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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 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: NINI 尼尼臺中店再訪意願高嗎? 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。TANG Zhan 湯棧適合多人分享嗎? 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。TANG Zhan 湯棧整體值得推薦嗎? 下一餐,不妨從這10家開始。三希樓CP 值高嗎? 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。印月餐廳適合約會嗎? 如果你有私心愛店,也歡迎留言分享,加分100%浜中特選昆布鍋物適合辦部門小聚嗎? 你的推薦,可能讓我下一趟美食旅程變得更精彩。TANG Zhan 湯棧人潮很多嗎? An illustration of viruses called phages infecting a bacterial cell. Researchers have developed a modified strain of Escherichia coli bacteria that is resistant to natural viral infections and has a low risk of escaping into the environment. This breakthrough in genetic engineering and synthetic biology is expected to decrease the risk of viral contamination in the production of medicines and other substances, such as biofuels. Currently, viral infections in bacteria can cause a halt in production, endanger drug safety, and result in high financial costs. Credit: Behnoush Hajian Researchers create virus-resistant, safely restrained E. coli for medical, industrial applications. In a step forward for genetic engineering and synthetic biology, researchers have modified a strain of Escherichia coli bacteria to be immune to natural viral infections while also minimizing the potential for the bacteria or their modified genes to escape into the wild. The work promises to reduce the threats of viral contamination when harnessing bacteria to produce medicines such as insulin as well as other useful substances, such as biofuels. Currently, viruses that infect vats of bacteria can halt production, compromise drug safety, and cost millions of dollars. Results are published today, March 15, in the journal Nature. Learn more about how codon deletion works in this video about a related project from the Church lab in 2016. Credit: Rick Groleau “We believe we have developed the first technology to design an organism that can’t be infected by any known virus,” said the study’s first author, Akos Nyerges, research fellow in genetics in the lab of George Church in the Blavatnik Institute at Harvard Medical School and the Wyss Institute for Biologically Inspired Engineering. “We can’t say it’s fully virus-resistant, but so far, based on extensive laboratory experiments and computational analysis, we haven’t found a virus that can break it,” Nyerges said. The work also provides the first built-in safety measure that prevents modified genetic material from being incorporated into natural cells, he said. The authors said their work suggests a general method for making any organism immune to viruses and preventing gene flow into and out of genetically modified organisms (GMOs). Such biocontainment strategies are of increasing interest as groups explore the safe deployment of GMOs for growing crops, reducing disease spread, generating biofuels, and removing pollutants from open environments. Building on What Came Before The findings build on earlier efforts by genetic engineers to achieve a helpful, safe, virus-resistant bacterium. In 2022, a group from the University of Cambridge thought they’d made an E. coli strain immune to viruses. But then Nyerges teamed up with research fellow Siân Owen and graduate student Eleanor Rand in the lab of co-author Michael Baym, assistant professor of biomedical informatics in the Blavatnik Institute at HMS. When they sampled local sites rife with E. coli, including chicken sheds, rat nests, sewage, and the Muddy River down the street from the HMS campus, they discovered viruses that could still infect the modified bacteria. Discovering that the bacteria weren’t fully virus-resistant “was a bummer,” Nyerges said. The initial method had involved genetically reprogramming E. coli to make all their life-sustaining proteins from 61 sets of genetic building blocks, or codons, instead of the naturally occurring 64. The idea was that viruses wouldn’t be able to hijack the cells because they couldn’t replicate without the missing codons. The HMS team, however, figured out that deleting codons wasn’t enough. Some viruses were bringing in their own equipment to get around the missing pieces. So, Nyerges and colleagues developed a way to change what those codons tell an organism to make — something scientists hadn’t done to this extent in living cells. Lost in Translation The key lay in transfer RNAs, or tRNAs. Each tRNA’s role is to recognize a specific codon and add the corresponding amino acid to a protein that’s being built. For instance, the codon TCG tells its matching tRNA to attach the amino acid serine. In this case, the Cambridge team had deleted TCG along with sister