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BioMed Research International
Volume 2013 (2013), Article ID 737358, 15 pages
Comparative Anatomy of the Hind Limb Vessels of the Bearded Capuchins (Sapajus libidinosus) with Apes, Baboons, and Cebus capucinus: With Comments on the Vessels' Role in Bipedalism
1Department of Anatomy, Howard University College of Medicine, 520 W Street NW, Numa Adams Building, Washington, DC 20059, USA
2Laboratory of Anthropology, Biochemistry, Neuroscience and Primates' Behavior (LABINECOP), Federal University of Tocantins, Avenida NS 15 ALC NO 14 109 Norte, 77001-090 Palmas, TO, Brazil
3Graduate School of Animal Biology, Institute of Biology, University of Brasilia, Darcy Ribeiro Campus, 70910-900 Brasília, DF, Brazil
4Department of Physiology, Laboratory of Neuroscience and Behavior, University of Brasilia, Darcy Ribeiro Campus, 70910-900 Brasília, DF, Brazil
5Graduate School of Veterinary, Federal University of Uberlândia, Rua Ceará S/N Bloco 2D Campus Umuarama, 38400-902 Uberlândia, MG, Brazil
Received 22 October 2013; Accepted 18 November 2013
Academic Editor: Hisao Nishijo
Copyright © 2013 Roqueline A. G. M. F. Aversi-Ferreira et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Capuchin monkeys are known to exhibit sporadic bipedalism while performing specific tasks, such as cracking nuts. The bipedal posture and locomotion cause an increase in the metabolic cost and therefore increased blood supply to lower limbs is necessary. Here, we present a detailed anatomical description of the capuchin arteries and veins of the pelvic limb of Sapajus libidinosus in comparison with other primates. The arterial pattern of the bearded capuchin hind limb is more similar to other quadrupedal Cebus species. Similarities were also found to the pattern observed in the quadruped Papio, which is probably due to a comparable pelvis and the presence of the tail. Sapajus' traits show fewer similarities when compared to great apes and modern humans. Moreover, the bearded capuchin showed unique patterns for the femoral and the short saphenous veins. Although this species switches easily from quadrupedal to bipedal postures, our results indicate that the bearded capuchin has no specific or differential features that support extended bipedal posture and locomotion. Thus, the explanation for the behavioral differences found among capuchin genera probably includes other aspects of their physiology.
There are numerous studies about Sapajus behavior, cognition, and bipedalism [1–5], but the anatomical descriptions of these species are scarce in scientific literature and the majority of those works concentrate on thoracic limbs [6–13]. Few descriptions are related to the nervous system of the hind limbs [14, 15]. It is not surprising that the anatomical descriptions available of the lower limbs that support the data about its bipedalism focusing mainly on muscles and bones, although these structures are supplied by the arterial system.
Indeed, some studies have focused on the kinematics of capuchin bipedalism  but few have addressed the metabolic cost of bipedal gait on hind limbs. Although this behavior requires higher energetic cost on hind limbs  and depends on an adequate arterial supply to muscles, only a handful of articles have emphasized the anatomical features of capuchin hind limbs vessels so far. Brown , for example, described the femoral artery of the apes and also mentioned Cebus with regard to the saphenous arteries. Manners-Smith  investigated the hind limb arteries of primates and compared two specimens of Cebus capucinus to other primates of different families, that is, Simiidae, Cercopithecidae, Hapalidae, and Prosimiae. Among New World primates, however, this work focused mostly on the genus Ateles. There were only few superficial descriptions of Cebus capucinus’ vessels and no pictures were provided for this species. Furthermore, neither of the authors mentioned above [18, 19] described the arteries supplying the muscles.
Indeed, the anatomical aspects of hind limb vessels could have considerable importance to keep the muscles working to support the weight when the animal is on a bipedal gait, because the more ramified arterial system could increase the area for the distribution of blood [20, 21]. Applying this rationale to different primate species, the comparative anatomical description of vessel plays important role to provide data about the physiology and behavior behind bipedalism.
Therefore, the main objective of this study was to generate modern and accurate data about the anatomical pattern of the vessels of Sapajus libidinosus (bearded capuchin) hind limbs and compare our findings with the anatomy of others species available in the scientific literature, namely, Cebus capucinus [19, 22], apes , baboons [24, 25], and modern humans .
We analyzed the vessels of the hind limbs of bearded capuchins, considering aspects as origin, distribution, and irrigation. We are discussing our results in comparison with other species and present our formatted data in a table. Moreover, we made an effort to identify associations of our data that would support the physiological anatomy of the bipedal position.
2. Material and Methods
Nine adult bearded capuchin specimens (three females, six males) were used in this study. Their weights were between one and four kilograms. No animal was killed for the purposes of this study; five of them suffered accidental deaths in their natural habitats and were deposited in the anatomical collection of the Anthropology, Biochemistry, Neuroscience and Behavior of Primates Laboratory (LABINECOP) from the Federal University of Tocantins, Tocantins State, Brazil. The other four belonged to the Brazilian Institute of Environment and Renewable Natural Resources (IBAMA) archive and were donated for studies in the 1970s. This work was approved by the Institutional Ethical Committee from the Federal University of Goiás, Goiás State, Brazil (CoEP-UFG 81/2008, authorization from the IBAMA number 15275).
