Results 51 to 60 of about 41,012 (269)

Jumping plant-lice of the Paurocephalinae (Insecta, Hemiptera, Psylloidea): systematics and phylogeny [PDF]

, 2003
Much confusion exists with respect to the content and definition of the psyUid subfamily Paurocephalinae. Based on a cladistic analysis of 22 morphological characters (16 adult and 6 larval), the subfamily is redefined to comprise the following five ...
Burckhardt, Daniel, Mifsud, David
core  

Spatial Relation of Bumblebees (Hymenoptera-Apidae) with Host-Plant and their Conservation Issues: An Outlook from Urban Ecosystem of Kathmandu Valley, Nepal [PDF]

, 2019
Ecology and conservation status of bumblebee species remains poorly understood, especially in rapidly degrading urban ecosystems, which is important considering the role of bumblebees in the pollinations. We collected more than 200 bumblebee (Bombus
Baniya, Pratikshya, Bhusal, Daya Ram, Dulal, Sabina, Ghimire, Kishor Chandra, Thakuri, Sudeep   +4 more
core   +2 more sources

Malvaceae novae americanae [PDF]

Repertorium novarum specierum regni vegetabilis, 1910
n ...
openaire   +2 more sources

Leveraging machine learning and citizen science data to describe flowering phenology across South Africa

PLANTS, PEOPLE, PLANET, EarlyView.
Recent shifts in flowering times are an index of, and a response to, human driven climate change. However, most information on these flowering changes is heavily skewed to the northern hemisphere. This imbalance limits our understanding of how climate change is affecting ecosystems, including the mismatches of flowering times between species, increased
Ross D. Stewart, Nicholas W. Bard, Michelle van der Bank, T. Jonathan Davies   +3 more
wiley   +1 more source

The Contributions of Neotropical Tree Families to the Structure of Common Amazon Forest-Types

International Journal of Plant Biology, 2023
In order to investigate how familial biodiversity structures forests in the critically important Amazon, I combined past plot samplings to investigate the contributions of tree families in those samplings to the structure of common Amazon forest types. I
Randall W. Myster
doaj   +1 more source

Paleogene monsoons across India and South China: Drivers of biotic change [PDF]

, 2017
Monsoonal climates at low latitudes (2. Fossil leaf form reveals that under such 'hothouse' conditions megathermal early Eocene to earliest Miocene forests were exposed to strong monsoonal climates typical of those experienced today arising from annual ...
Aleksandrova, Galina, Ding, Lin, Herman, Alexei, Jin, Jian-Hua, Kodrul, Tatiana, Liu, Xiao-Yan, Maslova, Natalia, Mehrotra, Rakesh, Shukla, Anumeha, Spicer, Robert, Spicer, Teresa, Srivastava, Gaurav, Xu, Qiang, Yang, Jian   +13 more
core   +1 more source

Climate‐induced shifts in long‐term tropical tree reproductive phenology: Insights from species dependent on and independent of biotic pollination

Functional Ecology, EarlyView.
Read the free Plain Language Summary for this article on the Journal blog. Abstract The dependence on biotic pollination may constrain plant phenological responses because flowering time ultimately defines reproductive success. We proposed a local‐scale study combining long‐term phenology and experimental data to evaluate how a key functional trait—the
Amanda Eburneo Martins, Priscilla de Paula de Loiola, Daniel Pareja‐Bonija, Leonor Patricia Cerdeira Morellato   +3 more
wiley   +1 more source

Pterocymbium R. Br ( Malvaceae , Sterculioideae ), a genus new to China

Xibei zhiwu xuebao
[ Objective ] The present study reports a newly recorded giant tropical deciduous tree , Pterocym- bium macranthum Kosterm. , which has been spotted in the border regions of Sino-Lao , Mengla County , Yunnan Province , and ...
ZHAO Mingxu , TAN Yunhong , YANG Zicheng , LI Jinhua , YAN Wende , CHEN Fei   +5 more
doaj   +1 more source

The complete chloroplast genome of Diplodiscus trichospermus and phylogenetic position of Brownlowioideae within Malvaceae

BMC Genomics, 2023
Background Malvaceae is an economically important plant family of 4,225 species in nine subfamilies. Phylogenetic relationships among the nine subfamilies have always been controversial, especially for Brownlowioideae, whose phylogenetic position remains
Mingsong Wu, Liu He, Guangyao Ma, Kai Zhang, Haijian Yang, Xinquan Yang   +5 more
doaj   +1 more source

An overview of anti-diabetic plants used in Gabon: Pharmacology and Toxicology [PDF]

