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29 December 2023 A historical collection of Greek spiders (Arachnida: Araneae) in the National Museum of the Czech Republic
Petr Dolejš
Author Affiliations +
Abstract

Greek spiders in the historical collection of the National Museum of the Czech Republic in Prague (NMPC) were mainly collected during expeditions organized by the NMPC before World War II. Some younger specimens are present in collections of the Czech arachnologists František Miller and Jan Buchar. The material was collected at 23 localities and includes 247 identifiable specimens from 74 species. Spiders were identified (or revised) according to current arachnological knowledge and thereafter databased. Among them, Leviellus stroemi (Thorell, 1870) is recorded for the first time from Greece.

Die historische Sammlung griechischer Spinnen des Nationalmuseums der Tschechischen Republik in Prag (NMPC) wurde maßgeblich während Expeditionen des NMPC vor dem Zweiten Weltkrieg gesammelt. Einige jüngere Exemplare sind auch in den Sammlungen der tschechischen Arachnologen František Miller und Jan Buchar vorhanden. Das Material stammt von 23 Standorten und umfasst 247 identifizierbare Exemplare von 74 Arten. Die Spinnen wurden nach aktuellem Wissenstand bearbeitet und digital erfasst. Bemerkenswert ist vor allem Leviellus stroemi (Thorell, 1870), die zum ersten Mal für Griechenland dokumentiert werden konnte.

One of the scientific roles of museums all over the world is keeping material for future generations and publishing checklists or catalogues of their collections. These collections, and data obtained from them, not only have faunistic and biogeographic value, but they also enable comparison with current conditions, and evaluation of change (e.g. climate changes, impact of human activity on the biotopes etc.) that has occurred since (e.g. Buchar 1997, Ewers-Saucedo et al. 2021, Gilgado et al. 2022, Punčochář 2021, 2022). Especially historical natural history collections might thus be very useful in nature protection and conservation (e.g. Drew 2011, Kitchener 1997, Suarez & Tsutsui 2004).

The National Museum of the Czech Republic in Prague (NMPC) has already published catalogues of various non-type zoological material (e.g. Dolejš 2016, Dolejš & Vaňousová 2015, Jiroušková et al. 2011, Mlíkovský et al. 2013, Subchev et al. 2017, Zamani et al. 2017, 2022). The present paper continues this work by providing information about spiders collected during expeditions to Greece in the 1920s and 1930s. The spider fauna of Greece was reviewed by Bosmans & Chatzaki (2005), summarizing data on 856 species from 49 families. Today, 1192 species from 50 families are known from Greece (Nentwig et al. 2023).

The collection of historical Greek spiders housed in the NMPC contains material from three distinct periods. The oldest originates from zoological expeditions organized by the NMPC before World War II (Štěpánek 1934, 1936, 1944, Štěpánek et al. 2016). Spiders were collected by the herpetologist Otakar Štěpánek (1903–1995), the entomologist Josef Mařan (1905–1978), and a volunteer, and later curator of invertebrates, Karel Táborský (1906–1988). They were collecting in western Greece – Ioannina, Katarraktis – and the island of Corfu (1927), in the Parnas Mts. and the Peloponnese (1935), Crete (1934–1936, 1938), northern Greece – Nausa cave (1937) – and the island of Gavdos (1938). Further material, consisting of only five specimens, comes from the collection of the Czech arachnologist František Miller (1902–1983). The youngest samples of wolf spiders (Lycosidae) from Greece were collected by another Czech arachnologist, Jan Buchar (1932–2015), in Thessaly, Thrace, Peloponnesus, Rhodes, etc. As he had already published the results of his collections (Buchar 2001, 2009, Buchar & Dolanský 2011, Buchar & Thaler 2002, Thaler et al. 2000), I do not treat his material further in this contribution. The aim of the present work is to provide historical, but unpublished, faunistic data on Greek spiders.

