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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 官網:http://www.marihuana.com.tw/yakiniku/index.html 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: 三希樓適合多人分享嗎? 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。三希樓小孩適合去嗎? 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。印月餐廳包廂適合尾牙嗎? 下一餐,不妨從這10家開始。加分100%浜中特選昆布鍋物節慶時段會不會太難訂位? 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。NINI 尼尼臺中店春酒場面夠體面嗎? 如果你有私心愛店,也歡迎留言分享,NINI 尼尼臺中店過年期間會開門嗎? 你的推薦,可能讓我下一趟美食旅程變得更精彩。一笈壽司平日好排隊嗎? Researchers have found that sound can influence cells directly, including suppressing fat cell development and activating certain genes – suggesting a future where acoustic therapy could aid medicine. Credit: SciTechDaily.com Sound doesn’t just enter your ears – it may actually talk to your cells. New research out of Kyoto University shows that acoustic waves, even those in the audible range, can alter cellular behavior. Using specially designed equipment, scientists found that sound can suppress the formation of fat cells and influence gene activity. These surprising findings open the door to non-invasive treatments that harness sound to affect our bodies at the cellular level. Sound You Can Feel You’ve probably felt it—standing near a plane as it takes off or beside massive speakers at a concert – when sound becomes so powerful it seems to vibrate through your entire body. In those moments, you’re not just hearing the sound with your ears – your whole body feels it. And as new research suggests, your cells might actually be responding to it, too. At its core, sound is made up of mechanical waves – compressions and rarefactions – that travel through substances like air, water, or tissue. It’s a fundamental feature of the physical world and a crucial source of information for living organisms. But scientists are only beginning to understand how sound might also influence the body at the cellular level. The fundamental relationship between life and sound. Credit: KyotoU/Kumeta lab Investigating Sound’s Effects on Cells Building on earlier work from 2018, researchers at Kyoto University are exploring how cells respond to sound, inspired by advances in mechanobiology and studies of body-conducted sound—the way vibrations move through tissues. Their findings suggest that the pressure from sound waves may be enough to trigger responses inside cells themselves. “To investigate the effect of sound on cellular activities, we designed a system to bathe cultured cells in acoustic waves,” says corresponding author Masahiro Kumeta. How the Experiment Worked The team first attached a vibration transducer upside-down on a shelf. Then using a digital audio player connected to an amplifier, they sent sound signals through the transducer to a diaphragm attached to a cell culture dish. This allowed the researchers to emit acoustic pressure within the range of physiological sound to cultured cells. Following this experiment, the researchers analyzed the effect of sound on cells using RNA-sequencing, microscopy, and other methods. Their results revealed cell-level responses to the audible range of acoustic stimulation. Suppressing Fat Cell Formation In particular, the team noticed the significant effect of sound in suppressing adipocyte differentiation, the process by which preadipocytes transform into fat cells, unveiling the possibility of utilizing acoustics to control cell and tissue states. “Since sound is non-material, acoustic stimulation is a tool that is non-invasive, safe, and immediate, and will likely benefit medicine and healthcare,” says Kumeta. The research team also identified about 190 sound-sensitive genes, noted the effect of sound in controlling cell adhesion activity, and observed the subcellular mechanism through which sound signals are transmitted. Rethinking Sound Perception In addition to providing compelling evidence of the perception of sound at the cell level, this study also challenges the traditional concept of sound perception by living beings, which is that it is mediated by receptive organs like the brain. It turns out that your cells respond to sounds, too. Reference: “Acoustic modulation of mechanosensitive genes and adipocyte differentiation” by Masahiro Kumeta, Makoto Otani, Masahiro Toyoda and Shige H. Yoshimura, 16 April 2025, Communications Biology. DOI: 10.1038/s42003-025-07969-1 Salk scientists developed a technique of using sound waves to control brain cells, dubbed sonogenetics, to selectively and noninvasively turn on groups of neurons. It was first used on