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Journal articles on the topic 'Eudromia'

Author: Grafiati

Published: 4 June 2021

Last updated: 2 February 2022

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1

Echarri, Fermín, Claudia Tambussi, and Carolina Acosta Hospitaleche. "Predicting the distribution of the crested tinamous, Eudromia spp. (Aves, Tinamiformes)." Journal of Ornithology 150, no. 1 (2008): 75–84. http://dx.doi.org/10.1007/s10336-008-0319-5.

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2

Smith, Paul, and Kimball L. Garrett. "The juvenile plumage of Quebracho Crested-Tinamou Eudromia formosa (Aves: Tinamidae)." Revista Brasileira de Ornitologia 24, no. 4 (2016): 335–37. http://dx.doi.org/10.1007/bf03544363.

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3

Ossiboff, R. J., M. M. Clancy, K. A. Terio, K. J. Conley, and D. McAloose. "Cerebral and Ocular Ochroconiasis in 2 Elegant Crested Tinamou (Eudromia elegans) Chicks." Veterinary Pathology 52, no. 4 (2014): 716–19. http://dx.doi.org/10.1177/0300985814556186.

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4

OGATA, Mitsuaki, Junichi KOIZUMI, Koki MORIKAKU, and Rei MATSUMOTO. "Sexing, the Elegant Crested-Tinamou, Eudromia elegans, Using a Molecular Biological Method." Japanese Journal of Zoo and Wildlife Medicine 11, no. 2 (2006): 79–81. http://dx.doi.org/10.5686/jjzwm.11.79.

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5

Hugot, J. P., C. A. Sutton, and S. Morand. "Morphological study of Eudromoxyura aspiculuris (Nematoda, Heteroxynematidae) from the tinamou Eudromia elegans (Aves, Tinamidae)." Systematic Parasitology 19, no. 1 (1991): 61–72. http://dx.doi.org/10.1007/bf00010303.

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6

Ronaldson, Hayley L., Paolo Monticelli, Andrew R. Cuff, Krijn B. Michel, Dario d'Ovidio, and Chiara Adami. "Anesthesia and Anesthetic-Related Complications of 8 Elegant-Crested Tinamous (Eudromia elegans) Undergoing Experimental Surgery." Journal of Avian Medicine and Surgery 34, no. 1 (2020): 17. http://dx.doi.org/10.1647/1082-6742-34.1.17.

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7

HANCOCK, JENNIFER A., NANCY J. STEVENS, and AUDRONE R. BIKNEVICIUS. "Whole-body mechanics and kinematics of terrestrial locomotion in the Elegant-crested Tinamou Eudromia elegans." Ibis 149, no. 3 (2007): 605–14. http://dx.doi.org/10.1111/j.1474-919x.2007.00688.x.

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8

Tisdale, Ryan K., Alexei L. Vyssotski, John A. Lesku, and Niels C. Rattenborg. "Sleep-Related Electrophysiology and Behavior of Tinamous (Eudromia elegans): Tinamous Do Not Sleep Like Ostriches." Brain, Behavior and Evolution 89, no. 4 (2017): 249–61. http://dx.doi.org/10.1159/000475590.

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The functions of slow wave sleep (SWS) and rapid eye movement (REM) sleep, distinct sleep substates present in both mammals and birds, remain unresolved. One approach to gaining insight into their function is to trace the evolution of these states through examining sleep in as many taxonomic groups as possible. The mammalian and avian clades are each composed of two extant groups, i.e., the monotremes (echidna and platypus) and therian (marsupial and eutherian [or placental]) mammals, and Palaeognaths (cassowaries, emus, kiwi, ostriches, rheas, and tinamous) and Neognaths (all other birds) among birds. Previous electrophysiological studies of monotremes and ostriches have identified a unique “mixed” sleep state combining features of SWS and REM sleep unlike the well-delineated sleep states observed in all therian mammals and Neognath birds. In the platypus this state is characterized by periods of REM sleep-related myoclonic twitching, relaxed skeletal musculature, and rapid eye movements, occurring in conjunction with SWS-related slow waves in the forebrain electroencephalogram (EEG). A similar mixed state was also observed in ostriches; although in addition to occurring during periods with EEG slow waves, reduced muscle tone and rapid eye movements also occurred in conjunction with EEG activation, a pattern typical of REM sleep in Neognath birds. Collectively, these studies suggested that REM sleep occurring exclusively as an integrated state with forebrain activation might have evolved independently in the therian and Neognath lineages. To test this hypothesis, we examined sleep in the elegant crested tinamou (Eudromia elegans), a small Palaeognath bird that more closely resembles Neognath birds in size and their ability to fly. A 24-h period was scored for sleep state based on electrophysiology and behavior. Unlike ostriches, but like all of the Neognath birds examined, all indicators of REM sleep usually occurred in conjunction with forebrain activation in tinamous. The absence of a mixed REM sleep state in tinamous calls into question the idea that this state is primitive among Palaeognath birds and therefore birds in general.

