Migratory Mass Research Articles

Leach's storm petrels Oceanodroma leucorhoa off southern Africa: breeding and migratory status, and measurements and mass of the breeding population

Leach's storm petrel Oceanodroma leucorhoa have bred at Dyer Island since at least 1995; a review of earlier records in the light of this discovery indicates that breeding has almost occurred since at least the 1970s. The South African offshore islands on which Leach's storm petrel almost certainly breeds are Jutten, Dassen, Dyer and St Croix. The South African population is probably of the order of 25 pairs. The migrant component of the Leach's storm petrel population visiting southern Africa is mainly confined to deep ocean waters (generally 2000–5000 m deep) and occurs in particularly high densities around Agulhas Rings where ring-edges apparently provided excellent foraging opportunities. Leach's storm petrels are comparatively scarce over the shelf areas (defined as coastal water of less than 2000 m depth) of Namibia and western South Africa. Given their abundance at sea, their distance offshore, the seasonality of their occurrence and their moult status, these birds cannot be part of the South African breeding population, and must therefore be mainly from colonies of the north Atlantic Ocean. The Leach's storm petrels breeding in South Africa appear to be relatively large, comparable in size to populations breeding in the north Atlantic Ocean. Molecular techniques should be used to determine the most closely related population, and possibly the period for which the South African population has been isolated.

Patterns of Frugivory and Energetic Condition in Nearctic Landbirds during Autumn Migration

Many species of Nearctic landbirds exhibit behavioral plasticity during migration, presumably to compensate for energetic demands of migratory flight. At Block Island, Rhode Island, a northern temperate site, I quantified the extent of one form of behavioral plasticity in Nearctic landbirds: dietary expansion from breeding season insectivory to high levels of frugivory during autumn. I also measured changes in energetic condition of migrants using recapture methods and diurnal regressions of mass change. Based on analyses of 1,568 fecal samples collected from 1993-1995, frugivory during migration was frequent within many species, extensive within individual birds, and widespread among taxa. Migratory species ranged from strict insectivory in the Winter Wren (Troglodytes troglodytes) to 96% fruit by volume in the fecal samples of Rose-breasted Grosbeaks (Pheucticus ludovicianus). Nine of 17 recaptured species demonstrated mass gains between first and last recapture. Only the Red-eyed Vireo (Vireo olivaceus) gained significant mass within a single day, suggesting that the site was suitable for migratory mass gain if a species remained longer than one day. Highly omnivorous species, with greater than one-third of the diet as fruit, gained significantly more mass while on Block Island than did strict insectivores, i.e., species with less than one-third of the diet as fruit. Insectivorous species on average declined in energetic condition during stopover. The extent of frugivory for a species was positively correlated with average change in energetic condition and fat score per day, suggesting that frugivory allowed species to gain mass more efficiently and extensively than exclusive insectivory. I conclude that frugivory in Nearctic landbirds is far more extensive during migration than previously thought, and that dietary plasticity may be an adaptation to energetic demands of migratory flights.

Basal Metabolic Rate and the Mass of Tissues Differing in Metabolic Scope: Migration-Related Covariation between Individual Knots Calidris canutus

To examine whether variability in the basal metabolic rate (BMR) of migrant shorebirds is a function of a variably sized metabolic machinery or of temporal changes in metabolic intensities at the tissue level, BMR, body composition and activity of cytochrome-c oxidase (CCO, a marker for maximum tissue respiration) were measured in 14 captive Knots Calidris canutus islandica in late spring, during the period of mass loss after the migratory body mass peak. Although the body mass cycle of captive birds closely followed the changes of free-living conspecifics, their fat-free mass of muscles and organs was somewhat lower and their fat content higher. BMR significantly declined during mass loss, as did the fat-free dry mass. BMR was an allometric function of both body mass (exponent=0.687) and lean dry mass (exponent=1.132). Fat-free dry mass of heart sind flight muscle decreased with the loss of fat. CCO-activity was determined in heart, flight muscle, leg muscle, liver and kidney. It was highest in heart and flight muscle and low in the other tissues. CCO-activity was not correlated with total fat mass. Intraspecific migration-related variation in BMR seems better explained by variation in the mass of organs with a high metabolic scope (as indicated by high CCO-activity), than by variation in the intensity of tissue metabolism.