worms and now has been used on mammalian cells. This technique could be a boon to science and medicine. Credit: Courtesy of the Salk Institute for Biological Studies Salk researchers pinpoint a sound-sensitive mammalian protein that lets them activate brain, heart or other cells with ultrasound. Salk scientists have engineered mammalian cells to be activated using ultrasound. The method, which the team used to activate human cells in a dish and brain cells inside living mice, paves the way toward non-invasive versions of deep brain stimulation, pacemakers and insulin pumps. The findings will be published in Nature Communications today (February 9, 2022). “Going wireless is the future for just about everything,” says senior author Sreekanth Chalasani, an associate professor in Salk’s Molecular Neurobiology Laboratory. “We already know that ultrasound is safe, and that it can go through bone, muscle, and other tissues, making it the ultimate tool for manipulating cells deep in the body.” Challenges and Discoveries in Protein Screening About a decade ago, Chalasani pioneered the idea of using ultrasonic waves to stimulate specific groups of genetically marked cells, and coined the term “sonogenetics” to describe it. In 2015, his group showed that, in the roundworm Caenorhabditis elegans, a protein called TRP-4 makes cells sensitive to low-frequency ultrasound. When the researchers added TRP-4 to C. elegans neurons that didn’t usually have it, they could activate these cells with a burst of ultrasound—the same sound waves used in medical sonograms. Neurons (magenta) in the mouse brain. The Chalasani lab made specific neurons express TRPA1 (white), so they can be activated by ultrasound. Credit: Salk Institute When the researchers tried adding TRP-4 to mammalian cells, however, the protein was not able to make the cells respond to ultrasound. A few mammalian proteins were reported to be ultrasound-sensitive, but none seemed ideal for clinical use. So Chalasani and his colleagues set out to search for a new mammalian protein that made cells highly ultrasound sensitive at 7 MHz, considered an optimal and safe frequency. “Our approach was different than previous screens because we set out to look for ultrasound-sensitive channels in a comprehensive way,” says Yusuf Tufail, a former project scientist at Salk and a co-first author of the new paper. TRPA1 Protein The researchers added hundreds of different proteins, one at a time, to a common human research cell line (HEK), which does not usually respond to ultrasound. Then, they put each cell culture under a setup that let them monitor changes to the cells upon ultrasound stimulation. Top from left: Sreekanth Chalasani and Corinne Lee-Kubli. Bottom from left: Marc Duque and Yusuf Tufail. Credit: Top: Salk Institute. Bottom from left: Marc Duque and Yusuf Tufail After screening proteins for more than a year, and working their way through nearly 300 candidates, the scientists finally found one that made the HEK cells sensitive to the 7 MHz ultrasound frequency. TRPA1, a channel protein, was known to let cells respond to the presence of noxious compounds and to activate a range of cells in the human body, including brain and heart cells. But Chalasani’s team discovered that the channel also opened in response to ultrasound in HEK cells. “We were really surprised,” says co-first author of the paper Marc Duque, a Salk exchange student. “TRPA1 has been well-studied in the literature but hasn’t been described as a classical mechanosensitive protein that you’d expect to respond to ultrasound.” To test whether the channel could activate other cell types in response to ultrasound, the team used a gene therapy approach to add the genes for human TRPA1 to a specific group of neurons in the brains of living mice. When they then administered ultrasound to the mice, only the neurons with the TRPA1 genes were activated. Expanding Sonogenetics Applications Beyond the Lab Clinicians treating conditions including Parkinson’s disease and epilepsy currently use deep brain stimulation, which involves surgically implanting electrodes in the brain, to activate certain subsets of neurons. Chalasani says that sonogenetics could one day replace this approach—the next step would be developing a gene therapy delivery method that can cross the blood-brain barrier, something that is already being studied. Perhaps sooner, he says, sonogenetics could be used to activate cells in the heart, as a kind of pacemaker that requires no implantation. “Gene delivery techniques already exist for getting a new gene—such as