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G F Striedter

Publications and source records attributed to G F Striedter.

17 recordsLinked to original sources
PubMed2000

Cell migration and aggregation in the developing telencephalon: pulse-labeling chick embryos with bromodeoxyuridine.

Previous studies had concluded that the avian telencephalon develops according to an outside-in schedule of neurogenesis, with relatively little migration of young neuroblasts past older cells. These previous studies had, however, been based on the "cumulative labeling" method, which is less accurate than the "pulse-labeling" method typically used in mammals. In the present study, we pulse-labeled chick embryos by injecting low doses of the thymidine analog bromodeoxyuridine (BrdU) directly into the circulatory system of chick embryos at 6 d of incubation. The brains of these embryos were then examined for anti-BrdU-labeled cells at postinjection survival times from 30 min to 10 d. Comparisons across different survival times, as well as with cases in which BrdU was injected on day 7, suggested that our effective pulse duration is <24 hr. This was confirmed by injecting tritiated thymidine 24 hr after the BrdU and seeing no double-labeled cells. Several deviations from the previously reported pattern of telencephalic neurogenesis were also noted. Most importantly, the cells born on day 6 in the avian Wulst, the likely homolog of mammalian neocortex, end up homogeneously distributed throughout the Wulst, which suggests that many of them are migrating past older cells. Furthermore, the cells born on day 6 in the ventral hyperstriatum and dorsal neostriatum gradually (over the course of 2-3 d) aggregate into distinct multicellular clusters, which suggests that isochronic cells in these regions adhere preferentially to one another. Finally, the data reveal a proliferative subventricular zone similar to that observed in the ganglionic eminences of mammalian embryos.

Animals↗
PubMed2000

Auditory responses in the vocal motor system of budgerigars.

Budgerigars (Melopsittacus undulatus) are small Australian parrots that can imitate novel sounds in adulthood and therefore serve as a convenient model system for the study of vocal learning in adult animals. Previous anatomical studies had indicated that known auditory regions in the telencephalon of budgerigars are connected, albeit indirectly and rather sparsely, to vocal motor nuclei. Physiological evidence for connections between the auditory and vocal motor systems in budgerigars had been lacking, however. Here, we show that neurons in a telencephalic vocal motor region, i.e., the central nucleus of the lateral neostriatum (NLc), are responsive to auditory stimuli in isoflurane-anesthetized budgerigars. These responses are highly variable from trial to trial and frequently have latencies in excess of 100 ms. Neurons in NLc generally respond better to a budgerigar's own contact call than to a white noise stimulus, but the response preferences of NLc neurons in budgerigars are generally weaker and more diverse than the response preferences of neurons in the high vocal center of songbirds, which is probably analogous to NLc. These data indicate that parrots and songbirds, which have evolved the ability to learn vocalizations independently of one another, have both evolved physiologically effective connections between their auditory and vocal motor systems. Interestingly, however, the anatomical pathways by which the auditory and vocal motor systems interact, and the physiological details of how they communicate, appear to be significantly different between the two taxa.

Acoustic Stimulation↗
PubMed1999

Homology in the nervous system: of characters, embryology and levels of analysis.

The establishment of homologies is critically dependent upon the process of character identification. Valid characters must reliably appear in many individuals and be delimitable from other characters. They are not defined by any essential attributes, but rather by the formation of distinct clusters in a multidimensional morphospace. Features in two or more species can be considered possible homologues only if they are identifiable as the same character, for it would be nonsensical to homologize them as different characters. In order to confirm that a character is indeed homologous between species, one must examine its phylogenetic distribution to determine that it is unlikely to have evolved several times independently in the taxa being compared. This method of homologue identification can be applied to embryonic as well as adult characters and to characters at various levels of organization, including cell types and cellular aggregates. Difficulties arise, however, when one attempts to link the homology of adult characters to that of their embryonic precursors, or the homology of cellular aggregates to that of their constituent cell types. These efforts are misguided because different characters cannot be homologized to each other (as different characters). This perspective suggests that many neural characters may lack homologues, and therefore be truly novel, in other taxa.

