 52 (3) species (number of species found only in the discussed region are
in brackets) are found in the Carpathian Mts., 18 genera and 65 (1) species in Polissya,
20 genera and 69 (2) species in Deciduous Forest zone, 20 genera and 70 (0) species in
Forest-Steppe, 25 genera and 87 (14) species in Steppe, and 28 genera and 87 (15) speciesin
the Crimean Mts. (see also fig. 1). As can be seen, the species and generic richness increas-
es from the mountain forests of Carpathians to the south and reaches its maximum in
the Steppe and Crimean Mts.
At the same time, comparison of ant fauna of different natural zones shows its high
heterogeneity. The highest similarity, which is not surprising, is observed between the adja-
cent forest regions – Polissya and Deciduous Forests (Jaccard index1 = 0.836). Similar,
although somewhat lower performance of the index is observed between Polissya and
Carpathians, Polissya and Forest-Steppe, Steppe and Deciduous Forests. It is important
to stress that the fauna of the Forest-Steppe zone is much more similar to those of the
adjacent forest zones that to the Steppe one (table 1, fig. 2). It is quite naturally that the
similarity of the faunae of forest areas with those of the steppes and the Crimean Mts.
is the lowest. It is noteworthy that the similarity of the Forest-Steppe ant fauna with that
of the Steppe significantly lower than with Polissya and Deciduous Forests zones.
Such difference can be easily explained: many of the major and widely distributed
genera, such as Formica, Myrmica and Camponotus include both mesophilic and xerophilic
re presentatives whose distribution is limited to one or other natural zones. For example,
genera found in all regions, account for more than 45% of their total number and species –
less than 30%.
514 A. G. Radchenko
1 Jaccard’sindex = ñ / (a + b) — c, where a and b are the number of species in two centres compared
and c is the number of species in common.
Fig. 1. Number of species and genera of ants in different natural zones of Ukraine.
Ðèñ. 1. Êîëè÷åñòâî âèäîâ è ðîäîâ ìóðàâüåâ â ðàçëè÷íûõ ïðèðîäíûõ çîíàõ Óêðàèíû.
0
10
20
30
40
50
60
70
80
90
100
Carpathian
Mts.
Deciduous
forests
Forest-
Steppe
Steppe Crimean
Mts.
number of genera
number of species
species only in region
Polissya
Of course, the quantity of different species vary greatly both in Ukraine as a whole
and in the separate regions. For example, red wood ants from the Formica rufa-group,
many members of the genera Lasius F., Myrmica, Camponotus and some others form the
basis of ant fauna in different ecosystems not only in our country but also in the whole
Palaearctic. At the same time, many species and even genera are extremely rare. To some
extent this may be associated with a cryptic style of life of some of them, however rig-
orous studies in many areas has confirmed the true rarity of at least about 20 species. For
example, Cryptopone ochracea (Mayr), Proceratium melinum (Roger), Liometopum micro-
cephalum (Panzer), Bothriomyrmex communistus Santschi, Formica cinereofusca Karawajew,
Myrmica stangeana Ruzsky, Aphaenogaster splendida (Roger), Temnothorax semenovi
(Ruzsky), T. recedens (Nylander) and some other species are known only by a single or
at most by a few rare finds.
There are also endemic ant species in Ukraine: Strongylognathus arnoldii Radchenko,
S. chelifer Radchenko, Solenopsis ilinei Santschi, Plagiolepis karawajewi Radchenko,
Chalepoxenus tauricus Radchenko. Tapinoma kinburni Karawajew was known only from
Ukraine until recently, but some years ago it had been recorded from the Belgorod region
of Russia (Prisny, 2003). It is characteristic that all of them distributed either in the Steppe
zone, or at the southern coast of Crimea.
515Zonal and zoogeographic characteristic of the ant fauna (Hymenoptera, Formicidae) of Ukraine
Ta b l e 1. Comparison of the ant faunas in different regions of Ukraine (at the species level)*
Ò à á ëèö à 1. Ñðàâíåíèå ôàóí ìóðàâüåâ ðàçëè÷íûõ ðåãèîíîâ Óêðàèíû (íà óðîâíå âèäîâ)*
* Diagonal indicate the number of species in the region; in the lower left side of the table – number of
species common to the compared regions; in the upper right side Jaccard index values .
Regions Polissya Carpathian
Mts.
Deciduous
Forests Forest-Steppe Steppe Crimean Mts.
Fig. 2. The similarity of ant fauna in different regions of Ukraine at the species level (Jaccard index).
Ðèñ. 2. Ñõîäñòâî ìèðìåêîôàóí ðàçëè÷íûõ ðåãèîíîâ Óêðàèíû íà âèäîâîì óðîâíå (èíäåêñ Æàêêàðà).
Polissya 65 0.696 0.836 0.688 0.382 0.382
Carpathian Mts. 48 52 0.613 0.525 0.264 0.264
Deciduous Forests 61 46 69 0.805 0.405 0.356
Forest-Steppe 55 42 62 70 0.554 0.481
Steppe 42 29 45 56 87 0.554
Crimean Mts. 42 29 41 51 62 87
Analysis of the distribution of ants and of the peculiarities of structure of the fau-
nistic complexes can shed light on the rather controversial question: is the Forest-
Steppe zone original, distinctive zone, or it is a transitional region between the Forests
and Steppe zones? Famous Russian myrmecologist K. V. Arnoldi stood for the first point
of view and pointed out the uniqueness of the ant fauna of the Forest-Steppe zone (Arnoldi,
1956, 1965, 1968). However, my data contradict this view.
