The western Antarctic Peninsula harbours a diverse benthic marine community where dense canopies of macroalgae can dominate the shallow subtidal zone (0–40 m or greater). In the lower portion of this range (below 25–35 m depending on topography), invertebrates such as sponges and echinoderms can be found in greater abundance due to reduced competition for space from the algal species. Dendrilla antarctica (previously Dendrilla membranosa) is a common demosponge that thrives in both communities and is known for producing diterpene secondary metabolites as a defence against sympatric sea star and amphipod predators. Omnivorous mesograzers such as amphipods inhabit both communities; however, they are in greatest abundance within the macroalgal canopy. Due to the differences between habitats, it was hypothesized that specific amphipod species not susceptible to the defensive metabolites of D. antarctica would take refuge from predators in the chemically defended sponge. Analysis of the metabolome and amphipod communities from sponges in both habitats found correlations of metabolic profile to both abundance and habitat. These studies serve to inform our understanding of the complex ecosystem of the Antarctic benthos that stands to be dramatically altered by the rapidly changing climate in the years to come.

Larvae of Plagiometriona aff. flavescens carry a structure on their back made of faeces and exuviae, called faecal shield, which may protect larvae against natural enemies. Previous investigations suggested that the nature of such protection was chemical. To test if chemicals found in the faecal shield of Plagiometriona aff. flavescens provided defence for larvae, experiments in the field and in the laboratory (using the ant Camponotus crassus, and chicks Gallus gallus as model predators) were undertaken. Both field and laboratory experiments showed that live larvae with faecal shields, as well as baits treated with faecal shield extracts, were rejected by predators, confirming the chemical nature of this kind of defence.

Studies were continued to investigate the ability of secondary metabolites sequestered in Antarctic sponges to cause feeding deterrent responses (tube foot retractions) in a common predator of Aritarctic sponges, the sea star Perknaster fuscus. Lipophilic (dichloromethane/methanol) and hydrophilic (methanol/water) extracts of 15 new species of Antarctic marine sponges were tested for their ability to induce sustained tubefoot retraction. One additional species, Cinchyra antarctica, was re-tested from a previous study because we discovered a colour morph that was of comparative interest. Employing established protocols, sponge extracts were imbedded in silicone and presented to an extended tube-foot on the tip of a glass rod. Extracts of ten of the 15 new species of sponges (67%) caused significantly longer tube-foot retractions than controls. Among all sponges tested, significant tube-foot retraction activity was primarily associated with dichloromethane/methanol extracts (eleven sponge species or colour morphs), while significant tube-foot retraction activity was less common in response to methanol/water extracts (three sponges species or colour morphs). Both lipophilic and hydrophilic extracts from the sponges C. antarctica (yellow morph) and Scolymastia joubini elicited significant tube-foot retraction activity, suggesting that more than one compound from these speciesmight elicit tube-foot retractions in P. fuscus. Overall these findings lend considerable support to the hypothesis that there has been significant evolutionary selection for chemical defences among Antarctic marine sponges in McMurdo Sound, in contrast to earlier biogeographic selection models that predicted low levels of chemical defences in polar marine invertebrates.

Mast-fruiting is the intermittent and synchronous production of large fruits by a population of plants at long intervals (Herrera et al. 1998, Kelly 1994). Several hypotheses have been proposed concerning the adaptive advantages of mast-fruiting (Janzen 1971, 1974; Kelly 1994), and some field observations have provided evidence for these hypotheses (Norton & Kelly 1988, Shibata et al. 1998, Sork 1993). The predator-satiation hypothesis is one well-known explanation for reproductive synchrony in plants and animals (Janzen 1971, 1974; Kelly 1994). This hypothesis claims that mast fruiting at irregular intervals of several years is an effective means of satiating vertebrate fruit predators: low seed production can only support low densities of predators during the periods between mast-fruiting events, but more fruits are produced than predators can consume in masting years (Janzen 1971, Kelly 1994). Thus, it may be said that mast-fruiting is a defence strategy of plants against post-dispersal vertebrate fruit predators.

Both within and between species, leaves of plants display wide ranges in structural features. These features include: gross investments of carbon and nitrogen substrates (e.g. leaf mass per unit area); stomatal density, distribution between adaxial and abaxial surfaces, and aperture; internal and external optical scattering structures; defensive structures, such as trichomes and spines; and defensive compounds, including UV screens, antifeedants, toxins, and silica abrasives. I offer a synthesis of selected publications, including some of my own. A unifying theme is the adaptive value of expressing certain structural features, posed as metabolic costs and benefits, for (1) competitive acquisition and use of abiotic resources (such as water, light and nitrogen) and (2) regulation of biotic interactions, particularly fungal attack and herbivory. Both acclimatory responses in one plant and adaptations over evolutionary time scales are covered where possible. The ubiquity of trade-offs in function is a recurrent theme; this helps to explain diversity in solutions to the same environmental challenges but poses problems for investigators to uncover numerous important trade-offs. I offer some suggestions for research, such as on the need for models that integrate biotic and abiotic effects (these must be highly focused), and some speculations, such as on the intensity of selection pressures for these structures.

The defensive glands of beetles, Tenebrio molitor, infected with metacestodes (cysticercoids) of Hymenolepis diminuta are everted less frequently upon stimulation, and contain less toluquinone (methylbenzoquinone) and m-cresol, than glands of uninfected controls. These differences, as shown in predation trials with wild rats, increase the likelihood that both cysticercoids and beetles will be ingested by the tapeworm's definitive host. This is the first documented case of a parasite inhibiting the chemical defence of an intermediate host, and one of only a few reports of parasite-induced manipulation of host biology supported by empirical evidence implicating facilitated parasite transmission between host species.