Florida faces a critical challenge in wetland management as invasive species threaten ecosystem integrity across the state. The South Florida Water Management District identifies approximately 200 introduced plant and animal species established in the region, with 66 non-native plant species designated as priorities for control. Current management strategies rely heavily on mechanical removal, prescribed burns, and herbicide applications—methods that are expensive, labor-intensive, and may have unintended ecological consequences.
Simultaneously, livestock grazing in wetland environments remains controversial and understudied, particularly in subtropical climates. While extensive research documents livestock impacts on wetlands, the vast majority focuses on cattle in temperate regions. Research on sheep grazing in subtropical wetlands, specifically using parasite-resistant hair sheep breeds, remains critically limited.

1579 Walsh Street Oviedo,
Florida 32765

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Katahdin sheep represent a unique opportunity for Florida wetland management due to their specific biological adaptations:
Parasite Resistance: Research demonstrates that Katahdin sheep possess significantly higher parasite resistance than conventional wool breeds. Studies conducted at Virginia Tech and Arkansas showed Katahdin sheep had fecal egg counts 45% lower than Dorper crosses and required substantially less anthelmintic treatment than wool breeds. Their Caribbean hair sheep ancestry provides genetic resistance evolved in hot, humid, high-parasite environments—precisely the conditions present in Florida wetlands.
Climate Adaptation: Katahdin sheep demonstrate well-developed heat tolerance in tropical and subtropical regions. Their hair coat (rather than wool) allows superior thermoregulation in humid conditions where wool breeds experience heat stress. University of Florida research identifies Katahdin as one of six meat breeds demonstrating ability to naturally minimize parasite burdens in Florida conditions.
Selective Grazing Behavior: Sheep exhibit different grazing patterns than cattle. Research indicates sheep nibble grass close to the ground and selectively consume flowers and certain vegetation types. This selective grazing could target specific invasive plant species while minimizing impact on desired native vegetation.
Reduced Wetland Impact: Sheep are lighter and more agile than cattle, causing less soil compaction and trampling damage. Studies in New Zealand and British Columbia specifically noted that sheep grazing can be preferable to cattle in fragile wetland environments vulnerable to poaching (soil damage from hoofprints in wet conditions).
Vegetation Management Without Chemicals: Multiple studies demonstrate that moderate grazing intensity can increase plant species diversity and control dominant invasive species that exclude less competitive native plants. Research in California vernal pools showed that reintroduced grazing at moderate stocking rates significantly increased both diversity and native cover after just two years. European wetland studies found that patchy, occasionally intense grazing increased protected plant species and habitat heterogeneity while benefiting both conservation and agricultural goals.
Cost-Effective Management: The solar grazing industry demonstrates that sheep can provide effective, economical vegetation management. While mechanical mowing requires expensive equipment, fuel, and risks panel/infrastructure damage, sheep provide continuous low-cost maintenance while generating potential revenue through meat production.
Ecosystem Services: Properly managed grazing can create habitat heterogeneity that benefits wildlife. Research in Hungarian marshes showed increases in wetland bird populations, protected plant species, and patches of open vegetation with grazing intensity gradients. The key is avoiding continuous heavy grazing while allowing patchy, varied grazing pressure.
Carbon Footprint Reduction: Replacing mechanical vegetation management eliminates fossil fuel consumption for mowers while integrating livestock production into ecosystem restoration.
Hypothesis: Katahdin sheep grazing at moderate stocking densities (2-4 sheep/acre for 2-4 week periods) will significantly reduce biomass of target invasive species compared to ungrazed control areas, while maintaining or increasing native plant species diversity.
Hypothesis: Moderate-intensity sheep grazing will maintain water quality parameters (turbidity, nitrogen, phosphorus, fecal coliform bacteria) within acceptable ranges for wetland ecosystem health, with impacts significantly lower than documented cattle grazing effects.
Hypothesis: Katahdin sheep grazing on Florida wetland vegetation will maintain adequate body condition scores and parasite resistance within acceptable management thresholds, requiring no more than 15% of animals to need anthelmintic treatment during the grazing period.
Hypothesis: Sheep grazing vegetation management costs will be ≤50% of equivalent mechanical mowing and herbicide application costs over a 12-month period, while producing marketable lamb weight gain.
Hypothesis: Sheep grazing vegetation management costs will be ≤50% of equivalent mechanical mowing and herbicide application costs over a 12-month period, while producing marketable lamb weight gain.
