VIRGIN ISLANDS RESOURCE MANAGEMENT COOPERATIVE BIOSPHERE RESERVE RESEARCH REPORT NO.20 A GENERAL REVIEW OF SEDIMENTATION AS IT RELATES TO ENVIRONMENTAL STRESS IN THE VIRGIN ISLANDS BIOSPHERE RESERVE AND THE EASTERN CARIBBEAN IN GENERAL Dennis K. Hubbard West Indies Laboratory Fairleigh Dickinson University St. Croix, U.S. Virgin Islands Virgin Islands National Park August, 1987 A GENERAL REVIEW OF SEDIMENTATION AS IT RELATES TO ENVIRONMENTAL STRESS IN THE VIRGIN ISLANDS BIOSPHERE RESERVE AND THE EASTERN CARIBBEAN IN GENERAL 1987 BIOSPHERE RESERVE REPORT NO. 20 DENNIS K. HUBBARD WEST INDIES LABORATORY FAIRLEIGH DICKINSON UNIVERSITY ST. CROIX, U.S. VIRGIN ISLANDS U.S. DEPARTMENT OF THE INTERIOR NATIONAL PARK SERVICE AND VIRGIN ISLANDS RESOURCE MANAGEMENT COOPERATIVE VIRGIN ISLANDS NATIONAL PARK P.O. BOX 7789, ST. THOMAS U.S. VIRGIN ISLANDS 00801 LOCAL CONTRACTING AGENT ISLAND RESOURCES FOUNDATION RED HOOK BOX 33, ST. THOMAS U.S. VIRGIN ISLANDS 00802 (NPS CONTRACT NO. CX-0001-3-0048) ABSTRACT This report discusses the impacts of sedimentation on tropical marine environments. Because of the greater susceptibility of reefs, the majority of the discussion is aimed at this specific environment. Included are: 1. A review of the general types of sediment stress that occur in marine systems. 2. A discussion of the critical parameters that should be measured in any study of sediment stress. 3. A discussion of sources of sediment stress in the Caribbean, including examples from within the v.I.. Biosphere Reserve, the U. S. Virgin Islands and the eastern Caribbean. 4. A more specific treatment of area-wide problems, along with strategies that exist or should exist to cope with them. This document is not meant to be an exhaustive review of the subject. Rather, it is intended to highlight the problems, provide some reasonable management guidelines, and serve as a starting point for developing future VIRMC projects dealing with this important topic. A synthesis such as this will never totally satisfy the needs of all individuals. Hopefully it can bea useful reference tool for those interested in pursuing the problem further. TABLE OF CONTENTS ABSTRACT... 0... ee wc cece cere e ewer nerves ec ee eee ew eee eee ees i TABLE OF CONTENTS........ Bem ee cece ee wre eet eee e eee eens wee aeee ii LIST OF TABLES.........ccccceesvenes cer ce eee ee eee ce ee ene teas ii INTRODUCTION. 1... ccc ccc esr c cece essnes cece ec eeee eae eeae . 21 BacKGround... cece cern ccc ces n ences ereneseeseensos wee 1 Statement of the Problem... . ccc cee etter cere eaens woe 2 TYPES OF SEDIMENTATION IMPACT. ...... cc ccccccccerceveces swe seas 4 Smothering........cce008 seme ewe wren rece nr een sesrseseseres & Shading.........ccesseeec00. eee cer eee tee eee eee eee en eae 6 Scouring and Inhibition of Recruitment..... Cece eee ew eae .» 8 WHAT ARE THE CRITICAL PARAMETERS?.......cccccccccccceccccceseee- AO Sedimentation Effects on Corals - a General Discussion....10 Important Parameters to Consider.........cccccccrecececeesld PRIMARY SOURCES OF SEDIMENT STRESS... .....0 ccc ccencsucsenene ...17 Dredging......seceseee sewer eee meee wc eee sens eee r een en nes 18 Upland Development... .. ccc ccc ccc ccc cere cee eee e eee e ren eees 19 GENERAL SEDIMENTATION PROBLEMS IN THE CARIBBEAN..........0000005 21 Land~-Based Development.......c.ccseeeee. Semen ee eee cen eens 22 Port Development... ... ccc cee ccacensons a earns: | SPECIFIC PROBLEMS AND STRATEGIES... .... ccc ccc c ence ree ccrsanense .26 ProblemS..... ccc ccc cee w ener cccce sce e wee eeee cee wee eee woes 26 Management Strategies..... em mee rere reese reer ence se reset ee dh Future Goals and Objectives............ meee eee eee aw eenee 35 LITERATURE CITED..... cece vesesace sac c ec eeee wee e eee tenes 0237 LIST OF TABLES Table 1. Sedimentation data from several marine environments... 