2.2. Preparation of the Animals for Dissection
All procedures involving the animals were done in accordance with the guidelines of the Brazilian Society of Animal Experimentation (COBEA). After the trichotomy with a razor blade, the animals received perfusion, by the femoral artery, with 10% of formaldehyde for fixation. The animals were conserved in 10% of formaldehyde, in covered opaque cubes.
We used the human nomenclature for the vessels whenever possible. In the cases where no human nomenclature was available we followed the terminology of .
3.1. Arterial Description (Table 1)
In the bearded capuchins investigated, the external iliac artery runs inferior and laterally in the pelvis lying on the ilium-psoas muscle. It emits a medial-inferior branch, the obturator artery (Figure 1(a)), immediately before crossing the aponeurosis of the external oblique muscle of the abdomen. We did not find a true inguinal ligament in any of the specimens studied here. The obturator artery emits the medial circumflex femoral artery, which crosses the aponeurosis of the external oblique abdomen muscle medially to iliac vein (Figures 1(a) and 1(b)). In one specimen, however, the medial circumflex femoral artery originates directly from external iliac artery but only at one side.
The medial circumflex femoral artery crosses inferiorly to the aponeurosis of the external oblique abdomen muscle, runs obliquely from the anterior to the posterior aspect of the thigh, and communicates branches to the gracilis and adductor muscles, one single branch to the femur head and emits the external pudenda artery (Figure 1(b)). The medial circumflex femoral artery is usually a branch from the obturator artery.
In the bearded capuchin the femoral artery (Figures 1(a), 1(b), 2(a), and 2(b)) emits first a lateral trunk that gives rise to the lateral circumflex femoral artery and the superficial epigastric artery (Figure 2(b)). The superficial epigastric artery turns laterally and superiorly and emits, superior-laterally, the superficial circumflex iliac artery. The lateral circumflex femoral artery emits two muscular branches to the vastus lateral and vastus intermedius muscles, a descendent branch, and a branch that runs inferiorly and laterally towards the femur’s head. We have identified the branches of the lateral circumflex femoral artery as the superficial epigastric artery (“ascendant branch”), and the lateral circumflex femoral artery (“descendent and transversal branches”).
In our specimens we observed that the first medial branch of the femoral artery is the profunda femoris artery that runs medial and posterior in the thigh (Figures 2(b) and 2(c)). It gives rise to muscular branches to the adductor muscles and quadriceps muscle in the medial side of the thigh, and one or two perforating branches that turn laterally. The profunda femoris artery terminates in muscular branches caudal in the lateral compartment of the thigh to the vastus lateralis muscle. The femoral artery continues in the thigh medially under the sartorius muscle through the adductor canal and inferiorly to the lower margin of the vastus medialis muscle, clearly giving rise to branches to the adductor muscles, the sartorius muscle and the vastus medialis muscle. In the distal quarter of the thigh the popliteal artery originates posteriorly and continues superficially as the saphenous artery (Figures 1(a) and 2(d)). In the bearded capuchins described here, the popliteal artery is a short vessel. It emits an ascendant trunk that gives off two inferior genicular arteries and later splits anteriorly into the common tibial artery and posteriorly into the fibular artery (Figure 2(d)).
The common tibial artery in the bearded capuchin (Figure 3(a)) divides into an anterior branch, the anterior tibial artery, and in the posterior and inferior branch, that is, the posterior tibial artery. The anterior tibial artery passes between the tibia and the fibula to turn proximately towards the anterior leg compartment and terminates into muscular branches supplying anterior superficial muscles of the leg (Figure 3(a)). The posterior tibial artery runs medially to the soleus muscle, lies at the posterior aspect of the interosseous membrane and penetrates in the middle third of the leg of this membrane to supply the deep anterior muscles of the leg in the anterior leg compartment (Figure 3(a)). The popliteal artery was considered here as the posterior tibial artery also due to position and function; the posterior and anterior tibial arteries do not reach the foot.
The fibular artery observed in the bearded capuchins (Figure 2(d)) is a branch from the popliteal artery. It gives rise to branches to the triceps sural muscles, continues superficially between the heads of the gastrocnemius muscle, and lies parallel to the short saphenous vein (Figure 4). Both, the fibular artery and the saphenous vein, run laterally to the gastrocnemius tendon along its lateral margin, passing posteriorly and inferiorly to the lateral malleolus into the foot’s dorsal area. From there the arteries distribute laterally and superficially as a calcaneal branch.
The saphenous artery (Figure 3(b)) is superficial, emits the superior genicular arteries, and divides into the anterior and posterior branches in the medial proximal third of the leg. The anterior branch generates a medium branch in the proximal third of the leg (Figures 3(b) and 3(c)). Initially, all branches from saphenous artery run under the skin of the leg (Figure 3(b)). In the foot, they split into the dorsal and the plantar arteries. The anterior ramus of the saphenous artery (Figure 3(c)) runs, after giving rise to the medium ramus, inferiorly and penetrates into the distal third of the leg underneath the retinaculum of the anterior leg muscles. It passes then obliquely to the lateral aspect into the retinaculum behind the tendon of the anterior tibial muscle. From there it emerges laterally on the foot, where finally it emits the dorsalis pedis lateral artery (Figures 3(c) and 4(a)).
