Tuesday, December 02, 2025

 

Moths detect bat attack signals: Ultrasonic pulse rates drive distinct escape responses



Playing specific bat-like ultrasounds can suppress moth reproduction, offering a smart way to protect crops with minimal pesticide use



Chiba University

Wing-flapping behavior of Autographa nigrisigna 

image: 

Researchers played simulated bat echolocation calls in the laboratory and found that egg-bearing A. nigrisigna stopped flying when exposed to high pulse repetition rates. This behavior could be harnessed in the field to reduce crop damage and support sustainable pest control.

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Credit: Professor Masashi Nomura from Chiba University, Japan





For many nocturnal moths, hearing sound waves is a matter of survival in night sky. Their ability to detect ultrasonic calls emitted by bats determines whether they escape or become prey. This predator-prey relationship has shaped the behavior, physiology, and sensory systems of both groups. Echolocating bats have developed complex call patterns to track insects in flight, while moths have evolved remarkable countermeasures, including evasive flight and sound-deflection tactics. The luna moth, for instance, spins its long hindwings to deflect the ultrasonic cries of bats and avoid capture. Although there are multiple studies on the auditory escape mechanisms of moths, the species-specific behavioral responses remain unexplored. 

Against this backdrop, Professor Masashi Nomura from the Graduate School of Horticulture at Chiba University, Japan, and Dr. Ryo Nakano from the Institute for Plant Protection at the National Agriculture and Food Research Organization (NARO), Japan —who has been studying bat-moth interactions and developed ultrasonic pest control techniques (Nakano et al. 2022 PNAS)— have been investigating the long-running evolutionary contest, which they describe as a "coevolutionary arms race" between bats and moths.

A study published online in the journal Pest Management Science on September 10, 2025, by Prof. Nomura and his team, including first author Dr. Ming Siang Lem from Chiba University , sheds new light on species-specific behavioral responses of moths. The study explores how a species of noctuid moth called Autographa nigrisigna (Walker) in the subfamily Plusiinae, which is widely distributed across East and South Asia, recognizes and reacts to bat echolocation calls. Their findings could help develop ultrasonic pest management strategies in agriculture, such as reducing moth egg-laying on vegetables.

"We wanted to quantify the auditory-mediated escape mechanisms of A. nigrisigna in response to controlled ultrasonic pulses under varying pulse rate regimes to understand egg-laying and flight characteristics," say Prof. Nomura and Dr. Nakano.

A key focus of the study was how the moths reacted to the pulse repetition rate (PRR), which measures how frequently bats emit their ultrasonic pulses. These pulse patterns signal different stages of a bat's hunt. When bats are searching for prey, their calls are slow and widely spaced. As they close in, the pulses become faster, ending in a rapid burst known as the "terminal buzz," just before the capture.

To explore how moths respond to these varying signals, the team recreated bat calls in the laboratory. They exposed 100 unmated adult plusiine moths­—50 males and 50 females­—to ultrasound pulses with different PRRs: low (1, 5, and 10 Hz), intermediate (20 and 40 Hz), and high (80 and 160 Hz).

Additionally, they tested how ultrasonic cues affect reproduction-related behavior by exposing gravid (egg-bearing) females to different PRRs. The moths adjusted their flight behavior depending on the pulse rate. At lower PRRs, they made simple avoidance turns, while at higher PRRs, they flew erratically or stopped flying altogether, showing stronger responses to sounds resembling an approaching bat. Gravid females were more likely to stop flying when exposed to higher PRRs, suggesting that moths balance survival and reproduction depending on the level of perceived danger.

"Mated females of A. nigrisigna selectively avoid ultrasonic PRRs that reflect high predation risk, the same rates emitted by bats during prey pursuit. This adaptive response highlights the evolutionary balance between predator evasion and reproductive investment in nocturnal moths," says Dr. Lem.

Ultimately, this finding gives us more insight into one of nature's most enduring rivalries: the silent evolutionary battle between bats and moths that has shaped both species for more than 60 million years. "Installing the ultrasonic emitters in fields to reduce nighttime moth activity could lead to reduced pesticide use. If ultrasonic treatment works for other pest moths as well, environmentally friendly pest control may become a reality," say Prof. Nomura and Dr. Nakano.

By taking inspiration from nature's own defense mechanisms, such as echolocation, this study could lead to novel pest control strategies and support more sustainable farming.

To see more news from Chiba University, click here.

 

About Professor Masashi Nomura from Chiba University

Dr. Masashi Nomura is a Professor and Vice Dean at the Graduate School of Horticulture, Chiba University, Japan. His research focuses on environmentally friendly pest management, employing biological and physical control methods to reduce pest populations without relying solely on chemical pesticides, and integrating these approaches through Integrated Pest Management. He also studies insect molecular phylogenetics and intraspecific variation, uncovering species differentiation and cryptic species within widely distributed insects. His current interests include Wolbachia lineage replacement, ultraviolet radiation effects on beneficial insects, and genetic variation in dragonflies.

