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Journal articles on the topic 'Whitii'

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Published: 4 June 2021

Last updated: 1 February 2022

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1

Milton, DA. "Genetic-Evidence for Sympatric Differentiation Between 2 Color Morphs of the Skink Egernia-Whitii." Australian Journal of Zoology 38, no. 2 (1990): 117. http://dx.doi.org/10.1071/zo9900117.

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The viviparous skink Egernia whitii is dimorphic for dorsal colour pattern. Both patterned and plain morphs coexist throughout the species' range. Adults live in family groups beneath exfoliating granite rocks. The closely related E. modesta also coexists in similar habitats in the northern part of the range of E. whitii. The plain E. whitii morph is intermediate in colour pattern between patterned E. whitii and E. modesta. Three populations of E. whitii and two populations of E. modesta were examined electrophoretically to assess the status of the plain morph of E. whitii. There were no fixed differences between the two morphs of E. whitii at any of the 55 loci examined, and loci polymorphic in both rnorphs of E. whitii showed no evidence of linkage disequilibria. Although heterozygosity values (H=0.017�0.002) and the level of polymorphism (P 0.95=0.015) were low, there were highly significant allele frequency differences between sympatric samples of the two morphs of E. whitii. This indicated that the two morphs were conspecific, yet they were not interbreeding at random. The established frequency of gene exchange between the two colour morphs in the three populations sampled varied from 3.6 to 6 individuals per generation. Reproductive data confirmed that both colour morphs of E. whitii produced young of the same dorsal colour pattern as their own in much greater frequency than random. However, females of both colours can and do breed with males of the other colour in very low frequency. Analysis of the lateral colour pattern of the two E. whitii morphs and E. modesta suggests that the colour patterns of the two E. whitii morphs are very similar, yet differ slightly from the colour pattern of E. modesta in the region of geographic overlap of these species. These results suggest that behavioural or microhabit differences between the two morphs may be involved in mate recognition.

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2

Donnellan, Stephen C., Mark N. Hutchinson, Paula Dempsey, and William S. Osborne. "Systematics of the Egernia whitii species group (Lacertilia : Scincidae) in south-eastern Australia." Australian Journal of Zoology 50, no. 5 (2002): 439. http://dx.doi.org/10.1071/zo01065.

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Allozyme electrophoresis was used to assess the taxonomic significance of colour pattern variation within and between populations of the Egernia whitii species group from 41 locations in south-eastern Australia. Analysis of the products of 39 presumed loci revealed that a minimum of three species are present in southern New South Wales among populations previously referred to Egernia whitii. Fixed allelic differences were maintained where pairs of species were sympatric. One of these three species is wide-ranging and is the one to which the name E. whitii is properly applied. The other two are more restricted ecologically and geographically and are described here as new. The three species are genetically and morphologically distinct from the other three eastern Australian members of the species group, E.�margaretae, E. modesta, and E. multiscutata. Genetic data and a review of the morphological evidence provide no support for the recognition of subspecies within either E. whitii (sensu stricto) or E. multiscutata.

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3

Milton, DA, and JM Hughes. "Habitat Selection by 2 Closely Related Skinks, Egernia-Modesta Storr and Egernia-Whitii Lacepede (Lacertilia, Scincidae)." Wildlife Research 13, no. 2 (1986): 295. http://dx.doi.org/10.1071/wr9860295.

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'The habitat and microhabitat preferences, and times of activity, of the skinks Egernia modesta and E. whitii were examined in southern Queensland where they coexist in a narrow zone. The above parameters were compared between locally sympatric and allopatric populations, in an attempt to determine whether there was evidence of niche separation in sympatry. E. modesta preferred open habitats with little canopy cover and high grass cover, adjacent to rocky retreats. E. whitii preferred rocky areas with well developed canopy and shrub layers. Both species were active throughout the day, although E. modesta was active later than E. whitii. No evidence was found of competition restricting habitat preferences where the two species coexisted. It is suggested that human disturbance has had some influence on current distributions of these species.

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4

Milton, DA. "Reproduction of 2 Closely Related Skinks, Egernia-Modesta and Egernia-Whitii (Lacertilia, Scincidae) in Southeast Queensland." Australian Journal of Zoology 35, no. 1 (1987): 35. http://dx.doi.org/10.1071/zo9870035.

