Search bioRxiv⌕ Search

Biology subjects

Doi, H.

Publications and source records attributed to Doi, H..

At least 19 recordsLinked to original sources

Time-series foundation modeling enables accurate lake ecosystem forecasting

Accurate ecological forecasting is increasingly essential for understanding and managing ecosystem responses to climate variability and anthropogenic pressures; however, prediction remains difficult in lakes because key biological variables, such as phytoplankton biomass, exhibit nonlinear dynamics, observational noise, data sparsity, and non-stationarity. This study aimed to test whether large pre-trained time-series foundation models can improve forecasts of lake phytoplankton dynamics, focusing on chlorophyll-a (Chl.a) and water-quality variables in two ecologically contrasting Japanese lakes, the deep-stratified Lake Biwa and the shallow nutrient-rich Lake Kasumigaura. Using extensive monthly monitoring records spanning up to 30 years, we benchmarked two time-series foundation models - Transformer-based Chronos-T5 and probabilistic Lag-Llama - against 15 statistical (AR, ARIMA, SARIMA, Prophet), machine learning (Random Forest, XGBoost, KNN, SVR), and deep learning (LSTM, CNN, TCN, and SSA-hybrid) approaches. Chronos-T5 achieved superior reproduction accuracy and stability across diverse environmental variables and outperformed all other tested models. This performance stemmed from its ability to capture long-term dependencies and complex temporal patterns through large-scale pre-training. We further identified an optimal training window of approximately 14 years, balancing data sufficiency with regime stability, beyond which model accuracy diminished owing to ecological regime shifts. Our findings highlight the transformative potential of time-series foundation models for ecological forecasting, providing a scalable, data-driven framework that can underpin robust early warning systems and adaptive management strategies for aquatic ecosystems worldwide.

ecology↗

Improving sensitivity in environmental DNA measurement by reconcentrating DNA extracts

Environmental DNA (eDNA) methodology is widely applied in the biomonitoring of organisms, but it requires the target DNA to be detected in a simple, stable, and highly sensitive manner. Detection sensitivity of eDNA measurement becomes particularly critical when monitoring species present at low abundance. In this study, we aimed to improve the detection sensitivity through a method of DNA-extract reconcentration. This approach involves reconcentrating eDNA samples that were originally extracted using the widely adopted DNeasy Blood and Tissue Kit (Qiagen), utilizing the same kits reagents, and does not require any additional equipment or reagents. We evaluated the ability of this DNA reconcentration method using field samples including river, lake and costal marine habitats. Evaluation of this DNA reconcentration method showed that when ten conventionally extracted samples were pooled, the DNA concentration increased by approximately sevenfold, as confirmed by DNA quantification and quantitative PCR analyses, demonstrating enhanced detection sensitivity.

ecology↗

Effects of Host-Dependent Niches and Biotic Constraints on Climate Change Driven Range Shifts in Anemonefish

We investigated how obligate mutualisms constrain species distributions under climate change, challenging the assumption that biotic interactions are negligible at macro-scales. By integrating host sea anemone distributions into Species Distribution Models for 17 anemonefish species, we found that host availability is a primary determinant of the realised niche, especially for specialists. Under future warming (SSP5-8.5), host immobility creates a biotic constraint, causing fish ranges to lag significantly behind their climatic potential. This mismatch generates over 3.2 million km2 of climatically suitable but ecologically inaccessible ocean. Furthermore, specialist anemonefish species with the narrowest niches face the highest climate velocities while being constrained to the most dispersal-limited hosts. These findings indicate that climate-only assessments underestimate extinction risk. Conservation should shift to a host-first management strategy to prevent the collapse of these mutualisms. Scientific Significance StatementClimate change assessments often assume species can freely track their preferred temperatures, ignoring the critical species they rely on for survival. We demonstrate that for obligate mutualists like anemonefish, the future is defined not just by where they can swim, but by where their host sea anemones can persist. Our models reveal that millions of square kilometers of ocean will become climatically perfect for fish but devoid of the hosts they need to survive. This mechanism of range loss disproportionately threatens specialist species. Our findings highlight the need to prioritise the conservation of immobile partner species, as their failure to migrate effectively traps their mobile symbionts in degrading environments.