codon TCA, which also calls for serine. The team had also removed the corresponding tRNAs. The HMS team now added new, trickster tRNAs in their place. When these tRNAs see TCG or TCA, they add leucine instead of serine. “Leucine is about as different from serine as you can get, physically and chemically,” said Nyerges. When an invading virus injects its own genetic code full of TCG and TCA and tries to tell the E. coli to make viral proteins, these tRNAs mess up the virus’s instructions. Inserting the wrong amino acids results in misfolded, nonfunctional viral proteins. That means the virus can’t replicate and go on to infect more cells. Viruses, however, also come equipped with their own tRNAs. These can still accurately turn TCG and TCA into serine. But Nyerges and colleagues provided evidence that the trickster tRNAs they introduced are so good at their jobs that they overpower their viral counterparts. “It was very challenging and a big achievement to demonstrate that it’s possible to swap an organism’s genetic code,” said Nyerges, “and that it only works if we do it this way.” The work may have cleared the last hurdle in rendering a bacterium immune to all viruses, although there’s still a chance something will appear that can break the protection, the authors said. The team takes confidence in knowing that overcoming the swapped codons would require a virus to develop dozens of specific mutations at the same time. “That’s very, very unlikely for natural evolution,” Nyerges said. Safety Measures The work incorporates two separate safeguards. The first protects against horizontal gene transfer, a constantly occurring phenomenon in which snippets of genetic code and their accompanying traits, such as antibiotic resistance, get transferred from one organism to another. Nyerges and colleagues short-circuited this outcome by making substitutions throughout genes in the modified E. coli cells so that all codons that call for leucine got replaced with TCG or TCA — the codons that in an unmodified organism would call for serine. The bacteria still correctly made leucine in those places because of their trickster tRNAs. If another organism were to incorporate any of the modified snippets into its own genome, though, the organism’s natural tRNAs would interpret TCG and TCA as serine and end up with junk proteins that don’t convey any evolutionary advantage. “The genetic information will be gibberish,” said Nyerges. Similarly, the team showed that if one of the E. coli’s trickster tRNAs gets transferred to another organism, its misreading of serine codons as leucine codons damages or kills the cell, preventing further spread. “Any modified tRNAs that escape won’t get far because they are toxic to natural organisms,” said Nyerges. The work represents the first technology that prevents horizontal gene transfer from genetically modified organisms into natural organisms, he said. For the second fail-safe, the team designed the bacteria themselves to be unable to live outside a controlled environment. The team used an existing technology developed by the Church lab to make the E. coli reliant on a lab-made amino acid that doesn’t exist in the wild. Workers cultivating these E. coli to produce insulin, for instance, would feed them the unnatural amino acid. But if any bacteria escaped, they would lose access to that amino acid and die. Therefore, no humans or other creatures are at risk of getting infected by “superbacteria,” Nyerges emphasized. Nyerges looks forward to exploring codon reprogramming as a tool for coaxing bacteria to produce medically useful synthetic materials that would otherwise require expensive chemistry. Other doors have yet to be opened. “Who knows what else?” he mused. “We’ve just started exploring.” Reference: “A swapped genetic code prevents viral infections and gene transfer” by Akos Nyerges, Svenja Vinke, Regan Flynn, Siân V. Owen, Eleanor A. Rand, Bogdan Budnik, Eric Keen, Kamesh Narasimhan, Jorge A. Marchand, Maximilien Baas-Thomas, Min Liu, Kangming Chen, Anush Chiappino-Pepe, Fangxiang Hu, Michael Baym and George M. Church, 15 March 2023, Nature. DOI: 10.1038/s41586-023-05824-z Church is the Robert Winthrop Professor of Genetics in the Blavatnik Institute at HMS. Additional authors are Svenja Vinke, Regan Flynn, Kamesh Narasimhan, Jorge Marchand, Maximilien Baas-Thomas, and Anush Chiappino-Pepe of HMS; Bogdan Budnik of the Wyss Institute; Eric Keen of Washington University School of Medicine; and Min Liu, Kangming Chen, and Fangxiang Hu of GenScript USA Inc. HMS has filed a provisional patent application related to this work on which Nyerges, Vinke, and Church are listed as inventors. GenScript had no role in designing or executing experiments. Church