The Azores diversity enigma: why are there so few Azorean endemic flowering plants and why are they so widespread?

Aim Endemism in the flora of the Azores is high (33%) but in other respects, notably the paucity of evolutionary radiations and the widespread distribution of most endemics, the flora differs markedly from the floras of the other Macaronesian archipelagos. We evaluate hypotheses to explain the distinctive patterns observed in the Azorean endemic flora, focusing particularly on comparisons with the Canary Islands. Location Azores archipelago. Methods Data on the distribution and ecology of Azorean endemic flowering plants are reviewed to ascertain the incidence of inter‐island allopatric speciation and adaptive, ecological speciation. These are contrasted with patterns for the Canary Islands. Patterns of endemism in the Azores and Canaries are further investigated in a phylogenetic context in relation to island age. beast was used to analyse a published molecular dataset for Pericallis (Asteraceae) and to investigate the relative ages of Azorean and Canarian lineages. Results There are few examples of inter‐island allopatric speciation in the Azorean flora, despite the considerable distances between islands and sub‐archipelagos. In contrast, inter‐island allopatric speciation has been an important process in the evolution of the Canary Islands flora. Phylogenetic data suggest that Azorean endemic lineages are not necessarily recent in origin. Furthermore, in Pericallis the divergence of the Azorean endemic lineage from its closest relative pre‐dates the radiation of a Canarian herbaceous clade by inter‐island allopatric speciation. Main conclusions The data presented do not support suggestions that hypotheses pertaining to island age, age of endemic lineages and ecological diversity considered individually explain the lack of radiations and the widespread distribution of Azorean endemics. We suggest that palaeoclimatic variation, a factor rarely considered in macroecological studies of island diversity patterns, may be an important factor. Palaeoclimatic data suggest frequent and abrupt transitions between humid and arid conditions in the Canaries during the late Quaternary, and such an unstable climate may have driven the recent diversification of the flora by inter‐island allopatric speciation, a process largely absent from the climatically more stable Azores. Further phylogenetic/phylogeographic analyses are necessary to determine the relative importance of palaeoclimate and other factors in generating the patterns observed.     

Species richness and endemicity in the Spanish vascular flora

Data from an updated and revised checklist of the Spanish flora is analyzed. The Spanish vascular plant flora is composed of 204 families, 1433 genera and 7071 species. Floristic data are analysed by considering three regions: mainland Spain with 5984 species, the Balearic Islands with 1521 species and Canary Islands with 2066 species. Extinct species are included in the analysis, with an extinction rate of 0.35% of the flora. A total of 1488 endemic species are recognized, which account for 21% of the Spanish flora. The rate of endemism in the Canary Islands is 25.9%, considerably higher than for the Balearic Islands (6.9%) and for mainland Spain (13.8%). A list of the 35 strict endemic genera is compiled, of which 65.7% are Canarian, and another list of 27 subendemic genera of which 48.1% are also Canarian. An estimated 12% of the Spanish flora is non‐native, with large variation between the 20.7% of the Canary flora, 10.5% of mainland Spain and 9.7% of the Balearic Islands. Finally, the composition of the Spanish flora for large groups and families is ana lysed. The data show that species richness and endemicity rates have been overestimated by previous authors, and are similar to other Mediterranean countries. It is concluded that a complete revision of the Macaronesian flora is strongly needed to obtain an accurate comparison with the flora of other areas.     