Funding:

This study was financially supported by the Agri-Net Scholarship Program under the Japan International Cooperation Agency (JICA) (Grant Number D2202241).

Reference:

Authors: Ming Siang Lem1, Ryo Nakano2, and Masashi Nomura1

Affiliations: 1Laboratory of Applied Entomology, Graduate School of Horticulture, Chiba

 University, Japan

2Migratory Insect Pests and Advanced Control Technology Group, Institute for Plant Protection, NARO, Japan

 

New method reveals pollen's UV resistance linked to sporopollenin chemistry





Maximum Academic Press





By analyzing the autofluorescence intensity of sporopollenin in the pollen wall, researchers have identified a significant link between UV absorption and environmental radiation levels.

Land plants, especially spores and pollen, face numerous environmental stressors, including harmful UV-B radiation. As sessile organisms, they are exposed to UV without the protective buffer of water, making their survival dependent on efficient UV defense mechanisms. Sporopollenin, a robust polymer found in the outer layer of pollen and spores, has been identified as a key player in absorbing UV radiation, preventing damage to the delicate DNA within these reproductive units. However, variations in sporopollenin chemistry across plant species have made it challenging to establish a universal marker for UV resistance. Existing research has focused on specific compounds like para-coumaric acid (p-CA) and ferulic acid (FA), which are known to absorb UV radiation. Yet, no single marker has universally linked sporopollenin chemistry to UV resistance across different plant species.

study (DOI: 10.48130/seedbio-0025-0016 ) published in Seed Biology on 10 October 2025 by Ying Xiao’s & Jing-Shi Xue’s team, Shanghai University of Traditional Chinese Medicine & Shanghai Normal University, offers new insights into how plants adapt to UV stress, with potential applications in plant evolution and environmental adaptation studies.

The research focused on quantifying the Integral of Sporopollenin Autofluorescence Intensity (ISAI) in pollen and spores using Laser Scanning Confocal Microscopy (LSCM). This method measures the autofluorescence emitted by the pollen wall when exposed to UV radiation, reflecting its capacity to convert harmful short-wave UV radiation into less damaging long-wave visible light. The researchers analyzed pollen from 55 plant species, including 18 Arabidopsis thaliana ecotypes, and found that ISAI values varied significantly depending on the ecological exposure to solar irradiance. Plants in high-radiation environments, such as seed plants exposed to direct sunlight, exhibited higher ISAI values compared to those in shaded habitats, like pteridophytes and bryophytes. This correlation indicates that ISAI can serve as a reliable indicator of UV resistance, with species flowering during high solar radiation seasons showing particularly elevated ISAI levels. Further analysis of Arabidopsis thaliana ecotypes demonstrated that ISAI is heritable, with a negative correlation between ISAI values and pollen germination decline under UV-B treatment. Genetic analysis showed that phenylpropanoid phenolics, including para-coumaric acid and ferulic acid, are essential components of sporopollenin responsible for the observed ISAI variations, confirming their role in UV-B protection. These findings highlight the importance of sporopollenin chemistry in pollen UV resistance and propose ISAI as a novel metric for studying plant adaptation to UV environments.

The ISAI method provides a non-destructive, efficient way to assess pollen UV resistance, a critical factor for plant reproductive success. This tool is especially useful for studying the effects of environmental factors on plant adaptation, offering a new approach to exploring how plants evolve to cope with changing UV radiation levels. By linking sporopollenin autofluorescence to UV resistance, ISAI could also be applied in ecological and evolutionary research, offering insights into plant responses to climate change and UV stress.

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References

DOI

10.48130/seedbio-0025-0016

Original Source URL

https://doi.org/10.48130/seedbio-0025-0016

Funding information

This work was supported by grants from the National Natural Science Foundation of China (31900165), Shanghai Municipal Education Commission (2019-01-07-00-02-E00006), Science and Technology Commission of Shanghai Municipality (17DZ2252700, 18DZ2260500, and 21DZ2202300), and the Postdoctoral Fellowship Program (Grade C) of China Postdoctoral Science Foundation (GZC20231699). We would like to thank Dr. Zong-Xin Ren (Kunming Institute of Botany, Chinese Academy of Sciences) for the helpful comments on the manuscript.

About Seed Biology

Seed Biology (e-ISSN 2834-5495) is published by Maximum Academic Press in partnership with Yazhou Bay Seed Laboratory. Seed Biology is an open access, online-only journal focusing on research related to all aspects of the biology of seeds, including but not limited to: evolution of seeds; developmental processes including sporogenesis and gametogenesis, pollination and fertilization; apomixis and artificial seed technologies; regulation and manipulation of seed yield; nutrition and health-related quality of the endosperm, cotyledons, and the seed coat; seed dormancy and germination; seed interactions with the biotic and abiotic environment; and roles of seeds in fruit development. Seed biology publishes a wide range of research approaches, such as omics, genetics, biotechnology, genome editing, cellular and molecular biology, physiology, and environmental biology. Seed Biology publishes high-quality original research, reviews, perspectives, and opinions in open access mode, promoting fast submission, review, and dissemination freely to the global research community.

