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文章數：93 |
 加分100%浜中特選昆布鍋物有生日驚喜或畫盤嗎？》台中公益路吃起來｜精選10家餐廳推薦 |
| 時事評論｜政治 2026/04/22 05:10:51 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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： 一笈壽司肉質如何？ 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。加分100%浜中特選昆布鍋物單點比較好嗎？ 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 尼尼臺中店過年期間會開門嗎？ 下一餐，不妨從這10家開始。印月餐廳值得推薦嗎？ 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。TANG Zhan 湯棧尾牙拍照效果好嗎？ 如果你有私心愛店，也歡迎留言分享，三希樓真的有那麼好吃嗎？ 你的推薦，可能讓我下一趟美食旅程變得更精彩。加分100%浜中特選昆布鍋物家庭過節聚會適合嗎？ This photo represents Cuesta et al.’s demonstration that cocaine exposure increases norepinephrine in the gut facilitating γ-Proteobacteria colonization. This gut microbiota shift toward γ-Proteobacteria leads to a depletion of glycine from the host, which, in turn, facilitates cocaine-induced addiction-like behaviors in mice. Credit: Florencia Cerchiara Common gut bacteria can enhance the effects of cocaine in mice, according to a report published recently in the journal Cell Host & Microbe. This study demonstrates how cocaine usage promotes the growth of gut bacteria, which in turn consume glycine, a chemical that contributes to normal brain function. As levels of glycine become depleted, mice exhibit a stronger response to cocaine with behavior abnormalities, such as substantially increasing drug-induced locomotion and seeking behaviors. In addition, by supplementing glycine back systemically or using a genetically modified bacteria that cannot use glycine, the response of the mice to cocaine falls back to normal levels. This demonstrates that this simple amino acid can act as an addiction-like behavior mediator in animal models. “I was interested in the gut-brain axis, and I found it very new and exciting,” says first author Santiago Cuesta a neuroscientist at the University of Wisconsin School of Medicine and Public Health. Mechanism of Bacterial Growth in Response to Cocaine Cuesta and colleagues found that when cocaine enters the gut of the mice, it triggers the activation of the QseC protein that supports the growth of γ-proteobacteria, such as E. coli. Fueled by glycine, these bacteria outcompete the normal gut bacteria that already exist in our digestive tracks, taking up most of the space and resources. “The gut bacteria are consuming all of the glycine and the levels are decreasing systemically and in the brain,” says senior author Vanessa Sperandio, a microbiologist from the University of Wisconsin School of Medicine and Public Health. “It seems changing glycine overall is impacting the glutamatergic synapses that make the animals more prone to develop addiction.” “Usually, for neuroscience behaviors, people are not thinking about controlling the microbiota, and microbiota studies usually don’t measure behaviors, but here we show they’re connected” says Cuesta. “Our microbiome can actually modulate psychiatric or brain-related behaviors.” “I think the bridging of these communities is what’s going to move the field forward, advancing beyond correlations towards causations for the different types of psychiatric disorders,” says Sperandio. Reference: “Gut colonization by Proteobacteria alters host metabolism and modulates cocaine neurobehavioral responses” by Santiago Cuesta, Paula Burdisso, Amir Segev, Saïd Kourrich and Vanessa Sperandio, 1 November 2022, Cell Host & Microbe. DOI: 10.1016/j.chom.2022.09.014 Financial support was provided by the National Institutes of Health (NIH). A human embryo in the lab at 9 days after fertilization. The hypoblast (a group of cells outside the main embryo) sends a message to the embryo that initiates the development of the head-to-tail body axis. Using immunofluorescence analysis, the hypoblast is shown in green – these cells are asymmetrically distributed. A cavity is visible at the center of the embryo marked by secretion of podocalyxin (red) and accumulation of F-actin (white). Nuclei are stained blue. The second week of gestation represents a critical stage of embryo development, or embryogenesis. Failure of development during this time is one of the major causes of early pregnancy loss. Using surplus human embryos voluntarily donated from in vitro fertilization clinics in the UK, scientists have extensively studied the pre-implantation period in the laboratory, the period before a developing embryo would implant into the mother’s uterus on the seventh day after fertilization. Very little is known about the development of the human embryo after implantation occurs, however, as the embryo becomes inaccessible for study. In 2016, Magdalena Zernicka-Goetz, now Caltech’s Bren Professor of Biology and Biological Engineering, and her team at the University of Cambridge developed a technique to culture human embryos outside the body of the mother beyond implantation. This enabled human embryos to be studied up until day 14 of development for the first time. In a new study, researchers in the Zernicka-Goetz lab examined what happens at the molecular level during this early stage of embryogenesis. Their findings provide the first evidence that a disc-shaped group of cells located outside of the embryo known as the hypoblast sends a message to the embryo that initiates the formation of the head-to-tail body axis, which gives the previously symmetrical embryo two distinct ends, a head and a “tail.” The findings reveal that the molecular signals involved in the formation of the body axis in human embryos are similar to those in other mammals, despite significant differences in the positioning and organization