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Artykuły w czasopismach na temat „Macrogeograhic”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 20 lutego 2023

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1

Pitocchelli, J. "Macrogeographic variation in the song of the Mourning Warbler (Oporornis philadelphia)." Canadian Journal of Zoology 89, no. 11 (November 2011): 1027–40. http://dx.doi.org/10.1139/z11-077.

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Studies of macrogeographic variation in birdsong involve populations incapable of interbreeding because of physical barriers or separation by large distances. Different patterns have emerged from these studies such as (i) little or no variation exists among individuals or populations from the breeding range, (ii) individual variation is greater than among population variation resulting in no geographic structure, (iii) clinal variation, and (iv) macrogeographic variation where all individuals from several populations on the breeding range share a common song type forming a regional dialect or

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2

Fore, Stephanie A., and Timothy P. Spira. "Macrogeographic Allozyme Variation in Passiflora incarnata." Journal of the Torrey Botanical Society 129, no. 4 (October 2002): 326. http://dx.doi.org/10.2307/3088703.

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3

McCalden, Gerald. "Macrogeographic Functions: A Review And Extension." Geographical Analysis 7, no. 4 (September 3, 2010): 411–20. http://dx.doi.org/10.1111/j.1538-4632.1975.tb01053.x.

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4

LIU, IRENE A., BERNARD LOHR, BRIAN OLSEN, and RUSSELL GREENBERG. "MACROGEOGRAPHIC VOCAL VARIATION IN SUBSPECIES OF SWAMP SPARROW." Condor 110, no. 1 (February 2008): 102–9. http://dx.doi.org/10.1525/cond.2008.110.1.102.

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5

Budka, Michał, Gunvar Mikkelsen, Lucia Turčoková, Yoan Fourcade, Svein Dale, and Tomasz S. Osiejuk. "Macrogeographic variation in the call of the corncrakeCrex crex." Journal of Avian Biology 45, no. 1 (December 3, 2013): 65–74. http://dx.doi.org/10.1111/j.1600-048x.2013.00208.x.

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6

Villela, Priscilla Marqui Schmidt, Luiz Lehmann Coutinho, Carlos Ignacio Piña, and Luciano M. Verdade. "Macrogeographic genetic variation in broad-snouted caiman (Caiman latirostris)." Journal of Experimental Zoology Part A: Ecological Genetics and Physiology 309A, no. 10 (December 1, 2008): 628–36. http://dx.doi.org/10.1002/jez.489.

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7

Pitocchelli, Jay, David Guerra, and Jaimie Kender. "Macrogeographic variation in song of the MacGillivray's Warbler (Geothlypis tolmiei)." Wilson Journal of Ornithology 130, no. 3 (September 2018): 716–29. http://dx.doi.org/10.1676/17-089.1.

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8

Plante, Yves, Peter T. Boag, and Bradley N. White. "Macrogeographic variation in mitochondrial DNA of meadow voles (Microtus pennsylvanicus)." Canadian Journal of Zoology 67, no. 1 (January 1, 1989): 158–67. http://dx.doi.org/10.1139/z89-021.

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Mitochondrial DNA (mtDNA) from 99 meadow voles (Microtus pennsylvanicus) collected in 13 localities and from 2 Townsend's voles (M. townsendii) from a single locality was assayed for restriction fragment length polymorphism (RFLP) with 13 restriction endonucleases. There was evidence of extensive mtDNA sequence heterogeneity within and among meadow vole populations. Thirty-eight different mtDNA composite phenotypes were found. Two common mtDNA composite phenotypes were shared among five populations, the other mtDNA composite phenotypes being characteristic of individual populations. Estimates

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9

Webster, Lucy M. I., Paul C. D. Johnson, Aileen Adam, Barbara K. Mable, and Lukas F. Keller. "Macrogeographic population structure in a parasitic nematode with avian hosts." Veterinary Parasitology 144, no. 1-2 (March 2007): 93–103. http://dx.doi.org/10.1016/j.vetpar.2006.09.027.

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10

Guttman, Sheldon I., and Lee A. Weigt. "Macrogeographic Genetic Variation in the Enchenopa binotata Complex (Homoptera: Membracidae)." Annals of the Entomological Society of America 82, no. 2 (March 1, 1989): 156–65. http://dx.doi.org/10.1093/aesa/82.2.156.

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11

Brown, Eleanor D., and Susan M. Farabaugh. "Macrogeographic Variation in Alarm Calls of the Australian Magpie Gymnorhina tibicen." Bird Behavior 9, no. 1 (December 1, 1990): 64–68. http://dx.doi.org/10.3727/015613890791749055.

