Enamel Microstructure of Rodent Molars, Classification, and Parallelisms, with a Note on the Systematic Affiliation of the Enigmatic Eocene Rodent Protoptychus

To investigate the diversity of the enamel structures in rodent molars, the schmelzmuster of more than 270 genera from the various fossil and extant groups was investigated. Only three basic types of schmelzmuster were recognized. The most prominent one, the C-type, is characterized by a basal ring of lamellar enamel (BRLE) surrounding the molars at the base of the crown. It occurs in most murids (cricetids) and other Myodonta. It is shared by the Dipodidea, Eomyidae, Geomyidae, and Gliridae. The C-type schmelzmuster was not found in any of the other rodents groups (Sciuromorpha, Anomaluromorpha, Sciuravida, Hystricognathi, Bathyergomorphi, and Caviida). Despite the rare occurrence of the P-type schmelzmuster with radial enamel only, most of these rodents have thick Hunter–Schreger bands (HSB) in their molars (S-type schmelzmuster). Although the C-type schmelzmuster is strictly limited to the Myomorpha (sensu McKenna and Bell), the fossil record shows that this structure does not form a synapomorphy but developed in parallel mostly from the P-type, but in Gliridae from the S-type schmelzmuster. On the basis of molar and incisor enamel the systematic position of Protoptychus can be evaluated.     

Functional symmetries in the schmelzmuster and morphology of rootless rodent molars

Morphology and schmelzmuster of rootless cheek teeth of 25 extant rodent genera were studied in relation to jaw movement. A differentiation between leading and trailing edges is observed regularly in enamel thickness and schmelzmuster. Similarities between antagonists are interpreted as 'functional symmetries'. Differences in the enamel thickness, the schmelzmuster and orientation of cutting edges are controlled by functional and phylogenetic constraints. The heterogenous sample allows discrimination between these two constraints. The most obvious functional constraint leads to the almost regular occurrence of radial enamel on the push sides of cutting edges. The degree of functional symmetry seems to be determined by phylogenetic limitations.     

First report of rodents from the late Hemphillian (late Miocene) Zwiebel Channel and a revised late Neogene biostratigraphy/biochronology of the Sand Draw area of Nebraska

A new late Hemphillian (late Miocene) rodent assemblage is reported from Zwiebel Channel, a channel cut into underlying Ash Hollow Miocene sediments along Sand Draw, Brown County, Nebraska. This locality extends the temporal range of rodent history in the Sand Draw area. A new biostratigraphic hypothesis proposes that previously described assemblages with Ogmodontomys are older than those with Ophiomys, as is the case in the Meade Basin of southwestern Kansas. Consequently, two Pliocene temporal zones are recognised. Based on a phylogenetic analysis of Ophiomys, rodent biostratigraphy, and paleomagnetic profiles, Sand Draw assemblages with Ogmodontomys are considered to have been deposited about 3.0–2.8 Ma, while those with Ophiomys were laid down between about 2.8–2.5 Ma. The 1.6 Ma date previously suggested for Ophiomys parvus from Froman Ferry, Idaho is probably too young; it is more likely that O. parvus became extinct in Idaho prior to the North American Microtus immigration event at about 2.0 Ma, inhabiting the Snake River basin until around 2.2 Ma.     

Dental wear,wear rate,and dental disease in the African apes

The African apes possess thinner enamel than do other hominoids, and a certain amount of dentin exposure may be advantageous in the processing of tough diets eaten by Gorilla. Dental wear (attrition plus abrasion) that erodes the enamel exposes the underlying dentin and creates additional cutting edges at the dentin‐enamel junction. Hypothetically, efficiency of food processing increases with junction formation until an optimal amount is reached, but excessive wear hinders efficient food processing and may lead to sickness, reduced fecundity, and death. Occlusal surfaces of molars and incisors in three populations each of Gorilla and Pan were videotaped and digitized. The quantity of incisal and molar occlusal dental wear and the lengths of dentin–enamel junctions were measured in 220 adult and 31 juvenile gorilla and chimpanzee skulls. Rates of dental wear were calculated in juveniles by scoring the degree of wear between adjacent molars M1 and M2. Differences were compared by principal (major) axis analysis. ANOVAs compared means of wear amounts. Pearson correlation coefficients were calculated to compare the relationship between molar wear and incidence of dental disease. Results indicate that quantities of wear are significantly greater in permanent incisors and molars and juvenile molars of gorillas compared to chimpanzees. The lengths of dentin–enamel junctions were predominantly suboptimal. Western lowland gorillas have the highest quantities of wear and the most molars with suboptimal wear. The highest rates of wear are seen in Pan paniscus and Pan t. troglodytes, and the lowest rates are found in P.t. schweinfurthii and G. g. graueri. Among gorillas, G. b. beringei have the highest rates but low amounts of wear. Coefficients between wear and dental disease were low, but significant when all teeth were combined. Gorilla teeth are durable, and wear does not lead to mechanical senescence in this sample. Am. J. Primatol. 72:481–491, 2010. © 2010 Wiley‐Liss, Inc.     