9 ii INTRODUCTION Background This is a final report to the Virgin Islands Resource Management Cooperative (VIRMC)- outlining a number of topics related to the impacts of sedimentation within the V. I. Biosphere Reserve (VIBR). Specifically, the tasks initially outlined include: 1) A review of the literature on the impacts of sedimentation on tropical marine ecosystems ,; 2) A review and evaluation of USVI and Federal legislation, policy and programs to control sedimentation in the USVI ; 3) A discussion of the general causes of sedimentation and its impacts within the V.I. Biosphere Reserve, the JU. S. Virgin Islands and the eastern Caribbean ; 4) Recommendations on specific watershed management tools that might be useful within and around the V.I. Biosphere Reserve ; 5) A prioritized list of future research projects that would address site-specific problems within the VIBR. This report is divided into two main sections. The first deals directly with sedimentation as it impacts marine systems (i.e. items 1 and 3). The primary focus will be on the coral reef system for two reasons. First, it is probably the most sensitive and least understood of the nearshore tropical marine ecosystems (mangroves, seagrass beds and reefs). Second, the focus of the management strategy within the VIBR with respect to sedimentation is likely to center primarily around reefs. The second section specifically discusses the state of present protection measures with respect to sedimentation. The focus is on present strategies to stem sedimentation (item 2), as well as potential management approaches that might be useful to provide additional protection (item 4). Consistent with. the embryonic state of our knowledge, the final recommendations must be somewhat general and cannot be imposed on every site-specific problem with equal vigor. Nevertheless, it is hoped that they will provide a useful framework from which to build a rational management plan within the VIBR. The following discussions are not intended to exhaust the subject of sedimentation in the nearshore tropical system. Nor do they purport to reference all the critical papers on the subject. The complexity of the process and the poor level of understanding largely preclude this possibility. Furthermore, the background of the author, and thus the interpretations of the available literature; must reflect a physical bias toward the subject. The primary goal of this report is to help the reader appreciate the state of our knowledge and the problems upon which we must focus if we are to understand these complex processes. Statement of the Problem The literature dealing with sedimentation in the marine environment is certainly extensive. However, despite the great number of papers dealing with the subject, our understanding of its impacts is still in its infancy. Central to the problem are two things: 1) the lack of baseline data before sedimentation events, and 2) the lack of long-term field measurements relating increasing levels of sedimentation to metabolic processes within individual organisms. As an example of the latter problem, several short-term or laboratory studies (e.g. Thompson, undated; Rogers, 1983) have demonstrated a surprising tolerance on the part of certain corals to short-term high doses of sediment. Yet, the literature is replete with what amounts to post-mortem autopsies of reefs destroyed by sedimentation during and after dredging in nearby environments. At the crux of this problem are the differences between high doses of sediment over a short period (acute stress) vs. much lower doses on a continuous basis (chronic stress). This is compounded by the general lack of baseline data on the condition of various marine areas prior to stress and subsequent degradation. This problem surrounds our ignorance of the specific metabolic processes that occur within potentially affected organisms as levels of stress progressively increase. For example, a storm will have a greater impact on a marine environment that is already stressed by background sedimentation than one which occurs in pristine conditions. Before we can understand these cumulative effects, however, we must come to grips with the organism-level response to individual stresses. Our attempts to model nearshore marine systems tell an unfortunate tale of confusion. Aller and Dodge (1974) and Dodge, et al. (1974) studied sedimentation in Discovery Bay, Jamaica. They concluded that the small size of the coral heads was an adaptation to sediment stress whereby smaller colonies would have a shorter distance to move sediment and clear the colony. Thus larger heads would eventually die, leaving the size distribution they observed. In contrast, Maragos (1974 a, b) interpreted the presence of all larger heads as a reflection of the same sediment