First of all, there are no ant species unique to the Ukrainian Forest-Steppe zone.
There are two main types of zonal ecosystems in this region: mainly deciduous, rarely
mixed island forest of valleys and beam type, as well as moderately dry upland meadows
and meadow-steppes. Correspondingly, the Forest-Steppe ants can be clearly divided into
mesophilous forest and more xerophilous grassland inhabitants. Simultaneously, fauna and
structure of multi-species associations of ants of forest ecosystems in the Forest-Steppe
are almost identical to that of the forests of the southern part of Polissya and of the zone
of Deciduous forests.
The ant fauna of meadow ecosystems is also more similar to those of forests than
of steppes what supported by a lower value of the Jaccard index between Forest-Steppe
and Steppe zones (0.357). The absence or extreme rarity of the steppe edificator species,
such as Cataglyphis aenescens (Förster), Proformica epinotalis (Ruzsky), several species
of Temnothorax Mayr, Bothriomyrmex Emery, etc., is also important. Many species com-
mon to the Forest-Steppe and Steppe fauna, in fact, are not typical steppe dwellers, but
also live in xerothermal habitats in the Central Europe and partly in the Mediterranean
region, i. e., are not interrelated with the origin and further development of the steppe
ecosystems.
Thus, based on the study of ants, I can make the following conclusions: – the for-
est dwellers are dominated in the Forest-Steppe zone, and virtually no true steppe
species here;– the Forest-Steppe ant fauna genetically related to the forest fauna, but
not to the steppe one;– the Forest-Steppe is not a substantive natural zone nor a tran-
sitional region between the forest and steppe zones;– the Forest-Steppe is likely to be
included in the southern sub-zone of the European forests.
Zoogeographical analysis of the fauna
The basic postulate of my zoogeographic studies was and remains a well-known fact:
the modern character of the area of any taxon is the result of historical development of
the latter, woven into the overall picture of phylogeneis, phylocenogenesis and fauno-
genesis (Chernov, 1984, Radchenko, 1998, 2003). Therefore, in the zoogeographical anal-
ysis I used not only chorological approach, but also take into account peculiarities of the
ecology and biology of species, their phylogenetic relationships, the history of the for-
mation of species and faunistic complexes. In addition, the data of systematic, paleon-
tology, paleogeography, florogenetic, physical geography, and other related sciences are
widely used. The classification of areas proposed below are based on the zonal-provin-
cial approach (Emelyanov, 1974; Kryzhanovsky, 1987, 2002; Czechowski et al., 2002;
Radchenko, 2007 a), it has a hierarchical structure and takes into account not only the
present distribution of species, but the history of the formation their areas.
All native ant species of Ukraine are assigned to 16 zoogeographical complexes, which
are grouped into three faunogenetic classes: class of the zone of coniferous forest (taiga),
zones of mixed and deciduous forests, and class of semi-arid and arid zones of Eurasia.
Such an association is based on the characters of areas, as well as on the ecological fea-
tures of species, included in the different classes, and also reflected the common histo-
ry of faunogenesis in these three vast regions.
Thus, the origin and subsequent evolution of the fauna of the semi-arid and arid zones
of Eurasia is closely related to the development of xerophytic landscape and vegetation
516 A. G. Radchenko
in the region of the drying Tethys Ocean starting in the Late Oligocene. Flora and fauna
of the zone of Deciduous and Mixed Forests of the Western Palaearctics, in essence, is
a derivative of the ancient Turgay flora (Krishtofovich, 1946), and fauna of the Taiga zone
is the youngest in the Palaearctic Region, it was the most exposed to the catastrophic effects
of the Pleistocene glaciations. A brief characteristic of the zoogeographical complexes,
discussed in this article is as follows.
I . C l a s s o f t h e c on i f e r o u s f o r e s t z on e ( t a i g a ) ( 2 3 s p e c i e s )
1) the boreo-montane complex (BM) – species distributed mainly in the northern-
most part of the Palaearctic Region (the Taiga zone), usually having a very wide range
from the Atlantic to Pacific Ocean. In the European plains, their southern limit as a rule
does not reach 50°N, often at most 55°N, but at the same time they occur in the moun-
tains of Europe and Caucasus; some species may penetrate by intrazonal habitats
(e. g. forests in valleys of large rivers) far to the south up to the Steppe zone. In Ukraine
11 species.
2) the montane complex (M) – species occurring only in the mountains of Europe
and Caucasus. Most probably, they are Tertiary relics. Two species are known in Ukraine:
Manica rubida (Latreille) (Carpathian and Crimean Mts.) and Formica cinereofusca
Karawajew (Carpathian Mts.).
3) the North-Palaearctic complex (Pn) – generally trans-Palaearctic forms whose
ranges cover the taiga zone together with the northern part of the mixed and deciduous
forest zones. Ecologically, they are mesophilous species living mostly in forests and in
mountain meadows. In Ukraine 10 species.
I I . C l a s s o f t h e m i x e d a nd d e c i d uou s f o r e s t z on e s ( 5 2 s p e c i e s )
4) the European forests complex (EF) – mesophilous and partly thermophilous species,
distributed mainly in the zones of deciduous and mixed forests and Wood-and-Steppe
of Europe; inhabit both forests and open areas. In Ukraine 9 species.
5) the Euro-West-Siberian complex (EWS) – species, widespread in Europe (usu-
ally also in the Caucasus) and in West Siberia, reaching to the east the Altai, rarely –
the Lake Baikal. Their range can cover several natural zones, but they are absent or extreme-
ly rare in the Mediterranean region and in the Taiga. Ecologically, they are quite diverse
and found both in forests and in open grasslands. In Ukraine 14 species.