Animals↗
PubMed1998

The "neostriatum" develops as part of the lateral pallium in birds.

Telencephalic organization in birds is so unusual that many homologies between avian and mammalian telencephalic areas remain controversial. Particularly contested is the avian "neostriatum," which has historically been homologized to either mammalian striatum, lateral neocortex, or endopiriform claustrum. Because homologies between these adult structures have been so difficult to resolve, we have begun to examine how telencephalic development diverges between birds and other vertebrates. To this end, biotinylated dextran was injected into the lateral telencephalon of chick embryos at 3 d of incubation, and the distribution of labeled cells was examined up to 14 d later. The data show that a definite boundary to cellular migration develops just ventral to the neostriatum between 5 and 8 d of incubation. Labeled polyclones within the neostriatum stretch from the ventricular zone to the brain surface and exhibit an increasingly rostrocaudal orientation as development proceeds. Individual polyclones contribute cells to several of the distinct auditory, visual, somatosensory, and olfactory regions within the neostriatum. A comparative analysis suggests that the avian neostriatum develops from a precursor region that in other vertebrates gives rise to olfactory cortex and, when present, to other components of the piriform lobe, such as the endopiriform claustrum and basolateral amygdala. Conclusions about lateral pallial homologies between birds and mammals remain uncertain, however, primarily because so little is known about the development of the lateral pallium in mammals. This lacuna might be filled by applying to mammals the novel fate-mapping method described in the present paper.

Animals↗
PubMed1998

Progress in the study of brain evolution: from speculative theories to testable hypotheses.

Darwin's theory of evolution raised the question of how the human brain differs from that of other animals and how it is the same. Early students of brain evolution had constructed rather grand but speculative theories which stated that brains evolved in a linear manner, from fish to man and from simple to complex. These speculations were soundly refuted, however, as contemporary comparative neurobiologists used powerful new techniques and methodologies to discover that complex brains have evolved several times independently among vertebrates (e.g., within teleost fishes and birds) and that brain complexity has actually decreased in the lineages leading to modern salamanders and lungfishes. Moreover, the old idea that brains evolved by the sequential addition of new components has now been replaced by the working hypothesis that brains generally evolve by the divergent modification of preexisting parts. Speculative theories have thus been replaced by testable hypotheses, and current efforts in the field are aimed at making phylogenetic hypotheses even more testable. Particularly promising new directions for comparative neurobiology include (1) the integration of comparative neuroanatomy with comparative embryology and developmental genetics in order to test phylogenetic hypotheses at a mechanistic level, (2) research into how evolutionary changes in the structure of neural circuits are related to evolutionary changes in circuit function and animal behavior, and (3) the analysis of independently evolved similarities to discover general rules about how brains may or may not change during the course of evolution.

Animals↗
PubMed1998

Stepping into the same river twice: homologues as recurring attractors in epigenetic landscapes.

The reunification of embryology with evolutionary biology is impeded by the perception that a phylogenetic view of homology is incompatible with a developmental approach. This dichotomy disappears when developmental information is viewed not as pre-existing within the zygote but as being constructed during development. Developmental information can be depicted as the surface of an epigenetic landscape. An epigenetic landscape, in turn, can be viewed as a series of aligned energy landscapes that change shape and become more complex as development proceeds. In this view, individual valley bottoms are attractors in state space that tend to reappear reliably in successive generations. Phylogeny can therefore be conceptualized as a succession of epigenetic landscapes, and homologues can be identified as corresponding valleys that have reappeared reliably since their origin in a single ancestral population. Epigenetic homologues can be robust to phylogenetic changes in developmental mechanisms, precursors, and lower level characters. Although application of the epigenetic homology concept is complicated by the lack of explicit information about the topography of epigenetic landscapes, comparative biologists can learn to identify recurring ontogenetic patterns in a manner that is analogous to the identification of input patterns by attractor neural networks. The correspondence of epigenetic valleys is therefore not defined by any essential criteria but by their overlap in multidimensional state space. Whether corresponding valleys are homologous to each other must be determined by a phylogenetic analysis using cladistic methods. Among the general implications of epigenetic homology for comparative neurobiology is that the concept of 'field homology' should be used with caution when dealing with novel characters. A case study, applying an epigenetic perspective to understand the variation in monkey visual cortex observed after developmental perturbations, is presented in a final section to make the concept of epigenetic homology more concrete.