Notes on the Poaceae of the Robinson Crusoe (Juan Fernández) Islands, Chile

Notes on the Poaceae of the Robinson Crusoe (Juan Fernández) Islands, Chile, Brittonia 54: 154–163. 2001.—Poaceae in the Robinson Crusoe (=Juan Fernández) Islands number 53 species in 32 genera, of which 9% of the species are endemic, 9% indigenous, and 81% adventitious. The endemic taxa (and their conservation status) are:Agrostis masafuerana (rare),Chusquea fernandeziana (not endangered),Megalachne berteroana (not endangered),M. masafuerana (not endangered), andPodophorus bromoides (extinct).Megalachne andPodophorus are endemic genera. Comparisons with Poaceae in the Bonin and Volcano Islands, Canary Islands, Galápagos Islands, and Hawaiian Islands show different levels of endemism: number of endemic taxa, respectively, 5, 10, 12, 40; percent specific endemism, 8, 6, 21, 19. No endemic genera occur.Anthoxanthum odoratum, Avena barbata andHordeum murinum are noxious weeds in the Robinson Crusoe Islands. Many adventives are shared among floras of the archipelagos, with the highest ties of Robinson Crusoe being to the Canaries (53% of total Poaceae known in Juan Fernández) and the Hawaiian Islands (47%). Low levels of adventives occur within the Bonin (5%) and Galápagos (7%) Islands. In contrast, there are many endemic genera of Asteraceae in these same archipelagos: Bonin and Volcano Islands (1), Canary Islands (8), Galápagos Islands (5), and Hawaiian Islands (6); percent of specific endemism is also higher (20, 53, 54 and 56, respectively). Hypotheses for greater levels of endemics among oceanic island Asteraceae include more efficient dispersal mechanisms by wind and birds, animal pollination systems that result in greater degrees of geographic populational genetic isolation, and a vascular cambium that offers enhanced growth-form evolutionary opportunities.     

Panbiogeography of New Caledonia,south‐west Pacific: basal angiosperms on basement terranes,ultramafic endemics inherited from volcanic island arcs and old taxa endemic to young islands

Aim To investigate areas of endemism in New Caledonia and their relationship with tectonic history. Location New Caledonia, south‐west Pacific. Methods Panbiogeographical analysis. Results Biogeographical patterns within New Caledonia are described and illustrated with reference to eight terranes and ten centres of endemism. The basement terranes make up a centre of endemism for taxa including Amborella, the basal angiosperm. Three of the terranes that accreted to the basement in the Eocene (high‐pressure metamorphic terrane, ultramafic nappe and Loyalty Ridge) have their own endemics. Main conclusions New Caledonia is not simply a fragment of Gondwana but, like New Zealand and New Guinea, is a complex mosaic of allochthonous terranes. The four New Caledonian basement terranes were all formed from island arc‐derived and arc‐associated material (including ophiolites) which accumulated in the pre‐Pacific Ocean, not in Gondwana. They amalgamated and were accreted to Gondwana (eastern Australia) in the Late Jurassic/Early Cretaceous, but in the Late Cretaceous they separated from Australia with the opening of the Tasman Sea and break‐up of Gondwana. An Eocene collision of the basement terranes with an island arc to the north‐east – possibly the Loyalty Ridge – is of special biogeographical interest in connection with New Caledonia–central Pacific affinities. The Loyalty–Three Kings Ridge has had a separate history from that of the Norfolk Ridge/New Caledonia, although both now run in parallel between Vanuatu and New Zealand. The South Loyalty Basin opened between Grande Terre and the Loyalty Ridge in the Cretaceous and attained a width of 750 km. However, it was almost completely destroyed by subduction in the Eocene which brought the Loyalty Ridge and Grande Terre together again, after 30 Myr of separation. The tectonic history is reflected in the strong biogeographical differences between Grande Terre and the Loyalty Islands. Many Loyalty Islands taxa are widespread in the Pacific but do not occur on Grande Terre, and many Grande Terre/Australian groups are not on the Loyalty Islands. The Loyalty Islands are young (2 Myr old) but they are merely the currently emergent parts of the Loyalty Ridge whose ancestor arcs have a history of volcanism dating back to the Cretaceous. Old taxa endemic to the young Loyalty Ridge islands persist over geological time as a dynamic metapopulation surviving in situ on the individually ephemeral islands and atolls found around subduction zones. The current Loyalty Islands, like the Grande Terre terranes, have inherited their biota from previous islands. On Grande Terre, the ultramafic terrane was emplaced on Grande Terre in the Eocene (about the same time as the collision with the island arc). The very diverse endemic flora on the ultramafics may have been inherited by the obducting nappe from prior base‐rich habitat in the region, including the mafic Poya terrane and the limestones typical of arc and intraplate volcanic islands.     

