The thorax of the cave cricket Troglophilus neglectus: anatomical adaptations in an ancient wingless insect lineage (Orthoptera: Rhaphidophoridae)
© Leubner et al. 2016
Received: 1 September 2015
Accepted: 9 February 2016
Published: 18 February 2016
Secondary winglessness is a common phenomenon found among neopteran insects. With an estimated age of at least 140 million years, the cave crickets (Rhaphidophoridae) form the oldest exclusively wingless lineage within the long-horned grasshoppers (Ensifera). With respect to their morphology, cave crickets are generally considered to represent a `primitive’ group of Ensifera, for which no apomorphic character has been reported so far.
We present the first detailed investigation and description of the thoracic skeletal and muscular anatomy of the East Mediterranean cave cricket Troglophilus neglectus (Ensifera: Rhaphidophoridae). T. neglectus possesses sternopleural muscles that are not yet reported from other neopteran insects. Cave crickets in general exhibit some unique features with respect to their thoracic skeletal anatomy: an externally reduced prospinasternum, a narrow median sclerite situated between the meso- and metathorax, a star-shaped prospina, and a triramous metafurca. The thoracic muscle equipment of T. neglectus compared to that of the bush cricket Conocephalus maculatus (Ensifera: Tettigoniidae) and the house cricket Acheta domesticus (Ensifera: Gryllidae) reveals a number of potentially synapomorphic characters between these lineages.
Based on the observed morphology we favor a closer relationship of Rhaphidophoridae to Tettigoniidae rather than to Gryllidae. In addition, the comparison of the thoracic morphology of T. neglectus to that of other wingless Polyneoptera allows reliable conclusions about anatomical adaptations correlated with secondary winglessness. The anatomy in apterous Ensifera, viz. the reduction of discrete direct and indirect flight muscles as well as the strengthening of specific leg muscles, largely resembles the condition found in wingless stick insects (Euphasmatodea), but is strikingly different from that of other related wingless insects, e.g. heel walkers (Mantophasmatodea), ice crawlers (Grylloblattodea), and certain grasshoppers (Caelifera). The composition of direct flight muscles largely follows similar patterns in winged respectively wingless species within major polyneopteran lineages, but it is highly heterogeneous between those lineages.
The evolution of wings is considered to be a key innovation responsible for the unrivaled evolutionary success of insects, improving dispersal capability, predator avoidance, as well as the access to scattered food sources and mating partners . Beyond flight, wings can provide additional advantages, contributing to thermoregulation, defensive behavior and acoustic communication [2–4]. Yet, wing loss is a common phenomenon among pterygotes . In Ensifera (long-horned grasshoppers), one of the most species-rich lineages among the Polyneoptera, wings are often reduced to tiny remnants whose only purpose appears to be the production of sound [5, 6]. Orthoptera in general have long been of interest to scientists studying intra-specific acoustic communication and hearing systems. Crickets (Gryllidae) and bush-crickets or katydids (Tettigoniidae) in particular are well known for their elaborate acoustic signaling via tegminal stridulation that is associated with mating and territorial behavior . In the last century, numerous biologists dedicated their research to bioacoustics and countless studies have been conducted illuminating the neuroanatomical [7, 8], behavioral  and evolutionary [10, 11] background of ensiferan bioacoustics.
Some ensiferan taxa have completely reduced their wings, nevertheless. To understand the evolution of bioacoustics within the Ensifera special attention was paid to these wingless and deaf taxa, such as the Rhaphidophoridae, commonly known as camel and cave crickets. The neuroanatomy of their chordotonal organs  as well as their vibratory communication through low frequencies  is assumed to reflect the ancestral condition of bioacoustics within the Ensifera. Also in regard of their overall morphology, cave crickets are considered a ´primitive` lineage among Ensifera preserving several characters in their plesiomorphic state, e.g. the morphology of the ovipositor, the absence of tarsal pulvilli and the absence of posterofurcal connectives in the thorax . With about 550 described species, these insects form an ecologically specialized group mainly adapted to cave life . Rhaphidophoridae has a disjunct geographical distribution restricted to the temperate areas of the Northern and Southern hemispheres as reflected by their phylogeny . Rhaphidophoridae comprises two major groups: Rhaphidophorinae, distributed in Eurasia and North America, and Macropthinae that is restricted to South Africa, South America and New Zealand [15, 16]. Although the monophyly of Rhaphidophoridae is well supported in molecular analyses [17–20], cladistic analyses of morphological characters indeed could not identify any supporting apomorphy for this clade yet [21, 22]. The species Troglophilus neglectus investigated in this study appears to branch off from a basal node, forming the sister taxon to the remaining Rhaphidophoridae . In this respect, T. neglectus likely retains characters from the last common ancestor of Rhaphidophoridae and can be considered representative for this taxon in general.
