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Miki, T.

Publications and source records attributed to Miki, T..

8 recordsLinked to original sources

Microscale nonrandomness revisited: An overlooked predictor of ecological change

Abrupt ecological transitions have driven the development of early warning signal metrics that track how ecological systems respond as external conditions gradually change and systems approach transitions between states. However, their generality and applicability remain uncertain, particularly for short-term ecological dynamics that can occur without directional external change. To address this gap, we propose a general framework based on the hypothesis that microscale nonrandomness, quantified from frequency distributions or spatial patterns, predicts subsequent short-term rates of change in populations and interactions, as well as current macroscale ecosystem states. We applied the framework to four datasets: time series from an incubation experiment of phytoplankton-parasitic chytrid interactions; spatiotemporal field observations of leaf beetles on willow trees and aphids in a crop system; and spatial snapshot data linking soil surface characteristics with aboveground and soil ecosystem properties in a forest vegetations-soil system. We quantified microscale nonrandomness using Morisita I_{delta} from frequency distributions and Moran's I and SADIE from spatial patterns. Across all systems, models incorporating microscale nonrandomness metrics consistently showed greater cross-validated predictive performance than those based on macroscale variables or spatial averages alone. Although their relative performance varied among systems, frequency-based metrics performed as well as or better than spatially explicit metrics in some cases. The consistent improvement across contrasting systems supports the broad applicability of this framework, including under limited data conditions. This framework broadens ecological forecasting to short-term, continuous dynamics beyond those associated with directional environmental change.

ecology↗

Hybrid eTFCE-GRF: Exact Cluster-Size Retrieval with Analytical p-Values for Voxel-Based Morphometry

Threshold-free cluster enhancement (TFCE) improves sensitivity in voxel-wise neuroimaging inference by integrating cluster extent across all thresholds, but its reliance on permutation testing makes it prohibitively slow for large datasets. Probabilistic TFCE (pTFCE) replaces permutations with analytical Gaussian random field (GRF) p-values, which reduces runtime by more than an order of magnitude, yet relies on a fixed threshold grid that introduces discretisation error. Exact TFCE (eTFCE) eliminates this discretisation by computing the integral exactly via a union-find data structure, but still requires permutations for inference. We propose a hybrid method that combines eTFCEs union-find data structure for exact cluster-size retrieval with pTFCEs analytical GRF inference. The union-find builds the full cluster hierarchy in a single pass over sorted voxels and enables exact cluster-size queries at any threshold in near-constant time; GRF theory then converts these sizes into analytical p-values without permutations. We validate the method through a six-experiment Monte Carlo study on synthetic phantoms (643, 80 subjects): null family-wise error rate is controlled at the nominal level (0/200 rejections, 95% CI [0.0%, 1.9%]); power curves match baseline pTFCE (Dice [≥] 0.999 at sufficient signal); smoothness estimation error is below 1%; and cross-variant concordance exceeds r = 0.99. On real brain data from UK Biobank (N = 500, within-vendor) and IXI (N = 563, cross-vendor), the method detects biologically plausible scanner, age, and sex effects; on IXI, significance maps form strict subsets of the reference R pTFCE output, which supports conservative family-wise error control. Both methods are implemented in pytfce, a pure-Python package with no R or FSL dependencies, available on PyPI. The baseline reimplementation completes whole-brain voxel-based morphometry in [~] 5 s (75 x faster than R pTFCE), while the hybrid variant completes in [~] 85 s (4.6 x faster) with the advantage of exact cluster-size retrieval; both are more than three orders of magnitude faster than permutation-based TFCE. HighlightsO_LIHybrid eTFCE-GRF: exact cluster-size retrieval with analytical inference C_LIO_LIFWER controlled at nominal level in Monte Carlo validation C_LIO_LIpytfce package 4.6 x (hybrid) to 75 x (baseline) faster than R pTFCE C_LIO_LIValidated on UK Biobank (N = 500) and IXI (N = 563) C_LIO_LIOpen-source Python package: pip install pytfce C_LI

neuroscience↗

Advancing marker-gene-based methods for prokaryote-mediated multifunctional redundancy: exploring random and nonrandom extinctions in a watershed

