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Experimental Addition (experimental + addition)
Selected AbstractsAromatic plants in blue tit Cyanistes caeruleus nests: no negative effect on blood-sucking Protocalliphora blow fly larvaeJOURNAL OF AVIAN BIOLOGY, Issue 2 2008Adèle Mennerat Nesting birds use several behavioural or physiological defence mechanisms against parasites. On Corsica, female blue tits Cyanistes caeruleus incorporate fresh fragments of a limited number of aromatic plants in the nest cup, from the end of nest construction until fledging. Some of these plants negatively affect bacterial growth and host location by blood-sucking mosquitoes in laboratory conditions. In natural populations, Corsican blue tit chicks are exposed to the highest levels of blood-sucking ectoparasitic blow flies Protocalliphora spp. reported in Europe. These ectoparasites can have severe negative effects on chick development and survival probabilities, especially when food constraints are elevated. Here we investigated in several natural Corsican blue tit populations the hypothesis that aromatic plants brought to the nest have anti-blow fly effects during the chick-rearing stage. We predicted that: 1) the amount of aromatic plants should be negatively related to blow fly infestation intensity across nests, 2) experimental addition of aromatic plants in nests should reduce blow fly infestation intensity, and 3) nestlings should be in better physical condition in nests where aromatic plants were experimentally added. No significant relation was found between amount of aromatic plants in nests and blow fly infestation intensity. Experimental addition of aromatic plants did not reduce blow fly infestation intensity and did not affect the chick phenotypic parameters we measured. We conclude that aromatic plants in blue tit nests are not used as a defence against ectoparasitic Protocalliphora blow flies in our study population. [source] Experimental addition of greenery reduces flea loads in nests of a non-greenery using species, the tree swallow Tachycineta bicolorJOURNAL OF AVIAN BIOLOGY, Issue 1 2007Dave Shutler Several bird species, including cavity-nesters such as European starlings Sturnus vulgaris, add to their nests green sprigs of plants such as yarrow Achillea millefolium that are rich in volatile compounds. In this field study on another cavity-nester, tree swallows Tachycineta bicolor, we tested whether yarrow reduced ectoparasite loads (the nest protection hypothesis), stimulated nestling immune systems (the drug hypothesis), or had other consequences for nestling growth or parental reproductive success (predicted by both preceding hypotheses). Tree swallows do not naturally add greenery to their nests, and thus offer several advantages in testing for effects of greenery independent of other potentially confounding explanations for the behaviour. We placed fresh yarrow in 23 swallow nests on the day the first egg was laid, replenishing every two days until clutch completion (=three times), and at 44 control nests, nesting material was simply touched. At 12 days of age, we measured nestling body size and mass, and took blood smears to do differential white blood cell counts. We subsequently determined the number and proportion of young fledging from nests and the number of fleas remaining after fledging. Higher humidity was associated with higher flea numbers whereas number of feathers in the nest was not. Our most significant finding was that an average of 773 fleas Ceratophyllus idius was found in control nests, versus 419 in yarrow nests. Possibly, parents compensate for blood that nestlings lose to ectoparasites by increasing food delivery, because we detected no differences between treatments in nestling mass, nestling leukocyte profiles, or proportion of young fledging, or relative to flea numbers. Our results provide no support for the drug hypothesis and strong support for the nest protection hypothesis. [source] Aromatic plants in blue tit Cyanistes caeruleus nests: no negative effect on blood-sucking Protocalliphora blow fly larvaeJOURNAL OF AVIAN BIOLOGY, Issue 2 2008Adèle Mennerat Nesting birds use several behavioural or physiological defence mechanisms against parasites. On Corsica, female blue tits Cyanistes caeruleus incorporate fresh fragments of a limited number of aromatic plants in the nest cup, from the end of nest construction until fledging. Some of these plants negatively affect bacterial growth and host location by blood-sucking mosquitoes in laboratory conditions. In natural populations, Corsican blue tit chicks are exposed to the highest levels of blood-sucking ectoparasitic blow flies Protocalliphora spp. reported in Europe. These ectoparasites can have severe negative effects on chick development and survival probabilities, especially when food constraints are elevated. Here we investigated in several natural Corsican blue tit populations the hypothesis that aromatic plants brought to the nest have anti-blow fly effects during the chick-rearing stage. We predicted that: 1) the amount of aromatic plants should be negatively related to blow fly infestation intensity across nests, 2) experimental addition of aromatic plants in nests should reduce blow fly infestation intensity, and 3) nestlings should be in better physical condition in nests where aromatic plants were experimentally added. No significant relation was found between amount of aromatic plants in nests and blow fly infestation intensity. Experimental addition of aromatic plants did not reduce blow fly infestation intensity and did not affect the chick phenotypic parameters we measured. We conclude that aromatic plants in blue tit nests are not used as a defence against ectoparasitic Protocalliphora blow flies in our study population. [source] The effect of initial seed density on the structure of a desert annual plant communityJOURNAL OF ECOLOGY, Issue 3 2002Christopher J. Lortie Summary 1,Few experiments directly test the role of density dependence in natural plant communities. 2,We tested (i) whether different initial seed densities of the entire seed bank of an annual plant community affected performance (emergence, mean plant biomass and survival) and (ii) whether density-dependent processes were operating within the communities. We also tested whether life-stage, year and soil moisture (both on a topographic gradient and in an experimental manipulation) influenced the effects of seed density. 3,We considered two distinct phases: seed to emergent seedlings, and emergent seedlings to established plants. 4,The seed bank was collected from a semistabilized sand dune in the Negev Desert, Israel. This was added to sieved sand in plots at the same site at four different initial seed densities: 1/16×, 1/4×, 1× (natural seed density) and 2×. The experiment was repeated for three consecutive growing seasons. 5,Emergence of seedlings was significantly influenced by initial seed density in all 3 years, with higher initial seed densities having lower rates of emergence. 6,Mean final plant size was negatively density dependent and consistently unaffected by the initial seed density sown. 7,In general, there were no strong interactions of topographic position with initial seed density, processes within the vegetation were not density dependent and the experimental addition of water did not influence any of the performance measures tested. Density-dependent processes vary from year to year, while moisture effects do not. 8,We conclude that seedling emergence and some processes in the established plant community are density dependent, but the established plant community is also affected by other processes, such as resource limitation. [source] | ||||||||||