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Artículos de revistas sobre el tema "Lemuroidea"

Autor: Grafiati
Publicado: 2 de julio de 2021
Última modificación: 7 de febrero de 2022

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Consulte los 16 mejores artículos de revistas para su investigación sobre el tema "Lemuroidea".

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1

Schreiber, A. y K. Bauer. "Strepsirhine dichotomy from a human perspective (Primates: Lorisoidea, Lemuroidea)". Journal of Zoological Systematics and Evolutionary Research 35, n.º 3 (27 de abril de 2009): 121–29. http://dx.doi.org/10.1111/j.1439-0469.1997.tb00413.x.

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2

Burrows, Anne M. y Timothy D. Smith. "Muscles of facial expression inOtolemur, with a comparison to Lemuroidea". Anatomical Record 274A, n.º 1 (11 de agosto de 2003): 827–36. http://dx.doi.org/10.1002/ar.a.10093.

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3

Sonntag, Charles F. "38. The Comparative Anatomy of the Tongues of the Mammalia. - V. Lemuroidea and Tarsioidea." Proceedings of the Zoological Society of London 91, n.º 4 (21 de agosto de 2009): 741–55. http://dx.doi.org/10.1111/j.1096-3642.1921.tb03289.x.

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4

Pollock, Jon I. "The song of the Indris (Indri indri; Primates: Lemuroidea): Natural history, form, and function". International Journal of Primatology 7, n.º 3 (junio de 1986): 225–64. http://dx.doi.org/10.1007/bf02736391.

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5

Wilson, Robyn F., Helene Marsh y John Winter. "Importance of canopy connectivity for home range and movements of the rainforest arboreal ringtail possum (Hemibelideus lemuroides)". Wildlife Research 34, n.º 3 (2007): 177. http://dx.doi.org/10.1071/wr06114.

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Roads and powerline corridors destroy canopy connectivity in the rainforest of north-east Australia. We tested the hypotheses that linear barriers affect (a) the alignment of home ranges, (b) use of habitat either side of linear barriers, and (c) the crossing of them by the strictly arboreal lemuroid ringtail possum (Hemibelideus lemuroides), which is known to be vulnerable to habitat fragmentation. Radio-tracking and a translocation experiment were conducted at a narrow 7-m-wide road and an 80-m-wide powerline. Homes ranges of lemuroid ringtails ranged from 0.15 to 1.67 ha (minimum convex polygon) and were aligned with the road but not powerline corridors. When lemuroid ringtails were experimentally translocated, wider canopy clearings over roads reduced their capacity to return to their original home range, and the powerline corridor was a nearly insurmountable barrier. No possums were observed crossing roads or the powerline corridor at ground level or residing in the intervening matrix, indicating that loss of canopy connectivity has a negative impact on their movements.
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6

Dickinson, Edwin, Emily Atkinson, Antonio Meza, Shruti Kolli, Ashley R. Deutsch, Anne M. Burrows y Adam Hartstone-Rose. "Visualization and quantification of mimetic musculature via DiceCT". PeerJ 8 (16 de junio de 2020): e9343. http://dx.doi.org/10.7717/peerj.9343.

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The muscles of facial expression are of significant interest to studies of communicative behaviors. However, due to their small size and high integration with other facial tissues, the current literature is largely restricted to descriptions of the presence or absence of specific muscles. Using diffusible iodine-based contrast-enhanced computed tomography (DiceCT) to stain and digitally image the mimetic mask of Eulemur flavifrons (the blue-eyed black lemur), we demonstrate—for the first time—the ability to visualize these muscles in three-dimensional space and to measure their relative volumes. Comparing these data to earlier accounts of mimetic organization with the face of lemuroidea, we demonstrate several novel configurations within this taxon, particularly in the superior auriculolabialis and the posterior auricularis. We conclude that DiceCT facilitates the study these muscles in closer detail than has been previously possible, and offers significant potential for future studies of this anatomy.
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7

Crowley, Brooke Erin. "Captive Dwarf and Mouse Lemurs Have Variable Fur Growth". Animals 10, n.º 8 (28 de julio de 2020): 1288. http://dx.doi.org/10.3390/ani10081288.

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Researchers typically assume constant fur and hair growth for primates, but the few studies that have investigated growth explicitly suggest this may not be the case. Instead, growth may vary considerably among individuals and across seasons. One might expect this variability to be most pronounced for species that have seasonally variable activity patterns (e.g., Madagascar’s Cheiorogaleidae). In particular, dwarf lemurs (Cheirogaleus spp.) undergo considerable changes in their daily activity levels (torpor) in the austral fall, when nights get shorter. I monitored regrowth of shaved fur patches for eight adult captive fat-tailed dwarf lemurs (Cheirogaleus medius) and gray mouse lemurs (Microcebusmurinus) on a bi-weekly basis for 21 months in total. Regrowth varied considerably both within and among individuals. Overall, fur regrew in spurts and was faster for mouse lemurs (0–14 to 215–229 days) than dwarf lemurs (27–40 to 313–327 days). There were significant differences between species and an obvious influence of season for dwarf lemurs, but no clear influence of shave location, age, or sex. Similar trends have been previously reported for captive lemurids, suggesting that seasonal fur growth may be widespread across Lemuroidea. Researchers are cautioned against using primate fur or hair to investigate variables confounded by seasonality (such as diet and body condition) until patterns of growth are better understood.
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8

