The functional morphology of hooding in cobras

One of the most dramatic visual displays in snakes is hooding, wherein a length of the neck is flared laterally and compressed dorsoventrally, sometimes displaying distinctive surface patterns. In cobras, the prevalence of this behavior is widely discussed and illustrated in both technical and popular works. Given this, it is somewhat surprising that the functional basis of this behavior has never been detailed. The only study specifically addressing hooding was that of Russell and Home (Russell and Home, 1804), which concluded that, ‘The mechanism by which the Cobra de Capello…expands the skin of the neck…consists intirely of muscles.’ This early work was cited by some of the more influential treatise on snakes (e.g. Wall, 1921; FitzSimons, 1962) but most references to hooding simply assert that it is due to a displacement of the ribs.

Reviews of the vertebrae and ribs (Hoffstetter and Gasc, 1969) and axial muscle (Gasc, 1981) have not explored the functional basis of hooding. The axial musculature of snakes has been detailed by several workers (e.g. Auffenberg, 1962; Gasc, 1981) including Mosauer who described the axial musculature of many species including two cobras (Mosauer, 1935). None of these studies explored regional differences between the trunk and neck regions. The musculature of the neck region of Vipera aspis was detailed by Kramer (Kramer, 1977), and Ruben (Ruben, 1977) described general functional correlates with cervical morphology. Pregill offered a detailed description of the neck musculature of Coluber constrictor and explored the myological specializations associated with the first few ribs, and the general differences between the neck and the remainder of the body (Pregill, 1977).

Given these earlier descriptions, and general accuracy we found in these earlier anatomical descriptions, this contribution will not detail the morphology of the neck and or hood region. Rather our purpose is to offer experimental evidence to establish the functional basis of hooding in cobras.

The six adult [snout–vent length (SVL) 1–1.5 m] cobras used for this study were obtained commercially (Glades Herp, Bushnell, FL, USA) and included three Egyptian (Naja haje Linnaeus 1758) and three Monocled (Naja kaouthia Lesson 1831) cobras. These snakes were maintained in individual terraria at temperatures of 27–31°C, with a 12 h:12 h light cycle, water ad libitum and a diet of pre-killed rodents. All maintenance and experimental use of these animals followed humane guidelines for reptiles and particularly for venomous snakes (Gans and Taub, 1964) (http://www.research.fsu.edu/acuc/policies_Guidelines/ASIH_HACC_GuidelinesAmphibians.pdf), and was approved by the Washburn University IACUC.

Individual cobras were placed on a table and the hooding kinematics were recorded using a TRV608 video camera (Sony, Tokyo, Japan) and a TroubleShooter 500S high-speed digital video camera (Fastec Imaging, San Diego, CA, USA) filming at 250 frames s⁻¹. One individual of each species was placed in a Plexiglas tube of adequate diameter to permit unencumbered hooding. The tubed snake was radiographed in the relaxed and hooded posture (and from both the dorsoventral and lateral perspective) using a General Electric MSI 850 unit (using Kodax T-mat L film exposed at 45 kVK and 400 MA for 0.01 s; Fairfield, CT, USA). Following the functional analyses (see below) costovertebral joints from the hood and mid-trunk region were removed from euthanized specimens of each species and skeletonized using bacterial maceration. The cleaned bones were dried, sputter coated with 15 Å of gold and the opposing articular surfaces were examined using a Hitachi S-570 scanning electron microscope (Lawrenceville, GA, USA). Upon completion of the functional analyses one individual of N. haje was euthanized, the viscera removed and the specimen posed in a hooding posture. The individual was pinned in this position and then fixed using 10% neutral buffered formalin (NBF). After fixation, the cobra was preserved in 70% ethanol and shipped to DigiMorph at the University of Texas at Austin where it was coated in lithium carbonate and scanned using high-resolution X-ray Computed Tomography (976 slices, each 0.1807 mm thick, with an interslice spacing of 0.1807 and a field resolution of 83 mm). This provided direct visual illustration of the underlying rib placement supporting the extended hood.