The dorsalis pedis lateral artery distributes blood to soft tissues and skin and emits the 3rd and 4th dorsal metatarsal branches. The medium ramus from the anterior branch of the saphenous artery (Figure 3(c)) runs inferiorly, passes anteriorly to the medial malleolus, superficially to the retinaculum (Figure 4(a)), and emerges on the medial portion of the foot emitting the dorsalis pedis medial artery (Figure 5(a)) that gives off the 2nd dorsal metatarsal, a perforating branch and the first dorsal metatarsal artery. The posterior ramus of the saphenous artery (Figure 3(b)) runs inferior and medially along the medial margin of the medial head of the gastrocnemius muscle, continues medially to the tendon of the triceps sural muscle, and penetrates the foot inferiorly (Figure 5(a)) and medially becoming the medial plantar artery (Figure 5(b)). The medial plantar artery is associated with the plantar nerve in the sole (Figure 5(b)). It splits into a branch to the hallux (the first plantar metatarsal branch), a branch to the second interosseous space, and a communicating branch and gives off the lateral plantar artery approximately in the proximal third of sole. The lateral plantar artery (Figure 5(b)) supplies the third and fourth interosseous spaces.
3.2. Vein Description
The veins in the hind limb form a superficial and a deep group in the bearded capuchins. The deep veins are “venae comitantes,” that is, companion veins that follow like duplicates the arteries (Figures 1(a), 1(b), 2(d), and 3(b)). A highlighted superficial vein in the bearded capuchin is the short saphenous vein (Figure 4) that originates dorsal and laterally in the foot follows laterally and turns around the lateral malleolus. It ascends superficially between the heads of the gastrocnemius muscle together with the fibular artery, is superficial and posterior in the knee (popliteal fossa) and thigh, and continues accompanying the muscular branch of the medial circumflex femoral artery in the proximal third of thigh (Figures 1(a) and 1(b)).
The short saphenous vein continues to merge with the external iliac vein in the pelvis. The other superficial veins are a group formed by companion veins of the saphenous artery’s branches that drain to the femoral vein, which represents the long saphenous. We found three superficial veins: two along each branch of the saphenous artery and a third one along the medium ramus of the anterior ramus of the saphenous artery.
The femoral vein receives the tributaries from veins accompanying the saphenous arteries. In the medial, aspect of the thigh of the bearded capuchin the femoral vein ascends passing into the femoral sheath, medial and deep to the femoral artery and lateral and anterior to the medial circumflex femoral artery and vein (Figure 2(a)). The external iliac and internal veins join to form the common iliac vein that drain to the inferior cava vena (Figure 2(a)).
4.1. Comparison with Other Primates: Arteries (Table 1)
Interestingly, few variations were found among the specimens of bearded capuchin observed in the present study. The main variation, the origin of the medial circumflex artery in one of nine cases, only allowed a general description of the pattern of vessels in the bearded capuchin. We also found that the inguinal ligament in general extends between the spina iliaca anterior superior of the ilium and the tuberculum pubicum of the pubis and separates a space for muscles and vessels between abdomen and leg. In contrast to the description of Manners-Smith  in Cebus we could not find a true inguinal ligament in any of the specimens of bearded capuchin studied here.
The origin of the obturator artery in monkeys and apes is quite diverse: it was found to originate from the external iliac artery in Cebus capucinus and in Pan ; from the internal iliac artery in Papio and in ca. 50% of Pan [23, 24]; directly from the femoral artery or from the profunda femoris artery in 25% of Papio ; and from the inferior epigastric artery in Gorilla, Pongo, and in ca. 50% of Pan . According to Gibbs , the obturator artery originates from the femoral artery as a variation in humans, while it originates from the profunda femoris, internal iliac , and inferior epigastric artery in 20 to 30% of all cases. The origin of obturator artery found here in bearded capuchin investigated here is similar to Cebus  and Pan . However, we found in one specimen that the medial circumflex femoral artery originates on one side directly from external iliac artery.
Manners-Smith  described that the external iliac arteries gives off a common trunk to the inferior epigastric, obturator, and medial circumflex femoral artery in C. capucinus. Also, the latter emits branches to the adductor muscles and its deep portion passes between the pectineus and psoas major muscle. The medial circumflex femoral artery originates from the profunda femoris artery in Homo [23, 24, 26] and in 50% of the Pan , from the external iliac artery in 50% of Pan and Hylobates, and from the obturator artery in Papio. An origin directly from the femoral artery occurs in Gorilla and Pongo  but is also described as a variation in Homo [23, 26]. The origin of the medial circumflex femoral artery observed here in bearded capuchin is similar to Papio . Nevertheless, the medial circumflex femoral artery is variable and may originate from external iliac, internal iliac, or obturator arteries in primates .
