A Reappraisal of the Feeding Adaptations in the Hairs of Nectar-Feeding Bats

1984 ◽  
Vol 65 (3) ◽  
pp. 481-484 ◽  
Author(s):  
D. W. Thomas ◽  
B. Crawford ◽  
S. Eastman ◽  
R. Glofscheskie ◽  
M. Heir
PeerJ ◽  
2016 ◽  
Vol 4 ◽  
pp. e1597 ◽  
Author(s):  
Florian Karolyi ◽  
Teresa Hansal ◽  
Harald W. Krenn ◽  
Jonathan F. Colville

Although anthophilous Coleoptera are regarded to be unspecialised flower-visiting insects, monkey beetles (Scarabaeidae: Hopliini) represent one of the most important groups of pollinating insects in South Africa’s floristic hotspot of the Greater Cape Region. South African monkey beetles are known to feed on floral tissue; however, some species seem to specialise on pollen and/or nectar. The present study examined the mouthpart morphology and gut content of various hopliine species to draw conclusions on their feeding preferences. According to the specialisations of their mouthparts, the investigated species were classified into different feeding groups. Adaptations to pollen-feeding included a well-developed, toothed molar and a lobe-like, setose lacinia mobilis on the mandible as well as curled hairs or sclerotized teeth on the galea of the maxillae. Furthermore, elongated mouthparts were interpreted as adaptations for nectar feeding. Floral- and folial-tissue feeding species showed sclerotized teeth on the maxilla, but the lacinia was mostly found to be reduced to a sclerotized ledge. While species could clearly be identified as floral or folial tissue feeding, several species showed intermediate traits suggesting both pollen and nectar feeding adaptations. Mismatches found between mouthpart morphology and previously reported flower visiting behaviours across different genera and species requires alternative explanations, not necessarily associated with feeding preferences. Although detailed examinations of the mouthparts allowed conclusions about the feeding preference and flower-visiting behaviour, additional morphological and behavioural investigations, combined with greater taxon sampling and phylogenetic data, are still necessary to fully understand hopliine host plant relationships, related to monkey beetle diversity.


1976 ◽  
Vol 148 (3) ◽  
pp. 329-336 ◽  
Author(s):  
D. J. Howell ◽  
Norman Hodgkin

Animals ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 2811
Author(s):  
Juan Francisco Pastor ◽  
Magdalena Natalia Muchlinski ◽  
Josep Maria Potau ◽  
Aroa Casado ◽  
Yolanda García-Mesa ◽  
...  

The mobility of the primate tongue allows for the manipulation of food, but, in addition, houses both general sensory afferents and special sensory end organs. Taste buds can be found across the tongue, but the ones found within the fungiform papillae on the anterior two thirds of the tongue are the first gustatory structures to come into contact with food, and are critical in making food ingestion decisions. Comparative studies of both the macro and micro anatomy in primates are sparse and incomplete, yet there is evidence that gustatory adaptation exists in several primate taxa. One is the distally feathered tongues observed in non-destructive nectar feeders, such as Eulemur rubriventer. We compare both the macro and micro anatomy of three lemurid species who died of natural causes in captivity. We included the following two non-destructive nectar feeders: Varecia variegata and Eulemur macaco, and the following destructive flower feeder: Lemur catta. Strepsirrhines and tarsiers are unique among primates, because they possess a sublingua, which is an anatomical structure that is located below the tongue. We include a microanatomical description of both the tongue and sublingua, which were accomplished using hematoxylin–eosin and Masson trichrome stains, and scanning electron microscopy. We found differences in the size, shape, and distribution of fungiform papillae, and differences in the morphology of conical papillae surrounding the circumvallate ones in all three species. Most notably, large distinct papillae were present at the tip of the tongue in nectar-feeding species. In addition, histological images of the ventro-apical portion of the tongue displayed that it houses an encapsulated structure, but only in Lemur catta case such structure presents cartilage inside. The presence of an encapsulated structure, coupled with the shared morphological traits associated with the sublingua and the tongue tip in Varecia variegata and Eulemur macaco, point to possible feeding adaptations that facilitate non-destructive flower feeding in these two lemurids.


2013 ◽  
Author(s):  
Fred C. Dyer ◽  
John Townsend-Mehler
Keyword(s):  

1979 ◽  
Vol 8 (3) ◽  
pp. 544-548 ◽  
Author(s):  
Louis A. Magnarelli ◽  
John F. Anderson ◽  
John H. Thorne
Keyword(s):  

2009 ◽  
Vol 179 (5) ◽  
pp. 553-562 ◽  
Author(s):  
Jorge Ayala-Berdon ◽  
Jorge E. Schondube ◽  
Kathryn E. Stoner

1982 ◽  
Vol 31 (3) ◽  
pp. 252 ◽  
Author(s):  
Michael W. Haiduk ◽  
Robert J. Baker
Keyword(s):  

Evolution ◽  
1962 ◽  
Vol 16 (3) ◽  
pp. 391-393 ◽  
Author(s):  
Robert K. Selander

Science ◽  
2021 ◽  
Vol 373 (6551) ◽  
pp. 226-231 ◽  
Author(s):  
Yasuka Toda ◽  
Meng-Ching Ko ◽  
Qiaoyi Liang ◽  
Eliot T. Miller ◽  
Alejandro Rico-Guevara ◽  
...  

Early events in the evolutionary history of a clade can shape the sensory systems of descendant lineages. Although the avian ancestor may not have had a sweet receptor, the widespread incidence of nectar-feeding birds suggests multiple acquisitions of sugar detection. In this study, we identify a single early sensory shift of the umami receptor (the T1R1-T1R3 heterodimer) that conferred sweet-sensing abilities in songbirds, a large evolutionary radiation containing nearly half of all living birds. We demonstrate sugar responses across species with diverse diets, uncover critical sites underlying carbohydrate detection, and identify the molecular basis of sensory convergence between songbirds and nectar-specialist hummingbirds. This early shift shaped the sensory biology of an entire radiation, emphasizing the role of contingency and providing an example of the genetic basis of convergence in avian evolution.


2018 ◽  
Vol 93 ◽  
pp. 118-123 ◽  
Author(s):  
Jorge Ayala-Berdon ◽  
Cesar García Corona ◽  
Margarita Martínez-Gómez

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