Literature DB >> 26085796

Collembolan species diversity of calcareous canyons in the Republic of Moldova.

Galina Buşmachiu1, Anne Bedos2, Louis Deharveng2.   

Abstract

The study of collembolan communities from the Vîşcăuți canyon in Moldova revealed 63 species belonging to 41 genera and 12 families, including four species new for the fauna of the Republic of Moldova. A checklist of collembolan species identified in the five calcareous canyons sampled so far in Moldova is included, with data on habitats, life form, occurrence and comments of distribution of most remarkable species. Of the 98 recognized species of these calcareous canyons, only 38 were shared by Vîşcăuți and the other canyons. The richness of calcareous habitats together with the high heterogeneity in faunal composition suggests that further significant increase in the species richness of the region may be expected.

Entities:  

Keywords:  Biodiversity; checklist; flotation method; life form

Year:  2015        PMID: 26085796      PMCID: PMC4467183          DOI: 10.3897/zookeys.506.8643

Source DB:  PubMed          Journal:  Zookeys        ISSN: 1313-2970            Impact factor:   1.546


Introduction

Republic of Moldova has a rather small territory (33,760 km2) but its heterogeneous natural conditions and its geographical position contributed to the formation of diverse types of soils, supporting high diversity of flora and fauna. The largest river in the country is the Dniester. Its length within the territory of Moldova is 657 km, its catchment representing about 70% of the territory of PageBreakcountry. The Dniester riverbed is sinuous in its upper course penetrating calcareous formations that emerge to the ground surface as cliffs and rocky banks. Along the course of water, petrophyte ecosystems are common and occupy a surface of 23 000 ha, being formed on the submarine coral reefs of Sarmatian Sea, emerged more than 10 million years ago. The petrophyte ecosystems in calcareous canyons of Dniester River are characteristic elements of the landscape – unique in the north-western part of Black Sea basin. The first result of the study concerning collembolan fauna of these canyons reported 56 species collected from five localities (Buşmachiu 2011a). The survey of Collembolan diversity on all riparian habitats of the Dniester revealed 138 species (Buşmachiu 2011b); however, it involved habitats such as natural steppe or natural flooded and xerothermic forests, which were not represented in Vîscăuți, the canyon object of the present study. Only 14 species were reported from Vîscăuți in our last paper. The present study was part of collembolan fauna survey carried out in the calcareous canyons of the Dniester River and allowed us to identify one genus () and four species new for the fauna of the Republic of Moldova.

Material and methods

Study sites

The samples were taken in a calcareous canyon near the locality of Vîşcăuți situated close to the Dniester River in the central part of Moldova (47°43'N, 29°07'E, altitude 52 m). Canyon slopes are steep and covered with natural deciduous forest (Fig. 1). The trees trunks growing on limestone slopes and calcareous rocks are covered with moss and lichens. After each rain, water is drained from the surroundings into the canyon, where soils at the bottom are usually very wet and covered with moss.
Figure 1.

Calcareous canyon on the bank of Dniester River near the locality of Vîșcăuți.

Calcareous canyon on the bank of Dniester River near the locality of Vîșcăuți. Several types of habitats and microhabitats of the canyon were sampled for the study (Table 1). The samples were collected randomly in November 2009 (8 samples), May 2010 (4 samples) and January 2014 (13 samples), amounting to a total number of 25. Litter and soil were sampled by a metallic square frame of 25 cm2 for 5 cm depth, each sample including 4 subsamples. Decaying wood, moss and lichens were taken additionally by hand. The winter 2013-2014 was very warm in Moldova and the first frosts began after our sampling within January, 2014, that could partly explain the richness of the collected fauna.
Table 1.

The types of studied habitats and number of samples from the Vîşcăuți canyon.

Studied habitatsLitter + soilSoilLitterLichen on woodMoss on soilMoss on rockBarks of treesDecaying woodNumber of samples
LSSLLWMSMRBDW
Bottom of the canyon311117
Forest on slopes3121310
Trees above the canyon23117
Pasture11
Number of samples8331142325
The types of studied habitats and number of samples from the Vîşcăuți canyon.