Following completion of the functional analyses (see below), blocks of tissue were removed from euthanized individuals of each species. Each block included two complete vertebrae and all surrounding tissue including the proximal quarter of the associated ribs; for comparison, similar tissue blocks were taken posterior to the hood from the mid-trunk region. The blocks were fixed in 10% NBF, decalcified in Cal-Ex (Fisher, Pittsburg, PA, USA), dehydrated through an ethanol series and Hemo-De (Fisher), and then embedded in Paraplast (Fisher). Each region was sectioned in both the frontal and transverse planes at 10 μm. Mounted sections were stained with Hematoxylin and Eosin, Milligan's trichrome and Verhoff's elastin stain. Staining procedures followed Humason (Humason, 1979) and Luna (Luna, 1968).

Wall (Wall, 1921), and subsequent workers, have noted how the body shape changes during hooding. To quantify this we examined three preserved specimens of N. kaouthia (SVL=85, 91 and 102 cm). From each specimen the first 20 anterior ribs were removed as were 20 consecutive ribs centered at the mid-body. Each rib was manually stripped of muscle and air-dried. Once dried, the ribs were positioned in the same orientation on graph paper, and digital calipers (Mitutoyo 500-322, Aurora, IL, USA) were used to measure the span (proximal-to-distal tip) and the height (maximum perpendicular distance between the span and the body of the rib) of each rib. To eliminate artifacts due to size differences, mean span and height values were calculated for the 20 mid-body ribs (no individual rib varied from this mean by more than 5%), and we used these mean values as the basis for comparison with the ribs from the hood region.

Four functional hypotheses were proposed guided by morphological dissection of the costal musculature with particular attention to the muscles' lines of action and by the observed displacement of the ribs during hooding (see below). The musculature acting on the ribs can be divided into four general groups (Fig. 1): muscles running between the rib tips and the skin, muscles running from rib to rib, muscles originating on vertebrae cranial to the rib of insertion (presumptive rib protractors), and muscles originating on vertebrae caudal to the rib of insertion (presumptive rib retractors). There are other muscles coursing between the ribs and the skin but none of these have a line of action that could produce the rib displacements observed during hooding (Fig. 2).

Hypothesis 1: our first functional hypothesis is that the rib-to-skin muscles act to move the skin along with the ribs, not erect the ribs. To test this hypothesis we experimented on three rib-to-skin muscles: costocutaneous inferior (ci), costocutaneous superior (cs) and obliquus abdominus internus (oai) (Figs 1 and 2).

Hypothesis 2: the muscles coursing from rib to rib are incapable alone of producing rib erection; our second functional hypothesis is that the rib-to-rib muscles act to transmit forces acting on the cranial ribs to the more caudal ribs. To test this hypothesis, we experimentally tested three rib-to-rib muscles: costovertebrocostalis (co), intercostalis externus (ie) and tuberculocostalis (tu) (Figs 1 and 2).

Hypothesis 3: our third functional hypothesis relates to two of the presumptive rib protractor muscles, the levator costae (lc) and the supracostalis lateralis superior (sls). These two muscles have a line of action corresponding to the rib displacements observed during hooding, and therefore we hypothesize that they function in hood erection.

Hypothesis 4: finally, our fourth functional hypothesis concerns two of the presumptive rib retractor muscles, the iliocostalis (il) and obliquus internus pars dorsalis (oid). These two muscles span the caudal surface of the costovertebral joint and have lines of action that correspond to the displacement of the ribs during hood relaxation; accordingly we hypothesize that these two muscles function to relax or retract the hood. These specified functional hypotheses, and the possible roles of other costal musculature, were tested electromyographically during hood erection and relaxation.

Electromyography (EMG) was performed on all six individual cobras. The cobras were anesthetized with isoflurane, and small incisions were made on the dorsal and lateral surface of the neck in the region of the hood. Bipolar EMG leads, 2 m in length, were constructed from 0.05 mm-diameter stainless steel wire with nylon insulation (California Fine Wire, Grover Beach, CA, USA). Hypodermic needles were used to implant the leads ipsilaterally using a binocular dissecting microscope (Nikon, Melville, NY, USA); all implantation sites spanned a maximum of three vertebrae. Because the muscles were directly exposed, placement could be visually confirmed. Once in place, back stimulation further confirmed successful electrode placement. Superficial muscles were carefully separated to visually expose deep, underlying muscles; the superficial muscles were allowed to fall back into their normal positions, and back stimulation further confirmed electrode placement. This approach has been previously used on complex muscle groups (Kardong et al., 1986; Young et al., 2004). This technique was used to implant leads into the following muscles: ci; cs; co; il; ie; lc; oai; obliquus internus pars ventralis (oiv) and oid; sls; and the tu. Surface incisions were closed with tissue glue (polyacrylamide adhesive, Vetbond®, St Paul, MN, USA), and the electrode leads were gently surrounded with rubber cement. A tether of silk suture was attached to the dorsal scalation above the neural spines at the dorsal midline and electrode leads glued to this tether.