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The reproductive cycles of two closely related skinks, Egernia modesta and E, whitii, in southern Queensland are described and compared in sympatric populations. They are very similar, both species produce 1-5 live young about 40 mm long in January-early February. Lizards mature at the end of their second year and litter size is positively related to female body length. Adults grow to 110 mm and appear to live at least 4 years. Two non-hybridising colour morphs of E. whitii were present in the study area and did not associate at random. Possible mechanisms explaining the evolution of these three closely related forms, which can coexist in similar habitats, are discussed.

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5

Chapple, DG. "Life history and reproductive ecology of White's skink, Egernia whitii." Australian Journal of Zoology 53, no. 6 (2005): 353. http://dx.doi.org/10.1071/zo05030.

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The life history and reproductive ecology of White’s skink, Egernia whitii, was examined in a population in the Australian Capital Territory using both field and genetic studies. Colour pattern polymorphism was evident within the population, with both patterned and plain-back morphs present. Lizards typically took 3 years to reach sexual maturity, with the size at maturity being ~75 mm snout–vent length (SVL) in both sexes. There was an even overall adult sex ratio, although a slight female-bias was evident in plain-back individuals. Sexual dimorphism was evident, with males having longer and wider heads, and females having larger body size. Females generally bred annually, with mating occurring in September–October and parturition in late January–February, although the litter was produced over several days (2–10 days, mean 4 days). Litter size ranged from one to four (mean of 2.5). There was a significant relationship between maternal SVL and both litter size and relative clutch mass, but these trends were not consistent between colour morphs. An inverse relationship between litter size and offspring size (SVL and mass) was found. Comparison of the results with previous investigations of E. whitii indicates substantial geographic variation in life-history traits that is presumably associated with latitudinal variation in climatic conditions.

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6

Hill, Peta, Foyez Shams, Christopher P. Burridge, Erik Wapstra, and Tariq Ezaz. "Differences in Homomorphic Sex Chromosomes Are Associated with Population Divergence in Sex Determination in Carinascincus ocellatus (Scincidae: Lygosominae)." Cells 10, no. 2 (February 1, 2021): 291. http://dx.doi.org/10.3390/cells10020291.

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Sex determination directs development as male or female in sexually reproducing organisms. Evolutionary transitions in sex determination have occurred frequently, suggesting simple mechanisms behind the transitions, yet their detail remains elusive. Here we explore the links between mechanisms of transitions in sex determination and sex chromosome evolution at both recent and deeper temporal scales (<1 Myr; ~79 Myr). We studied a rare example of a species with intraspecific variation in sex determination, Carinascincus ocellatus, and a relative, Liopholis whitii, using c-banding and mapping of repeat motifs and a custom Y chromosome probe set to identify the sex chromosomes. We identified both unique and conserved regions of the Y chromosome among C. ocellatus populations differing in sex determination. There was no evidence for homology of sex chromosomes between C. ocellatus and L. whitii, suggesting independent evolutionary origins. We discuss sex chromosome homology between members of the subfamily Lygosominae and propose links between sex chromosome evolution, sex determination transitions, and karyotype evolution.

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7

Chapple, David G., Mark N. Hutchinson, Brad Maryan, Mike Plivelich, Jennifer A. Moore, and J. Scott Keogh. "Evolution and maintenance of colour pattern polymorphism in Liopholis (Squamata:Scincidae)." Australian Journal of Zoology 56, no. 2 (2008): 103. http://dx.doi.org/10.1071/zo08040.