Avian distribution patterns in the Guiana Shield: implications for the delimitation of Amazonian areas of endemism

Aim To develop a methodology for defining the boundaries of the Guianan area of endemism using complementary approaches that include GIS tools, multivariate statistics and analyses of physical barriers in the distribution patterns of an entire endemic avifauna. As a case study, I used the distribution patterns of lowland terra firme forest birds. Location Guiana Shield, northern South America. Methods I identified Guianan endemics using the ornithological literature, subsequently gathering distributional data for these taxa using mainly museum collections and my own fieldwork in the region. I used these distributional data to map the spatial patterns of endemicity in the region and to compare distributions across taxa. I employed community composition data from 34 localities from throughout the Guiana Shield to identify spatial patterns of clustering using an ordination analysis (non‐metric multidimensional scaling), and to recognize the region’s main biogeographical barriers for birds using Monmonier’s algorithm. Results At least 88 avian taxa are restricted to the terra firme forests of the Guianan area of endemism, which is roughly delimited by the Amazon, Negro and Branco rivers. These large rivers, however, are not the only boundaries. I identified seven additional barriers, including medium‐sized rivers, non‐forested areas and mountains, which also contribute to delimiting the area of endemism. Within the endemic avifauna, I identified three distinct distribution patterns. The ordination analysis shows the presence of two distinct avifaunas within the Guiana Shield. Main conclusions Although the proposed boundaries of the Guianan area of endemism are consistent with previously postulated configurations, this study reveals a more complex delimitation than formerly recognized, highlighting the importance of several landscape features besides large rivers, and the existence of three distinct distributional patterns within one endemic avifauna. The Branco/Negro interfluvium, often included within this area of endemism, actually represents a transition zone between two distinct avifaunas. The longstanding view of the Amazon Basin as a mosaic of parapatric areas of endemism delimited by major rivers appears to be an oversimplification, at least for the Guiana Shield. This finding suggests the need for more rigorous approaches to re‐evaluate the traditional boundaries of such areas.     

Contradiction in Conservation of Island Ecosystems: Plants, Introduced Herbivores and Avian Scavengers in the Canary Islands

Introduction of alien herbivores in sensitive island systems has resulted in massive effects on vegetation cover, floristic richness and composition of communities; some species can be even totally extirpated by grazing pressure. Goats Capra hircus and wild rabbits Oryctolagus cuniculus were introduced in the Canary Islands around 500 B.C. Barbary ground squirrels Atlantoxerus getulus were introduced in 1967. Traditional extensive livestock exploitations have been maintained to the present but in the last decades the number of goats has sharply increased up to densities of 53 heads/km². Overgrazing and trampling have heavily affected eleven island endemic plant species. Some populations have been reduced to less than 10 viable individuals. On the other hand, goat carcasses and wild rabbit and squirrel populations help to maintain populations of three endangered endemic subspecies of birds. This conflict presents important economic and social ramifications: whereas public funds (mainly through European LIFE projects) are devoted to conservation of plant and avian endemic taxa, the number of goats increases rapidly thanks to subventions derived from the European Common Agricultural Policy (CAP). Similar conflicts are apparent in other Mediterranean Basin insular systems. It is urgently necessary to harmonize farming and conservation objectives in the Canary Islands. The impact of goats on the vegetation should be minimized through limitation of grazing in sensitive areas with high degree of endemism. Creation of ‘vulture restaurants’ may reduce the dependence of scavengers on extensive livestock exploitations. We recommend a careful study of ecological relationships within island communities where non-native species are susceptible of playing a keystonrole as occurs in the Mediterranean Basin archipelagos.     

