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or published in other medical journals. Posts must contain content related to one of the journal’s categories.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The content published\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The journal is divided into 3 categories:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Scientific research article: are valuable scientific works, which have been researched and accepted.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Overview of medicine, biology and pharmacy: serving the objective of continuing training in the fields of medicine, biology and pharmacy; to systematize classical and modern knowledge.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Update information on new knowledge about medicine, biology, pharmacy in the country and in the world.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Scope\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Publication and introduction of scientific research in the fields:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Medicine (internal medicine, surgery, pediatrics, obstetrics and gynecology, odonto-stomatology, laboratory, oncology, traditional medicine, nursing).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Biology (genetics, biotechnology).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Pharmacology (pharmaceutics, drug quality analysis-control, synthetic pharmaceutical chemistry, biochemistry, pharmacognosy, botany, clinical pharmacy).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- To enhance the quality of undergraduate, postgraduate education, scientifically researching and meet the necessary treatment in hospital.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Introducing the updated domestic and oversea information about science technology to promote scientific research and exchanging technology in local, other universities.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Exchanging pharmaceutical and medical information for social health developing in the Mekong Delta and Vietnam.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The object\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Postgraduate students, student of Can Tho University of Medicine and Pharmacy, scientists from schools, research institutes, hospitals, health centers, pharmaceutical companies of the Mekong Delta; other provinces and regions in Vietnam and other country.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Address\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Headquarters of Can Tho Journal of Medicine and Pharmacy, located Scientific Research and International Cooperation Office: 179 Nguyen Van Cu Street, An Khanh Ward, Ninh Kieu District, Can Tho City, Vietnam.\u003C\u002Fspan>\u003C\u002Fp>","\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Ngày 16\u002F7\u002F2015, Tạp chí Y Dược học Cần Thơ được cấp chỉ số quốc tế: ISSN 2354-1210.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 4\u002F2016, Tạp chí đã được Hội đồng Giáo sư ngành Y đưa vào danh sách các tạp chí khoa học Y học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Năm 2020 Tạp chí Y Dược học Cần Thơ đã được phê duyệt vào danh mục của các Hội đồng Giáo sư ngành Dược học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ ra 12 số\u002Fnăm, 180-200 trang\u002Fsố.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 12\u002F2022 Tạp chí Y Dược học Cần Thơ là thành viên của hệ thống Crossref và từ tháng 01\u002F2023 tạp chí thực hiện bình duyệt online kín 2 chiều nhằm tăng tính minh bạch, tin cậy của các công trình nghiên cứu khoa học và đảm bảo tốt nhất chất lượng khoa học của bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ, mục đích và phạm vi của tạp chí\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ và mục đích hoạt động của tạp chí: xuất bản nhằm mục đích phổ biến kết quả từ các đề tài nghiên cứu khoa học; giao lưu trao đổi khoa học, chia sẻ kinh nghiệm, học tập, đồng thời cập nhật thông tin khoa học mới trong các lĩnh vực y, sinh, dược học trong và ngoài nước.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phạm vi của tạp chí: Tạp chí xuất bản được chia thành 3 chuyên mục: (i) Bài báo nghiên cứu khoa học là kết quả công trình nghiên cứu khoa học có giá trị đã được triển khai nghiên cứu, (ii) Bài tổng quan y, sinh, dược học: phục vụ mục tiêu đào tạo liên tục trong lĩnh vực y, sinh, dược học; nhằm hệ thống hóa những kiến thức kinh điển và hiện đại; (iii) Thông tin cập nhật kiến thức mới về y, sinh, dược học trong nước và trên thế giới.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Chính sách truy cập mở\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ áp dụng chính sách truy cập mở đối với các bài báo đã xuất bản đến với độc giả, nhằm mở rộng cơ hội tiếp cận các kết quả nghiên cứu chất lượng cao và tăng cường trao đổi kiến thức. Tạp chí đăng tải trực tuyến (miễn phí) toàn văn các bài báo được công bố trên website của Tạp chí (https:\u002F\u002Ftapchi.ctump.edu.vn).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đạo đức xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ cam kết tuân thủ đạo đức xuất bản phù hợp với các hướng dẫn và tiêu chuẩn của the Committee on Publication Ethics (COPE), tuân thủ các nguyên tắc của COPE’s Core Practices, Best Practices Guidelines for Journal Editors và Guidelines on Good Publication Practices.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Bản thảo bài báo chỉ được chấp nhận khi được tác giả chịu trách nhiệm chính cam kết các nội dung sau: Các nội dung của bản thảo chưa được đăng tải toàn bộ hoặc một phần ở các tạp chí khác; Tất cả các tác giả đều có đóng góp một cách đáng kể vào quá trình nghiên cứu hoặc chuẩn bị bản thảo và cùng chịu trách nhiệm về các nội dung của bản thảo; Tuân thủ các biện pháp đảm bảo đạo đức nghiên cứu (ví dụ thỏa thuận đồng ý tham gia nghiên cứu).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Cam kết bảo mật\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí cam kết thực hiện và tuân thủ các quy định của luật và các văn bản hướng dẫn liên quan đến bảo mật thông tin cá nhân trên không gian mạng. Các thông tin mà người dùng (tác giả, độc giả, biên tập viên, người phản biện) nhập vào các biểu mẫu trên Hệ thống Quản lý xuất bản trực tuyến của tạp chí chỉ được sử dụng vào các mục đích đã được tuyên bố rõ ràng và sẽ không được cung cấp cho bất kỳ bên thứ ba nào khác, hay dùng vào bất kỳ mục đích nào khác.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phí gửi bài\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng bài: 1.000.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng nhanh: 1.500.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với tác giả là cán bộ viên chức thuộc Trường Đại học Y Dược Cần Thơ thì được hỗ trợ 50% lệ phí gửi đăng bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với sinh viên thực hiện đề tài nghiên cứu khoa học cấp trường được hỗ trợ 100% lệ phí đăng bài ( Tác giả gửi đính kèm “ Quyết định về việc giao tổ chức thực hiện đề tài nghiên cứu khoa học cấp Trường của sinh viên”).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Hình thức nộp lệ phí:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Tiền mặt:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Nộp trực tiếp tại Phòng Tài chính - Kế toán, Trường Đại học Y Dược Cần Thơ, số 179 Nguyễn Văn Cừ, P. An Khánh, Q. Ninh Kiều, thành phố Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Chuyển khoản:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tên Tài khoản: Trường ĐHYD Cần Thơ, Số TK: 0111000115668, tại ngân hàng Vietcombank chi nhánh Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Thời gian: Áp dụng từ ngày 01\u002F02\u002F2023.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">* Phí gửi bài không được hoàn trả khi bài viết bị từ chối hoặc tác giả xin rút bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Quy trình phản biện bài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ thực hiện quy trình phản biện kín hai chiều nghiêm ngặt. Danh tính của những người phản biện không được tiết lộ cho các tác giả và ngược lại. Quy trình thẩm định bài báo đăng gồm các bước sau:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tiếp nhận bản thảo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tác giả liên hệ gửi bản thảo đến Tạp chí qua hệ thống trực tuyến tại website: https:\u002F\u002Ftapchi.ctump.edu.vn. Hướng dẫn về cách đăng ký, gửi bài và chuẩn bị bản thảo được cung cấp trên website của Tạp chí.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sàng lọc sơ bộ\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sau khi Tòa soạn nhận được bài báo của tác giả, Ban Thư ký sẽ tiến hành kiểm tra sơ bộ bài báo (các yêu cầu về nội dung và hình thức). Những bài báo không đúng quy cách hoặc có nội dung không phù hợp hoặc vi phạm bản quyền sẽ bị từ chối (Ban Thư ký thông báo phản hồi đến tác giả trong vòng 1 tuần). Những bài báo đủ điều kiện, được Ban Thư ký tòa soạn chuyển đến Ban Biên tập có cùng chuyên môn với nội dung bài báo để đề xuất người phản biện. Thời gian kể từ khi Ban Biên tập nhận bài báo đến khi đề xuất người phản biện bài báo chậm nhất là 5 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Vòng phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký gửi bài và yêu cầu phản biện đến 02 phản biện độc lập.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Các phản biện gởi nhận xét cho Ban Thư ký. Thời gian từ khi gửi bài cho phản biện đến khi nhận ý kiến của phản biện tối đa là 20 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xử ký kết quả phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Nếu ý kiến đồng ý cho đăng và không cần chỉnh sửa, Ban Thư ký tiếp tục đăng bài theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Nếu ý kiến đồng ý đăng và cần chỉnh sửa, Ban Thư ký sẽ thông tin đến tác giả chỉnh sửa theo yêu cầu của người phản biện. Thời gian chỉnh sửa và gửi lại kéo dài không quá 2 tuần, từ khi tác giả bài báo nhận được thông tin (Quá trình này có thể lặp lại tối đa 2 lần\u002F1 bài báo). Khi có sự thống nhất, đồng ý của người phản biện; bài báo được tiếp tục đăng theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Những bài báo có chất lượng không đạt yêu cầu, cả 2 phản biện không đồng ý cho đăng sẽ bị Tòa soạn từ chối đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký tổng hợp các bản thảo đã được tác giả hoàn thiện sau thẩm định trình Ban Biên tập xem xét, Tổng Biên tập phê duyệt, quyết định bài đăng theo các tiêu chí: sự phù hợp nội dung với tôn chỉ và mục đích, thể loại bài viết (ưu tiên các bài có bài có nghiên cứu chuyên sâu, hàm lượng khoa học cao), đóng góp mới bài báo, bài báo được ưu tiên đăng trong số gần nhất của Tạp chí theo thứ tự: tính thời sự, chất lượng bài báo và thời gian gửi bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Ban Biên tập và Ban Thư ký biên tập bản thảo, chế bản, đọc rà soát lỗi. Thời gian hoàn thành từ 10-15 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Ban Thư ký có trách nhiệm thông báo cho tác giả bài báo (bằng e-mail) về tình hình phê duyệt bài báo, thời gian, số kỳ, tập xuất bản bài báo theo qui định.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">4. Danh sách bài báo theo số Tạp chí được in ấn và phát hành trong năm định kỳ được công bố chính thức trên website: https:\u002F\u002Ftapchi.ctump.edu.vn\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>",{"VOID":582},"wcQ1uqwAAAAJ","2023-05-30T08:17:21.868+00:00",[],[586],{"id":587,"createTime":24,"updateTime":24,"relativeEntities":588,"slug":24,"properties":589,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":599,"parentIds":600,"statistic":24},"6413896b-eca9-442b-a73f-182a58a0ce40",[],{"title":590,"address":593,"country":596,"abbreviation":597},{"EN":591,"VI":592},"Can Tho University of Medicine and Pharmacy","Trường Đại học Y Dược Cần Thơ",{"EN":594,"VI":595},"No 179, Nguyen Van Cu street, An Khanh ward, Ninh Kieu district, Can Tho city, Vietnam","Số 179, đường Nguyễn Văn Cừ, phường An Khánh, quận Ninh Kiều, thành phố Cần Thơ, Việt Nam",{"VOID":110},{"VOID":598},"ctump","http:\u002F\u002Fwww.ctump.edu.vn\u002F",[],[],"https:\u002F\u002Ftapchi.ctump.edu.vn\u002Findex.php\u002Fctump",{"impactFactor":25,"impactFactorByYear":604,"i10Index":25,"i10IndexLast5Year":25,"totalPublication":606,"totalPublicationByYear":607,"totalCitation":612,"totalCitationByYear":613,"totalCitationPerPublication":200,"totalCitationPerPublicationByYear":615,"hindexLast5Year":137,"hindex":137},{"2022":605,"2023":203,"2024":198},0.01,1556,{"2020":139,"2021":608,"2022":609,"2023":610,"2024":611,"2025":214},57,306,801,358,161,{"2021":238,"2022":372,"2023":614},99,{"2021":616,"2022":410,"2023":196},0.23,{"impactFactor":24,"impactFactorByYear":24,"i10Index":215,"i10IndexLast5Year":215,"totalPublication":618,"totalPublicationByYear":619,"totalCitation":618,"totalCitationByYear":620,"totalCitationPerPublication":132,"totalCitationPerPublicationByYear":623,"hindexLast5Year":141,"hindex":141},476,{"0":297,"2019":215,"2021":231,"2022":551,"2023":543,"2024":449,"2025":141,"2026":140},{"2021":134,"2022":215,"2023":253,"2024":621,"2025":452,"2026":622},136,83,{"2021":197,"2022":605,"2023":624,"2024":219,"2025":625,"2026":626},0.62,25.43,13.83,{"id":628,"createTime":629,"updateTime":474,"relativeEntities":630,"slug":631,"properties":632,"entityType":22,"verifyStatus":120,"verifyTime":24,"verifyNote":24,"languages":644,"translateLanguages":24,"viewCount":225,"subjectFields":645,"manageAffiliations":646,"indexDatabases":647,"url":648,"thumbnailPath":649,"statistic":650,"gsStatistic":686,"type":147,"analyzePriority":24},"6984a56a-db70-403b-9cc4-4013e1ceaffa","2023-05-09T06:47:40.346+00:00",[],"T%E1%BA%A1p%20ch%C3%AD%20Nghi%C3%AAn%20c%E1%BB%A9u%20n%C6%B0%E1%BB%9Bc%20ngo%C3%A0i",{"country":633,"issn":634,"title":636,"introduce":639,"gsId":642},{"VOID":110},{"VOID":635},"25252445",{"EN":637,"VI":638},"VNU Journal of Foreign Studies","Tạp chí Nghiên cứu nước ngoài",{"EN":640,"VI":641},"{\"ops\":[{\"insert\":\"\\n\\nThe \\n\"},{\"attributes\":{\"italic\":true},\"insert\":\"VNU Journal of Science\"},{\"insert\":\"\\n was established in 1985 for the publication of national and international research papers in all fields of natural sciences and technology, social sciences and humanities. Since then, the journal has grown in quality, size and scope and now comprises a dozen of serials spanning academic research. 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Although, the main text structure may vary based on the review subtopics, the articles should be formatted according to suitable Templates as research articles.\"},{\"attributes\":{\"align\":\"justify\"},\"insert\":\"\\n\"},{\"insert\":\"\\n\"}]}","{\"ops\":[{\"insert\":\"Tạp chí Khoa học Trường ĐHSP Hà Nội 2 nhằm mục đích cung cấp một nền tảng liên ngành của sự phổ biến những tiến bộ của khoa học và công nghệ. Tạp chí xuất bản các bài báo gốc có giá trị khoa học hoặc công nghệ trong tất cả các lĩnh vực khoa học tự nhiên, xã hội hoặc giáo dục.