6) the Euro-Caucasian complex (EC) – species distributed mainly in the zone of
deciduous forests and partly in mixed forests in Europe and the Caucasus. They may also
reach Asia Minor and the Near East. Many species are arboreal, but there are also poly-
topic representatives both in forests and in open areas. In Ukraine 15 species.
7) the South-Palaearctic complex (Ps) – generally trans-Palaearctic forms, often
distributed from the Atlantic to Pacific Oceans, whose ranges cover mainly the southern
part of the forest zones and the Forest-Steppe zone; ecologically associated with dry light
forests or dry grasslands; in southern Europe live mainly in mountains. They are associ-
ated mainly with moderately dry and light forests or with mesoxerophitous grasslands. In
Ukraine 14 species.
I I I . C l a s s o f t h e s em i - a r i d a nd a r i d z on e s ( 6 0 s p e c i e s )
8) the South-European complex (SE) – species occurring mainly in dry light forests
and xerothermal associations of southern Europe and partly Central Europe, they usu-
ally do not reach beyond 50° N northwards; at the same time they are quite rare in or
absent from the Mediterranean region. In Ukraine 10 species.
9) the Mediterranean complex (MD) – species distributed in the Mediterranean
region, i.e., in the Iberian and Apennine Peninsulas, southern France, the Balkans, Greece,
the southwestern part of North Africa, and in Asia Minor (or in a significant part of this
area). They occasionally occur also in the Near and Middle East, reaching in the east
the Kopet-Dagh Mts., but are absent in deserts of the Middle Asian plains; they can also
517Zonal and zoogeographic characteristic of the ant fauna (Hymenoptera, Formicidae) of Ukraine
reach Central Europe and the southern part of East Europe. Most typical habitats of these
species are those of the Mediterranean type (dry forests, macchia scrub, xerothermal plant
associations, often on stony mountain slopes). In Ukraine 16 species.
10) the Crimean-Caucasian complex (CC) – species occurring only in Crimean Mts.
and the Caucasus. Ecologically, they are similar to the species of previous complex; in
fact, this complex (as well as several ones below) can be considered as a particular case
of the wider Mediterranean complex. In Ukraine 2 species found in Crimea: Temnothorax
jajlensis (Arnoldi) and Strongylognathus karawajewi Pisarski.
11) the Balkan-Caucasian complex (BC) – the areas are similar to the previous com-
plex, but include the Balkans, the Crimea and the Caucasus. In Ukraine 3 species.
12) the Crimean-Balkan complex (CrB) – species distributed in the Crimea and
the Balkans; in the Ukraine found a single species – Bothriomyrmex communistus.
13) the Crimean (Cr) – all 4 known species are endemics of the southern coast of
Crimea.
14) the Tethyan complex (T) – species having a wide area that includes wholly or
at least mostly the Mediterranean region, southern part of Central and East Europe, the
Caucasus, Asia Minor, the Middle East, Iran, Kazakhstan, Middle Asia (i. e. so-called
“Ancient Mediterranean” region sensu Semenov-Tian-Shansky, 1936). All 6 species, found
in Ukraine, live in the steppes and dry meadows, and occasionally penetrate under the
canopy of light, dry, warm and sparse forests.
15) the Steppic (a synonym of this name – Scythian) (ST) – species, widely dis-
tributed in the steppes of Eurasia; all of them are associated with grasslands and avoid
forests, even dry and sparse ones. In Ukraine 12 species.
16) the Turano-Steppic (TST) – xerophilous and semi-xerofilous species living main-
ly in the steppes, but their areas also cover the Middle Asia, and some distributed in the
Transcaucasia, Asia Minor and the Mediterranean. In Ukraine 6 species.
Ratio of the zoogeographical complexes of ants in Ukraine as a whole seems to be
rather homogeneous, i.e., none of them is clearly dominant. Thus, 9 complexes that include
from 7 to 12% of the species in total cover more than 80% of species diversity (fig. 4).
At the same time, if the distribution of the zoogeographical complexes is compared
in the faunogenetic classes, the ratio of representatives of the “humid” (I and II) and
“arid” (III) classes will be approximately equal (56 vs. 44%) (fig. 3). This situation is
consistent with the natural environment in Ukraine, where semiarid regions occupy about
half of its territory.
The compositions and distributions of both zoogeographical complexes and fauno-
genetic classes in different regions vary quite significantly (table 2, fig. 5, 6) and reflect,
both the specificity of modern landscapes, and the history of the formation of ant fauna.
In zoogeographic respect, both by the composition of faunogenetic classes and of
the zoogeographic complexes, the ant faunas of Polissya and Deciduous forests are the
most similar among all the compared regions, although the first fauna is poorer and less
diverse (tabl. 1, 2).
Zoogeographic analysis confirms the above mentioned character of the ant fauna of
the Forest-Steppe zone that is much more similar to that of Forests than that of the Steppe
zones. A different pattern is observed in the Steppe zone, where the richness and diver-
sity of fauna not only increases , but very substantially increase the proportion of “arid”
representatives. Finally, the richest and the most diverse is the ant fauna of the Crimean
Mts., which includes representatives of all 16 zoogeographical complexes, and more than
half of them belong to the class of semi-arid and arid zones of Eurasia, mainly due to the
presence of the Mediterranean, Steppic, and Turano-Steppic elements (fig. 5, 6).