, 2018
© 2017 Elsevier B.V. All rights reserved.Ethnopharmacological relevance: The management of diabetes mellitus management in African communities, especially in Gabon, is not well established as more than 60% of population rely on traditional treatments as ...
A. Souza, Abdelgadir, Abdu-Aguye, Abdulrazaq, Abubakar, Adebayo, Adedoyin, Adelusi, Ademuyiwa, Adeneye, Adeneye, Adeneye, Adeneye, Aderibigbe, Adeyemi, Adisa, Adler, Agbor, Agnaniet, Agunbiabe, Agyare, Ajaiyeoba, Ajaiyoeba, Ajao, Ajayi, Akah, Akash, Akinloye, Akpanyung, Aladodo, Alaribe, Amole, Anaduaka, Anosike, Anowi, Anowi, Antia, Anyanwu, Apers, Areola, Arthur, Asadu, Asha, Ashraf, Asolkar, Assob, Asuquo, Atangwho, Atawodi, Atawodi, Aw, Awah, Awe, Aziba, B. Bading Taika, Balasubramanian, Bamisaye, Bapna, Bardi, Bayan, Bella, Ben-Chioma, Bera, Biney, Bisong, Brantley, Calapai, Campbell, Campbell-Tofte, Capasso, Chika, Chokshi, Chris-Ozoko, Coolborn, Coria-Téllez, Da-Costa-Rocha, Dadzeasah, Dahake, Das, Dhanabalan, Djeussi, Djimeli, Djomeni, Djomeni Dzeufiet, Effiong, Effiong, Effo, Eidi, Ejike, El-Demerdash, Elufioye, Elumalai, Eluwa, Eneh, Erharuyi, Erhirhie, Eteng, Etuk, Ewenighi, Ewere, Eyong, Eze, Ezeasor, Ezejindu, Ezejiofor, Ezeokeke, Ezike, Ezuruike, Fang-Chui, Farzaei, Fernand, Ferreira, Feuya Tchouya, Feuya Tchouya, Fongang, Fred-Jaiyesimi, Gandhare, Ganesh, Gbadegesin, Gboeloh, Gemede, Ghani, Ghiware, Gomez-Flores, Gondi, Goutarel, Gupta, Gutierrez, H.P. Bourobou Bourobou, Halim, Hamzah, Hansen, Helfer, Hossain, Houghton, Houël, Huang, Huang, Husain, Husin, Ibibia, Igbe, Igboasoiyi, Ilodigwe, Ilodigwe, Ilusanya, Inya-Agha, Iroanya, Irondi, Irondi, Ishola, Iwu, Iyamah, Jawonisi, Juárez-Rojop, Juárez-Rojop, Kadima, Kaiser, Kamagate, Kamboj, Karimi, Karioti, Kathirvel, Kazeem, Kazeem, Kengni, Kengni, Khodabakhsh, Kolawole, Kouakou, Koudou, Kouitcheu Mabeku, Krishna, Kubilienė, Kuete, Kuete, Kuete, Kulkarni, Kumar, Kumar, Kumar, Kupchan, L. Lione, L.S. MacKenzie, Lakshmi, Lamidi, Lawal, Lawal, Laxane, Lee, Li, Lima, Ludvik, Ludvik, Luka, M. Bouckandou, Mabeku, Madingou, Madingou, Malviya, Manga, Maniyar, Manjur, Manvitha, Mathur, Maurya, Mačiulaitis, Mbiantcha, Mebale, Mengome, Midawa, Miranda-Osorio, Mishra, Miura, Mohamed, Mohammed, Mohammed, Mohammed, Mohammed, Momoh, Montasser, Muhammad, Muhammad, Muhammad, Muhammad, Muttaka, Nabukenya, Nakavuma, Naseri, Naskar, Navghare, Ndam, Nessa, Ngoc, Ngondi, Ngondi, Ngueguim, Ngueguim, Nishimura, Niyonzima, Nkono Ya Nkono, Nkono Ya Nkono, Ntyonga-Pono, Nwamarah, Nweze, Nwodo, Nwokocha, Nyunaï, Nyunaï, N’doua, N’guessan, N’Guessan, Obiang, Obiudu, Ocho-Anin Atchibri, Oduola, Oduola, Ofusori, Ogbonnia, Ogunrinola, Ojewole, Ojewole, Ojewunmi, Ojewunmi, Ojiako, Okeke, Okokon, Okokon, Okokon, Okolie, Okolo, Okonkwo, Olajide, Olaleye, Olatokunboh, Olivier, Olowu, Olubomehin, Ombra, Omodamiro, Omonkhua, Ong, Onyekwe, Osabede, Osadebe, Osigwe, Ouédraogo, Oyewusi j, Ozsoy-Sacan, Padilla-Camberos, Palaksha, Panda, Panda, Parle, Passoni, Patel, Patil, Ping, Pochapski, Pour, Pérez, Rajesh, Raji, Rauf, Ravi, Renjith, Rong, Rosemary, Roy, Sabitha, Sagnia, Santas, Satyaprakash, Saxena, Seung, Shah, Sharma, Sharma, Sharma, Shittu, Silva, Singh, Singh, Sio, Somova, Souza, Sowemimo, Sudhakar, Sule, Sunday, Sunday, Suryawanshi, Sutar, Swargiary, Swathi, Taj Eldin, Talreja, Tan Paul, Tanayen, Tchamadeau, Teugwa, Thongsom, Titanji, Tjeck, Togola, Toma, Toma, Trabelsi, Uchechi, Ufelle, Umoh, Vannamalar, Varghese, Varghese, Vashishtha, Verma, Verma, Vijayalakshmi, Vikram, Vliet, Wang, Wang, Wauthoz, Woode, Yakubu, Yasir, Yeap, Yessoufou, Yokozawa, Yousuf, Yu, Zakiah, Zhang, Zhao, Zheng   +374 more
core   +3 more sources