All sheep management will follow American Veterinary Medical Association guidelines
Monitoring protocols ensure early detection of heat stress or health issues
Access to shade, clean water, and supplemental minerals as needed
Immediate veterinary intervention protocols established
Grazing exclusion during critical wildlife breeding/nesting periods
Monitoring for any decline in threatened or endangered species
Adaptive management to respond to unintended impacts
Coordination with Florida Fish and Wildlife Conservation Commission
Results may be specific to Black Hammock Farm's wetland types and may not generalize to all Florida wetlands
Seasonal variation requires multi-year data collection for robust conclusions
Initial infrastructure investment may limit adoption by other landowners
Weather variability in Florida may affect consistency of grazing schedules

Part 2 of 4: Katahdin Sheep & Florida Wetland Management Series
The transitional zone doesn't announce itself with signs or markers. You know you've entered it when your boots start sinking into soil that's neither quite solid nor truly saturated. The vegetation shifts—less pine, more palmetto. Vines begin their climb up tree trunks. The understory thickens until forward progress requires deliberate effort, pushing through layers of growth that seem designed to repel human passage.
This is the front line in Florida's war against invasive species. Not the deep wetlands where water stands year-round, nor the high ground where oaks and pines dominate, but the liminal space between—the wetland edge where invasions begin and from which they spread.
Understanding this battlefield requires more than knowing that invasive species threaten Florida's ecosystems. It demands intimate familiarity with the specific plants that colonize these transitional zones, the mechanisms by which they transform healthy wetlands into degraded monocultures, and critically, whether those plants represent targets that livestock grazing can effectively address.
Florida's wetland margins exist in a state of dynamic equilibrium. Water levels fluctuate seasonally and annually. Flooding pulses deposit nutrients and sediments. Fire sweeps through periodically, resetting succession and maintaining the mosaic of habitats that supports exceptional biodiversity. Native species evolved strategies to exploit this variability—germinating after fires, reproducing during floods, persisting through droughts.
Invasive species exploit the same variability, but with one crucial difference: they lack the natural controls that keep native populations in balance. No specialized herbivores consume them preferentially. No pathogens limit their spread. No competitors evolved specifically to exploit their weaknesses. The result is exponential growth, resource monopolization, and the creation of novel plant communities that native wildlife cannot utilize effectively.
The Florida Invasive Species Council maintains comprehensive lists of problematic species, dividing them into categories based on their documented ecological impact. Category I species are those already altering native plant communities by displacing native species, changing community structures or ecological functions, or hybridizing with natives. Category II species have increased in abundance or frequency but haven't yet altered Florida plant communities to the extent shown by Category I species—though they may reach that status if their ecological damage intensifies.[1]
The 2025 FISC list includes 145 plant species across these two categories.[1] Not all threaten wetlands specifically. Not all establish in transitional zones. But a significant subset of these invaders concentrates their assault on the exact habitats where prevention matters most—the edges where wetlands meet uplands, where seasonal flooding creates opportunities for establishment, and where early detection and control could prevent the wholesale transformation of wetland ecosystems.
Before examining true invasive species, we must acknowledge a complicating reality: some of the most problematic vegetation in Florida's wetland margins consists of native species behaving aggressively in response to altered conditions. These plants belong in Florida's ecosystems. They evolved here, support native wildlife, and serve legitimate ecological functions. But when fire suppression, altered hydrology, or other disturbances shift competitive dynamics, these natives can create management challenges nearly as severe as true invasives.
Several native grape species inhabit Florida wetlands and their margins. Vitis rotundifolia (muscadine grape) and Vitis aestivalis (summer grape) rank among the most common. Both produce the distinctive round to heart-shaped leaves with toothed margins that characterize the genus. Both climb vigorously into the forest canopy using tendrils that wrap around any available support.
Wild grapes serve important ecological functions. The fruit provides food for dozens of bird species, black bears, raccoons, and other wildlife.[2] The dense tangles of vines offer nesting sites and cover. The leaves feed larvae of several native moth species. In modest abundance, wild grapes contribute to the structural diversity that characterizes healthy forest edges.
The problem emerges when grapes escape control. In the absence of regular fire or in areas where overstory trees have been damaged, grape vines can explode across the landscape. They climb into tree canopies and form dense horizontal mats that block sunlight from reaching everything below. The accumulated weight of multiple vines can damage or kill host trees. A single vigorous vine can produce dozens of lateral shoots in a single growing season, each capable of climbing new support structures and expanding the colony.