The above data show the richness and high diversity of the ant fauna of Ukraine, as
well as its faunogenetic heterogeneity. Particularly clear these differences manifest them-
selves in the regional (both taxonomic and zoogeographic) analysis of ant fauna of dif-
518 A. G. Radchenko
ferent physiographic countries and natural zones of the country. This pattern reflects both
the modern character of natural complex and the history of formation of the ant fauna
of Ukraine.
519Zonal and zoogeographic characteristic of the ant fauna (Hymenoptera, Formicidae) of Ukraine
Fig. 3. Assignment of the ant fauna of Ukraine to the faunogeteic classes: I – class of the Zone of Coniferous
Forest (Taiga); II – class of the Zones of Mixed and Deciduous Forests; III – class of the Semi-Arid and
Arid Zones of Eurasia.
Ðèñ. 3. Ðàñïðåäåëåíèå ìèðìåêîôàóíû Óêðàèíû ïî ôàóíîãåíåòè÷åñêèì êëàññàì: ² – êëàññ çîíû õâîé-
íûõ ëåñîâ; ²² – êëàññ çîíû ñìåøàííûõ è ëèñòâåííûõ ëåñîâ; ²²² – êëàññ ñóáàðèäíîé è àðèäíîé çîí
Åâðàçèè.
Fig. 4. Zoogeographical composition of the ant fauna of Ukraine as a whole (abbreviations are given in the
text).
Ðèñ. 4. Çîîãåîãðàôè÷åñêèé ñîñòàâ ìèðìåêîôàóíû Óêðàèíû â öåëîì (ñîêðàùåíèÿ ïðèâåäåíû â òåêñòå).
I
II
III
3
Ta b l e 2. Zoogeographic characteristic of ant fauna in different regions of Ukraine*
Òà á ëèö à 2. Çîîãåîãðàôè÷åñêàÿ õàðàêòåðèñòèêà ìèðìåêîôàóíû ðàçëè÷íûõ ðåãèîíîâ Óêðàèíû*
* Abbreviations of the names of zoogeographical complexes see in the text above.
** in brackets: number of “ende mics” for regions.
Zoogeographical
complexes
Polissya
Carpathian
Mts.
Deciduous
Forests
Wood-and-
Steppe
Steppe
Crimean
Mts.
Total
BM 9 9 6 2 0 2 11
M 0 2 0 0 0 1 2
Pn 10 10 10 9 4 4 10
EF 5 3 6 5 5 3 9
EWS 12 9 12 13 12 11 14
EC 13 8 13 14 13 13 15
Ps 12 10 13 13 13 10 14
SE 1 0 4 2 8 6 10
MD 1 0 3 2 8 16 16
CC 0 0 0 0 0 2 2
BC 0 0 0 0 1 3 3
CrB 0 0 0 0 0 1 1
Cr 0 0 0 0 0 4 4
T 2 1 2 5 5 6 6
ST 0 0 0 3 12 1 12
TST 0 0 0 2 6 4 6
Total 65 (1) 52 (3) 69 (2) 70 (0) 87 (14) 87 (15)
% of “endemics “ 1.5 5.8 2.9 0 16.1 17.2
4
520 A. G. Radchenko
Fig. 5. Value of the faunogonetic classes of ants in different regions of Ukraine: I – class of the Zone of Coniferous
Forest (Taiga); II – class of the Zones of Mixed and Deciduous Forests; III – class of the Semi-Arid and
Arid Zones of Eurasia.
Ðèñ. 5. Ñîîòíîøåíèå ôàóíîãåíåòè÷åñêèõ êëàññîâ ìóðàâüåâ â ðàçëè÷íûõ ðåãèîíàõ Óêðàèíû: I – êëàññ
çîíû õâîéíûõ ëåñîâ; II – êëàññ çîíû ñìåøàííûõ è ëèñòâåííûõ ëåñîâ; III – êëàññ ñóáàðèäíîé è àðèä-
íîé çîí Åâðàçèè.
Fig. 6. Value of the zoogeographical complexes of the ant species in different regions of Ukraine (abbrevia-
tions are given in the text).
Ðèñ. 6. Ñîîòíîøåíèå çîîãåîãðàôè÷åñêèõ êîìïëåêñîâ âèäîâ ìóðàâüåâ â ðàçëè÷íûõ ðåãèîíàõ Óêðàèíû
(ñîêðàùåíèÿ ïðèâåäåíû â òåêñòå).
This work was supported by a grant of the State Fund for Fundamental Research of Ukraine (¹ DFFD
F40.4/043).
Arnoldi K. V. Sketch of the entomofauna and characterization of entomocomplexes of leaf litter in the Derkul
area // Trudy Instituta lesa AN SSSR. – 1956. – 30. – P. 13—34. – Russian : Àðíîëüäè Ê. Â. Î÷åðê
ýíòîìîôàóíû è õàðàêòåðèñòèêà ýíòîìîêîìïëåêñîâ ëåñíîé ïîäñòèëêè â ðàéîíå Äåðêóëà.
Arnoldi K. V. Wood-and-Steppe of the Russian Plain and its zoogeographical characteristics based on the study
of insects // Trudy Tsentralno-Chernozemnogo gosudarstvennogo zapovednika im. V. V. Alechina. –
1965. – Fasc. 8. – P. 135—166. – Russian : Àðíîëüäè Ê. Â. Ëåñîñòåïü Ðóññêîé ðàâíèíû è ïîïûò-
êà åå çîîãåîãðàôè÷åñêîé õàðàêòåðèñòèêè íà îñíîâàíèè èçó÷åíèÿ íàñåêîìûõ.