Extraction method and identification

The microarthropods were extracted from the soil using a modified flotation method (Fig. 2). A round plastic container of 1.8 litters and 22 cm in diameter was used for PageBreakextraction. The container is compound of two elements with handles and a cap, the internal one being perforated by many holes (Fig. 2a). The sample to be extracted is put into the internal container and water is added in the containers (Fig. 2b) and they are covered with a cap (Fig. 2c). The soaking of the sample takes no more than 5–15 minutes depending on the soil structure (Fig. 2d) for getting out of the PageBreaksubstrate. Then container is shaken slowly several times and the sample is stirred with a spatula. This process done carefully allows the collembolan specimens to move up to the surface of the water. and need more time than others to break surface. The floating collembolan specimens are collected one by one by hand under binocular (Fig. 2e), using entomological needle or disposable syringe with the end of the needle curved.
Figure 2.

Extraction of using flotation method (a plastic containers b filling the containers with sample and water c covering the containers d soaking the sample e collecting floating specimens under stereomicroscope).

Extraction of using flotation method (a plastic containers b filling the containers with sample and water c covering the containers d soaking the sample e collecting floating specimens under stereomicroscope). Specimens were stored in 96% ethyl alcohol and counted. They were cleared in lactic acid and KOH and mounted on slides using Marc Andre II medium. Identification was mainly done with a phase contrast microscope LEICA 2500 equipped with camera Lucida, using the standard determination keys and recently published Synopses on Palaearctic (Bretfeld 1999; Potapov 2001; Thibaud et al. 2004; Dunger and Schlitt 2011; Jordana 2012).

Results and discussion

As a result of our survey, 63 species of belonging to 41 genera and 12 families were found in the Vîşcăuți canyon. The family was represented by 14 species, followed by the families – 13, – 9, – 8, – 6, – 4, and – 2 species, PageBreak, , , and with one species each (Table 2). One genus – Stach, 1947 and four species – Rusek, 1978, (Ǻgrell, 1939), Rusek, 1966 and Martynova, 1967 are new for the Republic of Moldova.
Table 2.

Collembolan species found in the studied canyons. * – species new for the fauna of the Republic of Moldova; OC – other studied canyons; O – biogeographic occurrence (C – cosmopolitan, E – European, H – Holarctic, P – Palaearctic, M – Mediterranean, R – endemic); LF – life forms (e – epiedaphic, h – hemiedaphic, eu – euedaphic); abbreviations for habitats are given in Table 1.