From a livestock management perspective, wild grapes present an interesting paradox. Research on vineyard grazing demonstrates that sheep readily consume grape foliage. Studies indicate that fresh grape leaves offer medium to good digestibility, with in vitro dry matter digestibility ranging from 60 to 75 percent depending on grape variety and growth stage.[3] Voluntary dry matter intake of female sheep offered grape leaves reached approximately 1 kilogram per day in controlled studies—a relatively high intake rate suggesting good palatability.[3] The nutritive value of grape leaves roughly parallels hay quality, making them adequate forage for sheep with moderate nutritional requirements.[3]
Multiple vineyard operations across the United States and internationally now employ sheep specifically for their capacity to control grapevine vegetation. Winter grazing systems in vineyards demonstrate that sheep effectively manage cover crops and volunteers without damaging vines when properly timed and stocked.[4,5] Some operations have even extended grazing into the growing season, with sheep consuming sub-canopy vegetation and vine suckers while leaving mature fruit untouched.[5]
The implication for wetland margin management is clear: wild grape overgrowth represents a target that trained sheep flocks can address. The vines that smother native vegetation and create problematic thickets simultaneously provide nutritionally adequate forage for grazing animals.
If wild grapes represent a manageable challenge, greenbrier (Smilax spp.) presents something more formidable. Florida hosts at least nine common Smilax species, including S. rotundifolia (roundleaf greenbrier), S. bona-nox (saw greenbrier), S. laurifolia (laurel greenbrier), and several others.[6] All share certain characteristics: climbing or scrambling growth habits, tendrils for attachment, and—most notoriously—sharp prickles that make passage through dense stands an exercise in pain tolerance.
Greenbrier serves important ecological roles. The berries provide crucial winter food for songbirds when other resources grow scarce. White-tailed deer and rabbits browse the young foliage. The dense, thorny tangles offer protective cover for ground-nesting birds and small mammals. Black bears consume both the berries and, in some cases, the starchy roots.
But greenbrier can transform from beneficial native species to management nightmare when conditions favor its proliferation. Fire suppression allows greenbrier to accumulate biomass and expand vegetatively through extensive rhizome systems. Forest thinning or canopy disturbance triggers explosive growth of shoots that had persisted at low density in shaded understory. The result: impenetrable thickets that exclude human access, prevent wildlife movement, and suppress the growth of less competitive native plants.
Greenbrier presents a particularly vexing control challenge because it resists most herbicides and resprouts vigorously when cut.[7] The extensive rhizome networks store energy reserves sufficient to produce multiple crops of new shoots even after repeated top removal. Mechanical control proves labor-intensive and often ineffective. The thorns complicate every management intervention, turning simple brush clearing into hazardous work requiring heavy protective equipment.
Yet greenbrier's reputation as nearly unmanageable may be overstated—at least where grazing animals are concerned. Research from fire ecology studies reveals something remarkable about greenbrier: its nutritional quality actually increases following disturbance. Studies examining greenbrier foliage after prescribed fire found that protein content increased by 7.8 percent compared to unburned areas after low-severity fires, and by up to 19 percent following high-severity burns.[8]
In longleaf pine stands subjected to periodic prescribed fire in Florida, greenbrier occurred at moderate frequencies and experienced heavy spring browsing, with 90 percent of available twigs consumed by wildlife on one-year-old burns.[9] This utilization rate suggests that when greenbrier produces tender new growth, herbivores find it highly palatable despite the thorns that make mature stems so formidable.
The key insight for vegetation management: greenbrier becomes increasingly attractive to browsing animals when maintained in a state of active regrowth rather than allowed to mature into woody thickets. Repeated grazing pressure that forces continual resprouting may accomplish what mechanical and chemical control cannot—keeping greenbrier populations at functional levels that provide wildlife benefits without creating impenetrable barriers to ecological function.
Beyond the climbing vines, Florida's wetland margins support diverse communities of herbaceous plants—forbs, in botanical terminology. These non-woody, broadleaved plants include natives, naturalized species, and true invasives, often growing intermixed in ways that challenge simple classification.
Some forbs cause no management concerns. Native species like asters, goldenrods, and various legumes contribute to biodiversity and support pollinator populations. But other forbs exploit disturbance, forming dense monocultures that exclude more desirable species. Distinguishing between beneficial diversity and problematic weed infestations requires careful observation and ecological knowledge.
