Literature DB >> 26877671

Endonura Cassagnau in Iran, with a key to species of the genus (Collembola, Neanuridae, Neanurinae).

Adrian Smolis1, Morteza Kahrarian2, Agata Piwnik1, Dariusz Skarżyński1.   

Abstract

Three new species of Endonura are described from Iran. Endonura dichaeta sp. n. can be recognized by an ogival labrum, head without chaetae O and E, chaeta D connected with tubercle Cl, tubercle Dl with five chaetae on head, absence of tubercles Di on thorax I and tubercle (Di+Di) of thorax V with 2+2 chaetae. Endonura ceratolabralis sp. n. is characterized by large body size, reduction of labral chaetotaxy, ogival labrum, head without chaeta O and fusion of tubercles Di and De on first thoracic segment. Endonura persica sp. n. is distinguished from its congeners by a nonogival labrum, absence of chaeta O, tubercles Dl and (L+So) with five and eight chaetae respectively and claw with inner tooth. The key to all species of the genus is given.

Entities:  

Keywords:  Springtails; new species; taxonomy

Year:  2016        PMID: 26877671      PMCID: PMC4740980          DOI: 10.3897/zookeys.553.6009

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


Introduction

was established by Cassagnau (1979) as one of four subgenera within the genus MacGilliwray, 1893. Later, Deharveng (1982) raised it to the generic level. At present, is one of the largest (37 valid species) and most accurately studied genera within the subfamily (Dallai 1983, Deharveng 1979, 1982, Fanciulli and Dallai 2008, Pomorski and Skarżyński 2000, Pozo and Simón 1982, Smolis and Kaprus’ 2003, 2009, Smolis 2006, Smolis et al. 2007, 2011). It is mostly a Palaearctic genus and only one species, (Axelson, 1905), is known from the Nearctic (Alaska, Smolis et al. 2011). According to a recent definition (Smolis 2008), is characterized by the following characters: 0–2 ocelli, reduced mouth parts with a thin mandible and a styliform maxilla, separate tubercles Di and De on the head, the non-cross-type of chaetotaxy on the head and three or two tubercles on abdomen V. The highest species diversity is observed in Europe (32 from among the 37 known species). However, this may be a false picture because many areas of the Palaearctic have been poorly studied by collembologists. Undoubtedly, one of such regions is Central Asia, but in this case the situation is rapidly and positively changing (Arbea and Kahrarian 2015, Kahrarian 2014, Kahrarian et al. 2013, Mayvan et al. 2015, Shayanmehr et al. 2013, Smolis et al. 2012). In the present paper, three new non-European from the western part of Iran are described. An updated key to all species of the genus is included.

Terminology

Terminology for the description follows that given in Deharveng (1983), Deharveng and Weiner (1984), Smolis and Deharveng (2006) and Smolis (2008). Abbreviations used: General morphology: abd., ant., AOIII, Cx, Fe, Scx2, T, th., Tr, VT. – abdomen – antenna – sensory organ of antennal segment III – coxa – femur – subcoxa 2 – tibiotarsus – thorax – trochanter – ventral tube Groups of chaetae: Ag, An, ap, ca, cm, cp, d, Fu, vc, Ve or ve, Vea, Vem, Vep, Vel, Vec, Vei, Vi or vi, Vl. – antegenital – chaetae of anal lobes – apical – centroapical – centromedial – centroposterior – dorsal – furcal – ventrocentral – ventroexternal – ventroexternoanterior – ventroexternomedial – ventroexternoposterior – ventroexternolateral – ventroexternocentral – ventroexternointernal – ventrointernal – ventrolateral Tubercles: Af, Cl, De, Di, Dl, L, Oc, So. – antenno–frontal – clypeal – dorsoexternal – dorsointernal – dorsolateral – lateral – ocular – subocular Types of chaetae: Ml, Mc, Mcc, me, mi, ms, S or s, bs, miA, iv, or, brs, i, mou, x, L’, B4, B5. – long macrochaeta – short macrochaeta – very short macrochaeta – mesochaeta – microchaeta – s–microchaeta or microsensillum – chaeta s – border s–chaeta on ant. IV – microchaetae on PageBreakant. IV – ordinary chaetae on ventral ant. IV – organite of ant. IV – border s–chaeta on ant. IV – ordinary chaeta on ant. IV – cylindrical s–chaetae on ant. IV („soies mousses”) – labial papilla x – ordinary lateral chaeta on abd. V – ordinary chaetae on tibiotarsi

Materials and methods

The specimens were cleared in Nesbitt’s fluid, subsequently mounted on slides in Swan’s medium and observed using a phase contrast microscope Nikon E600. Photographs were made using a camera Nikon D5100 mounted on a microscope mentioned above. Photographs were stacked using Helicon Focus 6.2.2. and prepared for publication using Adobe Photoshop CS3. Material is deposited in the Department of Invertebrate Biology, Evolution and Conservation, Institute of Environmental Biology, University of Wrocław, Poland.