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12

Hafner, Mark S., John C. Hafner, James L. Patton, and Margaret F. Smith. "Macrogeographic Patterns of Genetic Differentiation in the Pocket Gopher Thomomys umbrinus." Systematic Zoology 36, no. 1 (March 1987): 18. http://dx.doi.org/10.2307/2413305.

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13

Andrade, S. C. S., C. A. Magalhaes, and V. N. Solferini. "Patterns of genetic variability in Brazilian Littorinids (Mollusca): a macrogeographic approach." Journal of Zoological Systematics and Evolutionary Research 41, no. 4 (November 2003): 249–55. http://dx.doi.org/10.1046/j.1439-0469.2003.00227.x.

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14

White, F. W. G. "Macrogeographic Variation in the Song of the Olive Whistler in Australia." Emu - Austral Ornithology 87, no. 1 (March 1987): 14–25. http://dx.doi.org/10.1071/mu9870014.

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15

Porter, J. S., J. S. Ryland, and G. R. Carvalho. "Micro- and macrogeographic genetic structure in bryozoans with different larval strategies." Journal of Experimental Marine Biology and Ecology 272, no. 2 (June 2002): 119–30. http://dx.doi.org/10.1016/s0022-0981(02)00042-4.

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16

Ouma, J. O., J. G. Marquez, and E. S. Krafsur. "Macrogeographic population structure of the tsetse fly, Glossina pallidipes (Diptera: Glossinidae)." Bulletin of Entomological Research 95, no. 5 (October 2005): 437–47. http://dx.doi.org/10.1079/ber2005376.

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AbstractTsetse flies are confined to sub-Saharan Africa where they occupy discontinuous habitats. In anticipation of area-wide control programmes, estimates of gene flow among tsetse populations are necessary. Genetic diversities were partitioned at eight microsatellite loci and five mitochondrial loci in 21 Glossina pallidipes Austin populations. At microsatellite loci, Nei's unbiased gene diversity averaged over loci was 0.659 and the total number of alleles was 214, only four of which were shared among all populations. The mean number of alleles per locus was 26.8. Random mating was observe

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17

Richmond, James A. "Macrogeographic Genetic Variation in Populations of the Webbing Cone worm (Lepidoptera: Pyralidae)." Journal of Entomological Science 30, no. 3 (July 1, 1995): 349–58. http://dx.doi.org/10.18474/0749-8004-30.3.349.

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Genetic variation among 14 populations of Dioryctria disclusa Heinrich adults was examined using starch gel electophoresis. The average number of alleles per locus exceeded 2.0 in all populations. The number of polymorphic loci exceeded 70% in 11 populations. Genetic structure data suggest moderate differentiation (average Fst, 0.111) among the populations. Most of the differentiation is attributable to three of the eight loci (MDH, ME, and IDH). Nei's genetic identity ranged from 0.77–1.00 between populations. A phenogram based on genetic identity and unweighted pair-group method of analysis

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18

Johnson, Ned K., and Jill A. Marten. "Macrogeographic Patterns of Morphometric and Genetic Variation in the Sage Sparrow Complex." Condor 94, no. 1 (February 1992): 1–19. http://dx.doi.org/10.2307/1368791.

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19

VIRGILIO, M., H. DELATTE, T. BACKELJAU, and M. DE MEYER. "Macrogeographic population structuring in the cosmopolitan agricultural pest Bactrocera cucurbitae (Diptera: Tephritidae)." Molecular Ecology 19, no. 13 (June 18, 2010): 2713–24. http://dx.doi.org/10.1111/j.1365-294x.2010.04662.x.

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20

Casaril, Aline Etelvina, Diego Peres Alonso, Karina Garcia Franco, Marcus Vinicius Niz Alvarez, Suellem Petilim Gomes Barrios, Wagner de Souza Fernandes, Jucelei de Oliveira Moura Infran, Ana Caroline Moura Rodrigues, Paulo Eduardo Martins Ribolla, and Alessandra Gutierrez de Oliveira. "Macrogeographic genetic structure of Lutzomyia longipalpis complex populations using Next Generation Sequencing." PLOS ONE 14, no. 10 (October 3, 2019): e0223277. http://dx.doi.org/10.1371/journal.pone.0223277.

