Award type：Honored in official journal of a scientific society, scientific journal  Country：Japan

http://square.umin.ac.jp/pl-morph/pdf/170810_Hirase_papers.pdf

Country：Germany

https://www.cell.com/pictureshow/biology-of-sex

Award type：Award from Japanese society, conference, symposium, etc.  Country：Japan

http://bsj.or.jp/jpn/members/information/622.php

Award type：Award from Japanese society, conference, symposium, etc.  Country：Japan

Award type：Award from Japanese society, conference, symposium, etc.  Country：Japan

https://www.nacos.com/jsb/07/07prize_2010.html

Award type：Award from Japanese society, conference, symposium, etc.  Country：Japan

Authorship：Lead author,　Corresponding author   Publisher：Cold Spring Harbor Laboratory  

ABSTRACT

In angiosperms, pollen tube guidance allows sperm cell delivery to the female gametes within the ovule, which are deeply embedded in a flower. However, when an ovary includes multiple pollen tubes and ovules, it is unclear how each ovule is fertilized one-to-one by a pollen tube. Here, our two-photon imaging revealed the pollen tube dynamics in living ovaries. The number of pollen tubes and ovule maturity affected the target selection among multiple ovules. On the inner surface of the septum epidermis within the transmitting tract, pollen tube behavior and emergence were regulated by the ovular sporophytic signals. In funicular guidance, the second pollen tube was strictly repelled by the FERONIA and LORELEI-dependent gametophytic signal, especially more than 45 minutes after the first pollen tube had passed. Such highly spatiotemporal regulation mechanisms in the one-to-one pollen tube guidance may allow angiosperms to produce more offspring in nature.

DOI： 10.1101/2023.04.19.537439

Authorship：Lead author,　Last author,　Corresponding author   Language：Japanese   Publisher：THE BOTANICAL SOCIETY OF JAPAN  

DOI： 10.24480/bsj-review.14a4.00239

CiNii Research

Language：Japanese   Publisher：公益社団法人 日本植物学会  

DOI： 10.24480/bsj-review.14a1.00236

CiNii Research

Authorship：Last author,　Corresponding author   Language：English   Publishing type：Research paper (scientific journal)   Publisher：Cambridge University Press (CUP)  

Abstract

Single-cell analysis is important to understand how individual cells work and respond at the cell population level. Experimental single-cell isolation techniques, including dilution, fluorescence-activated cell sorting, microfluidics, and micromanipulation, have been developed in recent decades. However, such applications typically require large cell populations and skilled professionals. Additionally, these methods are unsuitable for sequential analysis before and after cell isolation. In this study, we propose a method for target cell isolation using automated infrared laser-mediated disruption of pollen grains in pollen populations. Germination of the target pollen was observed at the same location as that before laser irradiation, and germinated pollen grains were enriched in the cell population. Pollination of laser-irradiated bulk pollen populations also showed that the target pollen preferentially germinated on the stigma. This method is expected to facilitate physiological analyses of target cells at the single-cell level and effectively produce seeds derived from target pollen.

DOI： 10.1017/qpb.2022.24

Open Access

Web of Science

Scopus

PubMed

Other Link： https://www.microscope.healthcare.nikon.com/ja_JP/resources/application-notes/automatic-isolation-of-pollen-using-nis-elements-general-analysis-ga-and-jobs-imaging-workflow-tools

Authorship：Last author,　Corresponding author   Language：English   Publishing type：Research paper (scientific journal)  

The recently developed clearing technology that eliminates refractive index mismatches and diminishes auto-fluorescent material has made it possible to observe plant tissues in three dimensions (3D) while preserving their internal structures. In rice (Oryza sativa L.), a monocot model plant and a globally important crop, clearing technology has been reported in organs that are relatively easy to observe, such as the roots and leaves. Applications of clearing technology in shoot apical meristem (SAM) and stems have also been reported, but only to a limited degree because of the poor penetration of the clearing solution (CS) in these tissues. The limited efficiency of the clearing solutions in these tissues has been attributed to auto-fluorescence, thickening, and hardening of the tissues in the stem as the vascular bundles and epidermis develop and layering of the SAM with water-repellent leaves. The present protocol reports the optimization of a clearing approach for continuous and 3D observation of gene expression from the SAM/young panicle to the base of the shoots during development. Fixed tissue samples expressing a fluorescent protein reporter were trimmed into sections using a vibrating micro-slicer. When an appropriate thickness was achieved, the CS was applied. By specifically targeting the central tissue, the penetration rate and uniformity of the CS increased, and the time required to make the tissue transparent decreased. Additionally, clearing of the trimmed sections enabled the observation of the internal structure of the whole shoot from a macro perspective. This method has potential applications in deep imaging of tissues of other plant species that are difficult to clear.