\\n\"},{\"attributes\":{\"bold\":true},\"insert\":\"Chuyên san Khoa học tự nhiên và công nghệ:\"},{\"insert\":\" Là các bài báo mô tả những phát hiện có giá trị trong vật lý, toán học, hóa học, sinh học; giải quyết các vấn đề kỹ thuật hoặc công nghệ.\"},{\"attributes\":{\"list\":\"bullet\"},\"insert\":\"\\n\"},{\"attributes\":{\"bold\":true},\"insert\":\"Chuyên san Khoa học Xã hội và Nhân văn:\"},{\"insert\":\" là các bài báo xuất bản chất lượng cao trong các lĩnh vực khác nhau của khoa học xã hội và nghiên cứu phát triển con người.\"},{\"attributes\":{\"list\":\"bullet\"},\"insert\":\"\\n\"},{\"attributes\":{\"bold\":true},\"insert\":\"Chuyên san Khoa học giáo dục:\"},{\"insert\":\" là các bài báo xuất bản trong lĩnh vực khoa học giáo dục và các ứng dụng của tiến bộ vào giáo dục để cải thiện và nâng cao giáo dục khoa học ở tất cả các cấp.\"},{\"attributes\":{\"list\":\"bullet\"},\"insert\":\"\\n\"},{\"insert\":\"Tạp chí trường ĐHSP Hà Nội 2 xuất bản được phản biện kín, xét duyệt bởi ít nhất 02 chuyên gia, và được đánh giá, chọn lựa từ ban biên tập và Tổng biên tập.\\n\"},{\"attributes\":{\"bold\":true},\"insert\":\"Các loại bài báo\"},{\"insert\":\":\\nBài báo nghiên cứu:\"},{\"attributes\":{\"list\":\"ordered\"},\"insert\":\"\\n\"},{\"insert\":\"Báo cáo học thuật về nghiên cứu ban đầu chưa từng được xuất bản ở bất kỳ nơi nào, hay bằng bất kỳ ngôn ngữ nào khác. Bản thảo thích hợp, nên chứa các phần sau theo thứ tự: Tiêu đề, Tác giả, Liên kết tác giả, Địa chỉ email của tác giả tương ứng, Tóm tắt, Từ khóa, Danh pháp (nếu có), Giới thiệu, Thử nghiệm, Lý thuyết, Kết quả và thảo luận, Kết luận, Xung đột quan tâm, Lời cảm ơn (nếu có), Tài liệu tham khảo, Phụ lục (nếu có). Bản xuất bản trước phải được định dạng theo Mẫu (phiên bản MS-Word).\\n2. Bài báo tổng quan:\\nNgoài các bài phê bình được mời, các bài phê bình tài liệu, bài phê bình có hệ thống và bài phê bình sẽ được chấp nhận để xem xét. Bản thảo cần được soạn thảo và sắp xếp theo trình tự yêu cầu: Tên sách, Tên tác giả, Liên kết, Địa chỉ email, Tóm tắt, Từ khóa, Nội dung chính, Kết luận, Xung đột lợi ích, Lời cảm ơn (nếu có), Tài liệu tham khảo. Mặc dù, cấu trúc văn bản chính có thể thay đổi dựa trên các chủ đề phụ của bài đánh giá, các bài báo nên được định dạng theo các Mẫu phù hợp như các bài báo nghiên cứu.\\n\"}]}",{"VOID":818},"YPoBvsIAAAAJ",[],[],[],"https:\u002F\u002Fsj.hpu2.edu.vn\u002Findex.php\u002Fjournal","\u002Fapi\u002Fpublic\u002Ffile\u002Fpublisher\u002F954132b5-ca74-461c-b819-45ad6e49a404\u002F2790ef1d0a7d7a40a504c2fc1647f670.jpg",{"impactFactor":25,"impactFactorByYear":825,"i10Index":25,"i10IndexLast5Year":25,"totalPublication":421,"totalPublicationByYear":827,"totalCitation":226,"totalCitationByYear":828,"totalCitationPerPublication":616,"totalCitationPerPublicationByYear":829,"hindexLast5Year":215,"hindex":215},{"2024":826},0.17,{"2022":228,"2023":370,"2024":234},{"2022":449,"2023":218,"2024":215},{"2022":261,"2023":316,"2024":257},{"impactFactor":24,"impactFactorByYear":24,"i10Index":137,"i10IndexLast5Year":137,"totalPublication":422,"totalPublicationByYear":831,"totalCitation":246,"totalCitationByYear":832,"totalCitationPerPublication":833,"totalCitationPerPublicationByYear":834,"hindexLast5Year":138,"hindex":138},{"0":215,"2022":226,"2023":228,"2024":161,"2025":237},{"2023":138,"2024":228,"2025":293,"2026":370},1.22,{"2023":205,"2024":432,"2025":835},4.56,{"id":837,"createTime":838,"updateTime":839,"relativeEntities":840,"slug":841,"properties":842,"entityType":22,"verifyStatus":120,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":161,"subjectFields":854,"manageAffiliations":855,"indexDatabases":863,"url":903,"thumbnailPath":24,"statistic":904,"gsStatistic":936,"type":147,"analyzePriority":24},"21ccdb34-414d-420f-8a60-a592a2fa848e","2023-05-29T10:42:53.358+00:00","2026-08-27T01:57:29.560+00:00",[],"Vietnam-Journal-of-Earth-Sciences",{"country":843,"eissn":844,"issn":846,"title":848,"introduce":850,"gsId":852},{"VOID":110},{"VOID":845},"26159783",{"VOID":847},"08667187",{"EN":849},"Vietnam Journal of Earth Sciences",{"EN":851},"Science of the Earth, formerly Vietnam Journal of Earth Sciences, is a peer-reviewed journal to publish high-quality articles on the entire range of earth sciences and the environment, focused on the Asia Pacific region and their correlations and connections to the globe. The journal publishes fundamental and applied research in earth sciences and the environment, including geology, geophysics, geography, soil science, hydrology, meteorology, oceanography, petroleum, geohazards, environmental sciences, environmental engineering, sustainable development, geoinformatics, geodesy, GIS, and remote sensing.",{"VOID":853},"5htfr3YAAAAJ",[],[856],{"id":165,"createTime":24,"updateTime":24,"relativeEntities":857,"slug":24,"properties":858,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":174,"parentIds":862,"statistic":24},[],{"title":859,"country":860,"abbreviation":861},{"EN":169,"VI":170},{"VOID":110},{"VOID":173},[],[864,876,887],{"id":865,"indexDatabase":866,"url":871,"indexYears":872,"academicFieldIds":873,"indexDatabaseRanking":875},"6ace2085-a177-4a27-b309-8813b832111e",{"id":64,"createTime":24,"updateTime":24,"relativeEntities":867,"label":868,"description":869,"key":70,"publicationTags":870,"standard":24},[],{"EN":67,"VI":67},{"EN":67,"VI":69},[72],"https:\u002F\u002Fwww.scopus.com\u002Fsourceid\u002F21101039869","2018-2024",[874],"1689391c-5702-4349-aaa7-d720ee4321fc","NONE",{"id":877,"indexDatabase":878,"url":883,"indexYears":884,"academicFieldIds":885,"indexDatabaseRanking":24},"dadb15a8-ee22-41c2-a287-49e969d9a998",{"id":180,"createTime":24,"updateTime":24,"relativeEntities":879,"label":880,"description":881,"key":186,"publicationTags":882,"standard":24},[],{"EN":183,"VI":183},{"EN":185,"VI":185},[188],"https:\u002F\u002Fasean-cites.org\u002Fjournal_info?jid=10629","2016-2022",[886],"e04f14cf-280b-4aa8-b711-b77ddd79cbaf",{"id":888,"indexDatabase":889,"url":900,"indexYears":24,"academicFieldIds":901,"indexDatabaseRanking":24},"06f278ee-37b9-41eb-a9b0-3d2d77fa502b",{"id":890,"createTime":24,"updateTime":24,"relativeEntities":891,"label":892,"description":894,"key":897,"publicationTags":898,"standard":24},"88bab0f7-443b-476c-a72a-7fa5222da393",[],{"EN":893,"VI":893},"ISI\u002FESCI  - 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Borgardt",{"id":989,"sortIndex":132,"researcher":24,"roles":990,"affiliations":991,"properties":998,"displayName":1000,"givenName":24,"familyName":24},"269cf75b-546d-4cc2-8804-657224b13435",[],[992],{"id":978,"sortIndex":25,"affiliation":993,"properties":24},{"id":978,"createTime":24,"updateTime":24,"relativeEntities":994,"slug":24,"properties":995,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":997,"statistic":24},[],{"title":996},{"EN":983},[],{"title":999},{"EN":1000},"Kevin C. Nixon","ARTICLE",{"url":24,"publisher":1003,"properties":1049},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":1004,"slug":10,"properties":1005,"entityType":22,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":25,"subjectFields":1010,"manageAffiliations":1023,"indexDatabases":1034,"url":97,"thumbnailPath":24,"statistic":24,"gsStatistic":24,"type":24,"analyzePriority":24},[],{"country":1006,"eissn":1007,"issn":1008,"title":1009},{"VOID":13},{"VOID":15},{"VOID":17},{"EN":19},[1011,1015,1019],{"id":28,"createTime":24,"updateTime":24,"relativeEntities":1012,"label":1013,"description":1014,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":31},{},{"id":34,"createTime":24,"updateTime":24,"relativeEntities":1016,"label":1017,"description":1018,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":37},{},{"id":40,"createTime":24,"updateTime":24,"relativeEntities":1020,"label":1021,"description":1022,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":43},{},[1024,1029],{"id":47,"createTime":24,"updateTime":24,"relativeEntities":1025,"slug":24,"properties":1026,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1028,"statistic":24},[],{"title":1027},{"EN":51},[],{"id":54,"createTime":24,"updateTime":24,"relativeEntities":1030,"slug":24,"properties":1031,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1033,"statistic":24},[],{"title":1032},{"EN":58},[],[1035,1042],{"id":62,"indexDatabase":1036,"url":73,"indexYears":74,"academicFieldIds":1041,"indexDatabaseRanking":79},{"id":64,"createTime":24,"updateTime":24,"relativeEntities":1037,"label":1038,"description":1039,"key":70,"publicationTags":1040,"standard":24},[],{"EN":67,"VI":67},{"EN":67,"VI":69},[72],[76,77,78],{"id":81,"indexDatabase":1043,"url":94,"indexYears":24,"academicFieldIds":1048,"indexDatabaseRanking":24},{"id":83,"createTime":24,"updateTime":24,"relativeEntities":1044,"label":1045,"description":1046,"key":90,"publicationTags":1047,"standard":24},[],{"EN":86,"VI":86},{"EN":88,"VI":89},[92,93],[96],{"issue":1050,"pages":1052,"volume":1054},{"VOID":1051},"11",{"VOID":1053},"1567-1584",{"VOID":1055},"90","2003-11-01",2003,[92,79],[],false,{"id":1062,"createTime":1063,"updateTime":1064,"relativeEntities":1065,"slug":1066,"properties":1067,"entityType":967,"verifyStatus":120,"verifyTime":1063,"verifyNote":968,"languages":1084,"translateLanguages":1085,"viewCount":25,"primaryUrl":1086,"fullTextUrl":24,"authors":1087,"publicationType":1001,"publisherRelationship":1184,"citationCount":1238,"citationInfo":1239,"publishDate":1248,"publishYear":1240,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":1249,"openAccess":24,"references":1250,"isForceReanalyzing":1060},"ec54393f-6f28-486e-9e8c-18aff8c39529","2024-09-24T23:27:36.123+00:00","2025-02-14T21:00:26.490+00:00",[],"Comparison-of-whole-chloroplast-genome-sequences-to-choose-noncoding-regions-for-phylogenetic-studies-in-angiosperms-the-tortoise-and-the-hare-III",{"mag":1068,"keywords":1070,"openalex":1072,"abstract":1074,"title":1077,"pm":1080,"doi":1082},{"VOID":1069},"2133559537",{"VI":1071},"",{"VOID":1073},"W2133559537",{"EN":1075,"VI":1076},"\u003Cjats:p>Although the chloroplast genome contains many noncoding regions, relatively few have been exploited for interspecific phylogenetic and intraspecific phylogeographic studies. In our recent evaluation of the phylogenetic utility of 21 noncoding chloroplast regions, we found the most widely used noncoding regions are among the least variable, but the more variable regions have rarely been employed. That study led us to conclude that there may be unexplored regions of the chloroplast genome that have even higher relative levels of variability. To explore the potential variability of previously unexplored regions, we compared three pairs of single‐copy chloroplast genome sequences in three disparate angiosperm lineages: \u003Cjats:italic>Atropa\u003C\u002Fjats:italic> vs. \u003Cjats:italic>Nicotiana\u003C\u002Fjats:italic> (asterids); \u003Cjats:italic>Lotus\u003C\u002Fjats:italic> vs. \u003Cjats:italic>Medicago\u003C\u002Fjats:italic> (rosids); and \u003Cjats:italic>Saccharum\u003C\u002Fjats:italic> vs. \u003Cjats:italic>Oryza\u003C\u002Fjats:italic> (monocots). These three separate sequence alignments highlighted 13 mutational hotspots that may be more variable than the best regions of our former study. These 13 regions were then selected for a more detailed analysis. Here we show that nine of these newly explored regions (\u003Cjats:italic>rpl32‐trnL\u003C\u002Fjats:italic>\u003Cjats:sup>(UAG)\u003C\u002Fjats:sup>, \u003Cjats:italic>trnQ\u003C\u002Fjats:italic>\u003Cjats:sup>(UUG)\u003C\u002Fjats:sup>‐\u003Cjats:italic>5′rps16\u003C\u002Fjats:italic>, \u003Cjats:italic>3′trnV\u003C\u002Fjats:italic>\u003Cjats:sup>(UAC)\u003C\u002Fjats:sup>‐\u003Cjats:italic>ndhC\u003C\u002Fjats:italic>, \u003Cjats:italic>ndhF‐rpl32\u003C\u002Fjats:italic>, \u003Cjats:italic>psbD‐trnT\u003C\u002Fjats:italic>\u003Cjats:sup>(GGU)\u003C\u002Fjats:sup>, \u003Cjats:italic>psbJ‐petA\u003C\u002Fjats:italic>, \u003Cjats:italic>3′rps16–5′trnK\u003C\u002Fjats:italic>\u003Cjats:sup>(UUU)\u003C\u002Fjats:sup>, \u003Cjats:italic>atpI‐atpH\u003C\u002Fjats:italic>, and \u003Cjats:italic>petL‐psbE\u003C\u002Fjats:italic>) offer levels of variation better than the best regions identified in our earlier study and are therefore likely to be the best choices for molecular studies at low taxonomic levels.\u003C\u002Fjats:p>","\u003Cjats:p>Mặc dù bộ gen ti thể chứa nhiều vùng không mã hóa, nhưng có rất ít vùng được khai thác cho các nghiên cứu phát sinh loài giữa các loài khác nhau và địa lý phát sinh giữa các cá thể trong cùng một loài. Trong đánh giá gần đây của chúng tôi về khả năng phát sinh loài của 21 vùng không mã hóa của bộ gen ti thể, chúng tôi nhận thấy rằng các vùng không mã hóa được sử dụng rộng rãi nhất lại là những vùng ít biến đổi, trong khi các vùng có tính biến đổi cao hơn lại hiếm khi được sử dụng. Nghiên cứu đó đã dẫn chúng tôi đến kết luận rằng có thể có những vùng chưa được khám phá trong bộ gen ti thể có mức độ biến đổi tương đối cao hơn nữa. Để khám phá khả năng biến đổi của các vùng chưa được nghiên cứu trước đó, chúng tôi đã so sánh ba cặp chuỗi gen ti thể đơn bản trong ba nhánh thực vật một lá mầm khác nhau: \u003Cjats:italic>Atropa\u003C\u002Fjats:italic> vs. \u003Cjats:italic>Nicotiana\u003C\u002Fjats:italic> (asterid); \u003Cjats:italic>Lotus\u003C\u002Fjats:italic> vs. \u003Cjats:italic>Medicago\u003C\u002Fjats:italic> (rosid); và \u003Cjats:italic>Saccharum\u003C\u002Fjats:italic> vs. \u003Cjats:italic>Oryza\u003C\u002Fjats:italic> (monocot). Ba lần căn chỉnh chuỗi gen này đã làm nổi bật 13 điểm đột biến có thể biến đổi nhiều hơn những vùng tốt nhất trong nghiên cứu trước đó của chúng tôi. 13 vùng này đã được chọn để phân tích chi tiết hơn. Tại đây, chúng tôi chỉ ra rằng chín trong số những vùng mới được khám phá này (\u003Cjats:italic>rpl32‐trnL\u003C\u002Fjats:italic>\u003Cjats:sup>(UAG)\u003C\u002Fjats:sup>, \u003Cjats:italic>trnQ\u003C\u002Fjats:italic>\u003Cjats:sup>(UUG)\u003C\u002Fjats:sup>‐\u003Cjats:italic>5′rps16\u003C\u002Fjats:italic>, \u003Cjats:italic>3′trnV\u003C\u002Fjats:italic>\u003Cjats:sup>(UAC)\u003C\u002Fjats:sup>‐\u003Cjats:italic>ndhC\u003C\u002Fjats:italic>, \u003Cjats:italic>ndhF‐rpl32\u003C\u002Fjats:italic>, \u003Cjats:italic>psbD‐trnT\u003C\u002Fjats:italic>\u003Cjats:sup>(GGU)\u003C\u002Fjats:sup>, \u003Cjats:italic>psbJ‐petA\u003C\u002Fjats:italic>, \u003Cjats:italic>3′rps16–5′trnK\u003C\u002Fjats:italic>\u003Cjats:sup>(UUU)\u003C\u002Fjats:sup>, \u003Cjats:italic>atpI‐atpH\u003C\u002Fjats:italic>, và \u003Cjats:italic>petL‐psbE\u003C\u002Fjats:italic>) cung cấp mức độ biến đổi tốt hơn so với các vùng tốt nhất được xác định trong nghiên cứu trước của chúng tôi và do đó có khả năng là lựa chọn tốt nhất cho các nghiên cứu phân tử ở các cấp độ phân loại thấp hơn.