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21

Gorbunova, A. Yu, D. I. Korobushkin, A. S. Zaitsev, and K. B. Gongalsky. "Forest fires increase variability of soil macrofauna communities along a macrogeographic gradient." European Journal of Soil Biology 80 (May 2017): 49–52. http://dx.doi.org/10.1016/j.ejsobi.2017.04.001.

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22

Confalonieri, VA. "Macrogeographic patterns in B-chromosome and inversion polymorphisms of the grasshopper Trimerotropis pallidipennis." Genetics Selection Evolution 27, no. 4 (1995): 305. http://dx.doi.org/10.1186/1297-9686-27-4-305.

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23

Korobushkin, D. I., A. Yu Gorbunova, A. S. Zaitsev, and K. B. Gongalsky. "Trait-specific response of soil macrofauna to forest burning along a macrogeographic gradient." Applied Soil Ecology 112 (April 2017): 97–100. http://dx.doi.org/10.1016/j.apsoil.2016.12.004.

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24

Zaslavskaya, N. I., and A. I. Pudovkin. "Macrogeographic genetic variability in the Gastropod Mollusk Littorina sitkana from the Northwest Pacific." Russian Journal of Genetics 41, no. 3 (March 2005): 291–300. http://dx.doi.org/10.1007/s11177-005-0087-8.

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25

Semenova, A. V., A. N. Stroganov, G. A. Rubtsova, and M. O. Rybakov. "Genetic Structure of the Pacific Herring Clupea pallasii Valenciennes, 1847 on a Macrogeographic Scale." Russian Journal of Genetics 57, no. 6 (June 2021): 697–710. http://dx.doi.org/10.1134/s1022795421060090.

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26

Doutrelant, Claire, and Marcel M. Lambrechts. "Macrogeographic Variation in Song - a Test of Competition and Habitat Effects in Blue Tits." Ethology 107, no. 6 (June 2001): 533–44. http://dx.doi.org/10.1046/j.1439-0310.2001.00688.x.

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27

TATARENKOV, ANDREY, and KERSTIN JOHANNESSON. "Micro- and macrogeographic allozyme variation in Littorina fabalis; do sheltered and exposed forms hybridize?" Biological Journal of the Linnean Society 67, no. 2 (June 1999): 199–212. http://dx.doi.org/10.1111/j.1095-8312.1999.tb01861.x.

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28

ANDERSON, T. J. C., and J. JAENIKE. "Host specificity, evolutionary relationships and macrogeographic differentiation among Ascaris populations from humans and pigs." Parasitology 115, no. 3 (September 1997): 325–42. http://dx.doi.org/10.1017/s0031182097001339.

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We describe a variety of restriction site polymorphisms in the introns of Ascaris nuclear genes and in the ribosomal DNA spacers. We use these markers, in addition to previously described mitochondrial variation, to clarify our understanding of the epidemiology of Ascaris in Guatemalan villages where humans and pigs occur in sympatry and to describe the genetic structure of host-associated Ascaris populations from world-wide locations. Intron sequences were amplified from individual worms and alleles defined by endonuclease digestion. Two loci were monomorphic, while 4 length variants and 22 p

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29

Sanjuan, Andrés, Angel S. Comesaña, and Alejandro De Carlos. "Macrogeographic differentiation by mtDNA restriction site analysis in the S.W. European Mytilus galloprovincialis Lmk." Journal of Experimental Marine Biology and Ecology 198, no. 1 (June 1996): 89–100. http://dx.doi.org/10.1016/0022-0981(95)00209-x.

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30

TATARENKOV, A. "Micro- and macrogeographic allozyme variation in Littorina fabalis ; do sheltered and exposed forms hybridize?" Biological Journal of the Linnean Society 67, no. 2 (June 1999): 199–212. http://dx.doi.org/10.1006/bijl.1998.0303.

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31

Mager, John Nicholas, Charles Walcott, and David Evers. "Macrogeographic Variation in the Body Size and Territorial Vocalizations of Male Common Loons (Gavia immer)." Waterbirds 30, no. 1 (March 2007): 64–72. http://dx.doi.org/10.1675/1524-4695(2007)030[0064:mvitbs]2.0.co;2.

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32

Sork, VL, S. Huang, and E. Wiener. "Macrogeographic and fine-scale genetic structure in a North American oak species, Quercus rubra L." annales des sciences forestières 50, Supplement (1993): 261s—270s. http://dx.doi.org/10.1051/forest:19930726.

