Biodiversity Data Journal :
Taxonomic Paper
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Corresponding author:
Academic editor: Pavel Stoev
Received: 24 Nov 2015 | Accepted: 17 May 2016 | Published: 19 May 2016
© 2016 Daniil Korobushkin, Irina Semenyuk, Ivan Tuf
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Korobushkin D, Semenyuk I, Tuf I (2016) An annotated checklist of the Chilopoda and Diplopoda (Myriapoda) of the Abrau Peninsula, northwestern Caucasus, Russia. Biodiversity Data Journal 4: e7308. https://doi.org/10.3897/BDJ.4.e7308
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The Abrau Peninsula is located in northwestern Caucasus between the cities of Novorossiysk and Anapa, Krasnodar Province, Russia. This paper contains an annotated checklist of the Chilopoda and Diplopoda inhabiting the Abrau Peninsula.
The fauna of the Abrau Peninsula comprises 17 centipede (4 orders) and 16 millipede (6 orders) species. Henia taurica, hitherto known only from the Crimea, has now been reported from several localities in the studied region. The study also reveals two possibly new millipede species. Statistical analyses showed that habitat preferences of myriapod species within the Abrau Peninsula are caused by species geographic distribution pattern and microbiotope preferences.
Myriapoda, taxonomy, Utrish Nature Reserve, soil fauna
The myriapod fauna of some parts of Russia still remains poorly known. This holds particularly true for the Caucasus, where most large-scale investigations of the group were performed a long time ago (
The Abrau Peninsula is located between the cities of Novorossiysk and Anapa, Krasnodar Region. Its 9065 ha area is occupied by the Utrish State Nature Reserve. The climate of the Abrau Peninsula is sub-Mediterranean with cool rainy winters without a stable snow cover and with hot dry summers. The mean annual precipitation is 500 mm, the mean July and February temperatures are 23.7°C and 2.7°C, respectively (
The abundance of millipedes and centipedes at the Abrau Peninsula averages from 784 to150 ind./m2, or ca. 65% and 10% of all soil macroinvertebrates (
The goal of this paper is to summarize and expand the current knowledge on the composition and the distribution of Chilopoda and Diplopoda in the Abrau Peninsula, which would help to improve the conservation policies in the Utrish Nature Reserve and facilitate further studies on these groups in the region.
The data presented in this paper are primarily based on the field studies of the myriapods collected by the authors (a description of the sampling sites is provided in Table
No. |
Habitat |
Coordinates and elevation (m a.s.l.) |
{1} |
Quercus petraea, Fagus orientalis, Carpinus caucasica forest |
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{2} |
Q. petraea, F. orientalis, C. caucasica forest |
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{3} |
Quercus pubescens – C. caucasica forest |
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{4} |
Q. pubescens – C. caucasica forest |
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{5} |
Mixed Q. pubescens, C. caucasica, Juniperus excelsa forest with Achnatherum bromoides, Physospermum cornubiense, Dictamnus albus |
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{6} |
Q. pubescens forest with Carpinus orientalis and steppe Graminaea species. |
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{7} |
Steppe meadow with Vitex agnus-castus, Q. pubescens and C. orientalis |
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{8} |
Q. pubescens – C. caucasica forest near the Lake Sukhoy Liman |
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{9} |
Mixed Q. pubescens C. caucasica, Fraxinus excelsior forest |
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{10} |
Tilia begoniifolia – Q. petraea forest with the oriental hornbeam and Acer laetum |
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{11} |
F. orientalis forest |
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{12} |
Q. pubescens – C. orientalis forest with Cotinus coggygria |
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{13} |
Q. pubescens – C. orientalis forest with Juniperus oxycedrus, J. excelsa, Ruscus ponticus and Graminaea. |
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{14} |
Marine station RAS; mixed Q. pubescens, C. orientalis, Pistacia mutica forest with J. excelsa and fruit-trees (Prunus avium, P. armeniaca, Ficus carica, Morus sp.). |
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{15} |
F. orientalis forest with C. caucasica |
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{16} |
T. begoniifolia forest with F. orientalis and C. caucasica |
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{17} |
F. orientalis forest with Q. petraea |
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{18} |
Q. petraea forest with A. laetum |
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{19} |
C. caucasica forest with Q. petraea |
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Photos of selected habitats in the Abrau Peninsula.
Sampling. The method of myriapod sampling differed from site to site, since the samples were collected by several authors in different years. In general sampling followed on of the four basic procedures described below.
The short quoted procedure names were used in the list below to specify the method of material collection for each species.
All specimens were preserved in 70% ethanol and stored in the collection of the Zoological Museum of Lomonosov Moscow State University or in personal collections of I.I. Semenyuk, I.H. Tuf and D.I. Korobushkin.