Hood displacement was recorded directly using a magneto-restrictive sensor (3503 SPREG chip, Allegro Industries, Worcester, MA, USA) and a 1.0 mm-diameter magnet (Neodymium Boron Iron ceramic magnet, Indigo Industries, Niagra Falls, NY, USA). Using polyacrylamide gel the SPREG chip was affixed along the dorsal midline of the hood, while the magnet was glued to the dorsal surface of the hood contralateral to the EMG leads. The leads from the SPREG magneto-restrictive sensor were integrated into the tether supporting the EMG leads. The EMG leads were coupled to P511 amplifiers (GRASS, West Warwick, RI, USA), the output of which, along with the signal from the SPREG sensor, was sampled at 16 kHz using an Instrunet data acquisition system (GW Instruments, Sommerville, MA, USA) and the SoundScope data analysis package (GW Instruments).

The cobras were allowed to recover from the anesthesia and were placed in a large box allowing full, natural, upright hooding. Electrodes and other leads were carried out of the top of the chamber through non-restricting slits and connected to the recording equipment. The activity of the researchers, viewed through the clear Plexiglas front to the chamber, was sufficient to induce hooding in the alert cobras. Each hooding episode provided data on muscle activation (from the EMG leads), correlated data on relative hood expansion (from the SPREG sensor) and kinematic data (from a synchronized video camera). Most of the hooding episodes were of fairly short duration (the entire cycle of hood erection, maintenance and relaxation occurring in under 5 min) so it was easy to record at least 10 hooding episodes from each cobra. Our goal was to explore the general patterns of muscle activity, rather than to quantify the electrical activity of individual muscles. Therefore, we combined the data from all of the recordings using repeated congruent signals to synchronize the activity patterns. The onset/offset of EMG signals were correlated to, or matched, three distinct phases: before hooding, during hooding, and during hood relaxation. Hooding duration was not fixed in length because this depended upon individual cobra ‘motivation’ making the length of the hood phase quite variable and therefore making quantification of EMG durations impractical.

Following the EMG analyses the cobras were re-anesthetized. The EMG leads were again checked for placement, then removed and the same muscles exposed on the contralateral side (where the magneto-restrictive sensor was anchored). With the snakes under anesthesia the functional role of each muscle was confirmed using a custom-fabricated microstimulator to apply stimulation (generated by a GRASS S88 stimulator) to the surface of each muscle. The hood was manually placed in varying postures (i.e. relaxed, fully erect), and the impact of the muscle contraction documented through the output of the magneto-restrictive sensor. Upon completion of the stimulation trials the specimens were either euthanized for anatomical analyses (see above) or allowed to recover from the anesthesia and returned to home cages. Muscle nomenclature follows Gasc (Gasc, 1981) with the addition of oai from Mosaur (Mosaur, 1935). Developmentally, the snake neck represents a forward extension of the thorax (Cohn and Tickle, 1999). However, anatomically the anterior axial column exhibits distinct morphological features of a neck, especially in its musculature (Kardong, 1980; Pregill, 1977) and atlas–axis complex (Romer, 1976), providing us with the use of the term ‘neck’ to identify this anatomically distinctive region of the anterior snake axial column.

In the cranial portion of the hood, the entire articular surface of the rib is concave (Fig. 3A). A second, convex, articular surface expands in size with each successive rib of the hood (Fig. 3B). The diapophyses of the vertebrae in the cranial portion of the hood project laterally beyond the centrum and support a convex articular surface (Fig. 3C). Three trends are evident in the diapophyses along the length of the hood from anterior to posterior: (1) the extent of lateral projection is reduced; (2) the convexity of the articular surface becomes less pronounced; and (3) a second, concave, articular surface enlarges (Fig. 3D). All of the articular surfaces of the costovertebral joint are covered with hyaline cartilage. Two ligaments span the costovertebral joint, one on the craniodorsal surface and a larger one on the caudoventral surface. The ligament spanning the caudoventral surface of the joint includes an abundance of elastic connective tissue (Fig. 4).