The external pudenda artery originates directly from the femoral artery in Homo  and Pan and unilaterally in Gorilla  Papio  and in 40% of the Papio anubis specimens . Within the bearded capuchin we observed high variability in the origin of the external pudenda artery with every specimen having a different one, but it originates mainly from medial circumflex femoral artery. The origin of the external pudenda artery is different in all species reported in previous study.
In the C. capucinus specimens studied by Manners-Smith  the lateral circumflex femoral artery arises like an independent branch from the femoral artery and divides into ascendant, descendent, and transversal ramus. The inferior epigastric artery is described as originating from the medial circumflex femoral artery or from a trunk of the external iliac artery. Nonetheless, the superficial epigastric artery was not mentioned. The lateral circumflex femoral artery is a branch from the profunda femoris in all apes (except half of the Gorilla) and divides directly from femoral artery into ramus ascendant and descendent in Gorilla . This is also described by Swindler and Wood , for Pan, Papio and Homo  although its origin in Homo may stem from the femoral and external iliac artery. In Papio anubis the lateral circumflex femoral artery originates from the femoral (35%) or the profunda femoris artery (65%) alone or in a common trunk with the medial circumflex femoral artery . Gibbs  described that the lateral circumflex femoral artery might arise directly from femoral artery in Homo.
In Gorilla the superficial epigastric artery is a branch from the lateral circumflex femoral artery in Pan it is a branch from the external iliac artery, and it originates from the femoral artery in Homo and 50% of the Pongo [23, 26]. According to Swindler and Wood , the superficial epigastric artery originates directly from the external iliac artery and gives off the superficial iliac artery in Papio, Pan and Homo. In Papio Anubis, however, it originates always from femoral, either alone or in a trunk together with the external pudenda artery and/or the superficial circumflex iliac artery .
The description of the lateral circumflex femoral artery in the bearded capuchin in the present work is similar to that in Manners-Smith  and in some cases of Homo  and Gorilla . Since Manners-Smith’s account is relatively unclear regarding its branches, we have identified them as the superficial epigastric artery (“ascendant branch”), and the lateral circumflex femoral artery (“descendent and transversal branches”). The origin of the superficial epigastric artery is similar to Homo [23, 26] and 50% of the Pongo . The superficial circumflex iliac artery was found to originate from the femoral artery in Homo and great apes [23, 26], from the inferior epigastric artery in Homo, Pan, and Papio [24, 26], but its origin was not described by Manners-Smith  in Cebus. Therefore, according to our data, the origin of the superficial circumflex iliac artery in bearded capuchins is similar to Papio and some of the apes and Homo.
According to Manners-Smith  the profunda femoris artery arises from the femoral artery, just below the lateral circumflex femoral, and gives off a branch to the adductor group and three perforating branches. The profunda femoris originates from the femoral artery and supplies the adductor muscles in all apes , Papio , and Homo [23, 24, 26]. It supplies the quadriceps in Homo, Pan, and Pongo and the hamstrings in Homo and Pan. The profunda femoris does not give rise to perforating branches in one third of Pongo, but emits two perforating branches in Pan and two-third of Pongo and three in Homo and Gorilla . Nevertheless, it usually gives off four perforating branches in Homo, Pan, and Papio, according to Swindler and Wood . Unfortunately, Dyl and Topol  did not describe the perforating branches of the profunda femoris in Papio anubis. The origin of the profunda femoris observed in our bearded capuchins is identical to the one in Cebus of Manners-Smith , Homo, and apes, but the number of perforating branches is more similar in Pan and in the majority of Pongo, according to Gibbs ; whereas in Cebus , the number of perforating branches is the same as in Homo and Gorilla.
Manners-Smith  describes in Cebus that the femoral artery runs in the adductor canal whence it emits branches to the adductor muscles and in the lower end of the canal divides into saphenous and popliteal arteries. Brown  (citing Meckel) stated that the femoral artery divides into two branches, a superficial muscular and a deep one. The latter supplies the anterior and posterior leg and probably represents the great saphenous artery, which divides into anterior small vessel that descends to dorsum foot and the posterior ones that descend to the sole. Gibbs  did not describe the trajectory of the femoral artery but mentioned that it has muscular branches t: the adductors in Homo, African apes, and Hylobates; to the vastus medialis muscle in Homo and African apes; and to the sartorius muscle in Homo. Swindler and Wood  did not mention the trajectory or division of the femoral artery in Homo, Pan, and Papio; but Dyl and Topol  found its division into popliteal and saphenous arteries in Papio anubis. The position and division of the femoral artery seem to be similar in all studied primates, as well as in the bearded capuchin observed here, except in Homo where the saphenous artery appears like a variation  or as a small branch from the descending genicular artery .
