taxonID	type	description	language	source
D837DC552165FFEAFD84DE2CFD43FC85.taxon	discussion	This genus was established by Mršić (1992) for the type and until now only species, B. mauriesi (from caves and pits on Mt. Biokovo, Dalmatia, Croatia). The name is regarded as a feminine noun.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552165FFEAFD84DE2CFD43FC85.taxon	diagnosis	Diagnosis This genus clearly differs from all other anthogonids in the presence of one pair of bristle apparatuses in combination with one pair of bristle-clad pseudoflagella on the anterior gonopods, while the posterior gonopods consist of coxal vesicles fused in the form of a medial process and telopodal remnants; without lateral coxal processes.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552165FFEAFD84DE2CFD43FC85.taxon	etymology	Etymology The genus is named after its type locality, Mt. Biokovo.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552165FFEAFD84DE2CFD43FC85.taxon	synonymic_list	Included species Biokoviella mauriesi Mršić, 1992 Biokoviella mosorensis Antić & Dražina sp. nov.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552164FFEEFDB4DA57FDD4FB0F.taxon	description	Figs 1 – 3, 9 A, 10 A	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552164FFEEFDB4DA57FDD4FB0F.taxon	diagnosis	Diagnosis Differs from B. mosorensis sp. nov. in larger body size, anterior gonopods that are more robust and several other details of their structure. Lateral valve of vulva with tooth-like subtriangular structures posteriorly.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552164FFEEFDB4DA57FDD4FB0F.taxon	etymology	Etymology The species was named in honor of the well-known world expert in diplopodology Dr. Jean-Paul Mauriès.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552164FFEEFDB4DA57FDD4FB0F.taxon	materials_examined	Material examined (total: 13 ♂♂, 7 ♀♀, 9 juveniles) Topotype CROATIA: ♂, Stara Ledenica Cave, 43.318 ° N, 17.050 ° E, 1350 m a. s. l., Biokovo Mountain, Dalmatia, 16 Jun. 2002, leg. R. Ozimec (IZB). Other material (total: 12 ♂♂, 7 ♀♀, 9 juveniles) CROATIA, Dalmatia, Mt. Biokovo: 4 ♂♂, Jama kraj Stare Škole Pit, Lokva, 12. Jul. 1989, leg. B. Jalžić (CBSS); 2 ♂♂, Jama Čavlenovača Pit, 18 Jun. 2002, leg. R. Ozimec (CBSS); 2 ♂♂, 2 ♀♀, 2 juveniles, Jama pod Sv. Jurom Pit, below Sv. Jure Peak, 20 Jun. 2002, leg. R. Ozimec (CBSS); 1 ♀, Kašogijeva Jama Pit, below Sv. Jure Peak, 21 Jul. 2002, leg. M. Lukić (CBSS); 1 ♀, 1 juvenile, Lovricia Jama 2 Pit, 26 Jul. 2002, leg. J. Bedek (CBSS); 1 ♂, 1 juvenile, Jezero Ledenica Cave, Stražbenica, Kaoci, 20 Jul. 2003, leg. R. Ozimec (CBSS); 1 juvenile, Led 1 Pit, below Sv. Jure Peak, 21 Jul. 2003, leg. J. Bedek (CBSS); 1 ♂, Crna Ledenica Cave, below Sv. Jure Peak, 24 Oct. 2006, leg. M. Lukić (CBSS); 1 ♀, same data except 18. Jun. 2011, leg. A. Kirin (CBSS); 1 ♂, 1 ♀, 3 juveniles, Velika Mačka Pit, Velika Mačka, 22 Jun. 2008, leg. M. Lukić (CBSS); 1 juvenile, same data except leg. S. Nižetić (CBSS); 1 ♂, 1 ♀, Lovricia 3 Pit, Lipi Doćić, 30 May 2015, leg. T. Delić (IZB). Type locality Stara Ledenica Cave, Mt. Biokovo, Dalmatia, Croatia.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552164FFEEFDB4DA57FDD4FB0F.taxon	description	Redescription Body indices PLEUROTERGITE 15 (Fig. 1). CIX ~ 0.8; MIX ~ 0.8; PIX = 0.25; MA ~ 160 °. Redescription of male sexual characters MALE SEXUAL CHARACTERS. Leg pairs 3 – 7 are somewhat larger than the rest of the legs, leg pairs 3 and 4 the most robust; without any peculiarities (see Discussion). ANTERIOR GONOPODS (Fig. 2). Anterior coxal processes (a) [= angiocoxites sensu Mršić (1992)] completely separated from each other, rising from the wide subquadrangular sternal plate (s); first ⅓ (base) very broad, remaining ⅔ very slender and long, curved caudad, apically with two branches (a 1 and a 2) opposite to each other. Posteriorly, anterior coxal processes equipped with bristle apparatuses (b) [= oval coxal intermediate process with bristles sensu Mršić (1992)]. Posterior coxal processes (p) [= syncoxal processes sensu Mršić (1992)] well-developed, broad at the base, “ C ” - curved in posterior view, apically divided into two parts, very wide in lateral view. The most posterior parts of the anterior gonopods are a pair of pseudoflagella (f) covered by bristles over almost their whole length, with tassels at the top (see Discussion). These pseudoflagella starting from the well-developed, rounded lobes (l). The only unpaired part of the anterior gonopods, apart from the sternum, is the rounded syncoxal vesicle (v) [= a small intermediate (medial) bridge sensu Mršić (1992)] situated between the coxal processes (deflated on the SEM photos). There are no traces of telopodites. POSTERIOR GONOPODS (Figs 2 C – D, 9 A). Very reduced in both size and structure. Consist of coxal vesicles fused in the form of a medial process (m) apically divided. Laterally with telopodal remnants (t). Lateral sternal processes (sp) high and subtriangular. Descriptions of vulvae VULVAE (Fig. 3). Somewhat elongated from lateral view. Mesal (mv) and lateral (lv) valves of bursae (bu) distally with long setae. Several setae are present on the lateral side of the lateral valvae. Lateral valvae posteriorly with tooth-like subtriangular structures (ts), which only partly cover the mesal valvae, so the bursa apertures can be seen from posterior view. Operculum (op) with long setae.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552164FFEEFDB4DA57FDD4FB0F.taxon	distribution	Distribution Croatia: known only from several caves on Mt. Biokovo (Fig. 11, red triangles).	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552164FFEEFDB4DA57FDD4FB0F.taxon	biology_ecology	Habitat Biokoviella mauriesi is limited to deep and cold caves on Mt. Biokovo with temperatures ranging from 0 to 7 ° C. The entrances of these caves are situated on an elevated plateau stretching from above 1300 m a. s. l. to the highest parts of Biokovo.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552160FFF8FE1EDDE2FCACFCE0.taxon	materials_examined	urn: lsid: zoobank. org: act: 6270477 C- 2572 - 4 DBC- 80 A 3 - 937677 DE 8949 Figs 4 – 8, 9 B, 10 B	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552160FFF8FE1EDDE2FCACFCE0.taxon	diagnosis	Diagnosis The new species can be clearly separated from B. mauriesi on the basis of the smaller body size, the presence of anterior gonopods that are much more gracile and differences in several other details of their structure. Lateral valve of vulva with shield-like structures posteriorly.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552160FFF8FE1EDDE2FCACFCE0.taxon	etymology	Etymology The new species is named after Mt. Mosor (Middle Dalmatia, Croatia), its terra typica.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552160FFF8FE1EDDE2FCACFCE0.taxon	materials_examined	Material studied (total: 14 ♂♂, 17 ♀♀, 4 juveniles) Holotype CROATIA: ♂, Balića Špilja Cave (= Kraljeva Peć Cave), 43.573 ° N, 16.570 ° E, 404 m a. s. l., Balići, village of Dugopolje, Mt. Mosor, Middle Dalmatia, Croatia, 7 Sep. 2015, leg. D. Antić & T. Rađa (NHMSC). Paratypes (total: 10 ♂♂, 10 ♀♀, 4 juveniles) CROATIA: 9 ♂♂, 7 ♀♀, 2 juveniles (IZB, NHMSC), same data as holotype; 1 ♂, 3 ♀♀, 2 juveniles, same data except 28 Apr. 2012, leg. M. Pavlek (CBSS). Other material (total: 3 ♂♂, 7 ♀♀) CROATIA, Mt. Mosor: 1 ♀, Ledenica pod Jabukovcem Pit, Jabukovac, 23 Jun. 2011, leg. P. Bregović (CBSS); 1 ♀, Maklutača Špilja Cave, Čevrljin Klen, Kute, 24 Jun. 2011, leg. R. Baković (CBSS); 1 ♂, Velika Gajna Pit, Gornje Sitno, 5 May 2012, leg. R. Cvitanić (CBSS); 2 ♂♂, 5 ♀♀, same data except 7 Jun. 2015, leg. B. Jalžić (CBSS). Type locality CROATIA: Balića Špilja Cave (= Kraljeva Peć Cave), Balići, village of Dugopolje, Mt. Mosor, Middle Dalmatia.