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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: 三希樓整體體驗如何? 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。永心鳳茶再訪意願高嗎? 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。KoDō 和牛燒肉會太油嗎? 下一餐,不妨從這10家開始。一笈壽司年節期間價格會變嗎? 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。一笈壽司好吃嗎? 如果你有私心愛店,也歡迎留言分享,一笈壽司有提供尾牙方案嗎? 你的推薦,可能讓我下一趟美食旅程變得更精彩。印月餐廳口味偏臺式還是日式? The development of the fetal brain involves the creation and migration of billions of neurons during the course of pregnancy. Credit: Veronika Mertens Researchers track the cellular migration of developing fetal brains for the first time by backtracking genetic mutations documented in deceased adult brains. The development of a human brain remains a mostly mysterious process that races from an embryonic neural tube and ends with more than 100 billion interconnected neurons in the brain of a newborn. To achieve this marvel of biological engineering, the developing fetal brain must grow, on average, at a rate of approximately 250,000 nerve cells per minute throughout the course of a pregnancy. These nerve cells are frequently created far from where they will eventually reside and function in the new brain, a migration that has been extensively researched in animal models using chemical or biological tracers but has never been directly studied in humans. That is, until now. In a new paper, published online on April 20, 2022, in the journal Nature, scientists at University of California San Diego (UCSD) School of Medicine and Rady Children’s Institute of Genomic Medicine describe novel methods for inferring the movement of human brain cells during fetal development by studying healthy adult individuals who have recently passed away from natural causes. Tracking Mutations to Reveal Brain Development “Every time a cell divides into two daughter cells, by chance, there arise one or more new mutations, which leave a trail of breadcrumbs that can be read out by modern DNA sequencers,” said senior author Joseph Gleeson, MD, Rady Professor of Neuroscience at UC San Diego School of Medicine and director of neuroscience research at the Rady Children’s Institute for Genomic Medicine. “By developing methods to read these mutations across the brain, we are able to reveal key insights into how the human brain forms, in comparison with other species.” The structure of the human neocortex underlies species-specific traits and reflects intricate developmental programs. Here we sought to reconstruct processes that occur during early development by sampling adult human tissues. We analyzed neocortical clones in a post-mortem human brain through a comprehensive assessment of brain somatic mosaicism, acting as neutral lineage recorders. We combined the sampling of 25 distinct anatomic locations with deep whole-genome sequencing in a neurotypical deceased individual and confirmed results with five samples collected from each of three additional donors. We identified 259 bona fide mosaic variants from the index case, then deconvolved distinct geographical, cell-type and clade organizations across the brain and other organs. We found that clones derived after the accumulation of 90–200 progenitors in the cerebral cortex tended to respect the midline axis, well before the anterior–posterior or entral–dorsal axes, representing a secondary hierarchy following the overall patterning of forebrain and hindbrain domains. Clones across neocortically derived cells were consistent with a dual origin from both dorsal and ventral cellular populations, similar to rodents, whereas the microglia lineage appeared distinct from other resident brain cells. Our data provide a comprehensive analysis of brain somatic mosaicism across the neocortex and demonstrate cellular origins and progenitor distribution patterns within the human brain. Although there are 3 billion DNA bases — and more than 30 trillion cells in the human body — Gleeson and colleagues focused their efforts on just a few hundred DNA mutations that likely arose during the first few cell divisions after fertilization of the embryo or during early development of the brain. By tracking these mutations throughout the brain in deceased individuals, they were able to reconstruct development of the human brain for the first time. Origins of Brain Cells To understand the type of cells displaying these breadcrumb mutations, they developed methods to isolate each of the major cell types in the brain. For instance, by profiling the mutations in excitatory neurons compared with inhibitory neurons, they confirmed the long-held suspicion that these two cell types are generated in different germinal zones of the brain, and then later mix together in the cerebral cortex, the outermost layer of the organ. However, they also discovered that the mutations found in the left and right sides of the brain were different from one another, suggesting that — at least in humans — the two cerebral hemispheres separate during development much earlier than previously suspected. The results have implications for certain human diseases, like intractable epilepsies, where patients show spontaneous convulsive seizures and require surgery to remove an epileptic brain focus, said Martin W. Breuss, PhD, former project scientist at UC San Diego and now an assistant professor at the University of Colorado School of Medicine. Breuss is co-first author with Xiaoxu Yang, PhD, postdoctoral scholar, and Johannes C. M. Schlachetzki, MD, project scientist, both at UC San Diego; and Danny Antaki, PhD, a former postdoctoral scholar at UC San Diego, now at Twist Biosciences. “This