scholarly journals THE RELATIVE IMPORTANCE OF THREE SPECIFIC CLIMATIC FACTORS ON NORTH AMERICAN BREEDING BIRD SPECIES RICHNESS

Author(s):  
M. Zhang ◽  
Y. Lin

Understanding of the relationships between bird species and environment facilitates protecting avian biodiversity and maintaining nature sustaining. However, the effects of many climatic factors on bird richness have not been fully grasped. To fill this gap, this study investigated the relationships between the richness of three typical North American breeding bird species and three climatic factors at the monthly scale. Based on the North American Breeding Bird Survey (BBS) data during 1967–2014, the relationships between the numbers of Carolina wren, Cerulean warbler, and Red-bellied woodpecker and the three climatic factors of precipitation, vapor pressure, and potential evapotranspiration were examined using the method of Pearson linear regression analysis. The results indicated that the three climatic factors have correlations with the richness of the breeding bird species but in different modes, e.g., strong correlations for the non-migratory species but weak correlations for the migratory species.

2019 ◽  
Author(s):  
Federico Morelli ◽  
Yanina

ContextThe negative association between elevation and species richness is a well-recognized pattern in macro-ecology. ObjectivesThe aim of this study was to investigate changes in functional evenness of breeding bird communities along an elevation gradient in Europe. MethodsUsing the bird data from the EBCC Atlas of European Breeding Birds we estimated an index of functional evenness which can be assumed as a measure of the potential resilience of communities.ResultsOur findings confirm the existence of a negative association between elevation and bird species richness in all European eco regions. However, we also explored a novel aspect of this relationship, important for conservation: Our findings provide evidence at large spatial scale of a negative association between the functional evenness (potential community resilience) and elevation, independent of the eco region. We also found that the Natura2000 protected areas covers the territory most in need of protection, those characterized by bird communities with low potential resilience, in hilly and mountainous areas.ConclusionsThese results draw attention to European areas occupied by bird communities characterized by a potential lower capacity to respond to strong ecological changes, and, therefore, potentially more exposed to risks for conservation.


1998 ◽  
Vol 76 (2) ◽  
pp. 278-287 ◽  
Author(s):  
J D Matheson ◽  
D W Larson

Cliffs along the Niagara Escarpment in Ontario, Canada, support a long, narrow presettlement forest that includes three distinct geomorphic and vegetation zones: cliff edge, cliff face, and talus slope. This unique landform provides an opportunity to evaluate differences in bird communities between the escarpment and adjacent forest relative to habitat features. We sampled forest birds 12 times during the summer of 1994 in plots located in plateau forests, on talus slope, at cliff edges, and on cliff faces. Eleven habitat variables considered important to birds were also sampled in the plots. We arranged plots along six randomly spaced transects at a south site and a north site. Both sites had the consistent habitat heterogeneity considered important to birds. Bird species richness and composition responded to this heterogeneity, but differently at each site: plateau deciduous forests always had the lowest richness and the simplest species composition, whereas both cliff edges and talus slopes had a higher diversity of birds. Cliff faces had large numbers of species in the south but smaller numbers in the north. Escarpment zones form a habitat mosaic that supports many species not found in the adjacent forest and is consistent with the effect of habitat edge. The results suggest that cliffs represent a significant additive influence on avian biodiversity, even when the cliff is a very narrow component of the landscape.


2018 ◽  
Author(s):  
Jin-Yong Kim ◽  
Sanghun Lee ◽  
Man-Seok Shin ◽  
Chang-Hoon Lee ◽  
Changwan Seo ◽  
...  

Altitudinal patterns in the population ecology of mountain bird species are useful for predicting species occurrence and behavior. Numerous hypotheses about the complex interactions among environmental factors have been proposed; however, these remain controversial. This study investigated the causes of altitudinal patterns in breeding bird species richness and density in relation to climate, habitat heterogeneity, and migration influence in Jirisan National Park, South Korea. We conducted a field survey of 142 plots at altitudes between 200 and 1400 m above mean sea level in the breeding season. A total of 2771 individuals from 53 breeding bird species were recorded. Altitudinal patterns of species richness and density showed a hump-shaped pattern, indicating that the highest richness and density could be observed at moderate altitudes. Models constructed with 16 combinations of six variables demonstrated that species richness was positively correlated with vertical and horizontal habitat heterogeneity, and that density was positively correlated with vertical, but not horizontal, habitat heterogeneity, and negatively correlated with migrant rate. No significant relationships were found between spring temperature and species richness or density. Therefore, the observed patterns in species richness support the hypothesis that habitat heterogeneity, rather than climate, is the main driver of species richness. And neither habitat heterogeneity nor climate hypotheses fully explains the observed patterns in density. However, vertical habitat heterogeneity does likely help explain observed patterns in density. The heterospecific attraction hypothesis did not apply to the distribution of birds along the altitudinal gradient. Appropriate management of vertical habitat heterogeneity, such as vegetation cover, should be maintained for the conservation of bird diversity in this area.