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552160FFF8FE1EDDE2FCACFCE0.taxon	description	Description SEGMENTS. Body with 30 segments (including telson) in adults. Juveniles with 28 and 26 segments (including telson), respectively. MEASUREMENTS. Males 9 – 12 mm long, vertical diameter of the largest pleurotergite 0.9 – 1 mm. Females 10.5 – 13 mm long, vertical diameter of the largest pleurotergite 1 – 1.05 mm. Holotype male 10.5 mm long, vertical diameter of its largest pleurotergite 1 mm. COLORATION. Pigmentless, whitish (Fig. 10 B). HEAD. Setose. Labrum with three medial labral teeth and with 4 + 4 labral and 1 + 1 supralabral setae. Gnathochilarium normal. Antennae elongated, 2.4 mm long in holotype male. Length of antennomeres (in mm): I (0.1), II (0.27), III (0.58), IV (0.3), V (0.7), VI (0.22), VII (0.2) and VIII (0.03). Length / breadth ratios of antennomeres I-VII: I (1), II (2.1), III (5.3), IV (2.7), V (5.4), VI (1.5) and VII (2). Antennomeres II, IV, V, VI and VII with one, three, one, four and one macrochaetae, respectively. Blind. COLLUM. Narrower than head, with six macrochaetae. BODY SEGMENTS (Fig. 4). Without lateral keels, metazonites with only small lateral swellings. Macrochaetae short, trichoid. CIX (pleurotergite 15) ~ 0.9; MIX (pleurotergite 15) ~ 1; PIX (pleurotergite 15) = 0.6; MA (pleurotergite 15) ~ 140 °. TELSON. Epiproct with a pair of spinnerets and six trichoid setae arranged in two rows (2 + 2 marginal and 1 + 1 paramedial setae). Hypoproct with two trichoid setae. Paraprocts with 3 + 3 marginal trichoid setae. WALKING LEGS. Elongated. Leg pairs 1 and 2 with tarsal combs in both sexes. MALE SEXUAL CHARACTERS. Leg pairs 3 – 7 somewhat larger than the rest of the legs, leg pairs 3 and 4 the most robust; without any peculiarities. Leg pairs 10 and 11 with coxal glands; leg pair 11 with posteriorly directed coxal horn. ANTERIOR GONOPODS (Figs 5, 6 A – E, 7). Anterior coxal processes (a) [= angiocoxites sensu Mršić (1992)] completely separated from each other, rising from the very wide sternal plate (s); first ⅓ (base) very broad, remaining ⅔ very gracile, long, thin and curved caudad, apically with two branches (a 1 and a 2) opposite to each other. Posteriorly anterior coxal processes with bristle apparatuses (b) [= oval coxal intermediate process with bristles sensu Mršić (1992)]. Posterior coxal processes (p) [= syncoxal processes sensu Mršić (1992)] well-developed, broad at the base, “ S ” - curved from posterior view, with only a small apical notch. The most posterior parts of the anterior gonopods are a pair of pseudoflagella (f), naked over their whole length, with tassels at the top. These pseudoflagella starting from the welldeveloped, rounded lobes (l). The only unpaired part of the anterior gonopods, apart from the sternum, is the rounded syncoxal vesicle (v) [= small intermediate (medial) bridge sensu Mršić (1992)] situated between the coxal processes (deflated on the SEM photos). There are no traces of telopodites. POSTERIOR GONOPODS (Figs 6 F, 9 B). Very reduced in both size and structure. Consisting of coxal vesicles fused in the form of a medial process (m) divided halfway. Laterally with telopodal remnants (t). Lateral sternal processes (sp) low and rounded. VULVAE (Fig. 8). Subquadrangular from lateral view. Mesal (mv) and lateral (lv) valvae of bursae (bu) distally with long setae. Lateral valvae posteriorly with shield-like structures (ss) which almost completely cover the mesal valvae, so that bursa apertures can’t be seen from posterior view. Operculum (op) with long setae.