TRPA1—into the human heart,” Chalasani says. “If we can then use an external ultrasound device to activate those cells, that could really revolutionize pacemakers.” For now, his team is carrying out more basic work on exactly how TRPA1 senses ultrasound. “In order to make this finding more useful for future research and clinical applications, we hope to determine exactly what parts of TRPA1 contribute to its ultrasound sensitivity and tweak them to enhance this sensitivity,” says Corinne Lee-Kubli, a co-first author of the paper and former postdoctoral fellow at Salk. They also plan to carry out another screen for ultrasound sensitive proteins—this time looking for proteins that can inhibit, or shut off, a cell’s activity in response to ultrasound. Reference: “Sonogenetic control of mammalian cells using exogenous Transient Receptor Potential A1 channels” by Marc Duque, Corinne A. Lee-Kubli, Yusuf Tufail, Uri Magaram, Janki Patel, Ahana Chakraborty, Jose Mendoza Lopez, Eric Edsinger, Aditya Vasan, Rani Shiao, Connor Weiss, James Friend and Sreekanth H. Chalasani, 9 February 2022, Nature Communications. DOI: 10.1038/s41467-022-28205-y The other authors of the paper were Uri Magaram, Janki Patel, Ahana Chakraborty, Jose Mendoza Lopez, Eric Edsinger, Rani Shiao and Connor Weiss of Salk; and Aditya Vasan and James Friend of UC San Diego. The work was supported by the National Institutes of Health (R01MH111534, R01NS115591), Brain Research Foundation, Kavli Institute of Brain and Mind, Life Sciences Research Foundation, W.M. Keck Foundation (SERF), and the Waitt Advanced Biophotonics and GT3 Cores (which receive funding through NCI CCSG P30014195 and NINDSR24). Image of a Melanocetus johnsonii anglerfish, also known as the black sea devil. Credit: Kory Evans/Rice University A new study on anglerfish evolution reveals how these deep-sea creatures adapted to the extreme bathypelagic zone, achieving unexpected diversity despite limited resources. Using genetic and morphological analyses, researchers uncovered adaptive radiation and evolutionary innovations, offering insights into biodiversity in extreme habitats. A groundbreaking study from Rice University sheds light on the extraordinary evolution of anglerfish, deep-sea dwellers whose bizarre adaptations have long captivated both scientists and the public. Published in Nature Ecology & Evolution, the research reveals how these enigmatic creatures defied the odds to diversify in the harsh, resource-scarce environment of the bathypelagic zone, an open-ocean region extending from 3,300 to 13,000 feet below the surface. Led by a team of biologists including Rice’s Kory Evans and his former undergraduate student Rose Faucher, the study analyzed the evolutionary journey of anglerfish (Lophiiformes) as they transitioned from seafloor habitats to the open waters of the deep sea. Through cutting-edge genetic analysis and 3D imaging of museum specimens, the researchers reconstructed the evolutionary tree of anglerfish and identified the morphological innovations that allowed these animals to thrive in an environment considered among the most challenging on Earth. Evolutionary Journey of Anglerfish Anglerfish are best known for their bioluminescent lures, which dangle from their foreheads to attract prey in the perpetual darkness of the deep sea. However, their evolutionary story goes far beyond this striking adaptation. The study reveals that the deep-sea pelagic anglerfish (ceratioids) originated from a benthic or seafloor-dwelling ancestor. This ancestor lived on the continental slope before transitioning to the open waters of the bathypelagic zone in a transition that set the stage for rapid evolutionary change. The ceratioids then developed features such as larger jaws, smaller eyes and laterally compressed bodies — adaptations tailored to life in an environment with limited food and no sunlight. Despite these directional trends, however, ceratioids also displayed remarkable variability in body shapes from the archetypical globose anglerfish to elongated forms like the “wolftrap” phenotype, which features a jaw structure resembling a trap. This finding is the most surprising of the study, for the bathypelagic zone did not constrain evolution as expected despite its apparent lack of ecological diversity. Instead, anglerfish achieved high levels of phenotypic disparity, greater than their benthic relatives in both shallow and deep waters. This suggests rather than being limited by the environmental challenges of the deep sea, ceratioids explored new evolutionary possibilities, diversifying