\u003C\u002Fjats:p>",{"EN":1078,"VI":1079},"Comparison of whole chloroplast genome sequences to choose noncoding regions for phylogenetic studies in angiosperms: the tortoise and the hare III","So sánh chuỗi gen toàn bộ của ti thể để lựa chọn các vùng không mã hóa cho các nghiên cứu hệ sinh thái ở thực vật một lá mầm: con rùa và con thỏ III",{"VOID":1081},"21636401",{"VOID":1083},"10.3732\u002Fajb.94.3.275",[124],[123],"https:\u002F\u002Fbsapubs.onlinelibrary.wiley.com\u002Fdoi\u002F10.3732\u002Fajb.94.3.275",[1088,1115,1138,1161],{"id":1089,"sortIndex":25,"researcher":24,"roles":1090,"affiliations":1091,"properties":1108,"displayName":1112,"givenName":24,"familyName":24},"70c18ad9-d1e5-499b-9739-bae4a11444fd",[],[1092,1100],{"id":1093,"sortIndex":25,"affiliation":1094,"properties":24},"c8f68cc1-3e92-426d-a0c5-6961d898a08d",{"id":1093,"createTime":24,"updateTime":24,"relativeEntities":1095,"slug":24,"properties":1096,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1099,"statistic":24},[],{"title":1097},{"EN":1098},"Department of Biological and Environmental Sciences, 615 McCallie Avenue, University of Tennessee, Chattanooga, Tennessee 37403 USA",[],{"id":1101,"sortIndex":132,"affiliation":1102,"properties":24},"41139a2a-5925-4b43-b759-fa54cf469109",{"id":1101,"createTime":24,"updateTime":24,"relativeEntities":1103,"slug":24,"properties":1104,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1107,"statistic":24},[],{"title":1105},{"EN":1106},"Department of Ecology and Evolutionary Biology, 442 Hesler Biology, University of Tennessee, Knoxville, Tennessee 37996 USA",[],{"orcid":1109,"title":1111,"openalex":1113},{"VOID":1110},"https:\u002F\u002Forcid.org\u002F0000-0003-4975-8122",{"EN":1112},"Joey Shaw",{"VOID":1114},"A5026239855",{"id":1116,"sortIndex":132,"researcher":24,"roles":1117,"affiliations":1118,"properties":1131,"displayName":1135,"givenName":24,"familyName":24},"45ebbb3a-2061-4c61-96a7-0c492d1117d1",[],[1119,1125],{"id":1093,"sortIndex":25,"affiliation":1120,"properties":24},{"id":1093,"createTime":24,"updateTime":24,"relativeEntities":1121,"slug":24,"properties":1122,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1124,"statistic":24},[],{"title":1123},{"EN":1098},[],{"id":1101,"sortIndex":132,"affiliation":1126,"properties":24},{"id":1101,"createTime":24,"updateTime":24,"relativeEntities":1127,"slug":24,"properties":1128,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1130,"statistic":24},[],{"title":1129},{"EN":1106},[],{"orcid":1132,"title":1134,"openalex":1136},{"VOID":1133},"https:\u002F\u002Forcid.org\u002F0000-0001-8687-6836",{"EN":1135},"Edgar B. 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Schilling",{"VOID":1160},"A5041150463",{"id":1162,"sortIndex":134,"researcher":24,"roles":1163,"affiliations":1164,"properties":1177,"displayName":1181,"givenName":24,"familyName":24},"269aef96-dfc6-45a3-9f67-bb9de62becbf",[],[1165,1171],{"id":1093,"sortIndex":25,"affiliation":1166,"properties":24},{"id":1093,"createTime":24,"updateTime":24,"relativeEntities":1167,"slug":24,"properties":1168,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1170,"statistic":24},[],{"title":1169},{"EN":1098},[],{"id":1101,"sortIndex":132,"affiliation":1172,"properties":24},{"id":1101,"createTime":24,"updateTime":24,"relativeEntities":1173,"slug":24,"properties":1174,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1176,"statistic":24},[],{"title":1175},{"EN":1106},[],{"orcid":1178,"title":1180,"openalex":1182},{"VOID":1179},"https:\u002F\u002Forcid.org\u002F0000-0001-5843-3261",{"EN":1181},"Randall L. 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J., 2002, Hybrid origin and parentage of Dendrochilum acuiferum (Orchidaceae) inferred in a phylogenetic context using nuclear and plastid DNA sequence data, Systematic Botany, 27, 209",{},{"id":24,"text":1258,"url":24,"identifiers":1259},"10.1046\u002Fj.1365-294x.1998.00466.x",{"doi":1258},{"id":24,"text":1261,"url":24,"identifiers":1262},"10.1093\u002Fbioinformatics\u002Fbti1200",{"doi":1261},{"id":24,"text":1264,"url":24,"identifiers":1265},"10.1073\u002Fpnas.91.15.6795",{"doi":1264},{"id":24,"text":1267,"url":24,"identifiers":1268},"Curtis S. E., 1984, Molecular evolution of chloroplast DNA sequences, Molecular Biology and Evolution, 1, 291",{},{"id":24,"text":1270,"url":24,"identifiers":1271},"10.1007\u002Fs00122-006-0254-x",{"doi":1270},{"id":24,"text":1273,"url":24,"identifiers":1274},"10.2307\u002F4135500",{"doi":1273},{"id":24,"text":1276,"url":24,"identifiers":1277},"10.1007\u002F978-1-4615-3276-7_1",{"doi":1276},{"id":24,"text":1279,"url":24,"identifiers":1280},"10.1007\u002Fs10592-005-9073-x",{"doi":1279},{"id":24,"text":1282,"url":24,"identifiers":1283},"10.1007\u002F978-1-4899-1751-5_4",{"doi":1282},{"id":24,"text":1285,"url":24,"identifiers":1286},"Gielly L., 1994, The use of chloroplast DNA to resolve plant phylogenies: noncoding versus rbcL sequences, Molecular Biology and Evolution, 11, 769",{},{"id":24,"text":1288,"url":24,"identifiers":1289},"10.1006\u002Fmpev.1993.1006",{"doi":1288},{"id":24,"text":1291,"url":24,"identifiers":1292},"10.1016\u002FS1055-7903(02)00022-2",{"doi":1291},{"id":24,"text":1294,"url":24,"identifiers":1295},"10.1098\u002Frspb.2002.2218",{"doi":1294},{"id":24,"text":1297,"url":24,"identifiers":1298},"10.1139\u002Fg05-093",{"doi":1297},{"id":24,"text":1300,"url":24,"identifiers":1301},"10.1111\u002Fj.1365-2699.2004.01082.x",{"doi":1300},{"id":24,"text":1303,"url":24,"identifiers":1304},"10.1098\u002Frstb.2005.1735",{"doi":1303},{"id":24,"text":1306,"url":24,"identifiers":1307},"10.1016\u002Fj.ympev.2005.12.003",{"doi":1306},{"id":24,"text":1309,"url":24,"identifiers":1310},"10.1080\u002F14620316.2003.11511612",{"doi":1309},{"id":24,"text":1312,"url":24,"identifiers":1313},"10.1073\u002Fpnas.0503123102",{"doi":1312},{"id":24,"text":1315,"url":24,"identifiers":1316},"Levinson G., 1987, Slipped‐strand mispairing: a major mechanism for DNA sequence evolution, Molecular Biology and Evolution, 4, 203",{},{"id":24,"text":1318,"url":24,"identifiers":1319},"Loayza M. D., 2005, Phragmipedium kovachii: molecular systematics of a new world orchid, Orchids, 72, 132",{},{"id":24,"text":1321,"url":24,"identifiers":1322},"10.1007\u002FBF00336789",{"doi":1321},{"id":24,"text":1324,"url":24,"identifiers":1325},"10.1007\u002FBF00351728",{"doi":1324},{"id":24,"text":1327,"url":24,"identifiers":1328},"10.1002\u002Fj.1537-2197.1994.tb15615.x",{"doi":1327},{"id":24,"text":1330,"url":24,"identifiers":1331},"10.1007\u002Fs00239-002-2333-y",{"doi":1330},{"id":24,"text":1333,"url":24,"identifiers":1334},"10.1600\u002F0363644054223648",{"doi":1333},{"id":24,"text":1336,"url":24,"identifiers":1337},"10.1111\u002Fj.1471-8286.2004.00636.x",{"doi":1336},{"id":24,"text":1339,"url":24,"identifiers":1340},"10.1021\u002Fjf0514569",{"doi":1339},{"id":24,"text":1342,"url":24,"identifiers":1343},"10.1016\u002Fj.tree.2005.10.019",{"doi":1342},{"id":24,"text":1345,"url":24,"identifiers":1346},"10.1111\u002Fj.1365-2699.2006.01462.x",{"doi":1345},{"id":24,"text":1348,"url":24,"identifiers":1349},"10.1111\u002Fj.1365-294X.2006.02821.x",{"doi":1348},{"id":24,"text":1351,"url":24,"identifiers":1352},"10.1111\u002Fj.1471-8286.2004.00635.x",{"doi":1351},{"id":24,"text":1354,"url":24,"identifiers":1355},"10.3732\u002Fajb.92.1.142",{"doi":1354},{"id":24,"text":1357,"url":24,"identifiers":1358},"10.3732\u002Fajb.92.12.2011",{"doi":1357},{"id":24,"text":1360,"url":24,"identifiers":1361},"10.2307\u002F2446640",{"doi":1360},{"id":24,"text":1363,"url":24,"identifiers":1364},"10.1111\u002Fj.1095-8339.2003.00265.x",{"doi":1363},{"id":24,"text":1366,"url":24,"identifiers":1367},"10.1007\u002FBF00037152",{"doi":1366},{"id":24,"text":1369,"url":24,"identifiers":1370},"10.1007\u002Fs00122-005-1990-z",{"doi":1369},{"id":24,"text":1372,"url":24,"identifiers":1373},"10.1111\u002Fj.1365-294X.2005.02462.x",{"doi":1372},{"id":24,"text":1375,"url":24,"identifiers":1376},"Thompson J. D. Higgins D. G. Gibson T. J.2001.ClustalXComputer program available atftp:\u002F\u002Fftp:\u002F\u002Fftp‐igbmc.u‐strasbg.fr\u002Fpub\u002Fclustalx\u002F.",{},{"id":24,"text":1378,"url":24,"identifiers":1379},"10.3732\u002Fajb.94.3.302",{"doi":1378},{"id":24,"text":1381,"url":24,"identifiers":1382},"10.1023\u002FA:1007564209282",{"doi":1381},{"id":24,"text":1384,"url":24,"identifiers":1385},"10.1111\u002Fj.1096-0031.2003.00008.x",{"doi":1384},{"id":24,"text":1387,"url":24,"identifiers":1388},"10.1093\u002Fjhered\u002Fesl001",{"doi":1387},{"id":24,"text":1390,"url":24,"identifiers":1391},"Wolfe K. H., 1991, Cell culture and somatic cell genetics of plants, vol. 7B, 467",{},{"id":24,"text":1393,"url":24,"identifiers":1394},"10.1073\u002Fpnas.84.24.9054",{"doi":1393},{"id":24,"text":1396,"url":24,"identifiers":1397},"10.1007\u002Fs00122-004-1588-x",{"doi":1396},{"id":24,"text":1399,"url":24,"identifiers":1400},"10.3732\u002Fajb.92.11.1887",{"doi":1399},{"id":1402,"createTime":1403,"updateTime":1404,"relativeEntities":1405,"slug":1406,"properties":1407,"entityType":967,"verifyStatus":120,"verifyTime":1403,"verifyNote":968,"languages":1422,"translateLanguages":1423,"viewCount":25,"primaryUrl":1424,"fullTextUrl":24,"authors":1425,"publicationType":1001,"publisherRelationship":1576,"citationCount":1630,"citationInfo":1631,"publishDate":1636,"publishYear":1238,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":1637,"openAccess":24,"references":1638,"isForceReanalyzing":1060},"3fc5fb3b-c27d-4915-9fde-804562311763","2024-09-24T23:27:38.248+00:00","2025-02-14T21:01:29.211+00:00",[],"The-tortoise-and-the-hare-II-relative-utility-of-21-noncoding-chloroplast-DNA-sequences-for-phylogenetic-analysis",{"mag":1408,"keywords":1410,"openalex":1411,"abstract":1413,"title":1416,"pm":1419,"doi":1421},{"VOID":1409},"2140038524",{"VI":1071},{"VOID":1412},"W2140038524",{"EN":1414,"VI":1415},"\u003Cjats:p>Chloroplast DNA sequences are a primary source of data for plant molecular systematic studies. A few key papers have provided the molecular systematics community with universal primer pairs for noncoding regions that have dominated the field, namely \u003Cjats:italic>trnL‐trnF\u003C\u002Fjats:italic> and \u003Cjats:italic>trnK\u002FmatK.\u003C\u002Fjats:italic> These two regions have provided adequate information to resolve species relationships in some taxa, but often provide little resolution at low taxonomic levels. To obtain better phylogenetic resolution, sequence data from these regions are often coupled with other sequence data. Choosing an appropriate cpDNA region for phylogenetic investigation is difficult because of the scarcity of information about the tempo of evolutionary rates among different noncoding cpDNA regions. The focus of this investigation was to determine whether there is any predictable rate heterogeneity among 21 noncoding cpDNA regions identified as phylogenetically useful at low levels. To test for rate heterogeneity among the different cpDNA regions, we used three species from each of 10 groups representing eight major phylogenetic lineages of phanerogams. The results of this study clearly show that a survey using as few as three representative taxa can be predictive of the amount of phylogenetic information offered by a cpDNA region and that rate heterogeneity exists among noncoding cpDNA regions.\u003C\u002Fjats:p>","\u003Cjats:p>Các trình tự DNA của ti thể lục lạp là nguồn dữ liệu chính cho các nghiên cứu hệ thống phân loại phân tử thực vật. Một vài tài liệu quan trọng đã cung cấp cho cộng đồng hệ thống phân loại phân tử những cặp mồi phổ quát cho các vùng không mã hóa chiếm ưu thế trong lĩnh vực này, cụ thể là \u003Cjats:italic>trnL‐trnF\u003C\u002Fjats:italic> và \u003Cjats:italic>trnK\u002FmatK.\u003C\u002Fjats:italic> Hai vùng này đã cung cấp thông tin đầy đủ để xác định mối quan hệ giữa các loài trong một số nhóm taxon, nhưng thường không cung cấp đủ độ phân giải ở các mức phân loại thấp. Để đạt được độ phân giải phát sinh chủng loài tốt hơn, dữ liệu trình tự từ các vùng này thường được kết hợp với các dữ liệu trình tự khác. Việc chọn lựa một vùng cpDNA phù hợp cho nghiên cứu phát sinh chủng loài là rất khó khăn do thiếu thông tin về tốc độ tiến hóa giữa các vùng cpDNA không mã hóa khác nhau. Mục tiêu của cuộc điều tra này là xác định xem có sự không đồng nhất về tốc độ nào có thể dự đoán được giữa 21 vùng cpDNA không mã hóa được xác định là hữu ích về mặt phát sinh chủng loài ở mức thấp hay không. Để kiểm tra sự không đồng nhất về tốc độ giữa các vùng cpDNA khác nhau, chúng tôi đã sử dụng ba loài từ mỗi nhóm trong số 10 nhóm đại diện cho tám dòng phát sinh chính của phanerogams. Kết quả của nghiên cứu này rõ ràng cho thấy rằng một khảo sát với chỉ ba loài đại diện cũng có thể dự đoán được lượng thông tin phát sinh chủng loài mà một vùng cpDNA cung cấp và rằng sự không đồng nhất về tốc độ tồn tại giữa các vùng cpDNA không mã hóa.\u003C\u002Fjats:p>",{"EN":1417,"VI":1418},"The tortoise and the hare II: relative utility of 21 noncoding chloroplast DNA sequences for phylogenetic analysis","Rùa và thỏ II: tính hữu ích tương đối của 21 trình tự DNA nhiễm sắc thể diệp lục không mã hóa cho phân tích phát sinh chủng loài",{"VOID":1420},"21652394",{"VOID":1354},[124],[123],"https:\u002F\u002Fbsapubs.onlinelibrary.wiley.com\u002Fdoi\u002F10.3732\u002Fajb.92.1.142",[1426,1442,1456,1471,1486,1503,1518,1533,1548,1562],{"id":1427,"sortIndex":25,"researcher":24,"roles":1428,"affiliations":1429,"properties":1438,"displayName":1112,"givenName":24,"familyName":24},"8583bf75-c0f2-4845-9097-2e67bbeddd5f",[],[1430],{"id":1431,"sortIndex":25,"affiliation":1432,"properties":24},"4ad63422-07c7-4cc6-b88a-94437bc4b998",{"id":1431,"createTime":24,"updateTime":24,"relativeEntities":1433,"slug":24,"properties":1434,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1437,"statistic":24},[],{"title":1435},{"EN":1436},"Department of Botany, 437 Hesler Biology, University of Tennessee, Knoxville, Tennessee 37996 USA.",[],{"orcid":1439,"title":1440,"openalex":1441},{"VOID":1110},{"EN":1112},{"VOID":1114},{"id":1443,"sortIndex":132,"researcher":24,"roles":1444,"affiliations":1445,"properties":1452,"displayName":1135,"givenName":24,"familyName":24},"7318a139-f766-461a-b430-1bd64383fd6d",[],[1446],{"id":1431,"sortIndex":25,"affiliation":1447,"properties":24},{"id":1431,"createTime":24,"updateTime":24,"relativeEntities":1448,"slug":24,"properties":1449,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1451,"statistic":24},[],{"title":1450},{"EN":1436},[],{"orcid":1453,"title":1454,"openalex":1455},{"VOID":1133},{"EN":1135},{"VOID":1137},{"id":1457,"sortIndex":215,"researcher":24,"roles":1458,"affiliations":1459,"properties":1466,"displayName":1468,"givenName":24,"familyName":24},"c297124c-18d4-4350-9c19-74af70cc301d",[],[1460],{"id":1431,"sortIndex":25,"affiliation":1461,"properties":24},{"id":1431,"createTime":24,"updateTime":24,"relativeEntities":1462,"slug":24,"properties":1463,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1465,"statistic":24},[],{"title":1464},{"EN":1436},[],{"title":1467,"openalex":1469},{"EN":1468},"John T. 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L., 1998, The intron in chloroplast gene rpL16 is missing from the flowering plant families Geraniaceae, Goodeniaceae, and Plumbaginaceae., Transactions of the Illinois State Academy of Science, 91, 1",{},{"id":24,"text":1714,"url":24,"identifiers":1715},"10.2307\u002F3558413",{"doi":1714},{"id":24,"text":1717,"url":24,"identifiers":1718},"10.1006\u002Fanbo.2000.1262",{"doi":1717},{"id":24,"text":1720,"url":24,"identifiers":1721},"10.2307\u002F2399846",{"doi":1720},{"id":24,"text":1723,"url":24,"identifiers":1724},"10.1007\u002Fs006060170015",{"doi":1723},{"id":24,"text":1726,"url":24,"identifiers":1727},"10.2307\u002F2419803",{"doi":1726},{"id":24,"text":1264,"url":24,"identifiers":1729},{"doi":1264},{"id":24,"text":1731,"url":24,"identifiers":1732},"Cranfill R. 