Biological Evolution↗
PubMed1998

Bilateral feedback projections to the forebrain in the premotor network for singing in zebra finches.

A discrete neural circuit mediates the production of learned vocalizations in oscine songbirds. Although this circuit includes some bilateral pathways at midbrain and medullary levels, the forebrain components of the song control network are not directly connected across the midline. There have been no previous reports of bilateral projections from medullary and midbrain vocal control nuclei back to the forebrain song system, but the existence of such bilateral corollary discharge pathways was strongly suggested by the recent observation that unilateral stimulation of a forebrain song nucleus during singing leads to a rapid readjustment of premotor activity in the contralateral forebrain. In the present study, we used neuroanatomical tracers to demonstrate bilateral projections from (a) the rostral ventrolateral medulla (RVL), which may control respiratory aspects of vocalization, to nucleus uvaeformis (Uva), and (b) the dorsomedial intercollicular nucleus (DM), a midbrain vocal control region, to Uva. Both RVL and DM receive descending projections from the forebrain song nucleus robustus archistriatalis, and Uva projects directly to the forebrain song nuclei interfacialis and high vocal center. We suggest that the bilateral feedback projections from DM and RVL to Uva function to coordinate the two hemispheres during singing in adult songbirds and to convey internal feedback of premotor signals to the forebrain in young birds that are learning to sing.

Animals↗
PubMed1997

Distribution of radial glia in the developing telencephalon of chicks.

Radial glia are known to have a sparse and uneven distribution in the telencephalon of adult birds. The present study utilizes antibodies against vimentin to reveal a more extensive, and more clearly radial, set of radial glia in the chicken telencephalon during the first half of embryogenesis. This initially extensive radial glial fiber system becomes distorted and reduced between 10 and 14 days of incubation. This reduction coincides with the cytoarchitectural differentiation of the telencephalon into its major adult subdivisions. Because developing neurons tend to migrate along radial glial fibers in both birds and mammals, a topological projection of these major subdivisions onto the embryonic ventricular zone along the radial glial fibers suggests hypotheses about lineage relationships that can be tested by subsequent experimental methods. This analysis suggests that the major components of the avian dorsal ventricular ridge, i.e., the ventral hyperstriatum, the neostriatum with its various subdivisions, part of the archistriatum, and probably also the piriform cortex, all derive from overlapping portions of the lateral pallial ventricular zone. Staining with antibodies against neurofilament suggests that this developmental parcellation of the lateral pallial complex is associated with the development of neuronal fiber systems.

Animals↗
PubMed1997

The telencephalon of tetrapods in evolution.