The forb component matters immensely for sheep-based vegetation management because forbs constitute a major portion of sheep dietary preference. Research on sheep feeding behavior consistently documents that forbs comprise approximately 30 percent of free-ranging sheep diets, compared to 50 percent grasses and legumes, and 20 percent browse from woody species.[10] This intermediate position between pure grazers (like cattle) and pure browsers (like goats) means sheep naturally target the forb-dominated understories characteristic of wetland margins.
The palatability of specific forb species varies, but sheep generally consume forbs more readily than grasses when given a choice. Forbs typically offer higher protein content and greater digestibility than mature grasses, making them preferred forage. This feeding preference aligns remarkably well with the vegetation control needs in wetland transitional zones, where problematic forbs often form dense stands that outcompete native grasses and sedges.
While native species behaving aggressively create legitimate management challenges, the true invasive species on the FISC Category I list represent more severe threats. These plants don't just overgrow—they fundamentally restructure the plant communities they invade, creating conditions that favor their own persistence while excluding natives.
Imperata cylindrica ranks among the ten worst weeds globally. It reached Florida accidentally in 1912 via packing material, then arrived intentionally in the 1930s for forage and soil stabilization—purposes for which it proved utterly inadequate.[11] What cogongrass does excel at is invasion.
The plant spreads through both seed dispersal and aggressive rhizome growth. A single cogongrass plant can produce thousands of seeds that disperse on wind currents. The rhizomes penetrate deeply into soil, creating dense mats of roots that exclude other vegetation. Cogongrass outcompetes nearly every native plant species through a combination of rapid growth, allelopathic chemical suppression of competitors, and the ability to thrive in both drought and flood conditions.
The ecological impacts extend beyond simple competitive exclusion. Cogongrass alters fire regimes dramatically. Its dense stands produce three times the fuel load of native vegetation and burn at higher temperatures.[11] These intense fires damage or kill native trees that would survive normal ground fires, creating gaps that cogongrass rapidly colonizes. The cycle reinforces itself: cogongrass invasion leads to hotter fires, which create disturbance that favors more cogongrass expansion.
Wildlife habitat value approaches zero. Cogongrass offers minimal food value for native herbivores. The dense growth excludes ground-foraging birds and small mammals. Even when cogongrass invades forests, deer and other browsers typically avoid it, leaving dense stands untouched while foraging pressure intensifies on remaining native vegetation.
Control proves extremely difficult. The deep rhizomes resist mechanical removal. Herbicide applications require repeated treatments over multiple years. Even intensive management often achieves only suppression rather than eradication. Biological control agents are under investigation but not yet deployed.
From a grazing perspective, cogongrass presents a particularly challenging target. Livestock generally avoid mature cogongrass. The leaf blades contain silica crystals that reduce palatability and digestibility. Nutritional quality is poor. Some research suggests that sheep and goats may consume young cogongrass shoots under high stocking pressure, but palatability remains low compared to native forages.[12]
This limitation doesn't render grazing irrelevant for cogongrass management, but it establishes realistic expectations. Sheep won't eagerly consume cogongrass the way they browse greenbrier or wild grape. However, intensive targeted grazing combined with other control methods might weaken cogongrass stands sufficiently to allow native species recovery—a question requiring field research to answer definitively.
Panicum repens enters Florida's waterways and wetland margins from southern Africa and Australia. True to its common name, torpedograss spreads rapidly through creeping rhizomes that can extend several feet horizontally in a single growing season. The plant tolerates both aquatic and terrestrial environments, forming dense colonies in shallow water, along shorelines, and in seasonally flooded areas.
Torpedograss stands crowd out native aquatic vegetation, reducing habitat quality for fish, wading birds, and aquatic invertebrates. The dense rhizome mats alter sediment deposition patterns and may affect nutrient cycling. Once established, torpedograss resists most control efforts. The rhizomes break easily when mechanically removed, and each fragment can generate a new plant. Herbicide treatments provide temporary suppression but rarely achieve permanent control.
The plant's intermediate habitat preference—thriving in both aquatic and terrestrial settings—makes it particularly well-suited to wetland margins where water levels fluctuate seasonally. These are precisely the zones where prevention matters most, as established torpedograss populations serve as source populations for invasion of deeper wetlands and upland buffers.