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We examined the evolution and maintenance of colour pattern polymorphism in an Australian lineage of scincid lizards, the genus Liopholis. Liopholis comprises 11 species, with representatives in both the temperate zone and arid zone. Specimens from all major Australian museums were examined to characterise colour pattern polymorphism within Liopholis, and investigate geographic variation in the relative abundance of morphs within polymorphic species. We used a previously published phylogeny for Liopholis to investigate the evolution and maintenance of colour pattern polymorphism within the group. Five species were found to exhibit colour pattern polymorphism (L. margaretae margaretae Storr, L. m. personata Storr, L. montana Donnellan et al., L. multiscutata Mitchell & Behrndt, L. pulchra Werner, L. whitii Lacépède), with six species being monomorphic (L. guthega Donnellan et al., L. inornata Rosén, L. kintorei Stirling & Zietz, L. modesta Storr, L. slateri Storr, L. striata Sternfeld). Three colour morphs occur in L. whitii, with the relative abundance of each varying significantly among latitudes. The patterned morph is most common, while the incidence of the plain-back morph decreases at latitudes higher than 35°S. The L. whitii patternless morph occurs only within a narrow latitudinal band (34–38°S). In L. multiscutata, the relative abundance of the patterned (~89–93%) and patternless morph (~7–11%) is consistent across regions, except for the Nullarbor Plain region where the patternless morph is more common (~39%). Our analyses suggest a single origin of colour pattern polymorphism in Liopholis, followed by the subsequent loss of polymorphism on four occasions. The secondary loss of polymorphism might be associated with climate or habitat, possibly as the result of shifts into the arid zone or alpine regions of Australia. This study provides the necessary framework for future studies of colour pattern polymorphism in Liopholis.

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8

Chapple, David G., and J. Scott Keogh. "Group Structure and Stability in Social Aggregations of White's Skink, Egernia whitii." Ethology 112, no. 3 (March 2006): 247–57. http://dx.doi.org/10.1111/j.1439-0310.2006.01153.x.

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9

CHAPPLE, DAVID G., and J. SCOTT KEOGH. "Complex mating system and dispersal patterns in a social lizard, Egernia whitii." Molecular Ecology 14, no. 4 (March 16, 2005): 1215–27. http://dx.doi.org/10.1111/j.1365-294x.2005.02486.x.

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10

Hugi, Jasmina, Christian Mitgutsch, and Marcelo R. Sánchez-Villagra. "Chondrogenic and ossification patterns and sequences in White's skink Liopholis whitii (Scincidae, Reptilia)." Zoosystematics and Evolution 86, no. 1 (March 24, 2010): 21–32. http://dx.doi.org/10.1002/zoos.200900011.

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11

Jordan, Emilio Ariel, Juan Ignacio Areta, and Ingrid Holzmann. "Mate recognition systems and species limits in a warbling-finch complex (Poospiza nigrorufa/whitii)." Emu - Austral Ornithology 117, no. 4 (August 16, 2017): 344–58. http://dx.doi.org/10.1080/01584197.2017.1360746.

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12

Cartledge, Victoria A., and Susan M. Jones. "Does adrenal responsiveness vary with sex and reproductive status in Egernia whitii, a viviparous skink?" General and Comparative Endocrinology 150, no. 1 (January 2007): 132–39. http://dx.doi.org/10.1016/j.ygcen.2006.07.021.

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13

Ponciano, Luiza Corral Martins de Oliveira, Deusana Maria da Costa Machado, Ana Carolina Gelmini de Faria, Ana Carolina Maciel, Juliana Matos, and Mariana Novaes. "Hábitos de vida dos Gastropoda e Bellerophontida da formação Maecuru, Devoniano Médio, Bacia do Amazonas, Brasil." Anuário do Instituto de Geociências 30, no. 1 (January 1, 2007): 197–203. http://dx.doi.org/10.11137/2007_1_197-203.

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The Maecuru Formation comprises the Devonian-Carboniferous sedimentary sequence of Amazonas Basin and consists of fluvialdeltaics to neritics sandstones and pelites layers. Its fossiliferous sediments (the uppermost part of the Lontra Member) consists of hummocky cross-stratified fine-grained to very coarse sandstones beds.With the purpose of adding more information about the palaeoecology of The Maecuru Formation fossils, the life habits of gastropods and bellerophontids were inferred based on functional analysis and similarities with the living forms. The more significant features used were: (1) total frontal cross-sectional area, (2) height and relative positions of pressure point and center of gravity, (3) apertural margin morphology, (4) kind of symmetry and (5) surface smoothness. The species Platyceras (Orthonychia) steinmanni; Platyceras (Tumbophalus) hartti; Platyceras (Platyostoma) darwini; Platyceras (Platyostoma) (?) agassizi; Platyceras (Orthonychia) meerwarthi; Platyceras (Orthonychia) gracilis; Platyceras (Tumbophalus) coutoanus; "Platyceras" tschernischewi; "Platyceras" subconicum; "Platyceras" (Ortonychia) hussaki; "Platyceras" (Ortonychia) whitii; "Platyceras" (Ortonychia) whitii var. curua and "Platyceras" symmetricum var. maecuruensis represent the epifaunal gastropods with low mobility (coprophagous/suspension feeders) of the Maecuru Formation, living symbiotically directly over the anus of a crinoid or nearby. This coprophagous mode of life was probably a non-obligate relationship, because only the closest organisms will get all the advantages of using the crinoid host as a nutrient source. The others adult platyceratids would have a broader feeding repertoire, like as suspension feeders. The bellerophonts Plectonotus (Plectonotus) derbyi, Plectonotus (?) (Plectonotus) salteri e Bucanella reissi would have an epifaunal medium to high mobility, showing a predator habit preferably. On the other hand Bucania freitasi, Ptomatis forbesi and Bellerophon steltzneri showed morphologies compable to a grazer habit with medium mobility. This relative high diversity of gastropods and bellerophonts corroborates the environment of medium and inner shelf inferred for the Maecuru Formation among the others macrofossils, since the majority of Paleozoic fauna of gastropods were typically from shallow seas.