DOI： 10.3791/64116

Web of Science

Scopus

PubMed

Language：English   Publishing type：Research paper (scientific journal)   Publisher：MyJove Corporation  

DOI： 10.3791/63428

Web of Science

Scopus

PubMed

Authorship：Last author,　Corresponding author   Language：English   Publishing type：Research paper (scientific journal)   Publisher：Springer Science and Business Media LLC  

Abstract

Key message

Biolistic delivery into pollen. Abstract

In recent years, genome editing techniques, such as the CRISPR/Cas9 system, have been highlighted as a new approach to plant breeding. Agrobacterium-mediated transformation has been widely utilized to generate transgenic plants by introducing plasmid DNA containing CRISPR/Cas9 into plant cells. However, this method has general limitations, such as the limited host range of Agrobacterium and difficulties in tissue culture, including callus induction and regeneration. To avoid these issues, we developed a method to genetically modify germ cells without the need for Agrobacterium-mediated transfection and tissue culture using tobacco as a model. In this study, plasmid DNA containing sequences of Cas9, guide RNA, and fluorescent reporter was introduced into pollen using a biolistic delivery system. Based on the transient expression of fluorescent reporters, the Arabidopsis UBQ10 promoter was found to be the most suitable promoter for driving the expression of the delivered gene in pollen tubes. We also evaluated the delivery efficiency in male germ cells in the pollen by expression of the introduced fluorescent marker. Mutations were detected in the target gene in the genomic DNA extracted from CRISPR/Cas9-introduced pollen tubes, but were not detected in the negative control. Bombarded pollen germinated pollen tubes and delivered their contents into the ovules in vivo. Although it is necessary to improve biolistic delivery efficiency and establish a method for the screening of genome-modified seeds, our findings provide important insights for the detection and production of genome-modified seeds by pollen biolistic delivery.

DOI： 10.1007/s00497-021-00418-z

Open Access

Web of Science

Scopus

PubMed

Other Link： https://link.springer.com/article/10.1007/s00497-021-00418-z/fulltext.html

Language：English   Publishing type：Research paper (scientific journal)   Publisher：Oxford University Press (OUP)  

Abstract

To understand how the body of plants is made, it is essential to observe the morphology, structure and arrangement of constituent cells. However, the opaque nature of the plant body makes it difficult to observe the internal structures directly under a microscope. To overcome this problem, we developed a reagent, ClearSee, that makes plants transparent, allowing direct observation of the inside of a plant body without inflicting damage on it, e.g. through physical cutting. However, because ClearSee is not effective in making some plant species and tissues transparent, in this study, we further improved its composition to prevent oxidation, and have developed ClearSeeAlpha, which can be applied to a broader range of plant species and tissues. Sodium sulfite, one of the reductants, prevented brown pigmentation due to oxidation during clearing treatment. Using ClearSeeAlpha, we show that it is possible to obtain clear chrysanthemum leaves, tobacco and Torenia pistils and fertilized Arabidopsis thaliana fruits—tissues that have hitherto been challenging to clear. Moreover, we show that the fluorescence intensity of purified fluorescent proteins emitting light of various colors was unaffected in the ClearSeeAlpha solution; only the fluorescence intensity of TagRFP was reduced by about half. ClearSeeAlpha should be useful in the discovery and analysis of biological phenomena occurring deep inside the plant tissues.

DOI： 10.1093/pcp/pcab033

Open Access

Web of Science

Scopus

PubMed

Other Link： https://academic.oup.com/pcp/article-pdf/62/8/1302/41119229/pcab033.pdf

Authorship：Lead author,　Last author,　Corresponding author   Language：English   Publishing type：Research paper (scientific journal)   Publisher：Oxford University Press (OUP)  

