Criteria of the homology and phylogeny of facial muscles in primates including man. I. Prosimia and Platyrrhina]

The facial muscles of primates are derivates of sphincter colli profundus muscle and platysma myoides. A third superficial muscle layer which is present in primitive mammals is found as a rest in Tupaiiformes. The facial muscles of some Lemuriformes must be considered as a model from which originate the facial musculature of other primates. The new formation of muscles takes place at the margine of the original muscle layers; marginal muscle fibers assume another run and get individualized. So it can be seen in facial muscles of prosimians and platyrrhine monkeys that the profound muscles of mouth and nose and some of the rostral margine of the auricle have orginated from sphincter colli muscle, all others from platysma myoides. Primitive and modified muscle forms and intermediate muscle forms can be observed among prosimians as well as among platyrrhine monkeys and by this it is possible to see the homology of the facial muscles.     

Cells of origin of the branches of the facial nerve: a retrograde HRP study in the rabbit

The origin of different branches of the facial nerve in the rabbit was determined by using retrograde transport of HRP. Either the proximal stump of specific nerves was exposed to HRP after transection, or an injection of the tracer was made into particular muscles innervated by a branch of the facial nerve. A clear somatotopic pattern was observed. Those branches which innervate the rostral facial musculature arise from cells located in the lateral and intermediate portions of the nuclear complex. Orbital musculature is supplied by neurons in the dorsal portion of the complex, with the more rostral orbital muscles receiving input from more laterally located cells while the caudal orbital region receives innervation from more medial regions of the dorsal facial nucleus. The rostral portion of the ear also receives innervation from cells located in the dorsomedial part of the nucleus, but the caudal aspect of the ear is supplied exclusively by cells located in medial regions. The cervical platysma, the platysma of the lower jaw, and the deep muscles (i.e., digastric and stylohyoid) receive input from cells topographically arranged in the middle and ventral portions of the nuclear complex. It is proposed that the topographic relationship between the facial nucleus and branches of the facial nerve reflects the embryological derivation of the facial muscles. Those muscles that develop from the embryonic sphincter colli profundus layer are innervated by lateral and dorsomedial portions of the nuclear complex. The muscles derived from the embryonic platysma layer, including the deep musculature, receive their input from mid to ventral regions of the nuclear complex.     

Epithelial behaviors and threshold effects in the development and evolution of internal and external cheek pouches in rodents

The internal and external cheek pouches found in certain rodents arise early in development by an evagination of the buccal epithelium. Differences in the epithelial evaginations that produce the internal pouches of the Syrian hamster (Mesocricetus auratus) and least chipmunk (Eutamias minimus) are consistent with the view that they evolved independently. The external cheek pouches of rodents of the superfamily Geomyoidea represent a macroevolutionary phenotype when compared to the internal pouches of other rodents. Externalization of an internal pouch rudiment found in the geomyoids Dipodomys and Thomomys can be explained by a simple change early in its development, the effect of which is greatly magnified by facial growth. In this example, the traditional dichotomy between microevolutonary and macroevolutionary theories is bridged by an understunding of developmental dynamics.     

THE MUSCULAR HYDROSTAT OF THE FLORIDA MANATEE (TRICHECHUS MANATUS LATIROSTRIS): A FUNCTIONAL MORPHOLOGICAL MODEL OF PERIORAL BRISTLE USE

Facial musculature was examined in the Florida manatee, Tricbecbus manatus latirostris , in order to develop a functional model of perioral bristle use. Muscles identified include the M. levator nasolabialis, M. buccinatorius, M. maxillonasolabialis, M. centralis nasi, M. lateralis nasi, M. spbincter colli profundus pars oris, M. orbicularis oris, M. mandibularis, and M. mentalis. A new muscle, M. centralis nasi , has been named and is an integral part of perioral bristle movement. The snout of the Florida manatee is capable of performing complex movements. The prehensile ability of Florida manatees can be explained in the context of a muscular hydrostat as defined by Kier and Smith (1985). Eversion of certain bristles in the upper lip occurs by shortening longitudinal, transverse, and semicircular muscles in combination with volume displacement due to compensatory changes in the shape of the snout. Midline sweeping of these bristles is accomplished by the contraction of M. centralis nasi. Eversion of bristles on the lower jaw is a result of shortening of M. mentalis. Contraction of M. orbicularis oris pushes vegetation into the oral cavity. All observed movement patterns and uses of perioral bristles can be explained by variation of these sequences within the context of muscular hydrostat function.     