Numerous hennigian (mental) and cladistic studies of Ensifera including Rhaphidophoridae have led to competing hypotheses with respect to the relative positions of the two most species-rich groups within the Ensifera, the true crickets (Gryllidae) and the bush-crickets (Tettigoniidae) (Additional file 1). Traditionally, ensiferan taxonomy is based on the morphology of wings and wing venation in particular. Interestingly, the phylogenetic hypotheses based on this specific character complex differ remarkably. Following the classification scheme of Handlirsch , Zeuner  proposed a closer relationship of crickets (‘Grylloidea’ therein) and bush-crickets (‘Tettigoniidae’ therein) and considered both taxa as having evolved from different fossil representatives of the Prophalangopsidae. He considered the tegminal stridulation and its specific wing morphology as an apomorphic character in the last common ancestor of crickets and bush-crickets. On the other hand, Karny [25, 26] and Sharov  shared the opinion that the true crickets and relatives (mole crickets, Gryllotalpidae, and antloving crickets, Myrmecophilinae) originated from the gryllacridids (including Rhaphidophoridae), whereas the bush-crickets (Tettigoniidae) were assumed to form an independent lineage within the Ensifera. However, the majority of hennigian and cladistic morphological studies [13, 21, 22, 28] as well as phylogenetic analyses based on molecular data [19, 29–33] propose a division of the Ensifera in two major groups: the “grylloid” clade, including true crickets (Gryllidae), mole crickets (Gryllotalpidae) and antloving crickets (Myrmecophilinae), and a “tettigonioid” clade, comprising the bush-crickets (Tettigoniidae), cave crickets (Rhaphidophoridae), wetas (Anostostomatidae), Jerusalem crickets (Stenopelmatidae) and raspy crickets (Gryllacrididae). Dune crickets (Schizodactylidae) are assigned to either of these two clades according to different authors [21, 22].
While studies solely based on molecular data may provide a robust phylogenetic framework for any given organismic group, comparative morphological research is essential for interpreting evolutionary scenarios  and tracing functional transformations and adaptations . In particular, the morphology of insect thoraces has repeatedly played a substantial role in understanding the systematics and evolution of certain insect groups [36–39]. In Ensifera this character complex is hitherto insufficiently studied, with publications that either give only a scarce description of the thoracic skeleton and/or merely include a part of the thoracic musculature. Very few detailed investigations of ensiferan thoraces provide characterizations of skeletal structures in addition to a complete description of the muscular equipment. These studies only consider representatives of the most species-rich ensiferan lineages: Voss [40–43] gives an exceedingly detailed description of the thorax of the house cricket Acheta domesticus (Gryllidae), whereas Maki  provides the only existing description of the thoracic musculature of a bush-cricket, Conocephalus maculatus (Tettigoniidae). Studies focusing on the thoracic morphology of Rhaphidophoridae are scarce. Carpentier  gives a brief description of the thoracic skeleton of the greenhouse stone cricket Diestrammena asynamora (Rhaphidophorinae) in addition to a study of its pleural musculature . Furthermore, Richards  presents a fragmentary description of the thoracic morphology of Macropathus filifer, a rhaphidophoridean species belonging to the southern group Macropathinae.
Here we present a detailed description of the skeletal structures and the muscular equipment of the thorax of the East Mediterranean cave cricket Troglophilus neglectus (Rhaphidophorinae). The thoracic morphology of T. neglectus is compared to the conditions found in other representatives of Orthoptera in order to detect possible apomorphic traits of Rhaphidophoridae. Furthermore, the investigated character complex is evaluated in the context of its phylogenetic information content, and potential synapomorphies of the competing phylogenetic hypotheses of ensiferan relationships are discussed. Moreover, the general nomenclature recently proposed for thoracic musculature of Neoptera  is critically reviewed in light of our results. It is evident that within the Neoptera wings were lost several times independently in evolution and this was a step-like process with numerous morphological transformations in each lineage. Therefore, our observations are compared to the thoracic morphology of other wingless polyneopteran representatives, such as Zoraptera , Mantophasmatodea  or Phasmatodea  in order to compile common adaptations of the thoracic skeletal and muscular system related to secondary winglessness. Based on our novel anatomical data we will provide a detailed description of the consequences of wing loss on the functional anatomy of insect thoraces and thoroughly address the question whether these transformations follow a similar pattern.
The specimens investigated in this study were collected in Brje pri Komnu, Slovenia, in July 2008 and identified as Troglophilus (Paratroglophilus) neglectus Krauss, 1879 . All specimens were preserved in 70% ethanol. For the sake of consistency in subsequent comparative studies, all investigated specimens are female adults. In total, four individuals were investigated using the following different methods.
Three specimens were used to investigate and illustrate the thoracic skeleton. One complete and undamaged specimen was dehydrated in a graded ethanol series and critical-point dried (Balzer CPD 030) to visualize the outer lateral and dorsal view. Another specimen was sagitally cut and macerated in 5% KOH (1 h in a heating cabinet with 60 °C) and likewise dried at critical point. Critical-point drying was applied to improve the contrast of the thoracic sclerites against the membranous areas and to visualize the sclerites in more detail. One specimen was fixed in a ventrally overstretched position to expose the neck region and subsequently dried using the HMDS (Hexamethyldisilazane, Carl Roth GmbH & Co KG, item number 3840.2) procedure . Photographs of the HMDS-dried specimen were taken using a digital camera (OLYMPUS Pen E-P2) mounted on a stereomicroscope ZEISS Stemi SV11. The critical-point dried specimens were photographed with a CANON EOS 550D equipped with a macro lens (100 mm) and a ring flash (METZ 15 MS-1). The overall sharp images are composed of image stacks edited in Helicon Focus® (Helicon Soft) and Adobe Photoshop® CS3.
Synchrotron radiation micro computer tomography (SRμCT) and 3D-reconstruction
In order to investigate the thoracic musculature, one specimen was dehydrated in a graded ethanol series, critical-point dried (Balzer CPD 030) and mounted on a specimen holder (aluminium stub). The scan was performed at the synchrotron radiation facility BESSY II (Berlin, Germany). The three-dimensional model of the thorax was created using AMIRA®5.4.3 and Autodesk Maya® 2013. Rendered images were edited using Adobe Illustrator® CS3.