study,” the authors said, “solves the mystery as to why these foci are almost always restricted to one hemisphere of the brain. Applying these results to other neurological conditions could help scientists understand more mysteries of the brain.” Reference: “Somatic mosaicism reveals clonal distributions of neocortical development” by Martin W. Breuss, Xiaoxu Yang, Johannes C. M. Schlachetzki, Danny Antaki, Addison J. Lana, Xin Xu, Changuk Chung, Guoliang Chai, Valentina Stanley, Qiong Song, Traci F. Newmeyer, An Nguyen, Sydney O’Brien, Marten A. Hoeksema, Beibei Cao, Alexi Nott, Jennifer McEvoy-Venneri, Martina P. Pasillas, Scott T. Barton, Brett R. Copeland, Shareef Nahas, Lucitia Van Der Kraan, Yan Ding, NIMH Brain Somatic Mosaicism Network, Christopher K. Glass and Joseph G. Gleeson, 20 April 2022, Nature. DOI: 10.1038/s41586-022-04602-7 Co-authors include: Xin Xu, Changuk Chung, Guoliang Chai, Valentina Stanley, Qiong Song, Traci F. Newmeyer, An Nguyen, Beibei Cao, Jennifer McEvoy-Venneri and Brett R. Copeland, all at UC San Diego and Rady Children’s Institute for Genomic Medicine; Addison J. Lana, Sydney O’Brien, Marten A. Hoeksema, Alexi Nott, Martina P. Pasilla, Scott T. Barton, and Christopher K. Glass, all at UC San Diego; Shareef Nahas, Lucitia Van Der Kraan and Yan Ding, Rady Children’s Institute for Genomic Medicine and the NIMH Brain Somatic Mosaicism Network. Funding for this research came, in part, from the Howard Hughes Medical Institute, the National Institute of Mental Health (grants MH108898, RO1 MH124890, R21 AG070462), the National Institute on Aging (grants RF1 AGO6106-02, R01 AGO56511-02, R01 NS096170-04) and the UC San Diego IGM Genomics Center (S10 OD026929). Rainbow Boa Boa constrictors breathe with different sections of rib cage when constricting prey and digesting dinner. The later stages of pregnancy can make life difficult as the fetus presses against the diaphragm making it hard to breathe. But snakes that constrict their victims before swallowing them whole have to overcome the challenges of breathing while their lungs are restricted each time they dine. “With no diaphragm, they rely entirely on motions of their ribs,” says John Capano (Brown University, USA), adding that the earliest snake ancestors must have overcome the challenge of breathing while squeezing and digesting dinner. But it wasn’t clear how modern snakes save themselves from suffocating while constricting their victims. One possibility was that the animals adjust which region of the ribcage they use to inhale, depending on whether they are resting, throttling an animal or digesting. But no one had monitored in detail the breathing patterns of snakes in the act of subduing their dinner to check whether the animals can adjust which section of the ribcage they use. Capano and Elizabeth Brainerd (Brown University) secured a blood pressure cuff around the ribs of boa constrictors to restrict their movements and discovered that the sinuous reptiles use different sections of the rib cage to breathe when their ribs are constricted. They publish their discovery that the hind section of the lung works like a bellows, pulling air into the lung when the ribs further forward can no longer move because they are squeezing prey to death, in Journal of Experimental Biology. But first, Capano attached minute metal markers to two ribs in each reptile – one a third of the way down the snake’s body and another halfway along – to visualize how the ribs moved using X-rays. Then he positioned a blood pressure cuff over the ribs in both regions and gradually increasing the pressure to immobilize them. “Either the animals did not mind the cuff or became defensive and hissed to try to get the researcher to leave,” recalls Capano, explaining that the reptiles really fill their lungs when hissing: “this was an opportunity to measure some of the biggest breathes snakes take,” he says. Ribs as Bellows: How Snakes Adapt Their Breathing Reconstructing the boa constrictors’ rib movements, it was clear that the animals were able to control the movements of ribs in different portions of the rib cage independently. When the boa constrictors were gripped by the blood pressure cuff a third of the way along the body, the animals breathed using the ribs further back, swinging the ribs backward while tipping them up to draw air into the lungs. However, when the ribs toward the rear of the lung were constricted, the snakes breathed using the ribs closer to the head. In fact, the ribs at the far end of the lung only moved when the forward ribs were gripped, drawing air deep into the region, even though it has a poor blood supply and does not provide the body with oxygen. The far end of the lung, was behaving like a bellows, pulling air through the front section of the lung when it could no longer breathe for itself. In addition, Capano, Scott Boback and Charles Zwemer (both from Dickinson College, USA), filmed and recorded the nerve signals controlling the rib muscles when constricted by the blood pressure cuff, while Boback also filmed a snake with a GoPro as it dined, revealing that the ribs were not simply being held immobile. There were no nerve signals in the constricted muscles; the snakes had shifted to breathing by activating a different set of ribs further along the body. Evolutionary Implications of Breathing Adaptations in Snakes As subduing and digesting a victim is one of the most energetic things these snakes can do, it was probably essential that they evolved the ability to adjust where they breathe before adopting their new rib-hindering lifestyle, to ensure that they didn’t suffocate themselves. “It