Abstract

Live and deep imaging play a significant role in the physiological and biological study of organisms. Two-photon excitation microscopy (2PEM), also known as multiphoton excitation microscopy, is a fluorescent imaging technique that allows deep imaging of living tissues. Two-photon lasers use near-infrared (NIR) pulse lasers that are less invasive and permit deep tissue penetration. In this review, recent advances in two-photon imaging and their applications in plant studies are discussed. Compared to confocal microscopy, NIR 2PEM exhibits reduced plant-specific autofluorescence, thereby achieving greater depth and high-resolution imaging in plant tissues. Fluorescent proteins with long emission wavelengths, such as orange–red fluorescent proteins, are particularly suitable for two-photon live imaging in plants. Furthermore, deep- and high-resolution imaging was achieved using plant-specific clearing methods. In addition to imaging, optical cell manipulations can be performed using femtosecond pulsed lasers at the single cell or organelle level. Optical surgery and manipulation can reveal cellular communication during development. Advances in in vivo imaging using 2PEM will greatly benefit biological studies in plant sciences.

DOI： 10.1093/pcp/pcab062

Open Access

Web of Science

Scopus

PubMed

Other Link： https://academic.oup.com/pcp/article-pdf/62/8/1224/41119175/pcab062.pdf

Language：English   Publishing type：Research paper (scientific journal)   Publisher：Elsevier BV  

Ovule development in Arabidopsis thaliana involves pattern formation, which ensures that ovules are regularly arranged in the pistils to reduce competition for nutrients and space. Mechanisms underlying pattern formation in plants, such as phyllotaxis, flower morphogenesis, or lateral root initiation, have been extensively studied, and genes controlling the initiation of ovules have been identified. However, the fundamental patterning mechanism that determines the spacing of ovule anlagen within the placenta remained unexplored. Using natural variation analysis combined with quantitative trait locus analysis, we found that the spacing of ovules in the developing gynoecium and fruits is controlled by two secreted peptides, EPFL2 and EPFL9 (also known as Stomagen), and their receptors from the ERECTA (ER) family that act from the carpel wall and the placental tissue. We found that a signaling pathway controlled by EPFL9 acting from the carpel wall through the LRR-receptor kinases ER, ERL1, and ERL2 promotes fruit growth. Regular spacing of ovules depends on EPFL2 expression in the carpel wall and in the inter-ovule spaces, where it acts through ERL1 and ERL2. Loss of EPFL2 signaling results in shorter gynoecia and fruits and irregular spacing of ovules or even ovule twinning. We propose that the EPFL2 signaling module evolved to control the initiation and regular, equidistant spacing of ovule primordia, which may serve to minimize competition between seeds or facilitate equal resource allocation. Together, EPFL2 and EPFL9 help to coordinate ovule patterning and thereby seed number with gynoecium and fruit growth through a set of shared receptors.

DOI： 10.1016/j.cub.2020.08.050

Web of Science

Scopus

PubMed

Language：Japanese   Publishing type：Research paper (scientific journal)   Publisher：Japanese Society of Breeding  

DOI： 10.1270/jsbbr.22.w03

CiNii Research

Authorship：Lead author,　Corresponding author   Language：English   Publishing type：Research paper (scientific journal)   Publisher：Company of Biologists Ltd  

Pollen tube guidance is a unique navigating system that is required for the successful sexual reproduction of plants. As plant sperm cells are non-motile and egg cells are embedded deep inside the female tissues, a pollen tube delivers the two sperm cells that it contains by growing towards the ovule, in which the egg cell resides. Pollen tube growth towards the ovule is precisely controlled and divided into two stages, preovular and ovular guidance. In this Cell Science at a Glance article and accompanying poster, we provide a comprehensive overview of pollen tube guidance and highlight some of the attractant peptides used during ovular guidance. We further discuss the precise one-to-one guidance system that exists in multi-ovular plants. The pollen tube-blocking system, which is mediated by male-female crosstalk communication, to avoid attraction of multiple pollen tubes, is also reviewed.

DOI： 10.1242/jcs.208447

Web of Science

Scopus

PubMed

CiNii Research

Authorship：Lead author,　Corresponding author   Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1007/978-1-4939-8657-6_15

Web of Science

Scopus

PubMed

Language：Japanese  

Authorship：Last author   Language：Japanese   Publisher：The Japanese Society of Plant Morphology  

<p>Fluorescent proteins enable us to visualize not only single cells but also organelles and molecules. However, plants have opaque bodies, complicated tissue structures containing air spaces, and autofluorescent compounds, which hinder fluorescence imaging of plants without mechanical sectioning. Recently, various clearing techniques have been developed for plant tissues to reduce the mismatch of refractive index and to remove the colored components. In this review, we will describe various clearing techniques for fluorescence imaging in plants.</p>