Material and methods

Specimens were collected at 23 localities (Tab. 1) and are kept in 80% ethanol. All material was identified in 2019 by the author (unless otherwise stated, namely in species difficult to identify) using Buchar et al. (2006), Isaia et al. (2018), Komnenov (2014), Levy (1985), Marusik et al. (2018), Nentwig et al. (2023), Oger (2022), Růžička (2018), Stäubli (2022) and Wunderlich (1995). Nomenclature follows the WSC (2022). After being identified, all material was databased in the internal database of the NMPC (the database will gradually become available online from 2024). Families and species are sorted alphabetically. The data are arranged as follows: locality number – number and sex of specimens. Photos of selected specimens (mostly those difficult to identify or those that have been rarely illustrated) were made using an Olympus SZX12 stereomicroscope equipped with an Olympus E-510 camera. Abbreviations: J = juvenile, sad = subadult. Juvenile specimens that were possible to identify to genus/family level only were omitted from this work.

Results

Agelenidae

  • Eratigena agrestis (Walckenaer, 1802): 4a – 1 ♀

  • Histopona strinatii (Brignoli, 1976): 23 – 1 ♀ (Fig. 1)

  • Maimuna cretica (Kulczyński, 1903): 18a – 2 ♀♀; 19 – 1 ♀

  • Maimuna vestita (C. L. Koch, 1841): 4a – 2 ♀♀

  • Tegenaria parietina (Fourcroy, 1785): 15c – 1 ♀; 20a – 1 ♀; 20b – 1 ♀

Tab. 1:

Names of the localities where the spiders were collected. If there are several collecting days or periods within the locality, they are distinguished by small letters. GPS coordinates and elevations cannot be provided as concrete collecting places are mostly unknown

img-z2-2_17.gif

Amaurobiidae

  • Amaurobius strandi Charitonov, 1937: 4b – 1 ♀ (Fig. 2a-c); 7 – 3 JJ

Araneidae

  • Aculepeira armida (Audouin, 1826): 8a – 1 ♀; 11b – 1 sad♀; 11c – 1 ♀

  • Agalenatea redii (Scopoli, 1763): 4a – 1 ♂, 2 ♀♀, 1 J; 11b – 1 ♀

  • Araneus angulatus Clerck, 1757: 6 – 3 ♀♀

  • Araniella cucurbitina (Clerck, 1757): 11d – 1 ♀

  • Cyrtophora citricola (Forsskål, 1775): 7 – 1 ♀

  • Larinioides suspicax (O. Pickard-Cambridge, 1876): 4a – 1 ♂, 2 ♀♀, 6 JJ; 4b – 1 ♀, 2 sad♂♂

  • Leviellus stroemi (Thorell, 1870): 4a – 3 ♀♀ (Fig. 3a-b)

  • Mangora acalypha (Walckenaer, 1802): 8a – 1 ♀

Ctenizidae

  • Cyrtocarenum grajum (C. L. Koch, 1836): 4b – 1 ♀

Dictynidae

  • Dictyna arundinacea (Linnaeus, 1758): 3 – 2 ♀♀

Dysderidae

  • Dysdera lata-group: 11a – 1 ♀; 12 – 1 ♂; 17 – 1 ♀; 20a – 1 sad♂(det. M. Řezáč)

  • Dysdera ninnii-group: 1b – 1 ♀ (Fig. 4a), 1 J; 10 – 1 J (Fig. 4b) (det. M. Řezáč)

  • Dysdera punctata-group: 2 – 1 ♀ (Fig. 5); 4b – 1 ♂ (det. M. Řezáč)

  • Note. Identification of highly endemic species of this group is very problematic at the above-mentioned sites (M. Řezáč, pers. comm.). Therefore, only species groups are provided.

Eresidae

  • Eresus walckenaeri Brullé, 1832: 9b – 1 ♀; 9c – 1 ♂; 20a – 1 ♂

  • Stegodyphus lineatus (Latreille, 1817): 13 – 1 ♀

Gnaphosidae

  • Aphantaulax trifasciata (O. Pickard-Cambridge, 1872): 8a – 1 ♂

  • Drassodes lapidosus (Walckenaer, 1802): 10 – 1 ♀

  • Haplodrassus signifer (C. L. Koch, 1839): 4b – 1 ♀, 2 JJ

  • Nomisia excerpta (O. Pickard-Cambridge, 1872): 18b – 1 ♀, 1 J

  • Pterotricha lentiginosa (C. L. Koch, 1837): 7 – 2 ♀♀; 18b – 1 ♀

  • Zelotes cingarus (O. Pickard-Cambridge, 1874): 1b – 1 ♀(Fig. 6a); 3 – 1 ♀ (Fig. 6b); 4b – 1 ♀ (det. J. Dolanský)

Fig. 1.

