Keita Fukasawa’s research while affiliated with National Institute for Environmental Studies and other places

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Publications (52)


Locations of camera-trapping arrays. A black dot indicates the centroid of camera-trap locations in an array.
Map of the number of taxa for (a) mammals and (b) birds and RAI of (c) mammals and (d) birds for each camera-trap array.
Biplot of principal component analysis for the relative abundance indices of the mammal community. The ellipsoids correspond to camera-trap arrays. The eight longest vectors of species are shown as arrows.
Biplot of principal component analysis for the relative abundance indices of the avian community. The ellipsoids correspond to camera-trap arrays. The eight longest vectors of species are shown as arrows.
Snapshot Japan 2023: the first camera trap dataset under a globally standardised protocol in Japan
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  • Full-text available

March 2025

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109 Reads

Keita Fukasawa

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Takahiro Morosawa

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Background There is an urgent need to develop global observation networks to quantify biodiversity trends for evaluating achievements of targets of Kunming-Montreal Global Biodiversity Framework. Camera traps are a commonly used tool, with the potential to enhance global observation networks for monitoring wildlife population trends and has the capacity to constitute global observation networks by applying a unified sampling protocol. The Snapshot protocol is simple and easy for camera trapping which is applied in North America and Europe. However, there is no regional camera-trap network with the Snapshot protocol in Asia. New information We present the first dataset from a collaborative camera-trap survey using the Snapshot protocol in Japan conducted in 2023. We collected data at 90 locations across nine arrays for a total of 6162 trap-nights of survey effort. The total number of sequences with mammals and birds was 7967, including 20 mammal species and 23 avian species. Apart from humans, wild boar, sika deer and rodents were the most commonly observed taxa on the camera traps, covering 57.9% of all the animal individuals. We provide the dataset with a standard format of Wildlife Insights, but also with Camtrap DP 1.0 format. Our dataset can be used for a part of the global dataset for comparing relative abundances of wildlife and for a baseline of wildlife population trends in Japan. It can also used for training machine-learning models for automatic species identifications.

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Example of simulated utility distributions under various dependencies of permeability on a hypothetical landscape variable. Black dots indicate cells with high permeability; other cells have low permeability. The red X indicates the activity center.
Example of simulated movement and the detection of an individual. The transparent solid line is the movement path. Open rectangles are traps, and blue circles indicate detection counts. The background tile map indicates zones with high (green) and low (pale red) permeability.
True versus estimated parameters by advection–diffusion capture–recapture. Dots and error bars indicate maximum likelihood estimates and 95% CIs. The solid black line is y = x.
Overlap between true and predicted home ranges by advection–diffusion capture–recapture (ADCR), spatial capture–recapture (SCR) with the least‐cost path, and basic SCR.
Estimated effect of landscape on (A) permeability by advection–diffusion capture–recapture (ADCR) and (B) cost by spatial capture–recapture (SCR) with the least‐cost path (SCR‐LCP) for black bear dataset. Dots and error bars are the maximum likelihood estimate and 95% CIs, respectively.
Mechanistic home range capture–recapture models for the estimation of population density and landscape connectivity

February 2025

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36 Reads

Spatial capture–recapture models (SCRs) provide an integrative statistical tool for analyzing animal movement and population patterns. Although incorporating home range formation with a theoretical basis of animal movement into SCRs can improve the prediction of animal space use in a heterogeneous landscape, this approach is challenging owing to the sparseness of recapture events. In this study, we developed an advection–diffusion capture–recapture model (ADCR), which is an extension of SCRs incorporating home range formation with advection–diffusion formalism, providing a new framework to estimate population density and landscape permeability. we tested the unbiasedness of the estimator using simulated capture–recapture data generated by a step selection function. We also compared the accuracy of population density estimates and home range shapes with those from SCR incorporating the least‐cost path and basic SCR. In addition, ADCR was applied to a real dataset of Asiatic black bear (Ursus thibetanus) in Japan to demonstrate the capacity of the ADCR to detect geographical barriers that constrain animal movements. Population density and permeability of ADCR were substantially unbiased for simulated datasets. ADCR could detect environmental signals on connectivity more sensitively and could estimate population density, home range shapes, and size variations better than the existing models. For the application to the bear dataset, ADCR could detect the effect of water bodies as a barrier to movement, which is consistent with previous studies, whereas estimates by SCR with the least‐cost path were difficult to interpret. ADCR provides unique opportunities to elucidate both individual‐ and population‐level ecological processes from capture–recapture data. By offering a formal link with step selection functions to estimate animal movement, it is suitable for simultaneously modeling capture–recapture data and animal movement data. This study provides a basis for studies of the interplay between animal movement processes and population patterns.