ecology↗

Peculiar Pigment Pattern and Population Profile of a Poisonous Pufferfish

Pufferfish are well-known for their toxicity, yet they also exhibit a remarkable diversity of pigment patterns. Mushifugu (Takifugu exascurus) is a pufferfish endemic to Japans coastal waters and is characterized by conspicuous labyrinthine patterns. Despite being recorded along both the Sea of Japan and the Pacific coasts, it has a limited distribution and is infrequently observed. Aside from its unique body pattern, mushifugu shows little to no morphological differences from other Takifugu species, often leading to speculation that it may be an interspecific hybrid. In addition, previous theoretical and empirical studies have shown that complex camouflage-like labyrinthine patterns can emerge through the pattern blending caused by hybridization between spotted species, providing support for this possibility. Here, we investigate the phylogenetic origin of mushifugu and its distinctive pattern through population structure analysis and demographic inference in comparison with its closest spotted relative, komonfugu (T. flavipterus). Mitochondrial DNA (mtDNA) analysis revealed two regional haplogroups within mushifugu--one in the Sea of Japan (SJ) and the other in the Pacific Ocean (PO). In the haplotype network, the SJ haplogroup formed a distinct cluster, whereas the PO haplogroup appeared as its own cluster connected to the komonfugu haplogroup. By contrast, genome-wide SNP analyses indicated limited structure between the SJ and PO mushifugu populations, while clearly separating mushifugu from komonfugu. Coalescent-based demographic inference suggested that the two species diverged following a bottleneck event in the early Pleistocene. These results confirm that mushifugu is a distinct species rather than a recent interspecific hybrid. Nevertheless, evidence of introgression was detected in both mitochondrial and nuclear genomes, suggesting multiple episodes of past hybridization between mushifugu and komonfugu, highlighting the potentially complex evolutionary processes shaping Takifugu species and their pigment patterns.

evolutionary biology↗

Evolutionary stasis and homogeneous selection structure microbial communities in the deep subseafloor sedimentary biosphere

The subseafloor biosphere, one of the Earths largest and most stable microbial habitats, mainly consists of energy-limited sediments where microbial life persists over geological timescales. However, the mechanisms governing microbial community assembly and evolution under condition of extreme energy limitation remains unclear. Here, we analysed a 296 m sediment core off the Shimokita Peninsula using amplicon sequencing, metagenomics, and genome-resolved analyses from 31 depth intervals spanning [~]480 kyr. The microbial community composition was governed primarily by homogeneous selection, consistent with persistent environmental uniformity during burial. Genome-resolved analyses of 224 high-quality metagenome-assembled genomes revealed highy conserved gene repertoires and uniformly low ratios of non-synonymous-to-synonymous substitutions, suggesting strong purifying selection with minimal genomic changes over this timescale. Our results indicate that evolutionary stasis is a pervasive feature of microbial life in deep subseafloor sediments, and propose a conceptual framework linking long-term environmental stability to genomic preservation in the Earths most persistent biosphere.

ecology↗

Revealing Long-Term Multi-Factor Climate Impacts on Antarctic Phytoplankton: A Trend-Based Approach Using STL and Piecewise SEM

Climate change imposes multiple interacting stressors on ocean ecosystems. The Southern Ocean is among the regions where these impacts are particularly pronounced. Phytoplankton, which perform the bulk of primary production, both maintain the Antarctic marine food web and contribute to the role of the Southern Ocean as the largest oceanic sink for atmospheric CO2. Previous observational and modeling studies have revealed certain drivers-phytoplankton relationships and highlighted the important confounding factors. In this study, we quantified how climate and environmental drivers interact and influence phytoplankton biomass over a 20-year period, across the entire Southern Ocean, within a multi-factor framework. Specifically, we examined the relationships among atmospheric CO2, surface water pH, sea ice concentration, sea surface temperature, mixed layer depth, dissolved iron concentration, and chlorophyll a concentration. To perform this analysis, we introduced and applied two novel methodological approaches. Firstly, to address seasonal autocorrelation, we combined seasonal trend decomposition using LOESS (STL) with piecewise structural equation modeling (SEM). This approach allowed for robust estimation of long-term driver magnitudes and causal pathways, even in the presence of limited sample sizes and complex data structures. Secondly, given the highly interconnected nature of environmental drivers, we employed a data-driven SEM approach to objectively identify causal structures and avoid biases associated with a priori pathway selection. Our results show a clear signal of ocean acidification driven by increasing CO2, iron limitation of phytoplankton biomass during spring, and seasonal differences in both the magnitude and structure of the causal pathways, demonstrating the dynamic nature of seasonal processes in the Southern Ocean. This study presents the first Southern Ocean-wide, multi-factor assessment of climate and environmental impacts on phytoplankton biomass over a two-decade period. It introduces a methodological framework mitigates seasonal autocorrelation to accurately capture long-term seasonal trends, and demonstrates the utility of data-driven causal discovery in resolving complex ecological interactions.

