Nodules Flow and Seaweeds Lie Low at West Flower Garden Bank
September 28, 2003
Catalina Martinez
NOAA Office of Ocean Exploration
Sarah Bernhardt
Flower Garden Banks National Marine Sanctuary, NOAA
Last night we arrived at the West Flower Garden Bank about 7:30 p.m., and the Sonsub crew launched the ROV (remotely operated vehicle) almost immediately.
Two transect surveys were conducted at the westernmost region of the West Flower Garden Bank, called the western mound (numbers 1 and 2 in Figure 1, below, indicate the two survey areas).
The western mound is a relatively shallow area (less than 100 m) featuring a wide variety of algal species, and many areas of the sea floor were literally covered with algal nodules. Also called rhodoliths, these spherical nodules consist of carbonate sand and gravel particles cemented together by coralline algae. The nodules range from 1-20 cm in diameter, and are the dominant sediment formers at depths of 45-75 m in the Flower Garden Banks. They remain as free-moving bodies on the sea floor, and can cover anywhere from 60 to 100 percent of the bottom.
Rhodoliths serve as the main substrate for leafy algae. Both light and substrate are necessary for leafy seaweeds to grow. The ROV dives here will provide a wide variety of algal specimens to team member Suzanne Fredericq, a phycologist from the University of Louisiana at Lafayette. After cataloguing and preserving the specimens collected at the western mound, Dr. Fredericq determined that at least two species in her bountiful collection are currently undescribed. For her, the two specimens made the entire cruise worthwhile (see How do we identify seaweeds? below).
Diverse assemblages of fishes, corals, and invertebrates also inhabit this region, and the Flower Garden Banks National Marine Sanctuary science team directed the Sonsub ROV pilot to collect a wide variety of representative organisms such as corals, invertebrates, sponges, algae, and even a few fish.
At 5:45 am this morning, the ROV went back in the water at the "southern bump" location of the West Flower Garden Bank (site 3 on Fig. 1), and had to come out of the water at 11 am because, as predicted, the weather had turned and the seas got rough and high. The lead scientists made the decision to start heading east, slowly acquiring multibeam data along the continental shelf edge, heading toward the final deep coral research site off the coast of Mississippi. The weather will be evaluated regularly to determine whether the ROV can return to the water sometime tomorrow. In the meantime, we have secured the equipment and are hunkered down for a rough ride!
How do we identify seaweeds?
Suzanne Fredericq
University of Louisiana at Lafayette
It is well known that seaweeds, especially the beautiful red algae, are notorious for being difficult or impossible to identify when certain reproductive structures are lacking. The result is that many checklists lack the appropriate data to confidently assign specimens to a certain species. Thus, there is a great need to identify nonreproductive specimens that lack diagnostic characters by other means. In most cases, vegetative and reproductive structures need to be sectioned by hand with a razor blade (Fig. 1). The sections are then placed on a glass slide, stained, covered by a cover slip, and observed with the light microscope (Fig. 2).
The samples needed for further morphological studies are typically fixed and wet-preserved in diluted (5 to 10 percent) Formalin/seawater and stored in bottles, or freshly pressed on herbarium sheets (Fig. 3). Specimens are then deposited in herbaria -- depositories of plant specimens -- where researchers can study and compare particular collections with specimens from other parts of the world (Fig. 6). While few may think to do it, pressed seaweeds also make beautiful and original Christmas cards!
One successful approach to help characterize and explain the relationships and distributions of seaweeds is the comparative analysis of their DNA sequences. A small DNA component of one species is compared with that from a number of other species in other parts of the world. Specimens for molecular studies are typically preserved in Ziploc bags in silica gel, the crystals used to dry flowers that are commonly found in hobby stores (Fig. 4). The silica gel removes most of the liquid in a sample but preserves the DNA. Back in the laboratory, total DNA is then extracted from representative specimens, and a suitable molecular marker is selected that will provide the appropriate phylogenetic (evolutionary) signal for addressing particular taxonomic and biogeographic (distributional) questions, such as: "what are the closest living relatives of seaweeds under study and in which group do they belong", or "where did the marine flora present in the Northwestern Gulf of Mexico come from"? Some exciting results from this cruise already include a new species of the red algal family Nemastomataceae, and an unknown species of Halymenia (see Figure 3). Just collecting these two specimens makes the whole trip worthwhile.
One goal we wish to accomplish during this exploratory trip is to identify and characterize the seaweeds, and assess the degree of their uniqueness, in each of the deep banks surveyed (Alderdice, McGrail, Rankin, Bright, Geyer, West Flower Garden). Seaweeds play a crucial role in our ability to assess the health of the deep banks, regulate species introductions, and monitor harmful algal blooms or global change. Thus, they need to be accurately characterized, and short- and long-term trends in the diversity of their assemblages must be thoroughly investigated.
In addition to clarifying distribution ranges of known species, our exploratory collecting efforts in these unique but poorly sampled benthic environments of the Northwestern Gulf of Mexico will lead to the discovery of more species new to science.