Predator satiation and extreme mast seeding in 11 species of Chionochloa (Poaceae)

Oikos ◽  
2000 ◽  
Vol 90 (3) ◽  
pp. 477-488 ◽  
Author(s):  
Dave Kelly ◽  
Andrea L. Harrison ◽  
William G. Lee ◽  
Ian J. Payton ◽  
Peter R. Wilson ◽  
...  
2008 ◽  
Vol 50 (4) ◽  
pp. 343-355 ◽  
Author(s):  
Dave Kelly ◽  
Matthew H. Turnbull ◽  
Richard P. Pharis ◽  
Michal S. Sarfati

2008 ◽  
Vol 276 (1657) ◽  
pp. 649-655 ◽  
Author(s):  
Stephen Takács ◽  
Hannah Bottomley ◽  
Iisak Andreller ◽  
Tracy Zaradnik ◽  
Joseph Schwarz ◽  
...  

Foraging animals use diverse cues to locate resources. Common foraging cues have visual, auditory, olfactory, tactile or gustatory characteristics. Here, we show a foraging herbivore using infrared (IR) radiation from living plants as a host-finding cue. We present data revealing that (i) conifer cones are warmer and emit more near-, mid- and long-range IR radiation than needles, (ii) cone-feeding western conifer seed bugs, Leptoglossus occidentalis (Hemiptera: Coreidae), possess IR receptive organs and orient towards experimental IR cues, and (iii) occlusion of the insects' IR receptors impairs IR perception. The conifers' cost of attracting cone-feeding insects may be offset by occasional mast seeding resulting in cone crops too large to be effectively exploited by herbivores.


Ecology ◽  
2010 ◽  
Vol 91 (9) ◽  
pp. 2673-2683 ◽  
Author(s):  
Quinn E. Fletcher ◽  
Stan Boutin ◽  
Jeffrey E. Lane ◽  
Jalene M. LaMontagne ◽  
Andrew G. McAdam ◽  
...  

2012 ◽  
Vol 16 (1) ◽  
pp. 90-98 ◽  
Author(s):  
Dave Kelly ◽  
Andre Geldenhuis ◽  
Alex James ◽  
E. Penelope Holland ◽  
Michael J. Plank ◽  
...  
Keyword(s):  

2008 ◽  
Vol 35 (1) ◽  
pp. 1 ◽  
Author(s):  
Andrew E. Fidler ◽  
Stephen B. Lawrence ◽  
Kenneth P. McNatty

An important goal in the intensive conservation management of New Zealand’s critically endangered nocturnal parrot, kakapo (Strigops habroptilus), is to increase the frequency of breeding attempts. Kakapo breeding does not occur annually but rather correlates with 3–5-year cycles in ‘mast’ seeding/fruiting of kakapo food plants, most notably podocarps such as rimu (Dacrydium cupressinum). Here we advance a hypothetical mechanism for the linking of kakapo breeding with such ‘mast’ seeding/fruiting. The essence of the hypothesis is that exposure to low levels of dietary phytochemicals may, in combination with hepatic gene ‘memory’, sensitise egg yolk protein genes, expressed in female kakapo livers, to oestrogens derived from developing ovarian follicles. Only in those years when the egg yolk protein genes have been sufficiently ‘pre-sensitised’ by dietary chemicals do kakapo ovarian follicles develop to ovulation and egg-laying occurs. While speculative, this hypothesis is both physiologically and evolutionarily plausible and suggests both future research directions and relatively simple interventions that may afford conservation workers some influence over kakapo breeding frequency.


2012 ◽  
Vol 9 (2) ◽  
pp. 220-228
Author(s):  
Baghdad Science Journal

This study evaluated the functional response of the larva of the predator Chrysoperla carnea by offering varying densities of cabbage aphid, Brevicoryne brassicae (L.) . Results showed conformity with type–II functional response, where the number of prey killed approaches asymptote hyperbolically as prey density increases (declining proportion of prey killed or the inverse density dependent) till it reached the stability stage determined by handling time and predator satiation. Also, the values of attack rate and handling time changed with age progress for both predator and prey. It has been observed an increase in the attack rate and reduction in handling time with the progress of the predator age when feeding on a particular nymphal instar. The attack rates of the predator was 1.779,3.406 and 4.219 ,while handling time was 0.015,0.010 and 0.008 (days) for 1st,2nd,3rd larval instars respectively, when fed on 1st nymphal instar. Also attack rates decreased and increases handling time with the progress in the prey. The attack rates were 1.779, 1.392, 1.096 and 1.059, due to an increase in size of the predator and in the growing efficiency in hunting the prey as well as in the increase in size of the prey and in developing its ability to defend itself and escape.


2016 ◽  
Vol 119 (1) ◽  
pp. 109-116 ◽  
Author(s):  
Zhishu Xiao ◽  
Xiangcheng Mi ◽  
Marcel Holyoak ◽  
Wenhua Xie ◽  
Ke Cao ◽  
...  

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