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The geographical scale factor in orientation of migrating birds

Migration routes of birds throw light on orientation performance at different geographic scales, over distances ranging from a few kilometres to more than 104 km. Detailed knowledge about the flight routes may be used to test predictions about optimal orientation according to theoretical principles and about the use of compasses based on celestial or magnetic cues. Ringing recoveries demonstrate that the migratory journey of many species, such as the wheatear and willow warbler, is divided into successive legs with different main orientation. Autumn and spring migration routes are often different, sometimes diverging on a continental scale. Aerial radiotracking of whooping cranes in North America and satellite tracking of brent geese migrating from Iceland across the Greenland ice cap point to the significant role of large-scale topography for the shaping of migration routes. Compass and position control are also required, e.g. during long passages across featureless sea or ice, but how these elements are integrated into the birds' orientation system remains unclear. Radar studies from the Arctic Ocean illustrate the importance of map projections for interpreting flight paths and suggest that birds accomplish approximate great circle orientation. Gradual course changes shown by migrating knots monitored by radar in Scandinavia are at variance with expected changes if the birds were to use a star, sun or magnetic compass over longer distances. Accurate recording of short flight segments shows how flying birds respond to visual, audible and electromagnetic cues, and also documents orientation precision and capacity to integrate rapidly shifting courses into a consistent resulting orientation. Analyses of flight patterns are crucial for understanding how birds find and follow their migration routes over different ranges of geographical scale.

Journal Article↗

Migration of luteinizing hormone-releasing hormone (LHRH) neurons in early human embryos.

Luteinizing hormone-releasing hormone (LHRH) neurons originate in the epithelium of the medial olfactory pit and migrate from the nose into the forebrain along nerve fibers rich in neural cell adhesion molecule (N-CAM). The present study examined the ontogenesis of LHRH neurons in early human embryos and found a similar pattern of development of these cells. Luteinizing hormone-releasing hormone immunoreactivity was detected in the epithelium of the medial olfactory pit and in cells associated with the terminal-vomeronasal nerves at 42 (but not 28-32) days of gestation. The migration route of these cells was examined with antibodies to N-CAM and antibodies to polysialic acid (PSA-N-CAM), which is present on N-CAM at certain stages of development. Neural cell adhesion molecule immunoreactivity was present in a population of cells in the olfactory placode of the earliest embryos examined (28-32 days) and later (42 and 46 days) throughout the migration route. The PSA-N-CAM immunoreactivity was not detected until 42 days and was present in a more limited distribution in nerve fibers streaming from the olfactory placode and along the caudal part of the migration route below the forebrain. Previous studies have indicated that the highly sialated form of N-CAM is less adhesive. The PSA-N-CAM may therefore facilitate the migration of these cells by lessening the adhesion between the fascicles that make up the migration route, expediting the passage of cords of LHRH cells between the nerve fibers as these cells move toward the brain.

Antibodies, Monoclonal↗

Antibody to neural cell adhesion molecule can disrupt the migration of luteinizing hormone-releasing hormone neurons into the mouse brain.

The neurons which synthesize and release luteinizing hormone-releasing hormone (LHRH), are hypothesized to originate in the epithelium of the medial olfactory pit and to migrate into the brain along a scaffolding made up of neural cell adhesion molecule (NCAM)-immunoreactive branches of the terminal and vomeronasal nerves. These LHRH neurons, studied by immunocytochemical and autoradiographic procedures, were found to originate within a very short period of embryogenesis, specifically day 10, in mice, and to follow a remarkably ordered spatiotemporal course along the migration route into the brain. The purpose of the present experiments was to determine whether perturbation of the NCAM-immunoreactive migration route, at a particular time in development, would arrest the migration of LHRH neurons into the brain. We found that a 1 microliter injection of antiserum to NCAM into the area of the olfactory pit, on day 10 of embryogenesis, significantly reduced the number of LHRH-immunoreactive neurons seen in the epithelium of the medial olfactory pit, with a concomitant significant reduction in the number of LHRH-immunoreactive cells seen outside of the placode, on the migration route. These results confirm our initial hypothesis that LHRH neurons migrate from the epithelium of the olfactory pit to the brain and indicate that NCAM plays a causal role in this phenomenon.

Animals↗

Human malignant astrocytoma xenografts migrate in rat brain: a model for central nervous system cancer research.

