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1.
Biology (Basel) ; 11(2)2022 Feb 12.
Article in English | MEDLINE | ID: mdl-35205168

ABSTRACT

Identifying appropriate indicator species for the impact of deer on forest vegetation is crucial for forest management in deer habitats and is required to be sensitive to temporal and spatial variations in deer density. Dryopteris crassirhizoma was selected as a new indicator to evaluate the response to these variations. We examined the population-level characteristics, morphological characteristics at the individual level, and grazing intensity of D. crassirhizoma at temporally different deer density sites in Hokkaido, Japan. The response of D. crassirhizoma to spatial variation in deer density was also examined within and between two regions in Hokkaido, Japan. Although the population-level characteristics and morphological characteristics did not significantly respond to short-term decreases in deer density, grazing intensity significantly decreased with decreasing deer density. The grazing intensity was also positively related to the spatial variation of deer density within both regions, but the estimated coefficient of the grazing intensity differed between regions. We concluded that D. crassirhizoma can be a useful indicator species of the impact of deer on forest vegetation. The grazing intensity of the indicator species was sensitive to temporal and spatial variations in deer density within the region.

2.
PeerJ ; 5: e3869, 2017.
Article in English | MEDLINE | ID: mdl-29038752

ABSTRACT

The sika deer (Cervus nippon yesoensis) population in the Ramsar-listed Kushiro Wetland has increased in recent years, and the Ministry of the Environment of Japan has decided to take measures to reduce the impact of deer on the ecosystem. However, seasonal movement patterns of the deer (i.e., when and where the deer inhabit the wetland) remain unclear. We examined the seasonal movement patterns of sika deer in the Kushiro Wetland from 2013 to 2015 by analyzing GPS location data for 28 hinds captured at three sites in the wetland. Seasonal movement patterns were quantitatively classified as seasonal migration, mixed, dispersal, nomadic, resident, or atypical, and the degree of wetland utilization for each individual was estimated. The area of overlap for each individual among intra-capture sites and inter-capture sites was calculated for the entire year and for each season. Our results showed that the movement patterns of these deer were classified not only as resident but also as seasonal migration, dispersal, and atypical. Approximately one-third of the individuals moved into and out of the wetland during the year as either seasonal migrants or individuals with atypical movement. Some of the individuals migrated to farmland areas outside the wetland (the farthest being 69.9 km away). Half of the individuals inhabited the wetland all or most of the year, i.e., 81-100% of their annual home range was within the wetland area. Even among individuals captured at the same site, different seasonal movement patterns were identified. The overlap areas of the home ranges of individuals from the same capture sites were larger than those for individuals from different capture sites (e.g., mean of annual home range overlap with intra-capture sites: 47.7% vs. inter-sites: 1.3%). To achieve more effective ecosystem management including deer management in the wetland, management plans should cover inside and outside of the wetland and separate the population into multiple management units to address the different movement patterns and wetland utilization of the population.

3.
Am J Primatol ; 76(6): 596-607, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24375432

ABSTRACT

Comparing animal consumption to plant primary production provides a means of assessing an animal's impact on the ecosystem and an evaluation of resource limitation. Here, we compared annual fruit and leaf consumption by Japanese macaques (Macaca fuscata) relative to the annual production of these foods in the lowlands and highlands of Yakushima Island, Japan. We estimated consumption by macaques by the direct observation of macaque groups for 1 year in each habitat. We estimated leaf production as the sum of leaf litter fall (corrected for the effect of translocated organic and inorganic matter) and folivory by insects (assumed to be 10%) and by macaques. We estimated fruit production as the sum of fruit litter fall and consumption by birds (estimated by the seed fall) and macaques. The impact of macaque folivory at the community level was negligible relative to production (∼0.04%) compared with folivory by insects (assumed to be 10%); however, for some species, macaque folivory reached up to 10.1% of production. Tree species on which macaques fed did not decline in abundance over 13 years, suggesting that their folivory did not influence tree species dynamics. For the three major fleshy-fruited species in the highland site, macaques consumed a considerable portion of total fruit production (6-40%), rivaling the consumption by birds (32-75%). We conclude that at the community level, macaque folivory was negligible compared with the leaf production, but frugivory was not.