stress. His logic centered around the inability of coral larvae to successfully recruit under conditions of high sediment load. Thus, the only corals that remain are those that recruited successfully prior to the existing conditions of high turbidity. The above example typifies the problems in dealing quantitatively with the topic of sediment stress. Either one set of researchers is wrong about the controls of sedimentation, or else the controls in the two areas of study are somehow different from one another. In either case, extreme confidence in our quantitative understanding of the problem is probably not warranted. Attempts to model the interactions of tropical marine systems (e.g. Berwick and Chamberlin, 1985) have raised some "interesting" possibilities, but unfortunately will do little to understand the complex nature of the problem until realistic input data for such models are available. In this respect, we are really back at the beginning. We certainly understand that sedimentation is (generally) detrimental to marine systems at some level. The problem centers around determining at what level that will occur, and how that might be incorporated into a rational management scheme that allows human entry into such fragile areas. Certainly mangroves are less susceptible to siltation than reefs; in fact, mangrove systems thrive under some conditions of high sedimentation in the absence of associated pollutants (e.g. heavy metals). Seagrasses, while more susceptible to sedimentation than mangrove complexes, can still tolerate a wide range of turbidity and sedimentation compared to coral reefs. As coral reefs are probably the best-represented of the major nearshore systems in the VIBR, and are profoundly affected by sediments at all levels, they become the most problematic in terms of management. This report will first look at the types of impacts typically occurring during sedimentation events. While seagrasses and mangroves are considered (although briefly), the main focus is on coral reefs. The impacts on mangrove and seagrass systems are more related to direct removal (i.e. dredging, deforestation) than to indirect sedimentation. Thus, the management strategy becomes less dependant on understanding a complex cause-and-effect relationship and more one of strict preservation. Coral reefs, in contrast, are potentially affected by any marine or upland activity. They therefore become the most problematic from a management standpoint, and are the primary focus of this report. The following section attempts to generally summarize the impacts of sedimentation on reefs. The discussion concentrates on scleractinean corals for three main reasons. First, they appear to be the most intolerant species present on the reef, and therefore represent the most critical problem in developing a management strategy. Second, the experience of the author is more broadly based with respect to scleractinean corals. And, finally, the available literature relating sedimentation to distributions of other organisms is limited and inconclusive. With respect to the latter point, it probably is safe to say that octocorals, sponges, crinoids and a host of other organisms are more tolerant of (and in some instances thrive on) sedimentation. While it is not intended to ignore the importance of these organisms on modern reefs, their usefulness in the context of this discussion is more related to identifying conditions less favorable to stony coral growth. Thus, their occurrence is more useful in establishing ambient conditions. With respect to management, they become less problematic (although not wholly unimportant) from the standpoint of preserving water quality. TYPES OF SEDIMENT IMPACTS Increased sedimentation can adversely impact coral reefs in a variety of ways. These include: 1) smothering of the coral by settling; 2) reducing incident light by turbidity; 3) scouring of the coral by bedload transport of primarily sand; 4) inhibiting recruitment by juvenile corals. Smothering of all the potential impacts, smothering is probably the easiest for a layperson to visualize. Dredging next to a reef suspends sediment and that material is moved in the prevailing currents until it settles on the nearby reefs. Certainly much of the damage documented from past dredging projects (Nichols, et al., 1972; Johannes, 