TaxonNumber of specimensHabitatsLFO
VîscăuțiOC
Hypogastruridae
Ceratophysella engadinensis (Gisin, 1949)2 ex.7 ex.LeC
Ceratophysella sp. juv.1 ex.DWe-
Hypogastrura manubrialis (Tullberg, 1869)2 ex.LeC
Schoettella ununguiculata (Tullberg, 1869)5 ex.LeH
Xenylla boerneri (Axelson, 1905)24 ex.B, MR, DWhE
Xenylla brevisimilis brevisimilis Stach, 194923 ex.L, LS, LWhE
Xenylla corticalis Börner, 190119 ex.MS, DWhE
Xenylla maritima Tullberg, 18698 ex.10 ex.L, LShC
Xenylla uniseta Gama, 196312 ex.MRhM
Neanuridae
Friesea mirabilis (Tullberg, 1871)7 ex.LhC
Deutonura albella (Stach, 1920)1 ex.5 ex.DWhE
Deutonura stachi (Gisin, 1952)4 ex.LhE
Endonura gracilirostris Smolis, Skarżyński, Pomorski & Kaprus’, 20072 ex.1 ex.DWhE
Lathriopyga nistru Buşmachiu, Deharveng & Weiner, 20103 ex.10 ex.L, DWhR
Neanura moldavica Buşmachiu & Deharveng, 200811 ex.15 ex.L, DWhR
Neanura minuta Gisin, 19631 ex.DWhE
Neanura muscorum (Templeton, 1835)2 ex.L, DWhC
Micranurida pygmaea Börner, 19017 ex.4 ex.L, MS, MR, DWeuC
Pseudachorutes parvulus Börner, 190335 ex.LeE
Pseudachorutes pratensis Rusek, 19731 ex.LeE
Pseudachorutes subcrassus Tullberg, 18715 ex.6 ex.L, MR, DWeP
Odontellidae
Axenyllodes bayeri Kseneman, 19353 ex.SeuE
Superodontella montemaceli Arbea & Weiner, 19921 ex.1 ex.LhE
Onychiuridae
Dimorphaphorura irinae (Thibaud & Taraschuk, 1997)3 ex.SeuE
Kalaphorura paradoxa (Schäffer, 1900)~ 47 ex.L, SeuE
Micraphorura uralica (Khanislamova, 1986)13 ex.25 ex.L, SeuP
Protaphorura armata (Tullberg, 1869)7 ex.SeuC
Protaphorura pannonica (Haybach, 1960)3 ex.SeuE
Protaphorura sakatoi (Yosii, 1966)79 ex.~ 37 ex.S, L, MSeuE
Protaphorura subarmata (Gisin, 1957)103 ex.~ 59 ex.S, L, MSeuE
Thalassaphorura tovtrensis (Kaprus’ & Weiner, 1994)81 ex.L, SeuE
Tullbergiidae
Doutnacia xerophila Rusek, 19744 ex.6 ex.SeuE
*Jevania fageticola Rusek, 19783 ex.SeuE
Jevania weinerae Rusek, 19783 ex.LeuE
Karlstejnia rusekiana Weiner, 19831 ex.SeuE
Mesaphorura critica Ellis, 197621 ex.5 ex.S, LWeuP
Mesaphorura florae Simón, Ruiz, Martin & Luciáňez, 19946 ex.SeuE
Mesaphorura jarmilae Rusek, 19821 ex.SeuE
Mesaphorura hylophila Rusek, 19824 ex.9 ex.SeuP
Mesaphorura italica (Rusek, 1971)2 ex.SeuP
Mesaphorura krausbaueri Börner, 19017 ex.SeuP
Mesaphorura macrochaeta Rusek, 19761 ex.SeuC
Mesaphorura sylvatica (Rusek, 1971)2 ex.SeuP
Mesaphorura yosii (Rusek, 1967)6 ex.SeuC
Metaphorura affinis (Börner, 1902)1 ex.2 ex.SeuP
Isotomidae
*Appendisotoma abiskoensis (Ågrell, 1939)24 ex.LeE
*Appendisotoma absoloni Rusek, 1966 juv.15 ex.LeE
Folsomia quadrioculata (Tullberg, 1871)11 ex.~ 26 ex.LhH
Folsomia manolachei Bagnall, 19397 ex.7 ex.LhP
Folsomia penicula Bagnall, 193911 ex.L, MRhP
*Folsomia volgensis Martynova, 196727 ex.LhP
Folsomides angularis (Axelson, 1905)7 ex.LShH
Folsomides marchicus (Frenzel, 1941)37 ex.LShE
Folsomides parvulus Stach, 19223 ex.~75 ex.LShC
Desoria olivacea (Tullberg, 1871)1 ex.LeH
Isotoma riparia (Nicolet, 1842)1 ex.BeE
Isotoma viridis Bourlet, 183914 ex.18 ex.L, MReH
Isotomiella minor (Schäffer, 1896)9 ex.13 ex.L, MS, DWeuH
Isotomodes productus (Axelson, 1906)1 ex.12 ex.LSeuC
Parisotoma notabilis (Schäffer, 1896)58 ex.~124 ex.LS, MR, MS, DWhC
Proisotomodes bipunctatus (Axelson, 1903)~ 23 ex.DWhE
Vertagopus sp.2 ex.Le-
Entomobryidae
Heteromurus major (Moniez, 1889)5 ex.~ 15 ex.LeM
Heteromurus nitidus (Templeton, 1835)3 ex.MReC
Entomobrya nigrocincta Denis, 19232 ex.LeE
Entomobrya marginata Tullberg, 187121 ex.MS, L, BeE
Entomobrya multifasciata (Tullberg, 1871)2 ex.5 ex.MeH
Entomobrya nivalis (Linnaeus, 1758)2 ex.MosseC
Lepidocyrtus curvicollis Bourlet, 18391 ex.LeH
Lepidocyrtus gr. lignorum (Fabricius, 1775)56 ex.~ 38 ex.LeH
Lepidocyrtus paradoxus Uzel, 18904 ex.L, MReH
Lepidocyrtus violaceus Lubbock, 18737 ex.LeH
Orchesella cincta (Linnaeus, 1758)1 ex.LeH
Orchesella maculosa Ionesco, 19157 ex.3 ex.MReE
Orchesella multifasciata Stscherbakow, 18982 ex.4 ex.L, MReE