Competition, predation, and the evolutionary significance of the cercopithecine cheek pouch: the case of Cercopithecus and Lophocebus

Reports of cercopithecine cheek pouch use and functional significance are largely anecdotal, and to date there have been no investigations into its use by species living in closed forest habitats. Here, I report on cheek pouch use in Cercopithecus ascanius and Lophocebus albigena in the Kibale National Park, Uganda, between July-October 1997. Two hypotheses were evaluated: this feature was selected for because of its role in 1) increasing feeding efficiency via a reduction in potential feeding competition, and/or 2) reducing vulnerability to predation. Results indicate that both species were more likely to use their cheek pouches when feeding on contestable foods and, after filling cheek pouches, retreated to more densely vegetated ("safer") positions for processing food. There was no influence of age and sex on L. albigena cheek pouch use. Subadult C. ascanius cheek-pouched less frequently than adults, although there were no differences between adult males and females. There was no relationship between feeding-patch size and number of plant food items cheek-pouched in either species. However, the diameter of breast height (dbh; a measure of patch size) of trees in which C. ascanius used their cheek pouches was significantly larger than the dbh of trees in which they did not. Both species were more likely to use their cheek pouches in the presence of greater numbers of conspecifics. These data provide insight into the relationship(s) among oral anatomy and feeding efficiency, and facilitate understanding into the selection for this important oral feature in stem cercopithecines.     

Cheek pouch use in relation to interspecific competition and predator risk for three guenon monkeys (Cercopithecus spp.)

Forest guenons (Cercopithecus spp.) are often found in polyspecific associations that may decrease predator risk while increasing interspecific competition for food. Cheek pouch use may mitigate interspecific competition and predator risk by reducing the time spent in areas of high competition/predator risk. I investigated these ideas in three forest guenons: Campbell’s monkey (Cercopithecus campbelli), spot-nosed monkey (C. petaurista), and Diana monkey (C. diana). I present 13 months of scan sample data from Taï Forest, Côte d’Ivoire, including 3,675, 3,330, and 5,689 records of cheek pouch distention, to quantify cheek pouch use, for Campbell’s, spot-nosed, and Diana monkeys, respectively. Cheek pouches are often used to hold fruit, so I first predicted that the most frugivorous species, Diana monkeys, would have the most cheek pouch distension. Spot-nosed monkeys ate the least amount of fruit over the study period and had the least distended cheek pouches, suggesting the importance of frugivory in relation to cheek pouch distension for this species. This was not a sufficient explanation for Campbell’s monkeys; Campbell’s ate fruit less than Diana monkeys, but had more distended cheek pouches, suggesting that cheek pouch use was not simply a reflection of high frugivory. From the interspecific competition hypothesis, I predicted that Campbell’s monkeys would have more distended cheek pouches than Diana and spot-nosed monkeys, and more distended cheek pouches when associated with Diana because Campbell’s monkeys have the highest potential for interspecific competition with dominant Diana monkeys. From the predator risk hypothesis, I predicted that Campbell’s would have more distended cheek pouches when not associated with highly vigilant Diana monkeys. Campbell’s monkeys had the most distended cheek pouches overall, but had more distended cheek pouches when not in association with Diana, suggesting the greater importance of predator risk rather than interspecific competition in Campbell’s cheek pouch use.     

Cheek pouch use, predation risk, and feeding competition in blue monkeys (Cercopithecus mitis stuhlmanni)

The adaptive function of cheek pouches in the primate subfamily Cercopithecinae remains unresolved. By analyzing the circumstances of cheek pouch use, we tested two hypotheses for the evolution of cercopithecine cheek pouches proposed in earlier studies: (1) cheek pouches reduce vulnerability to predation, and (2) cheek pouches increase feeding efficiency by reducing competition. We studied two groups of wild blue monkeys (Cercopithecus mitis stuhlmanni) in the Kakamega Forest, Kenya, conducting focal observations of feeding individuals. Monkeys were less exposed while emptying their cheek pouches than filling them, supporting the predation-avoidance hypothesis. We investigated several measures of competitive threat, but only one supported the competition-reduction hypothesis: when the nearest neighbor's rank increased, subjects were more likely to increase than to decrease cheek pouch use. Overall, our findings supported the predation-avoidance hypothesis more strongly than the competition-reduction hypothesis. We suggest that variation in cheek pouch use may reflect differing behavioral strategies used by cercopithecines to mitigate competition and predation, as well as factors such as resource size and distribution, home range size, and travel patterns.     

Composite rhytidectomy.