Taxonomy

sp. n.

http://zoobank.org/4CBE64B2-069B-4254-AF20-43D26E6CFE10 Figs 1–4 , Table 1
Figures 1–4.

sp. n.: 1 head (holotype), dorsal and lateral chaetotaxy 2 ventral sclerification of labrum 3 dorsal chaetotaxy of thorax 4 dorsal chaetotaxy of abdomen III–VI. Arrows indicate the position of eyes.

Table 1a.

Chaetotaxy of sp. n.: Cephalic chaetotaxy–dorsal side.

TubercleNumber of chaetaeTypes of chaetaeNames of chaetae
Cl 6 Ml McF D, G
Af 6 Ml McA B, C
Oc 3 Ml McOcm, Ocp Oca
Di 2 Ml McDi1 Di2
De 2 Ml McDe1 De2
Dl 5 Ml Mc Mcc miDl1, Dl5 Dl4 Dl2 Dl6
(L+So)8 Ml Mc meL1, L4, So1 L2, So6 So3–5

Type material.

Holotype: adult female on slide, Iran, Osmanevand area, near Golestan village (N33°55', E47°06', 1241 m a.s.l.), litter in oak forest, 13.XII.2013, leg. M. Kahrarian. Paratypes: female, two males and two juveniles on slides, same data as holotype.

Other material.

Two females and male on slide, Iran, Osmanevand area, near Chelkooshk village (N34°03', E47°12', 1516 m a.s.l.), litter in oak forest, 31.I.2014, leg. M. Kahrarian; three juveniles on slide, Iran, Paveh county, near Shabankereh village (N34°52.978', E46°30.760', 1632 m a.s.l.), litter in oak forest, 20.I.2014, leg. M. Kahrarian; two females and juvenile, Iran, Kermanshah county, near Chahar zebra-e-oliya village (N34°13', E46°40', 1592 m a.s.l.), litter in oak forest, 24.I.2014, leg. M. Kahrarian.

Etymology.

The species name refers to rare feature within the genus - only two chaetae Di on each side of tubercle (Di+Di) of abdomen V.

Diagnosis.

Habitus typical of the genus . Dorsal tubercles present and well developed, except tubercles Di on th. I. 2+2 unpigmented eyes. Buccal cone long, labrum ogival. Head with chaetae A, B, C, D, F and G. Chaetae O and E absent. Tubercles Cl and Af separate. Tubercle Cl with chaetae D. Tubercles Dl and (L+So) on head with five and eight chaetae respectively. Tubercles De on th. II and III with three and four chaetae respectively. Tubercles L on abd. III and IV with three and six chaetae respectively. Abd. IV and V with eight and three tubercles respectively. Claw without inner tooth. Tibiotarsi with chaetae B4 and B5 short.

Description.

Habitus typical of the genus. Body length (without antennae): 0.75–1.55 mm (holotype 1.30 mm). Colour of the body white. 2+2 medium unpigmented eyes (Fig. 1). sp. n.: 1 head (holotype), dorsal and lateral chaetotaxy 2 ventral sclerification of labrum 3 dorsal chaetotaxy of thorax 4 dorsal chaetotaxy of abdomen III–VI. Arrows indicate the position of eyes. Types of dorsal ordinary chaetae. Macrochaetae Ml relatively long, strongly thickened, almost cylindrical, arc-like or straight, narrowly sheathed, feebly serrated, apicalPageBreakly pointed (Figs 1, 3–4); macrochaetae Mc and Mcc thickened, straight and pointed; mesochaetae and microchaetae short, thin, feebly serrated and pointed. Head. Labrum ogival, with ventral sclerifications as in Fig. 2. Labrum chaetotaxy 2/2, 4. Labium with four basal, three distal and four lateral chaetae, papillae x absent. Maxilla styliform, mandible thin tridentate. Chaetotaxy of antennae as in Table 1c. Apical vesicle distinct, trilobed. S–chaetae of ant.IV long and moderately thickened. Chaetotaxy of head as in Table 1a, b, and Fig. 1. Chaeta D connected with tubercle Cl. Tubercle Af on head longer than tubercles Oc. Tubercle Dl with five chaetae, chaeta Dl3 absent, chaeta Dl6 as minute microchaeta and hard to detect (Fig. 1). Tubercle (L+So) with eight chaetae, chaetae So2 and L3 absent, chaeta So6 as Mc (Fig. 1). Elementary tubercles BE and CD present. Chaeta A shorter than B.
Table 1c.

Chaetotaxy of sp. n.: Chaetotaxy of antennae.

Segment, GroupNumber of chaetaeSegment, GroupNumber of chaetae adult
I7IV ap or, 8 S, i, 12 mou, 6 brs, 2 iv
II11
III ve5 sensilla AO III
58 bs, 5 miA
vc 4 ca 2 bs, 3 miA
vi 4 cm 3 bs, 1 miA
d 5 cp 8 miA, 1 brs
Table 1b.