DOI： 10.5685/plmorphol.29.81

CiNii Research

Language：Japanese   Publisher：The Japanese Society of Plant Morphology  

DOI： 10.5685/plmorphol.29.0

CiNii Research

Authorship：Lead author,　Corresponding author   Language：English  

Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1242/dev.127613

PubMed

Authorship：Lead author,　Corresponding author   Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1007/s00709-014-0754-5

PubMed

Authorship：Lead author   Language：Japanese  

Authorship：Lead author,　Corresponding author   Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1111/tpj.12461

PubMed

Language：English  

Authorship：Lead author   Language：Japanese  

Authorship：Lead author,　Corresponding author   Language：Japanese  

Language：English  

Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1093/pcp/pcq165

PubMed

Authorship：Lead author   Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1073/pnas.1003124107

PubMed

Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1093/pcp/pcn124

PubMed

Language：English   Publishing type：Research paper (scientific journal)  

DOI： 10.1093/pcp/pcn128

PubMed

Language：English   Publishing type：Research paper (scientific journal)  

Authorship：Lead author   Language：English  

Language：English  

Language：Japanese Book type：Image

Authorship：Lead author,　Corresponding author   Language：Japanese  

Authorship：Lead author,　Corresponding author   Language：Japanese   Publisher：The Japanese Society of Plant Morphology  

<p>In recent decades, various interdisciplinary technologies promote plant imaging research, such as MEMS (Micro-Electro-Mechanical-Systems), organic synthesis, genomics, and mathematical modeling. We have organized a symposium entitled ‘Plant imaging research promoted by interdisciplinary collaborations’ at the 84th Annual Meeting of the Botanical Society of Japan on September 21^st, 2020. This symposium was co-sponsored by The Birth of New Plant Species (Scientific Research on Innovative Areas, a MEXT Grant-in-Aid Project), Integrated Imaging Research Support (IIRS), and The Japanese Society of Plant Morphology. We had five young expert researchers’ presentations to introduce their innovative research with cutting-edge techniques for imaging. Current issues in the plant research, their solutions by the new imaging technologies, and plant imaging potential were interactively discussed involving speakers and audiences. This symposium was held using the online conference tool ‘Zoom’ under the first trial of the online Annual Meeting of the Botanical Society of Japan due to the influence of the COVID-19.</p>

DOI： 10.5685/plmorphol.33.1

CiNii Research

Authorship：Lead author   Language：Japanese  

<p>卓上型走査型電子顕微鏡によるシロイヌナズナめしべの観察像 めしべの片側の子房壁を取り除いて，キーエンスVHX-2000 およびVHX-D510 により撮影．</p>

DOI： 10.5685/plmorphol.29.0

Event date： 2025.5

Language：English   Presentation type：Oral presentation (general)  

Event date： 2025.3

Presentation type：Oral presentation (general)  

Event date： 2025.3

Presentation type：Oral presentation (general)  

Event date： 2025.3

Language：Japanese   Presentation type：Oral presentation (general)  

Event date： 2024.12

Presentation type：Symposium, workshop panel (nominated)  

Event date： 2024.9

Presentation type：Poster presentation  

Event date： 2024.9

Presentation type：Poster presentation  

Event date： 2024.9

Presentation type：Poster presentation  

Event date： 2024.9

Presentation type：Oral presentation (invited, special)  

Event date： 2024.3

Presentation type：Oral presentation (general)  

Event date： 2024.3

Presentation type：Oral presentation (general)  

Event date： 2024.3

Language：Japanese   Presentation type：Public lecture, seminar, tutorial, course, or other speech  

Venue：基礎生物学研究所  

Event date： 2024.3

Presentation type：Public lecture, seminar, tutorial, course, or other speech  

Event date： 2023.9

Presentation type：Oral presentation (general)  

Event date： 2023.9

Presentation type：Oral presentation (general)  

Event date： 2023.9

Presentation type：Poster presentation  

Event date： 2023.9

Presentation type：Poster presentation  

Event date： 2023.3

Presentation type：Oral presentation (general)  

Event date： 2023.3

Presentation type：Symposium, workshop panel (nominated)  

Event date： 2022.12

Presentation type：Oral presentation (general)  

Event date： 2022.12

Presentation type：Symposium, workshop panel (nominated)  

