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Articoli di riviste sul tema "Ants"

Autore: Grafiati

Pubblicato: 4 giugno 2021

Ultima modifica: 25 luglio 2025

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1

Karch, Jason, Michael J. Bround, Hadi Khalil, et al. "Inhibition of mitochondrial permeability transition by deletion of the ANT family and CypD." Science Advances 5, no. 8 (2019): eaaw4597. http://dx.doi.org/10.1126/sciadv.aaw4597.

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Abstract (sommario):

The mitochondrial permeability transition pore (MPTP) has resisted molecular identification. The original model of the MPTP that proposed the adenine nucleotide translocator (ANT) as the inner membrane pore-forming component was challenged when mitochondria from Ant1/2 double null mouse liver still had MPTP activity. Because mice express three Ant genes, we reinvestigated whether the ANTs comprise the MPTP. Liver mitochondria from Ant1, Ant2, and Ant4 deficient mice were highly refractory to Ca2+-induced MPTP formation, and when also given cyclosporine A (CsA), the MPTP was completely inhibite

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2

Marshall, Alan. "Ants/Anti-Ants!" Metascience 14, no. 2 (2005): 209–11. http://dx.doi.org/10.1007/s11016-005-3295-x.

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3

Mathis, Kaitlyn A., and Neil D. Tsutsui. "Dead ant walking: a myrmecophilous beetle predator uses parasitoid host location cues to selectively prey on parasitized ants." Proceedings of the Royal Society B: Biological Sciences 283, no. 1836 (2016): 20161281. http://dx.doi.org/10.1098/rspb.2016.1281.

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Abstract (sommario):

Myrmecophiles (i.e. organisms that associate with ants) use a variety of ecological niches and employ different strategies to survive encounters with ants. Because ants are typically excellent defenders, myrmecophiles may choose moments of weakness to take advantage of their ant associates. This hypothesis was studied in the rove beetle, Myrmedonota xipe , which associates with Azteca sericeasur ants in the presence of parasitoid flies. A combination of laboratory and field experiments show that M. xipe beetles selectively locate and prey upon parasitized ants. These parasitized ants are less

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4

David, Emmanuel M. General, Archival C. Buenavente Perry, and Jennifer V. Rodriguez Lillian. "A preliminary survey of nocturnal ants, with novel modifications for collecting nocturnal arboreal ants." Halteres 11 (March 16, 2020): 1–12. https://doi.org/10.5281/zenodo.3707151.

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<strong>Ants were surveyed in a 100-m horizontal transect by employing three collecting techniques: leaf litter sifting and Winkler extraction, pitfall trapping, and beating of low vegetation. Ants were surveyed during the day and again at night to record the temporal behavior of the ants. In aggregate, 23 species of ants were collected only during the day, 24 species during the night, and 36 species during both day and night. There was a large overlap between diurnal and nocturnal ground-foraging and leaf-litter ant communities. On the other hand, the diurnal arboreal ant community seems to b

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5

Graham, Paul, and Thomas S. Collett. "View-based navigation in insects: how wood ants (Formica rufaL.) look at and are guided by extended landmarks." Journal of Experimental Biology 205, no. 16 (2002): 2499–509. http://dx.doi.org/10.1242/jeb.205.16.2499.

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SUMMARYBees, wasps and ants learn landmarks as views from particular vantage points, storing the retinal positions of landmark edges. By moving so as to minimise the difference between their stored and current view, they can return to the vantage point from which a view was taken. We have examined what wood ants learn about a laterally placed, extended landmark, a wall, while walking parallel to it to reach a feeder and how they use this stored information to guide their path. Manipulation of the height of the wall and the ant's starting distance from it reveals that ants maintain a desired di

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6

Waxman, David. "Ants ordering ants to feed." Trends in Ecology & Evolution 17, no. 3 (2002): 103–4. http://dx.doi.org/10.1016/s0169-5347(01)02435-1.