ecology↗

Environmental DNA Surveys of Invertebrate Community on Forest Canopies Using Rainwater Analysis

Forest canopies, known for their high biodiversity, are essential for understanding forest ecosystems. Traditional methods for canopy surveys, such as tree climbing and canopy walkways, face challenges related to safety, cost, and time constraints. Environmental DNA (eDNA) analysis, which involves examining DNA from environmental samples, offers a promising alternative for these surveys. This study investigates the feasibility of using rainwater to collect eDNA from forest canopies, utilizing rains natural ability to wash away DNA from hard-to-reach areas. By comparing DNA analysis results from rainwater with conventional records obtained through visual and capture surveys, this research aims to validate the effectiveness and reliability of this method. Preliminary findings suggest that eDNA analysis from rainwater could provide an efficient approach to canopy biodiversity surveys, though further validation is required. This study marks an important first step towards developing eDNA analysis as a complementary tool for forest canopy research.

ecology↗

Body size is a better predictor of intra- than interspecific variation of animal stoichiometry across realms

Animal stoichiometry affects fundamental processes ranging from organismal physiology to global element cycles. However, it is unknown whether animal stoichiometry follows predictable scaling relationships with body mass and whether adaptation to life on land or water constrains patterns of elemental allocation. To test both interspecific and intraspecific body-size scaling relationships of the nitrogen (N), phosphorus (P), and N:P content of animals, we used a subset of the StoichLife database encompassing 9,933 individual animals (vertebrates and invertebrates) belonging to 1,543 species spanning 10 orders of magnitude of body size from terrestrial, freshwater, and marine realms. Across species, body mass did not explain much variation in %N and %P composition, although the %P of invertebrates decreased with size. The effects of body size on species elemental content were small in comparison to the effects of taxonomy. Body size was a better predictor of intraspecific than interspecific elemental patterns. Between 42 to 45% in intraspecific stoichiometric variation was explained by body size for 27% of vertebrate species and 35% of invertebrate species. Further, differences between organisms inhabiting aquatic and terrestrial realms were observed only in invertebrate interspecific %N, suggesting that the realm does not play an important role in determining elemental allocation of animals. Based on our analysis of the most comprehensive animal stoichiometry database, we conclude that (i) both body size and realm are relatively weak predictors of animal stoichiometry across taxa, and (ii) body size is a good predictor of intraspecific variation in animal elemental content, which is consistent with tissue-scaling relationships that hold broadly across large groups of animals. This research reveals a lack of general scaling patterns in the elemental content across animals and instead points to a large variation in scaling relationships within and among lineages.

ecology↗

Chemogenetic activation of target neurons expressing insect Ionotropic Receptors in the mammalian central nervous system by systemic administration of ligand precursors

