Avian species diversity in different habitat types in and around North Nandi Forest,Kenya

Forest fragmentation and degradation leads to formation of modified habitats whose ability to support existing avifaunal diversity is still largely unknown. Bird diversity in indigenous forest, disturbed forest, plantation forest and farmlands adjacent to North Nandi Forest reserve was studied between January 2015 and June 2015. The distribution of bird feeding guilds in these habitat patches was also evaluated. Birds were surveyed using point counts, timed species counts and line transects and classified into six feeding guilds. A total of 3,232 individual birds of 151 species were recorded in the four habitats. Significant difference on bird abundance across the four habitats (F = 15.141, P ≤ 0.05, df = 3, 1121) was noted. Shannon–Weiner diversity index H′ for bird community ranged from 3.06 for plantation forest to 4.05 for disturbed forest showing a relatively diverse bird community. Insectivores (F = 3.090, P ≤ 0.05, df = 3, 297) dominated the foraging species assemblage in all the habitats significantly. Linear regression analysis revealed a strong linear relationship on bird species richness and abundance with vegetation variables (P < 0.01 in all cases). The results indicate that disturbed forest and indigenous forest support high bird species richness than plantation forest and farmlands. However, high bird abundance was observed in farmlands and plantation forest as opposed to indigenous forest and disturbed forest as they provide dispersal routes over a short distance and are important for creating corridors between primary forests.     

Fluctuating Asymmetry and Environmental Stress: Understanding the Role of Trait History

While fluctuating asymmetry (FA; small, random deviations from perfect symmetry in bilaterally symmetrical traits) is widely regarded as a proxy for environmental and genetic stress effects, empirical associations between FA and stress are often weak or heterogeneous among traits. A conceptually important source of heterogeneity in relationships with FA is variation in the selection history of the trait(s) under study, i.e. traits that experienced a (recent) history of directional change are predicted to be developmentally less stable, potentially through the loss of canalizing modifiers. Here we applied X-ray photography on museum specimens and live captures to test to what extent the magnitude of FA and FA-stress relationships covary with directional shifts in traits related to the flight apparatus of four East-African rainforest birds that underwent recent shifts in habitat quality and landscape connectivity. Both the magnitude and direction of phenotypic change varied among species, with some traits increasing in size while others decreased or maintained their original size. In three of the four species, traits that underwent larger directional changes were less strongly buffered against random perturbations during their development, and traits that increased in size over time developed more asymmetrically than those that decreased. As we believe that spurious relationships due to biased comparisons of historic (museum specimens) and current (field captures) samples can be ruled out, these results support the largely untested hypothesis that directional shifts may increase the sensitivity of developing traits to random perturbations of environmental or genetic origin.     

Nest predation of grassland bird species increases with parental activity at the nest

Alexander Skutch predicted that nest predation will increase with activity at nests, and that predation should be greatest during the nestling stage when parents are feeding young. We tested this hypothesis using three ecologically similar grassland bird species nesting on the high altitude grasslands of Wakkerstroom, South Africa. Parental activity, measured as adult arrival and departure frequency from the nest, was greater during the nestling than incubation stage. Nest predation, however, did not increase with parental activity between these stages in all three study species. However, nest site effects could have confounded this result. We therefore conducted an experiment that controlled for parental activity (by reusing natural nests of the study species with artificial clutches) in order to test for nest site effects. Nests that had a high rate of predation when used by active parents had a correspondingly high rate of depredation when the same nests were reused with artificial clutches (i.e. after controlling for parental activity). This result supports the notion that variation in nest site quality is the primary factor affecting nest predation rate. We also tested whether high predation during incubation is related to nest site effects. Nest predation rates of experimental clutches placed in reused nests that had been originally (when active parents were present) depredated during incubation stage were significantly higher than those that were originally depredated during the nestling stage. Finally, once nest site effects were accounted for, nest predation showed a positive increase with parental activity during the nestling stage across species.     

Nest survival in year‐round breeding tropical red‐capped larks Calandrella cinerea increases with higher nest abundance but decreases with higher invertebrate availability and rainfall

Nest survival is critical to breeding in birds and plays an important role in life‐history evolution and population dynamics. Studies evaluating the proximate factors involved in explaining nest survival and the resulting temporal patterns are biased in favor of temperate regions. Yet, such studies are especially pertinent to the tropics, where nest predation rates are typically high and environmental conditions often allow for year‐round breeding. To tease apart the effects of calendar month and year, population‐level breeding activity and environmental conditions, we studied nest survival over a 64‐month period in equatorial, year‐round breeding red‐capped larks Calandrella cinerea in Kenya. We show that daily nest survival rates varied with time, but not in a predictable seasonal fashion among months or consistently among years. We found negative influences of flying invertebrate biomass and rain on nest survival and higher survival of nests when nests were more abundant, which suggests that nest predation resulted from incidental predation. Although an increase in nest predation is often attributed to an increase in nest predators, we suggest that in our study, it may be caused by altered predator activity resulting from increased activity of the primary prey, invertebrates, rather than activity of the red‐capped larks. Our results emphasize the need to conduct more studies in Afro‐tropical regions because proximate mechanisms explaining nest predation can be different in the unpredictable and highly variable environments of the tropics compared with the relatively predictable seasonal changes found in temperate regions. Such studies will aid in better understanding of the environmental influences on life‐history variation and population dynamics in birds.     