1975; Dodge and Vaisnys, 1977; Bak, 1978; Taylor and Saloman, 1978) is related to the direct impact of sediments smothering reef organisms. lLoya (1976) cited similar references to sediment damage in Australia (Fairbridge and Teichert, 1948), Johnston Island (Brock, et al, 1966), Hawaii (Johannes, 1975; Maragos, 1972), Puerto Rico (Kaye, 1959) and the Virgin Islands (van Eepoel and Grigg, 1970). Impacts due to increased runoff from the land have been discussed along the west coast of Puerto Rico by Morelock, et al. (1983). On Algarrobo Reef off Mayaguez, coral cover is presently below 2%, and is dominated by Porites asteroides and Montastrea cavernosa. At nearby Escollo Rodriguez Reef, increased runoff over recent decades has deposited up to 1 m of fine silt on the backreef and eliminated all coral cover. Even those corals that successfully cope with elevated levels of sedimentation must pay a price in the removal of that material. Energy must be expended in mucus production, polyp expansion, or whatever sediment-clearing strategy an individual organism might employ. Different corals deal with sediment in different ways. Some depend almost solely upon external physical energy (e.g. waves and currents) to remove sediment and therefore, are severely limited in the environments they can occupy. Some (e.g. Madracis mirabilis) move sediment by ciliary action, while others rely on polyp expansion or mucus generation. Madracis mirabilis appears to remove sand by tentacular action while muddy sediments are moved by active cilia (Bak and Elgershuizen, 1976). Thus, the state of this particular coral affects its ability to remove sediments of varying sizes. When the tentacles are extended, the colony will be more effective at removing larger particles. During retraction, increased ciliary action will facilitate mud _ removal, but will impede sand rejection. The ability of the reef to clear sediment has been difficult to quantify. Rogers (1977; 1983) demonstrated the ability of Diploria strigosa and D. clivosa to tolerate single, coarse sediment doses of 800 mg/sq cm and daily doses of 200 mg/sq cm for aperiod of 45 days. Acropora cervicornis also showed remarkable tolerance to short-term sediment loading. Thompson (undated) demonstrated a high tolerance of Porites to both carbonate sand and certain types of drilling mud. In contrast, Acropora palmata colonies died after single doses of 200 mg/sq cm (Rogers, 1983), and are likely susceptible to damage at much lower levels of stress. Bak (1978) felt that the platy form of Porites asteroides often found at depth on many Caribbean reefs ‘was almost totally incapable of clearing sediment settling on its surface. Montastrea annularis, probably the most important frame-builder in Caribbean scleractinian reefs has exhibited a wide range of tolerance in different studies. Lasker (1980) reported an ability to remove up to 16 mg/sq em-day of deposited sediment. In contrast, Dodge, et al. (1974) inferred a reduction in coral growth related to sedimentation (their "resuspension" ) rates as small as 1.1 mg/sq cm-day. In this latter study, however, it was not demonstrated that the sedimentation levels measured during the 8 days of their investigation were those necessarily responsible for the long-term growth rates measured in their coral samples. The impact of sedimentation on colony size is not well understood, and cannot be considered as much beyond speculation at this time. Dodge and Vaisnys (1977) felt that older colonies are more susceptible to sedimentation than younger colonies as they have to move sediment a greater distance to effect removal. Hubbard, et al. (1985) documented a gradual decrease over time of the growth rate of 100+ year-old Montastrea annularis colonies in Reef and Fish Bays on St. John. While they attributed the trend to subtle changes in runoff as the hillsides reforested, this decrease in growth rate may reflect a response similar to that described by Dodge and Vaisnys (1977). Maragos (1974a, b), however, described an opposite effect, whereby coral recruitment is inhibited by sedimentation. Therefore, older and larger corals formed prior to sedimentation will dominate on stressed reefs. There is probably at least some merit to both hypotheses which together point out the complexity of the problem. Corals have evolved a complex