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14

Chapple, David G., J. Scott Keogh, and Mark N. Hutchinson. "Molecular phylogeography and systematics of the arid-zone members of the Egernia whitii (Lacertilia: Scincidae) species group." Molecular Phylogenetics and Evolution 33, no. 3 (December 2004): 549–61. http://dx.doi.org/10.1016/j.ympev.2004.08.010.

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15

McEvoy, Jo, Geoffrey M. While, David L. Sinn, and Erik Wapstra. "The role of size and aggression in intrasexual male competition in a social lizard species, Egernia whitii." Behavioral Ecology and Sociobiology 67, no. 1 (October 10, 2012): 79–90. http://dx.doi.org/10.1007/s00265-012-1427-z.

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16

WHILE, GEOFFREY M., TOBIAS ULLER, and ERIK WAPSTRA. "Within-population variation in social strategies characterize the social and mating system of an Australian lizard,Egernia whitii." Austral Ecology 34, no. 8 (December 2009): 938–49. http://dx.doi.org/10.1111/j.1442-9993.2009.02002.x.

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17

Jones, Susan M., and Karyn Bell. "Plasma corticosterone concentrations in males of the skink Egernia whitii during acute and chronic confinement, and over a diel period." Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 137, no. 1 (January 2004): 105–13. http://dx.doi.org/10.1016/s1095-6433(03)00267-8.

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18

CHAPPLE, DAVID G., and J. SCOTT KEOGH. "Parallel adaptive radiations in arid and temperate Australia: molecular phylogeography and systematics of the Egernia whitii (Lacertilia: Scincidae) species group." Biological Journal of the Linnean Society 83, no. 2 (September 30, 2004): 157–73. http://dx.doi.org/10.1111/j.1095-8312.2004.00378.x.

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19

WHILE, G. M., S. M. JONES, and E. WAPSTRA. "Birthing asynchrony is not a consequence of asynchronous offspring development in a non-avian vertebrate, the Australian skink Egernia whitii." Functional Ecology 21, no. 3 (June 2007): 513–19. http://dx.doi.org/10.1111/j.1365-2435.2007.01272.x.

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20

CHAPPLE, DAVID G., J. SCOTT KEOGH, and MARK N. HUTCHINSON. "Substantial genetic substructuring in southeastern and alpine Australia revealed by molecular phylogeography of the Egernia whitii (Lacertilia: Scincidae) species group." Molecular Ecology 14, no. 5 (April 2005): 1279–92. http://dx.doi.org/10.1111/j.1365-294x.2005.02463.x.

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21

Cartledge, Victoria A., Brett Gartrell, and Susan M. Jones. "Adrenal and white cell count responses to chronic stress in gestating and postpartum females of the viviparous skink Egernia whitii (Scincidae)." Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 141, no. 1 (May 2005): 100–107. http://dx.doi.org/10.1016/j.cbpb.2005.04.008.

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22

Thornett, Elizabeth, Bertram Ostendorf, and David A. Taggart. "Interspecies co-use of southern hairy-nosed wombat (Lasiorhinus latifrons) burrows." Australian Mammalogy 39, no. 2 (2017): 205. http://dx.doi.org/10.1071/am15052.