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9

Black, Peter A., Michael Macek, Anne Tieber, and Martha Weber. "Reference Values for Hematology, Plasma Biochemical Analysis, Plasma Protein Electrophoresis, andAspergillusSerology in Elegant-crested Tinamou (Eudromia elegans)." Journal of Avian Medicine and Surgery 27, no. 1 (2013): 1–6. http://dx.doi.org/10.1647/2010-026.1.

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10

Schuster, Sophie, Sue Anne Zollinger, John A. Lesku, and Henrik Brumm. "On the evolution of noise-dependent vocal plasticity in birds." Biology Letters 8, no. 6 (2012): 913–16. http://dx.doi.org/10.1098/rsbl.2012.0676.

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Signal plasticity is considered an important step in the evolution of animal communication. In acoustic communication, signal transmission is often constrained by background noise. One adaptation to evade acoustic signal masking is the Lombard effect, in which an animal increases its vocal amplitude in response to an increase in background noise. This form of signal plasticity has been found in mammals, including humans, and some birds, but not frogs. However, the evolution of the Lombard effect is still unclear. Here we demonstrate for the first time the Lombard effect in a phylogentically basal bird species, the tinamou Eudromia elegans . By doing so, we take a step towards reconstructing the evolutionary history of noise-dependent vocal plasticity in birds. Similar to humans, the tinamous also raised their vocal pitch in noise, irrespective of any release from signal masking. The occurrence of the Lombard effect in a basal bird group suggests that this form of vocal plasticity was present in the common ancestor of all living birds and thus evolved at least as early as 119 Ma.

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11

Pigozzi, María Inés. "Diverse stages of sex-chromosome differentiation in tinamid birds: evidence from crossover analysis in Eudromia elegans and Crypturellus tataupa." Genetica 139, no. 6 (2011): 771–77. http://dx.doi.org/10.1007/s10709-011-9581-1.

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12

Cenizo, Marcos, Jorge Noriega, Juan Diederle, et al. "An unexpected large Crested Tinamou (Eudromia, Tinamidae, Aves) near to Last Glacial Maximum (MIS 2, late Pleistocene) of the Argentine Pampas." Historical Biology 32, no. 3 (2018): 330–38. http://dx.doi.org/10.1080/08912963.2018.1491568.

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13

Bishop, Peter J., Krijn B. Michel, Antoine Falisse, et al. "Computational modelling of muscle fibre operating ranges in the hindlimb of a small ground bird (Eudromia elegans), with implications for modelling locomotion in extinct species." PLOS Computational Biology 17, no. 4 (2021): e1008843. http://dx.doi.org/10.1371/journal.pcbi.1008843.