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7

Wilson, Edward O. "Ants." Bulletin of the American Academy of Arts and Sciences 45, no. 3 (1991): 13. http://dx.doi.org/10.2307/3824337.

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8

Lord, Richard. "Ants." American Biology Teacher 80, no. 5 (2018): 392. http://dx.doi.org/10.1525/abt.2018.80.5.392.

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9

Lapitskii, Viktor. "Ants." Index on Censorship 22, no. 10 (1993): 12–15. http://dx.doi.org/10.1080/03064229308535616.

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10

Brown, Bill. "Ants." Appalachian Heritage 30, no. 3 (2002): 71. http://dx.doi.org/10.1353/aph.2002.0082.

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11

Smith, Katherine. "Ants." Appalachian Heritage 33, no. 2 (2005): 104. http://dx.doi.org/10.1353/aph.2005.0109.

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12

Ward, Philip S. "Ants." Current Biology 16, no. 5 (2006): R152—R155. http://dx.doi.org/10.1016/j.cub.2006.02.054.

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13

Derrida, Jacques. "Ants." Oxford Literary Review 24, no. 1 (2002): 19–42. http://dx.doi.org/10.3366/olr.2002.003.

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14

Masini, Donna. "Ants." Italian Americana XXXIX, no. 1 (2021): 52. http://dx.doi.org/10.5406/2327753x.39.1.07.

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15

Wystrach, Antoine, Sebastian Schwarz, Alice Baniel, and Ken Cheng. "Backtracking behaviour in lost ants: an additional strategy in their navigational toolkit." Proceedings of the Royal Society B: Biological Sciences 280, no. 1769 (2013): 20131677. http://dx.doi.org/10.1098/rspb.2013.1677.

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Abstract (sommario):

Ants use multiple sources of information to navigate, but do not integrate all this information into a unified representation of the world. Rather, the available information appears to serve three distinct main navigational systems: path integration, systematic search and the use of learnt information—mainly via vision. Here, we report on an additional behaviour that suggests a supplemental system in the ant's navigational toolkit: ‘backtracking’. Homing ants, having almost reached their nest but, suddenly displaced to unfamiliar areas, did not show the characteristic undirected headings of sy

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16

Freeman, Theodore M. "Imported Fire Ants: The Ants from Hell!" Allergy and Asthma Proceedings 15, no. 1 (1994): 11–15. http://dx.doi.org/10.2500/108854194778816580.

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17

Razin, Nitzan, Jean-Pierre Eckmann, and Ofer Feinerman. "Desert ants achieve reliable recruitment across noisy interactions." Journal of The Royal Society Interface 10, no. 82 (2013): 20130079. http://dx.doi.org/10.1098/rsif.2013.0079.

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Abstract (sommario):

We study how desert ants, Cataglyphis niger , a species that lacks pheromone-based recruitment mechanisms, inform each other about the presence of food. Our results are based on automated tracking that allows us to collect a large database of ant trajectories and interactions. We find that interactions affect an ant's speed within the nest. Fast ants tend to slow down, whereas slow ones increase their speed when encountering a faster ant. Faster ants tend to exit the nest more frequently than slower ones. So, if an ant gains enough speed through encounters with others, then she tends to leave

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18

Fu, Jinwen. "Ant's Social Division of Labor and Its Influencing Factors." BIO Web of Conferences 142 (2024): 02002. https://doi.org/10.1051/bioconf/202414202002.

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As a higher social insect, ants have a clear hierarchy within them. According to the different divisions of labor, ant groups mainly include worker ants, soldier ants, male ants, and queen ants. In this paper, the social division of labor and its influencing factors on ants are studied in-depth. The main characteristics, physiological functions and behaviors of different grades of ants are explained, and the strong correlation between them and the social division of labor of ants is discussed from the aspects of gene differential expression, epigenetic regulation and brain specificity. From th

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19

Waruwu, Irena Santy, Marheni, and Lahmuddin Lubis. "Jumlah semut Myopopone castaneae (Hymenoptera:Formicidae) yang dihasilkan dengan pakan berbagai instar larva Oryctes rhinoceros L. (Coleoptera: Scarabaidae) di laboratorium." Jurnal Pertanian Tropik 5, no. 2 (2018): 170–76. http://dx.doi.org/10.32734/jpt.v5i2.2988.