The IR-mediated neuronal activation (IRNA) technology allows stimulation of neurons in the brain that heterologously-express members of the insect chemosensory IR repertoire in response to their cognate ligands. In the current protocol, a ligand against the complex consisting of IR84a and IR8a subunits, phenylacetic acid (PhAc), is locally injected into a brain region, because of a low efficiency of PhAc for the delivery into the brain across the blood-brain barrier. To circumvent this invasive injection, here we developed a strategy for activation of target neurons in the brain through peripheral administration with a precursor of PhAc, methyl ester of PhAc (PhAcM), which is efficiently transferred into the brain and converted to the mature ligand by endogenous esterase activities. Peripheral administration of with PhAcM activated IR84a/IR8a-expressing neurons in the locus coeruleus of mice and increased the release of neurotransmitters in their nerve terminal regions. (S)-2-phenylpropionic acid ((S)-PhPr) was newly identified as a ligand for IR84a/IR8a, and peripheral administration with the methyl ester of PhPr with the S-configuration [(S)-PhPrM] caused similar effects on the target neurons. In addition, cell-type specific expression of IR84a/IR8a complex in the striatum of rats was unilaterally induced with a viral vector based on the Cre-loxP system. Peripheral administration with PhAcM or (S)-PhPrM stimulated the neurotransmitter release in the ipsilateral terminal regions of the vector-injected striatum, and PhAcM administration resulted in rotational behavior. Finally, we demonstrated that the metabolites of the peripherally administered-radiolabeled (S)-PhPrM accumulated in the IR84a/IR8a-expressing region in the striatum of the vector-injected rats. These results demonstrate that the systemic IRNA technique provides a powerful strategy for remote manipulation of diverse types of target neurons in the mammalian central nervous system.

neuroscience↗

Sedimentary DNA can reveal past pelagic copepod population dynamics

O_LICopepods play a key trophic role as secondary producers, transferring primary production to higher trophic levels such as fish. Copepod production contributes significantly to successful fish recruitment. Despite their importance, knowledge of copepod dynamics over several decades remains limited due to the lack of long-term data series with adequate sampling and analysis. However, an understanding of long-term copepod dynamics is urgently required to strive toward better management for sustainable aquatic ecosystems and fish recruitment. C_LIO_LISedimentary DNA (sedDNA) has been developing as a useful tool for reconstructing past plankton dynamics. This study evaluates whether sedDNA targeting the pelagic copepod, Eodiaptomus japonicus, in Lake Biwa (Japan) can be an effective tool for elucidating its past population dynamics. C_LIO_LIWe applied a quantitative polymerase chain reaction method targeting the mitochondrial cytochrome c oxidase subunit I gene on two sediment cores and compared the detected sedDNA concentrations with the unique long-term dataset of demographic traits, biomass, specific growth rate, production, subitaneous eggs, and resting eggs of E. japonicus. C_LIO_LIThe sedDNA concentration of E. japonicus recovered from sediment layers correlated significantly with in situ production, biomass, and production of immediately hatching eggs but not with resting eggs or specific growth rate. Our study provides evidence for the effective use of sedDNA as a tracking tool for assessing past copepod production dynamics. C_LI

ecology↗

Fish environmental DNA in lake sediment overcomes the gap of reconstructing past fauna in lake ecosystems

O_LIUnderwater sediments are a natural archive of biological information. Reconstruction of past fauna has been conducted for various taxonomic groups using morphological remains and DNA derived from these remains. However, information on past occurrences of fish species, the top predator of lake ecosystems, could have been reproduced only in exceptional environments, and past quantitative information on fish, particularly in lake ecosystems, has been a knowledge gap in reconstructing past fauna. Tracking the quantitative fluctuations of fish is essential for reconstructing multiple trophic levels of organisms in lake ecosystems. C_LIO_LITo acquire past quantitative fish information from lake sediments, we collected approximately 30 cm-length of underwater sediments in Lake Biwa. We extracted sedimentary environmental DNA (eDNA) and measured temporal fluctuations in the eDNA concentration of the native and fishery target species Plecoglossus altivelis and Gymnogobius isaza. For P. altivelis, we examined the possibility of tracking quantitative fluctuations by comparing sedimentary eDNA with recorded catch per unit effort (CPUE). C_LIO_LIThe chronology of the sediments allowed us to obtain information on sediments collected in Lake Biwa over the past 100 years. The deepest depths at which sedimentary eDNA was detected were 30 and 13 cm for P. altivelis and G. isaza from the surface, corresponding to approximately 100 and 30 years ago, respectively. In the comparison of sedimentary eDNA concentrations and biomass, we found a significant correlation between the CPUE of P. altivelis and its sedimentary eDNA concentration adjusted to compensate for DNA degradation. Sedimentary eDNA fluctuations were observed in P. altivelis, possibly reflecting the abundance fluctuation due to variations in the main food resources of zooplankton. C_LIO_LIOur findings provide essential pieces for the reconstruction of past fauna of lake ecosystems. The addition of quantitative information on fish species will reach a new phase, for instance, by investigating population shifts or biological interactions in the reconstruction of past fauna in lake ecosystems. C_LI

ecology↗

Filtration extraction method using microfluidic channel for measuring environmental DNA

