美国纽约中部受管理的新兴湿地的野生蜜蜂群落和授粉网络

IF 2.6 2区 生物学 Q2 ECOLOGY Ecology and Evolution Pub Date : 2025-02-05 DOI:10.1002/ece3.70847
Molly M. Jacobson, Michael L. Schummer, Melissa K. Fierke, Paige R. Chesshire, Donald J. Leopold
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摘要

为了有效地保护野生蜜蜂传粉者及其提供的服务,收集其分布、生活史以及在多种栖息地类型中与植物相互作用的数据至关重要。在蜜蜂调查中,湿地的代表性不足,尽管湿地有多种开花植物,并且对数百种野生动物具有重要意义。在这项为期2年的调查中,在纽约中部的一个恢复湿地复合体中收集了9000多只蜜蜂,代表25属109种以上。我们记录了337种独特的植物-传粉者关系,包括那些以前未记载的湿地专性蒙面蜂,Hylaeus nelumbonis (Robertson)。花资源和蜂属的多样性在8月最为丰富,网络分析表明,9月蜂群网络的连通性、嵌套性和模块化程度最低。随着季节的推移,花卉资源也逐渐转向本地。结果表明,在生长季后半期,新兴湿地支持多种传粉媒介,湿地管理可以产生有利于野生蜜蜂栖息地的多样化条件。
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Wild Bee Assemblages and Pollination Networks of Managed Emergent Wetlands in Central New York, USA

To effectively protect wild bee pollinators and the services they provide, it is critical to gather data on their distributions, life histories, and interactions with plants among a diversity of habitat types. Wetlands are underrepresented in bee surveys, despite having a great diversity of flowering plants and known importance to hundreds of species of wildlife. In this 2-year survey of a restored wetland complex in Central New York, over 9000 bees were collected, representing ≥ 109 species in 25 genera. We recorded 337 unique plant–pollinator associations, including those previously undocumented for the wetland obligate masked bee, Hylaeus nelumbonis (Robertson). Floral resources and bee genera were most diverse in August, and network analyses indicated September networks were the most connected, nested, and least modular. Floral resources also shifted towards being more native over the course of the season. Results show that emergent wetlands support diverse guilds of pollinators in the latter half of the growing season, and that wetland management can produce diverse conditions conducive to wild bee habitat.

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来源期刊
CiteScore
4.40
自引率
3.80%
发文量
1027
审稿时长
3-6 weeks
期刊介绍: Ecology and Evolution is the peer reviewed journal for rapid dissemination of research in all areas of ecology, evolution and conservation science. The journal gives priority to quality research reports, theoretical or empirical, that develop our understanding of organisms and their diversity, interactions between them, and the natural environment. Ecology and Evolution gives prompt and equal consideration to papers reporting theoretical, experimental, applied and descriptive work in terrestrial and aquatic environments. The journal will consider submissions across taxa in areas including but not limited to micro and macro ecological and evolutionary processes, characteristics of and interactions between individuals, populations, communities and the environment, physiological responses to environmental change, population genetics and phylogenetics, relatedness and kin selection, life histories, systematics and taxonomy, conservation genetics, extinction, speciation, adaption, behaviour, biodiversity, species abundance, macroecology, population and ecosystem dynamics, and conservation policy.
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