The Enamel Microstructure of the Early Eocene Pantodont Coryphodonand the Nature of the Zigzag Enamel

An additional method for the investigation of the microstructure of enamel is described using the teeth of Coryphodon, Uintatherium, Entelodon, and Crocuta. Under low magnification natural surfaces or sections of teeth display details of the enamel microstructure when the light guide effect of prisms is used. Under the same low magnification even more details were obtained from sputter-coated surfaces of sections. The method is of particular significance for the investigation of large teeth with thick enamels when structures are somewhat irregular. The new method provides a better general survey, where scanning electron microscope images often show confusing details. The enamel of Coryphodon shows oblique lines of nested chevrons that are similar, to some degree, to the zigzag enamel in Crocuta, but a distinct asymmetry between ascending and descending lineaments was observed. This specific Coryphodon -enamel was also found in Uintatherium and Entelodon. This enamel type, which evolved several times in parallel, cannot be attributed to a specific diet, but must be regarded as one of the several ways to strengthen the enamel against breakage.     

The enamel microstructure ofAnchitheriomys (Rodentia, Mammalia) in comparison with that of other beavers and of porcupines

In the enamel microstructure of the incisors, porcupines (Hystricidae) are characterized by multiserial Hunter-Schreger bands (HSB) while beavers (Castoridae) basically have uniserial HSB. In addition, two groups can be differentiated among beavers based on enamel microstructure.Palaeocastor, Steneofiber andCastor show rather typical uniserial HSB. OnlyCastor shows a slight tendency of fusion of the bands. In contrast,Trogontherium andCastoroides are characterized by the regular occurrence of fused bands.Anchitheriomys, having uniserial HSB and a high frequency of fused bands fits well with theTrogontherium group, proving the castorid nature ofAnchitheriomys. Furthermore, the enamel differentiation observed among the Castoridae thus provides an important character for further systematic subdivision of the beavers. In the enamel of the cheek teeth, porcupines can be told apart from beavers as well.Anchitheriomys shows a two-layered schmelzmuster with inner radial enamel like other beavers. Porcupines have thick HSB throughout the enamel layer. This character in the cheek teeth facilitates the separation of isolated beaver teeth from porcupine teeth.     

Stable carbon and oxygen isotopes in human tooth enamel: Identifying breastfeeding and weaning in prehistory

This paper investigates the utility of stable carbon and oxygen isotopes in human dental enamel to reveal patterns of breastfeeding and weaning in prehistory. Enamel preserves a record of childhood diet that can be studied in adult skeletons. Comparing different teeth, we used δ¹³C to document the introduction of solid foods to infant diets and δ¹⁸O to monitor the decline of breastfeeding. We report enamel carbonate δ¹³C and δ¹⁸O of 33 first molars, 35 premolars, and 25 third molars from 35 burials from Kaminaljuyú, an early state in the valley of Guatemala. The skeletons span from Middle Preclassic through Late Postclassic occupations, ca. 700 B.C. to 1500 A.D. Sections of enamel were removed from each tooth spanning from the cusp to the cemento-enamel junction. Stable isotope ratios were measured on CO₂ liberated by reaction of enamel with H₃PO₄ in an automated carbonate system attached to a VG Optima mass spectrometer. Within a skeleton, teeth developing at older ages are more enriched in ¹³C and more depleted in ¹⁸O than teeth developing at younger ages. Premolars average 0.5% higher in δ¹³C than first molars from the same skeleton (P = 0.0001), but third molars are not significantly enriched over premolars. The shift from first molars to premolars may be due to the shift to solid foods from lipid-rich milk. After 2 years, when premolars begin to mineralize, the δ¹³C in childhood diets did not change systematically. First molars and premolars are similar in δ¹⁸O, but third molars average 0.7% lower than first molars (P = 0.0001) and 0.5% lower than premolars (P = 0.0003). First molar and premolar δ¹⁸O is heavier, because breast milk is more enriched in ¹⁸O than is drinking water. Hence, many children continued to nurse during the period of premolar formation. Together, these results indicate that Kaminaljuyú children had begun to eat solid maize foods before the age of 2 years but continued to drink breast milk until much later. Am J Phys Anthropol 106:1–18, 1998. © 1998 Wiley-Liss, Inc.     

