The relationship between species richness of vertebrate mutualists and their food plants in tropical and subtropical communities differs among hemispheres

Non-random statistical patterns have long been of interest to community ecologists. Recent studies of communities of mutualists have revealed non-random patterns in terms of connectance, degree of specialization, and nestedness. Currently unstudied, however, are the detailed statistical relationships between tropical vertebrate mutualists and their food plants in different parts of the world. Here, I review 87 studies that quantify the relationship between species richness of nectar- or fruit-eating birds and bats and species richness of their food plants in New and Old World, mostly tropical, communities. This analysis revealed that in the New World, number of plant-visiting birds and bats per community was significantly correlated with number of food plants and that the slopes of regression equations were the same for nectarivores and frugivores. The New World quantitative assembly rule states that it takes about three species of flowers or fruits to support one species of plant-visiting bird or bat. This relationship does not appear to exist in Old World communities, in which species richness of nectar- or fruit-eating birds or bats was independent of species richness of their food plants. These geographic differences likely reflect a greater degree of feeding specialization in plant-visiting vertebrates in the New World than in the Old World. I hypothesize that hemispheric differences in the spatio-temporal predictability (STP) of food resources ultimately determine levels of dietary specialization and structure in communities of New and Old World plant-visiting vertebrates.     

Latitudinal and elevational variation in fruiting phenology among western European bird-dispersed plants

I try to test the prediction that bird-dispersed plants should produce fruits when fruit-eating birds are most abundant by reviewing some phenological data of fleshy fruit production in western Europe The prediction that fruit ripening dates in populations of the same species should occur later at lower latitudes and elevations, to coincide with the maximum abundance of fruit-eating birds, is not supported by the data The patterns of seasonal variation in the total number and biomass of fruits, but not in the proportion of species in fruit, in communities at different latitudes and elevations do coincide with patterns of seasonal abundances of avian frugivores 1 suggest that this coincidence is due to the greater relative abundance (and contribution to total fruit production) in each locality of species that fruit at times of the year when birds are most abundant These species may have achieved a demographic advantage by getting more seeds dispersed than species that ripen fruits in other seasons     

Characterization of MHC class II B polymorphism in bottlenecked New Zealand saddlebacks reveals low levels of genetic diversity

The major histocompatibility complex (MHC) is integral to the vertebrate adaptive immune system. Characterizing diversity at functional MHC genes is invaluable for elucidating patterns of adaptive variation in wild populations, and is particularly interesting in species of conservation concern, which may suffer from reduced genetic diversity and compromised disease resilience. Here, we use next generation sequencing to investigate MHC class II B (MHCIIB) diversity in two sister taxa of New Zealand birds: South Island saddleback (SIS), Philesturnus carunculatus, and North Island saddleback (NIS), Philesturnus rufusater. These two species represent a passerine family outside the more extensively studied Passerida infraorder, and both have experienced historic bottlenecks. We examined exon 2 sequence data from populations that represent the majority of genetic diversity remaining in each species. A high level of locus co-amplification was detected, with from 1 to 4 and 3 to 12 putative alleles per individual for South and North Island birds, respectively. We found strong evidence for historic balancing selection in peptide-binding regions of putative alleles, and we identified a cluster combining non-classical loci and pseudogene sequences from both species, although no sequences were shared between the species. Fewer total alleles and fewer alleles per bird in SIS may be a consequence of their more severe bottleneck history; however, overall nucleotide diversity was similar between the species. Our characterization of MHCIIB diversity in two closely related species of New Zealand saddlebacks provides an important step in understanding the mechanisms shaping MHC diversity in wild, bottlenecked populations.     

Closing the gap: Avian lineage splits at a young,narrow seaway imply a protracted history of mixed population response

The evolutionary significance of spatial habitat gaps has been well recognized since Alfred Russel Wallace compared the faunas of Bali and Lombok. Gaps between islands influence population structuring of some species, and flightless birds are expected to show strong partitioning even where habitat gaps are narrow. We examined the population structure of the most numerous living flightless land bird in New Zealand, Weka (Gallirallus australis). We surveyed Weka and their feather lice in native and introduced populations using genetic data gathered from DNA sequences of mitochondrial genes and nuclear β‐fibrinogen and five microsatellite loci. We found low genetic diversity among extant Weka population samples. Two genetic clusters were evident in the mtDNA from Weka and their lice, but partitioning at nuclear loci was less abrupt. Many formerly recognized subspecies/species were not supported; instead, we infer one subspecies for each of the two main New Zealand islands. Although currently range restricted, North Island Weka have higher mtDNA diversity than the more wide‐ranging southern Weka. Mismatch and neutrality statistics indicate North Island Weka experienced rapid and recent population reduction, while South Island Weka display the signature of recent expansion. Similar haplotype data from a widespread flying relative of Weka and other New Zealand birds revealed instances of North Island—South Island partitioning associated with a narrow habitat gap (Cook Strait). However, contrasting patterns indicate priority effects and other ecological factors have a strong influence on spatial exchange at this scale.     

