Genetic differentiation and limited gene flow among fragmented populations of New Zealand endemic Hector’s and Maui’s dolphins

2012 ◽  
Vol 13 (4) ◽  
pp. 987-1002 ◽  
Author(s):  
Rebecca M. Hamner ◽  
Franz B. Pichler ◽  
Dorothea Heimeier ◽  
Rochelle Constantine ◽  
C. Scott Baker
2021 ◽  
Author(s):  
◽  
Luke Thomas

<p>Understanding patterns of gene flow across a species range is a vital component of an effective fisheries management strategy. The advent of highly polymorphic microsatellite markers has facilitated the detection of fine-scale patterns of genetic differentiation at levels below the resolving power of earlier techniques. This has triggered the wide-spread re-examination of population structure for a number of commercially targeted species. The aims of thesis were to re-investigate patterns of gene flow of the red rock lobster Jasus edwardsii throughout New Zealand and across the Tasman Sea using novel microsatellite markers. Jasus edwardsii is a keystone species of subtidal rocky reef system and supports lucrative export markets in both Australia and New Zealand. Eight highly polymorphic microsatellite markers were developed from 454 sequence data and screened across a Wellington south coast population to obtain basic diversity indices. All loci were polymorphic with the number of alleles per locus ranging from 6-39. Observed and expected heterozygosity ranged from 0.563-0.937 and 0.583-0.961, respectively. There were no significant deviations from Hardy-Weinberg equilibrium following standard Bonferroni corrections. The loci were used in a population analysis of J. edwardsii that spanned 10 degrees of latitude and stretched 3,500 km across the South Pacific. The analysis rejected the null-hypothesis of panmixia based on earlier mDNA analysis and revealed significant population structure (FST=0.011, RST=0.028) at a wide range of scales. Stewart Island was determined to have the highest levels of genetic differentiation of all populations sampled suggesting a high degree of reproductive isolation and self-recruitment. This study also identified high levels of asymmetric gene flow from Australia to New Zealand indicating a historical source-sink relationship between the two countries. Results from the genetic analysis were consistent with results from oceanographic dispersal models and it is likely that the genetic results reflect historical and contemporary patterns of Jasus edwardsii dispersal and recruitment throughout its range.</p>


Biology ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 71
Author(s):  
Hua Kong ◽  
Zhi Wang ◽  
Jing-Yuan Guo ◽  
Qi-Yu Xia ◽  
Hui Zhao ◽  
...  

Hypotheses regarding the association of increased species or genetic diversity with gradually warmer regions as a global pattern have been proposed, but no direct and solid experimental data are available to approve the association between plant genetic diversity and ambient temperatures. To test the diversity-temperature hypothesis, we studied genetic diversity and genetic differentiation of weedy rice (Oryza sativa f. spontanea) populations occurring naturally in early- and late-season rice fields that share nearly the same ecological conditions but with slightly different temperatures. Data collected from 10-year historical climatic records indicated a ~2 °C higher average air temperature in the late rice-cultivation seasons than in the early seasons. Results based on molecular fingerprints of 27 SSR (simple sequence repeat) loci showed a higher level of genetic diversity in the late-season weedy rice populations than in the early-season populations. In addition, a positive correlation was detected between the increased proportion of genetic diversity (ΔHe) and genetic differentiation among the weedy rice populations, suggesting limited gene flow. Therefore, we conclude from this study that increased genetic diversity in the late-season weedy rice populations is probably caused by the higher ambient temperatures. This finding provides evidence for the possible association between genetic diversity and ambient temperatures.