The environmental DNA (eDNA) method, which is widely applied for biomonitoring, is limited to laboratory analysis and processing. In this study, we developed a filtration/extraction component using a microfluidic channel, Biryu-Chip (BC), and a filtration/extraction method, BC method, to minimize the volume of the sample necessary for DNA extraction and subsequent PCR amplification. We tested the performance of the BC method and compared it with the Sterivex filtration/extraction method using aquarium and river water samples. We observed that using the BC method, the same concentration of the extracted DNA was obtained with 1/20-1/40 of the filtration volume of the Sterivex method, suggesting that the BC method can be widely used for eDNA measurement. In addition, we could perform on-site measurements of eDNA within 30 min using a mobile PCR device. Using the BC method, filtration and extraction could be performed easily and quickly. The PCR results obtained by the BC method were similar to those obtained by the Sterivex method. The BC method required fewer steps and therefore, the risk of DNA contamination could be reduced. When combined with a mobile PCR, the BC method can be applied to easily detect eDNA within 30 min from a few 10 mL of the water sample, even on-site.

ecology↗

Influence of DNA extraction kits on the fungal DNA metabarcoding for freshwater environmental DNA

BackgroundEnvironmental DNA (eDNA) metabarcoding is a common technique for efficient biodiversity monitoring, especially of microbes. Recently, the usefulness of aquatic eDNA in monitoring the diversity of both terrestrial and aquatic fungi has been suggested. In eDNA studies, different experimental factors, such as DNA extraction kits or methods, can affect the subsequent analyses and the results of DNA metabarcoding. However, few methodological studies have been carried out on eDNA of fungi, and little is known about how experimental procedures can affect the results of biodiversity analysis. In this study, we focused on the effect of DNA extraction method on fungal DNA metabarcoding using freshwater samples obtained from rivers and lakes. MethodsDNA was extracted from freshwater samples using the DNeasy PowerSoil kit, which is mainly used to extract microbial DNA from soil, and the DNeasy Blood & Tissue kit, which is commonly used for eDNA studies on animals. We then compared PCR inhibition and fungal DNA metabarcoding results; i.e., operational taxonomic unit (OTU) number and composition of the extracted samples. ResultsNo PCR inhibition was detected in any of the samples, and no significant differences in the number of OTUs and OTU compositions were detected between the samples processed using different kits. These results indicate that both DNA extraction kits may provide similar diversity results for the river and lake samples evaluated in this study. Therefore, it may be possible to evaluate the diversity of fungi using a unified experimental method, even with samples obtained for diversity studies on other taxa such as those of animals.

microbiology↗

Effect of salinity and water dilution on environmental DNA degradation in freshwater environments

Environmental DNA (eDNA) analysis methods have been developed to detect the distribution and abundance/biomass of organisms in various environments. eDNA generally degrades quickly, thus the study of eDNA degradation is critical for eDNA evaluation. However, there have only been a few studies of eDNA degradation experiments in which the salt concentration and water dilution were controlled. In this study, the effects of degradation were experimentally evaluated by controlling the salinity and water dilution of pond water. An experiment was conducted to evaluate the effects of salinity and dilution on eDNA detection with fragmental eDNA and free cell-derived eDNA using pond water, diluted pond water, and saline pond water. We quantified the eDNA copies of free cells, fragmental DNA, and the eDNA from Cyprinus carpio. In both the diluted and saline pond water, we found that the degradation rate of eDNA was much slower than that in pond water. Furthermore, the DNA concentration did not exponentially decrease in both the saline purified water and purified water samples. For the lower degradation rate in salt water, we interpreted that salts may affect DNA degradation factors such as microbe compositions and activities. The effect of salinity and dilution on eDNA detection provides fundamental information about the degradation process of eDNA, which is essential to understand the behavior of eDNA in natural environments.