Histopona strinatii, female from the Kastria Cave, epigyne

img-z3-1_17.jpg

Linyphiidae

  • Porrhomma convexum (Westring, 1851): 15c – 2 ♂♂, 5 ♀♀, 1 J

  • Prinerigone vagans (Audouin, 1826): 21 – 1 ♀

Lycosidae

  • Alopecosa albofasciata (Brullé, 1832): 1b – 1 sad♀; 2 – 1 ♀; 4a – 1 J

  • Alopecosa pentheri (Nosek, 1905): 4a – 1 ♀

  • Arctosa similis Schenkel, 1938: 20a – 1 ♀ (Fig. 7)

  • Hogna radiata (Latreille, 1817): 12 – 1 J; 18b – 1 J

  • Lycosa praegrandis C. L. Koch, 1836: 4a – 2 sad♀♀; 4b – 1 sad♀; 9a – 1 ♀; 10 – 1 sad♀; 11a – 1 sad♀; 11c – 1 sad♀; 20a – 1 sad♀; 20b – 1 sad♂, 7 sad♀♀; 20c – 1 sad♀

  • Pardosa prativaga (L. Koch, 1870): 3 – 1 ♂

  • Pardosa proxima (C. L. Koch, 1847): 3 – 1 ♂

  • Trochosa ruricola (De Geer, 1778): 4b – 1 ♂, 1 ♀, 1 J

Nemesiidae

  • Brachythele cf. icterica (C. L. Koch, 1838): 11c – 1 ♀ (det. V. Opatova)

  • Nemesia sp.: 4a – 1 ♂; 4b – 1 ♂

  • Note. The Nemesia males could belong to Nemesia daedali Decae, 1995, but unfortunately the original detailed description (Decae 1995) is based only on the female and in the supplementary article (Decae 2012), only the bulbus was redrawn, thus preventing precise identification. This species has been described from Crete, so given how endemic these spiders are, it would be better to keep it conservatively as Nemesia sp. (V. Opatova, in litt.)

Nesticidae

  • Nesticus cellulanus (Clerck, 1757): 15a – 1 J; 15b – 3 ♀♀, 4 JJ; 15c – 14 ♀♀, 6 JJ

Oecobiidae

  • Uroctea durandi (Latreille, 1809): 4b – 1 J

Fig. 2.

Amaurobius strandi, female from Ioannina. a. habitus; b. epigyne; c. vulva

img-z3-33_17.jpg

Oxyopidae

  • Oxyopes lineatus Latreille, 1806: 22 – 1 ♂

Palpimanidae

  • Palpimanus gibbulus Dufour, 1820: 9c – 1 ♀

  • Palpimanus orientalis Kulczyński, 1909: 1b – 1 ♀; 3 – 1 ♂; 7 – 2 ♀♀

Philodromidae

  • Philodromus margaritatus (Clerck, 1757): 9a – 1 ♀

  • Thanatus vulgaris Simon, 1870: 20a – 1 ♀

Fig. 3.

Leviellus stroemi, species new to Greece, female from Ioannina. a. habitus; b. epigyne

img-z4-1_17.jpg

Pholcidae

  • Holocnemus pluchei (Scopoli, 1763): 4a – 3 ♂♂

Salticidae

  • Euophrys sulphurea (L. Koch, 1867): 7 – 1 ♀

  • Evarcha jucunda (Lucas, 1846): 14 – 1 ♂

  • Heliophanus equester L. Koch, 1867: 8b – 1 ♀

  • Heliophanus lineiventris Simon, 1868: 4b – 1 ♂

  • Heliophanus melinus L. Koch, 1867: 11d – 1 ♀

  • Menemerus semilimbatus (Hahn, 1829): 4a – 1 ♂, 2 sad♀♀; 12 – 1 ♀

  • Philaeus chrysops (Poda, 1761): 4a – 2 ♂♂, 1 ♀; 10 – 1 ♂; 11d – 2 ♂♂; 21 – 1 ♀

  • Salticus propinquus Lucas, 1846: 4a – 1 ♂

Scytodidae

  • Scytodes thoracica (Latreille, 1802): 1b – 1 ♀

Selenopidae

  • Selenops radiatus Latreille, 1819: 16 – 1 J

Sicariidae

  • Loxosceles rufescens (Dufour, 1820): 1a – 1 ♀; 1b – 1 ♀; 10 – 1 sad♂; 12 – 1 J; 20 – 1 ♀

Fig. 4.

