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加分100%浜中特選昆布鍋物尾牙預算好掌控嗎?》公益路10家人氣餐廳|台中美食一網打盡 |
| 休閒生活|旅人手札 2026/04/20 06:37:53 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
身為一個熱愛美食、喜歡在城市裡挖掘驚喜的人,臺中公益路一直是我最常出沒的地方之一。這條路可說是「臺中人的美食戰場」,從精緻西餐到創意火鍋,從日式丼飯到義式早午餐,每走幾步,就會有完全不同的特色料理餐廳。 這次我特別花了一整個月,實際造訪了公益路上十間口碑不錯的餐廳。有的是網友熱推的打卡名店,也有隱藏在巷弄裡的小驚喜。我以環境氛圍、口味表現、價格CP值與再訪意願為基準,整理出這篇實測評比。希望能幫正在猶豫去哪裡吃飯的你,找到那一間「吃完會想再來」的餐廳。 評比標準與整理方向
這次我走訪的10家餐廳橫跨不同料理類型,從高質感牛排館到巷弄系早午餐,每一間都有自己獨特的風格。為了讓整體比較更客觀,我依照以下四大面向進行評比,並搭配實際用餐體驗來打分。
整體而言,我希望這份評比不只是「哪家好吃」,而是幫你在不同情境下(約會、家庭聚餐、朋友小聚、商業午餐)都能快速找到合適的選擇。畢竟,美食不只是味覺的滿足,更是一段段與朋友共享的生活記憶。 10間臺中公益路餐廳評比懶人包公益路向來是臺中人聚餐的首選地段,從火鍋、燒肉到中式料理與早午餐,每走幾步就有驚喜。以下是我實際造訪過的10間代表性餐廳清單,橫跨平價、創意、高級各路風格。
一頭牛日式燒肉|炭香濃郁的和牛饗宴,約會聚餐首選
走在公益路上,很難不被 一頭牛日式燒肉 的木質外觀吸引。低調卻不失質感的門面,搭配昏黃燈光與暖色調的內裝,讓人一進門就感受到濃濃的日式職人氛圍。店內空間不大,但桌距規劃得宜,每桌皆設有獨立排煙設備,烤肉時完全不怕滿身油煙味。 餐點特色
一頭牛的靈魂,絕對是他們招牌的「三國和牛拼盤」。 用餐體驗整體節奏掌握得非常好。店員會在你剛想烤下一片肉時貼心遞上夾子、幫忙換烤網,讓人完全不用分心。整場用餐過程就像一場表演,從視覺、嗅覺到味覺都被滿足。 綜合評分
地址:408臺中市南屯區公益路二段162號電話:04-23206800 小結語一頭牛日式燒肉不僅是「吃肉的地方」,更像是一場五感盛宴。從進門那一刻到最後一道甜點,都能感受到他們對細節的用心。 TANG Zhan 湯棧|文青系火鍋代表,麻香湯底與視覺美感並重
在公益路這條美食戰線上,TANG Zhan 湯棧 是讓人一眼就會想走進去的那一種。 餐點特色
湯棧最有名的當然是它的「麻香鍋」。 用餐體驗整體氛圍比一般火鍋店更有質感。 綜合評分
地址:408臺中市南屯區公益路二段248號電話:04-22580617 官網:https://www.facebook.com/TangZhan.tw/ 小結語TANG Zhan 湯棧 把傳統火鍋做出新的樣貌保留臺式鍋物的溫度,又結合現代風格與細節服務,讓吃鍋這件事變得更有品味。 如果你想找一間兼具「好吃、好拍、好放鬆」的火鍋店,湯棧會是公益路上最有風格的選擇之一。 NINI 尼尼臺中店|明亮寬敞的義式早午餐天堂
如果說前兩間是肉食愛好者的天堂,那 NINI 尼尼臺中店 絕對是想放鬆、聊聊天的好地方。餐廳外觀以白色系與大片玻璃窗為主,陽光灑進室內,讓人一踏入就有種度假般的輕盈感。假日早午餐時段特別熱鬧,建議提早訂位。 餐點特色
NINI 的菜單融合義式與臺灣人口味,選擇多樣且份量十足。主打的 松露燉飯 濃郁卻不膩口,米芯保留微Q口感;而 香蒜海鮮義大利麵 則以新鮮白蝦、花枝與淡菜搭配微辣蒜香,口感層次豐富。 用餐體驗店內氣氛輕鬆不拘謹,無論是一個人帶電腦工作、或朋友聚餐,都能找到舒服角落。餐點上桌速度穩定,服務人員態度親切、補水與收盤都非常主動。整體節奏讓人覺得「時間變慢了」,很適合想遠離忙碌日常的人。 綜合評分
地址:40861臺中市南屯區公益路二段18號電話:04-23288498 小結語NINI 尼尼臺中店是一間能讓人放下手機、慢慢吃飯的餐廳。餐點不追求浮誇,而是以「剛剛好」的份量與風味,陪伴每個平凡午後。如果你在找一間能邊吃邊聊天、拍照也漂亮的早午餐店,NINI 會是你在公益路上最不費力的幸福選擇。 加分100%浜中特選昆布鍋物|平價卻用心的湯頭系火鍋,家庭聚餐好選擇
在公益路這條高質感餐廳林立的戰場上,加分100%浜中特選昆布鍋物 走的是截然不同的路線。它沒有浮誇的裝潢、也沒有高價位的套餐,但靠著實在的湯頭與親切的服務,默默吸引許多回頭客。每到用餐時間,總能看到家庭或情侶三兩成群地圍著鍋邊聊天。 餐點特色
主打 北海道浜中昆布湯底,湯頭清澈卻不單薄,越煮越能喝出海藻與柴魚的自然香氣。 用餐體驗整體氛圍偏家庭取向,桌距寬敞、座位舒適,帶小孩來也不覺擁擠。店員態度親切,補湯、收盤都很勤快,給人一種「被照顧著」的安心感。 綜合評分
地址:403臺中市西區公益路288號電話:0910855180 小結語加分100%浜中特選昆布鍋物是一間「不浮誇、但會讓人想再訪」的火鍋店。它不追求豪華擺盤,而是用最簡單的湯頭與新鮮食材,傳遞出家常卻不平凡的溫度。 印月餐廳|中式料理的藝術演繹,宴客與家庭聚會首選
說到臺中公益路的中式料理代表,印月餐廳 絕對是榜上有名。這間開業多年的餐廳以「中菜西吃」的概念聞名,把傳統中式料理以現代手法重新詮釋。從建築外觀到餐具擺設,每個細節都散發著低調的典雅氣息。 餐點特色
印月最令人印象深刻的是他們將傳統中菜融入創意手法。 用餐體驗服務方面完全對得起餐廳的高級定位。從入座、點餐到上菜節奏,都拿捏得恰如其分。每道菜都會有服務人員細心介紹食材與吃法,讓人感受到「被款待」的尊榮感。 綜合評分
地址:408臺中市南屯區公益路二段818號電話:0422511155 小結語印月餐廳是一間「不只吃飯,更像品味生活」的地方。 KoDō 和牛燒肉|極致職人精神,專為儀式感與頂級味覺而生
若要形容 KoDō 和牛燒肉 的用餐體驗,一句話足以總結——「像在欣賞一場關於肉的表演」。 餐點特色
這裡主打 日本A5和牛冷藏肉,以「精切厚燒」的方式呈現。 用餐體驗KoDō 的最大特色是「儀式感」。 綜合評分
地址:403臺中市西區公益路260號電話:0423220312 官網:https://www.facebook.com/kodo2018/ 小結語KoDō 和牛燒肉不是日常餐廳,而是一場體驗。 永心鳳茶|在茶香裡用餐的優雅時光,臺味早午餐的新詮釋
走進 永心鳳茶公益店,彷彿進入一間有氣質的茶館。 餐點特色
永心鳳茶的餐點結合中式靈魂與西式擺盤,無論是「炸雞腿飯」還是「紅玉紅茶拿鐵」,都能讓人感受到熟悉卻不平凡的味道。 用餐體驗店內服務人員態度溫和,對茶品介紹詳盡。上餐節奏剛好,不急不徐。 綜合評分
地址:40360臺中市西區公益路68號三樓(勤美誠品)電話:0423221118 小結語永心鳳茶讓人重新定義「臺味」。 三希樓|老饕級江浙功夫菜,穩重又帶人情味的中式饗宴
位於公益路上的 三希樓 是許多臺中老饕的口袋名單。 餐點特色
三希樓的菜色以 江浙與港式料理 為主,兼顧傳統與現代風味。 用餐體驗三希樓的服務給人一種老派但貼心的感覺。 綜合評分
地址:408臺中市南屯區公益路二段95號電話:0423202322 官網:https://www.sanxilou.com.tw/ 小結語三希樓是一間「吃得出功夫」的餐廳。 一笈壽司|低調奢華的無菜單日料,職人手藝詮釋旬味極致
在熱鬧的公益路上,一笈壽司 低調得幾乎不顯眼。 餐點特色
一笈壽司採 Omakase(無菜單料理) 形式,每一餐都由主廚根據當日食材設計。 用餐體驗整場用餐約90分鐘,節奏緩慢但沉穩。 綜合評分
地址:408臺中市南屯區公益路二段25號電話:0423206368 官網:https://www.facebook.com/YIJI.sushi/ 小結語一笈壽司是一間真正讓人「放慢呼吸」的餐廳。 茶六燒肉堂|人氣爆棚的和牛燒肉聖地,肉香與幸福感同時滿分
若要票選公益路上「最難訂位」的餐廳,茶六燒肉堂 絕對名列前茅。 餐點特色
茶六主打 和牛燒肉套餐,價格約落在 $700–$1000 間,份量與品質兼具。 用餐體驗茶六的服務效率相當高。店員親切、換網勤快、補水速度快,整場用餐流程流暢無壓力。 綜合評分