Data analysis. To evaluate similarity of myriapod taxonomic composition in different microbiotopes with respect to the species' geographical distribution pattern, we applied Single Linkage Clustering analysis (Jaccard similarity index) with the presence/absence data standardization (
S. coleoptrata is an indigenous species in the Mediterranean region, which is largely introduced by human activities throughout Europe, Asia, North America and South America (
This species is widespread in the Caucasus (
The most common and abundant species in the European part of Russia (
This species is widespread in Central Asia, the Caucasus and the Crimea reaching the Chinese Karakoram in the east, and Greece and Romania in the west (
L. forficatus is an eurytopic species, showing a pan-Holarctic distribution pattern, widely distributed from Great Britain to Turkey and Georgia, the eastern boundary of its range reaching the Ural Mountains (
This species is known from mesophilous woodlands (e.g. beech and fir-beech forests) in Central Europe, Italy, Bulgaria, Greece, the southern part of Russia and Ukraine, including the Crimea (
L. peregrinus displays a mostly Mediterranean distribution pattern. The species is known from Italy, Croatia, Montenegro, Serbia, Macedonia, Albania, Greece, Bulgaria, Russian and Georgian sectors of Caucasus. It is also introduced into Great Britain, Panama, Bermuda Islands, and South Africa (
This South European species is distributed from Spain to Turkey and southern Ukraine (Askania Nova Biosphere Reserve). It is especially common in the Crimea Peninsula (
This Centralasiatic-European species ranges from Great Britain and Iceland in the north to Morocco and Turkey in the south and Uzbekistan and Tajikistan in the East. The species has also been introduced into North America, some Atlantic and Pacific islands (
This species is widely distributed in the Mediterranean. It is common in Crimea and the Caucasus, known from Iran, Turkey and Middle Asia (
This species was originally described by Seliwanoff in the Crimea Peninsula (
C. caucasicus is a species with the Caucasian and eastern Anatolian distribution (
This species inhabits soil and litter layers of various forests in Russia and Ukraine surrounding the Black Sea. It is also known to occur in the Balkans and extends to the Carpathians in the north. Several records are known from some Aegean islands and Anatolia (
D. conjungens is found in the Crimea, and also recorded in the Balkan Peninsula, throughout the entire Anatolia from the western coast and southern Sporades islands to the easternmost part of Western Armenia, northwards to the Pontic mountains and southwards to the Tauric mountains (
In habitus, the studied material strongly resembles G. oligopus, although our localities are situated far away from the currently known range of the species. Until now, G. oligopus has mostly been known from the Alpine-Dinaric area, being also recorded in the Carpathians (
P. ferrugineum is widely distributed through most parts of the Palaearctic (
A common soil-dwelling European species, distributed from the Great Britain to Macaronesia and through the Mediterranean region to Rostov region of Russia (
P. trivittatus is known from Israel, western Turkey and Greece; P. aegeus is found in Rhodes (
L. coecus is widespread throughout Europe, particularly in Eastern Europe with its distribution extending to Central Asia (
This species is known from Colchis, Georgian and Russian parts of the western Caucasus (
T. costata is known from parthenogenetic populations in Central and Eastern Europe, as well as in some areas in the Caucasus, while bisexual populations are restricted to southern Romania, the Balkans, Anatolia, Israel, most of the Caucasus, and Crimea (
The species distribution covers southern Russia, Abkhazia, Georgia, north-western Azerbaijan and eastern Turkey (
N. kochii is recorded widely across the continent. It has been introduced to New Zealand, North and South America (
The species is known from Turkey, Armenia, Azerbaidjan, Georgia and southern Russia (
Identification of the above species was difficult as only females and juveniles were found. C. flexum is a common and abundant species in the Krasnodar region (Chumachenko, in litt.), it was also reported from Georgia, Stavropol region and the montane parts of the Republic of Adygea, Russia (
This is most likely a new species that requires description. All specimens were collected from the leaf litter and under barks of fallen trees in all types of broad-leaf forests.
J. colchicus is known from Turkey, Georgia, Abkhazia and the southern regions of Russia (
M. rossicum is known from the south and center of European Russia, Crimea and the Caucasus, reaching Ural Mountains in the East (
P. krivolutskyi is mostly known from the Caucasus (
This is most likely a new, yet undescribed species. The specimens were found in broad-leaf forests, under the bark of fallen trees and branches, rarely in leaf litter.
B. furcatus was described in the Northern Caucasus (
The species is known from the western part of Turkey, Adsharia and Abkhasia (
The species is widespread in the Caucasus (Stavropol and Krasnodar regions of Russia and Western Georgia), where it occurs in a wide range of habitats (
In total, in the Abrau Peninsula 33 species of Chilopoda and Diplopoda were collected. The centipede fauna is represented by typical Caucasian (e.g. H. spinipes, C. caucasicus) as well as Mediterranean elements (D. conjungens, S. cingulata) and widespread Palearctic species (e.g. L. curtipes, P. ferrugineum). The millipede fauna consists mainly of Caucasian (e.g. B. furcatus, H. roseum, P. krivolutskyi) and some Euromediterranean species (M. rossicum, T. costata). The highest species diversity of Diplopoda is noted in the mountainous deciduous forests (all 16 species). However, in xerophytic forests presence of typically Mediterranean species is also notable (P. aegeus / P. trivittatus).
The PCA (Fig.
The cluster analysis revealed that habitat preferences of myriapods within the set of sampling plots (Table
Cluster analysis of similarity (Jaccard) of myriapod species distribution patterns across sampling plots in the Abrau Peninsula with respect to their distribution type and microbiotope preferences. The geographical distribution pattern of each species has been marked using color-key. The table to the left of the cluster tree demonstrates microbiotopes, in which the respective species were found.
The top two clusters in Fig.
Our results suggest that the Abrau Peninsula is identified as a unique vegetation formation (
We would like to thank S.I. Golovatch, K.B. Gongalsky, K.S. Onufrieva, M. Short, K.S. Speranskaya and A.S. Zaytsev for their support. T.Y. Lushnikova, D.M. Kuznetsova, K.B. Gongalsky and A.A. Panchenkov assisted during the collecting process. We would also like to thank V.S. Rudovsky for the photographs. The authors are grateful to L.M. Mukhametov, the Director of the Utrish Marine Biological Station RAS and O.N. Bykhalova, the Deputy Director of the Utrish State Nature Reserve. We greatly appreciate the improvements to the manuscript suggested by L. Danyi, P. Stoev, B. Vagalinsky and M. Zapparoli. The study was performed with the financial support of the Russian Science Foundation (project # 14-14-00894).