Dysdera ninnii-group. a. female from Corfu; b. juvenile from Kalamata

img-z4-4_17.jpg

Sparassidae

  • Eusparassus walckenaeri (Audouin, 1826): 10 – 2 JJ; 19 – 1 sad♂; 20a – 1 sad♂, 1 sad♀

Tetragnathidae

  • Meta bourneti Simon, 1922: 15b – 1 J; 15c – 5 ♀♀, 11 JJ

  • Meta menardi (Latreille, 1804): 23 – 1 ♀ (det. F. Miller)

  • Metellina merianae (Scopoli, 1763): 9c – 1 ♂; 15b – 1 ♀, 2 JJ; 15c – 1 ♂, 2 ♀♀, 3 JJ

  • Tetragnatha montana Simon, 1874: 3 – 2 ♀♀, 5 JJ; 9c – 2 ♂♂, 1 ♀

Theridiidae

  • Asagena phalerata (Panzer, 1801): 4a – 2 ♂♂

  • Crustulina scabripes Simon, 1881: 1b – 1 ♀; 11d – 1 ♀

  • Phycosoma inornatum (O. Pickard-Cambridge, 1861): 15b – 1 ♀

  • Steatoda paykulliana (Walckenaer, 1806): 4a – 3 ♀♀; 4b – 1 ♂, 3 ♀♀, 1 J

Thomisidae

  • Bassaniodes cf. tenebrosus (Šilhavý, 1944): 7 – 1 ♀ (Fig. 8a-b); 18b – 1 ♀

  • Runcinia grammica (C. L. Koch, 1837): 8a – 1 sad♂

  • Synema plorator (O. Pickard-Cambridge, 1872): 8a – 1 ♀

  • Thomisus onustus Walckenaer, 1805: 4a – 1 J; 8a – 1 J

  • Xysticus acerbus Thorell, 1872: 4a – 3 ♀♀

  • Xysticus cristatus (Clerck, 1757): 19 – 1 ♀

  • Xysticus thessalicus Simon, 1916: 4a – 2 ♂♂, 1 sad♂; 9c – 1 ♀(Fig. 9a-b) (det. J. Dolanský)

Fig. 5.

Dysdera punctata-group, female from Corfu

img-z5-1_17.jpg

Comments

This nearly century-old material revealed a presence of 74 species, or better said taxa, as some of them were identified only to species-group level. The most important discovery was Leviellus stroemi. This species is recorded here for the first time in Greece. The finding of this species confirms the general importance of revisions of historical collections. Other good examples of useful data obtained from such collections could include locating a bat, Pipistrellus nathusii (Keyserling & Blasius, 1839), in the collection of Natural History Museum of Crete, Irakleio, confirming thereafter its presence in Crete and its southernmost distribution margin (Benda et al. 2009); or locating a bird, Numenius tenuirostris Vieillot, 1817, in the collection of the NMPC, now apparently an extinct species in Poland (Mlíkovský 2007).

Fig. 6.

Zelotes cingarus, female. a. habitus (Corfu); b. epigyne (Preveza)

img-z5-10_17.jpg

Fig. 7.

Arctosa similis, female from Gavdos, epigyne

img-z5-3_17.jpg

Fig. 8.

Bassaniodes cf. tenebrosus, female from Anogia. a. habitus; b. epigyne

img-z5-13_17.jpg

Fig. 9.