is a founder of the following companies in which he has related financial interests: GRO Biosciences, EnEvolv, and 64x Bio. Funding for this research was provided by the U.S. Department of Energy (grant DE-FG02-02ER63445) and the National Science Foundation (award number 2123243). Nyerges was supported by an EMBO LTF 160-2019 long-term fellowship. Arabidopsis plants were used to develop the first CRISPR-Cas9-based gene drive in plants. Credit: Zhao Lab, UC San Diego Scientists Develop the First CRISPR/Cas9-Based Gene Drive in Plants New technology designed to breed more robust crops to improve agricultural yield and resist the effects of climate change. With a goal of breeding resilient crops that are better able to withstand drought and disease, University of California, San Diego (UCSD) scientists have developed the first CRISPR-Cas9-based gene drive in plants. While gene drive technology has been developed in insects to help stop the spread of vector-borne diseases such as malaria, researchers in Professor Yunde Zhao’s lab, along with colleagues at the Salk Institute for Biological Studies, demonstrated the successful design of a CRISPR-Cas9-based gene drive that cuts and copies genetic elements in Arabidopsis plants. Breaking from the traditional inheritance rules that dictate that offspring acquire genetic materials equally from each parent (Mendelian genetics), the new research uses CRISPR-Cas9 editing to transmit specific, targeted traits from a single parent in subsequent generations. Such genetic engineering could be used in agriculture to help plants defend against diseases to grow more productive crops. The technology also could help fortify plants against the impacts of climate change such as increased drought conditions in a warming world. A schematic representation of a new plant gene drive using CRISPR/Cas9 technology. Credit: Zhao Lab, UC San Diego The research, led by postdoctoral scholar Tao Zhang and graduate student Michael Mudgett in Zhao’s lab, is published in the journal Nature Communications. “This work defies the genetic constraints of sexual reproduction that an offspring inherits 50% of their genetic materials from each parent,” said Zhao, a member of the Division of Biological Sciences’ Section of Cell and Developmental Biology. “This work enables inheritance of both copies of the desired genes from only a single parent. The findings can greatly reduce the generations needed for plant breeding.” The study is the latest development by researchers in the Tata Institute for Genetics and Society (TIGS) at UC San Diego, which was built upon the foundation of a new technology called “active genetics” with potential to influence population inheritance in a variety of applications. Developing superior crops through traditional genetic inheritance can be expensive and time-consuming as genes are passed through multiple generations. Using the new active genetics technology based on CRISPR-Cas9, such genetic bias can be achieved much more quickly, the researchers say. “I am delighted that this gene drive success, now achieved by scientists affiliated with TIGS in plants, extends the generality of this work previously demonstrated at UC San Diego, to be applicable in insects and mammals,” said TIGS Global Director Suresh Subramani. “This advance will revolutionize plant and crop breeding and help address the global food security problem.” Reference: “Selective inheritance of target genes from only one parent of sexually reproduced F1 progeny in Arabidopsis” by Tao Zhang, Michael Mudgett, Ratnala Rambabu, Bradley Abramson, Xinhua Dai, Todd P. Michael and Yunde Zhao, 22 June 2021, Nature Communications. DOI: 10.1038/s41467-021-24195-5 Coauthors of the paper include: Tao Zhang, Michael Mudgett, Ratnala Rambabu, Bradley Abramson, Xinhua Dai, Todd Michael and Yunde Zhao. The research was funded by TIGS-UC San Diego and a training grant from the National Institutes of Health. The Scyphozoon Atolla sp., a deep-sea species, was an important prey for the blue wolffish, a demersal fish that lives at greater depths. Credit: Alfred Wegener Institute / Mario Hoppmann Jellyfish are consumed in greater quantities by fish in Greenlandic waters than previously thought, altering perceptions of the jellyfish’s role in marine ecosystems. Scientists long believed jellyfish to be a poor dietary choice for predatory fish, but recent research by a team from the Alfred Wegener Institute and the Thünen Institute has revealed that fish in the waters of Greenland actually do consume jellyfish. In two of the analyzed species, they even made up the majority of the food, as the researchers describe in a study published in the journal Royal Society Open Science. The results suggest