Chaetotaxy of sp. n.: Cephalic chaetotaxy–ventral side.

GroupNumber of chaetae
Vi6
Vea 3
Vem 3
Vep 4
labium11, 0x
Chaetotaxy of sp. n.: Cephalic chaetotaxy–dorsal side. Chaetotaxy of sp. n.: Cephalic chaetotaxy–ventral side. Chaetotaxy of sp. n.: Chaetotaxy of antennae. Thorax, abdomen, legs. Body s–chaeta thin and smooth, shorter than nearby macrochaetae (Figs 3, 4). Chaetotaxy of th. and abd. as in Table 1d and in Figs 3, 4. Tubercles Di on th.I not differentiated. Chaetae De3 on th. III and abd. I–III as Mcc. Chaetae De2 on th. II–III and De3 on th. III connected with tubercle De. Chaetae De3 on abd. I–III connected with tubercle De (Fig. 4). The line of chaetae De1–chaeta PageBreaks not perpendicular to the dorsomedian line on abd I–III. Furca rudimentary with 2–4 microchaetae. Tubercles Di on abd. V fused, with chaetae Di2 as Mc or Mcc, chaetae Di3 absent (Fig. 4). Chaetae L’ and Vl on abd. V present. IV abd. with 2+2 chaetae Ag. No cryptopygy. Chaetotaxy of legs as in Table 1d.
Table 1d.

Chaetotaxy of sp. n.: Postcephalic chaetotaxy.

DiTerga De Dl L Scx2 CxLegs Tr Fe T
th. I121-0361319
th. II32+s3+s+ms32761219
th. III33+s3+s32861118
Sterna
abd. I23+s23 VT: 4
abd. II23+s23Ve: 4–5Ve1 -present
abd. III23+s23 Vel:4–5 Fu:5–6me2–4mi
abd. IV22+s36 Vel: 4 Vec: 2 Vei: 2 Vl: 4
abd. V(2+2)5+s Ag: 2 Vl: 1 L’: 1
abd. VI7Ve:13–14 An: 2mi
Chaetotaxy of sp. n.: Postcephalic chaetotaxy.

Remarks.

In general appearance (shape of dorsal chaetae, chaetotaxy of central area of head and dorsal side of thorax and abdomen, complete absence of pigmentation and absence of cryptopygy), sp. n. strongly resembles Deharveng, 1980 described from Corsica. Nevertheless, both taxa differ in some essential characters, important from taxonomic point of view: presence/absence of chaetae E on head ( sp. n. absent, present), number of chaetae Dl on head ( sp. n. five, six), number of chaetae (L+So) ( sp. n. eight, nine), presence/absence of elementary tubercle EE on head ( sp. n. absent, present), presence/absence of tubercles Di on the first thoracic segment ( sp. n. absent, present), number of chaetae Di on abd. V ( sp. n. 2+2, 3+3) and presence/absence of tooth on claw ( sp. n. absent, present). In addition, the new species is characterized by only 2+2 antegenital chaetae ( 3+3) and ogival labrum (unknown in ), characters rarely observed within the genus. http://zoobank.org/FC09DDF3-EB60-416D-B31C-A290A4E812D5 Figs 5–9 , Table 2
Figures 5–9.

sp. n.: 5 head (holotype), dorsal and lateral chaetotaxy 6 ventral sclerification of labrum 7 dorsal chaetotaxy of thorax 8 dorsal chaetotaxy of abd. II 9 dorsal chaetotaxy of abdomen IV–VI. Arrows indicate the position of eyes.

Table 2a.

Chaetotaxy of sp. n.: Cephalic chaetotaxy–dorsal side.