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Ants of Myopopone castaneae (Hymenoptera: Formicidae) is a one potential predators of larvae palm stem borer Oryctes rhinoceros L. (Coleoptera: Scarabidae). These ants are able to prey on all stadia of larvae O. rhinoceros L. This research was aimed to know the number of ants Myopopone castaneae (Hymenoptera: Formicidae) generated by feeding the various instar larvae of palm stem borer Oryctes rhinoceros L. (Coleoptera: Scarabaidae) in the laboratory. The research was conducted at Laboratory of Plant Pest, Faculty of Agriculture, University of Sumatera Utara from April until September 2017. Th

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20

Hayashi, Masayuki, Masaru K. Hojo, Masashi Nomura, and Kazuki Tsuji. "Social transmission of information about a mutualist via trophallaxis in ant colonies." Proceedings of the Royal Society B: Biological Sciences 284, no. 1861 (2017): 20171367. http://dx.doi.org/10.1098/rspb.2017.1367.

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Partner discrimination is crucial in mutualistic interactions between organisms to counteract cheating by the partner. Trophobiosis between ants and aphids is a model system of such mutualistic interaction. To establish and maintain the mutualistic association, ants need to correctly discriminate mutualistic aphids. However, the mechanism by which ants recognize aphids as their partners is poorly understood, despite its ecological and evolutionary importance. Here, we show for the first time the evidence that interaction with nest-mates that have tended aphids ( Aphis craccivora ) allows ants

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21

Venable, Cameron P., and Tracy Langkilde. "Eastern Fence Lizards (Sceloporus undulatus) display an ontogenetic shift in relative consumption of native and invasive prey." Canadian Journal of Zoology 97, no. 5 (2019): 419–23. http://dx.doi.org/10.1139/cjz-2018-0228.

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Abstract (sommario):

Interactions between invasive prey and native predators can provide an opportunity to better understand predator–prey dynamics and how these may change through ontogeny. Eastern Fence Lizards (Sceloporus undulatus (Bosc and Daudin in Sonnini and Latreille, 1801)) are ant specialist, particularly as juveniles. Invasive red imported fire ants (Solenopsis invicta Buren, 1972) pose a lethal risk to S. undulatus that eat them, especially smaller-bodied juveniles. We examine ontogenetic shifts in S. undulatus consumption of toxic invasive fire ants versus palatable native pyramid ants (Dorymyrmex bu

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22

Wang, Bo, Min Lu, Yan-Qiong Peng, and Simon T. Segar. "Direct and Indirect Effects of Invasive vs. Native Ant-Hemipteran Mutualism: A Meta-Analysis That Supports the Mutualism Intensity Hypothesis." Agronomy 11, no. 11 (2021): 2323. http://dx.doi.org/10.3390/agronomy11112323.

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Mutualism can facilitate the colonization, establishment, and spread of invasive species. By modifying interactions with third parties, mutualisms can have cascading community-wide effects. Both native and invasive ants are capable of forming mutualisms with hemipteran insects, preying on non-hemipteran herbivores and indirectly affecting primary production. Comparative research on the effects of both native and invasive ant exclusions on multitrophic interactions is therefore crucial for understanding the invasive potential of ants, along with any ecological consequences that invasions may ha

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23

Zheng, Shanshan, Raquel Loreto, Philip Smith, Andrew Patterson, David Hughes, and Liande Wang. "Specialist and Generalist Fungal Parasites Induce Distinct Biochemical Changes in the Mandible Muscles of Their Host." International Journal of Molecular Sciences 20, no. 18 (2019): 4589. http://dx.doi.org/10.3390/ijms20184589.