Arnoldi K. V. Zonal zoogeographical and ecological peculiarities of the myrmecofauna and ants populations of
the Russian Plain // Zoologichesky Zhurnal. – 1968. – 47, fasc. 8. – P. 1155—1178. – Russian : Àðíîëüäè
Ê. Â. Çîíàëüíûå çîîãåîãðàôè÷åñêèå è ýêîëîãè÷åñêèå îñîáåííîñòè ìèðìåêîôàóíû è íàñåëåíèÿ
ìóðàâüåâ Ðóññêîé ðàâíèíû.
Arnoldi K. V., Dlussky G.M. Superfamily Formicoidea, Family Formicidae // Opredelitel’ nasekomykh
Evropeiskoi chasti SSSR / Ed. G. S. Medvedev. – Leningrad : Nauka, 1978. – Vol. 3 (1). –
P. 519—556. – Russian : Àðíîëüäè Ê. Â., Äëóññêèé Ã. Ì. Íàäñåìåéñòâî Formicoidea, Ñåìåéñòâî
Formicidae.
Blinov V. V. New ant species for the fauna of Byelorussia // Vestnik AN BSSR. Ser. Biol. – 1984. – N 5. –
P. 113—115. – Russian : Áëèíîâ Â. Â. Íîâûå äëÿ ôàóíû Áåëîðóññèè âèäû ìóðàâüåâ.
Blinov, V. V. The ants of the southern part of Byelorussia // Redaction of the Journal Izvestia AN BSSR, Ser.
Biological sciences. – 1985. – 21 p. – Dep. in VINITI 24.04.85, N 2757—85. – Russian :
Áëèíîâ Â. Â. Ìóðàâüè þãà Áåëîðóññèè.
Chernov Yu. I. The evolutionary process and the historical development of communities Faunogenez i phy-
locenogenez. – Moscow : Nauka, 1984. – P. 5—23. – Russian : ×åðíîâ Þ. È. Ýâîëþöèîííûé ïðî-
öåññ è èñòîðè÷åñêîå ðàçâèòèå ñîîáùåñòâ.
Csősz S., Markó B., Gallé L. The myrmecofauna (Hymenoptera: Formicidae) of Hungary: an updated check-
list // North-western journal of zoology. – 2011. – 7, N 1. – P. 55—62.
Czechowski W., Radchenko A., Czechowska W. The ants (Hymenoptera, Formicidae) of Poland. – Warsaw :
MIZ PAN, 2002. – 200 p.
Emelianov A. F. Propositions to the classification and nomenclature of the areas // Entomologicheskoe
Obozrenie. – 1974. – 53 (3). – P. 497—522. – Russian : Åìåëüÿíîâ À. Ô. Ïðåäëîæåíèÿ ïî êëàññè-
ôèêàöèè è íîìåíêëàòóðå àðåàëîâ.
Krishtofovich A. N. Main factors of the evolution of the flora in the past // Materialy po istorii flory i
rastitel’nosti SSSR. – Moscow ; Leningrad: Izd-vo AN SSSR, 1946. – Part 2. – P. 21—86. – Russian :
Êðèøòîôîâè÷ À. Í. Ýâîëþöèÿ ðàñòèòåëüíîãî ïîêðîâà â ãåîëîãè÷åñêîì ïðîøëîì è åå îñíîâíûå
ôàêòîðû.
Kryzhanovsky O. L. Principles of uniform zoogeographical divisions of a land on the basis of distribution land
invertebrates // Zhurnal obschei biologii. – 1987. – 48 (1). – P. 66—71. – Russian :
Êðûæàíîâñêèé Î. Ë. Ïðèíöèïû åäèíîãî çîîãåîãðàôè÷åñêîãî äåëåíèÿ ñóøè íà îñíîâå ðàñïðîñòðà-
íåíèÿ íàçåìíûõ áåñïîçâîíî÷íûõ.
Kryzhanovsky O. L. Composition and distribution of the entmophaunas of the Earth. – Moscow : KMK, 2002. –
237 p. – Russian : Êðûæàíîâñêèé Î. Ë. Ñîñòàâ è ðàñïðîñòðàíåíèå ýíòîìîôàóí Çåìëè.
Marinich O. M., Lanko A. I., Scherban’ P. G., Shystchenko P. G. Physical geography of the Ukrainian SSR. –
Kyiv : Vyscha shkola, 1982. – 206 p. – Ukrainian : Ìàðèíè÷ Î. Ì., Ëàíüêî À. ²., Ùåðáàíü Ì. ².,
Øèùåíêî Ï. Ã. Ô³çè÷íà ãåîãðàô³ÿ Óêðà¿íñüêî¿ ÑÐÑÐ.
Marinich O. M. Physical geography of the Ukraine. – Kyiv : Znannia, 2003. – 479 p. – Ukrainian :
Ìàðèíè÷ Î. Ì. Ô³çè÷íà ãåîãðàô³ÿ Óêðà¿íè.
Markó B., Sipos B., Csősz S. et al. A comprehensive list of the ants of Romania (Hymenoptera: Formicidae) //
Myrmecol. Nachrichten. – 2006. – 9. – S. 65—76.
Prisny A. V. Myrmecofauna of the Belgortod province, Russia // Evrazijsky entomologichesky zhurnal. – 2003. –
2 (2). – P. 125—134. – Russian : Ïðèñíûé À. Â. Ìèðìåêîôàóíà Áåëãîðîäñêîé îáëàñòè, Ðîññèÿ.