The terminology of the thoracic skeleton largely follows Snodgrass  and Friedrich & Beutel . Terms used by authors of ensiferan-specific literature e.g. [13, 40] are mentioned in the case of inconsistency. The thoracic musculature of Troglophilus (Paratroglophilus) neglectus is described and muscles are numbered consecutively. We homologize the observed muscles in Troglophilus, in addition to that of two other ensiferans, Conocephalus maculatus  (Xiphidion maculatum therein) and Acheta domesticus  (Gryllus domesticus therein) with the muscles described following the nomenclature of Friedrich & Beutel  for neopteran insects, allowing for comparison to studies of other authors. The distinctive set of thoracic muscles found in Troglophilus is compared with the condition in other polyneopteran taxa, i.e. two grasshoppers (Caelifera), Locusta migratoria migratorioides  (Locusta migratoria manilensis therein) and Atractomorpha sinensis  (Atractomorpha ambigua therein), two stick insects (Phasmatodea), Carausius morosus  (Dixippus morosus therein) and Megacrania tsudai , and one heelwalker (Mantophasmatodea), Austrophasma caledonensis . The current taxonomy of the examined species follows Eades et al.  and Brock .
The meso- and metathorax are almost identical in size. Like the pronotum nt1, also the pterothoracic nota nt2/nt3 show no external or internal sculpturing and are ventrally elongated covering the most part of the pterothoracic pleura (Fig. 1a, d). The mesopleura has a triangular form tapering at the dorsal side. The mesepisternum est2 is much broader than the epimeron em2 (Fig. 2). The mesepisternum is folded inwards at the anterior edge projecting into a median direction in an obtuse angle. This inwardly folded part of the episternum is referred to as anterior margin amest2 (Fig. 2a, e) and serves as an attachment area for several muscles (m38, m39). The anterior edge of the mesepisternum, connecting the episternum with its anterior margin, is forming a strongly sclerotized ridge (marked by white asterisks in Fig. 2a). The anterior margin of the mesepisternum extends medially onto the level of the trochantinocoxal joint. A massive and long pleural arm pla2 protrudes from the straight mesopleural ridge plr2 (Fig. 2d, e). A sclerotized bridge between the pleura and the sternum is absent in the mesothorax. The mesosternum st2 has a trapezoid shape, the longer edge orientated towards the head. The margins of the mesosternum are relatively indistinct because it is not delimited by strongly marked ridges as is the prosternum. The furcal pit fup2 and the spinal pit spp2 are located along a longitudinal groove at the posterior margin of the mesosternum st2 (Fig. 1e). The mesothoracic furca fu2 has a long lateral process lfup and a short posterolateral process plfup (Fig. 2d). The form of the mesothoracic spina sp2 is reminiscent of a butterfly with expanded wings consisting of paired dorsolateral and ventrolateral processes and an unpaired posterodorsal one (Figs. 2d, e; 4b). The mesospina is situated slightly posterior from and between the laterally exposed furcae. A distinct and isolated spinasternum is absent. Directly posterior to the mesospinal pit spp2, the sterna of the meso- and metathorax are flexibly connected by a lathy median sclerite ms (Mediansklerit in ), Fig. 1e). The slender and feather-shaped mesothoracic trochantin ti2 articulates anteroventrally with the coxa cx2.
In general, the morphology of the tergum and pleuron of the pterothoracic segments is similar. Compared to the mesopleuron, the anterior margin of the metepisternum amest3 has a broader basis (Fig. 2c, e). Main differences in the morphology of the pterothoracic segments are related to the sterna. The sternum of the metathorax st3 is trapezoid in shape. It is narrower but longer than the mesosternum (Fig. 1e). The posteromedian located furcal pit fup3 is more or less U-shaped. Internally, the metafurcae fu3 of each body side are joined in a short common stem fs (Fig. 2a, d). The laterally projecting metafurcal arms bear a lateral process lfup, a posterolateral process plfup, and an anterior process afup (Fig. 2c, e). A spina is absent in the metathorax.
Thoracic musculature of T. neglectus and its homologization with that of other Neoptera
List of thoracic muscles of the cave cricket Troglophilus neglectus, specifying origin and insertion of each muscle including noteworthy characteristics and corresponding figure in the article. Furthermore, homologization (Hom*) according to the nomenclature after  is provided
dorsal longitudinal muscles
median region of prophragma
dorsal area of occipital rim (close to m2)
prophragma (between m1 and m3)
anterior dorsomedial pronotal region
lateral region of prophragma
anterior process of lateral cervical sclerite
dorsolateral area of occipital rim (ventrad of m5)
posterior on inner face of lateral cervical sclerite
dorsolateral area of occipital rim
anterior part of pronotum (near m8)
posterior part of lateral cervical sclerites near cervicopleural articulation point
fan-shaped, long thin tendon
laterodorsal face of profural arm
ventrolateral area of prophragma
dorsolateral area of pronotum (above cryptopleura)
long thin tendon
lateral region of pronotum (posterior to cryptopleura)
posterolateral procoxal rim (close to m26)
posterolateral region of pronotum
posterolateral procoxal rim (close to pleurocoxal joint)
lateral area of pronotum (posterior to cryptopleura, beneath m9)
trochanter (with m16)
distal on ventral surface of profurcal arm
ventral part of anterior margin of mesepisternum
anterior procoxal rim
posterior face of anterior process of lateral cervical sclerite of opposite site (near cervicooccipital articulation point)
anterior margin of cryptopleura
anterior procoxal rim (close to m15)
anterodorsal area of cryptopleura
anterior procoxal rim (close to pleurocoxal joint)
anterolateral and anterodorsal area of cryptopleura
trochanter (with m11)
largest muscle in prothorax, strongly developed, 2 bundles
ventral longitudinal muscles
dorsal surface of profurcal arm
ventral area of occipital rim
posterior margin of profurcal arm