Subject(s)
Ecosystem , Feeding Behavior , Macaca , Animals , Female , Fruit , Japan , Male , Plant Leaves
4.
Ecology ; 94(12): 2873-85, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24597232

ABSTRACT

Numerous studies have revealed the existence of nonrandom trait distribution patterns as a sign of environmental filtering and/or biotic interactions in a community assembly process. A number of metrics with various algorithms have been used to detect these patterns without any clear guidelines. Although some studies have compared their statistical powers, the differences in performance among the metrics under the conditions close to actual studies are not clear. Therefore, the performances of five metrics of convergence and 16 metrics of divergence under alternative conditions were comparatively analyzed using a suite of simulated communities. We focused particularly on the robustness of the performances to conditions that are often uncertain and uncontrollable in actual studies; e.g., atypical trait distribution patterns stemming from the operation of multiple assembly mechanisms, a scaling of trait-function relationships, and a sufficiency of analyzed traits. Most tested metrics, for either convergence or divergence, had sufficient statistical power to distinguish nonrandom trait distribution patterns without uncertainty. However, the performances of the metrics were considerably influenced by both atypical trait distribution patterns and other uncertainties. Influences from these uncertainties varied among the metrics of different algorithms and their performances were often complementary. Therefore, under the uncertainties of an assembly process, the selection of appropriate metrics and the combined use of complementary metrics are critically important to reliably distinguish nonrandom patterns in a trait distribution. We provide a tentative list of recommended metrics for future studies.


Subject(s)
Ecosystem , Models, Biological , Uncertainty
5.
Primates ; 52(2): 187-98, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21340696

ABSTRACT

Habitat, diet and leaf chemistry are compared between Japanese and Barbary macaques to reveal the similarities and differences in dietary adaptations of temperate primates living at the eastern and western extremes of the genus Macaca. Tree species diversity and proportion of fleshy-fruited species are much higher in Japan than in North Africa. Both species spend considerable annual feeding time on leaves. Japanese macaques prefer fruits and seeds over leaves, and Barbary macaques prefer seeds. These characteristics are adaptive in temperate regions where fruit availability varies considerably with season, since animals can survive during the lean period by relying on leaf and other vegetative foods. The two species are different with respect to the higher consumption of herbs by Barbary macaques, and the leaves consumed contain high condensed and hydrolysable tannin for Barbary but not for Japanese macaques. Barbary macaques supplement less diverse tree foods with herbs. Because of the low species diversity and high tannin content of the dominant tree species, Barbary macaques may have developed the capacity to cope with tannin. This supports the idea that digestion of leaves is indispensable to survive in temperate regions where fruit and seed foods are not available for a prolonged period during each year.


Subject(s)
Adaptation, Physiological , Diet , Food Preferences , Macaca/physiology , Algeria , Animals , Behavior, Animal , Biodiversity , Ecosystem , Female , Fruit/classification , Japan , Plant Leaves/chemistry , Seeds/classification , Tannins/chemistry , Trees/chemistry , Trees/classification
6.
J Plant Res ; 122(5): 523-8, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19462156

ABSTRACT

Dwarf bamboos in the genus Sasa are believed to be long-lived, synchronously flowering, and monocarpic plants. However, the monocarpy of dwarf bamboo has not been confirmed, because whether all ramets within one genet flower at the same time cannot be determined without differentiating the genetic structure among ramets. This study aims to evaluate the reproductive traits of Sasa pubiculmis by verifying the monocarpy and physiological integration between flowering ramets and non-flowering ramets during a 4-year flowering period. One genotypically identified genet, which covered an area of approximately 3 ha, had both flowering and non-flowering patches of ramets during the 4-year flowering period (2004-2007). A fraction of the flowering genet remained non-flowering during the 4 years of observation, and did not die after mass flowering. Flowering ramets were physically connected to non-flowering ramets via rhizomes, and assimilated (13)C was allocated from non-flowering ramets to flowering ramets. Consequently, we clarified that this dwarf bamboo potentially has polycarpic reproductive traits rather than monocarpic, and a genet can keep rhizomes and non-flowering patches alive to sustain the organism after mass flowering.


Subject(s)
Flowers/genetics , Flowers/physiology , Sasa/genetics , Sasa/physiology , Carbon Isotopes , Sasa/growth & development
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