Genetic variation reveals broad-scale biogeographic patterns and challenges species’ classification in the Kunzea ericoides (kānuka; Myrtaceae) complex from New Zealand

Author(s):  
Peter B. Heenan ◽  
Matt S. McGlone ◽  
Caroline M. Mitchell ◽  
Dagmar F. Cheeseman ◽  
Gary J. Houliston
2021 ◽  
pp. 125789
Author(s):  
Michelle M McKeown ◽  
Edward A D Mitchell ◽  
Matthew J Amesbury ◽  
Quentin Blandenier ◽  
Dan Charman ◽  
...  

1961 ◽  
Vol 57 (3) ◽  
pp. 289-294 ◽  
Author(s):  
S. R. Searle

Part of the variation among butterfat yields in dairy cows arises from genetic differences among the animals. The proportion which this bears to the total variance is known as heritability. In the ‘narrow’ sense it is defined (Lush, 1940), as the proportion of the total variance that is due to additive gene effects; the ‘broad’ sense definition includes genetic variation arising from non-additive gene effects as well as that due to additive effects. Since related animals have a proportion of their genes in common the covariance among their production records can be used for estimating genetic variation and hence heritability. This paper discusses three groups of related animals most frequently used for this purpose, twins, daughter-dam pairs and paternal half-sibs, and presents the results of analysing production records of artificially bred heifers in New Zealand, including evidence of the magnitude of the sampling errors of the heritability estimates.


2021 ◽  
Author(s):  
◽  
Cherie Balls

<p>Introduced mammalian predators are one of the largest conservation threats to New Zealand native flora and fauna, and there is an increasing concern about their presence in urban environments, coupled with a recognition that cities present a unique opportunity for ecological restoration, due to the availability of a large number of volunteers and options for intensive management of green spaces and gardens. Predator control is an essential step towards the ecological restoration of urban environments, however, it requires an understanding of the factors influencing the distribution of these mammalian predators before successful control operations can be implemented. Few studies have investigated mammalian predators in urban environments, and there is little certainty about what drives their distribution in these environments. This thesis used simple mammal monitoring techniques and trapping data to investigate the distribution of mammalian predators within broad scale urban environments, with the aim of identifying drivers of their distribution.  Chew cards and tracking tunnels collected across three New Zealand cities were assessed for their efficacy as accurate monitoring devices in urban environments. In Chapter 2, monitoring devices were cross-checked between observers to assess the level of consistency in interpretation of chew and tracking marks. The consistency of chew card and tracking tunnel identifications was relatively high overall and were not substantially influenced by the city of identification, or the duration of card exposures. Monitoring devices were also assessed for their change in sensitivity between one and six-night exposures. Both devices were effective at detecting rats, however, tracking tunnels showed greater sensitivity and consistency in detecting mice and hedgehogs, whereas chew cards were better suited to the monitoring of possums. Neither device was particularly effective at detecting mustelids or cats.  In Chapter 3, mammalian predators were monitored across 24 monitoring lines in autumn, 2018, and results were compiled with spring 2017 and autumn 2018 data, pre-collected in two other cities, following the same procedures. There were distinct differences in the broad-scale habitat utilisation of rats, mice, hedgehogs, with possums being the only species to show a strong preference for urban forests. Only two of the tested microhabitat variables had an influence on species distributions. Detection of rats declined with increasing distance to the coast, and the increase in human population size was related to a significant increase in hedgehogs. There was a strong seasonal difference on the influence of local trap density and the detection of mammals. The increase in trap density within 25-50m radii was significantly related to a decrease in rat and hedgehog detections. Overall, there are substantial differences between the distributions of species in an urban environment.  Trapping is one of the main methods of predator control in New Zealand, and is already widespread within urban and suburban Wellington. In Chapter 4, I compiled trap data from 22 community trapping groups operating in residential and reserve areas in Wellington City. Residential groups (“backyard trappers”) used a high proportion of Victor and various rat and mouse traps, which was strongly linked to their high number of rat and mouse catches. Groups trapping in reserves used a high proportion of DOC 200, Victor and A24 traps, however, fewer hedgehogs were caught compared to residential areas. Catches were significantly influenced by various landscape variables. An increased distance of traps to streams led to significantly higher catches of rats, conversely, proximity to streams resulted in significantly higher catches of mice and hedgehogs. Although few catches of weasels were reported, traps closer to the coast and to forest fragments caught significantly more individuals.  The research in this thesis contributes to the small body of research conducted on mammalian predators within urban environments. The findings in this thesis can assist with the current and future predator management programmes, by highlighting areas of potential significance, particularly in Wellington.</p>