anterolateral process of prospina
posterior margin of profurcal arm (beneath m18)
anterior face of dorsolateral process of mesospina
proximal at posterior margin of profurcal arm
anterior margin of mesofurcal arm
posterior margin of posterolateral process of prospina
dorsal face of mesospina
posterolateral process of prospina
anterior margin of mesofurcal arm (proximad of m20 & m37)
lateral face of profurcal stem
anteromediad procoxal rim (mediad of m24)
3E, 4A, 4B
anterolateral face of profurcal stem
anterior procoxal rim (close to trochantinocoxal articulation point)
3D, 4A, 4B
medial face of profurcal stem and adjacent prosternum
anterior procoxal rim (laterad of m24)
3C, 4A, 4B
ventral face of profurcal arm
posterolateral procoxal rim
distal on ventral face of profurcal arm
posterior procoxal rim on inner median process
tip of anterolateral prospinal process
posterior procoxal rim on inner lateral process
3F, 4A, 4B
lateral processi of prospina
anterior mesocoxal rim
3F, 4A, 4B
dorsal longitudinal muscles
median region of prophragma
median region of mesophragma
several indistinct bundles as thin muscle layer
central region of mesonotum
posterior mesocoxal rim
two independent muscles sharing one insertion point
dorsal edge of mesepimeron (ventrad of m31)
posterior mesocoxal rim (close to pleurocoxal joint)
anterior region of mesonotum
trochanter (with m41 & m49)
largest muscle in mesothorax
epimeral face of mesopleural ridge
lateral region of mesonotum (ventrad of m32)
dorsal surface of mesofurca
ventral surface of mesopleural arm
posterior mesofurcal process
anterodorsal margin of metepisternum
anterior margin of mesofurcal arm (close to m20)
epimeral face of propleural ridge on cryptopleura
long thin tendon
anterior margin of mesepisternum (close to m39)
inner anterodorsal part of anterior margin of mesepisternum
anterior mesocoxal rim
episternal face of mesopleural ridge, few fibers from mesopleural arm
anterolateral mesocoxal rim
episternal face of mesopleural ridge and mesopleural arm
trochanter (with m33 & m49)
ventral longitudinal muscles
posterolateral process of mesofurcal arm
tip of anterior metafurcal process
lateral face of posterior mesospinal process
medial face of anterior metafurcal process
lateral at mesofurcal stem
anterior mesocoxal rim (close to trochantinocoxal articulation point)
anterior to mesofurcal stem at mesosternum
anterior mesocoxal rim (close to m44)
3E, 4A, 4B
ventral face of mesofurcal arm
mesal mesocoxal rim
ventral face of mesofurcal arm (posterior to m46 & m49)
lateral mesocoxal rim (close to pleurocoxal joint)
3F, 4A, 4B
ventrolateral and dorsolateral process of mesospina
posterior mesocoxal rim
3F, 4A, 4B
ventral face of mesofurcal arm (anterior to m46 & m47)
trochanter (with m33 & m41)
posterior face of lateral processi of mesospina
anterior metacoxal rim
3F, 4A, 4B
dorsal longitudinal muscles
median region of mesophragma
median region of metaphragma
several indistinct bundles as thin musle layer
mesophragme and anterior part of metanotum
runs partly behind m56
anterolateral region of metanotum
posterior metacoxal rim
anterolateral region of metanotum (dorsad of m53)
posterolateral metacoxal rim (close to m65)
osterolateral metacoxal rim (close to pleurocoxal joint)
dorsal epimeral face of metapleura (close to m57)
anterolateral region of metanotum (anterior to m54)
trochanter (with m63 & m68)
largest muscle in metathorax
epimeral face of metapleura (dorsad of m55)
lateral region of metanotum
dorsal surface of lateral metafurcal process
ventral surface of metapleural arm
posterior face of metafurcal stem
intersegmental membrane between metathorax and abdominal pleura
anterior margin of metepisternum
inner anterodorsal part of anterior margin of metepisternum (lateral to m60)
anterior metacoxal rim
dorsal metepisternum and dorsal episternal face of metapleural ridge, few fibers from metapleural arm
anterior metacoxal rim
dorsal part of metepisternum (dorsad of m62)
trochanter (with m56 & m68)
along lateral margin of metasternum
anterior metacoxal rim (close to trochantinocoxal joint)
3D, 4A, 4B
posteroventral face of metafurcal stem
along inner posterior metacoxal rim
strongly developed, broad insertion
3C, 4A, 4B
ventral face of anterior and lateral metafurcal process
inner mesal metacoxal rim
tip of posterolateral metafurcal process
lateral mesocoxal rim (close to pleurocoxal joint)
very thin and short
3C, 4A, 4B
distal at lateral metafurcal process
trochanter (with m56 & m63)
The nomenclature of neopteran thoracic muscles presented by Friedrich & Beutel  provides a solid basis for homologizing thoracic muscles across insect groups. In some cases, however, the homologization of the thoracic muscles of Troglophilus with the muscles of the “generalized neopteran thorax“ proves to be difficult, because muscles are solely defined by their origin and insertion points. While we were able to largely homologize the thoracic muscles unambiguously, we will discuss some problematic cases in the following:
The M. pronoto-trochantinalis anterior (Idvm13) and M. pronoto-trochantinalis posterior (Idvm14) both share the same insertion point on the trochantin and have only a slightly different origins on the pronotum: Idvm13 originates from the anterior region of the pronotum, whereas Idvm14 arises from the central region of the pronotum . In Troglophilus, the muscle m8 originates at the dorsolateral area of the pronotum slightly above the cryptopleura, inserting at the trochantin via a long and thin tendon. As m8 is the only muscle originating from the dorsal area of the pronotum it is questionable whether m8 is homologous to Idvm13 or Idvm14. Therefore, further criteria for homologization are necessary. A similar muscle with a long thin tendon is also present in other ensiferans . According to Ander , the point of origin of this pronotal muscle has shifted from an anterior laterodorsal area above the cryptopleura to the lateral or central area of the pronotum behind the cryptopleura. Thus, the muscle m8 of Troglophilus is most likely homologous to Idvm13 according to the nomenclature of Friedrich & Beutel .
