The skull and jaw musculature as guides to the ancestry of salamanders

The fossil record provides no evidence supporting a unique common ancestry for frogs, salamanders and apodans. The ancestors of the modern orders may have diverged from one another as recently as 250 million years ago, or as long ago as 400 million years according to current theories of various authors. In order to evaluate the evolutionary patterns of the modern orders it is necessary to determine whether their last common ancestor was a rhipidistian fish, a very primitive amphibian, a labyrimhodom or a ‘lissamphibian’. The broad cranial similarities of frogs and salamanders, especially the dominance of the braincase as a supporting element, can be associated with the small size of the skull in their immediate ancestors. Hynobiids show the most primitive cranial pattern known among the living salamander families and “provide a model for determining the nature of the ancestors of the entire order. Features expected in ancestral salamanders include: (1) Emargination of the cheek; (2) Movable suspensorium formed by the quadrate, squamosal and pterygoid; (3) Occipital condyle posterior to jaw articulation; (4) Distinct prootic and opisthotic; (5) Absence ol otic notch; (6) Stapes forming a structural link between braincase and cheek. In the otic region, cheek and jaw suspension, the primitive salamander pattern (resembles most closely the microsaurs among known Paleozoic amphibians, and shows no significant features in common with either ancestral frogs or the majority of labyrinth odonts. The basic pattern of the adductor jaw musculature is consistent within both frogs and salamanders, but major differences are evident between the two groups. The dominance of the adductor mandibulae externus in salamanders can be associated with the open cheek in all members of that order, and the small size of this muscle in frogs can be associated with the large otic notch. The spread of different muscles over the otic capsule, the longus head ol the adductor mandibulae posterior in frogs and the superficial head of the adductor mandibulae internus in salamanders, indicates that fenestration of the skull posterodorsal to the orbit occurred separately in the ancestors of the two groups. Reconstruction of the probable pattern of the jaw musculature in Paleozoic amphibians indicates that frogs and salamanders might have evolved from a condition hypothesized for primitive labyrinthodonts, but the presence of a large otic notch in dissorophids suggests specialization toward the anuran, not the urodele condition. The presence of either an einarginated cheek or an embayment of the lateral surface of the dentary and the absence of an otic notch in microsaurs indicate a salamander-like distribution of die adductor jaw muscles. The ancestors of frogs and salamanders probably diverged from one another in the early Carboniferous, Frogs later evolved from small labyrinthodonts and salamanders from microsaurs. Features considered typical of lissamphibians evolved separately in the two groups in the late Permian andTriassic.     

Temporalis function in anthropoids and strepsirrhines: an EMG study

The major purpose of this study is to analyze anterior and posterior temporalis muscle force recruitment and firing patterns in various anthropoid and strepsirrhine primates. There are two specific goals for this project. First, we test the hypothesis that in addition to transversely directed muscle force, the evolution of symphyseal fusion in primates may also be linked to vertically directed balancing-side muscle force during chewing (Hylander et al. [2000] Am. J. Phys. Anthropol. 112:469-492). Second, we test the hypothesis of whether strepsirrhines retain the hypothesized primitive mammalian condition for the firing of the anterior temporalis, whereas anthropoids have the derived condition (Weijs [1994] Biomechanics of Feeding in Vertebrates; Berlin: Springer-Verlag, p. 282-320). Electromyographic (EMG) activities of the left and right anterior and posterior temporalis muscles were recorded and analyzed in baboons, macaques, owl monkeys, thick-tailed galagos, and ring-tailed lemurs. In addition, as we used the working-side superficial masseter as a reference muscle, we also recorded and analyzed EMG activity of the left and right superficial masseter in these primates. The data for the anterior temporalis provided no support for the hypothesis that symphyseal fusion in primates is linked to vertically directed jaw muscle forces during mastication. Thus, symphyseal fusion in primates is most likely mainly linked to the timing and recruitment of transversely directed forces from the balancing-side deep masseter (Hylander et al. [2000] Am. J. Phys. Anthropol. 112:469-492). In addition, our data demonstrate that the firing patterns for the working- and balancing-side anterior temporalis muscles are near identical in both strepsirrhines and anthropoids. Their working- and balancing-side anterior temporalis muscles fire asynchronously and reach peak activity during the power stroke. Similarly, their working- and balancing-side posterior temporalis muscles also fire asynchronously and reach peak activity during the power stroke. Compared to these strepsirrhines, however, the balancing-side posterior temporalis of anthropoids appears to have a relatively delayed firing pattern. Moreover, based on their smaller W/B ratios, anthropoids demonstrate a relative increase in muscle-force recruitment of the balancing-side posterior temporalis. This in turn suggests that anthropoids may emphasize the duration and magnitude of the power stroke during mastication. This hypothesis, however, requires additional testing. Furthermore, during the latter portion of the power stroke, the late activity of the balancing-side posterior temporalis of anthropoids apparently assists the balancing-side deep masseter in driving the working-side molars through the terminal portion of occlusion.     