Microevolutionary patterns and processes of the Native Hawaiian colonizing fern Odontosoria chinensis (Lindsaeaceae)

Abstract.— The vascular‐plant flora of the Hawaiian Islands is characterized by one of the highest rates of species endemism in the world. Among flowering plants, approximately 89% of species are endemic, and among pteridophytes, about 76% are endemic. At the single‐island level, however, rates of species endemism vary dramatically between these two groups with 80% of angiosperms and only 6% of pteridophytes being single‐island endemics. Thus, in many groups of Hawaiian angiosperms, it is possible to link studies of phylogeny, evolution, and biogeographic history at the interspecific and interisland levels. In contrast, the low level of single‐island species endemism among Hawaiian pteridophytes makes similar interspecific and interisland studies nearly impossible. Higher levels of interisland gene flow may account for the different levels of single‐island endemism in Hawaiian pteridophytes relative to angiosperms. The primary question we addressed in the present study was: Can we infer microevolutionary patterns and processes among populations within widespread species of Hawaiian pteridophytes wherein gene flow is probably common? To address this broad question, we conducted a population genetic study of the native Hawaiian colonizing species Odontosoria chinensis. Data from allozyme analyses allowed us to infer: (1) significant genetic differentiation among populations from different islands; (2) historical patterns of dispersal between particular pairs of islands; (3) archipelago‐level patterns of dispersal and colonization; (4) founder effects among populations on the youngest island of Hawaii; and, (5) that this species primarily reproduces via outcrossing, but may possess a mixed‐mating system.     

Palaeo‐islands as refugia and sources of genetic diversity within volcanic archipelagos: the case of the widespread endemic Canarina canariensis (Campanulaceae)

Geographical isolation by oceanic barriers and climatic stability has been postulated as some of the main factors driving diversification within volcanic archipelagos. However, few studies have focused on the effect that catastrophic volcanic events have had on patterns of within‐island differentiation in geological time. This study employed data from the chloroplast (cpDNA haplotypes) and the nuclear (AFLPs) genomes to examine the patterns of genetic variation in Canarina canariensis, an iconic plant species associated with the endemic laurel forest of the Canary Islands. We found a strong geographical population structure, with a first divergence around 0.8 Ma that has Tenerife as its central axis and divides Canarian populations into eastern and western clades. Genetic diversity was greatest in the geologically stable ‘palaeo‐islands’ of Anaga, Teno and Roque del Conde; these areas were also inferred as the ancestral location of migrant alleles towards other disturbed areas within Tenerife or the nearby islands using a Bayesian approach to phylogeographical clustering. Oceanic barriers, in contrast, appear to have played a lesser role in structuring genetic variation, with intra‐island levels of genetic diversity larger than those between‐islands. We argue that volcanic eruptions and landslides after the merging of the palaeo‐islands 3.5 Ma played key roles in generating genetic boundaries within Tenerife, with the palaeo‐islands acting as refugia against extinction, and as cradles and sources of genetic diversity to other areas within the archipelago.     

Are plant communities on the Canary Islands resistant to plant invasion?

Oceanic islands are renowned for their unique flora and high levels of endemism. Native island plants, however, are imperilled by non-native species that can become invasive by outcompeting natives. The threat of native island assemblages generally increases with isolation and the number of endemics featured, but also with human-associated disturbance and land use. Based on this, the Canary Island native plant systems should be highly threatened by invasives, similar to other oceanic islands globally. However, Canarian native plant systems are only weakly infiltrated and are rarely directly threatened by invasive plants. Further, highly disturbed areas, usually among the first colonized by invasives on islands, are recolonized here by natives. Based on this, we postulate four hypotheses (climatic filter, well-preservation status, human legacy and permanent colonization) for explaining this unusual behaviour of plant systems on the Canary Islands, providing an opportunity to understand the drivers and processes behind invasion into plant communities on islands.     