set of strategies to deal with increasing sediment stress. These can be important at the level of the individual organism or the whole colony. At the organism level, Hubbard and Pocock (1972) related the sediment tolerance of individual corals to overall colony morphology, calyx structure and age of the coral. They felt that the more effective corals would have a greater number of more complex septa (related to the structural integrity of the skeleton/organism pair), higher calical relief (i.e. the polyps are elevated above the surrounding skeleton), V- or U-shaped calical floors anda lighter skeleton. Bak and Elgershuizen (1976) felt that long meandroid colonies (e.g. Diploria strigosa, Manicina aureolata, Colpophyllia natans) would be better at clearing sediment than those with short, reticulate valleys (e.g. Agaricia agqaricites). Colony shape and orientation are also important in determining the ability to shed sediment. Using Agaricia agaricites, Bak and Elgershuizen (1976) found that the ability of the colony to clear sediment could be progressively increased by tilting the coral away from the horizontal. This in fact appears to be the strategy by which otherwise sensitive species deal with sedimentation at depth. In Montastrea annularis, they showed that hemispherical colonies could remove sediment ina fraction of the time required by flatter morphs of the same coral. Also, hemispherical colonies were more effective at removing sand, while flatter colonies had an easier time with mud-sized sediment. Whether this is a long-term adaptation to the smaller sediment sizes introduced onto deeper-water corals (i.e. quieter energy) cannot be said with certainty, but is a tempting hypothesis. Shading In addition to settling on benthic organisms, sediment can reduce the amount of light reaching the bottom at any given depth. Inasmuch as a substantial portion of the carbohydrates required by corals are produced by photosynthetic algae (zooxanthellae), this raises another potentially limiting problem for the coral reef. Similar impacts are likely important in seagrass beds. Rogers (1977; 1979) clearly demonstrated the impacts of extreme shading on the corals of San Cristobal Reef in southwestern Puerto Rico. After 5 weeks of shading by black plastic, colonies of Acropora cervicornis showed significant bleaching of coral tissue and reductions in colony-extention rate. She proposed a relationship between polyp size and resistance to shading where corals with larger polyps would likely have a greater dependence on zooplankton and other in-water food sources. Corals with smaller polyps (A. cervicornis) were the first to show bleaching, followed by M. annularis (medium-size polyps) and two species of Diploria (largest polyps). There are several excellent discussions of this problem in the literature. However, none of them establish quantitative limits above which reefs or other marine systems can be expected to suffer specific levels of damage. Cortes and Risk (1985) described a reef system at Cahuita, Costa Rica along which coral growth (and probably cover) has been gradually reduced due to increasing development pressure. They cite an increase in the amount of terrigenous sediment trapped within the coral skeletons over time as a response to growing agriculture and logging since the late 50s. Their data on coral growth, however, do not make a convincing correlation between runoff, reduced water quality and actual coral-growth rate. Morelock, et al. (1979) described an environmental shift in the positions of reef zones within Guayanilla Canyon off the south coast of Puerto Rico. In the canyon, 18 m is the lower limit of coral growth, compared to 37 m along unstressed shelves. Furthermore, the corals within this zone were those typical of deeper-water environs in other areas, demonstrating an upward shift in depth zonation under conditions of higher turbidity (i.e. lower light). Dodge and Lang (1983) related a sudden drop in coral-growth rate in the Flower Gardens reef in the Gulf of Mexico with increased turbidity (and light reduction) during flooding of the Atchafalaya River. Rezak and Bright (1981) related it to submarine collapse of the underlying carbonate terrain , dropping the corals to a depth at which light level was significantly lower. In either case, the effect of lowered