Is tree diversity different in the Southern Hemisphere?

Questions: Is tree diversity higher in the southern hemisphere? Are latitudinal asymmetries in diversity sensitive to sampling effects? Location: 198 forested locales worldwide. Methods: I re‐analysed the Gentry database, which I augmented with an additional survey from New Zealand. Data were used to test whether latitudinal declines in tree diversity differ between the northern and southern hemispheres. Data were also used to test whether hemispheric asymmetries in diversity are sensitive to sampling effects, or geographic variation in tree densities. Results: Area‐based measurements of species diversity are higher in the southern hemisphere. However, southern forests house denser plant populations. After controlling for geographic variation in tree densities, diversity patterns reverse, indicating tree diversity is higher in the northern hemisphere. Conclusions: Latitudinal changes in tree diversity differ between hemispheres. However, the nature of hemispherical asymmetries in species diversity hinges on how diversity is defined, illustrating how different definitions of diversity can yield strikingly different solutions to common ecological problems.     

Is Avian Malaria Playing a Role in Native Bird Declines in New Zealand? Testing Hypotheses along an Elevational Gradient

The mosquito-borne disease avian malaria (Plasmodium spp.) has impacted both captive populations and wild individuals of native New Zealand bird species. However, whether or not it is a cause of concern to their wild populations is still unclear. In Hawaii, the disease has been a major factor in the population declines of some native forest bird species, often limiting their elevational distribution due to an inverse relationship between force of infection and elevation. While studies have investigated latitudinal patterns of infection in New Zealand, elevational patterns are unexplored. To address this, a survey was conducted in Nelson Lakes National Park, a site experiencing native bird declines in which disease has been suggested as playing a role, to investigate whether there is a similar inverse relationship in New Zealand. Results from blood samples (n = 436) collected over three seasons across a broad elevational range (650–1400 m) support there being such a relationship. In addition, an overall higher prevalence in non-native (14.1%) versus native birds (1.7%) may indicate differential impacts on these two groups, while particularly high prevalence in non-native Turdus spp. supports previous suggestions that they are key reservoir hosts for the disease. Overall, these findings add weight to the hypothesis that avian malaria is playing a role in ongoing declines of native New Zealand birds.     

Mapping Global Diversity Patterns for Migratory Birds

Nearly one in five bird species has separate breeding and overwintering distributions, and the regular migrations of these species cause a substantial seasonal redistribution of avian diversity across the world. However, despite its ecological importance, bird migration has been largely ignored in studies of global avian biodiversity, with few studies having addressed it from a macroecological perspective. Here, we analyse a dataset on the global distribution of the world’s birds in order to examine global spatial patterns in the diversity of migratory species, including: the seasonal variation in overall species diversity due to migration; the contribution of migratory birds to local bird diversity; and the distribution of narrow-range and threatened migratory birds. Our analyses reveal a striking asymmetry between the Northern and Southern hemispheres, evident in all of the patterns investigated. The highest migratory bird diversity was found in the Northern Hemisphere, with high inter-continental turnover in species composition between breeding and non-breeding seasons, and extensive regions (at high latitudes) where migratory birds constitute the majority of the local avifauna. Threatened migratory birds are concentrated mainly in Central and Southern Asia, whereas narrow-range migratory species are mainly found in Central America, the Himalayas and Patagonia. Overall, global patterns in the diversity of migratory birds indicate that bird migration is mainly a Northern Hemisphere phenomenon. The asymmetry between the Northern and Southern hemispheres could not have easily been predicted from the combined results of regional scale studies, highlighting the importance of a global perspective.     