of the cells of the embryos of different species. The results are described in a paper appearing in the journal Nature Communications. “We have revealed the patterns of gene expression in the developing embryo just after it implants in the womb, which reflect the multiple conversations going on between different cell types as the embryo develops through these early stages,” says Zernicka-Goetz. “We were looking for the genetic conversations that will allow the head to start developing in the embryo and found that these were initiated by cells in the hypoblast, which would not normally contribute to building the body itself. They send the message to the adjoining embryo cells, which respond by saying ‘OK, now we’ll set ourselves aside to develop into the head end.'” The study identified these gene conversations in the developing embryo by sequencing the code in the thousands of messenger RNA (mRNA) molecules made by individual cells; mRNA molecules are translated by cellular machinery into the protein molecules that perform vital functions and give cells their structure. This allowed the researchers to capture changes in the evolving molecular profile of developing embryos after their implantation in the womb and revealed the embryonic cells’ progressive loss of pluripotency (the ability to give rise to any type of cell) as they developed into the distinct cell types that eventually give rise to all the organs of the human body. “Our goal has always been to enable insight to very early human embryo development in a dish to understand how our lives start. By combining our new technology of culturing human embryos with advanced sequencing methods, we have delved deeper into the key changes that take place at this incredible stage of human development when the embryo becomes remodeled to undertake its critical decisions at a time when so many pregnancies fail,” says Zernicka-Goetz. For more on this research, see Key Molecular Events in the Developing Human Embryo Identified. Reference: “A single cell characterisation of human embryogenesis identifies pluripotency transitions and putative anterior hypoblast centre” by Matteo A. Molè, Tim H. H. Coorens, Marta N. Shahbazi, Antonia Weberling, Bailey A. T. Weatherbee, Carlos W. Gantner, Carmen Sancho-Serra, Lucy Richardson, Abbie Drinkwater, Najma Syed, Stephanie Engley, Philip Snell, Leila Christie, Kay Elder, Alison Campbell, Simon Fishel, Sam Behjati, Roser Vento-Tormo and Magdalena Zernicka-Goetz, 17 June 2021, Nature Communications. DOI: 10.1038/s41467-021-23758-w Matteo Molè of the University of Cambridge is the study’s first author. In addition to Zernicka-Goetz, additional co-authors are Tim Coorens and Carmen Sancho-Serra of the Wellcome Sanger Institute; Marta Shahbazi, Antonia Weberling, Bailey Weatherbee, and Carlos Gantner in the Zernicka-Goetz laboratory of the University of Cambridge; embryologists Lucy Richardson, Abbie Drinkwater, Najma Syed, and Stephanie Engley of the Herts & Essex Fertility Centre at Bishops College; Philip Snell, Leila Christie, and Kay Elder of Bourn Hall in Cambridge, UK; Alison Campbell of CARE Fertility group in Nottingham, UK; Simon Fishel of CARE Fertility group and Liverpool John Moores University in Liverpool, UK; and finally, the collaborators responsible for analyses of sequencing data: Sam Behjati of the Wellcome Sanger Institute and the University of Cambridge; and Roser Vento-Tormo of the Wellcome Sanger Institute. Funding was provided by European Molecular Biology Organisation, the UKRI Medical Research Council, the Gates Cambridge Trust, the Wellcome Trust, and in the U.S. by Open Philanthropy (Silicon Valley), and the Curci and Weston Havens foundations. Researchers have compared the genomes of woolly mammoths and modern-day elephants to identify the unique characteristics of woolly mammoths. In a study published in Current Biology, the team found that traits like woolly coats and large fat deposits were already genetically encoded in the earliest woolly mammoths, but became more defined throughout the species’ 700,000+ year existence. They also discovered a gene with several mutations that may have been responsible for the woolly mammoth’s small ears. The research gives insights into the evolution of woolly mammoths and their adaptations to cold environments. A study comparing woolly mammoth genomes with modern-day elephants revealed key traits that defined the species, such as woolly coats, large fat deposits, and small ears. These features were already present in early woolly mammoths and became more defined throughout their 700,000+ year existence. A team of researchers compared the genomes of woolly mammoths with modern day elephants to find out what made woolly mammoths unique, both as individuals and as a species. The investigators report today (April 7) in the journal Current Biology that many of the woolly mammoth’s trademark features—including their woolly coats and large fat deposits—were already genetically encoded in the earliest woolly mammoths, but these and other traits became more defined over the species’ 700,000+ year existence. They also identified a gene with several mutations that may have been responsible for the woolly mammoth’s miniscule ears. “We wanted to know what makes a mammoth a woolly mammoth,” says paleogeneticist and first author David Díez-del-Molino of the Centre for Palaeogenetics in Stockholm. “Woolly mammoths have some very characteristic morphological features, like their thick fur and small ears, that you obviously expect based on what frozen specimens look like, but there are also many