Inferior Competitor (inferior + competitor)

Distribution by Scientific Domains


Selected Abstracts


Parasitized Salamanders are Inferior Competitors for Territories and Food Resources

ETHOLOGY, Issue 4 2000
Daria S. Maksimowich
Parasites have been shown to impair the behaviour of their hosts, compromising the host's ability to exploit and compete for resources. We conducted two experiments to determine whether infestation with an ectoparasitic mite (Hannemania eltoni) was associated with changes in aggressive and foraging behaviour in the Ozark zigzag salamander, Plethodon angusticlavius. In a first experiment, male salamanders with high parasite loads were less aggressive overall than males with low parasite loads during territorial disputes. In addition, males with high parasite loads were more aggressive toward opponents with high parasite loads (symmetric contests) than toward opponents with low parasite loads (asymmetric contests). In contrast, males with low parasite loads did not adjust their level of aggression according to the parasite load of the opponent. In a second experiment, foraging behaviour of females was tested in response to ,familiar' (Drosophila) prey and ,novel' (termite) prey. Latency to first capture was significantly longer for parasitized than non-parasitized females when tested with ,familiar' prey, but not for ,novel' prey. Our results suggest that parasite-mediated effects may have profound influences on individual fitness in nature. [source]


Refuge-mediated apparent competition in plant,consumer interactions

ECOLOGY LETTERS, Issue 1 2010
John L. Orrock
Abstract At the intersection of consumer behaviour and plant competition is the concept of refuge-mediated apparent competition: an indirect interaction whereby plants provide a refuge for a shared consumer, subsequently increasing consumer pressure on another plant species. Here, we use a simple model and empirical examples to develop and illustrate the concept of refuge-mediated apparent competition. We find that the likelihood that an inferior competitor will succeed via refuge-mediated apparent competition is greater when competitors have similar resource requirements and when consumers exhibit a strong response to the refuge and high attack rates on the superior competitor. Refuge-mediated apparent competition may create an emergent Allee effect, such that a species invades only if it is sufficiently abundant to alter consumer impact on resident species. This indirect interaction may help explain unresolved patterns observed in biological invasion, such as the different physical structure of invasive exotic plants, the lag phase, and the failure of restoration efforts. Given the ubiquity of refuge-seeking behaviour by consumers and the ability of consumers to alter the outcome of direct competition among plants, refuge-mediated apparent competition may be an underappreciated mechanism affecting the composition and diversity of plant communities. Ecology Letters (2010) 13: 11,20 [source]


DNA analysis on fox faeces and competition induced niche shifts

MOLECULAR ECOLOGY, Issue 8 2004
LOVE DALÉN
Abstract Interference competition can force inferior competitors to change their distribution patterns. It is, however, possible that the dominant competitor poses a higher threat during certain times of the year, for example during reproduction. In such cases, the inferior competitor is expected to change its distribution accordingly. We used a molecular species identification method on faeces to investigate how the spatial overlap between arctic and red foxes changes between seasons. The results show that arctic and red foxes are sympatric during winter, but allopatric in summer as arctic foxes retreat to higher altitudes further from the tree-line during the breeding season. [source]


Breeding in high-elevation habitat results in shift to slower life-history strategy within a single species

JOURNAL OF ANIMAL ECOLOGY, Issue 2 2009
H. Bears
Summary 1Elevational gradients create environmental variation that is hypothesized to promote variation in life-history strategies. We tested whether differences in life-history strategies were associated with elevation in a songbird, the dark-eyed junco (Junco hyemalis; Aves; A.O.U. 1998). 2We monitored birds in four replicated sites per elevation, at 2000 m a.s.l. (high elevation) and 1000 m a.s.l. (low elevation), in the Rocky Mountains of Canada. 3Over 5 years, we measured the following traits and vital rates: egg-laying schedules, morphological indicators of reproductive stage, seasonal reproductive success, indicators of competitive class (age, size, arrival time), and survival rates. 4We found two main patterns: with an increase in breeding elevation, dark-eyed juncos delayed the development of structures necessary for reproduction (e.g. cloacal protuberance in males) and reduced the duration of their reproductive period to less than half of the time used by low-elevation birds; and 5Juncos at high-elevation sites had 55,61% lower annual reproductive success and 15 to 20% higher survival rates. While adult juncos at high elevations produced fewer offspring, those offspring were in better condition. Proportions of age and size classes in high- compared to low-elevation populations were similar, suggesting that a life-history trade-off is present, rather than competition forcing inferior competitors to breed in a peripheral habitat. The apparent trade-off between reproduction and survival corresponded to a shorter period of favourable weather and available food in high- compared to low-elevation habitats. 6Thus, elevation had a strong influence on life-history characteristics of a single species over a short spatial distance, suggesting a shift in life history from a high reproductive strategy at lower elevations to a high survivor strategy at high elevations. 7This is the first paper to show a shift in avian life-history strategies along an elevational gradient (in both genders, of multiple age classes) when region (latitude) and phylogenetic histories are controlled for. [source]


DNA analysis on fox faeces and competition induced niche shifts

MOLECULAR ECOLOGY, Issue 8 2004
LOVE DALÉN
Abstract Interference competition can force inferior competitors to change their distribution patterns. It is, however, possible that the dominant competitor poses a higher threat during certain times of the year, for example during reproduction. In such cases, the inferior competitor is expected to change its distribution accordingly. We used a molecular species identification method on faeces to investigate how the spatial overlap between arctic and red foxes changes between seasons. The results show that arctic and red foxes are sympatric during winter, but allopatric in summer as arctic foxes retreat to higher altitudes further from the tree-line during the breeding season. [source]


Sink habitats can alter ecological outcomes for competing species

JOURNAL OF ANIMAL ECOLOGY, Issue 6 2005
SEBASTIAN J. SCHREIBER
Summary 1Species often compete for breeding sites in heterogeneous landscapes consisting of sources and sinks. To understand how the presence or absence of sink breeding sites influence ecological outcomes, we extend Pulliam's source,sink model to competing species. 2In a homogeneous landscape consisting of source sites, we prove that one species, the ,superior' competitor, competitively excludes the other. Dominance is determined by a simple rule: the species that at equilibrium acquires new breeding sites at a faster rate dominates. 3We prove that the inclusion of sink sites can alter this ecological outcome by either mediating coexistence, reversing competitive dominance, or facilitating a priority effect. 4Sink-mediated coexistence requires the species to exhibit asymmetries in acquiring sink sites, the ,inferior' species to have a competitive advantage on sink sites and the ratio of sink to source sites be sufficiently low. 5For example, if the sink breeding sites are competitive refuges for the ,inferior' competitor and not too low in quality, coexistence occurs if the number of sink sites lies below a threshold. Alternatively, when the number of sink sites exceeds this threshold, competitive dominance is reversed and the ,superior' competitor is displaced. 6Counter-intuitively, despite being unable to support species in isolation, sink habitats embedded in a geographical mosaic of sources and sinks can enhance biodiversity by mediating coexistence or alter species composition by reversing competitive interactions. [source]