Xysticus thessalicus, female from Taygetos. a. habitus; b. epigyne

img-z6-1_17.jpg

The species composition of the spiders reflects the collecting method, general collecting effort and timing of the expeditions. As these were organized primarily for collecting vertebrates (reptiles) and insects during spring, and spiders were thus only collected as a “by-product”, only a restricted number of spider groups are represented. First, relatively large-bodied species that are unmissable and easy to collect during the day (e.g. large araneids, lycosids, sparassids or gnaphosids). Second, species that were collected by commonly used entomological collecting methods, e.g. sweeping (spiders dwelling on grass and shrubs, e.g. salticids, thomisids, linyphiids). Third, cave species that, despite their smaller size, were not overlooked during a presumably detailed investigation of these specific areas (e.g. nesticids or a blind Troglohyphantes juvenile from the Nausa Cave, that was, however, along with other unidentifiable juveniles, excluded from the text). On the other hand, species inhabiting other biotopes (e.g. the ground or canopies), night-active species (that could have been collected by pitfall traps or by hand during the night) or species occurring in autumn are largely underrepresented. Despite this “methodological bias”, the sampled species still contribute to the faunistics of Greece and again underline the importance of natural history collections.

Acknowledgements

I thank J. Dolanský (Pardubice), V. Opatova (Prague) and M. Řezáč (Prague) for help with identification of some specimens; L. Kardaki (Corfu), M. Chatzaki (Alexandroupolis) and J. Moravec (Prague) clarified several localities. I also thank E. Ašenbrenerová (formerly Kyralová; Prague) for technical assistance. Finally, I would like to thank Peter Jäger (Frankfurt am Main) and an anonymous reviewer for useful comments and suggestions that improved the earlier version of the manuscript. This work was financially supported by the Ministry of Culture of the Czech Republic (DKRVO 2019–2023/6.I.d–e, National Museum of the Czech Republic, 00023272).

References

1.

Benda P, Georgiakais P, Dietz C, Hanák V, Galanaki K, Markantonatou V, Chudárková A, Hulva P & Horáček I 2009 Bats (Mammalia: Chiroptera) of the Eastern Mediterranean and Middle East. Part 7. The bat fauna of Crete, Greece. – Acta Societatis Zoologicae Bohemicae 72 [2008]: 105–190 Google Scholar

2.

Bosmans R & Chatzaki M 2005 A catalogue of the spiders of Greece. A critical review of all spider species cited from Greece with their localities. – Newsletter of the Belgian Arachnological Society 20 (supplement 2): 1–124 Google Scholar

3.

Buchar J 1997 Změny ve složení arachnofauny Mohelenské hadcové stepi v letech 1942 až 1995 [Changes in the composition of the arachnofauna of the Mohelno Serpentine Stony Steppe between 1942 and 1995]. – Acta Scientiarum Naturalium Musei Moraviae Occidentalis Třebíč 28: 1–28 [in Czech, with English summary] Google Scholar

4.

Buchar J 2001 Two new species of the genus Alopecosa (Araneae: Lycosidae) from south-eastern Europe. – Acta Universitatis Carolinae – Biologica 45: 257–266 Google Scholar

5.

Buchar J 2009 Distribution patterns of wolf spiders (Araneae: Lycosidae) along a transect from Greece to the Czech Republic. – Contributons to Natural History 12: 315–340 Google Scholar

6.

Buchar J & Dolanský J 2011 New records of wolf spiders (Araneae: Lycosidae) in the Mediterranean. – Klapalekiana 47: 5–11 Google Scholar

7.

Buchar J, Knoflach B & Thaler K 2006 On the identity of Arctosa variana C. L. Koch and Artosa similis Schenkel, with notes on related species. – Bulletin of the British Arachnological Society 13: 329–336 Google Scholar

8.

Buchar J & Thaler K 2002 Über Pardosa atomaria (C. L. Koch) und andere Pardosa-Arten an Geröllufern in Süd- und Mitteleuropa (Araneae, Lycosidae). – Linzer biologische Beiträge 34: 445–465 Google Scholar

9.

Decae AE 1995 Two new trapdoor spider species in the genus Nemesia Audouin, 1827 and the first report of this genus from Greece (Araneae, Mygalomorphae, Nemesiidae). – Deinsea 2: 1–8 Google Scholar

10.

Decae AE 2012 Geography-related sub-generic diversity within the Mediterranean trapdoor spider genus Nemesia (Araneae, Mygalomorphae, Nemesiidae). – Arachnologische Mitteilungen 43: 24–28 –  https://doi.org/10.5431/aramit4304 Google Scholar

11.