Diverse bitter stimuli elicit highly similar patterns of Fos-like immunoreactivity in the nucleus of the solitary tract

Previous studies have demonstrated that oral stimulation with quinine elicits Fos-like immunoreactivity in the first-order gustatory nucleus, the NST, with a different topographic distribution than sucrose or citric acid. However, it is unknown whether the quinine pattern is unique to this alkaloid or common across bitter stimuli with different chemical structures. Indeed, recent physiological experiments suggest that taste receptor cells and primary afferent neurons may exhibit selectivity for various bitter tastants. The present investigation compared the distribution of FLI in NST following stimulation with three bitter chemicals: QHCl, denatonium and propylthiouracil, stimuli that evoked Ca(2+) currents in almost entirely different sets of receptor cells. The results demonstrate that the quinine pattern is not idiosyncratic but instead generalizes to the other two tastants. Although it remains possible that intermingled but different NST neurons are activated by these stimuli, these data suggest that a specialized region in the NST is preferentially involved in processing a common aspect of bitter tastants. In contrast to citric acid, quinine, denatonium and propylthiouracil all elicited vigorous oromotor rejection responses, consistent with our earlier hypothesis that the medial third of the NST may be an afferent trigger zone for oromotor rejection.     

Jaw muscles in older overdenture patients

Objective: To determine, using computer tomography (CT), whether the retention of a small number of teeth in the older adult used to support overdentures could affect the cross‐sectional area (CSA) and X‐ray density of two jaw closing muscles. Design: Cross‐sectional study of a group of older patients subdivided into dentate, edentulous and those wearing overdentures supported by two to five teeth. Subjects: The sample consisted of 24 subjects aged 55–68 years. Outcome measures: CSA and X‐ray density of two jaw closing muscles, masseter and medial pterygoid were measured and evaluated using CT. Results: There were no significant differences between left and right jaw muscles, but the CSA of the masseter muscles were significantly larger than the medial pterygoid muscles. The CSA of the masseter and medial pterygoid muscles was significantly smaller in edentulous subjects compared with dentate subjects but no significant difference was observed between subjects wearing overdentures and those with a natural dentition. No significant differences were observed with the X‐ray density between different muscles or dental states. Conclusion: The retention of a small number of teeth in the older adult used to support overdentures appears to sustain the CSA of two jaw closing muscles and therefore could enhance these patients’ masticatory ability compared with those who were edentulous.     

A catalogue of skulls and jaws of eastern tropical Pacific blennioid fishes (Blennioidei: Teleostei): A proposed evolutionary sequence of morphological change

Skulls and jaws are compared in 35 species of tropical eastern Pacific (mainly Gulf of California) blennioid fishes (5 species of Tripterygiidae, 13 Labrisomidae, 12 Chaenopsidae, 5 Blenniidae). Morphotypes are arranged in a series from relatively large-mouthed fishes (tripterygiids and a few labrisomids) with protrusible jaws and conical teeth to species with small, non-protrusible jaws and a single row of incisiform teeth. This polarity of arrangement probably reflects the direction of phylogenetic development, as suggested by outgroup comparison with other perciform fishes. Distribution patterns of morphotypes in a simple morphospace, obtained by combining dentition, shape of the jaw arch and jaw protrusibility, are discussed within an adaptive context.     

Suboccipital muscle of sharpnose sevengill shark Heptranchias perlo and its possible role in prey dissection

Skull and head muscles of Heptranchias perlo were studied. Its distinctive features include the suboccipital muscles, described for the first time, the absence of the palatoquadrate symphysis, a longitudinally extended mouth, and teeth unsuited for dissecting prey in typical method of modern sharks, which is cutting motions powered by head shaking from side to side. The palatoquadrate cartilages of H. perlo and closely related Hexanchidae articulate with the neurocranium via orbital and postorbital articulations, which together allow for lateral expansion of the jaws, but restrict retraction and protraction. We interpret these features as an adaptation to a different method of prey dissection, that is, ripping in a backward pull. It employs the specific postorbital articulation together with the suboccipital muscles as force-transmitting devices, and is powered by swimming muscles which produce a rearward thrust of the tail. During this type of dissection, the anterior part of the vertebral column should experience a tensile stress which explains the replacement of rigid vertebral bodies by a collagenous sheath around the notochord in H. perlo. The backward-ripping dissection could have been common among ancient Elasmobranchii based on the similarly developed postorbital articulation, a longitudinally extended mouth, and the absence of the palatoquadrate symphysis. A biomechanical comparison with the extinct Pucapampella indicates that ancient elasmobranchs could be also specialized in the backward-ripping prey dissection, but their mechanism was different from that inferred for H. perlo. We suggest that in the early evolution of sharks this mechanism was replaced by head-shaking dissection and then later was restored in H. perlo on a new morphological basis. A new position of the postorbital articulation below the vertebral axis is fraught with the braincase elevation when backward ripping the prey, and as a counter-mean, requires formation of suboccipital portions of the axial musculature unknown in other sharks. Homology and origin of these portions is considered.     