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Program available atftp:\u002F\u002Fftp‐igbmc.u‐strasbg.fr\u002Fpub\u002FClustalX\u002F.",{},{"id":24,"text":2101,"url":24,"identifiers":2102},"10.1007\u002FBF00279998",{"doi":2101},{"id":24,"text":2104,"url":24,"identifiers":2105},"10.3732\u002Fajb.90.10.1455",{"doi":2104},{"id":24,"text":2107,"url":24,"identifiers":2108},"10.1073\u002Fpnas.91.21.9794",{"doi":2107},{"id":24,"text":1381,"url":24,"identifiers":2110},{"doi":1381},{"id":24,"text":2112,"url":24,"identifiers":2113},"10.2307\u002F2656672",{"doi":2112},{"id":24,"text":2115,"url":24,"identifiers":2116},"10.1007\u002Fs006060170075",{"doi":2115},{"id":24,"text":2118,"url":24,"identifiers":2119},"Westhof E., 1996, Ribosomal RNA and group I introns",{},{"id":24,"text":2121,"url":24,"identifiers":2122},"10.1016\u002FS1055-7903(02)00210-5",{"doi":2121},{"id":24,"text":2124,"url":24,"identifiers":2125},"10.2307\u002F2446141",{"doi":2124},{"id":24,"text":1393,"url":24,"identifiers":2127},{"doi":1393},{"id":24,"text":2129,"url":24,"identifiers":2130},"10.1073\u002Fpnas.89.22.10648",{"doi":2129},{"id":24,"text":2132,"url":24,"identifiers":2133},"10.1007\u002Fs001220051537",{"doi":2132},{"id":24,"text":2135,"url":24,"identifiers":2136},"10.3732\u002Fajb.90.3.339",{"doi":2135},{"id":24,"text":2138,"url":24,"identifiers":2139},"10.1016\u002FS1055-7903(02)00026-X",{"doi":2138},{"id":24,"text":2141,"url":24,"identifiers":2142},"10.1006\u002Fmpev.1999.0729",{"doi":2141},{"id":24,"text":2144,"url":24,"identifiers":2145},"10.1046\u002Fj.1365-294x.2000.00963.x",{"doi":2144},{"id":24,"text":2147,"url":24,"identifiers":2148},"10.1146\u002Fannurev.pp.38.060187.002135",{"doi":2147},{"id":2150,"createTime":2151,"updateTime":2152,"relativeEntities":2153,"slug":2154,"properties":2155,"entityType":967,"verifyStatus":120,"verifyTime":2151,"verifyNote":968,"languages":2169,"translateLanguages":2170,"viewCount":25,"primaryUrl":2171,"fullTextUrl":24,"authors":2172,"publicationType":1001,"publisherRelationship":2190,"citationCount":2243,"citationInfo":2244,"publishDate":2247,"publishYear":2245,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":2248,"openAccess":24,"references":2249,"isForceReanalyzing":1060},"932d9c63-ad95-419b-88f5-84b1af9111a7","2024-09-21T11:45:45.289+00:00","2025-02-14T21:02:26.531+00:00",[],"CLASSIFICATION-OF-THE-ARCHITECTURE-OF-DICOTYLEDONOUS-LEAVES",{"openalex":2156,"mag":2158,"abstract":2160,"title":2163,"keywords":2166,"doi":2167},{"VOID":2157},"W2015423051",{"VOID":2159},"2015423051",{"EN":2161,"VI":2162},"\u003Cjats:p>A classification of the architectural features of dicot leaves—i.e., the placement and form of those elements constituting the outward expression of leaf structure, including shape, marginal configuration, venation, and gland position—has been developed as the result of an extensive survey of both living and fossil leaves. This system partially incorporates modifications of two earlier classifications: that of Turrill for leaf shape and that of Von Ettingshausen for venation pattern. After categorization of such features as shape of the whole leaf and of the apex and base, leaves are separated into a number of classes depending on the course of their principal venation. Identification of order of venation, which is fundamental to the application of the classification, is determined by size of a vein at its point of origin and to a lesser extent by its behavior in relation to that of other orders. The classification concludes by describing features of the areoles, i.e., the smallest areas of leaf tissue surrounded by veins which form a contiguous field over most of the leaf. Because most taxa of dicots possess consistent patterns of leaf architecture, this rigorous method of describing the features of leaves is of immediate usefulness in both modern and fossil taxonomic studies. In addition, as a result of this method, it is anticipated that leaves will play an increasingly important part in phylogenetic and ecological studies.\u003C\u002Fjats:p>","\u003Cjats:p>Đã phát triển một hệ thống phân loại các đặc trưng kiến trúc của lá song tính—tức là, vị trí và hình dạng của những yếu tố tạo nên biểu hiện bên ngoài của cấu trúc lá, bao gồm hình dạng, cấu hình lề, hệ thống gân, và vị trí tuyến—như là kết quả của một cuộc khảo sát rộng rãi về cả lá sống và lá hóa thạch. Hệ thống này một phần kết hợp các điều chỉnh từ hai phân loại trước đó: phân loại của Turrill về hình dạng lá và phân loại của Von Ettingshausen về mẫu gân. Sau khi phân loại các đặc trưng như hình dạng của toàn bộ lá và của đỉnh và đáy, các lá được phân tách thành một số lớp phụ thuộc vào hướng của hệ gân chính. Việc xác định thứ tự gân, điều này là nền tảng cho việc áp dụng phân loại, được xác định bởi kích thước của một gân tại điểm bắt đầu của nó và ở mức độ ít hơn là hành vi của nó liên quan đến các thứ tự khác. Phân loại kết thúc bằng việc mô tả các đặc trưng của các khoang tế bào, tức là, các khu vực nhỏ nhất của mô lá được bao quanh bởi các gân, tạo ra một trường liên tục trên hầu hết bề mặt lá. Bởi vì hầu hết các taxa của lá song tính đều sở hữu các mẫu kiến trúc lá nhất quán, phương pháp mô tả nghiêm ngặt này về các đặc trưng của lá là vô cùng hữu ích ngay cả trong các nghiên cứu phân loại hiện đại và hóa thạch. Ngoài ra, nhờ kết quả của phương pháp này, dự kiến rằng các lá sẽ đóng một vai trò ngày càng quan trọng trong các nghiên cứu phát sinh loài và sinh thái.\u003C\u002Fjats:p>",{"EN":2164,"VI":2165},"CLASSIFICATION OF THE ARCHITECTURE OF DICOTYLEDONOUS LEAVES","PHÂN LOẠI CÁC ĐẶC TRƯNG KIẾN TRÚC CỦA LÁ SONG TÍNH",{"VI":1071},{"VOID":2168},"10.1002\u002Fj.1537-2197.1973.tb10192.x",[124],[123],"https:\u002F\u002Fbsapubs.onlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fj.1537-2197.1973.tb10192.x",[2173],{"id":2174,"sortIndex":25,"researcher":24,"roles":2175,"affiliations":2176,"properties":2185,"displayName":2187,"givenName":24,"familyName":24},"6ddca9f8-2952-4020-b632-b2537453c08b",[],[2177],{"id":2178,"sortIndex":25,"affiliation":2179,"properties":24},"f72e8261-c2d8-422a-a84f-1f7e69ce935d",{"id":2178,"createTime":24,"updateTime":24,"relativeEntities":2180,"slug":24,"properties":2181,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":2184,"statistic":24},[],{"title":2182},{"EN":2183},"Division of Paleobotany, Smithsonian Institution, Washington, D. C.",[],{"title":2186,"openalex":2188},{"EN":2187},"Leo Hickey",{"VOID":2189},"A5004566707",{"url":24,"publisher":2191,"properties":2237},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":2192,"slug":10,"properties":2193,"entityType":22,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":25,"subjectFields":2198,"manageAffiliations":2211,"indexDatabases":2222,"url":97,"thumbnailPath":24,"statistic":24,"gsStatistic":24,"type":24,"analyzePriority":24},[],{"country":2194,"eissn":2195,"issn":2196,"title":2197},{"VOID":13},{"VOID":15},{"VOID":17},{"EN":19},[2199,2203,2207],{"id":28,"createTime":24,"updateTime":24,"relativeEntities":2200,"label":2201,"description":2202,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":31},{},{"id":34,"createTime":24,"updateTime":24,"relativeEntities":2204,"label":2205,"description":2206,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":37},{},{"id":40,"createTime":24,"updateTime":24,"relativeEntities":2208,"label":2209,"description":2210,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":43},{},[2212,2217],{"id":47,"createTime":24,"updateTime":24,"relativeEntities":2213,"slug":24,"properties":2214,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":2216,"statistic":24},[],{"title":2215},{"EN":51},[],{"id":54,"createTime":24,"updateTime":24,"relativeEntities":2218,"slug":24,"properties":2219,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":2221,"statistic":24},[],{"title":2220},{"EN":58},[],[2223,2230],{"id":62,"indexDatabase":2224,"url":73,"indexYears":74,"academicFieldIds":2229,"indexDatabaseRanking":79},{"id":64,"createTime":24,"updateTime":24,"relativeEntities":2225,"label":2226,"description":2227,"key":70,"publicationTags":2228,"standard":24},[],{"EN":67,"VI":67},{"EN":67,"VI":69},[72],[76,77,78],{"id":81,"indexDatabase":2231,"url":94,"indexYears":24,"academicFieldIds":2236,"indexDatabaseRanking":24},{"id":83,"createTime":24,"updateTime":24,"relativeEntities":2232,"label":2233,"description":2234,"key":90,"publicationTags":2235,"standard":24},[],{"EN":86,"VI":86},{"EN":88,"VI":89},[92,93],[96],{"issue":2238,"pages":2239,"volume":2241},{"VOID":1625},{"VOID":2240},"17-33",{"VOID":2242},"60",937,{"total":2243,"publishYear":2245,"statisticByYear":2246},1973,{"2012":214,"2013":233,"2014":234,"2015":214,"2016":222,"2017":214,"2018":526,"2019":691,"2020":233,"2021":781,"2022":240,"2023":230,"2024":221},"1973-01-01",[92],[2250,2254,2257,2260,2263,2266,2269,2272,2275,2278,2281,2284,2287,2290,2293,2296,2299,2302,2305,2308,2311,2314,2317,2321,2324,2327,2331,2335],{"id":24,"text":2251,"url":24,"identifiers":2252},"Berry E. W.1916.The lower Eocene floras of southeastern North America. U.S. Geol. Surv. Prof. Paper 91.",{"doi":2253},"10.3133\u002Fpp91",{"id":24,"text":2255,"url":24,"identifiers":2256},"10.1002\u002Fj.1537-2197.1971.tb10011.x",{"doi":2255},{"id":24,"text":2258,"url":24,"identifiers":2259},"10.1002\u002Fj.1537-2197.1971.tb09994.x",{"doi":2258},{"id":24,"text":2261,"url":24,"identifiers":2262},"10.1002\u002Fj.1537-2197.1970.tb09801.x",{"doi":2261},{"id":24,"text":2264,"url":24,"identifiers":2265},"10.5962\u002Fbhl.part.24686",{"doi":2264},{"id":24,"text":2267,"url":24,"identifiers":2268},"Ettingshausen C., 1861, Die Blattskelete des Dicotyledonen",{},{"id":24,"text":2270,"url":24,"identifiers":2271},"Federov A. A., 1956, Atlas po opisatelnoi morfologii visshich rastenii",{},{"id":24,"text":2273,"url":24,"identifiers":2274},"10.2307\u002F2437967",{"doi":2273},{"id":24,"text":2276,"url":24,"identifiers":2277},"10.2307\u002F2438624",{"doi":2276},{"id":24,"text":2279,"url":24,"identifiers":2280},"Goebel K.1905.Organography of plants. Eng. ed. byI. B.Balfour. Part II.Oxford.",{},{"id":24,"text":2282,"url":24,"identifiers":2283},"Hickey L. J., 1971, Leaf architectural classification of the Angiosperms (abstr.), Amer. J. Bot., 58, 450",{},{"id":24,"text":2285,"url":24,"identifiers":2286},"Hickey L. J., 1971, Evolutionary significance of leaf architectural features in the woody dicots (abstr.), Amer. J. Bot., 58, 469",{},{"id":24,"text":2288,"url":24,"identifiers":2289},"Hickey L. J.In press.Stratigraphy and Paleobotany of the Golden Valley Formation (Early Tertiary) of western North Dakota:Geol. Soc. Amer. Memoir.",{},{"id":24,"text":2291,"url":24,"identifiers":2292},"Hollick A.1936.The Tertiary floras of Alaska. U.S. Geol. Surv. Prof. Paper 182.",{},{"id":24,"text":2294,"url":24,"identifiers":2295},"Kerner von Marilaun A. J., 1895, The natural history of plants",{},{"id":24,"text":2297,"url":24,"identifiers":2298},"Krussmann G., 1960, Handbuch der Laubgehölze",{},{"id":24,"text":2300,"url":24,"identifiers":2301},"Lam H. J., 1925, The Sapotaceae, Sarcospermaceae, and Boerlagellaceae of the Dutch East Indies and surrounding countries, Bull. Jard. Bot. Buitenzorg III, 8, 1",{},{"id":24,"text":2303,"url":24,"identifiers":2304},"Lawrence G. H., 1951, Taxonomy of vascular plants",{},{"id":24,"text":2306,"url":24,"identifiers":2307},"Lee A. T., 1948, The genus Swainsona, Contrib. New South Wales Herb., 1, 131",{},{"id":24,"text":2309,"url":24,"identifiers":2310},"Lesquereux L.1878.Contributions to the fossil floras of the Western Territories.Part II. The Tertiary Flora. U.S. Geol. Geog. Surv. Terr. Rept. 7.",{},{"id":24,"text":2312,"url":24,"identifiers":2313},"Pacltová B., 1961, Zur Frage der gattung Eucalyptus in der böhmischen Dreideformation, Preslia, 33, 113",{},{"id":24,"text":2315,"url":24,"identifiers":2316},"Stearn W. T.1956.InP.Synge[ed.] Supplement to the Dictionary of Gardening.Oxford. p.318–322.",{},{"id":24,"text":2318,"url":24,"identifiers":2319},"Systematics Association Committee for Descriptive Terminology (SADT), 1962, Terminology of simple symmetrical plane shapes (Chart 1), Taxon, 11, 145, 10.2307\u002F1216718",{"doi":2320},"10.2307\u002F1216718",{"id":24,"text":2322,"url":24,"identifiers":2323},"Takhtajan A. L.1963.InA. L.Takhtajan V. A.Vakhremeev andG. P.Radchenko[ed.] Osnovy paleontologii Golosemennye i pokrytosemennye.Moskow. p.395–399.",{},{"id":24,"text":2325,"url":24,"identifiers":2326},"Troll W., 1938, Vergleichende Morphologie der höhern Pflanzen., 1",{},{"id":24,"text":2328,"url":24,"identifiers":2329},"Wolfe J. A.1966.Tertiary plants from the Cook Inlet Region Alaska. U.S. Geol. Surv. Prof. Paper 398‐B.",{"doi":2330},"10.3133\u002Fpp398B",{"id":24,"text":2332,"url":24,"identifiers":2333},"Wolfe J. A.1968.Paleogene biostratigraphy of nonmarine rocks in King Co. Washington. U.S. Geol. Surv. Prof. Paper 571.",{"doi":2334},"10.3133\u002Fpp571",{"id":24,"text":2336,"url":24,"identifiers":2337},"Wolfe J. A., 1969, Paleogene floras from the Gulf of Alaska Region",{},{"id":2339,"createTime":2340,"updateTime":2341,"relativeEntities":2342,"slug":2343,"properties":2344,"entityType":967,"verifyStatus":120,"verifyTime":2340,"verifyNote":968,"languages":2360,"translateLanguages":2361,"viewCount":25,"primaryUrl":2362,"fullTextUrl":24,"authors":2363,"publicationType":1001,"publisherRelationship":2421,"citationCount":664,"citationInfo":2474,"publishDate":2477,"publishYear":2475,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":2478,"openAccess":24,"references":2479,"isForceReanalyzing":1060},"2133d8ff-57c0-48b8-b85e-c141ba93e2ae","2024-10-08T21:15:03.735+00:00","2025-02-14T21:03:26.104+00:00",[],"A-phylogeny-of-legumes-Leguminosae-based-on-analysis-of-the-plastid-i-mat-i-i-K-i-gene-resolves-many-well-supported-subclades-within-the-family",{"mag":2345,"keywords":2347,"openalex":2348,"abstract":2350,"title":2353,"pm":2356,"doi":2358},{"VOID":2346},"2158152955",{"VI":1071},{"VOID":2349},"W2158152955",{"EN":2351,"VI":2352},"\u003Cjats:p>Phylogenetic analysis of 330 plastid\u003Cjats:italic>matK\u003C\u002Fjats:italic>gene sequences, representing 235 genera from 37 of 39 tribes, and four outgroup taxa from eurosids I supports many well‐resolved subclades within the Leguminosae. These results are generally consistent with those derived from other plastid sequence data (\u003Cjats:italic>rbcL\u003C\u002Fjats:italic>and\u003Cjats:italic>trnL\u003C\u002Fjats:italic>), but show greater resolution and clade support overall. In particular, the monophyly of subfamily Papilionoideae and at least seven major subclades are well‐supported by bootstrap and Bayesian credibility values. These subclades are informally recognized as the\u003Cjats:italic>Cladrastis\u003C\u002Fjats:italic>clade, genistoid sensu lato, dalbergioid sensu lato, mirbelioid, millettioid, and robinioid clades, and the inverted‐repeat‐lacking clade (IRLC). The genistoid clade is expanded to include genera such as\u003Cjats:italic>Poecilanthe\u003C\u002Fjats:italic>,\u003Cjats:italic>Cyclolobium\u003C\u002Fjats:italic>,\u003Cjats:italic>Bowdichia\u003C\u002Fjats:italic>, and\u003Cjats:italic>Diplotropis\u003C\u002Fjats:italic>and thus contains the vast majority of papilionoids known to produce quinolizidine alkaloids. The dalbergioid clade is expanded to include the tribe Amorpheae. The mirbelioids include the tribes Bossiaeeae and Mirbelieae, with Hypocalypteae as its sister group. The millettioids comprise two major subclades that roughly correspond to the tribes Millettieae and Phaseoleae and represent the only major papilionoid clade marked by a macromorphological apomorphy, pseudoracemose inflorescences. The robinioids are expanded to include\u003Cjats:italic>Sesbania\u003C\u002Fjats:italic>and members of the tribe Loteae. The IRLC, the most species‐rich subclade, is sister to the robinioids. Analysis of the\u003Cjats:italic>matK\u003C\u002Fjats:italic>data consistently resolves but modestly supports a clade comprising papilionoid taxa that accumulate canavanine in the seeds. This suggests a single origin for the biosynthesis of this most commonly produced of the nonprotein amino acids in legumes.