Fig. 1. (Top) Numbers of items and (bottom) average price for each item. (Left) trapping items and (right) control items. Shading indicates period after CSF arrived.
Fig. 2. Effects of CSF on (a) trapping items and (b) control items as wild boar countermeasures. The vertical dashed red line shows the start of the CSF outbreak.
Disease outbreak in wildlife changes online sales of management items

February 2025

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46 Reads

One Health

Infectious diseases of wildlife cause human health hazards and economic losses. However, it is unclear how outbreaks affect human behaviour in relation to countermeasures against human–wildlife conflict. To explore the effects of infectious disease outbreaks among wild boars on countermeasure choices, we analysed online auction data before and after an outbreak of classical swine fever in wild boar. Online sales of boar traps decreased by 17 % after the outbreak, whereas sales of control items increased by 73 %. These results imply that infectious disease outbreaks in wildlife shift people's countermeasures from active to passive management. Since active trapping for the control of wildlife populations is essential to the avoidance of human–wildlife conflict, our findings show that outbreaks of infectious disease can aggravate conflict. Governments, farmers and hunters need to improve population control after outbreaks of infectious disease.





Schematic of higher‐order dissimilarity (HOD). A spatial case of HOD is shown in (a). Although conventional dissimilarity has focused on dissimilarity among the same dimension, higher‐order dissimilarity can compare dissimilarity structures without regard to whether they are of the same dimension. For visualisation, only three compositional types are hypothesised, corresponding to three levels of darkness in each colour (e.g. blue, green and red). Specifically, we hypothesised that dissimilarities between sites (or time points) of the same level of darkness were zero (i.e. identical composition), those between sites of one darker or lighter difference were 0.5, and those between the darkest and lightest sites were 1.0. The grey arrows indicate conventional dissimilarity (i.e. first‐order dissimilarity) and the black arrows indicate HOD. Among compared datasets, black and white stars indicate identical sites or time points. The potential analytical framework for HOD based on spatial and temporal comparisons (i.e. spatial and temporal HOD) is shown in (b). The upper panel shows examples of spatial HOD, and the lower panel shows examples of temporal HOD. In both cases, the left‐hand side shows examples of community structure comparisons between different guilds and intraspecific genetic structure between species, while the right‐hand side shows examples of changes in spatial HOD or temporal HOD along a temporal or spatial axis.
Schematic representation of specific analytical procedures for higher‐order dissimilarity (HOD). For visualisation, only three compositional types are hypothesised, corresponding to three levels of darkness in each colour (e.g. blue, green and red). Specifically, we hypothesised that dissimilarities between sites (or time points) of the same level of darkness were zero (i.e. identical composition), between sites of one darker or lighter difference were 0.5, and between darkest and lightest sites were 1.0. The asterisk notes the necessity of the Kriging process if the specific sampling points are not identical.
Sample application of higher‐order dissimilarity (HOD) to genetic monitoring using two simulated datasets based on two types of scenarios from time 0 to time 100. In both scenarios, the stable conditions are hypothesised by time 30 (shared section in light green). After time 30, the genetic structure is stable in one scenario (upper section in orange) but homogenised in the other (lower section in blue). The change of the calculated HOD index (i.e. contrast RV coefficient) compared to the value at time 0 is shown in (a). The genetic structure is visualised in (b), and the colours were determined using the two axes of NMDS (details see Text S1).
Higher‐order dissimilarity in biodiversity: Identifying dissimilarities of spatial or temporal dissimilarity structures