In Cebus , the popliteal artery gives off an anterior tibial and a rudimentary posterior tibial artery and continues as fibular artery. It gives rise to the superior and medial genicular arteries. The popliteal artery lies deep in the popliteal fossa only in Homo. In all apes and Homo, it originates from the femoral artery, except in Pan where it divides into posterior tibial artery and a common branch for the anterior tibial and fibular arteries [23, 24]. In Homo, the popliteal artery is a continuation of the femoral artery. It emits the superior, middle, and inferior genicular arteries  and divides at the level of the proximal end of the crural interosseous space into tibial anterior and posterior arteries, in 90% of the cases . Nevertheless, Swindler and Wood  described that the femoral artery gives off the descending genicular artery before it passes to popliteal fossa to become popliteal artery and that the saphenous artery is a thin and insignificant end branch of the descending genicular artery placed in the medial side of knee and leg. In all apes and Homo, the popliteal artery gives rise to the superior, medial, (except in Hylobates) and inferior genicular arteries (except in Gorilla and Pongo) .
With respect to the branches of the popliteal artery, the pattern observed in the bearded capuchins is different from other primates described so far, but it is identical to the description by Manners-Smith for Cebus . Despite that, the nomenclature employed in the present work is different; that is, the “rudimentary posterior tibial artery” of Manners-Smith  is described here as posterior tibial artery and, since the “superior genicular artery” branches off inferiorly to the other genicular branch of saphenous artery, it was identified here, in bearded capuchin, as the inferior genicular artery. Furthermore, the main difference of the popliteal artery branches in bearded capuchins to other primates lies in its division into common tibial and fibular arteries, whereas the majority of the apes (except to Pan) present a division into anterior and posterior tibial arteries. Gibbs  described a division of the popliteal artery into anterior tibial and fibular arteries as a variation in Homo that is somewhat similar to the one observed here in the bearded capuchin.
Manners-Smith  did not describe in detail the distribution of anterior tibial artery and his “rudimentary posterior tibial artery” for Cebus. In Homo, Pan, and Pongo, the anterior tibial artery passes between tibia and fibula; it emits the fibular artery in Pan and Pongo and reaches the foot in Homo and Pan but not in Pongo and Gorilla, where it may be replaced distally by the saphenous artery. This replacement seems to appear in great apes , similarly to what has been observed here in bearded capuchins. The fibular artery arises from posterior tibial artery in Homo [23, 24, 26]. The posterior tibial artery is the terminal branch of popliteal artery in all apes, except in Pan; it branches off into medial and lateral plantar arteries in Pongo and Gorilla but not in Hylobates, Pan, and Homo [23, 24, 26].
In Papio, Manners-Smith  described that the popliteal artery divides into anterior tibial and fibular arteries, but Swindler and Wood  mentioned a large branch from popliteal artery that they called the posterior tibial artery due to its position and function. Indeed, in the bearded capuchin investigated here, a branch from popliteal artery was considered as the posterior tibial artery also due to position and function, in keeping with Swindler and Wood regarding the true posterior tibial artery. In the bearded capuchin, posterior and anterior tibial arteries do not reach the foot, similarly to the description in Papio where these vessels end near to ankle.
The trajectory of the fibular artery was not descripted by Manners-Smith  for Cebus. The fibular artery is a branch from the posterior tibial artery in Homo, Gorilla, and Hylobates, from the anterior tibial artery in Pongo and from the popliteal artery in Pan [23, 26]. Interestingly, according to Swindler and Wood , the fibular artery is a large branch from the posterior tibial artery in Pan, which is in disagreement with Gibbs , but this could also be just a variation from different studied specimens. The fibular artery gives rise to perforating and lateral calcaneal rami in all apes and Homo . The origin of the fibular artery in the bearded capuchin and Cebus  is similar to Pan , but the distribution is similar to all apes and Papio.
Manners-Smith  mentioned the saphenous artery in Cebus, which gives rise to the suprema genicular artery and splits into the anterior (dorsal) and posterior (plantar) branch. The dorsal branch was called posterior tibial artery (see above). The plantar artery divides into superficial and deep branches. This description is similar to our observation in the bearded capuchin regarding the region of the distribution, although different names and position were ascribed. With respect to the position, there seems to be a discrepancy in the Cebus descriptions of Manners-Smith : the dorsal division was first identified as “tibialis posterior” (page 120), and later the plantar division was also identified as “tibialis posterior” (page 121). The latter case seems to be correct as the dorsal division is associated with the posterior ramus of the saphenous.
The superficial part of the anterior division of saphenous artery subdivides into inner and outer branches according Manners-Smith . The inner branch is continuous as first dorsal metatarsal artery and communicates with arteries of the sole. The outer branch joins with the perforating branch of the fibular artery to form an arch. The deep part also forms an arch that emits the dorsal metatarsal arteries in Cebus. The posterior (plantar) division of the saphenous artery enters into the plantar region and divides into the lateral plantar and medial arteries. The saphenous artery runs medially to the knee in great apes and Homo and anastomoses with the medial inferior genicular artery, but in great apes it runs together with the saphenous nerve to the foot as dorsalis pedis artery and penetrates the first interosseus space to form the plantar arch .
Swindler and Wood  described also two branches from saphenous artery, the anterior and posterior, both supplying the distal leg and foot in Papio. In Pan there is a large saphenous artery to supply the dorsal foot and the sole is supplied by the posterior tibial artery. According to the authors cited here, the medium ramus from the anterior branch of the saphenous artery seems to be the dorsalis pedis artery. In this work, however, to bearded capuchin, the name “dorsalis pedis” was only used when this artery was located in the foot. In the bearded capuchin, we did not observe the perforating branch from the fibular artery and its communication with the anterior branch of the saphenous. Except for that, the rest of the description is similar to Cebus from Manners-Smith .