地址:403臺中市西區公益路268號電話:0423281167 官網:https://inline.app/booking/-L93VSXuz8o86ahWDRg0:inline-live-karuizawa/-LUYUEIOYwa7GCUpAFWA 小結語茶六燒肉堂用「穩定品質+輕奢氛圍」抓住了臺中年輕族群的心。 吃完10家公益路餐廳後的心得與結語吃完這十家餐廳後,臺中公益路不只是一條美食街,而是一段生活風景線。 有的餐廳講究細膩與儀式感,像 一頭牛日式燒肉 與 一笈壽司,讓人感受到食材最純粹的美好 有的則以親切與溫度打動人心,像 加分昆布鍋物、永心鳳茶,讓人明白吃飯不只是為了飽足,而是一種被照顧的幸福。 而像茶六燒肉堂、TANG Zhan 湯棧 這類人氣名店,則用穩定的品質與熱絡的氛圍,成為許多臺中人心中「想吃肉就去那裡」的代名詞。 這十家店,構成了公益路最動人的縮影 有華麗的,也有溫柔的;有傳統的,也有創新的。 每一家都在自己的風格裡發光,讓人吃到的不只是料理,而是一種生活的溫度與節奏。 對我而言,這不僅是一場美食旅程,更是一趟關於「臺中味道」的回憶之旅。 FAQ:關於臺中公益路美食常見問題Q1:公益路哪一區的餐廳最集中? Q2:需要提前訂位嗎? 最後的話若要用一句話形容這趟美食之旅,我會說: 一笈壽司氣氛如何? 如果你也和我一樣喜歡用味蕾探索一座城市,那就把這篇公益路美食攻略收藏起來吧。一笈壽司需要訂位嗎? 無論是約會、慶生、家庭聚餐,或只是想犒賞一下辛苦的自己——這條路上永遠會有一間剛剛好的餐廳在等你。NINI 尼尼臺中店適合跨年聚餐嗎? 下一餐,不妨從這10家開始。TANG Zhan 湯棧人潮很多嗎? 打開手機、約上朋友,讓公益路成為你生活裡最容易抵達的小確幸。印月餐廳情侶來合適嗎? 如果你有私心愛店,也歡迎留言分享,印月餐廳肉質如何? 你的推薦,可能讓我下一趟美食旅程變得更精彩。一笈壽司長官聚餐合適嗎? Artistic rendering of cellulose biosynthesis with zoomed in view. Individual cellulose chains (dark brown) are synthesized by plasma membrane-bound (purple) cellulose synthase enzyme complexes (cream) and associate into elementary fibrils (light brown) that further assemble into a microfibril network, forming the main scaffold for the cell wall. Credit: Ehsan Faridi/ Inmywork Studio/ Chundawat, Lee and Lam Labs In a breakthrough with promising real-world applications, a team of Rutgers biophysicists, bioengineers, and plant biologists has captured the first live images. In a groundbreaking study, researchers at Rutgers University-New Brunswick have captured continuous, 24-hour images of cellulose synthesis, the process by which plant cell walls are built, using living plant cells. This marks the first time the dynamic process of cell-wall construction has been observed in real time, offering critical insights that could lead to the development of more resilient crops, enhanced food production, and lower-cost biofuels. Published in the journal Science Advances, the study reveals cellular activity never before documented and opens new possibilities for practical applications in areas such as advanced textiles, biodegradable plastics, improved biofuels, and medical innovations. According to the researchers, the findings also deepen fundamental understanding of how plant cell walls are formed. The discovery is the result of more than six years of interdisciplinary collaboration among three Rutgers University laboratories, drawing on expertise from the School of Arts and Sciences, the School of Engineering, and the School of Environmental and Biological Sciences. Artistic rendering of cellulose regenerating on a plant protoplast cell surface with zoomed out view. Cellulose is synthesized by plasma membrane-bound enzyme complexes (green) and assembles into a microfibril network (brown), forming the main scaffold for the cell wall. Credit: Ehsan Faridi/ Inmywork Studio/ Chundawat, Lee and Lam Labs “This work is the first direct visualization of how cellulose synthesizes and self-assembles into a dense fibril network on a plant cell surface, since Robert Hook’s first microscopic observation of cell walls in 1667,” said Sang-Hyuk Lee, an associate professor in the Department of Physics and Astronomy and an author of the study. “This study also provides entirely new insights into how simple, basic physical mechanisms such as diffusion and self-organization may lead to the formation of complex cellulose networks in cells.” Watching Cellulose Build Itself The microscope-generated video images show protoplasts – cells with their walls removed – of cabbage’s cousin, the flowering plant Arabidopsis, chaotically sprouting filaments of cellulose fibers that gradually self-assemble into a complex network on the outer cell surface. “I was very surprised by the emergence of ordered structures out of the chaotic dance of molecules when I first saw these video images,” said Lee, who also is a faculty member at the Institute for Quantitative Biomedicine. “I thought plant cellulose would be made in a lot more of an organized fashion, as depicted in classical biology textbooks.” A time-lapse video showing Arabidopsis cells generate cellulose fibrils. Credit: Lee Lab/Rutgers University Cellulose is the most abundant biopolymer – large molecules naturally produced by living organisms – on Earth. A carbohydrate that is the primary structural component of plant cell walls, cellulose is widely used in industry to make a range of products, including paper and clothing. It also is used in filtration, trapping large particles more effectively and enhancing flow, and as a thickening agent in foods such as yogurt and ice cream. “This discovery opens the door for researchers to begin dissecting the genes that could play various roles for cellulose biosynthesis in the plant,” said Eric Lam, a Distinguished Professor in the Department of Plant Biology in Rutgers School of Environmental and Biological Sciences and an author on the study. “The knowledge gained from these future studies will provide new clues for approaches to design better plants for carbon capture, improve tolerance to all kinds of environmental stresses, from drought to disease, and optimize second-generation cellulosic biofuels production.” A Personal Dream Realized The work is the culmination of a childhood dream for Shishir Chundawat, an associate professor in the Department of Chemical and Biochemical Engineering in the Rutgers School of Engineering and an author on the study. “I have always been fascinated by plants and how they capture sunlight via leaves into reduced carbon forms like cellulose that form cell walls,” Chundawat said, who plans to explore new ways to produce new, sustainable biofuels and biochemicals from diverse feedstocks like terrestrial plants and marine algae. “I remember back in middle school when I had collected many leaves of different shapes, sizes, and colors for a science class report, and being very curious about how plants produce all this myriad complexity and diversity in nature. I was inspired by that experience to delve deeper into the fundamental phenomena of biomass production and its utilization using sustainable engineering to produce valuable bioproducts for societal benefit.” Animations for young students inspired to learn more about plants are available, however, the Rutgers study shows that the process of cellulose synthesis and cell wall formation is much more complex. Credit: Rutgers University Scientists from each of the three research teams made unique and critical contributions. When conventional lab microscopes wouldn’t do, providing at best blurry images of the cell wall-building process, the team turned to an advanced super-resolution and minimally invasive technique called total internal reflection fluorescence microscopy. The approach, which captured images only of the underside surface of cells, was sensitive enough to take videos for 24 hours without bleaching and destroying the cells. Lee, a biophysicist and an expert on using cutting-edge microscopy