Unrelated Host Plants Research Articles

RADIATION, DIVERSITY, AND HOST-PLANT INTERACTIONS AMONG ISLAND AND CONTINENTAL LEGUME-FEEDING PSYLLIDS

Island archipelagos and insect-plant associations have both independently provided many useful systems for evolutionary study. The arytainine psyllid (Sternorrhyncha: Hemiptera) radiation on broom (Fabaceae: Genisteae) in the Canary Island archipelago provides a discrete system for examining the speciation of highly host-specific phytophagous insects in an island context. Phylogenetic reconstructions based on three datasets (adult and nymph morphological characters, and two mitochondrial DNA regions: part of the small subunit rRNA, and part of cytochrome oxidase I, cytochrome oxidase II and the intervening tRNA leucine) are generally consistent. The combined molecular tree provides a well-supported estimate of psyllid relationships and shows that there have been several colonizations of the Macaronesian islands but that only one has resulted in a significant radiation. Psyllid diversification has apparently been constrained by the presence of suitable host groups within the genistoid legumes, and the diversity, distribution, and abundance of those groups. The phylogeny, by indicating pairs of sister species, allows putative mechanisms of speciation to be assessed. The most common conditions associated with psyllid speciation are geographical allopatry with a host switch to closely related hosts (six examples), or geographical allopatry on the same host (four examples). Where allopatric speciation involves a host switch, these have all been to related hosts. There is some evidence that switches between unrelated host plants may be more likely in sympatry. Only one sister pair (Arytainilla cytisi and A. telonicola) and the putative host races of Arytinnis modica are sympatric but on unrelated hosts, which may be a necessary condition for sympatric speciation in these insects. Where several psyllids share the same host, resources appear to be partitioned by ecological specialization and differing psyllid phenology.

Molecular data support a rapid radiation of aphids in the Cretaceous and multiple origins of host alternation

Many aphids display a remarkably complex life cycle of host alternation, in which cyclical parthenogenesis is combined with the obligate use of two unrelated host plants. We used mitochondrial ribosomal DNA (partial 12S and 16S) sequences to reconstruct the phylogeny of aphids, to determine how many origins of host alternation and correlated major host-plant shifts have occurred. Our results agreed with previous morphological studies in that species clustered with good support at the level of tribes. There was little well-supported phylogenetic structure at levels deeper than tribes, however, except for the monophyly of two subfamilies, Aphidinae and Lachninae. We argue that aphids experienced a rapid radiation at the tribal level, after host shifting from gymnosperms to angiosperms. A rapid radiation is consistent with aphid fossils, which record the presence of few subfamilies in the late Cretaceous, but most extant tribes by the early Tertiary. Plant fossils also record host plants of aphid tribes diversifying during this time. A hypothesized mechanism by which host alternation has evolved (fundatrix specialization), coupled with the rapid radiation, implies that this life cycle may have originated as often as in the ancestor of each tribe that displays it. We also consider, however, an alternative hypothesis of fewer origins. The basal radiation of Aphididae was dated from molecular sequences to have occurred at approximately 80–150 Mya.

Molecular data support a rapid radiation of aphids in the Cretaceous and multiple origins of host alternation

Many aphids display a remarkably complex life cycle of host alternation, in which cyclical parthenogenesis is combined with the obligate use of two unrelated host plants. We used mitochondrial ribosomal DNA (partial 12S and 16S) sequences to reconstruct the phylogeny of aphids, to determine how many origins of host alternation and correlated major host-plant shifts have occurred. Our results agreed with previous morphological studies in that species clustered with good support at the level of tribes. There was little well-supported phylogenetic structure at levels deeper than tribes, however, except for the monophyly of two subfamilies, Aphidinae and Lachninae. We argue that aphids experienced a rapid radiation at the tribal level, after host shifting from gymnosperms to angiosperms. A rapid radiation is consistent with aphid fossils, which record the presence of few subfamilies in the late Cretaceous, but most extant tribes by the early Tertiary. Plant fossils also record host plants of aphid tribes diversifying during this time. A hypothesized mechanism by which host alternation has evolved (fundatrix specialization), coupled with the rapid radiation, implies that this life cycle may have originated as often as in the ancestor of each tribe that displays it. We also consider, however, an alternative hypothesis of fewer origins. The basal radiation of Aphididae was dated from molecular sequences to have occurred at approximately 80–150 Mya.

Pestalotiopsis mangiferae . [Descriptions of Fungi and Bacteria

Abstract A description is provided for Pestalotiopsis mangiferae . Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On Mangifera indica ; also on Anacardium occidentale, Combretum decandrum, Eucalyptus spp., Mimusops spp., Vitis vinifera and many other unrelated host plants. DISEASE: Grey leaf spot of Mangifera indica . The spots vary in size from a few mm to several cm in length, are usually sharply delimited by a dark, raised border, and are silvery grey above and grey to brown below; leaf spots on other hosts are similar. Brown spot or rot of mango fruits is also known. GEOGRAPHICAL DISTRIBUTION: Ghana, Nigeria, Sierra Leone, Tanzania, Uganda, Zaire, Zambia; Bangladesh, Brunei, Burma, Hong Kong, India, Malaysia, Nepal, Sabah, Solomon Islands, Sri Lanka; Australia; Dominican Republic; Venezuela. TRANSMISSION: Inoculation studies with conidia and mycelium have shown P. mangiferae to be a weak parasite, capable of infecting young injured leaves, injured fruits, older uninjured leaves and healthy fruits if in contact with diseased tissue (35, 378; 40, 421). It has been isolated from soil, but the possibility of transmission through soil has not been investigated.