A new suiform (Artiodactyla,Mammalia) from the Early Miocene of East Africa

Fossils of an unnamed large suiform have been recovered from two Early Miocene localities in East Africa. The material is distinct from other species of the suborder, including the anthracothere Brachyodus aequatorialis, which is of similar size. The upper molars of the new form are bunodont, quadricuspidate (with a tiny paraconule), and have no buccal styles (parastyle, mesostyle, metastyle) and the enamel is thin and lightly wrinkled to smooth, which contrasts strongly with upper molars of Brachyodus which are pentacuspidate, selenodont, have pervasively wrinkled enamel and well-developed parastyle, mesostyle and metastyle. A new genus and species is erected for this suiform, which is most likely an anthracothere.     

Unique differentiation of radial enamel in Arsinoitherium (Embrithopoda,Tethytheria)

The enamel microstructure in molars of Arsinoitherium is reinvestigated and a new modification of radial enamel (RE), ‘arsinoitheriid radial enamel (ARE)’, is defined. It is characterised by alternating stripes with different organisation of the interprismatic matrix but no prism decussation. Recognition of this new subtype leads to a reinterpretation of structure previously identified as modified radial enamel and of Hunter–Schreger bands in Arsinoitherium. The newly differentiated ARE of Arsinoitherium is more derived in relation to corresponding microstructures of Palaeoamasia and Crivadiatherium. A careful reinvestigation of RE in other Paenungulata will be required to provide additional data bearing on phylogenetic reconstruction. The enamel of Phenacolophus argues against inclusion of this genus in the Embrithopoda.     

Dentition ofSivaladapis nagrii (Adapidae) from the late Miocene of India

Two genera and three species of adapid primates are known from the middle and late Miocene of India and Pakistan. Most fossil specimens are fragmentary, but the best-known species, Sivaladapis nagrii,is now represented by enough specimens to permit composite reconstruction of much of the dentition. The incisors of Sivaladapishave spatulate crowns, and the canines are large, projecting teeth. Premolars and molars exhibit complex occlusion involving simultaneous approximation of pointed leading cusps on upper and lower molars, with linear trailing lophs. The premolar eruption sequence in Sivaladapisappears to be P ₂-P₄-P₃, as in most extant prosimians. Symphyseal fusion of the mandibular rami occurred early in ontogeny, before the eruption of any of the anterior permanent teeth. We interpret Sivaladapisto have been a specialized arboreal folivore that became extinct near the end of the Miocene, when the distribution of forests was increasingly restricted and colobine monkeys first invaded South Asia.     

Coexistence of predatoryMuscina stabulans andophyra aenescens [Dipt.: Muscidae] with dipterous prey in poultry manure

Significant relationships between the emergence of adult predatory species,Ophyra aenescens (Wiedemann) andMuscina stabulans (Fallen) and prey,Musca domestica L.,Fannia femoralis (Stein) andF. canicularis (L.) existed on 10 poultry ranches in southern California. Predatory species may function in natural control at intervals throughout the year, especially on predominant prey,F. femoralis andF. canicularis. Dipterous species, especiallyO. aenescens andF. femoralis, were only moderately influenced by the surface area of breeding habitat available. Accuracy in the measurement of population trends in Diptere may be enhanced by increasing the number of samples at any given ranch rather than the addition of study ranches. Parasitism, ranging from 22.6–37.8% of collected puparia, involved principally 3 species,Muscidifurax zaraptor Kogan & Legner,M. raptor Girault & Sanders andSpalangia cameroni Perkins.      