\u003C\u002Fjats:p>","\u003Cjats:p>Phân tích hệ phát sinh chủng loại của 330 trình tự gen plastid \u003Cjats:italic>matK\u003C\u002Fjats:italic>, đại diện cho 235 giống từ 37 trên 39 tộc, và bốn taxa ngoài nhóm từ eurosids I hỗ trợ nhiều nhánh con được phân giải rõ ràng trong họ Đậu (Leguminosae). Những kết quả này nói chung nhất quán với những gì được rút ra từ dữ liệu trình tự plastid khác (\u003Cjats:italic>rbcL\u003C\u002Fjats:italic> và \u003Cjats:italic>trnL\u003C\u002Fjats:italic>), nhưng cho thấy mức độ phân giải và hỗ trợ nhánh cao hơn tổng thể. Cụ thể, tính đơn nguyên của tông Papilionoideae và ít nhất bảy nhánh lớn được hỗ trợ tốt bởi giá trị bootstrapping và độ tin cậy của Bayesian. Các nhánh này được công nhận không chính thức là nhánh \u003Cjats:italic>Cladrastis\u003C\u002Fjats:italic>, genistoid sensu lato, dalbergioid sensu lato, mirbelioid, millettioid, và robinioid, cùng với nhánh thiếu lặp lại đảo ngược (IRLC). Nhánh genistoid được mở rộng để bao gồm các giống như \u003Cjats:italic>Poecilanthe\u003C\u002Fjats:italic>, \u003Cjats:italic>Cyclolobium\u003C\u002Fjats:italic>, \u003Cjats:italic>Bowdichia\u003C\u002Fjats:italic>, và \u003Cjats:italic>Diplotropis\u003C\u002Fjats:italic> và do đó chứa hầu hết các giống papilionoid được biết đến có khả năng sản xuất alkaloid quinolizidine. Nhánh dalbergioid được mở rộng để bao gồm tông Amorpheae. Nhánh mirbelioid bao gồm các tông Bossiaeeae và Mirbelieae, với Hypocalypteae là nhóm chị em của nó. Nhánh millettioid bao gồm hai nhánh con lớn tương ứng với các tông Millettieae và Phaseoleae và đại diện cho nhánh papilionoid lớn duy nhất được đánh dấu bởi một apomorphy hình thái học vĩ mô, cụm hoa giả chùm. Nhánh robinioid được mở rộng để bao gồm \u003Cjats:italic>Sesbania\u003C\u002Fjats:italic> và các thành viên của tông Loteae. IRLC, nhánh có nhiều loài nhất, là chị em với robinioids. Phân tích dữ liệu \u003Cjats:italic>matK\u003C\u002Fjats:italic> liên tục xác định nhưng hỗ trợ khiêm tốn một nhánh bao gồm các taxa papilionoid tích lũy canavanine trong hạt. Điều này gợi ý một nguồn gốc đơn nhất cho sự tổng hợp sinh học của axit amin không protein được sản xuất phổ biến nhất trong họ đậu.\u003C\u002Fjats:p>",{"EN":2354,"VI":2355},"A phylogeny of legumes (Leguminosae) based on analysis of the plastid\u003Ci>mat\u003C\u002Fi>\u003Ci>K\u003C\u002Fi>gene resolves many well‐supported subclades within the family","Một phân loại học về cây họ Đậu (Leguminosae) dựa trên phân tích gen plastid \u003Ci>matK\u003C\u002Fi> giải quyết nhiều nhánh con được hỗ trợ tốt trong họ",{"VOID":2357},"21652332",{"VOID":2359},"10.3732\u002Fajb.91.11.1846",[124],[123],"https:\u002F\u002Fbsapubs.onlinelibrary.wiley.com\u002Fdoi\u002F10.3732\u002Fajb.91.11.1846",[2364,2383,2402],{"id":2365,"sortIndex":25,"researcher":24,"roles":2366,"affiliations":2367,"properties":2376,"displayName":2380,"givenName":24,"familyName":24},"70a5af13-e3ef-4384-ba55-18bfd29a64b5",[],[2368],{"id":2369,"sortIndex":25,"affiliation":2370,"properties":24},"cbeb8c8b-6cb2-448b-82d3-388eb06a31a0",{"id":2369,"createTime":24,"updateTime":24,"relativeEntities":2371,"slug":24,"properties":2372,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":2375,"statistic":24},[],{"title":2373},{"EN":2374},"2School of Life Sciences, Arizona State University, Tempe, Arizona 85287-4501 USA",[],{"orcid":2377,"title":2379,"openalex":2381},{"VOID":2378},"https:\u002F\u002Forcid.org\u002F0000-0002-0682-9034",{"EN":2380},"Martin F. 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L., 1981, Advances in legume systematics, part 1,, 403",{},{"id":24,"text":2787,"url":24,"identifiers":2788},"10.1046\u002Fj.1095-8339.2002.00051.x",{"doi":2787},{"id":24,"text":2790,"url":24,"identifiers":2791},"10.1016\u002FS0305-1978(03)00083-8",{"doi":2790},{"id":24,"text":2793,"url":24,"identifiers":2794},"10.1016\u002F0305-1978(93)90075-3",{"doi":2793},{"id":24,"text":2796,"url":24,"identifiers":2797},"Van Wyk B.‐E., 1995, Advances in legume systematics, part 7, Phylogeny,, 283",{},{"id":24,"text":2799,"url":24,"identifiers":2800},"Whiting M. F., 1997, The strepsiptera problem: phylogeny of the holometabolous insect orders inferred from 18S and 28S ribosomal DNA sequences and morphology., Systematic Biology, 46, 1",{},{"id":24,"text":2802,"url":24,"identifiers":2803},"10.1016\u002FS1055-7903(02)00244-0",{"doi":2802},{"id":24,"text":2805,"url":24,"identifiers":2806},"10.1016\u002FS0305-1978(03)00085-1",{"doi":2805},{"id":24,"text":2808,"url":24,"identifiers":2809},"Wojciechowski M. F., 2003, Advances in legume systematics, part 10, Higher leval systematics,, 5",{},{"id":24,"text":2811,"url":24,"identifiers":2812},"10.2307\u002F2419698",{"doi":2811},{"id":24,"text":2814,"url":24,"identifiers":2815},"Wojciechowski M. F., 2000, Advances in legume systematics, part 9,, 277",{},{"id":2817,"createTime":2818,"updateTime":2819,"relativeEntities":2820,"slug":2821,"properties":2822,"entityType":967,"verifyStatus":120,"verifyTime":2818,"verifyNote":968,"languages":2838,"translateLanguages":2839,"viewCount":25,"primaryUrl":2840,"fullTextUrl":24,"authors":2841,"publicationType":1001,"publisherRelationship":3342,"citationCount":3396,"citationInfo":3397,"publishDate":3401,"publishYear":3398,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":3402,"openAccess":24,"references":3403,"isForceReanalyzing":1060},"678f2d97-e377-47f2-98d1-a847e1efbe91","2024-10-10T08:41:22.697+00:00","2025-02-14T21:04:26.724+00:00",[],"Angiosperm-phylogeny-17-genes-640-taxa",{"mag":2823,"keywords":2825,"openalex":2826,"abstract":2828,"title":2831,"pm":2834,"doi":2836},{"VOID":2824},"2123023543",{"VI":1071},{"VOID":2827},"W2123023543",{"EN":2829,"VI":2830},"\u003Cjats:p>• \u003Cjats:italic>Premise of the study\u003C\u002Fjats:italic>: Recent analyses employing up to five genes have provided numerous insights into angiosperm phylogeny, but many relationships have remained unresolved or poorly supported. In the hope of improving our understanding of angiosperm phylogeny, we expanded sampling of taxa and genes beyond previous analyses.\u003C\u002Fjats:p>\u003Cjats:p>• \u003Cjats:italic>Methods\u003C\u002Fjats:italic>: We conducted two primary analyses based on 640 species representing 330 families. The first included 25260 aligned base pairs (bp) from 17 genes (representing all three plant genomes, i.e., nucleus, plastid, and mitochondrion). The second included 19846 aligned bp from 13 genes (representing only the nucleus and plastid).\u003C\u002Fjats:p>\u003Cjats:p>• \u003Cjats:italic>Key results\u003C\u002Fjats:italic>: Many important questions of deep‐level relationships in the nonmonocot angiosperms have now been resolved with strong support. Amborellaceae, Nymphaeales, and Austrobaileyales are successive sisters to the remaining angiosperms (\u003Cjats:italic>Mesangiospermae\u003C\u002Fjats:italic>), which are resolved into Chloranthales + \u003Cjats:italic>Magnoliidae\u003C\u002Fjats:italic> as sister to \u003Cjats:italic>Monocotyledoneae\u003C\u002Fjats:italic> + [Ceratophyllaceae + \u003Cjats:italic>Eudicotyledoneae\u003C\u002Fjats:italic>]. \u003Cjats:italic>Eudicotyledoneae\u003C\u002Fjats:italic> contains a basal grade subtending \u003Cjats:italic>Gunneridae\u003C\u002Fjats:italic>. Within \u003Cjats:italic>Gunneridae\u003C\u002Fjats:italic>, Gunnerales are sister to the remainder (\u003Cjats:italic>Pentapetalae\u003C\u002Fjats:italic>), which comprises (1) \u003Cjats:italic>Superrosidae\u003C\u002Fjats:italic>, consisting of \u003Cjats:italic>Rosidae\u003C\u002Fjats:italic> (including Vitaceae) and Saxifragales; and (2) \u003Cjats:italic>Superasteridae\u003C\u002Fjats:italic>, comprising Berberidopsidales, Santalales, \u003Cjats:italic>Caryophyllales\u003C\u002Fjats:italic>, \u003Cjats:italic>Asteridae\u003C\u002Fjats:italic>, and, based on this study, Dilleniaceae (although other recent analyses disagree with this placement). Within the major subclades of \u003Cjats:italic>Pentapetalae\u003C\u002Fjats:italic>, most deep‐level relationships are resolved with strong support.\u003C\u002Fjats:p>\u003Cjats:p>• \u003Cjats:italic>Conclusions\u003C\u002Fjats:italic>: Our analyses confirm that with large amounts of sequence data, most deep‐level relationships within the angiosperms can be resolved. We anticipate that this well‐resolved angiosperm tree will be of broad utility for many areas of biology, including physiology, ecology, paleobiology, and genomics.\u003C\u002Fjats:p>","\u003Cjats:p>• \u003Cjats:italic>Đặt vấn đề nghiên cứu\u003C\u002Fjats:italic>: Những phân tích gần đây sử dụng tối đa năm gen đã cung cấp nhiều hiểu biết về hệ phả hệ của thực vật hạt kín, nhưng nhiều mối quan hệ vẫn chưa được làm rõ hoặc hỗ trợ yếu. Với hy vọng cải thiện hiểu biết của chúng tôi về hệ phả hệ thực vật hạt kín, chúng tôi đã mở rộng mẫu vật và gen vượt ra ngoài những phân tích trước đây.\u003C\u002Fjats:p>\u003Cjats:p>• \u003Cjats:italic>Phương pháp\u003C\u002Fjats:italic>: Chúng tôi đã thực hiện hai phân tích chính dựa trên 640 loài đại diện cho 330 họ. Phân tích đầu tiên bao gồm 25260 cặp căn cứ đã căn chỉnh (bp) từ 17 gen (đại diện cho cả ba hệ gen thực vật, tức là nhân, plastid và ti thể). Phân tích thứ hai bao gồm 19846 bp đã căn chỉnh từ 13 gen (chỉ đại diện cho nhân và plastid).\u003C\u002Fjats:p>\u003Cjats:p>• \u003Cjats:italic>Kết quả chính\u003C\u002Fjats:italic>: Nhiều câu hỏi quan trọng về các mối quan hệ ở cấp độ sâu trong thực vật hạt kín không đơn lá đã được giải quyết với sự hỗ trợ mạnh mẽ. Amborellaceae, Nymphaeales và Austrobaileyales là các chi chị em liên tiếp với các thực vật hạt kín còn lại (\u003Cjats:italic>Mesangiospermae\u003C\u002Fjats:italic>), được phân thành Chloranthales + \u003Cjats:italic>Magnoliidae\u003C\u002Fjats:italic> như là chi chị em với \u003Cjats:italic>Monocotyledoneae\u003C\u002Fjats:italic> + [Ceratophyllaceae + \u003Cjats:italic>Eudicotyledoneae\u003C\u002Fjats:italic>]. \u003Cjats:italic>Eudicotyledoneae\u003C\u002Fjats:italic> chứa một nhánh cơ bản hỗ trợ \u003Cjats:italic>Gunneridae\u003C\u002Fjats:italic>. Trong \u003Cjats:italic>Gunneridae\u003C\u002Fjats:italic>, Gunnerales là chị em với phần còn lại (\u003Cjats:italic>Pentapetalae\u003C\u002Fjats:italic>), bao gồm (1) \u003Cjats:italic>Superrosidae\u003C\u002Fjats:italic>, bao gồm \u003Cjats:italic>Rosidae\u003C\u002Fjats:italic> (bao gồm Vitaceae) và Saxifragales; và (2) \u003Cjats:italic>Superasteridae\u003C\u002Fjats:italic>, bao gồm Berberidopsidales, Santalales, \u003Cjats:italic>Caryophyllales\u003C\u002Fjats:italic>, \u003Cjats:italic>Asteridae\u003C\u002Fjats:italic>, và, dựa trên nghiên cứu này, Dilleniaceae (mặc dù các phân tích gần đây khác không đồng ý với vị trí này). Trong các nhánh chính của \u003Cjats:italic>Pentapetalae\u003C\u002Fjats:italic>, hầu hết các mối quan hệ cấp độ sâu đã được giải quyết với sự hỗ trợ mạnh mẽ.\u003C\u002Fjats:p>\u003Cjats:p>• \u003Cjats:italic>Kết luận\u003C\u002Fjats:italic>: Các phân tích của chúng tôi xác nhận rằng với một lượng lớn dữ liệu trình tự, hầu hết các mối quan hệ cấp độ sâu trong các thực vật hạt kín có thể được giải quyết. Chúng tôi dự kiến rằng cây phả hệ được làm rõ tốt về thực vật hạt kín này sẽ có tính hữu dụng rộng rãi cho nhiều lĩnh vực sinh học, bao gồm sinh lý học, sinh thái học, cổ sinh vật học và gen học.\u003C\u002Fjats:p>",{"EN":2832,"VI":2833},"Angiosperm phylogeny: 17 genes, 640 taxa","Hệ phả hệ của thực vật hạt kín: 17 gen, 640 thu loại",{"VOID":2835},"21613169",{"VOID":2837},"10.3732\u002Fajb.1000404",[124],[123],"https:\u002F\u002Fbsapubs.onlinelibrary.wiley.com\u002Fdoi\u002F10.3732\u002Fajb.1000404",[2842,2861,2880,2899,2918,2935,2954,2973,2990,3009,3028,3047,3070,3087,3104,3129,3148,3165,3188,3205,3224,3241,3258,3274,3289,3306,3323],{"id":2843,"sortIndex":25,"researcher":24,"roles":2844,"affiliations":2845,"properties":2854,"displayName":2858,"givenName":24,"familyName":24},"d2b5841c-dfd9-45d1-8501-2606903e6104",[],[2846],{"id":2847,"sortIndex":25,"affiliation":2848,"properties":24},"e71ed117-dd45-4ba0-8f2a-d895984567ca",{"id":2847,"createTime":24,"updateTime":24,"relativeEntities":2849,"slug":24,"properties":2850,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":2853,"statistic":24},[],{"title":2851},{"EN":2852},"Department of Biology, University of Florida, Gainesville, Florida 32611-8525 USA",[],{"orcid":2855,"title":2857,"openalex":2859},{"VOID":2856},"https:\u002F\u002Forcid.org\u002F0000-0001-9310-8659",{"EN":2858},"Pamela S. 