Signs of aging in the face reflect the change in position of deep anatomic elements, which are the platysma muscle, cheek fat, and the orbicularis oculi muscle. These changes occur from progressive ptosis of these elements, which continue to keep their intimate relationship with each other throughout the aging process. Conventional face lift procedures disrupt this normal relationship by separating the skin from these elements. All SMAS techniques reposition only the platysma muscle without repositioning the cheek fat and orbicularis muscle. This composite rhytidectomy allows elevation of a composite musculocutaneous flap containing all three elements for repositioning while maintaining their intimate relationship with each other and with the skin. One-hundred and sixty-seven composite rhytidectomies have been done with impressive results and minimal complications.     

The differential use of cheek pouches in a troop ofPapio ursinus

Cheek pouches, one of the distinguishing characters of the Cercopithecinae, are structures used for the temporary storage of food. Their size and frequency of use within a given species are related primarily to the amount of conspecific competition for food. In relation to total body size, members of the genusPapio are considered to have relatively small cheek pouches which are said to be used only occasionally to maximize food harvest when local clusters of food are encountered. This investigation represents 165 hours of observation on a troop ofPapio ursinus at Mkuzi Game Reserve in Natal, South Africa. At the time of observation the choice of foods in the home range was restricted and usually found in abundance only in small clusters of trees. Given that conspecific competition would have been pronounced under these conditions, it was thought that any differences in the frequency of cheek pouch use related to age, sex, rank, or the reproductive state of an animal would be readily recognizable. The results indicated that cheek pouches were used differentially throughout the day, with virtually all ages of each sex displaying the same general pattern of maximal cheek pouch use during the middle of the day. In each sex there was an age graded diminution of the frequency of cheek pouch use from juveniles to adults. This trend was more pronounced in males resulting in a substantial sex difference in the use of cheek pouches between adult males and females. In addition, there was some indication that differences in the frequency of cheek pouch use between adult males were correlated with rank. Although a pattern of cheek pouch use and rank was not evident amongst adult females, there was an association between reproductive state and the frequency of cheek pouch use. Overall, body size, dominance, and energetic demands appeared to be the most significant factors underlying the differences in cheek pouch use in this troop.     

Cheek pouch capacities and loading rates of heteromyid rodents

Rodents of the family Heteromyidae are proficient gatherers and hoarders of seeds. A major component of their adaptive specialization for harvesting and transporting seeds is their spacious, fur-lined cheek pouches. Precise measurements of cheek pouch capacities are essential if ecologists are to understand the foraging ecology, possible constraints on locomotion patterns, and competitive relationships of heteromyid rodents. To measure the size of these cheek pouches and the rate at which animals load seeds into their pouches during seed harvest, we attracted 56 individuals representing ten species of heteromyid rodents to bait stations in the field and allowed them to fill their cheek pouches with seeds several times while we observed and timed the events with the aid of night-vision equipment. The largest load taken by each individual was used as an estimate of its cheek pouch capacity. At the end of observations, each subject was captured and its mass and other data gathered. The allometric relationship between cheek pouch capacity and body mass for ten species of heteromyids was significant [pouch capacity (ml) = 0.148 body mass (g)^0.992, r ²=0.91, P<0.0001]. The regression coefficient is ≈1.0, which indicates that the volume of the cheek pouches scales in direct proportion to body size. When the data were subdivided into quadrupeds (Perognathus and Chaetodipus) and bipeds (Dipodomys) (n=5 for each), the relationships between pouch capacity and body mass were significant, but the two regressions were not significantly different from each other. When all loads (full and partial) were considered, subjects filled their cheek pouches an average of 93 ± 10% of pouch capacity (n=185). Cheek pouch capacities from published studies of artificially filled pouches of heteromyids in the laboratory averaged about 40% below the field measurements obtained here. The allometric relationship between mean loading rate and body mass was also significant [seeds/s=1.067 bodymass (g)^0.830, r ²=0.85,P=0.0011), but when quadrupeds and bipeds were considered separately, the relationships were not significant. Seed densities and bulk densities were used to calculate packing coefficients for seed species, which, when used in conjunction with the allometric relationship between cheek pouch capacity and body size, can be used to estimate the maximum load carried by a heteromyid. Except for the very largest kangaroo rat species, a full pouch load of Indian ricegrass seeds represents less than the daily energy requirements of an active heteromyid. Received: 3 March 1997 / Accepted: 15 July 1997     