Multifunctional redundancy, the extent of loss in multiple ecosystem functions with decreasing biodiversity, stands as a crucial index for evaluating ecosystem resilience to environmental changes. We aimed to refine a marker-gene-based methodology for quantifying multifunctional redundancy in prokaryotic communities. Using PICRUSt2, we predicted KEGG orthologs (KOs) for each Amplicon Sequence Variant (ASV), assessed community-wide KO richness, and validated predictions against experimentally quantified phenotypic multifunctionality. Additionally, we introduced a refined regression on ASV richness-KO richness curves, providing a reliable estimate of the power-law exponent within computational time constraints, serving as the multifunctional redundancy index. Incorporating various non-random extinction scenarios alongside a random one allowed us to quantify estimate variations between scenarios, providing conservative estimates of multifunctional redundancy. Applied to Lake Biwa and four of its inlet rivers, the refined methodology unveiled spatio-temporal variations in multifunctional redundancy. Our analysis demonstrated lower redundancy in Lake Biwa compared to rivers, aiding in prioritizing conservation targets and inferring distinct community assembly processes. Future directions include a deeper exploration of KO composition information for detailed multifunctionality quantification and the refinement of extinction scenarios. This study demonstrates the promising integration of bioinformatic functional prediction and modeling biodiversity loss, offering a valuable tool for effective ecosystem management.

ecology↗

Non-destructive collection and metabarcoding of arthropod environmental DNA remained on a terrestrial plant

For the conservation and community ecology of arthropods and pest controls on terrestrial plants, survey of arthropods is a crucial step. However, efficient surveys are hindered by challenges in collecting small arthropods, and identifying the species. Environmental DNA (eDNA)-based techniques, such as eDNA metabarcording, help overcome these difficulties in aquatic systems. To apply eDNA metabarcording to terrestrial arthropods, we developed a non-destructive eDNA collection method. In this method, termed "plant flow collection," we spray distilled or tap water, or use rainfall, which eventually flows over the surface of the plant, and is collected in a container that is set at the plant base. DNA is extracted from the filtered water samples and a DNA barcode region, such as cytochrome c oxidase subunit I (COI) gene, of the extracted DNA is amplified and sequenced using a high-throughput sequencer. We identified more than 38 taxonomic groups of arthropods at the family level, of which 7 were visually observed or artificially introduced species, whereas the other 31 groups of arthropods, including 18 species, were not observed in the visual survey. Put together, these results show that the developed method is effective for detecting the presence of arthropods in plants.

ecology↗

Comparative whole-genome approach to identify traits underlying microbial interactions

Microbial interactions shape the structure and function of microbial communities with profound consequences for biogeochemical cycles and ecosystem health. Yet, most interaction mechanisms are studied only in model systems and their prevalence is unknown. To systematically explore the functional and interaction potential of sequenced marine bacteria, we developed a new trait-based approach, and applied it to 473 complete genomes (248 genera), representing a significant fraction of marine microbial communities. We identified genome functional clusters (GFCs) which condense bacterial diversity into groups with potentially common ecology and life history. Most GFCs revealed unique combinations of interaction traits, some widely distributed (e.g., antimicrobial activity), others less common (e.g., production of siderophores and phytohormones, biosynthesis and export of specific B vitamins). Specific GFCs, comprising Alpha- and Gammaproteobacteria, are predicted to preferentially interact synergistically and/or antagonistically with bacteria and phytoplankton. Moreover, linked trait clusters (LTCs) identify traits that may have evolved together and point to specific modes of interactions. Our approach translates multidimensional genomic information into an atlas of marine bacteria and their ecosystem functions, relevant for understanding the fundamental rules that govern community assembly and dynamics.