light levels remains a central control of the rate of coral growth. Roy and Smith (1971) described an area on Fanning Island (Pacific Ocean) where reefs are surviving (31% cover) under conditions of high natural turbidity. In turbid areas (3.5 mg/l Total Suspended Solids - TSS) coral cover was reduced to 31% compared to 62% in less turbid areas (1.0 mg/l TSS). This was accompanied by a shift in the importance of ramose corals in turbid water (50%) compared to clear water (10%). Based on their observations, they placed light attenuation at the top of the list of impacts, followed by smothering and larval inhibition by burial. Once again, however, there is some question as to whether the conditions measured during the brief study period were in fact those responsible for the differences observed in the coral population. Nevertheless, changes in turbidity at some level emerge as important controls of reef development. The critical question in this regard relates to the effects of specific levels of turbidity on various reefal organisms. Table 1 summarizes turbidity and sedimentation rates drawn from several literature sources. It appears that levels of TSS in the range of 1-2 mg/l can be considered as "normal" on most reef systems. Instances of reduced coral cover appear in areas where total suspended solids reach 3-5 mg/l over extended periods of time. Rogers (1982) did report storm-related turbidity levels of 10-30 mg/l on St. Thomas, however, with little environmental damage. Once again, these data together point to an ability for marine systems to tolerate significant short-term perturbations in water quality, while being relatively intolerant of much lower but chronic stresses. Rogers (1979) reported reductions of light levels in 2 m of water to less than 65 microeinsteins/ sq m - sec. These conditions corresponded to TSS values of 9-16 mg/l. Decreasing of the TSS levels to 1.4 mg/l resulted in an order-of-magnitude increase in light level to 700 microeinsteins at the same depth. If these levels of TSS are reasonable indicators of reef responses to sediment stress, then minor shifts in the water quality of a reef system over a long period of time would appear to have a very profound impact on reef structure. Certainly this is not good news to those interested in protection of reefs from impending stress. What is yet to be established, however, is whether these levels of suspended solids are those responsible for the observed patterns of reef development. At a minimum, long-term measurements of water quality in these areas are needed. These would provide a more reasonable estimate of the present conditions associated with these environments. Even more useful would be historical data on water quality and reef character, but these kinds of information are essentially nonexistent. gcouring and Inhibition of Recruitment The impact of scouring on corals is more likely related to the occurrence of bedload (i.e. sandy) transport. Therefore, this is probably more important as a natural control in areas adjacent to sand-dominated systems. For example, reefs close to the beach are often characterized by corals sitting on pedestals that elevate the main colony from the prevailing traction carpet of shifting sediments. Likewise, the dominance of A. palmata on many reef crests is likely a response to the energetic sand transport over the reef surface. By growing rapidly upward, this branching coral can quickly attain a position above the zone of periodic scour by shifting sands. There are other competitive strategies Table 1. LOCATION Costa Rica Grand Cayman San Cristobal, PR Guayanilla, PR Punta Ventana, PR Round Reef, Cstd, STX Long Reef, Cstd, STX Christiansted, STX Limetree Bay, STX Florida. Keys Discovery Bay, Jam. Negro Bank, PR Fanning Is. Discovery Bay, Jam. Virgin Gorda, BVI Brewers Bay, STT Sedimentation data from several marine environments. ZONE outer crest inner crest lagoon bay rivers general reef general reef canyon canyon backreef forereef east tip w. forereef e. forereef backreef general general general general e reef (steep) w reef (flat) turbid lagoon clear lagoon open ocean backreef general grassbed TSS(mg/1) 0.3-4.6 1.4-18.8 0.2-36.6 2.8-54.0 1.4-6200 0.1-2.4 0.8 4.5-6.1 11-17 OoOrw wooa 0.9-2.2 SETTLING (mg/cm-da) 12.8-1180 10.0 (1-21) 1.1-9.8 2.3 3-247 0.5-1.1 3-5 15