techniques to study living systems, developed a custom microscope for the project and oversaw the imaging efforts. Chundawat led a team that pioneered a technique allowing the scientists to tag the emerging cellulose tendrils with fluorescent protein dye. Chundawat is a bioengineer and expert on protein engineering and glycosciences, the study of complex carbohydrates such as cellulose. To make the cells fluorescent and detectable by the microscope, he and his team developed a probe derived from an engineered bacterial enzyme that binds specifically to cellulose. Lam, an expert on plant genetics and biotechnology, and his team found a way to remove the cell wall of individual cells of Arabidopsis to create a “blank slate” for new cell walls to be laid down by protoplast cells. “This provided little to no background cellulose to confound our visualization and tracking of newly synthesized cellulose under optimized conditions,” Lam said. Reference: “Time-resolved tracking of cellulose biosynthesis and assembly during cell wall regeneration in live Arabidopsis protoplasts” by Hyun Huh, Dharanidaran Jayachandran, Junhong Sun, Mohammad Irfan, Eric Lam, Shishir P. S. Chundawat and Sang-Hyuk Lee, 21 March 2025, Science Advances. DOI: 10.1126/sciadv.ads6312 Other Rutgers scientists on the study included: Hyun Huh, a postdoctoral scientist with the Institute for Quantitative Biomedicine; Dharanidaran Jayachandran, a doctoral student, and Mohammad Irfan, a postdoctoral scientist in the Department of Chemical and Biochemical Engineering; and Junhong Sun, a lab technician in the Department of Plant Biology. Funding: U.S. Department of Energy, U.S. National Science Foundation An international team has mapped the genome of Zygnema algae, ancestors of terrestrial plants, uncovering key evolutionary adaptations. This research could impact future studies in plant biology and environmental sustainability. Researchers have decoded the genomic sequence of Zygnema algae, revealing insights into the evolutionary transition from aquatic to terrestrial plant life. This breakthrough enhances our understanding of plant adaptation mechanisms and offers a basis for future studies in environmental resilience and bioenergy. Plant life first emerged on land about 550 million years ago, and an international research team co-led by University of Nebraska–Lincoln computational biologist Yanbin Yin has cracked the genomic code of its humble beginnings, which made possible all other terrestrial life on Earth, including humans. The team — about 50 scientists in eight countries – has generated the first genomic sequence of four strains of Zygnema algae, the closest living relatives of land plants. Their findings shed light on the ability of plants to adjust to the environment and provide a rich basis for future research. The study was published recently in the journal Nature Genetics. Evolutionary Insights Into Terrestrial Plant Life “This is an evolutionary story,” said Yin, who led the research team with a scientist from Germany. “It answers the fundamental question of how the earliest land plants evolved from aquatic freshwater algae.” Yin’s lab in the Nebraska Food for Health Center and the Department of Food Science and Technology has a long history of studying plant cell wall carbohydrates, a major component of dietary fibers for humans and farm animals; lignocelluloses for biofuel production; and natural barriers to protect crops from pathogens and environmental