Limited research exists on livestock utilization of torpedograss, though its classification in the genus Panicum suggests it may receive some grazing pressure when maintained in an actively growing state. The question of whether managed grazing can contribute to torpedograss suppression represents another area where practical field trials could yield valuable management insights.
Schinus terebinthifolia, the Brazilian pepper tree discussed extensively in Part 1 of this series, presents its most vulnerable stage during seedling establishment. Mature Brazilian pepper trees—with their dense canopies, allelopathic properties, and vigorous resprouting—resist most control efforts and require intensive mechanical or chemical intervention.
But every mature tree begins as a seedling. Brazilian pepper produces prodigious quantities of seed, dispersed widely by birds that consume the berries. Germination rates are high, and seedlings establish readily in disturbed areas. In the transitional zones of wetland margins, where periodic flooding creates bare soil and scattered canopy coverage provides adequate light, conditions favor Brazilian pepper recruitment.
Here, preventive management offers genuine promise. Brazilian pepper seedlings remain vulnerable to browsing during their first years of growth. The young foliage, while containing compounds that some wildlife find irritating, can be consumed by browsers without the intense chemical suppression that the plant directs at competing vegetation. Multiple browsers—including deer, goats, and potentially sheep—have been documented consuming young Brazilian pepper growth.
The window for effective browse control closes as seedlings mature into saplings with woody stems. Once Brazilian pepper develops trunk diameter exceeding a few inches, browsing animals cannot consume sufficient biomass to suppress growth. But in that early window—the first two or three years after germination—consistent browse pressure might prevent seedling recruitment, effectively limiting Brazilian pepper expansion without requiring intensive mechanical or chemical intervention.
This suggests a role for grazing in Brazilian pepper management that differs from simple vegetation clearing. Rather than attempting to browse mature trees, strategic grazing targets the seedling and sapling stages, preventing establishment before plants reach the size where control becomes exponentially more difficult and expensive.
Dioscorea bulbifera represents an African and Asian yam species that escapes from cultivation and invades Florida's wetland margins with remarkable success. The vine grows aggressively, often achieving 70 feet of growth in a single season. It produces aerial tubers—the "potatoes" of its common name—that drop to the ground and sprout new vines, enabling rapid vegetative spread.
Air potato vines climb into forest canopies, smothering native vegetation beneath dense layers of foliage that block sunlight and add tremendous weight to supporting trees. The vine shows particular affinity for wetland edges, where the combination of adequate moisture and forest structure provides ideal conditions for explosive growth.
Florida has deployed biological control for air potato with notable success. The air potato leaf beetle (Lilioceris cheni), released beginning in 2012, feeds voraciously on air potato foliage and has established populations across much of the plant's Florida range.[13] The beetle doesn't eradicate air potato but reduces vine vigor and tuber production substantially, making populations more manageable.
Whether grazing can complement biological control remains uncertain. The aerial tubers and mature vines aren't likely targets for livestock consumption, but young shoots and leaves might receive browse pressure, particularly from goats or trained sheep flocks. The rapid regrowth characteristic of air potato might actually favor browse-based management approaches, as the plant would repeatedly produce tender new growth in response to defoliation.
The complete list of Category I invasive species that threaten Florida's wetland margins extends far beyond these highlighted examples. Additional species of concern include:
Ardisia crenata (coral ardisia): A shade-tolerant shrub that invades wetland hammocks and floodplain forests, forming dense understories that exclude native groundcovers.[1]
Lantana camara (lantana): Despite some native Lantana species, the invasive form creates impenetrable thickets in disturbed areas and shows remarkable drought tolerance that allows establishment in transitional zones.[1]
Tradescantia spathacea (Moses-in-the-cradle): A ground cover species that forms dense colonies in moist, shaded areas, particularly along wetland edges.[1]
Ruellia simplex (Mexican petunia): An increasingly common invader of wetland margins that spreads both by seed and vegetatively, forming extensive monocultures.[1]
Each species presents unique control challenges. Each alters wetland ecology in specific ways. But collectively, they share the capacity to transform diverse native plant communities into species-poor invasive monocultures that provide minimal wildlife value and degrade essential ecosystem services.
Understanding which invasive species threaten wetland margins means little without the capacity to identify those species in field conditions. This proves more challenging than consulting reference guides and memorizing leaf shapes. Invasive plants don't announce themselves with labels. They grow intermixed with natives, often at various life stages simultaneously. Positive identification requires familiarity with growth habits, seasonal changes, and subtle morphological characters.