Evolutionary history of the flora of Mexico: Dry forests cradles and museums of endemism

Mexico is considered an exceptional biogeographic area with a varied endemic flora, however spatial phylogenetic measures of biodiversity have not yet been estimated to understand how its flora assembled to form the current vegetation. Patterns of species richness, endemism, phylogenetic diversity, phylogenetic endemism and centers of neo‐ and paleo‐endemism were determined to examine differences and congruence among these measures, and their implications for conservation. Of 24 360 vascular plant species 10 235 (42%) are endemic. Areas of endemism and phylogenetic endemism were associated with dry forests in zones of topographic complexity in mountain systems, in deserts, and in isolated xeric vegetation. Every single locality where seasonally tropical dry forests have been reported in Mexico was identified as an area of endemism. Significant phylogenetic diversity was the most restricted and occurred in the Trans‐Mexican Volcanic Belt and in the Sierra de Chiapas. Notably, the highest degree of phylogenetic clustering comprising neo‐, paleo‐, and super‐endemism was identified in southernmost Mexico. Most vascular plant lineages diverged in the Miocene (5–20 mya) when arid environments expanded across the world. The location of Mexico between two very large landmasses and the fact that more than fifty percent of its surface is arid favored the establishment of tropical lineages adapted to extreme seasonality and aridity. These lineages were able to migrate from both North and South America across Central America presumably during the Miocene and to diversify, illustrating the signature of the flora of Mexico of areas of endemism with a mixture of neo‐ and paleo‐endemism.     

Growth form diversity on the Canary Islands

An analysis is given of the growth form composition of the flora of the Canary Islands based on a checklist published by Hansen & Sunding (1985) and the authors' field studies. Results are compared with similar data available from Israel and California. Special attention is given to endemism, the Mediterranean-wides and introduced species, as well as to some special plant features such as succulence, spinescence and fleshy fruits. Long-distance dispersal is stressed as the mechanism by which the Canaries obtained their flora. The growth-form composition of the Canaries is discussed in the context of the prevailing present-day environmental conditions, not in the context of climatic conditions in geological time. Characteristic features are the low percentages of endemic and even of indigenous annuals, the high percentage of chamaephytes (many of whom are endemic), the strong development of arborescence, the richness in leaf succulents, and the paucity of spines.     

Spiders on a Hot Volcanic Roof: Colonisation Pathways and Phylogeography of the Canary Islands Endemic Trap-Door Spider Titanidiops canariensis (Araneae,Idiopidae)

Studies conducted on volcanic islands have greatly contributed to our current understanding of how organisms diversify. The Canary Islands archipelago, located northwest of the coast of northern Africa, harbours a large number of endemic taxa. Because of their low vagility, mygalomorph spiders are usually absent from oceanic islands. The spider Titanidiops canariensis, which inhabits the easternmost islands of the archipelago, constitutes an exception to this rule. Here, we use a multi-locus approach that combines three mitochondrial and four nuclear genes to investigate the origins and phylogeography of this remarkable trap-door spider. We provide a timeframe for the colonisation of the Canary Islands using two alternative approaches: concatenation and species tree inference in a Bayesian relaxed clock framework. Additionally, we investigate the existence of cryptic species on the islands by means of a Bayesian multi-locus species delimitation method. Our results indicate that T. canariensis colonised the Canary Islands once, most likely during the Miocene, although discrepancies between the timeframes from different approaches make the exact timing uncertain. A complex evolutionary history for the species in the archipelago is revealed, which involves two independent colonisations of Fuerteventura from the ancestral range of T. canariensis in northern Lanzarote and a possible back colonisation of southern Lanzarote. The data further corroborate a previously proposed volcanic refugium, highlighting the impact of the dynamic volcanic history of the island on the phylogeographic patterns of the endemic taxa. T. canariensis includes at least two different species, one inhabiting the Jandia peninsula and central Fuerteventura and one spanning from central Fuerteventura to Lanzarote. Our data suggest that the extant northern African Titanidiops lineages may have expanded to the region after the islands were colonised and, hence, are not the source of colonisation. In addition, T. maroccanus may harbour several cryptic species.     