Mutualisms with the wreckage of an avifauna: the status of bird pollination and fruit dispersal in New Zealand

Worldwide declines in bird numbers have recently renewed interest in how well bird?plant mutualisms are functioning. In New Zealand, it has been argued that bird pollination was relatively unimportant and bird pollination failure was unlikely to threaten any New Zealand plants, whereas dispersal mutualisms were widespread and in some cases potentially at risk because of reliance on a single large frugivore, the kereru (Hemiphaga novaeseelandiae). Work since 1989, however, has changed that assessment. Smaller individual fruits of most plant species can be dispersed by mid-sized birds such as tui (Prosthemadera novaezelandiae) because both fruits and birds vary in size within a species. Only one species (Beilschmiedia tarairi) has no individual fruits small enough for this to occur. Germination of 19 fleshy-fruited species, including most species with fruits >8 mm diameter, does not depend on birds removing the fruit pulp. The few studies of fruit removal rates mostly (7 out of 10) show good dispersal quantity. So dispersal is less at risk than once thought. In contrast, there is now evidence for widespread pollen limitation in species with ornithophilous flowers. Tests on 10 of the 29 known native ornithophilous-flowered species found that in 8 cases seed production was reduced by at least one-third, and the pollen limitation indices overall were significantly higher than the global average. Birds also frequently visit flowers of many other smaller-flowered native species, and excluding birds significantly reduced seed set in the three species tested. So pollination is more at risk than once thought. Finally, analyses of both species numbers and total woody basal area show that dependence on bird pollination is unexpectedly high. Birds have been recorded visiting the flowers of 85 native species, representing 5% of the total seed-plant flora (compared with 12% of those with fleshy fruit) and 30% of the tree flora (compared with 59% with fleshy fruit). A higher percentage of New Zealand forest basal area has bird-visited flowers (37% of basal area nationally) than fleshy fruit (31%). Thus, bird pollination is more important in New Zealand than was realised, partly because birds visit many flowers that do not have classic ?ornithophilous? flower morphology.     

Fruit–frugivore interactions in two southern hemisphere forests: allometry,phylogeny and body size

The size of fleshy fruits spans several orders of magnitude. However, the evolution of fruit size diversity is poorly understood. Fruit size diversity is hypothesised to result from several potential processes. The frugivore hypothesis postulates that different‐sized animal fruit consumers select for different‐sized fruits. The correlated selection hypothesis postulates that fruit size is allometrically related to other plant traits (e.g. leaf size, plant height); therefore differences in fruit size result from correlated evolution with other plant traits. We tested the frugivore and correlated selection hypotheses as potential explanations for fruit size diversity in two New Zealand study sites. We observed birds foraging for fruits over two fruiting seasons at each site and measured fruit size, leaf size and plant height in a total of 32 plant species. Relationships between average fruit size, leaf size, plant size and the average size of birds consuming each fruit species were then evaluated using phylogenetically independent contrasts. Similar results were obtained in both study sites. Fruit size was correlated with the size of avian fruit consumers, but was unrelated to leaf size or plant height. Therefore, results falsified the correlated selection hypothesis but failed to falsify the frugivore hypothesis. Although results suggest that frugivores may have influenced the evolution of fruit size in New Zealand, further study is needed to generate a mechanistic understanding of how frugivores may have selected for interspecific variation in fruit size.     

Heteroblasty on Chatham Island: A comparison with New Zealand and New Caledonia

We used a comparative approach to investigate heteroblasty in the Chatham Islands. Heteroblasty refers to abrupt changes in the morphology of leaves and shoots with plant height. Common on isolated islands such as New Caledonia and New Zealand, which once had flightless, browsing birds, heteroblasty is hypothesised to be an adaptation to deter bird browsing. The Chatham Islands are a small archipelago located 800 km off the east coast of New Zealand, which has clear floristic links to New Zealand. However, unlike New Caledonia and New Zealand, the Chathams never had flightless, browsing birds. We investigated heteroblasty on the Chatham Islands by: (1) comparing height-related changes in leaf morphology and branching architecture in several plant taxa with heteroblastic relatives on the New Zealand mainland; (2) characterising changes in leaf morphology in heteroblastic tree species endemic to the Chathams; and (3) comparing overall trends in leaf heteroblasty on the Chathams with New Caledonia and New Zealand. Reversions to homoblasty were observed in the three Chatham Island taxa with heteroblastic relatives on the New Zealand mainland. However, two endemic tree species were clearly heteroblastic; both produced dramatically larger leaves as juveniles than as adults. Inter-archipelago comparisons showed that this trend in leaf morphology is rare among heteroblastic species in New Caledonia and New Zealand. Therefore, while some of our results were consistent with the hypothesis that heteroblasty is an adaptation to avoid bird browsing, other processes also appear to have shaped the expression of heteroblasty on Chatham Island.     