TubercleNumber of chaetaeTypes of chaetaeNames of chaetae
Cl 4 Ml McF G
Af 10 Ml McA B, C, D, E
Oc 3 Ml meOcm, Ocp Oca
Di 2 Ml McDi1 Di2
De 2 Ml McDe1 De2
Dl 6 Ml Mc miDl1, Dl5 Dl2, Dl3, Dl4 Dl6
(L+So)9 Ml Mc meL1, L4, So1 L2, L3, So3 So4–6
Holotype: adult female on slide, Iran, Osmanevand area, near Markhor village (N33°53', E47°05', 1389 m a.s.l.), litter in oak forest, 13.XII.2013, leg. M. Kahrarian. Paratypes: 3 females on slide, same data as holotype. Three females on slide, Iran, Osmanevand area, near Ghader marz village (N34°01.030', E47°12.415', 1682 m a.s.l.), litter in oak forest, 31.I.2014, leg. M. Kahrarian. The species name refers to sharp labral apex which looks like a horn (“cera” in latin). Habitus typical of the genus . Dorsal tubercles present and well developed. 2+2 eyes darkly pigmented. Buccal cone long. Head with chaetae A, B, C, D, E, F and G. Chaeta O absent. Tubercles Cl and Af separate. Tubercles Dl and (L+So) on head with six and nine chaetae respectively. Tuberles Di and De on th. I fused. Tubercles De on th. II and III with three and four chaetae respectively. Tubercles L on abd. III and IV with three and 6–7 chaetae respectively. Abd. IV and V with eight and three tubercles respectively. Claw without inner tooth. Tibiotarsi with chaetae B4 and B5 short. Habitus typical of the genus. Body length (without antennae): 2.25–2.55 mm (holotype: 2.55 mm). Colour of the body bluish grey. 2+2 medium dark-pigmented eyes (Fig. 5). sp. n.: 5 head (holotype), dorsal and lateral chaetotaxy 6 ventral sclerification of labrum 7 dorsal chaetotaxy of thorax 8 dorsal chaetotaxy of abd. II 9 dorsal chaetotaxy of abdomen IV–VI. Arrows indicate the position of eyes. Types of dorsal ordinary chaetae. Macrochaetae Ml thickened, relatively long, arc-like or straight, narrowly sheathed, feebly serrated, apically pointed or rarely rounded (Figs 5, 7–9); macrochaetae Mc and Mcc thickened, straight, pointed or apically rounded; mesochaetae and microchaetae short, thin and pointed. Head. Buccal cone very long. Labrum ogival, with ventral sclerifications as in Fig. 6. Labrum chaetotaxy 0/2, 2. Labium with four basal, three distal and four lateral chaetae, papillae x absent. Maxilla styliform, mandible thin with two basal and two apical teeth. Chaetotaxy of antennae as in Table 2c. Apical vesicle distinct, trilobed. S–chaetae of ant.IV of medium length and moderately thickened. Chaetotaxy of head as in Table 2a, b, and Fig. 5. Tubercles Cl and Af separate. Tubercle Af on head longer than tubercles Oc. Chaeta O absent. Chaeta D free. Tubercle Dl with six chaetae, chaeta Dl3 present. Tubercle (L+So) with nine chaetae, chaeta So2 absent and chaeta So3 as Mc (Fig. 5). Elementary tubercles BE and CD present. Chaeta A shorter than B.
Table 2c.

Chaetotaxy of sp. n.: Chaetotaxy of antennae.

Segment, Group Number of chaetae Segment, Group Number of chaetae adult
I7IV ap or, 8 S, i, 12 mou, 6 brs, 2 iv
II12–14
III ve5 sensilla AO III
58 bs, 5 miA
vc 4 ca 2 bs, 3 miA
vi 4 cm 3 bs, 1 miA
d 5 cp 8 miA, 1 brs
Table 2b.

Chaetotaxy of sp. n.: Cephalic chaetotaxy–ventral side.

Group Number of chaetae
Vi6
Vea 3–4
Vem 3
Vep 4
Labium11, 0x
Chaetotaxy of sp. n.: Cephalic chaetotaxy–dorsal side. Chaetotaxy of sp. n.: Cephalic chaetotaxy–ventral side. Chaetotaxy of sp. n.: Chaetotaxy of antennae. Thorax, abdomen, legs. Body s–chaetae thin and smooth, shorter than nearby macrochaetae (Figs 7–9). Chaetotaxy of th. and abd. as in Table 2d and in Figs 7–9. Tubercles Di on th.I differentiated and fused with De (Fig. 7). Dorsal side of th. and abd. without free chaetae De. The line of chaetae De1–chaeta s perpendicular to the dorsomedian line on abd I–III. Furca rudimentary with two or without microchaetae. Tubercles Di on abd. V fused, with chaetae Di2 and Di3 as Mc (Fig. 9). Chaetae L’ and Vl on abd. V present. No cryptopygy. Chaetotaxy of legs as in Table 2d.
Table 2d.

Chaetotaxy of sp. n.: Postcephalic chaetotaxwy.

DiTerga De Dl L Scx2 CxLegs Tr Fe T
th. I121-0361319
th. II32+s3+s+ms32761219
th. III33+s3+s32861118
Sterna
abd. I23+s23 VT: 4
abd. II23+s23Ve: 5–6Ve1 -Present
abd. III23+s23 Vel:4–5 Fu:3–6me0–2mi
abd. IV22+s36–7 Vel: 4 Vec: 2 Vei: 2 Vl: 4
abd. V(3+3)5+s Ag: 3 Vl: 1 L’: 1
abd. VI7Ve: 13–14 An: 2mi
Chaetotaxy of sp. n.: Postcephalic chaetotaxwy. Because of the very characteristic long and pointed labrum, sp. n. seems to be most similar to (Ellis, 1976) (Crete) and Smolis et al. 2007 (Crimea). Nevertheless, the new species can be easily distinguished from these two taxa by the following combination of characters: maximum length of the body without antennae ( sp. n. 2.55 mm; PageBreak1.45 mm; 0.8 mm), labral formula ( sp. n. 0/2, 2; 0/2, 4; 2/2, 4), presence/absence of chaeta O on head ( sp. n. absent, in others present), number of chaetae Dl on head ( three, in others six), number of chaetae (L+So) on head ( seven, in others nine), fusion/separation of tubercles Di and de on th. I ( separate, in others fused), number of ordinary chaetae De on th. III ( two, others three), presence/absence of free chaetae on thorax ( sp. n. absent, in others present) and number of chaetae Di on abd. V ( 1-2, others three). http://zoobank.org/9CFE5947-62CC-4A3E-ABF7-5B84EA69A21A Figs 10–13 , Table 3
Figures 10–13.

sp. n.: 10 head and th. I, dorsal and lateral chaetotaxy 11 ventral sclerification of labrum 12 dorsal chaetotaxy of abdomen III–VI (holotype) 13 tibiotarsi and claw of leg III. Arrows indicate the position of eyes.