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33

Butler, Malcolm G., Iya I. Kiknadze, Veronica V. Golygina, Jon Martin, Albina G. Istomina, Wolfgang F. Wülker, James E. Sublette, and Mary F. Sublette. "Cytogenetic differentiation between Palearctic and Nearctic populations of Chironomus plumosus L. (Diptera, Chironomidae)." Genome 42, no. 5 (October 1, 1999): 797–815. http://dx.doi.org/10.1139/g99-014.

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Macrogeographic patterns of polytene chromosomal banding sequences were studied in natural populations of the Holarctic species Chironomus plumosus. Of the 31 inversion sequences now known, 16 are endemic to the Palearctic, 7 are endemic to the Nearctic, and 8 are Holarctic sequences common to both zoogeographic zones. Differences in the sets of inversion sequences found on each continent, plus differing frequencies of Holarctic sequences, result in great overall divergence of karyotypes on the two continents. The karyotype of Nearctic C. plumosus differs from that of Palearctic populations pr

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34

Costa, James T., and Kenneth G. Ross. "Hierarchical Genetic Structure and Gene Flow in Macrogeographic Populations of the Eastern Tent Caterpillar (Malacosoma americanum)." Evolution 48, no. 4 (August 1994): 1158. http://dx.doi.org/10.2307/2410375.

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35

Wei, K., AR Wood, and JPA Gardner. "Seascape genetics of the New Zealand greenshell mussel: sea surface temperature explains macrogeographic scale genetic variation." Marine Ecology Progress Series 477 (March 12, 2013): 107–21. http://dx.doi.org/10.3354/meps10158.

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36

Westlake, Robin L., and Gregory M. O'Corry-Crowe. "MACROGEOGRAPHIC STRUCTURE AND PATTERNS OF GENETIC DIVERSITY IN HARBOR SEALS (PHOCA VITULINA) FROM ALASKA TO JAPAN." Journal of Mammalogy 83, no. 4 (November 2002): 1111–26. http://dx.doi.org/10.1644/1545-1542(2002)083<1111:msapog>2.0.co;2.

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37

Hasson, Esteban, Constantina Rodriguez, Juan J. Fanara, Horacio Naveira, Osvaldo A. Reig, and Antonio Fontdevila. "The evolutionary history of Drosophila buzzatti. XXVI. Macrogeographic patterns of inversion polymorphism in New World populations." Journal of Evolutionary Biology 8, no. 3 (May 1995): 369–84. http://dx.doi.org/10.1046/j.1420-9101.1995.8030369.x.

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38

Costa, James T., and Kenneth G. Ross. "HIERARCHICAL GENETIC STRUCTURE AND GENE FLOW IN MACROGEOGRAPHIC POPULATIONS OF THE EASTERN TENT CATERPILLAR (MALACOSOMA AMERICANUM)." Evolution 48, no. 4 (August 1994): 1158–67. http://dx.doi.org/10.1111/j.1558-5646.1994.tb05302.x.

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39

Parry, Dylan, Richard A. Goyer, and Gerald J. Lenhard. "Macrogeographic clines in fecundity, reproductive allocation, and offspring size of the forest tent caterpillar Malacosoma disstria." Ecological Entomology 26, no. 3 (June 2001): 281–91. http://dx.doi.org/10.1046/j.1365-2311.2001.00319.x.

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40

Glaszmann, J. C. "Geographic pattern of variation among Asian native rice cultivars (Oryza sativa L.) based on fifteen isozyme loci." Genome 30, no. 5 (October 1, 1988): 782–92. http://dx.doi.org/10.1139/g88-126.

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The geographic pattern of isozyme variation among rice varieties (Oryza sativa L.) in Asia is described based on an electrophoretic survey of 1688 accessions for 15 loci. The distribution patterns are strongly determined by the existence of several varietal groups that are characterized by contrasting multilocus types with dissimilar environmental and macrogeographic distributions. The two main groups correspond to the indica and japonica subspecies. Other types are frequently found in the Indian subcontinent, especially along the Himalayan foothills. These types are predominant in the Indus R

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41

Pahl, B. C., J. M. Terhune, and H. R. Burton. "Repertoire and Geographic Variation in Underwater Vocalisations of Weddell Seals (Leptonychotes weddellii, Pinnipedia : Phocidae) at the Vestfold Hills, Antarctica." Australian Journal of Zoology 45, no. 2 (1997): 171. http://dx.doi.org/10.1071/zo95044.