The first rib is borne on the 2nd vertebra caudal to the axis; it is the smallest of the anterior ribs having a span and height that is 53% and 22%, respectively, of the mean mid-trunk values. Successive ribs increase in span until the 7th or 8th rib that reaches a maximum span slightly greater (108%) than the mean mid-trunk value (Fig. 5). Caudal ribs of the hood gradually decrease in span until around the 19th rib (which has a mean span of 87% of the mid-trunk value) after which the ribs gradually increase to the mid-trunk value. Rib height increases rapidly from the 1st to the 4th rib, then more slowly to the 10th rib, which has a height equal to 79% of the mid-trunk value (Fig. 5). Little change in rib height is evident between the 10th and 20th ribs of the hood, all of which are approximately 80% of the mean mid-trunk height.

Comparing radiographs of cobras in the relaxed and hooded posture reveals that erection of the hood is accomplished by rotation of the ribs in both the frontal and transverse planes (Fig. 6). These rotations displace the distal tip of the ribs cranially (protraction) and dorsally (elevation); the angular magnitudes of these displacements are greatest in the cranial portion of the hood and decrease throughout the length of the hood. As the rib rotates in the transverse plane, the head of the rib displaces dorsally on the parapophysis (Fig. 7).

The video records revealed the temporal pattern of hooding to be highly variable. The expansion of the hood always begins cranially then spreads caudally. Often hood erection and relaxation occur in stages; the hood can be maintained in a partially erect or partially relaxed stage for extended periods (>10 min). Similarly, the hood can be maintained in a fully erect position for long periods; the tendency to maintain the erect hood is highly dependent on the visual stimulus provided but may be influenced by intra- and inter-specific variation. Analysis of the video records suggests that the hood can be fully erected in approximately 80 ms. Hood relaxation, which proceeded in the reverse order from hood erection, typically was a slower process lasting several minutes.

Electrical activity patterns, synchronized to videographic records of hood displacement, were recorded from every muscle examined in this study (Fig. 8). When the results from all of the EMG studies are integrated there is a clear temporal pattern. Bursts are recorded in the sls and lc shortly before erection of the hood (Fig. 9). Lower level electrical activity continues in these two muscles throughout the duration of hooding, and in the case of the sls, into the early portions of hood relaxation.

Concurrent with, or slightly (~25 ms) subsequent to, the initial displacement of the cranial ribs, low level electrical activity was recorded in the oai and costocutaneus (ci and cs). These muscles remained active – although at low levels and with occasional gaps of inactivity – as long as the ribs were expanded (Fig. 9). The co, ie and tu – all of which span from rib to rib – were active concurrent with rib displacement. Activity within the tu continued throughout hood relaxation (although at a reduced level) whereas activity in the other two muscles generally terminated once the hood was fully erect (Fig. 9).

The onset of hood relaxation is marked by the onset of electrical activation in the il and the oid (Fig. 9). This electrical activity begins at a low level but generally increases in amplitude when the hood is actively reducing in size. There was typically a bit of a temporal offset between these two muscles with both the onset and termination of the il delayed relative to the oid.

Stimulation of the most cranial sls produced marked protraction and slight elevation in the first few cranial ribs (the exact number of ribs displaced depended on the site of muscle stimulation); stimulating the sls in more posterior portions of the hood produced less rib displacement (Fig. 10). Strong contraction in the cranial sls was enough to cause displacement in more caudal ribs but this displacement was not equivalent to that observed during true hooding. Stimulation of the lc produced elevation and slight protraction of the rib; the influence of this muscle appeared to be consistent throughout the length of the hood and – as with the sls – when stimulated separately was incapable of producing a ‘typical’ hood.

Stimulation of the costocutaneous (ci or cs) and tu produced only modest displacements involving a slight shift and buckling of the scalation and adduction of the adjacent ribs (respectively). Isolated stimulation of the il produced modest retraction of the corresponding rib. Stimulation of the oid resulted in distinct retraction of the rib and slight depression; as with the other separate muscle stimulations, these separate stimulations did not produce complete hood relaxation.