Table 3a.

Chaetotaxy of sp. n.: Cephalic chaetotaxy–dorsal side.

TubercleNumber of chaetaeTypes of chaetaeNames of chaetae
Cl 4 Ml McF G
Af 10 Ml Mc Mc or MccB A, C, E D
Oc 3 Ml Mc miOcm Ocp Oca
Di 2 Ml MccDi1 Di2
De 2 Ml MccDe1 De2
Dl 5 Ml Mc or MccDl1, Dl5 Dl2, Dl4, Dl6
(L+So)8 Ml Mc me or miL1, L4, So1 L2 So3–6
Holotype: adult female on slide, Iran, Kermanshah area, near Ghaleh shahin village (N34°25.590', E05°12.415', 566 m a.s.l.), litter in willow shrubs, 7.IV.2014, leg. M. Kahrarian. Paratypes: two females, four males and four juveniles on slides, same data as holotype. Female on slide, Iran, Kermanshah Province, Halashi County, near Sarfiroozabad village (N34°02', E47°10', 1624 m a.s.l.), litter in oak forest, 15.II.2014, leg. M. Kahrarian; female and male on slide, Iran, Osmanevand area, near Sarjoob village (N33°56', E47°08', 1240 m a.s.l.), litter in oak forest, 13.XII.2013, leg. M. Kahrarian. The species name refers to the historic name of Iran, Persia. Habitus typical of the genus . Dorsal tubercles present and generally well developed, only tubercles Di on th. I weakly differentiated. 2+2 large dark-pigmented eyes. Buccal cone rather short. Head with chaetae A, B, C, D, E , F and G. Chaeta O absent. Tubercles Cl and Af separate. Tubercles Dl and (L+So) on head with five and eight chaetae respectively. Tubercles De on th. II and III with three and four chaetae respectively. Tubercles L on abd. III and IV with four and 6–7 chaetae respectively. Abd. IV and V with eight and three tubercles respectively. Claw with inner tooth. Tibiotarsi with chaetae B4 and B5 long. Habitus typical of the genus. Body length (without antennae): 0.75–1.90 mm (holotype: 1.10 mm). Colour of the body bluish grey. 2+2 large dark pigmented eyes (Fig. 10). sp. n.: 10 head and th. I, dorsal and lateral chaetotaxy 11 ventral sclerification of labrum 12 dorsal chaetotaxy of abdomen III–VI (holotype) 13 tibiotarsi and claw of leg III. Arrows indicate the position of eyes. Types of dorsal ordinary chaetae. Macrochaetae Ml thickened, relatively long, arc–like or straight, narrowly sheathed, feebly serrated, apically rounded or rarely pointed (Figs 10, 12); macrochaetae Mc and Mcc thickened, straight and not pointed; mesochaetae and microchaetae short, thin and pointed. Head. Buccal cone short. Labrum rounded, with ventral sclerifications as in Fig. 11. Labrum chaetotaxy 4/2, 4. Labium with four basal, three distal and four lateral chaetae, papillae x absent. Maxilla styliform, mandible thin with two basal and two apical teeth. Chaetotaxy of antennae as in Table 3c. Apical vesicle distinct trilobed. S–chaetae of ant.IV of medium length and moderately thickened. Chaetotaxy of head as in Table 3a, b, and Fig. 10. Chaetae D and E free. Tubercles Cl and Af separate. PageBreakTubercle Af on head longer than tubercles Oc. Tubercle Dl with five chaetae, chaeta Dl3 absent. Tubercle (L+So) with eight chaetae, chaetae So2 and L3 absent (Fig. 10). Elementary tubercle BE absent. Chaeta A shorter than B.
Table 3c.

Chaetotaxy of sp. n.: Chaetotaxy of antennae.

Segment, GroupNumber of chaetaeSegment, GroupNumber of chaetaev adult
I7IV ap or, 8 S, i, 12 mou, 6 brs, 2 iv
II12–14
III ve5 sensilla AO III
58 bs, 5 miA
vc 4 ca 2 bs, 3 miA
vi 4 cm 3 bs, 1 miA
d 5 cp 8 miA, 1 brs
Table 3b.

Chaetotaxy of sp. n.: Cephalic chaetotaxy–ventral side.