Contrasting mtDNA diversity and population structure in a direct-developing marine gastropod and its trematode parasites

The comparative genetic structure of hosts and their parasites has important implications for their coevolution, but has been investigated in relatively few systems. In this study, we analysed the genetic structure and diversity of the New Zealand intertidal snail Zeacumantus subcarinatus ( n  =   330) and two of its trematode parasites, Maritrema novaezealandensis ( n  =   269) and Philophthalmus sp. ( n  =   246), using cytochrome c oxidase subunit I gene ( COI ) sequences. Snails and trematodes were examined from 11 collection sites representing three regions on the South Island of New Zealand. Zeacumantus subcarinatus displayed low genetic diversity per geographic locality, strong genetic structure following an isolation by distance pattern, and low migration rates at the scale of the study. In contrast, M. novaezealandensis possessed high genetic diversity, genetic homogeneity among collection sites and high migration rates. Genetic diversity and migration rates were typically lower for Philophthalmus sp. compared to M. novaezealandensis and it displayed weak to moderate genetic structure. The observed patterns likely result from the limited dispersal ability of the direct developing snail and the utilization of bird definitive hosts by the trematodes. In addition, snails may occasionally experience long-distance dispersal. Discrepancies between trematode species may result from differences in their effective population sizes and/or life history traits.     

Habitat selection in reintroduced bird populations: a case study of Stewart Island robins and South Island saddlebacks on Ulva Island

An understanding of the mechanisms influencing habitat selection in reintroduced bird populations is fundamental for successful translocation programmes. Plant species composition, abundance, structure and food availability are likely to influence animal movement and habitat choice, but few studies have evaluated their combined effect on habitat selection of translocated birds. Stewart Island robins (Petroica australis rakiura) and South Island saddlebacks (Philesturnus carunculatus carunculatus) are two threatened New?Zealand bird species that have been reintroduced to Ulva Island (Stewart Island). We hypothesised that their initial settlement patterns were driven by habitat quality. We tested this hypothesis by comparing habitat components between occupied and unoccupied habitats as the population grew after initial tanslocation. We also modelled probabilities of site selection as a function of the composition and structure of vegetation, availability of food (invertebrate composition) and nesting resources (cavity type). Founding pairs of both species first established territories in coastal habitat in the western part of the island, which is characterised by structurally complex broadleaved vegetation. Birds also selected sites with a greater abundance and diversity of food resources. Thus in the early stages of population establishment robins and saddlebacks appear to select high quality habitat that offers enhanced cover and foraging opportunities.     

The vegetation of a New Zealand dune slack

The vegetation of a dune slack at Mason Bay, Stewart Island, New Zealand was found to comprise a mosaic of communities. Although the broad vegetational patterns could be correlated with the depth of the water table, the patterns were far from simple. Species diversity over the whole slack was lower than values reported from European dune slacks; even the most diverse communities did not reach European mean values.For nomenclature see Wilson in press. Vascular plants of Stewart Island. D.S.I.R., Wellington, New Zealand; Sainsbury (1955). A handbook of the New Zealand mosses. N.Z. R. Soc. 5: 1–490 & Hamlin (1972). Hepaticae of New Zealand, Dominion Museum, Wellington.     

Enhanced niche opportunities: can they explain the success of New Zealand's introduced bird species?

Aim  The niche hypothesis could explain why some species introduced to new locations reach higher densities than in their native range: it posits that the new environment provides more abundant or higher quality resources or habitat, a more suitable physical environment or both. We investigate whether 11 bird species occur at higher densities in their introduced range than in their native range and whether the differences can be explained by the availability of preferred habitat or the suitability of climatic conditions in their introduced range relative to their native range.
Location  South Island, New Zealand (the introduced range); UK (the native range).
Methods  We first develop a series of models that accurately predict the density of 11 bird species at 54 UK farmland sites, which are closely matched to our New Zealand sites, from habitat and climatic variables. We then use these models to predict the density of the 11 species at 54 New Zealand farmland sites and compare the predicted and observed values.
Results  Actual densities at New Zealand sites were on average (median) 22 times (range: 1–6361) higher than predicted from the UK models and similarly higher than actually observed at comparable UK sites. Habitat and climatic variables can accurately predict bird densities in the UK but grossly underestimate densities for all species except Turdus merula in New Zealand.
Main conclusions  These findings indicate that factors other than the measured habitat and climatic variables must differ between the two regions and explain the much higher densities of New Zealand birds. We suggest that introduced birds, other than T. merula , in New Zealand may still experience enhanced niche opportunities due to greater availability of higher quality resources within habitats, release from natural enemy regulation, less exposure to extreme weather events, particularly during winter, or some combination of these processes.     

