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Abstract BackgroundWith the advances in high-throughput sequencing and bioinformatic pipelines, mitochondrial genomes have become increasingly popular for phylogenetic analyses across different clades of invertebrates. Despite the vast rise in available mitogenomic datasets of molluscs, one class of aplacophoran molluscs – Solenogastres (or Neomeniomorpha) – is still neglected. ResultsHere, we present six new mitochondrial genomes from five families of Solenogastres (Amphimeniidae, Gymnomeniidae, Proneomeniidae, Pruvotinidae, Simrothiellidae), including the first complete mitogenomes, thereby now representing three of the four traditional orders. Solenogaster mitogenomes are variable in size (ranging from approximately 15,000 bp to over 17,000 bp). The gene order of the 13 protein coding genes and two rRNA genes is conserved in three blocks, but considerable variation occurs in the order of the 22 tRNA genes. Based on phylogenetic analyses and reconstruction of ancestral mitochondrial genomes of Aculifera, the position of (1) trnD gene between atp8 and atp6, (2) trnT and P genes between atp6 and nad5, and (3) trnL1 gene between G and E, resulting in a ‘MCYWQGL1E’-block of tRNA genes, are all three considered synapomorphies for Solenogastres. The tRNA gene block ‘KARNI’ present in Polyplacophora and several conchiferan taxa is dissolved in Solenogastres. ConclusionOur study shows that mitogenomes are suitable to resolve the phylogenetic relationships among Aculifera and within Solenogastres, thus presenting a cost and time efficient compromise to approach evolutionary history in these clades. 

ABSTRACT AimStudies assessing large‐scale patterns of microbial diversity have predominantly focused on free‐living microorganisms, often failing to link observed patterns to established theories regarding the maintenance of global diversity patterns. We aimed to determine whether foliar fungi on two closely related grass hosts—Heteropogon contortusandThemeda triandra—display a commonly observed latitudinal gradient in species richness and determine whether host identity, energy (temperature and precipitation), climate seasonality, fire frequency and grass evolutionary history drive the observed patterns in species richness and composition. LocationPaleotropical. Time PeriodContemporary. Major Taxa StudiedFoliar fungi. MethodsFoliar fungal diversity was quantified from 201 leaf samples ofT. triandraandH. contortuscollected across the distributional range of these species. Mixed effects models were used to quantify patterns of diversity and their correlates among and within continents. Ordinations were used to assess drivers of composition. ResultsFoliar fungi displayed consistent latitudinal diversity gradients in richness. Energy was a strong driver of richness at inter‐continental and continental scales, while other factors had inconsistent impacts on richness among scales, hosts and guilds. Globally, richness was higher in regions of higher growing season temperatures and where hosts were present for longer periods. Composition was primarily structured by geographic region at the global scale, indicating that distance was a dominant driver of community composition. Within Australia, temperature and rainfall seasonality and the amount of growing season rainfall, were the dominant drivers of both richness and composition. Main ConclusionsWe find some support for the idea that foliar fungal species diversity is governed by the same factors as many macro‐organisms (energy availability and evolutionary history) at inter‐continental scales, but also that fungal diversity and composition in the highly seasonal continent of Australia were driven by factors that shape tropical grassy ecosystems, namely climate seasonality and fire.