In the bearded capuchin the dorsalis pedis lateralis is a branch from the anterior ramus of the saphenous artery and the dorsalis pedis medialis is a branch from the ramus medialis of the anterior ramus of the saphenous artery (present work). In Cebus according to Manners-Smith , the dorsalis pedis lateralis is a branch from the deep division of the saphenous artery. The dorsalis pedis medialis, on the other hand, is a division from the inner branch of the anterior division of the saphenous artery and therefore was identified as first dorsal metatarsal artery. The dorsalis pedis artery is the final branch of the anterior tibial artery in Homo , posterior tibial artery in Pan, the continuation of the saphenous in great apes, and completes the plantar arch in Homo, Pan, and Pongo . Therefore, our description of the dorsalis pedis artery in the bearded capuchin is more similar to Cebus and Papio.
In Homo and Pan the medial plantar arteries supply the first to third interosseous spaces and in Pongo the second and third ones. The lateral plantar artery is absent in Hylobates. It crosses the sole obliquely and emits a communicating branch to the dorsalis pedis artery to complete the plantar arch in great apes and Homo . The origin of the plantar arteries in the bearded capuchins is similar to Cebus and Papio.
In general, the pattern of arteries of the bearded capuchin hind limbs (Figure 6) is more similar to Cebus described by Manners-Smith  (Table 1). However, we observed specific differences in relation to origins, distribution, and names (see above discussion). The most likely explanation is that Manners-Smith  analyzed capuchin from Central America (Cebus genus) whereas we investigated the bearded capuchin from South America, which has been recently segregated as independent genus (Sapajus). On the other hand, as discussed by Swindler and Wood , problems in the interpretation were generated by the differences in nomenclature as for example, the posterior tibial artery to the posterior branch of the saphenous. Finally, other small differences could be explained by natural variation among specimens.
The arterial pattern observed for the hind limbs vessels in the bearded capuchin is somewhat similar to model observed in Papio. The similarities are probably due to a comparable pelvis and the presence of a tail. The characters become more different in great apes and Homo (Figure 7). Despite that, the anatomical descriptions in nonhuman primates are scarce and most of them are not thorough, rendering complete comparisons impossible. Future studies could focus on comparative analysis among bearded capuchin and other New World monkeys to supply data for taxonomy, phylogeny and evolution of apes and monkeys.
4.2. Comparison with Other Primates: Veins
According to Gibbs  in Gorilla the short saphenous vein splits into two branches, both of which merge with the popliteal vein in the popliteal space. It is a lateral vein in the human leg and one of two lateral veins in Pongo’s leg . The short saphenous vein begins on the lateral foot in Papio, runs in the lateral side of the thigh, and drains into the popliteal vein . Different from the observations in baboons, apes, and Homo, the short saphenous vein in the bearded capuchins continues to merge with the external iliac vein in the pelvis. The other superficial veins in the bearded capuchins are the group formed by companion veins of the saphenous artery’s branches that drain to the femoral vein, which represents the long saphenous. Gibbs  described one medial superficial vein in Homo, Pongo, and Pan and two in Gorilla as the long saphenous. Bearded capuchins on the other hand present three superficial veins: two along each branch of the saphenous artery and a third one along the medium ramus of the anterior ramus of the saphenous artery.
4.3. Comments on Bipedalism
The accurate studies considering the diameter of the vessels and number of branches of arteries to muscles and to compare them among the various primates was no yet made and could present many difficulties to be performed; therefore, the anatomical data about arterial distribution can give the more objective information to discuss deeply all subjects under the bipedalism evolution. In fact, it has been recently argued that the adoption of incremental terrestriality by arboreal primate species may have been crucial to the development of tool use in primates . Terrestrialism does not equate to bipedalism in terms of the conditions for complex manipulation, although as noted before, bipedalism does substantially spare the upper limbs from the locomotory function. Arguably, terrestriality without bipedalism could still be advantageous for the arboreal species since less effort is necessary to maintain balance on the ground and consequently one or both forelimbs could be freed for the handling of objects.
Capuchins are quadrupeds in strict sense  but switch easily from quadrupedal to bipedal postures and thus may be an important anthropological model for the evolution of human bipedalism . Interestingly, the intermittent bipedalism observed in the bearded capuchin is a strenuous or at least difficult activity , specially when coupled with other activities, such as nut-cracking . More morphological studies are required to provide important insights into this behavior as well as to associate behavior and morphology of the primate musculoskeletal system, to improve the understanding of the bipedalism evolution in the order primates. Indeed, most of the morphological studies in order to understand bipedalism in primates are focused on the musculoskeletal apparatus. However, the vascular supplement to muscles could play an important role in the aspect as they supply the muscles needed for the bipedal gait.