2021 ◽  
Author(s):  
◽  
Luke Thomas

<p>Understanding patterns of gene flow across a species range is a vital component of an effective fisheries management strategy. The advent of highly polymorphic microsatellite markers has facilitated the detection of fine-scale patterns of genetic differentiation at levels below the resolving power of earlier techniques. This has triggered the wide-spread re-examination of population structure for a number of commercially targeted species. The aims of thesis were to re-investigate patterns of gene flow of the red rock lobster Jasus edwardsii throughout New Zealand and across the Tasman Sea using novel microsatellite markers. Jasus edwardsii is a keystone species of subtidal rocky reef system and supports lucrative export markets in both Australia and New Zealand. Eight highly polymorphic microsatellite markers were developed from 454 sequence data and screened across a Wellington south coast population to obtain basic diversity indices. All loci were polymorphic with the number of alleles per locus ranging from 6-39. Observed and expected heterozygosity ranged from 0.563-0.937 and 0.583-0.961, respectively. There were no significant deviations from Hardy-Weinberg equilibrium following standard Bonferroni corrections. The loci were used in a population analysis of J. edwardsii that spanned 10 degrees of latitude and stretched 3,500 km across the South Pacific. The analysis rejected the null-hypothesis of panmixia based on earlier mDNA analysis and revealed significant population structure (FST=0.011, RST=0.028) at a wide range of scales. Stewart Island was determined to have the highest levels of genetic differentiation of all populations sampled suggesting a high degree of reproductive isolation and self-recruitment. This study also identified high levels of asymmetric gene flow from Australia to New Zealand indicating a historical source-sink relationship between the two countries. Results from the genetic analysis were consistent with results from oceanographic dispersal models and it is likely that the genetic results reflect historical and contemporary patterns of Jasus edwardsii dispersal and recruitment throughout its range.</p>


2021 ◽  
Author(s):  
◽  
Cong Zeng

<p>Knowledge about and understanding of population structure and connectivity of deep-sea fauna decreases with increasing depth, but such information is crucial for the management of vulnerable marine ecosystems (VMEs) in particular. As such, research using genetic markers, which does not require knowledge of ecological or environmental processes as a prerequisite for the analysis, is a practical method to investigate population connectivity of VME indicator taxa. However, population genetics studies are yet to be broadly conducted in the deep sea around New Zealand.  To provide background information and develop hypothesises for this research, 196 population genetic studies of deep-sea fauna were reviewed and analysed. Based on the collected studies, four different patterns of spatial genetic structure were observed: global homogeneous, oceanic, regional, and fine structure. These different structures were reported that they were related to depth, topography, distance between populations, temperature and other biological factors. Quantification of the relationship between these factors and the detection of barriers to gene flow (barrier detection) showed that depth, currents and topography contributed significantly to barrier detection and depth and topography were acting as a barrier to gene flow in the deep sea. Furthermore, different sampling strategies and different genetic marker types significantly influenced genetic barrier detection. Comparison amongst different habitats suggested that different conservation strategies should be developed for different habitat types (Chapter 2).  This study used different genetic markers to assess the genetic connectivity amongst VME indicator taxa Vulnerable Marine Ecosystems (VME). Seven VME indicator taxa were selected: 4 sponges (Neoaulaxinia persicum, Penares sp., Pleroma menoui and Poecillastra laminaris) and 3 corals (Goniocorella dumosa, Madrepora oculata and Solenosmilia variabilis), at different spatial scales. Due to lack of genetic information for these species, genetic markers were developed for Poecillastra laminaris (0) and S. variabilis (Chapter 4).  