other adaptations like fat metabolism and cold perception that are not so evident because they’re at the molecular level.” This is a photo of a woolly mammoth tusk, from which the authors sequenced the entire genome. The tusk was discovered in northeastern Siberia in 2015 and has been radiocarbon dated to ca 18,000 years before present. Credit: Love Dalén Ancient Adaptations to the Cold To identify genes that were “highly evolved” in woolly mammoths— meaning they had accrued a large number of mutations—the team compared the genomes of 23 Siberian woolly mammoth with 28 modern-day Asian and African elephant genomes. Twenty-two of these woolly mammoths were relatively modern, having lived within the past 100,000 years, and sixteen of the genomes had not been previously sequenced. The twenty-third woolly mammoth genome belonged to one of the oldest known woolly mammoths, Chukochya, who lived approximately 700,000 years ago. “Having the Chukochya genome allowed us to identify a number of genes that evolved during the lifespan of the woolly mammoth as a species,” says senior author Love Dalén, professor of evolutionary genomics at the Centre for Palaeogenetics in Stockholm. “This allows us to study evolution in real time, and we can say these specific mutations are unique to woolly mammoths, and they didn’t exist in its ancestors.” This is a photo of study co-author Love Dalén with the Yuka mammoth, whose genome was included in the analyses. Credit: Ian Watts Convergent Evolution with Other Arctic Mammals Not surprisingly, many genes that were adaptive for woolly mammoths are related to living in cold environments. Some of these genes are shared by unrelated modern-day Arctic mammals. “We found some highly evolved genes related to fat metabolism and storage that are also found in other Arctic species like reindeer and polar bears, which means there’s probably convergent evolution for these genes in cold-adapted mammals,” says Díez-del-Molino. While previous studies have looked at the genomes of one or two woolly mammoths, this is the first comparison of a large number of mammoth genomes. This large sample size enabled the team to identify genes that were common among all woolly mammoths, and therefore likely adaptive, as opposed to genetic mutations that might only have been present in a single individual. “We found that some of the genes that were previously thought to be special for woolly mammoths are actually variable between mammoths, which means they probably weren’t as important,” says Díez-del-Molino. This is a photo of study co-author Marianne Dehasque working in the ancient DNA lab at the Centre for Palaeogenetics in Stockholm. Credit: Jens Lasthein Evolutionary Milestones in Woolly Mammoths Overall, the 700,000-year-old Chukochya genome shared approximately 91.7% of the mutations that caused protein-coding changes in the more modern woolly mammoths. This means that many of the woolly mammoth’s defining traits—including thick fur, fat metabolism, and cold-perception abilities—were probably already present when the woolly mammoth first diverged from its ancestor, the steppe mammoth. However, these traits developed further in Chukochya’s descendants. “The very earliest woolly mammoths weren’t fully evolved,” says Dalén “They possibly had larger ears, and their wool was different—perhaps less insulating and fluffy compared to later woolly mammoths.” More modern woolly mammoths also had several immune mutations in T cell antigens that were not seen in their ancestor. The authors speculate that these mutations may have conferred enhanced cell-mediated immunity in response to emerging viral pathogens. Working with ancient mammoth DNA comes with a slew of hurdles. “Every step of the way, things are a bit more difficult, from fieldwork, to lab work, to bioinformatics,” says Díez-del-Molino. “Apart from the field work, where we have to battle both polar bears and mosquitos, another aspect that makes this much more difficult is that you have to work in an ancient DNA laboratory, and that means that you have to dress up in this full-body suit with a hood and face mask and visor and double gloves, so doing the lab work is rather uncomfortable to put it mildly,” says Dalén. “I would like to highlight Marianne Dehasque, the second author of this paper, who did the herculean effort of performing lab work on most of these samples.” All the mammoths whose genomes were included in this study were collected in Siberia, but the researchers hope to branch out and compare North American woolly mammoths in the future. “We showed a couple of years ago that there was gene flow between woolly mammoths and the ancestors of Colombian mammoths, so that’s something that we will need to account for because North American woolly mammoths might have been carrying non-woolly mammoth genes as well,” says Dalén. Reference: “Genomics of adaptive evolution in the woolly mammoth” by David Díez-del-Molino, Marianne Dehasque, J. Camilo Chacón-Duque, Patrícia Pečnerová, Alexei Tikhonov, Albert Protopopov, Valeri Plotnikov, Foteini Kanellidou, Pavel Nikolskiy, Peter Mortensen, Gleb K. Danilov, Sergey Vartanyan, M. Thomas P. Gilbert, Adrian M. Lister, Peter D. Heintzman, Tom van der Valk and Love Dalén, 7 April 2023, Current Biology. DOI: 10.1016/j.cub.2023.03.084 This research was supported by the Swedish Research Council, FORMAS, the Carl Tryggers Foundation, the SciLifeLab, the Wallenberg Data Driven Life Science Program, the Wallenberg Academy, and the Russian Science Foundation. RRG455KLJIEVEWWF |
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