Growth and the development of sexual size dimorphism in lorises and galagos.

Three fundamental ontogenetic pathways lead to the development of size differences between males and females. Males and females may grow at the same rate for different durations (bimaturism), grow for the same duration at different rates, or grow at a mix of rate and duration differences. While patterns of growth and the development of adult body size are well established for many haplorhines, the extent to which rate and duration differences affect strepsirrhine growth trajectories remains unclear. Here, we present iterative piecewise regression models that describe the ontogeny of adult body mass for males and females of five lorisoid species (i.e., lorises and galagos) from the Duke Lemur Center. We test the hypotheses that, like most haplorhines, sexual size dimorphism (SSD) is a result of bimaturism, and males and females of monomorphic species grow at the same rate for a similar duration. We confirm that the galagos in this sample (Galago moholi and Otolemur garnettii) show significant SSD that is achieved through bimaturism. Unlike monomorphic lemurids, the lorises in this sample show a diversity of ontogenetic patterns. Loris tardigradus does follow a lemur-like trajectory to monomorphism but Nycticebuscoucang and Nycticebus pygmaeus achieve larger adult female body sizes through a mixture of rate and duration differences. We show that contrary to previous assumptions, there are patterns of both similarity and difference in growth trajectories of comparably sized lorises and galagos. Furthermore, when ontogenetic profiles of lorisoid and lemurid growth are compared, it is evident that lorisoids grow faster for a shorter period of time.

Allometry and evolution in the galago skull.

To probe the ontogenetic bases of morphological diversity across galagos, we performed the first clade-wide analyses of growth allometries in 564 adult and non-adult crania from 12 galagid taxa. In addition to evaluating if variation in galago skull form results from the differential extension/truncation of common ontogenetic patterns, scaling trajectories were employed as a criterion of subtraction to identify putative morphological adaptations in the feeding complex. A pervasive pattern of ontogenetic scaling is observed for facial dimensions across galagids, with 2 genera also sharing relative growth trajectories for masticatory proportions (Galago, Galagoides). As the facial growth series and adult data are largely coincidental, interspecific variation may result from character displacement and consequent selection for size differentiation among sister taxa. Derived configurations of the jaw joint and jaw muscle mechanical advantage in Otolemur and Euoticus appear to facilitate increased gape during scraping behaviors. Differences in aspects of masticatory growth and form characterizing these 2 genera highlight selection to uncouple shared ontogenetic patterns, which occurred via transpositions that retained ancestral scaling patterns. Due to the lack of increased robusticity of load-resisting mandibular elements in Otolemur and Euoticus, there is little evidence to suggest that exudativory in galagos results in correspondingly higher masticatory stresses.

Limb growth in captive Galago senegalensis: getting in shape to be an adult.

Since primate infants are not simply miniature adults, adult shape results from differential growth patterns of individual body segments. Initially an infant relies on its mother for transportation, and later begins independent locomotion. Skeletal growth patterns must meet the functional demands of independent locomotion. In this study we sought to determine whether Galago senegalensis braccatus follow the general primate pattern of decreasing intermembral index (IMI) throughout ontogeny. We also asked whether ontogenetic attainment of adult limb proportions coincides with attainment of independent locomotion, i.e., do infants reach adult limb proportions near the time they begin independent locomotion (approximately 7 weeks of age)? Mixed-longitudinal data were taken from a sample of 10 captive-born Galago senegalensis. Linear lengths of the trunk, arm, forearm, thigh, and leg were measured in the animals from birth until they were approximately 500 days old. The IMI and the ratio of each limb segment to both trunk length and the cube root of body mass were calculated. The results of a Mann-Whitney Wilcoxon rank-sum test for unmatched samples indicate that G. senegalensis do exhibit the primate pattern of decreasing IMI throughout ontogeny, and that the IMIs of infants at the time of initial locomotor independence are significantly higher than those of adult IMIs. Some (but not all) measures of relative limb lengths differed between neonates or 7-week-old infants and adults. Therefore, the hypothesis that infants acquire adult limb proportions by the time they begin independent locomotion is not supported by this study. The current results indicate that ontogenetic shape changes in galagos are a complex process and apparently cannot be explained by simple initial locomotor competency.

Effects of monocular deprivation on the morphology of retinogeniculate axon arbors in a primate.

