Distinct Phylogeographic Patterns of Sympatric West Atlantic Exploited Seahorses PADRON, MARIANA Cohen, Sarah

Distinct Phylogeographic Patterns of Sympatric West Atlantic
Exploited Seahorses
PADRON,
1 Center
1,2
MARIANA
Cohen,
2
Sarah
and Hamilton,
1
Healy
for Applied Biodiversity Informatics, California Academy of Sciences, San Francisco, CA
2 Department of Biology, San Francisco State University, San Francisco, CA
.
Introduction
Results
One of the central questions in marine conservation biology is the
The results obtained for the mitochondrial DNA indicate that H.
extent of population connectivity in marine systems. Several studies
erectus and H. reidi exhibit distinct patterns of geographic genetic
have addressed this question in the past, with mixed success in
structure. An AMOVA revealed significant structure between the
resolving genetic structure in populations of marine fishes and
populations from the Caribbean and the Atlantic Ocean in both
invertebrates from the Indo-Pacific region and Atlantic Ocean.
cytochrome b (ФST = 0.737, P ‹ 0.0001; ФCT = 0.690, P ‹ 0.0001) and
We are particularly interested in examining the geographic patterns
control region (ФST = 0.877, P ‹ 0.0001; ФCT = 0.812, P ‹ 0.0001) for H.
of genetic connectivity in two seahorse species with largely
reidi; while no significant structure among regions was observed for
sympatric distributions: the long-snout seahorse (Hippocampus reidi)
H. erectus in both cytochrome b (ФST = 0.220, P ‹ 0.0001; ФCT = 0.006, P
and the lined seahorse (Hippocampus erectus). These two exploited
› 0.05) and control region (ФST = 0.109, P < 0.05; ФCT = 0.047, P › 0.05).
A
Fig. 6A & B.- Maximum Likelihood (ML) phylogenetic reconstructions for H. reidi (A) and
H. erectus (B) (with outgroups) using GeoPhylobuilder 1.1
Caribbean fish species demonstrate unique life history attributes,
that support a test of ecological vs. geographic population structure.
N = 38
H = 16
2
B
Gene diversity (Hd)
High
5
14
3
13
11
Low
16
8
9
4
10
6
15
7
1
12
Honduras
A
Venezuela
B
Brazil
Photo: Adriana Perez
www.flickr.com
Fig.1.- Hippocampus erectus
Fig.2.- Hippocampus reidi
Fig. 4.- Haplotype network of H. reidi (H = 16)
7
Honduras
Is there evidence of significant genetic population structure in H.
erectus or H. reidi from several populations sampled across their
15
4
29
30
26
Venezuela
43
20
Mexico
23
Can we determine the level of gene flow among populations, or
22
distributed seahorse species across the Caribbean, Gulf of Mexico and
32
Atlantic Ocean. The large break in the distribution of H. reidi from
33
36
37
3
1
38
42
Brazil to Honduras was also supported by reciprocal monophyly in
5
17
our phylogenetic reconstructions. This pattern is consistent with the
41
39
6
31
2
identify areas of high genetic diversity to assess the potential need for
distinct management units?
We document distinct patterns of genetic variation in two sympatric
27
8
19
high values of molecular divergence between the populations from
18
16
9
12
35
10
34
Brazil and the rest of the Caribbean (Dxy = 0.00857), relative to the
25
24
11
21
molecular divergence between the Caribbean populations of H. reidi
13
14
and its sister species from the Eastern Atlantic, H. algiricus (Dxy =
Methods
Fig. 5.- Haplotype network of H. erectus (H = 43)
A 820 bp fragment of the
0.00677). It seems that the populations of H. reidi from Brazil,
Venezuela and Honduras could be treated as distinct management
A total of 16 unique haplotypes were found for H. reidi , with no
mitochondrial cytochrome b
units. Additional sampling of Brazilian populations of H. reidi, as well
shared haplotypes between populations.
gene and a 285 bp fragment
as further comparative analysis with populations of H. algiricus, is
For H. erectus, 43 unique haplotypes were identified, with only 2
of the mitochondrial control
needed to help resolve taxonomic boundaries in H. reidi.
shared haplotypes. One shared between the populations from
region were analyzed from
On the other hand, H. erectus exhibit no signals of population
Florida (82.36%), Honduras (5.88%), Virginia (5.88%) and Colombia
Fig.3.- Map of the sampling distribution of H. erectus
and H. reidi in the Caribbean and Western Atlantic.
individuals of H. reidi from
3 locations of the Caribbean and Western Atlantic.
We used phylogenetic reconstructions using PAUP (v. 4.0, Swofford
2002) and MrBayes (v. 3.1, Huelsenbeck and Ronquist 2001),
haplotype network with TCS (v. 1.21, Posada and Crandall 2000) and
analysis of molecular variance (AMOVA) using Arlequin (v. 3.1,
Excoffier et al 2005) to infer population structure within the Atlantic
Ocean basin. Five variable microsatellite loci for each species are also
being analyzed to estimate population structure and gene flow
among populations.
28
Discussion
Colombia
40
from 6 locations and 40
N = 72
H = 43
Virginia, US
geographic ranges?
70 individuals of H. erectus
Fig. 7A & B.- Gene diversity interpolation for H. reidi (A) and H. erectus (B) using ArcMap 9.3
Florida, US
Our questions
structure between ocean basins, and the haplotype network
(5.88%); and another one shared only between the populations from
constructed for both the control region and cytochrome b showed a
Florida (42.86%) and Mexico (57.14%).
high degree of reticulation between the Caribbean and Gulf of
Summary of mtDNA for sampled populations of H. erectus and H. reidi from the Western Atlantic
Mexico, suggestive of incomplete lineage sorting. H. erectus appears
H. erectus
Population
Venezuela
Colombia
Mexico
Honduras
Florida
Virginia
H. reidi
Population
Venezuela
Honduras
Brazil
B
# of Seq.
n
6
13
15
12
24
2
# of Haplotypes
H
6
11
10
9
9
2
Gene diversity
Hd
1
0.914
0.914
0.909
0.659
1
Nucleotide div
π
0.01237
0.00276
0.00300
0.00574
0.00276
0.00385
# of Seq.
n
15
13
10
# of Haplotypes
H
2
9
5
Gene diversity
Hd
0.133
0.936
0.756
Nucleotide div
π
0.00024
0.00346
0.00130
to be a panmictic population that could probably be treated as one
management unit..
References
Mobley, K., et al.2010. Population structure of the dusky pipefish (Syngnathus floridae)
from the Atlantic and Gulf of Mexico, as revealed by mitochondrial DNA and
microsatellite analyses. Journal of Biogeography 37, 1362-1377.
Saarman, N., et al. 2010. Genetic differentiation avvross esatern Pacific oceanographic
barriers in the threatened seahorse Hippocampus ingens. Conservation Genetics
.
Acknowledgement
Lakeside Foundation – California Academy of Sciences Scholarship