Radchenko A. G. The ants (Hymenoptera, Formicidae) of the Palaearctic (evolution, systematic, genesis of fauna):
Avtoref. … dis. dok. boil. nauk. – Kyiv, 1988. – 48 p. – Ukrainian : Ðàä÷åíêî À. Ã. Ìóðàøêè
(Hymenoptera, Formicidae) Ïàëåàðêòèêè (åâîëþöiÿ, ñèñòåìàòèêà, ôàóíîãåíåç).
Radchenko A. G. Possible ways of forming of the Palaearctic myrmecofauna (Hymenoptera, Formicidae) //
Pryrodnychyi al’manakh. Ser. Biologichni nauky. – Kherson, 2003 (2002). – Fasc. 2(3). – P. 184—206. –
Russian : Ðàä÷åíêî À. Ã. Âåðîÿòíûå ïóòè ôîðìèðîâàíèÿ ìèðìåêîôàóíû (Hymenoptera, Formicidae)
Ïàëåàðêòèêè.
Radchenko A. Zoogeography of the East Palaearctic ants, with a special consideration of Korean Peninsula //
Proceed. Intern. Symp. Commemorating Innauguration Nat. Inst. Biol. Resors. October 11—12 2007. –
Incheon, Republic of Korea, 2007 à. – P. 104—120.
Radchenko A. Fauna Europea: Formicidae // Fauna Europea: Hymenoptera: Apocrita / Ed. J. Noyes. – 2007 b. –
Fauna Europea version 1.3, http: // www. faunaeur. org, accessed on 15 May 2007.
521Zonal and zoogeographic characteristic of the ant fauna (Hymenoptera, Formicidae) of Ukraine
Radchenko A., Czechowska W., Czechowski W. Mrówki – Formicidae. Klucze do Oznaczania Owadów
Polski. – Toruń : Polskie Towarzystwo Entomologiczne, 2004. – Cz. 24 (63). – 138 s.
Radchenko A., Elmes G. W., Czechowska W. et al. First records of Myrmica vandeli Bondroit and Myrmica
tulinae Elmes, Radchenko et Aktaç (Hymenoptera: Formicidae) for Poland, with a Key for the scabrin-
odis- and sabuleti-complexes // Fragm. faunist. – 2003. – N 46. – P. 47—57.
Radchenko A., Czechowska W., Czechowski W. et al. Myrmica lacustris Ruzsky (Hymenoptera: Formicidae),
an ant species new for Poland // Fragm. faunist. – 2005. – 48 (2). – P. 167—174.
Semenov-Tien-Shan’sky A. P. The limits and zoogeographical units of the Palaearctic Region for the terrestri-
al animals based on the distribution of coleopteran insects. – Moscow ; Leningrad, 1936. – 16 p. –
Russian : Ñåìåíîâ-Òÿí-Øàíñêèé À. Ï. Ïðåäåëû è çîîãåîãðàôè÷åñêèå ïîäðàçäåëåíèÿ Ïàëåàðêòè÷åñêîé
îáëàñòè äëÿ íàçåìíûõ ñóõîïóòíûõ æèâîòíûõ íà ïðèìåðå ãåîãðàôè÷åñêîãî ðàñïðîñòðàíåíèÿ
æåñòêîêðûëûõ íàñåêîìûõ.
Werner P., Wiezik M. Vespoidea: Formicidae (mravencovití) // Acta Entomol. Mus. Nat. Pragae. – 2007. –
Suppl. 11. – P. 133—164.
522 A. G. Radchenko
<<
/ASCII85EncodePages false
/AllowTransparency false
/AutoPositionEPSFiles true
/AutoRotatePages /None
/Binding /Left
/CalGrayProfile (Dot Gain 20%)
/CalRGBProfile (sRGB IEC61966-2.1)
/CalCMYKProfile (U.S. Web Coated \050SWOP\051 v2)
/sRGBProfile (sRGB IEC61966-2.1)
/CannotEmbedFontPolicy /Error
/CompatibilityLevel 1.4
/CompressObjects /Tags
/CompressPages true
/ConvertImagesToIndexed true
/PassThroughJPEGImages true
/CreateJDFFile false
/CreateJobTicket false
/DefaultRenderingIntent /Default
/DetectBlends true
/DetectCurves 0.0000
/ColorConversionStrategy /CMYK
/DoThumbnails false
/EmbedAllFonts true
/EmbedOpenType false
/ParseICCProfilesInComments true
/EmbedJobOptions true
/DSCReportingLevel 0
/EmitDSCWarnings false
/EndPage -1
/ImageMemory 1048576
/LockDistillerParams false
/MaxSubsetPct 100
/Optimize true
/OPM 1
/ParseDSCComments true
/ParseDSCCommentsForDocInfo true
/PreserveCopyPage true
/PreserveDICMYKValues true
/PreserveEPSInfo true
/PreserveFlatness true
/PreserveHalftoneInfo false
/PreserveOPIComments false
/PreserveOverprintSettings true
/StartPage 1
/SubsetFonts true
/TransferFunctionInfo /Apply
/UCRandBGInfo /Preserve
/UsePrologue false
/ColorSettingsFile ()
/AlwaysEmbed [ true
]
/NeverEmbed [ true
]
/AntiAliasColorImages false
/CropColorImages true
/ColorImageMinResolution 300
/ColorImageMinResolutionPolicy /OK
/DownsampleColorImages true
/ColorImageDownsampleType /Bicubic
/ColorImageResolution 300
/ColorImageDepth -1
/ColorImageMinDownsampleDepth 1
/ColorImageDownsampleThreshold 1.50000
/EncodeColorImages true
/ColorImageFilter /DCTEncode
/AutoFilterColorImages true
/ColorImageAutoFilterStrategy /JPEG
/ColorACSImageDict <<
/QFactor 0.15
/HSamples [1 1 1 1] /VSamples [1 1 1 1]
>>
/ColorImageDict <<
/QFactor 0.15
/HSamples [1 1 1 1] /VSamples [1 1 1 1]
>>
/JPEG2000ColorACSImageDict <<
/TileWidth 256
/TileHeight 256