Winter range compression of migrants in Central America

Where there is seasonal disparity among opportunities, the season with those in shortest supply is most likely to limit populations. Among migrant birds that travel between different breeding and winter ranges, any of breeding, migratory or winter conditions could exclusively constitute such population-limiting factors. In both the New and Old Worlds, landmass is disproportionately concentrated in temperate latitudes. In the Americas, most passerine bird species that breed in the USA and Canada spend the winter further south, commonly in parts of the tropics where landmass is significantly less. Using a sample of 89 migratory species (eight passerine families) that breed in eastern North America, I considered patterns of geographic breeding range size, winter range size and winter distribution. Winter range size is usually smaller than breeding range size (84 of 89 species), often substantially so (minimum 8%, mean 52%). Wintering latitude explains significant variation in both breeding range size and winter range size, as well as in winter range size relative to breeding range size. In particular, all three measures vary latitudinally in patterns similar to latitudinal variation in landmass. These patterns collectively suggest that the reduction in landmass in the latitudes of Central America and the Caribbean is a limiting factor for migrant bird populations, adding to other research concluding that winter conditions sometimes prevail over breeding conditions in the limitation of populations. Hectare for hectare, habitat destruction in the tropics is likely to have the greater impact on the welfare of passerine populations breeding in North America.     

EVOLUTIONARY ASPECTS OF FRUIT-EATING BY BIRDS

In spite of a considerable literature on fruit-eating, the general evolutionary implications of fruit as a source of food for birds have been neglected. A preliminary attempt is made to explore the evolutionary and ecological consequences of fruit-eating, considered as a mutual interaction between parent plant and dispersal agent. The relationship considered is that obtaining between fleshy fruits and the “legitimate” fruit-eating birds which digest the fleshy part of the fruit and void the seed intact. Evolutionary aspects of seed-eating are also briefly discussed. The “strategies” adopted by fruits for dispersal by birds result in the production of abundant food supplies which are easy of access and exploitable by many species of birds. By contrast, the predation of birds on insects leads to a heterogeneous, sparse and cryptic food supply, to exploit which many different hunting techniques are necessary. Two important evolutionary developments in birds are attributed to these differences in food supply: there tend to be more species in families of insectivorous than of frugivorous birds, and lek behaviour in tropical forest has evolved in predominantly frugivorous birds. The seasonal succession of fruits in temperate latitudes is discussed, and contrasted with the situation in the tropics, using examples from Europe and Trinidad. In general, the succession of ripe fruits in Europe seems to be adapted to the seasonal shifts of the bird populations, and the more nutritious fruits tend to have a more southerly distribution and to ripen later than the more succulent fruits. In the tropics the distinction between nutritious and succulent fruits seems to be largely one of habitat. The constant succession of ripe fruits throughout the year in the tropics probably depends on competition for dispersal by frugivorous birds, which thus ensure the maintenance of their own food supply. This may be regarded as a symbiosis at the level of the ecosystem.     

Winter range compression of migrants in Central America

Where there is seasonal disparity among opportunities, the season with those in shortest supply is most likely to limit populations. Among migrant birds that travel between different breeding and winter ranges, any of breeding, migratory or winter conditions could exclusively constitute such population‐limiting factors. In both the New and Old Worlds, landmass is disproportionately concentrated in temperate latitudes. In the Americas, most passerine bird species that breed in the USA and Canada spend the winter further south, commonly in parts of the tropics where landmass is significantly less. Using a sample of 89 migratory species (eight passerine families) that breed in eastern North America, I considered patterns of geographic breeding range size, winter range size and winter distribution. Winter range size is usually smaller than breeding range size (84 of 89 species), often substantially so (minimum 8%, mean 52%). Wintering latitude explains significant variation in both breeding range size and winter range size, as well as in winter range size relative to breeding range size. In particular, all three measures vary latitudinally in patterns similar to latitudinal variation in landmass. These patterns collectively suggest that the reduction in landmass in the latitudes of Central America and the Caribbean is a limiting factor for migrant bird populations, adding to other research concluding that winter conditions sometimes prevail over breeding conditions in the limitation of populations. Hectare for hectare, habitat destruction in the tropics is likely to have the greater impact on the welfare of passerine populations breeding in North America.     