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Some parasites have evolved the ability to adaptively manipulate host behavior. One notable example is the fungus Ophiocordyceps unilateralis sensu lato, which has evolved the ability to alter the behavior of ants in ways that enable fungal transmission and lifecycle completion. Because host mandibles are affected by the fungi, we focused on understanding changes in the metabolites of muscles during behavioral modification. We used High-Performance Liquid Chromatography-Mass/Mass (HPLC-MS/MS) to detect the metabolite difference between controls and O. unilateralis-infected ants. There was a si

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24

Reemer, Menno. "Review and Phylogenetic Evaluation of Associations between Microdontinae (Diptera: Syrphidae) and Ants (Hymenoptera: Formicidae)." Psyche: A Journal of Entomology 2013 (2013): 1–9. http://dx.doi.org/10.1155/2013/538316.

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Abstract (sommario):

The immature stages of hoverflies of the subfamily Microdontinae (Diptera: Syrphidae) develop in ant nests, as predators of the ant brood. The present paper reviews published and unpublished records of associations of Microdontinae with ants, in order to discuss the following questions. (1) Are all Microdontinae associated with ants? (2) Are Microdontinae associated with all ants? (3) Are particular clades of Microdontinae associated with particular clades of ants? (4) Are Microdontinae associated with other insects? A total number of 109 associations between the groups are evaluated, relating

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25

Hightower, Lawrence E. "Desert Ants." Science 268, no. 5216 (1995): 1417. http://dx.doi.org/10.1126/science.268.5216.1417.a.

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26

Jaffe, Klaus. "Surfing Ants." Florida Entomologist 76, no. 1 (1993): 182. http://dx.doi.org/10.2307/3496029.

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27

Kuzma, Greg. "The Ants." Iowa Review 37, no. 2 (2007): 53. http://dx.doi.org/10.17077/0021-065x.6343.

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28

Rhoades, Robert. "Stinging ants." Current Opinion in Allergy and Clinical Immunology 1, no. 4 (2001): 343–48. http://dx.doi.org/10.1097/01.all.0000011036.74215.95.

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29

Choi, Charles Q. "Sacrificial Ants." Scientific American 299, no. 6 (2008): 42. http://dx.doi.org/10.1038/scientificamerican1208-42c.

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30

Garner, Lynne. "Amazing ants." Practical Pre-School 2015, Sup175 (2015): 7–8. http://dx.doi.org/10.12968/prps.2015.sup175.7.

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31

Holloway, Marguerite. "Hot Ants." Scientific American 267, no. 3 (1992): 23. http://dx.doi.org/10.1038/scientificamerican0992-23b.

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32

Rohrer, Matthew. "The Ants." Issues in Science and Technology 41, no. 2 (2025): 40–41. https://doi.org/10.58875/wslf8485.

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33

Muller, Peter. "Why Ants?" Ballarat Naturalist (2016:Mar) (March 2016): 1–3. http://dx.doi.org/10.5962/p.385142.

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34

Dalman, Peter. "Excursion – Ants." Ballarat Naturalist (2016:Mar) (March 2016): 4–5. http://dx.doi.org/10.5962/p.385143.

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35

Pingyang, Lei, and Ming Di. "Happy Ants." Manoa 31, no. 1 (2019): 57. http://dx.doi.org/10.1353/man.2019.0032.

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36

Hightower, L. E. "Desert Ants." Science 268, no. 5216 (1995): 1417. http://dx.doi.org/10.1126/science.268.5216.1417.

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37

Blaeser, Kimberly M. "Red Ants." Wasafiri 32, no. 2 (2017): 3–5. http://dx.doi.org/10.1080/02690055.2017.1290389.