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552160FFF8FE1EDDE2FCACFCE0.taxon	distribution	Distribution Croatia, known only from several caves on Mt. Mosor (Fig. 11, blue circles).	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552160FFF8FE1EDDE2FCACFCE0.taxon	biology_ecology	Habitat Balića Špilja is a cave with a huge entrance enabling light to penetrate through almost the whole cave. Only the innermost part is in compete darkness and with various speleothems. Mean air temperature in the cave is 6.3 ºC and humidity is high (99.6 %). Altogether, the cave is 194 m long and 50 m deep. Balića Špilja is a very important biospeleological locality, being locus typicus for eight different taxa (Bedek et al. 2006; Makarov et al. 2011): Folkia boudewijni Deeleman-Reinhold, 1993, Troglohyphantes giromettai (Kulczyński, 1914) and Troglohyphantes strandi Absolon & Kratochvíl, 1932 (all Araneae); Neobisium dalmatinum Beier, 1938 (Pseudoscorpiones); Massarilatzelia dugopoljica Makarov & Rađa, 2011 (Diplopoda); and Neotrechus ganglbaueri bluehweissi (Hoffmann, 1913), Haplotropidius taxi subinflatus (Apfelbeck, 1907) and Spelaites grabowskii Apfelbeck, 1907 (all Coleoptera). Apart from the aforementioned taxa, the cave is also inhabited by another interesting troglobiont or trogophile fauna, including such species as: Oroniscus dalmaticus Strouhal, 1937, Alpioniscus balthasari (Frankenberger, 1937) and Armadillidium sp. (all Isopoda, Bedek et al. 2011 and CBSS); Apfelbeckia insculpta (L. Koch, 1867) and Brachydesmus subterraneus Heller, 1858 (both Diplopoda, present study); Nesticus eremita Simon, 1879, Rhode sp., Stygopholcus absoloni (Kulczyński, 1914) and Barusia maheni (Kratochvil & Miller, 1939) (all Aranea, CBSS); and Duvalius novaki (Müller, 1911) (Coleoptera, Pretner 1973). Biokoviella mosorensis sp. nov. is found in the middle part of the cave, walking on rocks or large stones on surfaces facing the dark. With a depth of 176 m, Velika Gajna Pit is one of the deepest pits on Mt. Mosor. Biokoviella mosorensis sp. nov. was collected near the bottom of this pit, where measured air temperature was 7 ºC and humidity 90 %. Other notable collected species of the pit’s fauna were: Alpioniscus sp. (Isopoda); Brachydesmus subterraneus Heller, 1858 (Diplopoda); and Duvalius erichsonii (Schaufuss, 1864), Haplotropidius taxi (Müller, 1903), Laemostenus cavicola (Schaum, 1858), S. grabowskii and Speoplanes giganteus (J. Müller, 1911) (all Coleoptera) (Jalžić et al. 1990 and CBSS). Maklutača is a cave almost 150 m long and 39 deep (Jalžić et al. 2013). Similar to Balića Špilja, Maklutača has a huge entrance, with light penetrating through the first half of the cave. Measured air temperature was 6.7 ºC. This cave is the type locality of Nicoletiella absoloni absoloni Willmann, 1940, a subspecies of small troglobitic mite (Acari). The following troglobitic or troglophilic forms were also recorded from this locality: T. giromettai and T. strandi (both Aranea); A. balthasari (Isopoda, Bedek et al. 2011); Onychiuridae indet., Heteromurus (Verhoeffiella) sp. and Pseudosinella sp. (all Collembola, CBSS); and Neotrechus ganglbaueri (Padewieth, 1891) and H. taxi (Pretner 1973 and CBSS). Furthermore, another diplopod species, Massarilatzelia dugopoljica Makarov & Rađa, 2011, was collected in Maklutača cave, which is the second known locality for this Mt. Mosor endemic species (present study). The Ledenica pod Jabukovcem Cave is situated in a deep dolina, and its specific position enables it to retain snow and ice up to the summer months. For that reason air temperature is extremely low, on average around 3.6 º C. The cave has a total length of 105 m and depth of 34 m (Jalžić et al. 2013). This speleological locality is an important locus typicus, with three described taxa: Neobisium maderi Beier, 1938 (Pseudoscorpiones), Traegardhia dalmatina gigantea Willmann, 1941 (Acari) and Speoplanes giganteus giganteus (J. Müller, 1911) (Coleoptera). Pretner (1973) mentioned two additional species of Coleoptera for this cave: H. taxi and S. grabowskii.