microbiology↗

Gsx2 is involved in specification of neurons in the inferior olivary nuclei from Ptf1a-expressing neuronal progenitors in zebrafish

Neurons in the inferior olivary nuclei (IO neurons) send climbing fibers to Purkinje cells to elicit functions of the cerebellum. IO neurons and Purkinje cells are derived from neural progenitors expressing the proneural gene ptf1a. In this study, we found that the homeobox gene gsx2 was co-expressed with ptf1a in IO progenitors in zebrafish. Both gsx2 and ptf1a zebrafish mutants showed a strong reduction or loss of IO neurons. The expression of ptf1a was not affected in gsx2 mutants and vice versa. In IO progenitors, the ptf1a mutation increased apoptosis whereas the gsx2 mutation did not, suggesting that ptf1a and gsx2 are independently regulated and have distinct roles. The fibroblast growth factors (Fgf) 3/8a and retinoic acid signals negatively and positively, respectively, regulated gsx2 expression and thereby the development of IO neurons. mafba and hox genes are at least partly involved in the Fgf- and retinoic acid-dependent regulation of IO neuronal development. Our results indicate that gsx2 mediates the rostro-caudal positional signals to specify the identity of IO neurons from ptf1a-expressing neural progenitors. SummaryThe homeobox gene gsx2 mediates rostro-caudal positional signaling to specify the identify of neurons in the inferior olivary nuclei from neural progenitors expressing the proneural gene ptf1a.

developmental biology↗

Intravenous edaravone plus therapeutic hypothermia offers limited neuroprotection in the hypoxic-ischaemic newborn piglet

Therapeutic hypothermia is a standard therapy for neonatal hypoxic-ischaemic encephalopathy. One potential additional therapy is the free radical scavenger edaravone (3-methyl-1-phenyl-2-pyrazolin-5-one). To compare the neuroprotective effects of edaravone plus therapeutic hypothermia with those of therapeutic hypothermia alone after a hypoxic-ischaemic insult in the newborn piglet, anaesthetized piglets were subjected to 40 min of hypoxia (3-5% inspired oxygen) and cerebral ischaemia was assessed by cerebral blood volume. Body temperature was maintained at 38.5 {degrees}C in the normothermia group (NT, n = 8) and at 34 {degrees}C (24 h after the insult) in the therapeutic hypothermia (TH, n = 7) and therapeutic hypothermia plus edaravone (3 mg intravenous every 12 h for 3 days after the insult; TH+EV, n = 6) groups under mechanical ventilation. Five days after the insult, the mean (standard deviation) neurological scores were 10.9 (5.7) in the NT group, 17.0 (0.4) in the TH group (p = 0.025 vs. NT) and 15.0 (3.9) in the TH+EV group. The histopathological score of the TH+EV group showed no significant improvement compared with that of the other groups. In conclusion, edaravone plus therapeutic hypothermia had no additive neuroprotective effects after hypoxia-ischaemia in neurological and histopathological assessments.

neuroscience↗

Long-term warming weakens stabilizing effects of biodiversity in aquatic ecosystems

Despite the consensus that warming will affect biodiversity, alter physicochemical environments, and disrupt biological interactions, the relative importance of these key processes and how they interact to determine overall ecosystem function is poorly understood. Here, we analyze long-term (16[~]39 years) time series data from ten aquatic ecosystems and use convergent cross mapping (CCM) to quantify the hidden causal network linking species diversity, ecosystem function, and physicochemical factors. We observe that aquatic ecosystems subject to stronger warming exhibit decreased stability (larger fluctuations in phytoplankton biomass). We further show that this effect can be attributed to a weakening of stabilizing causal pathways between biodiversity, nutrient cycling, and phytoplankton biomass. Thus, rather than thinking in terms of separate factors, a more holistic view, that causally links biodiversity and the other ecosystem components, is required to understand and predict climate impacts on the temporal stability of aquatic ecosystems.

ecology↗