Wild grapes demonstrate the identification challenge. Several native grape species inhabit Florida, along with escaped cultivated varieties. Distinguishing among them requires attention to details: tendril branching patterns, bark characteristics, leaf pubescence, fruit size, and seasonal timing. The muscadine grape (V. rotundifolia) typically shows unbranched tendrils and relatively smooth leaves, while summer grape (V. aestivalis) produces branched tendrils and leaves with dense reddish-brown hairs on the undersurface.[2] For vegetation management purposes, the distinction matters less than for botanical surveys, since all vigorous grape populations creating management problems respond similarly to grazing pressure. But accurate identification enables better record-keeping and more precise communication with other land managers.
Greenbrier identification presents similar complexity. The genus Smilax includes numerous species that share the characteristic prickles and climbing habit but differ in leaf shape, stem features, and habitat preferences. Smilax rotundifolia typically displays heart-shaped leaves and occurs in diverse habitats from dry forests to wetlands. Smilax laurifolia shows more elongated leaves and favors wetter sites. Smilax bona-nox exhibits the most formidable prickles—hence its common name "saw greenbrier"—and often displays variegated leaf patterns.[6]
For managers implementing grazing-based control, distinguishing greenbrier from superficially similar plants matters more than differentiating among Smilax species. Several non-Smilax vines receive common names including "brier" or "briar": dewberries (Rubus spp.), blackberries (Rubus spp.), and others. True greenbriers demonstrate distinctive features including parallel-veined leaves (unusual for dicots), stem prickles rather than thorns or spines, and unbranched tendrils emerging from leaf petioles. Learning these diagnostic characters enables rapid field identification.
The FISC Category I invasive species require even more careful attention. Many remain relatively uncommon in some regions, meaning field recognition builds slowly through repeated exposure. Brazilian pepper seedlings, for instance, bear little resemblance to mature trees and might be overlooked or misidentified during wetland surveys. Cogongrass displays distinctive characteristics—white midribs, compressed stems, windmill-like growth—but can be confused with other grasses when not closely examined. Torpedograss looks unremarkable among the diverse aquatic grasses in wetland edges until its aggressive growth habit reveals its identity.
Developing field identification skills requires time spent observing plants through their complete annual cycles, noting seasonal changes in appearance, and building the mental reference library that enables instant recognition. Photographs aid this process but can't replace direct experience. Three-dimensional structure, growth context, and tactile characteristics all contribute to accurate identification—information that two-dimensional images cannot fully convey.
Identifying problematic vegetation accomplishes little for grazing-based management unless livestock can obtain adequate nutrition while consuming target species. Sheep won't effectively control invasive populations if they must simultaneously receive intensive supplemental feeding to maintain body condition. The approach becomes economically sustainable only when problem plants provide at least maintenance-level nutrition, with supplements required only during the highest demand periods such as late pregnancy and early lactation.
The research on grape foliage consumption suggests cautious optimism. Fresh grape leaves demonstrate nutritive values roughly comparable to average-quality hay—adequate for maintenance and modest production demands but insufficient alone for supporting high milk production or rapid lamb growth.[3] Sheep in vineyard grazing operations typically receive grape foliage as part of a mixed diet including grass, forbs, and other browse species. This dietary diversity appears key to successful application.
Greenbrier offers more promising nutritional characteristics, at least when maintained in active growth. The documented increase in protein content following fire disturbance—reaching 19 percent crude protein in some studies[8]—places actively growing greenbrier among high-quality forages. The heavy wildlife utilization of tender greenbrier shoots supports the interpretation that young growth provides excellent nutrition.
The limitation is that mature, woody greenbrier stems offer far lower nutritional value. Fiber content increases, digestibility decreases, and palatability drops as greenbrier shoots lignify into tough, thorny canes. For grazing management to maintain greenbrier in a nutritionally valuable state requires continuous pressure that forces regular resprouting, preventing shoots from maturing into woody growth that livestock avoid.
The forb component of wetland margin vegetation likely provides the most consistently adequate nutrition for grazing sheep. Forbs generally demonstrate higher protein content and greater digestibility than grasses, particularly during active growth periods. The diverse forb communities in disturbed or invaded wetland edges typically include multiple palatable species that sheep readily consume. Even if some forbs prove unpalatable or low in nutritional value, the diversity of species available usually ensures sheep can select adequate diets.