Enamel Structure of Cuvieronius hyodon (Proboscidea, Gomphotheriidae) with a Discussion on Enamel Evolution in Elephantoids

Dental material of the South American elephantoid Cuvieronius hyodon from the Late Pleistocene of the Tarija Basin, Bolivia was sampled for a comprehensive analysis of the microstructure of the enamel. To examine variability at the dentition level, enamel samples of the upper incisor, second deciduous premolar, and molars were sectioned. The incisor and cheek teeth enamel is compared to that of other proboscideans in order to reveal phylogenetically and functional informative features useful to reconstruct the evolution of elephantoid enamel. Studies of the adaptations and evolution of proboscidean enamel have focused so far on molars. Nevertheless, given the possibility of an independent evolution of the enamel at different tooth positions, the variation of the enamel throughout the dentition needs to be taken into consideration when using enamel microstructural characters to infer proboscidean diversity and phylogeny. The results obtained from this study demonstrate the generality, among elephantoids, of the basic microstructural features of Cuvieronius hyodon enamel, allowing the characterization of the Elephantoid Enamel (EE). The differentiation between incisor and molar enamel seen in elephantoids is shown to represent a primitive elephantiform trait, as it also occurs in Phiomia. The three-layered enamel of the cheek teeth appears as the sole synapomorphy of the Elephantoidea, though the character might be homoplastic within the Proboscidea. Characters of the prisms cross-section might be used, on the other hand, to define less inclusive clades within the Elephantoidea.     

Tooth Wear Difference Between the Yuanmou Hominoid and <Emphasis Type="Italic">Lufengpithecus</Emphasis>

The Late Miocene hominoids recovered from Lufeng (Lufengpithecus) and Yuanmou of Yunnan Province, China, are among the most numerous hominoid fossils in Eurasia. They have yielded critical evidence for the evolutionary history, biogeography and paleobiology of Miocene hominoids. We examined and compared the wear pattern and differences of 804 molars of the Yuanmou hominoid and Lufengpithecus. Our results indicate that both the upper and lower molars of the Yuanmou hominoids were more heavily worn than those of Lufengpithecus. The wear patterns of the individual molars between the Yuanmou hominoid and Lufengpithecus also are different. The heaviest wear of lower molars of the Yuanmou hominoid occur in M₂, followed by M₁ and M₃. In Lufengpithecus, M₁ and M₃ were more heavily worn than M₂. There are differences in wear between the upper and lower molars for the two hominoids. Among the various factors related to tooth wear, we suggest that the main reason for the tooth wear differences between the Yuanmou hominoid and Lufengpithecus may be that they had different diets. More soft dietary items like leaves and berries were probably consumed by Lufengpithecus, and the Yuanmou hominoid may mainly have feed on harder or frugivorous diets. This result complements findings from previous studies of tooth size proportion, and the development of lower molar shearing crests in the 2 samples. Enamel thickness, living environment, behavior patterns, and population structure also might account for dental wear differences between the Yuanmou hominoid and Lufengpithecus.     

Some observations on enamel thickness and enamel prism packing in the miocene hominoid Otavipithecus namibiensis

Otavipithecus namibiensis is currently the sole representative of a Miocene hominoid radiation in subequatorial Africa. Several nondestructive techniques, such as computed tomography (CT) and confocal microscopy (CFM), can provide useful information about dental characteristics in this southern African Miocene hominoid. Our studies suggest that the molars of Otavipithecus are characterized by (1) thin enamel and (2) a predominance of pattern 1 enamel prism. Together, these findings provide little support for the recent suggestion of an Afropithecini clade consisting of Otavipithecus, Heliopithecus, and Afropithecus. Instead, they lend some (though not conclusive) support to the suggestion of an Otavipithecus/African ape clade distinct from Afropithecus. © 1995 Wiley-Liss, Inc.     

Pronghorn (Antilocapra americana) enamel phosphate δ18O values reflect climate seasonality: Implications for paleoclimate reconstruction

