Summary The advantages of guerrilla and phalanx growth for the guerrilla Elymus lanceolatus ssp. lanceolatus and phalanx E. l. ssp. wawawaiensis were evaluated over 2 years in two taxon mixtures with a range of densities of each subspecies and under two levels of watering. Ramet numbers and biomass of the guerrilla subspecies were higher than those of the phalanx grass in the first year but in the second year declined greatly, while the phalanx grass showed no change in biomass and an increase in ramet numbers. High neighbour densities affected the phalanx subspecies more strongly than the guerrilla subspecies in the first year, but in the second year there were few differences between subspecies. Biomass of the guerrilla grass remained greater than that of the phalanx grass but ramet numbers were similar in the second year. For both subspecies in both years, probability of flowering decreased at higher neighbour densities, indicating adaptation for competitive ability. In the first year, biomass was more strongly reduced by densities than flowering was, but in the second year, when crowding was apparently greater, flowering was more severely affected. Genet survival was high and similar for both subspecies. The presumed advantage of guerrilla subspecies in exploiting open space was supported. The guerrilla grass exploited resources more quickly in the first year by faster growth and greater ramet production, but its biomass, ramet numbers and rhizome growth, and thus its advantage, were reduced in the second year. The phalanx subspecies had slower growth, produced more ramets in later years, and delayed flowering until later years. Although less able to exploit open resources, it appeared adapted to more stressful conditions, and may be able to exploit temporal resource pulses more effectively.
Weaning conflict may represent an evolutionary conflict of interest between parent and offspring, an honest signal of need on the part of a weanling, or both. Accentuated lines visible in histological sections of teeth are indicators of stress during enamel formation and have been hypothesised to form in baboon teeth during weaning. We analysed growth increments in 5 tooth sections from 2 Ugandan baboons (Papio hamadryas anubis), using polarised light microscopy, to determine when stresses occurred during the weaning process. Dietary transitions were reconstructed using normalised strontium intensities (Sr/Ca) in enamel. Accentuated lines were cross-matched between teeth from the same animal and plotted by month. The highest frequency of stress was experienced at around 6 months in 1 baboon, coinciding with an inferred reduction in suckling frequency, and at 11 months in another, coinciding with the inferred cessation of suckling. Because accentuated lines appear to indicate weaning stress at dietary transitions, weaning conflict may represent an honest signal of need on the part of the weanling.
Cover data for plant species on eight environmentally similar sites that were each burned in a different year (from 2 to 36 years ago) were used to construct a composite sequence of vegetational change after fire on Artemisia-grassland sites in southeastern Idaho. Some species were early successional such as Lithospermum ruderale, and some late successional: Artemisia tridentata, A. tripartita, and Gutierreza sarothrae. But many species: Purshia tridentata, Symphoricarpos oreophilus, Amelanchier alnifolia, Chrysothamnus viscidiflorus, A chillea millefolium, Agropyron dasystachyum, and A. spicatum were present in both early and later stages. Shannon and Simpson indices of diversity and species richness indicated little change in alpha diversity through time. This was attributed mainly to the limited change in species composition from early to later stages. The general pattern of succession is compatible with the tolerance model of Connell & Slatyer (1977) in most respects. Species traits relating to persistence through a disturbance or re-establishment on the site, and tolerance of competition shape the course of succession on a site. Perennial grasses and forbs which sprout from the base after fire are the first species to dominate the sites. Sprouting shrubs, which require some years to regrow to their pre-fire form, are prominent by the sixth year. Shrubs which rely on dispersal become co-dominants in later stages, at which time some herbaceous species are reduced or eliminated. The pattern of succession can differ due to presence or absence of species with particular traits.
1 Foraging by means of plasticity in placement of tillers in response to low-and highnutrient patches was examined in the rhizomatous wheatgrass Elymus lanceolatus ssp. lanceolatus. Its ability to exploit soil nutrient patches was compared to that of the closely related but caespitose E. lanceolatus ssp. wawawaiensis. 2 Clones of 14 genets of each taxon were planted in boxes consisting of two 30 x 30 cm cells: the 'origin cell' where clones were planted, and the adjacent 'destination cell', with each cell containing soil with either low or high levels of nutrients. 3 The rhizomatous taxon, which can produce intravaginal, short-rhizome and longrhizome tillers, preferentially produced short-rhizome and intravaginal tillers in highnutrient destination cells. Effects of nutrient status of the origin cell as well as of the destination cell on total tiller numbers indicated clonal integration, yet tiller placement responded to local conditions. 4 Roots of both taxa accessed nutrients in destination cells (the caespitose subspecies by root growth only), and above-ground biomass of both taxa increased to a similar extent with high-nutrient destination cells. With the patch sizes used in this experiment, root growth was as important as ramet placement in exploiting nutrients in destination cells. 5 There was no relationship between degree of plasticity in ramet placement and biomass of the clone when high-nutrient destination cells were present.
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