Fresh cells from two grade 3 human malignant astrocytomas were prelabeled with Phaseolus vulgaris leucoagglutin (PHAL) and then xenografted into freshly made implantation pockets in rat host cerebral cortex. Animals were sacrificed at 7, 14, 21 days, and 1 month postimplantation (DPI). Paraffin sections were double-labeled for the presence of glial fibrillary acidic protein (GFAP), a specific marker for astrocytes and differentiated astrocytoma cells, and PHAL, utilized as a marker for graft-derived cells. Grafted human astrocytoma cells were found on the glia limitans along the entire circumference of the brain, in the corpus callosum, internal capsule, entopeduncular nucleus, optic tract, and median eminence. In addition, astrocytoma cells were observed in the cingulum, habenula, arcuate, and supraoptic nucleus. Astrocytoma cells entered the spaces of Virchow-Robin, and migrated along parenchymal blood vessels and between the ependymal and subependymal layers of the third and lateral ventricles. The corpus callosum was a major migration route for the astrocytoma cells. The presence of basal lamina or parallel nerve fiber bundles was a common factor for these migration routes. The migration of the human astrocytoma xenografted cells in the rat brain followed the spread of human malignant astrocytomas in the human brain and is a valuable basic science tool in brain cancer research.

Animals↗

[The social organization, behavior and ecological parameters of a migrating population of Siberian roe deer (Capreolus pygargus Pall.)].

Data obtained in 1988-1994 during a long-term study of the ecology and behavior of a seasonally migrating Siberian roe population in Amur Province are reviewed. Aerial surveillance of 24 roe marked with transmitters was used for tracing their migration routes under normal conditions and in the homing experiment. It was found that the routes of roe migrations can be as long as 200 km. These routes, as well as summer and winter territories and the sites where roe cross the rivers, remain unchanged year after year. In spring, roe migrate back along the same route as in autumn. In autumn, the average rate of migration is 6.1 km per day (the maximum rate is 26 km per day), and in summer it is 3.8 km per day. The urge to migrate is apparently innate. The roe memorize the route followed once and are capable of orienting themselves on expanses of land. The first frosts provide a stimulus for autumn migrations. Most roe start to migrate 30-45 days before the formation of snow cover, when forage is still abundant. This fact contradicts traditional views on roe migrations, which fall into the following scheme: thick snow cover; the absence of forage; migrations. A new hypothesis concerning the evolution of roe migrations is proposed. The social, sex, and age structures of the population are analyzed.

Animals↗

The route of migration of lymphocytes from blood to spleen and mesenteric lymph nodes in the pig.

Porcine peripheral blood lymphocytes were labelled with tritiated uridine in vitro and transfused into normal young pigs. Serial biopsies were taken from the spleen and mesenteric lymph nodes, and the localization of labelled lymphocytes determined on autoradiographs. Four to five hours after cell infusion samples of Peyer's patches, tonsils and small intestine were taken and the labelled lymphocytes classified by their localization in different organ compartments. In spleens most labelled cells were found in the red pulp and about 30% in the marginal zone. Within 4 to 5 h there was a constant increase in labelled lymphocytes in the compartment of the white pulp with more cells localized in the periarteriolar lymphatic sheath than in the corona. In lymph nodes about two thirds of all labelled cells were seen in the wall of high endothelial venules 15 min after cell infusion. Labelled cells then decreased in the vessel wall, but, at the same time, increased in the neighbourhood of these vessels and other parts of the paracortex. After 5 h about 10% of labelled lymphocytes had already migrated into the corona. In tonsils and Peyer's patches a comparable distribution of labelled cells was found in the organ compartments. The kinetics and the route of migration in the spleen and lymph nodes are therefore comparable to data for other species, despite the peculiar structure of pig lymph nodes and the paucity of lymphocytes in efferent lymphatics in pigs.

Animals↗

Routed protein migration after protein extravasation and water leakage caused by cold injury.

The movement of extravasated endogenous protein induced by cold injury was investigated in the rat. Extravasated proteins were observed around the cold injury immediately after injury; within 3 hr they had moved into the ipsi- and contralateral hemispheres along the nerve fibres (routed protein migration). The water content in the areas where the extravasated protein was observed was increased, and NMR-CT scans (TR 2000 msec, TE 90 msec) showed high intensity patterns whose distribution and progression coincided with those of extravasated protein. NMR relaxation time, T1, showed a slight increase in the area where the extravasated protein was observed, but T2 value did not show any significant changes. In the opposite hemisphere, CBF decreased within 3 to 6 hours after injury. Local cerebral glucose utilization was reduced, but this change occurred more than 6 hours after injury. These results indicate that water leakage and protein extravasation occur simultaneously after the injury without any significant change of water state or protein conformation. Subsequently, a reduction of CBF is induced, which is followed by changes in cerebral metabolism.