Ecological and historical factors affecting distribution pattern and richness of endemic plant species: the case of the Maritime and Ligurian Alps hotspot

The aim of this study was to test a method to locate all the foci, centres, and areas of endemism in a biodiversity hotspot in order to understand the influence of ecological and historical factors on the distribution pattern and to identify priority areas for future conservation projects. The study area was the Maritime and Ligurian Alps hotspot.
Analyses were performed on the presence/absence matrix of 36 vascular plant taxa endemic to the study area. For each operational geographical unit, the number of endemic taxa present was counted. Additionally, the weighted endemism value was calculated. Areas of endemism were distinguished using cluster analysis and parsimony analysis of endemicity. The influence of ecological characteristics and historical factors was evaluated using Multi-Response Permutation Procedure and the Nonparametric Multiplicative Regression. The Indicator Species Analysis (INDVAL) method was used to identify the species characterizing the areas of endemism. Our results show the importance and location of four main areas of endemism within the Maritime and Ligurian Alps and explain the distribution pattern of endemic plants. These areas are easily interpreted by historical and ecological factors, and INDVAL indicates which taxa took part in the history of each endemism area.     

Phytogeography of Lusitanian Macaronesia: biogeographic affinities in species richness and assemblage composition

Analysis of biogeographic affinities is a key tool to establish and improve the resolution of hierarchical biogeographic systems. We describe patterns of species richness of the marine macroalgal flora across Lusitanian Macaronesia (Azores, Madeira, the Salvage Islands and the Canary Islands), and test (i) whether such differences are related to differences in proximity to the nearest continental shore and size among islands. We also explore biogeographic affinities in the composition of macroalgal assemblages (= presence/absence of each taxon in multivariate datasets) to determine (ii) whether each archipelago is a biogeographic unit within this ecoregion and (iii) whether patterns in assemblage composition are related to proximity (i.e. distances) among islands. Presence/absence matrices were created to test and visualize multivariate affinities among archipelagos. A total of 872 taxa were compiled. Species richness peaked at the Canary Islands and decreased towards the Azores; the pattern matched a progressive increase in distance from the nearest continental shores, matching the classical island biogeography theory. Intra-archipelago differences in species richness were largely related to variations in island size. Biogeographic similarities among archipelagos were hierarchically structured. Madeira and the Salvage Islands constituted one biogeographic unit. Floras from the Azores, Madeira and the Salvage Islands were barely separable from each other, but were different from those at the Canary Islands. Such biogeographic similarities among islands were negatively correlated with the geographical separation (i.e. distances) among them. Proximity to nearby continental shores, in conjunction with large- and meso-scale oceanographic patterns, seems to interact to create patterns in richness and composition of algal assemblages across Lusitanian Macaronesia.     