The true invasive species on the FISC list present more challenging nutritional questions. Cogongrass offers poor forage value under most circumstances. Torpedograss has received little study regarding livestock nutrition. Brazilian pepper seedlings contain compounds that may limit intake or palatability. Air potato's suitability as livestock forage remains essentially unknown.
These limitations suggest that grazing-based management of wetland margins shouldn't be conceptualized as sheep consuming only invasive species. Rather, sheep working in these environments consume diverse diets including native and invasive plants, problematic natives, and desirable forages. The management objective becomes shifting plant community composition toward more native and desirable species by maintaining continuous pressure on invasives and overabundant natives, not by attempting to force sheep to subsist on problem species alone.
This nutritional reality shapes realistic expectations for what grazing can achieve. Sheep cannot eradicate cogongrass through grazing pressure alone when alternative forages remain available—the animals will preferentially consume natives and allow cogongrass to persist. But sheep might suppress cogongrass expansion, prevent seedling establishment of woody invasives, maintain greenbrier in a controlled state, and reduce wild grape populations to functional levels—all while obtaining adequate nutrition from the mixed plant communities characteristic of wetland margins.
Abstract discussions of which species sheep might control and what nutritional limitations apply yield hypotheses requiring field validation. Actual vegetation management demands real animals working in real landscapes with all their complexity, variability, and unpredictability.
Black Hammock Farms' experience with trained Katahdin flocks in densely vegetated wetland margins offers ground-truth data supporting several key conclusions. Photographic documentation of treatment areas shows dramatic reductions in vegetation density over the course of several months of managed grazing. Areas where human passage required forcing through thorny barriers became relatively open, with sight lines extending tens of feet rather than mere yards.
The before-and-after comparisons reveal that wild grape populations respond particularly well to sustained sheep pressure. Dense tangles of grape vines that created canopy-level coverage get systematically reduced, with sheep consuming both the leafy growing tips and older leaves. The vines don't disappear entirely—their woody trunks persist—but the suppression of new growth and gradual weakening of plants shifts the competitive balance away from grapes and toward species that can tolerate moderate shade and browsing pressure.

Greenbrier populations show similar responses. The documentation captures sections of wetland margin where greenbrier had formed nearly impenetrable thickets prior to sheep introduction. After several rotations of intensive grazing, the same areas support much reduced greenbrier populations. The thorny vines remain present but at densities that no longer preclude human or wildlife movement. Importantly, the greenbrier appears maintained in a state of continual regrowth, producing the tender shoots that sheep find palatable rather than the woody, mature canes they avoid.
Perhaps most telling, the photographic record shows signs of understory recovery. In areas where dense overgrowth had created near-monocultures of grape and greenbrier, the reduction in canopy coverage allowed light to reach the forest floor again. Native groundcovers began reestablishing. The structural complexity characteristic of healthy wetland margins—a layered community including canopy trees, midstory shrubs, and diverse groundcovers—started returning to areas that had been reduced to simplified tangle-and-shadow ecosystems.

The documentation also reveals limitations. Saw palmetto, a native species providing important wildlife habitat, persists essentially untouched by sheep grazing. The animals navigate around palmetto clumps rather than consuming them. This selectivity proves beneficial from a conservation perspective—palmetto should remain in these communities—but it demonstrates that sheep don't indiscriminately clear all vegetation.
Similarly, mature woody stems of invasive shrubs show little impact from sheep browsing. Brazilian pepper seedlings might receive browse pressure, but established shrubs with trunk diameters exceeding a few inches remain essentially unaffected. This limitation emphasizes that grazing-based management works preventively, suppressing seedling recruitment and maintaining existing populations at functional levels, rather than removing mature invasive woody plants already established.
The forb layer—diverse, dynamic, and difficult to characterize in before-and-after photographs—appears substantially reduced in grazed areas. This reduction might concern managers if the forb community consisted primarily of desirable native species. The reality in heavily disturbed wetland margins is that forb layers typically include problematic weeds, escaped ornamentals, and aggressive pioneers. Sheep grazing reduces this often-weedy component, creating opportunities for native species to reestablish from soil seed banks or colonize from adjacent populations.
This inventory of target species, nutritional considerations, and field observations generates several conclusions relevant to designing practical vegetation management strategies for Florida's wetland margins.