Morphology and relationships of the orangutan fatty cheek pads

The present paper examines the anatomical relationships as well as possible developmental and functional relationships of the fatty cheek pad characteristic of the adult male orangutan. The research involves the dissection of 11 orangutans of both sexes in a variety of age categories. All specimens possess either a fat pad or a subcutaneous connective tissue fascial compartment in the lateral face extending superiorly from slightly above the inferior border of the mandible to the temporal region. In immature specimens as well as adult females, fat deposits within the connective tissue compartment are scarce or nonexistent, whereas pubescent male specimens or older possess accumulations of fibro-fatty tissues in this region. The extensive fat accumulations of the adult male cheek flange are related to age and sex and to modifications in related facial musculature, especially mm. platysma, zygomaticus, orbicularis oculi, and orbitotemporalis and frontalis. These muscles are clearly related to the cheek pad structures in both sexes but appear to assume a supportive role in the males. The cheek pad has no direct bony attachments, but its mass may have a significant effect on facial morphology. The development of the cheek pad is temporally variable and its function remains speculative although the presence of a fully developed flange may be related to behavioral modifications.     

The relationship of the superficial and deep facial fascias: relevance to rhytidectomy and aging.

Controversy persists regarding the relationship of the superficial facial fascia (SMAS) to the mimetic muscles, deep facial fascia, and underlying facial nerve branches. Using fresh cadaver dissection, and supplemented by several hundred intraoperative dissections, we studied facial soft-tissue anatomy. The facial soft-tissue architecture can be described as being arranged in a series of concentric layers: skin, subcutaneous fat, superficial fascia, mimetic muscle, deep facial fascia (parotidomasseteric fascia), and the plane containing the facial nerve, parotid duct, and buccal fat pad. The anatomic relationships existing within the facial soft-tissue layers are (1) the superficial facial fascia invests the superficially situated mimetic muscles (platysma, orbicularis oculi, and zygomaticus major and minor); (2) the deep facial fascia represents a continuation of the deep cervical fascia cephalad into the face, the importance of which lies in the fact that the facial nerve branches within the cheek lie deep to this deep fascial layer; and (3) two types of relationships exist between the superficial and deep facial fascias: In some regions of the face, these fascial planes are separated by an areolar plane, and in other regions of the face, the superficial and deep fascia are intimately adherent to one another through a series of dense fibrous attachments. The layers of the facial soft tissue are supported in normal anatomic position by a series of retaining ligaments that run from deep, fixed facial structures to the overlying dermis. Two types of retaining ligaments are noted as defined by their origin, either from bone or from other fixed structures within the face.(ABSTRACT TRUNCATED AT 250 WORDS)     

The retaining ligaments of the cheek

The zygomatic ligaments (McGregor's patch) anchor the skin of the cheek to the inferior border of the zygoma just posterior to the origin of the zygomaticus minor muscle. The mandibular ligaments tether the overlying skin to the anterior mandible. Both these ligaments are obstacles to surgical maneuvers intended to advance the overlying skin. They also restrain the facial skin against gravitational changes, and they delineate the anterior border of the "jowl" area. The platysma-auricular ligament is a thin fascial sheet that extends from the posterosuperior border of the platysma and that is intimately attached to the periauricular skin; it serves as a surgical guide to the posterosuperior border of the platysma. The anterior platysma-cutaneous ligaments are variable fascial condensations that anchor the SMAS and platysma to the dermis. They can cause anatomic disorientation with dissection of false planes into the dermis. These four ligaments are useful as anatomic landmarks during facial dissections. The tethering effects of the zygomatic and mandibular ligaments must be interrupted if a maximum upward movement of the facial skin is desired.     

Free-radical inhibition of ATPase in hamster cheek pouch homogenates

The effects of free-radicals generated by either the oxidation of hypoxanthine by xanthine oxidase (HX/XO) or the lipoxidation of arachidonic acid (AA) on the ATPase of the hamster cheek pouch has been studied. Cheek pouches were removed from female golden syrian hamsters and homogenized. ATPase activity was measured by the production of Pi at 37 degrees. HX/XO and AA were added at a final concentration of 9.6 X 10(-5) M HX with 5 X 10(-2) units HX and 5 X 10(-5) M AA with and without 1 X 10(-4) M ouabain. HX/XO produced a 24.7% inhibition alone and 35.0% when combined with ouabain. Ouabain alone produced a 7.1% inhibition. AA produced a 23.6% inhibition alone and 24.3% inhibition when combined with ouabain. Ouabain alone produced a 5.4% inhibition in this series. When AA was added in doses ranging from 1 X 10(-5) to 2 X 10(-3) M, a plot of percent inhibition versus log dose followed a typical sigmoid type curve. The IC50 was 1.5 X 10(-4) M. These results suggest that free-radicals are capable of inhibiting the ATPase found in the hamster cheek pouch tissues. The possible modes of action of the free-radicals in producing this inhibition are discussed.     