stresses. Computational biologist Yanbin Yin (right) and postdoctoral researcher Xuehan Feng review algae samples. Credit: Craig Chandler/University Communication and Marketing;/University of Nebraska-Lincoln All current plant life on land burst from a one-off evolutionary event known as plant terrestrialization from ancient freshwater algae. The first land plants, known as embryophyta within the clade of streptophyta, emerged on land about 550 million years ago — their arrival fundamentally changing the surface and atmosphere of the planet. They made all other terrestrial life, including humans and animals, possible by serving as an evolutionary foundation for future flora and food for fauna. Pioneering Genomic Techniques in Algal Research The researchers worked with four algal strains from the genus Zygnema — two from a culture collection in the United States and two from Germany. Scientists combined a range of cutting-edge DNA sequencing techniques to determine the entire genome sequences of these algae. These methods enabled scientists to generate complete genomes for these organisms at the level of whole chromosomes — something that had never been done before on this group of algae. Comparing the genomes with those of other plants and algae led to the discovery of specific overabundances of cell wall enzymes, signaling genes, and environmental response factors. Unique Features of Zygnema Algae A unique feature of these algae revealed by microscopic imaging — performed at the University of Innsbruck in Austria, the Universität Hamburg in Germany and UNL’s Center for Biotechnology — is a thick and highly sticky layer of carbohydrates outside the cell walls, called the mucilage layer. Xuehuan Feng, the first author of the paper and a Husker postdoctoral research associate, developed a new and effective DNA extraction method to remove this mucilage layer for high purity and high molecular DNAs. “It is fascinating that the genetic building blocks, whose origins predate land plants by millions of years, duplicated and diversified in the ancestors of plants and algae and, in doing so, enabled the evolution of more specialized molecular machinery,” said Iker Irisarri of the Leibniz Institute for the Analysis of Biodiversity Change and co-first author of the paper. The team’s other co-leader, Jan de Vries of the University of Göttingen, said, “Not only do we present a valuable, high-quality resource for the entire plant scientific community, who can now explore these genome data, our analyses uncovered intricate connections between environmental responses.” Exploring Environmental Adaptations in Algae The four multicellular Zygnema algae belong to the class Zygnematophyceae, the closest living relatives of land plants; it is a class of freshwater and semi-terrestrial algae with more than 4,000 described species. Zygnematophyceae possess adaptations to withstand terrestrial stressors, such as desiccation, ultraviolet light, freezing, and other abiotic stresses. The key to understanding these adaptations is the genome sequences. Before this paper, genome sequences were only available for four unicellular Zygnematophyceae. Implications for Science and Society Yin said this research aligns with one of the National Science Foundation’s 10 Big Ideas — “Understanding the Rules of Life” — to address societal challenges, from clean water to climate resilience. The discovery also holds significance in applied sciences, such as bioenergy, water sustainability and