/Quality 30
>>
/JPEG2000ColorImageDict <<
/TileWidth 256
/TileHeight 256
/Quality 30
>>
/AntiAliasGrayImages false
/CropGrayImages true
/GrayImageMinResolution 300
/GrayImageMinResolutionPolicy /OK
/DownsampleGrayImages true
/GrayImageDownsampleType /Bicubic
/GrayImageResolution 300
/GrayImageDepth -1
/GrayImageMinDownsampleDepth 2
/GrayImageDownsampleThreshold 1.50000
/EncodeGrayImages true
/GrayImageFilter /DCTEncode
/AutoFilterGrayImages true
/GrayImageAutoFilterStrategy /JPEG
/GrayACSImageDict <<
/QFactor 0.15
/HSamples [1 1 1 1] /VSamples [1 1 1 1]
>>
/GrayImageDict <<
/QFactor 0.15
/HSamples [1 1 1 1] /VSamples [1 1 1 1]
>>
/JPEG2000GrayACSImageDict <<
/TileWidth 256
/TileHeight 256
/Quality 30
>>
/JPEG2000GrayImageDict <<
/TileWidth 256
/TileHeight 256
/Quality 30
>>
/AntiAliasMonoImages false
/CropMonoImages true
/MonoImageMinResolution 1200
/MonoImageMinResolutionPolicy /OK
/DownsampleMonoImages true
/MonoImageDownsampleType /Bicubic
/MonoImageResolution 1200
/MonoImageDepth -1
/MonoImageDownsampleThreshold 1.50000
/EncodeMonoImages true
/MonoImageFilter /CCITTFaxEncode
/MonoImageDict <<
/K -1
>>
/AllowPSXObjects false
/CheckCompliance [
/None
]
/PDFX1aCheck false
/PDFX3Check false
/PDFXCompliantPDFOnly false
/PDFXNoTrimBoxError true
/PDFXTrimBoxToMediaBoxOffset [
0.00000
0.00000
0.00000
0.00000
]
/PDFXSetBleedBoxToMediaBox true
/PDFXBleedBoxToTrimBoxOffset [
0.00000
0.00000
0.00000
0.00000
]
/PDFXOutputIntentProfile ()
/PDFXOutputConditionIdentifier ()
/PDFXOutputCondition ()
/PDFXRegistryName ()
/PDFXTrapped /False
/Description <<
/CHS <FEFF4f7f75288fd94e9b8bbe5b9a521b5efa7684002000410064006f006200650020005000440046002065876863900275284e8e9ad88d2891cf76845370524d53705237300260a853ef4ee54f7f75280020004100630072006f0062006100740020548c002000410064006f00620065002000520065006100640065007200200035002e003000204ee553ca66f49ad87248672c676562535f00521b5efa768400200050004400460020658768633002>
/CHT <FEFF4f7f752890194e9b8a2d7f6e5efa7acb7684002000410064006f006200650020005000440046002065874ef69069752865bc9ad854c18cea76845370524d5370523786557406300260a853ef4ee54f7f75280020004100630072006f0062006100740020548c002000410064006f00620065002000520065006100640065007200200035002e003000204ee553ca66f49ad87248672c4f86958b555f5df25efa7acb76840020005000440046002065874ef63002>
/DAN <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>
/DEU <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>
/ESP <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>
/FRA <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>
/ITA <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>
/JPN <FEFF9ad854c18cea306a30d730ea30d730ec30b951fa529b7528002000410064006f0062006500200050004400460020658766f8306e4f5c6210306b4f7f75283057307e305930023053306e8a2d5b9a30674f5c62103055308c305f0020005000440046002030d530a130a430eb306f3001004100630072006f0062006100740020304a30883073002000410064006f00620065002000520065006100640065007200200035002e003000204ee5964d3067958b304f30533068304c3067304d307e305930023053306e8a2d5b9a306b306f30d530a930f330c8306e57cb30818fbc307f304c5fc59808306730593002>
/KOR <FEFFc7740020c124c815c7440020c0acc6a9d558c5ec0020ace0d488c9c80020c2dcd5d80020c778c1c4c5d00020ac00c7a50020c801d569d55c002000410064006f0062006500200050004400460020bb38c11cb97c0020c791c131d569b2c8b2e4002e0020c774b807ac8c0020c791c131b41c00200050004400460020bb38c11cb2940020004100630072006f0062006100740020bc0f002000410064006f00620065002000520065006100640065007200200035002e00300020c774c0c1c5d0c11c0020c5f40020c2180020c788c2b5b2c8b2e4002e>
/NLD (Gebruik deze instellingen om Adobe PDF-documenten te maken die zijn geoptimaliseerd voor prepress-afdrukken van hoge kwaliteit. De gemaakte PDF-documenten kunnen worden geopend met Acrobat en Adobe Reader 5.0 en hoger.)
/NOR <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>
/PTB <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>
/SUO <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>
/SVE <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>
/ENU (Use these settings to create Adobe PDF documents best suited for high-quality prepress printing. Created PDF documents can be opened with Acrobat and Adobe Reader 5.0 and later.)