evolutionary biology↗

Application of augmented topic model to predicting biomarkers and therapeutic targets using multiple human disease-omics datasets

Human diseases are characterized by multiple features such as their pathophysiological, molecular, and genetic changes. The rapid expansion of such multi-modal disease-omics space provides an opportunity to re-classify diverse human diseases and uncover their latent molecular similarities, which could be exploited to repurpose a therapeutic-target for one disease to another. Herein, we probe this underexplored space by soft-clustering 6,955 human diseases by multi-modal generative topic-modeling. Focusing on chronic kidney disease and myocardial infarction, two most life-threatening diseases, unveiled are their previously underrecognized molecular similarities to neoplasia and mental/neurological-disorders, and 69 repurposable therapeutic-targets for these diseases. Using an edit-distance based pathway-classifier, we also find molecular pathways by which these targets could elicit their clinical effects. Importantly, for the 17 targets, the evidence for their therapeutic usefulness is retrospectively found in the pre-clinical and clinical space, illustrating the effectiveness of the method, and suggesting its broader applications across diverse human diseases.

bioinformatics↗

Evaluation of seasonal dynamics of fungal DNA assemblages in a flow-regulated stream in a restored forest using eDNA metabarcoding

Investigation of seasonal variation in fungal communities is essential for understanding biodiversity and ecosystem functions. However, the conventional sampling method, with substrate removal and high spatial heterogeneity of community composition, makes surveying the seasonality of fungal communities challenging. Recently, water environmental DNA (eDNA) analysis has been explored for its utility in biodiversity surveys. In this study, we assessed whether the seasonality of fungal communities can be detected by monitoring eDNA in a forest stream. We conducted monthly water sampling in a forest stream over two years and used DNA metabarcoding to identify fungal eDNA. The stream water contained DNA from functionally diverse aquatic and terrestrial fungi, such as plant decomposers, parasites, and mutualists. The variation in the fungal assemblage showed a regular annual periodicity, meaning that the assemblages in a given season were similar, irrespective of the year or sampling. Furthermore, the strength of the annual periodicity varied among functional groups. Our results suggest that forest streams may act as a "trap" for terrestrial fungal DNA derived from different habitats, allowing the analysis of fungal DNA in stream water to provide information about the temporal variation in fungal communities in both the aquatic and the surrounding terrestrial ecosystems.

ecology↗

Environmental DNA degradation simulation from water temperature and DNA fragment length: A meta-analysis approach

Environmental DNA (eDNA) analysis can detect aquatic organisms, including rare and endangered species, in a variety of habitats. The degradation of eDNA concentration is important to investigate their distribution and has also been experimentally evaluated. It is important to integrate these data to synthesize eDNA degradation in various environments. We collected the eDNA degradation rates and related factors, especially water temperature and fragment lengths of the measured DNA from 28 studies. Our results suggest that water temperature and fragment length are significantly related to the eDNA degradation rate. From the 95% quantile model simulation, we predicted the maximum eDNA degradation rate in various combinations of water temperature and fragment length. Predicting eDNA degradation could be important for evaluating species distribution and inducing innovation of eDNA methods, especially for rare and endangered species with lower DNA concentrations.

ecology↗

On-site eDNA detection of species using ultra-rapid mobile PCR

Molecular methods, including environmental DNA (eDNA) methods, provide essential information for biological and conservation sciences. Molecular measurements are often performed in the laboratory, which limits their scope, especially for rapid on-site analysis. eDNA methods for species detection provide essential information for the management and conservation of species and communities in various environments. We developed an innovative novel method for on-site eDNA measurements using an ultra-rapid mobile PCR platform. We tested the ability of our method to detect the distribution of silver carp, Hypophthalmichthys molitrix, an invasive fish in Japanese rivers and lakes. Our method reduced the measurement time to 30 min and provided high detectability of aquatic organisms compared to the national observation surveys using multiple fishing nets and laboratory extraction/detection using a benchtop qPCR platform. Our on-site eDNA method can be immediately applied to various taxa and environments.

ecology↗