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38

Reid, Judy. "Ancient ants." New Scientist 195, no. 2613 (2007): 23. http://dx.doi.org/10.1016/s0262-4079(07)61822-3.

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39

Rhoades, Robert. "Stinging ants." Current Opinion in Allergy and Clinical Immunology 1, no. 4 (2001): 343–48. http://dx.doi.org/10.1097/00130832-200108000-00010.

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40

Conway, John R. "Honey Ants." American Entomologist 40, no. 4 (1994): 229–34. http://dx.doi.org/10.1093/ae/40.4.229.

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41

Milius, Susan. "Ambush Ants." Science News 167, no. 17 (2005): 260. http://dx.doi.org/10.2307/4016241.

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42

Wheeler, Diana. "The Ants." Annals of the Entomological Society of America 84, no. 2 (1991): 212–13. http://dx.doi.org/10.1093/aesa/84.2.212.

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43

Kotsireas, Ilias, and Emil Volcheck. "ANTS VI." ACM SIGSAM Bulletin 38, no. 3 (2004): 93–107. http://dx.doi.org/10.1145/1040034.1040041.

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44

Elmes, Graham W. "The ants." Trends in Ecology & Evolution 5, no. 11 (1990): 380–81. http://dx.doi.org/10.1016/0169-5347(90)90111-p.

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45

Sendova-Franks, Ana B. "Exotic ants." Trends in Ecology & Evolution 9, no. 12 (1994): 497–98. http://dx.doi.org/10.1016/0169-5347(94)90327-1.

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46

Palmer, Todd M. "Acacia ants." Current Biology 33, no. 11 (2023): R469—R471. http://dx.doi.org/10.1016/j.cub.2023.02.002.

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47

Swenson, Jon E., Anna Jansson, Raili Riig, and Finn Sandegren. "Bears and ants: myrmecophagy by brown bears in central Scandinavia." Canadian Journal of Zoology 77, no. 4 (1999): 551–61. http://dx.doi.org/10.1139/z99-004.

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To determine general patterns of myrmecophagy in bears, we tested hypotheses regarding selection of ant species, factors important to bears when selecting ant species, factors influencing seasonal use of ants, and foraging behavior of brown bears (Ursus arctos) in central Sweden. Ants were an important food for these bears, constituting 12, 16, and 4% of fecal volume in spring, summer, and autumn, respectively. Ants were abundant, 30.5-38.5 tonnes per bear, and bears excavated 8-33% (mean 23%) of the mounds of red forest ants annually. Carpenter ants (Camponotus herculeanus) were highly prefer

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48

CARLIN, N. F. "Troublesome Insects: Fire Ants and Leaf-Cutting Ants." Science 235, no. 4796 (1987): 1682b—1683b. http://dx.doi.org/10.1126/science.235.4796.1682b.

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49

Stimac, Jerry L. "The Ants and Nothing but the Ants The Ants Bert Hölldobler Edward O. Wilson." BioScience 41, no. 3 (1991): 168. http://dx.doi.org/10.2307/1311458.

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50

Khafidhan, Abied, Rahayu Widyastuti, and Soetanto Abdoellah. "Ant Abundance, identification and relation with cocoa pest attacks under several shade trees." Pelita Perkebunan (a Coffee and Cocoa Research Journal) 37, no. 3 (2021): 219–28. http://dx.doi.org/10.22302/iccri.jur.pelitaperkebunan.v37i3.474.

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Abstract (sommario):

Ants are soil macrofauna that plays an essential role in preventing pods of cocoa (Theobroma cacao L.) from Helopeltis antonii and Conopomorpha cramerella attack. However, the method of those pests control primarily using pesticides and that will disturbed ant's life. This research aims to determine the abundance and diversity of ants in cocoa plantations with different shade and to determine the correlation between ant abundance and intensity of pest attack from Helopeltis antonii and Conopomorpha cramerella. Ants sample was carried out using pitfall traps and Berlese funnels based on purposi

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