Previous studies of the monocularly deprived (lid-sutured) primate (Galago crassicaudatus) have shown that magnocellular (M) and parvocellular (P) lateral geniculate nucleus (LGN) cells that receive input from the deprived eye are smaller than counterparts that receive input from the nondeprived eye; deprived koniocellular (K) cells show wide variability in size, but they do not differ from their nondeprived counterparts (Casagrande and Joseph, '80). Although deprivation results in cell-size changes, the physiological properties of deprived LGN cells do not change from normal (that is, P cells have normal X-like properties, M cells have normal Y-like properties, and K cells have normal W-like properties). Because of these findings, we were interested in determining how the morphology of retinogeniculate axon arbors is affected by deprivation. To this end, 104 horseradish-peroxidase-filled retinogeniculate arbors from galagos deprived from birth to maturity were completely reconstructed within the binocular segment of the LGN. These arbors were qualitatively and quantitatively compared with 56 arbors reconstructed from normal galagos as part of another study (Lachica and Casagrande, '88). Our main findings are as follows. Deprived M and P arbors are affected by deprivation in the same general manner: compared with normal arbors, they are altered in shape (rather than being round or columnar, respectively, both groups have terminals that are elongated parallel to laminar borders); they are smaller in area, and they have fewer boutons but innervate the LGN with a greater density of boutons. K arbors are affected by deprivation in the same manner, but less severely. Finally, our results show that nondeprived arbors are also affected by eyelid suture. Specifically, all nondeprived arbor groups are smaller in area than normal and possess more boutons/mm3. We interpret these changes in the morphology of deprived retinogeniculate axons to suggest that abnormal competitive interactions begin by affecting primarily immature LGN cells and their axons and that the retinogeniculate axons presynaptic to these cells experience secondary degenerative effects. Our results also show that similar manipulations of visual experience can result in changes that are not necessarily comparable across species such as cats and primates.

Embryonic epsilon and gamma globin genes of a prosimian primate (Galago crassicaudatus). Nucleotide and amino acid sequences, developmental regulation and phylogenetic footprints.

Sequence analysis of epsilon and gamma genes and encoded globins and high-pressure liquid chromatography analysis of globin compositions in blood hemolysates obtained from embryos, fetuses and adults show that the prosimian primate Galago crassicaudatus expresses its epsilon and gamma genes only embryonically. Since rabbit, mouse and galago all have embryonic gamma genes but simian primates have fetal gamma genes, we conclude that gamma E evolved into gamma F in stem-simians. An elevated non-synonymous substitution rate characterizes this transition. The alignment of epsilon and gamma nucleotide sequences and the parsimoniously reconstructed evolutionary history of these sequences identify several anciently conserved cis-regulatory elements (phylogenetic footprints) important for gamma expression in primates and also cis-mutations which may have been involved in the recruitment of the gamma gene to a fetal program in simian primates.

Scaling of growth and life history traits relative to body size, brain size, and metabolic rate in lorises and galagos (Lorisidae, primates).

A broad range of variation in body size, brain size, and metabolic rate occurs within the primate family Lorisidae, thus providing an opportunity to examine the relationship of these three parameters to variation in growth and life history traits. Data on adult body weight, gestation length, lactation length, age at first estrus, litter size, and growth parameters were collected from a captive colony of four lorisid species, Loris tardigradus, Nycticebus coucang, Galago crassicaudatus, and G. senegalensis. The data presented here constitute the most complete life history information available for these poorly understood prosimian species. Correlation and allometric analyses were performed to determine the relationships between variables. Among the lorisids studied, adult body weight, adult cranial capacity, and relative cranial capacity did not predict variation in life history traits. Adult basal metabolic rate predicted most of the variability in gestation length, lactation length, and growth parameters. Lorisines differ from similarly sized galagines in having lower basal metabolic rates, slower growth rates, slower developmental rates, and smaller litter sizes, resulting in reduced reproductive potential. This may be a consequence of lorisine adaptation to a diet of toxic insects. Metabolic rate and diet may be among the most important parameters to examine in any study of life history evolution.

Morphological effects of monocular deprivation and recovery on the dorsal lateral geniculate nucleus in galago.

The effects of monocular lid-suture deprivation on development were evaluated by measurement of cell sizes in the lateral geniculate nuclei of six deprived and three normally reared galagos. In all animals autoradiographic demonstration of the retino-thalamic projections from one eye was used to define the lamination and distinguish the monocular from the binocular segment of the nucleus. Our results indicate that monocular deprivation significantly affects cell growth in both the binocular and monocular geniculate segments, with the greater change occurring in the binocular segment, suggesting that both visual experience and binocular competitive interactions influence geniculate cell growth in these primates. In animals forced to use their deprived eye for 2 months or more by reverse suturing, disparity of cell sizes is reduced in the monocular segment, while differences in binocular segment cell sizes are maintained. Our results also show that monocular deprivation with or without later reverse suture has an unequal influence on different geniculate layers, such that cells in laminae 4 and 5 are not as severely affected as the remaining layers. This differential influence could relate either to the unique pattern of projection of these layers to cortex or to functional differences between layers.