The M. profurca-phragmalis (Idvm10) is a common feature among major polyneopteran taxa [36, 48]. This muscle usually connects the profurca with the prophragma. However, in some orthopteran species, like in the grasshopper Dissosteira carolina (muscle 59)  or the stick grasshopper Cephalocoema albrechti (muscle 59) , Idvm10 has an insertion point shifted to the anterior part of the mesopleura. In Troglophilus, both conditions are present at the same time (m7 and m12). The muscle m7 is undoubtedly homologous to Idvm10 as it arises on the dorsal face of the profurca and inserts at the ventrolateral part of the prophragma. The second muscle (m12) takes a more horizontal course and arises from the ventral surface of the profurca inserting ventrally at the anterior margin of the mesepisternum. Because of their diverging courses and their differing origins on the profurca, the muscles m7 and m12 are most likely two separate muscles and not portions of a single muscle. Therefore, we conclude that muscle m12 of Troglophilus is homologous to M. profurca-intersegmentalis posterior (Ispm5) . This assumption is also supported by the presence of serially homologues of m12 in the meso- and metathorax of Troglophilus (m36 and m59). Furthermore, a simultaneous presence of Idvm10 and Ispm5 is only known from Phasmatodea (Megacrania tsudai, Carausius morosus) and Embioptera (Oligotoma saundersii) . In contrast to the morphology of Troglophilus, the muscle Ispm5 is attached to the peritreme in Megacrania  and Oligotoma , but to the intersegmental fold in Carausius . These different attachment points cause uncertainties in regard to the homology of the muscle m12. Therefore, a question mark is added here (see Table 1).
In the generalized neopteran thorax, three pterothoracic dorsoventral muscles are attached to the posterior coxal rim : M. noto-coxalis anterior (II/III dvm4), M. noto-coxalis posterior (II/IIIdvm5) and M. coxa-subalaris (II/IIIdvm6). In winged Neoptera, the muscles II/IIIdvm4 and II/IIIdvm5 originate at the central region of the nota, while II/IIIdvm6 inserts at the subalare. According to literature data [48, 49], the insertion point of II/IIIdvm6 is translocated to the lateral region of the nota in wingless Neoptera. This interpretation is consistent with the assumed tergal origin of the subalare, as proposed before [44, 58, 59]. In winged orthopterans, all three dorsoventral muscles are also well developed with the muscle II/IIIdvm6 inserting at the subalare. In contrast, the same muscle inserts at the epimeral face of the pleura in wingless Orthoptera: in the cave crickets Troglophilus neglectus (m32 and m55; present study) and Diestrammena asynamora (cx-em2) , in the New Zealand tree weta Hemideina femorata (Ab4) , in the apterous proscopiids Cephalocoema albrechti (90a and 120) , in morabine grasshoppers (99 and 129) , in wingless females of Pamphagidae, Lamarckiana sp. (depressor extensor muscle) , and also in micropterous species of Acrididae, e.g. Barytettix psolus (99 and 129) . These findings are more consistent with the assumption of a pleural origin of the subalar sclerite, as suggested by other authors [40, 51, 64–66]. It is noteworthy that the hypothesis of a pleural origin of the basalar and subalar plates is exclusively based on developmental studies on orthopterans. With reference to Snodgrass , the aforementioned plates of nymphal Ensifera (Gryllus) and Caelifera (Melanoplus) are not yet differentiated from the pleura, and the M. coxa-subalaris (3E’ and 3E”) arises from the upper edge of the pterothoracic epimeron. Voss [41–43] who compared the thoracic musculature of different developmental stages of the house cricket Acheta domesticus also observed the epimeral insertion of the M. coxa-subalaris in the first instar (II and IIIpm6 in ; II and IIIldmv2 in [42, 43]), in which the basalar and subalar plates (Pleuralgelenkplatten) are not yet present.
Muscle m37 of T. neglectus is not described in Orthoptera or other insect taxa . Due to its sternal origin at the anterior face of the mesofurca and its pleural insertion at the posterior edge of the cryptopleura, this muscle should be assigned to the sternopleural muscles . Compared with the generalized neopteran thorax, muscle m37 is likely homologous to M. mesofurca-intersegmentalis anterior (IIspm7) with an insertion point shifted from the intersegmental membrane/ intersegmental sclerite to the posterior edge of the propleura. A muscle connecting the intersegmental sclerite between the pro- and the mesothorax with the mesothoracic furca is present in Corydalus (Megaloptera) . In Mantodea, a muscle that arises on the prosternum near the prothoracic spina inserting at the metafurca, is apparently homologous to muscle IIspm7 [36, 59]. The specific traits of m37 in Troglophilus cannot be compared with the conditions reported from the aforementioned insect taxa. For this reason, we cannot homologize this muscle with any muscle listed by Friedrich & Beutel (see Table 1).
