scholarly journals Two extended haplotype blocks are associated with adaptation to high altitude habitats in East African honey bees

PLoS Genetics ◽  
2017 ◽  
Vol 13 (5) ◽  
pp. e1006792 ◽  
Author(s):  
Andreas Wallberg ◽  
Caspar Schöning ◽  
Matthew T. Webster ◽  
Martin Hasselmann
1999 ◽  
Vol 22 (3) ◽  
pp. 321-323 ◽  
Author(s):  
Geraldo Moretto ◽  
Leonidas João de Mello Jr.

Different levels of infestation with the mite Varroa jacobsoni have been observed in the various Apis mellifera races. In general, bees of European races are more susceptible to the mite than African honey bees and their hybrids. In Brazil honey bee colonies are not treated against the mite, though apparently both climate and bee race influence the mite infestation. Six mixed colonies were made with Italian and Africanized honey bees. The percentage infestation by this parasite was found to be significantly lower in adult Africanized (1.69 ± 0.44) than Italian bees (2.79 ± 0.65). This ratio was similar to that found in Mexico, even though the Africanized bees tested there had not been in contact with varroa, compared to more than 20 years of the coexistence in Brazil. However, mean mite infestation in Brazil on both kinds of bees was only about a third of that found in Mexico.


Author(s):  
Cynthia M. Beall ◽  
Kingman P. Strohl

Biological anthropologists aim to explain the hows and whys of human biological variation using the concepts of evolution and adaptation. High-altitude environments provide informative natural laboratories with the unique stress of hypobaric hypoxia, which is less than usual oxygen in the ambient air arising from lower barometric pressure. Indigenous populations have adapted biologically to their extreme environment with acclimatization, developmental adaptation, and genetic adaptation. People have used the East African and Tibetan Plateaus above 3,000 m for at least 30,000 years and the Andean Plateau for at least 12,000 years. Ancient DNA shows evidence that the ancestors of modern highlanders have used all three high-altitude areas for at least 3,000 years. It is necessary to examine the differences in biological processes involved in oxygen exchange, transport, and use among these populations. Such an approach compares oxygen delivery traits reported for East African Amhara, Tibetans, and Andean highlanders with one another and with short-term visitors and long-term upward migrants in the early or later stages of acclimatization to hypoxia. Tibetan and Andean highlanders provide most of the data and differ quantitatively in biological characteristics. The best supported difference is the unelevated hemoglobin concentration of Tibetans and Amhara compared with Andean highlanders as well as short- and long-term upward migrants. Moreover, among Tibetans, several features of oxygen transfer and oxygen delivery resemble those of short-term acclimatization, while several features of Andean highlanders resemble the long-term responses. Genes and molecules of the oxygen homeostasis pathways contribute to some of the differences.


Author(s):  
Evert Kleynhans

Abstract Mountainous terrain has distinctly influenced combat operations throughout history. Warfare at high altitude often takes place in extreme weather conditions and over difficult terrain, which is largely considered to be inaccessible, inhospitable, and at times lacking any apparent strategic or operational value. As a result, combat operations at high altitudes are traditionally infantry affairs. The South African deployment to East Africa during the Second World War was for the most part characterised by highly mobile operations, across deserts and scrubland, where infantry, armour and artillery deployed in a mutually supportive role. The penultimate battles of the East African campaign were, however, fought in extremely severe terrain, where the South African troops would experience the harsh realities of mountain warfare for the first time during the war. This article broadly investigates the exigencies of mountain warfare, and critically reflects on the South African wartime experience of mountain warfare in East Africa.


BMC Genomics ◽  
2015 ◽  
Vol 16 (1) ◽  
Author(s):  
Zachary L. Fuller ◽  
Elina L. Niño ◽  
Harland M. Patch ◽  
Oscar C. Bedoya-Reina ◽  
Tracey Baumgarten ◽  
...  

Nature ◽  
1936 ◽  
Vol 138 (3484) ◽  
pp. 249-249
Author(s):  
T. D. A. COCKERELL

EDIS ◽  
2018 ◽  
Vol 2018 (2) ◽  
Author(s):  
James D Ellis ◽  
Mary Christine Bammer

African honey bees and European honey bees are the same species of honey bee, but the two are classified as different subspecies or races of honey bee. African honey bee x European honey bee hybrids present an unpredictable combination of both subspecies‹ behavioral traits. This 4-page fact sheet written by J. D. Ellis and M. Bammer and published by the UF/IFAS Department of Entomology and Nematology explains how to “bee-proof” your house and yard and develop a bee safety plan as well as what you can do if you encounter a swarm or a colony of bees and how to treat a bee sting. edis.ifas.ufl.edu/in1205


2000 ◽  
Vol 81 (8) ◽  
pp. 2111-2119 ◽  
Author(s):  
Neil Leat ◽  
Brenda Ball ◽  
Vandana Govan ◽  
Sean Davison

A virus with picorna-like biophysical properties was isolated from South African honey bees. On the basis of serology, it was identified as an isolate of black queen-cell virus (BQCV). Nucleotide sequence analysis revealed an 8550 nt polyadenylated genome containing two large ORFs. The 5′-proximal ORF (ORF 1) represented 4968 nt while the 3′-proximal ORF (ORF 2) represented 2562 nt. The ORFs were separated by a 208 nt intergenic region and were flanked by a 657 nt 5′-untranslated region and a 155 nt 3′-untranslated region. Deduced amino acid sequences for ORF 1 and ORF 2 were most similar to the non-structural and structural proteins, respectively, of Drosophila C virus (DCV), Rhopalosiphum padi virus (RhPV), Himetobi P virus (HiPV) and Plautia stali intestine virus (PSIV). It is proposed that BQCV belongs to the group of picorna-like, insect-infecting RNA viruses constituted by DCV, RhPV, HiPV and PSIV.


PEDIATRICS ◽  
1994 ◽  
Vol 94 (1) ◽  
pp. 115-117
Author(s):  
Barbara K. Ariue

African honey bees, Apis mellifera scutellata (formerly adsonii) were imported to Brazil in 1956 to introduce a strain of bees with increased honey production which were more suited for the tropical climate.1,2 A year later, 26 African queen bees and their accompanying colonies accidentally escaped.1,2 The African queen bees soon began mating with established European bee races resulting in the hybrid Africanized honey bees.2 Like the pure African bees, the Africanized bees are more defensive with a greater tendency to sting than European bees.3 They respond quickly to the slightest disturbance of their nest and can send out many thousands of bees.


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