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Burrows can provide refuge for both burrowing and non-burrowing species within harsh environments through protection from climatic extremes, water loss and predation. In Australia, however, despite having a rich diversity of burrowing mammals, little is known about the use of burrows by non-burrowing species. This study aimed to identify the extent of co-use of southern hairy-nosed wombat (Lasiorhinus latifrons) burrows on Wedge Island off the coast of South Australia. Burrow use was monitored using 34 motion-activated cameras placed outside wombat burrows between March and September 2015. Eleven species were found to use burrows, with six commensal species observed using burrows on numerous occasions. These included two mammal species (black-footed rock-wallaby, Petrogale lateralis pearsoni; brush-tailed bettong, Bettongia penicillata), three reptile species (peninsula dragon, Ctenophorus fionni; southern sand-skink, Liopholis multiscutata; White’s skink, Liopholis whitii), and one avian species (little penguin, Eudyptula minor). The most common species observed using burrows was the black-footed rock-wallaby, which was recorded using burrows 1795 times. Observations of wombats using burrows were made 1674 times. The prevalent use of burrows on Wedge Island by species other than wombats is an observation with potentially important and broad ecological, conservation, and management implications across Australia’s arid and semiarid zones.

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23

While, Geoffrey M., David L. Sinn, and Erik Wapstra. "Female aggression predicts mode of paternity acquisition in a social lizard." Proceedings of the Royal Society B: Biological Sciences 276, no. 1664 (March 4, 2009): 2021–29. http://dx.doi.org/10.1098/rspb.2008.1926.

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Individual differences in behaviour are ubiquitous in nature. Despite the likely role of selection in maintaining these differences, there are few demonstrations of their fitness consequences in wild populations and, consequently, the mechanisms that link behavioural variation to variation in fitness are poorly understood. Specifically, the consequences of consistent individual differences in behaviour for the evolution of social and mating strategies have rarely been considered. We examined the functional links between variation in female aggression and her social and mating strategies in a wild population of the social lizard Egernia whitii . We show that female Egernia exhibit temporally consistent aggressive phenotypes, which are unrelated to body size, territory size or social density. A female's aggressive phenotype, however, has strong links to her mode of paternity acquisition (within- versus extra-pair paternity), with more aggressive females having more offspring sired by extra-pair males than less aggressive females. We discuss the potential mechanisms by which female aggression could underpin mating strategies, such as the pursuit/acceptance of extra-pair copulations. We propose that a deeper understanding of the evolution and maintenance of social and mating systems may result from an explicit focus on individual-level female behavioural phenotypes and their relationship with key reproductive strategies.

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24

Greene, Mark E. "For whiter whites, use beetles." Materials Today 10, no. 3 (March 2007): 18. http://dx.doi.org/10.1016/s1369-7021(07)70014-7.

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25

Langkilde, Tracy, Dave O'Connor, and Richard Shine. "Shelter-site use by five species of montane scincid lizards in south-eastern Australia." Australian Journal of Zoology 51, no. 2 (2003): 175. http://dx.doi.org/10.1071/zo02073.

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Montane (cold-climate) habitats may impose severe thermal constraints on habitat use by ectotherms, favouring strong interspecific convergence in the attributes of suitable shelter-sites. We studied shelter-site use by five species of viviparous scincid lizards in Kanagra Boyd National Park, a montane (1200 m above sea level) forested region 160 km west of Sydney. We scored 21 attributes of 93 shelter-sites (13–20 per species), and the same attributes at unoccupied 'control' sites. These attributes included macrohabitat (e.g. canopy openness, substrate type, distance to waterbodies and logs) as well as shelter-site characteristics (e.g. type of cover-item, size of crevice). Hemispherical-lens photographs and gap-analysis software yielded estimates of solar radiation at each site, and data-loggers recorded temperature profiles in each occupied retreat-site. Principal Components Analysis of the data set identified eight axes of variation. Significant interspecific differences were evident on four of these axes, but with substantial overlap reflecting the broad syntopy of the taxa, plus similarities in characteristics of occupied retreat-sites (e.g. most lizard species utilised sun-exposed shelter-sites with logs nearby). Egernia species (cunninghami, saxatilis, whitii) typically used more open habitats than did Eulamprus (heatwolei, tympanum). Egernia cunninghami used very large crevices, whereas Eulamprus tympanum occupied heavily wooded macrohabitats. At this cold-climate site, interspecific similarities in the characteristics of utilised retreat-sites generated substantial overlap among species in the kinds of sites used, potentially intensifying interference competition among these taxa.