Stable oxygen isotope (δ¹⁸O) compositions from vertebrate tooth enamel are widely used as biogeochemical proxies for paleoclimate. However, the utility of enamel oxygen isotope values for environmental reconstruction varies among species. Herein, we evaluate the use of stable oxygen isotope compositions from pronghorn (Antilocapra americana Gray, 1866) enamel for reconstructing paleoclimate seasonality, an elusive but important parameter for understanding past ecosystems. We serially sampled the lower third molars of recent adult pronghorn from Wyoming for δ¹⁸O in phosphate (δ¹⁸O_PO4) and compared patterns to interpolated and measured yearly variation in environmental waters as well as from sagebrush leaves, lakes, and rivers (δ¹⁸O_w). As expected, the oxygen isotope compositions of phosphate from pronghorn enamel are enriched in ¹⁸O relative to environmental waters. For a more direct comparison, we converted δ¹⁸O_w values into expected δ¹⁸O_PO4* values (δ¹⁸O_W‐_PO4*). Pronghorn δ¹⁸O_PO4 values from tooth enamel record nearly the full amplitude of seasonal variation from Wyoming δ¹⁸O_W‐PO4* values. Furthermore, pronghorn enamel δ¹⁸O_PO4 values are more similar to modeled δ¹⁸O_W‐PO4* values from plant leaf waters than meteoric waters, suggesting that they obtain much of their water from evaporated plant waters. Collectively, our findings establish that seasonality in source water is reliably reflected in pronghorn enamel, providing the basis for exploring changes in the amplitude of seasonality of ancient climates. As a preliminary test, we sampled historical pronghorn specimens (1720 ± 100 AD), which show a mean decrease (a shift to lower values) of 1–2‰ in δ¹⁸O_PO4 compared to the modern specimens. They also exhibit an increase in the δ¹⁸O amplitude, representing an increase in seasonality. We suggest that the cooler mean annual and summer temperatures typical of the 18th century, as well as enhanced periods of drought, drove differences among the modern and historical pronghorn, further establishing pronghorn enamel as excellent sources of paleoclimate proxy data.     

A microscopic investigation of enamel in wombat (Vombatus ursinus)

Summary A study of the enamel of continuously growing Vombatus ursinus molars was carried out using the techniques of light microscopy, hardness testing, scanning electron microscopy and transmission electron microscopy. From the erupted end to within 8 mm of the growing end, mature enamel was observed and it was found that between comparable areas there were no significant ultrastructural differences in enamel; however, small (12nm diameter), loosely packed needle-like crystals characteristic of developing enamel were observed near the growing end. Mature enamel was found to consist of three optically-translucent regions interleaved with two opaque regions. Opaque enamel was softer than translucent enamel. The opacity and relative softness characteristic of two of the enamel regions was not related to prism pattern or orientation; it was, however, related to the presence of voids (28 nm diameter) in these regions.     

The Lectin from the Crustacean Liocarcinus depurator Recognizes O-acetylsialic Acids

A lectin that recognized sialic acids and agglutinated mouse erythrocytes was purified from hemolymph of the crab Liocarcinus depurator. It consisted of 38-kDa subunits and had a pI about 6.0. The specificity of the lectin was assayed by hemagglutination inhibition. N-acetylneuraminic acid (Neu5Ac) was a good inhibitor and its N-acetyl group at C-5 was critical for lectin-ligand interaction. Substitution of the C-9 hydroxyl on Neu5Ac with an O-acetyl group (9-O-Ac-Neu5Ac) increased the inhibitory potency of this molecule. Furthermore, O-acetyl substitution of all the hydroxyl groups yielded even better inhibitors (2,4,7,8,9-O-Ac-Neu5Ac and its 1-O-methyl ester). Removal of the hydroxyl or O-acetyl group connected to C-2 reduced the potency of these inhibitors. The lectin agglutinated and stimulated human but not mouse lymphocytes. It was also inhibited by Escherichia coli (O111:B4) lipopolysaccharide and agglutinated specific gram-negative bacteria. In vitro labeling with [³⁵S]methionine indicated that the lectin was synthesized in hepatopangreas of L. depurator. Immunofluorescence showed that among hemocytes it localized mainly in the large-granule population.     

Use of asymmetric somatic hybridization for transfer of the bacterial blight resistance trait from Oryza meyeriana L. to O. sativa L. ssp. japonica

Bacterial blight is one of the major diseases affecting rice productivity. To improve the resistance of cultivated rice to bacterial blight, we introduced a bacterial blight resistance trait from Oryza meyeriana, a wild rice species, into an elite japonica rice cultivar (Dalixiang) using asymmetric somatic hybridization. One hundred and thirty-two independent lines were regenerated. The hybrid plants possessed several morphological features of the donor species, O. meyeriana. Random amplified polymorphic DNA analysis revealed that hybrid plants exhibited banding patterns derived from their parental genotypes. For the majority of the hybrids, resistance to bacterial blight pathogens was intermediate to that observed for O. meyeriana and O. sativa (cv. Dalixiang). Four of the hybrid lines exhibited a high bacterial blight resistance, but it was less than that observed for O. meyeriana. These results demonstrate that O. meyeriana can be used as a good genetic source for improving bacterial blight resistance in commercial rice cultivars through asymmetric somatic hybridization.Abbreviations 2,4-D: 2,4-Dichlorophenoxyacetic acid - IOA: Iodoacetamide - NAA: -Naphthaleneacetic acid - PEG: Polyethylene glycol Communicated by P. Lakshmanan     