A geographic province (northern-southern province), region (north-central-south), and geomorphic feature hierarchical testing framework was employed to examine species-specific genetic variation in mitochondrial (COI, Cytb and 12S) and nuclear markers (microsatellites) amongst populations of four deep-sea sponges within the New Zealand region. For Poecillastra laminaris, significant mitochondrial and nuclear DNA genetic differences were revealed amongst biogeographic provinces. In contrast, no significant structure was detected across the same area for Penares sp. Both Neoaulaxinia persicum and Pleroma menoui were only available from the northern province, in which Pleroma menoui showed no evidence of genetic structure, but N. persicum exhibited a geographic differentiation in 12S. No depthrelated isolation was observed for any of the four species at the mitochondrial markers, nor at the microsatellite loci for Poecillastra laminaris. Genetic connectivity in Poecillastra laminaris is likely to be influenced by oceanic sub-surface currents that generate routes for gene flow and may also act as barriers to dispersal. Although data are limited, these results suggest that the differences in patterns of genetic structure amongst the species can be attributed to differences in life history and reproductive strategies. The results are discussed in the context of existing marine protected areas, and the future design of spatial management measures for protecting VMEs in the New Zealand region (Chapter 5).  To better understand the vulnerability of stony corals (Goniocorella dumosa, Madrepora oculata and Solenosmilia variabilis) to disturbance within the New Zealand region, and to guide marine protected area design, genetic structure and connectivity were determined using microsatellite loci and DNA sequencing. Analyses compared population genetic differentiation between two biogeographic provinces, amongst three sub-regions (north-central-south), and amongst geomorphic features. Population genetic differentiation varied amongst species and between marker types. For G. dumosa, genetic differentiation existed amongst regions and populations on geomorphic features, but not between provinces. For M. oculata, only a north-central-south regional structure was observed. For S. variabilis, genetic differentiation was observed between provinces, amongst regions and amongst geomorphic features based on microsatellite variation. Multivariate analyses indicated that populations on the Kermadec Ridge were genetically different from Chatham Rise populations in all three coral species. Furthermore, a significant isolation-by-depth pattern was observed for both marker types in G. dumosa, and also in ITS of M. oculata. An isolation-by-distance pattern was found in microsatellites of S. variabilis. Migrate analysis showed that medium to high self-recruitment were detected in all geomorphic feature populations, and different species presented different genetic connectivity patterns. These different patterns of population genetic structure and connectivity at a range of spatial scales indicate that flexible spatial management is required for the conservation of deep-sea corals around New Zealand (Chapter 6).  Understanding the deep-sea ecological processes that shape spatial genetic patterns of species is critical for predicting evolutionary dynamics and defining significant evolutionary and/or management units. In this study, the potential role of environmental factors in shaping the genetic structure of the 7 deep-sea habit-providing study species was investigated using a seascape genetics approach. The genetic data were acquired from nuclear and mitochondrial sequences and microsatellite genotype data, and 25 environmental variables (5 topographic, 17 physiochemical and 3 biological variables). The results indicated that environmental factors affected genetic variation differently amongst the species. However, factors related to current and food source explained the north-central-south genetic structure in sponges and corals, and environmental variation in these parameters may be acting as a barrier to gene flow. At the geomorphic feature level, the DistLM and dbRDA analysis showed that factors related to the food source and topography were most related to genetic variation in microsatellites of sponge and corals. This study highlights the utility of seascape genetic studies to better understand the processes shaping the genetic structure of organisms (Chapter 7).  The outcomes of this study provide vital information to assist in effective management and conservation of VME indicator taxa and contribute to an understanding of evolutionary and ecological processes in the deep sea (Chapter 8).</p>