Animals↗

Schistosoma mansoni: mechanism of attrition and routes of migration from lungs to hepatic portal system in the laboratory mouse.

The number of schistosomula in the axillary lymph nodes of mice was determined by compressed tissue autoradiography at 13 intervals from 0.5 to 28 days after exposure of abdominal skin to 75Se-labeled cercariae of S. mansoni. Significant accumulations were observed between days 3 and 6 and peaked on day 4 at which time 9.4 +/- 1.1% of the schistosomula present in the whole body were found in the axillary lymph nodes. The total number and distribution of schistosomula in all tissues of mice were likewise determined at 12 intervals from 3 to 24 days following exposure. The frequent appearance of small numbers of schistosomula in trachea and esophagus suggested that normal attrition resulted at least in part from physical expulsion of schistosomula from the body by way of the tracheobronchial tree and gastrointestinal tract. The distribution of schistosomula observed in heart chambers, caudal vena cava, hepatic portal vein, aorta, intestinal wall, thoracic cavity rinses, and diaphragm supported all 3 standing hypotheses regarding route of migration from lungs to hepatic portal system, i.e., that schistosomula migrate via (1) the pulmonary artery, right heart, caudal vena cava, and hepatic veins, (2) the pulmonary vein, left heart, aorta, and cranial mesenteric artery, and (3) the thoracic cavity and diaphragm.

Animals↗

Conflicting evidence about long-distance animal navigation.

Because of conflicting evidence about several fundamental issues, long-distance animal navigation has yet to be satisfactorily explained. Among the unsolved problems are the nature of genetic spatial control of migration and the relationships between celestial and magnetic compass mechanisms and between different map-related cues in orientation and homing, respectively. In addition, navigation is expected to differ between animal groups depending on sensory capabilities and ecological conditions. Evaluations based on modern long-term tracking techniques of the geometry of migration routes and individual migration history, combined with behavioral experiments and exploration of the sensory and genetic mechanisms, will be crucial for understanding the spatial principles that guide animals on their global journeys.

Animal Identification Systems↗

Origin and migration of luteinizing hormone-releasing hormone neurons in mammals.

Luteinizing hormone-releasing hormone (LHRH) neurons are unique among hypothalamic neurons in that they originate outside of the central nervous system. In most vertebrates, LHRH-immunoreactive (-ir) neurons are detected in the epithelium of the medial olfactory pit soon after its formation. The LHRH-ir neurons migrate out of the placodal epithelium and into the brain along a migration route that consists of the central processes of the terminal, olfactory, and vomeronasal nerves. LHRH-ir cell migration follows a highly ordered course from the initial appearance of the LHRH-ir cells in the epithelium of the medial olfactory pit, to the crossing of these cells in cords on the nasal septum, to their entrance into the forebrain. Here they separate and follow an arching trajectory to their final destinations in the septal and preoptic areas and in the hypothalamus. Examination of the molecular makeup of the developing migration route reveals the presence of neural cell adhesion molecule (N-CAM) in non-LHRH-ir cells. The N-CAM-ir cells migrate into the nasal mesenchyme, trailed by N-CAM-ir axons of the olfactory, vomeronasal, and terminal nerves. These N-CAM cells and axons link the olfactory epithelia with the developing forebrain and together form scaffolding along which the LHRH-ir cells migrate into the brain. The focus of this review is on the origin and migration of LHRH-ir neurons in mammals, including humans. A discussion of Kallmann's syndrome (hypogonadotropic hypogonadism with anosmia) is included, in which there is an absence of LHRH-ir in the brain but clusters of LHRH-ir cells in the nasal cavity. This "experiment of nature" lends support to the hypothesis that all LHRH-ir cells in humans originate in the olfactory placode.

Animals↗

Intraspecific molecular phylogeny, genetic variation and phylogeography of Reticulitermes speratus (Isoptera: Rhinotermitidae).