Numerous scientists have sought a homologue of mammalian isocortex in sauropsids (reptiles and birds) and a homologue of sauropsid dorsal ventricular ridge in mammals. Although some of the proposed theories were enormously influential, alternative theories continued to coexist, primarily because the striking differences in pallial organization between adult mammals, sauropsids, and amphibians enabled different authors to enlist different subsets of similarity data in support of different hypotheses of putative homology. A phylogenetic analysis based on parsimony cannot discriminate between such alternative hypotheses of putative homology, because sauropsids and mammals are sister groups. One solution to this dilemma is to include embryological patterns of telencephalic organization in the comparative analysis. Because early developmental stages in different taxa tend to resemble each other more than the adults do, the embryological data may reveal intermediate patterns of organization that provide unambiguous support for a single hypothesis of putative homology. The validity of this putative homology may then be supported by means of a phylogenetic analysis based on parsimony. A comparative analysis of pallial organization that includes embryological data suggests the following set of homologies. The lateral cortex in reptiles is homologous to the piriform cortex in birds and mammals. The anterior dorsal ventricular ridge in reptiles is probably homologous to the neostriatum and ventral hyperstriatum in birds and to the endopiriform nucleus in mammals. The posterior dorsal ventricular ridge in reptiles is most likely homologous to the archistriatum in birds and to the pallial amygdala in mammals. The pallial thickening in reptiles is probably homologous to the dorsal and intercalated portions of the hyperstriatum in birds and to the claustrum proper in mammals. Finally, the dorsal cortex in reptiles is probably homologous to the accessory hyperstriatum and parahippocampal area in birds and to the isocortex in mammals. These hypotheses of homology imply relatively minor evolutionary changes in development but major changes in neuronal connections. Most significantly, they imply the independent elaboration of thalamic sensory projections to derivatives of the lateral and dorsal pallia in sauropsids and mammals, respectively. They also imply the independent evolution of lamination in the pallium of birds and mammals.

Animals↗
PubMed1994

The vocal control pathways in budgerigars differ from those in songbirds.

Previous studies concluded that parrots and oscine songbirds, two taxa that have independently evolved the ability to learn vocalizations, possess similar neural circuits for vocal control. These investigations suggested, however, that the vocal control systems of parrots and songbirds may also differ in several respects. Most importantly, auditory inputs to the vocal control system derive from Field L in songbirds, but this area does not appear to project to the vocal control system in parrots. The principal aims in the present study were, therefore, to determine 1) exactly how similar the vocal control system in budgerigars is to that in songbirds and 2) whether the vocal control system in budgerigars receives auditory inputs from areas other than Field L. Biotinylated and fluorescently labeled dextrans were injected into five telencephalic nuclei of the vocal control system in budgerigars and into the physiologically identified auditory portions of the frontal neostriatum and nucleus basalis. The results indicate that the forebrain vocal control system in budgerigars is only superficially similar to that in songbirds. Many of the vocal control nuclei differ between the two taxa in both cytoarchitecture and connections. The nuclei in budgerigars that are comparable to those of the accessory loop of the vocal control system in songbirds, for example, do not form an accessory loop in budgerigars. The vocal control systems in the two taxa differ most significantly in the source of their auditory inputs. In songbirds, auditory information is conveyed to the vocal control system via Field L, whereas, in budgerigars, the auditory inputs to the vocal control system derive from nucleus basalis and the frontal neostriatum. A phylogenetic analysis suggests that the midbrain and medullary vocal control pathways are homologous across all birds, but that most of the vocal control circuits in the forebrain have probably evolved independently in parrots and songbirds.

Animals↗
PubMed1992

Phylogenetic changes in the connections of the lateral preglomerular nucleus in ostariophysan teleosts: a pluralistic view of brain evolution.

The connections of the lateral preglomerular nucleus were examined with the fluorescent tracer DiI in a cyprinid, a characin, a catfish and a gymnotoid species. In all of these taxa the lateral preglomerular nucleus receives inputs from the torus semicircularis and projects to the telencephalon. Cytoarchitectural and topological data further support the hypothesis that the lateral preglomerular nucleus is homologous among the species examined. A cladistic analysis of species differences, however, reveals that some connections of the lateral preglomerular nucleus have changed dramatically during the course of evolution. Some of the cell groups that are interconnected with the lateral preglomerular nucleus have increased in size, while others have decreased. Increases in the number of subdivisions of cell groups are frequently associated with size increases, but they may also be associated with size decreases. Some of the connections between cell groups have increased in strength, whereas others have decreased in strength, but these connectional changes bear no simple relationship to phylogenetic changes in the size of the cell groups. Phylogenetic increases in the number of subdivisions within a cell group may be associated with selective gains of connections, but they may be associated also with selective losses of connections or with no major changes in connections. Furthermore, several cell groups and connections appear to have evolved 'de novo', whereas others have disappeared during the course of evolution. Finally, the individual cell groups within this system of interconnected nuclei have changed largely independently of one another. These findings establish that brain evolution is not dominated by a single type of phylogenetic change.