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26

Lipkin, R. "A Quicker, Cooler Bleach for Whiter Whites?" Science News 145, no. 26 (June 25, 1994): 407. http://dx.doi.org/10.2307/3978256.

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27

Laden, Sonja. "Middle-class matters, or, how to keep whites whiter, colours brighter, and blacks beautiful." Critical Arts 11, no. 1-2 (January 1997): 120–41. http://dx.doi.org/10.1080/02560049785310101.

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28

Ratana, Donn. "“Reconnection”/Ka Whitiki." Cultural Studies ↔ Critical Methodologies 12, no. 1 (February 2012): 60–66. http://dx.doi.org/10.1177/1532708611430490.

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29

Gans, Herbert J. "“Whitening” and the Changing American Racial Hierarchy." Du Bois Review: Social Science Research on Race 9, no. 2 (2012): 267–79. http://dx.doi.org/10.1017/s1742058x12000288.

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AbstractAs a result of the increasing number of biracials and multiracials, and White reconstructions of previously non-White skin colors, the Whitening of selected immigrants and especially their children appears to be proceeding. Although there are many studies on the racial identity of biracials, too little research exists on how Whites identify them and light-skinned monoracials, which of these they Whiten, how, and why. Enough is known to suggest that if current trends continue, our picture of the country's racial hierarchy has to be revised. While Whites will likely remain on top and poor African Americans and other Blacks at the bottom, what happens in the middle cannot now even be guessed at with any hope of accuracy. For that reason alone, empirical and policy-oriented research on White identification patterns is badly needed.

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30

ROSENTHALL, JOANNA. "Whitby." Critical Quarterly 32, no. 3 (September 1990): 102–4. http://dx.doi.org/10.1111/j.1467-8705.1990.tb00613.x.

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31

White, Joel. "Protein Expression in Corynebacterium glutamicum." BioProcessing Journal 9, no. 2 (February 10, 2011): 53–55. http://dx.doi.org/10.12665/j92.white.

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32

Akresh, Ilana Redstone, and Reanne Frank. "Differential Returns?: Neighborhood Attainment among Hispanic and Non–Hispanic White New Legal Permanent Residents." City & Community 17, no. 3 (September 2018): 788–807. http://dx.doi.org/10.1111/cico.12313.

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We use data from the New Immigrant Survey to examine patterns of residential attainment among Hispanic immigrants who recently became legal permanent residents (LPRs) relative to new LPR non–Hispanic white immigrants. We focus on whether these Hispanic and non–Hispanic white immigrants differ in their ability to transform human capital into residential advantage. Our results suggest that the answer depends on the neighborhood attribute in question. When predicting residence in tracts with relatively more non–Hispanic whites, the answer is yes, with evidence in support of the place stratification model of residential attainment. We find that non–Hispanic white immigrants have access to relatively whiter neighborhoods than their Hispanic immigrant counterparts, irrespective of differences in education levels. When assessing Hispanic immigrants’ ability to enter socioeconomically advantaged neighborhoods, however, the differences we observe are mostly accounted for by compositional differences in sociodemographic and acculturation factors. Taken together, our findings suggest that Hispanic immigrants are more similar to their white immigrant counterparts when it comes to converting higher education into higher income neighborhoods than into increased residential integration with whites; although their exposure to more socioeconomically advantaged neighborhoods at all levels of education remains lower than that of their white immigrant counterparts.

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33

AMORY, Fr. "Whited Sepulchres." Recherches de Théologie et Philosophie Médiévales 53 (January 1, 1986): 5–39. http://dx.doi.org/10.2143/rtpm.53.0.2016356.

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34

Klitz, William. "Whitey crumbles." Trends in Genetics 30, no. 12 (December 2014): 516–18. http://dx.doi.org/10.1016/j.tig.2014.10.004.

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35

Jessop, Christopher. "Whiter skies." New Scientist 214, no. 2871 (June 2012): 30. http://dx.doi.org/10.1016/s0262-4079(12)61685-6.

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36

Floriani, Carol Milardo. "Nursing Whites." AJN, American Journal of Nursing 110, no. 5 (May 2010): 13. http://dx.doi.org/10.1097/01.naj.0000372053.50576.c2.