MOLAR OCCLUSION IN LATE TRIASSIC MAMMALS

1. A new genus and species of late Triassic mammal, Megazostrodon rudnerae, from Lesotho in southern Africa is described. The molars are similar to those of the British Eozostrodon parvus except that they are slightly larger and the upper molars have a large external cingulum supporting well-developed cusps. 2. Molar occlusion is discussed in two groups of late Triassic mammals: Eoxostrodon and the closely related Megazostrodon on one the hand and the unnamed primitive symmetrodonts on the other. It is shown that in Eoxostrodon the upper and lower molars did not have matching occlusal surfaces upon eruption but that wear produced matching occlusal surfaces. These surfaces are confined to the internal surface of the upper molars and the external surface of the lower molars and form a series of wide-angled triangles. The main cusp of an upper molar occluded between the main and posterior subsidiary cusp of the lower molar and the main cusp of the lower molar occluded between the main and anterior subsidiary cusp of the upper molar, 3. It is shown that the molars of Docodon and HaIdanodon were possibly derived from those of a primitive mammal such as Eozostrodon. The transition involved the development on the upper molars of an internal extension which, as it increased in size, established contact with the dorsal surfaces of two adjacent lower molars. The process involved is fundamentally different from that leading to tribosphenic molars. 4. In Megaxostrodon the main cusp of the upper molars occluded between the posterior and anterior subsidiary cusps of two adjacent lower molars, i.e. more posteriorly than in Eozostrodon. Primitive Rhaetic symmetrodonts were derived from mammals which had this type of occlusion and which were also closely related to Eoxostrodon and Megaxostrodon. The transition involved a rotation of the subsidiary cusps of the upper molars externally and those of the lower molars internally. This rotation increased the shearing surfaces between occluding upper and lower molars. Cusp rotation was carried further in the acute-angled symmetrodonts (Peralestes and Spalacotherium) and pantotheres. It appears that marked cusp rotation was coupled with the acquisition of transverse movements of the lower jaw during mastication. Transverse movement was apparently not possible in cynodonts, in Eoxostrodon (and related forms) and in Docodon. 5. The evolution of therian molars involves cusp rotation as originally proposed by the Cope—Osborn theory. Criticisms of the Cope—Osborn theory are re-evaluated in light of the new late Triassic material. 6. In Rhaetic symmetrodonts, molar wear produces matching occlusal facets, but the amount of attrition necessary to produce these facets was considerably less than in Eoxostrodon. In acute-angled symmetrodonts and in pantotheres, the molars erupt with more precise occlusal surfaces and attrition was not necessary to produce matching surfaces. 7. On the basis of the structure of the molar teeth it was concluded that Eozostrodon, Megazostrodon and Erythrotherium were closely related to the Rhaetic symmetrodonts. Slightly different occlusal relationships between upper and lower molars indicated that in these early mammals constant occlusal relations were being established. 8. Primitive cynodonts, such as Thrinaxodon, are characterized by alternate tooth replacement; there is a total lack of a constant occlusal relationship between upper and lower postcanine teeth. In Thrinaxodon individual postcanines were replaced several times. The crown structures of successive generations of postcanines were different so that a freshly erupted postcanine tooth had a crown structure quite distinct from the tooth which it replaced. It has been shown that the crown structure of one of the generations of postcanine teeth of Thrinaxodon is almost identical to that of Eozostrodon except that Thrinaxodon postcanines have a single root, On the basis of this similarity and the over-all structure of the primitive cynodont skull, it was concluded that Rhaetic mammals (excluding ictidosaurs and haramyids) could be derived from primitive cynodonts. 9. All the orders of Jurassic mammals (with the possible exception of multituber-culates) were probably derived from late Triassic mammals. The apparent close relationship of late Triassic mammals is evidence of a monophyletic origin of this class.