Animals↗
PubMed1991

Auditory, electrosensory, and mechanosensory lateral line pathways through the forebrain in channel catfishes.

The forebrain auditory, electrosensory, and mechanosensory lateral line pathways in the channel catfish, Ictalurus punctatus, were examined by applying the fluorescent tracer DiI to 1) the auditory part of the torus semicircularis, 2) the electrosensory part of the torus semicircularis, 3) the lateral preglomerular nucleus, and 4) the anterior tuberal nucleus. Three distinct pathways ascend from the torus semicircularis to the telencephalon; they course through either 1) the lateral preglomerular nucleus of the posterior tuberculum, 2) the anterior tuberal nucleus of the hypothalamus, or 3) the central posterior nucleus of the dorsal thalamus. The anatomical data suggest that each of these ascending pathways carries information from more than one sensory modality. The lateral preglomerular nucleus receives an electrosensory input from nucleus electrosensorius in the diencephalon, but it also receives auditory and mechanosensory inputs directly from the torus semicircularis. The anterior tuberal and central posterior nuclei receive primarily auditory and mechanosensory, but also minor electrosensory, inputs. The efferent projections of the central posterior nucleus are presently unknown, but the lateral preglomerular and anterior tuberal nuclei project to nonoverlapping portions of the telencephalon. A cladistic analysis of these indirect torotelencephalic pathways reveals that 1) the pathway through the dorsal thalamus is probably a primitive character for gnathostomes, 2) a well-developed pathway through the posterior tuberculum is probably a derived character for actinopterygian fishes, 3) the pathway through nucleus electrosensorius is probably a derived character for catfishes and gymnotoid teleosts, and 4) auditory pathways through the hypothalamus probably evolved independently in catfishes and frogs.

Afferent Pathways↗
PubMed1991

Biological hierarchies and the concept of homology.

Although most biologists agree that homology must be defined in terms of common ancestry, the details of this definition remain controversial. We review briefly the disagreements concerning the formal definition of homology and the methodology used to establish specific cases of homology. Our principal focus, however, is a third area of disagreement: whether morphological characters can be homologous even if their developmental and genetic bases are not homologous, and whether behavioral characters can be homologous even if their morphological substrates are not homologous. We contend that attempts to reduce behavioral homology to morphological homologies, and morphological homology to genetic and developmental homologies, are misguided and based on a failure to recognize the hierarchical nature of biological organization. Genes, developmental processes, morphological structures, physiological functions and behaviors all constitute different levels of biological organization. These levels are causally interrelated, but there is no one-to-one correspondence between characters at different levels. Furthermore, the causal relationships between characters at different levels may change during the course of evolution. As a result, higher level characters may be homologous, even though some of their constituent lower level characters are not homologous. In support of this assertion, we provide several examples of homologous morphological characters that are based on non-homologous developmental precursors and processes, and of homologous behavioral characters that are based on non-homologous morphological structures. In allowing one to recognize homologies at any level of organization, independently of homologies at other levels, the hierarchical concept of homology also allows one to ask important questions about how evolutionary changes at the various levels of organization are related to one another.

Animal Communication↗
PubMed1990

The diencephalon of the channel catfish, Ictalurus punctatus. I. Nuclear organization.