Patterns of endangerment in the hawaiian flora

The Hawaiian flora, because of its great isolation, high levels of endemism, known lineages, and high rates of endangerment, offers unique opportunities to explore patterns of endangerment related to phylogeny, ecological and life history traits, and geographic patterns. Nine percent of the native flora of 1159 taxa are already extinct, and 52.5% are at risk (extinct, endangered, vulnerable, or rare). Risk is strongly associated with limited geographic distribution at several scales: endemic taxa (native only to the Hawaiian Islands) are at far greater risk than indigenous taxa (with both Hawaiian and extra-Hawaiian ranges); single-island endemics are more at risk than multi-island endemics; small islands have the highest proportion of endemic taxa at risk; and endemics with more limited habitat distributions (elevation, community type) are more at risk. Historic population density is a strong predictor of risk, and taxa with low historic population densities are at greatest risk with rapid anthropogenic changes. Among the major islands, Maui Nui has the highest percent of taxa that are extinct. Kaua'i has the lowest percent of extinct taxa and the highest proportion of single-island endemic taxa that are rare. Endemic taxa at risk are associated with distributions in shrublands, forests, bogs, and cliff habitats. Endemic taxa with distributions in low elevation dry habitats have the highest proportion of taxa at risk, but the greatest absolute numbers of taxa at risk have distributions in mesic lowland and montane forests, and in wet montane forests. The life history patterns associated with risk are complicated, and inclusion of the effects of evolutionary relationships (lineages) changes some of these patterns. Species level analyses without respect to lineage shows risk associated with monomorphic (hermaphroditic) breeding systems and bird pollination because of the large number of hermaphroditic, bird-pollinated species in the Campanulaceae. Analyses incorporating the effect of lineage greatly reduce the impact of large lineages and result in an association of risk with insect pollination, and no effect of breeding system. There is no association of lineage size and the percent of taxa at risk within the lineage; endemic taxa from lineages with large radiations are at no greater risk than endemic single-taxon lineages. The percentages of taxa at risk at the family level in the Hawaiian Islands and worldwide (excluding Hawaiian taxa) are positively correlated, although flowering plant families in the Hawaiian Islands have a much greater proportion of taxa at risk. Some of the approaches described here may be useful to predict geographical and biological patterns of endangerment in island and island-like ecosystems under increasing pressures of endangerment and extinction.     

Diversification of the forest beetle genus Tarphius on the Canary Islands, and the evolutionary origins of island endemics

The flightless beetle genus Tarphius Erichson (Coleoptera: Colydiidae) is a distinctive element of the beetle fauna of the Canary Islands with 29 species distributed across the five western islands. The majority of Tarphius species are rare and intimately associated with the monteverde forest and only two species occur on more than one island. In this study we investigate the phylogeography of the Canary Island Tarphius, and their relationship to Tarphius from the more northerly archipelagos of Madeira and the Azores using maximum parsimony and Bayesian inference analysis of mitochondrial cytochrome oxidase I and II sequence data. We use geological datings for the Canary Islands, Azores, and Madeira to calibrate specific nodes of the tree for the estimation of divergence times using a penalized likelihood method. Data suggest that the Canary Island species assemblage is of some antiquity, however, much of this species diversity is relatively recent in origin. The phylogenetic relationships of species inhabiting the younger islands of El Hierro and La Palma indicate that colonization events between islands have probably been a significant factor in the evolutionary history of the Canary Island species assemblage. A comparison of molecular phylogenetic studies of arthropods on the Canary Islands suggests that, in the evolution of the arthropod species community of an island, the origin of endemic species is initially the result of colonizing lineages differentiating from their source populations. However, as an island matures a greater proportion of endemic species originate from intra-island speciation.     

Peculiarities of island endemism in Lasiocampidae (Lepidoptera)

The distinctive features of island endemism in Lasiocampidae are extensive adaptive radiation and vicariance. These phenomena are especially typical of archipelagoes, where different taxa occur on closely located islands. The diverse ecological conditions of the islands determine the presence of a great number of subordinate taxa. Owing to the reduced flight activity, the species of Lasiocampidae are characterized by a high level of endemism on isolated islands. Islands of continental origin (Sumatra, Borneo) have a lower level of endemism, with centers on the mountain ranges. The endemism level is much higher in islands of biogenic origin (the Philippines). The Pacific islands have a higher index of specific endemism. At the same time, the islands of mixed and oceanic origin have low species diversity by a large fraction of endemic taxa. The boundaries of species distribution are determined not only by the landscape or climatic factors but also by biological ones.     