Hill, J. P., Frances E. Ince y A. Subba Rau. "Development of the Fœtal Membranes in Loris, with special reference to the Mode of Vascularisation of the Chorion in the Lemuroidea and its Phylogenetic Significance." Proceedings of the Zoological Society of London 98, n.º 3 (7 de mayo de 2010): 699–716. http://dx.doi.org/10.1111/j.1469-7998.1928.tb07165.x.

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9

Harding, Elaine K. y Shirin Gomez. "Positive edge effects for arboreal marsupials: an assessment of potential mechanisms". Wildlife Research 33, n.º 2 (2006): 121. http://dx.doi.org/10.1071/wr04059.

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In this study we examined the potential for positive edge effects on folivorous arboreal marsupials inhabiting upland rainforest in the Wet Tropics region of far north Queensland, Australia. We predicted that the folivores should have increased densities at edges relative to interior forest 90 m from the edge owing to the following causal factors, either separately or in combination: (a) increased foliar biomass, measured as vertical foliage density; and/or (b) increased abundance of preferred food trees. To test these hypotheses, we conducted surveys of the lemuroid ringtail possum (Hemibelideus lemuroides), the green ringtail possum (Pseudochirops archeri), the Herbert River ringtail possum (Pseudochirulus herbertensis) and the coppery brushtail possum (Trichosurus vulpecula johnstonii) at two remnant rainforest sites with ‘hard’ edges such as roads or pasture. Because arboreal species are often difficult to survey accurately within forests, we utilised pellet counts as an index of the population and compared this to the common survey technique of night spotlighting. Our results indicated that pellet counts, combined over all species, were positively and strongly correlated with spotlighting results. Using pellet counts as a relative index of arboreal folivore populations, we found that edge transects contained a higher abundance of all species combined than did interior transects. Further, total foliage density in the 10–30-m vertical transect was found to be significantly correlated with total pellet counts at edge transects. Total preferred tree species was not significantly different between edge and interior transects. From these results we propose that foliage density, as a surrogate for biomass, is a possible mechanism explaining the higher abundance of arboreal marsupials at the edges of these two highland rainforest sites in north Queensland.
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10

DelPero, Massimiliano, Luca Pozzi y Judith C. Masters. "A Composite Molecular Phylogeny of Living Lemuroid Primates". Folia Primatologica 77, n.º 6 (2006): 434–45. http://dx.doi.org/10.1159/000095390.

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11

Rasmussen, D. Tab. "The phylogenetic position ofMahgarita stevensi: protoanthropoid or lemuroid?" International Journal of Primatology 11, n.º 5 (octubre de 1990): 439–69. http://dx.doi.org/10.1007/bf02196131.

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12

Seiffert, Erik R., Loïc Costeur y Doug M. Boyer. "Primate tarsal bones from Egerkingen, Switzerland, attributable to the middle Eocene adapiformCaenopithecus lemuroides". PeerJ 3 (23 de junio de 2015): e1036. http://dx.doi.org/10.7717/peerj.1036.

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13

Erhart, Elizabeth M. y Deborah J. Overdorff. "Rates of Agonism by Diurnal Lemuroids: Implications for Female Social Relationships". International Journal of Primatology 29, n.º 5 (29 de agosto de 2008): 1227–47. http://dx.doi.org/10.1007/s10764-008-9287-0.

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14

Walker, Alan, Timothy M. Ryan, Mary T. Silcox, Elwyn L. Simons y Fred Spoor. "The semicircular canal system and locomotion: The case of extinct lemuroids and lorisoids". Evolutionary Anthropology: Issues, News, and Reviews 17, n.º 3 (18 de junio de 2008): 135–45. http://dx.doi.org/10.1002/evan.20165.

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15

Smith, Timothy D., Laura J. Alport, Anne M. Burrows, Kunwar P. Bhatnagar, John C. Dennis, Praphul Tuladhar y Edward E. Morrison. "Perinatal size and maturation of the olfactory and vomeronasal neuroepithelia in lorisoids and lemuroids". American Journal of Primatology 69, n.º 1 (2006): 74–85. http://dx.doi.org/10.1002/ajp.20328.

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16

Preuss, Todd M. y Jon H. Kaas. "Cytochrome Oxidase 'Blobs' and Other Characteristics of Primary Visual Cortex in a Lemuroid Primate, Cheirogaleus medius". Brain, Behavior and Evolution 47, n.º 2 (1996): 103–12. http://dx.doi.org/10.1159/000113231.

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