Influence of ontogenetic changes in prey selection on the survival and growth of rohu, Labeo rohita and singhi, Heteropneustes fossilis larvae

When offered a mixed diet of different zooplanktonic items covering a body size range of 75–2200 μm, (a) rohu, Labeo rohita and (b) singhi, Heteropneustes fossilis larvae ingested progressively larger prey as they grew, due to age-related increase in gape. However, a nearly constant prey size/mouth size ratio was maintained for a period of 4wk after hatching. The dominance of rotifers in the diet during the first 2-wk was followed by cladocerans, particularly Moina macrocopa. Significant differences observed in the growth rates of the larvae reared on different diet regimes were related to ontogenetic changes in prey selection. An exclusive copepod diet throughout resulted in the lowest weight gain in the larvae of both species. However, copepods had no apparent adverse effects when present with the preferred rotifers and cladocerans. Although constituting a suboptimal prey size for the older larvae, rotifers alone, when present in sufficient densities, produced growth rates comparable to those obtained on a cladoceran diet. However, a mixed diet regime contributed to the maximum growth. The implications of these findings to rearing larvae of the economically important rohu and singhi are discussed.     

Morphological and functional diversity of the mandible in suckermouth armored catfishes (Siluriformes: Loricariidae)

We examined the mandibles of 377 individuals representing 25 species, 12 genera, 5 tribes, and 2 subfamilies of the Loricariidae, a species‐rich radiation of detritivorous–herbivorous neotropical freshwater fishes distinguished by having a ventral oral disk and jaws specialized for surface attachment and benthic feeding. Loricariid mandibles are transversely oriented and bilaterally independent, each rotating predominantly around its long axis, although rotational axes likely vary with mandibular geometry. On each mandible, we measured three traditional and three novel morphological parameters chosen primarily for their functional relevance. Five parameters were linear distances and three of these were analogous to traditional teleost in‐ and out‐levers for mandibular adduction. The sixth parameter was insertion area of the combined adductor mandibulae muscle (AM_area), which correlated with adductor mandibulae volume across a subset of taxa and is interpreted as being proportional to maximum force deliverable to the mandible. Multivariate analysis revealed distributions of phylogenetically diagnosed taxonomic groupings in mandibular morphospace that are consistent with an evolutionary pattern of basal niche conservatism giving rise to multiple adaptive radiations within nested clades. Correspondence between mandibular geometry and function was explored using a 3D model of spatial relationships among measured parameters, potential forces, and axes of rotation. By combining the model with known loricariid jaw kinematics, we developed explicit hypotheses for how individual parameters might relate to each other during kinesis. We hypothesize that the ratio [AM_area/tooth row length²] predicts interspecific variation in the magnitude of force entering the mandible per unit of substrate contacted during feeding. Other newly proposed metrics are hypothesized to predict variation in aspects of mandibular mechanical advantage that may be specific to Loricariidae and perhaps shared with other herbivorous and detritivorous fishes. 2011. © 2011Wiley Periodicals, Inc.     

THE GENETIC BASIS OF A COMPLEX FUNCTIONAL SYSTEM

The relationship between form and function can have profound effects on evolutionary dynamics and such effects may differ for simple versus complex systems. In particular, functions produced by multiple structural configurations (many‐to‐one mapping, MTOM) may dampen constituent trade‐offs and promote diversification. Unfortunately, we lack information about the genetic architecture of MTOM functional systems. The skulls of teleost fishes contain both simple (lower jaw levers) as well as more complex (jaws modeled as 4‐bar linkages) functional systems within the same craniofacial unit. We examined the mapping of form to function and the genetic basis of these systems by identifying quantitative trait loci (QTL) in hybrids of two Lake Malawi cichlid species. Hybrid individuals exhibited novelty (transgressive segregation) in morphological components and function of the simple and complex jaw systems. Functional novelty was proportional to the prevalence of extreme morphologies in the simple levers; by contrast, recombination of parental morphologies produced transgression in the MTOM 4‐bar linkage. We found multiple loci of moderate effect and epistasis controlling jaw phenotypes in both the simple and complex systems, with less phenotypic variance explained by QTL for the 4‐bar. Genetic linkage between components of the simple and complex systems partly explains phenotypic correlations and may constrain functional evolution.