Event date： 2022.10

Presentation type：Public lecture, seminar, tutorial, course, or other speech  

Event date： 2022.9

Presentation type：Symposium, workshop panel (nominated)  

Event date： 2022.9

Presentation type：Oral presentation (general)  

Event date： 2022.9

Presentation type：Symposium, workshop panel (nominated)  

Event date： 2022.9

Presentation type：Oral presentation (general)  

Event date： 2022.6

Language：Japanese   Presentation type：Symposium, workshop panel (nominated)  

Event date： 2021.12

Event date： 2021.10

Presentation type：Poster presentation  

Event date： 2021.9

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：弘前大学  

Event date： 2021.9

Language：Japanese   Presentation type：Poster presentation  

Venue：東京都立大学  

Event date： 2021.9

Language：Japanese   Presentation type：Symposium, workshop panel (nominated)  

Event date： 2021.3

Language：Japanese   Presentation type：Symposium, workshop panel (nominated)  

Event date： 2021.3

Language：Japanese   Presentation type：Poster presentation  

Venue：島根大学  

Event date： 2021.1

Language：Japanese   Presentation type：Public lecture, seminar, tutorial, course, or other speech  

Event date： 2020.9

Language：Japanese   Presentation type：Public lecture, seminar, tutorial, course, or other speech  

Event date： 2020.9

Language：Japanese   Presentation type：Oral presentation (general)  

Event date： 2020.9

Language：Japanese   Presentation type：Poster presentation  

Event date： 2020.9

Language：Japanese   Presentation type：Poster presentation  

Event date： 2020.6

Language：Japanese   Presentation type：Public lecture, seminar, tutorial, course, or other speech  

Event date： 2020.2

Language：Japanese   Presentation type：Symposium, workshop panel (nominated)  

Country：Japan  

Event date： 2019.10

Language：English   Presentation type：Oral presentation (general)  

Event date： 2019.9

Language：Japanese   Presentation type：Oral presentation (general)  

Country：Japan  

Event date： 2019.9

Language：Japanese   Presentation type：Poster presentation  

Country：Japan  

Event date： 2019.9

Language：Japanese   Presentation type：Poster presentation  

Country：Japan  

Event date： 2019.9

Language：Japanese   Presentation type：Symposium, workshop panel (nominated)  

Country：Japan  

Event date： 2019.3

Language：Japanese   Presentation type：Oral presentation (general)  

Country：Japan  

Event date： 2019.3

Language：Japanese   Presentation type：Symposium, workshop panel (nominated)  

Country：Japan  

Event date： 2019.2

Language：Japanese   Presentation type：Symposium, workshop panel (nominated)  

Country：Japan  

Event date： 2018.9

Language：Japanese   Presentation type：Poster presentation  

Country：Japan  

Event date： 2018.9

Language：Japanese   Presentation type：Poster presentation  

Country：Japan  

Event date： 2018.9

Language：Japanese   Presentation type：Poster presentation  

Country：Japan  

Event date： 2018.9

Language：Japanese   Presentation type：Poster presentation  

Country：Japan  

Event date： 2018.6

Language：English   Presentation type：Poster presentation  

Country：Japan  

Event date： 2017.12

Language：Japanese   Presentation type：Poster presentation  

Country：Japan  

Event date： 2017.12

Language：Japanese   Presentation type：Symposium, workshop panel (nominated)  

Country：Japan  

Event date： 2017.11

Language：Japanese   Presentation type：Symposium, workshop panel (nominated)  

Country：Japan  

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Language：Japanese   Presentation type：Oral presentation (general)  

Country：Japan  

Event date： 2017.2

Presentation type：Symposium, workshop panel (nominated)  

Event date： 2016.9

Language：Japanese   Presentation type：Symposium, workshop panel (nominated)  

Country：Japan  

Event date： 2016.9

Language：Japanese   Presentation type：Poster presentation  

Country：Japan  

Event date： 2016.6

Presentation type：Poster presentation  

Country：Japan  

Event date： 2016.3

Presentation type：Oral presentation (general)  

Country：Japan  

Event date： 2015.9

Language：Japanese   Presentation type：Symposium, workshop panel (nominated)  

Country：Japan  

Event date： 2015.9

Language：Japanese   Presentation type：Symposium, workshop panel (nominated)  

Country：Japan  

Event date： 2015.2

Language：English  

Country：Japan  

Event date： 2014.9

Language：Japanese   Presentation type：Oral presentation (general)  