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37

Spark, Ceridwen. "Whites Out?" Journal of Pacific History 40, no. 2 (September 2005): 213–19. http://dx.doi.org/10.1080/00223340500176624.

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38

Intan, Nadya, and Syahrul R.,. "PENGARUH MODEL DISCOVERY LEARNING BERBANTUAN MEDIA GAMBAR BERSERI TERHADAP KETERAMPILAN MENULIS TEKS EKSPLANASI SISWA KELAS VIII SMP NEGERI 4 PADANG." Pendidikan Bahasa Indonesia 9, no. 1 (February 20, 2020): 143. http://dx.doi.org/10.24036/108275-019883.

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ABSTRACT The purpose of the research are (1) to describe exsplanatory text writing skills of VIII grade students SMP Negeri 4 Padang before applying discovery learning model whitin serial piscture media, (2) to describe exsplanatory text writing skills of VIII grade students SMP Negeri 4 Padang after applying discovery learning model whitin serial piscture media, and (3) to analize effect of discovery learning model whitin serial piscture media to exsplanatory text writing skills of VIII grade students SMP Negeri 4 Padang. Based on the data analize the application of discovery learning model whitin serial piscture media affects the exsplanatory text writing skills of VIII grade students SMP Negeri 4 Padang. Kata kunci: pengaruh, discovery learning¸ media gambar berseri, menulis teks eksplanasi

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Jacobs, S. W. L. "An Earlier Name for Panicum whitei (Gramineae)." Kew Bulletin 40, no. 3 (1985): 662. http://dx.doi.org/10.2307/4109631.

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Pereira, Olivier, and Laurence Wolsey. "On the Wagner-Whitin Lot-Sizing Polyhedron." Mathematics of Operations Research 26, no. 3 (August 2001): 591–600. http://dx.doi.org/10.1287/moor.26.3.591.10586.

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Decraene, L. P. Ronse, and E. Smets. "The floral development of Popowia whitei (Annonaceae)." Nordic Journal of Botany 10, no. 4 (October 1990): 411–20. http://dx.doi.org/10.1111/j.1756-1051.1990.tb01781.x.

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Hanafizadeh, Payam, Amir Shahin, and Mehdi Sajadifar. "Robust Wagner–Whitin algorithm with uncertain costs." Journal of Industrial Engineering International 15, no. 3 (November 26, 2018): 435–47. http://dx.doi.org/10.1007/s40092-018-0298-y.

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Khan, A. R., and B. J. Selman. "Effect of pirimiphos methyl, Nosema whitei, and pirimiphos methyl-N. whitei doses on the growth of Tribolium castaneum adults." Journal of Invertebrate Pathology 49, no. 3 (May 1987): 336–38. http://dx.doi.org/10.1016/0022-2011(87)90067-x.

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Sokolova, Yuliya Y., Irma V. Issi, Elena V. Morzhina, Yuriy S. Tokarev, and Charles R. Vossbrinck. "Ultrastructural analysis supports transferring Nosema whitei Weiser 1953 to the genus Paranosema and creation a new combination, Paranosema whitei." Journal of Invertebrate Pathology 90, no. 2 (October 2005): 122–26. http://dx.doi.org/10.1016/j.jip.2005.06.009.

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Reddy, Maureen T., Karen Brodkin, and Abby L. Ferber. "White, Whiter, Whitest." Women's Review of Books 16, no. 6 (March 1999): 5. http://dx.doi.org/10.2307/4023120.

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James, V. Denise. "Whites, Tarry Here!" Radical Philosophy Review 16, no. 3 (2013): 805–8. http://dx.doi.org/10.5840/radphilrev201316360.

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Millington, Barry. "Wagner Washes Whiter." Musical Times 137, no. 1846 (December 1996): 5. http://dx.doi.org/10.2307/1004263.

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Alejandro de la Fuente. "The Whites' House." Transition, no. 122 (2017): 1. http://dx.doi.org/10.2979/transition.122.1.01.

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Levy, D. M., and Y. Tzabar. "Whiter than whiteout." Anaesthesia 48, no. 1 (February 22, 2007): 91. http://dx.doi.org/10.1111/j.1365-2044.1993.tb06828.x.

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Schmidt, Sigrid. "Snow Whitein Africa." Fabula 49, no. 3-4 (December 2008): 268–87. http://dx.doi.org/10.1515/fabl.2008.021.

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