GroupNumber of chaetae
Vi6
Vea 3–4
Vem 3
Vep 4
labium11, 0×
Chaetotaxy of sp. n.: Cephalic chaetotaxy–dorsal side. Chaetotaxy of sp. n.: Cephalic chaetotaxy–ventral side. Chaetotaxy of sp. n.: Chaetotaxy of antennae. Thorax, abdomen, legs. Body s–chaetae fine and smooth, distinctly shorter than nearby macrochaetae (Fig. 12). Chaetotaxy of th. and abd. as in Table 3d and in Figs PageBreak10, 12. Tubercles Di on th.I differentiated or not. Chaetae De2 on th. II–III and De3 on th. III free. Chaetae De3 on abd. I–III free (Fig. 12). The line of chaetae De1–chaeta s parallel to the dorsomedian line on abd. I–III. Furca rudimentary without microchaetae. Tubercles Di on abd. V fused, with chaetae Di2 as Mcc and Di3 as mi (Fig. 12). Chaetae Vl on abd. V present. Cryptopygy slightly developed. Chaetotaxy of legs as in Table 3d. Tibiotarsi with rather long chaetae B4 and B5. Claw with inner tooth (Fig. 13).
Table 3d.

Chaetotaxy of sp. n.: Postcephalic chaetotaxy.

DiTerga De Dl L Scx2 CxLegs Tr Fe T
th. I121-0361319
th. II32+s3+s+ms32761219
th. III33+s3+s32861118
Sterna
abd. I23+s23 VT: 4
abd. II23+s23Ve: 5–6Ve1 -present
abd. III23+s24 Vel: 5 Fu:5–10me0 mi
abd. IV22+s36–7 Vel: 4 Vec: 2 Vei: 2 Vl: 4
abd. V(3+3)8+s Ag: 3 Vl: 1 L’: 1
abd. VI7Ve: 13–14 An: 2mi
Chaetotaxy of sp. n.: Postcephalic chaetotaxy. In general appearance and presence of inner tooth on claw, characters rarely observed within the genus, sp. n. strongly resembles to Smolis et al. 2007 (described from Crimea). However, the new species can be reliably separated from Crimean species with the following characters: number of chaetae Dl on head ( sp. n. five, six), number of chaetae (L+So) on head ( sp. n. eight, ten), presence/absence of tubercles Di on the first thoracic segment ( sp. n. present, absent) and number of chaetae L of abd. IV ( sp. n. 6–7 chaetae, 8–9).

Key to the genus

In 1982, Deharveng, in his PhD thesis, elevated to the generic level and prepared a key to the genus that comprised 23 species. Nowadays, including the taxa described herein, the genus contains 40 members and is the second largest of the tribe , after Cassagnau, 1979. Moreover, after the publication of Deharveng’s paper (date), a few species were redescribed and one taxon was synonymised PageBreak(Smolis and Kaprus’ 2003, Smolis 2008, Smolis et al. 2007, 2011). Considering these facts, the preparation of an updated key to all species of the genus seemed to be highly recommended.