Phylogenetically informative characters
Characters unique for cave crickets
It is particularly noteworthy that in Troglophilus the well developed musculature is important for operating the legs. These muscles are attached to the coxal rim or the trochanter and enable diverse movements of the legs. These muscles are either strongly developed, like Mm. noto-trochanteralis (m11, m33, m56), or their number is increased, like in the pro- and mesothoracic sternocoxal muscles scm1 (m23-25, m44-45). This strengthening of the sternocoxal muscles through multiplication is also reported from the wingless New Zealand tree weta Hemideina thoracica . M. coxo-subalaris (II/IIIdvm6), which has an additional function as a flight muscle in winged insects , exclusively acts as leg retractor in Troglophilus. Additionally, Troglophilus has several sternopleural muscles that have not been described for other orthopterans. These include the serially homologous muscles m12 (Ispm5?), m36 (IIspm6) and m59 (IIIspm5) as well as the not homologized m37 (IIspm?). The connection of sternal and pleural elements by these muscles might lead to an enhanced movability of the thoracic segments (against each other), since there are no rigid connections of e.g. the pterothoracic sterna as in grasshoppers [13, 71]. Together with the strong leg musculature, the sternopleural musculature probably facilitates the scrambling movement of Troglophilus on cave walls and an increased jumping capability.
As suggested by authors of similar morphological studies [13, 72], the morphology of the thoracic sternum and associated sclerites in particular differs in decisive points between major ensiferan lineages. Including data on the thoracic skeletal anatomy of Diestrammena asynamora (Rhaphidophorinae) [45, 46] and Macropathus filifer (Macropathinae)  this specific character complex indeed provides some apomorphic traits for the Rhaphidophoridae. Prothoracic spinasternum and prospina. The characteristics of the prothoracic spinasternum and its internal protrusion, the prospina, have a unique appearance in rhaphidophorids. The prospinasternum of cave crickets is completely reduced externally (see Fig. 1e and ). Its presence is only noticeable by the existence of the prospina located in the membranous fold between the pro- and the mesosternum. In other ensiferan taxa, the prospinasternum is either exposed in the sternal intersegmental fold as a fully developed sclerite or merged with the posterior part of the prosternum or the anterior part of the mesosternum [13, 71, 72]. Also the star-shaped prospina, consisting of paired anterolateral and posterolateral processes and an unpaired anterior process, is a unique feature of rhaphidophorids. It has also been described in Diestrammena asynamora  and Macropathus filifer , two other representatives of cave crickets. In tettigoniids the prospina is triangular or t-shaped , when present. Voss  describes the prospina of Acheta domesticus as an irregular four-sided plate. The prospina of the mole cricket Gryllotalpa vulgaris is a long blade-like structure .
Median sclerite between meso- and metasternum. A narrow median sclerite, situated in a longitudinal arrangement between the sterna of the meso- and metathorax, is a typical feature of all rhaphidophorids . This sclerite is frequently present in other ensiferan taxa, but the specific condition is different. In tettigoniids it can be rectangular or trapezoid, mostly spanning the whole width of the metasternum . A triangular or semicircular sclerite is embedded at the anterior part of the metasternum in Anostostomatidae [13, 60], whereas in schizodactylids it is narrow and rectangular, inflexibly connecting meso- and metasternum (, unpublished observations for Comicus FL). Since the anatomical situation in rhaphidophorids is similar to that found in Grylloblatta, Ander  assumes that this sclerite is at least the posterior part of the mesothoracic spinasternum, since the mesospina is situated at the posterior end of the mesosternum right between the furcal apophyses. In contrast, Matsuda  and Naskrecki  refer to this sclerite as metathoracic presternum. As another alternative, Matsuda  characterizes the sclerite in question as the secondarily detached anterior part of the metathoracic basisternum. Due to these uncertainties, we simply refer to the sclerite as median sclerite ms following Ander .
Metafurca. The shape and specific structure of the metathoracic furca is another peculiarity of the thoracic skeleton of cave crickets. Rhaphidophorids possess a triramous furca with continuously tapered processes: an anterior, a lateral and a posterolateral one (see Fig. 2 and [45, 47]). Most other ensiferans have a biramous metafurca bearing a lateral and a posterior process [40, 72]. Like rhaphidophorids, the metafurca of Anostostomatidae has three processes, but the lateral one differs in shape from that of Rhaphidophoridae. In Anostostomatidae it is a flat, blade-like structure, termed apophysis wing, which directly projects beneath the pleural arm .
On the other hand, the alternative hypotheses also gain support by few characters of the thoracic musculature (Fig. 7). Gryllidae and Rhaphidophoridae share the presence of Ivlm6. However, this ventral longitudinal muscle frequently occurs within the Polyneoptera: in Austrophasma caledonensis (m26) , Periplaneta americana (101) , Grylloblatta campodeiformis (81) , Oligotoma saundersii (35) , and Zorotypus hubbardi (Ivlm6) . Considering the thoracic muscular system, the presence of muscle Iscm6 and IIspm3 are the unique common characters of Gryllidae and Tettigoniidae. Nevertheless, Iscm6 is also present in the outgroup representatives Atractomorpha sinensis (29)  and Austrophasma caledonensis (m34) . Muscle Iscm6 connects the profurca with the trochanter of the foreleg. In Troglophilus, the profurca is relatively short and does not extend beyond the opening of the coxa. This specific morphology would not allow lscm6 to reach the trochanter, which, from a functional point of view, could explain its secondary absence in Troglophilus. Although lacking in the representatives of the Caelifera, muscle IIspm3 appears to represent a common character of other polyneopteran taxa since it is present e.g. in Blattodea, Periplaneta americana (149) , Phasmatodea, Carausius morosus (IIildvm)  and Megacrania tsudai (148) , Mantophasmatodea, Austrophasma caledonensis (m51) , and Zoraptera, Zorotypus hubbardi (IIspm3) .