No downregulation of immune function during breeding in two year‐round breeding bird species in an equatorial East African environment

Some equatorial environments exhibit substantial within‐location variation in environmental conditions throughout the year and yet have year‐round breeding birds. This implies that breeding in such systems are potentially unrelated to the variable environmental conditions. By breeding not being influenced by environmental conditions, we become sure that any differences in immune function between breeding and non‐breeding birds do not result from environmental variation, therefore allowing for exclusion of the confounding effect of variation in environmental conditions. This create a unique opportunity to test if immune function is down‐regulated during reproduction compared to non‐breeding periods. We compared the immune function of sympatric male and female chick‐feeding and non‐breeding red‐capped Calandrella cinerea and rufous‐naped larks Mirafra africana in equatorial East Africa. These closely‐related species occupy different niches and have different breeding strategies in the same grassland habitat. Red‐capped larks prefer areas with short grass or almost bare ground, and breed during low rainfall periods. Rufous‐naped larks prefer areas of tall grass and scattered shrubs and breed during high rainfall. We measured the following immune indices: nitric oxide, haptoglobin, agglutination and lysis, and measured total monthly rain, monthly average minimum (T_min) and maximum (T_max) temperatures. Contrary to our predictions, we found no down‐regulation of immune function during breeding; breeding birds had higher nitric oxide than non‐breeding ones in both species, while the other three immune indices did not differ between breeding phases. Red‐capped larks had higher nitric oxide concentrations than Rufous‐naped larks, which in turn had higher haptoglobin levels than red‐capped larks. T_max was higher during breeding than during non‐breeding for red‐capped larks only, suggesting potential confounding effect of T_max on the comparison of immune function between breeding and non‐breeding birds for this species. Overall, we conclude that in the two year‐round breeding equatorial larks, immune function is not down‐regulated during breeding.     

Conservation planning in an agricultural landscape: the case of Sharpe's Longclaw

Lens, L., Muchai, M., Bennun, L.A. & Duchateau, L. 2000. Conservation planning in an agricultural landscape: the case of Sharpe's Longclaw. Ostrich 71 (1 & 2): 300–303.

We studied the distribution and habitat use of Sharpe's Longclaw, Macmnyx sharpei, a Kenyan montane grassland endemic, in a fragmented agricultural landscape at two spatial scales. Monthly counts in a fixed number of plots selected in contrasting habitat types provided insight in the species' distribution in relation to the available habitat. Simultaneously, focused ecological work in a smaller area provided information on its behaviour, movements and habitat choice, and allowed us to interpret the wider distribution patterns in a biologically meaningful way. Sharpe's Longclaw occurs only in grasslands, not in cultivated fields or plantations of exotic trees. It prefers short grassland with a well-developed tussock structure, apparently because tussocks provide good cover while foraging and nesting. However, as tussock grass is unpalatable to livestock, this grassland type is being ploughed up, re-seeded and converted to cultivation at an alarming rate, and the remaining patches are becoming ever more isolated from each other. Although only limited information on the species' population dynamics and dispersal ability is available, there is a clear need to conserve and manage the remaining natural grassland habitat. Since most of the land within the species' distribution range is privately owned, keeping viable populations of Sharpe's Longclaw may be extremely difficult.     

Home-ranges of tropical Red-capped Larks are influenced by breeding rather than vegetation,rainfall or invertebrate availability

Home-range studies have received considerable attention from ecologists but are greatly skewed towards the north temperate areas. Tropical areas offer an ideal setting to tease apart hypotheses about weather, food availability and social interactions as important factors influencing home-range. In this study, we investigated home-range and movement patterns of the tropical Red-capped Lark Callandrella cineria, a year-round breeding bird with a dynamic social structure. We tracked 56 individuals using radiotransmitters and colour-ring readings over a 23-month period. Our objective was to understand year-round variation in home-range size in the context of the highly aseasonal and unpredictable variation in weather and resources typical of many equatorial habitats, in addition to the birds’ changing social structure and year-round breeding. The mean composite monthly home-range of Red-capped Larks was 58.0 ha, and the mean individual home-range size was 19.9 ha, but this varied considerably between individuals. The total number of nests found per month (breeding intensity) best predicted home-range size of non-breeding birds, and of breeding and non-breeding birds combined. We show for the first time that breeding intensity decreases the home-range size of non-breeding individuals. Our study also underlines the relevance of conducting more studies in aseasonal tropical areas in order to disentangle effects of weather, food availability and breeding that vary in parallel, peaking simultaneously in most seasonal areas.