Classic problems in historical biogeography are where did penguins originate, and why are such mobile birds restricted to the Southern Hemisphere? Competing hypotheses posit they arose in tropical-warm temperate waters, species-diverse cool temperate regions, or in Gondwanaland approximately 100 mya when it was further north. To test these hypotheses we constructed a strongly supported phylogeny of extant penguins from 5851 bp of mitochondrial and nuclear DNA. Using Bayesian inference of ancestral areas we show that an Antarctic origin of extant taxa is highly likely, and that more derived taxa occur in lower latitudes. Molecular dating estimated penguins originated about 71 million years ago in Gondwanaland when it was further south and cooler. Moreover, extant taxa are inferred to have originated in the Eocene, coincident with the extinction of the larger-bodied fossil taxa as global climate cooled. We hypothesize that, as Antarctica became ice-encrusted, modern penguins expanded via the circumpolar current to oceanic islands within the Antarctic Convergence, and later to the southern continents. Thus, global cooling has had a major impact on penguin evolution, as it has on vertebrates generally. Penguins only reached cooler tropical waters in the Galapagos about 4 mya, and have not crossed the equatorial thermal barrier.
Galaxias vulgaris Stokell, which has until now been considered a single widespread freshwater fish species, may comprise several species. Comparative ethological investigations can contribute to determining taxonomic relationships; this laboratory study compares the anti-predator behaviour of Galaxias in the presence of brown trout (Salmo trutta L.). The response of three distinct genetic types (A, B, and C) to trout differed: Type A Galaxias exhibited more inactive behaviour (increasing the frequency of the cryptic "flat on the substrate" posture: FS) during the day but not the night. Type B Galaxias showed no significant effect of trout on the proportion of its behaviour that was inactive, either during the day or night, but the relative frequency of cryptic FS postures increased at both times. Type C Galaxias exhibited more active behaviour both during the day and the night. Nevertheless, the relative frequency of cryptic FS postures was greater during the day (but not the night). The proportions of fish feeding were reduced for all three types, but least marked for Type C. Feeding rate was reduced during both day and night for Types A and B, but not for Type C. These findings support the hypothesis that the three types are different species, but further critical evaluation is required. M93006
Abstract:In 2016, the New Zealand Government announced a policy to rid the country of key introduced predators (possums (Trichosurus vulpecula), ship rats (Rattus rattus), Norway rats (R. norvegicus) and mustelids (Mustela spp.)) by 2050. An interim goal under this policy is to remove all mammalian predators (the key species as well as mice (Mus musculus), kiore (R. exulans), cats (Felis catus), pigs (Sus scrofa) and hedgehogs (Erinaceus europaeus)) from island nature reserves by 2025. We identify the New Zealand islands over one hectare managed as reserves by the Department of Conservation (DOC) that have mammalian predators that can be eradicated. There are over 850 islands, islets, stacks and vegetated rocks in the New Zealand archipelago. We exclude islands in lakes and rivers and those smaller than one hectare, which leaves 616 islands, less than half of which are under some form of reserve status (286 islands entirely managed by DOC and 13 under mixed tenures but with some reserve land). One or more mammalian predators are known to occur on 48 of these islands, with the Government's 2050 target species on 42 islands and other predators (in the absence of the target species) on six islands. The Government's 2025 goal nominates one class of reserve, nature reserves. Of the 48 islands, just four islands are classed as nature reserves -two (Mauitaha and Araara Islands) with protected kiore in the Hen and Chickens group and two in the Auckland Islands group (Auckland with mice, cats and pigs; and Masked with mice and cats) -i.e. none with the key species of the wider 2050 goal. Therefore, we consider other reserve classes but place more or less strict risks of reinvasion, as indexed by known swimming ranges of the predators, to judge the feasibility of eradication. Relaxing the reserve class of the island, but not our selection of swimming ranges, results in 15 candidate islands where all mammalian predators present could be eradicated for the 2025 interim goal. Decisions on which islands to select for the programme need to consider costs and other constraints to eradicate different combinations of predators, and whether the island and its predators provide templates for the wider vision of a predator-free New Zealand, i.e. whether any of the key 2050 predators are present, the size of the island, and/or the presence of human inhabitants that complicate the predators to be targeted or constrain the use of some control methods.
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