carbon sequestration. “Our gene network analyses reveal co-expression of genes, especially those for cell wall synthesis and remodifications that were expanded and gained in the last common ancestor of land plants and Zygnematophyceae,” Yin said. “We shed light on the deep evolutionary roots of the mechanism for balancing environmental responses and multicellular cell growth.” The international research collaboration includes about 50 researchers from 20 research institutions in eight countries — the United States, Germany, France, Austria, Canada, China, Israel and Singapore. Other Husker researchers on the team are Chi Zhang, professor of biological sciences, and Jeffrey Mower, professor of agronomy and horticulture. Reference: “Genomes of multicellular algal sisters to land plants illuminate signaling network evolution” by Xuehuan Feng, Jinfang Zheng, Iker Irisarri, Huihui Yu, Bo Zheng, Zahin Ali, Sophie de Vries, Jean Keller, Janine M. R. Fürst-Jansen, Armin Dadras, Jaccoline M. S. Zegers, Tim P. Rieseberg, Amra Dhabalia Ashok, Tatyana Darienko, Maaike J. Bierenbroodspot, Lydia Gramzow, Romy Petroll, Fabian B. Haas, Noe Fernandez-Pozo, Orestis Nousias, Tang Li, Elisabeth Fitzek, W. Scott Grayburn, Nina Rittmeier, Charlotte Permann, Florian Rümpler, John M. Archibald, Günter Theißen, Jeffrey P. Mower, Maike Lorenz, Henrik Buschmann, Klaus von Schwartzenberg, Lori Boston, Richard D. Hayes, Chris Daum, Kerrie Barry, Igor V. Grigoriev, Xiyin Wang, Fay-Wei Li, Stefan A. Rensing, Julius Ben Ari, Noa Keren, Assaf Mosquna, Andreas Holzinger, Pierre-Marc Delaux, Chi Zhang, Jinling Huang, Marek Mutwil, Jan de Vries and Yanbin Yin, 1 May 2024, Nature Genetics. DOI: 10.1038/s41588-024-01737-3 Funding for UNL’s portion of the research came primarily from Yin’s NSF CAREER award, the Nebraska Tobacco Settlement Biomedical Research Enhancement Fund, the National Institutes of Health, and the U.S. departments of Agriculture and Energy. Funding: U.S. National Science Foundation, Nebraska Tobacco Settlement Biomedical Research Development Fund, Research & Artistry Fund of Northern Illinois University, Joint Genome Institute, U.S. Department of Agriculture, NIH/National Institutes of Health, German Research Foundation, European Research Council, Austrian Science Fund, Bill and Melinda Gates Foundation, UK Foreign, Commonwealth and Development Office, Laboratoires d’Excellence Likely the first extinction event of the 2000s in Europe, the sad history of the Pyrenean Ibex (Capra pyrenaica pyrenaica) is a powerful example of the ever-increasing species loss worldwide due to causes related to human activity. It can, however, give us valuable information on what should be done (or avoided) to halt this extinction vortex. Laña, the last surviving Pyrenean Ibex, returned as a mounted animal to Torla-Ordesa on the 6th November 2012 after its controversial cloning attempt. Her skin is now exhibited in the visitors centre of Ordesa & Monte Perdido National Park. Credit: Manolo Grasa The distribution of this subspecies of Iberian Ibex was limited to the French and Spanish Pyrenees. Its first mention in an official written document, dating back to 1767, already refers to it as extremely rare. Like many other mountain goats, it was almost hunted to extinction before its killing became prohibited in 1913. Neither the institution of a national park (Ordesa & Monte Perdido), nor a conservation project with European LIFE program funding could stop the extinction of the Pyrenean