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S. andP. O.Lewis.2001. PAUPRat: A tool to implement parsimony and likelihood ratchet searches using PAUP* [online computer program]. Websitehttp:\u002F\u002Fwww.ucalgary.ca\u002F∼dsikes\u002Fsoftware2.htm.",{},{"id":24,"text":3691,"url":24,"identifiers":3692},"10.2307\u002F2657021",{"doi":3691},{"id":24,"text":3694,"url":24,"identifiers":3695},"10.1006\u002Fmpev.2001.0937",{"doi":3694},{"id":24,"text":3697,"url":24,"identifiers":3698},"10.1186\u002F1471-2148-9-37",{"doi":3697},{"id":24,"text":3700,"url":24,"identifiers":3701},"10.1093\u002Fbioinformatics\u002Fbtm619",{"doi":3700},{"id":24,"text":3703,"url":24,"identifiers":3704},"10.1086\u002F509788",{"doi":3703},{"id":24,"text":3706,"url":24,"identifiers":3707},"10.2307\u002F2446027",{"doi":3706},{"id":24,"text":3709,"url":24,"identifiers":3710},"10.1038\u002F46528",{"doi":3709},{"id":24,"text":2719,"url":24,"identifiers":3712},{"doi":2719},{"id":24,"text":3714,"url":24,"identifiers":3715},"10.1002\u002Fj.1537-2197.1991.tb14517.x",{"doi":3714},{"id":24,"text":3717,"url":24,"identifiers":3718},"Soltis D. E., 2005, Phylogeny and evolution of the angiosperms",{},{"id":24,"text":3720,"url":24,"identifiers":3721},"10.2307\u002F2399952",{"doi":3720},{"id":24,"text":3723,"url":24,"identifiers":3724},"10.1093\u002Fbioinformatics\u002Fbtl446",{"doi":3723},{"id":24,"text":3726,"url":24,"identifiers":3727},"10.1080\u002F10635150802429642",{"doi":3726},{"id":24,"text":3729,"url":24,"identifiers":3730},"10.1016\u002Fj.aml.2009.08.009",{"doi":3729},{"id":24,"text":3732,"url":24,"identifiers":3733},"Stevens P. F.2001onward. Angiosperm Phylogeny Website version 9 June 2008 [and more or less continuously updated since]. Websitehttp:\u002F\u002Fwww.mobot.org\u002FMOBOT\u002Fresearch\u002FAPweb\u002F.",{},{"id":24,"text":3735,"url":24,"identifiers":3736},"Swofford D. L., 2002, PAUP*: Phylogenetic analysis using parsimony (*and other methods), version 4b10",{},{"id":24,"text":3738,"url":24,"identifiers":3739},"Sytsma K. J., 1994, DNA extraction from recalcitrant plants: Long, pure, and simple?, 69",{},{"id":24,"text":3741,"url":24,"identifiers":3742},"10.1086\u002F421066",{"doi":3741},{"id":24,"text":3744,"url":24,"identifiers":3745},"10.3732\u002Fajb.89.9.1531",{"doi":3744},{"id":24,"text":3747,"url":24,"identifiers":3748},"10.1080\u002F10635150701472164",{"doi":3747},{"id":24,"text":3750,"url":24,"identifiers":3751},"10.1600\u002F036364410791638306",{"doi":3750},{"id":24,"text":3753,"url":24,"identifiers":3754},"10.1086\u002F595288",{"doi":3753},{"id":24,"text":3756,"url":24,"identifiers":3757},"10.1073\u002Fpnas.0813376106",{"doi":3756},{"id":24,"text":3759,"url":24,"identifiers":3760},"10.1016\u002Fj.ppees.2009.01.001",{"doi":3759},{"id":24,"text":3762,"url":24,"identifiers":3763},"10.2307\u002F25065948",{"doi":3762},{"id":24,"text":2359,"url":24,"identifiers":3765},{"doi":2359},{"id":24,"text":3767,"url":24,"identifiers":3768},"10.3732\u002Fajb.0800207",{"doi":3767},{"id":24,"text":3770,"url":24,"identifiers":3771},"10.1073\u002Fpnas.092136399",{"doi":3770},{"id":24,"text":3773,"url":24,"identifiers":3774},"10.1086\u002F376882",{"doi":3773},{"id":24,"text":3776,"url":24,"identifiers":3777},"10.1600\u002F036364406775971778",{"doi":3776},{"id":24,"text":3779,"url":24,"identifiers":3780},"10.1016\u002Fj.ympev.2005.10.002",{"doi":3779},{"id":24,"text":3782,"url":24,"identifiers":3783},"10.1016\u002FS1055-7903(02)00303-2",{"doi":3782},{"id":24,"text":3785,"url":24,"identifiers":3786},"10.1186\u002F1471-2148-7-217",{"doi":3785},{"id":3788,"createTime":3789,"updateTime":3790,"relativeEntities":3791,"slug":3792,"properties":3793,"entityType":967,"verifyStatus":120,"verifyTime":3809,"verifyNote":968,"languages":3810,"translateLanguages":3811,"viewCount":25,"primaryUrl":3812,"fullTextUrl":24,"authors":3813,"publicationType":1001,"publisherRelationship":3887,"citationCount":3941,"citationInfo":3942,"publishDate":3945,"publishYear":3943,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":3946,"openAccess":24,"references":3947,"isForceReanalyzing":1060},"269fb9f1-fddf-41cc-b237-774b8acfbe14","2024-09-11T06:45:17.373+00:00","2025-02-14T21:05:24.024+00:00",[],"Size-and-function-in-conifer-tracheids-and-angiosperm-vessels",{"mag":3794,"keywords":3796,"openalex":3797,"abstract":3799,"title":3802,"pm":3805,"doi":3807},{"VOID":3795},"2150830640",{"VI":1071},{"VOID":3798},"W2150830640",{"EN":3800,"VI":3801},"\u003Cjats:p>The wide size range of conifer tracheids and angiosperm vessels has important consequences for function. In both conduit types, bigger is better for conducting efficiency. The gain in efficiency with size is maximized by the control of conduit shape, which balances end‐wall and lumen resistances. Although vessels are an order of magnitude longer than tracheids of the same diameter, they are not necessarily more efficient because they lack the low end‐wall resistance of tracheids with torus‐margo pits. Instead, vessels gain conducting efficiency over tracheids by achieving wider maximum diameters. End‐walls contributed 56–64% to total xylem resistance in both conduit types, indicating that length limits conducting efficiency. Tracheid dimensions may be more limited by unicellularity and the need to supply strength to homoxylous wood than by the need to protect against cavitation. In contrast, the greater size of the multicellular vessel is facilitated by fibers that strengthen heteroxylous wood. Vessel dimensions may be most limited by the need to restrict intervessel pitting and cavitation by air‐seeding. Stressful habitats that promote narrow vessels should favor coexistence of conifers and angiosperms. The evolution of vessels in angiosperm wood may have required early angiosperms to survive a phase of mechanic and hydraulic instability.\u003C\u002Fjats:p>","\u003Cjats:p>Phạm vi kích thước rộng rãi của tracheids ở thực vật hạt đứng và mạch của thực vật hạt kín có những hệ quả quan trọng cho chức năng. Trong cả hai loại ống dẫn, kích thước lớn hơn đem lại hiệu quả dẫn truyền tốt hơn. Lợi ích về hiệu quả khi tăng kích thước được tối đa hóa thông qua việc kiểm soát hình dạng của ống dẫn, giúp cân bằng giữa sức cản của tường cuối và lòng ống. Mặc dù mạch dài hơn một bậc so với tracheids cùng đường kính, chúng không nhất thiết phải hiệu quả hơn vì thiếu sức cản tường cuối thấp như ở các tracheids có lỗ torus-margo. Thay vào đó, mạch đạt được hiệu quả dẫn truyền cao hơn so với tracheids thông qua việc đạt được đường kính tối đa rộng hơn. Tường cuối đóng góp từ 56-64% vào tổng sức cản của xylem trong cả hai loại ống dẫn, cho thấy chiều dài giới hạn hiệu quả dẫn truyền. Kích thước của tracheid có thể bị giới hạn nhiều hơn bởi tính đơn bào và nhu cầu cung cấp độ bền cho gỗ đồng cấu hơn là bởi nhu cầu bảo vệ chống lại hiện tượng thủng khí. Ngược lại, kích thước lớn hơn của mạch đa bào được hỗ trợ bởi các sợi tăng cường độ bền cho gỗ dị cấu. Kích thước của mạch có thể bị giới hạn nhiều nhất bởi nhu cầu kiềm chế việc tạo lỗ và hiện tượng thủng khí. Những môi trường khắc nghiệt thúc đẩy sự hình thành mạch hẹp có thể ủng hộ sự đồng tồn tại của thực vật hạt đứng và thực vật hạt kín. Sự tiến hóa của mạch trong gỗ thực vật hạt kín có thể yêu cầu các cây hạt kín sớm phải sống sót qua một giai đoạn không ổn định về cơ học và thủy lực.\u003C\u002Fjats:p>",{"EN":3803,"VI":3804},"Size and function in conifer tracheids and angiosperm vessels","Kích thước và chức năng của tracheids ở thực vật hạt đứng và mạch ở thực vật hạt kín",{"VOID":3806},"21642096",{"VOID":3808},"10.3732\u002Fajb.93.10.1490","2024-09-11T06:45:17.371+00:00",[124],[123],"https:\u002F\u002Fbsapubs.onlinelibrary.wiley.com\u002Fdoi\u002F10.3732\u002Fajb.93.10.1490",[3814,3841,3864],{"id":3815,"sortIndex":25,"researcher":24,"roles":3816,"affiliations":3817,"properties":3834,"displayName":3838,"givenName":24,"familyName":24},"fcf82e37-da6d-46d7-a0bb-20bc8b7e94d3",[],[3818,3826],{"id":3819,"sortIndex":25,"affiliation":3820,"properties":24},"cfabca8a-7b96-4b49-9b29-ff3dc3788291",{"id":3819,"createTime":24,"updateTime":24,"relativeEntities":3821,"slug":24,"properties":3822,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":3825,"statistic":24},[],{"title":3823},{"EN":3824},"Department of Biology, University of Utah, 257S 1400E, Salt Lake City, Utah 84112 USA",[],{"id":3827,"sortIndex":132,"affiliation":3828,"properties":24},"3356b44f-0efe-4f69-b8ce-ff80b26fe39e",{"id":3827,"createTime":24,"updateTime":24,"relativeEntities":3829,"slug":24,"properties":3830,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":3833,"statistic":24},[],{"title":3831},{"EN":3832},"Department of Integrative Biology, University of California, 4007 Valley Life Sciences, Berkeley, California 94720 USA",[],{"orcid":3835,"title":3837,"openalex":3839},{"VOID":3836},"https:\u002F\u002Forcid.org\u002F0000-0001-7881-7393",{"EN":3838},"John S. 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J., 1951, The relation of differential collapse and shrinkage to wood anatomy in Eucalyptus regnans F. v. M. and E. Gigantea Hook. F., Australian Journal of Applied Science, 2, 175",{},{"id":24,"text":3961,"url":24,"identifiers":3962},"10.3732\u002Fajb.91.10.1599",{"doi":3961},{"id":24,"text":3964,"url":24,"identifiers":3965},"10.1525\u002F9780520320567",{"doi":3964},{"id":24,"text":3967,"url":24,"identifiers":3968},"10.1002\u002Fj.1537-2197.1992.tb14608.x",{"doi":3967},{"id":24,"text":3970,"url":24,"identifiers":3971},"10.1086\u002F297404",{"doi":3970},{"id":24,"text":3973,"url":24,"identifiers":3974},"10.2307\u002F2656805",{"doi":3973},{"id":24,"text":3976,"url":24,"identifiers":3977},"10.1016\u002FB978-012088457-5\u002F50021-6",{"doi":3976},{"id":24,"text":3979,"url":24,"identifiers":3980},"10.1093\u002Ftreephys\u002F11.1.73",{"doi":3979},{"id":24,"text":3982,"url":24,"identifiers":3983},"10.1104\u002Fpp.100.1.205",{"doi":3982},{"id":24,"text":3985,"url":24,"identifiers":3986},"10.1093\u002Ftreephys\u002F6.4.393",{"doi":3985},{"id":24,"text":3988,"url":24,"identifiers":3989},"10.1046\u002Fj.1469-8137.2000.00763.x",{"doi":3988},{"id":24,"text":3991,"url":24,"identifiers":3992},"Cronquist A., 1988, The evolution and classification of flowering plants",{},{"id":24,"text":3994,"url":24,"identifiers":3995},"10.2307\u002F2656919",{"doi":3994},{"id":24,"text":3997,"url":24,"identifiers":3998},"10.1093\u002Fjxb\u002Ferf100",{"doi":3997},{"id":24,"text":4000,"url":24,"identifiers":4001},"10.1093\u002Ftreephys\u002F22.2-3.91",{"doi":4000},{"id":24,"text":4003,"url":24,"identifiers":4004},"10.1163\u002F22941932-90000959",{"doi":4003},{"id":24,"text":4006,"url":24,"identifiers":4007},"10.1111\u002Fj.1469-8137.2005.01333.x",{"doi":4006},{"id":24,"text":4009,"url":24,"identifiers":4010},"10.1086\u002F314293",{"doi":4009},{"id":24,"text":4012,"url":24,"identifiers":4013},"10.1016\u002FB978-012276460-8\u002F50008-4",{"doi":4012},{"id":24,"text":4015,"url":24,"identifiers":4016},"10.3732\u002Fajb.91.3.386",{"doi":4015},{"id":24,"text":4018,"url":24,"identifiers":4019},"10.1016\u002FB978-012088457-5\u002F50018-6",{"doi":4018},{"id":24,"text":4021,"url":24,"identifiers":4022},"10.1007\u002Fs004420100628",{"doi":4021},{"id":24,"text":4024,"url":24,"identifiers":4025},"10.1093\u002Ftreephys\u002F26.6.689",{"doi":4024},{"id":24,"text":4027,"url":24,"identifiers":4028},"10.1046\u002Fj.1365-3040.2001.00660.x",{"doi":4027},{"id":24,"text":4030,"url":24,"identifiers":4031},"10.1104\u002Fpp.104.058404",{"doi":4030},{"id":24,"text":4033,"url":24,"identifiers":4034},"10.1111\u002Fj.1469-8137.2004.01097.x",{"doi":4033},{"id":24,"text":4036,"url":24,"identifiers":4037},"10.1111\u002Fj.1365-3040.1995.tb00352.x",{"doi":4036},{"id":24,"text":4039,"url":24,"identifiers":4040},"10.1093\u002Ftreephys\u002F12.2.119",{"doi":4039},{"id":24,"text":4042,"url":24,"identifiers":4043},"10.1093\u002Fjexbot\u002F53.373.1485",{"doi":4042},{"id":24,"text":4045,"url":24,"identifiers":4046},"Liese W., 1965, Cellular ultrastructure of woody plants, 271",{},{"id":24,"text":4048,"url":24,"identifiers":4049},"10.1111\u002Fj.1365-3040.1993.tb00898.x",{"doi":4048},{"id":24,"text":4051,"url":24,"identifiers":4052},"10.14214\u002Fsf.438",{"doi":4051},{"id":24,"text":4054,"url":24,"identifiers":4055},"10.1002\u002Fj.1537-2197.1994.tb15415.x",{"doi":4054},{"id":24,"text":4057,"url":24,"identifiers":4058},"Mayr S. Hacke U. Schmid P. Schwienbacher F. andGruber A.In press.frost drought in conifers at the alpine timberline: xylem dysfunction and adaptations.Ecology..",{},{"id":24,"text":4060,"url":24,"identifiers":4061},"10.1111\u002Fj.1558-5646.1985.tb00451.x",{"doi":4060},{"id":24,"text":4063,"url":24,"identifiers":4064},"10.1002\u002Fj.1537-2197.1990.tb14446.x",{"doi":4063},{"id":24,"text":4066,"url":24,"identifiers":4067},"Niklas K. J., 1994, Plant allometry",{},{"id":24,"text":4069,"url":24,"identifiers":4070},"Panshin A. J., 1970, Textbook of wood technology",{},{"id":24,"text":4072,"url":24,"identifiers":4073},"10.1098\u002Frspb.1972.0057",{"doi":4072},{"id":24,"text":4075,"url":24,"identifiers":4076},"10.1007\u002FBF00365299",{"doi":4075},{"id":24,"text":4078,"url":24,"identifiers":4079},"10.1046\u002Fj.1365-2435.2000.t01-1-00451.x",{"doi":4078},{"id":24,"text":4081,"url":24,"identifiers":4082},"10.1093\u002Ftreephys\u002F23.13.907",{"doi":4081},{"id":24,"text":4084,"url":24,"identifiers":4085},"10.1104\u002Fpp.105.067900",{"doi":4084},{"id":24,"text":4087,"url":24,"identifiers":4088},"10.1126\u002Fscience.1120479",{"doi":4087},{"id":24,"text":4090,"url":24,"identifiers":4091},"10.3732\u002Fajb.93.9.1265",{"doi":4090},{"id":24,"text":4093,"url":24,"identifiers":4094},"10.1111\u002Fj.1365-3040.2006.01539.x",{"doi":4093},{"id":24,"text":4096,"url":24,"identifiers":4097},"10.2307\u002F2656722",{"doi":4096},{"id":24,"text":4099,"url":24,"identifiers":4100},"10.1016\u002FS0065-2296(08)60361-4",{"doi":4099},{"id":24,"text":4102,"url":24,"identifiers":4103},"10.1139\u002Fb88-153",{"doi":4102},{"id":24,"text":4105,"url":24,"identifiers":4106},"10.1007\u002F978-3-642-69213-0",{"doi":4105},{"id":24,"text":4108,"url":24,"identifiers":4109},"10.3732\u002Fajb.91.10.1614",{"doi":4108},{"id":24,"text":4111,"url":24,"identifiers":4112},"10.1111\u002Fj.1438-8677.1988.tb00042.x",{"doi":4111},{"id":24,"text":4114,"url":24,"identifiers":4115},"10.1111\u002Fj.1365-3040.1988.tb01774.x",{"doi":4114},{"id":24,"text":4117,"url":24,"identifiers":4118},"10.3732\u002Fajb.91.3.369",{"doi":4117},{"id":24,"text":4120,"url":24,"identifiers":4121},"10.1111\u002Fj.1365-3040.2005.01287.x",{"doi":4120},{"id":24,"text":4123,"url":24,"identifiers":4124},"10.1111\u002Fj.1365-3040.1996.tb00334.x",{"doi":4123},{"id":24,"text":4126,"url":24,"identifiers":4127},"10.1111\u002Fj.1365-3040.1990.tb01319.x",{"doi":4126},{"id":24,"text":4129,"url":24,"identifiers":4130},"10.1163\u002F22941932-90001369",{"doi":4129},{"id":24,"text":4132,"url":24,"identifiers":4133},"10.1111\u002Fj.1469-8137.1991.tb00035.x",{"doi":4132},{"id":24,"text":4135,"url":24,"identifiers":4136},"10.1146\u002Fannurev.pp.40.060189.000315",{"doi":4135},{"id":24,"text":4138,"url":24,"identifiers":4139},"10.1002\u002Fj.1537-2197.1990.tb11401.x",{"doi":4138},{"id":24,"text":4141,"url":24,"identifiers":4142},"Vincent J. F. V., 1991, Biomechanics and evolution, 21",{},{"id":24,"text":4144,"url":24,"identifiers":4145},"10.1163\u002F22941932-90000400",{"doi":4144},{"id":24,"text":4147,"url":24,"identifiers":4148},"10.1111\u002Fj.1365-3040.2005.01330.x",{"doi":4147},{"id":24,"text":4150,"url":24,"identifiers":4151},"10.1007\u002F978-3-662-22627-8",{"doi":4150},{"id":24,"text":4153,"url":24,"identifiers":4154},"10.1139\u002Fb81-248",{"doi":4153},{"id":24,"text":4156,"url":24,"identifiers":4157},"10.1093\u002Fjexbot\u002F52.355.257",{"doi":4156},{"id":4159,"createTime":4160,"updateTime":4161,"relativeEntities":4162,"slug":4163,"properties":4164,"entityType":967,"verifyStatus":120,"verifyTime":4178,"verifyNote":968,"languages":4179,"translateLanguages":4180,"viewCount":25,"primaryUrl":4181,"fullTextUrl":24,"authors":4182,"publicationType":1001,"publisherRelationship":4230,"citationCount":4284,"citationInfo":4285,"publishDate":4288,"publishYear":4286,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":4289,"openAccess":24,"references":4290,"isForceReanalyzing":1060},"4656f5cf-0e63-41e1-8c27-add42f2bf761","2024-09-28T15:14:34.291+00:00","2025-02-14T21:06:26.362+00:00",[],"Chloroplast-DNA-systematics-a-review-of-methods-and-data-analysis",{"openalex":4165,"mag":4167,"abstract":4169,"title":4172,"keywords":4175,"doi":4177},{"VOID":4166},"W2069010522",{"VOID":4168},"2069010522",{"EN":4170,"VI":4171},"\u003Cjats:p>The field of plant molecular systematics is expanding rapidly, and with it new and refined methods are coming into use. This paper reviews recent advances in experimental methods and data analysis, as applied to the chloroplast genome. Restriction site mapping of the chloroplast genome has been used widely, but is limited in the range of taxonomic levels to which it can be applied. The upper limits (i.e., greatest divergence) of its application are being explored by mapping of the chloroplast inverted repeat region, where rates of nucleotide substitution are low. The lower limits of divergence amenable to restriction site study are being examined using restriction enzymes with 4‐base recognition sites to analyze polymerase chain reaction (PCR)‐amplified portions of the chloroplast genome that evolve rapidly. The comparison of DNA sequences is the area of molecular systematics in which the greatest advances are being made. PCR and methods for direct sequencing of PCR products have resulted in a mushrooming of sequence data. In theory, any degree of divergence is amenable to comparative sequencing studies. In practice, plant systematists have focused on two slowly evolving sequences (\u003Cjats:italic>rbc\u003C\u002Fjats:italic>L and rRNA genes). More rapidly evolving DNA sequences, including rapidly changing chloroplast genes, chloroplast introns, and intergenic spacers, and the noncoding portions of the nuclear ribosomal RNA repeat, also are being investigated for comparative purposes. The relative advantages and disadvantages of comparative restriction site mapping and DNA sequencing are reviewed. For both methods, the analysis of resulting data requires sufficient taxon and character sampling to achieve the best possible estimate of phylogenetic relationships. Parsimony analysis is particularly sensitive to the issue of taxon sampling due to the problem of long branches attracting on a tree. However, data sets with many taxa present serious computational difficulties that may result in the inability to achieve maximum parsimony or to find all shortest trees.