Dolejš P 2016 A collection of sea spiders (Pycnogonida: Pantopoda) in the National Museum, Prague (Czech Republic). – Arachnologische Mitteilungen 51: 12–15 –  https://doi.org/10.5431/aramit5103 Google Scholar

12.

Dolejš P & Vaňousová K 2015 A collection of horseshoe crabs (Chelicerata: Xiphosura) in the National Museum, Prague (Czech Republic) and a review of their immunological importance. – Arachnologische Mitteilungen 49: 1–9 –  https://doi.org/10.5431/aramit4901 Google Scholar

13.

Drew J 2011 The role of natural history institutions and bioinformatics in conservation biology. – Conservation Biology 25: 1250–1252 –  https://doi.org/10.1111/j.1523-1739.2011.01725.x Google Scholar

14.

Ewers-Saucedo C, Allspach A, Barilaro C, Bick A, Brandt A, Fiege D, Füting S, Hausdorf B, Hayer S, Husemann M, Joger U, Kamcke C, Küster M, Lohrmann V, Martin I, Michalik P, Reinicke G-B, Schwentner M, Stiller M & Brandis D 2021 Natural history collections recapitulate 200 years of faunal change. – Royal Society Open Science 8 (201983): 1–19 –  https://doi.org/10.1098/rsos.201983 Google Scholar

15.

Gilgado JD, Rusterholz H-P & Baur B 2022 Millipedes step up: species extend their upper elevational limit in the Alps in response to climate warming. – Insect Conservation and Diversity 15: 61–72 –  https://doi.org/10.1111/icad.12535 Google Scholar

16.

Isaia M, Kronestedt T, Ballarin F & Chiarle A 2018 On the morphological separation of two sibling species: Pardosa proxima (P. vlijmi syn. nov.) and P. tenuipes (Araneae: Lycosidae). – Arachnologische Mitteilungen 56: 6–16 –  https://doi.org/10.30963/aramit5602 Google Scholar

17.

Jiroušková J, Kandert J, Mlíkovský J & Šámal M (eds) 2011 Emil Holub's collection in the National Museum. National Museum, Prague. 204 pp. Google Scholar

18.

Kitchener AC 1997 The role of museums and zoos in conservation biology. – International Zoo Yearbook 35: 325–336 –  https://doi.org/10.1111/j.1748-1090.1997.tb01228.x Google Scholar

19.

Komnenov M 2014 Spider fauna of the Osogovo Mt. Range, Northeastern Macedonia. – Fauna Balkana 2 (2013): 1–267 Google Scholar

20.

Levy G 1985 Araneae: Thomisidae. In: Fauna Palaestina, Arachnida II. Israel Academy of Sciences and Humanities Jerusalem. 115 pp. Google Scholar

21.

Marusik YM, Nadolny AA & Koponen S 2018 A survey of the Alopecosa cursor species group (Aranei: Lycosidae) from Asia. – Arthropoda Selecta 27: 348–362 –  https://doi.org/10.15298/arthsel.27.4.12 Google Scholar

22.

Mlíkovský J 2007 Nieznany okaz kulika cienkodziobego Numenius tenuirostris z Polski [An unknown specimen of the Slender-billed Curlew Numenius tenuirostris from Poland]. – Notatki Ornitologiczne 48: 281–282 [in Polish, with English summary] Google Scholar

23.

Mlíkovský J, Benda P, Dolejš P, Moravec J & Šanda R 2013 Jirušův odkaz a zoologické sbírky Národního muzea v Praze [ Jiruš's bequest and zoological collections of the National Museum in Prague]. – Acta Musei Nationalis Pragae, Series A – Historia 67: 47–52 [in Czech, with English abstract] Google Scholar

24.

Nentwig W, Blick T, Bosmans R, Gloor D, Hänggi A & Kropf C 2023 Spiders of Europe. Version 3.2023. –  https://araneae.nmbe.ch https://doi.org/10.24436/1 Google Scholar

25.

Oger P 2022 Les araignées de Belgique et de France. – Internet:  https://arachno.piwigo.com/ (30. Nov. 2022) Google Scholar

26.

Punčochář P 2021 Fauna vodulí několika rybníků v České republice v r. 2020 v porovnání s nálezy Dr. Karla Thona publikovanými v r. 1900 [Fauna of water mites in several ponds in the Czech Republic in 2020 in comparison with the findings of Dr. Karl Thon published in 1900]. – Ochrana přírody 68: 35–35 [in Czech, with English summary] Google Scholar

27.