Discussion

Considering the data presented here and those obtained from the literature (Mayvan et al. 2015, Shayanmehr et al. 2013, Smolis et al. 2012), fauna of Iran PageBreakcomprises ten species and seven genera: (Caroli, 1912), Smolis et al., 2012, Smolis et al., 2012, (Gama & Gisin, 1964) (Gisin 1964), sp. n., sp. n., , sp. n., (Templeton, 1835), Mayvan et al. 2015, (Kos, 1940). It should be noted, however, that until now only the western part of Iran has been roughly studied. Although future research may change the present picture of the subfamily diversity in the studied country and region, some preliminary conclusions can be drawn. The first is related to the higher systematic pattern and composition of of Iran. This fauna consists almost exclusively of members of the tribe , the most diverse and dominant among in the western Palaearctic. To date, none of the and genera have been found in Iran, although they are numerous and widely distributed in south, south-east and east Asia. The second conclusion seems to be more expected, species from Iran resemble those known from south-east Europe. It suggests their close affinity and the historical connection between these faunas. The third conclusion sheds light on the distribution and the history of this genus. Most species were recorded from Mediterranean and temperate zones of Europe, where they live predominantly in forests. It is worth saying that the greatest diversity of the genus through the continent is more or less correlated to the areas of land that have never been subjected to glaciations. Till now, the occurrence of only a few species is documented outside Europe, especially in the Middle East (Smolis and Kaprus 2003, 2009; Smolis et al. 2011). The recent and present discoveries of species in Kyrgyzstan (Smolis et al. 2011) and Iran significantly expand the list of species and also our knowledge on the genus. Undoubtedly, diverse forest habitats of the coastal and montane regions of Iran and adjacent countries hide a rich fauna of . We therefore hope that a more comprehensive study in the future will allow us to present a better picture of the distribution of in Iran and the near East.
1Head with fusion of tubercles Af and Cl 2
Head with separation of tubercles Af and Cl 7
2.Chaeta O on head present 3
Chaeta O on head absent 4
3Tubercles Di on th. I present and fused with De, tubercle (Di+Dl+L) on abd. V with nine chaetae Endonura poinsotae Deharveng, 1980 (France, Corsica)
Tubercles Di on th. I absent, tubercle (Di+Dl+L) on abd. V with seven chaetae Endonura ichnusae Dallai, 1983 (Italy, Sardinia)
4Tubercles De on abd. I–III with four chaetae 5
Tubercles De on abd. I–III with three chaetae Endonura granulata (Cassagnau & Delamare Deboutteville, 1955) (Lebanon)
5Tubercles Di and De on th. I fused, cryptopygy strongly developed Endonura gladiirostra Smolis & Kaprus’, 2003 (Israel)
Tubercles Di and De on th. I separate, cryptopygy absent or weakly developed 6
6Chaeta E on head present, Tubercle Dl on head with four chaetae Endonura tyrrhenica Dallai, 1983 (Italy, Sardinia)
Chaeta E on head absent, Tubercle Dl on head with six chaetae Endonura pejai Deharveng, 1980 (France, Corsica)
7Tubercle Af on head equal or shorter than tubercles Oc 8
Tubercle Af on head longer than tubercles Oc 9
8Labrum with ventral sclerifications ogival and without prelabral chaetae Endonura gracilirostrisSmolis et al., 2007 (Crimea, Moldova)
Labrum with ventral sclerifications nonogival and with prelabral chaetae Endonura taurica (Stach, 1951) (Crimea)
9Chaeta O on head present 10
Chaeta O on head absent 26
10Eyes completely absent 11
Eyes present 12
11Tubercles Di on th. I present Endonura arbasensis Deharveng, 1979 (France, Spain)
Tubercles Di on th. I absent Endonura caeca (Gisin, 1963) (Bosnia and Herzegovina)
12Anterior eye present and located outside tubercle Oc Endonura asiaticaSmolis et al., 2011 (Kyrgyzstan)
Anterior eye present or absent, if present located within tubercle Oc 13
13Anterior eye present 14
anterior eye absent Endonura immaculata Deharveng, 1980 (France, Corsica)
14Claw with inner tooth, tibiotarsi with long chaetae B4 and B5 15
Claw without tooth, tibiotarsi with short chaetae B4 and B5 16
15Tubercle Dl on head with three chaetae, tubercles Di on th. II–III with two chaetae Endonura tetrophtalma (Stach, 1929) (Hungary)
Tubercle Dl on head with five chaetae, tubercles Di on th. II–III with three chaetae Endonura lusatica (Dunger, 1966) (Germany, Poland, Ukraine)
16Chaeta E on head absent 17
Chaeta E on head present 18
17Tubercle Cl on head with chaetae D, elementary tubercle DF present Endonura colorata (Gama, 1964) (Portugal)
Tubercle Cl on head without chaetae D, elementary tubercle DF absent Endonura cantabrica (Deharveng, 1979) (Spain)
18Tubercle Dl on head with six chaetae 19
Tubercle Dl on head with less number of chaetae 25
19Tubercles Di on head present 20
Tubercles Di on head absent Endonura dalensi Deharveng, 1979 (Andorra, France, Spain, Italy)
20Body white 21
Body blue or bluish–grey 22
21.Tubercle (L+So) on head with nine chaetae, macrochaetae thin and pointed Endonura deharvengi Cassagnau & Péja, 1979 (Greece)
Tubercle (L+So) on head with eight chaetae, macrochaetae thickened and blunt Endonura levanticaSmolis et al., 2011 (Israel)
22Tubercle De on th. III with two ordinary chaetae Endonura gladiolifer (Cassagnau, 1954) (Algeria, Spain)
Tubercle De on th. III with three ordinary chaetae 23
23Tubercle Cl on head with chaetae D, furca rudimentary with microchaetae Endonura alavensis Pozo & Simon, 1982 (Spain)
Tubercle Cl on head without chaetae D, furca rudimentary without microchaetae 24
24Tubercle (L+So) on head with nine chaetae, free chaeta L on abd. IV present Endonura quadriseta Cassagnau & Péja, 1979 (Greece, Turkey, Crimea)
Tubercle (L+So) on head with ten chaetae, free chaeta L on abd. IV absent Endonura reticulata (Axelson, 1905) (Finland; Russia; Sweden; United States, Alaska)
25Tubercle Dl on head with four chaetae, tubercles Di and De on th. I separate Endonura occidentalis (Deharveng, 1979) (Spain)
Tubercle Dl on head with three chaetae, tubercles Di and De on th. I fused Endonura cretensis (Ellis, 1976) (Greece, Israel)
26Cryptopygy strong and complete, tubercles of abd. VI invisible in dorsal view Endonura ludovicae (Denis, 1948) (France, Corsica)
Cryptopygy absent or weak, tubercles of abd. VI well or partially visible in dorsal view 27
27Body bluish–grey 28
Body white 30
28Claw with inner tooth, labrum chaetotaxy 4/2, 4 29
Claw without inner tooth, labrum chaetotaxy 0/2, 2 Endonura ceratolabralis sp. n. (Iran)
29Tubercle Dl on head with five chaetae, tubercles Di on th. I present Endonura persica sp. n. (Iran)
Tubercle Dl on head with six chaetae, tubercles Di on th. I absent Endonura dentiferaSmolis et al., 2007 (Crimea)
30Chaeta C on head absent 31
Chaeta C on head present 33
31Macrochaetae Di1 on abd. V distinctly thickened and club–like Endonura baculifer Deharveng, 1979 (Portugal)
Macrochaetae Di1 on abd. V slightly thickened and cylindrical 32
32Eyes present, tubercles Di on th. I present Endonura transcaucasica (Stach, 1951) (Georgia)
Eyes absent, tubercles Di on th. I absent Endonura carpatica Smolis, 2006 (Poland)
33Tubercle Cl on head with chaetae D, elementary tubercle DF present 34
Tubercle Cl on head without chaetae D, elementary tubercle DF absent 35
34Chaeta E on head present, tubercle Dl on head with six chaetae Endonura tartaginenis Deharveng, 1980 (France, Corsica)
Chaeta E on head absent, tubercle Dl on head with five chaetae Endonura dichaeta sp. n. (Iran)
35Chaeta E on head present Endonura urotuberculata Pomorski & Skarżyński, 2000 (Bulgaria)
Chaeta E on head absent 36
36Chaeta L4 on head free, eyes absent or present unpigmented 37
Chaeta L4 within tubercle (L+So), eyes present and pigmented 39
37Abd. V with two tubercles Endonura incolorata (Stach, 1951) (Poland, Ukraine, Romania)
Abd. V with three tubercles 38
38Abd. IV with eight tubercles, macrochaetae Ml relatively short Endonura tatricola (Stach, 1951) (Poland, Slovakia)
Abd. IV with five tubercles, macrochaetae Ml long Endonura dudichi (Loksa, 1967) (Hungary, Poland, Slovakia)
39Tubercle Dl on head with six chaetae, tubercle L on abd. III with three chaetae Endonura centaurea Cassagnau & Péja, 1979 (Greece)
Tubercle Dl on head with five chaetae, tubercle L on abd. III with four chaetae Endonura saleri Fanciulli & Dallai, 2008 (Italy)
  4 in total