The thorax of Troglophilus neglectus and the evolution of secondary winglessness in general
The consequence of wing reduction and flight loss largely affects thorax morphology in insects, both cuticular structures and the muscular system, which includes secondarily undifferentiated terga, less extensive phragmata and reduced or poorly developed dorsal longitudinal muscles (II/IIIdlm1, II/IIIdlm2), as well as the absence of wing base sclerites and associated wing-steering muscles [36, 60]. These distinctive traits are also found in the thorax of Troglophilus. In contrast to other wingless taxa like Grylloblatta  and the wingless morph of Zorotypus , the pleural arms in the pterothorax of Troglophilus are still well pronounced. Additionally, well developed pleural arms seem to be a common feature of Orthoptera, regardless the wing status, either fully winged [40, 56], micropterous  or wingless [46, 57]. In Mantophasmatodea, the well-developed pleural arms are explained by the climbing lifestyle among shrubs .
M. pleura-sternalis (II/IIIspm1), which is attached dorsally on the basalare and ventrally on the lateral part of the sternum, is thought to act as an extensor and flexor of the wing, and therefore is considered to be a direct flight muscle . With the exception of Grylloblattodea and Mantophasmatodea, the general trend among wingless insects is the reduction of this muscle . This trend is also observed within Orthoptera. In Caelifera, M. pleura-sternalis is present in the meso- and metathorax of winged locusts [44, 56], whereas it is absent in the micropterous Mexican grasshopper Barytettix psolus , and also reduced in wingless Proscopiidae  and morabine grasshoppers . The assumption that M. pleura-sternalis is at least present in the mesothorax of Ensifera is based on the description of a single cricket species [41–43]. After investigation of several additional ensiferan species, we can now reliably conclude that muscle IIspm1 is only present in Grylloidea, e.g. Acheta domesticus (IIpm14)  and Gryllus campestris (ls-es1) , and in the mole cricket Gryllotalpa gryllotalpa (LS-EP2) . The muscle is lacking in the meso- and the metathorax of the cave cricket Troglophilus, the schizodactylid Comicus calcaris (unpublished observations FL) and the winged bush-cricket Conocephalus maculatus . This reduction of muscle spm1 in the pterothorax, especially in Tettigoniidae, might be a phylogenetically informative character, which needs to be tested in a future cladistic analysis based on an enlarged taxon sampling.
In the pterothorax of Troglophilus, dorsal longitudinal (II/IIIdlm2), dorsoventral (II/IIIdvm1) and tergopleural muscles (tpm) are absent, muscles that are indirectly or directly involved in flying [36, 48]. Most notably, the number of wing-steering tergopleural muscles is reduced, as has also been reported from other wingless taxa, e.g. Phasmatodea [49, 52] or Orthoptera [57, 60]. The only tergopleural muscle retained in both pterothoracic segments of Troglophilus is M. epimero-subalaris (II/IIItpm10). In winged species, this muscle connects the dorsal part of the epimeron with the subalar sclerite . As in Troglophilus, the insertion point of tpm10 is translocated to the notum in wingless species of Phasmatodea  or Mantophasmatodea .
Regarding the two major lineages of Orthoptera, Caelifera (grasshoppers) and Ensifera (katydids and crickets), muscle tpm10 is only known to exist in the meso- and metathorax of ensiferan taxa [41, 44, 76]. Only Maki  described a muscle tpm10 in the mesothorax of the African Migratory Locust Locusta migratoria migratorioides (see Additional file 2), but neither Albrecht  observed this muscle in the European Migratory Locust Locusta migratoria migratoria, nor did Snodgrass  in his study about the thoracic morphology of the Carolina Grasshopper Dissosteira carolina. In general, the number of tergopleural muscles that have been described for Locusta (II/IIItpm1, II/IIItpm2, II/IIItpm5, II/IIItpm9 and IItpm10) is exceptionally large . Somewhat surprisingly, only M. epimero-axillaris tertius (II/IIItpm9) is known in Locusta migratoria migratoria (85 and 114) , Dissosteira carolina (85 and 114) , the wingless morabine grasshoppers (tergopleural muscle) , and even in the brachypterous Atractomorpha sinensis (37/38 and 62/63) . In wingless Caelifera, like Lentula callani  and Cephalocoema albrechti , even this muscle is reduced and not a single tergopleural muscle has ever been reported. In summary, the distinctive set of tergopleural muscles differs significantly between Caelifera and Ensifera and the role of these muscles after wing loss is markedly dissimilar.
In Euphasmatodea (the majority of extant stick insects) on the other hand, thoracic morphology of wingless species largely resembles conditions found in Ensifera. Klug  observed a significantly reduced set of tergopleural muscles in wingless stick insects, only consisting of muscles II/IIItpm10 and II/IIItpm13 (tpm13 is a unique muscle of Phasmatodea). These partly comparable patterns imply that the mechanism and morphology of secondary winglessness may follow similar routes in closely related taxa. In contrast, in Embioptera (webspinners), the assumed sister taxon of Phasmatodea , the set of tergopleural muscles (II/IIItpm1, II/IIItpm5, II/IIItpm6, II/IIItpm7, II/IIItpm10; homologized in ) does not differ between winged males and wingless females of the same species [78, 79].