The functional hypotheses were tested through a combination of EMG and muscle stimulation. We hypothesized that the muscles connecting the ribs to the skin [cs, ci and oai] function primarily to keep the skin taut, rather than to displace the ribs relative to the vertebrae. Experimental results corroborate this. Stimulation of these muscles caused limited superficial deformation of the skin but no noticeable deflection of the ribs. Further, the muscle activity patterns of three of these muscles (ci, cs and oai; see Fig. 9) do not coincide with either hood erection or relaxation. Rather, the electrical activity is concentrated during the time when the hood is erect. This activity pattern is somewhat surprising for the cs, which shows morphological specializations in the cranial portion of the hood (covering the first four scutes). Since rib displacement begins in this region, tensile forces on the skin may be most important (in terms of coordinating erection of the entire hood). The signals recorded from these muscles were complicated by the fact that the cobras almost always hood while lifting the anterior portion of the trunk off of the substrate, sometimes in a nearly vertical orientation. As such, some of the muscle activity we observed may be associated with this change in posture rather than with hooding per se.

We hypothesized second that the muscles coursing between the ribs [co, ie and tu] function primarily to transmit forces between adjacent ribs, rather than to move the ribs relative to the vertebrae. This hypothesis was supported by the stimulation experiments (during which the intercostals gap was reduced, rather than the ribs displaced relative to the vertebrae) and by the electrical activity recorded from the co, ie and tu. The activity pattern of each muscle revealed that low-level activity might begin before hood erection, the maximum activity only occurred after the initiation of rib displacement (Fig. 9). These results may oversimplify the functional role of the co. This muscle originates as two heads; a medial head covering much of the ventral surface of the vertebra and the costovertebral joint, and a lateral head that originates on the proximal end of the rib (near the tubercle). Thus, one portion of this muscle spans the costovertebral joint, while the other portion does not. Only the lateral head of this muscle was implanted with electrodes during the current experiments.

The third hypothesis that the lc and sls are responsible for hood erection was supported by the muscle stimulation experiments during which stimulation of these muscles caused rib displacements similar to those observed during hooding. The electrical activity pattern of these muscles (Fig. 9) also supported this hypothesis in that both muscles were active shortly before the onset of rib displacement and remained active throughout the maintenance of the erect hood. While other muscles may also contribute to the erection of the hood, the lever arms, activity patterns and regional morphological specializations of these two muscles (see below) suggest that they are the primary effectors of hood erection.

The fourth hypothesized function, the bases for hood relaxation, was more difficult to test; in part this was due to the greater levels of temporal and spatial variation present in hood relaxation (when compared with hood erection) and in part because we did not quantify the relative contribution of elastic recoil. Nevertheless, the two costal muscles with lever arms most in line with the displacements of the ribs during hood relaxation – il and oid – both had an onset of electrical activity shortly before hood relaxation and some electrical activity during relaxation (Fig. 9). Electrical stimulation of these muscles produced rib displacements similar to those observed during hood relaxation.

Collectively, our results suggest the following model for hooding in cobras (Fig. 11). Hood erection begins with the contraction of the cranial-most sls and lc. The most cranial of these muscles have specialized origins (both more dorsal and more robust) and specialized insertions (covering the entire cranial and lateral surfaces of the first ribs). The contraction of these two muscles simultaneously elevates and protracts the ribs; the forces acting on the ribs are strong enough that the articular facet is displaced dorsally at the costovertebral joint (see Hoffstetter, 1939). The displacement of the rib stretches the elastic ligament that courses over the caudoventral surface of the costovertebral joint (Fig. 11). Once displacement of the anterior ribs begins, the intercostal muscles (including co, ie and tu) contract to assist in the displacement of the more posterior ribs, and the costocutaneous (cs and ci) and oai muscles contract to keep the skin relatively taut across the hood.

In many hooding episodes the cobra stops at the early stage of hooding and only presents a ‘partial’ hood. To fully spread the hood, the sls and lc that insert on the more posterior ribs of the hood are contracted. The force generated, coupled with the ongoing contraction of the other muscles, is adequate to fully protract and elevate all of the ribs of the hood. The combined displacements of the ribs rotate the distal ends of the ribs laterally (producing the flared expansion of the hood) as well as dorsally (which dorso-ventrally compresses the region of the hood). The movements of the ribs, coupled with the contractions of the cs, spread the dorsal and lateral scalation leading to prominent visual displays in many cobra species (e.g. Wall, 1921). The hood can be maintained in the erect posture through sustained contraction of the sls and lc; the specific shape and relative rigidity of the hood is enhanced through regular (but not continual) activation of the tu and cs. Maintenance of the hood in the erect position, despite the displacement of the rib relative to the diapophysis, appears to be active, not passive, as evidenced by the continued contraction of the sls and lc during hood maintenance.