\u003C\u002Fjats:p>","\u003Cjats:p>Lĩnh vực hệ thống phân loại phân tử thực vật đang mở rộng nhanh chóng, đi kèm với đó là sự xuất hiện của các phương pháp mới và cải tiến. Bài báo này tổng hợp những tiến bộ gần đây trong các phương pháp thí nghiệm và phân tích dữ liệu, ứng dụng cho bộ gen lạp thể. Việc lập bản đồ vị trí cắt của bộ gen lạp thể đã được sử dụng rộng rãi, nhưng bị hạn chế về mức độ phân loại mà nó có thể áp dụng. Các giới hạn trên (tức là, độ phân ly lớn nhất) của ứng dụng này đang được khám phá bằng cách lập bản đồ vùng đảo ngược của lạp thể, nơi mà tỷ lệ thay thế nucleotide khá thấp. Các giới hạn dưới của độ phân ly có thể nghiên cứu bằng vị trí cắt đang được kiểm tra bằng cách sử dụng các enzym cắt có vị trí nhận diện 4 base để phân tích các phần của bộ gen lạp thể được khuếch đại qua phản ứng chuỗi polymerase (PCR) có tốc độ tiến hóa nhanh. So sánh các trình tự DNA là lĩnh vực hệ thống phân loại phân tử đang có những tiến bộ lớn nhất. PCR và các phương pháp trực tiếp phân tích trình tự các sản phẩm PCR đã dẫn đến việc dữ liệu trình tự gia tăng mạnh mẽ. Về lý thuyết, bất kỳ mức độ phân ly nào đều có thể áp dụng cho các nghiên cứu trình tự so sánh. Trong thực tế, các nhà hệ thống phân loại thực vật đã tập trung vào hai trình tự tiến hóa chậm (\u003Cjats:italic>rbc\u003C\u002Fjats:italic>L và các gen rRNA). Các trình tự DNA tiến hóa nhanh hơn, bao gồm các gen lạp thể thay đổi nhanh chóng, các intron trong lạp thể, và các khoảng không gian giữa các gen, cũng như các phần không mã hóa của lặp ribosomal RNA hạt nhân, cũng đang được nghiên cứu cho mục đích so sánh. Những lợi thế và bất lợi tương đối của việc lập bản đồ vị trí cắt so sánh và phân tích trình tự DNA được đánh giá. Đối với cả hai phương pháp, phân tích dữ liệu thu được yêu cầu đủ mẫu phân loại và đặc điểm để đạt được ước lượng tốt nhất có thể về mối quan hệ phát sinh loài. Phân tích parsimony đặc biệt nhạy cảm với vấn đề lấy mẫu phân loại do sự cố gắng của các nhánh dài trên một cây. Tuy nhiên, các tập dữ liệu với nhiều loài có thể gây ra những khó khăn tính toán nghiêm trọng mà có thể dẫn đến việc không thể đạt được tối đa tính parsimony hoặc tìm ra tất cả các cây ngắn nhất.",{"EN":4173,"VI":4174},"Chloroplast DNA systematics: a review of methods and data analysis","Hệ thống phân loại DNA lạp thể: một cái nhìn tổng quan về các phương pháp và phân tích dữ liệu",{"VI":4176},"hệ thống phân loại phân tử, bộ gen lạp thể, PCR, trình tự DNA, phân tích parsimony",{"VOID":1327},"2024-09-28T15:14:34.290+00:00",[124],[123],"https:\u002F\u002Fbsapubs.onlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fj.1537-2197.1994.tb15615.x",[4183,4207],{"id":4184,"sortIndex":25,"researcher":24,"roles":4185,"affiliations":4186,"properties":4203,"displayName":3303,"givenName":24,"familyName":24},"6d4430a6-d70b-447d-ac56-7dcc14fe8005",[],[4187,4195],{"id":4188,"sortIndex":25,"affiliation":4189,"properties":24},"ee2fdda3-9215-4c8e-8dac-d99082af16b6",{"id":4188,"createTime":24,"updateTime":24,"relativeEntities":4190,"slug":24,"properties":4191,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":4194,"statistic":24},[],{"title":4192},{"VI":4193},"Department of Biology, Indiana University, Bloomington, Indiana 47405",[],{"id":4196,"sortIndex":132,"affiliation":4197,"properties":24},"29d77f1a-cf05-4c93-8c5f-30dfe0c1f684",{"id":4196,"createTime":24,"updateTime":24,"relativeEntities":4198,"slug":24,"properties":4199,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":4202,"statistic":24},[],{"title":4200},{"EN":4201},"Department of EPO Biology University of Colorado Boulder, Colorado 80309",[],{"orcid":4204,"title":4205,"openalex":4206},{"VOID":3301},{"EN":3303},{"VOID":3305},{"id":4208,"sortIndex":132,"researcher":24,"roles":4209,"affiliations":4210,"properties":4223,"displayName":4227,"givenName":24,"familyName":24},"8efef2cb-b003-4b9f-b367-925e983e31d8",[],[4211,4217],{"id":4188,"sortIndex":25,"affiliation":4212,"properties":24},{"id":4188,"createTime":24,"updateTime":24,"relativeEntities":4213,"slug":24,"properties":4214,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":4216,"statistic":24},[],{"title":4215},{"VI":4193},[],{"id":4196,"sortIndex":132,"affiliation":4218,"properties":24},{"id":4196,"createTime":24,"updateTime":24,"relativeEntities":4219,"slug":24,"properties":4220,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":4222,"statistic":24},[],{"title":4221},{"EN":4201},[],{"orcid":4224,"title":4226,"openalex":4228},{"VOID":4225},"https:\u002F\u002Forcid.org\u002F0000-0002-4626-2220",{"EN":4227},"Jeffrey D. 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H., 1991, Phylogenetic consequences of cytoplasmic gene flow in plants, Evolutionary Trends in Plants, 5, 65",{},{"id":24,"text":4706,"url":24,"identifiers":4707},"10.1111\u002Fj.1558-5646.1988.tb04127.x",{"doi":4706},{"id":24,"text":2028,"url":24,"identifiers":4709},{"doi":2028},{"id":24,"text":4711,"url":24,"identifiers":4712},"Ritland K., 1990, Molecular evolution, UCLA symposia on molecular and cellular biology, new series, 289",{},{"id":24,"text":4714,"url":24,"identifiers":4715},"10.1073\u002Fpnas.81.24.8014",{"doi":4714},{"id":24,"text":4717,"url":24,"identifiers":4718},"10.1126\u002Fscience.2448875",{"doi":4717},{"id":24,"text":4720,"url":24,"identifiers":4721},"Sambrook J., 1989, Molecular cloning: a laboratory manual, 2d ed",{},{"id":24,"text":4723,"url":24,"identifiers":4724},"10.1111\u002Fj.1096-0031.1989.tb00559.x",{"doi":4723},{"id":24,"text":4726,"url":24,"identifiers":4727},"10.1093\u002Fsysbio\u002F41.1.4",{"doi":4726},{"id":24,"text":4729,"url":24,"identifiers":4730},"10.1038\u002F343027a0",{"doi":4729},{"id":24,"text":4732,"url":24,"identifiers":4733},"10.1002\u002Fj.1537-2197.1989.tb15167.x",{"doi":4732},{"id":24,"text":4735,"url":24,"identifiers":4736},"10.1086\u002F284690",{"doi":4735},{"id":24,"text":4738,"url":24,"identifiers":4739},"10.1002\u002Fj.1460-2075.1986.tb04464.x",{"doi":4738},{"id":24,"text":4741,"url":24,"identifiers":4742},"10.2307\u002F2419348",{"doi":4741},{"id":24,"text":4744,"url":24,"identifiers":4745},"10.1073\u002Fpnas.87.12.4640",{"doi":4744},{"id":24,"text":4747,"url":24,"identifiers":4748},"10.1007\u002F978-1-4615-3276-7_6",{"doi":4747},{"id":24,"text":4750,"url":24,"identifiers":4751},"Soltis P. S. andD. E.Soltis. In press.Plant molecular systematics: inferences of phylogeny and evolutionary processes.Evolutionary Biology..",{},{"id":24,"text":4753,"url":24,"identifiers":4754},"10.1007\u002F978-1-4615-3276-7",{"doi":4753},{"id":24,"text":4756,"url":24,"identifiers":4757},"10.1007\u002FBF00937800",{"doi":4756},{"id":24,"text":4759,"url":24,"identifiers":4760},"Steele K. P., 1991, Assessing the reliability of 5S rRNA sequence data for phylogenetic analysis in green plants, Molecular Biology and Evolution, 8, 240",{},{"id":24,"text":2081,"url":24,"identifiers":4762},{"doi":2081},{"id":24,"text":4764,"url":24,"identifiers":4765},"10.1146\u002Fannurev.cb.05.110189.000411",{"doi":4764},{"id":24,"text":4767,"url":24,"identifiers":4768},"10.1002\u002Fj.1537-2197.1993.tb15332.x",{"doi":4767},{"id":24,"text":4770,"url":24,"identifiers":4771},"Swofford D. L., 1991, Phylogenetic analysis of DNA sequences, 295, 10.1093\u002Foso\u002F9780195066982.003.0014",{"doi":4772},"10.1093\u002Foso\u002F9780195066982.003.0014",{"id":24,"text":4774,"url":24,"identifiers":4775},"Swofford D. L., 1993, PAUP: phylogenetic analysis using parsimony, version 3.1",{},{"id":24,"text":4777,"url":24,"identifiers":4778},"Swofford D. 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C., 1989, The hierarchy of life, 407",{},{"id":24,"text":4810,"url":24,"identifiers":4811},"10.1002\u002Fj.1537-2197.1993.tb15241.x",{"doi":4810},{"id":24,"text":4813,"url":24,"identifiers":4814},"Wolfe K. H., 1991, The photosynthetic apparatus: molecular biology and operation, vol. 7B, Cell culture and somatic cell genetics in plants, 467, 10.1016\u002FB978-0-12-715010-9.50022-0",{"doi":4815},"10.1016\u002FB978-0-12-715010-9.50022-0",{"id":24,"text":1393,"url":24,"identifiers":4817},{"doi":1393},{"id":24,"text":2129,"url":24,"identifiers":4819},{"doi":2129},{"id":24,"text":4821,"url":24,"identifiers":4822},"10.1016\u002F0378-1119(88)90358-7",{"doi":4821},{"id":24,"text":4824,"url":24,"identifiers":4825},"10.1016\u002FS0959-437X(05)80116-9",{"doi":4824},{"id":24,"text":4827,"url":24,"identifiers":4828},"10.1073\u002Fpnas.77.4.2158",{"doi":4827},{"id":4830,"createTime":4831,"updateTime":4832,"relativeEntities":4833,"slug":4834,"properties":4835,"entityType":967,"verifyStatus":120,"verifyTime":4831,"verifyNote":968,"languages":4851,"translateLanguages":4852,"viewCount":25,"primaryUrl":4853,"fullTextUrl":24,"authors":4854,"publicationType":1001,"publisherRelationship":4889,"citationCount":4943,"citationInfo":4944,"publishDate":4947,"publishYear":4945,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":4948,"openAccess":24,"references":4949,"isForceReanalyzing":1060},"153c76fa-8c7c-4329-a084-50a00b3bb2d6","2024-09-20T20:15:36.684+00:00","2025-02-14T21:07:24.752+00:00",[],"Interspecific-variation-in-plant-responses-to-mycorrhizal-colonization-in-tallgrass-prairie",{"mag":4836,"keywords":4838,"openalex":4839,"abstract":4841,"title":4844,"pm":4847,"doi":4849},{"VOID":4837},"2054987373",{"VI":1071},{"VOID":4840},"W2054987373",{"EN":4842,"VI":4843},"\u003Cjats:p>Symbiotic associations between plants and arbuscular mycorrhizal fungi are ubiquitous and ecologically important in many grasslands. Differences in species responses to mycorrhizal colonization can have a significant influence on plant community structure. The growth responses of 36 species of warm‐ and cool‐season tallgrass prairie grasses and 59 tallgrass prairie forbs to arbuscular mycorrhizal (AM) fungal colonization were assessed in greenhouse studies to examine the extent of interspecific variation in host‐plant benefit from the symbiosis and patterns of mycorrhizal dependence among host plant life history (e.g., annual, perennial) and taxonomic (e.g., grass, forb, legume, nonlegume) groups and phenological guilds. There was a strong and significant relationship between phenology of prairie grasses and mycorrhizal responsiveness, however this relationship was less apparent in forbs. Perennial warm‐season C\u003Cjats:sub>4\u003C\u002Fjats:sub> grasses and forbs generally benefited significantly from the mycorrhizal symbiosis, whereas biomass production of the cool‐season C\u003Cjats:sub>3\u003C\u002Fjats:sub> grasses was not affected. The root systems of the cool‐season grasses were also less highly colonized by the AM fungi, as compared to the warm‐season grasses or forbs. Unlike the native perennials, annuals were generally not responsive to mycorrhizal colonization and were lower in percentage root colonization than the perennial species. Plant growth responsiveness and AM root colonization were positively correlated for the nonleguminous species, with this relationship being strongest for the cool‐season grasses. In contrast, root colonization of prairie legumes showed a significant, but negative, relationship to mycorrhizal growth responsiveness.\u003C\u002Fjats:p>","\u003Cjats:p>Các liên kết hợp sinh giữa cây trồng và nấm mycorrhiza arbuscular rất phổ biến và có tầm quan trọng sinh thái ở nhiều vùng thảo nguyên. Những khác biệt trong phản ứng của các loài đối với sự thực dân mycorrhiza có thể ảnh hưởng đáng kể đến cấu trúc cộng đồng thực vật. Phản ứng sinh trưởng của 36 loài cỏ thảo nguyên mùa nóng và mùa mát cùng với 59 loài cây hoa thảo nguyên đã được đánh giá trong các nghiên cứu trong nhà kính nhằm kiểm tra mức độ biến thiên giữa các loài về lợi ích từ sự cộng sinh cũng như các mô hình phụ thuộc vào mycorrhiza giữa các nhóm thực vật chủ theo lịch sử sống (ví dụ: hàng năm, lâu năm) và phân loại (ví dụ: cỏ, cây hoa, đậu, không phải đậu) cùng với các nhóm phenology. Có mối quan hệ mạnh mẽ và đáng kể giữa hiện tượng phenology của cỏ thảo nguyên và khả năng phản ứng với mycorrhiza, tuy nhiên mối quan hệ này ít rõ ràng hơn ở các loài cây hoa. Các loài cỏ C\u003Cjats:sub>4\u003C\u002Fjats:sub> mùa nóng lâu năm và cây hoa thường được hưởng lợi đáng kể từ sự cộng sinh mycorrhiza, trong khi sản lượng sinh khối của các loài cỏ C\u003Cjats:sub>3\u003C\u002Fjats:sub> mùa mát không bị ảnh hưởng. Hệ rễ của các loài cỏ mùa mát cũng bị thực dân ít hơn bởi nấm AM, so với các loài cỏ mùa nóng hoặc cây hoa. Khác với các loài lâu năm bản địa, các loài hàng năm thường không phản ứng với sự thực dân mycorrhiza và có tỷ lệ thực dân rễ thấp hơn so với các loài lâu năm. Phản ứng sinh trưởng của cây và sự thực dân rễ AM có mối tương quan tích cực với nhau ở các loài không phải đậu, trong đó mối quan hệ này mạnh nhất ở các loài cỏ mùa mát. Ngược lại, sự thực dân rễ của các loài đậu thảo nguyên cho thấy mối quan hệ đáng kể nhưng tiêu cực với khả năng phản ứng sinh trưởng của mycorrhiza.