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The arrangement and physiology of muscle fibres can strongly influence musculoskeletal function and whole-organismal performance. However, experimental investigation of muscle function duringin vivoactivity is typically limited to relatively few muscles in a given system. Computational models and simulations of the musculoskeletal system can partly overcome these limitations, by exploring the dynamics of muscles, tendons and other tissues in a robust and quantitative fashion. Here, a high-fidelity, 26-degree-of-freedom musculoskeletal model was developed of the hindlimb of a small ground bird, the elegant-crested tinamou (Eudromia elegans, ~550 g), including all the major muscles of the limb (36 actuators per leg). The model was integrated with biplanar fluoroscopy (XROMM) and forceplate data for walking and running, where dynamic optimization was used to estimate muscle excitations and fibre length changes throughout both gaits. Following this, a series of static simulations over the total range of physiological limb postures were performed, to circumscribe the bounds of possible variation in fibre length. During gait, fibre lengths for all muscles remained between 0.5 to 1.21 times optimal fibre length, but operated mostly on the ascending limb and plateau of the active force-length curve, a result that parallels previous experimental findings for birds, humans and other species. However, the ranges of fibre length varied considerably among individual muscles, especially when considered across the total possible range of joint excursion. Net length change of muscle–tendon units was mostly less than optimal fibre length, sometimes markedly so, suggesting that approaches that use muscle–tendon length change to estimate optimal fibre length in extinct species are likely underestimating this important parameter for many muscles. The results of this study clarify and broaden understanding of muscle function in extant animals, and can help refine approaches used to study extinct species.

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14

Tsuda, Yayoi, Chizuko Nishida-Umehara, Junko Ishijima, Kazuhiko Yamada, and Yoichi Matsuda. "Comparison of the Z and W sex chromosomal architectures in elegant crested tinamou (Eudromia elegans) and ostrich (Struthio camelus) and the process of sex chromosome differentiation in palaeognathous birds." Chromosoma 116, no. 2 (2007): 159–73. http://dx.doi.org/10.1007/s00412-006-0088-y.

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15

Романов, А. А., та В. В. Тарасов. "Биология размножения хрустана ( Eudromias morinellus ) на плато Путорана, Средняя Сибирь". Зоологический журнал 100, № 8 (2021): 914–26. http://dx.doi.org/10.31857/s0044513421060118.

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16

Bassi, Enrico, Enrico Viganò, and Gianfranco Scieghi. "New breeding of Eurasian Dotterel Eudromias morinellus in the Italian Alps." Rivista Italiana di Ornitologia 84, no. 1 (2015): 5. http://dx.doi.org/10.4081/rio.2014.198.

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Eurasian Dotterel Eudromias morinellus is a summer visitor to northern Europe, but occurs more patchily farther south, with Europe accounting for less than half of its global breeding range. It has an extremely large range with an European breeding population relatively small (&lt;42,000 pairs), but was stable between 1970-1990. Spain hosts the largest breeding population of Southern Europe (Gutiérrez 1997; Valle &amp; Scarton 1999). Over the Alps the species is threatened of extinction due to its small population size. The main breeding alpine population settled in Austria with a maximum of ten reproductive pairs since 2003. In Switzerland after two breeding events recorded in the Grisons in 1965 and 1998, three more broods occurred in 2012 and 2013. In Italy the main reproductive population, varying from 1 to 6 pairs, is located in Abruzzo’s Apennines whereas from 1974 to 1994 several breeding events were recorded. Last breeding was confirmed up to 1994. In the Italian Alps breeding was suspected in few instances, but it was only confirmed in 1978 (one pair plus another possible one in South Tyrol) and 1994-95 in Lombardy region (one pair in Upper Valtellina).

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17

Rittinghaus, Hans. "Untersuchungen zur Biologie des Mornellregenpfeifers (Eudromias morinellus L.) in Schwedisch Lappland1,2." Zeitschrift für Tierpsychologie 19, no. 5 (2010): 539–58. http://dx.doi.org/10.1111/j.1439-0310.1962.tb00788.x.

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18

Horak, M., and IFB Common. "A Revision of the Austrlian Genus Epitymbia Meyrick, with Remarks on the Epitymbiini (Lepidoptera: Tortricidae)." Australian Journal of Zoology 33, no. 4 (1985): 577. http://dx.doi.org/10.1071/zo9850577.