1.  A new species and new records of the genus Hypogastrura Bourlet, 1839 (Collembola, Hypogastruridae) from Iran.

Authors:  Morteza Kahrarian; Reza Vafaei-Shoushtar; Dariusz Skarżyński; Marta Konikiewicz; Ebrahim Soleymannezhadyan; Masoumeh Shayan Mehr; Bahman Shams
Journal:  Zootaxa       Date:  2013       Impact factor: 1.091

2.  Persanura hyrcanica, a new genus and species of Neanurinae (Collembola: Neanuridae) from Iran, with a key to genera of the tribe Neanurini.

Authors:  Mahmood Mehrafroz Mayvan; Masoumeh Shayanmehr; Adrian Smolis; Dariusz Skarżyński
Journal:  Zootaxa       Date:  2015-02-13       Impact factor: 1.091

3.  The genus Folsomides Stach (Collembola, Isotomidae) in Kermanshah Province (W Iran) with the description of two new species.

Authors:  Javier I Arbea; Morteza Kahrarian
Journal:  Zootaxa       Date:  2015-02-27       Impact factor: 1.091

4.  An introduction to Iranian Collembola (Hexapoda): an update to the species list.

Authors:  Masoumeh Shayanmehr; Elliyeh Yahyapour; Morteza Kahrarian; Elham Yoosefi Lafooraki
Journal:  Zookeys       Date:  2013-09-25       Impact factor: 1.546

  4 in total
  3 in total

1.  Paravietnura gen. n., a new intriguing genus of Neanurini from the Caucasus (Collembola, Neanuridae, Neanurinae).

Authors:  Adrian Smolis; Nataliya Kuznetsova
Journal:  Zookeys       Date:  2018-02-22       Impact factor: 1.546

2.  The genera Albanura Deharveng, 1982 and Persanura Mayvan et al., 2015 are no longer monotypic: description of new species from the Caucasus (Collembola, Neanuridae, Neanurinae, Neanurini).

Authors:  Adrian Smolis; Nataliya Kuznetsova
Journal:  Zookeys       Date:  2018-02-12       Impact factor: 1.546

3.  Three new remarkable species of the genus Endonura Cassagnau, 1979 from the Middle East and Central Asia (Collembola, Neanuridae, Neanurinae, Neanurini).

Authors:  Adrian Smolis; Masoumeh Shayanmehr; Nataliya Kuznetsova; Elham Yoosefi Lafooraki
Journal:  Zookeys       Date:  2017-05-15       Impact factor: 1.546

  3 in total

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