Orchesella orientalis Stach, 19602 ex.MReE
Orchesella pseudobifasciata Stach, 196037 ex.4 ex.M, LeE
Orchesella xerothermica Stach, 19604 ex.L, MReE
Pseudosinella horaki Rusek, 198524 ex.~ 32 ex.L, MS, DWhE
Pseudosinella imparipunctata Gisin, 19531 ex.11 ex.LhE
Pseudosinella moldavica Gama & Buşmachiu, 20023 ex.28 ex.LhE
Pseudosinella octopunctata Börner, 190118 ex.LhC
Seira domestica (Nicolet, 1842)1 ex.1 ex.LeE
Tomoceridae
Pogonognathellus flavescens (Tullberg, 1871)5 ex.DWhH
Tomocerus minor (Lubbock, 1862)2 ex.LhC
Tomocerus vulgaris (Tullberg, 1871)2 ex.DWhC
Cyphoderidae
Cyphoderus albinus Nicolet, 18423 ex.LeuP
Cyphoderus bidenticulatus Parona, 18887 ex.S, LeuM
Neelidae
Megalothorax minimus Willem, 19008 ex.12 ex.L, SeuC
Neelus murinus Folsom, 18966 ex.6 ex.L, SeuC
Sminthurididae
Sphaeridia pumilis (Krausbauer, 1898)1 ex.~21 ex.L, MRhC
Arrhopalitidae
Pygmarrhopalites sp.3 ex.DWeu-
Katiannidae
Sminthurinus aureus (Lubbock, 1862)7 ex.2 ex.LeP
Sminthurinus elegans (Fitch, 1863)4 ex.LeE
Sminthurinus niger (Lubbock, 1868)5 ex.LeP
Sminthuridae
Caprainea marginata (Schott, 1893)2 ex.LeP
Dicyrtomidae
Dicyrtoma minuta (Fabricius, 1763)1 ex.1 ex.L, MReE
Ptenothrix leucostrigata Stach, 19572 ex.LeE
Total number of species: 986373
Collembolan species found in the studied canyons. * – species new for the fauna of the Republic of Moldova; OC – other studied canyons; O – biogeographic occurrence (C – cosmopolitan, E – European, H – Holarctic, P – Palaearctic, M – Mediterranean, R – endemic); LF – life forms (e – epiedaphic, h – hemiedaphic, eu – euedaphic); abbreviations for habitats are given in Table 1. The first study concerning collembolan fauna of calcareous canyons near the localities Lalova, Țipova, Saharna, Vîşcăuți and Butuceni with similar ecological settings recorded 56 species (Buşmachiu 2011a). One additional species was included in the next paper (Buşmachiu 2011b). The present research increases the number of species revealed from the calcareous canyons of the Republic of Moldova from 57 to 98, which belong to 49 genera and 15 families. In Vîşcăuți were recorded 63 species, in other four localities 73. Only 38 species were shared by Vîşcăuți and the other canyons. Because none of the species of the canyons are considered local micro-endemics, this high divergence in faunal composition may result from important differences in sampled habitats. The comparison with canyons of Lalova, Țipova, Saharna and Butuceni (below named as “other canyons” – OC) revealed that contribution of the different Collembolan families to local biodiversity was similar, with the dominance of two families (Table 2): with 21 species (14 species in Vîşcăuți and 17 in OC) and with 17 species (13 and 11). They are followed by the families with 14 species (9 and 9), with 12 species (8 and 10), with 9 species (6 and 5) and with 8 species (4 and 7). Two families comprised three species: (1 and 2) and (1 and 3); four families – two species: (2 and 1), (2 and 2), (1 and 2) and (0 and 2); other three families, , and were represented by one species each. The family missed in the other canyons, while and were not found in Vîşcăuți (Table 2). The distribution and ecology of the most interesting and rare taxa through the country is commented below. Among the collected in the canyons, the family includes 9 species and 4 genera. In the Republic of Moldova the genus is represented by seven species (Buşmachiu and Weiner 2008). Five of them were present in studied canyons. Populations of this genus are usually represented by numerous specimens in moss, litter and sometimes on the bark of trees. Though all species are largely distributed in Europe, their distribution among studied canyons differs greatly, with only one species shared by Vîşcăuți and other canyons. This may point again to differences in sampled habitats. The family was represented by 12 