Population structure was investigated in Reticulitermes speratus populations in the Korean Peninsula and the Japanese Archipelago. All trees derived from analyses of the combined sequence dataset of two mitochondrial genes, COII and COIII, showed that R. speratus populations cluster into two major clades comprising the Korean/southern Japanese populations and the north-ern Japanese populations. Analysis of population ge-netic structure showed strong genetic partitioning between populations of the two clades. To understand historical migration routes and current distributions, the phylogeographic history of R. speratus was inferred from intra-/interspecific phylogeny and diver-gence times estimated between the clades of the phylogenetic tree. The estimated migration route and divergence time of ancestral R. speratus are congruent with recent paleogeographic hypotheses involving land-bridge connections between the Asian continent and the Japanese Archipelago. We suggest that ancestral R. speratus separated into northern and southern Japanese populations after its migration into the Japanese main islands from East China during the early Pleistocene via the East China Sea basin, which may have been exposed during that period. The Korean populations seem to have diverged recently from southern Japanese populations; this may explain the current distribution of R. speratus in the Japanese Arachipelago, and account for why it is restricted to northern areas of the Tokara Strait.

Animals↗

ITS 2 sequences heterogeneity in Phlebotomus sergenti and Phlebotomus similis (Diptera, Psychodidae): possible consequences in their ability to transmit Leishmania tropica.

An intraspecific study on Phlebotomus sergenti, the main and only proven vector of Leishmania tropica among the members of the subgenus Paraphlebotomus was performed. The internal transcribed spacer 2 (ITS2) sequences of 12 populations from 10 countries (Cyprus, Egypt, Italy, Lebanon, Morocco, Pakistan, Portugal, Spain, Syria, and Turkey) were compared. Samples also included three species closely related to P. sergenti: Phlebotomus similis (three populations from Greece and Malta), Phlebotomus jacusieli and Phlebotomus kazeruni. Our results confirm the validity of the taxa morphologically characterised, and imply the revision of their distribution areas, which are explained through biogeographical events. At the Miocene time, a migration route, north of the Paratethys sea would have been followed by P. similis to colonise the north of the Caucasus, Crimea, Balkans including Greece and its islands, and western Turkey. Phlebotomus sergenti would have followed an Asiatic dispersion as well as a western migration route south of the Tethys sea to colonise North Africa and western Europe. This hypothesis seems to be well supported by high degree of variation observed in the present study, which is not related to colonisation or to intra-populational variation. Two groups can be individualised, one oriental and one western in connection with ecology, host preferences and distribution of L. tropica. We hypothesise that they could be correlated with differences in vectorial capacities.

Africa, Northern↗

Does climate at different scales influence the phenology and phenotype of the River Warbler Locustella fluviatilis?

Weather and climatic conditions may impact on the phenology and morphology of birds, and thereby affect their survival rate and population dynamics. We examined the North Atlantic Oscillation (NAO), precipitation in the Sahel zone, temperatures in the wintering grounds, on the migration route, and in the breeding area in relation to arrival dates and six morphological measures (wing, tarsus, bill, and tail lengths, body mass, body condition) in a Slovak population of the River Warbler Locustella fluviatilis. Arrival dates did not change significantly over the study period, but were significantly positively correlated with NAO, although not with temperatures in wintering areas, migration route or breeding area, nor with Sahel precipitation. Four of the six morphological traits changed during the study period and part of the change in condition index can be attributed to climatic variables. We suggest changes in birds' phenotype vary with food availability, which fluctuate according to climate events.

Animals↗

Birds, migration and emerging zoonoses: west nile virus, lyme disease, influenza A and enteropathogens.

Wild birds are important to public health because they carry emerging zoonotic pathogens, either as a reservoir host or by dispersing infected arthropod vectors. In addition, bird migration provides a mechanism for the establishment of new endemic foci of disease at great distances from where an infection was acquired. Birds are central to the epidemiology of West Nile virus (WNV) because they are the main amplifying host of the virus in nature. The initial spread of WNV in the U.S. along the eastern seaboard coincided with a major bird migration corridor. The subsequent rapid movement of the virus inland could have been facilitated by the elliptical migration routes used by many songbirds. A number of bird species can be infected with Borrelia burgdorferi, the etiologic agent of Lyme disease, but most are not competent to transmit the infection to Ixodes ticks. The major role birds play in the geographic expansion of Lyme disease is as dispersers of B. burgdorferi-infected ticks. Aquatic waterfowl are asymptomatic carriers of essentially all hemagglutinin and neuraminidase combinations of influenza A virus. Avian influenza strains do not usually replicate well in humans, but they can undergo genetic reassortment with human strains that co-infect pigs. This can result in new strains with a marked increase in virulence for humans. Wild birds can acquire enteropathogens, such as Salmonella and Campylobacter spp., by feeding on raw sewage and garbage, and can spread these agents to humans directly or by contaminating commercial poultry operations. Conversely, wild birds can acquire drug-resistant enteropathogens from farms and spread these strains along migration routes. Birds contribute to the global spread of emerging infectious diseases in a manner analogous to humans traveling on aircraft. A better understanding of avian migration patterns and infectious diseases of birds would be useful in helping to predict future outbreaks of infections due to emerging zoonotic pathogens.