July 2024

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132 Reads

Elucidating biodiversity patterns and their background processes is critical in biodiversity science. Dissimilarity, which is calculated based on multivariate biological quantities, is a major component of biodiversity. As spatial and temporal biodiversity information availability increases, the scope of dissimilarity studies has been expanded to cover various levels and types of spatiotemporal biodiversity facets (e.g. gene, community and ecosystem function), and diverse pairwise dissimilarity indices have been developed. However, further development of the dissimilarity concept is required in comparative studies on spatiotemporal structures of biodiversity compositional patterns, such as those exploring commonalities of biogeographical boundaries among taxa, compared to the conventional ones to consider higher dimensions of dissimilarity: dissimilarity of dissimilarity structures. This study proposes a novel and general concept, higher‐order dissimilarity (HOD), for quantitatively evaluating the dissimilarities of spatial or temporal dissimilarity structures among different datasets, proposes specific implementations of HOD as operational indices, and illustrates the potential resolution of scientific and practical questions through HOD. We further demonstrate the advantages of the HOD concept by applying it to actual patterns, such as long‐term and/or large‐spatial hypothetical monitoring datasets. Our conceptual framework on HOD extends the existing framework of biodiversity science and is versatile, with many potential applications in acquiring more valuable information from ever‐increasing biodiversity data.



Kernel density estimation of allele frequency including undetected alleles

April 2024

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3 Reads

Whereas undetected species contribute to estimation of species diversity, undetected alleles have not been used to estimated genetic diversity. Although random sampling guarantees unbiased estimation of allele frequency and genetic diversity measures, using undetected alleles may provide biased but more precise estimators useful for conservation. We newly devised kernel density estimation (KDE) for allele frequency including undetected alleles and tested it in estimation of allele frequency and nucleotide diversity using population generated by coalescent simulation as well as well as real population data. Contrary to expectations, nucleotide diversity estimated by KDE had worse bias and accuracy. Allele frequency estimated by KDE was also worse except when the sample size was small. These might be due to finity of population and/or the curse of dimensionality. In conclusion, KDE of allele frequency does not contribute to genetic diversity estimation.


Wait to promote high sighting rates of wildlife in tourism: Evidence from a Wildlife Disturbance Experiment

March 2024

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76 Reads

Ecotourism is often viewed as a mutually beneficial solution for both people and nature; however, unregulated wildlife tourism can inadvertently harm the wildlife. To enhance management practices, we conducted a study on rabbit tourism involving Amami rabbits (Pentalagus furnessi) which can be sighted by car driving at a Natural World Heritage Site in Japan. Because the sighting rate of wildlife under different car schedules and in varying density scenarios remains unknown, our study employed wildlife disturbance experiments and model simulation to estimate the recovery rate of rabbits after being flushed by tourists in different density and car schedule scenarios. Our analysis revealed that implementing a 20-minute time lag for the following car resulted in a 90% recovery rate for Amami rabbits. Additionally, adhering to a regular car schedule provided an increase in sighting rates of the rabbit compared to random and normal schedules by approximately 1.85 and 2.4 times, respectively, under optimal conditions (maximum density and 50 cars). Finally, we evaluated the profitability of the tourism industry under different densities of rabbits and rates of the money-back guarantee. Though introducing more cars appears to generate greater profits, it may simultaneously lead to a decrease in the rabbit sighting rate and an increased likelihood of activating the money-back guarantee. In conclusion, our findings clearly showed that considering both animal behavior in response to humans and human interest (i.e., MBG) in developing a tourism management system can achieve a simultaneous resolution of profitability and reduction in the impact of overutilization.


Citations (25)


... 2024; Puica and Benth, 2023) [115,116] could potentially address these interactions, the lack of spatially detailed water quality data near the study site made such modeling technically infeasible at this stage. ...

Reference:

Stochastic volatility model with long memory for water quantity-quality dynamics
Spatiotemporal smoothing of water quality in a complex riverine system with physical barriers
  • Citing Article
  • July 2024

The Science of The Total Environment

... With a single phylogenetic signal parameter over all covariate effects, the form of the covariance function for Σ allows inversion by repeatedly applying the Sherman-Morrison formula for computationally cheap rank-one updates to the inverse of C, but this still has O(m 2 ) computational complexity, so further improvement is warranted. Recently, (Matsuba et al. 2024) employed a nearest neighbor Gaussian Process (NNGP) approximation to quickly and accurately retrieve the inverse of the phylogenetic matrix, although with a different model parameterisation than that we use here. We also adopt NNGPs as our fourth and final approximation here. ...