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The underwater vocalisations of Weddell seals (Leptonychotes weddellii) near Davis, Antarctica, were many and varied. A total of 11029 vocalisations recorded throughout and immediately after the breeding season were analysed. Vocalisations were classified by cluster analysis techniques, based on differences in frequency, duration, call shape, waveform and number of elements. Thirteen broad call categories (many with subdivisions) were identified. Twelve call types (belonging to nine categories) made up 91· 9% of the vocalisations and were present at all seven study sites within the Vestfold Hi

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42

Hebert, Paul D. N., and Terrie L. Finston. "Macrogeographic patterns of breeding system diversity in the Daphnia pulex group from the United States and Mexico." Heredity 87, no. 2 (August 2001): 153–61. http://dx.doi.org/10.1046/j.1365-2540.2001.00885.x.

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43

Pérez de Rosas, Alicia R., Elsa L. Segura, Laura Fichera, and Beatriz Alicia García. "Macrogeographic and microgeographic genetic structure of the Chagas’ disease vector Triatoma infestans (Hemiptera: Reduviidae) from Catamarca, Argentina." Genetica 133, no. 3 (September 21, 2007): 247–60. http://dx.doi.org/10.1007/s10709-007-9208-8.

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44

Takezaki, Toshiro, Toshinobu Fujiyoshi, and Kazuo Tajima. "Macrogeographic and micrographic comparative study of risk factors for gastric cancer in Japan, China and South America." Estudios Atacameños. Arqueología y antropología surandinas., no. 15 (1998): 13–20. http://dx.doi.org/10.22199/s07181043.1998.0015.00003.

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45

Hebert, Paul D. N., Steven S. Schwartz, Robert D. Ward, and Terrie L. Finston. "Macrogeographic patterns of breeding system diversity in the Daphnia pulex group. I. Breeding systems of Canadian populations." Heredity 70, no. 2 (February 1993): 148–61. http://dx.doi.org/10.1038/hdy.1993.24.

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46

Gordillo, Sandra, Mariano E. Malvé, Gisela A. Morán, and Gabriella M. Boretto. "Naticid drilling predation from tidal flats in northern Patagonia, SW Atlantic." Journal of the Marine Biological Association of the United Kingdom 100, no. 6 (September 2020): 909–19. http://dx.doi.org/10.1017/s0025315420000892.

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AbstractNaticids and muricids are the main drilling gastropod families that leave a characteristic hole in their shelled prey. Drilling predation can be evaluated along spatial scales, and different latitudinal patterns (equatorward, poleward, mid-latitude peaks or no trend at all) have already been described. For Argentine Patagonia, most studies have analysed muricid predation, but scant information is available on naticid predation. This study provides evidence of predation by the moon snail Notocochlis isabelleana on a thin and fragile burrowing bivalve, Darina solenoides, along the intert

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47

Johnson, Ned K. "Speciation in Vireos. I. Macrogeographic Patterns of Allozymic Variation in the Vireo solitarius Complex in the Contiguous United States." Condor 97, no. 4 (November 1995): 903–19. http://dx.doi.org/10.2307/1369530.

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48

Arias, Maria Belen, Samia Elfekih, and Alfried P. Vogler. "Population genetics and migration pathways of the Mediterranean fruit fly Ceratitis capitata inferred with coalescent methods." PeerJ 6 (August 7, 2018): e5340. http://dx.doi.org/10.7717/peerj.5340.

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Background Invasive species are a growing threat to food biosecurity and cause significant economic losses in agricultural systems. Despite their damaging effect, they are attractive models for the study of evolution and adaptation in newly colonised environments. The Mediterranean fruit fly, Ceratitis capitata, as a member of the family Tephritidae, is one of the most studied invasive species feeding on many fruit crops in the tropics and subtropics worldwide. This study aims to determine the global macrogeographic population structure of Ceratitis capitata and reconstruct its potential migra

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49

Ruiz-Garcia, Manuel, and Keith K. Klein. "Genetic structure of populations of the domestic cat in Catalonia (Spain) and upper midwestern USA: A microgeographic and macrogeographic study." Journal of Genetics 76, no. 2 (August 1997): 99–115. http://dx.doi.org/10.1007/bf02923555.

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50

Förschler, Marc I., and Elisabeth K. V. Kalko. "Macrogeographic variations in food choice of mainland citril finches Carduelis [citrinella] citrinella versus insular Corsican (citril) finches Carduelis [citrinella] corsicanus." Journal of Ornithology 147, no. 3 (December 6, 2005): 441–47. http://dx.doi.org/10.1007/s10336-005-0032-6.

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