Four elements contribute to the relaxation of the hood: (1) cessation of contractile activity in the sls and lc; (2) elastic recoil in the ligament spanning the caudoventral surface of the costovertebral joint; (3) onset of contraction in the il and oid; and (4) contractile activity within the tu and costocutaneous (ci and cs), which presumably function to synchronize and coordinate the displacements of the ribs with scalation (Fig. 11). The il and oid are smaller and have shorter lever arms than their antagonists (the sls and lc). This may be one reason why relaxation of the hood is generally a much slower process than is hood erection, although clearly the two actions are associated with different behavioral pressures. Hood relaxation, like hood erection, often occurs in several stages. Presumably the elastic recoil is most important during the initial relaxation stage (because retraction of the rib would reduce the stored elastic energy); however, at the present time the relative contributions to hood relaxation of the torques generated by the il and oid and the elastic recoil of the costovertebral ligament, are unknown.

Although the hood is widely recognized as one of the characteristic features of cobras, the presence, shape and size of the hood are highly variable within the Najini radiation. There are true cobras (e.g. Naja pallida) as well as related species (e.g. Paranaja) in which the hood is very narrow or absent. Among the hooded cobras some (e.g. N. kaouthia) have broad but relatively short hoods while others (e.g. N. nivea) have elongated narrow hoods. The differences in the shape of the hood presumably reflect underlying variation in the degree of elongation and curvature in the ribs that form the hood (Fig. 4). The ability of a cobra to erect a hood, like the caudal termination of the hood itself, appears to be due more to neuro-muscular control rather than specific morphological specializations beyond elongation of the ribs.

In addition to the true cobras (Naja), and some closely related elapids (e.g. Ophiophagus), hoods are also known from a variety of other snakes (e.g. Hydrodynastes). Myers postulated that hooding may be a synapomorphy for Xenodontine snakes (Myers, 1986). Other species (e.g. Acanthophis) lack regional specialization of the ribs but displace the ribs – often nearly all the ribs in the body – in a similar fashion resulting in a pronounced broad but flattened defensive display (see Carpenter and Fergusson, 1977; Greene, 1988). Elevation of the ribs is also a key component of some specialized ophidian locomotions, particularly gliding (e.g. Socha, 2002) and burrowing (e.g. Young and Morain, 2003). All of these costal displacements are dependent on one of the key features of snakes, the absence of any sternal skeleton (e.g. Romer, 1976); and may all ultimately be a cooption of the regional costal displacements used by snakes for ventilation (e.g. Rosenberg, 1973).

Although some fanciful alternatives for the function of the hood have been suggested – such as serving as an expansive receptive area for the sense organs – most researchers regard the hooding as an aposematic display that increases the apparent size of the cobra, advertising its venomous danger. In this respect hooding is viewed as similar to a variety of other ophidian visual displays that involve inflation or expansion of head and/or neck (e.g. Young et al., 1999; Young et al., 2000) The visual significance of the hood is further demonstrated by the presence in some species of eye spots or similar patterns on the dorsal surface of the hood (e.g. Wall, 1921). Agitated cobras will often turn their back to display the dorsal surface of the hood to their assailant, a pose that renders the snake highly vulnerable. Interestingly enough, despite all of the accounts and photographs of hooded cobras, there does not appear to have been a single study that examined just how effective the hood is as a defensive display.

We thank DigiMorph at the University of Texas at Austin, and especially Timothy Rowe and Jessie Maisano, both of who we particularly helpful with arranging and completing the cobra images.

 
• ci

  costocutaneous inferior

 
• co

  costovertebrocostalis

 
• cs

  costocutaneous superior

 
• CT

  computed tomography

 
• EMG

  electromyography

 
• ie

  intercostalis externus

 
• il

  iliocostalis

 
• iq

  intercostalis quadrangularis

 
• lc

  levator costae

 
• oai

  obliquus abdominus internus

 
• oid

  obliquus internus pars dorsalis

 
• oiv

  obliquus internus pars ventralis

 
• sli

  supracostalis lateralis inferior

 
• sls

  supracostalis lateralis superior

 
• ta

  transversus abdominus

 
• tu

  tuberculocostalis