their body forms and hunting strategies. Adaptive Radiation in the Deep Sea “With their unique traits like bioluminescent lures and large oral gapes, deep-sea anglerfish may be one of the few documented examples of adaptive radiation in the resource-limited bathypelagic zone,” said Evans, a co-corresponding author on the paper and assistant professor of biosciences. “These traits likely gave anglerfish an edge in exploiting scarce resources and navigating the extreme conditions of their environment, although we don’t have strong evidence directly linking this diversity to this kind of resource specialization.” Evans noted that the research leaves room for the possibility that nonadaptive processes, such as relaxed selection or random mutations, could also have contributed to the observed variability. The researchers also compared anglerfish clades across different habitats and found more unexpected results. Coastal species like frogfish, which live in diverse and productive coral reef environments, exhibited much lower rates of evolutionary change than their counterparts in the deep sea. “The idea that a resource-poor, homogenous environment — like being surrounded on all sides by nothing but water — would produce diverse body and skull plans is really counterintuitive in this field,” said Faucher, who was co-first author of the paper along with Elizabeth Christina Miller, a postdoctoral fellow at University of California, Irvine. “When fish have different features to interact with, like corals and plants in shallow water or sand and rocks on the seafloor, that’s when we would expect fish to have a lot of variation in shape. Instead, we’re seeing it in these deep-sea fish who have nothing but water to interact with.” The researchers used a combination of advanced methods to conduct this study. They constructed a phylogeny of anglerfish using data from 1,092 genetic loci across 132 species, representing approximately 38% of described species, complemented by fossil calibrations and genomic data to estimate divergence times and ancestral habitats. Morphological data were collected from museum specimens, including linear body measurements and 3D skull shape analyses via micro-CT scans. To evaluate evolutionary trends, the researchers applied phylogenetic comparative methods to assess phenotypic and lineage diversification, while disparity analyses quantified the extent of morphological variation across anglerfish clades and habitats. They then employed Bayesian models to reconstruct ancestral habitats, revealing that ceratioids originated from benthic ancestors before transitioning to the pelagic zone. Finally, principal component analyses visualized how anglerfish occupied different regions of phenotypic space, shedding light on evolutionary trends in body, skull, and jaw shapes. Broader Implications of the Study “Anglerfish are a perfect example of how life can innovate under extreme constraints,” said Evans. “This work not only enhances our understanding of deep-sea biodiversity but also illustrates the resilience and creativity of evolution.” This study’s significance extends beyond the evolutionary history of anglerfish. It provides valuable insights into how life adapts to extreme environments. The deep sea is one of the least understood ecosystems on Earth, yet it plays a critical role in global biodiversity and the planet’s carbon cycle. Understanding how organisms like anglerfish thrive in such conditions helps scientists predict how life might respond to environmental changes, including those caused by climate change. Moreover, the study touches on broader questions of macroevolution: how new species arise, adapt, and diversify. By showing that even resource-poor environments can foster significant evolutionary radiation, the research challenges conventional wisdom and opens new avenues for studying evolution in extreme habitats. Reference: “Reduced evolutionary constraint accompanies ongoing radiation in deep-sea anglerfishes” by Elizabeth Christina Miller, Rose Faucher, Pamela B. Hart, Melissa Rincón-Sandoval, Aintzane Santaquiteria, William T. White, Carole C. Baldwin, Masaki Miya, Ricardo Betancur-R, Luke Tornabene, Kory Evans and Dahiana Arcila, 27 November 2024, Nature Ecology & Evolution. DOI: 10.1038/s41559-024-02586-3 This research was supported in part by FishLife (National Science Foundation DEB-1541554 and NSF DEB-2144325); NSF Postdoctoral Fellowships (DBI-1906574 and DBI-2109469); NSF DEB-2237278; NSF DEB-2144325 and NSF DEB-2015404. 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