\u003C\u002Fjats:p>",{"EN":4845,"VI":4846},"Interspecific variation in plant responses to mycorrhizal colonization in tallgrass prairie","Sự biến thiên giữa các loài trong phản ứng của thực vật đối với sự thực dân mycorrhiza trong thảo nguyên cỏ cao",{"VOID":4848},"21680333",{"VOID":4850},"10.2307\u002F2446507",[124],[123],"https:\u002F\u002Fbsapubs.onlinelibrary.wiley.com\u002Fdoi\u002F10.2307\u002F2446507",[4855,4874],{"id":4856,"sortIndex":25,"researcher":24,"roles":4857,"affiliations":4858,"properties":4867,"displayName":4871,"givenName":24,"familyName":24},"efc57967-7924-4cbf-b811-c8a3c4eaca6a",[],[4859],{"id":4860,"sortIndex":25,"affiliation":4861,"properties":24},"c2067815-ff4f-4e06-8dfe-0706e83a476a",{"id":4860,"createTime":24,"updateTime":24,"relativeEntities":4862,"slug":24,"properties":4863,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":4866,"statistic":24},[],{"title":4864},{"EN":4865},"3Division of Biology, 232 Ackert Hall, Kansas State University, Manhattan, Kansas 66506‐5502",[],{"orcid":4868,"title":4870,"openalex":4872},{"VOID":4869},"https:\u002F\u002Forcid.org\u002F0000-0003-1396-6480",{"EN":4871},"Gail W. T. Wilson",{"VOID":4873},"A5076288410",{"id":4875,"sortIndex":132,"researcher":24,"roles":4876,"affiliations":4877,"properties":4884,"displayName":4886,"givenName":24,"familyName":24},"e4eda96e-dd0c-46f5-87e4-910efe90fa08",[],[4878],{"id":4860,"sortIndex":25,"affiliation":4879,"properties":24},{"id":4860,"createTime":24,"updateTime":24,"relativeEntities":4880,"slug":24,"properties":4881,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":4883,"statistic":24},[],{"title":4882},{"EN":4865},[],{"title":4885,"openalex":4887},{"EN":4886},"David C. Hartnett",{"VOID":4888},"A5009352347",{"url":24,"publisher":4890,"properties":4936},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":4891,"slug":10,"properties":4892,"entityType":22,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":25,"subjectFields":4897,"manageAffiliations":4910,"indexDatabases":4921,"url":97,"thumbnailPath":24,"statistic":24,"gsStatistic":24,"type":24,"analyzePriority":24},[],{"country":4893,"eissn":4894,"issn":4895,"title":4896},{"VOID":13},{"VOID":15},{"VOID":17},{"EN":19},[4898,4902,4906],{"id":28,"createTime":24,"updateTime":24,"relativeEntities":4899,"label":4900,"description":4901,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":31},{},{"id":34,"createTime":24,"updateTime":24,"relativeEntities":4903,"label":4904,"description":4905,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":37},{},{"id":40,"createTime":24,"updateTime":24,"relativeEntities":4907,"label":4908,"description":4909,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":43},{},[4911,4916],{"id":47,"createTime":24,"updateTime":24,"relativeEntities":4912,"slug":24,"properties":4913,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":4915,"statistic":24},[],{"title":4914},{"EN":51},[],{"id":54,"createTime":24,"updateTime":24,"relativeEntities":4917,"slug":24,"properties":4918,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":4920,"statistic":24},[],{"title":4919},{"EN":58},[],[4922,4929],{"id":62,"indexDatabase":4923,"url":73,"indexYears":74,"academicFieldIds":4928,"indexDatabaseRanking":79},{"id":64,"createTime":24,"updateTime":24,"relativeEntities":4924,"label":4925,"description":4926,"key":70,"publicationTags":4927,"standard":24},[],{"EN":67,"VI":67},{"EN":67,"VI":69},[72],[76,77,78],{"id":81,"indexDatabase":4930,"url":94,"indexYears":24,"academicFieldIds":4935,"indexDatabaseRanking":24},{"id":83,"createTime":24,"updateTime":24,"relativeEntities":4931,"label":4932,"description":4933,"key":90,"publicationTags":4934,"standard":24},[],{"EN":86,"VI":86},{"EN":88,"VI":89},[92,93],[96],{"issue":4937,"pages":4939,"volume":4941},{"VOID":4938},"12",{"VOID":4940},"1732-1738",{"VOID":4942},"85",402,{"total":4943,"publishYear":4945,"statisticByYear":4946},1998,{"2012":214,"2013":228,"2014":214,"2015":222,"2016":228,"2017":219,"2018":228,"2019":223,"2020":415,"2021":214,"2022":222,"2023":297,"2024":297},"1998-12-01",[92,79],[4950,4953,4956,4959,4962,4965,4968,4971,4974,4977,4980,4983,4986,4989,4992,4995,4998,5001,5004,5007,5010,5013,5016,5019,5022,5025,5028,5031,5034,5037,5040,5043,5046,5049,5052,5055,5058,5061,5064,5067,5070,5073,5076,5079,5082,5085,5088,5091,5094,5097,5100,5103,5106,5109,5112,5115],{"id":24,"text":4951,"url":24,"identifiers":4952},"10.1111\u002Fj.1469-8137.1986.tb00656.x",{"doi":4951},{"id":24,"text":4954,"url":24,"identifiers":4955},"Grace J. R., 1990, Perspectives on plant competition, 367",{},{"id":24,"text":4957,"url":24,"identifiers":4958},"Allen M. F., 1985, Proceedings of the Sixth North American Conference on Mycorrhizae, 158",{},{"id":24,"text":4960,"url":24,"identifiers":4961},"Azcon‐Aguilar C, 1992, Mycorrhizal functioning, an integrative plant‐fungal process, 163",{},{"id":24,"text":4963,"url":24,"identifiers":4964},"Baylis G. T. S., 1975, Endomycorrhizas, 373",{},{"id":24,"text":4966,"url":24,"identifiers":4967},"10.1016\u002FS0065-2113(08)60351-X",{"doi":4966},{"id":24,"text":4969,"url":24,"identifiers":4970},"10.1146\u002Fannurev.es.16.110185.002051",{"doi":4969},{"id":24,"text":4972,"url":24,"identifiers":4973},"10.1139\u002Fb88-166",{"doi":4972},{"id":24,"text":4975,"url":24,"identifiers":4976},"10.1111\u002Fj.1469-8137.1981.tb02319.x",{"doi":4975},{"id":24,"text":4978,"url":24,"identifiers":4979},"Skipper H. A., 1982, Methods and principles on mycorrhizal research, 29",{},{"id":24,"text":4981,"url":24,"identifiers":4982},"10.1007\u002FBF02370406",{"doi":4981},{"id":24,"text":4984,"url":24,"identifiers":4985},"10.1111\u002Fj.1469-8137.1988.tb00238.x",{"doi":4984},{"id":24,"text":4987,"url":24,"identifiers":4988},"Fitter A. H., 1992, Mycorrhizas in ecosystems, 26",{},{"id":24,"text":4990,"url":24,"identifiers":4991},"10.1007\u002FBF00000091",{"doi":4990},{"id":24,"text":4993,"url":24,"identifiers":4994},"10.2307\u002F3627880",{"doi":4993},{"id":24,"text":4996,"url":24,"identifiers":4997},"10.2307\u002F2390139",{"doi":4996},{"id":24,"text":4999,"url":24,"identifiers":5000},"10.1111\u002Fj.1469-8137.1994.tb03989.x",{"doi":4999},{"id":24,"text":5002,"url":24,"identifiers":5003},"10.1007\u002F978-94-015-7934-6_52",{"doi":5002},{"id":24,"text":5005,"url":24,"identifiers":5006},"Great Plains Flora Association, 1986, Flora of the Great Plains",{},{"id":24,"text":5008,"url":24,"identifiers":5009},"10.1111\u002Fj.1469-8137.1987.tb00674.x",{"doi":5008},{"id":24,"text":5011,"url":24,"identifiers":5012},"10.2307\u002F2261676",{"doi":5011},{"id":24,"text":5014,"url":24,"identifiers":5015},"10.1007\u002FBF00317079",{"doi":5014},{"id":24,"text":5017,"url":24,"identifiers":5018},"10.1007\u002FBF00937189",{"doi":5017},{"id":24,"text":5020,"url":24,"identifiers":5021},"10.1111\u002Fj.1744-7348.1979.tb06524.x",{"doi":5020},{"id":24,"text":5023,"url":24,"identifiers":5024},"10.1139\u002Fb88-193",{"doi":5023},{"id":24,"text":5026,"url":24,"identifiers":5027},"10.1139\u002Fb91-016",{"doi":5026},{"id":24,"text":5029,"url":24,"identifiers":5030},"10.1139\u002Fb90-061",{"doi":5029},{"id":24,"text":5032,"url":24,"identifiers":5033},"10.1139\u002Fb92-191",{"doi":5032},{"id":24,"text":5035,"url":24,"identifiers":5036},"10.1139\u002Fb96-003",{"doi":5035},{"id":24,"text":5038,"url":24,"identifiers":5039},"10.1016\u002FS0580-9517(08)70176-4",{"doi":5038},{"id":24,"text":5041,"url":24,"identifiers":5042},"10.2307\u002F2388157",{"doi":5041},{"id":24,"text":5044,"url":24,"identifiers":5045},"10.2307\u002F3627486",{"doi":5044},{"id":24,"text":5047,"url":24,"identifiers":5048},"10.1046\u002Fj.1469-8137.1997.00672.x",{"doi":5047},{"id":24,"text":5050,"url":24,"identifiers":5051},"Martensson A., 1994, Variability among Pea varieties for infection with arbuscular mycorrhizal fungi, Swedish Journal of Agricultural Research, 24, 13",{},{"id":24,"text":5053,"url":24,"identifiers":5054},"Miller R. M., 1987, Ectophysiology of VA mycorrhizal plants, 135",{},{"id":24,"text":5056,"url":24,"identifiers":5057},"Millikin G. A., 1984, Analysis of messy data",{},{"id":24,"text":5059,"url":24,"identifiers":5060},"Munns D. N., 1980, Advances in legume science, 115",{},{"id":24,"text":5062,"url":24,"identifiers":5063},"10.1016\u002FS0169-5347(00)89157-0",{"doi":5062},{"id":24,"text":5065,"url":24,"identifiers":5066},"10.2307\u002F2261180",{"doi":5065},{"id":24,"text":5068,"url":24,"identifiers":5069},"10.2307\u002F2390007",{"doi":5068},{"id":24,"text":5071,"url":24,"identifiers":5072},"10.1007\u002FBF02370104",{"doi":5071},{"id":24,"text":5074,"url":24,"identifiers":5075},"10.1016\u002FS0007-1536(70)80110-3",{"doi":5074},{"id":24,"text":5077,"url":24,"identifiers":5078},"Read D. J., 1991, Frontiers in mycology, 101",{},{"id":24,"text":5080,"url":24,"identifiers":5081},"10.1071\u002FPP9810427",{"doi":5080},{"id":24,"text":5083,"url":24,"identifiers":5084},"Rock H. W., 1977, Prairie propagation handbook",{},{"id":24,"text":5086,"url":24,"identifiers":5087},"Salisbury F. B., 1985, Plant physiology",{},{"id":24,"text":5089,"url":24,"identifiers":5090},"SAS, 1988, SAS user's guide: statistics, version 6 edition",{},{"id":24,"text":5092,"url":24,"identifiers":5093},"Schenk N. C., 1990, Manual for the identification of VA mycorrhizal fungi",{},{"id":24,"text":5095,"url":24,"identifiers":5096},"10.1016\u002FS0065-2296(08)60055-5",{"doi":5095},{"id":24,"text":5098,"url":24,"identifiers":5099},"10.2307\u002F2960650",{"doi":5098},{"id":24,"text":5101,"url":24,"identifiers":5102},"Trappe J. M., 1987, Ecophysiology of VA Mycorrhizalplants, 5",{},{"id":24,"text":5104,"url":24,"identifiers":5105},"Weaver J. E., 1954, North American Prairie",{},{"id":24,"text":5107,"url":24,"identifiers":5108},"Whitson T. D., 1992, Weeds of the West",{},{"id":24,"text":5110,"url":24,"identifiers":5111},"10.2307\u002F2446024",{"doi":5110},{"id":24,"text":5113,"url":24,"identifiers":5114},"10.1007\u002FBF02812100",{"doi":5113},{"id":24,"text":5116,"url":24,"identifiers":5117},"10.2307\u002F3545818",{"doi":5116},{"id":5119,"createTime":5120,"updateTime":5121,"relativeEntities":5122,"slug":5123,"properties":5124,"entityType":967,"verifyStatus":120,"verifyTime":5120,"verifyNote":968,"languages":5141,"translateLanguages":5142,"viewCount":25,"primaryUrl":5143,"fullTextUrl":24,"authors":5144,"publicationType":1001,"publisherRelationship":5223,"citationCount":5275,"citationInfo":5276,"publishDate":5278,"publishYear":2475,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":5279,"openAccess":24,"references":5280,"isForceReanalyzing":1060},"e6d891f6-11e8-4eb0-9f30-29a767707721","2025-01-06T01:46:13.915+00:00","2025-02-14T21:08:23.751+00:00",[],"Dinoflagellates-a-remarkable-evolutionary-experiment",{"mag":5125,"keywords":5127,"openalex":5129,"abstract":5131,"title":5134,"pm":5137,"doi":5139},{"VOID":5126},"2145913874",{"VI":5128},"Cá tảo độc, sinh thái học, độc tố, hồ sơ hóa thạch, phân tích phylogenetic phân tử, gene, plastid.",{"VOID":5130},"W2145913874",{"EN":5132,"VI":5133},"\u003Cjats:p>In this paper, we focus on dinoflagellate ecology, toxin production, fossil record, and a molecular phylogenetic analysis of hosts and plastids. Of ecological interest are the swimming and feeding behavior, bioluminescence, and symbioses of dinoflagellates with corals. The many varieties of dinoflagellate toxins, their biological effects, and current knowledge of their origin are discussed. Knowledge of dinoflagellate evolution is aided by a rich fossil record that can be used to document their emergence and diversification. However, recent biogeochemical studies indicate that dinoflagellates may be much older than previously believed. A remarkable feature of dinoflagellates is their unique genome structure and gene regulation. The nuclear genomes of these algae are of enormous size, lack nucleosomes, and have permanently condensed chromosomes. This chapter reviews the current knowledge of gene regulation and transcription in dinoflagellates with regard to the unique aspects of the nuclear genome. Previous work shows the plastid genome of typical dinoflagellates to have been reduced to single‐gene minicircles that encode only a small number of proteins. Recent studies have demonstrated that the majority of the plastid genome has been transferred to the nucleus, which makes the dinoflagellates the only eukaryotes to encode the majority of typical plastid genes in the nucleus. The evolution of the dinoflagellate plastid and the implications of these results for understanding organellar genome evolution are discussed.\u003C\u002Fjats:p>","\u003Cjats:p>Trong bài báo này, chúng tôi tập trung vào sinh thái học của cá tảo độc, sự sản xuất độc tố, hồ sơ hóa thạch và phân tích hệ gen phân tử của các vật chủ và plastid. Những vấn đề sinh thái đáng quan tâm là hành vi bơi lội và ăn uống, hiện tượng phát quang sinh học và sự hợp sinh của cá tảo độc với san hô. Nhiều loại độc tố của cá tảo độc, ảnh hưởng sinh học của chúng và kiến thức hiện tại về nguồn gốc của chúng được thảo luận. Kiến thức về tiến hóa của cá tảo độc được hỗ trợ bởi một hồ sơ hóa thạch phong phú có thể được sử dụng để ghi chép sự xuất hiện và đa dạng hóa của chúng. Tuy nhiên, các nghiên cứu sinh hóa sinh học gần đây cho thấy cá tảo độc có thể cổ xưa hơn nhiều so với suy nghĩ trước đây. Một đặc điểm đáng chú ý của cá tảo độc là cấu trúc gen độc đáo và sự điều hòa gen của chúng. Bộ gen hạt nhân của tảo thuộc nhóm này có kích thước khổng lồ, thiếu nucleosome và có nhiễm sắc thể vĩnh viễn bị ngưng tụ. Chương này tổng hợp kiến thức hiện tại về sự điều hòa gen và phiên mã ở cá tảo độc liên quan đến những khía cạnh độc đáo của bộ gen hạt nhân. Các công trình trước đây cho thấy bộ gen plastid của cá tảo độc điển hình đã được giảm xuống thành các vòng nhỏ chứa một gen duy nhất chỉ mã hóa một số lượng nhỏ protein. Các nghiên cứu gần đây đã chứng minh rằng phần lớn bộ gen plastid đã được chuyển đến hạt nhân, làm cho cá tảo độc trở thành nhóm eukaryote duy nhất mã hóa phần lớn các gen plastid điển hình trong hạt nhân. Sự tiến hóa của plastid ở cá tảo độc và ý nghĩa của những kết quả này đối với việc hiểu sự tiến hóa của bộ gen ti thể được thảo luận.\u003C\u002Fjats:p>",{"EN":5135,"VI":5136},"Dinoflagellates: a remarkable evolutionary experiment","Cá tảo độc: Một thí nghiệm tiến hóa đáng chú ý",{"VOID":5138},"21652307",{"VOID":5140},"10.3732\u002Fajb.91.10.1523",[124],[123],"https:\u002F\u002Fbsapubs.onlinelibrary.wiley.com\u002Fdoi\u002F10.3732\u002Fajb.91.10.1523",[5145,5162,5181,5198],{"id":5146,"sortIndex":25,"researcher":24,"roles":5147,"affiliations":5148,"properties":5157,"displayName":5159,"givenName":24,"familyName":24},"b45b63da-f007-43e0-8e94-fca02d923be3",[],[5149],{"id":5150,"sortIndex":25,"affiliation":5151,"properties":24},"348963c8-2fd4-485b-8e50-e92762c5a02d",{"id":5150,"createTime":24,"updateTime":24,"relativeEntities":5152,"slug":24,"properties":5153,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":5156,"statistic":24},[],{"title":5154},{"EN":5155},"2Department of Biological Sciences and Center for Comparative Genomics, University of Iowa, Iowa City, Iowa 52242 USA",[],{"title":5158,"openalex":5160},{"EN":5159},"Jeremiah D. 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