Expression of 9-O-acetylated gangliosides during development of the rat olfactory system.

The expression of 9-O-acetylated gangliosides recognized by the Jones monoclonal antibody (mAb) correlates with cell migration and axonal outgrowth in the developing rat nervous system. We studied the expression of these gangliosides during the development and maturation of the rat olfactory system. Beginning on embryonic day 13 (E13) the olfactory epithelium and the migratory mass were intensely stained with Jones mAb. However, though this immunoreactivity disappeared from the olfactory epithelium at E19, it remained in a few fascicles and some glomeruli of the newborn and adult olfactory bulbs. We concluded that the expression of 9-O-acetylated gangliosides by olfactory axons and/or migrating cells may facilitate axonal outgrowth during development and might be involved in the formation of new glomeruli in the mature olfactory bulb.

Formation of an olfactory glomerulus: Morphological aspects of development and organization

We have studied the development of olfactory nerves in the rat from their first contact with the telencephalic vesicle until the formation of glomerular structures in the olfactory bulb at early postnatal period. The study is based on serial semithin and ultrathin sections of material prepared for electron microscopy and antibodies to label radial glial cells, glial fibrillary acidic protein and Rat-401. Beginning on embryonic day 12, developing olfactory axons from the olfactory placode are accompanied by migratory cells, also derived from the olfactory placode, that reach the prospective olfactory bulb by embryonic day 13. The mass of migratory cells accumulate superficial to the telencephalic vesicle. The cells increase in number by mitotic divisions. The majority of these cells represent precursor elements that will later develop into the ensheathing cells of the olfactory nerves and olfactory nerve layer of the adult. Some migratory cells penetrate into the prospective olfactory bulb early during development. The first synaptic contacts of olfactory axons with dendritic processes in the olfactory bulb were observed at embryonic day 18. Glomerular formation is initiated by penetration of cells from the migratory mass into the prospective glomerular layer by embryonic day 20 to postnatal day 0. These cells form walls surrounding zones of high synaptic density forming protoglomeruli. Postnatally, the peripheral processes of radial glial cells branch profusely delimiting glomerular formations and transform into periglomerular astrocytes. Rat-401 stains radial glial cells from embryonic day 14. Immunoreactivity becomes restricted to the olfactory glomeruli during the first postnatal weeks and it virtually disappears by the end of the first postnatal month. We conclude that the early penetration of cells from the migratory mass into the prospective olfactory bulb, observed immediately after the first synaptic contacts were established, initiates the formation of olfactory glomeruli which becomes completed by the transformation of radial glial cells into periglomerular astrocytes.

The contribution of the mesonephros to the development of the sheep fetal testis.

In this study, which was performed on 52 sheep fetuses aged 24 to 85 days, we examined the relationship between testicular development and the "giant" mesonephric nephron, a peculiar structure consisting of a large glomerulus and multiple tubules. The development of the testis occurred in two phases. The preparatory phase began at day 24 of gestation, evolved simultaneously with the involution of the glomerulus of the giant nephron, and was characterized by mobilization of the glomerular cells and by their colonization of the genital ridge. By day 31, a prominent mass of migrating mesonephric cells had developed; it extended uninterrupted from the giant glomerulus into the gonad where the mesonephric cells associated with the germinal cells forming the cellular template from which the testicular cords later became assembled. At complete involution of the glomerulus (day 52), the migratory mass implanted on the tubules of the giant nephron, which thus became continuous with the gonad. During the organizational phase, which began at day 29 with the formation of the tunica albuginea, the various components of this continuum became progressively organized along a testis-to-mesonephros direction into seminiferous cords, tubuli recti, the cords of the rete testis, and the ductules efferentes. These observations show that, in the sheep, the precursors of the Sertoli cells are mesonephric in origin, and that the genital tract proximal to the epididymis differentiates from a single mesonephric nephron.