Scalable phylogenetic Gaussian process models improve the detectability of environmental signals on local extinctions for many Red List species
  • Citing Article
  • February 2024

... In Hyogo Prefecture, Japan, »50% of female bears captured were accompanied by cubs in 2004 and 2006 (Hyogo Prefecture 2009). Additionally, it has been reported that more than half of the female bears reproduce biennially in the Echigo-Mikuni population in Japan (Tochigi et al. 2023). It is likely that the RAI values for females with unweaned offspring in our study were lower than expected, based on the birth rates observed in the Hyogo and Echigo-Mikuni populations. ...

Demographic Parameters of Asian Black Bears in Central Japan
  • Citing Article
  • July 2023

Mammal Study

... Therefore, the ease of acquiring species-identification skills varies from species to species (Louw and Sanford-Dolly, 2024;Starr et al., 2014), making some learning methods more effective than others. A study that introduced an algorithm focusing on training species that users find difficult to remember reported that the algorithm increased the correct answer rate of the participants, but it was not as effective as the conventional method (Ogawa et al., 2023). Although algorithms that automatically personalize and/or optimize quiz items are expected to make the training more effective, these algorithms have not been adequately investigated (Ogawa et al., 2023). ...

Quiz-style online training tool helps to learn birdsong identification and support citizen science

... In Idaho, the state requires wolves to be checked in after they are harvested, at which time Idaho Department of Fish and Game (IDFG) personnel can record the sex of the individual and collect samples to determine the age and obtain a genetic sample for individual identification. Using such samples and associated data multilocus genotypes can be used to reconstruct pedigrees and estimate relatedness among individuals, which can then be used to investigate mating systems and relationships among harvested individuals (Stenglein et al. 2011, Clendenin et al. 2020, Shimozuru et al. 2022. Such genetic approaches can give biologists insights into whether who dies in a group and when matters for group persistence and reproductive success (Ausband et al. 2017b). ...

Estimation of breeding population size using DNA‐based pedigree reconstruction in brown bears

... Although we found a slightly increasing trend in bird diversity, habitat heterogeneity of the Satoyama landscape has been lost due to human depopulation, and associated land abandonment can be linked to the reduction of many butterfly species in Japan (Sugimoto et al. 2022). Our findings suggest that if further depopulation, abandonment and the loss of open habitats such as paddy fields and water bodies occur in the future, bird diversity may decline. ...

Positive and negative effects of land abandonment on butterfly communities revealed by a hierarchical sampling design across climatic regions

... This event is characterized by a higher emergence of piglets during the January-February period in years following mast events, indicating a longer reproductive season. Another study [7] in wildlife biology identified digging marks in a specific area as a key indicator of wild boar abundance in that place. Besala et al. ...

Effectiveness of signs of activity as relative abundance indices for wild boar

... Many cervid species find human communities to be a suitable habitat and, in some cases, seek out these habitats, increasing human-cervid interactions. Worldwide, expanding cervid populations impact ecosystem dynamics [21], browse on economically important crops [164], increase risks of vehicle collisions [165], and contribute to a risk of disease spread among wildlife, humans, and livestock. For example, sika deer (Cervus nippon) contribute to more than 50 million dollars in agricultural damage every year in Japan [164], and, in the United States, millions of cervid-vehicle collisions occur annually, posing a threat to wildlife and human health, as well as causing economic damage for drivers [165,166]. ...

Occurrence patterns of crop-foraging sika deer distribution in an agriculture–forest landscape revealed by nitrogen stable isotopes

... The datasets, program codes and model predictions shown in figure 4 and electronic supplementary material, figures S2, S3 and S4 are available from the Dryad Digital Repository (https://doi.org/10.5061/dryad.6hdr7sr0z [73]), except specific records of endangered species. ...

Hierarchical trait-based model reveals positive and negative effects of land abandonment on butterfly communities across climatic regions in Japan

... The management and control of these weeds are crucial for maintaining the productivity and profitability of canola crops (Asaduzzaman et al. 2020). Wild oats (Avena fatua L.), belonging to the Gramineae family, is one of the most dominant weeds in canola and is currently found in approximately 50 countries globally (Matsuhashi et al. 2021). Some studies have shown that A. fatua can significantly reduce crop yield, highlighting their severe impact on agricultural productivity . ...

Estimations and projections of Avena fatua dynamics under multiple management scenarios in crop fields using simplified longitudinal monitoring