Indeed, the aspect to be considered is the relation between volume of muscle, that is, the tissue to be supplied, and the surface covered by vessels that supply these muscles. The surface-to-volume ratio plays an important role in the metabolism in general and to muscles physiology and this might depend on the volume of body or an organ. In fact, the capuchins must have higher relative superficial area than other larger primates, and it could explain the high muscles capacity to support the weight of animal when in bipedal gait; however, this knowledge is not enough to generate a conclusion on the special behavior about the Sapajus bipedalism rather than others primates with same proportions. Interestingly, occasional bipedal gait has been observed in several primate species; few of them adopt this posture while handling tools. This is the case even for closely related species, for example, Cebus albifrons, C. olivaceus, C. capucinus, and Sapajus libidinosus have all been shown to engage in bipedal locomotion, but this behavior has only been observed in association with tool use in the Sapajus.
Probably, as small-bodied primates, all capuchin species would benefit from the higher surface-to-volume ratio in hind limb vessels to stay in a bipedal gait. Since only a few such species present prolonged bipedal posture during tool use, higher surface-to-volume may be a necessary but not sufficient condition for occasional bipedalism in capuchins. Moreover, the results presented here indicate that the bearded capuchin has no specific anatomical circulatory apparatus for this behavior, because it was not possible to analyze whether the Sapajus libidinosus has more arterial ramification than others studied primates or to verify the diameter of the arteries comparatively. Indeed, there are no data available in literature that would specifically relate to this question.
Compared to all primates included in the present study, the arterial pattern observed in bearded capuchins is closest to the description of Cebus capucinus made by Manners-Smith . There are however a few differences regarding the origin, trajectory, and branching of the tibial artery, which may support the recent Cebus/Sapajus separation . Bearded capuchins also show a high degree of similarity to baboons, which is probably due to the presence of tails in both genera. As expected from the phylogeny, the degree of similarity to apes and humans is lower. Nevertheless, the pattern of superficial veins observed in bearded capuchins is not similar to any of the primates in comparison, namely, the short saphenous does not drain to popliteal but to extern iliac vein. The pattern of the deep veins, on the other hand, shows very few discrepancies among all studied primates. As a whole, the hind limb vessels observed in the bearded capuchin do not seem to have any fundamental influence on the intermittent bipedalism displayed by these primates in relation to other primates with similar proportions. Future studies should focus on comparative anatomical analysis among capuchin genera and other New World monkeys, apes, and monkeys to responds fundamental questions as the interesting behavior associated to Sapajus.
Roqueline A. G. M. F. Aversi-Ferreira was recipient of a doctoral fellowship from CAPES/Brazil and Tales A. Aversi-Ferreira received a research fellowship from National Council of Technology and Development (CNPq/Brazil).
- E. B. Ottoni and P. Izar, “Capuchin monkey tool use: overview and implications,” Evolutionary Anthropology, vol. 17, no. 4, pp. 171–178, 2008.
- B. Demes, “Three-dimensional kinematics of capuchin monkey bipedalism,” American Journal of Physical Anthropology, vol. 145, no. 1, pp. 147–155, 2011.
- E. Visalberghi, D. M. Fragaszy, P. Izar, E. B. Ottoni, P. C. Lee, and A. C. D. A. Moura, “Terrestriality and tool use,” Science, vol. 308, no. 5724, pp. 951–952, 2005.
- J. W. Lynch Alfaro, J. P. Boubli, L. E. Olson et al., “Explosive Pleistocene range expansion leads to widespread Amazonian sympatry between robust and gracile capuchin monkeys,” Journal of Biogeography, vol. 39, no. 2, pp. 272–288, 2012.
- J. W. L. Alfaro, J. D. S. E. Silva Jr., and A. B. Rylands, “How different are robust and gracile capuchin monkeys? An argument for the use of sapajus and cebus,” American Journal of Primatology, vol. 74, no. 4, pp. 273–286, 2012.
- T. A. Aversi-Ferreira, R. A. E. G. M. F. Aversi-Ferreira, Z. Silva, L. F. Gouvêa-E-Silva, and N. Penha-Silva, “Anatomical study of the forearm deep muscles in Cebus apella (Linnaeus, 1766),” Acta Scientiarum, vol. 27, no. 3, pp. 297–301, 2005.
- T. A. Aversi-Ferreira, M. S. L. Silva, J. P. Paula, L. F. G. Silva, and N. Penha-Silva, “Anatomia comparativa dos nervos do braço de Cebus apella. Descrição do músculo dorso epitroclear,” Acta Scientiarum Biological Sciences, vol. 27, no. 3, pp. 291–296, 2005.
- T. A. Aversi-Ferreira, L. G. Vieira, R. M. Pires, Z. Silva, and N. Penha-Silva, “Estudo anatômico dos músculos flexores superficiais do antebraço no macaco Cebus apella,” Bioscience Journal, vol. 22, no. 1, pp. 139–144, 2006.
- T. A. Aversi-Ferreira, J. Pereira-de-Paula, M. D. S. Lima-e-Silva, and Z. Silva, “Anatomy of the arteries of the arm of Cebus libidinosus (Rylands et al., 2000) monkeys,” Acta Scientiarum, vol. 29, no. 3, pp. 247–254, 2007.