Country：Japan  

Event date： 2014.9

Language：Japanese   Presentation type：Poster presentation  

Country：Japan  

Event date： 2014.7

Language：English   Presentation type：Symposium, workshop panel (nominated)  

Country：Japan  

Event date： 2014.7

Language：English   Presentation type：Poster presentation  

Country：Portugal  

Event date： 2014.1

Language：Japanese   Presentation type：Poster presentation  

Country：Japan  

Event date： 2013.9

Language：Japanese   Presentation type：Symposium, workshop panel (nominated)  

Country：Japan  

Event date： 2013.9

Language：Japanese   Presentation type：Poster presentation  

Country：Japan  

Event date： 2013.8

Language：Japanese   Presentation type：Oral presentation (general)  

Event date： 2013.6

Language：English   Presentation type：Poster presentation  

Country：Australia  

Event date： 2013.5

Language：Japanese   Presentation type：Oral presentation (general)  

Event date： 2012.9

Language：Japanese   Presentation type：Oral presentation (general)  

Country：Japan  

Event date： 2012.9

Language：Japanese   Presentation type：Poster presentation  

Country：Japan  

Event date： 2012.5

Language：Japanese   Presentation type：Oral presentation (general)  

Event date： 2012.3

Language：Japanese   Presentation type：Oral presentation (general)  

Country：Japan  

Event date： 2011.9

Language：Japanese   Presentation type：Oral presentation (general)  

Country：Japan  

Event date： 2011.9

Language：Japanese   Presentation type：Poster presentation  

Country：Japan  

Event date： 2010.9

Language：Japanese  

Country：Japan  

Event date： 2010.3

Language：Japanese   Presentation type：Oral presentation (general)  

Country：Japan  

Event date： 2010.3

Language：Japanese   Presentation type：Oral presentation (general)  

Country：Japan  

Event date： 2010.3

Language：English   Presentation type：Poster presentation  

Country：Japan  

Event date： 2009.12

Language：Japanese   Presentation type：Poster presentation  

Country：Japan  

Event date： 2009.9

Language：Japanese   Presentation type：Oral presentation (general)  

Country：Japan  

Event date： 2008.10

Language：Japanese   Presentation type：Oral presentation (general)  

Country：Japan  

Event date： 2008.7

Language：English   Presentation type：Poster presentation  

Country：Germany  

Event date： 2007.9

Language：Japanese   Presentation type：Oral presentation (general)  

Country：Japan  

Event date： 2007.9

Language：Japanese   Presentation type：Oral presentation (general)  

Country：Japan  

Event date： 2007.3

Language：Japanese   Presentation type：Oral presentation (general)  

Event date： 2005.10

Language：Japanese   Presentation type：Oral presentation (general)  

Work type：Artistic work   Location：日本植物学会第79回大会  

File： ロゴマーク ユキツバキ（日本植物学会第79回大会）.pdf

Work type：Artistic work   Location：科学技術の美パネル展  

File： 生きている花粉管の花火（科学技術の美パネル展） .pdf

Date applied：2019.4

Announcement no：2020-171262  Date announced：2020.10

Country of applicant：Domestic   Country of acquisition：Domestic

Applicant：Nagoya University

Application no：特願2019-076650  Date applied：2019.4

Announcement no：特開2020-171262  Date announced：2020.10

Patent/Registration no：特許7334898  Date registered：2023.8 

Applicant：国立大学法人名古屋大学

Application no：特願2018-79316  Date applied：2018.4

Announcement no：2019-180373  Date announced：2019.10

Patent/Registration no：特許第6614622号  Date registered：2019.11  Date issued：2019.12

Country of applicant：Domestic  

Audience： Infants,　Schoolchildren

Type：Seminar, workshop

File： 211001_591e5814.jpg

最先端の科学が明らかにする“新しい進化の物語”を、圧巻の映像美で描く大型シリーズ。第１集は、陸の王者、植物。「おとなしくて鈍感な生き物」のイメージを覆す、驚異的な能力の数々。植物がまるで“おしゃべり”するかのようにコミュニケーションする様子を、世界初の映像で紹介！さらに、多様な命が暮らす森の地下には“支え合いの世界”が広がっていた！特殊撮影と最先端のＶＦＸ技術で、植物の驚きの新世界を描き尽くす。

Author：Other 

Author：Other 

Author：Other 

Author：Other 

Type：Academic society, research group, etc. 

Type：Competition, symposium, etc.