A newly identified gene boosts wheat regeneration and transformation efficiency




Maximum Academic Press





By directly suppressing cytokinin degradation genes (TaCKXs) and promoting key developmental genes (TaWOX5 and TaGIF1), TaDOF4.7-B dramatically increases shoot regeneration and callus proliferation.

Wheat is a globally vital food crop, yet its limited regeneration ability has long hampered genetic transformation and molecular breeding efforts. Plant regeneration—the ability to develop new organs or tissues—is a cornerstone of modern crop biotechnology, enabling genetic transformation and variety improvement. Among plant hormones, cytokinin plays a central role in stimulating callus formation and shoot development. Its homeostasis is tightly regulated by synthesis enzymes (IPTs) and degradation enzymes (CKXs). While manipulating cytokinin levels has shown promise in improving regeneration, the transcriptional mechanisms that coordinate this balance in wheat remain poorly understood. Based on these challenges, identifying key transcription factors that control cytokinin homeostasis is essential for advancing wheat regeneration and transformation efficiency.

study (DOI: 10.48130/seedbio-0025-0018 ) published in Seed Biology on 03 November 2025 by Haixia Yu’s & Chen Wang’s team, Shandong Agricultural University, provides crucial insights into the molecular mechanisms underlying plant regeneration and paves the way for more efficient genome editing and variety improvement in wheat.

To investigate the role of the TaDOF4.7-B transcription factor in wheat regeneration, several experimental techniques were employed. First, chromatin accessibility analysis identified that the promoters of TaDOF4.7-B and TaDOF4.7-D had higher chromatin accessibility compared to TaDOF4.7-A during the early stages of callus induction. RT-qPCR confirmed that TaDOF4.7-B was more highly expressed than the other DOF family members during wheat regeneration. To explore its function, TaDOF4.7-B was fused with green fluorescent protein (GFP) and expressed in Nicotiana benthamiana, revealing its nuclear localization. In wheat, RNA in-situ hybridization showed TaDOF4.7-B was primarily expressed in regions of callus where shoot primordia would emerge. Further, overexpression of TaDOF4.7-B in Fielder wheat led to earlier shoot primordia formation, better callus growth, and higher regeneration frequencies. Specifically, regeneration frequency increased from 22.65% in controls to 60.57% in transgenic lines, while regenerating shoot frequency and callus proliferation also significantly improved. Next, transcriptome analysis was performed on calli collected at different regeneration stages. Overexpression of TaDOF4.7-B resulted in the upregulation of genes related to cell division, shoot formation, and cytokinin signaling, including TaWOX5 and TaGIF1. ChIP-qPCR demonstrated that TaDOF4.7-B directly binds to the promoters of these genes, suggesting it regulates their expression during shoot regeneration. The overexpression lines also showed altered cytokinin levels, as the expression of TaCKX genes—responsible for cytokinin degradation—was downregulated. This regulation of cytokinin homeostasis by TaDOF4.7-B significantly enhanced shoot regeneration, even in the absence of exogenous cytokinin. These results highlight the critical role of TaDOF4.7-B in wheat regeneration and provide valuable insights for improving wheat transformation efficiency.

The discovery of TaDOF4.7-B offers a new genetic tool for improving transformation efficiency in wheat, a major bottleneck in cereal biotechnology. By modulating cytokinin metabolism rather than relying on hormone supplementation, this approach enables faster and more reliable regeneration across genotypes. Integrating TaDOF4.7-B into transformation pipelines could accelerate the production of gene-edited or transgenic wheat varieties with improved yield, quality, and stress tolerance. Beyond wheat, this regulatory mechanism provides a model for enhancing regeneration in other recalcitrant crops, offering broad applications in plant breeding and agricultural biotechnology.

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References

DOI

10.48130/seedbio-0025-0018

Original Source URL

https://doi.org/10.48130/seedbio-0025-0018

Funding information

This research was funded by the Biological Breeding-National Science and Technology Major Project (2024ZD04077).

About Seed Biology

Seed Biology (e-ISSN 2834-5495) is published by Maximum Academic Press in partnership with Yazhou Bay Seed Laboratory. Seed Biology is an open access, online-only journal focusing on research related to all aspects of the biology of seeds, including but not limited to: evolution of seeds; developmental processes including sporogenesis and gametogenesis, pollination and fertilization; apomixis and artificial seed technologies; regulation and manipulation of seed yield; nutrition and health-related quality of the endosperm, cotyledons, and the seed coat; seed dormancy and germination; seed interactions with the biotic and abiotic environment; and roles of seeds in fruit development. Seed biology publishes a wide range of research approaches, such as omics, genetics, biotechnology, genome editing, cellular and molecular biology, physiology, and environmental biology. Seed Biology publishes high-quality original research, reviews, perspectives, and opinions in open access mode, promoting fast submission, review, and dissemination freely to the global research community.