>>
/Namespace [
(Adobe)
(Common)
(1.0)
]
/OtherNamespaces [
<<
/AsReaderSpreads false
/CropImagesToFrames true
/ErrorControl /WarnAndContinue
/FlattenerIgnoreSpreadOverrides false
/IncludeGuidesGrids false
/IncludeNonPrinting false
/IncludeSlug false
/Namespace [
(Adobe)
(InDesign)
(4.0)
]
/OmitPlacedBitmaps false
/OmitPlacedEPS false
/OmitPlacedPDF false
/SimulateOverprint /Legacy
>>
<<
/AddBleedMarks false
/AddColorBars false
/AddCropMarks false
/AddPageInfo false
/AddRegMarks false
/ConvertColors /ConvertToCMYK
/DestinationProfileName ()
/DestinationProfileSelector /DocumentCMYK
/Downsample16BitImages true
/FlattenerPreset <<
/PresetSelector /MediumResolution
>>
/FormElements false
/GenerateStructure false
/IncludeBookmarks false
/IncludeHyperlinks false
/IncludeInteractive false
/IncludeLayers false
/IncludeProfiles false
/MultimediaHandling /UseObjectSettings
/Namespace [
(Adobe)
(CreativeSuite)
(2.0)
]
/PDFXOutputIntentProfileSelector /DocumentCMYK
/PreserveEditing true
/UntaggedCMYKHandling /LeaveUntagged
/UntaggedRGBHandling /UseDocumentProfile
/UseDocumentBleed false
>>
]
>> setdistillerparams
<<
/HWResolution [2400 2400]
/PageSize [612.000 792.000]
>> setpagedevice
|
| id | nasplib_isofts_kiev_ua-123456789-65838 |
| institution | Digital Library of Periodicals of National Academy of Sciences of Ukraine |
| issn | 0084-5604 |
| language | English |
| last_indexed | 2025-12-07T15:46:23Z |
| publishDate | 2011 |
| publisher | Інститут зоології ім. І.І. Шмальгаузена НАН України |
| record_format | dspace |
| spelling | Radchenko, A.G. 2014-07-03T20:03:17Z 2014-07-03T20:03:17Z 2011 Zonal and Zoogeographic Characteristic of the Ant Fauna (Hymenoptera, Formicidae) of Ukraine / A.G. Radchenko // Вестник зоологии. — 2011. — Т. 45, № 6. — С. 513–522. — Бібліогр.: 26 назв. — англ. 0084-5604 https://nasplib.isofts.kiev.ua/handle/123456789/65838 595.796 (477) One hundred fourty ant species belonging to 38 genera of 5 subfamilies are known to occur in Ukraine nowadays. All the species are attributed to 16 zoogeographic complexes that are grouped into three faunogenetic classes. Comparative zonal and zoogeographical analysis of the fauna of different geographical regions of Ukraine has revealed their essential heterogeneity. The ant fauna of the Forest-Steppe zone is not original. At the same time, it is not transitive between the faunae of the Forest and Steppe zones. Ant fauna of the Forest-Steppe is related to those not the Steppe but the Forests zones, and the Forest-Steppe can be included in the southern subzone of a Forest zone of t Europe. В Украине известно 140 видов муравьев из 38 родов 5 подсемейств. Выделены 16 зоогеографических комплексов, отнесенных к трем фауногенетическим классам. Сравнительный зональный и зоогеографический анализ фаун различных физико-географических регионов Украины выявил их существенную разнородность. Показано, что фауна муравьев Лесостепи не является самобытной. В то же время, она не является переходной между фаунами лесов и степной зоны. По происхождению мирмекофауна Лесостепи связана с таковой не степной, а лесных зон, и, на основании данных о распространении муравьев, Лесостепь может быть включена в состав южной подзоны лесной зоны Европы. This work was supported by a grant of the State Fund for Fundamental Research of Ukraine (№ DFFD F40.4/043). en Інститут зоології ім. І.І. Шмальгаузена НАН України Вестник зоологии Экология Zonal and Zoogeographic Characteristic of the Ant Fauna (Hymenoptera, Formicidae) of Ukraine Зональная и зоогеографическая характеристика мирмекофауны (Hymenoptera, Formicidae) Украины Article published earlier |
| spellingShingle | Zonal and Zoogeographic Characteristic of the Ant Fauna (Hymenoptera, Formicidae) of Ukraine Radchenko, A.G. Экология |
| title | Zonal and Zoogeographic Characteristic of the Ant Fauna (Hymenoptera, Formicidae) of Ukraine |
| title_alt | Зональная и зоогеографическая характеристика мирмекофауны (Hymenoptera, Formicidae) Украины |
| title_full | Zonal and Zoogeographic Characteristic of the Ant Fauna (Hymenoptera, Formicidae) of Ukraine |
| title_fullStr | Zonal and Zoogeographic Characteristic of the Ant Fauna (Hymenoptera, Formicidae) of Ukraine |
| title_full_unstemmed | Zonal and Zoogeographic Characteristic of the Ant Fauna (Hymenoptera, Formicidae) of Ukraine |
| title_short | Zonal and Zoogeographic Characteristic of the Ant Fauna (Hymenoptera, Formicidae) of Ukraine |
| title_sort | zonal and zoogeographic characteristic of the ant fauna (hymenoptera, formicidae) of ukraine |
| topic | Экология |
| topic_facet | Экология |
| url | https://nasplib.isofts.kiev.ua/handle/123456789/65838 |
| work_keys_str_mv | AT radchenkoag zonalandzoogeographiccharacteristicoftheantfaunahymenopteraformicidaeofukraine AT radchenkoag zonalʹnaâizoogeografičeskaâharakteristikamirmekofaunyhymenopteraformicidaeukrainy |