species from 7 genera. The most interesting and most diversified among them are , all linked to litter and decaying wood in Moldova, with two species probably endemic for the country (PageBreakPageBreakPageBreakPageBreak and ), and one species originally described as endemic of Crimea () (Buşmachiu and Deharveng 2008; Buşmachiu et al. 2010; Smolis et al. 2007). These three species are frequent in all or most of the canyons. All are typical species for calcareous soils situated along the Dniester River, but are also present in the natural forest and under lower shrubs throughout the country (Buşmachiu 2008). , of much larger distribution in Europe, is a very rare species in Moldova, only found in low number in the litter of the Saharna canyon (Buşmachiu 2011b). In the calcareous canyons the family was represented by 8 species from 5 genera. The species typical for calcareous soil – was found in every canyon covered with natural forest or rare lower shrubs except Vîşcăuți. Pomorski (1998) cited it as living in humid litter of mountains, under stones and pieces of wood: this is a rather different ecology, and suggests that two forms may be included under this species name. was found along a streamlet in Butuceni, i.e. in same ecological conditions as its occurrence outside Moldova (Kaprus’ and Weiner 1994; Thibaud et al. 1999). The species is widespread from Bashkiria in the south part of Ural Mountain (Khanislamova 1986) to Ukraine, and inhabits forest litter and moss on stone (Kaprus’ and Weiner 1994, Kaprus’ et al. 2002). The smallest species of belong to , which are well diversified in European soils. In Moldavian calcareous canyons, 14 species and 5 genera were collected. Among them, 5 species are only present in Vîşcăuți, while 5 are absent from this canyon, pointing once again to the originality of its faunal composition. Few species (4 out of 14) were present in Vîşcăuți and in OC. PageBreak, , and were especially observed in open habitats of calcareous canyons covered with low shrubs, and are not present in Vîşcăuți. The species and , only cited previously from the soils of natural deciduous forest, are here recorded in Vîşcăuți. The genus includes only two rare silvicolous species in Europe. Both of them inhabit the soils in Moldova, with only cited from calcareous soil of Lalova canyon (Buşmachiu and Weiner 2010) and cited from Vîşcăuți (first record for Moldova). is a silvicolous euedaphic species described from a cave of southern Poland in beech and oak-hornbeam forest area (Weiner 1983) and cited from Ukrainian forest (Kaprus’ et al. 2006). Family was represented in the canyons by 17 species from 10 genera. The most speciose genera were and . The most interesting, and new for Moldova, was the genus . and were present in some of the studied canyons, mostly in open habitat or under lower shrubs, but not found in Vîşcăuți; they have a similar ecology in Europe (Potapov 2001). Species from genus may inhabit several types of ecosystems, including disturbed ones. Four species of the genus were found in Moldavian calcareous canyons, of which one, , is cited for the first time in the country. This species inhabits forest – steppe region in central part of the Palaearctic region, being common in dry forest biotopes (Potapov 2001) and is very rare in the Ukrainian fauna (Kaprus’ et al. 2006). Two species of , (Fig. 3A) and (Fig. 3B), were identified. Both are first records for Moldova, and so far restricted to Vîşcăuți canyon where they were collected in January, in litter. The first species is considered rare, recorded in litter and moss near the streams (Potapov 2001) and also cited from the Ukrainian steppe (Kaprus’ et al. 2006). is rather common in Czech deciduous forest, mostly abundant in autumn (Rusek 1968). Remarkably, these two species were collected in a same sample, both in large number.
Figures 3.