1981 ◽  
Vol 8 (4) ◽  
pp. 543-550 ◽  
Author(s):  
Charles H. Daugherty ◽  
Ben D. Bell ◽  
Mark Adams ◽  
Linda R. Maxson

Author(s):  
Rob D. Smissen ◽  
Kerry A. Ford ◽  
Paul D. Champion ◽  
Peter B. Heenan

While examining herbarium specimens of Trithuria inconspicua Cheeseman, we observed differences in the stigmatic hairs among plants from New Zealand’s North and South Islands. This motivated us to assess genetic and morphological variation within this species and its sister T. filamentosa Rodway from Tasmania. Samples were collected from lakes in the three disjunct geographic areas where the two species occur. Genetic variation in both species was assessed with simple sequence-repeat (SSR, microsatellite) markers and analyses of genetic distances. We also compared the morphology of northern and southern New Zealand T. inconspicua using fresh material. Samples of each species clustered together in a minimum evolution tree built from genetic distances. Trithuria filamentosa had more genetic diversity than did T. inconspicua. Within T. inconspicua, plants from lakes in the North Island and the South Island formed discrete genetic groups diagnosable by subtle morphological differences. Low levels of heterozygosity in both species are consistent with a high level of selfing, as suggested for other co-sexual Trithuria species, but unusual for a putative apomict. On the basis of genetic and morphological variation, we propose recognition of the northern New Zealand and southern New Zealand lineages of T. inconspicua at subspecies rank.


2002 ◽  
Vol 29 (5-6) ◽  
pp. 663-676 ◽  
Author(s):  
Sebastian Holzapfel ◽  
Marty Z. Faville ◽  
Chrissen E. C. Gemmill

2009 ◽  
Vol 22 (3) ◽  
pp. 143 ◽  
Author(s):  
A. D. Mitchell ◽  
P. B. Heenan ◽  
B. G. Murray ◽  
B. P. J. Molloy ◽  
P. J. de Lange

Phylogenetic analyses of nuclear DNA external transcribed spacer (ETS) and chloroplast DNA trnL–trnF markers were undertaken to reconstruct the evolutionary history of the South Pacific genus Melicytus. Bayesian analyses of the ETS sequence data produced a phylogenetic tree with several well supported groups, including clades comprising: (1) species from Australia, Tasmania and Lord Howe Island; (2) the Norfolk Island M. latifolius and New Zealand off-shore island M. novae-zelandiae subsp. novae-zelandiae; (3) the large-leaved M. ramiflorus complex; (4) M. fasciger and M. micranthus; and (5) M. obovatus and allies from the Cook Strait region. Phylogenetic analysis of trnL–trnF sequence data also retrieved some of these groups although, in general, was not as well resolved. The relationships of M. lanceolatus are equivocal, as in the ETS phylogeny it is sister to a clade comprising the large-leaved tree species M. fasciger and M. ramiflorus complex and the small-leaved M. micranthus, whereas in the trnL–trnF phylogeny it is sister to a clade of small-leaved shrub species such as M. alpinus and M. crassifolius. Several biogeographic patterns are evident, with dispersal to the west from New Zealand, to Australia, involving small-leaved shrub species. Dispersal to the north from New Zealand, to Norfolk Island and Fiji, involves large-leaved tree species. The sex expression is documented for all named species and undescribed entities, with these being either hermaphroditic or dioecious. When sex expression is mapped onto the phylogeny, the hermaphroditic system is inferred to have evolved from the dioecious system. New chromosome counts are presented for M. angustifolius (2n = 64) and M. dentatus (2n = 32), and earlier counts of 2n = 64 are confirmed for M. crassifolius and M. alpinus. An additional 17 counts are provided for two natural hybrids and several undescribed entities from Australia and New Zealand. The polyploid chromosome number of 2n = 64 occurs most frequently in small-leaved divariate plants with hermaphroditic flowers. When chromosome numbers are plotted onto the phylogeny it is inferred that high polyploids (e.g. 2n = 64) and small-leaved shrubs have evolved from large-leaved trees with functional diploid (e.g. 2n = 32) chromosome numbers.


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