A detailed cytoarchitectonic description of the diencephalon in the channel catfish reveals more than 40 distinct cell groups. Of these, 4 are located in the preoptic area, 8 in the hypothalamus, 7 in the thalamus, 2 in the epithalamus, 15 in the posterior tuberculum and 7 in the synencephalon. A comparison of the diencephalon of Ictalurus punctatus to that of goldfish, which has previously been described, indicates major differences in the diencephalon between these two species. Channel catfish lack the superficial pretectum and the nucleus 'glomerulosus' of goldfish, whereas the anterior tuberal nucleus of the hypothalamus, the paracommissural nucleus of the synencephalon and the nucleus lobobulbaris of the posterior tuberculum are all better developed in channel catfish than in goldfish. The nucleus electrosensorius in the synencephalon of channel catfish is probably homologous to the nucleus of the same name in gymnotoid teleosts, but it appears to have no homologue in the diencephalon of goldfish. An analysis of interspecific variation in the diencephalon among catfishes, goldfish and several other teleosts reveals that some areas of the diencephalon are more variable across species than others. Specifically, the migrated portions of both the posterior tuberculum and the synencephalon appear to be most variable, whereas the epithalamus and the preoptic area are the most conservative. It is hypothesized that the relatively conservative areas of the brain may have a greater number of afferent connections, and probably also a greater number of distinct behavioral functions, than the more variable areas.

Animals↗
PubMed1990

The diencephalon of the channel catfish, Ictalurus punctatus. II. Retinal, tectal, cerebellar and telencephalic connections.

In a companion paper, the nuclear organization of the diencephalon of the channel catfish, Ictalurus punctatus, was described and compared to that of other teleosts. The present paper describes the connections of the diencephalon with the retina, optic tectum, corpus of the cerebellum and telencephalon. The principal tracer employed is the indocarbocyanine dye DiI which diffuses along neuronal membranes in fixed tissues. Almost all of the nuclei that were recognized as distinct in the companion study are found to also exhibit distinct sets of connections. Most of these connections have not been described previously in catfishes or other teleosts. When combined with connectional data from the existing literature, the results of the present study allow one to recognize a great number of distinct pathways through the diencephalon of channel catfish, including several visual, auditory, gustatory, electrosensory and mechanosensory pathways to the telencephalon. Almost all of the species differences in diencephalic organization noted in the companion study can be accounted for by changes in one of the major sensory pathways. In contrast, the multimodal and integrative areas of the diencephalon appear to be relatively conservative. A comparison between the diencephalon of teleosts and that of other vertebrates suggests that the dorsal thalamus, the ventral thalamus and the posterior tuberculum are homologous, at least in part, to the dorsal thalamus, the zona incerta and the subthalamic nucleus of mammals, respectively. All three areas project to the telencephalon in both mammals and teleosts. In most vertebrates, however, the dorsal thalamus provides the dominant input to the telencephalon, whereas in teleosts the main telencephalic input derives instead from the posterior tuberculum.

Animals↗
PubMed1989

Two distinct visual pathways through the superficial pretectum in a percomorph teleost.

The connections of the superficial pretectum and of nucleus isthmi were examined in a percomorph teleost, Lepomis cyanellus. Horseradish peroxidase was injected either with a pin into the parvicellular nucleus of the superficial pretectum or pressure injected into nucleus isthmi; the isthmal injections retrogradely labelled the neurons of the magnocellular nucleus of the superficial pretectum. Two main visual pathways can be recognized: The first projects from the retina to the parvicellular nucleus, and then to the intermediate nucleus of the superficial pretectum, the inferior raphe nucleus, and the trochlear nucleus. The second projects from the retina via the optic tectum to the magnocellular nucleus of the superficial pretectum, and from there to nucleus isthmi and the lateral thalamic nucleus; nucleus isthmi and the lateral thalamic nucleus project back to the optic tectum, and nucleus isthmi also projects back to the magnocellular nucleus. The two pathways are interconnected to some extent because both nucleus isthmi and the optic tectum project to the parvicellular nucleus; nevertheless, we suggest that they may be functionally and evolutionarily distinct. Compared to percomorphs, the first pathway appears reduced in cyprinid teleosts such as goldfish. Furthermore, the magnocellular nucleus of the second pathway is completely different in cyprinids, both in cellular architecture and in efferent connections. A phylogenetic analysis suggests that cyprinid ancestors went through a period of reduced vision and that the magnocellular nucleus of the superficial pretectum in modern cyprinids has been either extensively modified from the primitive condition or lost entirely and replaced by a superficially similar structure.

Animals↗