Author(s):  
Adam C. Smith ◽  
Brandon P.M. Edwards

ABSTRACTThe status and trend estimates derived from the North American Breeding Bird Survey (BBS), are critical sources of information for bird conservation. However, the estimates are partly dependent on the statistical model used. Therefore, multiple models are useful because not all of the varied uses of these estimates (e.g. inferences about long-term change, annual fluctuations, population cycles, recovery of once declining populations) are supported equally well by a single statistical model. Here we describe Bayesian hierarchical generalized additive models (GAM) for the BBS, which share information on the pattern of population change across a species’ range. We demonstrate the models and their benefits using data a selection of species; and we run a full cross-validation of the GAMs against two other models to compare predictive fit. The GAMs have better predictive fit than the standard model for all species studied here, and comparable predictive fit to an alternative first difference model. In addition, one version of the GAM described here (GAMYE) estimates a population trajectory that can be decomposed into a smooth component and the annual fluctuations around that smooth. This decomposition allows trend estimates based only on the smooth component, which are more stable between years and are therefore particularly useful for trend-based status assessments, such as those by the IUCN. It also allows for the easy customization of the model to incorporate covariates that influence the smooth component separately from those that influence annual fluctuations (e.g., climate cycles vs annual precipitation). For these reasons and more, this GAMYE model is a particularly useful model for the BBS-based status and trend estimates.LAY SUMMARYThe status and trend estimates derived from the North American Breeding Bird Survey are critical sources of information for bird conservation, but they are partly dependent on the statistical model used.We describe a model to estimate population status and trends from the North American Breeding Bird Survey data, using a Bayesian hierarchical generalized additive mixed-model that allows for flexible population trajectories and shares information on population change across a species’ range.The model generates estimates that are broadly useful for a wide range of common conservation applications, such as IUCN status assessments based on trends or changes in the rates of decline for species of concern; and the estimates have better or similar predictive accuracy to other models., and


2021 ◽  
Author(s):  
Lars Witting

I use the North American Breeding Bird Survey (Sauer et al. 2017) to construct 462 population trajectories with about 50 yearly abundance estimates each. Applying AIC model-selection, I find that selection-regulated population dynamics is 25,000 (95%:0.42-1.7e17) times more probable than density-regulated growth. Selection is essential in 94% of the best models explaining 82% of the population dynamics variance across the North American continent. Similar results are obtained for 111, 215, and 420 populations of British birds (BTO 2020), Danish birds (DOF 2020), and birds and mammals in the Global Population Dynamic Database (GPDD 2010). The traditional paradigm---that the population dynamic growth rate is a function of the environment, with maximal per-capita growth at low population densities, and sub-optimal reproduction from famine at carrying capacities with strong competition for limited resources---is not supported. Selection regulation generates a new paradigm where the world is green and individuals are selected to survive and reproduce at optimal levels at population dynamic equilibria with sufficient resources. It is only the acceleration of the population dynamic growth rate, and not the growth rate itself, that is determined by the density-dependent environment, with maximal growth occurring at the densities of the population dynamic equilibrium.


The Condor ◽  
2016 ◽  
Vol 118 (3) ◽  
pp. 502-512 ◽  
Author(s):  
Jessica M. Gorzo ◽  
Anna M. Pidgeon ◽  
Wayne E. Thogmartin ◽  
Andrew J. Allstadt ◽  
Volker C. Radeloff ◽  
...  

2017 ◽  
Vol 8 (1) ◽  
pp. 154-172 ◽  
Author(s):  
John R. Sauer ◽  
Daniel K. Niven ◽  
Keith L. Pardieck ◽  
David J. Ziolkowski ◽  
William A. Link

Abstract The North American Breeding Bird Survey (BBS) contains data for >700 bird species, but analyses often focus on a core group of ∼420 species. We analyzed data for 122 species of North American birds for which data exist in the North American Breeding Bird Survey (BBS) database but are not routinely analyzed on the BBS Summary and Analysis Website. Many of these species occur in the northern part of the continent, on routes that fall outside the core survey area presently analyzed in the United States and southern Canada. Other species not historically analyzed occur in the core survey area with very limited data but have large portions of their ranges in Mexico and south. A third group of species not historically analyzed included species thought to be poorly surveyed by the BBS, such as rare, coastal, or nocturnal species. For 56 species found primarily in regions north of the core survey area, we expanded the scope of the analysis, using data from 1993 to 2014 during which ≥3 survey routes had been sampled in 6 northern strata (Bird Conservation regions in Alaska, Yukon, and Newfoundland and Labrador) and fitting log-linear hierarchical models for an augmented BBS survey area that included both the new northern strata and the core survey area. We also applied this model to 168 species historically analyzed in the BBS that had data from these additional northern strata. For both groups of species we calculated survey-wide trends for the both core and augmented survey areas from 1993 to 2014; for species that did not occur in the newly defined strata, we computed trends from 1966 to 2014. We evaluated trend estimates in terms of established credibility criteria for BBS results, screening for imprecise trends, small samples, and low relative abundance. Inclusion of data from the northern strata permitted estimation of trend for 56 species not historically analyzed, but only 4 of these were reasonably monitored and an additional 13 were questionably monitored; 39 of these species were likely poorly monitored because of small numbers of samples or very imprecisely estimated trends. Only 4 of 66 “new” species found in the core survey area were reasonably monitored by the BBS; 20 were questionably monitored; and 42 were likely poorly monitored by the BBS because of inefficiency in precision, abundance, or sample size. The hierarchical analyses we present provide a means for reasonable inclusion of the additional species and strata in a common analysis with data from the core area, a critical step in the evolution of the BBS as a continent-scale survey. We recommend that results be presented both 1) from 1993 to the present using the expanded survey area, and 2) from 1966 to the present for the core survey area. Although most of the “new” species we analyzed were poorly monitored by the BBS during 1993–2014, continued expansion of the BBS will improve the quality of information in future analyses for these species and for the many other species presently monitored by the BBS.


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