A B .

A B . The total number of represented in the studied canyons was 21 species from 6 genera. Among species living preferentially in moss on limestone in Moldova are several and species. One of them, was found in most studied canyons and not in other ecological conditions. This species was first cited from calcareous places near caves in south-western Romania (Ionesco 1915), and then from meadows near the Dniester canyon of the Ukrainian part of the river (Chernobai et al. 2003). The microhabitats of the studied locality are rich in rare species from families (, , ), (, ) and (), but poor in species. species are rare not only in microhabitats of calcareous canyons, but also in the riparian habitats exposed to periodical flooding on the bank of Dniester River (Buşmachiu and Weiner 2013). The species of this group, especially from the families , and , are abundant in the herbaceous plants of open habitats (Buşmachiu 2011b). Their rarity (3 species, versus 7 for OC) in our samples may result from a lack of favourable open habitats in Vîşcăuți, but also by unadapted sampling techniques, as suggested by the abundance of and soil-dependent species of (, , sp.). The Dniester flows through Ukraine and Moldova. It is therefore not surprising that more than 90 collembolan species revealed in our study are shared with Ukraine. PageBreakThe analysis of collembolan species from studied calcareous canyons brings new information on the peculiarities of species distribution and on their ecological preferences. Of special interest is the fact that, for several families, a large proportion of the species are not shared by Vîşcăuți and other canyons. This may be due to differences more important than estimated at first sight that may exist in sampled habitats. The three classical morpho-functional groups of epiedaphic, hemiedaphic and euedaphic were represented by a quite similar number of species, i.e. 35 epiedaphic, 31 hemiedaphic, and 32 euedaphic (Table 2). These groups differ in dispersal ability and other life traits such as reproduction, mobility, metabolic activity and feeding behaviour (Hopkin 1997). In our dataset, they usually match the vertical gradient from surface to deep soil. So the petrophyte ecosystems covered by natural forest, with moss and decayed wood, provide diversified micro-microhabitats to a large diversity in each of these three functional groups. The most part of identified species in the calcareous canyons have a wide occurrence (Fig. 4). Between them 43.3% have European, 20.7% – cosmopolitan, 15.3% – Palaearctic and 13.4% – Holarctic distribution. Only three species have Mediterranean distribution and two species were described from the Republic of Moldova; for the description of two other species, supplementary material is needed.
Figure 4.

Percentage of identified collembolan species per biogeographical categories in the studied calcareous canyons.

Percentage of identified collembolan species per biogeographical categories in the studied calcareous canyons.

Conclusions

With a total of 98 species of in 49 genera and 15 families, the fauna of the calcareous canyons of Moldova can be qualified of rich, though comparative data are lacking in other areas. Enlarging the spectrum of sampled habitats and collecting techniques (pitfall, berlesing, beating vegetation) will probably increase significantly this number, especially for . A second important result is the large differences in the composition of fauna between canyons. It is suggested that the relative importance of open versus forest habitats may explain most of these differences. At least, the presence PageBreakof rare and even of a few endemic species may be noticed, giving a further interest to this Collembolan fauna of calcareous habitats. Additional sampling is currently carried out to check whether the originality of Vîşcăuți is real or an effect of sampling bias.
  2 in total

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  2 in total

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