Population structure and biogeography of Hemiphaga pigeons (Aves: Columbidae) on islands in the New Zealand region

Aim The New Zealand avifauna includes lineages that lack close relatives elsewhere and have low diversity, characteristics sometimes ascribed to long geographic isolation. However, extinction at the population and species levels could yield the same pattern. A prominent example is the ecologically important pigeon genus Hemiphaga. In this study, we examined the population structure and phylogeography of Hemiphaga across islands in the region. Location New Zealand, Chatham Islands and Norfolk Island. Methods Mitochondrial DNA was sequenced for all species of the genus Hemiphaga. Sixty‐seven individuals from mainland New Zealand (Hemiphaga novaeseelandiae novaeseelandiae), six of the Chatham Islands sister species (Hemiphaga chathamensis), and three of the extinct Norfolk Island subspecies (Hemiphaga novaeseelandiae spadicea) were included in this study. Novel D‐loop and cytochrome b primers were designed to amplify DNA from museum samples. Additionally, five other mitochondrial genes were used to examine placement of the phylogenetic root. Results Analyses of mitochondrial DNA sequences revealed three Hemiphaga clades, consistent with the allopatric populations of recognized (sub)species on oceanic islands. Of the 23 D‐loop haplotypes among 67 New Zealand pigeons (Hemiphaga n. novaeseelandiae), 19 haplotypes were singletons and one haplotype was common and widespread. Population genetic diversity was shallow within and between New Zealand populations, indicating range expansion with high inter‐population exchange. Tentative rooting of the Hemiphaga clade with cyt b data indicates exchange between mainland New Zealand and the Chatham Islands prior to colonization of Norfolk Island. We found low genetic divergence between populations on New Zealand, the Chatham Islands and Norfolk Island, but deep phylogenetic divergence from the closest living relatives of Hemiphaga. Main conclusions The data are consistent with the hypothesis of population reduction during the Pleistocene and subsequent expansion from forest refugia. Observed mobility of Hemiphaga when feeding helps explain the shallow diversity among populations on islands separated by many hundreds of kilometres of ocean. Together with comparison of distribution patterns observed among birds of the New Zealand region, these data suggest that endemicity might represent not long occupancy of an area, but descent from geologically recent colonizations. We consider the role of lineage pruning in creating the impression of old endemicity.     

Body size trends in a Holocene island bird assemblage

Despite the robust observation in macroecology that there are many small-bodied species, recent comparative studies have found little evidence for elevated net rates of diversification among small-bodied species within taxa. Here we examine the relationship between body size and species richness using the New Zealand land bird fauna, a well resolved palaeoecological Holocene assemblage. We test whether there is any evidence that net cladogenesis depended on body size in an assemblage prior to the impact of human-induced extinction. We also test whether net cladogenesis depends on the level at which taxa are endemic to New Zealand, to see whether there is evidence for bursts of cladogenesis following taxon establishment, and examine how the body sizes of New Zealand land birds relate to those in Australia, the most likely source pool for colonising taxa. Most New Zealand land bird species are small-bodied. We find no evidence, however, that this is due to higher net cladogenesis in small-bodied taxa. The body mass distributions of endemic and recent colonist species do not differ statistically, but recent colonists tend to be smaller-bodied than their closest endemic relative. This tendency is more marked for small-bodied than large-bodied taxa. More endemic taxa do not tend to be more species rich in New Zealand, although there is a positive relationship between level of endemism and species richness for forest taxa. The body mass distribution of New Zealand birds is very similar to that for Australia. Body mass does not dictate the likelihood that a family has colonised New Zealand from Australia, but the number of species in the family does: it is the species rich Australian families that have successfully colonised. We discuss the implications of these results for the evolution of body size distributions, and for the "island rule" of body size evolution on islands.     

Weta and the evolution of fleshy fruits in New Zealand

Fleshy fruits are typically coloured either red or black and are displayed in conspicuous locations where they can be easily located by birds. However, fleshy fruits in New Zealand are often white or translucently coloured and are displayed in the inner recesses of plant canopies. These characteristics have been attributed to coevolution with reptiles. I describe seed dispersal by a ground weta in Nelson lakes National Park, and hypothesise that the unusual characteristics of fleshy fruits in New Zealand may result from coevolution with weta.