Punčochář P 2022 Changes in the fauna of water mites (Acari: Parasitengona: Hydrachnidia) in small streams of the Bohemian-Moravian Highlands between the years 1964 and 2018. – Acta Societatis Zoologicae Bohemicae 85 [2021]: 34–44 Google Scholar

28.

Růžička V 2018 A review of the spider genus Porrhomma (Araneae, Linyphiidae). – Zootaxa 4481: 1–75 –  https://doi.org/10.11646/zootaxa.4481.1.1 Google Scholar

29.

Stäubli A 2022 Interactive key to linyphiid species. In: Nentwig W et al. Spiders of Europe. – Internet:  http://www.araneae.nmbe.ch (30. Nov. 2022) Google Scholar

30.

Štěpánek O 1934 Poznámky k herpetologii Krety [Sur l'herpétologie de l'ile de Crête]. – Sborník zoologického oddělení Národního Musea v Praze 1: 7–10 [in Czech, with French abstract] Google Scholar

31.

Štěpánek O 1936 Kréta a nástin její obratlovčí fauny [Crete and outline of its vertebrate fauna]. – Věda přírodní 17: 53–58 [in Czech] Google Scholar

32.

Štěpánek O 1944 Zur Herpetologie Griechenlands. – Věstník České zoologické společnosti v Praze 9: 123–147 Google Scholar

33.

Štěpánek O, Moravec J & Lymberakis P 2016 V zemi Mínótaura – Vzpomínky přírodovědce [In the Land of Minotaur – Memoirs of a naturalist]. Národní muzeum, Praha, 208 pp. [in Czech; with one chapter in English] Google Scholar

34.

Suarez AV & Tsutsui ND 2004 The value of museum collections for research and society. – BioScience 54: 66–74 –  https://doi.org/10.1641/0006-3568(2004)054[0066:TVOMCF]2.0.CO;2 Google Scholar

35.

Subchev M, Dolejš P & Kilmajerova V 2017 Branchiobdellida (Annelida: Clitellata) from collections of the National Museum (Prague) and recent samples from Slovakia, with a synopsis of branchiobdellidans from Czechia, Slovakia, and Bosnia and Herzegovina. – Acta zoologica bulgarica 69: 467–476 Google Scholar

36.

Thaler K, Buchar J & Knoflach B 2000 Notes on wolf spiders from Greece (Araneae, Lycosidae). – Linzer biologische Beiträge 32: 1071–1091 Google Scholar

37.

Wunderlich J 1995 Zur Kenntnis west-paläarktischer Arten der Gattungen Psammitis Menge 1875, Xysticus C. L. Koch 1835 und Ozyptila Simon 1864 (Arachnida: Araneae: Thomisidae). – Beiträge zur Araneologie 4 (1994): 749–774 Google Scholar

38.

WSC 2022. World Spider Catalog. Version 23.5. Natural History Museum Bern – Internet:  http://wsc.nmbe.ch https://doi.org/10.24436/2 Google Scholar

39.

Zamani A, Mirshamasi O, Dolejš P, Marusik YM, Esyunin SL, Hula V & Ponel P 2017 New data on the spider fauna of Iran (Arachnida: Araneae), Part IV. – Acta Arachnologica 66: 55–71 –  https://doi.org/10.2476/asjaa.66.55 Google Scholar

40.

Zamani A, Nadolny AA & Dolejš P 2022 New data on the spider fauna of Iran (Arachnida: Araneae), Part X. – Arachnology 19: 551–573 –  https://doi.org/10.13156/arac.2022.19.2.551 Google Scholar
Petr Dolejš "A historical collection of Greek spiders (Arachnida: Araneae) in the National Museum of the Czech Republic," Arachnologische Mitteilungen: Arachnology Letters 66(1), 17-23, (29 December 2023). https://doi.org/10.30963/aramit6603
Received: 8 January 2023; Accepted: 18 April 2023; Published: 29 December 2023
KEYWORDS
Crete
expeditions
faunistics
Greece
Leviellus stroemi
new records
Peloponnese
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