Inglis Peter W, Custodio Adriana R, Seijo José G, Valls José F M, Moretzsohn Marcio C
Embrapa Recursos Genéticos e Biotecnologia, Parque Estação Biológica, PqEB, Av. W5 Norte (final), Brasília, DF CEP 70770-917, Brazil.
Instituto de Botánica del Nordeste (IBONE, UNNE-CONICET), Sargento Cabral 2131, Corrientes 3400, Argentina.
Ann Bot. 2025 Sep 26;136(4):795-820. doi: 10.1093/aob/mcaf139.
Arachis contains 84 accepted species, including peanut (Arachis hypogaea), all endemic to South America. To better understand evolutionary patterns in Arachis, we studied its phylogeny and biogeographical history.
We sequenced ITS, ETS, psbA-trnH, rpoB-trnCGCA and ycf1 regions and constructed maximum likelihood trees based on aligned matrices and on a concatenation of all five regions. We then conducted a fossil-calibrated Bayesian phylogenetic analysis and a biogeographical analysis.
We hypothesize that Arachis diverged from its sister Stylosanthes in the Middle Miocene, about 15 Ma, in the area now occupied by the Brazilian Caatinga and Northeastern Cerrado, accompanied by the innovation of geocarpy as a possible adaptation to increasing aridity. Arachis began to diversify about 10 Ma, and the deepest branching, and more species-poor lineages remain associated with the Caatinga. Expansion of two distinct lineages to the contiguous and nascent Cerrado occurred in the late Miocene by ∼7.4 and ∼5.5 Ma, respectively. The Cerrado remains the major centre of diversity of Arachis and is the area of progressive expansion of the genus along the broad corridor of the north-eastern-south-western Neotropical Dry Diagonal, during the late Miocene and Pliocene. Further Pliocene expansion of distinct Arachis lineages from the Cerrado to the Pantanal and Chaco regions are also hypothesized, where the latter two ecoregions are identified as secondary centres of diversification of the genus. Frequent diversifications occurred in section Arachis from the Middle Pleistocene (∼0.774 Ma), probably driven by climate change, and accompanied by expansion of distinct Cerrado lineages: two into the Chaco, comprising a subclade of A genome species and another of all K-genome species, and a third comprising a subset of B genome species into the Chiquitano.
Our results clarify phylogenetic relationships in Arachis and provide a new framework to understand its evolutionary history.
落花生属包含84个公认的物种,其中包括花生(Arachis hypogaea),所有物种均原产于南美洲。为了更好地理解落花生属的进化模式,我们研究了其系统发育和生物地理历史。
我们对ITS、ETS、psbA-trnH、rpoB-trnCGCA和ycf1区域进行了测序,并基于比对矩阵以及所有五个区域的串联构建了最大似然树。然后,我们进行了化石校准的贝叶斯系统发育分析和生物地理分析。
我们推测,落花生属在中新世中期(约1500万年前)与其姐妹属链荚豆属分化,分化地点在现今巴西卡廷加和东北塞拉多所占据的区域,同时发生了地下结果的创新,这可能是对日益干旱环境的一种适应。落花生属大约在1000万年前开始多样化,最深的分支以及物种较少的谱系仍然与卡廷加有关。两个不同的谱系分别在中新世晚期(约740万年前和约550万年前)扩展到相邻的新生塞拉多。塞拉多仍然是落花生属的主要多样性中心,并且是该属在中新世晚期和上新世沿着东北 - 西南新热带干燥对角线的广阔走廊逐步扩张的区域。我们还推测,在上新世,落花生属的不同谱系进一步从塞拉多扩展到潘塔纳尔湿地和查科地区,后两个生态区域被确定为该属的次生多样化中心。从更新世中期(约77.4万年前)开始,落花生组频繁发生多样化,可能是由气候变化驱动的,同时伴随着不同的塞拉多谱系的扩张:两个谱系进入查科,其中一个包含A基因组物种的一个亚分支,另一个包含所有K基因组物种;第三个谱系包含B基因组物种的一个子集进入奇基塔诺地区。
我们的结果阐明了落花生属的系统发育关系,并提供了一个理解其进化历史的新框架。