A Recurrent Epiphytotic of Guava Rust on Rose Apple, Syzygium jambos, in Hawaii.

A Neotropical rust of the Myrtaceae, Puccinia psidii Winter, was described from Psidium guajava L., or guava, in Brazil in 1884 (1). It was first discovered in Hawaii on potted Metrosideros polymorpha Gaud. on Oahu in April 2005 (2) with pathogenicity and identity established (3). It spread quickly, and by January 2006, severe outbreaks of this rust occurred statewide on new leaves of Syzygium jambos (L.) Alston, or rose apple. Rose apple, a native to South and Southeast Asia, was introduced to Hawaii in 1825 and is locally abundant to invasive from just above sea level to as high as 1,000 m in elevation in wet sites. Healthy, reddish green immature leaves on new twigs become deformed, yellow-red, and covered with masses of yellow urediniospores following infection. As the disease progresses, infected leaves are blackened and defoliate, with no functional leaves formed. Stem tips and branches are killed and the canopy becomes progressively smaller. Repeated mortality of juvenile leaves was observed to kill 8 to12 m tall trees in the Haiku area of Maui. Wind dispersal of urediniospores resulted in heavy infection of even small groups of S. jambos isolated by 1 km or more and billions of urediniospores covered the ground under diseased trees. On Hawaii, Maui, and Oahu, trees with many dead branches are becoming common with concerns about the fire hazard of these dead trees surrounded by dry grasses. At low humidity levels, or on more mature leaves characterized by soft expanded yellow-green tissue, fewer, mostly circular spots are formed that do not expand. S. jambos is an example of a highly vulnerable host in Hawaii and represents one of approximately 3,500 species of Myrtaceae outside the Neotropics growing in Australasia, Southeast Asia, the Pacific, and tropical Africa, which have evolved unexposed to P. psidii. Severely infected S. jambos plants have been the major source of spores in the environment, exposing many Myrtaceae hosts to P. psidii. The pathogenicity of P. psidii has been consistent among and within islands with S. jambos severely infected and M. polymorpha, Melaleuca quinquenervia, Rhodomyrtus tomentosa, Myrtus communis, and Eugenia species commonly infected. Other hosts such as S. cumini, S. malaccense, and Myriciaria cauliflora are also infected, although guava and Eucalyptus spp. are rarely infected. Strain differences within P. psidii are suspected (4). In the tropics, it is rare for mature trees to be killed by a foliar pathogen, but given the devastation of new growth, death of more S. jambos trees is likely. References: (1) T. A. Coutinho et al. Plant Dis. 82:819, 1998. (2) E. M. Killgore and R. A. Heu. New Pest Advisory No. 05-04. Hawaii Department of Agriculture, 2007. (3) J. Y. Uchida et al. Plant Dis. 90:524, 2006. (4) S. Zhong et al. Mol. Ecol. Res. 8:348. 2008.

Determinants of thermal balance in the Hawaiian giant rosette plant, Argyroxiphium sandwicense.

The effects of leaf pubescence and rosette geometry on thermal balance were studied in a subspecies of a Hawaiian giant rosette plant, Argyroxiphium sandwicense. This species, a member of the silversword alliance, grows above 2000 m elevation in the alpine zone of two Hawaiian volcanoes. Its highly pubescent leaves are very reflective (absorptance in the 400-700 nm waveband=0.44). Temperature of the expanded leaves was very similar to, or even lower than, air temperature during clear days, which was somewhat surprising given that solar radiation at the high elevation sites where this species grows can exceed 1100 W m-2. However, the temperature of the apical bud, which is located in the center of the parabolic rosette, was usually 25°C higher than air temperature at midday. Experimental manipulations in the field indicated that incoming solar radiation being focussed towards the center of the rosette resulted in higher temperatures of the apical bud. Attenuation of wind speed inside the rosette, which increased the thickness of the boundary layer surrounding the apical bud, also contributed to higher temperatures. The heating effect on the apical bud of the large parabolic rosette, which apparently enhances the rates of physiological processes in the developing leaves, may exclude the species from lower elevations by producing lethal tissue temperatures. Model simulations of apical bud temperatures at different elevations and laboratory estimates of the temperature threshold for permanent heat injury predicted that the lower altitude limit should be approximately 1900 m, which is reasonably close to the lower limit of distribution of A. sandwicense on Haleakala volcano.

Introduced species in Hawaii. biological effects and opportunities for ecological research.

The articles in this volume illustrate that the Hawaiian islands are perhaps the most extraordinary living museum of evolution on the planet. However, Hawaii's value as a museum has diminished as the products of millions of years of evolutionary radiation have been lost to habitat destruction and biological invasions by exotic species. Human-caused habitat destruction can largely be controlled in parks and preserves, but exotic species do not respect park boundaries and can degrade native communities within protected areas. On the other hand, invasions by exotic species provide a dynamic laboratory of ecological processes at the same time as they erode the value of the evolutionary museum.