Autumnal migration routes of the eastern population of the monarch butterfly (Danaus p. plexippus L.; Danaidae; Lepidoptera) in North America to the overwintering site in the Neovolcanic Plateau of Mexico

1978 ◽  
Vol 56 (8) ◽  
pp. 1759-1764 ◽  
Author(s):  
F. A. Urquhart ◽  
N. R. Urquhart

Based upon numerous recaptures of alar-tagged migrating monarch butterflies, together with extensive field expeditions through various parts of North and Central America, the migrating routes of monarchs have been plotted with considerable accuracy.Five overwintering areas have been defined representing 13 loci of concentrations, in the Neovolcanic Plateau of Mexico.It appears that migrants from the breeding areas of the Great Plains region overwinter in the western mountains of Mexico and those from breeding areas east of the Great Plains region overwinter in the eastern mountains. The greatest concentration occurs in the central mountains and represents migrations from parts of the Great Plains regions and parts of the eastern regions.

1979 ◽  
Vol 111 (1) ◽  
pp. 15-18 ◽  
Author(s):  
F. A. Urquhart ◽  
N. R. Urquhart

AbstractThe vernal migration routes of the eastern population of the monarch butterfly (Danaus p. plexippus L.) in North America were plotted from data resulting from the recapture of migrants alar tagged in the overwintering site of the Neo-volcanic Plateau of Mexico. One migrant, which had been alar tagged at Decorah, Iowa, on 3 September 1973, and recaptured 7 months later on 8 April 1974 at Richmond, Texas, led to the conclusion that this particular migrant had flown to the Mexican overwintering site and was recaptured on its return vernal flight. This recapture also gave data indicating that it was not returning to the original breeding area, from which it is concluded that although some migrants may return to the original breeding grounds many may not do so.


1979 ◽  
Vol 111 (11) ◽  
pp. 1281-1286 ◽  
Author(s):  
F. A. Urquhart ◽  
N. R. Urquhart

AbstractStrong westerly winds occurring during autumnal migration of the eastern population of the monarch butterfly in North America, affect those butterflies migrating from areas east of long. 90°. The following aberrant migratory routes are presented: (1) Migrants moving down the Atlantic coast pass through the Florida peninsula to western Cuba thence to the overwintering site in Guatemala and Honduras; (2) migrants forced over the Atlantic ocean eventually reach the Bahama islands and thence to Yucatan, or Honduras via Jamaica and other islands of the Caribbean Sea, to the overwintering site in Guatemala and Honduras; (3) migrants arriving in the eastern islands of the Greater Antilles may eventually arrive in the Cordilleran mountains of Columbia and northwestern Venezuela; (4) migrants from the Lesser Antilles may return, along with members of a first generation, in the spring without establishing an overwintering site—the fate of these few occasional spring migrants is unknown.


1977 ◽  
Vol 109 (12) ◽  
pp. 1583-1589 ◽  
Author(s):  
F. A. Urquhart ◽  
N. R. Urquhart

AbstractAs a result of alar tagging migrating specimens of the monarch butterfly (Danaus p. plexippus L.) in North America over a period of 25 years, it was possible to plot the migration routes establishing two large overwintering colonies, one located in California and the other in mountains of the Sierra Madré Occidentale in Mexico. Photographs of the two overwintering populations are presented together with release–recapture lines showing the direction of migration from breeding areas to the two overwintering sites. Data, presented for the first time, show the migration routes of the Western population from the breeding areas in the mountains and west of the mountains to California.


Paleobiology ◽  
2011 ◽  
Vol 37 (1) ◽  
pp. 50-71 ◽  
Author(s):  
Caroline A. E. Strömberg ◽  
Francesca A. McInerney

The rapid ecological expansion of grasses with C4 photosynthesis at the end of the Neogene (8–2 Ma) is well documented in the fossil record of stable carbon isotopes. As one of the most profound vegetation changes to occur in recent geologic time, it paved the way for modern tropical grassland ecosystems. Changes in CO2 levels, seasonality, aridity, herbivory, and fire regime have all been suggested as potential triggers for this broadly synchronous change, long after the evolutionary origin of the C4 pathway in grasses. To date, these hypotheses have suffered from a lack of direct evidence for floral composition and structure during this important transition. This study aimed to remedy the problem by providing the first direct, relatively continuous record of vegetation change for the Great Plains of North America for the critical interval (ca. 12–2 Ma) using plant silica (phytolith) assemblages.Phytoliths were extracted from late Miocene-Pliocene paleosols in Nebraska and Kansas. Quantitative phytolith analysis of the 14 best-preserved assemblages indicates that habitats varied substantially in openness during the middle to late Miocene but became more uniformly open, corresponding to relatively open grassland or savanna, during the late Miocene and early Pliocene. Phytolith data also point to a marked increase of grass short cells typical of chloridoid and other potentially C4 grasses of the PACMAD clade between 8 and 5 Ma; these data suggest that the proportion of these grasses reached up to ∼50–60% of grasses, resulting in mixed C3-C4 and highly heterogeneous grassland communities by 5.5 Ma. This scenario is consistent with interpretations of isotopic records from paleosol carbonates and ungulate tooth enamel. The rise in abundance of chloridoids, which were present in the central Great Plains since the early Miocene, demonstrates that the “globally” observed lag between C4 grass evolution/taxonomic diversification and ecological expansion occurred at the regional scale. These patterns of vegetation alteration imply that environmental change during the late Miocene-Pliocene played a major role in the C3-C4 shift in the Great Plains. Specifically, the importance of chloridoids as well as a decline in the relative abundance of forest indicator taxa, including palms, point to climatic drying as a key trigger for C4 dominance.


2013 ◽  
Vol 280 (1768) ◽  
pp. 20131087 ◽  
Author(s):  
D. T. Tyler Flockhart ◽  
Leonard I. Wassenaar ◽  
Tara G. Martin ◽  
Keith A. Hobson ◽  
Michael B. Wunder ◽  
...  

Insect migration may involve movements over multiple breeding generations at continental scales, resulting in formidable challenges to their conservation and management. Using distribution models generated from citizen scientist occurrence data and stable-carbon and -hydrogen isotope measurements, we tracked multi-generational colonization of the breeding grounds of monarch butterflies ( Danaus plexippus ) in eastern North America. We found that monarch breeding occurrence was best modelled with geographical and climatic variables resulting in an annual breeding distribution of greater than 12 million km 2 that encompassed 99% occurrence probability. Combining occurrence models with stable isotope measurements to estimate natal origin, we show that butterflies which overwintered in Mexico came from a wide breeding distribution, including southern portions of the range. There was a clear northward progression of monarchs over successive generations from May until August when reproductive butterflies began to change direction and moved south. Fifth-generation individuals breeding in Texas in the late summer/autumn tended to originate from northern breeding areas rather than regions further south. Although the Midwest was the most productive area during the breeding season, monarchs that re-colonized the Midwest were produced largely in Texas, suggesting that conserving breeding habitat in the Midwest alone is insufficient to ensure long-term persistence of the monarch butterfly population in eastern North America.


2014 ◽  
Vol 102 (6) ◽  
pp. 1374-1385 ◽  
Author(s):  
Zak Ratajczak ◽  
Jesse B. Nippert ◽  
John M. Briggs ◽  
John M. Blair

2001 ◽  
Vol 20 (1-3) ◽  
pp. 301-314 ◽  
Author(s):  
Carole A.S Mandryk ◽  
Heiner Josenhans ◽  
Daryl W Fedje ◽  
Rolf W Mathewes

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