- T. A. Aversi-Ferreira, J. Pereira-de-Paula, Y. C. L. do Prado, M. S. Lima-e-Silva, and J. R. da Mata, “Anatomy of the shoulder and arm muscles of cebus libidinosus,” Brazilian Journal for Morphological Sciences, vol. 24, no. 2, pp. 63–74, 2007.
- T. A. Aversi-Ferreira, P. J. Paula, M. S. L. Silva, Y. C. L. Prado, and Z. Silva, “Estudo anatômico das artérias do ombro de Cebus libidinosus (Rylands, 2000, Primates-Cebidae),” Ciência Animal Brasileira, vol. 8, no. 2, pp. 273–284, 2007.
- T. A. Aversi-Ferreira, R. Diogo, J. M. Potau, G. Bello, J. F. Pastor, and M. A. Aziz, “Comparative anatomical study of the forearm extensor muscles of Cebus libidinosus (Rylands et al., 2000; primates, cebidae), modern humans, and other primates, with comments on primate evolution, phylogeny, and manipulatory behavior,” Anatomical Record, vol. 293, no. 12, pp. 2056–2070, 2010.
- R. A. G. M. F. Aversi-Ferreira, K. A. Marin, F. O. Carneiro e Silva, and T. A. Aversi-Ferreira, “Comparative anatomy of the thigh nerves of Cebus libidinosus (Rylands et al., 2000),” Pesquisa Veterinaria Brasileira, vol. 31, no. 3, pp. 261–266, 2011.
- T. A. Aversi-Ferreira, R. S. Maior, F. O. Carneiro-e-Silva et al., “Comparative anatomical analyses of the forearm muscles of Cebus libidinosus (Rylands et al. 2000): manipulatory behavior and tool use,” PLoS ONE, vol. 6, no. 7, Article ID e22165, 2011.
- T. Abreu, G. A. Pfrimer, R. A. G. M. F. Aversi-Ferreira, L. D. Brandão, H. Nishijo, and T. A. Aversi-Ferreira, “Comparative anatomical study of the leg's nerves of Cebus (barbed capuchins) with baboons, chimpanzees and modern humans,” Pesquisa Veterinária Brasileira, vol. 32, 1, pp. 113–117, 2012.
- M. Duarte, J. Hanna, E. Sanches, Q. Liu, and D. Fragaszy, “Kinematics of bipedal locomotion while carrying a load in the arms in bearded capuchin monkeys (Sapajus libidinosus),” Journal of Human Evolution, vol. 63, no. 6, pp. 851–858, 2012.
- B. Demes and M. C. O'Neill, “Ground reaction forces and center of mass mechanics of bipedal capuchin monkeys: implications for the evolution of human bipedalism,” American Journal of Physical Anthropology, vol. 150, no. 1, pp. 76–86, 2013.
- J. M. Brown, “The femoral artery in apes,” Journal of Anatomy and Physiology, vol. 15, pp. 525–535, 1881.
- T. Manners-Smith, “The limb arteries of primates,” Journal of Anatomy and Physiology, vol. 46, pp. 95–172, 1912.
- J. R. Mata, F. R. Mata, M. C. Souza, H. Nishijo, and T. A. Aversi-Ferreira, “Arrangement and prevalence of branches in the external carotid artery in humans,” Italian Journal of Anatomy and Embryology, vol. 117, no. 2, pp. 65–74, 2012.
- J. C. Penereiro, “Some considerations about Galileo regarding the physics likeness, theory of strength materials and bending theory,” Caderno Brasileiro De Ensino De Física, vol. 27, pp. 288–312, 2010.
- T. Manners-Smith, “The limb arteries of primates,” Journal of Anatomy and Physiology, vol. 45, pp. 23–64, 1910.
- S. Gibbs, Comparative soft tissue morphology of the extant Hominoidea, including man [Ph.D. thesis], The University of Liverpool, Inglaterra, England, 1999.
- D. R. Swindler and C. D. Wood, An Atlas of Primates Gross Anatomy: Baboon, Chimpanzee and Man, University of Washington Press, Seattle, Wash, USA, 1973.
- Ł. Dyl and M. Topol, “The femoral artery and its branches in the baboon Papio anubis,” Folia Morphologica, vol. 66, no. 4, pp. 291–295, 2007.
- S. Standring, “Pelvis girdle and lower limb,” in Gray's Anatomy: The Anatomical basis of Clinical Practice, Churchill Livingstone, London, UK, 2008.
- E. J. M. Meulman, C. M. Sanz, E. Visalberghi, and C. P. van Schaik, “The role of terrestriality in promoting primate technology,” Evolutionary Anthropology, vol. 21, no. 2, pp. 58–68, 2012.
- D. M. Fragaszy, E. Visalberghi, and L. M. Fedigan, The Complete Capuchin: The Biology of the Genus Cebus, Cambridge University Press, Cambridge, Mass, USA, 2004.
- Q. Liu, K. Simpson, P. Izar, E. Ottoni, E. Visalberghi, and D. Fragaszy, “Kinematics and energetics of nut-cracking in wild capuchin monkeys (Cebus libidinosus) in Piauí, Brazil,” American Journal of Physical Anthropology, vol. 138, no. 2, pp. 210–220, 2009.