Author(s):  
Richard Frankham ◽  
Jonathan D. Ballou ◽  
Katherine Ralls ◽  
Mark D. B. Eldridge ◽  
Michele R. Dudash ◽  
...  

Evidence of population structure and limited gene flow often leads to the questionable conclusion that populations should be managed as separate unit. A paradigm shift is needed where evidence of genetic differentiation among populations is followed by an assessment of whether populations are suffering genetic erosion, whether there are other populations to which they could be crossed, and whether the crosses would be beneficial, or harmful, and if beneficial, whether the benefits would be large enough to justify a genetic rescue attempt. Here we address these questions based on the principles established in the preceding chapters.


2021 ◽  
Author(s):  
◽  
Cong Zeng

<p>Knowledge about and understanding of population structure and connectivity of deep-sea fauna decreases with increasing depth, but such information is crucial for the management of vulnerable marine ecosystems (VMEs) in particular. As such, research using genetic markers, which does not require knowledge of ecological or environmental processes as a prerequisite for the analysis, is a practical method to investigate population connectivity of VME indicator taxa. However, population genetics studies are yet to be broadly conducted in the deep sea around New Zealand.  To provide background information and develop hypothesises for this research, 196 population genetic studies of deep-sea fauna were reviewed and analysed. Based on the collected studies, four different patterns of spatial genetic structure were observed: global homogeneous, oceanic, regional, and fine structure. These different structures were reported that they were related to depth, topography, distance between populations, temperature and other biological factors. Quantification of the relationship between these factors and the detection of barriers to gene flow (barrier detection) showed that depth, currents and topography contributed significantly to barrier detection and depth and topography were acting as a barrier to gene flow in the deep sea. Furthermore, different sampling strategies and different genetic marker types significantly influenced genetic barrier detection. Comparison amongst different habitats suggested that different conservation strategies should be developed for different habitat types (Chapter 2).  This study used different genetic markers to assess the genetic connectivity amongst VME indicator taxa Vulnerable Marine Ecosystems (VME). Seven VME indicator taxa were selected: 4 sponges (Neoaulaxinia persicum, Penares sp., Pleroma menoui and Poecillastra laminaris) and 3 corals (Goniocorella dumosa, Madrepora oculata and Solenosmilia variabilis), at different spatial scales. Due to lack of genetic information for these species, genetic markers were developed for Poecillastra laminaris (0) and S. variabilis (Chapter 4).  A geographic province (northern-southern province), region (north-central-south), and geomorphic feature hierarchical testing framework was employed to examine species-specific genetic variation in mitochondrial (COI, Cytb and 12S) and nuclear markers (microsatellites) amongst populations of four deep-sea sponges within the New Zealand region. For Poecillastra laminaris, significant mitochondrial and nuclear DNA genetic differences were revealed amongst biogeographic provinces. In contrast, no significant structure was detected across the same area for Penares sp. Both Neoaulaxinia persicum and Pleroma menoui were only available from the northern province, in which Pleroma menoui showed no evidence of genetic structure, but N. persicum exhibited a geographic differentiation in 12S. No depthrelated isolation was observed for any of the four species at the mitochondrial markers, nor at the microsatellite loci for Poecillastra laminaris. Genetic connectivity in Poecillastra laminaris is likely to be influenced by oceanic sub-surface currents that generate routes for gene flow and may also act as barriers to dispersal. Although data are limited, these results suggest that the differences in patterns of genetic structure amongst the species can be attributed to differences in life history and reproductive strategies. The results are discussed in the context of existing marine protected areas, and the future design of spatial management measures for protecting VMEs in the New Zealand region (Chapter 5).  To better understand the vulnerability of stony corals (Goniocorella dumosa, Madrepora oculata and Solenosmilia variabilis) to disturbance within the New Zealand region, and to guide marine protected area design, genetic structure and connectivity were determined using microsatellite loci and DNA sequencing. Analyses compared population genetic differentiation between two biogeographic provinces, amongst three sub-regions (north-central-south), and amongst geomorphic features. Population genetic differentiation varied amongst species and between marker types. For G. dumosa, genetic differentiation existed amongst regions and populations on geomorphic features, but not between provinces. For M. oculata, only a north-central-south regional structure was observed. For S. variabilis, genetic differentiation was observed between provinces, amongst regions and amongst geomorphic features based on microsatellite variation. Multivariate analyses indicated that populations on the Kermadec Ridge were genetically different from Chatham Rise populations in all three coral species. Furthermore, a significant isolation-by-depth pattern was observed for both marker types in G. dumosa, and also in ITS of M. oculata. An isolation-by-distance pattern was found in microsatellites of S. variabilis. Migrate analysis showed that medium to high self-recruitment were detected in all geomorphic feature populations, and different species presented different genetic connectivity patterns. These different patterns of population genetic structure and connectivity at a range of spatial scales indicate that flexible spatial management is required for the conservation of deep-sea corals around New Zealand (Chapter 6).  Understanding the deep-sea ecological processes that shape spatial genetic patterns of species is critical for predicting evolutionary dynamics and defining significant evolutionary and/or management units. In this study, the potential role of environmental factors in shaping the genetic structure of the 7 deep-sea habit-providing study species was investigated using a seascape genetics approach. The genetic data were acquired from nuclear and mitochondrial sequences and microsatellite genotype data, and 25 environmental variables (5 topographic, 17 physiochemical and 3 biological variables). The results indicated that environmental factors affected genetic variation differently amongst the species. However, factors related to current and food source explained the north-central-south genetic structure in sponges and corals, and environmental variation in these parameters may be acting as a barrier to gene flow. At the geomorphic feature level, the DistLM and dbRDA analysis showed that factors related to the food source and topography were most related to genetic variation in microsatellites of sponge and corals. This study highlights the utility of seascape genetic studies to better understand the processes shaping the genetic structure of organisms (Chapter 7).  The outcomes of this study provide vital information to assist in effective management and conservation of VME indicator taxa and contribute to an understanding of evolutionary and ecological processes in the deep sea (Chapter 8).</p>