Bird–flower interactions in the Macaronesian islands

Aims Several bird‐pollinated or ornithophilous flowers are present on the Macaronesian archipelagos, the Canary Islands and Madeira, but absent from nearby NW Africa and Europe. In Macaronesia, no specialist nectar‐feeding birds are found, but several generalist passerine bird species visit flowers for nectar. Two hypotheses attempt to explain the origin and evolution of ornithophily in the Macaronesian flora. According to ‘the island de novo hypothesis’, bird‐flowers evolved from mainland insect‐pollinated ancestors after island colonization. Alternatively, ancestors of the ornithophilous Macaronesian plant species evolved bird‐flowers before reaching the islands (‘the relict hypothesis’). In this study we first compile information of Macaronesian bird–flower interactions from the literature and our own field observations. Secondly, we discuss the two hypotheses of origin of ornithophily in the light of evidence from recent molecular plant phylogenies, palaeontology, historical biogeography of the African avifauna and flora, and present‐day ecological patterns. Location Madeira and Canary Islands. Results At least eleven endemic Macaronesian plant species from six genera have typical ornithophilous floral traits. These genera are: Canarina and Musschia (Campanulaceae), Isoplexis (Scrophulariaceae), Echium (Boraginaceae), Lotus (Fabaceae) and Lavatera (Malvaceae). These lineages have clear affinities to the Mediterranean region, except for Canarina whose closest relatives grow in East African mountains. Six generalist passerine bird species of Sylvia, Phylloscopus (Sylviidae), Serinus (Fringillidae) and Parus (Paridae) visit this flora for nectar. Main conclusion We suggest that the origin and evolution of ornithophilous traits in these plant species took place mostly in mainland areas prior to island colonization. In Canarina and Lavatera, it is well supported that ornithophily is a relict condition, which originated in mainland areas possibly in association with specialist nectar‐feeding birds. For the remaining plant species except Echium wildpretii bird floral traits probably also are a relict condition. These species may be derived from ancestors, which were visited by specialist nectar‐feeding birds during geological periods when the Mediterranean and the Ethiopian vegetation were intermingled in mainland Africa. Probably, these mainland ancestors went extinct due to severe climatic fluctuations, while their Macaronesian descendants survived in ‘refuge’ on the islands. Finally, the island de novo hypothesis may explain the evolution of a mixed bird/insect‐pollination system in the neo‐endemic red‐flowered Echium wildpretii.     

The Greater Cape Floristic Region

Aim The Cape Floristic Region (CFR) (Cape Floristic Kingdom) is currently narrowly delimited to include only the relatively mesic Cape fold mountains and adjacent intermontane valleys and coastal plains. We evaluate the floristic support for expanding the delimitation to include the whole winter‐rainfall area (arid and mesic climates) into a Greater CFR. Location Southern Africa, particularly the south‐western tip. Methods The initial divisive hierarchical classification analysis twinspan used the presence/absence of vascular plant genera to obtain major floristic groupings in southern Africa. For the more detailed analyses, we scored the flora as present/absent within a set of centres, among which the floristic relationships were investigated (agglomerative methods, upgma and minimum spanning trees). These analyses were conducted with species, genera and families separately. The centres were grouped into five regions. The species richness and endemism was calculated for the centres, regions and combination of regions. The dominant floristic components of each region were sought by calculating the percentage contribution of each family to the flora. Results The divisive method showed that the winter‐rainfall areas are floristically distinct from the rest of southern Africa. The species‐ and generic‐level analyses revealed five regions: CFR, Karoo Region, Hantam‐Tanqua‐Roggeveld Region, Namaqualand Region and Namib‐Desert Region. The CFR has the highest endemism and richness. However, the combination of the CFR, the Hantam‐Tanqua‐Roggeveld Region and the Namaqualand Region results in a higher total endemism. Combined, these three regions almost match the region delimited by the twinspan analysis, and together constitute the Greater CFR. Main conclusions The CFR constitutes a valid floristic region. This is evident from the endemism and the distinctive composition of the flora. However, the total endemism is higher for the whole winter‐rainfall area, and this supports the recognition of the larger unit. If floristic regions are to be delimited only on endemism, then the Greater CFR is to be preferred. If floristic regions are delimited on the composition of their floras at family level, then the support for such a grouping is weaker.