Ibex eventually officialized on January 6, 2000. But the story of this charismatic animal did not end there — a controversial cloning program was started instantly with no scientific agreement, nor support from regional environmental NGOs, claiming that de-extinction was possible even in the absence of further DNA studies. To find out more about the drivers of its extinction, an international team composed of 7 nationalities built a database of all known museum specimens and reconstructed the demographic history of the Pyrenean Ibex based on DNA evidence. Their research is published in the open-access, peer-reviewed journal Zoosystematics and Evolution. The research found that after a population expansion between 14,000 and 29,000 years ago (which is quite recent from a genetic point of view), a significant loss of genetic diversity followed between approximately 15,000 and 7,500 years BP, and continued until present. By that time, the Pyrenean Ibex also lived outside the Pyrenean mountain chain, but, gradually, its distribution was reduced to only one valley in the Ordesa National Park in the Spanish Pyrenees. The adventures of the British hunter E.N. Buxton were published in 1893. This engraving represents a hunting party in the Ordesa Valley (Spanish Pyrenees). Written sources confirm hunting of the Pyrenean Ibex from as early as the 14th century, and during the 19th and 20th century it became a common target for trophy hunters. Undoubtedly, hunting played an important role in reducing its population numbers and distribution area, but it is not possible — with the information currently available — to pinpoint it as the straw that broke the camel’s back. Infectious diseases that originate from livestock (for instance, those caused by the bluetongue virus, BTV, and sarcopses) are capable of decimating other subspecies of Iberian Ibex in extremely short periods of time. While the relative contribution of various factors remains largely unknown, it seems that hunting and diseases transmitted from other animals have been effective in drastically reducing the number of Pyrenean ibexes over the last two centuries, because they were acting on an already genetically weakened population. This low genetic diversity, combined with inbreeding depression and reduced fertility, brought the population beyond the minimum viable size — from that point onwards, extinction was inevitable. Only the French mountaineer and photographer Bernhard Clos managed to take a series of good photos of the Bucardo, as the Pyrenean Ibex is called on the Spanish side. Credit: Bernhard Clos This case study shows the importance of historical biological collections for genetic analyses of extinct species. A privately owned 140-year-old trophy preserved in Pau, France, was genotyped as part of this research, showing that private individuals may possess material of high value. As there is little knowledge of such resources, the authors call for the creation of an online public database of private collections hosting biological material for the benefit of biodiversity studies. Reference: “Demography reveals populational expansion of a recently extinct Iberian ungulate” by Giovanni Forcina, Kees Woutersen, Santiago Sánchez-Ramírez, Samer Angelone, Jean P. Crampe, Jesus M. Pérez, Paulino Fandos, José Enrique Granados and Michael J. Jowers, 1 April 2021, Zoosystematics and Evolution. DOI: 10.3897/zse.97.61854 RRG455KLJIEVEWWF |
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