2011 ◽  
Vol 4 (2) ◽  
pp. 102-114 ◽  
Author(s):  
Evgenyi N. Panov ◽  
Larissa Yu. Zykova

Field studies were conducted in Central Negev within the breeding range of Laudakia stellio brachydactyla and in NE Israel (Qyriat Shemona) in the range of an unnamed form (tentatively “Near-East Rock Agama”), during March – May 1996. Additional data have been collected in Jerusalem at a distance of ca. 110 km from the first and about 170 km from the second study sites. A total of 63 individuals were caught and examined. The animals were marked and their subsequent movements were followed. Social and signal behavior of both forms were described and compared. Lizards from Negev and Qyriat Shemona differ from each other sharply in external morphology, habitat preference, population structure, and behavior. The differences obviously exceed the subspecies level. At the same time, the lizards from Jerusalem tend to be intermediate morphologically between those from both above-named localities, which permits admitting the existence of a limited gene flow between lizard populations of Negev and northern Israel. The lizards from NE Israel apparently do not belong to the nominate subspecies of L. stellio and should be regarded as one more subspecies within the species.


Author(s):  
Richard Frankham ◽  
Jonathan D. Ballou ◽  
Katherine Ralls ◽  
Mark D. B. Eldridge ◽  
Michele R. Dudash ◽  
...  

Most species now have fragmented distributions, often with adverse genetic consequences. The genetic impacts of population fragmentation depend critically upon gene flow among fragments and their effective sizes. Fragmentation with cessation of gene flow is highly harmful in the long term, leading to greater inbreeding, increased loss of genetic diversity, decreased likelihood of evolutionary adaptation and elevated extinction risk, when compared to a single population of the same total size. The consequences of fragmentation with limited gene flow typically lie between those for a large population with random mating and isolated population fragments with no gene flow.


The Auk ◽  
2019 ◽  
Vol 136 (4) ◽  
Author(s):  
Catalina Palacios ◽  
Silvana García-R ◽  
Juan Luis Parra ◽  
Andrés M Cuervo ◽  
F Gary Stiles ◽  
...  

Abstract Ecological speciation can proceed despite genetic interchange when selection counteracts the homogenizing effects of migration. We tested predictions of this divergence-with-gene-flow model in Coeligena helianthea and C. bonapartei, 2 parapatric Andean hummingbirds with marked plumage divergence. We sequenced putatively neutral markers (mitochondrial DNA [mtDNA] and nuclear ultraconserved elements [UCEs]) to examine genetic structure and gene flow, and a candidate gene (MC1R) to assess its role underlying divergence in coloration. We also tested the prediction of Gloger’s rule that darker forms occur in more humid environments, and examined morphological variation to assess adaptive mechanisms potentially promoting divergence. Genetic differentiation between species was low in both ND2 and UCEs. Coalescent estimates of migration were consistent with divergence with gene flow, but we cannot reject incomplete lineage sorting reflecting recent speciation as an explanation for patterns of genetic variation. MC1R variation was unrelated to phenotypic differences. Species did not differ in macroclimatic niches but were distinct in morphology. Although we reject adaptation to variation in macroclimatic conditions as a cause of divergence, speciation may have occurred in the face of gene flow driven by other ecological pressures or by sexual selection. Marked phenotypic divergence with no neutral genetic differentiation is remarkable for Neotropical birds, and makes C. helianthea and C. bonapartei an appropriate system in which to search for the genetic basis of species differences employing genomics.


Crustaceana ◽  
1993 ◽  
Vol 65 (2) ◽  
pp. 265-277 ◽  
Author(s):  
Barbara A. Stewart

AbstractThe use of protein electrophoretic data for determining species boundaries in amphipods is addressed. Analysis of published literature on genetic differentiation in amphipods showed that pairs of allopatric populations which have genetic identities (I) above a value of 0.85 probably represent intraspecific populations, whereas pairs of populations which have genetic identities below about 0.45 probably represent different species. It was recommended that if I values fall between 0.45 and 0.85, additional factors such as evidence of a lack of gene flow between the populations, and concordant morphological variation should be considered.


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