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Nine species of Epitymbia Meyrick are recognized in this revision: alaudana Meyrick [=periopa (Meyrick); =cydropis (Meyrick)], cosmota (Meyrick) [=heliochares (Lower), syn. nov.; =callizyga (Lower)], scotinopa (Lower), eudrosa (Turner), comb, nov. [=pyrrhocremna (Meyrick), syn. nov.], apatela, sp. nov., eutypa (Turner), sp. rev. and comb. nov., passalotana (Meyrick), comb. nov. [=semiophora (Turner), syn. nov.], dialepta, sp. nov., and isoscelana (Meyrick), comb. nov. [=thetis (Butler), syn. nov.]. One generic and three specific synonymies are confirmed and one generic and four specific synonymies are newly established. Two lectotypes are designated and four new combinations are proposed. All species except eudrosa, which is also found in New Guinea, are endemic to eastern and south-eastem mainland Australia and Tasmania, and known larvae feed on fallen leaves. Adults and genitalia of both sexes are figured, and heads, wing venation and other structures if relevant. The larval chaetotaxy is illustrated and the unusual biology is described. A tentative cladogram for the species of Epitymbia is given and the phylogeny of the genus is discussed with a view to clarifying the taxonomic status of the Epitymbiini.

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19

Buono, Paolo, Fabio Cassano, Alessandra Legretto, and Antonio Piccinno. "EUDroid: a formal language specifying the behaviour of IoT devices." IET Software 12, no. 5 (2018): 425–29. http://dx.doi.org/10.1049/iet-sen.2017.0347.

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20

HICKMAN, V. V., and J. L. HICKMAN. "NOTES ON THE HABITS OF THE TASMANIAN DORMOUSE PHALANGERS CERCAERTUS NANUS (DESMAREST) AND EUDROMICIA LEPIDA (THOMAS)." Proceedings of the Zoological Society of London 135, no. 3 (2009): 365–74. http://dx.doi.org/10.1111/j.1469-7998.1960.tb05853.x.

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21

Gomes, Vitor. "Elegant Crested-Tinamou (Eudromia elegans)." Neotropical Birds, March 7, 2014. http://dx.doi.org/10.2173/nb.elctin1.01.

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22

Smith, Paul. "Quebracho Crested-Tinamou (Eudromia formosa)." Neotropical Birds, April 11, 2014. http://dx.doi.org/10.2173/nb.quctin1.01.

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23

Urantówka, Adam Dawid, Aleksandra Kroczak, and Paweł Mackiewicz. "New view on the organization and evolution of Palaeognathae mitogenomes poses the question on the ancestral gene rearrangement in Aves." BMC Genomics 21, no. 1 (2020). http://dx.doi.org/10.1186/s12864-020-07284-5.

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Abstract Background Bird mitogenomes differ from other vertebrates in gene rearrangement. The most common avian gene order, identified first in Gallus gallus, is considered ancestral for all Aves. However, other rearrangements including a duplicated control region and neighboring genes have been reported in many representatives of avian orders. The repeated regions can be easily overlooked due to inappropriate DNA amplification or genome sequencing. This raises a question about the actual prevalence of mitogenomic duplications and the validity of the current view on the avian mitogenome evolution. In this context, Palaeognathae is especially interesting because is sister to all other living birds, i.e. Neognathae. So far, a unique duplicated region has been found in one palaeognath mitogenome, that of Eudromia elegans. Results Therefore, we applied an appropriate PCR strategy to look for omitted duplications in other palaeognaths. The analyses revealed the duplicated control regions with adjacent genes in Crypturellus, Rhea and Struthio as well as ND6 pseudogene in three moas. The copies are very similar and were subjected to concerted evolution. Mapping the presence and absence of duplication onto the Palaeognathae phylogeny indicates that the duplication was an ancestral state for this avian group. This feature was inherited by early diverged lineages and lost two times in others. Comparison of incongruent phylogenetic trees based on mitochondrial and nuclear sequences showed that two variants of mitogenomes could exist in the evolution of palaeognaths. Data collected for other avian mitogenomes revealed that the last common ancestor of all birds and early diverging lineages of Neoaves could also possess the mitogenomic duplication. Conclusions The duplicated control regions with adjacent genes are more common in avian mitochondrial genomes than it was previously thought. These two regions could increase effectiveness of replication and transcription as well as the number of replicating mitogenomes per organelle. In consequence, energy production by mitochondria may be also more efficient. However, further physiological and molecular analyses are necessary to assess the potential selective advantages of the mitogenome duplications.

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