First, the species most amenable to control through sheep grazing include those that maintain high palatability and nutritional value when actively growing: wild grapes, young greenbrier shoots, diverse forbs, and the seedling stages of some woody invasives. These targets align well with sheep dietary preferences and provide adequate nutrition to maintain animal condition without intensive supplemental feeding.
Second, the most problematic invasive species from an ecological perspective—cogongrass, mature torpedograss stands, established Brazilian pepper—rank among the least suitable targets for grazing-based control. Sheep won't preferentially consume these species when alternative forages exist, and forcing consumption through extreme stocking pressure or forage limitation would compromise animal welfare and productivity.
This apparent paradox—the worst invaders make the poorest grazing targets—doesn't invalidate grazing as a management tool. It reframes the strategic question. Rather than asking "Can sheep remove existing cogongrass infestations?" the relevant question becomes "Can sheep working in wetland margins suppress the expansion of cogongrass from existing patches, prevent new establishment, maintain native vegetation resilience, and create conditions that resist invasion?"
Reframed thus, the answer trends more positive. Sheep maintaining continuous grazing pressure in transitional zones can prevent woody plant seedling establishment, suppress aggressive native vines, reduce fuel loads, consume forbs that might otherwise outcompete native grasses, and maintain overall vegetation density at levels that resist the establishment of new invasive populations.
Third, successful application requires thinking of grazing animals not as standalone vegetation control tools but as components of integrated management systems. Sheep work best in combination with other approaches: initial mechanical removal of mature invasive woody plants, followed by sheep grazing to suppress resprouting and prevent seedling recruitment; prescribed fire to reset vegetation communities, followed by sheep grazing to prevent undesirable species from dominating during the recovery period; herbicide treatment of discrete invasive patches that sheep avoid, while sheep manage the broader matrix of vegetation surrounding those patches.
Fourth, the timing and intensity of grazing interventions matter as much as the choice to employ livestock at all. Continuous grazing at moderate intensity produces different outcomes than short-duration, high-intensity grazing rotations. Different seasons favor control of different species. Young greenbrier shoots emerging in spring offer the most palatable target. Grape vines putting on new growth after rain events provide temporarily abundant forage. Matching grazing timing to phenology improves both vegetation control outcomes and livestock nutrition.
Finally, documenting outcomes remains essential. The field evidence from Black Hammock Farms demonstrates proof-of-concept, but expanding application to diverse sites across Florida's varied wetland systems requires systematic monitoring. Which species actually decrease under grazing pressure? Which persist or even increase? Do native species recover, or do grazed areas simply shift from one problematic community composition to another? These questions demand data—vegetation surveys, photographic monitoring, assessments of wildlife use—not assumptions.
This examination of specific target species establishes the foundation for practical application. We know now which plants threaten Florida's wetland margins. We understand, at least preliminarily, which of those species might respond to grazing-based management and which require alternative control approaches. We've seen field evidence that trained Katahdin flocks can navigate dense vegetation and effect measurable changes in plant community composition.
What remains is translating this knowledge into implementable management systems. That translation requires understanding not just which plants to target but how to deploy livestock most effectively—the grazing strategies, stocking rates, rotation schedules, seasonal timing, and integration with other management tools that transform individual observations into repeatable, scalable approaches.
It requires understanding what makes Katahdin sheep specifically—rather than sheep generally or livestock broadly—particularly well-suited to this application. The climatic challenges of Florida's subtropical wetlands eliminate most livestock options. The parasite pressures inherent in warm, wet environments where animals must work through dense vegetation create health management challenges that conventional sheep breeds cannot withstand. The need for year-round operation rather than seasonal use demands animals that maintain fertility and productivity across Florida's minimal seasonal variation.
These requirements describe not just any grazing animal but a specifically adapted breed with characteristics shaped by both natural selection in challenging tropical environments and deliberate breeding for performance under subtropical conditions. Understanding why Katahdin sheep can thrive where other breeds fail completes the foundation for practical application.
In Part 3 of this series, we'll shift focus from the problem and the targets to the solution. We'll examine the Katahdin breed's unique adaptations to subtropical environments, document the scientific evidence supporting their suitability for Florida applications, and analyze the specific characteristics that enable these animals to work effectively in the challenging conditions of wetland margin vegetation management. The pieces are coming together—problematic vegetation identified, grazing targets selected, field evidence gathered. Now we turn to the animals themselves and what makes them uniquely qualified for this critical work.

1579 Walsh Street Oviedo,
Florida 32765

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