Correction of extracapsular temporomandibular joint ankylosis with a cervical subcutaneous pedicle flap

A new method of correcting extracapsular temporomandibular joint ankylosis with a cervical subcutaneous pedicle flap is described. In this procedure, a cervical subcutaneous pedicle flap with or without platysma is introduced into the oral cavity through a tunnel to repair the defect after the buccal scar is excised and the normal oral opening is restored. Sixteen consecutive patients underwent the surgery, and good results were obtained.     

Strain and load thresholds for cervical muscle recruitment in response to quasi-static tensile stretch of the caprine C5–C6 facet joint capsule

The aim of this study was to investigate the response of cervical muscles to physiologic tensile stretch of cervical facet joint capsule (FJC) at a quasi-static displacement rate of 0.5 mm/s. In vivo caprine left C5–C6 FJC preparations were subjected to an incremental tensile displacement paradigm. EMG activity was recorded during FJC stretch from the right trapezius (TR) and multifidus (MF) muscle groups at the C5 and C6 levels and bilaterally from the sternomastoid (SM) and longus colli (LC) muscle groups at the C5–C6 level. Onset of muscular activity was later analyzed using visual and computer-based methods. Capsule load and strain at the time of onset were recorded and compared between the muscle groups. Results indicated capsule load was a better indicator of the tensile stretch thresholds for muscular recruitment than capsule strain. MF responded at significantly smaller capsule loads than TR and LC, while TR and LC activation loads were not significantly different. SM did not respond to physiologic FJC stretch. Muscle group recruitment order reflected the muscles’ fiber type compositions and functional roles in the spine. This study provides the first evidence that the cervical ligamento-muscular reflex pathways are activated via tensile FJC stretch and extend to superficial and deep musculature on the anterior and posterior aspects of the neck, ipsilateral and contralateral to the side of FJC stretch.     

Rhytidectomy and the nasolabial fold.

I describe a technical modification in the Skoog face lift procedure that releases the deep attachments of the SMAS to the muscles of facial expression for maximal mobility of the medial cheek yet elevates the cheek flap as a composite of skin, subcutaneous tissue, and SMAS to enhance skin perfusion. My results with the procedure in 100 patients are analyzed by using functional zones of the nasolabial fold corresponding to underlying musculature and a simple grading system based on preoperative and postoperative photographs. Marked improvement in the nasolabial fold was noted in over 80 percent of patients by 6 and 12 months postoperatively. This effect seemed to last up to 4 years.     

Repositioning the orbicularis oculi muscle in the composite rhytidectomy.

While blepharoplasties are routinely done with face lift procedures, the improvement is accomplished by removing excess orbital fat with eyelid skin and muscle along the incisional line. The orbicularis oculi muscle remains intact as its inferior border, which has become ptotic and redundant with aging, and actually remains in the same position following a conventional lower lid blepharoplasty and rhytidectomy. However, by elevating the orbicularis oculi with the cheek fat and platysma in a composite face lift flap, and by excising the redundant inferior border of the orbicularis muscle, a total rejuvenation of the malar area is accomplished. The descent of the orbicularis oculi muscle is in an inferolateral vector, whereas the vector of facial aging is inferomedial. Thus, repositioning the orbicularis oculi is in a superomedial vector and is obligatory in a composite rhytidectomy.     

Two patterns of differentiation in the jaw musculature of teleostean fishes

In its most generalized configuration among modern teleosts the M. adductor mandibulae comprises a single, almost continuous mass of musculature extending from the cheek to the inner surface of the mandible. In more advanced teleosts this muscle is usually divided into sections. Two basically different pathways of differentiation in the cheek part of the adductor mandibulae are dealt with here. One is that in the ostariophysine fishes. The other is represented in at least the great majority of acanthopterygians. Only certain of the differentiated sections are homologous in these two large groups of fishes.     

Distribution of different fiber types in whole cross-sections of human platysma. A histological and morphometric study

Analysis of cryostat cross-sections of the entire platysma muscle from human autopsies revealed enzyme histochemical and morphometric differences between normal human limb and facial muscles. The mean diameter of platysma fibers was about 50% of that of normal limb muscle fibers. Fiber type diameter increased from the medial to the lateral parts of the platysma. A variability coefficient of 356 indicated great variation in fiber caliber, with many fibers of 10 microns and less. Type I fibers showed an increase in density from the medial to the lateral parts of the muscle. The arrangement of histochemical fiber types was irregular with a tendency to form fiber type groupings.