Animal Migration↗

Hepatic damage in experimental and clinical paragonimiasis.

The hepatic damage induced by Paragonimus skrjabini, and the migration route of this species and that of P. westermani, were investigated in a series of animal experiments and in 34 clinical and four autopsy cases of paragonimiasis. The major symptoms and signs of an unique case reported from Sichuan Province included hepatic tenderness, disturbance of hepatic functions, remittent fever, and cough with bloody sputum. Laparotomy revealed marked adhesions surrounding the liver, spleen and duodenum. Diagnosis was made by finding P. skrjabini in a bulla on the abdominal wall about 5 months after the onset of illness. After specific treatment with bithional, body temperature and liver functions returned to normal. Twenty-three of 33 cases independently studied from Fujian Province also showed similar hepatic function disturbance. Autopsy cases showed hepatic chronic eosinophilic abscesses with Charcot-Leyden crystals. Experimentally, P. skrjabini infection caused hepatic damage in all laboratory animals used. The main pathologic changes were initially acute eosinophilic abscesses in the liver, worms being found sometimes in the necrotic cavities of the abscesses; hepatomagaly also occurred. Some cysts containing mature worms were found in the liver of dogs 3-9 months after infection. Numerous eggs were deposited in the cyst walls. The migration route of P. skrjabini was studied in young dogs. Worms appeared in the liver initially on day 3 and reached their highest level on day 14. P. westermani also migrated into liver, but their numbers were less than those of P. skrjabini.

Acute Disease↗

A morphological study of the lymphocyte traffic in Peyer's patches after an in vivo antigenic stimulation.

BACKGROUND: Lymphoid cells have often been observed in the intestinal lumen and it has been hypothesized that M cells could represent one of the most important migration routes for the immunocompetent cells from the lymphoid follicle to the lumen. However, a direct evidence of the passage was lacking. In this study we describe a morphological analysis of the lymphocyte traffic in rabbit Peyer's patches after an in vivo stimulation with an antigen normally not present in the intestine. METHODS: The antigenic stimulation of a large number of Peyer's patches was carried out using the isolated ileal loop technique and then the samples from stimulated and control Peyer's patches were analysed by light and transmission electron microscopy. RESULTS: We have been able to describe details of lymphocyte migration through M cells, from the follicle to the intestinal lumen, and a marked increase of intraluminal lymphocytes by counting the immunocompetent cells after periods of antigenic stimulation of varying lengths. CONCLUSIONS: Our finding is that the passage of lymphocytes to the lumen is an antigen-dependent event and we also provide direct evidence that M cells are one of the migration routes. Our observations also indicate that lymphoid cells in the intestinal lumen may play an immunologic role in mucosal immunity.

Animals↗

Identification of novel allele on the locus 47z (DXYS5) in the Korean population.

Two homogenous sequences of 47z (DXYS5) are located on the X (DXYS5X) and Y (DXYS5Y) chromosomes, and these are known to be useful polymorphic markers for tracing male-specific gene flow such as the migration routes of human populations. Using the 47z/StuI PCR-RFLP system, we found a novel allele which showed two bands, in contrast to the previous two allele types, one band (Y1) and three bands (Y2). This means that copies of PCR products derived from both the DXYS5X and DXYS5Y loci were clearly cut by the StuI enzyme, implying that the DXYS5X locus of the X chromosome is polymorphic. Allelic frequencies examined in 267 male Korean individuals showed that 95.8% had Y1, 3.4% Y2, and 0.8% had the novel allele. Our findings should contribute to a better understanding of genetic polymorphism on X and Y chromosomes, the molecular evolution mechanism of sex chromosomes, and how the migration route of Koreans is related to those of other East Asian populations.

Base Sequence↗