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552176FFF8FF5BDA7BFB32FAA7.taxon	biology_ecology	Biokoviella mosorensis sp. nov. inhabits cold caves on Mt. Mosor, those in which the air temperature does not exceed 7 º C and humidity ranges from 95 to 100 %. A similar ecological preference is also characteristic of B. mauriesi. Chordeumatidans are known to tolerate low temperature, and they can be active in the soil and in rocky crevices below the snow cover (Mauriès 1986, 1988). Thus, this group of diplopods is well adapted for colonization of cold underground habitats. The subterranean habitats of Mts Biokovo and Mosor have diverse and endemic troglobiotic faunas. Turbulent geological history and the role of the Dinaric area as a refuge during glacial periods promoted continuous colonization of suitable underground habitats. A high rate of endemism is present throughout the entire Dinarides, and Mosor is no exception – even after more than 100 years of speleological and biospeleological research (Girometta 1914), new species are still being discovered.	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552176FFF8FF5BDC74FAC8FA6B.taxon	materials_examined	CROATIA: 2 ♂♂, 1 ♀, Pećina Čakovec Cave, Javorinske Drage, Mlakva, Perušić, 2 Aug. 2015, leg. B. Jalžić (CBSS); 2 ♂♂, 1 ♀, Kalvarija Cave, Bužin, Gospić, 1 Sep. 2015, leg. H. Cvitanović (CBSS).	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552176FFF8FF5BDF07FEBEF9C6.taxon	materials_examined	SLOVENIA: 1 ♂, 1 juvenile, Veliki Mižuk Pit, Mokri Potok, 15 Dec. 2015, leg. T. Delić & S. Polak (IZB).	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552176FFF8FF5BDF9AFD7AF805.taxon	materials_examined	CROATIA: 1 ♂, 2 ♀♀, Pepelarica Pit, Middle Velebit, 4 Jul. 2015, leg. G. Rnjak (CBSS); 1 ♂, 3 ♀♀, Meduza Pit, Crikvena, North Velebit National Park, 4 Aug. 2015, leg. B. Jalžić (CBSS). SLOVENIA: 1 ♀, Velika Ledenica u Paradani Pit, Lokve, Batuje, Nova Gorica, 6 Apr. 2014, leg. T. Delić & Š. Borko (IZB); 1 ♂, same data except Jun. 2014, leg. Š. Borko (IZB); 2 ♂♂, 1 juvenile, Brezno Treh Src, Cifre, Snežnik, 12 Sep. 2015, leg. T. Delić (IZB); 1 ♂, 2 ♀♀, 2 juveniles, Brajnice Pit, Dobec, Bezuljak, 14 Nov. 2015, leg. T. Delić (IZB).	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552175FFFBFF5BD80CFEBEFEC3.taxon	materials_examined	MONTENEGRO: 2 juveniles, Trzy Kopce Pit, Prokletije Mountains, 17 Jul. 2015, leg. M. Petković (IZB).	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
D837DC552175FFFBFF5BD89FFDCFFD26.taxon	materials_examined	CROATIA: 1 ♂, 4 juveniles, Jama pod Gažnovcem Pit, Stilja, Vrgorac, 3 Aug. 2014, leg. T. Rađa (IZB); 3 juveniles, Martina Jama Pit, Stilja, Vrgorac, 9 Aug. 2015, leg. T. Rađa (IZB). MONTENEGRO: 1 ♀, Jama u Dubokomdolu Pit, Njeguši, no dates or leg. (IZB); 2 ♀♀, Ericova Jama Pit, Krivošije Mt., Crkvice, 20 Sep, 2006, leg. M. Perreau (IZB); 1 ♀, Opasna Jama Pit, Kučka Korita, 21 Jun. 2015, leg. M. Petković (IZB).	en	Dragan Ž. Antić, Tvrtko Dražina, Tonći Rađa, Luka R. Lučić, Slobodan E. Makarov (2016): Taxonomic status of the family Biokoviellidae Mršić, 1992 (Diplopoda, Chordeumatida): reconsideration, with a description of one new species. European Journal of Taxonomy 205: 1-23, DOI: 10.5852/ejt.2016.205
