Constant-Effort Mist Net Bird Monitoring During the Breeding Season in a Lowland Deciduous Forest in Western Hokkaido, Japan

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Using a standardized method to track long-term fluctuations in avian populations is important for proposing effective conservation strategies for birds. From 2013 to 2022, we conducted constant-effort mist netting and bird banding during the breeding season in a lowland deciduous forest in western Hokkaido, Japan. A total of 1,327 individuals of 30 species were banded or recaptured. Twenty-four species bred in the study area, two species periodically passed through the site, and four species were considered accidental visitors. Breeding adult Asian Stubtail Urosphena squameiceps and Eastern Crowned Leaf Warbler Phylloscopus coronatus declined significantly during the study period, although, there was no decline in their rate of reproduction. In the absence of forest deterioration, this suggests that their declines may have resulted from environmental changes along their migration routes or on their wintering grounds. Significantly more adult male Asian Stubtail than females were captured annually. This was assumed to be because of the unique breeding habits of this species. The recapture probabilities (p) of males were higher than those of females in four species (Asian Stubtail, Eastern Crowned Leaf Warbler, Japanese Thrush Turdus cardis, and Black-faced Bunting Emberiza spodocephala), but vice versa in Narcissus Flycatcher Ficedula narcissina. Among these five species, the adult apparent survival rate (φ) was highest for Black-faced Bunting and lowest for Eastern Crowned Leaf Warbler. The number of sites comparing the vital indices of birds in Japan should be increased in the future, as in the Constant Effort Sites (CES) ringing scheme in Europe and the Monitoring Avian Productivity and Survivorship (MAPS) program in North America.

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Nonetheless, nest site selection has been studied in alligators (Alligator mississippensis; Garrick and Lang, 1977), green iguanas (Iguana iguana; Rand, 1968), turtles (Burger and Montevecchi, 1975; 430 This content downloaded from 157.55.39.153 on Mon, 19 Sep 2016 04:52:46 UTC All use subject to http://about.jstor.org/terms BURROW SELECTION BY IGUANAS Ewert, 1976; Stoneburner and Richardson, 1981), and pine snakes (Pituophis melanoleucus; Burger and Zappalorti, 1986). Most reptiles do not regularly dig burrows for daily occupation (see Wright and Wright, 1957), although many reptiles use subterranean burrows dug by mammals. However some lizards (Rand and Dugan, 1983) and a snake (Carpenter, 1982; Burger et al., 1988) dig burrows for nests or for use throughout the year. Presumably the location of these burrows reflects evolutionary constraints such as predation pressures, conspecific competition, and thermoregulation. In this paper we examine burrow site selection in black iguana (Ctenosaura similis) at Palo Verde, Guanacaste, Costa Rica. We were interested in whether the same burrows were used from year to year, whether burrow site characteristics varied between years, and whether burrow sites differed from the available habitat. Black iguanas are large iguanid lizards ranging from southern Mexico to Panama. The flesh is edible, and they are often hunted for food (Fitch and Hackforth-Jones, 1983). They range in size from 20-50 cm snout-vent length (SVL), with overlap between the sexes, although males are generally larger (Fitch and Hackforth-Jones, 1983). METHODS AND STUDY AREA We studied black iguanas at the Palo Verde National Park in Guanacaste, northwestern Costa Rica, in March of 1989 and 1990. Palo Verde contains mainly tropical lowland deciduous forest that borders the extensive marshes of the Tempisque River. Further description of the study area can be found in Gill (1989) and Burger and Gochfeld (1991). In 1989 we surveyed the area immediately around the OTS biological station, the deciduous forest within 25 m of the road between the OTS station and the park headquarters (hereafter called the hacienda), and around the hacienda (1 km from the station). We searched by walking transects through each area in a manner that allowed us to see nearly all of the habitat. Burrows included all holes where iguanas lived, but did not include nests or spaces under buildings. We included only burrows actively being used by black iguanas. We used photographs and sketches from 1989 to locate the sites of all burrows for comparison with 1990. To compare overall habitat choice (bank, ground, flat rock, rock or trees, see Table 2) with available habitat, we used a table of random numbers to generate coordinates for a grid used to select points for the entire study site. General habitat types included bank (slope over 15?), ground (flat area), flat rock, rocks or boulders, and trees, logs or roots. We recorded specific site characteristics (see Table 3) from all burrows and from an equal number of random points in each of the three plac s (OTS station, deciduous forest, hacienda). Specific site characteristics recorded included: slope; substrate (ground, rock, bank); percent cover over the opening; percent vegetation cover within 1 m of the point (or burrow entrance estimated); percent rock within 1 m; percent overall cover (vegetation, trees, rock) within 1 m; distance to the closest burrow and closest tree; and temperature of the air and at the mouth of the burrow entrance or spot. We so recorded the height and width of the burrow entrance for all burrows whether they were dug or were in rock crevices. Random points were selected by using a table of random numbers to generate a compass direction and a distance (1 to 4 m) from each burrow. Thus, each random point was matched to a burrow site. We estimated iguana length by noting where an iguana started and ended on the habitat and then measuring this distance, and checked our estimates against iguanas of known length (N = 20 from marked individuals, r = 0.9, P < 0.001). We were usually only 1-3 m from the iguana, so the estimates were possible. In 1989 both general habitat type (bank, ground, flat rock, rock, logs) and specific site characteristics were recorded for random points and for burrow sites. In 1990 we recorded the general habitat types for burrows at the OTS station, hacienda, and forest in between, but we tripled the size of the areas searched in equal proportion to the three types. We also recorded some site characteristics, including location, height and width of burrow entrance, percent cover at the entrance, overall slope of area with burrow, slope at the burrow entrance, nearestneighbor distance, and the length of the burrow. 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  • Preprint Article
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Chemical Profiles and Anti-Inflammatory Activities of the Copal Resin and Its Volatile Fraction of &lt;em&gt;Bursera bipinnata&lt;/em&gt;
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Bursera bipinnata is known as “copal chino, is a small tree that grows in steep areas and is part of the transitional populations of pine and oak forests and lowland deciduous forests. It is the taxon with the widest geographic distribution in México and considered a source of high-grade copal resin used in ceremonies and offerings. Also, B. bipinnata is considered to have great value in traditional medicine to treat ailments related to in-flammation. In this work, the anti-inflammatory effects of the volatile fraction and resin of B. bipinnata in LPS-stimulated RAW 264.7 macrophage cells were demonstrated. The resin extract was the best inhibitor with a 65.83 ± 8.53 % of inhibition of NO production with IC50 = 30 ± 3.3 µg/mL. In contrast, its volatile fraction showed a 37.43± 7.13 % of inhibition at 40 µg/mL. GC/MS and LC analysis of the total resin allowed the chemical characterization of eleven pentacyclic triterpenes with ursane, oleanane, and lupane skeletons, and eight monoterpenes. The structures of compounds (15, 17, 29-35) are reported for the first time from the resin of Bursera bipinnata. The anti-inflammatory activity of the most abundant constituents of the resin of B. bipinnata (α-amyrin (15), 3-epilupeol (17) and α-phellandrene (1) has been previously demonstrated which con-firms the activity showed by the resin as well as the traditional use of this important copal resin. The chemical profile of B. bippinata differs from that of other copal resins (e.g. B. copallifera) in the presence of a greater variety of triterpenes in the resin.

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