Another pattern providing support for the assumption of similar evolutionary trajectories in closely related taxa can be observed in the entirely wingless Xenonomia  comprising heelwalkers (Mantophasmatodea) and ice crawlers (Grylloblattodea). Here, the set of tergopleural muscles is different from that of wingless representatives of Orthoptera, Phasmatodea or Embioptera. Grylloblatta campodeiformis (Grylloblattodea) is characterized by a set of IItpm1/5 and IIItpm1/5  (homologized in ). Based on the description of Klug , Austrophasma caledonensis (Mantophasmatodea) exhibits the same set of tergopleural muscles in the pterothorax, IItpm1/5 and IIItpm1/5. According to the reinvestigation of the same species  a considerably higher number of tergopleural muscles is reported: IItpm1/2/3/4/5/?10 and IIItpm1/2/3/4/5/?10. These studies used different µCT data sets for analysis. Depending on the quality of the data sets, it is possible that some muscles were initially overlooked, e.g. tpm10 characterized as a flat muscle closely fitting the skeletal elements. Nevertheless, muscle tpm1 in Klug  and the four muscles tpm1/2/3/4 described for Austrophasma by Wipfler et al.  are located in the same small area between the anterior part of the tergum and the dorsal part of the pleural ridge. A further explanation of these striking differences might lie in the different life stages or sexes investigated in both studies. Klug  examined a nymphal stage of unknown sex of Austrophasma caledonensis, whereas in the study of Wipfler et al.  no explicit information about the developmental stage or the sex of the investigated specimens is provided. However, studies about the postembryonic development of the flight musculature of hemimetabolous insects show that these muscles are less developed in early nymphal stages, significantly increasing in size during their ontogenesis [81–84]. Other studies comparing the thoracic musculature report a differing number of muscles in nymphs and adults of the same species [41, 42, 85]. In consequence, the presence of tpm1 and tpm5 in the meso- and metathorax of Grylloblattodea and Mantophasmatodea might still be considered a synapomorphic character of both taxa.
Principally, the flight ability and performance of insects also depend on the total mass of flight muscles present, and not only on the concrete set of direct and indirect flight muscles . Nonetheless, the concrete set of tergopleural muscles differs between major insect groups . Regarding the Orthoptera, their flight ability and performance become of secondary importance, since many species primarily move by jumping. In these cases, wings are mainly used to control the direction and trajectory during the jumping process [5, 86]. For instance, the house cricket Acheta domesticus , with a set of IItpm1/2/5/9/10 and IIItpm1/2/5/9/10, and the tettigoniid Conocephalus (Anisoptera) maculatus , with a reduced set of IItpm2/5/9 and IIItpm2/9/10, exhibit similar flight capability [44, 86]. On the other hand, the absence of specific tergopleural muscles as in the brachypterous gaudy grasshopper Atractomorpha sinensis  having only a single duplicated tergopleural muscle in the meso- and metathorax (II/IIItpm9) causes a low vagility . In contrast, Sipyloidea sipylus, a winged stick insect, only has the ability to control its speed and trajectory during free fall with a set of six different metathoracic tergopleural muscles in the flight apparatus (tpm1/3/4/6/9/10) [49, 88]. In conclusion, there appears to be no correlation between an increased number of pterothoracic tergopleural muscles and an enhanced flight capability. However, an extremely reduced set of tergopleural muscles does consequently lead to the inability to fly.
Anatomical structures that are no longer used will be reduced in the course of evolution, and the degree of reduction can be an indicator of the time elapsed . Nevertheless, conservative anatomical elements can be retained although associated traits of the periphery are lost . As we have outlined, the loss of wings in insect groups like Orthoptera, Xenonomia  or Phasmatodea  has been followed by a number of anatomical adaptations of skeletal and muscular elements in the thorax. The insect lineages compared above exhibit significantly different evolutionary histories in regard of the time span since wing loss, affecting the degree of reduction or anatomical adaptations towards flightlessness. The radiation of Rhaphidophoridae began at least 140 million years ago [16, 19]. Thus, the Rhaphidophoridae may represent the oldest exclusively wingless lineage within Ensifera , and wing loss occurred most probably in the last common ancestor (autapomorphy) of all Rhaphidophoridae. The likewise wingless Xenonomia, heelwalkers (Mantophasmatodea) and ice crawlers (Grylloblattodea), are roughly the same age as the Rhaphidophoridae . We have demonstrated that the thoracic musculature differs significantly in both lineages. In comparison, the wingless representatives of Euphasmatodea are significantly younger. The diversification of their major extant lineages took place during a period of about 20 million years, and presumably started after the Cretaceous-Tertiary boundary ~66 million years ago [91, 92]. The thoracic musculature of wingless Ensifera, Rhaphidophoridae in particular, is most similar to the conditions found in the much younger wingless representatives of Euphasmatodea than in the equally old Xenonomia, refuting any dependency between level of reduction and evolutionary time. This might be explained by the degree of correlation of the structures in question to other, still adaptive features .
Secondary winglessness, a widespread phenomenon among pterygote insects, largely affects the thoracic anatomy including skeletal structures and the muscular system. By comparing the thoracic morphology of various wingless representatives of Polyneoptera, we demonstrate that anatomical adaptations towards flightlessness, especially regarding the flight musculature, are highly homogenous within major lineages, viz. Ensifera, Caelifera, Xenonomia, or Euphasmatodea. However, in most cases these specific adaptations are strikingly different between the aforementioned taxa indicating a markedly dissimilar role of these muscles after wing loss.
The thoracic morphology of Ensifera is a highly structured character complex whose investigation is a worthwhile endeavor, leading to a deeper understanding of functional adaptations during the evolution of Ensifera in general. We have shown that the thoracic morphology can be a valuable source for characterizing individual ensiferan taxa, providing a number of potential apomorphies for cave crickets (Rhaphidophoridae). Based on our comparison with other ensiferans, we can provide arguments for a closer relationship of Rhaphidophoridae to Tettigoniidae, rather than to Gryllidae. These findings are consistent with previous assumptions [19, 21, 22].
We thank Dr. Christian Fischer, University of Göttingen, for providing useful critiques and helpful comments on the manuscript. FL thanks Dr. Benjamin Wipfler, University of Jena, for his introduction and useful hints in dealing with the 3D-software Autodesk Maya® 2013. The project was funded through the DFG grant HO2306/10-1 and publication was supported by the Open Access Publication Funds of the University of Göttingen.
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