would have been difficult for snakes to evolve those behaviors without the ability to breathe,” he concludes. Reference: “Modular lung ventilation in Boa constrictor” by John G. Capano, Scott M. Boback, Hannah I. Weller, Robert L. Cieri, Charles F. Zwemer and Elizabeth L. Brainerd, 24 March 2022, Journal of Experimental Biology. DOI: 10.1242/jeb.243119 Vampire Bats Study tracks foraging behavior of 50 bats in the wild. Vampire bats that form bonds in captivity and continue those “friendships” in the wild also hunt together, meeting up over a meal after independent departures from the roost, according to a new study. Researchers attached tiny “backpack” computers to 50 vampire bats – some that had previously been in captivity together and others that had lived only in the wild – to track their movement during their nightly foraging outings. By day, the bats shared a hollow tree in Panama, and at night they obtained their meals by drinking blood from wounds they made on cows in nearby pastures. Tracking data showed that vampire bats set out to forage separately rather than as a group – and those that had established social relationships would reunite during the hunt for what the researchers speculated was some sort of coordination over food. Common vampire bats (Desmodus rotundus). The findings suggest “making friends” in the roost could create more interdependence among socially bonded vampire bats – meaning they could benefit from each other’s success at obtaining blood meals and join forces when competing with other groups of bats for food resources. “Everything we’ve been studying with vampire bats has looked at what they’re doing inside of a roost. What nobody has really known up until now is whether these social relationships serve any function outside the roost,” said study co-author Gerald Carter, assistant professor of evolution, ecology, and organismal biology at The Ohio State University. “Understanding their interactions with a completely different group of bats out on the pasture can help us understand what’s going on inside the colony. If every time they leave the roost they’re getting into battles, that can increase the amount of cooperation within the colony.” Co-author Simon Ripperger, a former postdoctoral researcher in Carter’s lab, later supplemented the tracking data by capturing video and audio of foraging vampire bats. He observed bats clustered together on one cow and others atop separate cows, some drinking from different wounds and some fighting over food access. He also made what are likely the first audio recordings of a specific type of vampire bat vocalization associated with foraging. The research is published today (Sept. 23, 2021) in PLOS Biology. The high-tech proximity sensors had already given the team a rare look at how vampire bats maintained friendships they formed in captivity when they returned to the wild. Over the course of two weeks, the backpack computers placed on the 50 wild and formerly captive female bats produced data on almost 400,000 individual meetings – the information analyzed for this new study. By tracking the foraging behaviors of both groups of bats, the researchers were able to use the wild group as a control and simultaneously gauge whether the lengthy captivity interfered with bats’ ability to hunt – which was not the case. Carter and Ripperger considered a number of possible methods vampire bat “friends” would use to seek out food, ranging from not coordinating at all to leaving the roost together and foraging as a group. Though the proximity sensors couldn’t provide details of where exactly the bats were or what they were doing, the data on foraging encounters and previously published data on which bats groomed and shared food during captivity combined to tell a pretty convincing story. “We looked at the possibility of different scenarios, and we found that they leave the roost to forage independently of each other, but then the ones that have a relationship are somehow finding each other and associating out on the cattle pasture – and we think they’re coordinating,” Carter said. Bats that spent more time near each other in the roost during the day also spent more time together outside at night and encountered each other while foraging more frequently than bats not showing signs of social bonds. Foraging encounters between bats that had close relationships were, on average, longer in duration as well. “If you think about it, a longer interaction is more likely to be cooperative or affiliative than a short encounter, which could be neutral or aggressive,” Ripperger said. The recorded vocalizations may eventually provide other insights into vampire bats’ social behaviors. Downward sweeping calls inside roosts and “buzz” calls during arguments had been documented before, but the calls recorded during the hunt, which increased and then decreased in frequency, were distinct from those. “I could see them vocalize even if they were alone on a cow, and they vocalize back and forth, so we can tell that they interact while they’re feeding,” Ripperger said. Reference: “Social foraging in vampire bats is predicted by long-term cooperative relationships” by Simon P. Ripperger and Gerald G. Carter, 23 September 2021, PLOS Biology. DOI: 10.1371/journal.pbio.3001366 This work was conducted at and supported by the Smithsonian Tropical Research Institute in Panama. The study was funded by the National Science Foundation, the German Research Foundation, a Smithsonian Scholarly Studies Awards grant and a National Geographic Society Research Grant. RRG455KLJIEVEWWF |
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