that the role of jellyfish as prey in marine food webs should be reconsidered, especially in regard to the fact that they could be profiting from climate change and spreading farther and farther north. Jellyfish are found in all oceans, from polar to tropical regions. In the future, gelatinous zooplankton could spread even further, as it is generally one of the winners of climate change: unlike other species, jellyfish are able to better cope with the fact that the global oceans are becoming warmer and more acidic. “Therefore, it is important that we rethink and understand how jellyfish and gelatinous zooplankton generally fit into marine food webs,” says Dr Charlotte Havermans, head of the ARJEL junior research group at the Alfred Wegener Institute, Helmholtz Centre for Polar and Marine Research (AWI). In a new study, she and her team have therefore investigated the role of gelatinous zooplankton as prey for fish in Greenlandic waters. Greenlandic waters are home to large quantities of various types of gelatinous zooplankton. However, whether and to what extent jellyfish and co. are on the menu of the fish that live here was previously unclear. “We analyzed the stomach contents of seven fish species, including commercially used species such as Atlantic cod, haddock, and redfish,” says Charlotte Havermans. “With the help of DNA metabarcoding, we were able to determine very precisely what the animals fed on.” The results were surprising: “We found DNA of jelly in the stomachs of all examined fish species, albeit in varying quantities,” says Annkathrin Dischereit, first author of the study and doctoral student in ARJEL. For two species, the greater silver smelt and the northern wolffish, they even made up the largest proportion of the food. This is despite the fact that gelatinous zooplankton is widely considered a trophic dead end and emergency food for some fish species at best. “This assumption is based on the fact that their tissue is quickly digested by predator fish and jellyfish are therefore rarely recorded as prey in studies,” explains Annkathrin Dischereit. Modern method shows that the role of jellyfish is greater than previously thought DNA metabarcoding provided a solution to this situation: Using this state-of-the-art method, researchers were able to detect short gene fragments in the stomachs, compare them with genetic reference databases, and thus identify those prey species to which the fragments belonged. “We were able to see that every species we analyzed fed on jellyfish or other gelatinous zooplankton,” explains Annkathrin Dischereit. “We detected up to 59 species of gelatinous invertebrates in the stomachs of the fish. This clearly shows that they play a significant but previously overlooked role in the subarctic food web.” The stomach contents of some of these species had never been analyzed before in this area. The study shows that we need to rethink our view of the role of jellyfish and co. in marine food webs. Gelatinous zooplankton is more than just stop-gap food. It is regular prey for predator fish higher up the food chain. “Our results raise the question of why fish seem to eat jellyfish surprisingly frequently,” says Charlotte Havermans. Despite their low energy density, their contribution to the energy budget of predator fish could be more significant than previously assumed: They could be digested more quickly, are easier to hunt, are increasingly common, and provide energy-rich components thanks to their diet. “There is still a need for research here,” says Annkathrin Dischereit. “Our study provides a snapshot in time that only takes into account recently digested prey. We need to collect continuous samples throughout the year and link these to how the gelatinous zooplankton communities change over this period of time. Only then can we understand the trophic links between fish and gelatinous zooplankton.” This is absolutely necessary, as Charlotte Havermans says: “Only trophic insights can provide information on why jellyfish are important for fish and other organisms.” So far, no proper trophic studies have yet been carried out on several species, such as redfish. “The results of our current study raise doubts about how well we understand subpolar ecosystems and how the recently observed increase in gelatinous zooplankton might affect them.” Reference: “A belly full of jelly? DNA metabarcoding shows evidence for gelatinous zooplankton predation by several fish species in Greenland waters” by Annkathrin Dischereit, Julia Katharina Throm, Karl Michael Werner, Stefan Neuhaus and Charlotte Havermans, 1 August 2024, Royal Society Open Science. DOI: 10.1098/rsos.240797 RRG455KLJIEVEWWF |
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